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A combined in situ infrared spectroscopy and scanning tunneling microscopy study of ethyl xanthate adsorption on Au(111)

机译:黄原酸乙酯吸附在Au(111)上的原位红外光谱和扫描隧道显微镜相结合

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We have used in situ FTIR and STM in a complementary study of chemisorbed ethyl xanthate on gold. We have limited the potential region to avoid the formation of oxidation products of ethyl xanthate. The FTIR results show a clear adsorbate band at ca. 1210 cm~(-1), which is assigned to the asymmetric C-O-C stretch of the chemisorbate. Notably, no asymmetric CS_2 stretch is observed. This data favours an adsorbate structure, in which both sulfur atoms bond to the surface, the molecular plane of the S_2C-O group is perpendicular to the surface and the alkyl chain of the molecule face towards the electrolyte. Two ordered ethyl xanthate overlayers are imaged on Au(111) by in situ STM. We propose a unit cell for one of these overlayers.
机译:我们在化学吸附的黄原酸乙酯在金上的补充研究中使用了原位FTIR和STM。我们限制了潜在区域,以避免形成黄药酸乙酯的氧化产物。 FTIR结果表明,在约℃处有清晰的吸附带。 1210 cm〜(-1),对应于化学吸附物的不对称C-O-C延伸。值得注意的是,未观察到不对称的CS_2拉伸。该数据有利于吸附物结构,其中两个硫原子均键合到表面,S_2C-O基团的分子平面垂直于表面,并且分子的烷基链面向电解质。通过原位STM在Au(111)上成像了两个有序的黄药酸乙酯覆盖剂。我们为这些叠加器之一提出了一个晶胞。

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