The surface evolution of LiNi0.8Co0.15Al0.05O2 (NCA) and Li4Ti5O12 (LTO) electrodes cycled in a carbonate-based electrolyte was systematically investigated using the high lateral resolution and surface sensitivity of x-ray photoemission electron microscopy combined with x-ray absorption spectroscopy and x-ray photoelectron spectroscopy. On the cathode, we attest that the surface of the pristine particles is composed of adventitious Li2CO3 together with reduced Ni and Co in a +2 oxidation state, which is directly responsible for the overpotential observed during the first de-lithiation. This layer decomposes at 3.8 V vs Li+/Li, leaving behind a fresh surface with Ni and Co in a +3 oxidation state. The charge compensation upon Li+ extraction takes place above 4.0 V and is assigned to the oxidation of both Ni and oxygen, while Co remains in a +3 oxidation state during the whole redox process. We also identified the formation of an inactive surface layer already at 4.3 V, rich in reduced Ni and depleted in oxygen. However, at 4.9 V, NiO-like species are detected accompanied with reduced Co. Despite the highly oxidative potential, the surface of the cathode after long cycling is free of oxidized solvent byproducts but contains traces of LiPF6 byproducts (LiF and POxFy). On the LTO counter electrode, transition metals are detected only after long cycling vs NCA to 4.9 V as well as PVdF and LiPF6 byproducts originating from the cathode. Finally, harvested cycled electrodes prove that the influence of the crosstalk on the electrochemical performance of LTO is limited.
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14 May 2020
Research Article|
May 13 2020
Multi-length-scale x-ray spectroscopies for determination of surface reactivity at high voltages of LiNi0.8Co0.15Al0.05O2 vs Li4Ti5O12
Special Collection:
Interfacial Structure and Dynamics for Electrochemical Energy Storage
Marta Mirolo
;
Marta Mirolo
1
Electrochemistry Laboratory, Paul Scherrer Institut
, CH-5232 Villigen PSI, Switzerland
2
Swiss Light Source, Paul Scherrer Institut
, CH-5232 Villigen PSI, Switzerland
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Carlos A. F. Vaz
;
Carlos A. F. Vaz
a)
2
Swiss Light Source, Paul Scherrer Institut
, CH-5232 Villigen PSI, Switzerland
a)Author to whom correspondence should be addressed: mario.el-kazzi@psi.ch
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Petr Novák
;
Petr Novák
1
Electrochemistry Laboratory, Paul Scherrer Institut
, CH-5232 Villigen PSI, Switzerland
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Mario El Kazzi
Mario El Kazzi
a)
1
Electrochemistry Laboratory, Paul Scherrer Institut
, CH-5232 Villigen PSI, Switzerland
a)Author to whom correspondence should be addressed: mario.el-kazzi@psi.ch
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a)Author to whom correspondence should be addressed: mario.el-kazzi@psi.ch
Note: This paper is part of the JCP Special Topic on Interfacial Structure and Dynamics for Electrochemical Energy Storage.
J. Chem. Phys. 152, 184705 (2020)
Article history
Received:
March 02 2020
Accepted:
April 16 2020
Citation
Marta Mirolo, Carlos A. F. Vaz, Petr Novák, Mario El Kazzi; Multi-length-scale x-ray spectroscopies for determination of surface reactivity at high voltages of LiNi0.8Co0.15Al0.05O2 vs Li4Ti5O12. J. Chem. Phys. 14 May 2020; 152 (18): 184705. https://doi.org/10.1063/5.0006269
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