Title Distinct Oxygen Redox Activities in Li2MO3 (M = Mn, Ru, Ir)
Authors Zhuo, Zengqing
Dai, Kehua
Wu, Jinpeng
Zhang, Liang
Tamura, Nobumichi
Chuang, Yi-de
Feng, Jun
Guo, Jinghua
Shen, Zhi-xun
Liu, Gao
Pan, Feng
Yang, Wanli
Affiliation Peking Univ, Sch Adv Mat, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China
Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
Tianjin Normal Univ, Coll Chem, Tianjin 300387, Peoples R China
Stanford Inst Mat & Energy Sci, SLAC Natl Accelerator Lab, Menlo Pk, CA 94025 USA
Stanford Univ, Geballe Lab Adv Mat, Stanford, CA 94305 USA
Tsinghua Univ, Dept Elect Engn, Beijing 100084, Peoples R China
South Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen 518055, Peoples R China
Stanford Univ, Dept Phys & Appl Phys, Stanford, CA 94305 USA
Lawrence Berkeley Natl Lab, Energy Storage & Distributed Resources Div, Energy Technol Area, Berkeley, CA 94720 USA
Keywords LI-ION
LATTICE OXYGEN
LAYERED OXIDES
CAPACITY
LI2MNO3
CHALLENGES
CHEMISTRY
BATTERIES
PAIR
Issue Date 8-Oct-2021
Publisher ACS ENERGY LETTERS
Abstract Li2MO3 (M = transition metal) systems are parent compounds of Li-rich materials and widely considered to offer oxygen redox for high-energy batteries. However, recent clarifications have revealed that, among the three representative Li2MO3 (M = Mn, Ru, Ir) compounds, no reversible oxygen redox takes place in the Mn and Ir systems. Here, we reevaluate the redox reactions in Li2RuO3 through advanced spectroscopy, which shows both Ru redox and highly reversible O redox (96% initial-cycle reversibility, 80% retained after 10 cycles, and 77% after 50 cycles). This is in sharp contrast with the Li2MnO3 and Li2IrO3 systems and concludes the three distinct oxygen behaviors in the Li2MO3 systems during charging: (i) only irreversible oxygen oxidation in Li2MO3; (ii) reversible Ru and O redox in Li2RuO3; (iii) only cationic redox in Li2IrO3. This work suggests the critical role of transition metals and their coupling to oxygen for maintaining reversible oxygen redox activities for high-energy batteries.
URI http://hdl.handle.net/20.500.11897/628525
ISSN 2380-8195
DOI 10.1021/acsenergylett.1c01101
Indexed SCI(E)
Appears in Collections: 新材料学院

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