Activation Energy of Ion Desorption at Ionic Liquid/Pt Electrode Interfaces: A Sum-Frequency Generation Vibrational Spectroscopic Study.

Abstract

Electrolyte/electrode interfaces of room-temperature ionic liquids (RTILs) exhibit hysteretic responses to different applied potentials owing to the differences in the ion adsorption/desorption processes; the ion desorption requires excess potential, which reflects the activation energy of ion desorption. Thus far, the contributions of the ion adsorption energy and the activation barrier for ion desorption toward the ion-dependent excess potential have not been quantified. Herein, we report on our infrared-visible sum-frequency generation vibrational spectroscopy study of the hysteretic responses of the anion adsorption/desorption at Pt electrode interfaces using neat, binary, and diluted RTILs composed of 1-butyl-3-methylimidazolium cations ([C4mim]+) and bis(trifluoromethanesulfonyl)amide ([TFSA]-) and trifluoromethanesulfonate ([OTf]-) anions. Experimental results are compared to the theoretical calculations for the electric double layer model. The hysteretic response of the RTIL/Pt interface derives predominantly from the activation energy of anion desorption, which causes the negative excess potential required for anion desorption. A comparison of the anion adsorption/desorption behaviors of neat RTILs with those of binary and diluted RTILs reveals that the large activation energy of anion desorption at the neat RTIL/Pt interface originates largely from the activation barrier for restructuring ionic layering in the diffuse layer.