The growing demand for portable electronic devices means that lightweight power sources are increasingly sought after. Electric double layer capacitors (EDLCs) are promising candidates for use in lightweight power sources due to their high power densities and outstanding charge/discharge cycling stabilities. Three-dimensional (3D) self-supporting carbon-based materials have been extensively studied for use in lightweight EDLCs. Yet, a major challenge for 3D carbon electrodes is the limited ion diffusion rate in their internal spaces. To address this limitation, hierarchically porous 3D structures that provide additional channels for internal ion diffusion have been proposed. Herein, we report a new chemical method for the synthesis of an ultralight (9.92 mg/cm³) 3D porous carbon foam (PCF) involving carbonization of a glutaraldehydecross-linked chitosan aerogel in the presence of potassium carbonate. Electron microscopy images reveal that the carbon foam is an interconnected network of carbon sheets containing uniformly dispersed macropores. In addition, Brunauer–Emmett–Teller measurements confirm the hierarchically porous structure. Electrochemical data show that the PCF electrode can achieve an outstanding gravimetric capacitance of 246.5 F/g at a current density of 0.5 A/g, and a remarkable capacity retention of 67.5% was observed when the current density was increased from 0.5 to 100 A/g. A quasi-solid-state symmetric supercapacitor was fabricated via assembly of two pieces of the new PCF and was found to deliver an ultra-high power density of 25 kW/kg at an energy density of 2.8 Wh/kg. This study demonstrates the synthesis of an ultralight and hierarchically porous carbon foam with high capacitive performance.

Graphene oxide (GO) can be reduced to graphene in a normal aerobic setup under ambient conditions as mediated by microbial respiration of Shewanella cells. The microbially-reduced graphene (MRG) exhibited excellent electrochemical properties. Extracellular electron transfer pathways at the cell/GO interface were systematically investigated, suggesting both direct electron transfer and electron mediators are involved in the GO reduction.