Abstract
Carbon-supported NiMo catalysts (NiMo/C) were synthesized and investigated for the electrooxidation of hydrazine. Their morphology and composition were determined with physicochemical characterizations (TEM-EDS, XPS and XRD) and further bridged to their electrocatalytic activity. The electrochemical performances measured in rotating disk electrode experiments reached 7.68±0.96 kAgmetal−1 for hydrazine electrooxidation at E=0.4V vs. RHE for the carbon-supported NiMo (9:1)/C. This value is amongst the highest reported in the literature. The large activity of the carbon-supported NiMo (9:1)/C catalyst was ascribed to the effect of a low but non-negligible (<15 at. %) molybdenum content, as molybdenum atoms stabilize the hydrazine N-N bond, thereby preventing the chemical decomposition of hydrazine into ammonia, and improving the catalyst selectivity towards the complete (and desired) hydrazine oxidation into N2 gas.
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