Journal
CATALYSIS TODAY
Volume 388, Issue -, Pages 79-86Publisher
ELSEVIER
DOI: 10.1016/j.cattod.2020.11.012
Keywords
Hydrogenation; Hydrogen evolution; Photocatalysis; Bimetallic; X-ray absorption spectra
Funding
- Ministry of Science and Technology, Taiwan [MOST 108-2112-M-213-002-MY3, MOST 108-2218-E-009-039-MY3, MOST108-3017-F-009-004]
- Center for Emergent Functional Matter Science of National Chiao Tung University from The Featured Areas Research Center Program by the Ministry of Education (MOE) in Taiwan
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The efficacy of treatment with hydrogen and Ag-Cu co-deposition on TiO2 photocatalysts has been investigated computationally and experimentally. The results show that the hydrogenated Ag-Cu with co-loaded TiO2 achieved a photoactivity about 110 times greater than that of pristine TiO2. This enhancement is attributed to the synergy between new electronic states and lattice distortion. Soft X-ray spectra and quantum-chemical calculations provide evidence for this mechanism. The photocatalytic process involves the transfer of photo-excited electrons from the bimetallic Ag-Cu to the TiO2 conduction band, as observed through in situ soft X-ray absorption spectra (XAS). The coupling of hydrogenation with bimetallic Ag-Cu onto TiO2-based photocatalysis offers a promising solution for environmental and energy applications.
The efficacy of treatment with hydrogen and Ag-Cu co-deposition on TiO2 photocatalysts has been investigated computationally and experimentally. The hydrogenated Ag-Cu with co-loaded TiO2 (H:(Ag-Cu/TiO2)) achieved a photoactivity about 110 times that of pristine TiO2, which corresponds to a rate of 1.16 mmol h(-1) g(-1) for hydrogen generation. Soft X-ray spectra and quantum-chemical calculations indicate that the notable promotion of photoactivity on H:(Ag-Cu/TiO2) is ascribable to the synergy between new electronic states and a lattice distortion. The soft X-ray absorption spectra (XAS) indicated that the TiO6 octahedral symmetry and the Ti 3d-orbital orientation are significantly affected by the Ag-Cu decoration and the hydrogenation treatment. The mechanisms involved in this photocatalysis were studied with soft XAS in situ, which showed that the photo-excited electrons transfer from the bimetallic Ag-Cu to the TiO2 conduction band as the photoresponse of this composite photocatalyst. The strategy of coupling hydrogenation with bimetallic Ag-Cu onto TiO2-based photocatalysis provides a facile and promising solution to other environmental and energy applications.
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