Vibrational dynamics of CO at the (100) platinum electrochemical interface

被引:36
作者
Peremans, A [1 ]
Tadjeddine, A [1 ]
GuyotSionnest, P [1 ]
机构
[1] UNIV CHICAGO,JAMES FRANCK INST,CHICAGO,IL 60637
基金
美国国家科学基金会;
关键词
D O I
10.1016/0009-2614(95)01221-8
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 vibrational relaxation of the CO stretching vibration when the molecule is adsorbed at a (100) platinum single crystal electrode in aqueous electrolyte is investigated by sum-frequency generation, The measured vibration lifetime of 1.5 +/- 0.5 ps is in line with those previously observed for dry CO/metal interfaces. No lifetime modification upon electrode potential shift of 0.5 V could be detected. Consequently, the electrolyte or the interfacial electric field has little effect on the fast vibrational dynamics resulting from the non-adiabatic coupling of the vibration to the substrate electrons. It is speculated that the observation of a significant lifetime modification upon electrode potential shift would require non-aqueous electrolytes where the CO/Pt interface can be stable over a larger potential range.
引用
收藏
页码:243 / 248
页数:6
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