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Chloride ion-dependent surface-enhanced Raman scattering study of biotin on the silver surface

机译:氯离子依赖性表面增强的银素生物素的散射研究

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In the present paper, the surface enhanced Raman scattering (SERS) technique was employed to study the SERS spectra of biotin molecules formed on the silver surface. The adsorption geometries of biotin molecules on the silver surface were analyzed based on the SERS data. It can be found that most vibration modes show a Raman shift in silver sol after the addition of sodium chloride solution. In addition, The Raman signals of biotin become weaker and weaker with the increase of the concentration of sodium chloride. This may be due to that the interaction between chloride ions and silver particles is stronger than the interaction between biotin molecules and silver particles. When the concentration of sodium chloride in silver colloid is higher than 0.05mol/L, superfluous chloride ions may form an absorption layer so that biotin can not be adsorbed on silver surface directly. The changes in intensity and profile shape in the SERS spectra suggest different adsorption behavior and surfacecoverage of biotin on silver surface. The SERS spectra of biotin suggest that the contribution of the charge transfer mechanism to SERS may be dominant.
机译:在本文中,采用表面增强拉曼散射(SERS)技术研究在银表面上形成的生物素分子的SERS光谱。基于SERS数据分析银表面上的生物素分子的吸附几何形状。可以发现,在加入氯化钠溶液后,大多数振动模式显示银溶胶中的拉曼换档。此外,Biotin的拉曼信号随着氯化钠浓度的增加而变弱和较弱。这可能是由于氯离子和银颗粒之间的相互作用比生物素分子和银颗粒之间的相互作用更强。当银胶体中氯化钠的浓度高于0.05mol / L时,氯离子离子可以形成吸收层,使得生物素不能直接吸附在银表面上。 SERS光谱中强度和型材形状的变化表明了银表面上生物素的不同吸附行为和Surfacecoverage。生物素的SERS光谱表明,电荷转移机制对SERS的贡献可能是显性的。

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