材料科学
钙钛矿(结构)
卤化物
钝化
接受者
光电流
电子受体
能量转换效率
光化学
无机化学
图层(电子)
化学工程
纳米技术
光电子学
凝聚态物理
化学
工程类
物理
作者
Minchao Qin,Jie Cao,Tiankai Zhang,Jiangquan Mai,Tsz‐Ki Lau,Shu Zhou,Yang Zhou,Jiayu Wang,Yao‐Jane Hsu,Ni Zhao,Jianbin Xu,Xiaowei Zhan,Xinhui Lu
标识
DOI:10.1002/aenm.201703399
摘要
Abstract Solution‐processed perovskite solar cells have great potential for low‐cost roll‐to‐roll fabrication. However, the degradation of aged precursor solutions will become a critical obstacle to mass production. In this report, a small molecule (ITIC‐Th) is employed to stabilize the perovskite precursor solution containing mixed cations and halides. It is found that ITIC‐Th can effectively suppress the formation of yellow δ‐phase in the films made from aged precursor solutions. Consequently, the devices fabricated from the aged precursor solution with ITIC‐Th experience much less efficiency drop with the increase of the precursor aging time—from 19.20% (fresh) to 16.55% (39 d), compared with the devices made from conventional precursor solutions dropping from 18.07% (fresh) to 1.76% (39 d). The characterizations suggest that ITIC‐Th is beneficial for CH 3 NH 3 + cations to be incorporated into the crystal structure, facilitating the formation of perovskite phase. Furthermore, the presence of ITIC‐Th in the perovskite thin film gives rise to additional photocurrent as well as improved fill factor due to the well‐matched energy levels, the passivation of defects, and the complementary absorption spectra, suggesting a new route toward future high‐efficiency solar cells—incorporating organic non‐fullerene acceptors and halide perovskite materials into the same active layer.
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