材料科学
钝化
钙钛矿(结构)
结晶
能量转换效率
卤化物
化学工程
碳纤维
相(物质)
无机化学
图层(电子)
纳米技术
光电子学
复合材料
有机化学
复合数
化学
工程类
作者
Jinqing Lü,Xiaonan Huo,Weifeng Liu,Weiwei Sun,Sai Ji,Tingting You,Kexiang Wang,Lu Wei,Shiwei Wang
标识
DOI:10.1016/j.mtener.2024.101628
摘要
Hole transport layer (HTL)-free all-inorganic CsPbIxBr3-x carbon-based perovskite solar cells (C-PSCs) have attracted much attention due to its low cost and excellent stability. The poor device efficiency is a barrier to constrain its commercialization, mainly due to the large amount of interfacial and bulk defects existed in inorganic perovskite films. In this study, an organic small molecule dicyandiamide (DCD) is added into perovskite precursor as an additive to adjust the crystallization kinetics and passivate defects of inorganic perovskite films, simultaneously. It is demonstrated that the introduction of DCD can not only accelerate the transition process from intermediate phase DMAPbI3 to inorganic perovskite, but also passivate defects through Lewis acid-base interaction between cyano (C≡N), imine (C=N) groups and uncoordinated Pb2+. Meanwhile, the energy level alignment was optimized, which effectively improves the charge transport efficiency of CsPbIxBr3-x C-PSCs. As a result, optimized device shows an enhanced efficiency from 14.07% to 15.84%, accompanied by the improved long-term stability.
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