非阻塞I/O
串联
材料科学
钙钛矿(结构)
带隙
钝化
能量转换效率
光电子学
纳米技术
结晶学
图层(电子)
化学
生物化学
复合材料
催化作用
作者
Xing Zhang,Qiaoyan Ma,Yousheng Wang,Jianzha Zheng,Quanxi Liu,Liming Liu,Peng Yang,Wujie He,Ye Cao,Weiyuan Duan,Kaining Ding,Yaohua Mai
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-06-03
卷期号:18 (24): 15991-16001
被引量:1
标识
DOI:10.1021/acsnano.4c04341
摘要
Phase heterogeneity of bromine–iodine (Br–I) mixed wide-bandgap (WBG) perovskites has detrimental effects on solar cell performance and stability. Here, we report a heterointerface anchoring strategy to homogenize the Br–I distribution and mitigate the segregation of Br-rich WBG-perovskite phases. We find that methoxy-substituted phenyl ethylammonium (x-MeOPEA+) ligands not only contribute to the crystal growth with vertical orientation but also promote halide homogenization and defect passivation near the buried perovskite/hole transport layer (HTL) interface as well as reduce trap-mediated recombination. Based on improvements in WBG-perovskite homogeneity and heterointerface contacts, NiOx-based opaque WBG-perovskite solar cells (WBG-PSCs) achieved impressive open-circuit voltage (Voc) and fill factor (FF) values of 1.22 V and 83%, respectively. Moreover, semitransparent WBG-PSCs exhibit a PCE of 18.5% (15.4% for the IZO front side) and a high FF of 80.7% (79.4% for the IZO front side) for a designated illumination area (da) of 0.12 cm2. Such a strategy further enables 24.3%-efficient two-terminal perovskite/silicon (double-polished) tandem solar cells (da of 1.159 cm2) with a high Voc of over 1.90 V. The tandem devices also show high operational stability over 1000 h during T90 lifetime measurements.
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