Enhancing hydroxyl adsorption for methanol oxidation reaction (MOR) of Pt-loaded on carbon support 3D network Magnéli phase V4O7 composite
[Display omitted] •Carbon composited Magnéli compound V4O7 was prepared.•The different Pt loaded 3D network Pt/V4O7-C electrocatalysts were synthesized.•The Pt/V4O7-C could enhance the performance of catalyze methanol oxidation reaction.•The designed experiments proved the mechanism of enhance MOR p...
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Veröffentlicht in: | Journal of electroanalytical chemistry (Lausanne, Switzerland) Switzerland), 2023-03, Vol.932, p.117270, Article 117270 |
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Sprache: | eng |
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•Carbon composited Magnéli compound V4O7 was prepared.•The different Pt loaded 3D network Pt/V4O7-C electrocatalysts were synthesized.•The Pt/V4O7-C could enhance the performance of catalyze methanol oxidation reaction.•The designed experiments proved the mechanism of enhance MOR performance.
Carbon-composited 3D network V-O Magnéli compounds V4O7-C were prepared through the colloid-impregnation-carbonthermic method. After Pt nanoparticles loading, electrocatalysts for the methanol oxidation reaction (MOR) with different Pt contents Pt/V4O7-C were obtained. The specific activity of 15% Pt/V4O7-C was 3847 mA/g, which was 2.4 times that of commercial Pt/C. After 3000s durability tests the 15% Pt/V4O7-C had a stability similar to the Pt/C (38% activity retention), and the 20% Pt/V4O7-C showed better durability (45% activity retention) than commercial materials. XPS results implied that a strong metal-support interaction occurred between the Pt and V4O7-C, which may enhance the MOR performance. Moreover, a designed CO stripping experiment proved that V4O7 could enhance the adsorption of OH− and the oxidation reaction of intermediates and restrain the adsorption of carbonyl species of MOR. The synergistic effect between Pt and V4O7-C was summarized. The interaction between Pt and Magnéli oxides may provide a new idea for the design of high performance catalytic materials for electrocatalytic oxidation in the view of the adsorption of the reaction species. |
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ISSN: | 1572-6657 1873-2569 |
DOI: | 10.1016/j.jelechem.2023.117270 |