Intermediate-phase engineering via dimethylammonium cation additive for stable perovskite solar cells

钙钛矿(结构) 甲脒 材料科学 结晶度 结晶 能量转换效率 化学工程 二甲基亚砜 微晶 晶界 相(物质) 纳米技术 微观结构 光电子学 化学 有机化学 复合材料 冶金 工程类
作者
David P. McMeekin,Philippe Holzhey,Sebastian O. Fürer,Steven P. Harvey,Laura T. Schelhas,James M. Ball,Suhas Mahesh,Seongrok Seo,Nicholas Hawkins,Jianfeng Lu,Michael B. Johnston,Joseph J. Berry,Udo Bach,Henry J. Snaith
出处
期刊:Nature Materials [Springer Nature]
卷期号:22 (1): 73-83 被引量:75
标识
DOI:10.1038/s41563-022-01399-8
摘要

Achieving the long-term stability of perovskite solar cells is arguably the most important challenge required to enable widespread commercialization. Understanding the perovskite crystallization process and its direct impact on device stability is critical to achieving this goal. The commonly employed dimethyl-formamide/dimethyl-sulfoxide solvent preparation method results in a poor crystal quality and microstructure of the polycrystalline perovskite films. In this work, we introduce a high-temperature dimethyl-sulfoxide-free processing method that utilizes dimethylammonium chloride as an additive to control the perovskite intermediate precursor phases. By controlling the crystallization sequence, we tune the grain size, texturing, orientation (corner-up versus face-up) and crystallinity of the formamidinium (FA)/caesium (FA)yCs1-yPb(IxBr1-x)3 perovskite system. A population of encapsulated devices showed improved operational stability, with a median T80 lifetime (the time over which the device power conversion efficiency decreases to 80% of its initial value) for the steady-state power conversion efficiency of 1,190 hours, and a champion device showed a T80 of 1,410 hours, under simulated sunlight at 65 °C in air, under open-circuit conditions. This work highlights the importance of material quality in achieving the long-term operational stability of perovskite optoelectronic devices.
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