NaLiFe(C2O4)2: A polyanionic Li/Na-ion battery cathode exhibiting cationic and anionic redox

Recently, polyanionic compounds have received great interest as alternative cathode materials to conventional oxides due to their different advantages in cost, safety, structural stability, as well as being environmentally friendly. However, the vast majority of polyanionic materials reported so far rely exclusively upon the redox reaction of the transition metal for lithium/sodium transfer. The development of multielectron redox-active cathode materials is a top priority for achieving high energy density with long cycle life in the next-generation secondary battery applications. Triggering anion redox activity is a promising strategy to enhance the energy density of polyanionic cathode materials for Li/Na-ion batteries. In addition to transition metal redox activity, the oxalate group also shows redox behavior enabling reversible charge/discharge and high capacity without gas evolution. Herein, we report NaLiFe(C 2 O 4 ) 2 as a new positive electrode and use different characterization techniques such as Raman spectroscopy and Mössbauer analyses to characterise this dual-ion redox process experimentally. First-principles calculations also help to understand the interactions between the transition metal and the oxalate group as the main factor that modulates the cationic and polyanionic redox couples in these materials.

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Publication Details

Journal
Energy storage materials
Published
2024-10-02
DOI
https://doi.org/10.1016/j.ensm.2024.103821
Citations
6
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
1.25

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article

NaLiFe(C2O4)2: A polyanionic Li/Na-ion battery cathode exhibiting cationic and anionic redox

Lennart Häggström, A. Robert Armstrong, David B. Cordes, Fredrik Lindgren et al.
6 citations
Energy storage materials
Advancements in Battery Materials
1.25
article

NaLiFe(C2O4)2: A polyanionic Li/Na-ion battery cathode exhibiting cationic and anionic redox

Lennart Häggström, A. Robert Armstrong, David B. Cordes, Fredrik Lindgren, Alexis G. Manche, Tore Ericsson, Atin Pramanik
article en
6 citations

Abstract

Recently, polyanionic compounds have received great interest as alternative cathode materials to conventional oxides due to their different advantages in cost, safety, structural stability, as well as being environmentally friendly. However, the vast majority of polyanionic materials reported so far rely exclusively upon the redox reaction of the transition metal for lithium/sodium transfer. The development of multielectron redox-active cathode materials is a top priority for achieving high energy density with long cycle life in the next-generation secondary battery applications. Triggering anion redox activity is a promising strategy to enhance the energy density of polyanionic cathode materials for Li/Na-ion batteries. In addition to transition metal redox activity, the oxalate group also shows redox behavior enabling reversible charge/discharge and high capacity without gas evolution. Herein, we report NaLiFe(C 2 O 4 ) 2 as a new positive electrode and use different characterization techniques such as Raman spectroscopy and Mössbauer analyses to characterise this dual-ion redox process experimentally. First-principles calculations also help to understand the interactions between the transition metal and the oxalate group as the main factor that modulates the cationic and polyanionic redox couples in these materials.

Energy storage materialsVol. 73
Uppsala University (SE), University of St Andrews (GB), The Faraday Institution (GB)
Faraday Institution, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 20%
Advancements in Battery Materials
1.25
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