文献类型：期刊文献

英文题名：Breaking through the Peak Height Limit of the Volcano-Shaped Activity Curve for Metal Catalysts: Role of Distinct Surface Structures on Transition Metal Oxides

作者：Chen, Jianfu[1,2];Jia, Menglei[1,2,3];Wang, Jinglin[1,2];Hu, Peijun[1,2,3];Wang, Haifeng[1,2]

机构：[1]East China Univ Sci & Technol, Key Lab Adv Mat, Ctr Computat Chem, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Res Inst Ind Catalysis, Shanghai 200237, Peoples R China;[3]Queens Univ Belfast, Sch Chem & Chem Engn, Belfast BT9 5AG, Antrim, North Ireland

年份：2022

卷号：126

期号：1

起止页码：183

外文期刊名：JOURNAL OF PHYSICAL CHEMISTRY C

收录：;EI(收录号：20220111410912);WOS:【SCI-EXPANDED(收录号:WOS:000759636200020)】；

基金：This project was supported by National Key R&D Program of China (2018YFA0208602), NSFC (91945302, 21873028, 21703067, and 92045303), National Ten Thousand Talent Program for Young Top-notch Talents in China, Shanghai ShuGuang project (17SG30), Postdoctoral Science Foundation of China (2017M611471), and the Fundamental Research Funds for the Central Universities. M.J. thanks the China Scholarship Council for sponsorship.

语种：英文

外文关键词：Oxide minerals - Titanium dioxide - Calculations - Dissociation - Transition metals - Volcanoes - Catalyst activity - Molecules

摘要：The volcano-shaped activity curve has long been used to reveal the activity trends among different catalysts and is a fundamental tool for catalyst screening. Although generally the peak height of the curve is considered as the highest possible activity, the understanding for its origin and inherent constraints is still a comparatively open issue. Herein, on the basis of microkinetic analysis and first-principles calculations, we quantitatively demonstrate that the peak height is strongly affected by the structural features of catalyst surfaces and could be largely improved by reducing the intercept of the Bronsted-Evans-Polanyi (BEP) relation. Focusing on various transition metal oxides (TMOs), we explore the BEP relations for the dissociation of small molecules, and the intercepts are shown to be smaller than those of flat metals. This reduction in intercept originates from the distinct local structure of oxide surfaces, which contributes to the weak binding ability and more final-state-like transition state. Taking NO oxidation as an example, we illustrate that the activity curve of rutile-type oxides is obviously higher than metals at typical medium-high temperatures, suggesting that rutile-type oxides possess inherently superior activity. Furthermore, general application of TMOs in breaking through the activity limit of metals for molecule dissociation is discussed.