甲脒
钙钛矿(结构)
乙二胺
卤化物
材料科学
结晶
化学工程
薄膜
光谱学
纳米技术
化学
结晶学
无机化学
量子力学
物理
工程类
作者
Margherita Taddei,Joel Smith,Benjamin M. Gallant,Suer Zhou,Robert J. E. Westbrook,Yangwei Shi,Jian Wang,James N. Drysdale,Declan P. McCarthy,Stephen Barlow,Seth R. Marder,Henry J. Snaith,David S. Ginger
出处
期刊:Cornell University - arXiv
日期:2022-01-01
标识
DOI:10.48550/arxiv.2209.15100
摘要
We show that adding ethylenediamine (EDA) to perovskite precursor solution improves the photovoltaic device performance and material stability of high-bromide-content, methylammonium-free, formamidinium cesium lead halide perovskites FA1-xCsxPb(I1-yBry)3 which are currently of interest for perovskite-on-Si tandem solar cells. Using spectroscopy and hyperspectral microscopy, we show that the additive improves film homogeneity and suppresses the phase instability that is ubiquitous in high-Br perovskite formulations, producing films that remain stable for over 100 days in ambient conditions. With the addition of 1 mol% EDA we demonstrate 1.69 eV-gap perovskite single-junction p-i-n devices with a VOC of 1.22 V, and a champion maximum power point tracked power conversion efficiency of 18.8%, comparable to the best reported methylammonium-free perovskites. Using nuclear magnetic resonance (NMR) spectroscopy and X-ray diffraction techniques, we show that EDA reacts with FA+ in solution, rapidly and quantitatively forming imidazolinium cations. It is the presence of imidazolinium during crystallization which drives the improved perovskite thin-film properties.
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