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通过同时固定甲铵和补偿空位提高超卤代钙钛矿太阳能电池的光伏性能和稳定性

Boosting Photovoltaic Performance and Stability of Super-Halogen-Substituted Perovskite Solar Cells by Simultaneous Methylammonium Immobilization and Vacancy Compensation.

作者信息

Xu Shendong, Liu Guozhen, Zheng Haiying, Xu Xiaoxiao, Zhang Liying, Xu Huifen, Zhu Liangzheng, Kong Fantai, Li Yongtao, Pan Xu

机构信息

Key Laboratory of Photovoltaic and Energy Conservation Materials, Institute of Applied Technology, Hefei Institutes of Physical Science , Chinese Academy of Sciences , Hefei 230031 , China.

University of Science and Technology of China , Hefei 230026 , China.

出版信息

ACS Appl Mater Interfaces. 2020 Feb 19;12(7):8249-8259. doi: 10.1021/acsami.9b21074. Epub 2020 Feb 10.

DOI:10.1021/acsami.9b21074
PMID:31999094
Abstract

Perovskite solar cells (PSCs) are susceptible to intrinsic structural instability associated with the presence of inorganic halide anions and organic cation vacancies, thus leading to the deterioration or even premature failure of devices. Herein, we develop an efficient strategy using super-halogen BH substitution to simultaneously immobilize methylammonium and substitute iodide vacancy for high-performance PSCs based on the dihydrogen bonding interactions. The introduced super-halogen BH groups not only significantly reduce the vacancy density but also effectively inhibit the decomposition of the CHNH group by forming perovskite CHNHPbI(BH). The power conversion efficiency (PCE) of the assembled mesoporous devices is remarkably promoted from 18.43 to 21.10%, accompanied by significant increase of both and without obvious hysteresis. The superior PSCs can retain 90 and 80% of their initial PCE even after being stored for 1200 h under environmental conditions (50 ± 10% RH) and 240 h at 85 °C in the dark, respectively. Moreover, it delivers excellent optical stability under ultraviolet illumination. This work provides an avenue to improve both the long-term stability and photovoltaic performance of PSCs.

摘要

钙钛矿太阳能电池(PSCs)易受与无机卤化物阴离子和有机阳离子空位的存在相关的固有结构不稳定性影响,从而导致器件性能恶化甚至过早失效。在此,我们基于双氢键相互作用,开发了一种利用超卤素BH取代的有效策略,以同时固定甲铵并替代碘空位,用于高性能PSCs。引入的超卤素BH基团不仅显著降低了空位密度,还通过形成钙钛矿CHNHPbI(BH)有效地抑制了CHNH基团的分解。组装的介观器件的功率转换效率(PCE)从18.43%显著提高到21.10%,同时开路电压和填充因子均显著增加,且无明显滞后现象。即使在环境条件(50±10%相对湿度)下储存1200小时以及在85°C黑暗环境中储存240小时后,优异的PSCs仍可分别保留其初始PCE的90%和80%。此外,它在紫外光照下具有出色的光学稳定性。这项工作为提高PSCs的长期稳定性和光伏性能提供了一条途径。

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