4.7 Article

Ag-doped TiO2 photocatalysts with effective charge transfer for highly efficient hydrogen production through water splitting

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 45, Issue 4, Pages 2729-2744

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2019.11.127

Keywords

Photocatalytic water splitting; Renewable energy; Bandgap reduction; Hydrogen production

Funding

  1. Department of Science and Technology (DST), New Delhi, India under the special scheme Clean Energy Research Initiative (CERI) [DST/TM/CERI/C19(G)]
  2. Center for Excellence in Nano electronics & Theranostic Devices, MEITY, GOI [5(9/2012/NANO)]

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The development of efficient metal doped semiconductors for solar energy harvesting to produce hydrogen has attracted significant attention. Herein, the H-2 generation over Ag-doped TiO2 photocatalyst, synthesized using a simple and cost-effective method based on chemical reduction, was reported. The Ag/TiO2 exhibited an absorption peak in the visible region and the reduction of the bandgap to 2.5 eV due to surface plasmonic resonance (SPR). X-ray photoelectron spectroscopy revealed the presence of oxygen vacancies and 11% of Ag in Ti-Ag-O phase. The effect of reaction time and photocatalyst loading in the absence and presence of sacrificial reagents (alcohols and sulfur) on water splitting was studied and compared the activity of Ag/TiO2 with that of bare TiO2. The H-2 production rate of 23.5 mmol g(-1) h(-1) (with an apparent quantum yield of 19%), over 1.5Ag/TiO2, was the highest ever reported so far. The observed higher activity could mainly be attributed to the existence of oxygen vacancies and the Ti-Ag-O phase. The photocatalyst was stable for three consecutive cycles in both the presence and absence of sacrificial reagents. This study offers new insights into the rational design of metal-support hybrid structures for hydrogen production through photocatalytic water splitting. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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