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MoO3/C-supported Pd nanoparticles as an efficient bifunctional electrocatalyst for ethanol oxidation and oxygen reduction reactions
metal oxide electronic interactions in composite electrocatalysts have a considerable impact on their catalytic capability. In this study, we successfully synthesized an electrocatalytic material composed of MoO 3 /C species-supported Pd nanoparticles (Pd-MoO 3 /C) using a convenient hydrothermal me...
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Published in: | Rare metals 2023-05, Vol.42 (5), p.1516-1525 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | metal oxide electronic interactions in composite electrocatalysts have a considerable impact on their catalytic capability. In this study, we successfully synthesized an electrocatalytic material composed of MoO
3
/C species-supported Pd nanoparticles (Pd-MoO
3
/C) using a convenient hydrothermal method, which exhibited excellent catalytic activities for both ethanol oxidation and oxygen reduction in KOH media. The specific activity of Pd-MoO
3
/C toward ethanol oxidation with MoO
3
loading (40 wt%) was ~ 2.6 times greater than that for the commercial Pd/C (10 wt%) with the same Pd content. In particular, the activity could effectively hold up to ~ 60% of its maximum activity after 500-cycle tests, demonstrating improved cyclical stability. Notably, the fast electron transfer kinetics toward oxygen reduction for Pd-MoO
3
/C (40%) were also comparable to those of commercial Pt/C (20 wt%) catalysts. These superior electrochemical features are primarily derived from the stronger electronic coupling between Pd and MoO
3
through charge transfer, which can supply more active centers and improve the anti-poisoning ability. Meanwhile, the MoO
3
species in the Pd-MoO
3
/C composite may provide additional benefits in terms of electrical conductivity and dispersion.
Graphical Abstract |
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ISSN: | 1001-0521 1867-7185 |
DOI: | 10.1007/s12598-022-02211-x |