2018
DOI: 10.1016/j.colsurfa.2018.08.007
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Facile preparation and electrochemical characterization of self-assembled core-shell diamond-polypyrrole nanocomposites

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Cited by 15 publications
(6 citation statements)
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“…41 The spectrum of polypyrrole shows characteristic C-H in-plane and C-N stretching vibrations at 1376 cm À1 and 1213 cm À1 , respectively. 42 The peak observed at 3399 cm À1 is due the N-H functional group. The characteristic O-H stretching peak of chitosan is obtained at around 3439 cm À1 , and the peak at 2905 cm À1 is ascribed to axial stretching of the C-H bond, while the peak at 1663 cm À1 is ascribed to the amide group.…”
Section: Ftir Analysismentioning
confidence: 99%
“…41 The spectrum of polypyrrole shows characteristic C-H in-plane and C-N stretching vibrations at 1376 cm À1 and 1213 cm À1 , respectively. 42 The peak observed at 3399 cm À1 is due the N-H functional group. The characteristic O-H stretching peak of chitosan is obtained at around 3439 cm À1 , and the peak at 2905 cm À1 is ascribed to axial stretching of the C-H bond, while the peak at 1663 cm À1 is ascribed to the amide group.…”
Section: Ftir Analysismentioning
confidence: 99%
“…The two peaks at 1050 and 1078 cm − 1 belong to the in-plane deformation vibration of C-H, and the other two peaks at 1384 and 1330 cm − 1 belong to the stretching vibration of the ring. The ring deformation vibration of PPy at 927 cm − 1 , and the stretching vibration peak of C-N at 1434 cm − 1 [ 47 ].…”
Section: Resultsmentioning
confidence: 99%
“…The C=C stretching peak at 1598 cm − 1 is considered to be an overlap of the two oxidized structures, which should be attributed to the conversion of C=C from the neutral state component to the oxidized state component after the combination of PPy and CNC. The peak at 1381 and 1316 cm − 1 can be assigned to antisymmetric C-H in-plane bending, and the deformation vibration peak in C-H plane at 1243 cm − 1 [ 45 , 47 ]. The ring deformation vibration of PPy at 932 cm − 1 , and the stretching vibration peak of C-N at 1474 cm − 1 .…”
Section: Resultsmentioning
confidence: 99%
“…Following polymerization of pyrrole on the surface-modified MWCNTs, prominent characteristic Raman bands emerged at 1421, 1164, 1051, 987, and 925 cm −1 , which were identical to those of pure polypyrrole. The first four bands are attributed to antisymmetrical C-N stretching, N-H in-plane deformation, N-H ring stretching, and symmetrical C-H in-plane bending of polypyrrole, respectively [ 18 , 19 , 20 ]. The peaks at 925 and 987 cm −1 are associated with dications (bipolarons) and radical cations (polarons), respectively [ 21 ].…”
Section: Resultsmentioning
confidence: 99%