Liu Si, Zhang Qiankui, Wang Xianshu, Xu Mengqing, Li Weishan, Lucht Brett L
School of Chemistry, South China Normal University, Guangzhou 510006, China.
National and Local Joint Engineering Research Center of MPTES in High Energy and Safety LIBs, Engineering Research Center of MTEES (Ministry of Education), and Key Lab of ETESPG (GHEI), South China Normal University, Guangzhou 510006, China.
ACS Appl Mater Interfaces. 2020 Jul 29;12(30):33719-33728. doi: 10.1021/acsami.0c08094. Epub 2020 Jul 14.
Metallic lithium (Li) has great potential as an anode material for high-energy-density batteries due to its high specific capacity. However, the uncontrollable dendritic lithium growth on the metallic lithium surface limits its practical application owing to the instability of the solid electrolyte interphase (SEI). A tailored SEI composition/structure can mitigate or inhibit the lithium dendrites' growth, thereby enhancing the cyclability of the Li-metal anode. In this work, excellent cycling stability of lithium metal anodes was achieved by utilizing a novel dual-salt electrolyte based on lithium bis(fluorosulfonyl) imide (LiFSI) and lithium difluorobis(oxalato) phosphate (LiDFBOP) in carbonate solvents. By combining surface/microstructural characterization and computations, we reveal that the preferential reduction of LiDFBOP occurs prior to LiFSI and carbonate solvents and its reduction products (LiCO and P-O species) bind to LiF, resulting in a favorable compact and protective SEI on the Li electrodes. It was found that the improved oxidative stability was accompanied by reduced corrosion of the current collector. A Li/Li symmetrical cell with a designed dual-salt electrolyte system exhibits stable polarization voltage over 1000 h of cycle time. In addition, the LiFSI-LiDFBOP advantage of this dual-salt electrolyte system enables the Li/LiFePO cells with significantly enhanced cycling stability. This work demonstrates that constructing a tailored SEI using a dual-salt electrolyte system is vital for improving the interfacial stability of lithium metal batteries.
金属锂(Li)因其高比容量而作为高能量密度电池的负极材料具有巨大潜力。然而,由于固体电解质界面(SEI)的不稳定性,金属锂表面不可控的枝晶锂生长限制了其实际应用。定制的SEI组成/结构可以减轻或抑制锂枝晶的生长,从而提高锂金属负极的循环性能。在这项工作中,通过在碳酸盐溶剂中使用基于双(氟磺酰)亚胺锂(LiFSI)和二氟双(草酸根)磷酸锂(LiDFBOP)的新型双盐电解质,实现了锂金属负极优异的循环稳定性。通过结合表面/微观结构表征和计算,我们发现LiDFBOP优先于LiFSI和碳酸盐溶剂发生还原,其还原产物(LiCO和P-O物种)与LiF结合,从而在锂电极上形成有利的致密且具有保护作用的SEI。研究发现,氧化稳定性的提高伴随着集流体腐蚀的减少。具有设计的双盐电解质系统的Li/Li对称电池在1000小时的循环时间内表现出稳定的极化电压。此外,这种双盐电解质系统的LiFSI-LiDFBOP优势使Li/LiFePO电池的循环稳定性显著提高。这项工作表明,使用双盐电解质系统构建定制的SEI对于提高锂金属电池的界面稳定性至关重要。