4.6 Article

Solid state synthesis of a RuNiO3 perovskite nanomaterial as an electro-catalyst for direct alcohol (ethanol, methanol and ethylene glycol) fuel cell applications

Journal

NEW JOURNAL OF CHEMISTRY
Volume 47, Issue 8, Pages 3870-3879

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3nj00032j

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In this study, a solid-state synthesis of ruthenium nickel oxide (RuNiO3) modified nickel foam (RNO/NF) is reported as a cost-effective perovskite based electrocatalyst for direct alcohol fuel cells (DAFCs). The RNO/NF catalyst electrode shows high current density and good stability at different concentrations and levels of ethanol, methanol, and ethylene glycol. Therefore, the RNO/NF electrode is considered as an ideal electrocatalyst for low-cost DAFC applications.
Direct alcohol fuel cells (DAFCs) are considered as reliable, clean and sustainable energy conversion technologies. However, most of them are reported using noble metal based electro-catalysts such as platinum (Pt), palladium (Pd) etc. which suffer from low cycling stability due to intermediate CO poisoning during the alcohol oxidation reaction (AOR). Herein, we report the solid-state synthesis of ruthenium nickel oxide (RuNiO3) modified nickel foam (RNO/NF) as a cost-effective perovskite based electrocatalyst for DAFC applications. The RNO/NF catalyst electrode exhibits a high current density of similar to 711.15 mA cm(-2) (0.4 M; ethanol), similar to 475.05 mA cm(-2) (0.3 M; methanol) and similar to 579.1 mA cm(-2) (0.3 M; ethylene glycol) at a potential of 0.8 V (vs. Hg|HgO). This superior performance of the RNO/NF electrode is ascribed to the presence of the Ni2+/3+ redox couple at the tetrahedral sites favouring the AOR with the oxidation of CO into CO2. The electrochemical active surface area of RNO/NF is estimated to be similar to 175% greater than that of the bare NF which proves the activity of the electrode. The RNO/NF electrode displays high stability with a capacity retention of 88.79% (ethanol), 82.283% (methanol) and 95.54% (ethylene glycol) for 10 000 s which is higher than that of the commercial platinum-on-carbon (Pt/C) electro-catalyst, proving to be an ideal electrocatalyst for low-cost DAFC applications.

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