甲脒
钙钛矿(结构)
碘化物
化学物理
化学
亚稳态
中子散射
相(物质)
四方晶系
材料科学
结晶学
无机化学
晶体结构
散射
有机化学
光学
物理
作者
Kacper Drużbicki,Rasmus Lavén,Jeff Armstrong,Lorenzo Malavasi,Félix Fernández-Alonso,Maths Karlsson
标识
DOI:10.1021/acs.jpclett.1c00616
摘要
The vibrational dynamics of pure and methylammonium-doped formamidinium lead iodide perovskites (FAPbI3) has been investigated by high-resolution neutron spectroscopy. For the first time, we provide an exhaustive and accurate analysis of the cation vibrations and underlying local structure around the organic moiety in these materials using first-principles electronic-structure calculations validated by the neutron data. Inelastic neutron scattering experiments on FAPbI3 provide direct evidence of the formation of a low-temperature orientational glass, unveiling the physicochemical origin of phase metastability in the tetragonal structure. Further analysis of these data provides a suitable starting point to explore and understand the stabilization of the perovskite framework via doping with small amounts of organic cations. In particular, we find that the hydrogen-bonding interactions around the formamidinium cations are strengthened as a result of cage deformation. This synergistic effect across perovskite cages is accompanied by a concomitant weakening of the methylammonium interactions with the surrounding framework.
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