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最小化锂氧电池中与氧化还原介质相关的异常高电位放电过程。

Minimizing the Abnormal High-Potential Discharge Process Related to Redox Mediators in Lithium-Oxygen Batteries.

作者信息

Wu Shichao, Qiao Yu, Deng Han, He Yibo, Zhou Haoshen

机构信息

Energy Technology Research Institute , National Institute of Advanced Industrial Science and Technology (AIST) , 1-1-1 Umezono , Tsukuba 305-8568 , Japan.

Center of Energy Storage Materials & Technology, College of Engineering and Applied Sciences, National Laboratory of Solid State Microstructures, Collaborative Innovation Center of Advanced Microstructures , Nanjing University , Nanjing 210093 , China.

出版信息

J Phys Chem Lett. 2018 Dec 6;9(23):6761-6766. doi: 10.1021/acs.jpclett.8b02899. Epub 2018 Nov 14.

Abstract

Nonaqueous lithium-oxygen batteries can achieve a reduced charge potential when an available redox mediator is introduced. However, there are accompanying problems, such as the shuttle effect and the abnormal high-potential discharge process (>2.96 V) after the first cycle. The shuttle effect can be addressed by developing a blocking separator or resistant solid electrolyte interphase on the anode. No attention has been paid to the abnormal discharge process. Here, we unravel the underlying mechanism causing the undesired abnormal phenomenon. Our results show that the slow reaction rate between the discharged lithium peroxide and redox mediator and the low yield of lithium peroxide should take primary responsibility for the abnormal discharge issue. The sluggish reaction kinetics results from the formed byproducts covering lithium peroxide. We propose developing redox mediator-containing hydrate-melt lithium-oxygen batteries. The lithium hydroperoxide intermediator shows high reaction activity with the redox mediator and improves battery charge ability, thus solving the abnormal discharge problem. This work sheds light on the further design of lithium-oxygen batteries using a redox mediator.

摘要

当引入可用的氧化还原介质时,非水锂氧电池可以实现降低的充电电位。然而,随之而来的问题包括穿梭效应以及首次循环后异常的高电位放电过程(>2.96 V)。穿梭效应可以通过开发阳极上的阻挡隔膜或抗性固体电解质界面来解决。人们尚未关注异常放电过程。在此,我们揭示了导致这种不良异常现象的潜在机制。我们的结果表明,放电的过氧化锂与氧化还原介质之间缓慢的反应速率以及过氧化锂的低产率应主要归咎于异常放电问题。反应动力学迟缓是由覆盖过氧化锂的副产物形成所致。我们建议开发含氧化还原介质的水合物 - 熔体锂氧电池。过氧化氢锂中间体与氧化还原介质表现出高反应活性,并提高了电池充电能力,从而解决了异常放电问题。这项工作为使用氧化还原介质的锂氧电池的进一步设计提供了思路。

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