4.7 Article Proceedings Paper

Effective excitons separation on graphene supported ZrO2-TiO2 heterojunction for enhanced H2 production under solar light

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 43, Issue 8, Pages 3905-3919

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2017.09.091

Keywords

Hydrogen production; Graphene; Mesoporous; Heterojunction; Solar light

Funding

  1. Department of Science and Technology, New Delhi [SR/FT/CS -14/2011]
  2. INSPIRE fellowship [IF131053]

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A novel photocatalyst comprises of ZrO2-TiO2 immobilized on reduced graphene oxide (rGO) a ternary heterojunction (ZrO2 TiO2/rGO) was synthesized by using facile chemical method. The nanocomposite was prepared with a strategy to achieve better utilization of excitons for catalytic reactions by channelizing from metal oxide surfaces to rGO support. TEM and XRD analysis results revealed the heterojunction formed between ZrO2 and single crystalline anatase TiO2. The mesoporous structure of ZrO2-TiO2 was confirmed using BET analysis. The red shift in absorption edge position of ZrO2-TiO2/rGO photocatalyst was characterized by using diffuse reflectance UV-Visible spectra. ZrO2-TiO2/rGO showed greater interfacial charge transfer efficiency than ZrO2-TiO2, which was evidenced by well suppressed PL intensity and high photocurrent of ZrO2-TiO2/rGO. The suitable band gap of 1.0 wt% ZrO2-TiO2/rGO facilitated the utilization of solar light in a wide range by responding to the light of energy equal to as well as greater than 2.95 eV by the additional formation of excited high-energy electrons (HEEs). ZrO2-TiO2/rGO showed the enhanced H-2 production than TiO2/rGO, which revealed the role of ZrO2 for the effective charge separation at the heterojunction and the solar light response. The optimum loading of 1.0 wt% of ZrO2 and rGO on TiO2 showed the highest photocatalytic performance (7773 mu molh(-1)g(cat)(-1)) for hydrogen (H-2) production under direct solar light irradiation. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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