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Characterization of Water Structure on Silver Electrode Surfaces by SERS with Two-Dimensional Correlation Spectroscopy

机译:二维相关光谱法通过SERS表征银电极表面的水结构

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Surface-enhanced Raman scattering (SERS) spectra were collected continuously during cyclic voltammetric measurements on silver electrodes in alkaline aqueous solution at room temperature. Three water librational modes as well as the bending mode peak were observed in cathodic potential range. The 2D-COS analysis of spectra collected in LiOH and KOH solutions showed that the librational bands appear prior to the bending band on the cathodic scan, while in CsOH solution the potential dependence of these bands was identical. A comparison of librational band frequencies revealed that the water molecules around Cs~(+) cations arranged on the electrode surface were poorly hydrogen bonded in contrast to Li~(+) and K~(+). The water bending band of spectra collected in LiOH solution was found to be the convolution of two contributions, consistent with a two state model of water arranged on an electrode surface.
机译:在室温下在碱性水溶液中的银电极上进行循环伏安法测量期间,连续收集表面增强拉曼散射(SERS)光谱。在阴极电位范围内观察到三种水释放模式以及弯曲模式峰。在LiOH和KOH溶液中收集的光谱的2D-COS分析表明,在阴极扫描中,自由带出现在弯曲带之前,而在CsOH溶液中,这些带的电位依赖性相同。释放带频率的比较表明,与Li〜(+)和K〜(+)相比,排列在电极表面的Cs〜(+)阳离子周围的水分子氢键差。发现在LiOH溶液中收集的光谱的水弯曲带是两个贡献的卷积,这与电极表面上的水的两个状态模型一致。

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