Capillary Condensation of Ionic Liquid Solutions in Porous Electrodes

被引:13
|
作者
Szparaga, Ryan [1 ]
Woodward, Clifford E. [2 ]
Forsman, Jan [1 ]
机构
[1] Chem Ctr Lund, S-22100 Lund, Sweden
[2] Univ New S Wales, ADFA Canberra, Univ Coll, Sch Phys Environm & Math Sci, Canberra, ACT 2600, Australia
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2013年 / 117卷 / 04期
关键词
DENSITY-FUNCTIONAL THEORY; DOUBLE-LAYER; SURFACE FORCES; DIFFERENTIAL CAPACITANCE; CARBON MATERIALS; PORE-SIZE; SIMULATION; PREDICTION; MIXTURES; FLUIDS;
D O I
10.1021/jp309794w
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
We use classical density functional theory to investigate room temperature ionic liquid + solvent mixtures in porous electrodes. We consider those mixtures that display a miscibility gap in the bulk fluid and hence have the capacity to undergo capillary condensation in pores which preferentially attract the ionic liquid component. A novel aspect of this transition is that, when the system is at or near the critical point for this transition, we find an extraordinary increase in the capacitance, which derives from the fact that the capacitance is a thermodynamic response function, diverging at spinodal points.
引用
收藏
页码:1728 / 1734
页数:7
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