Journal
SMALL
Volume 14, Issue 5, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201700979
Keywords
CoSe2; oxygen evolution reaction; reaction mechanism; selenization reaction; supercapacitor
Categories
Funding
- National High Technology Research and Development Program [2015AA050601]
- National Natural Science Foundation of China [11674252, 61376013, 91433203]
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Metal selenides have great potential for electrochemical energy storage, but are relatively scarce investigated. Herein, a novel hollow core-branch CoSe2 nanoarray on carbon cloth is designed by a facile selenization reaction of predesigned CoO nanocones. And the electrochemical reaction mechanism of CoSe2 in supercapacitor is studied in detail for the first time. Compared with CoO, the hollow core-branch CoSe2 has both larger specific surface area and higher electrical conductivity. When tested as a supercapacitor positive electrode, the CoSe2 delivers a high specific capacitance of 759.5 F g(-1) at 1 mA cm(-2), which is much larger than that of CoO nanocones (319.5 F g(-1)). In addition, the CoSe2 electrode exhibits excellent cycling stability in that a capacitance retention of 94.5% can be maintained after 5000 charge-discharge cycles at 5 mA cm(-2). An asymmetric supercapacitor using the CoSe2 as cathode and an N-doped carbon nanowall as anode is further assembled, which show a high energy density of 32.2 Wh kg(-1) at a power density of 1914.7 W kg(-1), and maintains 24.9 Wh kg(-1) when power density increased to 7354.8 W kg(-1). Moreover, the CoSe2 electrode also exhibits better oxygen evolution reaction activity than that of CoO.
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