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dc.contributor.authorLiu, J.
dc.contributor.authorKe, J.
dc.contributor.authorLi, Y.
dc.contributor.authorLiu, B.
dc.contributor.authorWang, L.
dc.contributor.authorXiao, H.
dc.contributor.authorWang, Shaobin
dc.date.accessioned2018-06-29T12:26:42Z
dc.date.available2018-06-29T12:26:42Z
dc.date.created2018-06-29T12:08:46Z
dc.date.issued2018
dc.identifier.citationLiu, J. and Ke, J. and Li, Y. and Liu, B. and Wang, L. and Xiao, H. and Wang, S. 2018. Co<inf>3</inf>O<inf>4</inf>quantum dots/TiO<inf>2</inf>nanobelt hybrids for highly efficient photocatalytic overall water splitting. Applied Catalysis B: Environmental. 236: pp. 396-403.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/68684
dc.identifier.doi10.1016/j.apcatb.2018.05.042
dc.description.abstract

© 2018 Elsevier B.V. Solar-light driven water splitting to hydrogen and oxygen without sacrificial agents has gained tremendous attention due to the clean and renewable energy supply of the future. Herein, we report construction of Co3O4quantum dots (QDs)/TiO2nanobelts (NBs) hybrids via a facile hydrothermal method for simultaneous H2and O2productions from pure water, with high evolution rates of 41.8 and 22.0 µmol h-1g-1, respectively, which are significantly enhanced compared with TiO2NBs and Co3O4materials. The Co3O4QDs not only improve light sensitivity but also change the work function of TiO2, promoting the transfer of electrons from TiO2to Co3O4QDs and H2generation on the surface of Co3O4QDs. Moreover, the size effect of Co3O4QDs (~3 nm) facilitates the electron trapping due to the shorter pathway, and the generation of heterojunctions favors to suppress the recombination of photo-excited carries.

dc.publisherElsevier BV
dc.titleCo<inf>3</inf>O<inf>4</inf>quantum dots/TiO<inf>2</inf>nanobelt hybrids for highly efficient photocatalytic overall water splitting
dc.typeJournal Article
dcterms.source.volume236
dcterms.source.startPage396
dcterms.source.endPage403
dcterms.source.issn0926-3373
dcterms.source.titleApplied Catalysis B: Environmental
curtin.departmentWASM: Minerals, Energy and Chemical Engineering (WASM-MECE)
curtin.accessStatusFulltext not available


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