钙钛矿(结构)
材料科学
相(物质)
基质(水族馆)
配体(生物化学)
方向(向量空间)
散射
结晶学
光学
化学
几何学
数学
物理
有机化学
生物化学
海洋学
受体
地质学
作者
Han Wang,Zhaotong Qin,Jiangsheng Xie,Shenghe Zhao,Kuan Liu,Xinlu Guo,Gang Li,Xinhui Lu,Keyou Yan,Jianbin Xu
出处
期刊:Small
[Wiley]
日期:2020-09-30
卷期号:16 (42)
被引量:40
标识
DOI:10.1002/smll.202003098
摘要
Abstract The crystalline orientation and phase distribution are two important parameters for high‐performance 2D perovskite solar cells. Therefore, it is essential to understand how the structure of spacer ligands influences the orientation and phase distribution of resulting 2D perovskite films. In this work, a new member of Dion–Jacobson (DJ) phase 2D perovskites based on trans‐1,4‐cyclohexanediamine (CHDA) is demonstrated and it is found that the crystalline orientation is self‐aligned spontaneously, which is different from the well‐known graded distribution in controlled sample with its isomer 1,6‐diaminohexane (HDA) as spacer ligand. Grazing incident X‐ray scattering suggests that the exact alignment is strongly slantwise to the substrate while it is still beneficial for charge transfer along the vertical structure of devices. The devices can achieve high efficiency up to 15.01% for (CHDA)MA 3 Pb 4 I 13 ( n = 4), one of the highest efficiencies reported by now. The encapsulated (CHDA)MA 3 Pb 4 I 13 ( n = 4) devices can retain 80.7% efficiency for 270 min under continuous maximum power point tracking. (CHDA)MA 3 Pb 4 I 13 ( n = 4) devices can retain 96.5% efficiency under 60 °C and 74.4% efficiency under 70 °C heating for 68 h. The results demonstrate the slantwise aligned DJ phase perovskite solar cells with excellent stability.
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