材料科学
钙钛矿(结构)
电极
串联
制作
纳米技术
同质性(统计学)
光电子学
金属氢氧化物
异质结
氢氧化物
图层(电子)
电导率
分子
光伏系统
金属
微晶
化学工程
石墨烯
热的
润湿
表面电荷
聚合物太阳能电池
曲面(拓扑)
空间电荷
光活性层
作者
Rik Hooijer,Sunwoo Kim,Sinja Klenk,Hao Zhu,Cem Yilmaz,Yenal Yalçinkaya,Doyun Im,Anna S. Backeberg,Jian Huang,M. Bouraoui,Ali Buyruk,Esma Ugur,Clément Maheu,Achim Hartschuh,Frédéric Laquai,Lukas Schmidt‐Mende,Georg S. Duesberg,Sangwook Lee,Erkan Aydin
摘要
ABSTRACT Self‐assembled molecules (SAMs) as a molecular charge selective contact and interface with metal oxides are the new benchmark in p‐i‐n devices. Yet, transparent electrode (i.e., ITO) surface preparation is often performed with established protocols that do not exploit the full potential of self‐assembly. We introduce a simple, solution‐based ITO surface treatment strategy that enables improved contact formation by simultaneously tuning surface chemistry, conductivity and homogeneity. Contrary to the prevailing assumption that maximizing surface hydroxylation is the key for phosphonic‐acid‐based SAMs, we show that synthetic design with moderate hydroxyl and hydroxide content yields more uniform and electronically favourable interfaces for SAM anchoring. Electronically, the resulting contacts enable enhanced charge extraction, while offering improved layer homogeneity and operational stability. The treated interfaces further demonstrate improved resilience under extreme thermal cycling between −80°C and 80°C, relevant for low‐earth‐orbit (LEO) space operation. Importantly, we demonstrated the broad applicability of our approach across various materials, fabrication environments, and device structures, including single junction and tandem solar cells. These findings establish surface preparation as a design parameter on par with molecular engineering for robust perovskite optoelectronic devices.
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