串联
钙钛矿(结构)
光伏
带隙
材料科学
纳米技术
卤化物
光电子学
化学
光伏系统
无机化学
电气工程
结晶学
工程类
复合材料
作者
Keyou Yan,Chenghao Duan,Kaicheng Zhang,Zijian Peng,Shiang Li,Feilin Zou,Feng Wang,Jiong Li,Zheng Zhang,Chang Chen,Qiliang Zhu,Jianhang Qiu,Xinhui Lu,Ning Li,Liming Ding,Christoph J. Brabec,Feng Gao
出处
期刊:Research Square - Research Square
日期:2024-06-12
标识
DOI:10.21203/rs.3.rs-4400007/v1
摘要
Abstract Inorganic perovskite tandem solar cells (IPTSCs) are promising candidates to break the efficiency bottleneck and address the stability issue. However, challenges remain in fabricating 2-terminal (2T) IPTSCs due to the inferior film formation and deep trap states induced by tin cations. Herein, a green ligand evolution (GLE) strategy with p-toluenesulfonyl hydrazide is employed to regulate film formation and eliminate deep traps in inorganic narrow bandgap perovskite, enabling the successful development of 2T IPTSCs. Accordingly, the 1.31 eV CsPb0.4Sn0.6I3:GLE device delivers a record efficiency of 17.41%. Combined with the 1.92 eV CsPbI2Br top-cell, 2T-IPTSCs exhibit a champion efficiency of 22.57% (certified 21.92%). Additionally, IPTSCs are engineered to deliver remarkable operation durability under maximum power point tracking, maintaining 80% of the initial efficiency at 65 ℃ for 1510 h and 85℃ for 800 h, respectively.
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