Lithium/Sulfur Cell Discharge Mechanism: An Original Approach for Intermediate Species Identification

多硫化物 化学 电解质 歧化 电化学 硫黄 电子顺磁共振 无机化学 锂(药物) 氧化还原 电极 有机化学 物理化学 催化作用 内分泌学 物理 医学 核磁共振
作者
Céline Barchasz,Florian Molton,Carole Duboc,Jean‐Claude Leprêtre,Sébastien Patoux,Fannie Alloin
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:84 (9): 3973-3980 被引量:937
标识
DOI:10.1021/ac2032244
摘要

The lithium/sulfur battery is a promising electrochemical system that has a high theoretical capacity of 1675 mAh g(-1), but its discharge mechanism is well-known to be a complex multistep process. As the active material dissolves during cycling, this discharge mechanism was investigated through the electrolyte characterization. Using high-performance liquid chromatography, UV-visible absorption, and electron spin resonance spectroscopies, we investigated the electrolyte composition at different discharge potentials in a TEGDME-based electrolyte. In this study, we propose a possible mechanism for sulfur reduction consisting of three steps. Long polysulfide chains are produced during the first reduction step (2.4-2.2 V vs Li(+)/Li), such as S(8)(2-) and S(6)(2-), as evidenced by UV and HPLC data. The S(3)(•-) radical can also be found in solution because of a disproportionation reaction. S(4)(2-) is produced during the second reduction step (2.15-2.1 V vs Li(+)/Li), thus pointing out the gradual decrease of the polysulfide chain lengths. Finally, short polysulfide species, such as S(3)(2-), S(2)(2-), and S(2-), are produced at the end of the reduction process, i.e., between 2.1 and 1.9 V vs Li(+)/Li. The precipitation of the poorly soluble and insulating short polysulfide compounds was evidenced, thus leading to the positive electrode passivation and explaining the early end of discharge.
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