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Electrocatalytic performance of Pt-Ni nanoparticles supported on an activated graphite electrode for ethanol and 2-propanol oxidation

Platinum (Pt) and platinum-nickel (Pt-Ni) electrocatalysts were prepared on activated graphite electrodes by an electrochemical deposition process. The electrocatalysts were analyzed by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD). The el...

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Bibliographic Details
Published in:RSC advances 2020-10, Vol.1 (61), p.36941-36948
Main Authors: Chelaghmia, M. L, Nacef, M, Fisli, H, Affoune, A. M, Pontié, M, Makhlouf, A, Derabla, T, Khelifi, O, Aissat, F
Format: Article
Language:English
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Summary:Platinum (Pt) and platinum-nickel (Pt-Ni) electrocatalysts were prepared on activated graphite electrodes by an electrochemical deposition process. The electrocatalysts were analyzed by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD). The electrocatalytic activity of the prepared electrocatalysts, their stability, and the effect of temperature toward ethanol and 2-propanol oxidation were evaluated by cyclic voltammetry (CV), chronoamperometry and electrochemical impedance spectroscopy (EIS). The results showed that the Pt-Ni/C exhibited higher catalytic activity, better stability and better tolerance to poisoning by ethanol and 2-propanol oxidation intermediate species compared to Pt/C, which was interpreted as synergistic and electronic effects between Pt and Ni. A study of the temperature dependence of ethanol and 2-propanol oxidation in the temperature range of 298-318 K, shows that the apparent activation energy for ethanol and 2-propanol oxidation on Pt-Ni/C was lower than on Pt/C. The results also revealed that the electro-oxidation of ethanol and 2-propanol on Pt/C were improved by raising the temperature and Ni modification. Platinum (Pt) and platinum-nickel (Pt-Ni) electrocatalysts were prepared on activated graphite electrodes by an electrochemical deposition process.
ISSN:2046-2069
2046-2069
DOI:10.1039/d0ra07331h