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The charging of the carbon nanotube/oligothiophene interphase as studied by in situ electron spin resonance/UV-Vis-NIR spectroelectrochemistry

机译:原位电子自旋共振/ UV-Vis-NIR光谱电化学研究碳纳米管/低聚噻吩中间相的电荷

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摘要

A detailed in situ Electron Spin Resonance (ESR)/UV-Vis-NIR spectroelectrochemical study of the oligothiophene/single walled carbon nanotube (SWCNT) interphase is presented to provide an insight into the interaction of nanotubes with oligothiophenes. Used as electrode materials these composites are followed in situ with respect to the paramagnetic and diamagnetic states formed upon electrochemical charging. The variation of the oligomer chain length and the type, position and number of substituents at the oligomer is used to understand the structural influence on the formation of the charged states in the material upon electrochemical reaction. For β,β'-dihexylsexithiophene (β,β'-DHST)-SWCNT the enlarged current in the composite and a decreased radical cation concentration can be explained by the formation of π-dimers. By interaction with SWCNTs the π-dimerization of oligothiophenes and the formation of multi π-stack structures occur. For α,ω-dicyano-β,β'-dibutylquaterthiophene (DCNDBQT)-SWCNT a new paramagnetic structure of the oligomer is formed as an intermediate which undergoes follow-up reactions. Using different substituted oligothiophenes their interaction with nanotubes can be understood with respect to the structure of the oligomer.
机译:提出了详细的原位电子自旋共振(ESR)/ UV-Vis-NIR光谱电化学研究寡聚噻吩/单壁碳纳米管(SWCNT)中间相的方法,以提供对纳米管与寡聚噻吩相互作用的了解。这些复合材料用作电极材料时,会根据电化学充电时形成的顺磁性和反磁性状态进行原位跟踪。低聚物链长的变化以及低聚物上取代基的类型,位置和数目的变化用于理解在电化学反应中对材料中带电态形成的结构影响。对于β,β'-二己基己基噻吩(β,β'-DHST)-SWCNT,复合物中的增大电流和降低的自由基阳离子浓度可以通过形成π-二聚体来解释。通过与SWCNT的相互作用,发生了低聚噻吩的π-二聚化和多个π-堆叠结构的形成。对于α,ω-二氰基-β,β′-二丁基四噻吩(DCNDBQT)-SWCNT,形成低聚物的新的顺磁性结构作为中间体,该中间体经历后续反应。使用不同的取代的低聚噻吩,可以从低聚物的结构上理解它们与纳米管的相互作用。

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