Gao Daqiang, Xia Baorui, Wang Yanyan, Xiao Wen, Xi Pinxian, Xue Desheng, Ding Jun
Key Laboratory for Magnetism and Magnetic Materials of MOE, Key Laboratory of Special Function Materials and Structure Design of MOE, Lanzhou University, Lanzhou, 730000, P. R. China.
Department of Materials Science and Engineering, National University of Singapore, 9 Engineering Drive 1, Singapore, 117575, Singapore.
Small. 2018 Apr;14(14):e1704150. doi: 10.1002/smll.201704150. Epub 2018 Feb 20.
Although transition metal dichalcogenide MoSe is recognized as one of the low-cost and efficient electrocatalysts for the hydrogen evolution reaction (HER), its thermodynamically stable basal plane and semiconducting property still hamper the electrocatalytic activity. Here, it is demonstrated that the basal plane and edges of 2H-MoSe toward HER can be activated by introducing dual-native vacancy. The first-principle calculations indicate that both the Se and Mo vacancies together activate the electrocatalytic sites in the basal plane and edges of MoSe with the optimal hydrogen adsorption free energy (ΔG ) of 0 eV. Experimentally, 2D MoSe nanosheet arrays with a large amount of dual-native vacancies are fabricated as a catalytic working electrode, which possesses an overpotential of 126 mV at a current density of 100 mV cm , a Tafel slope of 38 mV dec , and an excellent long-term durability. The findings pave a rational pathway to trigger the activity of inert MoSe toward HER and also can be extended to other layered dichalcogenide.
尽管过渡金属二硫属化物MoSe被认为是用于析氢反应(HER)的低成本且高效的电催化剂之一,但其热力学稳定的基面和半导体性质仍然阻碍了电催化活性。在此,证明了通过引入双本征空位可以激活2H-MoSe的基面和边缘以用于HER。第一性原理计算表明,Se和Mo空位共同激活了MoSe基面和边缘的电催化位点,其最佳氢吸附自由能(ΔG)为0 eV。在实验上,制备了具有大量双本征空位的二维MoSe纳米片阵列作为催化工作电极,该电极在电流密度为100 mV cm时的过电位为126 mV,塔菲尔斜率为38 mV dec,并且具有优异的长期耐久性。这些发现为激发惰性MoSe对HER的活性开辟了一条合理途径,并且也可以扩展到其他层状二硫属化物。