Stable tin perovskite solar cells enabled by widening the time window for crystallization

被引:13
作者
Dai, Zhensheng [1 ,2 ]
Tang, Wentao [1 ,2 ]
Wang, Tao [1 ,2 ]
Lv, Taoyuze [1 ,2 ,3 ]
Luo, Xinhui [1 ,2 ]
Cui, Danyu [1 ,2 ]
Sun, Ruitian [1 ,2 ]
Qiao, Liang [1 ,2 ]
Chen, Han [1 ,2 ]
Zheng, Rongkun [3 ]
Yang, Xudong [1 ,2 ]
Han, Liyuan [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Joint Res Ctr Clean Energy Mat, Shanghai 200240, Peoples R China
[3] Univ Sydney, Australian Ctr Microscopy & Microanal, Sch Phys, Sydney Nano Inst, Sydney, NSW 2006, Australia
基金
中国国家自然科学基金;
关键词
lead-free perovskite; FASnI(3); perovskite solar cells; crystallization; stability;
D O I
10.1007/s40843-020-1581-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Tin perovskite solar cells (TPSCs) are the most promising candidates for lead-free perovskite solar cells (PSCs). However, the poor crystallization and chemical stability of Sn perovskites are the two challenging issues for further application of TPSCs. Here, we present a strategy to stabilize CH(NH2)(2)SnI3 (FASnI(3)) perovskite enabled by an amine complex, CH3NH3I center dot 3CH(3)NH(2), which can hinder the major degradation issue caused by the oxidation of Sn2+ to Sn4+. The resulting Sn perovskite films exhibit enhanced crystallinity and stability in comparison with those made with conventional inorganic SnF2 additives. Finally, the device achieved a higher external quantum efficiency for charge extraction and a power conversion efficiency (PCE) of 9.53%, which maintained more than 90% of the initial efficiency after 1000 h of light soaking under the standard AM 1.5 G solar illumination.
引用
收藏
页码:1849 / 1857
页数:9
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