Search

A new ternary phosphidopolysilicate (IV), KSi2P3, has been synthesized by high temperature solid state reaction. The compound crystallizes in a new structure type in the monoclinic space group C2/c with a=10.1327(5)Å, b=10.1382(5)Å, c=21.1181(10)Å, β=96.88(0)°, and Z=8. In the structure, all SiP4 tetrahedra are connected with each other by corner-sharing P atoms to form layers, which are stacked along c direction and separated by K+ cations. The two-dimensional structure of KSi2P3 contrasts with those of the two known members in the ternary A/Si/P (A=alkali metal) system, namely Na5SiP3 (zero-dimensional) and K2SiP2 (one-dimensional), which contains less amount of Si. The band gap deduced from UV–vis–IR diffuse reflectance spectrum is 1.72eV. [ABSTRACT FROM AUTHOR]

The new ternary sulfide Sn 2 SiS 4 has been synthesized via high-temperature solid state reaction. It crystallizes in the centrosymmetric space group P2 1 / c of the monoclinic system. In the structure, the Sn 2+ cations are coordinated to a heavily-distorted octahedron of six S atoms or a pentagonal pyramid of six S atoms, both geometries clearly demonstrating the effect of the stereo-chemically active electron lone pair on the Sn coordination environment. These SnS 6 polyhedra and the SiS 4 tetrahedra are connected to each other via corner and edge-sharing to generate a three-dimensional framework. Based on the diffuse reflectance measurement and the electronic structure calculation, Sn 2 SiS 4 has an indirect band gap of 2.00 eV. Interestingly, Sn 2 SiS 4 exhibits an efficient visible-light-driven photocatalytic activity pertaining to Rhodamine B (RhB) degradation, which is superior to the important photocatalyst C 3 N 4 . Moreover, the photocatalytic mechanism was also elucidated based on the active species trapping experiments. [ABSTRACT FROM AUTHOR]

The first two members in the quaternary A/A′/M/Q (A = alkali metal; A′ = alkaline-earth metal; M = As, Sb, Bi; Q = S, Se, Te) system, namely the KBaMSe 3 (M = As, Sb) selenides, have been synthesized by solid state reactions. They are isostructural and crystallize in the centrosymmetric space group P 2 1 / c of the monoclinic system. In the structure, the trivalent M atom (M = As, Sb) is coordinated to three Se atoms forming a trigonal pyramid with the Se atoms serving as the triangle base, showing the stereochemical activity of the ns 2 lone pair electron. The MSe 3 (M = As, Sb) trigonal pyramids are totally isolated from each other with K + and Ba 2+ cations located between them. The optical band gaps of 2.26 (2) eV for KBaAsSe 3 and 2.04 (2) eV for KBaSbSe 3 , were deduced from the diffuse reflectance spectra. The first principles calculations were performed to study the electronic structures of KBaMSe 3 (M = As, Sb) compounds and the results indicated that these two compounds are indirect band gap semiconductors. [ABSTRACT FROM AUTHOR]