钙钛矿(结构)
材料科学
有机太阳能电池
串联
光电子学
钝化
带隙
氧化铟锡
硒化铜铟镓太阳电池
开路电压
能量转换效率
电压
薄膜
图层(电子)
纳米技术
太阳能电池
化学工程
复合材料
聚合物
电气工程
工程类
作者
Wei Chen,Yudong Zhu,Jingwei Xiu,Guocong Chen,Haoming Liang,Shunchang Liu,Hansong Xue,Erik Birgersson,J. Ho,Xinshun Qin,Jingyang Lin,Ruijie Ma,Tao Liu,Yanling He,Alan Man Ching Ng,Xugang Guo,Zhubing He,He Yan,Aleksandra B. Djurišić,Yi Hou
出处
期刊:Nature Energy
[Springer Nature]
日期:2022-01-20
卷期号:7 (3): 229-237
被引量:188
标识
DOI:10.1038/s41560-021-00966-8
摘要
Due to the large chemical composition and bandgap tunability of both perovskite and organic semiconductors, perovskite/organic tandem solar cells are attractive for next-generation thin-film photovoltaics. However, their efficiency is limited by the open-circuit voltage loss of wide-bandgap perovskite subcells and the non-ideal interconnecting layers. Here we report that the passivation of nickel oxide hole-transporting layers with benzylphosphonic acid leads to the suppression of interfacial recombination, boosting the voltage up to 1.26 V in a 1.79-eV-bandgap perovskite subcell. Then, we develop an optimized interconnecting layer structure based on a 4-nm-thick sputtered indium zinc oxide layer inserted between organic bathocuproine and molybdenum oxide with enhanced electrical properties and transmittance in the near-infrared region. Through these improvements, we achieve a maximum efficiency of 23.60% (22.95% certified) in the perovskite/organic tandem solar cell. In addition, the tandem device retained 90% initial efficiency after 500 h maximum power point tracking under continuous one sun illumination.
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