1. Voltage fade mitigation in the cationic dominant lithium-rich NCM cathode
- Author
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Chung-Chieh Chang, Po-Wei Chi, Heng-Liang Wu, Kai-Han Su, Horng-Yi Tang, Phillip M. Wu, T. W. Huang, Kuo-Wei Yeh, Maw-Kuen Wu, Ming-Jye Wang, Yu-Wen Lee, Chui-Chang Chiu, Wei-Fan Hsu, H.W. Chang, Dong-Ze Wu, and Prem Chandan
- Subjects
NI ,Materials science ,Chemistry, Multidisciplinary ,ELECTRODES ,Metal ions in aqueous solution ,chemistry.chemical_element ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Biochemistry ,Redox ,CAPACITY ,law.invention ,lcsh:Chemistry ,ANIONIC REDOX ,law ,Materials Chemistry ,Environmental Chemistry ,ION ,Dissolution ,Science & Technology ,Cationic polymerization ,General Chemistry ,021001 nanoscience & nanotechnology ,Cathode ,MN ,0104 chemical sciences ,Chemistry ,CYCLING PERFORMANCE ,lcsh:QD1-999 ,Chemical engineering ,chemistry ,Physical Sciences ,Lithium ,Fade ,0210 nano-technology ,Capacity loss - Abstract
In the archetypal lithium-rich cathode compound Li1.2Ni0.13Co0.13Mn0.54O2, a major part of the capacity is contributed from the anionic (O2−/−) reversible redox couple and is accompanied by the transition metal ions migration with a detrimental voltage fade. A better understanding of these mutual interactions demands for a new model that helps to unfold the occurrences of voltage fade in lithium-rich system. Here we present an alternative approach, a cationic reaction dominated lithium-rich material Li1.083Ni0.333Co0.083Mn0.5O2, with reduced lithium content to modify the initial band structure, hence ~80% and ~20% of capacity are contributed by cationic and anionic redox couples, individually. A 400 cycle test with 85% capacity retention depicts the capacity loss mainly arises from the metal ions dissolution. The voltage fade usually from Mn4+/Mn3+ and/or On−/O2− reduction at around 2.5/3.0 V seen in the typical lithium-rich materials is completely eliminated in the cationic dominated cathode material.
- Published
- 2019