n-type absorber by Cd2+ doping achieves high-performance carbon-based CsPbIBr2 perovskite solar cells

被引:33
作者
Xu, Yuan [1 ,2 ,3 ]
Li, Guodong [1 ,2 ,3 ]
Jing, Yu [1 ,2 ,3 ]
Zhang, Huayan [1 ,2 ,3 ]
Wang, Xin [1 ,2 ,3 ]
Lu, Yan [3 ]
Wu, Jihuai [1 ,2 ,3 ]
Lan, Zhang [1 ,2 ,3 ]
机构
[1] Minist Educ, Engn Res Ctr Environm Friendly Funct Mat, Beijing, Peoples R China
[2] Fujian Key Lab Photoelect Funct Mat, Xiamen, Peoples R China
[3] Huaqiao Univ, Coll Mat Sci & Engn, Xiamen 361021, Peoples R China
基金
中国国家自然科学基金;
关键词
Power conversion efficiency; CsPbIBr2; Carbon electrode; All-inorganic perovskite solar cell; N-doping; ALL-INORGANIC PEROVSKITE; EFFICIENT; STABILITY; SUBSTITUTION; CSPBBR3; SURFACE; ENERGY; FILMS;
D O I
10.1016/j.jcis.2021.09.117
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
High efficiency and stability have long been the key issues faced by perovskite solar cells (PSCs). It is found that the CsPbIBr2 all-inorganic perovskite has a suitable band gap and satisfactory stability, so it has attracted much attention. However, the many defects in the CsPbIBr2 film are one of the main prob-lems hindering the improvement of power conversion efficiency (PCE) of the CsPbIBr2 PSCs. The substi-tution of trace impurities is undoubtedly a simple, cost-effective and efficient strategy. In this work, an appropriate amount of Cd2+ (1.0% mol of Pb2+) is added into the CsPbIBr2 precursor solution to fabricate high quality CsPbIBr2 film with improved crystallinity, reduced trap density, suppressed photo-generated carrier recombination, displayed n-type doping and optimized energy level alignment. The corresponding carbon-based all-inorganic Cd2+-doped CsPbIBr2 PSCs achieve a maximum PCE of 10.63% with a high open circuit voltage (V-OC) of 1.324 V, which are much higher than those of the control one with a PCE of 8.48% and an V-OC of 1.235 V. The unencapsulated device can still retain more than 92% of the initial PCE when stored at ambient atmosphere (25 degrees C, relative humidity about 30%) for 40 days. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:40 / 47
页数:8
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