Issue 25, 2017

Biomass-derived hierarchical porous carbons: boosting the energy density of supercapacitors via an ionothermal approach

Abstract

High mass energy density coupled with high power density is highly desired for electrical double-layer capacitors. Usually the capacitive performance is improved by optimizing the pore size and volume distribution. Herein, the authors report an efficient approach to optimize the porous structure through a facile ionothermal carbonization method. A series of hierarchical porous carbons with unique sub-micrometer sized morphology, high surface area and abundant mesopores (e.g. SBET = 2532 m2 g−1 and Vmeso = 1.077 cm3 g−1) have been synthesized, using Jujun grass as a nitrogen-containing precursor. The ionic liquid acts not only as a reaction medium for the conversion of biomass to carbon but also as a porogenic agent for inducing mesoporosity. The results indicate that the ionothermal method can balance the micro- and mesoporosity of the optimized porous carbon, making it one of the competent alternatives to the state-of-the-art electrodes for ultra-high energy density supercapacitors. The optimized ionothermal carbon (ITC-JG-900) shows an impressively high specific capacitance of 336 F g−1 at 1 A g−1 in 6 M KOH, and even retained a capacitance of 222 F g−1 at 10 A g−1, which is 66% of the initial capacitance. The maximum energy density of ITC-JG-900 as a supercapacitor is found to be over 72.7 W h kg−1 when the power density is 1204 W kg−1, which is higher than those of most of the equivalent benchmarks tested in aqueous electrolytes.

Graphical abstract: Biomass-derived hierarchical porous carbons: boosting the energy density of supercapacitors via an ionothermal approach

Associated articles

Article information

Article type
Paper
Submitted
27 Apr 2017
Accepted
18 May 2017
First published
19 May 2017

J. Mater. Chem. A, 2017,5, 13009-13018

Biomass-derived hierarchical porous carbons: boosting the energy density of supercapacitors via an ionothermal approach

Y. Liu, B. Huang, X. Lin and Z. Xie, J. Mater. Chem. A, 2017, 5, 13009 DOI: 10.1039/C7TA03639F

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