Wang Xuemin, Zhang Ke, Xie Yuhan, Yu Dehua, Tian Haoze, Lou Yongbing
School of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, China.
Dalton Trans. 2023 Oct 24;52(41):15091-15100. doi: 10.1039/d3dt02467a.
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 on a nickel foam (NF) substrate, with the interface structure formed through the electrodeposition of MnOH. The resulting heterostructure MnOH/CoMoP/NF exhibited remarkable hydrogen evolution reaction (HER) activity, achieving overpotentials as low as 61 and 138 mV at 10 and 100 mA cm, respectively. Moreover, MnOH/CoMoP/NF demonstrated efficient oxygen evolution reaction (OER) activity with an overpotential of 330 mV at 100 mA cm. Remarkably, MnOH/CoMoP/NF maintained its catalytic properties and structural integrity even after working continuously for 20 h facilitating the HER at 10 mA cm and the OER at 100 mA cm. The Tafel slopes of the HER and OER were determined to be as small as 14 and 55 mV dec, respectively, confirming that the coupled interface conferred fast reaction kinetics on the catalyst. When applied in overall water splitting, MnOH/CoMoP/NF delivered a voltage of 1.91 V at 100 mA cm 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.
人们普遍认为,界面工程策略可以显著提高催化剂的活性。在本研究中,我们开发了一种直接生长在泡沫镍(NF)基底上的CoMoP纳米阵列,其界面结构是通过MnOH的电沉积形成的。所得的异质结构MnOH/CoMoP/NF表现出显著的析氢反应(HER)活性,在10和100 mA cm时的过电位分别低至61和138 mV。此外,MnOH/CoMoP/NF在100 mA cm时表现出高效的析氧反应(OER)活性,过电位为330 mV。值得注意的是,即使在10 mA cm的HER和100 mA cm的OER连续工作20小时后,MnOH/CoMoP/NF仍保持其催化性能和结构完整性。HER和OER的塔菲尔斜率分别低至14和55 mV dec,证实了耦合界面赋予了催化剂快速的反应动力学。当应用于全水解时,MnOH/CoMoP/NF在100 mA cm时提供1.91 V的电压,具有优异的稳定性。本研究证明了利用简单的电沉积技术制备具有双功能催化活性的异质结构的可行性,为各种工业应用奠定了坚实的基础。