Deuk Yong Leea and Young-Jei Ohb,c,*
aDepartment of Biomedical Engineering, Daelim University, Anyang 13916,
Korea
bOpto-electronic Materials & Devices Research Center, Korea
Institute of Science and Technology, Seoul 02792, Korea
cDepartment of Nano Material Science and Engineering, Korea University
of Science and Technology, Daejeon 34113, Korea
The Ni-Mn hydroxide/carbon
cryogel (20 to 80 wt%) composite electrodes were synthesized by freeze-drying
to improve electrochemical properties of the Ni-Mn hydroxide. XRD results
revealed that the composite electrode showed a distorted spinel-like structure
similar to the Ni-Mn hydroxide plus the graphitized carbon. The crystallinity
of carbon cryogel in composite electrode was improved dramatically with
increasing the carbon cryogel content. The presence of the carbon cryogel
played a significant role in inhibiting the crystal growth of Ni-Mn hydroxide
on the surface of carbon cryogel. Electrochemical properties of the composite
electrodes, such as capacitance, power density, and energy density, were observed
to be always higher than those of the Ni-Mn electrodes. The highest specific
capacitance of 221 F/g was observed for the electrodes containing 20 wt% of
carbon cryogel at a scan rate of 5 mV/s and an electrode loading amount of 15
mg/cm2 due to easy transport of the ions into pores. However, the
highest energy density of 10.8 Wh/kg and power density of 927 W/kg were
observed for the composite electrodes containing 80 wt% of carbon cryogel.
Experimental results suggested that tunable electrochemical properties of the
composite electrodes can be adjusted by varying the carbon cryogel content.
Keywords: Ni-Mn hydroxide, Carbon cryogel, Capacitance, Power density, Energy density, Supercapacitor
2019; 20(6): 649-654
Published on Dec 31, 2019
bOpto-electronic Materials & Devices Research
Center, Korea Institute of Science and Technology, Seoul 02792, Korea
cDepartment of Nano Material Science and Engineering, Korea University
of Science and Technology, Daejeon 34113, Korea
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