4.5 Article

Modified surficial chemistry micro-circumstance and mid-gap effect on photocatalytic ability of tetracycline by introducing of nitrogen in Fe2(MoO4)3

期刊

MOLECULAR CATALYSIS
卷 434, 期 -, 页码 106-115

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.mcat.2017.02.034

关键词

Photocatalytic; Nitrogen-doped Fe-2(MoO4)(3); Oxygen vacancy; Tetracyclines

资金

  1. Project of the National Natural Science Foundation of China [21271022]

向作者/读者索取更多资源

A novel non-metal doped Fe-2(MoO4)(3) photocatalyst with flower-like microstructure was synthesized by a hydrothermal method. The incorporation location of nitrogen was proved by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). UV-Vis diffuse reflectance spectroscopy (DRS) revealed mid-gap from the dope of nitrogen strongly enhanced the visible-light absorption ability. Scanning electron microscopy (SEM) showed that the morphology of dbped samples was greatly influenced by nitrogen dopant. Significantly, N-doped Fe-2(MoO4)(3) exhibits an ideal tetracycline (TC) photocatalytic ability, which can be a potential function material for antibiotics degradation. Photoluminescence (PL) and photocurrent indicated that constract of oxygen vacancy, which modified the surficial chemistry micro-circumstance, greatly depressed the recombination rate of the photo-generated electron-hole pairs. In order to investigate the possible mechanism of promoted TC degradation efficiency, radical trapping experiments of pure Fe-2(MoO4)(3) and N-doped samples were examined. It was found that superoxide radicals (center dot O-2(-)) and hydroxyl radical (center dot OH) formed in the visible light excitation process play an important role in the fragmentation reaction. Moreover, the possible ring-opening intermediates were deduced and a reasonable enhancement mechanism of N-doped Fe-2(MoO4)(3) TC degradation was also investigated in this study. This investigation could provide an effective reference for doping non-metallic species for improving the photocatalytic activity of Fe-2(MoO4)(3). (C) 2017 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据