单层
钙钛矿(结构)
能量转换效率
烷基
连接器
材料科学
部分
离域电子
共轭体系
钝化
轨道能级差
光化学
纳米技术
光电子学
化学
结晶学
有机化学
聚合物
图层(电子)
分子
复合材料
操作系统
计算机科学
作者
Shuo Zhang,Ruihan Wu,Chenkai Mu,Yanbo Wang,Liyuan Han,Yongzhen Wu,Weihong Zhu
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2022-09-09
卷期号:4 (10): 1976-1983
被引量:70
标识
DOI:10.1021/acsmaterialslett.2c00799
摘要
The alkyl linker-based self-assembled monolayer (SAM) has emerged as an efficient hole-selective contact (HSC) for inverted perovskite solar cells (PSCs). Despite being effective in hole-extraction and interfacial passivation, its hole-transporting capability is limited by the insulating alkyl linker, along with poor stability due to the isolated and nonconjugated electron-rich moiety. Here, we report a series of conjugated SAMs that exhibit excellent photo- and electrical stabilities. The conjugated molecular structure not only enhances charge transport but also stabilizes the electron-rich arylamines through electron/charge delocalization. Moreover, it enables convenient modulation of frontier orbital energy levels for interfacial band alignment. By scrutinization of the conjugation-linker and hole-transporting head, an optimal conjugated SAM (MPA-Ph-CA) in combination with the standard triple cation perovskite Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3 achieved an efficient inverted PSC with a power conversion efficiency (PCE) of 22.53% (certified 22.12%). Moreover, the MPA-Ph-CA based devices showed excellent stability, retaining over 95% of their initial PCEs under one sun constant irradiation for 800 h. The synchronously enhanced efficiency and stability suggest that conjugated SAM-based HSCs are promising for further advancing inverted PSCs.
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