Jinlong Wang , Dongni Liu , Mingyang Li , Xiaoyi Gu , Shiqun Wu , Jinlong Zhang
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引用次数: 0
Abstract
The photoreduction of greenhouse gas CO2 using photocatalytic technologies not only benefits environmental remediation but also facilitates the production of raw materials for chemicals. However, the efficiency of CO2 photoreduction remains generally low due to the challenging activation of CO2 and the limited light absorption and separation of charge. Defect engineering of catalysts represents a pivotal strategy to enhance the photocatalytic activity for CO2, with most research on metal oxide catalysts focusing on the creation of anionic vacancies. The exploration of metal vacancies and their effects, however, is still underexplored. In this study, we prepared an In2O3 catalyst with indium vacancies (VIn) through defect engineering for CO2 photoreduction. Experimental and theoretical calculations results demonstrate that VIn not only facilitate light absorption and charge separation in the catalyst but also enhance CO2 adsorption and reduce the energy barrier for the formation of the key intermediate *COOH during CO2 reduction. Through metal vacancy engineering, the activity of the catalyst was 7.4 times, reaching an outstanding rate of 841.32 µmol g‒1 h‒1. This work unveils the mechanism of metal vacancies in CO2 photoreduction and provides theoretical guidance for the development of novel CO2 photoreduction catalysts.
利用光催化技术对温室气体二氧化碳进行光还原,不仅有利于环境治理,还有助于生产化工原料。然而,由于二氧化碳的活化难度大、光吸收和电荷分离能力有限,二氧化碳的光催化效率普遍较低。催化剂的缺陷工程是提高 CO2 光催化活性的关键策略,金属氧化物催化剂的大部分研究都集中在阴离子空位的产生上。然而,对金属空位及其影响的探索仍然不足。在本研究中,我们通过缺陷工程制备了一种含有铟空位(VIn)的 In2O3 催化剂,用于 CO2 光还原。实验和理论计算结果表明,VIn 不仅能促进催化剂的光吸收和电荷分离,还能增强对 CO2 的吸附,降低 CO2 还原过程中形成关键中间产物 *COOH 的能垒。通过金属空位工程,催化剂的活性提高了 7.4 倍,达到了 841.32 µmol g-1 h-1 的优异速率。这项研究揭示了金属空位在 CO2 光还原中的作用机理,为新型 CO2 光还原催化剂的开发提供了理论指导。
期刊介绍:
The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.