In-Situ Fabrication of g-C₃N₄/ZnO Nanocomposites for Photocatalytic Degradation of Methylene Blue: Synthesis Procedure Does Matter

• Published in: Nanomaterials (Basel, Switzerland) Vol. 9; no. 2; p. 215
• Main Authors: Zhang, Shengqiang, Su, Changsheng, Ren, Hang, Li, Mengli, Zhu, Longfeng, Ge, Shuang, Wang, Min, Zhang, Zulei, Li, Lei, Cao, Xuebo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 06.02.2019; MDPI AG
• Subjects: dye photodegradation; graphitic carbon nitride; in situ synthesis; nanocomposites; ZnO nanorods; ZnO nanorods; in situ synthesis; nanocomposites; dye photodegradation; graphitic carbon nitride
• ISSN: 2079-4991; 2079-4991
• DOI: 10.3390/nano9020215

The nanocomposite preparation procedure plays an important role in achieving a well-established heterostructured junction, and hence, an optimized photocatalytic activity. In this study, a series of g-C₃N₄/ZnO nanocomposites were prepared through two distinct procedures of a low-cost, environmentally-friendly, in-situ fabrication process, with urea and zinc acetate being the only precursor materials. The physicochemical properties of synthesized g-C₃N₄/ZnO composites were mainly characterized by XRD, UV⁻VIS diffuse reflectance spectroscopy (DRS), N₂ adsorption-desorption, FTIR, TEM, and SEM. These nanocomposites' photocatalytic properties were evaluated in methylene blue (MB) dye photodecomposition under UV and sunlight irradiation. Interestingly, compared with ZnO nanorods, g-C₃N₄/ZnO nanocomposites ( :1, obtained from urea and ZnO nanorods) exhibited weak photocatalytic activity likely due to a "shading effect", while nanocomposites ( :1 CN, made from g-C₃N₄ and zinc acetate) showed enhanced photocatalytic activity that can be ascribed to the effective establishment of heterojunctions. A kinetics study showed that a maximum reaction rate constant of 0.1862 min can be achieved under solar light illumination, which is three times higher than that of bare ZnO nanorods. The photocatalytic mechanism was revealed by determining reactive species through adding a series of scavengers. It suggested that reactive ∙O₂ and h⁺ radicals played a major role in promoting dye photodegradation.