材料科学
聚乙烯亚胺
法拉第效率
阴极
聚合物
成核
化学工程
电解质
涂层
相间
沉积(地质)
纳米技术
锂(药物)
纳米尺度
集电器
聚合物电解质
电化学
吸附
胺气处理
纳米颗粒
基质(化学分析)
枝晶(数学)
复合材料
同种类的
金属
储能
作者
Hyeong Seop Jeong,Daehyun Kim,Ga Hyeon Lee,Liting Zhang,Y. Kim,Junyeong Lee,Min Kyeong Kim,DongIl Kim,Jin Pyo Hong,Jin Pyo Hong,Woon Bae Park,Jung Inn Sohn,John Hong,John Hong
标识
DOI:10.1002/adfm.202527860
摘要
ABSTRACT Anode‐free lithium‐metal batteries (AFLMBs), wherein Li is plated onto a bare Cu current collector during the initial charge, feature a simplified architecture and high energy density. However, in AFLMBs employing high‐mass‐loading cathodes, the intrinsically poor lithiophilicity of bare Cu induces uncontrolled dendrite growth, irreversible lithium loss, and an unstable solid electrolyte interphase (SEI), resulting in rapid capacity decay and a low Coulombic efficiency (CE). Herein, an ultrathin, cross‐linked polyethylenimine (PEI) coating is proposed as a simple yet effective interfacial engineering strategy to stabilize the anode–electrolyte interface through dual mechanisms. Abundant amine groups coordinate strongly with Li⁺, promoting homogeneous nucleation and vertical deposition while restricting lateral diffusion. The flexible polymer matrix acts as a robust barrier against parasitic reactions and corrosion. Consequently, Cu||Li half‐cells with PEI‐coated Cu sustain 350 cycles at 0.5 mA cm −2 and 0.5 mAh cm −2 , delivering an average CE of 95.29%. Full cells with high‐loading LiFePO 4 cathodes (26.52 mg cm −2 ) retain 57.65% of their initial capacity (3.26 to 1.87 mAh cm −2 ) after 100 cycles. These findings highlight nanoscale polymer coatings as a promising strategy for constructing stable artificial SEI layers in AFLMBs, yielding high‐energy and durable Li‐ion batteries.
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