材料科学
电极
电解质
化学工程
储能
电池(电)
惰性
石墨
收缩率
离子
相(物质)
纳米技术
相变
电流密度
阳极
复合材料
锂离子电池
光电子学
格子(音乐)
化学稳定性
容量损失
工作(物理)
电位梯度
表面改性
极化(电化学)
基质(化学分析)
作者
Chenrui Zeng,Ruixin Zheng,Yiqi Cao,Fengxia Fan,Yan Huang,Yang Zhang,Haoruo Xiao,Chaozhu Shu,Bingsen Zhang
标识
DOI:10.1002/adfm.202519504
摘要
Abstract Ni‐rich layered oxides are promising positive electrode materials for lithium‐ion batteries (LIBs) owing to their high energy density and cost efficiency. Nevertheless, the intrinsic chemicophysical instability of Ni‐rich layered oxides severely limits the massive application. Herein, a unique gradient structure design from coherent rock‐salt phase surface structure to quasi super‐lattice matrix on the sub‐surface of single‐crystalline LiNi 0.83 Co 0.11 Mn 0.06 O 2 (GS‐SC‐NCM) is proposed to improve their stability. The introduced Ti 4+ /Nb 5+ /Zr 4+ ions are able to alleviate the overlay of O 2p and Ni 3d bands at the highly delithiated state, remarkably improving the stability of anion skeleton. Moreover, intragranular cracks and undesired lattice shrinkage during the H2‐H3 phase transition are greatly suppressed due to the ultra‐stable gradient structure design. In addition, the inert rock‐salt‐like phase on the surface of GS‐SC‐NCM hinders continuous evolution of interphase. Consequently, the superior cycling stability of GS‐SC‐NCM with high capacity retention of 92.9% after 150 cycles is achieved. Moreover, an Ah‐level pouch cell consisting of GS‐SC‐NCM positive electrode and commercial graphite negative electrode exhibits extraordinary cycling stability at 1C with 89.8% capacity retention after 450 cycles. This work represents significant progress in stabilizing single‐crystalline Ni‐rich layered oxides for an advanced secondary battery system, which is pivotal for accelerating the current electrification process.
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