A review and outlook on anionic and cationic redox in Ni-, Li- and Mn-rich layered oxides LiMeO2 (Me = Li, Ni, Co, Mn)

Fuente: arXiv
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Autores principales: Ying, Bixian, Teng, Zhenjie, Day, Sarah, Porter, Dan, Winter, Martin, Jonas, Adrian, Frenzel, Katja, Mathies, Lena, Beckhoff, Burkhard, Nagel, Peter, Schuppler, Stefan, Merz, Michael, Pfeiffer, Felix, Weiling, Matthias, Baghernejad, Masoud, Kleiner, Karin
Formato: Preprint
Publicado: 2023
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author Ying, Bixian
Teng, Zhenjie
Day, Sarah
Porter, Dan
Winter, Martin
Jonas, Adrian
Frenzel, Katja
Mathies, Lena
Beckhoff, Burkhard
Nagel, Peter
Schuppler, Stefan
Merz, Michael
Pfeiffer, Felix
Weiling, Matthias
Baghernejad, Masoud
Kleiner, Karin
author_facet Ying, Bixian
Teng, Zhenjie
Day, Sarah
Porter, Dan
Winter, Martin
Jonas, Adrian
Frenzel, Katja
Mathies, Lena
Beckhoff, Burkhard
Nagel, Peter
Schuppler, Stefan
Merz, Michael
Pfeiffer, Felix
Weiling, Matthias
Baghernejad, Masoud
Kleiner, Karin
contents The present work reviews the charge compensation in Ni based layered oxides (LiNi1-xMexO2 with x <= 0.2, Me = Co, Mn, space group R-3m) relating performance parameters to changes in the electronic and crystallographic structure of the cathode materials. Upon charge and discharge two fundamentally different redox mechanisms are observed: At low and medium states of charge (SOCs) charge compensation takes mainly place at oxygen sites while electron density is shifted from the oxygen lattice to nickel (formation of sigma bonds). At high SOCs the shift of electron density from the transition metals to oxygen (formation of pi bonds) enables an additional redox process but also oxygen release from the transition metal host structure and subsequent detrimental reactions. Depending on the Ni:Co:Mn content, both processes lead to characteristic features in the voltage profile of the cathode materials and performance parameters like the capacity, the cycling stability and the open cell voltage become a function of the composition.
format Preprint
id arxiv_https___arxiv_org_abs_2310_01295
institution arXiv
publishDate 2023
record_format arxiv
spellingShingle A review and outlook on anionic and cationic redox in Ni-, Li- and Mn-rich layered oxides LiMeO2 (Me = Li, Ni, Co, Mn)
Ying, Bixian
Teng, Zhenjie
Day, Sarah
Porter, Dan
Winter, Martin
Jonas, Adrian
Frenzel, Katja
Mathies, Lena
Beckhoff, Burkhard
Nagel, Peter
Schuppler, Stefan
Merz, Michael
Pfeiffer, Felix
Weiling, Matthias
Baghernejad, Masoud
Kleiner, Karin
Materials Science
The present work reviews the charge compensation in Ni based layered oxides (LiNi1-xMexO2 with x <= 0.2, Me = Co, Mn, space group R-3m) relating performance parameters to changes in the electronic and crystallographic structure of the cathode materials. Upon charge and discharge two fundamentally different redox mechanisms are observed: At low and medium states of charge (SOCs) charge compensation takes mainly place at oxygen sites while electron density is shifted from the oxygen lattice to nickel (formation of sigma bonds). At high SOCs the shift of electron density from the transition metals to oxygen (formation of pi bonds) enables an additional redox process but also oxygen release from the transition metal host structure and subsequent detrimental reactions. Depending on the Ni:Co:Mn content, both processes lead to characteristic features in the voltage profile of the cathode materials and performance parameters like the capacity, the cycling stability and the open cell voltage become a function of the composition.
title A review and outlook on anionic and cationic redox in Ni-, Li- and Mn-rich layered oxides LiMeO2 (Me = Li, Ni, Co, Mn)
topic Materials Science
url https://arxiv.org/abs/2310.01295