High Efficient Hole Extraction and Stable All-Bromide Inorganic Perovskite Solar Cells via Derivative-Phase Gradient Bandgap Architecture

被引:86
作者
Tong, Guoqing [1 ,2 ]
Chen, Taotao [1 ]
Li, Huan [1 ]
Song, Wentao [2 ]
Chang, Yajing [1 ]
Liu, Jingjing [3 ,4 ]
Yu, Linwei [3 ,4 ]
Xu, Jun [3 ,4 ]
Qi, Yabing [2 ]
Jiang, Yang [1 ]
机构
[1] Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China
[2] Okinawa Inst Sci & Technol Grad Univ OIST, EMSSU, 1919-1 Tancha, Onna Son, Okinawa 9040495, Japan
[3] Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[4] Nanjing Univ, Sch Elect Sci & Engn, Collaborat Innovat Ctr Adv Microstruct, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
derivative phase; gradient bandgap; inorganic perovskite; solar cells; vapor deposition; QUANTUM DOTS; HETEROJUNCTION; CSPBBR3; NANOCRYSTALS; PERFORMANCE; STABILITY; BR;
D O I
10.1002/solr.201900030
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Inorganic perovskite materials have demonstrated outstanding performance in the field of photovoltaic devices due to their superior charge carrier transport properties and excellent thermal stability. In particular, the inorganic perovskite derivative phases show special properties in terms of phase stability and optoelectronic application, especially in the phase transition investigation. However, their commercial applications still face challenges due to the large recombination at the interface, resulting in poor efficiency and metastable phases such as iodide perovskite existing in the film. Herein, an all-bromide inorganic perovskite solar cell has been developed by introducing the derivative phases (CsPb2Br5 and Cs4PbBr6) to construct gradient bandgap architecture. This graded heterojunction device is realized with a controllable sequential vapor deposition procedure. The valance band maximum elevates gradually with the presence of derivative phases and effectively blocks electrons and boosts the hole extraction efficiency at the counter electrode, which promotes charge separation and reduces the interface recombination. Ultimately, an impressive power conversion efficiency of 10.17% is achieved through a CsPbBr3/CsPbBr3-CsPb2Br5/CsPbBr3-Cs4PbBr6 architecture strategy with excellent stability above 3000h (85% of initial performance) in a humid environment (@RH approximate to 45%) and 700h (83% of initial efficiency) under thermal conditions (@ 100 degrees C).
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页数:9
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