journal article·2019-11-25Open access

Ag–TiO2 Hybrid Nanocrystal Photocatalyst: Hydrogen Evolution under UV Irradiation but Not under Visible-Light Irradiation

Shelton J. P. Varapragasam, Shahzahan Mia, Carly Wieting, Choumini Balasanthiran, Md Yeathad Hossan, Aravind Baride, Robert M. Rioux, James D. Hoefelmeyer

ACS Applied Energy Materials· Volume 2· Issue 11

Abstract

We report a thermolytic reduction of silver precursors in the presence of anatase TiO2 nanorods to form Ag–TiO2 hybrid nanocrystals (HNCs). Upon changing the reaction conditions, the size and number density of Ag on the HNCs could be adjusted. The size and number density of Ag on the HNCs were found to have an inverse relation. We assess the hydrogen evolution of TiO2 nanorods, P25 TiO2, and Ag–TiO2 HNCs in methanol/water under xenon lamp irradiation. The turnover frequency for hydrogen evolution on silica-supported Ag–TiO2 was 1.4 × 10–4 s–1, greater than that of the anatase TiO2 nanorods (9.8 × 10–6 s–1) or the coupled anatase/rutile TiO2 (P25 catalyst; 5.2 × 10–5 s–1).
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · TiO2 Photocatalysis and Solar Cells · Advanced Nanomaterials in Catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, University of South Dakota, 414 East Clark Street, Vermillion, South Dakota 57069, United States

Funding

U.S. Department of Energy · National Science Foundation

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