Liu Xu, Dong Xu, Adenusi Henry, Wu Yuping, Passerini Stefano
School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing, China.
Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Ulm, Germany.
Nat Rev Chem. 2025 Apr 28. doi: 10.1038/s41570-025-00714-6.
The potential increase in cost of lithium-ion batteries owing to the limited supply of lithium has prompted investigations into alternative and complementary rechargeable batteries that use post-lithium charge carriers with higher elemental abundance. However, achieving highly reversible post-lithium metal anodes with sufficient kinetics remains challenging. The addition of co-solvents to conventional electrolytes is emerging as an important strategy to resolve these issues. In this Perspective, we discuss the progress of the co-solvent strategy for sodium, potassium, magnesium, calcium, zinc and aluminium post-lithium metal batteries. The coordination ability of co-solvents with post-lithium charge carriers is presented as a useful guide for selecting co-solvents for the respective battery electrolytes, owing to its correlation with several influential factors that affect the electrochemical performance of the metal anodes, such as solvation structure, de-solvation process and solid electrolyte interphase formation. Additionally, a discussion is provided on the importance of unravelling the effects beyond the solvation sheath of cationic charge carriers and for the development of sustainable electrolytes.
由于锂供应有限,锂离子电池成本可能增加,这促使人们对使用具有更高元素丰度的后锂电荷载体的替代和互补可充电电池进行研究。然而,实现具有足够动力学的高度可逆后锂金属阳极仍然具有挑战性。在传统电解质中添加共溶剂正成为解决这些问题的重要策略。在这篇综述中,我们讨论了用于钠、钾、镁、钙、锌和铝后锂金属电池的共溶剂策略的进展。共溶剂与后锂电荷载体的配位能力被认为是为相应电池电解质选择共溶剂的有用指南,因为它与影响金属阳极电化学性能的几个重要因素相关,如溶剂化结构、去溶剂化过程和固体电解质界面的形成。此外,还讨论了揭示阳离子电荷载体溶剂化鞘层之外的影响以及开发可持续电解质的重要性。