材料科学
法拉第效率
阴极
电解质
化学工程
无定形固体
电化学
涂层
氧气
锂(药物)
电极
电流密度
离子键合
金属
析氧
纳米技术
能量密度
金属锂
氧化物
储能
快离子导体
容量损失
动能
电化学窗口
比能量
作者
Yuehua Chen,Ling Huang,Awais Ghani,Xiaodong Chen,Xin Gao,Tao Meng,Hongchao Sun,Runjing Xu,Peiyi Ji,Xianghong Deng,Long Bao,Sui‐Dong Wang,Nana Wang,Gang Tan,G. Wang,Zhiyong Huang
标识
DOI:10.1002/adma.202521690
摘要
ABSTRACT The Li‐rich manganese‐based oxides (LRMO) with high operating voltage and large reversible capacities can demonstrate comprehensive advantages of intrinsic safety and high energy density when employed in all‐solid‐state lithium batteries (ASSLBs). However, severe interfacial incompatibility with solid electrolytes (SEs) arising from unstable lattice oxygen and sluggish Li + ionic transport hinders their practical application. In this contribution, the gradient‐modified structure containing S, Zr co‐doping near‐surface and amorphous Zr(SO 4 ) 2 coating is simultaneously established onto LRMO cathode by a one‐step mechano‐fusion process. The synergistic co‐functionalization stabilizes the oxygen framework, enhances charge transport, and suppresses oxygen dimerization under high potential. Besides, the amorphous Zr(SO 4 ) 2 coating evenly adhering onto LRMO bulk ensures long‐term intimate contact with SEs to guarantee electrochemical activities and restrains interfacial parasitic reactions. Consequently, the optimized A‐LRMO cathode exhibits a high discharge capacity of 292 mAh/g at 0.1 C and 81.8% capacity retention after 2000 cycles at 1 C. Pouch cells delivered an areal capacity of 8.5 mAh/cm 2 with >99.6% Coulombic efficiency. This gradient‐modification strategy offers an effective pathway to improve interfacial stability and accelerate the practical application of LRMO‐based ASSLBs.
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