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In situ addition of graphitic carbon into a NiCo(2)O(4)/CoO composite: enhanced catalysis toward the oxygen evolution reaction
We present a rapid, environmentally benign one-pot synthesis technique for the production of a NiCo(2)O(4)/CoO and graphite composite that demonstrates efficient electrocatalysis towards the Oxygen Evolution Reaction (OER), in 1.0 M KOH. The NiCo(2)O(4)/CoO/graphitic carbon composite that displayed...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069886/ https://www.ncbi.nlm.nih.gov/pubmed/35528657 http://dx.doi.org/10.1039/c9ra05195c |
Sumario: | We present a rapid, environmentally benign one-pot synthesis technique for the production of a NiCo(2)O(4)/CoO and graphite composite that demonstrates efficient electrocatalysis towards the Oxygen Evolution Reaction (OER), in 1.0 M KOH. The NiCo(2)O(4)/CoO/graphitic carbon composite that displayed optimal OER catalysis was synthesized by nitrate decomposition in the presence of citric acid (synthesized glycine and sucrose variants displayed inferior electro kinetics towards the OER). Screen-printed electrodes modified with ca. 530 μg cm(−2) of the citric acid NiCo(2)O(4)/CoO/graphite variant displayed remarkable OER catalysis with an overpotential (η) of +323 mV (vs. RHE) (recorded at 10 mA cm(−2)), which is superior to that of IrO(2) (340 mV) and RuO(2) (350 mV). The composite also exhibited a large achievable current density of 77 mA cm(−2) (at +1.5 V (vs. RHE)), a high O(2) turnover frequency of 1.53 × 10(−2) s(−1) and good stability over the course of 500 repeat cycles. Clearly, the NiCo(2)O(4)/CoO composite has the potential to replace precious metal based catalysts as the anodic material within electrolysers, thereby providing a reduction in the associated costs of hydrogen production via water splitting. |
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