Ouhbi Hassan, Ambrosio Francesco, De Angelis Filippo, Wiktor Julia
Department of Physics, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden.
Computational Laboratory for Hybrid/Organic Photovoltaics (CLHYO), Istituto CNR di Scienze e Tecnologie Chimicie "Giulio Natta" (CNR-SCITEC), Via Elce di Sotto 8, 06123 Perugia, Italy.
J Phys Chem Lett. 2021 Jun 10;12(22):5339-5343. doi: 10.1021/acs.jpclett.1c01326. Epub 2021 Jun 1.
Tin halide perovskites (THPs) have been established as a lower-toxicity alternative to lead halide perovskites. In spite of the increasing interest, the behavior of photoexcited charges has not been well understood in this class of materials. We here investigate the behavior of excess electrons in a series of tin halide perovskites by employing advanced electronic-structure calculations. We first focus on CsSnBr and show that electron localization is favorable in this compound and that bipolaronic states are the most stable form of self-trapped electrons. We then extend the analysis to CsSnI, CsSnCl, MASnBr, FASnBr, and DMASnBr and show that electron bipolarons are stable in all these compounds, thus indicating that strong electron localization is recurrent in THPs.
卤化锡钙钛矿(THPs)已被确立为卤化铅钙钛矿的低毒性替代品。尽管人们对其兴趣日益浓厚,但这类材料中光激发电荷的行为尚未得到很好的理解。我们在此通过先进的电子结构计算来研究一系列卤化锡钙钛矿中多余电子的行为。我们首先聚焦于CsSnBr,结果表明电子定域在该化合物中是有利的,并且双极化子态是自陷电子最稳定的形式。然后我们将分析扩展到CsSnI、CsSnCl、MASnBr、FASnBr和DMASnBr,结果表明电子双极化子在所有这些化合物中都是稳定的,从而表明强电子定域在卤化锡钙钛矿中是普遍存在的。