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新型三元 CuO/gCN/BiO 光催化剂的结构性能和催化活性。

Structural properties and catalytic activity of a novel ternary CuO/gCN/BiO photocatalyst.

机构信息

Division of Computational Physics, Institute for Computational Science, Ton Duc Thang University, Ho Chi Minh City 70000, Viet Nam; Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City 70000, Viet Nam.

Department of Environmental and Renewable Energy Systems, Graduate School of Engineering, Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.

出版信息

J Colloid Interface Sci. 2018 Aug 15;524:227-235. doi: 10.1016/j.jcis.2018.04.020. Epub 2018 Apr 6.

Abstract

In the present study, CuO/gCN/BiO composite is constructed as a ternary visible light active photocatalyst. Since CuO plays a critical role in enhancing the photocatalytic activity of the formed composite, its structural properties are particularly studied using synchrotron X-ray absorption spectroscopy (XAS), including X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS). XANES confirms the presence of Cu species with +2 oxidation state in the form of CuO. EXAFS furthermore confirms that each Cu cation is coordinated to four O anions in an approximately square planar configuration. The length of the Cu-O coordination is estimated to be 1.92 Å, slightly shorter than that of bulk CuO (1.95 Å). The CuO/gCN/BiO composite exhibits highly enhanced photocatalytic activity in the 2,4-dichlorophenol decomposition under visible light. The enhanced photocatalytic activity is due to the increased population of electrons and the successful consumption of the photoproduced electrons by the dissolved oxygen through the one-electron transfer reaction.

摘要

在本研究中,构建了 CuO/gCN/BiO 复合物作为一种三元可见光活性光催化剂。由于 CuO 在提高形成的复合材料的光催化活性方面起着关键作用,因此使用同步加速器 X 射线吸收光谱(XAS),包括 X 射线吸收近边结构(XANES)和扩展 X 射线吸收精细结构(EXAFS)对其结构特性进行了特别研究。XANES 证实了以 CuO 形式存在的+2 氧化态的 Cu 物种。EXAFS 进一步证实,每个 Cu 阳离子以近似平面正方形的构型与四个 O 阴离子配位。Cu-O 配位的长度估计为 1.92Å,略短于体相 CuO(1.95Å)。CuO/gCN/BiO 复合物在可见光下 2,4-二氯苯酚分解中表现出高度增强的光催化活性。增强的光催化活性归因于电子密度的增加,以及通过单电子转移反应成功地用光产生的电子消耗溶解氧。

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