UV-Vis and Raman spectroelectrochemistry of electrodeposited polypyrrole in hexafluorophosphate

A1 Originalartikel i en vetenskaplig tidskrift (referentgranskad)


Interna författare/redaktörer


Publikationens författare: Kepas A, Grzeszczuk M, Kvarnstrom C, Lindfors T, Ivaska A
Förläggare: POLISH CHEMICAL SOC
Publiceringsår: 2007
Tidskrift: Polish Journal of Chemistry
Tidskriftsakronym: POL J CHEM
Volym: 81
Nummer: 12
Artikelns första sida, sidnummer: 2207
Artikelns sista sida, sidnummer: 2214
Antal sidor: 8
ISSN: 0137-5083


Abstrakt

UV-Vis and Raman spectroscopy are very useful and powerful techniques to characterize the structure of conjugated polymers in various states. Spectroelectrochemical measurements were performed in a three-electrode cell containing polypyrrole (PPY) films as active layers in contact with NaPF6 aqueous electrolyte. UV-Vis spectroscopy was used to characterize the neutral (undoped) and oxidized (p-doped) states of polypyrrole upon electrochemical p-doping. Raman measurements were done with the excitation wavelengths of 5 14, 633 and 780 nm. It is shown how the vibrational modes of PPY were influenced by the applied laser wavelength. The neutral form was found to be strongly resonance enhanced with the 514 nm excitation wavelength and the corresponding Raman bands dominate the spectra. Spectra obtained using the 633 nm excitation wavelength displayed a strong contribution of the neutral form, but noticeable bands due to the radical cation and dication were also visible. The spectra recorded using the 780 nm excitation line are dominated by Raman bands of the radical cation and dication.


Nyckelord

conducting polymers, in situ spectroelectrochemistry, polypyrrole, sodium hexafluorophosphate, UV-Vis and Raman spectroscopy

Senast uppdaterad 2019-14-11 vid 02:42