Theoretical Insight into the Imidazolium-Based Ionic Liquid Interface Structure and Differential Capacitance on...

Electric double layers (EDLs) play a key role in the electrochemical and energy storage of supercapacitors. It is important to understand the structure and properties of EDLs. In this work, quantum chemical calculations and molecular dynamics (MD) simulations are used to study the microstructure of EDLs of four different substituents of imidazolium-based bis(trifluoromethylsulfonyl)imide ionic liquids (ILs) on the Au(111) surface. It is shown that the particle interactions influence the different arrangements of the anion and cation. More alkyl substitutions and longer alkyl chains result in a higher E_LUMO and thus a stronger interaction energy between cations and electrodes. Strong interactions produce linear patterns of anions/cations on the electrode and a maximum value of differential capacitance near PZC, whereas weak interactions generate worm-like patterns of anions/cations on Au(111) and a minimum value of differential capacitance near the PZC. We hold the opinion that the alkyl substitution has more effects on the EDLs. Our analysis provides a new perspective on EDLs structures at the atomic and molecular level. This study provides a good basis and guidance for further understanding the interface phenomena and characteristics of ionic liquids in electrochemical and energy device applications.