Methyl on Cu(111) - structural determination including influence of co-adsorbed iodine

被引:23
|
作者
Pascal, M
Lamont, CLA [1 ]
Kittel, M
Hoeft, JT
Constant, L
Polcik, M
Bradshaw, AM
Toomes, RL
Woodruff, DP
机构
[1] Univ Huddersfield, Ctr Appl Catalysis, Dept Chem & Biol Sci, Huddersfield HD1 3DH, W Yorkshire, England
[2] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[3] Univ Warwick, Dept Phys, Coventry CV4 7AL, W Midlands, England
关键词
photoelectron diffraction; copper; iodine; alkanes; single crystal surfaces;
D O I
10.1016/S0039-6028(02)01724-7
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 geometry of the methyl species on Cu(111) with and without coadsorbed iodine has been determined using scanned energy mode photoelectron diffraction. Under all circumstances the three-fold-coordinated hollow sites are occupied. At saturation coverage of pure methyl species only the 'fcc' site, directly above a third layer Cu atom is occupied, whereas at half saturation coverage similar to70% of the methyl species occupy these fcc hollows and similar to30% occupy the 'hcp' sites above second layer Cu atoms. Best agreement between theory and experiment corresponded to a methyl group adsorbed with C-3v symmetry, but the possibility that the species was tilted on the surface could not be excluded. The height of the C above the surface in a pure methyl layer was 1.66 +/- 0.02 Angstrom, but was reduced to 1.62 +/- 0.02 Angstrom in the presence of co-adsorbed iodine, suggesting that iodine may increase the strength of adsorption. Iodine was also found to occupy the fcc hollow sites with a Cu-I bondlength of 2.61 +/- 0.02 k (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:173 / 184
页数:12
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