研究活性表面物种的通用方法 CT-SKAn:电荷转移谱动力学分析

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Catalysis Pub Date : 2024-04-21 DOI:10.1016/j.jcat.2024.115508
Alejandra Torres-Velasco , Bhagyesha S. Patil , Hongda Zhu , Yue Qi , Simon G. Podkolzin , Juan J. Bravo-Suárez
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引用次数: 0

摘要

结合操作紫外-可见光谱和电荷转移动力学模型,开发了一种光谱动力学方法来确定反应性表面物种。该方法包括三个一般步骤:1) 通过紫外-可见光谱同时测量反应速率和电荷转移;2) 根据涉及相关吸附物种的动力学模型开发速率表达式。这些速率表达式将反应速率、电荷转移和气相物种的分压联系起来;以及 3)评估速率表达式与实验数据的拟合程度。速率表达式拟合度最好的物种更有可能是所研究反应的表面活性物种。以测定金/二氧化钛上乙醇氧化过程中的活性氧物种为例进行说明。电荷转移谱动力学分析表明,表面过氧化氢、羟基和原子氧是反应性表面中间产物,而表面分子氧则不是。
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A general method for studying reactive surface species, CT-SKAn: Charge-transfer spectrokinetic analysis

A spectrokinetic methodology was developed to determine reactive surface species by combining operando ultraviolet–visible spectroscopy and charge transfer kinetic models. The methodology consisted of three general steps: 1) concomitant measurement of reaction rates and charge transfer via ultraviolet–visible spectroscopy; 2) development of rate expressions from kinetic models involving the adsorbed species of interest. These rate expressions relate reaction rates, charge transfer, and partial pressures of gas phase species; and 3) evaluation of the goodness of fit of the rate expressions to the experimental data. The species whose rate expressions show the best fit are the more likely reactive surface species for the studied reaction. An example is presented for the determination of reactive oxygen species during ethanol oxidation over Au/TiO2. The charge transfer spectrokinetic analysis showed that surface hydroperoxyl, hydroxyl, and atomic oxygen species were reactive surface intermediates, whereas surface molecular oxygen was not.

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来源期刊
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
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