材料科学
钙钛矿(结构)
钝化
堆积
光电子学
能量转换效率
接口(物质)
载流子寿命
小分子
载流子
分子
晶体缺陷
纳米技术
光伏系统
功率(物理)
化学物理
化学工程
重组
作者
Xiaoshan Zhang,F. Liu,Ziqing Yang,Zhihong Liu,Lidong Guo,Pengfei Huang
标识
DOI:10.1002/adfm.202524231
摘要
ABSTRACT Although [4‐(3,6‐dimethyl‐9H‐carbazol‐9‐yl)butyl] phosphonic acid (Me‐4PACz) self‐assembled molecules have been widely used in inverted perovskite solar cells (PSCs), their strong hydrophobicity is difficult to form a dense perovskite film, and the defect passivation ability is weak, resulting in serious non‐radiative recombination loss of carriers between them and the perovskite film, which limits the further improvement of device performance. Here, we introduce 2‐phenylethylamine hydrochloride (PEACl) to modify the buried interface in PSCs. The incorporation of PEACl molecules not only reduces the substrate's hydrophobicity, enabling uniform growth of perovskite film, but also enhances carrier transport at the interface through π‐π stacking interaction with Me‐4PACz, thereby reducing charge accumulation. Furthermore, PEACl reacts with PbI 2 at the bottom interface to form a 2D structure that effectively passivated interface defects and suppressed non‐radiative recombination. Consequently, the PEACl‐treated PSCs demonstrate an impressive power conversion efficiency of 26.08%. Notably, these PEACl‐treated PSCs exhibit exceptional stability, retaining 90.80% of their initial efficiency after 2 500 h of continuous operation at the maximum power point under ambient conditions at 55°C, using 1‐sun illumination without a UV filter. The effectively suppressed of interface defects by PEACl at the buried perovskite interface offers a promising strategy for advancing the commercial viability of PSCs.
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