2017
DOI: 10.1134/s0022476617060178
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Functional composition and electrochemical characteristics of oxidized nanosized carbon

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Cited by 7 publications
(4 citation statements)
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“…It was reported previously that oxygen functional groups enhance the electrochemical capacitance due to an increased number of functional groups on the surface facilitating a higher charge transfer. These results are consistent with the previous studies. …”
Section: Resultssupporting
confidence: 94%
“…It was reported previously that oxygen functional groups enhance the electrochemical capacitance due to an increased number of functional groups on the surface facilitating a higher charge transfer. These results are consistent with the previous studies. …”
Section: Resultssupporting
confidence: 94%
“…Figure 4 presents the XPS spectra of carbon, oxygen, and iron in the samples before and after hydrogen plasma treatment. The deconvolution of C 1s spectra ( Figure 4 a) indicates the presence of graphite-like sp 2 carbon (component at 284.5 eV), disordered regions in the hexagonal carbon network (C dis component at 285.1 eV) [ 48 ], carbon in oxygen-containing groups C–O, C=O (286.6 eV), and COOH (288.5 eV), and π plasmon at 290.5 eV [ 49 , 50 , 51 , 52 ]. The plasma-treated sample shows the higher intensity of the peaks from C dis and the oxygen-containing groups, indicative of a larger number of defect states on the CNT surface [ 53 ].…”
Section: Resultsmentioning
confidence: 99%
“…The more extended plateau capacities of activated samples are supposed to appear due to the presence of micropores developed during the hydrothermal treatments. CV curves measured for the samples at a scan rate of 0.5 mV s −1 are presented in Figure 8a-c. A sharp peak at 0-0.2 V in the cathodic scans is related to the insertion of Na + ions between the carbon layers, while the broad peak at 0.3 V in the reverse anodic scans corresponds to the extraction process [51]. The broad peaks at 0.6-0.8 V in the cathodic scans observed in the CV curves of all samples.…”
Section: Electrochemical Propertiesmentioning
confidence: 82%
“…These reversible Faradaic processes occur with the proton-coupled electron transfer reaction of nitrogen-or oxygen-containing moieties due to the intercalation and absorption of H + into material depth. Only carbonyl oxygen (C=O), pyridinic nitrogen (>N), and pyrrolic nitrogen (>N-H) are electrochemically active in acidic electrolytes [5,9,11,51]. At a scan rate of 5 mV s −1 , the redox peaks from the reversible reduction/oxidation of carbonyl oxygen appear between 0.2 and 0.4 V [12], while the Faradaic process involving the pyridinic nitrogen gave a redox peak in the cathodic scans at a higher potential of~0.7 V [52].…”
Section: Electrochemical Propertiesmentioning
confidence: 99%