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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Published in: | RSC advances Vol. 1; no. 61; pp. 36941 - 36948 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Royal Society of Chemistry
07-10-2020
The Royal Society of Chemistry |
Subjects: | |
Online Access: | Get full text |
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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. |
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Bibliography: | 10.1039/d0ra07331h Electronic supplementary information (ESI) available. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d0ra07331h |