论文标题
纳米孔的当前波动揭示了聚合物壁吸附电位
Current fluctuations in nanopores reveal the polymer-wall adsorption potential
论文作者
论文摘要
通过聚合物吸附对表面特性的修饰是一种广泛使用的技术,用于调整分子实验(例如纳米孔传感)中的相互作用。在这里,我们研究了通过固态纳米孔的离子电流噪声如何反映短而中性聚合物对孔隙表面的吸附。噪声的功率光谱密度在吸附聚合物后显示出特征的变化,其大小强烈取决于聚合物长度和盐浓度。特别是,对于低盐浓度的短聚合物,尽管使用石英晶体微生物测量值验证了这些系统中可比吸附的可比吸附,但仍未观察到任何变化。我们提出,特征性噪声是由聚合物在表面和表面上的运动产生的,并执行模拟以评估该模型的可行性。与实验数据的良好一致性是使用有力动机的模拟参数获得的,从而深入了解吸附电位和潜在过程的形状。这为使用噪声频谱分析的原位表征铺平了道路。
Modification of surface properties by polymer adsorption is a widely used technique to tune interactions in molecular experiments such as nanopore sensing. Here, we investigate how the ionic current noise through solid-state nanopores reflects the adsorption of short, neutral polymers to the pore surface. The power spectral density of the noise shows a characteristic change upon adsorption of polymer, the magnitude of which is strongly dependent on both polymer length and salt concentration. In particular, for short polymers at low salt concentrations no change is observed, despite verification of comparable adsorption in these systems using quartz crystal microbalance measurements. We propose that the characteristic noise is generated by the movement of polymers on and off the surface and perform simulations to assess the feasibility of this model. Excellent agreement with experimental data is obtained using physically motivated simulation parameters, providing deep insight into the shape of the adsorption potential and underlying processes. This paves the way towards using noise spectral analysis for in situ characterisation of functionalised nanopores.