Vacuum thermal evaporation of polyaniline doped with camphor sulfonic acid

被引:6
|
作者
Boyne, Devon [1 ]
Menegazzo, Nicola [1 ]
Pupillo, Rachel C. [1 ]
Rosenthal, Joel [1 ]
Booksh, Karl S. [1 ]
机构
[1] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
来源
基金
美国国家科学基金会;
关键词
PLASMA-POLYMERIZED ANILINE; ELECTRONIC-PROPERTIES; SENSITIVE LAYER; EMERALDINE BASE; FILMS; CONDUCTIVITY; PERFORMANCE; DEPOSITION; XPS;
D O I
10.1116/1.4916990
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Intrinsically conducting polymers belong to a class of organic polymers with intriguing electronic and physical properties specifically for electro-optical applications. Significant interest into doped polyaniline (PAni) can be attributed to its high conductivity and environmental stability. Poor dissolution in most solvents has thus far hindered the successful integration of PAni into commercial applications, which in turn, has led to the investigations of various deposition and acidic doping methods. Physical vapor deposition methods, including D.C. magnetron sputtering and vacuum thermal evaporation, have shown exceptional control over physical film properties (thickness and morphology). However, resulting films are less conductive than films deposited by conventional methods (i.e., spin and drop casting) due to interruption of the hyperconjugation of polymer chains. Specifically, vacuum thermal evaporation requires a postdoping process, which results in incorporation of impurities and oxidation of surface moieties. In this contribution, thermally evaporated films, sequentially doped by vacuum evaporation of an organic acid (camphorsulfonic acid, CSA) is explored. Spectroscopic evidence confirms the successful doping of PAni with CSA while physical characterization (atomic force microscopy) suggests films retain good morphology and are not damaged by the doping process. The procedure presented herein also combines other postpreparation methods in an attempt to improve conductivity and/or substrate adhesion. (C) 2015 American Vacuum Society.
引用
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页数:6
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