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研究碳化物表面捕获CO的Mars-van Krevelen机理。

Investigating the Mars-van Krevelen Mechanism for CO Capture on the Surface of Carbides.

作者信息

Ashraf Naveed, Abghoui Younes

机构信息

Science Institute of the University of Iceland, 102 Reykjavik, Iceland.

出版信息

Molecules. 2025 Sep 6;30(17):3637. doi: 10.3390/molecules30173637.

Abstract

Electrochemical reduction processes enable the CO to be converted into a useful chemical fuel. Our study employs density functional theory calculations to analyze the (110) facets of the transition metal carbide surfaces for CO capture, incorporating the Mars-van Krevelen (MvK) mechanism. All the possible adsorption sites on the surface, including carbon, metal, and bridge sites, were fully investigated. The findings indicate that the carbon site is more active relative to the other adsorption sites examined. The CO hydrogenation paths have been comprehensively investigated on all the surfaces, and the free energy diagrams have been constructed towards the product. The results conclude that the TiC is the most promising candidate for the formation of methane, exhibiting an onset potential of -0.44 V. The predicted onset potential for CrC, MoC, NbC, VC, WC, ZrC, and HfC are -0.86, -0.61, -0.61, -0.93, -0.87, -0.61, and -0.81 V, respectively. Our calculated results demonstrate that MvK is selectively relevant to methane synthesis. Additionally, we investigated the stability of these surfaces against decomposition and conversion to pure metals concerning thermodynamics and kinetics. It was found that these carbides could remain stable under ambient conditions. The exergonic adsorption of hydrogen on carbon sites, requiring smaller potential values for product formation, and stability against decomposition indicate that these surfaces are highly suitable for CO reduction reactions using the MvK mechanism.

摘要

电化学还原过程能使一氧化碳转化为有用的化学燃料。我们的研究采用密度泛函理论计算,结合Mars-van Krevelen(MvK)机理,分析过渡金属碳化物表面的(110)晶面用于一氧化碳捕获的情况。对表面上所有可能的吸附位点,包括碳原子位点、金属原子位点和桥连位点,都进行了充分研究。研究结果表明,相对于所考察的其他吸附位点,碳原子位点更具活性。在所有表面上全面研究了一氧化碳加氢路径,并构建了产物的自由能图。结果得出,TiC是生成甲烷最有前景的候选物,起始电位为-0.44 V。预测CrC、MoC、NbC、VC、WC、ZrC和HfC的起始电位分别为-0.86、-0.61、-0.61、-0.93、-0.87、-0.61和-0.81 V。我们的计算结果表明,MvK与甲烷合成选择性相关。此外,我们从热力学和动力学方面研究了这些表面抵抗分解以及转化为纯金属的稳定性。发现这些碳化物在环境条件下可保持稳定。氢在碳原子位点上的放能吸附,生成产物所需的电位值较小,以及抗分解稳定性表明,这些表面非常适合使用MvK机理进行一氧化碳还原反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d7e/12430208/81c8a40789b8/molecules-30-03637-g001.jpg

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