Cross‐Linked g‐C3N4/rGO Nanocomposites with Tunable Band Structure and Enhanced Visible Light Photocatalytic Activity

纳米复合材料 光催化 石墨烯 材料科学 罗丹明B X射线光电子能谱 氧化物 石墨氮化碳 化学工程 傅里叶变换红外光谱 可见光谱 光化学 纳米技术 化学 有机化学 催化作用 光电子学 冶金 工程类
作者
Yibing Li,Haimin Zhang,Porun Liu,Dan Wang,Ying Li,Huijun Zhao
出处
期刊:Small [Wiley]
卷期号:9 (19): 3336-3344 被引量:618
标识
DOI:10.1002/smll.201203135
摘要

Abstract Cross‐linked rather than non‐covalently bonded graphitic carbon nitride (g‐C 3 N 4 )/reduced graphene oxide (rGO) nanocomposites with tunable band structures have been successfully fabricated by thermal treatment of a mixture of cyanamide and graphene oxide with different weight ratios. The experimental results indicate that compared to pure g‐C 3 N 4 , the fabricated CN/rGO nanocomposites show narrowed bandgaps with an increased in the rGO ratio. Furthermore, the band structure of the CN/rGO nanocomposites can be readily tuned by simply controlling the weight ratio of the rGO. It is found that an appropriate rGO ratio in nanocomposite leads to a noticeable positively shifted valence band edge potential, meaning an increased oxidation power. The tunable band structure of the CN/rGO nanocomposites can be ascribed to the formation of C−O−C covalent bonding between the rGO and g‐C 3 N 4 layers, which is experimentally confirmed by Fourier transform infrared (FT‐IR) and X‐ray photoelectron (XPS) data. The resulting nanocomposites are evaluated as photocatalysts by photocatalytic degradation of rhodamine B (RhB) and 4‐nitrophenol under visible light irradiation (λ > 400 nm). The results demonstrate that the photocatalytic activities of the CN/rGO nanocomposites are strongly influenced by rGO ratio. With a rGO ratio of 2.5%, the CN/rGO‐2.5% nanocomposite exhibits the highest photocatalytic efficiency, which is almost 3.0 and 2.7 times that of pure g‐C 3 N 4 toward photocatalytic degradation of RhB and 4‐nitrophenol, respectively. This improved photocatalytic activity could be attributed to the improved visible light utilization, oxidation power, and electron transport property, due to the significantly narrowed bandgap, positively shifted valence band‐edge potential, and enhanced electronic conductivity.
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