Accelerating the Screening of Perovskite Compositions for Photovoltaic Applications through High-Throughput Inkjet Printing

被引:45
|
作者
Chen, Shi [1 ,2 ,3 ]
Zhang, Lihua [2 ,3 ,4 ]
Yan, Lijia [2 ,3 ]
Xiang, Xiaodong [2 ]
Zhao, Xingzhong [5 ]
Yang, Shihe [4 ,6 ]
Xu, Baomin [2 ,3 ]
机构
[1] Southern Univ Sci & Technol, SUSTech Acad Adv Interdisciplinary Studies, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China
[3] Southern Univ Sci & Technol, Shenzhen Engn Res & Dev Ctr Flexible Solar Cells, Shenzhen 518055, Guangdong, Peoples R China
[4] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[5] Wuhan Univ, Dept Phys, Wuhan 430072, Hubei, Peoples R China
[6] Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Guangdong Key Lab Nanomicro Mat Res, Shenzhen 518055, Guangdong, Peoples R China
关键词
high throughput fabrication; inkjet printing; perovskites; photovoltaic applications; SOLAR-CELLS; HYBRID PEROVSKITES; LEAD-FREE; EFFICIENT; DESIGN; CATIONS; LAYERS; TIO2;
D O I
10.1002/adfm.201905487
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The exploration and optimization of numerous mixed perovskite compositions are causing a strong demand for high-throughput synthesis. Nevertheless high-throughput fabrication of perovskite films with representative film properties, which can efficiently screen the perovskite compositions for photovoltaic applications, has rarely been explored. A high-throughput inkjet printing approach that can automatically fabricate perovskite films with various compositions with high reproducibility and high speed is developed. The automatic sequential printing of four precursors forms 25 mixed films in a fast and reproducible manner. The obtained bandgaps, photoluminescence (PL) peak positions, and PL lifetimes allow for the efficient screening of perovskite compositions for photovoltaic applications. To exemplify this concept, among 25 tested films, two compositions CH3NH3PbBr0.75I2.25 (MA) and (HC(NH2)(2))(0.75)(CH3NH3)(0.25)PbBr0.75I2.25 (FA(0.75)MA(0.25)) with a long (237 ns) and short (49.0 ns) PL lifetime, respectively, are screened out for device investigations. As expected, the MA-based device exhibits a much higher efficiency (19.0%) than that (15.3%) of the FA(0.75)MA(0.25) counterpart. This efficiency improvement is mainly ascribed to a smaller dark saturate current density, a lower level of energetic disorder, more efficient charge transfer and decreased charge recombination losses, which are consistent with the much longer PL lifetime in the database.
引用
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页数:9
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