共价键
兴奋剂
材料科学
薄膜
共价有机骨架
纳米技术
化学
光电子学
有机化学
作者
Dayanni D. Bhagwandin,Brian M. Everhart,Kirt A. Page,Michael Altvater,Yao Yao,Rahul Rao,Kara L. Martin,K. Mahalingam,Cheri M. Hampton,Jonathan Ludwick,Griffin W. Roberts,Drake Austin,Md. Sherajul Islam,Ly D. Tran,Arthur R. Woll,Lawrence F. Drummy,Ajit K. Roy,Tobin J. Marks,Antonio Facchetti,Tyson C. Back
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-07-10
卷期号:19 (28): 25720-25731
标识
DOI:10.1021/acsnano.5c03065
摘要
Strict control of both crystallographic orientation and band structure is crucial in realizing future high performing semiconducting microelectronic devices based on 2D covalent organic frameworks (COFs). Due to the insoluble nature from extensive aromaticity, processing of these materials into well-ordered, highly crystalline thin films presents a great challenge. In this work, a strategy to enable controlled covalent doping of imine COF thin films with thiophene linkers is presented. By incorporating different aldehyde ratios of terephthalaldehyde (PDA) and 2,5-thiophenedicarboxaldehyde (TDA) with 1,3,5-tris(4-aminophenyl)benzene (TAPB) in a liquid-solid synthesis approach, a series of highly crystalline and uniformly oriented TAPB-PDA-TDA COF thin films with varying percentages of TDA linkers incorporated into the framework were obtained. In this case, incorporation of thiophene linkers up to 20% resulted in minimal disruption of the long-range crystallographic ordering. Moreover, a small amount of thiophene molecules covalently doped into the highly ordered structure results in a small reduction in the band gap and a corresponding increase in the work function and decrease in the valence band maximum, effectively behaving like a p-type dopant in conventional semiconductors. The covalently doped thiophene unit is shown to increase the π-conjugation through enhanced crystallinity in the framework, improving the electron delocalization in the structure.
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