DocumentCode
3488913
Title
Investigation of characteristics of PEDOT obtained under controlled polymerization conditions
Author
Yang Yaiie ; Yadong, Jiang ; Jianhua, Xu ; Yun, Ye ; Hongjuan, Zeng
Author_Institution
Sch. of Opto-Electron. Inf., Univ. of Electron. Sci. & Technol. of China, Chengdu, China
fYear
2005
fDate
11-14 Sept. 2005
Firstpage
509
Lastpage
511
Abstract
An organic chemical accelerant was added into the mixed solution during the in situ polymerization process of conductive polymer 3,4-polyethylenedioxythiophene (PEDOT). The conductivity change of PEDOT films was measured by four-probe technique. Morphology images of films were observed by atomic force microscopy (AFM). The experimental results showed that higher conductivity PEDOT films (about 120S/cm) was obtained after molar ratio of 0.05-0.15% accelerant was added into solution and high quality PEDOT films was obtained. We suggested that the accelerant changed polymerization speed of PEDOT and longer conjugated chain was formed and PEDOT films had better orientation. Furthermore, the decomposition temperature of PEDOT was influenced by accelerant. About 40 °C change of decomposition temperature was observed by thermogravimetry (TG). The explanation of advantage of lower decomposition temperature of PEDOT was also included in this paper.
Keywords
atomic force microscopy; conducting polymers; decomposition; electrical conductivity; organic semiconductors; polymer films; polymerisation; semiconductor thin films; thermal analysis; 3,4-polyethylenedioxythiophene film; PEDOT films; atomic force microscopy; conductive polymer; conductivity; decomposition temperature; four-probe technique; organic chemical accelerant; polymerization process; thermogravimetry; Atomic force microscopy; Capacitors; Conductive films; Conductivity measurement; Electrodes; Morphology; Polymer films; Stability; Substrates; Temperature; Accelerant; Four-probe; PEDOT; TG;
fLanguage
English
Publisher
ieee
Conference_Titel
Electrets, 2005. ISE-12. 2005 12th International Symposium on
Print_ISBN
0-7803-9116-0
Type
conf
DOI
10.1109/ISE.2005.1612437
Filename
1612437
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