Electrolyte Design for High-Voltage Lithium-Metal Batteries with Synthetic Sulfonamide-Based Solvent and Electrochemically Active Additives.

Considering practical viability, Li-metal battery electrolytes should be formulated by tuning solvent composition similar to electrolyte systems for Li-ion batteries to enable the facile salt-dissociation, ion-conduction, and introduction of sacrificial additives for building stable electrode-electrolyte interfaces. Although 1,2-dimethoxyethane with a high-donor number enables the implementation of ionic compounds as effective interface modifiers, its ubiquitous usage is limited by its low-oxidation durability and high-volatility. Regulation of the solvation structure and construction of well-structured interfacial layers ensure the potential strength of electrolytes in both Li-metal and LiNi0.8Co0.1Mn0.1O2 (NCM811). This study reports the build-up of multilayer solid-electrolyte interphase by utilizing different electron-accepting tendencies of lithium difluoro(bisoxalato) phosphate (LiDFBP), lithium nitrate, and synthetic 1-((trifluoromethyl)sulfonyl)piperidine. Furthermore, a well-structured cathode-electrolyte interface from LiDFBP effectively addresses the issues with NCM811. The developed electrolyte based on a framework of highly- and weakly-solvating solvents with interface modifiers enables the operation of Li|NCM811 cells with a high areal capacity cathode (4.3 mAh cm-2) at 4.4 V versus Li/Li+.

Operando Spatial Pressure Mapping Analysis for Prototype Lithium Metal Pouch Cells Under Practical Conditions.

Monitoring and diagnosing the battery status in real-time are of utmost importance for clarifying failure mechanism, improving battery performance, and ensuring safety, particularly under fast charging conditions. Recently, advanced operando techniques have been developed to observe changes in the microstructures of lithium deposits using laboratory-scale cell designs, focusing on understanding the nature of Li metal electrodes. However, the macroscopic spatial inhomogeneity of lithium electroplating/stripping in the prototype pressurized pouch cells has not been measured in real-time under practical conditions. Herein, a new noninvasive operando technique, spatial pressure mapping analysis, is introduced to macroscopically and quantitatively measure spatial pressure changes in a pressurized pouch cell during cycling. Moreover, dynamic spatial changes in the macroscopic morphology of the lithium metal electrode are theoretically visualized by combining operando pressure mapping data with mechanical analyses of cell components. Additionally, under fast charging conditions, the direct correlation between abrupt capacity fading and sudden increases in spatial pressure distribution inhomogeneity is demonstrated through comparative analysis of pouch cells under various external pressures, electrolyte species, and electrolyte weight to cell capacity (e/c) ratios. This operando technique provides insights for assessing the current battery status and understanding the complex origin of cell degradation behavior in pressurized pouch cells.

Correlation between Redox Potential and Solvation Structure in Biphasic Electrolytes for Li Metal Batteries.

The activity of lithium ions in electrolytes depends on their solvation structures. However, the understanding of changes in Li+ activity is still elusive in terms of interactions between lithium ions and solvent molecules. Herein, the chelating effect of lithium ion by forming [Li(15C5)]+ gives rise to a decrease in Li+ activity, leading to the negative potential shift of Li metal anode. Moreover, weakly solvating lithium ions in ionic liquids, such as [Li(TFSI)2 ]- (TFSI = bis(trifluoromethanesulfonyl)imide), increase in Li+ activity, resulting in the positive potential shift of LiFePO4 cathode. This allows the development of innovative high energy density Li metal batteries, such as 3.8 V class Li | LiFePO4 cells, along with introducing stable biphasic electrolytes. In addition, correlation between Li+ activity, cell potential shift, and Li+ solvation structure is investigated by comparing solvated Li+ ions with carbonate solvents, chelated Li+ ions with cyclic and linear ethers, and weakly solvating Li+ ions in ionic liquids. These findings elucidate a broader understanding of the complex origin of Li+ activity and provide an opportunity to achieve high energy density lithium metal batteries.

Three-Dimensional Porous Frameworks for Li Metal Batteries: Superconformal versus Conformal Li Growth.

Li metal batteries have been considered a promising alternative to Li-ion batteries because of the high theoretical capacity of the Li metal. There have been remarkable improvements in the electrochemical performance of Li metal electrodes, although the current Li metal technology is not sufficiently practical in terms of cycle performance, safety, and volume change during cycling. Herein, the role of pore size distribution in the Li metal plating behavior of porous frameworks is clarified to attain the ideal pore structure of the framework as a Li metal host. The monodisperse pore framework shows the conformal electrodeposition of the Li metal, whereas the pore size gradient framework exhibits the superconformal plating of the Li metal. The conformal and superconformal electrodepositions of the Li metal are elucidated in terms of variations along the pore depth direction in the charge-transfer resistance on the pore walls and the ionic resistance of electrolytes confined in pores. The pore size gradient framework also shows excellent electrochemical performance, such as stable capacity retention over 760 cycles with 0.5 mAh cm-2 at 2 mA cm-2. These findings provide fundamental insights into strategies to improve the electrochemical performance of porous frameworks for Li metal batteries.