Promotional nature of Sn on Pt/CeO_(2)for the oxidative dehydrogenation of propane with carbon dioxide  

作　　者：Guo-Qing Yang Xing Ren Vita A.Kondratenko Heng-Bo Zhang Evgenii V.Kondratenko Zhong-Wen Liu 

机构地区：[1]Key Laboratory of Syngas Conversion of Shaanxi Province,School of Chemistry&Chemical Engineering,Shaanxi Normal University,Xi’an 710119,China [2]Leibniz-Institut für Katalyse e.V,Albert-Einstein-Strasse 29 a,Rostock 18059,Germany

出　　处：《Nano Research》2023年第5期6237-6250,共14页纳米研究（英文版）

基　　金：the National Natural Science Foundation of China(No.21636006);the Fundamental Research Funds for the Central Universities(No.GK201901001).G.Q.Y.acknowledges support from the China Scholarship Council.

摘　　要：The oxidative dehydrogenation of propane with CO_(2)(CO_(2)-ODP)is a promising technology for the efficient production of propene in tandem with CO_(2)reduction to CO.However,the rational design of high-performance catalysts for this green process is still challenged by limited understanding of the nature of active sites and the reaction mechanism.In this work,the effects of SnO_(2) promoter on Pt/CeO_(2)activity and propene selectivity in CO_(2)-ODP are elucidated through varying the Sn/Pt molar ratio.When the ratio increases,propane conversion gradually decreases,while the propene selectivity increases.These dependences are explained by increasing the electron density of Pt through the promoter.The strength of this effect is determined by the Sn/Pt ratio.Owing to the electronic changes of Pt,CO_(2)-ODP becomes more favorable than the undesired CO_(2)reforming of propane.Sn-modified Pt–O–Ce bonds are reasonably revealed as the active sites for CO_(2)-ODP occurring through a redox mechanism involving the activation of CO_(2)over oxygen vacancies at Sn-modified Pt and CeO_(2)boundaries.These atomic-scale understandings are important guidelines for purposeful development of high-performance Pt-based catalysts for CO_(2)-ODP.

关 键 词：oxidative dehydrogenation carbon dioxide supported PtSn CERIA 

分 类 号：O64[理学—物理化学]