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Issue 20, 2018
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Controllable synthesis and photoreduction performance towards Cr(VI) of BiOCl microrods with exposed (110) crystal facets

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Bismuth oxyhalides have been of great interest, since they induce a strong internal static electric field and promote the effective separation of photoinduced electron–hole pairs, which enables good photocatalytic performance. However, simple synthesis and easily controllable facet exposure remain great challenges in this regard. Here, BiOCl microrods were synthesized via a simple hydrothermal method, using sodium citrate as a capping agent. High-resolution transmission electron microscopy (HRTEM) images show that the BiOCl microrods have (110) facets (BiOCl-110) exposed and grow with a [1[1 with combining macron]2] orientation. X-ray photoelectron spectroscopy (XPS) and FT-IR spectra show a number of citrate ions on the surface of BiOCl-110. An Ostwald ripening growth mechanism for BiOCl-110 has been demonstrated in our study. In addition, the photocatalytic performance of BiOCl-110 was evaluated via the degradation of hexavalent chromium (Cr(VI)) under solar light irradiation. From this, BiOCl-110 exhibits more excellent photoreduction performance towards Cr(VI) than BiOCl-001, and Cr(VI) at a concentration of 30 mg L−1 can be completely photoreduced within 4 and 10 min under acidic and neutral conditions, respectively. This enhanced photoreduction performance is ascribed to the more negative conductive band position of the (110) crystal facets, which enhances the reductive ability of photoelectrons.

Graphical abstract: Controllable synthesis and photoreduction performance towards Cr(vi) of BiOCl microrods with exposed (110) crystal facets

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Publication details

The article was received on 04 Jul 2018, accepted on 11 Sep 2018 and first published on 12 Sep 2018

Article type: Paper
DOI: 10.1039/C8NJ03323D
Citation: New J. Chem., 2018,42, 16911-16918

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    Controllable synthesis and photoreduction performance towards Cr(VI) of BiOCl microrods with exposed (110) crystal facets

    Y. Peng, Y. G. Mao, P. F. Kan, J. Y. Liu and Z. Fang, New J. Chem., 2018, 42, 16911
    DOI: 10.1039/C8NJ03323D

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