Nurdillayeva Raushan N, Moral Raphael F, Pols Mike, Lee Do-Kyoung, Altoe Virginia, Schwartz Craig P, Tao Shuxia, Sutter-Fella Carolin M
Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Khoja Akhmet Yassawi International Kazakh-Turkish University, Turkistan 161200, Kazakhstan.
ACS Nano. 2025 Mar 25;19(11):11348-11357. doi: 10.1021/acsnano.5c00480. Epub 2025 Mar 16.
Chiral two-dimensional (2D) hybrid organic-inorganic metal halide perovskite semiconductors have emerged as an exceptional material platform with many design opportunities for spintronic applications. However, a comprehensive understanding of changes to the crystal structure and chiroptical properties upon exposure to atmospheric humidity has not been established. We demonstrate phase degradation to the 1D (MBA)PbI (MBA = methylbenzylammonium) and the hypothetical (MBA)PbI·HO hydrate phases, accompanied by a reduction and disappearance of the chiroptical response. First-principle simulations show that water molecules preferentially locate at the interface between the organic cations and the inorganic framework, thereby disrupting the hydrogen bonding, impacting both the structural chirality and stability of the material. These findings provide critical insights into phase degradation mechanisms and their impact on chiroptical activity in chiral 2D perovskites.
手性二维(2D)有机-无机杂化金属卤化物钙钛矿半导体已成为一种特殊的材料平台,为自旋电子学应用提供了许多设计机会。然而,对于暴露在大气湿度下时晶体结构和手性光学性质的变化,尚未形成全面的认识。我们证明了(MBA)PbI(MBA = 甲基苄基铵)一维相和假设的(MBA)PbI·H₂O水合物相发生了相降解,同时伴随着手性光学响应的降低和消失。第一性原理模拟表明,水分子优先位于有机阳离子与无机骨架之间的界面处,从而破坏氢键,影响材料的结构手性和稳定性。这些发现为手性二维钙钛矿中的相降解机制及其对手性光学活性的影响提供了关键见解。