Published October 2013 | Version v1
Journal article

Ag/AgBr/g-C3N4: A highly efficient and stable composite photocatalyst for degradation of organic contaminants under visible light

  • 1. State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China)
  • 2. College of Chemistry and Materials Science, Huaibei Normal University, Huaibei 235000, Anhui (China)

Description

Graphical abstract: Ag/AgBr/g-C3N4 composite photocatalysts displayed excellent photocatalytic activities on the degradation of methyl orange (MO) under visible light. The improved photocatalytic performance and stability of Ag/AgBr/g-C3N4 originated from the synergetic effects of AgBr/g-C3N4 interface and metallic Ag nanoparticles. ·O2−, one of the reactive species, was responsible for the photodegradation of MO compared to H+ and ·OH. - Highlights: • Novel Ag/AgBr/g-C3N4 composite photocatalyst was reported. • Ag/AgBr/g-C3N4 had novel energy band combination between AgBr and g-C3N4. • Synergetic effects of AgBr/g-C3N4 interface and metallic Ag nanoparticles. • Electron trapping role of metallic Ag dominated the stability of Ag/AgBr/g-C3N4. - Abstract: Novel Ag/AgBr/g-C3N4 composite photocatalysts were constructed via deposition–precipitation method and extensively characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and UV–vis diffuse reflectance spectroscopy (DRS). Under visible light (λ > 420 nm), Ag/AgBr/g-C3N4 composite photocatalysts displayed much higher photocatalytic activities than those of Ag/AgBr and g-C3N4 for degradation of methyl orange (MO). 50% Ag/AgBr/g-C3N4 presented the best photocatalytic performance, which was mainly attributed to the synergistic effects of AgBr/g-C3N4 interface and the in situ metallic Ag nanoparticles for efficiently separating electron–hole pairs. Furthermore, Ag/AgBr/g-C3N4 remained good photocatalytic activity through 5 times of cycle experiments. Additionally, the radical scavengers experiment indicated that ·O2− was the main reactive species for the MO degradation under visible light

Availability note (English)

Available from http://dx.doi.org/10.1016/j.materresbull.2013.05.120

Additional details

Identifiers

DOI
10.1016/j.materresbull.2013.05.120;
PII
S0025-5408(13)00518-7;

Publishing Information

Journal Title
Materials Research Bulletin
Journal Volume
48
Journal Issue
10
Journal Page Range
p. 3873-3880
ISSN
0025-5408
CODEN
MRBUAC

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.