| JOURNAL OF COLLOID AND INTERFACE SCIENCE | 卷:459 |
| Poly(vinyl pyrrolidone)-assisted hydrothermal synthesis and enhanced visible-light photocatalytic performance of oxygen-rich bismuth oxychlorides | |
| Article | |
| Chang, Fei1  Luo, Jieru1  Wang, Xiaofang1  Xie, Yunchao1  Deng, Baoqing1  Hu, Xuefeng2  | |
| [1] Univ Shanghai Sci & Technol, Sch Environm & Architecture, Shanghai 200093, Peoples R China | |
| [2] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Environm Proc & Ecol Remediat, Yantai 264003, Shandong, Peoples R China | |
| 关键词: Bi12O17Cl2; Poly(vinyl pyrrolidone); Photocatalysis; Rhodamine B; 2,4-Dichlorophenol; Mechanism; | |
| DOI : 10.1016/j.jcis.2015.08.023 | |
| 来源: Elsevier | |
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【 摘 要 】
A series of novel oxygen-rich bismuth oxychloride (Bi12O17Cl2) were synthesized through a facile poly (vinyl pyrrolidone) (PVP)-assisted hydrothermal route. These obtained Bi12O17Cl2 samples were characterized by various physicochemical techniques. It was found that a proper addition amount of PVP could promote the transformation of Bi12O17Cl2 morphology from irregular clusters to three-dimensional hierarchical flower-like microspheres that were nominated as sample BP2. As-synthesized samples were subjected to a photocatalytic degradation of dye Rhodamine B (RhB) or 2,4-dichlorophenol (2,4-DCP) under visible light. Among all candidates, the sample BP2 with a hierarchical flower-like morphology showed the best degradation efficiency for RhB and 2,4-DCP. The apparent rate constant of sample BP2 in terms of degradation of RhB was nearly 5.7 and 45 times that of unmodified BP0 and N-TiO2. The enhanced photocatalytic performance could be ascribed to synergetic effects including unique hierarchical morphologies, large specific surface area, small particle size, good crystallinity, and suitable band structures. A possible mechanism of catalytic degradation was finally proposed basing upon the active species trapping experiments. (C) 2015 Elsevier Inc. All rights reserved.
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| 10_1016_j_jcis_2015_08_023.pdf | 3347KB |
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