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机构地区:[1]河南大学物理与信息光电子学院,开封475001
出 处:《高等学校化学学报》2004年第10期1920-1923,共4页Chemical Journal of Chinese Universities
基 金:国家自然科学基金 (批准号 :10 2 740 19);河南省自然科学基金 (批准号 :0 2 110 10 10 0 )资助
摘 要:报道了 C70 分子吸附于铜表面的增强拉曼光谱 .通过与正常拉曼光谱以及银表面 SERS谱的比较发现 ,C70 分子与铜表面之间的吸附属于物理吸附 ,增强机制主要是电磁增强 .C70 分子在银表面上的吸附状态与铜表面上的不同 ,这导致了两者特征峰谱线强度分布存在差异 .以 C6 0 的振动模式为参考 ,推断出 C70 分子在 2种金属表面上的吸附状态可能分别处于使碳笼的挤压振动模接近于“平躺”和“竖直”的The SERS effect of C 70 molecules adsorbed on the surface of copper was reported for the first time. By comparing with the normal Raman and the SERS on the surface of silver, it sounds reasonable that the adsorption between the copper and C 70 is a physical adsorption, and electromagnetic enhance mechanism dominates over the surface enhanced effect. The difference of relative intensities between the SERS spectra of C 70 adsorbed on the silver surface and copper surface originates from different adsorption states of C 70 molecules on them. Judged by the vibration mode of C 70, the adsorption states on the two different metal surfaces could be described as near “horizontal” and near “upending” directions, respectively. This investigation is valuable for the research of interaction between C 70 molecules and different metal surfaces.
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