A Near‐Surface Structure Reconfiguration Strategy to Regulate Mn3+/Mn4+and O2−/(O2)n−Redox for Stabilizing Lithium‐Rich Oxide Cathode

Author:

Zhang Ying12,Zheng Shuanghao13,Meng Caixia134,Liu Hanqing12,Dong Cong12,Shi Xiaoyu1,Das Pratteek1,Huang Rong5,Yu Yan6,Wu Zhong‐Shuai13ORCID

Affiliation:

1. State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences 457 Zhongshan Road Dalian 116023 China

2. University of Chinese Academy of Sciences 19 A Yuquan Road Beijing 100049 China

3. Dalian National Laboratory for Clean Energy Chinese Academy of Sciences 457 Zhongshan Road Dalian 116023 China

4. Division of Energy Research Resources Dalian 116023 China

5. Vacuum Interconnected Nanotech Workstation Suzhou Institute of Nano‐Tech and Nano‐Bionics Chinese Academy of Sciences Suzhou 215123 China

6. Hefei National Research Center for Physical Sciences at the Microscale Department of Materials Science and Engineering CAS Key Laboratory of Materials for Energy Conversion University of Science and Technology of China Hefei 230026 China

Abstract

AbstractLithium‐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 Mn3+/Mn4+and O2−/(O2)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 Fimpact becomes easier for the O sites at the lattice interface ofC2/mandRmto sufficiently buffer lattice stress. Moreover, lithium ions coupled to the doped F atoms at the lattice interface migrate to the Ni‐richRmlattice 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.

Funder

National Natural Science Foundation of China

Dalian Institute of Chemical Physics

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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