钝化
非阻塞I/O
钙钛矿(结构)
材料科学
氧化镍
吡啶
图层(电子)
氧化物
能量转换效率
无机化学
化学工程
纳米技术
光电子学
化学
冶金
催化作用
有机化学
工程类
作者
Yinyan Xu,Hyoungmin Park,Urasawadee Amornkitbamrung,Hyeon Jun Jeong,Canjie Wang,Yongjae In,Ashleigh E. Gibson,Hyunjung Shin
标识
DOI:10.1002/solr.202400765
摘要
Nickel oxide (NiO) is a promising hole transport layer (HTL) that can be used to fabricate efficient, large‐scale inverted‐type perovskite solar cells (PSCs). However, depositing a high‐quality perovskite layer on NiO substrates comparable to those realized in the normal structure still presents a challenge. Herein, a pyridinium tetrafluoroborate (PyBF 4 ) additive is introduced to passivate the intrinsic defects in the bulk perovskite films. The nitrogen Lewis base in the PyBF 4 molecule interacts well with uncoordinated Pb 2+ cations, leading to high‐quality perovskite films with minimized defects. Meanwhile, the pseudohalide BF 4 − can fill halogen vacancies in the perovskite films to enable defect passivation. As a result, the perovskite precursor solution with PyBF 4 shows better reproducibility for high‐efficiency devices. The optimal PSC based on PyBF 4 modification yields a champion power conversion efficiency of 22.7% with atomic layer deposited NiO as the HTL.
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