Conformational Disordering of Organic Cations during Moisture-Induced Structural Collapse in Organic-Inorganic Hybrid Perovskites

被引:1
作者
Lai, Jing [1 ]
Tan, Junjun [2 ]
Zhu, Renlong [1 ]
Lv, Wenyu [1 ]
Ye, Shuji [1 ,2 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Lab, Hefei 230088, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
organic-inorganic hybrid perovskites; stability; sum frequency generation; aromatic cations; structure-property relationship; CHARGE-CARRIER DYNAMICS; VIBRATIONAL SPECTROSCOPY; HALIDE; DEGRADATION; GENERATION; EFFICIENCY; STABILITY; SURFACE; SPACER;
D O I
10.1021/acsaem.4c02147
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Moisture-induced structural collapse is an important factor hindering the commercialization of organic-inorganic hybrid perovskites, where organic cations play a crucial role. However, owing to the softness and complexity of organic cations, very few techniques can be used to characterize the collapse process in situ and in real time. In this study, we used a phenylpropylamine (PPA)-based 2D perovskite as a model and demonstrated that femtosecond sum frequency generation vibrational spectroscopy (SFG-VS) provides a powerful probe for the conformational disordering evolution of organic cations during perovskite collapse. Photoluminescence (PL) spectroscopy was used to monitor perovskite structural collapse. Following the collapse of the perovskite from a 2D confinement effect to a 1D confinement effect, the effective in-plane charge carrier mobility (phi mu) and 2D exciton ratio of the films decreased. The decreases in the 2D exciton ratio and phi mu are strongly correlated with the relative conformational disordering degree of the organic cations, revealing the structural origin of perovskite collapse. Coating the perovskite film surface with a Teflon layer can effectively retard structural collapse and maintain the conformational ordering of organic cations.
引用
收藏
页码:10521 / 10527
页数:7
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