材料科学
钙钛矿(结构)
甲脒
石墨烯
能量转换效率
离子键合
化学工程
相(物质)
纳米技术
离子
光电子学
有机化学
量子力学
物理
工程类
化学
作者
Meng Li,Weiwei Zuo,Qiong Wang,Kai‐Li Wang,Ming‐Peng Zhuo,Hans Köbler,Christian E. Halbig,Siegfried Eigler,Yingguo Yang,Xingyu Gao,Zhao‐Kui Wang,Yongfang Li,Antonio Abate
标识
DOI:10.1002/aenm.201902653
摘要
Abstract Mixed cation/halide perovskites have led to a significant increase in the efficiency and stability of perovskite solar cells. However, mobile ionic defects inevitably exacerbate the photoinduced phase segregation and self‐decomposition of the crystal structure. Herein, ultrathin 2D nanosheets of oxo‐functionalized graphene/dodecylamine (oxo‐G/DA) are used to solve ion migration in cesium (Cs)‐formamidinium (FA)‐methylammonium (MA) triple‐cation‐based perovskites. Based on the superconducting carbon skeleton and functional groups that provide lone pairs of electrons on it, the ultrathin 2D network structure can fit tightly on the crystals and wrap them, isolating them, and thus reducing the migration of ions within the built‐in electric field of the perovskite film. As evidence of the formation of sharp crystals with different orientation within the perovskite film, moiré fringes are observed in transmission electron microscopy. Thus, a champion device with a power conversion efficiency (PCE) of 21.1% (the efficiency distribution is 18.8 ± 1.7%) and a remarkable fill factor of 81%, with reduced hysteresis and improved long‐term stability, is reported. This work provides a simple method for the improvement of the structural stability of perovskite in solar cells.
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