ABSTRACT
Conductive metal-organic frameworks (c-MOFs) and ionic liquids (ILs) have emerged as auspicious combinations for high-performance supercapacitors. However, the nanoconfinement from c-MOFs and high viscosity of ILs slow down the charging process. This hindrance can, however, be resolved by adding solvent. Here, constant-potential molecular simulations are performed to scrutinize the solvent impact on charge storage and charging dynamics of MOF-IL-based supercapacitors. Conditions for >100% enhancement in capacity and ≈6 times increase in charging speed are found. These improvements are confirmed by synthesizing near-ideal c-MOFs and developing multiscale models linking molecular simulations to electrochemical measurements. Fundamentally, the findings elucidate that the solvent acts as an "ionophobic agent" to induce a substantial enhancement in charge storage, and as an "ion traffic police" to eliminate convoluted counterion and co-ion motion paths and create two distinct ion transport highways to accelerate charging dynamics. This work paves the way for the optimal design of MOF supercapacitors.
ABSTRACT
Optimizing the synergy between nanoporous carbons and ionic liquids can significantly enhance the energy density of supercapacitors. The highest energy density has been obtained as the size of porous carbon matches the size of ionic liquids, while it may result in slower charging dynamics and thus reduce the power density. Enhancing energy storage without retarding charging dynamics remains challenging. Herein, we designed porous electrodes by introducing an optimized horn-like entrance to the nanopore, which can concurrently improve supercapacitors' charging dynamics and energy storage. Our results revealed the mechanism of improved charging lies in the gradual desolvation process and optimized ion motion paths: the former expedites the adsorption of the counterion by reducing the transitional energy barrier for ions entering the pores, and the latter accelerates the co-ion desorption and eliminates ion overfilling. Meanwhile, the enhancement of energy density could be attributed to the multi-ion coordinated migration.
