Silver nanoparticle-decorated NiFeO/CuWO heterostructure electrocatalyst for oxygen evolution reactions
In this work, Ag nanoparticles decorated with NiFe 2 O 4 /CuWO 4 heterostructure were synthesized using the step-wise precipitation method. The influence of varying Ag loading on the NiFe 2 O 4 /CuWO 4 heterostructure and its electrochemical OER performance was extensively studied in 1 M KOH electro...
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Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2024-05, Vol.26 (2), p.14883-14897 |
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Zusammenfassung: | In this work, Ag nanoparticles decorated with NiFe
2
O
4
/CuWO
4
heterostructure were synthesized using the step-wise precipitation method. The influence of varying Ag loading on the NiFe
2
O
4
/CuWO
4
heterostructure and its electrochemical OER performance was extensively studied in 1 M KOH electrolyte. The obtained LSV profile was analyzed to determine the overpotential, Tafel slope, and onset potential. The heterostructure with an optimal Ag loading of 5 wt% required the least overpotential (1.60 V
vs.
RHE) for generating a current density of 10 mA cm
−2
with a lower Tafel slope of 44.5 mV dec
−1
, indicating its faster OER kinetics. Furthermore, the composite remained stable over a period of 24 hours with a minimum rise in the overpotential after the stability test. The enhanced OER performance of the as-prepared catalyst can be attributed to the presence of multiple metallic elements in the Ag-loaded NiFe
2
O
4
/CuWO
4
composite, which created a diverse array of oxygen-vacant sites with varying reactivity, enhancing the charge-transfer kinetics; and thus contributing to the overall efficiency of OER. Therefore, optimizing the Ag concentration and engineering a microstructure represents an encouraging strategy for developing cost-effective catalysts for next-generation energy-conversion applications.
Ag nanoparticles decorated onto the NiFe
2
O
4
/CuWO
4
heterostructure, with induced oxygen vacancies, improve the electrocatalytic properties of the oxygen evolution reaction. |
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ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/d4cp00473f |