Construction of BiVO4@ NiCo2O3 Heterojunction to Promote Photocatalytic CO2 Reduction

IF 3 4区 化学 Q3 CHEMISTRY, PHYSICAL ChemPhotoChem Pub Date : 2024-06-26 DOI:10.1002/cptc.202400152
Wenjie Fu, Guanhong Lu, Dr. Xiao Wang, Prof. Xiaofeng Xie, Prof. Jing Sun
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Abstract

Constructing a catalyst capable of reducing CO2 through photoreduction in aqueous environments presents a significant challenge. In this study, we present the synthesis of BiVO4@NiCo2O3 heterojunction using a straightforward hydrothermal method for CO2 photoreduction. The sample with the optimal loading ratio demonstrates a CO generation rate of 7.202 μmol ⋅ g−1 ⋅ h−1, which is twice that of pure BiVO4 (3.626 μmol ⋅ g−1 ⋅ h−1) and 1.5 times that of pure NiCo2O3 (4.726 μmol ⋅ g−1 ⋅ h−1). Analysis using XPS and EPR techniques suggests that electron transfer at the interface of the heterojunction facilitates the separation of photogenerated charge carriers, thereby enhancing the efficiency of the photocatalytic process. This investigation offers a viable approach for developing photocatalysts for CO2 reduction in aqueous environments.

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构建 BiVO4@ NiCo2O3 异质结以促进光催化还原二氧化碳
构建一种能够在水环境中通过光还原作用还原二氧化碳的催化剂是一项重大挑战。在本研究中,我们采用直接的水热法合成了 BiVO4@NiCo2O3 异质结,用于 CO2 光还原。具有最佳负载率的样品的 CO 生成率为 7.202 μmol-g-1-h-1,是原始 BiVO4(3.626 μmol-g-1-h-1)的两倍,纯 NiCo2O3(4.726 μmol-g-1-h-1)的 1.5 倍。利用 XPS 和 EPR 技术进行的分析表明,异质结界面上的电子转移促进了光生电荷载流子的分离,从而提高了光催化过程的效率。这项研究为开发用于在水环境中还原二氧化碳的光催化剂提供了一种可行的方法。
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ChemPhotoChem
ChemPhotoChem Chemistry-Physical and Theoretical Chemistry
CiteScore
5.80
自引率
5.40%
发文量
165
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