Carbonate on Ag(110): a complex system clarified by STM

被引:26
作者
Guo, XC [1 ]
Madix, RJ [1 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
scanning tunneling microscopy; surface chemical reaction; silver; inorganic compounds; carbon dioxide; oxygen; single crystal surfaces;
D O I
10.1016/S0039-6028(01)01095-0
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
In the present work we have used scanning tunneling microscopy (STM) in conjunction with temperature programmed reaction spectroscopy (TPRS) to study the formation of surface carbonate on Ag(110) by the reaction of CO2 With atomic oxygen. Recently, we have found and reported that the STM images attributed previously to carbonate are actually due to chemisorbed CO2. STM images reported here reveal that the surface carbonate species on Ag(110) has a very different appearance from chemisorbed CO2. Chemisorbed CO2 appears as round protrusions, whereas carbonate forms thick rods along the [1 (1) over bar0] direction consisting of double or single chains. An adsorption structure model consistent with the STM observation and the (1 x 2) reconstruction is suggested. Images recorded at various oxygen coverages show that the carbonate rods form between the -Ag-O- rows and accumulate near step edges. In situ STM imaging during carbonate formation demonstrates that the reaction may initiate at the end or from the side of the -Ag-O- rows. The reaction progresses along the rows. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:37 / 44
页数:8
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