材料科学
阴极
尖晶石
电场
电解质
化学物理
化学工程
氧化物
电极
物理化学
冶金
量子力学
物理
工程类
化学
作者
Jun Chen,Guoqiang Zou,Wentao Deng,Zhaodong Huang,Xu Gao,Cheng Liu,Shouyi Yin,Huanqing Liu,Xinglan Deng,Ye Tian,Jiayang Li,Chi-Wei Wang,Di Wang,Hanwen Wu,Li Yang,Hongshuai Hou,Xiaobo Ji
标识
DOI:10.1002/adfm.202004302
摘要
Abstract The practical application of Li‐rich Mn‐based oxide cathode is predominately retarded by the capacity decline and voltage fading, associated with the structure distortion and anionic redox reactions. Here, a linkage‐functionalized modification approach to tackle these challenges via a synchronous lithium oxidation strategy is reported. The doping of Ce in the bulk phase activates the pseudo‐bonding effect, effectively stabilizing the lattice oxygen evolution and suppressing the structure distortion. Interestingly, it also induces the formation of spinel phase Li 4 Mn 5 O 12 in the subsurface, which in turn constructs the phase boundaries, thereby arousing the interior self‐built‐in electric field to prevent the outward migration of bulk oxygen anions and boost the charge transfer. Moreover, the formed coating layer Li 2 CeO 3 with oxygen vacancies accelerates Li + diffusion and mitigates electrolyte cauterization. The corresponding cathode exhibits superior long‐cycle stability after 300 cycles with only a 0.013% capacity drop and 1.76 mV voltage decay per cycle. This work sheds new light on the development of Li‐rich Mn‐based oxide cathodes toward high energy density applications.
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