钙钛矿(结构)
材料科学
光伏系统
磁滞
能量转换效率
偶极子
钙钛矿太阳能电池
工作职能
吡啶
表面能
化学工程
光电子学
纳米技术
图层(电子)
化学
结晶学
有机化学
复合材料
凝聚态物理
物理
工程类
生物
生态学
作者
Junjie Qian,Jingjing He,Q. Q. Zhang,Chenyue Zhu,Shilin Chen,Zhanpeng Wei,Xuesong Leng,Ziren Zhou,Benben Shen,Yu Peng,Qiang Niu,Shuang Yang,Yu Hou
标识
DOI:10.1016/j.jechem.2023.11.039
摘要
Inverted perovskite solar cells (PSCs) have attracted broad research and industrial interest owing to their suppressed hysteresis, cost-effectiveness, and easy-fabrication. However, the issue of non-radiative recombination losses at the n-type interface between the perovskite and fullerene has impeded further improvement of photovoltaic performance. Here, we modify the n-type interface of FAPbI3 perovskite films by constructing a stereochemical two-dimensional (2D) perovskite interlayer, in which the organic cations comprise both pyridine and ammonium groups. The pyridine N donor can create stable bonding with the surface-uncoordinated Pb on the perovskite, thereby passivating the shallow-level defects and enhancing the air stability of the film. Furthermore, the pyridine N donor also offers a positive polar interface to decrease the surface work function of the perovskite film, enabling n-type modification. Ultimately, we employ a p-i-n photovoltaic (PV) device with the positive dipole interlayer at perovskite/fullerene contact and achieve remarkable photoelectric conversion efficiency (PCE) of 22.0%.
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