光催化
X射线光电子能谱
可见光谱
材料科学
漫反射红外傅里叶变换
纳米复合材料
光化学
傅里叶变换红外光谱
透射电子显微镜
化学工程
化学
分析化学(期刊)
纳米技术
光电子学
催化作用
有机化学
工程类
作者
Shen Shen,Kunlin Chen,Hongbo Wang,Jiajia Fu
标识
DOI:10.1016/j.diamond.2022.108896
摘要
Element decomposition is a promising modification technique for enhancing the photocatalytic activity of TiO 2 . Firstly, (i) It may accelerate photogenerated electron–hole separation as electron traps, (ii) broaden the sunlight absorption region into the visible range and promote surface electron excitation by plasmon resonances excited under visible light and (iii) modify the surface performance of semiconductors. Herein, we describe the introduction of carbon dots (CDs) as solid-state electron mediator on TiO 2 sheets (TNs) via a highly effective hydrothermal process. The as-prepared CDs/TNs nanocomposites was measured by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, UV–visible diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy analysis. The results proved that CDs were firmly scattered in the TNs interface. Furthermore, the resultant CDs/TNs nanocomposites exhibited remarkable photocatalytic activity for the degradation of different model pollutants under visible light, which is considerably superior to that of bare TNs. The enhanced photocatalytic activity highlights that CDs can promote the separation and migration efficiency of photoexcited electron–hole pairs. The striking stability of CDs/TNs was investigated by performing five successive cycles of degradation of Congo red. Moreover, the degradation intermediates of three pollutants were monitored by liquid chromatography-tandem mass spectrometry, and potential removal pathways are proposed. We firmly believe that this work may inspire new insights and approaches for the design of highly efficient photocatalysts. • Ammonium citrate carbon dots were effectively grew on TiO 2 surface. • CR, RhB, and TC were removed quickly in Carbon dots/TiO 2 system (CDs/TNs) under visible light irradiation. • Most of decomposed hazardous fragments were converted to CO 2 , H 2 O, and small molecules, respectively. • Possible transformation mechanism of CR, RhB and TC in carbon dots/TiO 2 were proposed.
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