Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University , Nishikyo-ku, Kyoto 615-8510, Japan.
Research Center for Advanced Computing Infrastructure, JAIST , Asahidai 1-1, Nomi, Ishikawa 923-1292, Japan.
J Am Chem Soc. 2017 Dec 27;139(51):18725-18731. doi: 10.1021/jacs.7b11497. Epub 2017 Dec 14.
A layered oxychloride BiNbOCl is a visible-light responsive catalyst for water splitting, with its remarkable stability ascribed to the highly dispersive O-2p orbitals in the valence band, the origin of which, however, remains unclear. Here, we systematically investigate four series of layered bismuth oxyhalides, BiOX (X = Cl, Br, I), BiNbOX (X = Cl, Br), BiGdOX (X = Cl, Br), and SrBiOX (X = Cl, Br, I), and found that Madelung site potentials of anions capture essential features of the valence band structures of these materials. The oxide anion in fluorite-like blocks (e.g., [BiO] slab in BiNbOCl) is responsible for the upward shift of the valence band, and the degree of electrostatic destabilization changes depending on building layers and their stacking sequence. This study suggests that the Madelung analysis enables a prediction and design of the valence band structures of bismuth and other layered oxyhalides and is applicable even to a compound where DFT calculation is difficult to perform.
层状氧氯化物 BiNbOCl 是一种对可见光响应的水分解催化剂,其显著的稳定性归因于价带中高度分散的 O-2p 轨道,但其起源尚不清楚。在这里,我们系统地研究了四类层状铋卤化物,BiOX(X = Cl、Br、I)、BiNbOX(X = Cl、Br)、BiGdOX(X = Cl、Br)和 SrBiOX(X = Cl、Br、I),并发现阴离子的Madelung 位势捕获了这些材料价带结构的基本特征。萤石型块体中的氧化物阴离子(例如,BiNbOCl 中的 [BiO] 片层)负责价带的向上移动,而静电去稳定化的程度取决于建筑层及其堆叠顺序。这项研究表明,Madelung 分析能够预测和设计铋和其他层状卤氧化物的价带结构,即使对于 DFT 计算难以进行的化合物也是如此。