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

被引:2
|
作者
Wang, Xuemin [1 ]
Zhang, Ke [1 ]
Xie, Yuhan [1 ]
Yu, Dehua [1 ]
Tian, Haoze [1 ]
Lou, Yongbing [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Peoples R China
关键词
ELECTROCATALYSTS; EFFICIENT;
D O I
10.1039/d3dt02467a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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.
引用
收藏
页码:15091 / 15100
页数:10
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