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27 results on '"Novel Advanced Nano-Objects (LCMCP-NANO)"'

1. Revealing the Elusive Structure and Reactivity of Iron Boride α-FeB

Author: Fernando Igoa Saldaña, Emile Defoy, Daniel Janisch, Gwenaëlle Rousse, Pierre-Olivier Autran, Anissa Ghoridi, Amandine Séné, Marzena Baron, Leopoldo Suescun, Yann Le Godec, David Portehault, Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Design et étude de nouveaux matériaux à propriété remarquables [IMPMC] (IMPMC_DEMARE), Institut de minéralogie, de physique des matériaux et de cosmochimie (IMPMC), Muséum national d'Histoire naturelle (MNHN)-Institut de recherche pour le développement [IRD] : UR206-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Muséum national d'Histoire naturelle (MNHN)-Institut de recherche pour le développement [IRD] : UR206-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Collège de France - Chaire Chimie du solide et énergie, Chimie du solide et de l'énergie (CSE), Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Réseau sur le stockage électrochimique de l'énergie (RS2E), Aix Marseille Université (AMU)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Collège de France (CdF (institution))-Université de Picardie Jules Verne (UPJV)-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP ), Université Grenoble Alpes (UGA)-Université Grenoble Alpes (UGA)-Nantes Université (Nantes Univ)-Université de Montpellier (UM)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM), Université de Montpellier (UM), European Synchroton Radiation Facility [Grenoble] (ESRF), Laboratorio de Cristalografıa, Estado Solido y Materiales [UCUR] (Cryssmat-Lab), Universidad de la República [Montevideo] (UDELAR), and Doctoral School ED397ESRF proposal MA-5188
Subjects: Inorganic Chemistry, crystal structure, borides, intergrowth, in situ XRD, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, Physical and Theoretical Chemistry, FAULTS
Abstract: International audience; Crystal structures can strongly deviate from bulk states when confined into nanodomains. These deviations may deeply affect properties and reactivity and then call for a close examination. In this work, we address the case where extended crystal defects spread through a whole solid and then yield an aperiodic structure and specific reactivity. We focus on iron boride, α-FeB, whose structure has not been elucidated yet, thus hindering the understanding of its properties. We synthesize the two known phases, α-FeB and β-FeB, in molten salts at 600 and 1100 °C, respectively. The experimental X-ray diffraction (XRD) data cannot be satisfactorily accounted for by a periodic crystal structure. We then model the compound as a stochastic assembly of layers of two structure types. Refinement of the powder XRD pattern by considering the explicit scattering interference of the different layers allows quantitative evaluation of the size of these domains and of the stacking faults between them. We, therefore, demonstrate that α-FeB is an intergrowth of nanometer-thick slabs of two structure types, β-FeB and CrB-type structures, in similar proportions. We finally discuss the implications of this novel structure on the reactivity of the material and its ability to perform insertion reactions by comparing the reactivities of α-FeB and β-FeB as reagents in the synthesis of a model layered material: Fe2AlB2. Using synchrotron-based in situ X-ray diffraction, we elucidate the mechanisms of the formation of Fe2AlB2. We highlight the higher reactivity of the intergrowth α-FeB in agreement with structural relationships.
Published: 2023
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2. Liquid Processing of Bismuth–Silica Nanoparticle/Aluminum Matrix Nanocomposites for Heat Storage Applications

Author: Binghua Ma, Walid Baaziz, Léo Mazerolles, Ovidiu Ersen, Bernard Sahut, Clément Sanchez, Stéphane Delalande, David Portehault, Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Stellantis - PSA Centre Technique de Vélizy, Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et Nanosciences Grand-Est (MNGE), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie et des Matériaux Paris-Est (ICMPE), Institut de Chimie du CNRS (INC)-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)-Centre National de la Recherche Scientifique (CNRS), Portehault, David, and Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et nanosciences d'Alsace (FMNGE)
Subjects: heat storage, [CHIM.INOR] Chemical Sciences/Inorganic chemistry, [CHIM.MATE] Chemical Sciences/Material chemistry, phase change, aluminum, bismuth, nanoparticles, General Materials Science, [CHIM.MATE]Chemical Sciences/Material chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, composites, core−shell
Abstract: International audience; Metal matrix nanocomposites encompassing low-melting point metal nano-inclusions are promising candidates for thermal regulation of devices at high temperature. They are usually processed by solid-state routes that provide access to a limited range of materials and are hardly compatible with complex shaping processes and with large-scale applications. Herein, we develop a liquid-phase processing technique to design aluminum matrix nanocomposites made of phase change nanoparticles, using bismuth nanoparticles as a proof-of-concept. The bismuth nanoparticles derived from colloidal chemistry are first encapsulated in a silica shell and then dispersed by ultrasonication into molten aluminum. Using X-ray diffraction, electron microscopy, and X-ray photoelectron spectroscopy, we probe the evolution of the bismuth particles and of the inorganic shell. We demonstrate that the silica shell acts as a barrier against extensive coalescence of particles during the dispersion process, thus enabling a decrease and a widening of the phase change temperature range.
Published: 2022
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3. Hydroxyapatites as Versatile Inorganic Hosts of Unusual Pentavalent Manganese Cations

Author: María Hernando, José M. González-Calbet, Marina Parras, Christel Laberty-Robert, Aurea Varela, Gwenaëlle Rousse, José Luis Martínez, Laura Serrador, David Portehault, María Teresa Fernández-Díaz, Francisco Gonell, E. Matesanz, Clément Sanchez, Isabel Gómez-Recio, Almudena Torres-Pardo, Universidad Complutense de Madrid = Complutense University of Madrid [Madrid] (UCM), Institut Laue-Langevin (ILL), ILL, Laboratoire des Sciences du Numérique de Nantes (LS2N), IMT Atlantique Bretagne-Pays de la Loire (IMT Atlantique), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-Université de Nantes - UFR des Sciences et des Techniques (UN UFR ST), Université de Nantes (UN)-Université de Nantes (UN)-École Centrale de Nantes (ECN)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Sorbonne Université (SU), Chaire Chimie des matériaux hybrides, and Reactive Materials for Electrochemical Systems (LCMCP-RMES )
Subjects: Chemistry, General Chemical Engineering, chemistry.chemical_element, [CHIM.MATE]Chemical Sciences/Material chemistry, 02 engineering and technology, General Chemistry, Manganese, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, Polymer chemistry, Materials Chemistry, Hydroxyapatites, 0210 nano-technology
Abstract: International audience; Contrary to molecular species, only very few solids are reported to host manganese (V) species. Herein, we report three new compounds with a hydroxyapatite structural backbone built on the Mn V O 4 3− anion: Sr 5 [(Mn 1−x Si x)O 4 ] 3 (OH) 1−3x (x =0 and 0.053), Sr 5 (MnO 4) 3 (OH) 1−y F y (y = 0.90), and Sr 5 [(Mn 1−x Si x)-O 4 ] 3 F 1−3x (x = 0.058). These solids are fully characterized using powder X-ray and neutron powder diffraction, scanning transmission electron microscopy, electron energy loss spectroscopy (EELS), thermogravimetric analysis, and magnetic measurements. Especially, we report for the first time EELS Mn−L 2,3 spectra of manganese with the oxidation state (V). Contrary to other Mn(V) oxides, these solids and the nominal compound Sr 5 (MnO 4) 3 OH do not comprise Ba 2+ cations but rely only on Sr 2+ cations, showing that barium is not a required element to stabilize Mn(V) species in inorganic solids. We show that by tuning soft chemistry conditions on the one hand and post-treatment topological transformation conditions on the other hand, Mn(V) and hydroxyl groups can be substituted by Si(IV) and fluoride ions, respectively. Hence, we deliver solids with a potentially wide composition range. These compounds show significant oxygen anionic conduction, thus suggesting the emergence of new functional materials built from high-oxidation state manganese cations.
Published: 2020
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4. Ultrasound-Assisted Liquid-Phase Synthesis and Mechanical Properties of Aluminum Matrix Nanocomposites Incorporating Boride Nanocrystals

Author: Ma, Binghua, Gómez-Recio, Isabel, Gómez‐recio, Isabel, Mazerolles, L., Mazeran, Pierre‐emmanuel, Sanchez, Clément, Delalande, Stéphane, Portehault, David, Institut de Chimie et des Matériaux Paris-Est (ICMPE), Institut de Chimie du CNRS (INC)-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)-Centre National de la Recherche Scientifique (CNRS), Stellantis France, Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Roberval (Roberval), and Université de Technologie de Compiègne (UTC)
Subjects: Materials science, Nucleation, Nanoparticle, 02 engineering and technology, mechanical properties, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 01 natural sciences, Biomaterials, chemistry.chemical_compound, Boride, 0103 physical sciences, metal matrix nanocomposites, General Materials Science, ComputingMilieux_MISCELLANEOUS, Grain boundary strengthening, 010302 applied physics, Nanocomposite, boride nanoparticles, [CHIM.MATE]Chemical Sciences/Material chemistry, General Chemistry, Nanoindentation, 021001 nanoscience & nanotechnology, Grain size, Nanocrystal, Chemical engineering, chemistry, 0210 nano-technology, Biotechnology
Abstract: International audience; Incorporating boride nanocrystals could significantly impact the mechanical properties of aluminum alloys. Molten salts synthesis offers opportunities to fabricate superhard boride nanoparticles, which can sustain the harsh conditions during the liquid-phase design of metallic nanocomposites. Here hafnium diboride-aluminum nanocomposites are unveiled from molten salt-derived HfB2 nanoparticles sequentially dispersed in aluminum by ultrasound treatment. The structure and size of the nanocrystals are retained in the final nanocomposites, supporting their high chemical stability. Semicoherent interfaces between the nanoparticles and the matrix are then evidenced by TEM, suggesting that the nanocrystals could promote heterogeneous nucleation of Al and then limit the Al grain size to ≈20 µm. Nanoindentation measurements reveal significant grain boundary strengthening and grain refinement effects. It is finally shown that HfB2 nanoparticles also enable a decrease in matrix grain size and an increase in the hardness of the AlSi7Cu0.5Mg0.3 alloy. These proof-of-concept materials are paving the way to light-weight Al matrix nanocomposites doped by molten-salt synthesized nanoparticles.
Published: 2021
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5. Alkoxysilane effect in hybrid material: A comparison of pHEMA-TiO2 and pMAPTMS-TiO2 nanoparticulate hybrids

Author: François Ribot, Andrei Kanaev, Arseniy I. Kuznetsov, Laurence Rozes, A.P. Diaz-Gomez, Mamadou Kaba Traoré, Pavlo Gorbovyi, Boris N. Chichkov, Clément Sanchez, Luc Museur, Laboratoire d'Ingénierie des Matériaux et des Hautes Pressions (LIMHP), Centre National de la Recherche Scientifique (CNRS)-Institut Galilée-Université Paris 13 (UP13), Laboratoire des Sciences des Procédés et des Matériaux (LSPM), Université Paris 13 (UP13)-Institut Galilée-Université Sorbonne Paris Cité (USPC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Physique des Lasers (LPL), Université Paris 13 (UP13)-Centre National de la Recherche Scientifique (CNRS), Chaire Chimie des matériaux hybrides, Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Procédés (LCMCP-MHP ), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Novel Advanced Nano-Objects (LCMCP-NANO), and Laser Zentrum Hannover e.V. (LZH)
Subjects: Materials science, Mechanical Engineering, Nanoparticle, 02 engineering and technology, 010402 general chemistry, 021001 nanoscience & nanotechnology, Condensed Matter Physics, Methacrylate, 01 natural sciences, 0104 chemical sciences, [SPI]Engineering Sciences [physics], Hydrolysis, Chemical engineering, Photoinduced charge separation, Polymerization, Mechanics of Materials, [CHIM]Chemical Sciences, Molecule, General Materials Science, Quantum efficiency, 0210 nano-technology, Hybrid material, ComputingMilieux_MISCELLANEOUS
Abstract: We report on a comparative study of photonic sensitivities of organic-inorganic hybrids prepared with size-selected 5 nm titanium-oxo-alkoxo nanoparticles and two different organic phases: HEMA (2-hydroxyethyl methacrylate) and MAPTMS (3-methacryloxypropyltrimethoxysilane). After organic polymerization, the obtained pHEMA-TiO2 and pMAPTMS-TiO2 hybrids are solids with different inter-component bindings. While surface exchange fixes organic (HEMA than pHEMA) groups on the nanoparticle surface, the titanium-oxo-alkoxo nanoparticles do not interact with the organic component in the pMAPTMS-TiO2 hydrid. Indeed, MAPTMS molecules are hydrolyzed forming condensed Si O Si species. The formation of Si O Ti bonds is observed at the organic thermal polymerization stage, which may be a signature of the silica layer formation at the particles surface. Consequently, the quantum efficiency of the photoinduced charge separation and storage in pMAPTMS-TiO2 hybrids is found considerably lower compared to that in pHEMA-TiO2 hybrids. The 3D micro-structuring of the hybrid solutions has been realized using 2-photon laser polymerization. The structures were mechanically more stable and easier to achieve in pMAPTMS-TiO2 compared to pHEMA-TiO2. Moreover, higher density of the photoinduced electrons decreases the damage threshold in the pHEMA-TiO2 hybrids.
Published: 2019
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6. The origin of the high electrochemical activity of pseudo-amorphous iridium oxides

Author: Cédric Boissière, Marine Elmaalouf, Clément Sanchez, Mounib Bahri, Jean-Yves Piquemal, Mateusz Odziomek, Andrea Zitolo, Ovidiu Ersen, Benedikt Lassalle-Kaiser, Maxime Gayrard, Marion Giraud, Silvia Duran, Jennifer Peron, Marco Faustini, Cédric Tard, HAL-SU, Gestionnaire, Interfaces, Traitements, Organisation et Dynamique des Systèmes (ITODYS (UMR_7086)), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Procédés (LCMCP-MHP ), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie moléculaire (LCM), École polytechnique (X)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et Nanosciences Grand-Est (MNGE), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Synchrotron SOLEIL (SSOLEIL), Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-École polytechnique (X), Université de Strasbourg (UNISTRA)-Matériaux et nanosciences d'Alsace (FMNGE), and Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique
Subjects: [CHIM.INOR] Chemical Sciences/Inorganic chemistry, Materials science, Science, General Physics and Astronomy, chemistry.chemical_element, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, Electrocatalyst, 01 natural sciences, Article, General Biochemistry, Genetics and Molecular Biology, law.invention, X-ray photoelectron spectroscopy, law, Oxidation state, Porous materials, Calcination, Iridium, Crystallization, [CHIM.MATE] Chemical Sciences/Material chemistry, Energy, Multidisciplinary, Structural properties, 010405 organic chemistry, Oxygen evolution, [CHIM.MATE]Chemical Sciences/Material chemistry, General Chemistry, 0104 chemical sciences, Amorphous solid, Chemical engineering, chemistry, 13. Climate action, Nanoparticles, Electrocatalysis
Abstract: Combining high activity and stability, iridium oxide remains the gold standard material for the oxygen evolution reaction in acidic medium for green hydrogen production. The reasons for the higher electroactivity of amorphous iridium oxides compared to their crystalline counterpart is still the matter of an intense debate in the literature and, a comprehensive understanding is needed to optimize its use and allow for the development of water electrolysis. By producing iridium-based mixed oxides using aerosol, we are able to decouple the electronic processes from the structural transformation, i.e. Ir oxidation from IrO2 crystallization, occurring upon calcination. Full characterization using in situ and ex situ X-ray absorption spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction and transmission electron microscopy allows to unambiguously attribute their high electrochemical activity to structural features and rules out the iridium oxidation state as a critical parameter. This study indicates that short-range ordering, corresponding to sub-2nm crystal size for our samples, drives the activity independently of the initial oxidation state and composition of the calcined iridium oxides., The origins of the superior catalytic activity of poorly crystallized Ir-based oxide material for the OER in acid is still under debate. Here, authors synthesize porous IrMo oxides to deconvolute the effect of Ir oxidation state from short-range ordering and show the latter to be a key factor.
Published: 2021
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7. Electron Precise Sodium Carbaboride Nanocrystals from Molten Salts: Single Sources to Boron Carbides

Author: Gwenaëlle Rousse, Cristina Coelho-Diogo, Christel Gervais, Simon Delacroix, Fernando Igoa, Yann Le Godec, David Portehault, Yang Song, Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut de minéralogie, de physique des matériaux et de cosmochimie (IMPMC), Muséum national d'Histoire naturelle (MNHN)-Institut de recherche pour le développement [IRD] : UR206-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut des matériaux de Paris-Centre (IMPC), Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Spectroscopie, Modélisation, Interfaces pour L'Environnement et la Santé (LCMCP-SMiLES), Chimie du solide et de l'énergie (CSE), Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), HPC resources from GENCI-IDRIS (Grant 097535), and Centre National de la Recherche Scientifique (CNRS)-Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)
Subjects: Octahedral cluster, 010405 organic chemistry, chemistry.chemical_element, Nanoparticle, Crystal structure, Boron carbide, [CHIM.MATE]Chemical Sciences/Material chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 01 natural sciences, 0104 chemical sciences, Inorganic Chemistry, chemistry.chemical_compound, chemistry, X-ray photoelectron spectroscopy, Chemical engineering, Physical and Theoretical Chemistry, Boron, Powder diffraction, Solid solution
Abstract: International audience; Boron-rich solids exhibit specific crystal structures and unique properties, which are only very scarcely addressed in nanoparticles. In this work, we address the original inorganic structural chemistry and reactivity of boron-rich nanoparticles, by reporting the first occurrence of sodium carbaboride nanocrystals based on the NaB 5 C crystal structure. To design these sub-10 nm nano-objects, we use liquid-phase synthesis in molten salts at 900°C. By combining a set of characterization tools including powder Xray powder diffraction, transmission electron microscopy, solid-state nuclear magnetic resonance coupled to DFT modeling, and X-ray photoelectron spectroscopy, we demonstrate that these nanocrystals deviate from the ideal stoichiometry reported for the bulk compound. We suggest that the carbon and sodium contents compensate each other to ensure that the octahedral cluster-based framework is stabilized by fulfilling an electron counting rule. These nanocrystals encompass substituted octahedral covalent structural building units not reported in the related bulk compound. They then shed new light on the ability of nanoparticles to host wide solid solution ranges in covalent solids and then to yield new solids. We finally show that these nanocrystals are efficient single sources of boron and carbon to form a nanostructured boron carbide, thus paving the way to new nanostructured materials.
Published: 2021
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8. Phase selective synthesis of nickel silicide nanocrystals in molten salts for electrocatalysis of the oxygen evolution reaction

Author: Ovidiu Ersen, Ram Kumar, Mounib Bahri, Christel Laberty-Robert, Cyril Thomas, Yang Song, David Portehault, Francisco Gonell, Clément Sanchez, Portehault, David, Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et Nanosciences Grand-Est (MNGE), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Réactivité de Surface (LRS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Chaire Chimie des matériaux hybrides, Reactive Materials for Electrochemical Systems (LCMCP-RMES ), Université de Strasbourg (UNISTRA)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, and Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)
Subjects: [PHYS]Physics [physics], chemistry.chemical_classification, [CHIM.MATE] Chemical Sciences/Material chemistry, Materials science, Oxygen evolution, Intermetallic, chemistry.chemical_element, Salt (chemistry), [CHIM.MATE]Chemical Sciences/Material chemistry, 02 engineering and technology, 010402 general chemistry, 021001 nanoscience & nanotechnology, Electrocatalyst, 01 natural sciences, [PHYS] Physics [physics], 0104 chemical sciences, Sodium silicide, chemistry.chemical_compound, Nickel, chemistry, Chemical engineering, General Materials Science, Iridium, 0210 nano-technology, Eutectic system
Abstract: International audience; We report phase selective synthesis of intermetallic nickel silicide nanocrystals in inorganic molten salts. NiSi and Ni2Si nanocrystals are obtained by reacting a nickel (II) salt and sodium silicide Na4Si4 in the molten LiI-KI inorganic eutectic salt mixture. We report that nickel silicide nanocrystals are precursors to active electrocatalysts in the oxygen evolution reaction (OER) and may be low-cost alternatives to iridium-based electrocatalysts.
Published: 2020
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9. Origin of transparency in scattering biomimetic collagen materials

Author: Flore Salviat, Milena Lama, Nadine Nassif, Clément Sanchez, Marco Faustini, Marc Robin, Jean-Marie Chassot, Rémi Carminati, Elodie Moulongui, Arnaud Bardouil, Mohamed Selmane, Yan Wang, Marie-Madeleine Giraud-Guille, Alba Marcellan, Elora Bessot, Chrystelle Salameh, Franck Artzner, Institut Européen des membranes (IEM), Centre National de la Recherche Scientifique (CNRS)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Université Montpellier 2 - Sciences et Techniques (UM2)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM), Chaire Chimie des matériaux hybrides, Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut Laue-Langevin (ILL), ILL, Institut de Physique de Rennes (IPR), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS), Institut des matériaux de Paris-Centre (IMPC), Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Sciences et Ingénierie de la Matière Molle (UMR 7615) (SIMM), Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut Langevin - Ondes et Images (UMR7587) (IL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), Collège de France (CdF)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), ESPCI ParisTech, Ecole Nationale Supérieure de Chimie de Paris- Chimie ParisTech-PSL (ENSCP)-ESPCI ParisTech-Sorbonne Université (SU), Sciences et Ingénierie de la Matière Molle (SIMM), PSL Research University (PSL)-Sorbonne Université (SU)-ESPCI ParisTech-Centre National de la Recherche Scientifique (CNRS), Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Procédés (LCMCP-MHP ), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), and Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Subjects: collagen, Materials science, [SDV]Life Sciences [q-bio], [PHYS.PHYS.PHYS-BIO-PH]Physics [physics]/Physics [physics]/Biological Physics [physics.bio-ph], Fibrillar Collagens, 02 engineering and technology, mechanical properties, 010402 general chemistry, 01 natural sciences, Light scattering, Photonic metamaterial, Cornea, Biomimetic Materials, Biomimetics, Phase (matter), Animals, Transparency (data compression), Microscale chemistry, Phase diagram, transparency, [PHYS]Physics [physics], [PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics], Multidisciplinary, Scattering, self-assembly, [CHIM.MATE]Chemical Sciences/Material chemistry, 021001 nanoscience & nanotechnology, photonic materials, 0104 chemical sciences, Order (biology), [CHIM.POLY]Chemical Sciences/Polymers, Chemical physics, Physical Sciences, [PHYS.PHYS.PHYS-MED-PH]Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph], [PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph], 0210 nano-technology
Abstract: International audience; Living tissues, heterogeneous at the microscale, usually scatter light. Strong scattering is responsible for the whiteness of bones, teeth, and brain and is known to limit severely the performances of biomedical optical imaging. Transparency is also found within collagen-based extracellular tissues such as decalcified ivory, fish scales, or cornea. However, its physical origin is still poorly understood. Here, we unveil the presence of a gap of transparency in scattering fibrillar collagen matrices within a narrow range of concentration in the phase diagram. This precholesteric phase presents a three-dimensional (3D) orientational order biomimetic of that in natural tissues. By quantitatively studying the relation between the 3D fibrillar network and the optical and mechanical properties of the macroscopic matrices, we show that transparency results from structural partial order inhibiting light scattering, while preserving mechanical stability, stiffness, and nonlinearity. The striking similarities between synthetic and natural materials provide insights for better understanding the occurring transparency.
Published: 2020
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10. Following in Situ the Degradation of Mesoporous Silica in Biorelevant Conditions: At Last, a Good Comprehension of the Structure Influence

Author: Zeinab Chehadi, Corinne Chanéac, David Grosso, Omar Azzaroni, Clément Sanchez, Cédric Boissière, Pierre-Antoine Albouy, Marco Faustini, Andrea Cattoni, Elisa Bindini, Chaire Chimie des matériaux hybrides, Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Centre de Nanosciences et de Nanotechnologies (C2N), Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Physique des Solides (LPS), Institut des Matériaux, de Microélectronique et des Nanosciences de Provence (IM2NP), Université de Toulon (UTLN)-Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU), Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas [La Plata] (INIFTA), Facultad de Ciencias Exactas [La Plata], Universidad Nacional de la Plata [Argentine] (UNLP)-Universidad Nacional de la Plata [Argentine] (UNLP), Matériaux Hybrides et Procédés (LCMCP-MHP ), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Aix Marseille Université (AMU)-Université de Toulon (UTLN)-Centre National de la Recherche Scientifique (CNRS), and Novel Advanced Nano-Objects (LCMCP-NANO)
Subjects: In situ, Materials science, Nanoparticle, Nanotechnology, 02 engineering and technology, therapeutic vectors, 010402 general chemistry, 01 natural sciences, dissolution kinetic, Drug Delivery Systems, Ellipsometry, [CHIM]Chemical Sciences, Humans, General Materials Science, mesoporous silica, Porosity, Drug Carriers, High loading, Proteins, Mesoporous silica, 021001 nanoscience & nanotechnology, Silicon Dioxide, 0104 chemical sciences, Drug Liberation, Kinetics, Drug delivery, Degradation (geology), Nanoparticles, 0210 nano-technology, protein, ellipsometry
Abstract: International audience; Mesoporous silica nanoparticles (MSNs) have seen a fast development as drug delivery carriers thanks to their tunable porosity and high loading capacity. The employ of MSNs in biomedical applications requires a good understanding of their degradation behavior both to control drug release and to assess possible toxicity issues on human health. In this work, we study mesoporous silica degradation in biologically relevant conditions through in situ ellipsometry on model mesoporous nanoparticle or continuous thin films, in buffer solution and in media containing proteins. In order to shed light on the structure/dissolution relationship, we performed dissolution experiments far from soluble silicate species saturation. Via a complete decorrelation of dissolution and diffusion contributions, we proved unambiguously that surface area of silica vectors is the main parameter influencing dissolution kinetics, while thermal treatment and open mesoporous network architecture have a minor impact. As a logical consequence of our dissolution model, we proved that the dissolution lag-time can be promoted by selective blocking of the mesopores that limits the access to the mesoporous internal surface. This study was broadened by studying the impact of the organosilanes in the silica structure, of the presence of residual structuring agents, and of the chemical composition of the dissolution medium. The presence of albumin at blood concentration was found affecting drastically the dissolution kinetics of the mesoporous structure, acting as a diffusion barrier. Globally, we could identify the main factors affecting mesoporous silica materials degradation and proved that we can tune their structure and composition for adjusting dissolution kinetics in order to achieve efficient drug delivery.
Published: 2020
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11. Modified Synthesis Strategies for the Stabilization of low n Tin O2n-1 Magnéli Phases

Author: Clément Sanchez, David Portehault, Luisa Ruiz-González, Marina Parras, Alberto Azor-Lafarga, José M. González-Calbet, Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), and Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Materials science, General Chemical Engineering, Superlattice, chemistry.chemical_element, Nanoparticle, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Biochemistry, Metal, Transition metal, Materials Chemistry, ComputingMilieux_MISCELLANEOUS, Sol-gel, Electron energy loss spectroscopy, [CHIM.MATE]Chemical Sciences/Material chemistry, General Chemistry, 021001 nanoscience & nanotechnology, 0104 chemical sciences, chemistry, Chemical physics, visual_art, visual_art.visual_art_medium, 0210 nano-technology, Tin, Titanium
Abstract: Titanium reduced oxides TiO2-x occupy, since long time, a prominent place on the landscape of binary metal oxides because of their intriguing ability to form extended defects that affect both the formation of new superlattices and different electronic behaviours. Related to these features, a wide range of practical applications has been achieved. Moved by the conviction of the great potential of understanding the influence of the reactivity, compositional variations and size effects on their functional properties, the aim of this personal account is the optimization of a recently developed strategy for the stabilization of low n Tin O2n-1 terms. In particular, we will focus on the Ti4 O7 composition as well as the incorporation of transition metals, like Mn, in order to deal with new reduced Magneli phases.
Published: 2018
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12. Multicationic Sr4Mn3O10 mesostructures: molten salt synthesis, analytical electron microscopy study and reactivity

Author: Irma N. González-Jiménez, Juan C. Hernández-Garrido, Christel Laberty-Robert, David Portehault, Clément Sanchez, Miguel López-Haro, Almudena Torres-Pardo, José M. González-Calbet, Marina Parras, Simon Rano, José J. Calvino, Aurea Varela, Universidad Complutense de Madrid = Complutense University of Madrid [Madrid] (UCM), Chaire Chimie des matériaux hybrides, Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Reactive Materials for Electrochemical Systems (LCMCP-RMES ), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Universidad de Cádiz (UCA), and Novel Advanced Nano-Objects (LCMCP-NANO)
Subjects: Materials science, Nanostructure, Process Chemistry and Technology, Electron energy loss spectroscopy, 02 engineering and technology, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, Surface energy, 0104 chemical sciences, chemistry.chemical_compound, Electron tomography, chemistry, Chemical engineering, Mechanics of Materials, Transmission electron microscopy, Strontium hydroxide, General Materials Science, Surface charge, Electrical and Electronic Engineering, Molten salt, 0210 nano-technology
Abstract: International audience; Inorganic molten salts are known as fluxes for the synthesis of novel bulk inorganic compounds and of mesostructures and nanostructures with crystal habits different from those observed in more conventional solvents. However, they have not demonstrated the ability to provide mesostructures and nanostructures of complex metal oxides that are currently unreported at the mesoscale and nanoscale. In this report, we show the first occurrence of Sr4Mn3O10 at the mesoscale, as platelets synthesized in molten strontium hydroxide at 600 °C with basal faces of few hundreds of nanometers and thicknesses ranging from 20 to 100 nm. We address carefully the atom-scale structure by transmission electron microscopy, including electron energy loss spectroscopy and electron tomography. We then propose that the final morphology is driven by the surface charge of each facet through surface energy. The reactivity of these platelets is then addressed, highlighting cation leaching when in contact with acidic water, which results in crystalline–amorphous core–shell platelets that are active electrocatalysts towards the oxygen reduction reaction.
Published: 2018
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13. Metal-Dependent Interplay between Crystallization and Phosphorus Diffusion during the Synthesis of Metal Phosphide Nanoparticles

Author: Sophie Carenco, Nicolas Mézailles, Ileana Florea, Cédric Boissière, Ovidiu Ersen, Clément Sanchez, Y. Hu, Laboratoire Hétéroéléments et Coordination (DCPH), École polytechnique (X)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Procédés (LCMCP-MHP ), and Chaire Chimie des matériaux hybrides
Subjects: Materials science, Amorphous metal, White Phosphorus, Phosphide, General Chemical Engineering, Inorganic chemistry, Nanoparticle, 02 engineering and technology, General Chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, law.invention, Amorphous solid, chemistry.chemical_compound, chemistry, law, Materials Chemistry, [CHIM]Chemical Sciences, Reactivity (chemistry), Crystallization, 0210 nano-technology, Stoichiometry
Abstract: International audience; The interplay between crystallization and phosphorus diffusion in the versatile synthesis of metal phosphide nanoparticles from well-defined metal nanoparticles is studied by using a favorable "P(0)" source for mechanistic studies: white phosphorus. In this study, the reaction of Ni, Fe, Pd, and Cu nanoparticles with P 4 was quantitative even at relatively low temperatures thanks to the high reactivity of this soluble "P" source. Intermediate amorphous alloys could be identified for the first time in the case of Fe and Pd, while the quantitative character of the reaction provided a selective and controlled access to Pd 5 P 4 versus PdP 2 and Cu 3 P versus CuP 2. Morphological evolution of the nanoparticles with temperature and M/P stoichiometry was also discussed and provided new insights in the kinetics of the reaction in each case. Hollow Ni 2 P and FeP nanoparticles were finally obtained while the particularly high stability of the amorphous plain Pd 3 P nanoparticles was uncovered.
Published: 2012
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14. Probing Ionic Association on Metal Oxide Clusters by Pulsed Field Gradient NMR Spectroscopy: The Example of Sn12–Oxo Clusters

Author: Laurent Ghys, Virginie Escax, François Ribot, José C. Martins, Ingrid Verbruggen, Monique Biesemans, Rudolph Willem, Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), High-Resolution NMR Centre, Vrije Universiteit Brussel (VUB), High Resolution NMR Centre, and Vrije Universiteit Brussel
Subjects: Magnetic Resonance Spectroscopy, Diffusion, Analytical chemistry, Ionic bonding, 02 engineering and technology, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 01 natural sciences, Catalysis, chemistry.chemical_compound, Hydroxides, Organometallic Compounds, Spectroscopy, ComputingMilieux_MISCELLANEOUS, Organometallic chemistry, Ion exchange, Organic Chemistry, Oxides, General Chemistry, Nuclear magnetic resonance spectroscopy, 021001 nanoscience & nanotechnology, 0104 chemical sciences, chemistry, Tin, Proton NMR, Physical chemistry, 0210 nano-technology, Pulsed field gradient
Abstract: Pulsed field gradient 1 H NMR spectroscopy has been applied to investigate the association behavior of the Sn 1 2 -oxo cluster macrocation [(BuSn) 1 2 O 1 4 (OH) 6 ] 2 + with two different and smaller anions, p-toluenesulfonate (PTS - ) and diphenylphosphinate (Ph 2 PO 2 -). By monitoring the translational diffusion coefficients of the various species involved, it is shown that the association depends on the anion involved and on the solvent used. Moreover, the possibility to individually monitor the diffusion characteristics of multiple anionic and cationic species in mixtures, by virtue of resolved 1 H resonances available from each species, allows us to evidence the occurrence of ion exchange in such systems. Thus when [(BuSn) 1 2 O 1 4 (OH) 6 ](PTS) 2 is mixed with two equivalents of Ph 2 PO 2 NMe 4 , PTS- is displaced by Ph 2 PO 2 -, highlighting the greater affinity of the organotin macrocation for the diphenylphosphinate. This example clearly illustrates the potential of pulsed field gradient 1 H NMR spectroscopy in inorganic/organometallic chemistry, to follow preferential ion pairing in multi-ion systems at the level of each individually charged species.
Published: 2004
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15. Design of functional nano-structured materials through the use of controlled hybrid organic–inorganic interfaces

Author: François Ribot, David Grosso, Galo J. A. A. Soler-Illia, Clément Sanchez, Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)), Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), and Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Nanostructure, Materials science, General Chemical Engineering, Nanoparticle, Nanotechnology, [CHIM.MATE]Chemical Sciences/Material chemistry, 02 engineering and technology, General Chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, Nanomaterials, Nano, Self-assembly, Thin film, 0210 nano-technology, Hybrid material, ComputingMilieux_MISCELLANEOUS, Sol-gel
Abstract: The chemical strategies offered by combining sol-gel processes together with the templated growth of inorganic or hybrid networks involving self-assembly with surfactant mesophases or organogels, and with external solicitations allows us, through an intelligent and tuned coding, to develop innovative materials having complex architectures. These methods where chemistry and process are strongly coupled, allow directing the assembling of a large variety of molecular precursors, oligomers, clusters or nanoparticles (nanobuilding blocks) into functional hierarchical structures. In this short review article, the different strategies allowing to design nanostructured and/or microtextured inorganic and hybrid materials shaped as thick or thin films, microparticles and fibres are illustrated with several striking examples developed in our research group. To cite this article: C. Sanchez et al., C. R. Chimie 6 (2003).
Published: 2003
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16. New Photochromic Hybrid Organic–Inorganic Materials Built from Well-Defined Nano-Building Blocks

Author: Clément Sanchez, Christophe Eychenne-Baron, François Ribot, Aurelie Lafuma, Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), and Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Poly ethylene glycol, Materials science, Mechanical Engineering, [CHIM.MATE]Chemical Sciences/Material chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, Photochromism, Chemical engineering, Mechanics of Materials, Nano, Organic inorganic, Organic chemistry, General Materials Science, Self-assembly, Well-defined, ComputingMilieux_MISCELLANEOUS
Abstract: International audience
Published: 2002
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17. Designed Hybrid Organic−Inorganic Nanocomposites from Functional Nanobuilding Blocks

Author: Thierry Lalot, Cédric R. Mayer, G. J. de A. A. Soler-Illia, Clément Sanchez, Valérie Cabuil, François Ribot, Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Liquides Ioniques et Interfaces Chargées (LI2C), Université Pierre et Marie Curie - Paris 6 (UPMC)-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), and Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Materials science, Nanocomposite, Nanostructure, General Chemical Engineering, chemistry.chemical_element, Nanoparticle, Nanotechnology, [CHIM.MATE]Chemical Sciences/Material chemistry, 02 engineering and technology, General Chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, Soft chemistry, 0104 chemical sciences, [CHIM.POLY]Chemical Sciences/Polymers, chemistry, Materials Chemistry, Surface modification, Self-assembly, 0210 nano-technology, Tin, Hybrid material, ComputingMilieux_MISCELLANEOUS
Abstract: This article describes hybrid materials and systems in which the core integrity of inorganic nanobuilding blocks (NBBs) is preserved and reviews the main synthetic procedures presented in the literature. The relation between the NBB and the resulting hybrid networks is discussed for several striking examples: silicon and tin oxo clusters, polyoxometalates, and transition metal−oxo-based clusters. This approach is extended to nanoparticule-based hybrids. The chemical strategies offered by the coupling of soft chemistry processes and this approach based on functional NBBs allows, through an intelligent and tuned coding, to develop a new vectorial chemistry that is able to direct the assembly of a large variety of structurally well-defined clusters or nanoparticles into complex architectures.
Published: 2001
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18. Mn(V) polyhedron size in Ba10((P,Mn)O4)6F2: vibrational spectroscopy and EXAFS study

Author: G. Chottard, François Ribot, D. Huguenin, K. Dardenne, Daniel Vivien, Laboratoire de Chimie Appliquée de l'État Solide (LCAES), Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie Inorganique et Matériaux Moléculaires (CIM2), and Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Extended X-ray absorption fine structure, Analytical chemistry, Infrared spectroscopy, chemistry.chemical_element, Barium, [CHIM.MATE]Chemical Sciences/Material chemistry, 02 engineering and technology, General Chemistry, Manganese, Crystal structure, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, Inorganic Chemistry, symbols.namesake, Crystallography, chemistry, K-edge, symbols, 0210 nano-technology, Raman spectroscopy, ComputingMilieux_MISCELLANEOUS, Solid solution
Abstract: This paper reports the study of manganese substituted barium fluoroapatite Ba10(P1−xMnxO4)6F2 with 0 ≤ × ≤ 0.20. X-rays diffraction investigation indicates that the phosphate-manganate solid solution is complete, at least for this composition range, and follows Vegard's law, while diffuse reflectance and fluorescence spectra confirm that Mn(V) substitutes for P(V) in the barium apatite lattice. EXAFS experiment, at the manganese K edge, performed on the x = 0.2 compound, indicates that the Mn(V)-O distance is 1.73 A, a much larger value than the P-O distance equal to 1.54 A. The (MnO4)3− vibrational mode frequencies, deduced from the IR and Raman spectra are almost independent of the x value. This indicates that, even at very low manganese content (x = 0.001), the Mn-O distance is also very close to 1.73 A. The Mn(V) ion distorts the barium apatite lattice to a large extent when it substitutes for P(V) and imposes its own size to the host sites.
Published: 1998
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19. Homogeneity-Related Problems in Solution Derived Powders

Author: François Ribot, P. Barboux, P. Griesmar, Léo Mazerolles, Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)), Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Gestion Territoriale de l'Eau et de l'environnement (UMR GESTE), École Nationale du Génie de l'Eau et de l'Environnement de Strasbourg (ENGEES)-Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA), Centre d'études de chimie métallurgique (CECM), and Centre National de la Recherche Scientifique (CNRS)
Subjects: Inorganic chemistry, Thermodynamics, 02 engineering and technology, Quaternary compound, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 01 natural sciences, law.invention, Inorganic Chemistry, law, Metastability, Homogeneity (physics), Materials Chemistry, Cuprate, Calcination, Physical and Theoretical Chemistry, Inorganic compound, ComputingMilieux_MISCELLANEOUS, Superconductivity, chemistry.chemical_classification, [CHIM.MATE]Chemical Sciences/Material chemistry, 021001 nanoscience & nanotechnology, Condensed Matter Physics, Ferroelectricity, 0104 chemical sciences, Electronic, Optical and Magnetic Materials, chemistry, Ceramics and Composites, 0210 nano-technology
Abstract: The role of homogeneity in the reactivity of multicomponent powders resulting from solution synthesis is discussed. Examples have been given in perovskite-derived systems, such as superconducting cuprates and ferroelectric PbTi 1- x Zr x O 3 , which are of technological interest. Also, metastable structures may be obtained by low-temperature synthesis, as observed in the PbO-ZrO 2 system. In this system, we discuss the opposing effects of homogeneity and diffusion kinetics during the calcination steps and heating process.
Published: 1995
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20. General Routes to Functional Organotin Trichlorides and Trialkoxides Involving the Tricyclohexylstannyl Group

Author: Clément Sanchez, Bernard Jousseaume, François Ribot, Marie-Claude Rascle, Mohammed Lahcini, Laboratoire de chimie organique et organométallique (LCOO), Université Sciences et Technologies - Bordeaux 1-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)), Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), and Université Sciences et Technologies - Bordeaux 1 (UB)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Inorganic Chemistry, 010405 organic chemistry, Group (periodic table), Chemistry, Organic Chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, Physical and Theoretical Chemistry, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, ComputingMilieux_MISCELLANEOUS, 0104 chemical sciences, 3. Good health
Abstract: International audience
Published: 1995
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21. EXAFS, Raman and 31P NMR study of amorphous titanium phosphates

Author: M Verdaguer, P Barboux, François Ribot, Francis Taulelle, Concha Fernández-Lorenzo, C Schmutz, Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)), Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie Inorganique et Matériaux Moléculaires (CIM2), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Departamento Química Física, and Facultad de Ciencias
Subjects: Materials science, Coordination number, Inorganic chemistry, chemistry.chemical_element, 02 engineering and technology, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 01 natural sciences, chemistry.chemical_compound, symbols.namesake, Materials Chemistry, Phosphoric acid, ComputingMilieux_MISCELLANEOUS, Extended X-ray absorption fine structure, [CHIM.MATE]Chemical Sciences/Material chemistry, Nuclear magnetic resonance spectroscopy, 021001 nanoscience & nanotechnology, Condensed Matter Physics, 0104 chemical sciences, Electronic, Optical and Magnetic Materials, Amorphous solid, Crystallography, chemistry, Alkoxide, Ceramics and Composites, symbols, 0210 nano-technology, Raman spectroscopy, Titanium
Abstract: The reaction of phosphoric acid with titanium alkoxides for a PO4/Ti ratio ranging from 0.5 to 2 was investigated. For these compositions, amorphous precipitates are obtained. Their microstructure has been studied by means of Raman, nuclear magnetic resonance and X-ray absorption spectroscopies. The phosphatation of titanium alkoxide increases the Ti coordination number to 6 and the symmetry becomes purely octahedral for a P/Ti ratio of 2. For the composition range 0 < PO4/Ti ⩽ 2, phosphate anions are homogeneously dispersed in the precipitate and bound to titanium, the coordination of which is completed by oxo-, hydroxo- and remaining alkoxy- groups. Short TiO distances are observed in the materials having the lowest P/Ti ratios.
Published: 1994
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22. Vanadium clusters in doped ZrO2-SiO2 toughened ceramic composites obtained from alkoxides

Author: J.B. Carda, G. Monrós, Purificación Escribano, François Ribot, Clément Sanchez, M. A. Tena, Universitat Jaume I, Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), and Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Materials science, Composite number, Inorganic chemistry, Vanadium, chemistry.chemical_element, 02 engineering and technology, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 01 natural sciences, law.invention, law, 0103 physical sciences, General Materials Science, Ceramic, Crystallization, Electron paramagnetic resonance, ComputingMilieux_MISCELLANEOUS, 010302 applied physics, Doping, [CHIM.MATE]Chemical Sciences/Material chemistry, General Chemistry, 021001 nanoscience & nanotechnology, Condensed Matter Physics, Crystallography, chemistry, visual_art, visual_art.visual_art_medium, 0210 nano-technology, Solid solution, Zircon
Abstract: Gels of ZrO 2 -SiO 2 doped with small amounts of vanadium have been prepared from alkoxides. The stabilization of tetragonal zirconia in the amorphous silica matrix at low firing temperatures and a blue solid solution of vanadium in zircon structure above 1200°C has been identified. Electron paramagnetic resonance (EPR) shows that vanadium (IV) occupies three kinds of sites in the composite: one with C 4 v symmetry located at the solid surface like [VO(H 2 O) 5 ] 2+ , another diluted in the solid and coordina ted to oxygens like in V 2 O 5 structure, and the latest, forming clusters of V(IV) in dipolar interaction. The EPR signal of these clusters increases with the zircon crystallization.
Published: 1993
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23. Molecular and supramolecular dynamics of hybrid organic-inorganic interfaces for the rational construction of advanced hybrid nanomaterials

Author: François Ribot, David Grosso, Clément Sanchez, Cédric Boissière, Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), and Chaire Chimie des matériaux hybrides
Subjects: Chemistry, Supramolecular chemistry, Nanoparticle, Nanotechnology, [CHIM.MATE]Chemical Sciences/Material chemistry, 02 engineering and technology, General Chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, Nanomaterials, Characterization (materials science), Organic inorganic, Soft matter, 0210 nano-technology, Pulsed field gradient, Hybrid material, ComputingMilieux_MISCELLANEOUS
Abstract: Today the capability to rationally design and construct hybrid materials utilizing a performance-property driven methodology is strongly dependent on our ability to control the structure and the dynamics of hybrid interfaces. This control needs a deep knowledge of their molecular and supramolecular dynamics that must be evaluated in situ, in the soft matter or colloidal states. For this purpose the use of modern methodologies of characterization such as time resolved synchrotron experiments and advanced pulsed field gradient NMR methods (DOSY) is particularly relevant. In this critical review, two important examples are discussed. They concern, first, the study of surface capping organic components' affinity towards nanoparticle surfaces by DOSY NMR. The knowledge and therefore the tuning of this affinity is paramount because it controls solubility, transferability and stability of colloidal dispersions of nanoparticles (NPs). In the second part, the mechanism of micellar templated formation of hybrid mesophases will be discussed in the frame of the main results obtained via in situ SAXS (107 references).
Published: 2010
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24. Hydrolysis-condensation process of .beta.-diketonates-modified cerium(IV) isopropoxide

Author: Clément Sanchez, Paul Toledano, François Ribot, Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)), Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), and Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Materials science, General Chemical Engineering, Condensation process, chemistry.chemical_element, 02 engineering and technology, General Chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, Hydrolysis, Cerium, chemistry, Polymer chemistry, Materials Chemistry, 0210 nano-technology, Beta (finance), ComputingMilieux_MISCELLANEOUS
Abstract: International audience
Published: 1991
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25. The first structure of a cerium(IV) phosphate: ab initio Rietveld analysis of CeIV(PO4)(HPO4)(0.5)(H2O)0.5

Author: François Ribot, Elisabeth Tronc, Corinne Chanéac, Jean-Pierre Jolivet, Gilles Wallez, Micaela Nazaraly, Michel Quarton, Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)), Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), and Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Subjects: 010405 organic chemistry, Rietveld refinement, Inorganic chemistry, Ab initio, chemistry.chemical_element, General Medicine, 02 engineering and technology, General Chemistry, Nuclear magnetic resonance spectroscopy, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 021001 nanoscience & nanotechnology, Phosphate, 01 natural sciences, Catalysis, 0104 chemical sciences, Crystallography, Cerium, chemistry.chemical_compound, chemistry, [CHIM.CRIS]Chemical Sciences/Cristallography, 0210 nano-technology, ComputingMilieux_MISCELLANEOUS
Abstract: International audience
Published: 2005
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26. Controlled Formation of Highly Organized Mesoporous Titania Thin Films: From Mesostructured Hybrids to Mesoporous Nanoanatase TiO2

Author: Florence Cagnol, François Ribot, Galo J. A. A. Soler-Illia, Eduardo L. Crepaldi, David Grosso, Clément Sanchez, Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) (LCMCP (site Paris VI)), Université Pierre et Marie Curie - Paris 6 (UPMC)-Collège de France (CdF (institution))-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), and Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Oxide, Mineralogy, 02 engineering and technology, Thermal treatment, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, Catalysis, law.invention, chemistry.chemical_compound, Colloid and Surface Chemistry, law, Crystallization, Thin film, ComputingMilieux_MISCELLANEOUS, Extended X-ray absorption fine structure, Chemistry, [CHIM.MATE]Chemical Sciences/Material chemistry, General Chemistry, 021001 nanoscience & nanotechnology, XANES, 0104 chemical sciences, Characterization (materials science), Chemical engineering, 0210 nano-technology, Mesoporous material
Abstract: In this paper, we report the complete synthesis and characterization procedures to generate highly organized and oriented mesoporous titania thin films, using poly(ethylene oxide) (PEO)-based templates. Controlled conditions in the deposition, postsynthesis, and thermal treatment steps allow one to tailor the final mesostructure (2D hexagonal, p6m, or 3D cubic, Im3m). Various techniques were used to determine the time evolution of the mesostructure. Spectroscopic techniques (UV/vis, (17)O NMR) and EXAFS/XANES have been used to follow the chemical changes in the Ti(IV) environment. Crossing these techniques spanning all ranges permits a complete description of the chemistry all the way from solution to the mesostructured metal oxide. A critical discussion on all important chemical and processing parameters is provided; the understanding of these features is essential for a rational design and the reproducible construction of mesoporous materials.
Published: 2003
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27. A DFT and HF quantum chemical study of the tin nanocluster [(RSn)12O14(OH)6]2+ and its interactions with anions and neutral nucleophiles: confrontation with experimental data

Author: Frank De Proft, Clément Sanchez, Paul Geerlings, Ricardo Vivas-Reyes, François Ribot, Monique Biesemans, Rudolph Willem, General Chemistry, High Resolution NMR Centre, Vrije Universiteit Brussel, Eenheid Algemene Chemie, Vrije Universiteit Brussel (VUB), High-Resolution NMR Centre, Matériaux Hybrides et Nanomatériaux (LCMCP-MHN), Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Novel Advanced Nano-Objects (LCMCP-NANO), Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), and Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Subjects: Hydrogen, 010405 organic chemistry, chemistry.chemical_element, Protonation, General Chemistry, [CHIM.INOR]Chemical Sciences/Inorganic chemistry, 010402 general chemistry, Electrostatics, 01 natural sciences, Catalysis, 0104 chemical sciences, [CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry, chemistry, Nucleophile, Computational chemistry, Materials Chemistry, HSAB theory, Cluster (physics), Reactivity (chemistry), Tin, ComputingMilieux_MISCELLANEOUS
Abstract: Calculations of traditional wave function and DFT based reactivity descriptors are reported for the nanocluster [(RSn)12O14(OH)6]2+ (R = CH3) in order to get insight into the factors determining the exact nature of its interactions with anions or neutral nucleophiles (F−, Cl−, OH−, H2O, acetone, DMSO). Two levels of calculation (Hartree–Fock and DFT) were used in this study, giving the opportunity to compare the performance of both aproaches. As a whole the HF and DFT results, despite some numerical differences, are qualitatively and in most cases quantitatively similar, since no interchanges in the sequences are found. Calculated charge distributions indicate that the hexacoordinated tin atoms are expected to be harder, the pentacoordinated ones softer. This result is confirmed by the condensed local softness and experimental observations provided by the literature (X-ray, 119Sn NMR), thereby matching predictions made on the basis of the HSAB principle. Molecular electrostatic potential (MEP) calculations further confirm this selectivity, indicating that nucleophiles will approach preferentially the macrocation around the poles rather than at the equator of the cage. Calculated stabilization energies indicate that the charged (F−, Cl− and OH−) and uncharged (DMSO, acetone and water) nucleophiles tested all interact preferentially with the cage pole region around the hexacoordinated tin atoms. This feature appears related to the electrostatic nature of the interaction for the charged nucleophiles and to the tendency, for all the nucleophiles, to form hydrogen bridges with the μ2-OH moieties. The basicity of the three types of oxygen atoms [μ2-OH, μ3-O(I), μ3-O(P)] present in [(RSn)12O14(OH)6)]2+ has been addressed by protonation energy and MEP calculations, taking into account accessibility factors not represented by atomic charges. Summarizing, it turns out that the hardness/softness properties of tin atoms are modulated by their coordination; however, the sole consideration of these quantities is not sufficient to predict in all cases the strength and orientation of the interaction between various nucleophiles and the cluster, since electrostatic interactions and H-bonding play a major role.
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27 results on '"Novel Advanced Nano-Objects (LCMCP-NANO)"'

1. Revealing the Elusive Structure and Reactivity of Iron Boride α-FeB

2. Liquid Processing of Bismuth–Silica Nanoparticle/Aluminum Matrix Nanocomposites for Heat Storage Applications

3. Hydroxyapatites as Versatile Inorganic Hosts of Unusual Pentavalent Manganese Cations

4. Ultrasound-Assisted Liquid-Phase Synthesis and Mechanical Properties of Aluminum Matrix Nanocomposites Incorporating Boride Nanocrystals

5. Alkoxysilane effect in hybrid material: A comparison of pHEMA-TiO2 and pMAPTMS-TiO2 nanoparticulate hybrids

6. The origin of the high electrochemical activity of pseudo-amorphous iridium oxides

7. Electron Precise Sodium Carbaboride Nanocrystals from Molten Salts: Single Sources to Boron Carbides

8. Phase selective synthesis of nickel silicide nanocrystals in molten salts for electrocatalysis of the oxygen evolution reaction

9. Origin of transparency in scattering biomimetic collagen materials

10. Following in Situ the Degradation of Mesoporous Silica in Biorelevant Conditions: At Last, a Good Comprehension of the Structure Influence

11. Modified Synthesis Strategies for the Stabilization of low n Tin O2n-1 Magnéli Phases

12. Multicationic Sr4Mn3O10 mesostructures: molten salt synthesis, analytical electron microscopy study and reactivity

13. Metal-Dependent Interplay between Crystallization and Phosphorus Diffusion during the Synthesis of Metal Phosphide Nanoparticles

14. Probing Ionic Association on Metal Oxide Clusters by Pulsed Field Gradient NMR Spectroscopy: The Example of Sn12–Oxo Clusters

15. Design of functional nano-structured materials through the use of controlled hybrid organic–inorganic interfaces

16. New Photochromic Hybrid Organic–Inorganic Materials Built from Well-Defined Nano-Building Blocks

17. Designed Hybrid Organic−Inorganic Nanocomposites from Functional Nanobuilding Blocks

18. Mn(V) polyhedron size in Ba10((P,Mn)O4)6F2: vibrational spectroscopy and EXAFS study

19. Homogeneity-Related Problems in Solution Derived Powders

20. General Routes to Functional Organotin Trichlorides and Trialkoxides Involving the Tricyclohexylstannyl Group

21. EXAFS, Raman and 31P NMR study of amorphous titanium phosphates

22. Vanadium clusters in doped ZrO2-SiO2 toughened ceramic composites obtained from alkoxides

23. Molecular and supramolecular dynamics of hybrid organic-inorganic interfaces for the rational construction of advanced hybrid nanomaterials

24. Hydrolysis-condensation process of .beta.-diketonates-modified cerium(IV) isopropoxide

25. The first structure of a cerium(IV) phosphate: ab initio Rietveld analysis of CeIV(PO4)(HPO4)(0.5)(H2O)0.5

26. Controlled Formation of Highly Organized Mesoporous Titania Thin Films: From Mesostructured Hybrids to Mesoporous Nanoanatase TiO2

27. A DFT and HF quantum chemical study of the tin nanocluster [(RSn)12O14(OH)6]2+ and its interactions with anions and neutral nucleophiles: confrontation with experimental data

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27 results on '"Novel Advanced Nano-Objects (LCMCP-NANO)"'

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