1992
DOI: 10.1016/0379-6779(92)90233-9
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Infrared investigations of pristine, doped and partially doped polypyrrole

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Cited by 97 publications
(43 citation statements)
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References 18 publications
(11 reference statements)
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“…FTIR spectra of PPy with different morphologies showed no obvious difference. The characteristic bands of the PPy samples were consistent with those in [127]: the pyrrole ring fundamental vibration at 1544 and 1457 cm À1 , the = C -H in-plane vibration at 1303 and 1040 cm À1 , and the C -N stretching vibration at 1175 cm À1 . The results indicate that the molecular structure of the PPy chain is identical to that of PPy synthesized by a common method.…”
Section: Nanostructuressupporting
confidence: 56%
“…FTIR spectra of PPy with different morphologies showed no obvious difference. The characteristic bands of the PPy samples were consistent with those in [127]: the pyrrole ring fundamental vibration at 1544 and 1457 cm À1 , the = C -H in-plane vibration at 1303 and 1040 cm À1 , and the C -N stretching vibration at 1175 cm À1 . The results indicate that the molecular structure of the PPy chain is identical to that of PPy synthesized by a common method.…”
Section: Nanostructuressupporting
confidence: 56%
“…The peaks at 1634, 1550, and 1470 cm -1 indicate the presence of pyrrole, whereas the peaks at 1385 and 1308 cm -1 arise from the N-C vibration and the deformation of pyrrole. The peaks in the 750~930 cm -1 range and at 1043 cm -1 originate from C-H absorption [23,24]. Further, the FTIR peak at 690 cm -1 is attributed to C-S stretching, as reported previously in the literature [23].…”
Section: Resultsmentioning
confidence: 72%
“…The peaks in the 750~930 cm -1 range and at 1043 cm -1 originate from C-H absorption [23,24]. Further, the FTIR peak at 690 cm -1 is attributed to C-S stretching, as reported previously in the literature [23]. The characteristics of polypyrrole are independent of the synthesis method.…”
Section: Resultsmentioning
confidence: 75%
“…1b) shifted to lower wavenumbers (1170 cm À1 , Fig. 1c) possibly due to the formation of H-bond between the lone electron pair of N atom in pyrrole and C-O group of CGO [20]. It can be found from Fig.…”
Section: Resultsmentioning
confidence: 86%