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@ARTICLE{Kasnatscheew:829298,
author = {Kasnatscheew, J. and Evertz, M. and Streipert, B. and
Wagner, R. and Klöpsch, R. and Vortmann, B. and Hahn, H.
and Nowak, S. and Amereller, M. and Gentschev, A.-C. and
Lamp, P. and Winter, M.},
title = {{T}he truth about the 1st cycle {C}oulombic efficiency of
{L}i{N}i $_{1/3}$ {C}o $_{1/3}$ {M}n $_{1/3}$ {O} $_{2}$
({NCM}) cathodes},
journal = {Physical chemistry, chemical physics},
volume = {18},
number = {5},
issn = {1463-9084},
address = {Cambridge},
publisher = {RSC Publ.},
reportid = {FZJ-2017-03028},
pages = {3956 - 3965},
year = {2016},
abstract = {The 1st cycle Coulombic efficiency (CE) of
LiNi1/3Co1/3Mn1/3O2 (NCM) at 4.6 V vs. Li/Li+ has been
extensively investigated in NCM/Li half cells. It could be
proven that the major part of the observed overall specific
capacity loss (in total 36.3 mA h g−1) is reversible and
induced by kinetic limitations, namely an impeded lithiation
reaction during discharge. A measure facilitating the
lithiation reaction, i.e. a constant potential (CP) step at
the discharge cut-off potential, results in an increase in
specific discharge capacity of 22.1 mA h g−1. This
capacity increase during the CP step could be proven as a
relithiation process by Li+ content determination in NCM via
an ICP-OES measurement. In addition, a specific capacity
loss of approx. 4.2 mA h g−1 could be determined as an
intrinsic reaction to the NCM cathode material at room
temperature (RT). In total, less than 10.0 mA h g−1
$(=28\%$ of the overall capacity loss) can be attributed to
irreversible reactions, mainly to irreversible structural
changes of NCM. Thus, the impact of parasitic reactions,
such as oxidative electrolyte decomposition, on the
irreversible capacity is negligible and could also be proven
by on-line MS. As a consequence, the determination of the
amount of extracted Li+ (“Li+ extraction ratio”) so far
has been incorrect and must be calculated by the charge
capacity (=delithiation amount) divided by the theoretical
capacity. In a NCM/graphite full cell the relithiation
amount during the constant voltage (CV) step is smaller than
in the half cell, due to irreversible Li+ loss at graphite.},
cin = {IEK-12},
ddc = {540},
cid = {I:(DE-Juel1)IEK-12-20141217},
pnm = {131 - Electrochemical Storage (POF3-131)},
pid = {G:(DE-HGF)POF3-131},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000369508100069},
pubmed = {pmid:26771035},
doi = {10.1039/C5CP07718D},
url = {https://juser.fz-juelich.de/record/829298},
}