Synergistic Effect of Anti‐Solvent and Component Engineering for Effective Passivation to Attain Highly Stable Perovskite Solar Cells

钝化 钙钛矿(结构) 材料科学 化学工程 成核 能量转换效率 光伏系统 溶剂 晶界 钙钛矿太阳能电池 氧化铟锡 纳米技术 开路电压 化学 无机化学 图层(电子) 有机化学 光电子学 电压 冶金 微观结构 物理 工程类 生物 量子力学 生态学
作者
Yetai Cheng,Qingbo Wei,Zhangwen Ye,Xinyu Zhang,Peixin Ji,Nannan Wang,Lingxing Zan,Feng Fu,Shengzhong Liu
出处
期刊:Solar RRL [Wiley]
卷期号:6 (9) 被引量:21
标识
DOI:10.1002/solr.202200418
摘要

Defect passivation is a crucial process for achieving high‐performance perovskite solar cells (PSCs). Herein, the synergistic effect of anti‐solvent and component engineering for effective passivation to attain highly stable PSCs is demonstrated, specifically, for ethyl acetate as the anti‐solvent and CsBr as the additive in the MAPbI 3 precursor solution. It is found that the rapid solvent evaporation results in fast nucleation, and the CsBr assists the perovskite grain growth. The synergistic effect of anti‐solvent and additive engineering leads to increased perovskite grain size, reduced defect density, improved quality of the perovskite thin film, and finally, enhanced efficiency and stability of the indium tin oxide/SnO 2 /perovskite/carbon device. The influence of this synergistic effect on the morphology and photovoltaic performance is systematically investigated. Printable PSCs with hole‐transport‐layer‐free carbon electrodes are designed and constructed, which achieve a champion photoelectric conversion efficiency of 16.45%, fill factor of 72.63%, short circuit current of 19.90 mA cm −2, and open circuit voltage of 1.14 V. Herein, a facile and low‐cost approach is demonstrated to obtain highly stable C‐PSCs and a promising strategy for future commercial application is provided.
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