论文标题

横跨纳米颗粒悬浮液的无链层双层和结构力

Untangling superposed double layer and structural forces across confined nanoparticle suspensions

论文作者

Ludwig, Michael, von Klitzing, Regine

论文摘要

由于不同贡献的可能重叠,对跨密闭复合流体的力的描述仍然存在许多挑战。在这里,试图解开纳米颗粒悬浮液之间带电表面之间的相互作用。使用胶体探针原子力显微镜测量相互作用力。实验力剖面被认为是双层和结构力的叠加。为了独立描述双层力的衰减,悬浮液的离子强度由电解电导率测量确定。 Jellium近似用于定义流体对筛选表面电势的影响。在那里,纳米颗粒被认为均匀分布在整个流体上,并且仅通过颗粒柜台和添加盐进行筛选。由于两个表面接近纳米颗粒的层驱动,结构力遵循阻尼的振荡曲线。振荡性结构力的描述是通过狭窄表面旁边的耗竭层扩展的,没有纳米颗粒。耗竭层的厚度与来自类似的表面的带电纳米颗粒的静电排斥有关。结果表明,总力谱是独立力贡献的叠加,而没有任何互相影响。使用这个相当简单的模型,从几百个纳米的表面分离到几乎接触的表面,从几百个纳米的表面分离中很好地描述了完整的实验确定的相互作用曲线。

The description of forces across confined complex fluids still holds many challenges due to the possible overlap of different contributions. Here, an attempt is made to untangle the interaction between charged surfaces across nanoparticle suspensions. Interaction forces are measured using colloidal-probe atomic force microscopy. The experimental force profiles are considered as a superposition of double layer and structural forces. In order to independently describe the decay of the double layer force, the ionic strength of the suspension is determined by electrolytic conductivity measurements. Jellium approximation is used to define the impact of the fluid on screening the surface potential. There, the nanoparticles are considered homogeneously distributed across the fluid and screening is only carried out via the particles counterions and added salt. The structural force follows a damped oscillatory profile due to the layer-wise expulsion of the nanoparticles upon approach of both surfaces. The description of the oscillatory structural force is extended by a depletion layer next to the confining surfaces, with no nanoparticles present. The thickness of the depletion layer is related to the electrostatic repulsion of the charged nanoparticles from the like-charged surfaces. The results show that the total force profile is a superposition of independent force contributions without any mutual effects. Using this rather simple model describes the complete experimentally determined interaction force profiles very well from surface separations of a few hundred nanometres down to the surfaces being almost in contact.

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