Dually‐Passivated Perovskite Solar Cells with Reduced Voltage Loss and Increased Super Oxide Resistance

钝化 钙钛矿(结构) 光电流 能量转换效率 材料科学 二亚胺 微晶 开路电压 钙钛矿太阳能电池 化学工程 光电子学 纳米技术 化学 电压 有机化学 物理 工程类 量子力学 冶金 图层(电子) 分子
作者
Qin Zhou,Yifeng Gao,C.S. Cai,Zhuangzhuang Zhang,Jianbin Xu,Zhongyi Yuan,Peng Gao
出处
期刊:Angewandte Chemie [Wiley]
卷期号:133 (15): 8384-8393 被引量:29
标识
DOI:10.1002/ange.202017148
摘要

Abstract In recent years, the power conversion efficiency (PCE) of perovskite solar cells (PSCs) has witnessed rapid progress. Nevertheless, the pervasive defects prone to non‐radiative recombination and decomposition exist at the surface and the grain boundaries (GBs) of the polycrystalline perovskite films. Herein, we report a comprehensive dual‐passivation (DP) strategy to effectively passivate the defects at both surface and GBs to enhance device performance and stability further. Firstly, a fluorinated perylene‐tetracarboxylic diimide derivative is permeated in the perovskite metaphase during antisolvent treatment, and then a fluorinated bulky aromatic ammonium salt is introduced over the annealed perovskite. The reduction of defect density can be unambiguously proved by the superoxide species generation/quenching reaction. As a result, optimized planar PSCs demonstrate a decreased open‐circuit voltages deficit from 0.47 to 0.39 V and the best efficiency of 23.80 % from photocurrent scanning with a stabilized maximum power output efficiency of 22.99 %. Without encapsulation, one typical device can maintain over 85 % of the initial efficiency after heating on a hot plate at 100 °C for 30 h under relative humidity (RH) of 70 %. When the device is aged under 30±5 % RH, over 97 % of its initial PCE is retained after 1700 h.
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