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Stabilization of a mixed iron vanadium based hexagonal tungsten bronze hydroxyfluoride HTB–(Fe 0.55 V 0.45 )F 2.67 (OH) 0.33 as a positive electrode for lithium-ion batteries

Authors :
Marc Leblanc
Jean-Marie Tarascon
Romain Moury
Jérôme Lhoste
Jean-Marc Greneche
Kévin Lemoine
Vincent Maisonneuve
Annie Hémon-Ribaud
Institut des Molécules et Matériaux du Mans (IMMM)
Le Mans Université (UM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Chaire Chimie du solide et énergie
Chimie du solide et de l'énergie (CSE)
Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Source :
Dalton Transactions, Dalton Transactions, Royal Society of Chemistry, 2020, 49 (24), pp.8186-8193. ⟨10.1039/D0DT01310B⟩
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

International audience; In our search for novel insertion compounds for Li-based batteries, we have identified a new mixed iron vanadium based Hexagonal Tungsten Bronze (HTB) type phase. Its synthesis involves two steps which consist first of preparing mixed metal hydrated fluoride Fe1.64V1.36F8(H2O)2 by a microwave assisted thermal process, followed by thermal treatment under air to obtain metastable HTB–(Fe0.55V0.45)F2.67(OH)0.33 hydroxyfluoride. 57Fe Mössbauer spectrometry demonstrates the presence of oxidation states Fe2+ and Fe3+ in Fe1.64V1.36F8(H2O)2 as opposed to only Fe3+ in HTB–(Fe0.55V0.47)F2.67(OH)0.33. Moreover, the Mössbauer spectra recorded at 77 K reveal that none of the compounds shows magnetic ordering owing to the presence of V3+ distributed over the crystallographic sites of Fe3+. Complementary X-ray spectroscopy and Rietveld refinement further confirm the successful synthesis of HTB–(Fe0.55V0.45)F2.67(OH)0.33. Electrochemically, the new HTB–(Fe0.55V0.45)F2.67(OH)0.33 shows a first discharge capacity of 181 mA h g−1 with 67% of this capacity remaining upon cycling. Unlike HTB–FeF2.66(OH)0.34, the structure remains stable after the first discharge confirming the positive effect of vanadium in the HTB network.

Details

Language :
English
ISSN :
14779226 and 14779234
Database :
OpenAIRE
Journal :
Dalton Transactions, Dalton Transactions, Royal Society of Chemistry, 2020, 49 (24), pp.8186-8193. ⟨10.1039/D0DT01310B⟩
Accession number :
edsair.doi.dedup.....4f75ff2842dc9044621ea2a5f9255257