枝晶(数学)
电解质
溶剂化
化学物理
电极
材料科学
锂(药物)
再分配(选举)
电化学
金属锂
金属
电荷(物理)
电极电位
电化学电位
化学
分析化学(期刊)
表面电荷
基本电荷
纳米技术
纳米尺度
分子动力学
电荷密度
工作(物理)
快离子导体
作者
Xuezhong Li,Genming Lai,Wei Deng,Zhifang Wei,Jianwei Li,Chi Fang,Taisen Zuo,He Cheng,Phakkhananan Pakawanit,Suihan Cui,Bao Qiu,Xufeng Zhou,Jiaxin Zheng,Yongbing Tang
标识
DOI:10.1038/s41467-026-72472-y
摘要
Unraveling the origins of Li dendrite growth remains a critical challenge for lithium metal batteries. Existing studies often treat diffusion-reaction mismatches or electrode surface excess charge in isolation, overlooking the coupled interfacial processes at the nanoscale solid-liquid interface that govern Li dendrite growth. Herein, we introduce the interfacial excess charge distribution factor, a quantitative descriptor that captures the dynamic equilibrium by integrating the contributions of electrode surface excess charge, charge depletion rate and solvation chemistry. We further propose an electrochemical method to monitor Li dendrite growth rates, confirming that electrolytes with rapid excess charge redistribution ability favor planar Li plating. Our findings reveal that the depletion rate of interfacial excess charge governed by Li⁺-dipole-anion interactions, and the degree of electrode excess charge modulated by solvation structures and cation screening, competitively determine the interfacial excess charge dynamics. Guided by these insights, we designed an electrolyte with optimized excess charge redistribution capability, which suppresses dendrite formation and enables stable cycling in ~6.4 Ah lithium metal batteries. This work provides mechanistic insight into how competitive interfacial processes dictate Li dendrite growth.
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