Published December 2023 | Version v1
Journal article

Orbital hybridization in kagome metal GdV6Sn6 revealed by resonant ARPES

  • 1. Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing, 100049 (China)
  • 2. Center for Excellence in Superconducting Electronics, State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai, 200050 (China)
  • 3. Center for Transformative Science, ShanghaiTech University, Shanghai, 201210 (China)
  • 4. Research Center for Intelligent Chips and Devices, Zhejiang Lab, Hangzhou, 311121 (China)
  • 5. School of Physical Science and Technology, ShanghaiTech University, Shanghai, 201210 (China)
  • 6. Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Shanghai, 201210 (China)

Description

Novel quantum materials have broad application prospects in spintronic devices and low-power-consumption devices. The kagome-type lattice has special corner-sharing triangle geometry, providing a rich platform to investigate the relationship of novel correlated topological states, geometry, and strong electron interactions. However, the orbital hybridization in the presence of flat band that originated from the electron localization due to the unique kagome lattice configuration is still unclear. Resonant-angle-resolved photoemission spectroscopy is utilized to study the valence band structures of a new vanadium-based kagome material GdV6Sn6, combined with density functional theory calculation. Herein, a significant hybridization between V3d and Sn5p electrons, which paves the way to understand the formation of long-range magnetic ordering of GdV6Sn6 and other kagome materials at low temperature, is unambiguously revealed in the results. (© 2023 Wiley‐VCH GmbH)

Additional details

Identifiers

Publishing Information

Journal Title
Physica Status Solidi. Rapid Research Letters (Online)
Journal Volume
17
Journal Issue
12
Journal Page Range
p. 1-5
ISSN
1862-6270
CODEN
PSSRCS

Optional Information

Notes
AID: 2300083