串联
钙钛矿(结构)
材料科学
光电子学
纳米技术
化学
复合材料
结晶学
作者
Fawad Aslam,Hengyue Li,Jianhui Chang,Ding Yang,Fang Yang,Xiangxiang Feng,Xiang Liao,Qiang Zeng,Muhammad Zahid,Muhammad Irfan Sadiq,Muhammad Tahir,Fangyang Liu,Junliang Yang
摘要
The wide bandgap perovskite solar cells (PSCs) are promising candidates for high-efficiency tandem photovoltaics. However, these devices encounter challenges arising from defects within the perovskite lattice and at interfaces, which lead to non-radiative recombination and voltage losses. To address these issues, we have developed a synergistic approach that combines bulk passivation using l-cystine dihydrochloride as an additive with subsequent surface passivation treatments. This compound effectively passivates Pb2+ and halide defects through its carbonyl and amine functional groups. Both experimental and simulation results demonstrate that l-cystine dihydrochloride effectively reduces trap states, retards nucleation kinetics, promotes grain growth, and enhances crystallinity. Consequently, the device [FA0.8Cs0.2Pb(I0.6Br0.4)3, energy gap: 1.77 eV] incorporating l-cystine dihydrochloride achieved a power conversion efficiency (PCE) of approximately 16.00%, which was further increased to 17.03% with an additional octylammonium iodide surface passivation. Expanding our approach, we have fabricated the wide bandgap semitransparent device, yielding a PCE of 15.62%. When integrated with narrow-bandgap organic solar cells in four-terminal (4T) perovskite/organic tandem solar cells, a remarkable efficiency of 23.14% was attained. This strategy effectively improves the performance of wide bandgap PSCs, which exhibit great potential in advancing perovskite/organic photovoltaic technologies.
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