Quantifying Effects of Ligand-Metal Bond Covalency on Oxygen-Redox Electrochemistry in Layered Oxide Cathodes
Jianyue Jiao1, Hongquan Song2,3, Enyue Zhao2
1College of Materials Science and Opto-electronic Technology, Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, China.
Abstract:
Oxygen-redox electrochemistry is attracting tremendous attention due to its enhanced energy density for layered oxide cathodes. However, quantified effects of ligand-metal bond covalency on the oxygen-redox behaviors are not fully understood, limiting a rational structure design for enhancing the oxygen redox reversibility. Here, using Li2Ru1-MnO3 (0 ≤ x ≤ 0.8) which includes both 3d- and 4d-based cations as model compounds, we provide a quantified relation between the ligand-metal bond covalency and oxygen-redox electrochemistry. Supported by theoretical calculations, we reveal a linear positive correlation between the transition metal (TM)-O bond covalency and the overlap area of TM nd and O 2p orbitals. Furthermore, based on the electrochemical tests on the Li2Ru1-MnO3 systems, we found that the enhanced TM-O bond covalency can increase the reversibility of oxygen-redox electrochemistry. Due to the strong Ru-O bond covalency, the thus designed Ru-doped Li-rich Li1.2Mn0.54Ni0.13Co0.13O2 cathode shows an enhanced initial coulombic efficiency, increased capacity retention, and suppressed voltage decay during cycling. This systematic study provides a rational structure design principle for the development of oxygen-redox-based layered oxide cathodes.
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