The double perovskite halides A2BIBIIIX6 provide flexibility for various formulation adjustments and are of less toxicity in comparison with well-discussed complex lead halide derivatives. Such type of structure can be formed by replacing two Pb2+ ions in the cubic lattice with a pair of non-toxic heterovalent (monovalent and trivalent) metal cations, such as silver and indium. The aim of this work is to briefly characterize the phase equilibria in the ternary system CsBr-AgBr-InBr3 and investigate the thermodynamic availability of synthesis of Cs2AgInBr6 double perovskite phase by solid-state sintering or melt crystallization. The results demonstrate the unfeasibility of the Cs2AgInBr6 phase but high stability of the corresponding binary bromides perspective for optoelectronics.

An alkoxysilane derivative bearing a 10-vertex closodecaborate nanocluster (B 10 H 10 2−) was successfully synthesized and immobilized in a SiO 2 aerogel matrix. closo-Decaboratecontaining SiO 2 aerogels showed high specific surface (∼750 m 2 / g), open porosity (∼95%), and extremely low apparent density (80 mg/cm 3 ) as well as increased thermal stability of the closodecaborate moiety. Despite the low boron content (∼1.2 mol % of boron nanoclusters comprising natural mixture of boron isotopes), the aerogel nanomaterial demonstrated excellent neutron capture properties exceeding lightweight polymer-based analogues. Cell viability assessment indicated the pronounced dose-dependent toxicity of the borylated aerogel with respect to malignant cells (U251 MG glioblastoma line) and low toxicity with respect to normal cells (dental pump stem cells). The combination of the properties of closo-decaborate-modified silica aerogels makes them good candidate material for shielding of patients and healthcare personnel during boron neutron capture therapy procedures.

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New bromide compounds A2BIBIIIBr6 with a double perovskite structure provide variety and flexibility of optoelectronic properties, and some of them are of poor toxicity in comparison with such popular lead halides. The promising compound with a double perovskite structure was proposed recently for the ternary system of CsBr-CuBr-InBr3. Analysis of phase equilibria in the CsBr-CuBr-InBr3 ternary system showed stability of the quasi-binary section of CsCu2Br3–Cs3In2Br9. Formation of the estimated phase Cs2CuInBr6 by melt crystallization or solid-state sintering was not observed, most likely, as a result of higher thermodynamic stability of binary bromides CsCu2Br3 and Cs3In2Br9. The existence of three quasi-binary sections was observed, while no ternary bromide compounds were found.