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Issue 41, 2011
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Sunlight-driven plasmonic photocatalysts based on Ag/AgCl nanostructures synthesized via an oil-in-water medium: enhanced catalytic performance by morphology selection

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Abstract

Herein, we have demonstrated that spherical and quasi-cubic Ag/AgCl-based plasmonic photocatalysts could be controllably synthesized by means of a one-pot surfactant-assisted method, wherein an oil-in-water system is employed as synthesis medium. We have found that thus-produced nanostructures can display stable photocatalytic performance for the photodegradation of Methyl Orange (MO) pollutant when energized with sunlight or visible light, where morphology dependent and enhanced photocatalytic activity could be realized. Compared with the Ag/AgCl nanospheres, their quasi-cubic counterparts exhibit much higher photocatalytic activity, which could be further enhanced upon hybridization with graphene oxide (GO). Moreover, in contrast to the spherical Ag/AgCl nanospecies formulated via a water-in-oil medium, those synthesized through the oil-in-water system display higher photocatalytic activity. On the basis of our experimental facts, a plausible explanation has been proposed for these significant findings. The investigation has not only one-pot controllably produced sunlight energized Ag/AgCl-based plasmonic photocatalysts with morphology dependent catalytic performance, but also essentially increased their catalytic activity.

Graphical abstract: Sunlight-driven plasmonic photocatalysts based on Ag/AgCl nanostructures synthesized via an oil-in-water medium: enhanced catalytic performance by morphology selection

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Publication details

The article was received on 15 Jul 2011, accepted on 15 Aug 2011 and first published on 23 Sep 2011


Article type: Paper
DOI: 10.1039/C1JM13326H
Citation: J. Mater. Chem., 2011,21, 16413-16419
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    Sunlight-driven plasmonic photocatalysts based on Ag/AgCl nanostructures synthesized via an oil-in-water medium: enhanced catalytic performance by morphology selection

    M. Zhu, P. Chen and M. Liu, J. Mater. Chem., 2011, 21, 16413
    DOI: 10.1039/C1JM13326H

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