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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >X-ray Photoelectron Spectroscopy and Differential Capacitance Study of Thiol-Functional Polysiloxane Films on Gold Supports
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X-ray Photoelectron Spectroscopy and Differential Capacitance Study of Thiol-Functional Polysiloxane Films on Gold Supports

机译:金载体上硫醇官能化聚硅氧烷薄膜的X射线光电子能谱和微分电容研究

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摘要

Polymeric molecules containing multiple thiol groups(polythiols)provide tenacious attachment to metal surfaces such as gold.Polythiol films are also well suited for subsequent derivatization with biomacro-molecules through remnant free thiol groups of the film.In this study,1-3 nm thick layers of a commercial polythiol,poly((mercaptopropyl)methylsiloxane)(PMPMS),are investigated with X-ray photoelectron spectroscopy(XPS)and electrochemical impedance spectroscopy.XPS is used to reveal the surface coverage of thiolate-Au bonds between the polythiol and the metal support,which is found to be approximately 30% lower than that in alkanethiol self-assembled monolayers.The surface density of thiolate-Au bonds did not depend on film thickness provided sufficient PMPMS material was present.Differential capacitance measurements show that the effective dielectric barrier presented by PMPMS films under aqueous environments corresponds closely to their physical thickness,with even approx nm films remaining impermeable to electrolyte species.Modification of the films with an oligoethylene glycol compound was also examined,in anticipation of future applications in label-free,impedance-based biomolecular diagnostics.
机译:包含多个硫醇基团的聚合物分子(聚硫醇)牢固地附着在金等金属表面上。多硫醇薄膜也非常适合随后通过生物大分子通过剩余的硫醇基团进行衍生化。在本研究中,厚度为1-3 nm用X射线光电子能谱(XPS)和电化学阻抗谱研究了商用多硫醇,聚(巯基丙基)甲基硅氧烷)(PMPMS)的各层.XPS用于揭示多硫醇与金属载体比链烷硫醇自组装单层膜低约30%。如果存在足够的PMPMS材料,则硫醇盐-Au键的表面密度不取决于膜厚。差分电容测量表明有效PMPMS膜在水性环境下呈现的介电势垒与它们的物理厚度非常接近,甚至约nm膜预期将在无标签,基于阻抗的生物分子诊断中的未来应用领域中,还对低聚乙二醇化合物对薄膜的改性进行了研究。

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