In situ encapsulation of tin oxide and cobalt oxide composite in porous carbon for high-performance energy storage applications
Herein, we report the preparation of porous carbon from palm kernel shell and loading of tin oxide‑cobalt oxide in its pores using a facile in-situ encapsulation synthesis strategy. The as-synthesized SnO2/Co3O4@C composite was characterized by powder X-ray diffraction, X-ray photoelectron spectrosc...
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Published in | Journal of electroanalytical chemistry (Lausanne, Switzerland) Vol. 817; pp. 217 - 225 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
15.05.2018
Elsevier Science Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | Herein, we report the preparation of porous carbon from palm kernel shell and loading of tin oxide‑cobalt oxide in its pores using a facile in-situ encapsulation synthesis strategy. The as-synthesized SnO2/Co3O4@C composite was characterized by powder X-ray diffraction, X-ray photoelectron spectroscopy and field-emission scanning electron microscopy techniques. This composite was used as an electrode for supercapacitors. Electrochemical charge storage capabilities of the composite were measured using cyclic voltammetry, charge-discharge cycling and electrochemical impedance spectroscopy in aqueous 6 M KOH and 1 M Na2SO4 electrolytes. The SnO2/Co3O4@C composite showed over 70% higher specific capacitance (177 F g−1) than the pure porous carbon (106 F g−1) in 6 M KOH. Among these electrolytes, the composite exhibited an enhanced electrochemical performance in KOH electrolyte due to its smaller hydrated ion radius, high ionic mobility and lower equivalent series resistance than Na2SO4.
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•In situ encapsulation of tin oxide and cobalt oxide in porous carbon.•The SnO2/Co3O4@C composite showed 70% higher CS than porous carbon in 6 M KOH.•Best electrochemical behaviors are shown in 6 M KOH electrolyte than 1 M Na2SO4.•The SnO2/Co3O4@C composite showed lower resistance in 6 M KOH than 1 M Na2SO4.•The mobility and conductivity of hydrated ions play vital in electrode performance. |
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ISSN: | 1572-6657 1873-2569 |
DOI: | 10.1016/j.jelechem.2018.04.019 |