钙钛矿(结构)
材料科学
单层
热稳定性
太阳能电池
氧化镍
自组装单层膜
粒度
分子
接触角
氧化物
光电子学
载流子寿命
表面改性
化学工程
萃取(化学)
光伏系统
纳米技术
硅
化学
复合材料
色谱法
有机化学
工程类
冶金
生物
生态学
作者
Gisung Kim,Hyojung Kim,Mijoung Kim,Jaegwan Sin,Moonhoe Kim,Jaeho Kim,Haoran Zhou,Sung Ho Kang,Hye Min Oh,JungYup Yang
出处
期刊:Nanomaterials
[Multidisciplinary Digital Publishing Institute]
日期:2024-01-19
卷期号:14 (2): 214-214
被引量:8
摘要
Perovskite solar cells (PSCs) have been significantly improved by utilizing an inorganic hole-transporting layer (HTL), such as nickel oxide. Despite the promising properties, there are still limitations due to defects. Recently, research on self-assembled monolayers (SAMs) is being actively conducted, which shows promise in reducing defects and enhancing device performance. In this study, we successfully engineered a p-i-n perovskite solar cell structure utilizing HC-A1 and HC-A4 molecules. These SAM molecules were found to enhance the grain morphology and uniformity of the perovskite film, which are critical factors in determining optical properties and device performance. Notably, HC-A4 demonstrated superior performance due to its distinct hydrophilic properties with a contact angle of 50.3°, attributable to its unique functional groups. Overall, the HC-A4-applied film exhibited efficient carrier extraction properties, attaining a carrier lifetime of 117.33 ns. Furthermore, HC-A4 contributed to superior device performance, achieving the highest device efficiency of 20% and demonstrating outstanding thermal stability over 300 h.
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