Hydration Shell Water Surrounding Citrate-Stabilised Gold Nanoparticles

Martin, Rabe, Taritra, Mukherjee
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Abstract

Presence of gold nanoparticles in an aqueous dispersion perturbs water molecules in their vicinity. Such water molecules form what is known as hydration shell and possess different vibrational attributes than those in the bulk dispersion. Raman spectroscopy was utilised to study these hydration shell water molecules around citrate-stabilised gold nanoparticles. Aqueous dilution series of three sizes of gold nanoparticle samples were prepared. Hydration shell spectral response, recovered by applying multivariate curve resolution technique, were compared against the spectra of the bulk phase. Once correlated with an increasing aqueous content in the respective samples, it could be inferred from the comparison that the hydration shell contains a less extensive hydrogen-bonding network with a smaller number of hydrogen-bonding interactions being possible than that in bulk. The results also suggest the hydrogen-bonding network in the hydration shells to be structurally more rigid and stronger, if compared against the intermolecular hydrogen-bonding prevalent in bulk.
柠檬酸盐稳定金纳米粒子周围的水合壳水
金纳米粒子在水分散体中的存在会扰动其附近的水分子。这些水分子形成了所谓的水合壳,并具有不同于分散体中水分子的振动属性。拉曼光谱被用来研究柠檬酸盐稳定金纳米粒子周围的水合壳水分子。制备了三种尺寸的金纳米粒子水稀释系列样品。应用多元曲线解析技术恢复的水合壳光谱响应与体相的光谱进行了比较。一旦与各样品中水溶液含量的增加相关联,就可以从比较中推断出水合壳包含的氢键网络范围较小,可能发生的氢键相互作用的数量也比体相少。结果还表明,如果与块体中普遍存在的分子间氢键作用相比,水合壳中的氢键网络在结构上更加坚硬和牢固。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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