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首页> 外文期刊>Vibrational Spectroscopy: An International Journal devoted to Applications of Infrared and Raman Spectroscopy >Surface-enhanced Raman spectroscopy of molecules adsorbed on silver nanoparticles dispersed an agarose gel and their adsorption isotherms
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Surface-enhanced Raman spectroscopy of molecules adsorbed on silver nanoparticles dispersed an agarose gel and their adsorption isotherms

机译:吸附在银纳米粒子上的分子的表面增强拉曼光谱分散在琼脂糖凝胶及其吸附等温线上

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摘要

Surface-enhanced Raman scattering (SERS) was used to obtain adsorption isotherms for two types of SERS-active substrates: silver nanoparticles (AgNPs) dispersed in water (AgNP/sol); and AgNPs dispersed in agarose gel (AgNP/Agar). Rodhamine 6G (R6G) was chosen as the probe molecule to evaluate the two substrates. R6G adsorbs on both substrates following Langmuir isotherms with very similar adsorption constants. The SERS from R6G in AgNP/Agar is ca. 10 times more intense than in AgNP/sol due to the confinement of the R6G molecules within the gel matrix. The AgNP/Agar was further evaluated for the adsorption of methylene blue (MB), crystal violet (CV) and benzotriazole (BTA). The results showed that, for lower surface coverages (theta < 0.1), the observed SERS (or SERRS) spectra corresponded to single molecule events. In this case, each single spectrum presented different relative intensities than from the ensemble averaged spectrum. On the other hand, for higher coverages (theta approximate to 1), the relative intensities of a single spectrum were quite similar to those of the ensemble average. Single molecule SERRS events were well identified for MB, because the spectra of the monomer and of the aggregated state differ considerably for this dye. The results also indicate that R6G and CV adsorb on the SERS-active sites forming ion pairs with the adsorbed chloride, while MB and BTA form covalent bonds with Ag atoms on the AgNP surface. In all cases the Gibbs free energy of adsorption were below -30 kJ mol(-1), characterizing chemical adsorption. (C) 2016 Elsevier B.V. All rights reserved.
机译:表面增强的拉曼散射(SERS)用于获得两种类型的SERS-活性基材的吸附等温线:分散在水中的银纳米颗粒(AgNP);和分散在琼脂糖凝胶(AgNP /琼脂)中的酰度。选择Rodhamine 6G(R6G)作为探针分子以评估两个基材。在Langmuir等温线后的两个底物上的R6G吸附具有非常相似的吸附常数。 agnp / agar中的R6G的SERS是CA。由于凝胶基质内的R6G分子限制,而不是AgNP /溶胶中的10倍。进一步评价AgNP /琼脂对亚甲基蓝(MB),晶体紫(CV)和苯并三唑(BTA)的吸附。结果表明,对于下表面覆盖(Theta <0.1),观察到的SERS(或SERRS)光谱对应于单分子事件。在这种情况下,每个单频谱呈现不同于来自集合平均频谱的相对强度。另一方面,对于更高的覆盖范围(近似为1),单谱的相对强度与集合平均值的相对强度非常相似。单分子SERRS事件均得到良好的MB,因为单体和聚集状态的光谱对该染料相当不同。结果还表明R6G和CV吸附在与吸附氯化物形成离子对的SERS-活性位点,而MB和BTA在AgNP表面上形成共价键。在所有情况下,吉布斯吸附的自由能量低于-30 kJ摩尔(-1),表征化学吸附。 (c)2016年Elsevier B.v.保留所有权利。

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