Intercalation of Cu into layered polychalcogenide LaOS was demonstrated to be viable both under solvothermal conditions at 200 °C and mechanical ball milling at ambient temperature. This result evidences the soft-chemical nature of metal intercalation into layered polychalcogenides driven by the redox reactivity of anion-anion bonds.
View Article and Find Full Text PDFDesigning and synthesising new metastable compounds is a major challenge of today's material science. While exploration of metastable oxides has seen decades-long advancement thanks to the topochemical deintercalation of oxygen as recently spotlighted with the discovery of nickelate superconductor, such unique synthetic pathway has not yet been found for chalcogenide compounds. Here we combine an original soft chemistry approach, structure prediction calculations and advanced electron microscopy techniques to demonstrate the topochemical deintercalation/reintercalation of sulfur in a layered oxychalcogenide leading to the design of novel metastable phases.
View Article and Find Full Text PDFAfter decades of speculation without material proof, the yellow-orange luminescence of scapolite is definitely assigned to (S) activators trapped in [Na] square cages. Synthetic sulfur-doped scapolites confirm the implication of sulfur species in luminescence. Formally, the emission and excitation spectra of various polysulfide species were calculated.
View Article and Find Full Text PDFSeveral new materials with four structure-types (e.g., CuInGaS (CIGS), CuInGaS (CIGS), CuInGaS (CIGS), and CuInGaS (CIGS)) have been evidenced in the CuS-InS-GaS pseudo-ternary system.
View Article and Find Full Text PDFWe demonstrate here the low temperature topochemical insertion of transition elements (Fe, Ni, and Cu) in precursors containing pre-formed (Sn)2- (n = 2 and 3) oligomers. Indeed, this soft chemistry route opens the door to the easy, orientated synthesis of low dimensional transition metal compounds provided that the elemental metal can retrocede electron(s) to empty antibonding sulfur σ* levels.
View Article and Find Full Text PDFCdInS and InS compounds were both previously studied as buffer layers in CIGS-based thin-film solar cells, each of them exhibiting advantages and disadvantages. Thus, we naturally embarked on the study of the CdInS-InS system, and a series of CdInS (0 ≤ x ≤ 1) materials were prepared and characterized. Our results show that two solid solutions exist.
View Article and Find Full Text PDFLayered transition metal compounds represent a major playground to explore unconventional electric or magnetic properties. In that framework, topochemical approaches that mostly preserve the topology of layered reactants have been intensively investigated to tune properties and/or design new materials. Topochemical reactions often involve the insertion or deinsertion of a chemical element accompanied by a change of oxidation state of the cations only.
View Article and Find Full Text PDFThe cationic and anionic disorder in the CuZnSnSe-CuZnSnS (CZTSe-CZTS) system has been investigated through a chemical crystallography approach including X-ray diffraction (in conventional and resonant setup), Sn and Se NMR spectroscopy, and high-resolution transmission electron microscopy (HRTEM) techniques. Single-crystal XRD analysis demonstrates that the studied compounds behave as a solid solution with the kesterite crystal structure in the whole S/(S + Se) composition range. As previously reported for pure sulfide and pure selenide compounds, the Sn NMR spectroscopy study gives clear evidence that the level of Cu/Zn disorder in mixed S/Se compounds depends on the thermal history of the samples (slow cooled or quenched).
View Article and Find Full Text PDFSuspensions of carbon blacks and spherical carbon particles are studied experimentally and numerically to understand the role of the particle shape on the tendency to percolation. Two commercial carbon blacks and one lab-synthesized spherical carbon are used. The percolation thresholds in suspensions are experimentally determined by two complementary methods: impedance spectroscopy and rheology.
View Article and Find Full Text PDFThe inherently oxygen-deficient compounds Ln26O27 square(BO3)8 (Ln=La, Nd) react with water vapor leading to Ln26O26(OH)2(BO3)8 phases, and this reaction is reversible. The crystal structure of Nd26O27 square(BO3)8 has been determined from single-crystal data (space group P with a=6.7643(10) A, b=12.
View Article and Find Full Text PDF