2014
DOI: 10.1016/j.electacta.2014.03.129
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Based on a new support for synthesis of highly efficient palladium/hydroxyapatite catalyst for ethanol electrooxidation

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Cited by 41 publications
(23 citation statements)
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“…XRD analysis showed larger crystal formation due to the palladium metal deposited upon the HAP surface, indicated by sharper (narrower) XRD peaks, when compared to the JCPDS pattern presented in Figure 4B,C. Also, patterns reveal face-centred-cubic crystalline palladium metal, with all the peaks shifted slightly, corresponding to a lower binding energy of the material (shown in Figure 4D) [42,43]. This scenario is also accompanied by an increased intensity of the peaks, which is characteristic behaviour for material with changed centre of symmetry of the material.…”
Section: Palladium Doped Hapmentioning
confidence: 99%
“…XRD analysis showed larger crystal formation due to the palladium metal deposited upon the HAP surface, indicated by sharper (narrower) XRD peaks, when compared to the JCPDS pattern presented in Figure 4B,C. Also, patterns reveal face-centred-cubic crystalline palladium metal, with all the peaks shifted slightly, corresponding to a lower binding energy of the material (shown in Figure 4D) [42,43]. This scenario is also accompanied by an increased intensity of the peaks, which is characteristic behaviour for material with changed centre of symmetry of the material.…”
Section: Palladium Doped Hapmentioning
confidence: 99%
“…According to the Ostwald ripening mechanism, surface atoms could detach from the smaller nanoparticles, followed by reattachment to generate the more stable surfaces of the larger nanoparticles [45]. Therefore, the better electro-catalytic activities of Pd/CB can be ascribed to the narrow distribution of Pd NPs, which suppresses the Ostwald ripening and thus improves the stability of the catalyst [13].…”
Section: Resultsmentioning
confidence: 99%
“…It can be observed from CV curves that all onset potentials of the ethanol electro‐oxidation begin at ∼ –0.70 V, and the peak potentials of ethanol oxidation are in the range of –0.17 to –0.22 V for positive‐going potential scan. In the forward‐going scan, the oxidation peak is corresponding to the oxidation of freshly chemisorbed species coming from ethanol adsorption . The reverse scan peak is primarily associated with removal of carbonaceous species not completely oxidized in the forward‐going scan than the oxidation of freshly chemisorbed species , .…”
Section: Resultsmentioning
confidence: 99%