• 文献标题:   Three-dimensional reduced graphene oxide/carbon nanotube nanocomposites anchoring of amorphous and crystalline molybdenum sulfide: Physicochemical characteristics and electrocatalytic hydrogen evolution performances
  • 文献类型:   Article
  • 作  者:   GUO YL, WANG R, XU X, SHANG YN, GAO BY
  • 作者关键词:   graphene oxide, carbon nanotube, nanocomposite, hydrogen evolution reaction, amorphous mosx
  • 出版物名称:   ELECTROCHIMICA ACTA
  • ISSN:   0013-4686 EI 1873-3859
  • 通讯作者地址:   Shandong Univ
  • 被引频次:   5
  • DOI:   10.1016/j.electacta.2018.04.078
  • 出版年:   2018

▎ 摘  要

The three-dimensional (3D) reduced graphene oxide/carbon nanotube nanocomposites (rGO/CNTs nanocomposites) and reduced graphene oxide nanocomposites (rGO nanocomposites) were anchored with amorphous MoSx, forming the MoSx-rGO/CNTs and MoSx-rGO nanocomposites. Their hydrogen evolution reaction (HER) activities were intensively evaluated. Results indicated that the rGO/CNTs nanocomposite provided more sites for the amorphous MoSx as compared with that of CNTs nanocomposite. Raman spectra of MoSx-rGO and MoSx-rGO/CNTs nanocomposites confirmed the amorphous state of MoSx in all MoSx anchored nanocomposites. TEM and SEM morphology indicated that the amorphous MoSx was well-dispersed on the rGO/CNTs and rGO nanocomposites. The amorphous MoSx nanoparticles in MoSx-rGO/CNTs and MoSx-rGO nanocomposites could provide more S atoms at their edges, and therefore greatly improve the HER activity. HER performances indicated that the rGO/CNTs and rGO nanocomposites anchored with crystalline MoS2 exhibited poor HER performance. In contrast, MoSx-rGO/CNTs and MoSx-rGO nanocomposites anchored with a small amount of MoSx exhibited the excellent HER activity (179 mV of overpotential at 10mA cm(-2)). Results also indicated that the HER activities of the MoSx-@rGO nanocomposites were a bit smaller than those of MoSx-rGO/CNTs nanocomposites. The CNTs in the rGO/CNTs nanocomposites would improve the intimate electrolyte/electrode contact and promote the high-rate charge transfer, which further strengthened their electrocatalytic hydrogen evolution performances. (c) 2018 Elsevier Ltd. All rights reserved.