Electrochemical attenuated total reflectance spectroscopy in far- and deep-ultraviolet regions

I. Tanabe, Ken-ichi Fukui
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Abstract

Recently, we developed a novel attenuated total reflectance (ATR) spectroscopic system in far- and deep-ultraviolet (FUV and DUV) regions that operates under electrochemical conditions in order to investigate the electronic states of materials near the electrode surface. We succeeded to record the FUV-DUV spectra of various ionic liquids systematically using the ATR-FUV-DUV spectroscopy and theoretically assign the obtained spectra based on quantum chemical calculations. Subsequently, upon application of voltage to an ionic liquid consisting of imidazolium cations and iodide anions, electronic transition spectra in the 150−450 nm range varied. In particular, absorbance due to charge transfer from the anion to the cation drastically increased at positive potentials. According to the molecular dynamics simulations, the density of iodide anion near the electrode surface drastically changed depending on the electrode potential, which contributed to the spectral changes. Now, this technique is applied for organic semiconductor materials.
远紫外和深紫外区的电化学衰减全反射光谱
最近,我们开发了一种在电化学条件下工作的远紫外和深紫外(FUV和DUV)区域的新型衰减全反射(ATR)光谱系统,以研究电极表面附近材料的电子状态。我们成功地利用ATR-FUV-DUV光谱系统地记录了各种离子液体的FUV-DUV光谱,并基于量子化学计算对得到的光谱进行了理论分配。随后,对由咪唑阳离子和碘化物阴离子组成的离子液体施加电压后,150 ~ 450 nm范围内的电子跃迁光谱发生了变化。特别是,由于电荷从阴离子转移到阳离子而引起的吸光度在正电位下急剧增加。分子动力学模拟表明,电极表面碘离子的密度随电极电位的变化而急剧变化,从而导致光谱的变化。现在,该技术被应用于有机半导体材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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