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Development of supercapacitors with high-energy density and high-power density is a tremendous challenge. Although the use of conductive carbon materials is promising, other methods are needed to reach high cyclability, which cannot be achieved by fully utilizing the surface-oxygen redox reactions of carbon. Here we introduce an effective strategy that utilizes Cu(2+) reduction with carbon-oxygen surface groups of the binder-free electrode in a new redox-active electrolyte. We report a 10-fold increase in the voltammetric capacitance (4,700 F g(-1)) compared with conventional electrolyte. We measured galvanostatic capacitances of 1,335 F g(-1) with a retention of 99.4% after 5,000 cycles at 60 A g(-1) in a three-electrode cell and 1,010 F g(-1) in a two-electrode cell. This improvement is attributed to the synergistic effects between surface-oxygen molecules and electrolyte ions as well as the low charge transfer resistance (0.04 Ω) of the binder-free porous electrode. Our strategy provides a versatile method for designing new energy storage devices and is promising for the development of high-performance supercapacitors for large-scale applications.

Synergistic interaction between redox-active electrolyte and binder-free functionalized carbon for ultrahigh supercapacitor performance