Understanding the role of promoters in catalysis: operando XAFS/DRIFTS study of CeOx/Pt/Al2O3 during CO oxidation

Q1 Materials Science Catalysis Structure & Reactivity Pub Date : 2017-02-14 DOI:10.1080/2055074X.2017.1278890
E. Gibson, E. Crabb, D. Gianolio, A. Russell, D. Thompsett, P. Wells
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引用次数: 7

Abstract

Abstract A combined operando XAFS/DRIFTS study on CeOx/Pt/Al2O3 catalysts has been performed during CO oxidation and provides insights into the changes in nanoparticle structure and adsorbed species during the reaction profile. The onset of CO2 formation is shown to be concurrent with a rapid re-oxidation of the Pt nanoparticles, evidenced by XAFS spectroscopy, and the loss of bridge bonded CO adsorbed on Pt, as shown by simultaneous DRIFTS acquisition. The continued appearance of linear bound CO on the catalyst surface is shown to remain long after catalytic light off. The interaction of Pt and CeOx is evidenced by the improved performance towards CO oxidation, compared to the non-CeOx modified Pt/Al2O3, and changes in the CO adsorption properties on Pt previously linked to Pt-CeO2 interfaces.
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CO氧化过程中CeOx/Pt/Al2O3的XAFS/DRIFTS研究促进剂在催化中的作用
摘要/ Abstract摘要:采用XAFS/DRIFTS方法研究了CO氧化过程中CeOx/Pt/Al2O3催化剂的纳米粒子结构和吸附物质的变化。XAFS光谱显示,CO2的形成与Pt纳米颗粒的快速再氧化同时发生,同时DRIFTS采集数据显示,桥键CO吸附在Pt上的损失也同时发生。在催化熄灯后很长一段时间内,在催化剂表面继续出现线性结合的CO。与非CeOx修饰的Pt/Al2O3相比,Pt和CeOx的相互作用证明了Pt/Al2O3对CO氧化性能的改善,以及之前连接到Pt- ceo2界面的Pt上CO吸附性能的变化。
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来源期刊
Catalysis Structure & Reactivity
Catalysis Structure & Reactivity CHEMISTRY, PHYSICAL-
CiteScore
4.80
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