纳米孔
吸附
化学物理
噪音(视频)
解吸
低频
缩放比例
扩散
离子
材料科学
动力学
光谱密度
次声
指数
分子物理学
分析化学(期刊)
纳米技术
化学
物理
物理化学
热力学
声学
经典力学
哲学
数学
人工智能
图像(数学)
语言学
计算机科学
几何学
色谱法
统计
有机化学
天文
作者
Simon Gravelle,Roland R. Netz,Lydéric Bocquet
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-08-30
卷期号:19 (10): 7265-7272
被引量:34
标识
DOI:10.1021/acs.nanolett.9b02858
摘要
Ionic current measurements through solid-state nanopores consistently show a power spectral density that scales as 1/f α at low frequency f, with an exponent α ∼ 0.5–1.5, but strikingly, the physical origin of this behavior remains elusive. Here, we perform simulations of particles reversibly adsorbing at the surface of a nanopore and show that the fluctuations in the number of adsorbed particles exhibit low-frequency pink noise. We furthermore propose theoretical modeling for the time-dependent adsorption of particles on the nanopore surface for various geometries, which predicts a frequency spectrum in very good agreement with the simulation results. Altogether, our results highlight that the low-frequency noise takes its origin in the reversible adsorption of ions at the pore surface combined with the long-lasting excursions of the ions in the reservoirs. The scaling regime of the power spectrum extends down to a cutoff frequency which is far smaller than simple diffusion estimates. Using realistic values for the pore dimensions and the adsorption–desorption kinetics, this predicts the observation of pink noise for frequencies down to the hertz for a typical solid-state nanopore, in good agreement with experiments.
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