The Dynamic Behavior of Charged Particles During the Relaxation Process of Electrophoretic Displays

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Sheng Mai, Xuekai Liu, Juncheng Zhao, Zhihang Yu, Jing Jin, Liuyong Shi, Teng Zhou
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Abstract

Electrophoretic displays (EPDs) are commonly employed in applications like e-books and electronic price tags due to their benefits of minimal power consumption, excellent contrast, and broad viewing angles. This article establishes a dynamic model for nanoparticles after the removal of the applied electric field. The model combines the Poisson equation, the Navier–Stokes equation, and the Nernst–Planck equation. The Arbitrary Lagrangian–Eulerian method is applied to simulate nanoparticle diffusion motion under varying conditions, such as solution viscosity, particle radius, and reverse micelle radius, after the electric field is removed. The results indicate that after the electric field is removed, high-viscosity solutions exert a stronger hindrance on the particles, resulting in a shorter displacement over the same time period. With equal charge, smaller particle radius exhibits higher surface charge density, allowing them to travel further within the same time frame. Additionally, a smaller reverse micelle radius facilitates the rapid neutralization of surface charge on the particles, thereby limiting their diffusion distance. These findings provide theoretical support for a deeper understanding of the operating mechanism of EPDs.

电泳显示器弛豫过程中带电粒子的动态行为。
电泳显示器(epd)通常用于电子书和电子价格标签等应用,因为它们具有最小功耗,出色对比度和宽视角的优点。本文建立了外加电场去除后纳米颗粒的动力学模型。该模型结合了泊松方程、纳维-斯托克斯方程和能斯特-普朗克方程。采用任意拉格朗日-欧拉方法模拟了去除电场后溶液粘度、粒子半径、反胶束半径等不同条件下纳米粒子的扩散运动。结果表明,在去除电场后,高粘度溶液对颗粒施加更强的阻力,导致相同时间内的位移更短。在电荷相等的情况下,粒子半径越小,表面电荷密度越高,从而使它们在相同的时间范围内运动得更远。此外,较小的反胶束半径有利于粒子表面电荷的快速中和,从而限制了它们的扩散距离。这些发现为深入了解epd的运行机制提供了理论支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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