材料科学
电解质
铜
法拉第效率
导电体
集电器
电池(电)
氧化铜
锂(药物)
电化学
纳米技术
氧化物
电流(流体)
原子层沉积
锂离子电池
快离子导体
储能
合金
离子
阳极
电极
离子注入
化学工程
表面工程
数码产品
氧气
光电子学
金属
锂离子电池的纳米结构
沉积(地质)
锂电池
作者
Yue Li,Xiaomeng Ren,Caihong Feng,Lingcheng Kong,Fengping Luo,Yang Xu,Qian Liu,Yusheng Ye,Ziqiang Zhao,Xin Gao,Jinli Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-06-22
卷期号:20 (26): 18688-18699
标识
DOI:10.1021/acsnano.6c02968
摘要
Interfaces govern reaction pathways and stability in electrochemical systems, yet creating clean, well-defined metal interfaces at scale remains challenging. In anode-free lithium metal batteries (AFLMBs), the current-collector interface is decisive for lithium nucleation and solid electrolyte interphase (SEI) formation, and ideally should support efficient charge transport, uniform reaction distribution, and long-term chemical and structural stability. Here we report an ion-implantation strategy that produces an atomically clean and oxidation-resistant copper interface. Implanting copper ions into commercial foils removes the native oxide while generating subsurface vacancy clusters directly beneath the surface─an atomic-scale modification that does not increase the collector thickness but fundamentally alters interfacial chemistry. Experiments and multiscale simulations reveal that these vacancies act as strong oxygen traps, preventing reoxidation, enhancing interfacial conductivity, and guiding the formation of an ultrathin, Li 2 O-enriched SEI that promotes uniform lithium deposition and suppresses parasitic reactions. Applied in AFLMBs, the engineered current collectors deliver long-term stability with a Coulombic efficiency of 98.8% over 600 cycles under lean-electrolyte conditions. These findings demonstrate atomic-scale interface control of copper current collectors as a route toward stable and practical lithium metal batteries.
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