钙钛矿(结构)
材料科学
异质结
能量转换效率
带隙
哌啶
碘化物
非阻塞I/O
光电子学
化学工程
纳米技术
无机化学
有机化学
催化作用
化学
工程类
作者
Jiafan Zhang,Nan Yan,Yang Cao,Yanyan Li,Rongguang Wang,Danyang Qi,Jiacheng Pi,Nan Li,Xiaolong Feng,Jiarong Wu,Xinyi Liu,Xingyu Gao,Yucheng Liu,Shengzhong Liu,Jiangshan Feng
标识
DOI:10.1002/adma.202511162
摘要
Abstract The 3D/2D perovskite heterostructure has emerged as a promising strategy to simultaneously enhance both the efficiency and stability of perovskite solar cells (PSCs). This work introduced a fluorinated piperidine derivative, 4‐trifluoromethylpiperidine (p‐CF 3 PiP), as a precise surface reconstruction agent for 3D perovskite. By harnessing the strong hydrophobicity of the ─CF 3 groups and the coordination interaction between the piperidine ring and lead iodide, this approach promotes the growth of high‐n‐value ( n = 4) 2D perovskite, resulting in significantly improved film stability. The 3D/2D structure significantly facilitates the extraction and transport of electrons, effectively reducing the density of defect states at the interface, leading to suppressed carrier recombination. The resulting inverted PSC (with a 1.55 eV bandgap) achieved a remarkable power conversion efficiency (PCE) of 26.17%, along with a high open‐circuit voltage ( V OC ) of 1.194 V. This strategy demonstrates broad applicability, as flexible devices reached a PCE of 24.26%, and wide‐bandgap (1.68 eV) systems achieved 22.72%. Notably, the 3D/2D heterojunction exhibits exceptional long‐term stability, maintaining 99% of its initial PCE after 1730 h under ISOS‐L‐1 protocols at 25 °C, and displaying only 20% PCE degradation after 423 h of maximum power point (MPP) tracking under 85 °C.
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