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@ARTICLE{Klein:892524,
author = {Klein, Sven and Harte, Patrick and Henschel, Jonas and
Bärmann, Peer and Borzutzki, Kristina and Beuse, Thomas and
Wickeren, Stefan and Heidrich, Bastian and Kasnatscheew,
Johannes and Nowak, Sascha and Winter, Martin and Placke,
Tobias},
title = {{O}n the {B}eneficial {I}mpact of {L}i 2 {CO} 3 as
{E}lectrolyte {A}dditive in {NCM}523 ∥ {G}raphite
{L}ithium {I}on {C}ells {U}nder {H}igh‐{V}oltage
{C}onditions},
journal = {Advanced energy materials},
volume = {11},
number = {10},
issn = {1614-6840},
address = {Weinheim},
publisher = {Wiley-VCH},
reportid = {FZJ-2021-02132},
pages = {2003756 -},
year = {2021},
abstract = {Lithium ion battery cells operating at high‐voltage
typically suffer from severe capacity fading, known as
‘rollover’ failure. Here, the beneficial impact of
Li2CO3 as an electrolyte additive for state‐of‐the‐art
carbonate‐based electrolytes, which significantly improves
the cycling performance of NCM523 ∥ graphite full‐cells
operated at 4.5 V is elucidated. LIB cells using the
electrolyte stored at 20 °C (with or without Li2CO3
additive) suffer from severe capacity decay due to parasitic
transition metal (TM) dissolution/deposition and subsequent
Li metal dendrite growth on graphite. In contrast, NCM523
∥ graphite cells using the Li2CO3‐containing electrolyte
stored at 40 °C display significantly improved capacity
retention. The underlying mechanism is successfully
elucidated: The rollover failure is inhibited, as Li2CO3
reacts with LiPF6 at 40 °C to in situ form lithium
difluorophosphate, and its decomposition products in turn
act as ‘scavenging’ agents for TMs (Ni and Co), thus
preventing TM deposition and Li metal formation on
graphite.},
cin = {IEK-12},
ddc = {050},
cid = {I:(DE-Juel1)IEK-12-20141217},
pnm = {122 - Elektrochemische Energiespeicherung (POF4-122)},
pid = {G:(DE-HGF)POF4-122},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000611080200001},
doi = {10.1002/aenm.202003756},
url = {https://juser.fz-juelich.de/record/892524},
}