Short communicationGraphitic carbon nitride nanocrystals decorated AgVO3 nanowires with enhanced visible-light photocatalytic activity
Graphical abstract
Introduction
The development of visible-light-driven photocatalysts with excellent performance and good stability is a prerequisite for harvesting more sunlight and realizing efficient photocatalysis [1], [2]. AgVO3 has been demonstrated to be an efficient visible photocatalyst, due to its narrow band gap and well crystallization [3]. However, poor quantum yield and poor visible light absorption efficiency are still challenges to improve the photocatalytic performance of AgVO3 for meeting the practical application requirements. To solve this issue, great effort has been devoted to the exploration and preparation of novel photocatalytic materials for improving photocatalytic performance of the catalysts [3], [4], [5], including dye-sensitization [5], [6], [7], development of new narrow-band gap semiconductors and band engineering of semiconductor heterojunction [8], [9], [10], [11], [12]. Among these works, the construction of a semiconductor heterojunction has attracted great attention because of its perfect effectiveness in improving photocatalytic activity [13], [14], [15], [16], [17].
Recently, graphitic carbon nitride (g-C3N4) as a metal-free polymeric semiconductor has attracted much attention [18]. In this context, it would be of great significance to develop g-C3N4 based materials for photocatalysis application. Recently, there are a few reports concentrated on g-C3N4 based photocatalysts, such as g-C3N4 quantum dots/g-C3N4, g-C3N4/graphene, g-C3N4/BiPO4, and g-C3N4/TiO2 [19], [20], [21], [22]. Herein, we report a successful attempt at the fabrication of g-C3N4/AgVO3 nanowires via a facile in situ precipitation method, and the photocatalytic activity of the nanoheterostructures was investigated by measuring the degradation of rhodamine B (Rh B) under visible light (λ > 420 nm).
Section snippets
Preparation of g-C3N4 nanocrystals
Bulk g-C3N4 was prepared by heating melamine for 4 h to 550 °C and kept at this temperature for another 4 h in air [19]. The g-C3N4 nanocrystals were prepared by using the Yu method [19]: First, 1 g of bulk g-C3N4 was treated in the mixture of concentrated sulfuric acid (H2SO4) (20 mL) and nitric acid (HNO3) (20 mL) for about 2 h at room temperature. The mixture was then diluted with deionized water (1 L) and washed for several times. Second, 50 mg of the obtained solid was dispersed in 30 mL
Results and discussion
Fig. 1 shows the XRD patterns of the as-prepared AgVO3, g-C3N4, and g-C3N4 (2%)/AgVO3 samples. The diffraction peaks for the AgVO3 sample are well indexed to monoclinic structure of β-AgVO3 (JCPDS: 29-1154) [3]. When coupling the two compounds, the main characteristic diffraction peaks of AgVO3 did not change obviously. In addition, there is no any diffraction peaks of g-C3N4 can be detected for g-C3N4/AgVO3 sample, which may be resulted from small crystal size or low percentage of g-C3N4
Conclusions
High-efficiency visible-light-driven g-C3N4/AgVO3 photocatalyst was successfully synthesized. The as-prepared g-C3N4/AgVO3 nanowires exhibited excellent photocatalytic efficiency on the decolorization of Rh B, which was superior to those of pure g-C3N4 and AgVO3. The enhanced photocatalytic activity of the g-C3N4/AgVO3 may originate from the efficient separation of photogenerated electron–hole pairs through the heterostructure composed of g-C3N4 and AgVO3.
Acknowledgment
This work was supported by the National Natural Science Foundation of China (21407059, 21576112, 51404108, 61308095), the Science Development Project of Jiangsu Province (BK20140527), and Science and Technology Research Project of the Department of Education of Jilin Province (2015220).
References (28)
- et al.
Chem. Eng. J.
(2012) - et al.
Appl. Catal. B Environ.
(2004) - et al.
Sep. Purif. Technol.
(2013) - et al.
Appl. Catal. B Environ.
(2015) - et al.
Mater. Lett.
(2014) - et al.
Appl. Catal. B Environ.
(2016) - et al.
Catal. Comm.
(2015) - et al.
Adv. Mater.
(2012) - et al.
Am. Chem. Soc.
(2006) - et al.
J. Mater. Chem. A
(2013)
Chem. Soc. Rev.
Energy Environ. Sci.
Energy Environ. Sci.
Chem. Soc. Rev.
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