Single-Layered MXene Nanosheets Doping TiO2 for Efficient and Stable Double Perovskite Solar Cells

被引:161
作者
Li, Zhenxing [1 ]
Wang, Ping [1 ]
Ma, Chang [1 ,2 ]
Igbari, Femi [3 ]
Kang, Yikun [1 ]
Wang, Kai-Li [3 ]
Song, Weiyu [1 ]
Dong, Chong [3 ]
Li, Yanjie [1 ]
Yao, Jiasai [1 ]
Meng, Dong [4 ]
Wang, Zhao-Kui [3 ]
Yang, Yang [4 ]
机构
[1] China Univ Petr, Coll New Energy & Mat, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] BTR New Energy Mat Inc, Shenzhen 518106, Peoples R China
[3] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
[4] Univ Calif Los Angeles, Dept Mat Sci & Engn, Los Angeles, CA 90095 USA
基金
北京市自然科学基金;
关键词
36;
D O I
10.1021/jacs.0c12739
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The inorganic lead-free Cs2AgBiBr6 double perovskite structure is the promising development direction in perovskite solar cells (PSCs) to solve the problem of the instability of the APbX(3) structure and lead toxicity. However, the low short-circuit current and power conversion efficiency (PCE) caused by the low crystallization of Cs2AgBiBr6 greatly limit the optoelectronic application. Herein, we adopt a simple strategy to dope single-layered MXene nanosheets into titania (Ti3C2Tx@TiO2) as a multifunctional electron transport layer for stable and efficient Cs(2)AgBiBr(6 )double PSCs. The single-layered MXene nanosheets significantly improve the electrical conductivity and electron extraction rate of TiO2; meanwhile, the single-layered MXene nanosheets change the surface wettability of the electron transport layer and promote the crystallization of the Cs2AgBiBr6 double perovskite in solar cell devices. Therefore, the PCE went up by more than 40% to 2.81% compared to that of a TiO2 based device, and the hysteresis was greatly suppressed. Furthermore, the device based on Ti3C2Tx@TiO(2 )showed the long-term operating stability. After storing the device for 15 days under ambient air conditions, the PCE still remained a retention rate of 93% of the initial one. Our finding demonstrates the potential of Ti3C2Tx@TiO2 in electron transfer material of high-performance double PSCs.
引用
收藏
页码:2593 / 2600
页数:8
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