4.8 Article

Dense-Packed RuO2 Nanorods with In Situ Generated Metal Vacancies Loaded on SnO2 Nanocubes for Proton Exchange Membrane Water Electrolyzer with Ultra-Low Noble Metal Loading

Journal

SMALL
Volume -, Issue -, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202301516

Keywords

electrochemical catalysis; material synthesis; oxygen evolution reaction; ruthenium oxide; water electrolysis

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In this study, a catalyst with RuO2 nanorods coated outside SnO2 nanocubes is designed, which forms continuous networks and provides high conductivity, allowing for the reduction of Ru contents in catalysts. Furthermore, the structure evolutions on the RuO2 surface are carefully investigated, and the etched RuO2 surfaces are seen as the consequence of Co leaching, which is more effective in driving oxygen evolution. Electrochemical tests show that the catalysts with 23 wt% Ru exhibit an overpotential of 178 mV at 10 mA cm(-2), which is higher than most state-of-art oxygen evolution catalysts. In practical PEMWE, the noble metal Ru loading on the anode side is only 0.3 mg cm(-2), and the cell achieves 1.61 V at 1 A cm(-2) and proper stability at 500 mA cm(-2), demonstrating the effectiveness of the designed catalyst.
Proton exchange membrane water electrolyzer (PEMWE) is a green hydrogen production technology that can be coupled with intermittent power sources such as wind and photoelectric power. To achieve cost-effective operations, low noble metal loading on the anode catalyst layer is desired. In this study, a catalyst with RuO2 nanorods coated outside SnO2 nanocubes is designed, which forms continuous networks and provides high conductivity. This allows for the reduction of Ru contents in catalysts. Furthermore, the structure evolutions on the RuO2 surface are carefully investigated. The etched RuO2 surfaces are seen as the consequence of Co leaching, and theoretical calculations demonstrate that it is more effective in driving oxygen evolution. For electrochemical tests, the catalysts with 23 wt% Ru exhibit an overpotential of 178 mV at 10 mA cm(-2), which is much higher than most state-of-art oxygen evolution catalysts. In a practical PEMWE, the noble metal Ru loading on the anode side is only 0.3 mg cm(-2). The cell achieves 1.61 V at 1 A cm(-2) and proper stability at 500 mA cm(-2), demonstrating the effectiveness of the designed catalyst.

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