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• W2572979815 startingPage "39" @default.
• W2572979815 abstract "Methanol, being a high energy density liquid fuel, with 12.5 wt% hydrogen content, is an attractive energy storage and energy transport media. Methanol assisted water electrolysis for hydrogen production has the potential to reduce the electric energy input by more than 50% compared to conventional electrolysis. However, high electro-catalytic activity and stable performance are key factors for sustainable hydrogen production by this route. In this paper, a number of Pt based catalysts with or without the addition of nano-sized SnO2 and CeO2 to reduce noble metal loading have been investigated for methanol assisted water electrolysis. A controlled spraying technique was used for catalyst deposition on the catalyst supports in a polymer electrolyte membrane-based zero-gap electrolysis cell. The performance has been investigated under different cell operating conditions of temperature, methanol concentration and current loading. The V–I curves extrapolated to zero current density showed that the cell approach the thermo-neutral voltage of 0.22 V for the methanol assisted water electrolysis compared with 1.48 V for conventional electrolysis. Electrochemical impedance spectroscopy was used to elucidate information on the methanol oxidation reaction. Although the PtRu/C catalyst showed the best performance, SnO2-modified Pt/C catalyst was found to be superior to Pt/C as well as PtRu/C-SnO2 catalysts with low degradation rates. This approach for pure hydrogen generation has the potential to drastically decrease the electric energy input by ∼60%." @default.
• W2572979815 created "2017-01-26" @default.
• W2572979815 creator A5062665232 @default.
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• W2572979815 date "2017-03-01" @default.
• W2572979815 modified "2023-10-10" @default.
• W2572979815 title "The role of nanosized SnO 2 in Pt-based electrocatalysts for hydrogen production in methanol assisted water electrolysis" @default.
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• W2572979815 doi "https://doi.org/10.1016/j.electacta.2017.01.106" @default.
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