材料科学
钙钛矿(结构)
非阻塞I/O
基质(水族馆)
化学工程
异质结
能量转换效率
钝化
纳米技术
图层(电子)
光电子学
有机化学
催化作用
海洋学
地质学
工程类
化学
作者
Mingyang Gao,Zeping Ou,Can Wang,Lei Liu,Dingqin Hu,Wei Wan,Peidong Chen,Yi Pan,Shisong Nie,Yuanyi Luo,Pengyan Zhang,Peng Dong,Ke Zhao,Meirong Fu,Wei Liu,Xia Wang,Wei Zhang,Guo Haoxuan,Yujie Zheng,Zeyun Xiao
标识
DOI:10.1002/adma.202514273
摘要
Abstract Carbazole‐based self‐assembled monolayers (SAMs) as an effective hole transportation layer have tremendously advanced the power conversion efficiency (PCE) of inverted perovskite solar cells (PSCs). However, the inhomogeneous distribution of SAMs on substrate and non‐intimate interface contact can bring about significant interfacial energy loss at SAM/perovskite heterojunction. Herein, a small molecule 4‐Bromobenzylphosphnic acid (4Br‐BPA) is constructed as a molecule bridge connecting [4‐(3,6‐dimethyl‐9 H ‐carbazol‐9‐yl) butyl] phosphonic acid (Me‐4PACz) and perovskite, exhibiting multifunctionality on improving the interfacial characteristics. First, the small‐size 4Br‐BPA molecules can partly fill some voids on NiO x /Me‐4PACz anchored with NiO x via phosphonic acid group, meanwhile ameliorating the NiO x surface state. Second, the 4Br‐BPA post‐deposited onto Me‐4PACz interacting with Me‐4PACz via π – π stacking has suppressed charge accumulation at interface, aligned the energy level of NiO x /Me‐4PACz consequently promoting the hole transportation. Third, the interplay between 4Br‐BPA and perovskite enables effective passivation of interfacial traps, and the substrate NiO x /Me‐4PACz/4Br‐BPA with improved wettability has facilitated the perovskite film growth with enhanced crystallization and released residual stress. Consequently, all these benefits have been transformed to an impressive PCE of 26.59% (certified 26.12%). The device based on 4Br‐BPA also demonstrates much improved operational stability, maintaining ≈90% of initial efficiency under 1400 h continuous one‐sun illumination.
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