钙钛矿(结构)
粘附
材料科学
能量转换效率
单层
光伏
成核
光伏系统
光电子学
纳米技术
复合材料
化学工程
工程类
化学
有机化学
生物
生态学
作者
Zhenghong Dai,Shuai You,Dwaipayan Chakraborty,Shunran Li,Yadong Zhang,Anush Ranka,Stephen Barlow,Joseph J. Berry,Seth R. Marder,Peijun Guo,Yue Qi,Kai Zhu,Nitin P. Padture
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-04-02
卷期号:9 (4): 1880-1887
被引量:6
标识
DOI:10.1021/acsenergylett.4c00510
摘要
Carbazole-based self-assembled monolayers (SAMs) at the interface between the metal-halide perovskite (MHP) and the transparent conducting oxide (TCO) serve the function of hole-transport layers in p-i-n "inverted" perovskite solar cells (PSCs). Here we show that the use of an iodine-terminated carbazole-based SAM increases the interfacial mechanical adhesion dramatically (2.6-fold) and that this is responsible for substantial improvements in the interfacial morphology, photocarrier transport, and operational stability. While the improved morphology and optoelectronic properties impart high efficiency (up to 25.39%) to the PSCs, the enhanced adhesion suppresses nucleation and propagation of pores/cracks during PSC operation, resulting in the retention of 96% of the initial efficiency after 1000 h of continuous-illumination testing at the maximum power-point. This demonstrates the strong connection between judicious interfacial adhesion toughening and simultaneous enhancement in the efficiency and operational stability of p-i-n PSCs, with broader implications for the reliability and durability of perovskite photovoltaics before they can be commercialized.
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