材料科学
电解质
成核
阴极
化学工程
复合数
煅烧
硝酸银
纳米技术
储能
铜
锂(药物)
银纳米粒子
涂层
纳米颗粒
枝晶(数学)
能量密度
电池(电)
图层(电子)
碘化银
电流密度
锂离子电池
集电器
电极
快离子导体
镁
阳极
作者
Hui‐Tae Sim,Myung‐Keun Oh,Ji‐Back Cho,Chae‐Young Kim,Seong‐Ho Kang,Hae‐Gon Lee,Y. R. Cho,Seong‐Jin Park,Dong‐Won Kim
标识
DOI:10.1002/adfm.202527688
摘要
ABSTRACT Anodeless all‐solid‐state batteries (ALASSBs) represent a transformative energy storage technology with the potential to maximize energy density and improve safety. The strategic incorporation of lithiophilic materials such as silver and magnesium has recently shown remarkable enhancements in cycling performance, particularly in sulfide‐based ALASSBs. Here, we report a solution‐assisted strategy employing poly(ethylene‐co‐maleic anhydride) (PEMA) to fabricate an ultrathin (∼120 nm) layer containing uniformly dispersed silver nanoparticles (10–20 nm), derived from silver nitrate (AgNO 3 , ANO), on a copper current collector, denoted as ANO_PEMA@Cu. PEMA simultaneously facilitated controlled silver nucleation and enhanced cohesion, leading to the formation of chemically and electrochemically stable interface with solid electrolyte (Li 6 PS 5 Cl). The ANO_PEMA@Cu promoted highly uniform lithium plating/stripping and effectively suppressed lithium dendrite growth, thereby ensuring interfacial stability. The anodeless all‐solid‐state cell incorporating ANO_PEMA@Cu, solid electrolyte, and composite LiNi 0.82 Co 0.10 Mn 0.08 O 2 (NCM) cathode with an areal capacity of 3.0 mAh cm −2 exhibited excellent cycling stability, retaining 80.6% of its initial capacity after 300 cycles at 0.33 C and 30°C without short‐circuiting.
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