钠金属负极界面失效机理与多尺度稳定策略OA
Failure Mechanisms of the Sodium Metal Anode Interface and Multiscale Stabilization Strategies
钠金属电池因其高理论比容量(1 166 mA·h/g)和低还原电势(-2.71 V(vs.SHE))成为新一代高能量密度储能体系的有力候选.然而,钠金属负极在循环过程中存在易形成枝晶、界面副反应剧烈、固体电解质界面膜(SEI)不稳定等问题,严重制约了其实际应用进程.为实现钠金属电池的稳定高效运行,构建稳定的负极界面成为研究的关键方向.近年来,研究者从电解液优化、人工界面膜构建、固态/凝胶电解质应用、合金化策略等角度出发,提出了一系列界面调控方法.系统梳理了钠金属负极界面稳定性的研究进展,重点讨论了界面调控策略的作用机制及其对电化学性能的影响,并对当前面临的挑战与未来发展方向进行了展望.
Sodium metal batteries(SMBs)are regarded as highly promising candidates for next-generation high-energy-density energy storage systems,owing to the high theoretical specific capacity(1 166 mA•h/g)and low redox potential(-2.71 V(vs.SHE))of sodium metal.However,the practical implementation of sodium metal anodes is significantly impeded by several critical issues,including uncontrollable dendrite growth,vigorous interfacial side reactions,and instability of the solid electrolyte interphase(SEI).Consequently,engineering a stable and robust anode interface has become a pivotal research focus for achieving high-performance SMBs.In recent years,researchers have proposed a variety of interfacial regulation strategies,including electrolyte optimization,artificial interfacial layer construction,application of solid-state or gel electrolytes,and alloying approaches.This review systematically summarizes recent progress in stabilizing the sodium metal anode interface,with a focus on the mechanismsof various interface engineering strategies and their effects on electrochemical performance.The challenges and future perspectives in this field are also discussed.
薛锐;王文举
南京工程学院 能源与动力工程学院,江苏 南京 210000南京理工大学 能源与动力工程学院,江苏 南京 210000
化学化工
钠金属电池负极界面SEI膜界面调控枝晶抑制
Sodium metal batteriesAnode interfaceSEI layerInterface engineeringDendrite suppression
《石油化工高等学校学报》 2026 (2)
1-8,8
国家自然科学基金项目(BK20230933).
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