• Highly-dispersed ultrafine Pt nanoparticles on reduced graphene oxide nanosheets In situ sacrificial template synthesis and superior electrocatalytic performance for methanol oxidation

    分类: 材料科学 >> 材料化学 提交时间: 2017-11-01

    摘要: We report a simple and environment-friendly route to prepare platinum/reduced graphene oxide (Pt/rGO) nanocomposites (NCs) with highly reactive MnOx colloids as reducing agents and sacrificial templates. The colloids are obtained by laser ablation of a metallic Mn target in graphene oxide (GO)-containing solution. Structural and morphological investigations of the as-prepared NCs revealed that ultrafine Pt nanoparticles (NPs) with an average size of 1.8 (± 0.6) nm are uniformly dispersed on the surfaces of rGO nanosheets. Compared with commercial Pt/C catalysts, Pt/rGO NCs with highly electrochemically active surface areas show remarkably improved catalytic activity and durability toward methanol oxidation. All of these superior characteristics can be attributed to the small particle size and uniform distribution of the Pt NPs, as well as the excellent electrical conductivity and stability of the rGO catalyst support. These findings suggest that Pt/rGO electrocatalysts are promising candidate materials for practical use in fuel cells.

  • Co-doped Ni hydroxide and oxide nanosheet networks Laser-Assisted Synthesis Effective Doping, and Ultrahigh Pseudocapacitor Performance

    分类: 材料科学 >> 材料化学 提交时间: 2017-11-01

    摘要: Morphology control and impurity doping are two widely applied strategies to improve the electrochemical performance of nanomaterials. Herein, we report an environmentally friendly approach to obtain Co-doped Ni(OH)2 nanosheet networks using a laser-induced cobalt colloid as a doping precursor followed by an aging treatment in a hybrid medium of nickel ions. The shape and specific surface area of the doped Ni(OH)2 can be successfully adjusted by changing the concentration of sodium thiosulfate. Furthermore, a Co-doped Ni(OH)2 nanosheet network was further converted into Co-doped NiO with its pristine morphology retained via facile thermal decomposition in air. The structure and electrochemical performance of the as-prepared samples are investigated with scanning and transmission electron microscopy, energy dispersive x-ray analysis, x-ray diffraction, Fourier transform infrared spectroscopy, the nitrogen adsorption-desorption isotherm technique, and electrochemical measurements. The Co-doped Ni(OH)2 electrode shows an ultrahigh specific capacitance of 1421 F/g at a current density of 6 A/g, and a good retention level of 76% after 1000 cycles, in sharp contrast with only a 47% retention level of the pure Ni(OH)2 electrode at the same current density. In addition, the Co-doped NiO electrode exhibits a capacitance of 720 F/g at 6 A/g and 92% retention after 1000 cycles, which is also superior to those values for relevant pure NiO electrodes. The Co2+ partially substitutes for Ni2+ in the metal hydroxide and oxide, resulting in an increase of free holes in the valence band, and, therefore, enhancement of the p-type conductivity of Ni(OH)2 and NiO. Moreover, such novel mesoporous nanosheet network structures are also able to enlarge the electrode-electrolyte contact area and shorten the path length for ion transport. The synergetic effect of these two results is responsible for the observed ultrahigh pseudocapacitor performance.