4.7 Article

Surface acid etching of (BiO)2CO3 to construct (BiO)2CO3/BiOX (X = Cl, Br, I) heterostructure for methyl orange removal under visible light

Journal

APPLIED SURFACE SCIENCE
Volume 266, Issue -, Pages 294-299

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2012.11.172

Keywords

(BiO)(2)CO3; Acid etching method; Photocatalytic activity; Heterostructure

Funding

  1. Natural Science Foundation of China [20973071, 51172086]
  2. Natural Science Foundation of Educational Committee of Anhui Province [KJ2012Z356, KJ2009B107]
  3. Foundation for Excellent Young Talents of Higher Education institution of Anhui Province [2009SQRZ151ZD]

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A series of (BiO)(2)CO3/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 (lambda > 400 nm), (BiO)(2)CO3/BiOX displayed much higher photocatalytic activity than pure (BiO)(2)CO3 and corresponding BiOX for the degradation of methyl orange (MO). The photocatalytic activities of the as-prepared samples increased following this order: (BiO)(2)CO3/BiOCl < (BiO)(2)CO3/BiOBr < (BiO)(2)CO3/BiOI. The enhanced photocatalytic activities could be attributed to the function of heterojunction interface between (BiO)(2)CO3 and BiOX. Moreover, except for the role of heterostructure, the excellent photocatalytic performance of (BiO)(2)CO3/BiOI also originated from its good visible light absorption. (c) 2012 Elsevier B.V. All rights reserved.

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