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Electric Birefringence of Electrolytes near Charged Surfaces,I

机译:带电表面附近电解质的电双折射I

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We investigate electric birefringence of aqueous electrolyte solutions near a negatively charged silica glass surface using evanescent wave laser polarimetry(EWLP).By probing changes in the polarization state of visible light totally internally reflected at the solid-liquid interface,EWLP facilitates unprecedented measurements of electric-field-induced birefringence in a thin electrolyte film,O(150 nm),adsorbed on the glass surface.For aqueous NaCl and MgCl2 solutions(1-100 mM),these measurements reveal Kerr law behavior over a range of pH and solution concentrations.The Kerr coefficients are,however,several orders of magnitude larger than values normally obtained from bulk electric birefringence measurements.We propose that formation of anisotropic,polarizable ionic clusters near the glass surface is the source of these observations.Orientation of the clusters by the electric field is confined in the plane defined by the glass/electrolyte interface and is attributed to rearrangement of the constituent ions.Birefringence relaxation measurements reveal relaxation times,r,many orders of magnitude larger than typically observed in molecular fluids.These measurements also show that t is independent of both the electrolyte concentration,c,and pH.We discuss these latter observations in terms of an ion redistribution process,wherein the intrinsic surface adsorption- desorption rates of ions in the clusters determine the time constant for relaxation of surface birefringence.
机译:我们使用e逝波激光偏振法(EWLP)研究带负电的石英玻璃表面附近电解质水溶液的电双折射。通过探测固液界面全内反射的可见光的偏振态变化,EWLP促进了前所未有的电学测量在玻璃表面上吸附的O(150 nm)薄膜中的磁场引起的双折射。对于NaCl和MgCl2水溶液(1-100 mM),这些测量结果显示了在一定pH和溶液浓度下的克尔定律行为但是,Kerr系数比通常通过体电双折射测量获得的值大几个数量级。我们建议在玻璃表面附近形成各向异性的可极化离子簇是这些观察的来源。电场被限制在由玻璃/电解质界面定义的平面中,并归因于双折射弛豫测量揭示了弛豫时间,r,比分子流体中通常观察到的弛豫时间大许多数量级。这些测量结果还表明,t与电解质浓度,c和pH无关。我们讨论了后面的这些观察结果就离子再分布过程而言,簇中离子的固有表面吸附-解吸速率决定了表面双折射松弛的时间常数。

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