4.7 Article

In situ loading of Ag2WO4 on ultrathin g-C3N4 nanosheets with highly enhanced photocatalytic performance

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 313, Issue -, Pages 219-228

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhazmat.2016.04.011

Keywords

Photocatalysis; Heterojunction; Nanosheets; g-C3N4; Composite materials

Funding

  1. National Natural Science Foundation of China [21473027]
  2. Jilin Provincial Key Laboratory of Advanced Energy Materials (Northeast Normal University)
  3. project development plan of science and technology of Jilin Province [20140101110JC]
  4. Research Fund for the Doctoral Program of Higher Education of China [20120043110005]
  5. Opening Fund of State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences

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The g-C3N4 nanosheets (g-C3N4-NS) exhibit more excellent property than common bulk g-C3N4 (g-C3N4-B) due to their large surface areas, improved electron transport ability and well dispersion in water. In this work, ultrathin g-C3N4-NS with a thickness of about 2.7 nm have been synthesized by a simple thermal exfoliation of bulk g-C3N4, and then Ag2WO4 nanoparticles are in situ loaded on their surface to construct the Ag2WO4/g-C3N4-NS heterostructured photocatalysts. Due to their unique physicochemical properties, the as-prepared heterostructures possess a fast interfacial charge transfer and increased lifetime of photo-excited charge carriers, and exhibit much higher photocatalytic activity. Under visible light irradiation, the optimum photocatalytic activity of Ag2WO4/g-C3N4-NS composites is almost 53.6 and 26.5 times higher than that of pure g-C3N4-B and Ag2WO4/g-C3N4-B heterostructures towards the degradation of rhodamine B, respectively, and is almost 30.6 and 9.8 times higher towards the degradation of methyl orange, respectively. In addition, the natural sunlight photocatalytic activities of the as-prepared samples are also investigated. (C) 2016 Elsevier B.V. All rights reserved.

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