The effect of explicit counterion binding on the transference number of polyelectrolyte solutions

被引:1
|
作者
Lytle, T. K. [1 ]
Yethiraj, A. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2022年 / 156卷 / 10期
基金
美国国家科学基金会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; SODIUM POLYSTYRENE SULFONATE; INTEGRAL-EQUATION THEORY; BROWNIAN DYNAMICS; FLEXIBLE POLYELECTROLYTES; TRANSPORT-PROPERTIES; LIQUID ELECTROLYTES; SALT; GROMACS; LI+;
D O I
10.1063/5.0083414
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Polyelectrolyte solutions have been proposed as a method to improve the efficiency of lithium-ion batteries by increasing the cation transference number because the polymer self-diffusion coefficient is much lower than that of the counterion. However, this is not necessarily true for the polymer mobility. In some cases, negative transference numbers have been reported, which implies that the lithium ions are transporting to the same electrode as the anion, behavior that is often attributed to a binding of counterions to the polyion. We use a simple model where we bind some counterions to the polymer via harmonic springs to investigate this phenomenon. We find that both the number of bound counterions and the strength of their binding alter the transference number, and, in some cases, the transference number is negative. We also investigate how the transference number depends on the Manning parameter, the ratio of the Bjerrum length to charge separation along the chain. By altering the Manning parameter, the transference number can almost be doubled, which suggests that charge spacing could be a way to increase the transference number of polyelectrolyte solutions. Published under an exclusive license by AIP Publishing.
引用
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页数:10
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