Issue 43, 2014

CO2-assisted synthesis of mesoporous carbon/C-doped ZnO composites for enhanced photocatalytic performance under visible light

Abstract

Visible-light-responsive mesoporous carbon/C-doped ZnO (mC/C-ZnO) composites were fabricated using a facile, fast, one-step process in CO2-expanded ethanol solution. It is a green and sustainable process that does not need tedious pretreatment, surfactants or precipitants. CO2 played triple roles in the synthesis of mC/C-ZnO composites; the first was to provide a simple physical expansion to evenly dope the carbon in the ZnO; the second was to offer some chemical groups such as CO32− and HCO3, facilitating the uniform and complete deposition through the coordination of a metallic cation with these anions; and the third was to offer CO32− acting as a template for the formation of mesoporosity in the carbon. When used as a photocatalyst for the photodegradation of RhB and the organic pollutant phenol, the mC/C-ZnO composites with glucose content at 22 wt% (mC/C-ZnO-CE-2) synthesized in CO2-expanded ethanol exhibited better recycling stability and photodegradation rate than the corresponding sample synthesized in pure ethanol. Such improved photocatalytic performance was attributed to the well-mixing of the mesoporous carbon and the small sized C-doped ZnO particles in the mC/C-ZnO-CE-2 composites. The facile and fast synthesis method could be extended to other mesoporous carbon/C-doped metal oxide composites, which are expected to be good photocatalyst candidates, or in other application fields.

Graphical abstract: CO2-assisted synthesis of mesoporous carbon/C-doped ZnO composites for enhanced photocatalytic performance under visible light

Article information

Article type
Paper
Submitted
10 Jul 2014
Accepted
06 Sep 2014
First published
08 Sep 2014

Dalton Trans., 2014,43, 16441-16449

CO2-assisted synthesis of mesoporous carbon/C-doped ZnO composites for enhanced photocatalytic performance under visible light

F. Wang, L. Liang, L. Shi, M. Liu and J. Sun, Dalton Trans., 2014, 43, 16441 DOI: 10.1039/C4DT02098G

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