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Journal Article | PUBDB-2024-01989 |
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2023
RSC Publ.
Cambridge
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Please use a persistent id in citations: doi:10.1039/D3EE03258B doi:10.3204/PUBDB-2024-01989
Abstract: Electrochemical urea splitting provides a sustainable and environmentally benign route for facilitating energy conversion. Nonetheless, the sustained efficiency of urea splitting is impeded by a scarcity of active sites during extended operational periods. Herein, an atomic heterostructure engineering strategy is proposed to promote the generation of active species via synthesizing unique Ru–O$_4$ coordinated single atom catalysts anchored on Ni hydroxide (Ru$_1$–Ni(OH)$_2$), with ultralow Ru loading mass of 40.6 μg cm$^{−2}$ on the nickel foam for commercial feasibility. Leveraging in situ spectroscopic characterizations, the structure-performance relationship in low and high urea concentrations was investigated and exhibited extensive universality. The boosted generation of dynamic Ni$^{3+}$ active sites ensures outstanding activity and prominent long-term durability tests in various practical scenarios, including 100 h Zn–urea–air battery operation, 100 h alkaline urine electrolysis, and over 400 h stable hydrogen production in membrane electrode assembly (MEA) system under industrial-level current density.
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