Open AccessEnforced Freedom: Electric‐Field‐Induced Declustering of Ionic‐Liquid Ions in the Electrical Double Layer
Author(s) -
Zhang Yufan,
Ye Ting,
Chen Ming,
Goodwin Zachary A.H.,
Feng Guang,
Huang Jun,
Kornyshev Alexei A.
Publication year - 2020
Publication title -
energy and environmental materials
Language(s) - English
Resource type - Journals
ISSN - 2575-0356
DOI - 10.1002/eem2.12107
Subject(s) - ion , electric field , dipole , dielectric , chemical physics , multipole expansion , ionic bonding , chemistry , molecular dynamics , ionic liquid , ionic potential , materials science , molecular physics , physics , computational chemistry , quantum mechanics , optoelectronics , biochemistry , organic chemistry , catalysis
Ions in the bulk of solvent‐free ionic liquids bind into ion pairs and clusters. The competition between the propensity of ions to stay in a bound state, and the reduction of the energy when unbinding in electric field, determines the portion of free ions in the electrical double layer. We present the simplest possible mean‐field theory to study this effect. “Cracking” of ion pairs into free ions in electric field is accompanied by the change of the dielectric response of the ionic liquid. The predictions from the theory are verified and further explored by molecular dynamics simulations. A particular finding of the theory is that the differential capacitance vs potential curve displays a bell shape, despite the low concentration of free charge carriers, because the dielectric response reduces the threshold concentration for the bell‐ to camel‐shape transition. The presented theory does not take into account overscreening and oscillating charge distributions in the electrical double layer. But in spite of the simplicity of the model, its findings demonstrate a clear physical effect: a preference to be a charged monopole rather than a dipole (or higher order multipole) in strong electric field.