Structured oligo(aniline) nanofilms via ionic self-assembly

被引:41
作者
Dane, Thomas G. [1 ]
Cresswell, Philip T. [1 ]
Bikondoa, Oier [2 ,3 ]
Newby, Gemma E. [2 ,3 ]
Arnold, Thomas [4 ]
Faul, Charl F. J. [1 ]
Briscoe, Wuge H. [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[2] ESRF, F-38043 Grenoble, France
[3] Univ Warwick, XMaS, Coventry CV4 7AL, W Midlands, England
[4] Diamond Light Source Ltd, Harwell OX11 0DE, Berks, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
POLYANILINE EMERALDINE SALT; DOPED POLYANILINE; CHARGE-TRANSPORT; THIN-FILMS; ACID; POLYMER; CRYSTALLINE; CONFORMATIONS; CONDUCTIVITY; CELLS;
D O I
10.1039/c2sm06492h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Conducting polymers have shown great potential for application in electronic devices. A major challenge in such applications is to control the supramolecular structures these materials form to optimise the functionality. In this work we probe the structure of oligo(aniline) thin films (of sub-mm thickness) drop cast on a silicon substrate using synchrotron surface diffraction. Self-assembly was induced through doping with an acid surfactant, bis(ethyl hexyl) phosphate (BEHP), resulting in the formation of well-ordered lamellae with the d-spacing ranging from 2.15 nm to 2.35 nm. The exact structural characteristics depended both on the oligomer chain length and film thickness, as well as the doping ratio. Complementary UV/Vis spectroscopy measurements confirm that such thin films retain their bulk electronic properties. Our results point to a simple and effective ionic self-assembly approach to prepare thin films with well-defined structures by tailoring parameters such as the oligomer molecular architecture, the nanofilm composition and the interfacial roughness.
引用
收藏
页码:2824 / 2832
页数:9
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