Abstract
Electrolyte engineering is emerging as a key strategy for enhancing the cycle life of lithium metal batteries (LMBs). Fluorinated electrolytes have dramatically extended cycle life; however, intractable challenges in terms of rate capability and fluorine overuse persist. Here, we introduce a lithiophilic, solvent-interactive, and fluorine-free nano-Si3N4 additive that facilitates the fine-tuning of weak Li+ solvation to form inorganic-rich solid-electrolyte interphase (SEI) layers. Additionally, the alloying and conversion reactions between nano-Si3N4 and Li generated a fast Li+-conductive SEI, overcoming the poor rate performance of weakly solvating electrolytes. Simultaneously, nano-Si3N4 interacts with ethylene carbonate (EC), minimizing hydrogen (H)-transfer reactions and scavenging HF, thus increasing the high-voltage tolerance. Consequently, nano-Si3N4 extends the cyclability of the commercial carbonate-based electrolyte in 360 W h kg−1-level Li||LiNi0.8Co0.1Mn0.1O2 (NCM811) pouch-cells, resulting in 74% capacity retention after 100 cycles, whereas failure occurred without it. Our study provides an in-depth understanding of the working mechanisms of suspension electrolytes through comprehensive analysis.
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CITATION STYLE
Kim, J., Lee, D. G., Lee, J. H., Kim, S., Park, C. Y., Lee, J., … Lee, J. (2025). Concurrent electrode-electrolyte interfaces engineering via nano-Si3N4 additive for high-rate, high-voltage lithium metal batteries. Energy and Environmental Science, 18(7), 3148–3159. https://doi.org/10.1039/d4ee03862b
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