氧化还原
材料科学
电解质
离子
氧气
氧化态
锂(药物)
溶解
阴极
金属
无机化学
物理化学
化学
电极
有机化学
冶金
内分泌学
医学
作者
Ying Zhang,Shuanghao Zheng,Caixia Meng,Hanqing Liu,Cong Dong,Xiaoyu Shi,Pratteek Das,Rong Huang,Yan Yu,Zhong‐Shuai Wu
标识
DOI:10.1002/adfm.202300987
摘要
Abstract Lithium‐rich layered oxides (LROs) are one class of the most competitive high‐capacity cathode materials due to their anion/cation synergistic redox activity. However, excessive oxidation of the oxygen sublattices can induce serious oxygen loss and structural imbalance. Hence, a near‐surface reconfiguration strategy by fluorinating graphene is proposed to precisely regulate Mn 3+ /Mn 4+ and O 2− /(O 2 ) n− redox couples for remarkably stabilizing high‐capacity LROs and realizing the simultaneous reduction of the lattice stress, regulation of the Mn metal at a lower charge state, and construction of 3D Li + diffusion channels. Combining with a highly conductive graphene‐coating layer, the surface oxygen loss, transition metal dissolution, and electrolyte catalytic decomposition are suppressed. Benefiting from this synergy, the modified LROs disclose higher initial Coulombic efficiency and discharge‐specific capacity and improve cyclability compared with pristine LROs. Further, it is revealed that the F − impact becomes easier for the O sites at the lattice interface of C 2 /m and R m to sufficiently buffer lattice stress. Moreover, lithium ions coupled to the doped F atoms at the lattice interface migrate to the Ni‐rich R m lattice sites with lower migration energies. This consolidated understanding will open new avenues to regulate reversible oxygen redox of LROs for high‐energy‐density lithium‐ion batteries.
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