材料科学
钙钛矿(结构)
再现性
偶极子
水分
串联
光电子学
结晶
能量转换效率
接口(物质)
缩放比例
湿度
纳米技术
化学工程
分子
聚二甲基硅氧烷
化学物理
保形涂层
生物污染
压力(语言学)
雾
作者
SungWon Cho,Seong Chan Cho,Padmini Pandey,Sun‐Ho Lee,Sun‐Ho Lee,Hyungju Ahn,In‐Wook Hwang,Jun Yeong Ryu,Hyosung Choi,Jitendra Bahadur,Jincheol kim,Sang Uck Lee,Sang Uck Lee,Dong‐Won Kang
标识
DOI:10.1002/aenm.202505598
摘要
ABSTRACT The advancement of wide‐bandgap (WBG) Sn‐perovskite devices is substantially hindered by seasonal instability and limited reproducibility, primarily due to moisture‐induced over‐doping of PEDOT:PSS and Sn 2+ oxidation. Here, we introduce a hydrophobic proton‐locking interface engineering strategy by incorporating a novel S‐benzyl‐L‐cysteine (SBLC) molecule into PEDOT:PSS. The hydrophobic benzyl backbone, amine groups, and significant dipole moment of SBLC facilitate strong coordination with Sn 2+ , effectively preventing moisture ingress and stabilizing buried interfacial energetics. This multifunctional modulation suppresses defects and promotes uniform crystallization across varying humidity and seasonal conditions. The optimized Target device, based on a WBG Sn‐perovskite composition of PEA 0.10 FA 0.75 EA 0.15 SnI 2.15 Br 0.85 , achieves a power conversion efficiency of 11.50% and retains >80% of its average performance across 279 devices fabricated monthly over 11 months, thereby establishing the first seasonal reproducibility benchmark. Furthermore, this approach exhibits increased stability of various stress conditions and enables a record efficiency of 17.40% in all‐perovskite tandem devices featuring a WBG Sn‐perovskite. These findings provide a scalable pathway toward reproducible, tandem‐compatible, lead‐free photovoltaics.
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