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Metal-organic framework-derived CoSe2/(NiCo) Se-2 box-in-box hollow nanocubes with enhanced electrochemical properties for sodium-ion storage and hydrogen evolution

Authors
Park, Seung-KeunKim, Jin KooKang, Yun Chan
Issue Date
21-9월-2017
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.5, no.35, pp.18823 - 18830
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MATERIALS CHEMISTRY A
Volume
5
Number
35
Start Page
18823
End Page
18830
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/82201
DOI
10.1039/c7ta05571d
ISSN
2050-7488
Abstract
Multishell structured metal selenide nanocubes, namely, Co/(NiCo)Se-2 box-in-box structures with different shell compositions, were successfully synthesized by applying zeolitic imidazolate framework-67 (ZIF-67) as a template. This strategy involved the fabrication of cube-shaped ZIF-67/Ni-Co layered double hydroxides with a yolk-shell structure and then transformation into Co/(NiCo)Se-2 with a box-in-box structure by a selenization process under Ar/H-2 conditions. During the selenization step, hollow structured CoSe2 cores were generated by Ostwald ripening, resulting in the formation of Co/(NiCo)Se-2 with a box-in-box structure composed of an inner CoSe2 shell and an outer (NiCo)Se-2 shell. Due to the synergetic effect of the unique structure and multicomponent selenide composition, the Co/(NiCo)Se-2 with the box-in-box structure offered excellent dual functionality as both an anode for sodium ion batteries (SIBs) and an electrocatalyst for the hydrogen evolution reaction (HER). Electrochemical tests on the Co/(NiCo)Se-2 with the box-in-box structure demonstrated a low Tafel slope (39.8 mV dec(-1)) andexcellent stability. In addition, it delivered a high specific capacity of 497 mA h g(-1) after 80 cycles, with a current density of 0.2 A g(-1) and excellent cycling stability as an anode material for SIBs.
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