Preparation and activity evaluation of B4C/ZnO composite photocatalyst

光催化 材料科学 傅里叶变换红外光谱 复合数 扫描电子显微镜 核化学 可见光谱 漫反射红外傅里叶变换 光化学 亚甲蓝 降级(电信) 化学工程 复合材料 催化作用 化学 有机化学 光电子学 工程类 电信 计算机科学
作者
Özcan Köysüren,Hafize Nagehan Köysüren
出处
期刊:Journal of Sol-Gel Science and Technology [Springer Nature]
卷期号:103 (1): 172-184 被引量:11
标识
DOI:10.1007/s10971-022-05797-x
摘要

In this study, B4C/ZnO composite photocatalysts were obtained by the heat treatment of polyvinyl borate composite, synthesized using the crosslinking reaction of polyvinyl alcohol and boric acid in the presence of ZnO nanoparticles. The photocatalytic activity of B4C/ZnO was evaluated by photocatalytic degradation of a model dye, methylene blue. The relationship between the photocatalytic degradation of methylene blue and the temperature of the reaction medium, and the pH of the reaction medium was also studied. The structural and optical properties of B4C/ZnO photocatalyst were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD) analysis, fluorescence spectroscopy, scanning electron microscopy (SEM), and UV–Vis absorption spectroscopy. The B4C and B4C/ZnO composite nanoparticles were synthesized successfully, which was proven by the FTIR, XRD, and SEM analyses. The photocatalytic degradation experiments illustrated that the photocatalytic activity of the composite photocatalysts was higher than that of B4C on the photocatalytic degradation of the model dye. The heterojunction structure formed between ZnO and B4C might have decreased the recombination rate, which was determined by the fluorescence spectroscopy. The B4C/ZnO composites possessed wider optical bandgap compared to pure B4C, which was determined by Tauc’s plot analysis. When compared with pure B4C, approximately three times faster degradation rate was obtained by the B4C/ZnO composite. After four cycles of the photocatalytic degradation experiments, approximately 26% loss in the photocatalytic degradation efficiency was observed. Based on the scavenger experiments to reveal the photocatalytic degradation mechanism, the photoinduced holes, the superoxide radicals, and the hydroxyl radicals were the main active species for the degradation of methylene blue. Graphical abstract

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