Institute of Physics, Martin-Luther-University, D-06099 Halle, Germany.
J Chem Phys. 2009 Sep 21;131(11):114903. doi: 10.1063/1.3223724.
Based on the Poisson-Nernst-Planck equations (PNP), the spatiotemporal charge, concentration profile, and the electric field in polyelectrolytes are analyzed. The system is subjected to a dc applied voltage. Different to recent papers we obtain an exact analytical solution of the PNP in the linear regime, which is characterized by an inevitable coupling between the spatial and the temporal behavior. In the long time limit the systems tends in a nonexponential manner to the steady state predicted by the Debye-Hueckel theory, where the time scale for the crossover into the steady state is determined by the Debye screening length and the initial concentration. The higher the initial concentration is the faster the system evolves into the stationary state. The Debye screening length characterizes not only the asymptotic behavior but also the spatiotemporal evolution of the system at finite times. Using experimental data the concentration profile and the electric field is shown to be on a master curve parametrized by the screening length.
基于泊松-纳斯特-普朗克方程(PNP),分析了聚电解质中的时空电荷、浓度分布和电场。该系统受到直流外加电压的作用。与最近的论文不同,我们得到了 PNP 在线性区域的精确解析解,其特征是空间和时间行为之间不可避免的耦合。在长时间限制下,系统以非指数方式趋于德拜-休克尔理论预测的稳态,其中进入稳态的时间尺度由德拜屏蔽长度和初始浓度决定。初始浓度越高,系统进入稳态的速度就越快。德拜屏蔽长度不仅表征了渐近行为,还表征了系统在有限时间内的时空演化。利用实验数据,我们发现浓度分布和电场呈标度参数为屏蔽长度的主曲线。