电解质
化学
离子键合
超级电容器
化学物理
离子
介孔材料
电容
功率密度
准固态
密度泛函理论
电极
计算化学
热力学
物理化学
功率(物理)
色素敏化染料
有机化学
催化作用
物理
作者
Xuehang Wang,Aleksandar Y. Mehandzhiyski,Bjørnar Arstad,Katherine L. Van Aken,Tyler S. Mathis,Alejandro Gallegos,Ziqi Tian,Dingding Ren,Edel Sheridan,Brian A. Grimes,De‐en Jiang,Jianzhong Wu,Yury Gogotsi,De Chen
摘要
Ion-ion interactions in supercapacitor (SC) electrolytes are considered to have significant influence over the charging process and therefore the overall performance of the SC system. Current strategies used to weaken ionic interactions can enhance the power of SCs, but consequently, the energy density will decrease due to the increased distance between adjacent electrolyte ions at the electrode surface. Herein, we report on the simultaneous enhancement of the power and energy densities of a SC using an ionic mixture electrolyte with different types of ionic interactions. Two types of cations with stronger ionic interactions can be packed in a denser arrangement in mesopores to increase the capacitance, whereas only cations with weaker ionic interactions are allowed to enter micropores without sacrificing the power density. This unique selective charging behavior in different confined porous structure was investigated by solid-state nuclear magnetic resonance experiments and further confirmed theoretically by both density functional theory and molecular dynamics simulations. Our results offer a distinct insight into pairing ionic mixture electrolytes with materials with confined porous characteristics and further propose that it is possible to control the charging process resulting in comprehensive enhancements in SC performance.
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