钝化
材料科学
钙钛矿(结构)
化学工程
基质(水族馆)
能量转换效率
吸附
无机化学
图层(电子)
光电子学
化学
纳米技术
物理化学
海洋学
地质学
工程类
作者
Shengwen Li,Junmin Xia,Chao Liang,Zhaorui Wen,Zhen Mu,Kaiyang Wang,Hao Gu,Shiliang Mei,Hui Pan,Jiangzhao Chen,Guichuan Xing,Shi Chen
标识
DOI:10.1016/j.cej.2022.135895
摘要
Surface passivation is a promising technique to improve the power conversion efficiency (PCE) and stability of perovskite solar cells (PSCs). Upper surface passivation has been widely used to passivate surface traps responsible for interfacial recombination loss. The bottom surface (or substrate) passivation has also been studied using similar additives but with lesser improvement. Here we investigated the passivation effect of SnO2 substrates by two potassium salts with different functional sulfate anions, namely K-FSI and K-OTf. From calculation and experimental data, we found that anions play three roles in substrate passivation: removal of the hydroxyl group on SnO2 substrates, improving perovskite crystallinity and promoting electron extraction. The OTf- anion is more effective than FSI- due to its larger adsorption energy on the SnO2 substrate. K-OTf passivation also improves interfacial contact and energy level alignment, but K-FSI passivation induced an upward band bending from workfunction mismatch. As a result, K-FSI salts passivation only slightly increase the PCE from 21.00% to 21.86%, while the K-OTf further increases PCE to 22.33%. Our study suggests a viable method of bottom surface passivation by selecting a proper combination of anions and cations.
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