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Ce3+ self-doped CeOx/FeOCl: an efficient Fenton catalyst for phenol degradation under mild conditions†
Dalton Transactions ( IF 3.5 ) Pub Date : 2019-02-11 00:00:00 , DOI: 10.1039/c8dt04269a
Jian Zhang 1, 2, 3, 4 , Mengxue Yang 1, 2, 3, 4 , Ye Lian 1, 2, 3, 4 , Mingliang Zhong 1, 2, 3, 4 , Jingquan Sha 1, 2, 3, 4 , Guodong Liu 1, 2, 3, 4 , Xinfu Zhao 5, 6, 7, 8, 9 , Shaojie Liu 8, 9, 10, 11
Affiliation  

Herein, a novel Ce3+ self-doped CeOx/FeOCl composite was successfully prepared by a facile method for the first time, which showed remarkable catalytic activity as a Fenton catalyst in the degradation of phenol under the conditions of a neutral solution, room temperature and natural light. In CeOx/FeOCl, 5.23% CeOx is the optimal condition, and the degradation constant (k) of CeOx/FeOCl is greater than that of FeOCl by a factor of 10.8. CeOCl in the composite plays a more important role than CeO2, which greatly increases the production of ˙OH radicals. Furthermore, the Ce-doping in FeOCl accelerates the separation efficiency of the photogenerated electron–hole pairs. The increased surface area and surface potential of CeOx/FeOCl than those of FeOCl effectively promote the adsorption of phenol, which is 4.05 times that of FeOCl. According to the DFT calculations, the Ce-doping in FeOCl enhances the structural stability by increasing the strength of the chemical bonds. The adsorption of H2O2 with Ce3+ is energetically favorable, which promotes the production of ˙OH radicals. A synergistic mechanism for the enhanced catalytic performance of CeOx/FeOCl is proposed.

中文翻译:

Ce 3+自掺杂CeO x / FeOCl:在温和条件下用于苯酚降解的高效Fenton催化剂

本文首次通过一种简便的方法成功制备了一种新型的Ce 3+自掺杂CeO x / FeOCl复合材料,在中性溶液,室温条件下,该化合物作为Fenton催化剂对苯酚的降解具有显着的催化活性。温度和自然光。在CeO x / FeOCl中,最佳条件为5.23%CeO x,并且CeO x / FeOCl的降解常数(k)比FeOCl大10.8倍。CeOCl在复合材料中的作用比CeO 2更重要,大大增加了˙OH自由基的产生。此外,FeOCl中的Ce掺杂可加速光生电子-空穴对的分离效率。CeO x / FeOCl比FeOCl增加的表面积和表面电势有效地促进了苯酚的吸附,这是FeOCl的4.05倍。根据DFT计算,FeOCl中的Ce掺杂通过增加化学键的强度来增强结构稳定性。H的吸附2 ö 2被Ce 3+是积极有利的,这促进了生产OH自由基。提出了增强CeO x / FeOCl催化性能的协同机理。
更新日期:2019-02-11
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