Elucidating the electrochemical reaction mechanism of lithium-rich antiperovskite cathodes for lithium-ion batteries as exemplified by (Li2Fe)SeO

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Lennart Singer - , Heidelberg University  (Author)
  • M. A.A. Mohamed - , Chair of Experimental Solid State Physics, Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Henrik Hahn - , Heidelberg University  (Author)
  • Ignacio G. Gonzalez-Martinez - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Martin Hantusch - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Karolina Wenelska - , West Pomeranian University of Technology (Author)
  • Ewa Mijowska - , West Pomeranian University of Technology (Author)
  • Bernd Büchner - , Chair of Experimental Solid State Physics, Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Silke Hampel - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Nico Gräßler - , Chair of Opto-Electronics, Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Rüdiger Klingeler - , Heidelberg University  (Author)

Abstract

We report in the context of lithium-rich antiperovskite cathode materials outstanding electrochemical properties of (Li2Fe)SeO, which for the first time was synthesized via direct ball-milling. The unique structured material displays an electrochemical cycling performance of 250 mA h g−1 at 0.1C when used as a cathode in lithium-ion batteries. Comprehensive electrochemical analysis combined with detailed transmission electron microscopy studies reveal that, above 2.5 V, the multi electron storage mechanism involves conversion of (Li2Fe)SeO to Fe1−xSex. Our results furthermore demonstrate the general relevance of our findings to the whole class of antiperovskite cathode materials and present a route to strongly enhance their cell performance by avoiding the degradation path deciphered by our studies.

Details

Original languageEnglish
Pages (from-to)14294-14303
Number of pages10
JournalJournal of Materials Chemistry A
Volume11
Issue number26
Publication statusPublished - 8 Jun 2023
Peer-reviewedYes