Ni and Co-based bifunctional electrocatalysts supported on TiO2@C for oxygen evolution and reduction reactions
•Ni and Co-based electrocatalysts supported on bifunctional TiO2@C.•Electrocatalytic studies on OER and ORR processes.•Biomass influences the properties of hybrid TiO2@C supports and electroactivity.•The number of electrons involved in OER and ORR was determined.•Co-based catalysts are alternative c...
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Published in | Electrochimica acta Vol. 506; p. 145030 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.12.2024
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Subjects | |
Online Access | Get full text |
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Summary: | •Ni and Co-based electrocatalysts supported on bifunctional TiO2@C.•Electrocatalytic studies on OER and ORR processes.•Biomass influences the properties of hybrid TiO2@C supports and electroactivity.•The number of electrons involved in OER and ORR was determined.•Co-based catalysts are alternative catalysts in fuel cells-related reactions.
In the search for affordable, ecofriendly, and sustainable catalysts for energy-related processes, series of Ni and Co-based bifunctional hybrid electrocatalysts supported on TiO2@C were prepared and studied in the oxygen evolution (OER) and oxygen reduction reactions (ORR). The hybrid TiO2@C supports were prepared using three biomass precursors: furfural, chitosan and saccharose. The nature and dispersion of the metallic phases on those supports was evaluated as a function of the biomass-derived precursors. The prepared materials showed electrocatalytic activity towards ORR and OER reaction, being more active for the latter. Despite a lower performance than Pt/C benchmark, these materials are clearly at much lower costs. The long-term stability and performance of the catalysts were also performed. The number of electrons involved in both processes was determined and a mechanism is proposed for the understanding of the mechanism of reactions using the present materials. It can be concluded that the Ni and mainly Co-based electrocatalysts show a remarkable potential for use as alternative catalysts in fuel cells-related reactions.
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ISSN: | 0013-4686 |
DOI: | 10.1016/j.electacta.2024.145030 |