Reactivity of oxygen states at caesium surfaces towards carbon monoxide and carbon dioxide

被引:11
作者
Kulkarni, GU [1 ]
Laruelle, S [1 ]
Roberts, MW [1 ]
机构
[1] UNIV WALES COLL CARDIFF,DEPT CHEM,CARDIFF CF1 3TB,S GLAM,WALES
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1996年 / 92卷 / 23期
关键词
D O I
10.1039/ft9969204793
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
The development of oxygen states at caesium surfaces at 80 K has been studied by X-ray photoelectron spectroscopy. Core-level O Is spectra have enabled three distinct oxygen states to be assigned to isolated oxygen adatoms, O-delta-, peroxo-type species, O-2(delta-), and oxide, O2-. The O-delta- State is only observed at low coverages and is the precursor to oxide formation. The reactivity of these species towards carbon monoxide and carbon dioxide has been studied through monitoring the O Is and C Is spectra and quantitative analysis of the stoichiometry of the reactions. Both the anionic form of chemisorbed carbon dioxide, CO2delta-, and surface carbonate species can be formed through reactions of the individual oxygen species with either CO or CO2 while the CO2delta- species can be transformed to carbonate species by exposure to dioxygen. All reactions are of low activation energy and occur at 80 K. A reaction scheme is proposed which illustrates the various reaction pathways available when carbon monoxide-dioxygen mixtures are exposed to a caesium surface at 80 K; for oxygen rich mixtures surface oxidation dominates while for carbon monoxide rich mixtures both chemisorbed carbon dioxide, CO2delta-, and surface carbonate form.
引用
收藏
页码:4793 / 4798
页数:6
相关论文
共 24 条
[1]   REACTION PATHWAYS IN THE OXYDEHYDROGENATION OF AMMONIA AT CU(110) SURFACES [J].
AFSIN, B ;
DAVIES, PR ;
PASHUSKY, A ;
ROBERTS, MW ;
VINCENT, D .
SURFACE SCIENCE, 1993, 284 (1-2) :109-120
[2]  
[Anonymous], SURFACE SCI REPT
[3]   THE PROMOTION OF SURFACE-CATALYZED REACTIONS BY GASEOUS ADDITIVES - THE ROLE OF A SURFACE OXYGEN TRANSIENT [J].
AU, CT ;
ROBERTS, MW .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1987, 83 :2047-2059
[4]   SPECIFIC ROLE OF TRANSIENT O-(S) AT MG(0001) SURFACES IN ACTIVATION OF AMMONIA BY DIOXYGEN AND NITROUS-OXIDE [J].
AU, CT ;
ROBERTS, MW .
NATURE, 1986, 319 (6050) :206-208
[5]  
AU CT, 1993, ADSORPTION ORDERED S, P241
[6]   X-RAY PHOTOELECTRON SPECTROSCOPIC STUDY OF INTERACTION OF OXYGEN AND NITRIC-OXIDE WITH ALUMINUM [J].
CARLEY, AF ;
ROBERTS, MW .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 1978, 363 (1714) :403-424
[7]   OXYGEN-INDUCED DISSOCIATION OF CARBON-MONOXIDE AT AN SP-METAL (ALUMINUM) SURFACE [J].
CARLEY, AF ;
ROBERTS, MW .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1987, (05) :355-356
[8]   ACTIVATION OF CARBON-MONOXIDE AND CARBON-DIOXIDE AT CESIUM-PROMOTED CU(110) AND CU(110)-O SURFACES [J].
CARLEY, AF ;
ROBERTS, MW ;
STRUTT, AJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (37) :9175-9181
[9]   HYDROXYLATION OF MOLECULARLY ADSORBED WATER AT AG(111) AND CU(100) SURFACES BY DIOXYGEN - PHOTOELECTRON AND VIBRATIONAL SPECTROSCOPIC STUDIES [J].
CARLEY, AF ;
DAVIES, PR ;
ROBERTS, MW ;
THOMAS, KK .
SURFACE SCIENCE, 1990, 238 (1-3) :L467-L472
[10]  
FREUND HJ, IN PRESS SURF SCI RE