钙钛矿(结构)
异质结
材料科学
钙钛矿太阳能电池
卤化物
晶界
化学工程
微晶
光电子学
图层(电子)
纳米技术
无机化学
化学
复合材料
冶金
工程类
微观结构
作者
Seid Yimer Abate,Surabhi Jha,Abdul Kalam Shaik,Guorong Ma,Jada Emodogo,Nihar Pradhan,Xiaodan Gu,Derek L. Patton,Nathan I. Hammer,Qilin Dai
标识
DOI:10.1016/j.orgel.2023.106984
摘要
Organic-inorganic halide perovskites achieved tremendous success in solar cells, however, their commercialization has not yet been realized. The primary reason is the intrinsic property of perovskite film. The significant density of defects in the polycrystalline perovskite layers influenced not only the performance of the solar cell as well its long-term stability. Here, we employed a post-surface treatment of the perovskite layer by tetrabutylammonium tetrafluoroborate (TBATFB). TBATFB interacted through hydrogen bonding with the 3D perovskite and formed an in situ a 1D TBAPbI1.66Br0.34BF4 on the surface of the 3D perovskite. This low-dimensional 1D perovskite (perovskitoid) capping layer represses the defects in perovskite by blocking the nonradiative recombination centers and minimizing the surface and grain boundary defects. Our experimental results verified both the electron and hole defects were significantly suppressed by the TBATFB modification. As a result, the 1D/3D heterostructure device exhibited a champion performance of 21.68% PCE compared to 20.03% PCE for the control device. Intriguingly, the 1D TBAPbI1.66Br0.34BF4 capping layer safeguards the 3D perovskite from the infiltration of moisture thus the TBATFB modified devices maintained 99% of their initial performance after 720h in the air (RH = 40–60%).
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