Stabilization of Highly Efficient and Stable Phase-Pure FAPbI3Perovskite Solar Cells by Molecularly Tailored 2D-Overlayers

被引:229
作者
Liu, Yuhang [1 ]
Akin, Seckin [1 ,4 ]
Hinderhofer, Alexander [2 ]
Eickemeyer, Felix T. [1 ]
Zhu, Hongwei [1 ]
Seo, Ji-Youn [1 ]
Zhang, Jiahuan [3 ]
Schreiber, Frank [2 ]
Zhang, Hong [1 ]
Zakeeruddin, Shaik M. [1 ]
Hagfeldt, Anders [3 ]
Dar, M. Ibrahim [1 ]
Graetzel, Michael [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Dept Chem & Chem Engn, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[2] Univ Tubingen, Inst Angew Phys, D-72076 Tubingen, Germany
[3] Ecole Polytech Fed Lausanne, Lab Photomol Sci, Stn 6, CH-1015 Lausanne, Switzerland
[4] Karamanoglu Mehmetbey Univ, Dept Met & Mat Engn, Karaman, Turkey
基金
瑞士国家科学基金会;
关键词
additive engineering; FAPbI(3); perovskite solar cells; thermal stability; HALIDE PEROVSKITES; LEAD IODIDE; LAYERS;
D O I
10.1002/anie.202005211
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As a result of their attractive optoelectronic properties, metal halide APbI(3)perovskites employing formamidinium (FA(+)) as the A cation are the focus of research. The superior chemical and thermal stability of FA(+)cations makes alpha-FAPbI(3)more suitable for solar-cell applications than methylammonium lead iodide (MAPbI(3)). However, its spontaneous conversion into the yellow non-perovskite phase (delta-FAPbI(3)) under ambient conditions poses a serious challenge for practical applications. Herein, we report on the stabilization of the desired alpha-FAPbI(3)perovskite phase by protecting it with a two-dimensional (2D) IBA(2)FAPb(2)I(7)(IBA=iso-butylammonium overlayer, formed via stepwise annealing. The alpha-FAPbI(3)/IBA(2)FAPb(2)I(7)based perovskite solar cell (PSC) reached a high power conversion efficiency (PCE) of close to 23 %. In addition, it showed excellent operational stability, retaining around 85 % of its initial efficiency under severe combined heat and light stress, that is, simultaneous exposure with maximum power tracking to full simulated sunlight at 80 degrees C over 500 h.
引用
收藏
页码:15688 / 15694
页数:7
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