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Abstract

Photocatalytic production of green oxidation reagents as an economical and environmental-friendly process is a promising strategy to replace the traditional production processes. In the present study, a series of 1.0 wt% Pt/WO3 photocatalysts with different surface chemical states of Pt were successfully fabricated. The different surface metallic Pt (Pt0) and oxidized Pt (PtOx) ratios on WO3 showed significant effects on the photocatalytic activities for strong oxidants of peroxydisulfate (S2O82-) and hydrogen peroxide (H2O2) formations. It is proposed that surface Pt0 and PtOx functioned as reduction site for O2 reduction to H2O and oxidation site for H2O oxidation to H2O2, respectively, during the photocatalytic process. As a result, a higher surface composition of Pt0 prepared using photodeposition (PD) method led to the formation of higher amount of S2O82-. On the other hand, PtOx-loaded WO3 using impregnation (IM) method showed significant formations of S2O82- and H2O2 simultaneously. This work provided a new idea for the design of noble metal Pt-supported WO3 for efficiently photocatalytic generation of S2O82- and H2O2.

Details

Title
Metallic Pt and PtOx dual-cocatalyst-loaded WO3 for photocatalytic production of peroxydisulfate and hydrogen peroxide
Author
Xie Wenwen 1 ; Huang Zeai 1   VIAFID ORCID Logo  ; Wang, Ruiqi 2 ; Cheng, Wen 2 ; Zhou, Ying 1   VIAFID ORCID Logo 

 Southwest Petroleum University, State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation, Chengdu, China (GRID:grid.437806.e) (ISNI:0000 0004 0644 5828); Southwest Petroleum University, The Center of New Energy Materials and Technology, School of New Energy and Materials, Chengdu, China (GRID:grid.437806.e) (ISNI:0000 0004 0644 5828) 
 Southwest Petroleum University, The Center of New Energy Materials and Technology, School of New Energy and Materials, Chengdu, China (GRID:grid.437806.e) (ISNI:0000 0004 0644 5828) 
Pages
11829-11840
Publication year
2020
Publication date
Sep 2020
Publisher
Springer Nature B.V.
ISSN
00222461
e-ISSN
15734803
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2416040273
Copyright
© Springer Science+Business Media, LLC, part of Springer Nature 2020.