单独一对
铁电性
材料科学
凝聚态物理
单斜晶系
结晶学
价(化学)
卤化物
锡
钙钛矿(结构)
化学物理
电介质
物理
化学
晶体结构
无机化学
量子力学
光电子学
分子
冶金
作者
Michael W. Swift,John L. Lyons
出处
期刊:Cornell University - arXiv
日期:2023-08-04
被引量:1
标识
DOI:10.1021/acs.chemmater.3c02201
摘要
The lone-pair s states of germanium, tin, and lead underlie many of the unconventional properties of the inorganic metal halide perovskites. Dynamic stereochemical expression of the lone pairs is well established for perovskites based on all three metals, but previously only the germanium perovskites were thought to express the lone pair crystallographically. In this work, we use advanced first-principles calculations with a hybrid functional and spin-orbit coupling to predict stable monoclinic polar phases of $\mathrm{CsSnI}_3$ and $\mathrm{CsSnBr}_3$, which exhibit a ferroelectric distortion driven by stereochemical expression of the tin lone pair. We also predict similar metastable ferroelectric phases of $\mathrm{CsPbI}_3$ and $\mathrm{CsPbBr}_3$. In addition to ferroelectricity, these phases exhibit the Rashba effect. Spin splitting in both the conduction and valence bands suggests that nanostructures based on these phases could host bright ground-state excitons. Finally, we discuss paths toward experimental realization of these phases via electric fields and tensile strain.
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