钝化
X射线光电子能谱
材料科学
钙钛矿(结构)
单独一对
电解质
红外光谱学
能量转换效率
开路电压
极化(电化学)
分析化学(期刊)
光谱学
化学
无机化学
氧气
介电谱
离子键合
极地的
溶剂
光化学
钙钛矿太阳能电池
光伏系统
光电效应
光电子学
激发态
塔菲尔方程
离解(化学)
电子光谱学
泄漏(经济)
光电发射光谱学
色素敏化染料
电子
作者
Huimeng Shen,Chen Wang,Huidan Gao,Zhen Chang,Huawei Zhou,Xianxi Zhang,Federico Rosei
标识
DOI:10.20517/energymater.2025.166
摘要
A major unresolved challenge in inverted organic-inorganic hybrid perovskite solar cells (I-PSCs) is interfacial non-radiative recombination. To tackle this issue, we introduced trace dimethylformamide (tDMF) in isopropanol (tDMF/IPA) as a passivation material, carefully modifying the interface between FA<sub>0.95</sub>Cs<sub>0.05</sub>PbI<sub>3</sub> and [6,6]-phenyl-C61-butyric acid methyl ester. The experimental results of energy dispersive X-ray spectroscopy at different voltages and angles, infrared spectroscopy, and X-ray photoelectron spectroscopy indicate that oxygen lone pair of electrons in carbonyl group (-C=O) of polar solvent N,N-dimethylformamide form coordination bonds (Pb<sup>2+</sup> → O=C) with Pb²⁺ suspension bond on the surface of perovskite. Tafel polarization curve and dark current results reveal decrease in the charge recombination rate at the interface and decrease in leakage current, respectively, after tDMF/IPA passivation. The photoelectric conversion efficiency (PCE) of I-PSCs treated with tDMF/IPA is significantly increased from 21.44% to 23.24%, and the open-circuit voltage is also increased from 1.01 to 1.12 V. Encapsulated devices based on tDMF/IPA passivation retained over 77% of their initial PCE after being stored in ambient air for 2,736 h.
科研通智能强力驱动
Strongly Powered by AbleSci AI