Eu-Bi12O17Cl2/Bi14W2O27 2D/0D heterojunction for efficient photocatalytic reduction of CO2 to CO

IF 5.8 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
Yi-Nan Zheng, Wen-Ze Liu, Shu-Yan Wang, Li-Guo Gao
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引用次数: 0

Abstract

In order to improve the utilisation of sunlight and expand the photoresponsive range of the photocatalyst, a visible light responsive 2D/0D binary heterojunction: Eu-Bi12O17Cl2/Bi14W2O27, was prepared in this paper by a controlled solvent-thermal method. The enhancement of photocatalytic activity originates from the following synergistic effects, including the unique 2D/0D contact interface, the enhancement of the photoresponsive range, and the introduction of the elemental Eu which makes the light-absorbing edge towards the visible light direction. The results of characterisation and photocatalysis experiments show that the 2D/0D catalyst has good spectral absorption range and redox capacity. In the experiments conducted with a xenon lamp as a simulated sunlight, the CO yield reached 44 μmol·g-1·h-1. The mechanism of electron transfer was analysed in conjunction with Density functional theory (DFT) calculations, laying the foundation for the subsequent development of photocatalysts in this field.
Eu-Bi12O17Cl2/Bi14W2O27 2D/0D 异质结用于将 CO2 高效光催化还原为 CO
为了提高对太阳光的利用率并扩大光催化剂的光致发光范围,本文采用可控溶剂热法制备了一种可见光响应型 2D/0D 二元异质结:Eu-Bi12O17Cl2/Bi14W2O27。光催化活性的增强源于以下协同效应,包括独特的 2D/0D 接触界面、光致发光范围的增强,以及 Eu 元素的引入使得光吸收边缘朝向可见光方向。表征和光催化实验结果表明,2D/0D 催化剂具有良好的光谱吸收范围和氧化还原能力。在用氙灯模拟太阳光进行的实验中,CO 产率达到 44 μmol-g-1-h-1。结合密度泛函理论(DFT)计算分析了电子转移的机理,为后续开发该领域的光催化剂奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
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