钇
钙钛矿(结构)
基质(水族馆)
材料科学
氧化锡
氧化物
介孔材料
扩散阻挡层
纳米技术
串联
光电子学
化学工程
光伏
兴奋剂
热稳定性
离子
蒸发
透明导电膜
成核
导电体
金属
法拉第效率
太阳能电池
原子层沉积
扩散
真空蒸发
能量转换效率
作者
Haibing Wang,Yansong Ge,Wenlong Shao,Xingyu Xiong,Guang Li,Nengxu Li,Xuzhi Hu,Guoyi Chen,Kailian Dong,Wei Ai,Zhenhua Yu,Zhimiao Zheng,Chen Wang,Fang Yao,Xiaojuan Cao,Songzhan Li,Jianwei Zhao,Weijun Ke,Chen Tao,Yi Hou
标识
DOI:10.1038/s41467-025-64548-y
摘要
Transparent conductive oxides (TCOs)-foundation of perovskite solar cells (PSCs)-have long been assumed to be stable, and thus their impact on device longevity is frequently overlooked. Herein, we unveil that fluorine doped tin oxide (FTO) suffers from instability under operational stress, exacerbating PSC stability issue. To address this issue, we propose a universal interface engineering strategy employing a scalable thermal evaporation followed by natural oxidation to form an atomically bonded yttrium oxide (Y2O3) to strengthen structural stability of FTO. Evaporated yttrium effectively anchors a portion of lattice oxygen within FTO, preventing elemental dissociation. Moreover, the formed Y2O3 featured conformal deposition on rough FTO increases the interfacial adhesion energy, establishing a robust barrier against ion diffusion and carrier nonradiative recombination loss. This approach fortifies the structural integrity of the PSC, leading to dramatically improved operational stability. Unencapsulated devices exhibit negligible performance loss after 1,200 h of continuous illumination. Notably, we achieve power conversion efficiencies of 26.48% (certified at 26.12%) in regular (n-i-p) architectures, 26.34% in inverted (p-i-n) configurations, and 28.47% in tandem structures-among one of the highest reported in their respective categories-underscoring its strong generality and potential for commercialization.
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