钙钛矿(结构)
材料科学
锡
降级(电信)
图层(电子)
氧化锡
接口(物质)
氧化物
基质(水族馆)
化学工程
分解
相(物质)
光电子学
不稳定性
聚合物
离子
纳米技术
化学稳定性
结构稳定性
作者
Wenxin Yang,Yepin Zhao,Zhen-Yang Suo,Yu‐Che Lin,Minhuan Wang,Weixuan Huang,Jian-Guo Zheng,Joo‐Hong Lee,Mingjie Xu,Yiushun Tong,Zhichao Shen,Dong Meng,Ran Zheng,Ming Gong,Yingke Zhu,Ying Zhang,Haoxiang Duan,Enxi Zhang,Yuran Shi,Chia‐Yu Lin
标识
DOI:10.1038/s41467-026-77624-8
摘要
Abstract The buried interface between the charge transport layer and the overlying perovskite absorber is critical yet difficult to probe in perovskite solar cells. Because light enters through the transparent substrate and is predominantly absorbed near this region, photo-induced degradation processes are partially initiated at the hidden buried interface. Here, we reveal that instability at the buried SnO 2 /perovskite interface triggers structural and chemical decomposition of the perovskite layer. To address this issue, we introduce polymeric interlayers that simultaneously reinforce interfacial bonding and suppress tin-ion migration. Poly(1-ethenylpyrrolidine-2,5-dione) (PED) forms a robust and chemically compatible interface, yielding enhanced phase purity, reduced defect density, and significantly mitigated tin diffusion. These findings identify the buried SnO 2 /perovskite interface as a key degradation-sensitive region under light aging and highlight interfacial polymer design as an effective strategy for improving the intrinsic stability of perovskite photovoltaics.
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