A Link Between Lithium Diffusivity, Interplane Distance and Ni Redox State in Ni-Rich Ncm
Both enhanced Li diffusivity and high discharge capacities make Ni-rich LiNi 1-x-y Co x Mn y O 2 (NCM) cathodes attractive for application in high energy density Li-ion batteries with good power [1]. However, further improvement in power density requires a thorough understanding of the mechanisms un...
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Veröffentlicht in: | Meeting abstracts (Electrochemical Society) 2016-06, Vol.MA2016-03 (2), p.145-145 |
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Sprache: | eng |
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Zusammenfassung: | Both enhanced Li diffusivity and high discharge capacities make Ni-rich LiNi
1-x-y
Co
x
Mn
y
O
2
(NCM) cathodes attractive for application in high energy density Li-ion batteries with good power [1]. However, further improvement in power density requires a thorough understanding of the mechanisms underlying the Li diffusion kinetics. Here, we investigate changes in Li diffusion coefficient (
D
Li
) during charging of NCM/Li cells and link the evolution of
D
Li
to the atomic structure and material resistivity.
Results from galvanostatic intermittent titration technique show that Li diffusivity in NCM cathodes evolves non-monotonically during charge and discharge. The most significant changes are observed in the potential range from 3.6 to 4.0 V with respect to Li/Li
+
. Electrochemical impedance spectroscopy suggests that the lithium intercalation kinetics is primarily controlled by the charge transfer resistance at the cathode/electrolyte interface, while
in operando
X-ray diffraction indicates that the spacing along the
c
-axis increases, which we attribute to an increase of the repulsion between the oxygen slabs in the absence of screening Li. Furthermore, we observe a drastic decrease in the interplane spacing between 4.0 and 4.3 V, and a gradual decrease of the in-plane spacing (
a
,
b
-axis) during Li-deintercalation. The latter indicates shortage of the O-Me bonds with oxidation of Ni. Overall, our research data demonstrate that Li diffusion in Ni-rich LiNi
1-x-y
Co
x
Mn
y
O
2
is strongly controlled by the interplane spacing of the host structure, and the overall kinetics appears to be limited by high interfacial charge transfer resistance at the beginning of charge.
References
[1] Wei, Y.; Zheng, J.; Cui, S.; Song, X.; Su, Y.; Deng, W.; Wu, Z.; Wang, X.; Wang, W.; Rao, M.; Lin, Y.; Wang, C.; Amine, K. & Pan, F. Kinetics Tuning of Li-Ion Diffusion in Layered Li(Ni
x
Mn
y
Co
z
)O
2
, Journal of the American Chemical Society, 2015, 137, 8364-8367. |
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ISSN: | 2151-2043 2151-2035 |
DOI: | 10.1149/MA2016-03/2/145 |