Synergistic effect of alkali metal doping and thiocyanate passivation in CsPbBr3 for HTM-free all-inorganic perovskite solar cells

钝化 钙钛矿(结构) 硫氰酸盐 碱金属 兴奋剂 掺杂剂 材料科学 无机化学 金属 化学工程 化学 纳米技术 光电子学 冶金 图层(电子) 有机化学 工程类
作者
Shiqiang Jiang,Haojie Sui,Benlin He,Xinyi Zhang,Zhihao Zong,Haiyan Chen,Qunwei Tang
出处
期刊:Dalton Transactions [Royal Society of Chemistry]
卷期号:52 (28): 9772-9779 被引量:7
标识
DOI:10.1039/d3dt01618h
摘要

All-inorganic CsPbBr3 perovskite solar cells (PSCs) without hole-transport materials (HTMs) have attracted widespread attention because of their significant environmental stability. However, the poor quality of perovskite film and the energetics mismatch between CsPbBr3 and charge-transport layers limit the further improvement of the CsPbBr3 PSC performance. To solve this issue, the synergistic effect of alkali metal doping and thiocyanate passivation in NaSCN and KSCN dopants is utilized to improve the properties of the CsPbBr3 film. The Na+ and K+ with smaller ionic radii are doped at the A-site of CsPbBr3 to cause a lattice contraction, which contributes to the formation of CsPbBr3 film with enhanced grain size and crystallinity. The SCN- exerts the function of passivating the uncoordinated Pb2+ defects of CsPbBr3 film, leading to a reduction of trap state density. The incorporation of NaSCN and KSCN dopants also adjusts the band structure of CsPbBr3 film to improve the interfacial energetics match of the device. As a result, the charge recombination is suppressed, and the charge transfer and extraction are effectively promoted, delivering a highly enhanced power conversion efficiency of 10.38% for the champion KSCN doped CsPbBr3 PSCs without HTMs compared to 6.72% efficiency for the original device. Moreover, the stability of the unencapsulated PSCs under ambient conditions with high humidity (85% RH, 25 °C) is distinctly improved, retaining 91.1% of the initial efficiency after 30 days of aging.
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