Zhou Rui, Xu Yan-Song, Han Chong, Li Yun-Nuo, Wang Jun, Liang Xiongyi, Jing Tian-Tian, Liu Rui, Chen Guanhua, Cao Fei-Fei
College of Chemistry, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
Department of Chemistry, The University of Hong Kong, Pok Fu Lam Road, Hong Kong, 999077, P. R. China.
Adv Mater. 2025 Mar;37(10):e2416748. doi: 10.1002/adma.202416748. Epub 2025 Jan 26.
Sodium-based rechargeable batteries are some of the most promising candidates for electric energy storage with abundant sodium reserves, particularly, sodium-based dual-ion batteries (SDIBs) perform advantages in high work voltage (≈5.0 V), high-power density, and potentially low cost. However, irreversible electrolyte decomposition and co-intercalation of solvent molecules at the electrode interface under a high charge state are blocking their development. Herein, a high-salt concentration microenvironment is created and proposed by tailoring the solvation structures of charge carriers including both cations and anions, which maintains highly oxidation-resistant contact ion pairs and ion aggregates and provides a high ion conductivity. The tailored solvation structure makes a great contribution to protecting the graphite cathode from electrolyte oxidation, solvent co-intercalation, and structural degradation by constructing a robust cathode-electrolyte interphase with standout electrochemical stability. Based on this, the SDIBs achieved an excellent high-voltage cycling stability with 81% capacity retention after 10 000 cycles and the battery showed an improved rate performance with 97.4 mAh g maintained at 100 C. It is identified that regulating anion solvation structure is responsible for the stable interface chemistry and enhanced reaction kinetics, which provides deep insight into the compatibility design between the electrolyte and specialized charge storage in electrodes.
钠基可充电电池是电能存储最有前景的候选者之一,因为钠储量丰富。特别是,钠基双离子电池(SDIBs)在高工作电压(约5.0V)、高功率密度和潜在的低成本方面具有优势。然而,在高充电状态下,电极界面处不可逆的电解质分解和溶剂分子的共嵌入阻碍了它们的发展。在此,通过调整包括阳离子和阴离子在内的电荷载体的溶剂化结构,创建并提出了一种高盐浓度微环境,该微环境维持了高度抗氧化的接触离子对和离子聚集体,并提供了高离子电导率。定制的溶剂化结构通过构建具有出色电化学稳定性的坚固的阴极-电解质界面,为保护石墨阴极免受电解质氧化、溶剂共嵌入和结构降解做出了巨大贡献。基于此,SDIBs实现了出色的高压循环稳定性,在10000次循环后容量保持率为81%,并且该电池在100C下保持97.4mAh g的倍率性能有所提高。研究发现,调节阴离子溶剂化结构有助于稳定界面化学和增强反应动力学,这为深入了解电解质与电极中特定电荷存储之间的兼容性设计提供了思路。