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Unraveling the Voltage Decay Phenomenon in Li‐Rich Layered Oxide Cathode of No Oxygen Activity
Author(s) -
Li Ning,
Hwang Sooyeon,
Sun Meiling,
Fu Yanbao,
Battaglia Vincent S.,
Su Dong,
Tong Wei
Publication year - 2019
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201902258
Subject(s) - oxide , materials science , decoupling (probability) , oxygen , electrochemistry , lattice (music) , cathode , oxygen evolution , chemical physics , nanotechnology , electrode , chemistry , physics , metallurgy , control engineering , acoustics , engineering , organic chemistry
Extensive efforts have been devoted to unraveling the true cause of voltage decay in Li, Mn‐rich layered oxides. An initial consensus was reached on structural rearrangement, then leaned toward the newly discovered lattice oxygen activity. It is challenging to differentiate their explicit roles because these events typically coexist during the electrochemical reaction of most Li‐rich layered oxides. Here, the voltage decay behavior is probed in Li 1.2 Ni 0.2 Ru 0.6 O 2 , a structurally and electrochemically relevant compound to Li, Mn‐rich layered oxide, but of no oxygen activity. Such intriguing characteristics allow the explicit decoupling of the contribution of transition metal migration and lattice oxygen activity to voltage decay in Li‐rich layered oxides. The results demonstrate that the microstructural evolution, mainly originating from transition metal migration, is a direct cause of voltage decay, and lattice oxygen activity likely accelerates the decay.