Issue 47, 2013

Natural leaves-assisted synthesis of nitrogen-doped, carbon-rich nanodots-sensitized, Ag-loaded anatase TiO2 square nanosheets with dominant {001} facets and their enhanced catalytic applications

Abstract

Extending the UV response of anatase TiO2 photocatalysts into the visible light range can play a pivotal role in promoting the practical applications of these catalysts. Nitrogen and carbon co-doped, silver loaded anatase TiO2 (Ag@NC–TiO2) single-crystal nanosheets dominated by {001} facets were prepared for the first time using leaves as the nitrogen and carbon source by a facile, low cost method. The size of the Ag particles on NC–TiO2 nanosheets can be tuned from 1.5 nm to 15 nm using a photo-reduction strategy. The synthesized Ag@NC–TiO2 nanosheets show higher photocatalytic activity in the photodecomposition of organic pollutants compared to NC–TiO2, TiO2 and P25 under visible light irradiation. The enhanced photocatalytic efficiency was ascribed to a synergistic effect between N, C and Ag. In addition, the formed Ag@NC–TiO2 heteronanosheets are highly dispersible in aqueous solution and are capable of efficient catalysis for the reduction of p-nitrophenol. The present synthesis gives a promising method of forming non-metal co-doped, metal nanoparticles (NPs) loaded anatase TiO2 with dominant {001} facets and for broad applications in catalysis and photocatalysis.

Graphical abstract: Natural leaves-assisted synthesis of nitrogen-doped, carbon-rich nanodots-sensitized, Ag-loaded anatase TiO2 square nanosheets with dominant {001} facets and their enhanced catalytic applications

Supplementary files

Article information

Article type
Paper
Submitted
16 Aug 2013
Accepted
03 Oct 2013
First published
03 Oct 2013

J. Mater. Chem. A, 2013,1, 14963-14972

Natural leaves-assisted synthesis of nitrogen-doped, carbon-rich nanodots-sensitized, Ag-loaded anatase TiO2 square nanosheets with dominant {001} facets and their enhanced catalytic applications

Z. Jiang, X. Lv, D. Jiang, J. Xie and D. Mao, J. Mater. Chem. A, 2013, 1, 14963 DOI: 10.1039/C3TA13248J

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