4.6 Article

Methanol-assisted energy-saving green hydrogen production using electrodeposited 3D-metallic tin as an electrocatalyst

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 11, Issue 41, Pages 22419-22429

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ta03014h

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Efficient water-splitting devices are crucial for sustainable hydrogen production and achieving carbon neutrality. This study investigates the use of tin as a bifunctional catalyst in a hybrid water electrolyzer, replacing the sluggish oxygen evolution reaction with the more feasible methanol oxidation reaction. The results show that the 3D Sn/NF catalyst exhibits excellent performance in hydrogen evolution, oxygen evolution, and methanol oxidation, paving the way for the development of monometallic catalysts for future electrochemical energy conversion devices.
Sustainable hydrogen production via developing an efficient water-splitting device plays a major role in achieving carbon neutrality. However, the efficiency of traditional water electrolysis is severely hindered by the sluggish kinetics of the oxygen evolution reaction (OER). To overcome this limitation and boost hydrogen production, the OER can be replaced by the thermodynamically feasible methanol oxidation reaction (MOR). Herein, we electrochemically deposited 3D metallic tin on nickel foam (3D Sn/NF) and explored the bi-functional electrocatalytic properties of tin when used in a hybrid water electrolyzer. The 3D Sn/NF grown with 15 min of Sn deposition (3D Sn/NF-15) exhibited excellent HER, OER, and MOR performances with low overpotentials of 130, 300, and 160 mV at a current density of 10 mA cm(-2). Furthermore, we designed a MOR-mediated water electrolyzer using 3D Sn/NF-15 as a bifunctional catalyst, which required a cell voltage of only 1.54 V to achieve a current density of 10 mA cm(-2), which is 70 mV lower than that required by a conventional water electrolyzer. Furthermore, a real-time hybrid water electrolysis system built with an H-type electrolytic cell showed exceptional hydrogen production, with a faradaic efficiency of 98%. Overall, this work paves the way for the facile preparation of monometallic catalysts for next-generation electrochemical energy conversion devices.

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