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Updated: Jul 28, 2025

Evaluating the Electrochemical Properties of Supercapacitors using the Three-Electrode System
Published on: January 7, 2022
Biomass-Derived Carbon Electrodes for High-Performance Supercapacitors
Liqiong Zhang1,2, Yujie Zhang3, Shenghui Jiao2
1Key Lab of Biomass Energy and Material, Jiangsu Province, Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing, 210042, P. R. China.
Abstract:
Supercapacitors with the performance advantages of high-power density are emerging materials for energy storage/conversion systems that can combat climate change caused by CO2 emissions and are of importance with the development of electronic products and artificial intelligence. But rationally preparing high-performance electrode with high mass-loading quantity remains challenge. Herein, we have opted for chitosan as well-structured binding agent to combine with active carbon (SSP-900), a 3D hierarchical micro-meso-macro porous biochar previously obtained, to synthesize high mass-loading freestanding electrode. Especially, the freestanding material (C1000 G0.2 ), owning 0.2 g SSP-900 and suffering carbonization at 1000 °C exhibits high specific surface area of 389.3 cm2 g-1 , and self-doped N, O (2.75 %, 5.64 %). That awards C1000 G0.2 outstanding electrochemical properties, including high specific mass capacitance of 199.2 F g-1 , splendid specific area capacitance of 4.37 F cm-2 in 21.93 g cm-2 , which is more competitive than conventional freestanding materials. Symmetrical supercapacitor with mass loading of 12 mg is assembled and exhibits large specific capacitance of 65 F g-1 , high energy density of 32.5 Wh kg-1 under the power density of 90.4 W kg-1 , and capacitance stability of 98 % after 10,000 cycles. The distinguished electrochemical performance of freestanding electrodes supplies prospective application for storing/converting electrical energy from intermittent solar and wind.
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