posted on 2014-02-27, 00:00authored bySong Li, Katherine L. Van Aken, John K. McDonough, Guang Feng, Yury Gogotsi, Peter T. Cummings
The
electrical double layer (EDL) structure formed by ions at a
charged surface, which is the key to determining the performance of
supercapacitors, has been extensively studied for many monocationic
ionic liquids (MILs). However, it is not known what effect replacing
MILs with dicationic ionic liquids (DILs) will have on the EDL structure.
In this work, the interfacial structure and electrochemical performance
of DILs [Cn(mim)2](BF4)2 (n = 3, 6, 9) and [C6(mim)2](Tf2N)2 were investigated using classical
molecular dynamics (MD) simulation for comparison with their monocationic
counterparts. Different EDL structures formed by DILs and MILs near
an onion-like carbon (OLC) electrode were observed. The interfacial
orientation of the imidazolium plane in dications was verified to
be similar to that of monocations. Moreover, the dissimilar sizes
of the cation/anion and the specific ion adsorption on OLC were found
to contribute to the distinctive shape of the differential capacitance–electric
potential (C–V) curves, which were also dependent on the type
of anions. Increased capacitance in BF4-containing DILs
was not observed in comparison with their counterpart MILs, whereas
dicationic [C6(mim)2](Tf2N)2 yielded higher differential capacitance in contrast to monocationic
[C6mim][Tf2N], which was substantiated by cyclic
voltammetry measurements as well. This work provides molecular insights
into the EDL structure and C–V curves of imidazolium-based
DILs in OLC-based supercapacitors.