Hyperactive Selenium Source Yields Kesterite Solar Cells with 12.86% Efficiency

被引:0
|
作者
Wang, Mengyang [1 ,2 ]
Geng, Hang [2 ]
Zhu, Jichun [3 ]
Cui, Yubo [1 ]
Zhao, Shanheng [1 ,2 ]
Fu, Junjie [1 ]
Kou, Dongxing [2 ]
Sun, Jie [4 ]
Zhao, Chaoliang [1 ]
Wu, Sixin [2 ]
Ding, Liming [4 ]
Zheng, Zhi [1 ]
机构
[1] Xuchang Univ, Inst Surface Micro & Nano Mat, Coll Chem & Mat Engn, Key Lab Micronano Mat Energy Storage & Convers He, Xuchang 461000, Henan, Peoples R China
[2] Henan Univ, Key Lab Special Funct Mat MOE, Kaifeng 475004, Peoples R China
[3] Henan Univ, Miami Coll, Kaifeng 475004, Peoples R China
[4] Ctr Excellence Nanosci CAS, Natl Ctr Nanosci & Technol, Key Lab Nanosyst & Hierarch Fabricat CAS, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
chemical environment; hyperactive selenium source; intrinsic defects; kesterite solar cells; open circuit voltage deficit;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
One of the main issues that limits the efficiency of kesterite solar cells is the low diffusion and chemical activity of selenium clusters. Here, this work proposes a simple and effective pre-selenization strategy using Na-2(Se2S) solution, which enables the direct introduction of hyperactive Se-2, Se-3, and Se-4 into the precursors. The results demonstrate that Se-2, Se-3, and Se-4 promote the formation of the Cu2-xSe liquid phase and enhance the diffusion of elements from different micro-regions. Consequently, the ratios of Cu/(Zn + Sn) and Sn/Zn in different micro-regions of the absorber are controlled within the optimal range, exhibiting reduced fluctuations. The controlled environment suppresses the formation of Cu-Zn and Sn-Zn defects, as well as [2Cu(Zn) + Sn-Zn] defect clusters. Finally, a power conversion efficiency (PCE) of 12.86% is achieved, which is the highest PCE for kesterite solar cells made under ambient pressure and with N,N-dimethylformamide solvent.
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页数:10
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