Constructing an inorganic-rich solid electrolyte interphase by adjusting electrolyte additives for stable Li metal anodes

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Vol. 12; no. 17; pp. 172 - 18
• Main Authors: Li, Minghui, Chen, Cai, Luo, Hongze, Xu, Qingshuai, Yan, Keyou, Qiu, Yongcai, Zhou, Guangmin
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 30.04.2024
• Subjects: Additives; Anodes; Cycles; Electrochemical potential; Electrochemistry; Electrolytes; Electrolytic cells; Energy levels; Interface stability; Ion migration; Lithium batteries; Metals; Molecular orbitals; Molten salt electrolytes; Side reactions; Solid electrolytes
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/d3ta07655e

Li metal anodes are considered among the most ideal candidates for next generation batteries owing to their lowest electrochemical potential and high theoretical capacity. However, the highly reactive Li metal is subject to continuous side reactions with conventional carbonate electrolytes. The resulting unsatisfying solid electrolyte interface (SEI) induces severe Li dendritic growth. Therefore, there is an urgent need to effectively control the components of SEI to solve the electrolyte/anode interface electrochemical instability. Herein, LiDFP and LiNO 3 are introduced into the electrolyte to modulate the composition of the SEI. Owing to the lower lowest unoccupied molecular orbital (LUMO) energy levels of LiDFP and LiNO 3 relative to those of the solvents, LiDFP and LiNO 3 have preferential reducibility and thus generate a stable SEI containing LiF and Li 3 N, which has swift ion migration kinetics and homogeneous Li deposition behaviors. As a result, our electrolyte modified by additives enables the anode to achieve an excellent coulombic efficiency of 98% and exhibits an ultra-long cycling life of over 700 h in symmetrical cells. Li metal full cells paired with the LFP or NCM811 cathode also have excellent long cycling performance. This work demonstrates that additive-modified electrolytes are a viable and simple strategy for the evolution of Li metal batteries. The SEI formation mechanism in the absence/presence of LiDFP and LiNO 3 additives.