Orientation change of adsorbed pyrazine on roughened rhodium electrodes as probed by surface-enhanced Raman spectroscopy

被引:18
作者
Cui, L
Liu, Z
Duan, S
Wu, DY
Ren, B [1 ]
Tian, ZQ
Zou, SZ
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
[3] Miami Univ, Dept Chem & Biochem, Oxford, OH 45056 USA
关键词
D O I
10.1021/jp052983y
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
A surface-enhanced Raman spectroscopic (SERS) study of pyrazine adsorbed on roughened Rh electrodes was performed. Potential and concentration effects on the adsorption behavior of pyrazine were investigated. The SER spectra display four pairs of overlapping bands with the relative intensity of each pair being highly potential dependent, which has not been observed on other metals. The orientation change of the adsorbed pyrazine from the end-on to N/pi bonded edge-on configuration is proposed to account for this potential dependent relative intensity change. This hypothesis is further supported by the SERS results obtained at different pyrazine concentrations. In conjunction with the orientation effect, the interaction of Rh with hydrogen and oxygen generated at different potentials has a great influence on the adsorption configuration of pyrazine.
引用
收藏
页码:17597 / 17602
页数:6
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