Synthesis, Characterization, and Electrochemistry of Layered Chalcogenides LiCu Ch (Ch = Se, Te)

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Martin Valldor - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Daria Mikhailova - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Lars Giebeler - , Chair of Materials Synthesis and Analysis, Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Kwing To Lai - , Chinese University of Hong Kong (Author)
  • Lena Spillecke - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Hans Joachim Grafe - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Bernd Büchner - , Chair of Experimental Solid State Physics, Leibniz Institute for Solid State and Materials Research Dresden (Author)

Abstract

Two novel compounds, LiCuCh (Ch = Se or Te), were synthesized by direct reaction between elements in closed ampules inside corundum crucibles. Both compounds are highly air-sensitive and possess an anti-PbClF crystal structure, which contains CuCh layer analogues to the Fe[As/Se] layers in Fe-based superconductors. In electrochemical battery cells, Li can be almost completely extracted from LiCuSe, but the reverse reaction is only partly successful and Li2Se and Cu2-xSe are formed instead. LiCuSe exhibits a temperature independent and slightly positive magnetic susceptibility. From 7Li NMR measurements, the activation energy of the Li ion diffusion process is about 0.5 eV but is slightly lower for LiCuTe as compared to LiCuSe. Also, the small and almost temperature independent NMR shifts of the 7Li nucleus indicate the absence of Pauli paramagnetism in these compounds, consistent with a 3d10 full valence state of the Cu ions.

Details

Original languageEnglish
Pages (from-to)7201-7207
Number of pages7
JournalInorganic chemistry
Volume57
Issue number12
Publication statusPublished - 18 Jun 2018
Peer-reviewedYes

External IDs

PubMed 29808682