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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >Dual visible-light active components containing self-doped Bi2O2CO3/g-C3N4 2D-2D heterojunction with enhanced visible-light-driven photocatalytic activity
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Dual visible-light active components containing self-doped Bi2O2CO3/g-C3N4 2D-2D heterojunction with enhanced visible-light-driven photocatalytic activity

机译:包含自掺杂Bi2O2CO3 / g-C3N4 2D-2D异质结的双可见光活性组分,具有增强的可见光驱动的光催化活性

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摘要

The (CO3)(2-)self-doped Bi2O2CO3/g-C3N4 (C-BOC/g-C3N4) unique 2D-2D heterostructure has been developed via a mixed-calcination method. This heterostructure is confirmed by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), SEM-mapping, and diffuse reflection spectroscopy (DRS). Due to the charge interaction, it is interesting to observe that C-BOC nanosheets are assembled on g-C3N4 in a surface-surface coupling way, which enables an intimate interfacial interaction between the two components. The photocatalytic activity is evaluated by photodegradation of Rhodamine B (RhB) under visible light (lambda>420nm). It is found that all the C-BOC/g-C3N4 composites showed highly enhanced photocatalytic activity. Electrochemical impedance spectra (EIS) measurement revealed that the largely promoted charge transfer derived from the well matchable band structure and intimate interfacial interactions between the two visible-light active components is responsible for the photoactivity enhancement. Besides, the active species trapping and center dot O(2)(-)quantitation experiments are conducted to disclose the photocatalytic mechanism. (C) 2016 Elsevier B.V. All rights reserved.
机译:(CO3)(2-)自掺杂Bi2O2CO3 / g-C3N4(C-BOC / g-C3N4)独特的2D-2D异质结构是通过混合煅烧方法开发的。通过X射线衍射(XRD),傅里叶变换红外光谱(FTIR),X射线光电子光谱(XPS),扫描电子显微镜(SEM),SEM映射和漫反射光谱(DRS)确认了这种异质结构。由于电荷相互作用,有趣的是观察到C-BOC纳米片以表面-表面耦合的方式组装在g-C3N4上,这使得两个组件之间可以进行紧密的界面相互作用。通过在可见光(λ> 420nm)下若丹明B(RhB)的光降解来评价光催化活性。发现所有的C-BOC / g-C3N4复合材料都表现出高度增强的光催化活性。电化学阻抗谱(EIS)测量表明,由良好匹配的能带结构和两个可见光活性组分之间的紧密界面相互作用所引起的电荷转移大大促进了光活性的提高。此外,进行了活性物种捕获和中心点O(2)(-)定量实验以揭示光催化机理。 (C)2016 Elsevier B.V.保留所有权利。

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