钝化
甲脒
结晶度
钙钛矿(结构)
光致发光
材料科学
带隙
能量转换效率
锡
光电子学
化学
纳米技术
化学工程
结晶学
工程类
冶金
复合材料
图层(电子)
作者
Jianchao Yang,Weijian Tang,Ruihan Yuan,Yu Chen,Jing Wang,Yihui Wu,Wan‐Jian Yin,Xiaoshuang Zhou,Jianning Ding,Wen‐Hua Zhang
出处
期刊:Chemical Science
[The Royal Society of Chemistry]
日期:2021-01-01
卷期号:12 (6): 2050-2059
被引量:92
摘要
Trap-dominated non-radiative charge recombination is one of the key factors that limit the performance of perovskite solar cells (PSCs), which was widely studied in methylammonium (MA) containing PSCs. However, there is a need to elucidate the defect chemistry of thermally stable, MA-free, cesium/formamidinium (Cs/FA)-based perovskites. Herein, we show that d-penicillamine (PA), an edible antidote for treating heavy metal ions, not only effectively passivates the iodine vacancies (Pb2+ defects) through coordination with the -SH and -COOH groups in PA, but also finely tunes the crystallinity of Cs/FA-based perovskite film. Benefiting from these merits, a reduction of non-radiative recombination and an increase in photoluminescence lifetime have been achieved. As a result, the champion MA-free device exhibits an impressive power conversion efficiency (PCE) of 22.4%, an open-circuit voltage of 1.163 V, a notable fill factor of 82%, and excellent long-term operational stability. Moreover, the defect passivation strategy can be further extended to a mini module (substrate: 4 × 4 cm2, active area: 7.2 cm2) as well as a wide-bandgap (∼1.73 eV) Cs/FA perovskite system by delivering PCEs of 16.3% and 20.2%, respectively, demonstrating its universality in defect passivation for efficient PSCs.
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