阳极
材料科学
阴极
电解质
利加
导电体
堆栈(抽象数据类型)
电化学
分离器(采油)
锂(药物)
电流密度
枝晶(数学)
化学工程
纳米技术
能量密度
金属锂
快离子导体
光电子学
锂离子电池的纳米结构
储能
环境压力
电化学窗口
相容性(地球化学)
作者
Jeong‐Myeong Yoon,Pugalenthiyar Thondaiman,Je‐Hyeon Han,Young Han Lee,Do‐Hyeon Kim,Cheol‐Min Park
标识
DOI:10.1002/aenm.202505248
摘要
ABSTRACT Lithium all‐solid‐state batteries (LASSBs) with sulfide‐type solid electrolytes (SEs) offer enhanced safety and higher energy densities compared to conventional Li‐ion batteries. However, Li‐metal anodes are incompatible with sulfide‐type SEs and prone to dendrite formation, which severely limits their practical applicability. Although various strategies, including the use of Li‐free, carbon‐based, alloy‐based, or oxide‐based anodes, as well as interfacial protection layers, have been explored, they typically deliver poor rate performance and suffer from dendrite growth. Herein, we introduce a Li–Ga compound anode, specifically the LiGa phase, predicted through density functional theory simulations, which exhibits dendrite‐free behavior, high ionic/electronic conductivities, stable operation at low stack pressures, room temperature stability, and excellent interfacial compatibility with SEs. Benefiting from these properties, a full cell comprising a LiGa anode and the LiNi 0.6 Co 0.2 Mn 0.2 O 2 (NCM622) cathode (LiGa|NCM622) delivers a high areal capacity of 14.47 mAh cm −2 at a high cathode loading of 100 mg cm −2 , along with fast rate capability and stable cycling at a low stack pressure of 3 MPa at room temperature. Furthermore, a LiGa|NCM622 pouch cell demonstrates outstanding electrochemical performance, highlighting the potential of LiGa as a high‐performance anode for next‐generation LASSBs, with the concept broadly applicable to diverse Li‐based compounds.
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