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The effect of illumination on the formation of metal halide perovskite films

碘化物 卤化物 钙钛矿(结构) 扫描电子显微镜 化学工程 沉积(地质) 材料科学 化学 太阳能电池 插层(化学) 金属 光化学 无机化学 薄膜 纳米技术 光电子学 有机化学 古生物学 工程类 复合材料 生物 沉积物
作者
Amita Ummadisingu,Ludmilla Steier,Ji‐Youn Seo,Taisuke Matsui,Antonio Abate,Wolfgang Tress,Michaël Grätzel
出处
期刊:Nature [Springer Nature]
卷期号:545 (7653): 208-212 被引量:240
标识
DOI:10.1038/nature22072
摘要

Optimizing the morphology of metal halide perovskite films is an important way to improve the performance of solar cells when these materials are used as light harvesters, because film homogeneity is correlated with photovoltaic performance. Many device architectures and processing techniques have been explored with the aim of achieving high-performance devices, including single-step deposition, sequential deposition and anti-solvent methods. Earlier studies have looked at the influence of reaction conditions on film quality, such as the concentration of the reactants and the reaction temperature. However, the precise mechanism of the reaction and the main factors that govern it are poorly understood. The consequent lack of control is the main reason for the large variability observed in perovskite morphology and the related solar-cell performance. Here we show that light has a strong influence on the rate of perovskite formation and on film morphology in both of the main deposition methods currently used: sequential deposition and the anti-solvent method. We study the reaction of a metal halide (lead iodide) with an organic compound (methylammonium iodide) using confocal laser scanning fluorescence microscopy and scanning electron microscopy. The lead iodide crystallizes before the intercalation of methylammonium iodide commences, producing the methylammonium lead iodide perovskite. We find that the formation of perovskite via such a sequential deposition is much accelerated by light. The influence of light on morphology is reflected in a doubling of solar-cell efficiency. Conversely, using the anti-solvent method to form methyl ammonium lead iodide perovskite in a single step from the same starting materials, we find that the best photovoltaic performance is obtained when films are produced in the dark. The discovery of light-activated crystallization not only identifies a previously unknown source of variability in opto-electronic properties, but also opens up new ways of tuning morphology and structuring perovskites for various applications.
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