塔菲尔方程
石墨烯
材料科学
单层
成核
催化作用
GSM演进的增强数据速率
化学工程
氧化物
纳米技术
电流密度
胶体
化学
有机化学
物理化学
电化学
冶金
工程类
物理
电信
量子力学
计算机科学
电极
作者
Yugang Sun,Farbod Alimohammadi,Dongtang Zhang,Guangsheng Guo
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-02-10
卷期号:17 (3): 1963-1969
被引量:256
标识
DOI:10.1021/acs.nanolett.6b05346
摘要
By selectively promoting heterogeneous nucleation/growth of MoS2 on graphene monolayer sheets, edge-oriented (EO) MoS2 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 MoS2 nanosheets per area of graphene sheets were tuned by controlling the reaction time in the microwave-assisted solvothermal reduction of ammonium tetrathiomolybdate [(NH4)2MoS4] in dimethylformamide. The edge-oriented and interlayer-expanded (EO&IE) MoS2/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 MoS2 sheets without edge-oriented geometry, highlighting the importance of synergistic effect between edge-oriented geometry and interlayer expansion on determining HER activity of MoS2 nanosheets. Quantitative analysis clearly shows the linear dependence of current density on the edge length of MoS2 nanosheets.
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