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Surface-enhanced Raman Spectroscopy of Ethephone Adsorbed on Silver Surface

机译:银表面吸附的乙烯表面增强拉曼光谱

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We investigated the Surface-enhanced Raman Spectroscopy (SERS) spectrum of ethephone (2- chloroethylphosphonic acid). We observed significant signals in the ordinary Raman spectrum for solid-state ethephone as well as when it was adsorbed on a colloidal silver surface, strong vibrational signals were obtained at a very low concentration. The SERS spectra were obtained by silver colloids that were prepared by the ャ - irradiation method. The influence of pH and the influence of anion (Cl-, Br-, I-) on the adsorption orientation were investigated. Two different adsorption mechanisms were deduced, depending on the experimental conditions. The chlorine atom or the chlorine and two oxygen atoms were adsorbed on the colloidal silver surface. Among halide ions, Br- and I- were more strongly adsorbed on the colloidal silver surfaces. As a result, the adsorption of ethephone was less effective due to their steric hinderance.
机译:我们研究了电子琴(2-氯乙基膦酸)的表面增强拉曼光谱(SERS)光谱。我们在普通拉曼光谱中观察到了固态电子琴的重要信号,以及当它吸附在胶体银表面上时,在很低的浓度下就获得了强烈的振动信号。 SERS光谱是由通过ャ-辐照法制备的银胶体获得的。研究了pH值和阴离子(Cl -,Br -,I -)对吸附方向的影响。根据实验条件,推导了两种不同的吸附机理。氯原子或氯和两个氧原子吸附在胶体银表面上。在卤离子中,Br -和I -更强地吸附在胶体银表面。结果,由于其空间位阻,对乙烯的吸附效果较差。

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