材料科学
双层
钙钛矿(结构)
能量转换效率
图层(电子)
单层
热稳定性
化学工程
纳米技术
光电子学
化学
膜
生物化学
工程类
作者
Bitao Dong,Mingyang Wei,Yuheng Li,Yingguo Yang,Wei Ma,Yueshuai Zhang,Yuge Ran,Meijie Cui,Zhongbo Su,Qunping Fan,Zhaozhao Bi,Tomas Edvinsson,Zhiqin Ding,Huanxin Ju,Shuai You,Shaik M. Zakeeruddin,Xiong Li,Anders Hagfeldt,Michael Gräetzel,Yuhang Liu
标识
DOI:10.1038/s41560-024-01689-2
摘要
The adoption of perovskite solar cells (PSCs) requires improved resistance to high temperatures and temperature variations. Hole-selective self-assembled monolayers (SAMs) have enabled progress in the performance of inverted PSCs, yet they may compromise temperature stability owing to desorption and weak interfacial contact. Here we developed a self-assembled bilayer by covalently interconnecting a phosphonic acid SAM with a triphenylamine upper layer. This polymerized network, formed through Friedel–Crafts alkylation, resisted thermal degradation up to 100 °C for 200 h. Meanwhile, the face-on-oriented upper layer exhibited adhesive contact with perovskites, leading to a 1.7-fold improvement in adhesion energy compared with the SAM–perovskite interface. We reported power conversion efficiencies exceeding 26% for inverted PSCs. The champion devices demonstrated less than 4% and 3% efficiency loss after 2,000 h damp heat exposure (85 °C and 85% relative humidity) and over 1,200 thermal cycles between −40 °C and 85 °C, respectively, meeting the temperature stability criteria outlined in the International Electrotechnical Commission 61215:2021 standards. To improve the tolerance of perovskite solar cells against high temperatures and temperature variations, Dong et al. covalently cross-link two molecules in the charge transport layer to strengthen adhesion with the perovskite layer.
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