4.7 Article

Carbon Nanotube with Vertical 2D Molybdenum Sulphoselenide Nanosheet Arrays for Boosting Electrocatalytic Hydrogen Evolution

期刊

ACS APPLIED ENERGY MATERIALS
卷 1, 期 12, 页码 7035-7045

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.8b01466

关键词

transition metal dichalcogenides; vertical nanosheet array; carbon nanotube; high-temperature sulfidation; hydrogen evolution

资金

  1. National Natural Science Foundation of China [51433001, 21504012, 51773035, 11774136, 11404144]
  2. Program of Shanghai Subject Chief Scientist [17XD1400100]
  3. Natural Science Foundation of Shanghai [17ZR1439900]
  4. Shanghai Rising-Star Program [18QA1400200]
  5. China Postdoctoral Science Foundation [2016M601722]
  6. Shanghai Scientific and Technological Innovation Project [18JC1410600]

向作者/读者索取更多资源

Transition metal dichalcogenides (TMDs) are a promising non-noble-metal electrocatalyst toward the hydrogen evolution reaction (HER). However, the sluggish HER kinetics and poor electric conductivities of the TMDs severely restrict their practical applications for high-efficient water splitting. Herein, a nanosheet array of 2D anion-tailored MoSexS2-x on carbon nanotubes (CNTs) was prepared through an anionic substitution reaction. The all-solid-state sulfidation of the CNT-MoSe2 precursor using the sulfur powder as the sulfur source indicates a green and easily scalable strategy for the preparation of the CNT-MoSexS2-x hybrid. As a result, the CNT-MoSexS2-x hybrid delivers an excellent HER performance including a low onset overpotential (83 mV), small Tafel slope (40 mV dec(-1)) and long-term stability (overpotential at 10 mA cm(-2) from 160 to 166 mV after 6000 cycles). The superior electrocatalytic activities of the CNT-MoSexS2-x hybrid are originated from decreased hydrogen adsorption energy associated with altering arrangements of Se and S atoms within the MoSexS2-x nanosheets. In addition, the MoSexS2-x nanosheet array on the highly conductive backbones of CNTs also enables an efficient electron/ion transport thus manifesting fast HER kinetics.

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