Insight into the Role of Metal-Oxygen Bond and O 2p Hole in High-Voltage Cathode LiNixMn2-xO4

Insight into the Role of Metal-Oxygen Bond and O 2p Hole in High-Voltage Cathode LiNixMn2-xO4
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深入了解金属氧键和 O 2p 空穴在高压正极 LiNixMn2-xO4 中的作用

DOI:
10.1021/acs.jpcc.7b03875
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发表时间:
2017
影响因子:
3.7
通讯作者:
Zhang Shuo
Zhang Shuo
中科院分区:
化学3区
文献类型:
--
作者:
Liu Hengjie;Zhou Jing;Zhang Linjuan;Hu Zhiwei;Kuo Changyang;Li Jiong;Wang Yu;Tjeng Liu Hao;Pi Tun-Wen;Tanaka Arata;Song Li;Wang Jian-Qiang;Zhang Shuo

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The role of transition-metal d and ligand p hybridization continues to be of immense interest in Li-ion battery cathode, and yet it is still poorly understood. Using combined experimental and theoretical soft X-ray absorption spectroscopic study and density functional theory calculation, we investigated the fundamental electronic structure of the high-voltage spinel LiNixMn2–xO4. An oxygen-participating charge rebalance between manganese and nickel ions was found; that is, the content of O 2p holes close to the Fermi level increases along with the increasing Ni content. Moreover, these unstable oxygen holes primarily congregate around the redox active dopants. The underlying mechanism accounting for this charge-compensated occurrence is the reverse of two bonding levels when manganese ions are oxidized from +3 to +4 states. On the basis of these new findings, we further exposed the role of oxygen in electrochemical performance. First, oxygen ions afford the charge variation together with the cations during Li insertion/deinsertion process. Second, the O 2p holes can largely screen the strong electrostatic repulsion between Mn4+and Li+ions to effectively enhance the rate capacity. Lastly, the excessive amount of O 2p holes is disadvantageous to the thermal stability associated with the O2evolution. Also, we point out that O 2p holes concentration can be modified by the metal–oxygen bonding character, and the “charge-transfer energy” is a crucial point for designing high-capacity positive electrodes for Li-ion battery.