Fischer Sebastian, Netz Roland R
Fachbereich Physik, Freie Universität Berlin, Arnimallee 14, 14195, Berlin, Germany.
Eur Phys J E Soft Matter. 2013 Oct;36(10):117. doi: 10.1140/epje/i2013-13117-9. Epub 2013 Oct 25.
We study the frequency-dependent dielectric response of flexible polyelectrolyte chains in aqueous salt-free dilute solution as a function of polymer concentration and length by means of Brownian dynamics simulations including hydrodynamic interactions. We show that condensed and uncondensed counter ions are characterized by different dielectric response spectra and thus confirm long-held scaling assumptions used for the interpretation of experimental data. In addition to the well-known relaxation modes of condensed and uncondensed counter ions we observe for a single polyelectrolyte chain, we find in many-chain simulations a novel spectral feature at low frequencies that essentially corresponds to an exchange of counter ions between neighboring polyelectrolytes. Our results suggest that the experimental low-frequency dielectric mode might not be due to condensed counter ions, as is commonly assumed, but rather due to a collective many-chain process. This could resolve a long-standing puzzle in the comparison of experimental results and scaling predictions.
我们通过包含流体动力学相互作用的布朗动力学模拟,研究了无盐水溶液中柔性聚电解质链的频率相关介电响应随聚合物浓度和长度的变化。我们表明,凝聚态和非凝聚态抗衡离子具有不同的介电响应光谱,从而证实了长期以来用于解释实验数据的标度假设。除了在单个聚电解质链中观察到的凝聚态和非凝聚态抗衡离子的众所周知的弛豫模式外,我们在多链模拟中还发现了低频处的一个新光谱特征,该特征本质上对应于相邻聚电解质之间抗衡离子的交换。我们的结果表明,实验中的低频介电模式可能并非如通常所假设的那样是由于凝聚态抗衡离子,而是由于集体多链过程。这可能解决了实验结果与标度预测比较中一个长期存在的难题。