Mutual Conservation of Redox Mediator and Singlet Oxygen Quencher in Lithium-Oxygen Batteries

Authors
Kwak, Won-JinFreunberger, Stefan A.Kim, HunPark, JiwonTrung Thien NguyenJung, Hun-GiByon, Hye RyungSun, Yang-Kook
Issue Date
2019-11
Publisher
AMER CHEMICAL SOC
Citation
ACS CATALYSIS, v.9, no.11, pp.9914 - 9922
Abstract
Li-O-2 batteries are plagued by side reactions that cause poor rechargeability and efficiency. These reactions were recently revealed to be predominantly caused by singlet oxygen, which can be neutralized by chemical traps or physical quenchers. However, traps are irreversibly consumed and thus only active for a limited time, and so far identified quenchers lack oxidative stability to be suitable for typically required recharge potentials. Thus, reducing the charge potential within the stability limit of the quencher and/or finding more stable quenchers is required. Here, we show that dimethylphenazine as a redox mediator decreases the charge potential well within the stability limit of the quencher 1,4-diazabicyclo[2.2.2]octane. The quencher can thus mitigate the parasitic reactions without being oxidatively decomposed. At the same time the quencher protects the redox mediator from singlet oxygen attack. The mutual conservation of the redox mediator and the quencher is rational for stable and effective Li-O-2 batteries.
Keywords
LI-O-2 BATTERIES; SUPEROXIDE ANION; SOLID-ELECTROLYTE; STABILITY; RECHARGEABILITY; DISMUTATION; LIMITATIONS; GENERATION; DISCHARGE; CELLS; LI-O-2 BATTERIES; SUPEROXIDE ANION; SOLID-ELECTROLYTE; STABILITY; RECHARGEABILITY; DISMUTATION; LIMITATIONS; GENERATION; DISCHARGE; CELLS; lithium oxygen batteries; redox mediator; singlet oxygen; singlet oxygen quencher
ISSN
2155-5435
URI
https://pubs.kist.re.kr/handle/201004/119388
DOI
10.1021/acscatal.9b01337
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KIST Article > 2019
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