2019
DOI: 10.1007/978-3-319-92067-2_3-1
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Electrochemical Polymerization

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Cited by 12 publications
(11 citation statements)
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“…The anodic wave at 1.1 V in the very first anodic scan (SI Figure S3a) coincides with the initial increase in absorbance showing a predominant band with a maximum at 420 nm, which indicates the start of the formation of PANI related to the presence of aniline radicals and dimers. 31 During the cathodic scan, this peak at 420 nm remained almost constant, whereas there is one at 700 nm that increased up to an applied potential of 200 mV and then gradually decreased displaying a maximum in absorbance.…”
Section: Analytical Chemistrymentioning
confidence: 96%
“…The anodic wave at 1.1 V in the very first anodic scan (SI Figure S3a) coincides with the initial increase in absorbance showing a predominant band with a maximum at 420 nm, which indicates the start of the formation of PANI related to the presence of aniline radicals and dimers. 31 During the cathodic scan, this peak at 420 nm remained almost constant, whereas there is one at 700 nm that increased up to an applied potential of 200 mV and then gradually decreased displaying a maximum in absorbance.…”
Section: Analytical Chemistrymentioning
confidence: 96%
“…112,113 This form of polymerisation is initiated by the oxidation (voltage- or current-induced) of a specific monomer in an electrochemical cell, facilitating polymer growth. 114 Electropolymerisation enables precise control over film thickness and shows good compatibility with aqueous media. 115…”
Section: Mechanisms Of Molecularly Imprinted Polymersmentioning
confidence: 99%
“…The pair O 3 R 3 (0.77 V, 0.56 V) was due to oxidation of emeraldine base state to the oxidized pernigraniline state, and vice versa. The O 2 R 2 (0.54 V, 0.45 V) peaks were attributed to either presence of ortho-coupled polymers [86] or the oxidation of segments of PANI chain to benzoquinone and hydroquinone species, whose potentials are very close to one another and tend to disappear after several scans [87,88]. The oxidation peak at O 3 exhibited a broad oxidation wave compared to that of O 1 , which could signify that charge transfer was more difficult for the second oxidation step than the first [85].…”
Section: Electroanalysis Of Pani and Composite Materialsmentioning
confidence: 99%
“…The increase of the second oxidation peak (i.e., peak b of Figure 7A), which corresponds to the doping process of counterions as they are inserted into the film to neutralize positive charge by H + protonation during PANI oxidation, indicates that the doping behavior of these supporting electrolytes is controlled consistently by the surface electron transfer process [88]. Using the anodic peaks (b) from Figure 7 for PANI-GCE (Figure 7A), AgNP-PANI-GCE (Figure 7B), ZnONP-PANI-GCE (Figure 7C), and Ag-ZnONP-PANI-GCE (Figure 7D), the slopes for peak current vs. square root of scan rate (Figure 7F) were used to obtain the diffusion coefficients of the counter ion (Cl − ) across the modified electrodes.…”
Section: Electroanalysis Of Pani and Composite Materialsmentioning
confidence: 99%