Publications by authors named "Clement Sanchez"

For photodetection applications using 3D hybrid perovskites (HPs), dense and thick films or compacted powders in wafer form are needed and generally require large amounts of HPs. HPs are also often combined with a graphene/carbon layer to improve their conductivity. Among HP synthesis methods, mechanosynthesis, a green synthesis method, provides a large amount of powders, which are furthermore easily densified in compact wafers due to their mechanical activation.

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The development of nanozeolites is crucial for advancing applications in catalysis, adsorption, and separation due to their unique structural and functional properties. Herein, we demonstrate the ultra-fast crystallization of RHO-type nanozeolite (in just a few tenths of a seconds) in a colloidal aluminosilicate suspension is demonstrated and is observed by transmission electron microscopy. Nucleation occurs almost instantaneously, within 5 s, under electron beam irradiation, followed by rapid, homogeneous crystal growth completed within 14-20 s.

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Understanding the condensation process of two precursors in the Stöber process is crucial to enhance the complexity and applicability of silica hybrids. We present a simple and effective method to prepare functional silica hybrid particles with tunable properties through the co-condensation of tetraethoxysilane and an organoalkoxide precursor using a modified Stöber process. Three organoalkoxide precursors have been studied: (3-mercaptopropyl)triethoxysilane, (3-cyanopropyl)triethoxysilane, and (3-aminopropyl)triethoxysilane.

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The deposition of conformal films from redox-active biological molecules, such as catechols, catecholamines, and other polyphenols, has demonstrated great versatility in terms of the substrate used. Precursors of allomelanins, mainly found in plants and fungi, have been largely overlooked as precursors for the design of conformal and robust coatings. Moreover, their potential application for the electrodeposition of films on conductive substrates has not yet been investigated.

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Self-assembly and characteristics of hybrid mesoporous silica film templates remain a subject of inquiry. The short time scale of the inorganic condensation and formation of micelles makes our understanding of this process insufficient. To provide an insight into the evaporation-induced self-assembly of such films, we synthesized an efficient molecular probe of the triethoxysilane precursor bearing a pyrene derivative.

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The physical properties of many modern multi-component materials are determined by their internal microstructure. Tools capable of characterizing complex nanoscale architectures in composite materials are, therefore, essential to design materials with targeted properties. Depending on the morphology and the composition, structures may be measured by laser diffraction, scattering methods, or by electron microscopy.

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Calcium carbonate (CaCO) is one of the most significant biominerals in nature. Living organisms are able to control its biomineralization by means of an organic matrix to tailor a myriad of hybrid functional materials. The soluble organic components are often proteins rich in acidic amino-acids such as l-aspartic acid.

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We have investigated the early stages of the formation of iron oxide nanoparticles from iron stearate precursors in the presence of sodium stearate in an organic solvent by liquid phase transmission electron microscopy (IL-TEM). Before nucleation, we have evidenced the spontaneous formation of vesicular assemblies made of iron polycation-based precursors sandwiched between stearate layers. Nucleation of iron oxide nanoparticles occurs within the walls of the vesicles, which subsequently collapse upon the consumption of the iron precursors and the growth of the nanoparticles.

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Solution-processed inorganic nanoporous films are key components for the vast spectrum of applications ranging from dew harvesting to solar cells. Shaping them into complex architectures required for advanced functionality often needs time-consuming or expensive fabrication. In this work, crack formation is harnessed to pattern porous inorganic films in a single step and without using lithography.

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Article Synopsis
  • Thermal decomposition is an effective method for creating nanosized metal oxides with specific properties, especially iron oxide nanoparticles.
  • The study examines the nucleation process in this synthesis, finding that it doesn't occur homogeneously but instead within vesicle-like nanoreactors.
  • The new mechanism involves steps like melting iron stearate particles, forming a unique crystalline phase, and producing iron oxide nuclei inside these nanoreactors, enhancing control over nanoparticle characteristics.
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ConspectusThe properties of a material depend upon its physical characteristics, one of these being its crystalline state. Next generation solid-state technologies will integrate crystalline oxides into thermal sensitive processes and composite materials. Crystallization of amorphous phases of metal oxides in the solid state typically requires substantial energy input to induce the amorphous to crystalline phase transformation.

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A family of iron-doped manganese-related hollandites, K Mn Fe O (0 ≤ ≤ 0.15), with high performance in CO oxidation have been prepared. Among them, the most active catalyst, KMnFeO(OH), is able to oxidize more than 50% of CO at room temperature.

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  • Incorporating boride nanocrystals into aluminum alloys enhances their mechanical properties, particularly strength and hardness.
  • Using molten salts synthesis, researchers created superhard hafnium diboride nanoparticles that remain stable during the manufacturing of aluminum nanocomposites.
  • Structural analysis shows strong interactions between the nanoparticles and aluminum matrix, resulting in reduced grain size and improved hardness, indicating potential for lightweight applications.
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Enantiopure α-Tfm-proline and α-Tfm-pipecolic acid were synthesized starting from commercially available diesters and ethyl trifluoroacetate. A Strecker type reaction on intermediate chiral Tfm-oxazolo-pyrrolidine and -piperidine provided the corresponding nitrile precursor of enantiopure (R) and (S) α-Tfm-proline and α-Tfm-pipecolic acid. The C-terminal peptide coupling reaction of α-Tfm-pipecolic acid has been successfully achieved.

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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.

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The straightforward synthesis of enantiopure 5-()-and 5-()-trifluoromethylproline is reported. The key steps are a Ruppert-Prakash reagent addition on l-pyroglutamic esters followed by an elimination reaction and a selective reduction. The solution-phase and solid-phase incorporation of this unprotected enantiopure fluorinated amino acid in a short peptide chain was demonstrated.

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Here, we present a correlative microscopic analysis of electrodeposited films from catechol solutions in aqueous electrolytes. The films were prepared in a miniaturized electrochemical cell and were analyzed by identical location transmission electron microscopy, scanning transmission X-ray microscopy, and atomic force microscopy. Thanks to this combined approach, we have shown that the electrodeposited films are constituted of ultrathin graphite oxide nanosheets.

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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.

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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.

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Article Synopsis
  • New research reveals important details about iron or titanium-doped KxMnO2 hollandites.
  • Techniques like neutron diffraction and advanced electron microscopy help to understand where the dopant cations are positioned within the material.
  • This localization of dopants is suggested to significantly influence the performance and functionality of these nanomaterials.
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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.

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Extracellular matrices (ECM) rich in type I collagen exhibit characteristic anisotropic ultrastructures. Nevertheless, working in vitro with this biomacromolecule remains challenging. When processed, denaturation of the collagen molecule is easily induced in vitro avoiding proper fibril self-assembly and further hierarchical order.

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In the field of heterogeneous catalysis, the successful integration of enzymes and inorganic catalysts could pave the way to multifunctional materials which are able to perform advanced cascade reactions. However, such combination is not straightforward, for example in the case of zeolite catalysts for which enzyme immobilization is restricted to the external surface. Herein, this challenge is overcome by developing a new kind of hybrid catalyst based on hollow zeolite microspheres obtained by the aerosol-assisted assembly of zeolite nanocrystals.

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Unveiling the mechanism of electrocatalytic processes is fundamental for the search of more efficient and stable electrode materials for clean energy conversion devices. Although several techniques are now available to track structural changes during electrocatalysis, especially of water oxidation, a direct observation, in real space, of morphological changes of nanostructured electrocatalysts is missing. Herein, we implement an electrochemical Transmission Electron Microscopy ( EC-TEM) methodology for studying electrocatalysts of the oxygen evolution reaction (OER) during operation, by using model cobalt oxide CoO nanoparticles.

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