1986
DOI: 10.1016/0379-6779(86)90130-x
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Auger and infrared study of polypyrrole films: Evidence of chemical changes during electrochemical deposition and aging in air

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Cited by 38 publications
(4 citation statements)
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“…Step-2 corresponds to the oxidative degradation reactions of polymer backbone producing segments of various conjugation lengths (Mohammad et al 1993) involve substitution, addition and chain scission. The presence of resonances due to broad H-bonded -OH and C=O groups in the FTIR spectra of degraded polythiophene (BF4) (Mohammad 1988) are further supported by the work of Hahn et al (1986) Oxidative degradation of most polymers proceeds via chemical reactions of peroxy radicals. Yang and Chien (1985) reported autooxidation of polyacetylene, a typical unsaturated polymer with a long conjugated system, and a value of 9 x 10 ~ mol(g)s-1 for the rate constant at 70°C and 760 torr O z.…”
Section: It(k)mentioning
confidence: 91%
“…Step-2 corresponds to the oxidative degradation reactions of polymer backbone producing segments of various conjugation lengths (Mohammad et al 1993) involve substitution, addition and chain scission. The presence of resonances due to broad H-bonded -OH and C=O groups in the FTIR spectra of degraded polythiophene (BF4) (Mohammad 1988) are further supported by the work of Hahn et al (1986) Oxidative degradation of most polymers proceeds via chemical reactions of peroxy radicals. Yang and Chien (1985) reported autooxidation of polyacetylene, a typical unsaturated polymer with a long conjugated system, and a value of 9 x 10 ~ mol(g)s-1 for the rate constant at 70°C and 760 torr O z.…”
Section: It(k)mentioning
confidence: 91%
“…In most studies, electrochemical (11)(12)(13)(14) and spectroscopic (7,(15)(16)(17)(18)(19)(20) properties, conductivity data (4,20,21), and chemical degradations (22) were reported.…”
mentioning
confidence: 99%
“…The series of sharp peaks between 1600 and 600 cm -1 is similar to those observed in the spectra of unsubstituted PPyr. [22][23][24] The peaks at around 1500 cm -1 can be assigned to CdC stretching modes of the pyrrole and benzene rings and C-N stretching vibration modes. The relative strong absorption above 2500 cm -1 indicates the presence of pyrrole CH (3100 cm -1 ), aliphatic CH (∼2900 cm -1 ), and probably hydrogenbridged pyrroles, carboxy groups, and water.…”
Section: Resultsmentioning
confidence: 99%