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首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >One-pot controllable synthesis of BiOBr/beta-Bi2O3 nanocomposites with enhanced photocatalytic degradation of norfloxacin under simulated solar irradiation
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One-pot controllable synthesis of BiOBr/beta-Bi2O3 nanocomposites with enhanced photocatalytic degradation of norfloxacin under simulated solar irradiation

机译:BioBR /β-Bi2O3纳米复合材料的一锅可控合成,模拟太阳辐照下诺氟沙星的光催化降解增强

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The low quantum yield and weak catalytic ability of bismuth oxyhalides retard their applications in photocatalytic degradation. To promote the performances of bismuth oxyhalides in photodegradation of antibiotics, a series of BiOBr/beta-Bi2O3 nanocomposites was synthesized via a facile solvothermal process in which one-pot strategy was adopted to accomplish the purpose by adjusting the mole ratio of the bismuth and bromine. The formation of heterojunction at the BiOBr/beta-Bi2O3 surface boundary was confirmed by XRD, PL, DRS, XPS and HR-TEM. The photocatalytic properties of these BiOBr/beta-Bi2O3 nanocomposites were evaluated by the photodegradation of norfloxacin under simulated sunlight irradiation. The BiOBr/beta-Bi2O3 nanocomposites obtained at the molar ratio of 3:1 (Bi:Br) exhibit the best photodegradation activity. The photocurrent density of BiOBr/beta-Bi(2)O(3 )nanocomposites (Bi:Br = 3:1) is twice higher than that of the pristine BiOBr, indicating the in-situ generating Bi2O3 on the BiOBr surface can effectively promote the separation of photogenerated electron-hole pairs and thus improving the photocatalytic performance. Furthermore, the photocatalytic mechanism was investigated using trapping experiments and ESR study. The results reveal that the matched energy band structure between BiOBr and Bi2O3 was able to facilitate the charge transfer and reduce the recombination of the photogenerated carriers. This work supplies a simple procedure for the in-situ growing Bi2O3 on Bi-based photocatalysts and an effective measurement for degrading norfloxacin. (C) 2019 Published by Elsevier B.V.
机译:氧化铋的低量子产率和弱催化能力延迟了它们在光催化降解中的应用。为了促进氧化铋的性能在抗生素的光降解中,通过体面的溶剂热法合成一系列BioBR /β-Bi2O3纳米复合材料,其中采用单锅策略来调节铋和溴的摩尔比来实现目的。通过XRD,PL,DRS,XPS和HR-TEM确认BioBR / Beta-Bi2O3表面边界中的异质结的形成。通过在模拟阳光照射下的光降解,评价这些BIOBR /β-BI2O3纳米复合材料的光催化性能。以摩尔比为3:1(Bi:Br)的BioBR /β-Bi2O3纳米复合材料表现出最佳的光降解活性。 BioBR / Beta-Bi(2)O(3)纳米复合材料(Bi:Br = 3:1)的光电流密度比原始BioBR的两倍高,指示BioBR表面上的原位生成Bi2O3可以有效地促进光静电电子 - 空穴对的分离,从而改善光催化性能。此外,使用诱捕实验和ESR研究研究了光催化机制。结果表明,BioBR和Bi2O3之间的匹配能带结构能够促进电荷转移并减少光源载体的重组。这项工作为BI基光催化剂的原位生长BI2O3提供了一种简单的过程,以及降解NORFLOXACIN的有效测量。 (c)2019年由elestvier b.v发布。

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