Issue 50, 2018, Issue in Progress

Rotating-disk electrode analysis of the oxidation behavior of dissolved Li2O2 in Li–O2 batteries

Abstract

The development of the rechargeable Li–O2 battery (LOB) has encountered several bottlenecks till date. One of the biggest challenges is to lower the oxidation potential of Li2O2, which is the insulating and insoluble discharge product. A possible solution to this problem is to use high acceptor number (AN) or donor number (DN) solvents to increase the solubility of Li2O2, so that the dissolved Li2O2 can diffuse to the cathode surface and get oxidized at a relatively low potential. Herein, we explored the efficiency and side-reactions in the LOB charge process with different Li2O2 soluble electrolytes. The relationship between the solubility of Li2O2 and charging rate was analyzed quantitatively with ultraviolet-visible (UV-Vis) spectroscopy and rotating disk electrode experiments. As a result, electrolytes with high AN usually have higher solubility for Li2O2 than electrolytes with high DN, and thus exhibit higher Li2O2 oxidation rates. Nevertheless, higher Li2O2 solubility in high AN electrolytes also induces more severe side reactions and easily passivates the electrode surface. The trade-off between charging reaction rate and electrolyte stability is a key issue to be considered when designing high performance LOB electrolytes.

Graphical abstract: Rotating-disk electrode analysis of the oxidation behavior of dissolved Li2O2 in Li–O2 batteries

Supplementary files

Article information

Article type
Paper
Submitted
20 Apr 2018
Accepted
10 Jul 2018
First published
10 Aug 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 28496-28502

Rotating-disk electrode analysis of the oxidation behavior of dissolved Li2O2 in Li–O2 batteries

J. Ren, Z. Huang, P. K. Kalambate, Y. Shen and Y. Huang, RSC Adv., 2018, 8, 28496 DOI: 10.1039/C8RA03416H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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