The formation of a NO-NH3 coadsorption complex on a Pt(111) surface: A NEXAFS study

被引:39
作者
Esch, F [1 ]
Greber, T [1 ]
Kennou, S [1 ]
Siokou, A [1 ]
Ladas, S [1 ]
Imbihl, R [1 ]
机构
[1] UNIV HANNOVER,INST PHYS CHEM & ELEKTROCHEM,D-30167 HANNOVER,GERMANY
关键词
catalytic NO reduction; coadsorption complexes; NEXAFS;
D O I
10.1007/BF00806563
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 NO and the coadsorption of NO and NH3 on Pt(111) has been studied with TDS, work function measurements and near-edge X-ray absorption fine structure spectroscopy (NEXAFS). Pure NO was found to be adsorbed upright at low coverages (theta(NO) < 0.25) with a bond length of 1.24 +/- 0.05 Angstrom which corresponds to an elongation by 0.1 Angstrom as compared to the gas phase. An additional tilted species forms at high coverages. The formation of a coadsorption complex of NH3 and low coverage NO shows up in an elongation of NO to 1.28 +/- 0.05 Angstrom. In the coadsorption complex NO is adsorbed upright. The formation of such a complex which is held together by strong attractive interactions explains the high abundance of the mixed (NN)-N-14-N-15 reaction product in experiments with isotopically labeled educts in the NO + NH3 reaction.
引用
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页码:165 / 170
页数:6
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