Issue 35, 2017

Metal–organic framework-derived CoSe2/(NiCo)Se2 box-in-box hollow nanocubes with enhanced electrochemical properties for sodium-ion storage and hydrogen evolution

Abstract

Multishell structured metal selenide nanocubes, namely, Co/(NiCo)Se2 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)Se2 with a box-in-box structure by a selenization process under Ar/H2 conditions. During the selenization step, hollow structured CoSe2 cores were generated by Ostwald ripening, resulting in the formation of Co/(NiCo)Se2 with a box-in-box structure composed of an inner CoSe2 shell and an outer (NiCo)Se2 shell. Due to the synergetic effect of the unique structure and multicomponent selenide composition, the Co/(NiCo)Se2 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)Se2 with the box-in-box structure demonstrated a low Tafel slope (39.8 mV dec−1) and excellent 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.

Graphical abstract: Metal–organic framework-derived CoSe2/(NiCo)Se2 box-in-box hollow nanocubes with enhanced electrochemical properties for sodium-ion storage and hydrogen evolution

Supplementary files

Article information

Article type
Paper
Submitted
27 Jun 2017
Accepted
11 Aug 2017
First published
11 Aug 2017

J. Mater. Chem. A, 2017,5, 18823-18830

Metal–organic framework-derived CoSe2/(NiCo)Se2 box-in-box hollow nanocubes with enhanced electrochemical properties for sodium-ion storage and hydrogen evolution

S. Park, J. K. Kim and Y. Chan Kang, J. Mater. Chem. A, 2017, 5, 18823 DOI: 10.1039/C7TA05571D

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