Reactivity and deconstruction of the (1x2)-Rh(110) surface studied by scanning tunneling microscopy

被引:14
作者
Africh, C
Esch, F [1 ]
Comelli, G
Rosei, R
机构
[1] INFM, Lab TASC, I-34012 Trieste, Italy
[2] Univ Trieste, Dept Phys, I-34127 Trieste, Italy
关键词
D O I
10.1063/1.1465411
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 titration of a (2x2)p2mg-O/Rh(110) surface by hydrogen and the subsequent deconstruction of the nonequilibrium (1x2) reconstructed surface has been studied by scanning tunneling microscopy (STM) in a temperature range between 380 and 405 K. The titration reaction is seen to occur via reaction fronts, which start at steps, are elongated in the [1 (1) over bar0] direction and leave behind a surface covered by diffusing oxygen atoms. Two deconstruction mechanisms are active: A long-range row pairing of adjacent (1x2) rows, which propagates over several hundreds of Angstrom in the [1 (1) over bar0] direction, and a local hole formation in which Rh atoms detach from the ends of broken [1 (1) over bar0] rows, diffuse over up to 100 Angstrom and condense into (1x1) islands. Both mechanisms lead to the formation of correlated up-down islands; at step edges, the second one leads to a step retraction. The deconstruction is strongly defect mediated and the STM results indicate that the (1x2) reconstructed surface is most probably metastable. (C) 2002 American Institute of Physics.
引用
收藏
页码:7200 / 7206
页数:7
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