工作职能
电极
单层
自组装单层膜
材料科学
工作(物理)
功能(生物学)
曲面(拓扑)
纳米技术
光电子学
化学
机械工程
工程类
数学
生物
进化生物学
物理化学
几何学
作者
Ricardo Ruvalcaba,Zhongzhe Liu,Mohamad Insan Nugraha,George T. Harrison,Yuying Yang,Marco Thaler,Adam V. Marsh,Matthias Zeilerbauer,Chrysa Aivalioti,Raul Ricardo Aguileta-Vazquez,Leonidas Tsetseris,Laerte L. Patera,Percy Zahl,Martin Heeney,Thomas D. Anthopoulos,Shadi Fatayer
标识
DOI:10.1021/acsmaterialslett.4c02267
摘要
Self-assembled monolayers (SAMs) help improve the performance of organic electronic devices through interface passivation and enhanced carrier transport. Yet, there is limited information regarding the chemical structure of the SAMs upon functionalization and subsequent thermal treatment. Here, we studied the on-surface reaction of carbazole-derived SAMs on model gold electrodes, focusing on the chemical structure changes induced by thermal treatments. Furthermore, we correlate the microscopic changes with their impact on the electrode’s work function. The carbazole-based SAMs first transform into organometallic complexes. At higher annealing temperatures, SAMs convert to oligomeric complexes. The observed chemical reactions significantly reduce the electrode work function and facilitate electron injection in n-type organic thin-film transistors. Our results highlight the on-surface synthesis of electronically active SAMs as an alternative approach for modifying the work function of electrodes for organic electronics.
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