Accelerated aging of all-inorganic, interface-stabilized perovskite solar cells

被引:203
|
作者
Zhao, Xiaoming [1 ]
Liu, Tianran [1 ,2 ]
Burlingame, Quinn C. [3 ]
Liu, Tianjun [4 ]
Holley, Rudolph [1 ]
Cheng, Guangming [5 ]
Yao, Nan [5 ]
Gao, Feng [4 ]
Loo, Yueh-Lin [1 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Elect & Comp Engn, Princeton, NJ 08544 USA
[3] Princeton Univ, Andlinger Ctr Energy & Environm, Princeton, NJ 08544 USA
[4] Linkoping Univ, Dept Phys Chem & Biol IFM, SE-58183 Linkoping, Sweden
[5] Princeton Univ, Princeton Inst Sci & Technol Mat, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
EFFICIENT; PHOTOVOLTAICS; LIGHT; PASSIVATION; PERFORMANCE; IODIDE; FILM;
D O I
10.1126/science.abn5679
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To understand degradation routes and improve the stability of perovskite solar cells (PSCs), accelerated aging tests are needed. Here, we use elevated temperatures (up to 110 degrees C) to quantify the accelerated degradation of encapsulated CsPbI3 PSCs under constant illumination. Incorporating a two-dimensional (2D) Cs2PbI2Cl2 capping layer between the perovskite active layer and hole-transport layer stabilizes the interface while increasing power conversion efficiency of the all-inorganic PSCs from 14.9 to 17.4%. Devices with this 2D capping layer did not degrade at 35 degrees C and required >= 2100 hours at 110 degrees C under constant illumination to degrade by 20% of their initial efficiency. Degradation acceleration factors based on the observed Arrhenius temperature dependence predict intrinsic lifetimes of 51,000 +/- 7000 hours (>5 years) operating continuously at 35 degrees C.
引用
收藏
页码:307 / 310
页数:4
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