TY - JOUR
T1 - Constructing a Thin Disordered Self-Protective Layer on the LiNiO2 Primary Particles Against Oxygen Release
AU - Chen, Jinniu
AU - Yang, Yang
AU - Tang, Yushu
AU - Wang, Yifan
AU - Li, Hang
AU - Xiao, Xianghui
AU - Wang, Suning
AU - Darma, Mariyam Susana Dewi
AU - Etter, Martin
AU - Missyul, Alexander
AU - Tayal, Akhil
AU - Knapp, Michael
AU - Ehrenberg, Helmut
AU - Indris, Sylvio
AU - Hua, Weibo
N1 - Publisher Copyright:
© 2022 The Authors. Advanced Functional Materials published by Wiley-VCH GmbH.
PY - 2023/2/2
Y1 - 2023/2/2
N2 - One of the major challenges facing the application of layered LiNiO2 (LNO) cathode materials is the oxygen release upon electrochemical cycling. Here it is shown that tailoring the provided lithium content during synthesis process can create a disordered layered Li1-xNi1+xO2 phase at the primary particle surface. The disordered surface, which serves as a self-protective layer to alleviate the oxygen loss, possesses the same layered rhombohedral structure (R (Formula presented.) m) as the inner core of primary particles of the Li1-xNi1+xO2 (x ≈ 0). With advanced synchrotron-based x-ray 3D imaging and spectroscopic techniques, a macroporous architecture within the agglomerates of LNO with ordered surface (LNO-OS) is revealed after only 40 cycles, concomitant with the reduction of nickel on the primary particle surface throughout the whole secondary particles. Such chemomechanical degradation accelerates the deterioration of LNO-OS cathodes. Comparably, there are only slight changes in the nickel valence state and interior architecture of LNO with a thin disordered surface layer (LNO-DS) after cycling, mainly arising from an improved robustness of the oxygen framework on the surface. More importantly, the disordered surface can suppress the detrimental H2 ⇋ H3 phase transition upon cycling compared to the ordered one.
AB - One of the major challenges facing the application of layered LiNiO2 (LNO) cathode materials is the oxygen release upon electrochemical cycling. Here it is shown that tailoring the provided lithium content during synthesis process can create a disordered layered Li1-xNi1+xO2 phase at the primary particle surface. The disordered surface, which serves as a self-protective layer to alleviate the oxygen loss, possesses the same layered rhombohedral structure (R (Formula presented.) m) as the inner core of primary particles of the Li1-xNi1+xO2 (x ≈ 0). With advanced synchrotron-based x-ray 3D imaging and spectroscopic techniques, a macroporous architecture within the agglomerates of LNO with ordered surface (LNO-OS) is revealed after only 40 cycles, concomitant with the reduction of nickel on the primary particle surface throughout the whole secondary particles. Such chemomechanical degradation accelerates the deterioration of LNO-OS cathodes. Comparably, there are only slight changes in the nickel valence state and interior architecture of LNO with a thin disordered surface layer (LNO-DS) after cycling, mainly arising from an improved robustness of the oxygen framework on the surface. More importantly, the disordered surface can suppress the detrimental H2 ⇋ H3 phase transition upon cycling compared to the ordered one.
KW - LiNiO cathodes
KW - chemomechanical degradation
KW - oxygen release
KW - self-protecting layers
KW - tomography
UR - https://www.scopus.com/pages/publications/85142873871
U2 - 10.1002/adfm.202211515
DO - 10.1002/adfm.202211515
M3 - 文章
AN - SCOPUS:85142873871
SN - 1616-301X
VL - 33
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 6
M1 - 2211515
ER -