烷基
碘化物
铵
钝化
卤化物
碘化铵
结晶度
钙钛矿(结构)
氢键
能量转换效率
化学
化学工程
盐(化学)
材料科学
无机化学
有机化学
图层(电子)
结晶学
分子
工程类
光电子学
作者
Xiaofang Ye,Hongkun Cai,Qinghe Sun,Tie Xu,Jian Ni,Juan Li,Jianjun Zhang
标识
DOI:10.1016/j.orgel.2022.106542
摘要
Recently, 2D/3D halide perovskites solar cells (PSCs) attract extensive attention due to simultaneous improved efficiency and stability. However, the types of alkyl ammonium salts, including the type of functional groups, the number of carbon atoms in the hydrocarbon chain, as well as the arrangement and distribution of the molecular structure, have a great impact on the performance and stability of films and devices. Herein, we compare the passivation capacity and moisture resistance of 2D capping layer based on three structurally similar alkyl ammonium salts (Butyl Ammonium Iodide (BAI), Propyl Ammonium Iodide (PAI), Ethyl Ammonium Iodide (EAI)) on triple cation perovskite thin films. As the number of carbon atoms in the alkane increases, the water contact angle gradually increases. Moreover, the defect state density is reduced to a certain extent compared to untreated 3D perovskite. The optimal PSCs with PAI-based 2D capping layer exhibit a power conversion efficiency (PCE) of 21.22% and remain 79.5% of initial PCE after 720 h. In addition, the reduced defect state density and improved crystallinity can be attributed to the hydrogen bonding interaction between the amine group and the [PbI6]4- framework. The emergence and development of 2D/3D perovskites have brought greater hope to commercialize the PSCs.
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