1995
DOI: 10.1016/0928-4931(95)00063-1
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Influence of pH on the electroactivity of polycarbazole

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Cited by 20 publications
(7 citation statements)
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“…In CPHC, which contains carbazole units, an absorption peak is visible at 310 nm and a shoulder at 335 nm is observed, which are typically due to the π−π* transition in polycarbazole. , In the case of spectroelectrochemical observation done under monomer free conditions, we observed that with increasing voltage the peak at 310 nm bleaches and the film starts to turn green giving rise to two new peaks at 418 and 699 nm during the stepwise oxidation of the cross-linked polymer film. The peaks at 310, 418, and 699 nm have been understood to arise from the valence band to conduction band, polaron bonding level to π* conduction band, and bonding level to antibonding state of polaron transitions, respectively. , …”
Section: Resultsmentioning
confidence: 98%
“…In CPHC, which contains carbazole units, an absorption peak is visible at 310 nm and a shoulder at 335 nm is observed, which are typically due to the π−π* transition in polycarbazole. , In the case of spectroelectrochemical observation done under monomer free conditions, we observed that with increasing voltage the peak at 310 nm bleaches and the film starts to turn green giving rise to two new peaks at 418 and 699 nm during the stepwise oxidation of the cross-linked polymer film. The peaks at 310, 418, and 699 nm have been understood to arise from the valence band to conduction band, polaron bonding level to π* conduction band, and bonding level to antibonding state of polaron transitions, respectively. , …”
Section: Resultsmentioning
confidence: 98%
“…Because of the absorption of the low energy charged state, the absorption in the visible range due to the π−π* transition bleaches. , In CP−CBZ, at 1.0 V, the peak due to the π−π* transition at 310 nm bleaches and shows a chromic shift from colorless to green, giving rise to two new peaks at 424 and 605 nm (Figure b). The peaks at 424 and 605 nm have been understood to arise from the polaron bonding level to the π* conduction band and bonding level to antibonding state of polaron transitions, respectively 7a, …”
Section: Resultsmentioning
confidence: 99%
“…[5] Above all, a good environmental stability and photoconductivity of PCz with and without substitution have made it a subject of exploration for various applications especially in electroluminescence, [6] light-emitting diodes, [7] electrochromic displays, [8] organic transistors, [9] rechargeable batteries, [10] and so forth. However, a relatively low electrical conductivity (>10 À9 S Á cm À1 in the undoped state and >10 À3 S Á cm À1 in the doped state [11] ) may inhibit its applications. Synthesis of PCz (substituted and unsubstituted) extensively studied by electrochemical polymerization method.…”
Section: Introductionmentioning
confidence: 99%