Triple Hierarchical Porous Carbon Spheres as Effective Cathodes for Li-O-2 Batteries

Authors
Jeong, Min-GiKwak, Won-JinIslam, MobinulPark, JiwonByon, Hye RyungJang, MinchulSun, Yang-KookJung, Hun-Gi
Issue Date
2019-02-07
Publisher
ELECTROCHEMICAL SOC INC
Citation
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, v.166, no.4, pp.A455 - A463
Abstract
This paper presents the synthesis and characterization of triple hierarchical porous carbon spheres as cathodes in lithium-oxygen batteries. The porous carbon cathode exhibits a higher discharge capacity and average discharge potential compared to a typical carbon black cathode. This superior electrochemical result can be attributed to the triple hierarchical pores of the cathode: micropores that act as channels for oxygen to flow without interruption by the accumulated discharge product, abundant mesopores that shape the size of the discharge product and transport the electrolyte, and macropores that easily accommodate the accumulation of discharge product. To further promote Li2O2 formation/decomposition, the cathode can be decorated with a Ru catalyst, which strongly influences the oxygen evolution reaction performance. Conspicuously, triple hierarchical porous carbon spheres exhibit a homogeneous distribution of the Ru catalyst and thus provide an appropriate architecture. The synergistic effect from the unique structure and catalytic competence of Ru increases the capacity and rate capability with lower over-potential, and facilitates the formation of Li2O2. This can be decomposed at a low potential during recharge and thus contributes to the very high energy efficiency. (C) 2019 The Electrochemical Society.
Keywords
ORDERED MESOPOROUS CARBON; OXYGEN REDUCTION REACTION; SURFACE-AREA; METAL; PERFORMANCE; GRAPHENE; RECHARGEABILITY; REVERSIBILITY; ELECTRODES; CATALYSTS; ORDERED MESOPOROUS CARBON; OXYGEN REDUCTION REACTION; SURFACE-AREA; METAL; PERFORMANCE; GRAPHENE; RECHARGEABILITY; REVERSIBILITY; ELECTRODES; CATALYSTS
ISSN
0013-4651
URI
https://pubs.kist.re.kr/handle/201004/120357
DOI
10.1149/2.0021904jes
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KIST Article > 2019
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