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THE ADSORPTION OF AG ON CO, O, AND H COVERED W(110) .1. OVERLAYER FORMATION AND STABILITY
被引:15
作者:
ZHAO, YB
[1
]
GOMER, R
[1
]
机构:
[1] UNIV CHICAGO,DEPT CHEM,CHICAGO,IL 60637
关键词:
D O I:
10.1016/0039-6028(93)90362-N
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 adsorption of Ag mono- and multilayers on O/W(110), CO/W(110), and H/W(110) was investigated, from 90 K to Ag desorption temperatures. Auger measurements indicate that Ag growth occurs layer by layer at 90 K on all substrates. For Ag/O/W(110) dewetting, i.e. partial balling up of Ag occurs from 200 to 400 K. At T greater-than-or-equal-to 500 K segregation sets in, with O forced into p(1 X 1) islands, and Ag pushed into islands which can be several layers thick. This behavior is similar to that seen previously with 0 and Cu and 0 and Pd on W(110). There is also a slight amount of 0 left trapped under the Ag covered surface. In the case of CO partial dewetting also seems to set in at 200-300 K. Ag adsorption does not cause CO desorption. However, with an Ag overlayer there is a slight decrease from 400 to 350 K in the virgin-CO desorption peak, and the ratio of virgin to beta-desorption increases with Ag coverage. This suggests that Ag competes with remaining CO for sites which could be used for dissociative, i.e. beta-adsorption. CO is only very weakly adsorbed on Ag1/W(110); this explains the relatively small effect on v-CO desorption, since there is no driving force for CO-Ag interchange, as in the case of Cu/CO/W(110), where CO is still strongly bound on Cu1/W(110). The effect of Ag on H2 desorption from H/W(110) is quite dramatic, with the appearance of a sharp low temperature peak at 150 K and a second sharp peak at 400 K, also lower than the broad main peak for H/W(110). This behavior is very similar to what was seen previously for Hg/H/W(110) and Pd/H/W(110) and may result from a modification of H binding sites on W(110) by the overlayer metal, even if the latter does not interact directly with H.
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页码:125 / 137
页数:13
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