Methodological Studies of the Mechanism of Anion Insertion in Nanometer-Sized Carbon Micropores

Dual-ion hybrid capacitors (DIHCs) are a promising class of electrochemical energy storage devices intermediate between batteries and supercapacitors, exhibiting both high energy and power density, and generalizable across wide chemistries beyond lithium. In this study, a model carbon framework material with a periodic structure containing exclusively 1.2 nm width pores, zeolite-templated carbon (ZTC), was investigated as the positive electrode for the storage of a range of anions relevant to DIHC chemistries. Screening experiments were carried out across 21 electrolyte compositions within a common stable potential window of 3.0-4.0 V vs. Li/Li+ to determine trends in capacity as a function of anion and solvent properties. To achieve fast rate capability, a binary solvent balancing a high dielectric constant with a low viscosity and small molecular size was used; optimized full-cells based on LiPF6 in binary electrolyte exhibited 146 Wh kg(-1) and >4000 W kg(-1) energy and power densities, respectively.

Automated summary

Dual-ion hybrid capacitors (DIHCs) are electrochemical energy storage devices that have both high energy density and high power density, and can be applied in chemistry beyond lithium. This study investigated a carbon framework material as the positive electrode for DIHCs and determined the effect of different anions and solvents on capacity through screening experiments. By using a specific binary solvent, optimized full-cells achieved high energy and power densities.