钙钛矿(结构)
光伏
卤化物
相(物质)
光伏系统
光电子学
带隙
材料科学
量子阱
物理
结晶学
化学
光学
电气工程
无机化学
工程类
有机化学
激光器
作者
Yiting Zheng,Tingting Niu,Jian Qiu,Lingfeng Chao,Bixin Li,Yingguo Yang,Qian Li,Changqing Lin,Xingyu Gao,Chunfeng Zhang,Yingdong Xia,Yonghua Chen,Wei Huang
出处
期刊:Solar RRL
[Wiley]
日期:2019-05-08
卷期号:3 (9)
被引量:114
标识
DOI:10.1002/solr.201900090
摘要
Dion–Jacobson (DJ) phase halide perovskites have attracted extensive attention in photovoltaic devices due to their significantly enhanced stability when compared with conventional 3D analogs. However, fundamental questions concerning the quantum well (QW) barrier thicknesses, which are critical to design efficient DJ phase perovskite photovoltaics, remain unknown. Herein, it is unambiguously demonstrated that QW barrier thickness, depending on bulky organic ammonium spacers with different chain lengths, such as 1.3‐propanediamine (PDA), 1.4‐butanediamine (BDA), 1.5‐pentamethylenediamine (PeDA), and 1.6‐hexamethylenediamine (HDA), allows the control of orientation and QW distribution. The DJ phase perovskites based on PDA and BDA have suitable QW barrier thicknesses, which exhibit excellent orientation and more uniform QW distribution, allowing a smooth bandgap transition that leads to longer carrier diffusion length, higher charge mobility, and lower defect density. Conversely, PeDA and HDA, with thicker QW barriers, result in lower orientation and multiple DJ perovskite phases. DJ phase perovskite photovoltaic devices based on PDA and BDA show significantly improved power conversion efficiencies (PCEs) of 14.16% and 16.38% compared with PCEs of 12.95% and 10.55% for PeDA and HDA analogs, respectively.
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