4.7 Article

MnOxHy-modified CoMoP/NF nanosheet arrays as hydrogen evolution reaction and oxygen evolution reaction bifunctional catalysts under alkaline conditions

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DALTON TRANSACTIONS
卷 52, 期 41, 页码 15091-15100

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d3dt02467a

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The study developed a new interface engineering strategy by electrodeposition, resulting in a heterostructure MnOxHy/CoMoP/NF with remarkable catalytic activity for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The study demonstrated the feasibility of fabricating a heterogeneous structure with bifunctional catalytic activity and excellent stability.
It is widely acknowledged that interface engineering strategies can significantly enhance the activity of catalysts. In this study, we developed a CoMoP nanoarray directly grown in situ on a nickel foam (NF) substrate, with the interface structure formed through the electrodeposition of MnOxHy. The resulting heterostructure MnOxHy/CoMoP/NF exhibited remarkable hydrogen evolution reaction (HER) activity, achieving overpotentials as low as 61 and 138 mV at 10 and 100 mA cm(-2), respectively. Moreover, MnOxHy/CoMoP/NF demonstrated efficient oxygen evolution reaction (OER) activity with an overpotential of 330 mV at 100 mA cm(-2). Remarkably, MnOxHy/CoMoP/NF maintained its catalytic properties and structural integrity even after working continuously for 20 h facilitating the HER at 10 mA cm(-2) and the OER at 100 mA cm(-2). The Tafel slopes of the HER and OER were determined to be as small as 14 and 55 mV dec(-1), respectively, confirming that the coupled interface conferred fast reaction kinetics on the catalyst. When applied in overall water splitting, MnOxHy/CoMoP/NF delivered a voltage of 1.91 V at 100 mA cm(-2) with excellent stability. This study demonstrated the feasibility of utilizing a simple electrodeposition technique to fabricate a heterogeneous structure with bifunctional catalytic activity, establishing a solid foundation for diverse industrial applications.

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