成核
钙钛矿(结构)
能量转换效率
溶剂
材料科学
配体(生物化学)
化学工程
结晶
钙钛矿太阳能电池
光电子学
纳米技术
化学
有机化学
生物化学
工程类
受体
作者
Yibo Xu,Chenguang Zhou,Xinzhu Li,Kaihuai Du,Yue Li,Dong Xu,Ningyi Yuan,Lvzhou Li,Jianning Ding
出处
期刊:Small methods
[Wiley]
日期:2024-05-14
卷期号:8 (12): e2400428-e2400428
被引量:13
标识
DOI:10.1002/smtd.202400428
摘要
Efficiency reduction in perovskite solar cells (PSCs) during the magnification procedure significantly hampers commercialization. Vacuum-flash (VF) has emerged as a promising method to fabricate PSCs with consistent efficiency across scales. However, the slower solvent removal rate of VF compared to the anti-solvent method leads to perovskite films with buried defects. Thus, this work employs low-toxic Lewis base ligand solvent N-ethyl-2-pyrrolidone (NEP) to improve the nucleation process of perovskite films. NEP, with a mechanism similar to that of N-methyl-2-pyrrolidone in FA-based perovskite formation, enhances the solvent removal speed owing to its lower coordination ability. Based on this strategy, p-i-n PSCs with an optimized interface attain a power conversion efficiency (PCE) of 24.19% on an area of 0.08 cm2. The same nucleation process enables perovskite solar modules (PSMs) to achieve a certified PCE of 23.28% on an aperture area of 22.96 cm2, with a high geometric fill factor of 97%, ensuring nearly identical active area PCE (24%) in PSMs as in PSCs. This strategy highlights the potential of NEP as a ligand solvent choice for the commercialization of PSCs.
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