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层状卤化物双钙钛矿:CsAgBiBr 的维度降低。

Layered Halide Double Perovskites: Dimensional Reduction of CsAgBiBr.

机构信息

Department of Chemistry , Stanford University , Stanford , California 94305 , United States.

Institute of Physics , University of Bayreuth , 95440 Bayreuth , Germany.

出版信息

J Am Chem Soc. 2018 Apr 18;140(15):5235-5240. doi: 10.1021/jacs.8b01543. Epub 2018 Apr 9.

Abstract

We investigate the consequences of dimensional confinement on halide double perovskites by synthesizing two-dimensional analogues of the recently reported three-dimensional double perovskite CsAgBiBr. The layered perovskites (BA)AgBiBr (1) and (BA)CsAgBiBr (2) (BA = CH(CH)NH) feature metal-halide sheets of mono and bilayer thickness, respectively, where the ordered double-perovskite lattice is partitioned by organic cations. Electronic structure calculations indicate that the indirect bandgap of CsAgBiBr becomes direct when the infinitely thick inorganic lattice is reduced to monolayer thickness. Calculations on model systems allow us to separate the effects of dimensional reduction from those of the accompanying structural distortions in the inorganic sublattice. Detailed optical characterization shows that the photophysical properties of 1 and 2 are markedly different than those of their well-studied lead-halide analogs. Hybrid layered derivatives of double perovskites substantially expand on the substitutional flexibility of halide perovskites to encompass greater compositional and electronic diversity.

摘要

我们通过合成最近报道的三维双钙钛矿 CsAgBiBr 的二维类似物,研究了维度限制对卤化物双钙钛矿的影响。层状钙钛矿(BA)AgBiBr(1)和(BA)CsAgBiBr(2)(BA = CH(CH)NH)的金属卤化物片分别具有单层和双层厚度,其中有序的双钙钛矿晶格由有机阳离子隔开。电子结构计算表明,当无限厚的无机晶格减薄至单层厚度时,CsAgBiBr 的间接带隙变为直接带隙。对模型体系的计算使我们能够将维度降低的影响与无机子晶格伴随的结构变形的影响分开。详细的光学特性表明,1 和 2 的光物理性质明显不同于其经过充分研究的铅卤化物类似物。双钙钛矿的混合层状衍生物大大扩展了卤化物钙钛矿的取代灵活性,从而包含更大的组成和电子多样性。

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