Search

Antibacterial coatings are becoming increasingly attractive for application in the field of biomaterials. In this framework, we developed polymer coating zirconia with antibacterial activity using the "grafting from" methodology. First, 1-(4-vinylbenzyl)-3-butylimidazolium chloride monomer was synthesized. Then, the surface modification of zirconia substrates was performed with this monomer via surface-initiated photo atom transfer radical polymerization for antibacterial activity. X-ray photoelectron spectroscopy, ellipsometry, static contact angle measurements, and an atomic force microscope were used to characterize the films for each step of the surface modification. The results revealed that cationic polymers could be successfully deposited on the zirconia surfaces, and the thickness of the grafted layer steadily increased with polymerization time. Finally, the antibacterial adhesion test was used to evaluate the antibacterial activity of the modified zirconia substrates, and we successfully showed the antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa strains. [ABSTRACT FROM AUTHOR]

In the search of low cost and more efficient electronic devices, here the properties of SrVO3 transparent conductor oxide (TCO) thin film are investigated, both visible‐range optically transparent and highly conductive, it stands as a promising candidate to substitute the standard indium‐tin‐oxide (ITO) in applications. Its surface stability under water (both liquid and vapor) and other gaseous atmospheres is especially addressed. Through the use of spectroscopy characterizations, X‐ray photoemission and operando X‐ray absorption measurements, the formation of a thin Sr‐rich V5+ layer located at the surface of the polycrystalline SrVO3 film with aging is observed, and for the first time how it can be removed from the surface by solvating in water atmosphere. The surface recovery is associated to an etching process, here spectroscopically characterized in operando conditions, allowing to follow the stoichiometric modification under reaction. Once exposed in oxygen atmosphere, the Sr‐rich V5+ layer forms again. The findings improve the understanding of aging effects in perovskite oxides, allowing for the development of functionalized films in which it is possible to control or to avoid an insulating surface layer. This constitutes an important step towards the large‐scale use of V‐based TCOs, with possible implementations in oxide‐based electronics. [ABSTRACT FROM AUTHOR]

Although vanadium compounds are well recognized for their ability to change from insulator to metal, they may also be used therapeutically to address significant medical issues. In this study, we used vanadium oxide thin films synthesized by the pulsed laser deposition (PLD) technique to examine human stem cells generated from bone marrow. According to x-ray reflectivity (XRR) measurements, the films' thickness ranged from 6 to 26 nm. The water contact angle method has been employed to probe the surface energy and wettability of the films, which influence the cell behavior significantly. We also used a variety of techniques, such as differentiation staining, phase contrast microscopy, and real-time reverse transcription-polymerase chain reaction (RT-PCR), to examine the growth, adhesion, proliferation, and differentiation of human bone marrow mesenchymal stem cells (hBMMSCs) on these oxide films over time. Our results indicated that vanadium oxide films alter hBMMSCs adhesion and growth and affect their differentiation. The application of VOx films in biological and medical materials, as well as future research on cells, is all made possible by these findings, which also improve our understanding of the biological actions of vanadium compounds. [ABSTRACT FROM AUTHOR]

The strain coupling, microstructural evolution, and functional properties of a series of BaTi[O.sub.3] (BTO) films with different second-phase oxide additions, Ti[O.sub.2], MgO, Zr[O.sub.2], [Sm.sub.2][O.sub.3] and [Y.sub.2][O.sub.3] (YO), is studied. The studies have shown that the strain state in BTO is tuned by different additions and compared with BFO, which is switched from tensile for a pure film on STO to compressive by the presence of the second phase (SmO).

Indium‐tin‐oxide (ITO) is a widely employed transparent conducting oxide (TCO), but the indium scarcity and price encourage developing some alternatives. The correlated metals CaVO3 and SrVO3 have been recently identified as new TCOs with functional properties being comparable to ITO. However, their technological potential is limited by the critical requirement of a perovskite structure of the film, impossible to achieve via direct growth on substrates commonly used for applications. In this article, the authors tackle this limitation by demonstrating the crystalline growth of vanadate TCOs on glass at temperatures below 600 °C, with the help of 2D nanosheets as transparent seed layers. The functional properties do not suffer from the textured structure of the films, as confirmed by an in‐depth spectroscopic ellipsometry study, allowing for an industrially viable approach to integrate vanadate TCOs on virtually any surface and to exploit their promising performances as a new generation TCO. [ABSTRACT FROM AUTHOR]

Since SrVO3 (SVO) can be used as a highly conductive material for perovskite heterostructures, the control of surface morphology and chemistry of such thin‐films are essential. Using pulsed laser deposition, two distinct topographies can be produced. Thus, by tuning oxygen pressure in the growth chamber during cooling, smooth or partially covered by self‐oriented Sr3V2O8 nanorods surfaces can be grown. This study manages to correlate the two typical topographies, revealed by atomic force microscopy (AFM), with their chemical compositions obtained by X‐ray photoelectron spectroscopy (XPS). At first, a model describes their initial surface chemistry through the Sr/V cationic ratio and the (Sr+V)/Oox ratio. Furthermore, using sputter‐depth profiling, post‐thermal treatments and wet chemical etching, SVO thin‐film chemical compositions are extensively studied. We demonstrate that they are composed of stoichiometric SVO phase covered by Sr‐rich layer on top. Finally, treatment in water for 180 seconds helps to remove Sr‐rich phases. Sr3V2O8 nanorods are found selectively dissolved leaving a surface nano‐imprint. Moreover, on smooth SVO surfaces, a balanced Sr/V cationic ratio of 1.0±0.1 is obtained. These results appear very promising for SVO thin‐films surface preparation and further development as electrodes for electronic devices. [ABSTRACT FROM AUTHOR]

SrVO3 (SVO) is a model system for strongly correlated oxides and is highly promising as conductive layer in heterostructures. Therefore, the control of electronic properties and morphology are essential for the advanced applications. Here, the oxygen stability during and after the deposition is explored, as SVO film is expected to undergo different postdeposition thermal and atmosphere treatments during its integration in a heterostructure. Hence, the influence of oxygen stability on morphology and electrical properties of the metallic SrVO3 grown by pulsed laser deposition has been investigated. Films grown under vacuum (SrVO3− δ ) exhibit a very smooth surface while films grown under higher oxygen pressure roughen and present nanostructures at the surface. These nanostructures are found to be of Sr3V2O8 phase and their apparition can be controlled by the oxygen supply. Subsequent thermal treatments at different temperatures under same oxygen pressure prevent formation of the Sr3V2O8 phase, lead to the stoichiometric SrVO3, and thus improve the transport properties. In this study is shown the extreme sensitivity of SVO to oxygen and the conditions to obtain high quality smooth SVO films with improved electrical properties for electrode application. [ABSTRACT FROM AUTHOR]

We have studied the chemical and electronic properties of LaAlO3/SrVO3 (SVO) ultrathin films by combining hard x-ray photoemission spectroscopy and transport measurements. We compare single SrVO3 (SVO) ultrathin films and SrVO3 buried below a polar LaAlO3 (LAO) thin layer, both epitaxially grown on SrTiO3. While ultrathin films (4 unit cells) of SVO do show insulating behavior over the entire temperature range, the LAO/SVO interface has a resistivity minimum at 250 K. When increasing the SVO layer thickness, the minimum is observed to shift to higher temperatures, but the resistivity always stays smaller than that of comparable SVO single films. Hard x-ray photoemission spectroscopy reveals a surface or interface related V5+ component in the V 2p spectra for SVO films and LAO/SVO heterostructures, respectively, attributed to a strongly oxidized component. This chemical reconstruction is weaker in LAO/SVO heterostructures compared to single SVO films. We show that this dead layer in SVO ultrathin films has to be considered when the film thickness reaches the few unit-cells limit and propose solutions on how to prevent this detrimental effect. [ABSTRACT FROM AUTHOR]

In situ optical characterizations of metal-insulator (MI) transition have been developed in a pulsed laser deposition (PLD) chamber. It consists of associating a spectroscopic ellipsometer and an infrared camera. The first one is sensitive to modifications of the optical indexes and the second one to the emissivity changes. We focus onto the metallic LaNiO3 and the insulating SrTiO3, which present opposite electrical properties as a function of their oxygen content. Using a combinatorial synthesis approach during fabrication by PLD onto LaAlO3 substrate, we observe the evolution of the apparent temperature for different area corresponding to single LaNiO3 or SrTiO3 layers and heterostructures during reduction and reoxygenation process at constant temperature. Thus, the possibility to grow off-stochiometric samples by PLD or to reduce them by heating under high vacuum, associated to the ability of injecting controlled quantity of oxygen by pulsed valve, provide us an original tool in order to study the (MI) transition. [ABSTRACT FROM AUTHOR]

Two-phase, vertical nanocomposite heteroepitaxial films hold great promise for (multi)functional device applications. In order to achieve practical devices, a number of hurdles need to be overcome, including the creation of ordered structures (and their formation on a large scale), achieving different combinations of materials and control of strain coupling between the phases. Here we demonstrate major advances on all these fronts: remarkable spontaneously ordered structures were produced in newly predicted compositions, vertical strain was proven to dominate the strain state in films above 20 nm thickness and strain manipulation was demonstrated by selection of phases with the appropriate elastic moduli. The work opens up a new avenue for strain control in relatively thick films and also promises new forms of ordered nanostructures for multifunctional applications. [ABSTRACT FROM AUTHOR]

This article reports on the magnetism of continuous and patterned bismuth iron garnet (Bi3Fe5O12 or BIG) thin films for magnetophotonic crystal (MPC) applications. The exact knowledge of the magnetic properties is crucial for the design of fully functional MPC. BIG thin films were grown on several types of isostructural substrates by pulsed laser deposition. The growth conditions and bismuth transfer were optimized to obtain good quality magneto-optically active films compatible with nanostructuring process. MPC were successfully fabricated from BIG/GGG(001) films with low roughness and high Faraday rotation. Magnetic characteristics (magnetization, anisotropy, magnetic domains, magnetization reversal) of the continuous BIG films and MPC were extensively studied and compared to the results of the micromagnetic simulations performed for MPC with different anisotropy. The present study shows that the fabrication of the MPC structure lowers the magnetocrystalline and uniaxial in-plane anisotropies and induces a partial out-of-plane magnetization. External field smaller than 2000 G is sufficient to ensure the out-of-plane saturation of magnetization for optimum device operation, in agreement with micromagnetic calculations. The experimentally determined magnetic properties of MPC are fully compatible with the device operation. [ABSTRACT FROM AUTHOR]

The vanadate SrVO3 is a transparent conductor perovskite with optical and electrical properties competing with those of the most‐used indium tin oxide material. Although its charge density is comparable to that of metals, SrVO3 shows a plasma frequency below the visible range due to strong electronic correlations characterizing the electronic transport in this material and enhancing the effective mass. Therefore, the well‐known interplay between the structure and the electronic properties of strongly correlated systems can be used in such transparent conductor to tune the optical properties, as the plasma frequency also depends on the effective mass. In this study, SrVO3 films are grown by pulsed laser deposition onto different lattice mismatched perovskite substrates such as SrTiO3, LaAlO3, and (LaAlO3)0.3(Sr2TaAlO6)0.7 at different growth temperatures. The structural, electronic, and optical properties are analyzed, illustrating the influence of the strain on the structure of the films and on a shift of the plasma frequency. The electronic correlations in this new group of transparent conducting oxides can be therefore used as a supplementary lever for the tuning of the functional properties. SrVO3 thins films are grown by pulsed laser deposition onto SrTiO3, LaAlO3, and (LaAlO3)0.3(Sr2TaAlO6)0.7. Both optical and electrical properties of the films are investigated and demonstrate that such strongly correlated system is competing with the indium tin oxide as new transparent conducting oxide. The plasma frequency of the films depends on the substrate and can be easily tuned toward the infrared region. [ABSTRACT FROM AUTHOR]

We investigate the spin-dependent electronic density of states near and above the Fermi level in bismuth iron garnet (BIG), Bi3Fe5O12, by magnetic circular dichroism and magneto-optical Faraday spectroscopy. BIG is a recently synthesized material, as its preparation requires special nonequilibrium conditions. Its scientific and applicative interest resides in huge specific Faraday rotation of the incident light, useful for magneto-optic applications. We show experimentally the presence of spin gaps in the conduction band as recently predicted theoretically by Oikawa et al. [T. Oikawa, S. Suzuki, and K. Nakao, J. Phys. Soc. Jpn. 74, 401 (2005)]. In the range of photon energies, where full spin polarization is expected, completely asymmetric Faraday hysteresis loops were observed, similar to those observed in half-metals such as (Pr,La)0.7Ca0.3MnO3 and Fe3O4. These results were modeled using even and odd (with respect to magnetization) contributions into hysteresis loops. The odd contribution appears only in the energy ranges where the density of states is fully spin polarized and vanishes at the Curie temperature. These results open a new perspective for the use of bismuth iron garnet in optic spintronics at room temperature and above. [ABSTRACT FROM AUTHOR]

Zirconia surfaces were functionalized by polymer grafting according to a simple and successful two-steps procedure. In the first step, the initiator bearing a N , N -dimethyl amine group was grafted on the surface by co-deposition with dopamine. Secondly, different monomers such as styrene, methyl methacrylate, 2-hydroxyethylmethacrylate, 2,2,2-trifluoroethyl methacrylate and styrene sulfonate were polymerized on the surface using photochemical activation. The efficiency of the two steps, initiator grafting and photopolymerization, were checked by several analytical techniques including X-ray photoelectron spectroscopy (XPS), spectroscopic ellipsometry (SE) and water contact angle measurements. Theses characterizations highlighted the surface chemical change after each step and the possibility to modulate surface hydrophilicity and hydrophobicity by grafting-from polymerizations. [Display omitted] • A novel initiator for radical photopolymerization bearing a catechol group was prepared by a simple two-step procedure. • Zirconia surfaces were functionalized by grafting of a polymer layer using photopolymerization with blue led activation. • The hydrophilicity and hydrophobicity of zirconia surfaces could be modulated according to the nature of the monomer used. [ABSTRACT FROM AUTHOR]

• Self organized epitaxial Sr 3 V 2 O 8 nanorods on SrVO 3 metallic matrix. • Specific local electric properties by conductive Atomic Force Microscopy and scanning tunneling microscopy. • Three dimensional resistance mapping of the nanorods by 3D-Spreading Resistance Microscopy mode. Self-organized epitaxial nanorods, obtained by an adapted annealing process after deposition of metallic strontium vanadate perovskite (SrVO 3) thin films, are analyzed to determine their structural, chemical and electrical properties. After the identification of the Sr 3 V 2 O 8 phase of the nanorods by electron diffraction; Electron Energy Loss Spectroscopy investigations show the vanadium oxidation state (V5+) for the nanorods. Two scanning probe techniques are deployed to determine the specific local electrical properties of these Sr 3 V 2 O 8 nanorods. In ambient conditions, local electrical properties are studied by Scanning Spreading Resistance Microscopy based on an Atomic Force Microscope and multiple probe scanning tunneling microscopy is used for the study in ultrahigh vacuum. Both techniques reveal that local electrical resistances of the nanorods are five order of magnitude higher than the resistance of the perovskite SrVO 3 matrix. Futhermore, the nanorods are found to be etched by repeating scanning of the conductive Atomic Force Microcopy probe, enabling a three-dimensional depth profile of the nanorods resistance with 3D-Spreading Resistance Microscopy mode. A partial embedding of the nanorods in the underlying SrVO 3 film is proved and the impact of the water meniscus at the origin of the selective etching observed during Scanning Spreading Resistance Microscopy, in ambient conditions, is discussed. [ABSTRACT FROM AUTHOR]

We have investigated the effects of low-energy ion beam irradiations using argon clusters on the chemical and electronic properties of LaAlO 3 / SrTiO 3 (LAO/STO) heterointerfaces by combining x-ray photoelectron spectroscopy (XPS) and electrical transport measurements. Due to its unique features, we demonstrate that a short-time cluster ion irradiation of the LAO surface induces significant modifications in the chemical properties of the buried STO substrate with (1) a lowering of Ti atoms oxidation states (from Ti 4 + to Ti 3 + and Ti 2 + ) correlated to the formation of oxygen vacancies at the LAO surface and (2) the creation of new surface states for Sr atoms. Contrary to what is generally observed by using higher energy ion beam techniques, this leads to an increase of the electrical conductivity at the LAO/STO interface. Our XPS data clearly reveal the existence of dynamical processes on the titanium and strontium atoms, which compete with the effect of the cluster ion beam irradiation. These relaxation effects are in part attributed to the diffusion of the ion-induced oxygen vacancies in the entire heterostructure since an increase of the interfacial metallicity is also evidenced far from the irradiated area. This paper highlights the possibility of tuning the electrical properties of LAO/STO interfaces by surface engineering, confirming experimentally the intimate connection between LAO chemistry and electronic properties of LAO/STO interfaces. [ABSTRACT FROM AUTHOR]

Correlated transparent conducting oxides (TCOs) have gained great attention, because of their unique combination of transparency and metallic character. SrVO 3 (SVO) was identified as a high-performance TCO in the visible range. Few studies have investigated band structure engineering through chemical doping to enhance the optical properties of SVO. Here, we use two different strategies by exploiting the band-filling and width of the bands derived from Vanadium to tune the screened plasma frequency ω p * and the interband transition E p - d energy, corresponding to the optical transparency window edges. For control of the band-filling strategy, it is found that Titanium doped SVO has a wide transparency window, but such a composition does not maintain the high electrical conductivity required for TCO applications. Concerning the bandwidth strategy, the doping of SrVO 3 by Calcium shows that ω p * remains located in the IR range (1.12 eV), while E p - d is blue-shifted into the UV region (3.43 eV) due to reinforced electronic correlations. By an appropriate choice of dopant, we successfully increased the size of the transparency window by around 11% from 1.94 eV (SVO) to 2.30 eV (Calcium-doped SVO), while retaining high conductivity of around 2.30 × 10 4 (S·cm -1 ) and high charge carrier density of 2.93 × 10 22 cm -3 .

SrVO 3 (SVO) is a prospective candidate to replace the conventional indium tin oxide (ITO) among the new generation of transparent conducting oxide (TCO) materials. In this study, the structural, electrical, and optical properties of SVO thin films, both epitaxial and polycrystalline, are determined during and after heat treatments in the 150-250 °C range and under ambient environment in order to explore the chemical stability of this material. The use of these relatively low temperatures speeds up the natural aging of the films and allows following the evolution of their related properties. The combination of techniques rather sensitive to the film surface and of techniques sampling the film volume will emphasize the presence of a surface oxidation evolving in time at low annealing temperatures, whereas the perovskite phase is destroyed throughout the film for treatments above 200 °C. The present study is designed to understand the thermal degradation and long-term stability issues of vanadate-based TCOs and to identify technologically viable solutions for the application of this group as new TCOs.

We have probed the structural and magnetic properties of PrVO 3 (PVO) thin films grown on the (001)-, (110)-, and (111)-oriented SrTiO 3 (STO) substrates. By changing the substrate orientation, the film out-of-plane orientation can be tuned to [110], [100]/[010], and [011]/[311], with different in-plane crystallographic variants. Accommodation of these variants on the different substrates implies different strain states, which have direct influence on the magnetic properties of PVO films. The magnetic moment of PVO films radically enhances from 0.4 μ B /f.u. for STO(001) to 2.3 μ B /f.u. for STO(111). While films on the (001)-oriented STO substrate display out-of-plane anisotropy, an in-plane anisotropy is observed for films grown on the (110)- and (111)-oriented STO substrates. In addition, a strong uniaxial magnetic anisotropy is also extracted for a partially relaxed film on the (110)-oriented STO substrate. Such findings can help oxide community for the better understanding of magnetic anisotropy in vanadate thin films, a subject that still suffer from significant lack of scientific investigations.

The integration of functional thin film materials with adaptable properties is essential for the development of new paradigms in information technology. Among them, complex oxides with perovskite structures have huge potential based on the particularly vast diversity of physical properties. Here, we demonstrate the possibility of transferring perovskite oxide materials like SrTiO 3 onto a silicon substrate using an environmentally friendly process at the nanoscale by means of a water-soluble perovskite sacrificial layer, SrVO 3 . Based on in situ monitoring atomic force microscopy and photoemission studies, we reveal that the dissolution is initiated from a strontium-rich phase at the extreme surface of SrVO 3 . The nanothick SrTiO 3 -transferred layer onto silicon presents appropriate morphology and monocrystalline quality, providing a proof of concept for the integration and development of all-perovskite-oxide electronics or "oxitronics" onto any Si-based substrate.