Highly Conductive and Stable Naphthalenediimide-Based Organic Salt Cathode for Robust Lithium-Ion Batteries
Corresponding Author: Yuan Chen
Nano-Micro Letters,
Vol. 18 (2026), Article Number: 322
Abstract
Organic lithium salts are promising cathode candidates for sustainable lithium-ion batteries (LIBs) due to their synthetic simplicity and environmental friendliness. However, their practical application is often thwarted by active material dissolution and sluggish redox kinetics, stemming from limited conjugation and deficient electronic conductivity. Herein, we report a naphthalenediimide-based lithium salt (NDI-OLi) designed with a robust π-conjugated structure and high aromaticity to enhance electronic transport. Experimental and theoretical studies reveal that the relatively high electronic conductivity, rapid reaction kinetics, and stable delocalized electronic geometry of the NDI-OLi cathode are key factors enabling sufficient coordination between carbonyl sites and lithium ions. As a result, the NDI-OLi electrode presents a high reversible capacity of 160 mAh g−1 at 0.1 A g−1, excellent rate performance (99.9 mAh g−1 at 8 A g−1), and exceptional cycling stability with 85% capacity retention after 5000 cycles at 1 A g−1. This work opens up new avenues for developing highly conductive and stable organic salt cathodes toward high-performance and durable LIBs.
Highlights:
1 A naphthalenediimide-based lithium salt (NDI-OLi) featuring a stable π-conjugated structure and high aromaticity is proposed as a cathode, which facilitates relatively high electronic conductivity and rapid electron transfer.
2 Experimental and theoretical investigations reveal that the stable delocalized electronic geometry and fast reaction kinetics enable sufficient coupling between carbonyl sites and lithium ions, ensuring excellent energy storage performance.
3 The NDI-OLi electrode demonstrates superior rate capability and long-term cyclability (85% capacity retention after 5000 cycles), outperforming previously reported organic lithium salt cathodes.
Keywords
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References
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Z. Liu, X. Yang, K. Wang, B. Li, W. Liu et al., P-type semiconducting covalent organic frameworks for Li-ion battery cathodes with high-energy density. Energy Storage Mater. 68, 103337 (2024). https://doi.org/10.1016/j.ensm.2024.103337
M. Guo, W. Li, W. Tang, C. Tang, B. Cao et al., A p-type small-molecule organic cathode simultaneously for high-voltage Li/Na-based dual-ion full batteries. Energy Storage Mater. 74, 103979 (2025). https://doi.org/10.1016/j.ensm.2024.103979
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W. Li, H. Ma, W. Tang, K. Fan, S. Jia et al., Single organic electrode for multi-system dual-ion symmetric batteries. Nat. Commun. 15(1), 9533 (2024). https://doi.org/10.1038/s41467-024-53803-3
Z. Song, Y. Qian, X. Liu, T. Zhang, Y. Zhu et al., A quinone-based oligomeric lithium salt for superior Li–organic batteries. Energy Environ. Sci. 7(12), 4077–4086 (2014). https://doi.org/10.1039/c4ee02575j
J. Liu, J. Jiang, Q. Zhou, Z. Chen, R. Zhang et al., Manipulation of π-aromatic conjugation in two-dimensional sn-organic materials for efficient lithium storage. eScience 3(2), 100094 (2023). https://doi.org/10.1016/j.esci.2023.100094
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H. Chen, M. Armand, M. Courty, M. Jiang, C.P. Grey et al., Lithium salt of tetrahydroxybenzoquinone: toward the development of a sustainable Li-ion battery. J. Am. Chem. Soc. 131(25), 8984–8988 (2009). https://doi.org/10.1021/ja9024897
M. Yao, S. Umetani, H. Ando, T. Kiyobayashi, N. Takeichi et al., Rechargeable organic batteries using chloro-substituted naphthazarin derivatives as positive electrode materials. J. Mater. Sci. 52(20), 12401–12408 (2017). https://doi.org/10.1007/s10853-017-1368-z
L. Huang, Z. Hu, M. Li, L. Luo, J. Wang et al., Trilithium salt of tetrahydroxyanthraquinone: a high-voltage and stable organic cathode material for rechargeable lithium metal and lithium-ion batteries. Chem. Eng. J. 481, 148447 (2024). https://doi.org/10.1016/j.cej.2023.148447
Q. Zhao, J. Wang, C. Chen, T. Ma, J. Chen, Nanostructured organic electrode materials grown on graphene with covalent-bond interaction for high-rate and ultra-long-life lithium-ion batteries. Nano Res. 10(12), 4245–4255 (2017). https://doi.org/10.1007/s12274-017-1580-9
C. Wang, Weak intermolecular interactions for strengthening organic batteries. Energy Environ. Mater. 3(4), 441–452 (2020). https://doi.org/10.1002/eem2.12076
C. Wang, Y. Xu, Y. Fang, M. Zhou, L. Liang et al., Extended π-conjugated system for fast-charge and-discharge sodium-ion batteries. J. Am. Chem. Soc. 137(8), 3124–3130 (2015). https://doi.org/10.1021/jacs.5b00336
Q. Zhao, J. Wang, Y. Lu, Y. Li, G. Liang et al., Oxocarbon salts for fast rechargeable batteries. Angew. Chem. Int. Ed. 55(40), 12528–12532 (2016). https://doi.org/10.1002/anie.201607194
K. Lei, F. Li, C. Mu, J. Wang, Q. Zhao et al., High K-storage performance based on the synergy of dipotassium terephthalate and ether-based electrolytes. Energy Environ. Sci. 10(2), 552–557 (2017). https://doi.org/10.1039/C6EE03185D
C. Wang, Y. Fang, Y. Xu, L. Liang, M. Zhou et al., Manipulation of disodium rhodizonate: factors for fast-charge and fast-discharge sodium-ion batteries with long-term cyclability. Adv. Funct. Mater. 26(11), 1777–1786 (2016). https://doi.org/10.1002/adfm.201504537
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