有色金属功能化策略在无负极碱金属电池中的应用研究
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作者单位:

1.化学电源湖南省重点实验室,湖南长沙 410083 ;2.中南大学 化学化工学院,湖南长沙 410083

作者简介:

卢骏辉(2002-),广东广州人,硕士,主要研究方向为无负极钠金属电池;

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中图分类号:

TM912.2

基金项目:

国家自然科学基金项目(No. 22579191);湖南省科技计划项目(No. 2017TP1001)


Non-ferrous metal functionalization strategies for anode-free alkali metal batteries
Author:
Affiliation:

1. Hunan Provincial Key Laboratory of Chemical Power Sources, Changsha 410083 , China ;2. School of Chemistry and Chemical Engineering, Central South University, Changsha 410083 , China

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    摘要:

    无负极碱金属电池(Anode-Free Alkali Metal Batteries,AFAMBs)具有高能量密度、低制造成本和简化结构特点,是极具潜力的下一代储能技术。然而,其负极侧因碱金属高反应活性引发的固态电解质界面(SEI)不稳定、枝晶生长、不可逆沉积及体积变化等问题,严重制约其循环寿命和商业化进程。针对这些问题,兼具优异导电性、良好机械性能及对碱金属诱导特性的有色金属,在构建负极侧功能化界面中发挥关键作用。本文重点阐述了相关策略与机制:通过Au、In等构建亲碱金属界面降低成核势垒,诱导均匀沉积;借助Ru、Zn等构筑原位/人工SEI增强界面稳定性,抑制副反应与枝晶生长;采用三维多孔骨架结构缓解体积应变,优化离子/电子传输;开发新型合金及复合集流体调控沉积行为,提升循环可逆性。进一步分析了有色金属在晶格匹配、电子结构调控等方面的深层机理。通过引入高界面亲和性的有色金属或重构晶面,可降低能垒并引导均匀成核,具有特定原子半径的有色金属可在碱金属沉积时原位合金化,生成适配的合金相,确保碱金属的可逆沉积。通过引入具备特定活性位点的有色金属纳米团簇、单原子配位键或异质结构,可调节集流体的局部电流密度,改善界面游离离子的传输动力学,均匀极化电场,抑制枝晶生长。该领域未来研究重点应加速开发低成本有色金属改性材料;开发绿色、简易且兼容现有产线的功能化技术;设计先进计算方法,预测有色金属改性集流体的界面演化路径,为设计高性能AFAMBs提供支撑。

    Abstract:

    Anode-free alkali metal batteries (AFAMBs) are regarded as a promising next-generation energy storage technology, featuring high energy density, low manufacturing cost and simple structure. However, the anode side is confronted with challenges such as unstable solid electrolyte interface (SEI), dendrite growth, irreversible deposition and severe volume changes, caused by the high reactivity of alkali metals. These issues severely limit the cycle life and commercialization of AFAMBs. In response to these issues, non-ferrous metals play key roles in the construction of the functionalized interfaces on the anode side of AFAMBs due to their excellent electrical conductivity, favorable mechanical properties and the ability to induce alkali metals. This article focuses on various strategies and mechanisms: (i) constructing alkaliphlic interface layers (e. g. , Au, In) to reduce the nucleation barrier and guide uniform deposition; (ii) building in-situ/artificial SEI with Ru, Zn, etc. , to enhance interface stability and suppress side reactions and dendrite growth; (iii) implementing three-dimensional porous scaffolds to alleviate volume strain and optimize ion/electron transport; (iv) developing advanced alloys and composite current collectors to regulate interface deposition behavior and improve cycle reversibility. This article further analyzes the research progress in the mechanism of non-ferrous metals in aspects such as lattice matching and electronic structure modulation. By introducing high affinity non-ferrous species or reconfiguring crystal planes, the energy barrier can be reduced and homogeneous nucleation can be guided. Certain non-ferrous metals with specific atomic radii facilitate in-situ alloying during deposition, forming stable alloy phases, ensuring reversible deposition. Moreover, by integrating non-ferrous nanoclusters, single-atom coordination bonds, or heterostructures with specific active sites, the local current density can be regulated, thereby accelerating ion transport kinetics, homogenizing the electric field and inhibiting dendrite growth. Future research should prioritize the development of cost-efficient modification materials; develop green, simple, and compatible functionalization techniques with existing production lines; and design advanced computational models to predict interface evolution, ultimately providing support for high-performance AFAMBs.

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引用本文

卢骏辉,黄友,戴嘉文,等 . 有色金属功能化策略在无负极碱金属电池中的应用研究[J]. 中国有色冶金,2026,55 (3):28-42.

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  • 收稿日期:2025-12-30
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  • 在线发布日期: 2026-07-08
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