Sulfur-containing C2H2O8S2 molecules as an overall-functional electrolyte additive for high-voltage LiNi0.5Co0.2Mn0.3O2/graphite batteries with enhanced performance

法拉第效率 电解质 阳极 石墨 阴极 锂(药物) 材料科学 化学工程 电化学 化学 电极 工程类 复合材料 物理化学 医学 内分泌学
作者
Tianxiang Yang,Wenlian Wang,Shuai Li,Jing Lü,Weizhen Fan,Xiaoxi Zuo,Junmin Nan
出处
期刊:Journal of Power Sources [Elsevier BV]
卷期号:470: 228462-228462 被引量:53
标识
DOI:10.1016/j.jpowsour.2020.228462
摘要

The optimization of electrode-electrolyte interfacial properties plays a key role in the stable operation of high-energy density lithium-ion batteries (LIBs) over a wide temperature range. In this work, a functional electrolyte using dihydro-1,3,2-dioxathiolo [1,3,2]dioxathiole-2,2,5,5-tetraoxide (D-DTD) molecules as an overall-functional additive is designed and used to enhance the comprehensive performance of LiNi0.5Co0.2Mn0.3O2/graphite batteries under extreme conditions, namely, a high 4.4 V working potential and a wide temperature range of −30 °C–60 °C. The batteries with D-DTD exhibit stable coulombic efficiency, enhanced cycling stability, and superior rate performance. Specifically, the batteries with D-DTD retain 89.1% of their original reversible capacities after 150 cycles at room temperature, while only 55.4% and 84.0% capacity retentions are obtained from the batteries without additive and with 1,3,2-dioxathiolane-2,2-dioxide (DTD), respectively. Interestingly, the addition of D-DTD to the baseline electrolyte promotes higher cycling retentions of 77.2% (45 °C) and 92.5% (−10 °C) after 100 cycles in comparison to 14.7% and 82.1% with DTD-added electrolyte, respectively. It is demonstrated that D-DTD can participate in the construction of interfacial films on both cathode and anode, which contributes to stabilizing the electrode-electrolyte interfaces and reducing parasitic interfacial reactions of LIBs.
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