Issue 44, 2022

Strong electron–phonon coupling driven charge density wave states in stoichiometric 1T-VS2 crystals

Abstract

A charge density wave (CDW) transition is one of the fundamental quantum phenomena used to unveil the interactions between electrons and phonons that are coexisting or competing with other intriguing quantum phases, such as superconducting and ferromagnetic phases. Layered van der Waals materials, especially the family of vanadium dichalcogenides (VS2, VSe2, and VTe2), have previously demonstrated CDW transition and ferromagnetic ordering, although these demonstrations lacked critical evidence. Among them, VS2 single crystals in bulk form are challenging materials due to their thermodynamical instability; thus, experiments involving these materials have been rare. Herein, we report the multiple CDW states of a perfect 1T-phase VS2 single crystal fabricated by chemical vapor transport and annealing treatment. The metastable phase comprising VS2 and V5S8 turned into a stoichiometric 1T-phase VS2 single crystal, confirmed by high-resolution microscopy. The fine structure formed at low temperature exhibits two clear CDW orders with the absence of nesting vectors on the Fermi surface, confirmed by scanning tunneling microscopy and density functional theory calculations. Our findings provide insight into obtaining a stable crystallographic phase of VS2, stimulating further research into its compelling physical properties.

Graphical abstract: Strong electron–phonon coupling driven charge density wave states in stoichiometric 1T-VS2 crystals

Supplementary files

Article information

Article type
Communication
Submitted
01 অক্টো 2022
Accepted
27 অক্টো 2022
First published
28 অক্টো 2022

J. Mater. Chem. C, 2022,10, 16657-16665

Author version available

Strong electron–phonon coupling driven charge density wave states in stoichiometric 1T-VS2 crystals

S. Lee, Y. C. Park, J. Chae, G. Kim, H. J. Kim, B. K. Choi, I. H. Lee, Y. J. Chang, S. Chun, M. Jung, J. Seo and S. Lee, J. Mater. Chem. C, 2022, 10, 16657 DOI: 10.1039/D2TC04186C

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