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Three-dimensional reduced graphene oxide/carbon nanotube nanocomposites anchoring of amorphous and crystalline molybdenum sulfide: Physicochemical characteristics and electrocatalytic hydrogen evolution performances
Electrochimica Acta ( IF 5.5 ) Pub Date : 2018-04-12
Yali Guo, Rui Wang, Xing Xu, Yanan Shang, Baoyu Gao

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 10 mA 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.



中文翻译:

三维还原氧化石墨烯/碳纳米管纳米复合材料锚固无定形和结晶性硫化钼:理化特性和电催化制氢性能

将三维(3D)还原氧化石墨烯/碳纳米管纳米复合材料(rGO / CNTs纳米复合材料)和还原氧化石墨烯纳米复合材料(rGO纳米复合材料)与非晶态MoS x锚固,形成MoS x -rGO / CNT和MoS x -rGO纳米复合材料。他们的放氢反应(HER)活性进行了深入评估。结果表明,与CNTs纳米复合材料相比,rGO / CNTs纳米复合材料为非晶态MoSx提供了更多的位点。MoS x -rGO和MoS x -rGO / CNTs纳米复合材料的拉曼光谱证实了MoS x在所有MoS x中的非晶态锚定的纳米复合材料。TEM和SEM的形态表明,非晶态的MoS x很好地分散在rGO / CNT和rGO纳米复合材料上。MoS x -rGO / CNT和MoS x -rGO纳米复合材料中的无定形MoS x纳米颗粒可以在其边缘提供更多S原子,因此大大提高了HER活性。HER性能表明,锚固有结晶MoS 2的rGO / CNT和rGO纳米复合材料表现出较差的HER性能。相反,锚固有少量MoS x的MoS x -rGO / CNT和MoS x -rGO纳米复合材料表现出出色的HER活性(在10 mA cm -2时过电势为179 mV)。结果还表明,MoS x- @ rGO纳米复合材料的HER活性比MoS x -rGO / CNTs纳米复合材料的小。rGO / CNTs纳米复合材料中的CNTs将改善电解质/电极的紧密接触并促进高速率的电荷转移,从而进一步增强了它们的电催化制氢性能。

更新日期:2018-04-12
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