In Situ intercalating expandable graphite for mesoporous carbon/graphite nanosheet composites as high-performance supercapacitor electrodes
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Updated: May 17, 2026

Evaluating the Electrochemical Properties of Supercapacitors using the Three-Electrode System
Published on: January 7, 2022
Lei Wang1, Guang Mu, Chungui Tian
1Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, Heilongjiang University, Harbin 150080, PR China.
Abstract:
Mesoporous-carbon-coated graphite nanosheet (GNS@MC) composites have been synthesized by the intercalation of resol prepolymer into the interlayers of expandable graphite (EG) under vacuum-assisted conditions, followed by the exfoliation of EG through in situ polymerization, the growth of resol under hydrothermal conditions, and carbonization under Ar. The GNS@MC composites exhibit enhanced capacitive performance compared to mesoporous carbon (MC), microwaved EG after thermal treatment (T-EG), and the physical mixture of MC and T-EG (MC+T-EG). In particular, the GNS@MC-35-800 composite carbonized at 800 °C, which has a graphite-nanosheet content of 35 % and a Brunauer-Emmett-Teller surface area (S(BET) ) of 432.3 m(2) g(-1) , exhibits the highest capacitance of 203 F g(-1) at 1 A g(-1) in 6 M KOH electrolyte. Furthermore, the GNS@MC-35-800 composite exhibits a good cyclic stability with 95 % capacitance retention and a high columbic efficiency of 99 % after 5000 cycles. The energy density of the symmetric supercapacitor GNS@MC-35-800/GNS@MC-35-800 achieved was as high as 11.5 Wh kg(-1) at a high power density of 10 kW kg(-1) . This good performance is attributable to the GNSs in the GNS@MC composite facilitating electron transport owing to its excellent conductivity; moreover, the MC in GNS@MC favors the rapid diffusion of ions by providing low-resistance pathways. The GNS@MC composite may find application in high-performance energy storage and conversion devices.
