Stabilizing efficient wide-bandgap perovskite in perovskite-organic tandem solar cells

被引:37
作者
Guo, Xiao [1 ,2 ]
Jia, Zhenrong [1 ,2 ]
Liu, Shunchang [1 ,2 ]
Guo, Renjun [2 ]
Jiang, Fangyuan [3 ]
Shi, Yangwei [4 ,5 ]
Dong, Zijing [1 ,2 ]
Luo, Ran [1 ,2 ]
Wang, Yu-Duan [1 ,2 ]
Shi, Zhuojie [1 ,2 ]
Li, Jia [2 ]
Chen, Jinxi [1 ,2 ]
Lee, Ling Kai [2 ]
Mueller-Buschbaum, Peter [5 ,6 ]
Ginger, David S. [3 ,7 ]
Paterson, David J. [8 ]
Hou, Yi [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117585, Singapore
[2] Natl Univ Singapore, Solar Energy Res Inst Singapore SERIS, Singapore 117574, Singapore
[3] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[4] Univ Washington, Mol Engn & Sci Inst, Seattle, WA 98195 USA
[5] Tech Univ Munich, TUM Sch Nat Sci, Dept Phys, Chair Funct Mat, James Franck Str 1, D-85748 Garching, Germany
[6] Tech Univ Munich, Heinz Maier Leibnitz Zent MLZ, Lichtenbergstr 1, D-85748 Garching, Germany
[7] Pacific Northwest Natl Lab, Phys & Computat Sci Directorate, Phys Sci Div, Richland, WA 99352 USA
[8] Australian Synchrotron ANSTO, Clayton, VIC 3168, Australia
基金
新加坡国家研究基金会;
关键词
PHOTOINDUCED HALIDE SEGREGATION; SUPPRESSED PHASE SEGREGATION; LENGTHS;
D O I
10.1016/j.joule.2024.06.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Iodide and bromide integration facilitate bandgap tunability in wide-bandgap perovskites, yet high concentrations of bromide lead to halide phase segregation, adversely affecting the efficiency and stability of solar cell devices. In this work, 2-amino-4,5-imidazoledicarbonitrile (AIDCN), with highly polarized charge distribution and compact molecular configuration, is incorporated into a 1.86 eV wide-bandgap perovskite to effectively suppress photoinduced iodine escape and phase segregation. Hyperspectral photoluminescence microscopy reveals that AIDCN mitigates phase segregation under continuous laser exposure. Concurrent in situ grazing-incidence wide-angle X-ray scattering and X-ray fluorescence measurements further validate suppressed iodine escape, evidenced by a notable slowing down of lattice shrinkage and a well-maintained overall chemical composition of the perovskite under continuous illumination. Applying this approach, we achieve a power conversion efficiency (PCE) of 18.52% in 1.86 eV wide-bandgap perovskite solar cells. By integrating this perovskite subcell with the PM6:BTP-eC9 organic subcell, the tandem attains a maximum PCE of 25.13%, with a certified stabilized PCE of 23.40%.
引用
收藏
页码:2554 / 2569
页数:17
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