In-Situ Synthesis of CQDs/BiOBr Material via Mechanical Ball Milling with Enhanced Photocatalytic Performances

被引:0
|
作者
Xingwang Yan [1 ]
Bin Wang [1 ]
Mengxia Ji [1 ]
Qi Jiang [1 ]
Gaopeng Liu [1 ]
Pengjun Liu [2 ]
Sheng Yin [1 ]
Huaming Li [1 ]
Jiexiang Xia [1 ]
机构
[1] School of Chemistry and Chemical Engineering, Institute for Energy Research, Jiangsu University
[2] Key Laboratory of Medicinal and Edible Plants Resources of Hainan Province, Hainan Vocational University of Science and Technology
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
D O I
10.14102/j.cnki.0254-5861.2022-0141
中图分类号
O643.36 [催化剂]; O644.1 [光化学]; X703 [废水的处理与利用];
学科分类号
摘要
Designing simple, efficient, and environmentally friendly methods to construct high-efficient photocatalysts is an important strategy to promote the further development of the field of photocatalysis. Herein, flower-like carbon quantum dots(CQDs)/Bi OBr composite photocatalysts have been prepared via in-situ synthesis by mechanical ball milling in the existence of ionic liquid. The CQDs/Bi OBr composites exhibit higher photo-degradation performance for tetracycline(TC) than Bi OBr monomer and the commercial Bi2O3under visible light irradiation. For comparison, the different Br sources and synthetic methods are chosen to prepare Bi OBr and CQDs/Bi OBr composites. Photocatalysts prepared by ball milling and ionic liquid present significantly enhanced photocatalytic performance for removing TC. In addition, the introduction of CQDs could distinctly enhance the photocatalytic performances of pure Bi OBr. The reason is that CQDs as electron acceptor effectively separate electrons and holes and inhibit their recombination. The intermediates during photocatalytic degradation were tested using liquid chromatography-mass spectrometry(LC-MS) and possible degradation pathways were given. During degradation, ·OH, O2·-and h~+ were identified to be the main active species based on electron spin resonance(ESR) spectra and free radical trapping experiments. A possible mechanism of CQDs/Bi OBr with enhanced photocatalytic performances was further proposed.
引用
收藏
页码:44 / 51
页数:8
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