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Investigations on the adsorption behavior of water on Ag electrode/acetanitrile interface by using surface-enhanced Raman spectroscopy

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表面增强拉曼光谱研究银电极_乙腈界面微量水的吸附行为.pdf (176.1Kb)
Date
2002
Author
Gu, RA
顾仁敖
Sun, YH
孙玉华
Cao, PG
曹佩根
Yao, JL
姚建林
Ren, B
任斌
Tian, ZQ
田中群
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  • 化学化工-已发表论文 [14237]
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Abstract
The surface-enhanced Raman scattering (SERS) spectrum of the trace amount of water on the silver/acetonitrile interface was investigated as a function of the applied potential and the concentration of water. The results show that several adsorption modes of water exist in the electrochemical double layer of silver. At relatively positive potentials, the water molecule was co-adsorbed with acetonitrile through weak hydrogen bond, which was hardly affected by the increase of the concentration of water. The frequency of nu(O-H) appears at 3 487 cm(-1). When the scanning potentials were negative values, the water molecule turned to interact with the surface complex [Ag(CN)(n)]((n-1)-) produced by the dissociation reaction of the solvent acetonitrile. The frequency of nu(O-H) centered at ca. 3 583 cm(-1) which red-shifted with the increase of the concentration of water. At more negative potentials, the hydrogen evolution reaction of water occurs seriously, and the quantity of OH- produced led to the formation of the crystallite LiOH which had the vibration of nu(O-H) locating at 3 665 cm(-1). The formation of LiOH . H2O, in which the frequency of nu(O-H) was at 3 563 cm(-1), becomes possible when increasing the quantity of water to 1.0 mol/L in the bulk solution.
Citation
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,2002,23(10):1960-1964
URI
https://dspace.xmu.edu.cn/handle/2288/12311

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