States of Pt/CeO2 catalysts for CO oxidation below room temperature

被引:27
作者
Slavinskaya, Elena M. [1 ]
Stadnichenko, Andrey I. [1 ]
Dominguez, Jon E. Quinlivan [2 ,3 ]
Stonkus, Olga A. [1 ]
Vorokhta, Mykhailo [4 ]
Smid, Bretislav
Castro-Latorre, Pablo [2 ,3 ]
Bruix, Albert [2 ,3 ]
Neyman, Konstantin M. [2 ,3 ,5 ]
Boronin, Andrei I. [1 ]
机构
[1] RAS, SB, Boreskov Inst Catalysis, Pr Ak Lavrentieva 5, Novosibirsk 630090, Russia
[2] Univ Barcelona, Dept Ciencia Mat & Quim Fis, C Marti & Franques 1, Barcelona 08028, Spain
[3] Univ Barcelona, Inst Quim Teor & Computac IQTCUB, C Marti & Franques 1, Barcelona 08028, Spain
[4] Charles Univ Prague, Fac Math & Phys, Dept Surface & Plasma Sci, V Holesovickach 2, Prague 18000 2, Czech Republic
[5] ICREA Inst Catalana Recerca & Estudis Avancats, Barcelona 08010, Spain
关键词
Pt; CeO2; low-temperature CO oxidation; PtOx clusters; Single atom; METAL-SUPPORT INTERACTION; WATER-GAS SHIFT; IN-SITU; PD/CEO2; CATALYSTS; CARBON-MONOXIDE; CERIA; STABILITY; SINGLE; CEO2; TRANSFORMATION;
D O I
10.1016/j.jcat.2023.03.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CO molecules can be efficiently oxidized over Pt/CeO2 catalysts, but the stability and reactivity of differ-ent states of Pt in the catalysts are still unclear. Here we combine experimental and computational meth-ods to characterize Pt/CeO2 catalysts subjected to reductive and oxidative pre-treatments and exposed CO oxidation reaction conditions. Particles of metallic Pt, known to be catalytically active at elevated tem-perature, are shown to be precursors for the formation, under operando conditions, of more stable PtOx particles that enable CO oxidation below room temperature. These PtOx particles are similarly stable to - but more active than - atomically dispersed Pt2+ species. The results and approaches presented this study illustrate the complex response of catalytic materials to reaction conditions and pave the way for future efforts to improve Pt/CeO2 and similar catalysts using dedicated pre-treatment strategies.(c) 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:285 / 299
页数:15
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