Journal
ENERGY & FUELS
Volume 35, Issue 17, Pages 14157-14168Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.energyfuels.1c01922
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Funding
- National Natural Science Foundation of China [31971794]
- Key Research and Development Project of Zhejiang Province [2019C02080]
- Department of Education of Zhejiang Province [FX2019077]
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Corncob-derived Fe/N co-doped porous carbon spheres were successfully synthesized and optimized for superior ion transfer kinetics and rate performances, demonstrating high capacitance and supreme cyclability in supercapacitor applications. These properties were attributed to the unique packing architecture, developed micro-mesoporous structure, and multiple redox possibilities of the carbon spheres, showcasing potential for high-tech applications.
Corncob, as a sustainable biomass waste, is mainly composed of hemicellulose. Herein, on the basis of natural corncob as substrates, Fe/N co-doped porous carbon spheres were designed via a consecutive FeCl3-mediated hydrothermal reaction and mild KHCO3 activation route for supercapacitor electrode materials. Owing to the low hydrolysis temperature of hemicellulose and hydrolysis promotion of Fe3+, the corncob-derived hydrochar exhibited special carbon sphere morphology. Interestingly, the carbon sphere morphology was well-preserved upon the melamine-mediated KHCO3 activation. As a result of the short ion diffusion distance, unique packing architecture, and developed micro-mesoporous structure of the carbon spheres, optimized CCAC-Fe-M-50% manifested superior ion transfer kinetics and rate performances (87% up to 20 A g(-1)). Meanwhile, the electrochemical investigation of CCAC-Fe-M-50% in a three-electrode setup illustrated high capacitance (338 F g(-1) at 1 A g(-1)). In a two-electrode setup, the CCAC-Fe-M-50%parallel to CCAC-Fe-M-50% device revealed supreme cyclability (102.7% retention after 5000 cycles) and extremely low R-ct (0.59 Omega) and R-s (4.54 Omega). These superior properties were attributed to the large S-BET (2305.7 m(2) g(-1)), the multiple redox possibilities (Fe3+, Fe2+, and N functional groups), and the carbon sphere morphology with a micro-mesoporous structure, which enhanced ion physisorption, pseudocapacitance, and electrolyte/ion diffusion, respectively. Besides, the fabricated CCAC-Fe-M-50%parallel to CCAC-Fe-M-50% device in a neutral electrolyte demonstrated a superb energy density (E-D) of 18.60 Wh kg(-1) at the power density (P-D) of 455 W kg(-1). The currently presented strategy with superior results might lead to the novel development of biomass-based ultraperformance electrode materials for supercapacitors and other high-tech applications.
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