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机构地区:[1]固体表面物理化学国家重点实验室,厦门大学化学化工学院,福建厦门361005 [2]近海海洋环境科学国家重点实验室,厦门大学环境与生态学院,福建厦门361102
出 处:《电化学》2016年第1期32-36,共5页Journal of Electrochemistry
基 金:国家自然科学基金项目(No.21227004,No.21321062,No.J1310024,No.21473140);科技部973项目(No.2013CB933703,No.2011YQ03012406);教育部创新团队基金(No.IRT13036)资助
摘 要:罗丹明6G(Rhodamine 6G,R6G)是单分子表面增强拉曼光谱(SM-SERS)研究中最常用的探针分子之一,对R6G分子在表面吸附行为的研究有助于了解R6G分子和表面的相互作用.本文应用电化学和电化学表面增强拉曼光谱技术,研究不同电位下R6G的银电极表面的吸附行为.结果表明,随着电位负移罗丹明6G在银表面上从垂直吸附转为倾斜吸附,该变化和碱性条件下吸附于金纳米粒子上R6G的吸附构象一致.这说明,在部分单分子实验中所发现的R6G反常光谱其来源是单个R6G分子在表面吸附取向变化.本研究对后续详细分析SM-SERS研究中单分子SERS谱峰变化的机制有一定的参考价值.Rhodamine 6G (R6G) is one of the most common probe molecules employed in single molecule surface-enhanced Raman spectroscopy (SM-SERS). The study in adsorption behavior of R6G will help understand the interactions between R6G and surface. In this paper, we used electrochemical surface-enhanced Raman spectroscopy (SERS) to study the potential-dependent adsorp- tion behavior of R6G on silver electrodes. Our results show that when the potential moved negatively, the orientation of R6G on silver surface changed from vertical to inclined adsorption. This result indicates that the abnormal SM-SERS spectra of R6G observed in the former SM-SERS studies from other research groups are due to the reorientation in the R6G molecule on the surface rather than the change in resonance effect of R6G. Such a detailed study will assist the understanding for the spectral change of SERS in SM-SERS studies.
关 键 词:罗丹明6G 吸附取向 电化学 电化学表面增强拉曼光谱
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