4.6 Article

Microwave-assisted hydrothermal synthesis of graphene based Au-TiO2 photocatalysts for efficient visible-light hydrogen production

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 2, Issue 11, Pages 3847-3855

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ta14908k

Keywords

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Funding

  1. 973 program [2013CB632402]
  2. 863 Program [2012AA062701]
  3. NSFC [51272199, 51320105001, 51372190, 21177100]
  4. Fundamental Research Funds for the Central Universities [2013-VII-030]
  5. Self-determined and Innovative Research Funds of SKLWUT [2013-ZD-1]

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The construction and application of visible-light-driven photocataLysts falls in the central focus for the efficient utilization of renewable solar energy, which provides unprecedented opportunities for addressing the increasing concerns on energy and environmental sustainability. Herein, graphene based Au-TiO2 photocataLysts were fabricated by a simple, one-step microwave-assisted hydrothermal method, using Degussa P25 TiO2 powder (P25), graphene oxide and HAuCl4 aqueous solution as the raw materials. The effects of graphene introduction and gold Loading on the photocatalytic hydrogen production rates of the as-prepared samples in a methanolic aqueous solution were investigated. The results indicated that Au-TiO2-graphene composite had a significanty increased visible Light absorption and enhanced photocatalytic H-2-production activity compared to the Au-TiO2 composite. In comparison, the pure TiO2, graphene-TiO2 and graphene-Au had no appreciable visible-light-driven H-2 production. The enhanced photocatalytic H-2-production activity of the Au-TiO2-graphene composite is ascribed to (1) the Load of the Au nanoparticles which broadens the visible Light response of TiO2 due to the surface plasmon resonance (SPR) effect, and (2) the introduction of graphene, which functions as rapid electron transfer units, facilitating the space separation of photoelectron and hole pairs. The proposed H-2-production activity enhancement mechanism was further confirmed by the transient photocurrent response and electrochemical impedance spectroscopy (EIS) experiments.

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