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.2017.01.121Additional 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
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49002065
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CAPACITY; CARBON; COBALT OXIDES; CURRENT DENSITY; ELECTRIC CONDUCTIVITY; ENERGY DENSITY; ENERGY STORAGE; LITHIUM ION BATTERIES; NANOPARTICLES; ORGANOMETALLIC COMPOUNDS; OXIDATION; POROUS MATERIALS
- Descriptors DEC
- CHALCOGENIDES; CHEMICAL REACTIONS; COBALT COMPOUNDS; ELECTRIC BATTERIES; ELECTRICAL PROPERTIES; ELECTROCHEMICAL CELLS; ELEMENTS; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; MATERIALS; NONMETALS; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PARTICLES; PHYSICAL PROPERTIES; STORAGE; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.