The movement of electrolyte solutions within nanometer-scale channels is central to understanding nanofluidic phenomena. Ion transport within small (nm) scale pores is also key to electrochemical energy storage, where the energy storage process is dependent on ionic ingress into porous carbon materials [1,2]. Although very significant advances in the understanding of ion movement within electrically charged pores have been made [3], a key barrier is that porous carbon materials contain a complex distribution of interconnected pores of varying size, making it difficult to de-convolute specific size effects. A further connection between the fields of nanofluidics and electrochemistry arises because electrochemical control, based on the phenomenon of electrowetting, may be used to drive liquids into small channels [4]. This restriction has been overcome by applying the nanochannel technology developed by Radha et al [5,6] in the electrochemical context, where one “wall” of the graphene channel is used as an electrode. We are therefore able to observe the effects of differing ion sizes on electrical double-layer capacitance, additionally, the effects of such extreme confinement on electrochemical processes (both capacitive and Faradaic) can also be discerned.
References:
1. B.E. Conway, Electrochemical Supercapacitors, Springer, 1999.
2. Z. Chen et al, Adv. Mater., 23, (2011), 791
3 J. Chmiola, G. Yushin, Y. Gogotsi, C. Portet, P. Simon, P.L. Taberna, Science, 313, (2006), 1760
4 D.J. Lomax et al, Soft Matter, 12, (2016), 8798.
5 B. Radha et al, Nature, 538, (2016), 222
6 A. Esfandiar et al, Science, 358, (2017), 511