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Solvent vapor annealing-assisted mesoporous PbBr2 frameworks for high-performance inorganic CsPbBr3 perovskite solar cells

材料科学 退火(玻璃) 化学工程 介孔材料 钙钛矿(结构) 开路电压 能量转换效率 钙钛矿太阳能电池 短路 分析化学(期刊) 纳米技术 光电子学 催化作用 电压 复合材料 有机化学 化学 电气工程 工程类
作者
Kaibo Liang,Yunjia Wu,Qingshui Zhen,Yu Zou,Xiuchun Zhang,Chen‐Hao Wang,Puyao Shi,Yangyang Zhang,Weihai Sun,Yunlong Li,Jihuai Wu
出处
期刊:Surfaces and Interfaces [Elsevier]
卷期号:37: 102707-102707 被引量:10
标识
DOI:10.1016/j.surfin.2023.102707
摘要

In recent years, CsPbBr3 perovskite solar cells (PSCs) have attracted the attention of a large number of researchers due to their excellent temperature and humidity stability. And in the current studies, due to the lack of suitable solvents to dissolve PbBr2 and CsBr at the same time, most studies have used sequential solution-processing techniques (SSPTs) to prepare CsPbBr3 films. However, in the process of the sequential deposition of PbBr2 and CsBr, the uneven reaction could lead to the generation of impure phase (e.g. CsPb2Br5 and Cs4PbBr6), which would deteriorate the photoelectric performance of the device. Here, a solvent-vapor annealing (SA) method has been proposed for fabricating mesoporous PbBr2 films by exposing the PbBr2 films in N,N-Dimethylformamide (DMF) vapor environment. The porous PbBr2 frameworks could facilitate the reaction with CsBr to fully convert into inorganic perovskite CsPbBr3. A series of characterization results show that a compact, uniform and high-quality CsPbBr3 film with large grains was obtained, where the porosity of PbBr2 scaffold could be tuned by the volume of DMF. Consequently, the devices based on optimized PbBr2 films treated by SA method achieved a champion power convention efficiency (PCE) of 9.60%, an open-circuit voltage (VOC) of 1.54 V, a short-circuit current density (JSC) of 7.57 mA cm−2 and a fill factor (FF) of 82.37%, compared with the devices treated by conventional thermal annealing (TA) method achieved a PCE of 8.42%, a VOC of 1.49 V, JSC of 7.31 mA cm−2 and FF of 77.30%. Furthermore, the SA treated devices exhibit more durable stability than TA treated devices, and the SA treated devices still retain 94.28% of its original PCE without any encapsulation in the ambient atmosphere after 30 days.
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