| Literature DB >> 32031283 |
Gi-Hyeok Lee1, Jinpeng Wu2,3, Duho Kim4, Kyeongjae Cho5, Maenghyo Cho6, Wanli Yang2, Yong-Mook Kang7.
Abstract
Redox reactions of oxygen have been considered critical in controlling the electrochemical properties of lithium-excessive layered-oxide electrodes. However, conventional electrode materials without overlithiation remain the most practical. Typically, cationic redox reactions are believed to dominate the electrochemical processes in conventional electrodes. Herein, we show unambiguous evidence of reversible anionic redox reactions in LiNi1/3 Co1/3 Mn1/3 O2 . The typical involvement of oxygen through hybridization with transition metals is discussed, as well as the intrinsic oxygen redox process at high potentials, which is 75 % reversible during initial cycling and 63 % retained after 10 cycles. Our results clarify the reaction mechanism at high potentials in conventional layered electrodes involving both cationic and anionic reactions and indicate the potential of utilizing reversible oxygen redox reactions in conventional layered oxides for high-capacity lithium-ion batteries.Entities:
Keywords: X-ray absorption spectroscopy; electrochemistry; lithium-ion batteries; redox chemistry; resonant inelastic X-ray scattering
Year: 2020 PMID: 32031283 DOI: 10.1002/anie.202001349
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336