Ten times of LiNO3 solubility increase in co-solvents free ester-based carbonate electrolytes enables 450 Wh/kg lithium metal batteries

• A two-step method dissolves 0.1 M LiNO 3 into carbonate ester-based electrolytes. • MD simulation: negative enthalpy drives LiNO 3 dissolution without co-solvents. • Performance boost is exhibited in Li||Cu, Li||Li, Li||LiNi 0.83 Mn 0.06 Co 0.11 O 2 coin cells. • A pouch cell with 450 Wh kg -1 is fabricated. • Solvation structure–SEI/CEI–performance correlation is studied. LiNO 3 is a promising additive for high-energy-density lithium metal batteries (LMBs) via regulating the solid electrolyte interphase (SEI) layer. However, the extremely low solubility of LiNO 3 in carbonate ester-based electrolytes limits applications. In this study, a two-step physical method successfully dissolves 0.1 M LiNO 3 into carbonate ester-based electrolytes without co-solvents (∼10 × higher solubility than conventional systems), where EC disrupts Li⁺–NO 3 ⁻ interactions and the subsequent mixing with a preformed LiFSI/LiPF 6 –DMC/FEC electrolyte releases part of the coordinated species, increasing entropy, while the remaining solvents/anions stabilize Li⁺ - making the process both enthalpically and entropically favorable. This facile, scalable, cost-effective way is confirmed by theoretical simulation and experimental investigations. With the synergistic effect of 4-fluoro-1,3-dioxolan-2-one (FEC), the NO 3 - anions preferentially enter the Li + solvation layer. Therefore, the enhanced SEI layer with LiF, Li x C, and Li 2 O homogenizes lithium deposition. The robust cathode–electrolyte interphase (CEI) composed of NSO x F y and LiF supports high-voltage Ni-rich cathodes. Notably, Li||LiNi 0.83 Mn 0.06 Co 0.11 O 2 cells retain 82.5% capacity after 300 cycles at 1 C (1 C=200 mA g -1 ) with a 4.3 V cut-off voltage and an 85.5% capacity after 100 cycles at 1 C with a 4.5 V cut-off voltage. Importantly, a pouch cell with 450 Wh kg -1 energy density further demonstrates the practical potential in industry. Additionally, this strategy also demonstrates the potential application of LiNO 3 in some carbonated ester-based electrolytes for other alkali metal batteries.

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Publication Details

Journal
Energy storage materials
Published
2025-11-29
DOI
https://doi.org/10.1016/j.ensm.2025.104779
Citations
1
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.73
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article

Ten times of LiNO3 solubility increase in co-solvents free ester-based carbonate electrolytes enables 450 Wh/kg lithium metal batteries

Siqi Shi, Jie Gao, Meilan Peng, Zhuijun Xu et al.
1 citations
Energy storage materials
Advanced Battery Materials and Technologies
0.73
article

Ten times of LiNO3 solubility increase in co-solvents free ester-based carbonate electrolytes enables 450 Wh/kg lithium metal batteries

Siqi Shi, Jie Gao, Meilan Peng, Zhuijun Xu, Ya‐Jun Cheng, Baohu Wu, Yiyao Xiao, Peter Müller‐Buschbaum, Guangjiu Pan, Yinghui Li, Shanshan Yin, Tianle Zheng, Qing Ji, Weiping Xie, Yonggao Xia, Ji Miu
article en
1 citations

Abstract

• A two-step method dissolves 0.1 M LiNO 3 into carbonate ester-based electrolytes. • MD simulation: negative enthalpy drives LiNO 3 dissolution without co-solvents. • Performance boost is exhibited in Li||Cu, Li||Li, Li||LiNi 0.83 Mn 0.06 Co 0.11 O 2 coin cells. • A pouch cell with 450 Wh kg -1 is fabricated. • Solvation structure–SEI/CEI–performance correlation is studied. LiNO 3 is a promising additive for high-energy-density lithium metal batteries (LMBs) via regulating the solid electrolyte interphase (SEI) layer. However, the extremely low solubility of LiNO 3 in carbonate ester-based electrolytes limits applications. In this study, a two-step physical method successfully dissolves 0.1 M LiNO 3 into carbonate ester-based electrolytes without co-solvents (∼10 × higher solubility than conventional systems), where EC disrupts Li⁺–NO 3 ⁻ interactions and the subsequent mixing with a preformed LiFSI/LiPF 6 –DMC/FEC electrolyte releases part of the coordinated species, increasing entropy, while the remaining solvents/anions stabilize Li⁺ - making the process both enthalpically and entropically favorable. This facile, scalable, cost-effective way is confirmed by theoretical simulation and experimental investigations. With the synergistic effect of 4-fluoro-1,3-dioxolan-2-one (FEC), the NO 3 - anions preferentially enter the Li + solvation layer. Therefore, the enhanced SEI layer with LiF, Li x C, and Li 2 O homogenizes lithium deposition. The robust cathode–electrolyte interphase (CEI) composed of NSO x F y and LiF supports high-voltage Ni-rich cathodes. Notably, Li||LiNi 0.83 Mn 0.06 Co 0.11 O 2 cells retain 82.5% capacity after 300 cycles at 1 C (1 C=200 mA g -1 ) with a 4.3 V cut-off voltage and an 85.5% capacity after 100 cycles at 1 C with a 4.5 V cut-off voltage. Importantly, a pouch cell with 450 Wh kg -1 energy density further demonstrates the practical potential in industry. Additionally, this strategy also demonstrates the potential application of LiNO 3 in some carbonated ester-based electrolytes for other alkali metal batteries.

Energy storage materialsVol. 84
Shanghai University (CN), Ningbo University of Technology (CN), Hohai University (CN), Forschungszentrum Jülich (DE), Chinese Academy of Sciences (CN), Heinz Maier-Leibnitz Zentrum (DE), Jiangsu University of Technology (CN), Changzhou University (CN), University of Chinese Academy of Sciences (CN), Ningbo Institute of Industrial Technology (CN), Technical University of Munich (DE)
Openalex Percentile: Top 21%
Advanced Battery Materials and Technologies
0.73
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