钙钛矿(结构)
热稳定性
光伏
理论(学习稳定性)
分解
材料科学
吞吐量
动能
化学工程
化学物理
纳米技术
化学
计算机科学
结晶学
光伏系统
物理
机器学习
有机化学
电气工程
工程类
电信
量子力学
无线
作者
Yicheng Zhao,Jiyun Zhang,Zhengwei Xu,Shijing Sun,Stefan Langner,Noor Titan Putri Hartono,Thomas Heumueller,Yi Hou,Jack Elia,Ning Li,Gebhard J. Matt,Xiaoyan Du,Wei Meng,Andres Osvet,Kaicheng Zhang,Tobias Stubhan,Yexin Feng,Jens Hauch,Edward H. Sargent,Tonio Buonassisi,Christoph J. Brabec
标识
DOI:10.1038/s41467-021-22472-x
摘要
Abstract Stability of perovskite-based photovoltaics remains a topic requiring further attention. Cation engineering influences perovskite stability, with the present-day understanding of the impact of cations based on accelerated ageing tests at higher-than-operating temperatures (e.g. 140°C). By coupling high-throughput experimentation with machine learning, we discover a weak correlation between high/low-temperature stability with a stability-reversal behavior. At high ageing temperatures, increasing organic cation (e.g. methylammonium) or decreasing inorganic cation (e.g. cesium) in multi-cation perovskites has detrimental impact on photo/thermal-stability; but below 100°C, the impact is reversed. The underlying mechanism is revealed by calculating the kinetic activation energy in perovskite decomposition. We further identify that incorporating at least 10 mol.% MA and up to 5 mol.% Cs/Rb to maximize the device stability at device-operating temperature (<100°C). We close by demonstrating the methylammonium-containing perovskite solar cells showing negligible efficiency loss compared to its initial efficiency after 1800 hours of working under illumination at 30°C.
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