钝化
钙钛矿(结构)
溶剂
化学工程
材料科学
能量转换效率
制作
光化学
化学
纳米技术
光电子学
图层(电子)
有机化学
工程类
医学
病理
替代医学
作者
Pengfei Xie,Hui Xiao,Ying Qiao,Geping Qu,Jiangzhao Chen,Xiaoyuan Liu,Zong‐Xiang Xu
标识
DOI:10.1016/j.cej.2023.142328
摘要
Compared with traditional processes for perovskite solar cell (PSC) fabrication using toxic anti-solvents in an inert environment, the air process using a green anti-solvent is significantly more eco-friendly and economical. However, such perovskite films contain more defects owing to moisture and non-optimal anti-solvents. To solve this problem, a new radical-strengthened defect passivation strategy is proposed, for enhancing the electron density of Lewis bases to reduce defect states in perovskite films. By introducing a donor–acceptor structure and free radical to improve the electron donation ability of Cl groups, a stable radical derivative (OTTM) with methoxy and multiple Cl groups was designed and used as a green anti-solvent additive for perovskite passivation. The mechanisms of radical-enhanced defect passivation are uncovered by theoretical and experimental results. As a consequence, a 21% power conversion efficiency with high stability was achieved based on the air process with a green anti-solvent for MAPbI3 PSCs.
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