Electrically assisted water splitting is an endurable strategy for hydrogen production, but the sluggish kinetics of oxygen evolution reaction (OER) extremely restrict the large-scale production of hydrogen. Developing highly efficient and non-precious catalytic materials is essential to accelerate the sluggish kinetics of OER. However, currently used catalyst supports, such as copper foam, suffer from inferior corrosion resistance and structural stability, resulting in the disabled functionality of 3D conductive networks. To this end, a novel 3D freestanding electrode with corrosion-resistant and robust Ti-6Al-4V titanium alloy lattice as the catalyst support is designed via a 3D printing technology of selective laser melting. After the coating of core-shell Cu(OH)2@CoNi carbonate hydroxides (CoNiCH) on the designed lattice, a unique micro/nano-sized hierarchical porous structure is formed, which endows the electrocatalyst with a promising electrocatalytic activity (a low overpotential of 355 mV at 30 mA cm-2 and Tafel slope of 125.3 mV dec-1 ). Computational results indicate that the CoNiCH exhibits optimized electron transfer and the catalytic activity of the Ni site is higher than that of the Co site in the CoNiCH. Therefore, the integration of robust catalyst supports and highly active materials opens up an avenue for reliable and high-performance OER electrocatalysts.
Keywords: 3D Printing; Ti-6Al-4V titanium alloy; lattice; oxygen evolution reaction; selective laser melting.
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