001     1025084
005     20250203103432.0
024 7 _ |a 10.1149/MA2023-012665mtgabs
|2 doi
024 7 _ |a 1091-8213
|2 ISSN
024 7 _ |a 2151-2043
|2 ISSN
037 _ _ |a FZJ-2024-02672
082 _ _ |a 540
100 1 _ |a Arifiadi, Anindityo
|0 0000-0002-1329-1295
|b 0
245 _ _ |a Establishing an Appropriate Voltage Window for Stable Cycling of Li/Mn-Rich Layered Oxide || Graphite Full Cells
260 _ _ |a Pennington, NJ
|c 2023
|b Soc.
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1712833346_17869
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
500 _ _ |a Hierbei handelt es sich lediglich um einen Abstract.
520 _ _ |a Li/Mn-rich layered oxide cathode active materials (LMR) have gained attention due to their exceptionally high practical specific discharge capacity (>250 mAh g-1) originating from both conventional cationic as well as anionic oxygen redox contributions. To achieve this high capacity, the Li2MnO3-like regions of the material, which give rise to oxygen redox need to be electrochemically activated at high voltage (above 4.6 V versus Li+/Li0). This high voltage activation, however, results in the destabilization of lattice oxygen that creates subsequent adverse phenomena such as first-cycle hysteresis and the evolution of redox couples. The latter happens continuously during cycling and results in the activation of Mn3+/Mn4+ redox couple. This redox couple involving Mn3+ is problematic because, at this oxidation state, Mn disproportionation reaction can occur, resulting in the formation of highly soluble Mn2+ species. In a half-cell setup, the impact of Mn dissolution may be subtle, however, in LMR||Graphite full cells, the impact is consequential.This work focuses on investigating the degradation mechanism of LMR||Graphite full cells at different voltage windows applied during the activation cycles and the long-term cycling. These different voltage windows alter the redox contributions and thus affect the long-term performance of the cells. We observe that lowering the upper cut-off voltage (UCV) from 4.7 V to 4.5 V during the entire cycling process can increase capacity retention, although rapid degradation can still be observed. Only when the UCV during the long-term cycling is lowered to 4.3 V, can we obtain incremental degradation of the cells. We also show that lowering the activation cycles UCV to 4.5 V is beneficial for long-term cycling due to the lower contribution of Mn3+/Mn4+ redox couple after the activation cycles. Finally, we observe that increasing the lower cut-off voltage from 1.9 V to 2.4 V results in higher discharge voltage. Nevertheless it is followed by a reduction in discharge capacity, resulting in a lower specific energy. This study offers insights into the high-voltage cycling performance of practical LMR||Gr full cells that can be used for the foundation of material design to alleviate the adverse effect of oxygen redox in LMR.
536 _ _ |a 1221 - Fundamentals and Materials (POF4-122)
|0 G:(DE-HGF)POF4-1221
|c POF4-122
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, Journals: juser.fz-juelich.de
700 1 _ |a Schmuch, Richard
|b 1
700 1 _ |a Kasnatscheew, Johannes
|0 P:(DE-Juel1)171865
|b 2
700 1 _ |a Winter, Martin
|0 P:(DE-Juel1)166130
|b 3
773 _ _ |a 10.1149/MA2023-012665mtgabs
|g Vol. MA2023-01, no. 2, p. 665 - 665
|0 PERI:(DE-600)2438749-6
|n 2
|p 665 - 665
|t Meeting abstracts
|v MA2023-01
|y 2023
|x 1091-8213
909 C O |o oai:juser.fz-juelich.de:1025084
|p VDB
910 1 _ |a Forschungszentrum Jülich
|0 I:(DE-588b)5008462-8
|k FZJ
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|6 P:(DE-Juel1)171865
910 1 _ |a Forschungszentrum Jülich
|0 I:(DE-588b)5008462-8
|k FZJ
|b 3
|6 P:(DE-Juel1)166130
913 1 _ |a DE-HGF
|b Forschungsbereich Energie
|l Materialien und Technologien für die Energiewende (MTET)
|1 G:(DE-HGF)POF4-120
|0 G:(DE-HGF)POF4-122
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-100
|4 G:(DE-HGF)POF
|v Elektrochemische Energiespeicherung
|9 G:(DE-HGF)POF4-1221
|x 0
914 1 _ |y 2024
920 1 _ |0 I:(DE-Juel1)IEK-12-20141217
|k IEK-12
|l Helmholtz-Institut Münster Ionenleiter für Energiespeicher
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-Juel1)IEK-12-20141217
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IMD-4-20141217


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