CsPbl3-Based Phase-Stable 2D Ruddlesden-Popper Perovskites for Efficient Solar Cells

被引:35
作者
Xu, Zhiyuan [1 ,2 ]
Li, Ling [3 ,4 ]
Dong, Xiyue [1 ,2 ]
Lu, Di [1 ,2 ]
Wang, Rui [1 ,2 ]
Yin, Wan-Jian [3 ,4 ]
Liu, Yongsheng [1 ,2 ,5 ]
机构
[1] Nankai Univ, Coll Chem, Ctr Nanoscale Sci & Technol, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Chem, Inst Polymer Chem, Key Lab Funct Polymer Mat, Tianjin 300071, Peoples R China
[3] Soochow Univ, Soochow Inst Energy & Mat Innovat SIEMIS, Light Ind Inst Electrochem Power Sources, Coll Energy, Suzhou 300071, Peoples R China
[4] Soochow Univ, Jiangsu Prov Key Lab Adv Carbon Mat & Wearable En, Suzhou 300071, Peoples R China
[5] Nankai Univ, Renewable Energy Convers & Storage Ctr, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
inorganic perovskite; two-dimensional perovskite; solar cells; organic spacer; stability; CESIUM LEAD IODIDE; HALIDE PEROVSKITE;
D O I
10.1021/acs.nanolett.2c00002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inorganic CsPbI3 perovskite has shown great promise in highly stable perovskite solar cells due to the lack of volatile organic components. However, the inferior phase stability in ambient conditions resulted from the very small Cs+, limiting their practical applications. Here, CsPbI3-based 2D Ruddlesden-Popper (RP) perovskites were developed using two thiophene-based aromatic spacers, namely, 2-thiophenemethylamine hydroiodide (ThMA) and 2-thiopheneformamidine hydroiodide (ThFA), which significantly improved the phase stability by releasing the large inner stress of black-phase CsPbI3. The optimized ThFA-based 2D RP perovskite (n = 5, ThFA-Cs) device achieves a record efficiency of 16.00%. Importantly, the ThFA-Cs devices could maintain an average of 98% of their initial efficiencies after being stored in N-2 at room temperature for 3000 h and 92% of their initial value at 80 degrees C for 960 h. This work provides a new perspective for exploration of the phase-stable CsPbI3-based perovskite with reduced dimensions for high-performance solar cells.
引用
收藏
页码:2874 / 2880
页数:7
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