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The prompt management of patients with massive burns is essential to maximize survival by preventing infection, hemorrhage, fluid and heat loss, and to optimally prepare the wound bed for the application of autografts or cultured tissue-engineered artificial autologous skin. Acute treatments are typically based on temporary bio-dressings, commonly cadaveric skin allografts, but supply challenges, high costs and increasingly stringent regulatory requirements preclude their widespread use. Nanostructured fibrin-agarose hydrogels (NFAH) have been proven to be safe and effective biomaterials in preclinical and clinical studies, and show good hemostatic and biomechanical properties. Here we generated and tested NFAH with embedded allogeneic dermal fibroblasts (NFAH-F) under Good Manufacturing Practice (GMP) conditions. Fibroblasts were first expanded and characterized to create a GMP bank and the NFAH-F was manufactured on demand. Three patients with major burns were treated with this product as a temporary bio-dressing under compassionate use. Our results suggest that NFAH-F product was a safe product and no adverse reactions were observed. In all cases, the patients survived until definitive treatment. Therefore, the application of NFAH-F might be a temporary bio-dressing for patients with massive burns when cadaveric skin allografts are not available.

Strain sensors for wearable electronic devices have received attention due to their potential application in medicine for physiological monitoring or as part of advanced prosthetics. However, low sensitivity values as well as complex fabrication procedures remain significant challenges limiting the applicability. This work presents the fabrication of a strain sensor based on the separation of silver microplates immobilized on a stretchable substrate. The deposition of the microplates is achieved through the exposition of a glucosamine‐functionalized surface to the Tollens' reagent, being a versatile fabrication methodology able to be implemented in a wide range of substrates. The obtained sensors present a high stretchability (>100%), high conductivity (105 S m–1), good linearity (R2 > 0.98 under 30% strain), good hysteresis properties, and high sensitivity (up to GF = 900 000). Hence, the sensors allow the measurement of very small deformations even in dynamic range, where it presents a stable linear response for the quantification of cyclic deformations of 0.02% strain. Moreover, the applicability of these sensors has been studied in motion‐sensing devices and in a pressure sensor revealing that this technology may expand the potential applications of wearable electronic devices. [ABSTRACT FROM AUTHOR]

The eco-responsible lead-free piezoelectric ceramics have been intensively searched for more than a decade, however, the final goal to replace toxic ceramics like lead zirconate titanate (PZT) with lead-free compounds, having comparable or even better performance has not yet been reached. In this road, the lead-free ceramics Ba0.85Ca0.15Zr0.1Ti0.9O3 (BCZT), possessing excellent dielectric, ferroelectric, and piezoelectric properties are regarded as serious candidates for the PZT replacement. Besides, nanostructuring BCZT is of paramount importance to enhance these functionalities even more. Here, BCZT multipodes are designed by template-growth hydrothermal synthesis using hydrogen zirconate titanate nanowires. We demonstrate that the fabricated BCZT multipodes exhibit high dielectric permittivity of 5300 with a temperature stability coefficient of ±5.9% between 20 and 140 °C. A significant recovered energy density of 315.0 mJ/cm3 with high thermal stability and high energy storage efficiency of 87.4%, and enhanced large-signal piezoelectric coefficient d33∗ (310 pm/V) are found. Compared to the traditional BCZT ceramics reported in the literature, relying on high-temperature processing, our sample exhibits boosted energy storage parameters at a much lower temperature. These outcomes may offer a new strategy to tailor eco-responsible relaxor ferroelectrics toward superior energy storage performance for ceramic capacitor applications.

Abstract Strain sensors for wearable electronic devices have received attention due to their potential application in medicine for physiological monitoring or as part of advanced prosthetics. However, low sensitivity values as well as complex fabrication procedures remain significant challenges limiting the applicability. This work presents the fabrication of a strain sensor based on the separation of silver microplates immobilized on a stretchable substrate. The deposition of the microplates is achieved through the exposition of a glucosamine‐functionalized surface to the Tollens’ reagent, being a versatile fabrication methodology able to be implemented in a wide range of substrates. The obtained sensors present a high stretchability (>100%), high conductivity (105 S m–1), good linearity (R2 > 0.98 under 30% strain), good hysteresis properties, and high sensitivity (up to GF = 900 000). Hence, the sensors allow the measurement of very small deformations even in dynamic range, where it presents a stable linear response for the quantification of cyclic deformations of 0.02% strain. Moreover, the applicability of these sensors has been studied in motion‐sensing devices and in a pressure sensor revealing that this technology may expand the potential applications of wearable electronic devices.

[Display omitted] • The thermal behavior of DBN and DBU PILs with carboxylic acids of varying chain length was explored. • The effects of base, acid, and temperature on C p , m 0 of the PILs were studied. • The T g and C p , m 0 of the PILs show a significant dependence with the base. • PILs can display high values of excess heat capacities, depending on their ionicity. • Evidence for the occurrence of nanostructuration in PILs with acids of longer chain length. Herein, we report the thermal behavior and high-precision heat capacity values, at T = 298.15 K, and in the range from 283 to 363 K, for several protic ionic liquids (PILs), derived from the 1:1 liquid mixtures of the organic superbases 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) with some carboxylic acids (propionic, butyric, hexanoic and octanoic). Glass transition, T g , crystallization, T c , cold-crystallization, T cc , and melting, T m , temperatures were determined for the PILs studied, showing marked differences with the base – T g is lower for all DBN PILs, and no T m , T c , and T cc could be obtained for the DBU PILs. The standard molar heat capacities, C p , m 0 , were obtained with an uncertainty of less than ±0.3 % and their dependence on the base and on the acid's chain length was studied in detail. The C p , m 0 of the DBU PILs were found to be significantly higher than those of the corresponding DBN PILs, which corroborates the greater ionic character of DBU PILs. The heat capacity data suggested the existence of a trend-shift with the chain length of the carboxylic acid. Similar to aprotic ionic liquids, the shift occurs around n = 5 (pentanoic acid) and suggests the existence of some degree of nanostructuration into polar and non-polar domains in PILs with larger acids. Moreover, PILs can display abnormally high excess heat capacities, resulting from the formation of an ionic mixture from neutral species. Analysis of the calculated excess heat capacities indicates that PILs tend to become less ionic as the temperature increases, which goes in accordance with the acid-base equilibrium shift. [ABSTRACT FROM AUTHOR]

Iridium Oxide (IrO2) is a metal oxide with a rutile crystalline structure, analogous to the TiO2 rutile polymorph. Unlike other oxides of transition metals, IrO2 shows a metallic type conductivity and displays a low surface work function. IrO2 is also characterized by a high chemical stability. These highly desirable properties make IrO2 a rightful candidate for specific applications. Furthermore, IrO2 can be synthesized in the form of a wide variety of nanostructures ranging from nanopowder, nanosheets, nanotubes, nanorods, nanowires, and nanoporous thin films. IrO2 nanostructuration, which allows its attractive intrinsic properties to be enhanced, can therefore be exploited according to the pursued application. Indeed, IrO2 nanostructures have shown utility in fields that span from electrocatalysis, electrochromic devices, sensors, fuel cell and supercapacitors. After a brief description of the IrO2 structure and properties, the present review will describe the main employed synthetic methodologies that are followed to prepare selectively the various types of nanostructures, highlighting in each case the advantages brought by the nanostructuration illustrating their performances and applications. [ABSTRACT FROM AUTHOR]

The terbium(III) ion is a particularly suitable candidate for the creation of surface-based magnetic and luminescent devices. In the present work, we report the epitaxial growth of needle-like objects composed of [Tb(hfac)3·2H2O]n (where hfac = hexafluoroacetylacetonate) polymeric units on muscovite mica, which is observed by atomic force microscopy. The needle-like shape mimics the structure observed in the crystalline bulk material. The growth of this molecular organization is assisted by water adsorption on the freshly air-cleaved muscovite mica. This deposition technique allows for the observation of a significant amount of nanochains grown along three preferential directions 60° apart from another. The magnetic properties and the luminescence of the nanochains can be detected without the need of surface-dedicated instrumentation. The intermediate value of the observed luminescence lifetime of the deposits (132 µs) compared to that of the bulk (375 µs) and the CHCl3 solution (13 µs) further reinforces the idea of water-induced growth.

Iridium Oxide (IrO2) is a metal oxide with a rutile crystalline structure, analogous to the TiO2 rutile polymorph. Unlike other oxides of transition metals, IrO2 shows a metallic type conductivity and displays a low surface work function. IrO2 is also characterized by a high chemical stability. These highly desirable properties make IrO2 a rightful candidate for specific applications. Furthermore, IrO2 can be synthesized in the form of a wide variety of nanostructures ranging from nanopowder, nanosheets, nanotubes, nanorods, nanowires, and nanoporous thin films. IrO2 nanostructuration, which allows its attractive intrinsic properties to be enhanced, can therefore be exploited according to the pursued application. Indeed, IrO2 nanostructures have shown utility in fields that span from electrocatalysis, electrochromic devices, sensors, fuel cell and supercapacitors. After a brief description of the IrO2 structure and properties, the present review will describe the main employed synthetic methodologies that are followed to prepare selectively the various types of nanostructures, highlighting in each case the advantages brought by the nanostructuration illustrating their performances and applications.

This article reports a study to identify optimal synthesis parameters for a pure boron precursor prepared following a patented process developed at CNR-SPIN laboratories, performed in the framework of a collaboration between CNR-SPIN and CERN. Boron is a precursor that plays a crucial role in the MgB2 wire manufacturing, as a consequence, the synthesis parameters of the superconducting phase have been investigated. In this article, we report results for MgB2 samples synthesized at 870 °C for 17nbsp;h under Ar/5% H2 flow and 760 °C for 0.2 h. Magnesiothermic amorphous nanoboron (MANB) and commercial boron nanopowders (purchased from Pavezyum) have been compared in terms of morphological features. MgB2 derived from both sources has been characterized and the superconductive properties in the wire form have been compared. Results demonstrate that the MANB performance is comparable with the nanoboron obtained via gas synthesis. [ABSTRACT FROM AUTHOR]

This article presents a study on Metal-Assisted Chemical Etching (MACE) of silicon in HF-H2O2 using silver nanoparticles as catalysts. Our aim is a better understanding of the process to elaborate new 3D submicrometric surface structures useful for light management. We investigated MACE over the whole range of silicon doping, i.e., p++, p+, p, p−, n, n+, and n++. We discovered that, instead of the well-defined and straight mesopores obtained in p and n-type silicon, in p++ and n++ silicon MACE leads to the formation of cone-shaped macropores filled with porous silicon. We account for the transition between these two pore-formation regimes (straight and cone-shaped pores) by modeling (at equilibrium and under polarization) the Ag/Si/electrolyte (HF) system. The model simulates the system as two nanodiodes in series. We show that delocalized MACE is explained by a large tunnel current contribution for the p-Si/Ag and n-Si/HF diodes under reverse polarization, which increases with the doping level and when the size of the nanocontacts (Ag, HF) decreases. By analogy with the results obtained on heavily doped silicon, we finally present a method to form size-controlled cone-shaped macropores in p silicon with silver nanoparticles. This shape, instead of the usual straight mesopores, is obtained by applying an external anodic polarization during MACE. Two methods are shown to be effective for the control of the macropore cone angle: one by adjusting the potential applied during MACE, the other by changing the H2O2 concentration. Under appropriate etching conditions, the obtained macropores exhibit optical properties (reflectivity ~3 %) similar to that of black silicon.

The prompt management of patients with massive burns is essential to maximize survival by preventing infection, hemorrhage, fluid and heat loss, and to optimally prepare the wound bed for the application of autografts or cultured tissue-engineered artificial autologous skin. Acute treatments are typically based on temporary bio-dressings, commonly cadaveric skin allografts, but supply challenges, high costs and increasingly stringent regulatory requirements preclude their widespread use. Nanostructured fibrin-agarose hydrogels (NFAH) have been proven to be safe and effective biomaterials in preclinical and clinical studies, and show good hemostatic and biomechanical properties. Here we generated and tested NFAH with embedded allogeneic dermal fibroblasts (NFAH-F) under Good Manufacturing Practice (GMP) conditions. Fibroblasts were first expanded and characterized to create a GMP bank and the NFAH-F was manufactured on demand. Three patients with major burns were treated with this product as a temporary bio-dressing under compassionate use. Our results suggest that NFAH-F product was a safe product and no adverse reactions were observed. In all cases, the patients survived until definitive treatment. Therefore, the application of NFAH-F might be a temporary bio-dressing for patients with massive burns when cadaveric skin allografts are not available. [Display omitted] • Fibroblasts were efficiently expanded and banked under GMP compliant conditions. • A bio-dressing based on nanostructured fibrin-agarose hydrogels with embedded allogeneic fibroblasts (NFAH-F) was designed. • Three massively burned patients were treated with NFAH-F under compassionate use and no adverse reactions were observed. • The application of NFAH-F might be a temporary bio-dressing for patients when cadaveric skin allografts are not available. [ABSTRACT FROM AUTHOR]

More people, more cities; the energy demand increases in consequence and much of that will rely on next-generation smart materials. Zn-ferrites (ZnFe2O4) are nonconventional ceramic materials on account of their unique properties, such as chemical and thermal stability and the reduced toxicity of Zn over other metals. Furthermore, the remarkable cation inversion behavior in nanostructured ZnFe2O4 extensively cast-off in the high-density magnetic data storage, 5G mobile communication, energy storage devices like Li-ion batteries, supercapacitors, and water splitting for hydrogen production, among others. Here, we review how aforesaid properties can be easily tuned in various ZnFe2O4 nanostructures depending on the choice, amount, and oxidation state of metal ions, the specific features of cation arrangement in the crystal lattice and the processing route used for the fabrication.

The recent advances in the supramolecular control in nanostructured films have improved the performance of organic-based devices. However, the effect of different supramolecular arrangement on the sensor or biosensor performance is poorly studied yet. In this paper, we show the role of the composition and nanostructuration of the films on the impedance and voltammetric-based sensor performance to catechol detection. The films here studied were composed by a perylene derivative (PTCD-NH2) and a metallic phthalocyanine (FePc), using Langmuir-Blodgett (LB) and physical vapor deposition (PVD) techniques. The deposition technique and intrinsic properties of compounds showed influence on electrical and electrocatalytic responses. The PVD PTCD-NH2 shows the best sensor performance to the detection of catechol. Quantification of catechol contents in mate tea samples was also evaluated, and the results showed good agreement compared with Folin-Ciocalteu standard method for polyphenol detection.

Nanostructuration is one of the most promising strategies to develop performant electrode materials for energy storage devices, such as hybrid supercapacitors. In this work, we studied the influence of precipitation medium and the use of a series of 1-alkyl-3-methylimidazolium bromide ionic liquids for the nanostructuration of β(III) cobalt oxyhydroxides. Then, the effect of the nanostructuration and the impact of the different ionic liquids used during synthesis were investigated in terms of energy storage performances. First, we demonstrated that forward precipitation, in a cobalt-rich medium, leads to smaller particles with higher specific surface areas (SSA) and an enhanced mesoporosity. Introduction of ionic liquids (ILs) in the precipitation medium further strongly increased the specific surface area and the mesoporosity to achieve well-nanostructured materials with a very high SSA of 265 m2/g and porosity of 0.43 cm3/g. Additionally, we showed that ILs used as surfactant and template also functionalize the nanomaterial surface, leading to a beneficial synergy between the highly ionic conductive IL and the cobalt oxyhydroxide, which lowers the resistance charge transfer and improves the specific capacity. The nature of the ionic liquid had an important influence on the final electrochemical properties and the best performances were reached with the ionic liquid containing the longest alkyl chain.

Organic polymers can be made porous via continuous or discontinuous expansion processes in scCO2. The resulting foams properties are controlled by the interplay of three groups of parameters: (i) Chemical, (ii) physico-chemical, and (iii) technological/process that are explained in this paper. The advantages and drawbacks of continuous (extrusion, injection foaming) or discontinuous (batch foaming) foaming processes in scCO2, will be discussed in this article; especially for micro or nano cellular polymers. Indeed, a challenge is to reduce both specific mass (e.g., ρ < 100 kg·m−3) and cell size (e.g., average pore diameter ϕaveragepores < 100 nm). Then a particular system where small “objects” (coreshells CS, block copolymer MAM) are perfectly dispersed at a micrometric to nanometric scale in poly(methyl methacrylate) (PMMA) will be presented. Such “additives”, considered as foaming aids, are aimed at “regulating” the foaming and lowering the pore size and/or density of PMMA based foams. Differences between these additives will be shown. Finally, in a PMMA/20 wt% MAM blend, via a quasi one-step batch foaming, a “porous to nonporous” transition is observed in thick samples. A lower limit of pore size (around 50 nm) seems to arise.

CeF 3 is largely used due to its technological importance for applications in various domains such as photonics, sensors, energy and catalysis and its nanostructuration represents a real challenge. In this paper, we report on the novel and environmentally friendly synthetic route of monodisperse CeF 3 nanoparticles (NP) with a diameter of about 10 nm and a high surface area (≈130 m2 g−1) by a surfactant-free aqueous precipitation route at room temperature (yield ≈ 90%). The dispersion of the NP as a stable colloidal suspension allows to prepare for the first time 3D interconnected macroporous CeF 3 through the assembly of as-prepared NP and home-made poly(methyl methacrylate) (PMMA) beads as template. These Organized Porous Inorganic Fluorides (OPIF) materials have been deeply characterized at different synthesis stages by means of powder X-ray diffraction (XRD), N 2 sorption, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses. CeF 3 OPIF present a macroporosity (pore diameter ≈ 200 nm) as well as well as intergranular mesoporosity emerging from the voids between the CeF 3 NP (D TEM ≈ 7 nm) composing the OPIF walls resulting in a surface area of 33 m2 g−1. The thermal stability under nitrogen of the CeF 3 crystal structure is increased for the 3D interconnected macroporous materials in comparison with the NP as the CeF 3 crystal structure remains stable until 550 °C for CeF 3 OPIF and only 400 °C for CeF 3 NP. Finally, the porous structuration of CeF 3 materials considerably slows down the crystallite growth during thermal treatment under nitrogen. The crystallite size of CeF 3 NP constantly increases from 10 nm (120 °C) to 30 nm (420 °C). At the opposite, the crystallite size of CeF 3 OPIF remains unchanged until 460 °C (17 nm). [Display omitted] • CeF 3 nanoparticles (NP) obtained by a surfactant-free aqueous precipitation route. • Preparation of 3D interconnected macroporous CeF 3. • Thermal stability of the crystal structure increased for macroporous CeF 3 vs. NP. • Porous structuration of CeF 3 slows down the crystal growth during thermal treatment. [ABSTRACT FROM AUTHOR]

PbTe-based alloys have the best thermoelectric properties for intermediate temperature applications (500−900 K). We report on the preparation of pristine PbTe and two doped derivatives (Pb0.99Sb0.01Te and Ag0.05Sb0.05Pb0.9Te, so-called LAST18) by a fast arc-melting technique, yielding nanostructured polycrystalline pellets. XRD and neutron powder diffraction (NPD) data assessed the a slight Te deficiency for PbTe, also yielding trends on the displacement factors of the 4a and 4b sites of the cubic Fm-3m space group. Interestingly, SEM analysis shows the conspicuous formation of layers assembled as stackings of nano-sheets, with 20−30 nm thickness. TEM analysis shows intra-sheet nanostructuration on the 50 nm scale in the form of polycrystalline grains. Large numbers of grain boundaries are created by this nanostructuration and this may contribute to reduce the thermal conductivity to a record-low value of 1.6 Wm−1K−1 at room temperature. In LAST18, a positive Seebeck coefficient up to 600 μV K−1 at 450 K was observed, contributing further towards improving potential thermoelectric efficiency.

A key factor for dental implant success is a good sealing between the implant surface and both soft (gum) and hard (bone) tissues. Surface nanotopography can modulate cell response through mechanotransduction. The main objective of this research was the development of nanostructured titanium (Ti) surfaces that promote both soft and hard tissue integration with potential application in dental implants. Nanostructured Ti surfaces were developed by electrochemical anodization—nanopores (NPs) and nanonets (NNs)—and characterized by atomic force microscopy, scanning electronic microscopy, and contact angle analysis. In addition, nanoparticle release and apoptosis activation were analyzed on cell culture. NP surfaces showed nanoparticle release, which increased in vitro cell apoptosis. Primary human gingival fibroblasts (hGFs) and human bone marrow mesenchymal stem cells (hBM-MSCs) were used to test cell adhesion, cytotoxicity, metabolic activity, and differentiation markers. Finally, cell orientation on the different surfaces was analyzed using a phalloidin staining. NN surfaces induced an oriented alignment of both cell types, leading in turn to an improved expression of differentiation markers. Our results suggest that NN structuration of Ti surfaces has great potential to be used for dental implant abutments to improve both soft and hard tissue integration.

The influence of the synthesis and sintering methods on the structural, microstructural, stoichiometry and thus the magnetocaloric properties of the La 0.7 Ca 0.3 MnO 3 compound has been thoroughly studied. Soft-chemistry (sol-gel and polyol) synthesis and spark plasma sintering (SPS) procedures, used to obtain nanostructured materials, were compared to the traditional ceramic ones. This work evidences that SPS treatment not only reduces the grain size but also leads to oxygen sub-stoichiometry. This entails a lower Mn 4+ content in the manganite, and probably heterogeneity in the Mn 4+ grain distribution, which have consequences on the magnetic and magnetocaloric properties: a lower maximum entropy variation which is compensated by a larger transition temperature range. The sample prepared by combining polyol soft-chemistry synthesis and SPS sintering displays a higher maximum relative cooling power value, equal to 70% of that of gadolinium, the most effective material for domestic magnetic refrigeration. [ABSTRACT FROM AUTHOR]

The heat capacity and thermal behavior trend along the 1-alkyl-3-methylimidazolium hexafluorophosphate [C n C 1 im][PF 6 ] (with n = 2–10, 12) ionic liquids series, is used to explore the effect of the alkyl chain length in the nanostructuration. The heat capacities of the studied ILs were measured with an uncertainty better than ± 0.15% and are in excellent agreement with the available data in the literature. An odd-even effect for the specific and volumic heat capacities of the [C n C 1 im][PF 6 ] series was found. The observed odd-even effect in the liquid heat capacity was rationalized considering the preferential orientation of the terminal CH 3 group. The higher specific/volumic heat capacities shown for the [C 6 C 1 im][PF 6 ] and [C 8 C 1 im][PF 6 ] are an indication of an additional conformational disorder increase in the liquid phase that could be related with a weaker alkyl chain interdigitation capability of the even number chain ILs. The melting temperatures and consequent ∆ s l H m o and ∆ s l S m o trend along the alkyl series present a V-shape profile that is explained based on the analysis of the balance between the initial decrease of the electrostatic interaction potential and the increase of the van der Waals interactions with the increasing size of the alkyl side chain of the cation. The inhibition of crystallization for intermediate alkyl chain size (from [C 5 C 1 im][PF 6 ] to [C 8 C 1 im][PF 6 ]) seems to arise from the overlapping of the hypothetical cold crystallization temperature by the melting temperature. Above the critical alkyl size, CAS, a regular increase in the entropy and enthalpy profiles presents a similar shape than the observed in other alkane series and is a strong support of the intensification of the ILs nanostructuration. [ABSTRACT FROM AUTHOR]

We investigated the fabrication of large-area (cm2) nanostructured glasses for solar cell modules with hydrophobic and hydrophilic properties using soft lithography and colloidal lithography. Both of these techniques entail low-cost and ease of nanofabrication. We explored the use of simple 1D and 2D nanopatterns (nanowires and nanocones) and the effect of introducing disorder in the nanostructures. We observed an increase in the transmitted light for ordered nanostructures with a maximum value of 99% for wavelengths >600 nm when ordered nanocones are fabricated on the two sides of the solar glass. They produced an increment in the efficiency of the packaged solar cell with respect to the glass without nanostructures. On the one hand, the wettability properties showed that the ordering of the nanostructures improved the hydrophobicity of the solar glasses and increased their self-cleaning capacity. On the other hand, the disordered nanostructures improved the hydrophilic properties of solar glasses, increasing their anti-fogging capacity. The results show that by selecting the appropriate nanopattern, the wettability properties (hydrophobic or hydrophilic) can be easily improved without decreasing the efficiency of the solar cell underneath. [ABSTRACT FROM AUTHOR]

Metal nanostructures are, nowadays, extensively used in applications such as catalysis, electronics, sensing, optoelectronics and others. These applications require the possibility to design and fabricate metal nanostructures directly on functional substrates, with specifically controlled shapes, sizes, structures and reduced costs. A promising route towards the controlled fabrication of surface-supported metal nanostructures is the processing of substrate-deposited thin metal films by fast and ultrafast pulsed lasers. In fact, the processes occurring for laser-irradiated metal films (melting, ablation, deformation) can be exploited and controlled on the nanoscale to produce metal nanostructures with the desired shape, size, and surface order. The present paper aims to overview the results concerning the use of fast and ultrafast laser-based fabrication methodologies to obtain metal nanostructures on surfaces from the processing of deposited metal films. The paper aims to focus on the correlation between the process parameter, physical parameters and the morphological/structural properties of the obtained nanostructures. We begin with a review of the basic concepts on the laser-metal films interaction to clarify the main laser, metal film, and substrate parameters governing the metal film evolution under the laser irradiation. The review then aims to provide a comprehensive schematization of some notable classes of metal nanostructures which can be fabricated and establishes general frameworks connecting the processes parameters to the characteristics of the nanostructures. To simplify the discussion, the laser types under considerations are classified into three classes on the basis of the range of the pulse duration: nanosecond-, picosecond-, femtosecond-pulsed lasers. These lasers induce different structuring mechanisms for an irradiated metal film. By discussing these mechanisms, the basic formation processes of micro- and nano-structures is illustrated and justified. A short discussion on the notable applications for the produced metal nanostructures is carried out so as to outline the strengths of the laser-based fabrication processes. Finally, the review shows the innovative contributions that can be proposed in this research field by illustrating the challenges and perspectives.

Ultra-hydrophobic bilayer coatings on a glass surface were fabricated by sol-gel process using hexadecyltrimethoxysilane (C16TMS) and tetramethoxysilane (TMOS) (1:4 molar ratio) as precursors. After coating, silica nanoparticles (SiO2 NPs) functionalized with different mono-alkoxy derivatives (methoxytrimethylsilane, TMeMS; ethoxydimethylvinylsilane, DMeVES; ethoxydimethylphenylsilane, DMePhES; and methoxydimethyloctylsilane, DMeC8MS) were added, assuring the microscale roughness on the glass surface. Influences of the functionalized SiO2 NPs and surface morphology on the hydrophobicity of the hybrid films were discussed. The successful functionalization of SiO2 NPs with hydrophobic alkyl groups were confirmed by Fourier transform infrared spectroscopy (FTIR). The thermal stability of hydrophobic SiO2 NPs showed that the degradation of the alkyl groups takes place in the 200-400°C range. Bilayer coating with C16TMS/TMOS and SiO2 NPs modified with alkoxysilane substituted with C8 alkyl chain (SiO2 NP-C8) has micro/nano structure. Hydrophobicity of functionalized SiO2 NPs-C8 and its higher degree of nanometer-scale roughness gave rise to ultra-hydrophobicity performance for bilayer coating C16TMS/TMOS + SiO2 NPs-C8 (145°), compared to other similar hybrid structures. Our synthesis method for the functionalization of SiO2 NPs is useful for the modification of surface polarity and roughness. [ABSTRACT FROM AUTHOR]

Pure tysonite La 0.95 Ba 0.05 F 2.95 is nanostructured by using the ball-milling technique. Size and pollution rate are minimized using the statistical method of Design of Experiment. The nanocrystalline powders are studied by X-ray and TEM analyses and by 19 F solid state NMR and impedance spectroscopies. Specific surface area and F/OH substitution rate are estimated by BET measurements and thermal analysis (TGA-MS), respectively. Fluorine environments and mobilities are discussed on the basis of 19 F solid state NMR data, both prior and after thermal treatment. The ionic conductivity, evaluated from sintered pellets, is compared at different thermal treatment temperatures. Thermal treatment tends to reduce microstrains up to 500 °C and to increase the grain size above this temperature. Optimal conductivity is obtained for a thermal treatment from 700 °C and no significant improvement of the conductivity by nanostructuration is observed. [ABSTRACT FROM AUTHOR]

In competitive thermoelectric devices for energy conversion and generation, high-efficiency materials of both n-type and p-type are required. For this, BiTe-based alloys have the best thermoelectric properties in room temperature applications. Partial replacement of tellurium by selenium is expected to introduce new donor states in the band gap, which would alter electrical conductivity and thermopower. We report on the preparation of n-type Bi(TeSe) solid solutions by a straightforward arc-melting technique, yielding nanostructured polycrystalline pellets. X-ray and neutron powder diffraction was used to assess Se inclusion, also indicating that the interactions between quintuple layers constituting this material are weakened upon Se doping, while the covalency of intralayer bonds is augmented. Moreover, scanning electron microscopy shows large surfaces perpendicular to the c crystallographic axis assembled as stacked sheets. Grain boundaries related to this 2D nanostructuration affect the thermal conductivity reducing it below 0.8 WmK at room temperature. Furthermore, Se doping increases the absolute Seebeck coefficient up to −140 μV K at 400 K, which is also beneficial for improved thermoelectric efficiency. [ABSTRACT FROM AUTHOR]

We investigated the fabrication of large-area (cm2) nanostructured glasses for solar cell modules with hydrophobic and hydrophilic properties using soft lithography and colloidal lithography. Both of these techniques entail low-cost and ease of nanofabrication. We explored the use of simple 1D and 2D nanopatterns (nanowires and nanocones) and the effect of introducing disorder in the nanostructures. We observed an increase in the transmitted light for ordered nanostructures with a maximum value of 99% for wavelengths >600 nm when ordered nanocones are fabricated on the two sides of the solar glass. They produced an increment in the efficiency of the packaged solar cell with respect to the glass without nanostructures. On the one hand, the wettability properties showed that the ordering of the nanostructures improved the hydrophobicity of the solar glasses and increased their self-cleaning capacity. On the other hand, the disordered nanostructures improved the hydrophilic properties of solar glasses, increasing their anti-fogging capacity. The results show that by selecting the appropriate nanopattern, the wettability properties (hydrophobic or hydrophilic) can be easily improved without decreasing the efficiency of the solar cell underneath.

Thermoelectric materials constitute an alternative source of sustainable energy, harvested from waste heat. BiTe is the most utilized thermoelectric alloy. We show that it can be readily prepared in nanostructured form by arc-melting synthesis, yielding mechanically robust pellets of highly oriented polycrystals. This material has been characterized by neutron powder diffraction (NPD), scanning electron microscopy (SEM), and electronic and thermal transport measurements. A microscopic analysis from NPD data demonstrates a near-perfect stoichiometry of BiTe and a fair amount of anharmonicity of the chemical bonds. The as-grown material presents a metallic behavior, showing a record-low resistivity at 320 K of 2 μΩ m, which is advantageous for its performance as a thermoelectric material. SEM analysis shows a stacking of nanosized sheets, each of them presumably single-crystalline, with large surfaces perpendicular to the c crystallographic axis. This nanostructuration notably affects the thermoelectric properties, involving many surface boundaries that are responsible for large phonon scattering factors, yielding a thermal conductivity as low as 1.2 W m K around room temperature. [ABSTRACT FROM AUTHOR]

Ultra-hydrophobic bilayer coatings on a glass surface were fabricated by sol–gel process using hexadecyltrimethoxysilane (C16TMS) and tetramethoxysilane (TMOS) (1:4 molar ratio) as precursors. After coating, silica nanoparticles (SiO2 NPs) functionalized with different mono-alkoxy derivatives (methoxytrimethylsilane, TMeMS; ethoxydimethylvinylsilane, DMeVES; ethoxydimethylphenylsilane, DMePhES; and methoxydimethyloctylsilane, DMeC8MS) were added, assuring the microscale roughness on the glass surface. Influences of the functionalized SiO2 NPs and surface morphology on the hydrophobicity of the hybrid films were discussed. The successful functionalization of SiO2 NPs with hydrophobic alkyl groups were confirmed by Fourier transform infrared spectroscopy (FTIR). The thermal stability of hydrophobic SiO2 NPs showed that the degradation of the alkyl groups takes place in the 200–400 °C range. Bilayer coating with C16TMS/TMOS and SiO2 NPs modified with alkoxysilane substituted with C8 alkyl chain (SiO2 NP-C8) has micro/nano structure. Hydrophobicity of functionalized SiO2 NPs-C8 and its higher degree of nanometer-scale roughness gave rise to ultra-hydrophobicity performance for bilayer coating C16TMS/TMOS + SiO2 NPs-C8 (145°), compared to other similar hybrid structures. Our synthesis method for the functionalization of SiO2 NPs is useful for the modification of surface polarity and roughness.

In this work, we produce bulk nanostructured Mg 2 Si 0.4 Sn 0.6 thermoelectric materials made of nanograins with sizes below 200 nm and containing a fine distribution of Sn-rich nanoparticles. These materials are obtained by the mechanical alloying followed by spark plasma sintering. The microstructure and transport properties, and their evolutions upon aging, are investigated. A model is developed to capture the different contributions to the phonon scattering processes arising from the nano/microstructural parameters. The calculations show quantitative agreement with the temperature and the temporal dependence of the lattice thermal conductivity of the nanostructured Mg 2 Si 0.4 Sn 0.6 alloy. This work provides a general analytic approach for identifying the individual contributions of the microstructural parameters on the thermal conductivity which is a very important property controlling the performance of thermoelectric materials. [ABSTRACT FROM AUTHOR]

The low vapor pressure of explosives makes the gaseous detection challenging and drives even the particle detection. There is a need to provide easy portable systems, highly spreadable. A bio-inspired concept was developed to detect explosive vapors with unprecedent sensitivities. Vertically aligned TiO2 nanotubes were grown on a cantilever. The sensors successfully detected trinitrotoluene (TNT) and pentaerythritol tetranitrate (PETN) with a minimum threshold concentration down to 0.8 ppt. This work describes also the investigations undertaken to develop the characterization of explosives by nanocalorimetry, which is able to identify explosives in form of single particles. [ABSTRACT FROM AUTHOR]

Abstract: Densities, viscosities and refractive index, as a function of temperature, and isobaric thermal expansion coefficient, were determined for 1-alkyl-3-methylimidazolium hexafluorophosphate, [CN−1C1im][PF6] (where N=5 to 10) series of ionic liquids. The density presents a regular decrease along the ionic liquid series, with no detectable alkyl chain length dependence of the thermal expansion coefficient. Both the refractive index and viscosity show a trend shift along the series around the [C6C1im][PF6] that could be associated to the impact of the change in the nanostructuration of the ionic liquids. The experimental results are compared with the analogous [CN−1C1im][NTf2] series and the effect of the anion is analyzed. The sphericity of the [PF6]− anion is reflected in the lower pre-exponential VTF parameter, Aη , and the higher viscosity of the [CN−1C1im][PF6], when compared with the [CN−1C1im][NTf2] series, is ruled by the higher energy barriers, which are related with stronger electrostatic interaction due to the low charge dispersion of the [PF6]−.anion. [Copyright &y& Elsevier]

Highlights: [•] Shear alignment of a block copolymer/epoxy thermosetting system is achieved. [•] Pre-shearing conditions play a key role in the orientation of the system. [•] Long-range order is investigated by TEM and SAXS. [ABSTRACT FROM AUTHOR]