Department of Chemistry, Temple University , 1901 North 13th Street, Philadelphia, Pennsylvania 19122, United States.
Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Chemical Engineering, Beijing University of Technology , Beijing, 100124, People's Republic of China.
Nano Lett. 2017 Mar 8;17(3):1963-1969. doi: 10.1021/acs.nanolett.6b05346. Epub 2017 Feb 13.
By selectively promoting heterogeneous nucleation/growth of MoS on graphene monolayer sheets, edge-oriented (EO) MoS nanosheets with expanded interlayer spacing (∼9.4 Å) supported on reduced graphene oxide (rGO) sheets were successfully synthesized through colloidal chemistry, showing the promise in low-cost and large-scale production. The number and edge length of MoS nanosheets per area of graphene sheets were tuned by controlling the reaction time in the microwave-assisted solvothermal reduction of ammonium tetrathiomolybdate [(NH)MoS] in dimethylformamide. The edge-oriented and interlayer-expanded (EO&IE) MoS/rGO exhibited significantly improved catalytic activity toward hydrogen evolution reaction (HER) in terms of larger current density, lower Tafel slope, and lower charge transfer resistance compared to the corresponding interlayer-expanded MoS sheets without edge-oriented geometry, highlighting the importance of synergistic effect between edge-oriented geometry and interlayer expansion on determining HER activity of MoS nanosheets. Quantitative analysis clearly shows the linear dependence of current density on the edge length of MoS nanosheets.
通过选择性地促进 MoS 在石墨烯单层片上的异质成核/生长,通过胶体化学成功合成了负载在还原氧化石墨烯(rGO)片上的具有扩展层间间距(∼9.4 Å)的边缘取向(EO)MoS 纳米片,展示了低成本和大规模生产的前景。通过控制在二甲基甲酰胺中微波辅助溶剂热还原四硫代钼酸铵[(NH)MoS]的反应时间,可以调节石墨烯片上 MoS 纳米片的数量和边缘长度。与没有边缘取向几何形状的相应层间扩展 MoS 片相比,边缘取向和层间扩展(EO&IE)MoS/rGO 表现出显著提高的析氢反应(HER)催化活性,表现为更大的电流密度、更低的塔菲尔斜率和更低的电荷转移电阻,突出了边缘取向几何形状和层间扩展之间的协同效应对确定 MoS 纳米片的 HER 活性的重要性。定量分析清楚地表明电流密度与 MoS 纳米片边缘长度呈线性关系。