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Abstract
Operating fuel cells in alkaline environments permits the use of platinum-group-metal-free (PGM-free) catalysts and inexpensive bipolar plates, leading to significant cost reduction. Of the PGM-free catalysts explored, however, only a few nickel-based materials are active for catalyzing the hydrogen oxidation reaction (HOR) in alkali; moreover, these catalysts deactivate rapidly at high anode potentials owing to nickel hydroxide formation. Here we describe that a nickel–tungsten–copper (Ni5.2WCu2.2) ternary alloy showing HOR activity rivals Pt/C benchmark in alkaline electrolyte. Importantly, we achieved a high anode potential up to 0.3 V versus reversible hydrogen electrode on this catalyst with good operational stability over 20 h. The catalyst also displays excellent CO-tolerant ability that Pt/C catalyst lacks. Experimental and theoretical studies uncover that nickel, tungsten, and copper play in synergy to create a favorable alloying surface for optimized hydrogen and hydroxyl bindings, as well as for the improved oxidation resistance, which result in the HOR enhancement.
The lack of efficient and cost-effective catalysts for H2 oxidation reaction (HOR) hinders the application of anion exchange membrane fuel cells. Here, authors report a ternary nickel-tungsten-copper nanoalloy with marked HOR activity and stability that rivals the benchmark platinum catalyst.
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1 University of Science and Technology of China, Division of Nanomaterials & Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, Hefei, China (GRID:grid.59053.3a) (ISNI:0000000121679639)
2 Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, China (GRID:grid.418741.f) (ISNI:0000 0004 0632 3097)
3 University of Science and Technology of China, Department of Materials Science and Engineering, Hefei, China (GRID:grid.59053.3a) (ISNI:0000000121679639)
4 University of Science and Technology of China, National Synchrotron Radiation Laboratory, Hefei, China (GRID:grid.59053.3a) (ISNI:0000000121679639)