原位
氧化还原
钝化
聚合
串联
能量转换效率
热稳定性
化学工程
材料科学
聚合物
催化作用
无机化学
热氧化
工作(物理)
集中太阳能
氧气
限制
磁滞
钙钛矿太阳能电池
热的
太阳能电池
能量转换
光伏系统
钙钛矿(结构)
纳米技术
化学稳定性
作者
Ji-Hong Zheng,Qingyun He,Yang Jiang,Zhiwen Yin,Hong‐Qiang Du,Yu-Song Xiao,Qi-Bo Yuan,Xie Zheng-wen,Yichen Zhou,Junbo Wang,Chang Guo,Yu‐Chen Wang,Fangfang Wang,Mathias Uller Rothmann,Yibing Cheng,Wei Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-01-14
卷期号:11 (2): 2126-2134
被引量:1
标识
DOI:10.1021/acsenergylett.5c03960
摘要
Tin–lead (Sn–Pb) narrow-bandgap perovskites have emerged as promising absorbers for single-junction and all-perovskite tandem solar cells. However, Sn2+ oxidation remains a key factor limiting both the performance and long-term stability of Sn–Pb perovskite solar cells (PSCs). Here, we report a multifunctional polymer strategy that integrates chemical passivation with physical sealing at grain boundaries. During thermal annealing, the hydroxyl-functionalized additive 4-(bis(4-vinylphenyl)amino)-2,6-di-tert-butylphenol undergoes in situ polymerization to form a cross-linked network which coordinates Sn2+ ions, stabilizes their oxidation state, and blocks oxygen ingress along grain boundaries. This dual-function strategy effectively suppresses Sn2+ oxidation and enhances operational stability of PSCs. As a result, FA0.7MA0.3Pb0.5Sn0.5I3 PSCs achieve a power conversion efficiency of 23.27% and retain 90% of the initial efficiency after 1060 h of maximum power point tracking at 25 °C under one-sun illumination in nitrogen. This work advances the practical deployment of Sn–Pb perovskite photovoltaics.
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