Discovery of temperature-induced stability reversal in perovskites using high-throughput robotic learning

Yicheng Zhao(Friedrich-Alexander-Universität Erlangen-Nürnberg), Jiyun Zhang(Friedrich-Alexander-Universität Erlangen-Nürnberg), Zhengwei Xu(Hunan University), Shijing Sun(Massachusetts Institute of Technology), Stefan Langner(Friedrich-Alexander-Universität Erlangen-Nürnberg), Noor Titan Putri Hartono(Massachusetts Institute of Technology), Thomas Heumueller(Friedrich-Alexander-Universität Erlangen-Nürnberg), Yi Hou(University of Toronto), Jack Elia(Friedrich-Alexander-Universität Erlangen-Nürnberg), Ning Li(Friedrich-Alexander-Universität Erlangen-Nürnberg), Gebhard J. Matt(Friedrich-Alexander-Universität Erlangen-Nürnberg), Xiaoyan Du(Helmholtz Institute Erlangen-Nürnberg), Wei Meng(Friedrich-Alexander-Universität Erlangen-Nürnberg), Andres Osvet(Friedrich-Alexander-Universität Erlangen-Nürnberg), Kaicheng Zhang(Friedrich-Alexander-Universität Erlangen-Nürnberg), Tobias Stubhan(Helmholtz Institute Erlangen-Nürnberg), Yexin Feng(Hunan University), Jens Hauch(Helmholtz Institute Erlangen-Nürnberg), Edward H. Sargent(University of Toronto), Tonio Buonassisi(Massachusetts Institute of Technology), Christoph J. Brabec(Friedrich-Alexander-Universität Erlangen-Nürnberg)
Nature Communications
April 13, 2021
Cited by 173Open Access
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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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