4.7 Article

A facile green synthesis of porous hexagonal cobalt pyrovanadate electrode for supercapacitors by deep eutectic solvent

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 892, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.162205

关键词

Co2V2O7; Supercapacitors; Deep eutectic solvent; Porous hexagonal nanoplatelets; Transition metal vanadates

资金

  1. Fundamental Research Grant Scheme of Northwest Geological and Mining for Nonferrous Metals Group Co., Ltd. in China [XBDK201904]

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In this study, cobalt pyrovanadate was successfully fabricated using an ionothermal method and exhibited excellent electrochemical performance in the electrolyte solution. It showed a specific capacitance of 304 F g(-1) and maintained outstanding cycle performance, providing a new approach for the preparation of electrode materials for pseudo-supercapacitors.
Cobalt vanadate is a kind of promising electrode material for pseudo-supercapacitors because of their higher electrical conductivity, better electrochemical activity, and prominent specific capacitance than single metal oxides. In this paper, cobalt pyrovanadate (Co2V2O7) was primarily fabricated by a facile environment-friendly ionothermal method using a green deep eutectic solvent (DES) and followed the heat treatment in the air. The eutectic mixture discussed here was consisted of a hydrogen bond donor (urea) and acceptor (ChCl) in a 2:1 molar ratio. The as-prepared Co2V2O7 was porous hexagonal nanoplatelets, and its electrochemical performances were characterized by cycle voltammetry, galvanostatic charge/discharge and cycling stability tests in a three-electrode system with 2 M KOH electrolyte solution. The specific capacitance of the synthesized Co2V2O7 revealed 304 F g(-1) at the current density of 1 A g(-1). Surprisingly, it remained an excellent cycle performance with 103% in 100 charge/discharge cycles. Therefore, we have successfully presented a deep eutectic solvent derived routine to prepare porous hexagonal Co2V2O7 nanoplatelets electrode material. (C) 2021 Elsevier B.V. All rights reserved.

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