光催化
吸附
材料科学
复合材料
异质结
电子顺磁共振
猝灭(荧光)
化学工程
比表面积
金属
电子转移
降级(电信)
光化学
化学
催化作用
有机化学
冶金
工程类
物理
计算机科学
荧光
电信
量子力学
光电子学
核磁共振
作者
Qingsong Hu,Yong Chen,Ming Li,Yi Zhang,Bin Wang,Yaping Zhao,Jiexiang Xia,Sheng Yin,Huaming Li
标识
DOI:10.1016/j.colsurfa.2019.123625
摘要
Abstract Metal-organic framework (MOF) have gained significant interest for photocatalysis, mainly due to the advantages of the regulable semiconducting characteristics and tunable porous structure. In this work, a novel heterojunction of NH2-UiO-66/BiOBr composites were successfully synthesized via the growth of BiOBr nanosheets on the surface of these NH2-UiO-66 octahedrons. The as-prepared composites showed a large interface contact area, which ensured preferable charge carriers transfer between NH2-UiO-66 and BiOBr. In addition, the increased specific surface area endowed NH2-UiO-66/BiOBr composites with high adsorption capacity for contaminants. As a consequence, the composites displayed enhanced photocatalytic performance for tetracycline hydrochloride (TC) degradation and Cr(VI) reduction in comparison with BiOBr or NH2-UiO-66, and the ideal NH2-UiO-66 content was around 15 wt%. Superoxide radical (O2 −) and holes (h+) acted as a key role in the degradation of TC, while electrons (e−) and O2 − were the major active groups involved in Cr(VI) reduction owing to reactive-species-quenching experiments and electron spin resonance (ESR) technique. Furthermore, a possible TC degradation pathway was explored based on the mass spectroscopy (MS) analysis. The introduction of MOF into inorganic photocatalysts exhibits a promising strategy to enhance the photoreactivity of the catalysts in the field of water purification.
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