Low-Temperature CO Oxidation by the Pt/CeO2 Based Catalysts

被引:7
作者
Stadnichenko, Andrey I. [1 ]
Slavinskaya, Elena M. [1 ]
Stonkus, Olga A. [1 ]
Boronin, Andrei I. [1 ]
机构
[1] SB RAS, Boreskov Inst Catalysis, Pr Lavrentieva 5, Novosibirsk 630090, Russia
关键词
Pt/CeO2; low temperature CO oxidation; PtOx clusters; metallic clusters; single atoms; RAY PHOTOELECTRON-SPECTROSCOPY; METAL-SUPPORT INTERACTIONS; SINGLE-ATOM; IN-SITU; LIGHT-OFF; PLATINUM NANOPARTICLES; REDUCING CONDITIONS; THERMAL-STABILITY; DISPERSED PT/CEO2; COMBUSTION METHOD;
D O I
10.1002/cctc.202301727
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
This review analyzes the literature data and the results of studies of the Pt/CeO2-based catalysts that are capable of providing the low-temperature CO oxidation (LTO CO). The review summarizes the catalytic characteristics and the main properties of Pt/CeO2-based catalysts necessary for the low-temperature oxidation at T<50 degrees C. Analysis of the literature data on the use of physical methods of investigation and their correlation with the activity of Pt/CeO2 catalysts allowed us to conclude that the main active forms of platinum are small metallic clusters, single atoms Pt2+-SA and oxide clusters PtOx interacting with ceria nanoparticles. It has been established that the most active forms are PtOx clusters, which provide a high reaction rate in the temperature range from -50 to +50 degrees C. Forms of ionic Pt2+ with different coordination with oxygen ensure the activity of catalysts starting at temperatures above 100 degrees C. Finally, small metallic clusters occupy an intermediate position, providing activity above 0 degrees C, but their instability and gradual transition to the oxidized state Pt2+/PtOx are noted. At the conclusion of the review, the results of mathematical modeling demonstrate the correct kinetics description of the low-temperature CO oxidation based on the Mars-van Krevelen and associative mechanisms.
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页数:25
相关论文
共 176 条
[1]   Pt/CeO2 catalysts in crotonaldehyde hydrogenation:: Selectivity, metal particle size and SMSI states [J].
Abid, M ;
Paul-Boncour, V ;
Touroude, R .
APPLIED CATALYSIS A-GENERAL, 2006, 297 (01) :48-59
[2]   Surface-structure sensitivity of CO oxidation over polycrystalline ceria powders [J].
Aneggi, E ;
Llorca, J ;
Boaro, M ;
Trovarelli, A .
JOURNAL OF CATALYSIS, 2005, 234 (01) :88-95
[3]  
Aneggi E, 2020, METAL OXIDES, P45, DOI 10.1016/B978-0-12-815661-2.00003-7
[4]  
[Anonymous], 2009, N 43 1002 POWDER DIF
[5]   Introducing Time Resolution to Detect Ce3+ Catalytically Active Sites at the Pt/CeO2 Interface through Ambient Pressure X-ray Photoelectron Spectroscopy [J].
Artiglia, Luca ;
Orlando, Fabrizio ;
Roy, Kanak ;
Kopelent, Rene ;
Safonova, Olga ;
Nachtegaal, Maarten ;
Huthwelker, Thomas ;
van Bokhoven, Jeroen A. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2017, 8 (01) :102-108
[6]   Evolution of the Atomic Structure of Ceria-Supported Platinum Nanocatalysts: Formation of Single Layer Platinum Oxide and Pt-O-Ce and Pt-Ce Linkages [J].
Avakyan, Leon A. ;
Kolpacheva, Natalia A. ;
Paramonova, Ekaterina V. ;
Singh, Jagdeep ;
Hartfelder, Urs ;
van Bokhoven, Jeroen A. ;
Bugaev, Lusegen A. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2016, 120 (49) :28057-28066
[7]   Local structure of Pt and Pd ions in Ce1-xTixO2:: X-ray diffraction, x-ray photoelectron spectroscopy, and extended x-ray absorption fine structure [J].
Baidya, Tinku ;
Priolkar, K. R. ;
Sarode, P. R. ;
Hegde, M. S. ;
Asakura, K. ;
Tateno, G. ;
Koike, Y. .
JOURNAL OF CHEMICAL PHYSICS, 2008, 128 (12)
[8]   The influence of the preparation methods on the catalytic activity of platinum and gold supported on TiO2 for CO oxidation [J].
Bamwenda, GR ;
Tsubota, S ;
Nakamura, T ;
Haruta, M .
CATALYSIS LETTERS, 1997, 44 (1-2) :83-87
[9]   Dynamics, structure and energetics of the (111), (011) and (001) surfaces of ceria [J].
Baudin, M ;
Wójcik, M ;
Hermansson, K .
SURFACE SCIENCE, 2000, 468 (1-3) :51-61
[10]   Promoting effect of CeO2 in combustion synthesized Pt/CeO2 catalyst for CO oxidation [J].
Bera, P ;
Gayen, A ;
Hegde, MS ;
Lalla, NP ;
Spadaro, L ;
Frusteri, F ;
Arena, F .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (25) :6122-6130