Published March 10, 2017 | Version v1
Journal article

Metal–organic frameworks-derived porous carbon/Co3O4 composites for rechargeable lithium–oxygen batteries

  • 1. School of Integrated Technology, Yonsei Institute of Convergence Technology, Yonsei University, 85 Songdogwahak-ro, Yeonsu-gu, Incheon 21983 (Korea, Republic of)
  • 2. Underwood International College, Yonsei University, 85 Songdogwahak-ro, Yeonsu-gu, Incheon 21983 (Korea, Republic of)

Description

Highlights: • We develop porous carbon/Co3O4 composites for Li–O2 batteries. • Porous carbon/Co3O4 composites are derived from cobalt-containing MOFs. • Co3O4 nanoparticles catalyze both ORR and OER in a rechargeable Li–O2 system. • The porous structure of the composites realizes a high discharge capacity. • The uniform distribution of Co3O4 realizes effective catalytic effects. - Abstract: Lithium–oxygen (Li–O2) batteries are promising candidates for high-performance energy storage systems because of their tremendous energy density, which significantly exceeds that of conventional Li–ion batteries. Cobalt oxide (Co3O4) is considered an effective catalyst for non-aqueous Li-O2 batteries owing to its excellent oxygen reduction and oxygen evolution reaction activity. However, low electrical conductivity and agglomeration of Co3O4 can degrade the electrochemical performance properties. We present a facile method of synthesizing porous carbon/Co3O4 composites derived from metal–organic frameworks (MOFs) via post-thermal treatment for use as the cathode in rechargeable Li–O2 batteries. Use of cobalt-containing MOFs as a sacrificial template produces uniformly distributed Co3O4 nanoparticles in the carbonaceous matrix, alleviating the problems of using only Co3O4 as the cathode material. As-synthesized porous carbon/Co3O4 composites show superior electrochemical performance, for example, a low overpotential and high reversible capacity of about 9850 mA h g−1 at a current density of 100 mA g−1. They also exhibit excellent cyclability up to the 320th cycle, with a limited capacity of 500 mA h g−1 at a current density of 200 mA g−1. The improvement is attributed to the catalytic activity and mesoporous structure of uniformly distributed Co3O4 nanoparticles in the carbonaceous matrix.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2017.01.121

Additional details

Identifiers

DOI
10.1016/j.electacta.2017.01.121;
PII
S0013-4686(17)30159-7;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
230
Journal Page Range
p. 73-80
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.