钝化
钙钛矿(结构)
电子
共轭体系
醛
分子
酮
光化学
材料科学
芘
化学
有机化学
聚合物
催化作用
物理
图层(电子)
量子力学
作者
Xiaoqing Jiang,Lina Zhu,Bingqian Zhang,Guangyue Yang,Likai Zheng,Kaiwen Dong,Yanfeng Yin,Minhuan Wang,Shiwei Liu,Shuping Pang,Xin Guo
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-12-12
卷期号:64 (8): e202420369-e202420369
被引量:13
标识
DOI:10.1002/anie.202420369
摘要
Carbonyl-containing aromatic ketones or aldehydes have been demonstrated to be effective defect passivators for perovskite films to improve performances of perovskite solar cells (PSCs). It has been claimed that both π-electrons within aromatic units and carbonyl groups can, separately, interact with ionic defects, which, however, causes troubles in understanding the passivation mechanism of those aromatic ketone/aldehyde molecules. Herein, we clarify the effect of both moieties in one molecule on the defect passivation by investigating three aromatic aldehydes with varied conjugation planes, namely, biphenyl-4-carbaldehyde (BPCA), naphthalene-2-carbaldehyde (NACA) and pyrene-1-carbaldehyde (PyCA). Our findings reveal that the π-electrons located in the conjugated system do not directly present strong passivation for defects, but enhance the electron cloud density of the carbonyl group augmenting its interaction with defect sites; thereby, with the extended conjugation plane of the three molecules, their defect passivation ability is gradually improved. PSCs incorporating PyCA with the most extended π-electrons delocalization achieve maximum power conversion efficiencies of 25.67 % (0.09 cm2) and 21.76 % (14.0 cm2). Moreover, these devices exhibit outstanding long-term stability, retaining 95 % of their initial efficiency after operation for 1000 hours at the maximum power point.
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