摘要
The antagonism between porosity and graphitization critically limits carbon supercapacitor performance. Here, we demonstrate a structural engineering strategy that converts Sargentodoxa Cuneata residue (SCR) into hierarchically porous graphitic carbons (SCR-HPCs). By precisely regulating biomass precursor porous architecture, this methodology decouples the antagonism between porosity development and graphitization progression in KOH-mediated activation, achieving simultaneous high specific surface area (2465.1 m 2 g −1 ) and graphitization (I D /I G of 0.73). In 6 m KOH electrolyte, the specific capacitance of the optimized SCR-HPC-900 electrode reaches 415.6 F g −1 at 0.5 A g −1 , with a capacitance retention of 75.1% even at an ultra-high current density of 200 A g −1 . The fabricated symmetric supercapacitor achieves an energy density of 8.5 Wh kg −1 at a power density of 37 803 W kg −1 , retaining over 100.8% of its capacitance after 100 000 cycles. Remarkably, in 1 m TEABF 4 /PC organic electrolyte, the supercapacitor achieves maximum energy and power densities of 45.6 Wh kg −1 and 41 750 W kg −1 , respectively. This study presents an effective methodology for decoupling the antagonism between porosity and graphitization in conventional processes, offering a new idea for converting biomass waste into high-performance energy storage materials.
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