School of Physical Sciences, Ingram Building, University of Kent, Canterbury, Kent CT2 7NH, UK.
Institute of Physics, University of Silesia, ul. Uniwersytecka 4, 40007 Katowice, Poland.
Nat Commun. 2017 May 11;8:15152. doi: 10.1038/ncomms15152.
Hybrid perovskites form an emerging family of exceptional light harvesting compounds. However, the mechanism underpinning their photovoltaic effect is still far from understood, which is impeded by a lack of clarity on their structures. Here we show that iodide ions in the methylammonium lead iodide migrate via interstitial sites at temperatures above 280 K. This coincides with temperature dependent static distortions resulting in pseudocubic local symmetry. Based on bond distance analysis, the migrating and distorted iodines are at lengths consistent with the formation of I molecules, suggesting a 2I→I+2e redox couple. The actual formula of this compound is thus (CHNH)PbI(I) where x∼0.007 at room temperature. A crucial feature of the tetragonal structure is that the methylammonium ions do not sit centrally in the A-site cavity, but disordered around two off-centre orientations that facilitate the interstitial ion migration via a gate opening mechanism.
杂化钙钛矿形成了一类新兴的卓越的光捕获化合物家族。然而,它们的光伏效应的机制仍然远未被理解,这是由于它们的结构缺乏清晰度所阻碍的。在这里,我们表明在 280 K 以上的温度下,碘化甲基铵中的碘离子通过间隙位点迁移。这与温度相关的静态畸变相吻合,导致伪立方局部对称。基于键长分析,迁移和畸变的碘处于与 I 分子形成一致的长度,表明 2I→I+2e 的氧化还原对。因此,该化合物的实际分子式为(CHNH)PbI(I),其中室温下 x∼0.007。四方结构的一个关键特征是,甲基铵离子不在 A 位腔的中心,而是在两个偏离中心的取向周围无序排列,通过一个开闸机制促进了间隙离子的迁移。