Atomistic Insight on the Charging Energetics in Subnanometer Pore Supercapacitors

被引:52
作者
Feng, Guang [1 ]
Qiao, Rui [1 ]
Huang, Jingsong [2 ]
Sumpter, Bobby G. [2 ]
Meunier, Vincent [3 ]
机构
[1] Clemson Univ, Coll Engn & Sci, Clemson, SC 29634 USA
[2] Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
[3] Rensselaer Polytech Inst, Dept Phys Appl Phys & Astron, Troy, NY 12180 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-DYNAMICS; CARBON; CAPACITANCE; SIMULATIONS; SELECTIVITY;
D O I
10.1021/jp107125m
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
Electrodes featuring subnanometer pores are favorable to the capacitance and energy density of supercapacitors. However, there is an energy penalty to enter subnanometer pores as ions have to shed part of their salvation shell. The magnitude of such an energy penalty plays a key role in determining the accessibility and charging/discharging of these subnanometer pores. Here, we report on the atomistic simulation of Na+ and Cl- ions entering a polarizable slit pore with a center-to-center width of 0.82 tun We show that the free energy penalty for these ions to enter the pore is less than 14 kJ/mol for both Na+ and Cl- ions. The surprisingly small energy penalty is caused by the van der Waals attractions between ions and pore walls, the image charge effects, the moderate (19-26%) dehydration of the ions inside the pore and the strengthened interactions between ions and their hydration water molecules in the subnanometer pore. The results provide strong impetus for further developing nanoporous electrodes featuring subnanometer pores.
引用
收藏
页码:18012 / 18016
页数:5
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