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dc.contributor.authorCao, J.
dc.contributor.authorLi, Xin Yong
dc.contributor.authorLin, H.
dc.contributor.authorXu, B.
dc.contributor.authorChen, S.
dc.contributor.authorGuan, Q.
dc.date.accessioned2017-01-30T11:28:10Z
dc.date.available2017-01-30T11:28:10Z
dc.date.created2015-10-29T04:09:37Z
dc.date.issued2013
dc.identifier.citationCao, J. and Li, X.Y. and Lin, H. and Xu, B. and Chen, S. and Guan, Q. 2013. Surface acid etching of (BiO)2CO3 to construct (BiO)2CO3/BiOX (X = Cl, Br, I) heterostructure for methyl orange removal under visible light. Applied Surface Science. 266: pp. 294-299.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/12014
dc.identifier.doi10.1016/j.apsusc.2012.11.172
dc.description.abstract

A series of (BiO)2CO3/BiOX (X = Cl, Br, I) heterostructured photocatalysts were synthesized through acid etching method and characterized by XRD, DRS, SEM and HRTEM, respectively. Under visible light (λ > 400 nm), (BiO)2CO3/BiOX displayed much higher photocatalytic activity than pure (BiO)2CO3 and corresponding BiOX for the degradation of methyl orange (MO). The photocatalytic activities of the as-prepared samples increased following this order: (BiO)2CO3/BiOCl < (BiO)2CO3/BiOBr < (BiO)2CO3/BiOI. The enhanced photocatalytic activities could be attributed to the function of heterojunction interface between (BiO)2CO3 and BiOX. Moreover, except for the role of heterostructure, the excellent photocatalytic performance of (BiO)2CO3/BiOI also originated from its good visible light absorption.

dc.titleSurface acid etching of (BiO)2CO3 to construct (BiO)2CO3/BiOX (X = Cl, Br, I) heterostructure for methyl orange removal under visible light
dc.typeJournal Article
dcterms.source.volume266
dcterms.source.startPage294
dcterms.source.endPage299
dcterms.source.issn0169-4332
dcterms.source.titleApplied Surface Science
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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