Au deposits on graphite:: On the nature of high desorption peaks in CO thermal desorption spectra

被引:7
作者
Nowitzki, T.
Nickut, P.
Deiter, C.
Wollschlaeger, J.
Al-Shamery, K.
Baeumer, M.
机构
[1] Univ Bremen, Inst Angew & Phys Chem, D-28334 Bremen, Germany
[2] Carl von Ossietzky Univ Oldenburg, D-25111 Oldenburg, Germany
关键词
gold; graphite; carbon monoxide; scanning tunneling microscopy; temperature programmed desorption; photoelectron spectroscopy;
D O I
10.1016/j.susc.2006.01.063
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
Due to the discovery of An as a catalyst for low temperature CO oxidation, the adsorption of CO on Au surfaces has attracted a lot of attention recently. On stepped and rough single crystal surfaces as well as on deposited particles two characteristic desorption states above 100 K have been observed via TPD. We have studied An deposits on graphite in order to elucidate the nature of these desorption peaks in more detail. For this purpose, Au was deposited at 100 K and 300 K on HOPG as a weakly interacting support. In analogy to other supports, we obtain two desorption states (similar to 140 K and similar to 170 K) whose relative intensities depend strongly on the deposition temperature with the high temperature peak being much more pronounced for the 100 K deposits. After annealing to 600 K, both states drastically lose intensity. XP spectra, on the other hand, show virtually no decrease of the An 4f intensity as would be expected for desorption or significant changes of the particle morphologies. We conclude that both desorption peaks are defect-related and connected with under-coordinated An atoms that are lost for the most part upon annealing. These sites could be located at the perimeter of dendritic islands or on small, defect-rich particles in addition to larger particles not adsorbing CO at 100 K. Preliminary STM results are in favour of the second interpretation. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:3595 / 3599
页数:5
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