Visible light photocatalytic degradation of MB using UiO-66/g-C3N4 heterojunction nanocatalyst

光催化 降级(电信) 异质结 材料科学 光化学 可见光谱 化学工程 催化作用 化学 计算机科学 有机化学 电信 光电子学 工程类
作者
Ying Zhang,Jiabin Zhou,Qinqin Feng,Xin Chen,Zeshu Hu
出处
期刊:Chemosphere [Elsevier BV]
卷期号:212: 523-532 被引量:197
标识
DOI:10.1016/j.chemosphere.2018.08.117
摘要

A unique hybrid of Zr-based metal-organic framework (UiO-66) with graphitic carbon nitride (g-C3N4) nanosheets was synthesized by a facile annealing method. Photocatalytic effect was measured by the photodegradation of methylene blue (MB) under visible light irradiation. The morphology, structure, and porous properties of the as-synthesized composites were characterized by using transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), the thermogravimetric and differential scanning calorimetry analysis (TG-DSC), diffuse reflectance UV–vis spectroscopy (UV–vis DRS), photoluminescence (PL), and N2 sorption-desorption isotherms (BET). The results showed that about 100% of MB (200 mL of 10 mg L−1) photodegradation was achieved by the UiO-66/g-C3N4 hybrids (UC 10:10) in 240 min under visible light. The enhanced photocatalytic activity could be attributed to the heterojunction between UiO-66 and g-C3N4 therefore the photoelectron transfers efficiently from the conduction band (CB) of g-C3N4 to the CB of UiO-66 through the inner electric field generated by the heterojunction resulting the decreasing of recombination of electron/hole and the porous structures which enhance adsorption of the dye molecules on the catalyst surface thereby facilitates the electron/hole transfer within the framework. The trapping experiment and electron spin resonance (ESR) results showed that superoxide radicals (•O2−) was the main oxidative species in the photodegradation of MB and the enhanced photocatalytic mechanism of UiO-66/g-C3N4 heterojunction hybrids was also proposed.
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