4.6 Article

Template-assisted synthesis of porous carbon derived from biomass for enhanced supercapacitor performance

Journal

DIAMOND AND RELATED MATERIALS
Volume 128, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.diamond.2022.109219

Keywords

Fe-SA-C; 3D porous carbon; In-situ hard template; Electrochemical capacitor

Funding

  1. Na-tional Natural Science Foundation of China [21776026, 22075034, 22178037]
  2. Natural Science Foundation of Liaoning Province of China [2021-MS-303]
  3. Liaoning Revitalization Talents Program [XLYC1902037, XLYC2002114]

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Carbon-based electrode materials have attracted attention in supercapacitors due to their tunable structure, stability, and low cost. This study proposes a simple and low-cost method using alginate as a precursor to fabricate biomass-derived porous carbon with a controllable structure. The in-situ formation of Fe(OH)3 nanoparticles is used as a hard template to construct interconnect microchannels, enhancing capacitive active sites and electrolyte diffusion. The optimized sample exhibits high specific capacitance and cycling stability, and a symmetric supercapacitor assembled with these electrodes demonstrates high energy density.
Carbon-based electrode materials have received widespread interest in supercapacitors because of their tunable structure, high chemical and physical stability, and low cost. The hard template method is considered as a potential strategy for fabricating porous carbons with controllable structures. However, porous carbons with satisfactory capacitance are always fabricated using an expensive template. Therefore, a simple and low-cost template strategy is necessary to construct high specific capacity porous carbon for supercapacitors. Herein, we proposed a facile and cost-effective method to fabricate biomass-derived porous carbon with a controllable structure using alginate as precursor. The in-situ formation of Fe(OH)3 nanoparticles was employed as a hard template to construct interconnect microchannels, which could effectively increase capacitive active sites and promote electrolyte diffusion during the electrochemical process. The optimized sample displayed a high specific capacitance of 302 F g(-1) at a current density of 0.5 A g(-1) in 6 M KOH electrolyte and outstanding cycling stability with the capacitance retention of 88.39 % after 10,000 cycles at 5 A g(-1). In addition, a symmetric supercapacitor assembled by Fe-SA-C-1.5 electrodes showed an energy density of 11.32 W h kg(-1) at a power density of 250 W kg(-1). This work offers a promising approach to construct high-performance electrodes for supercapacitors.

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