Abstract

The recent discovery of superconductivity in paramagnetic UTe2 turns spotlight on a serious candidate for spin-triplet state. To draw a complete picture of the superconducting state in UTe2 precise knowledge of the electronic properties of the 5 f states of Uranium is missing. We report on x-ray absorption and magnetic circular dichroism experiments performed at the U M4,5 edges at 2.7 K. At ambient pressure the 5 f electron count is found to be in-between 2.6 and 2.8. Partial delocalization of the 5 f electrons is further confirmed by the reduced value of the U orbital to spin magnetic moment ratio. The 5 f count is reduced by as large as 7 percent at the transition to a magnetically ordered state at Pc ≈ 1.5 GPa. At pressures above 4 GPa, the 5 f count increases back towards U3+ in the tetragonal phase. The observed “valence instabilities” and their interplay with magnetism seem to be important ingredients to understand the electronic structure in UTe2 in different phases.

UTe2 is a strong candidate for spin-triplet superconductivity; however, to fully understand its superconducting properties a more complete understanding of its general electronic structure is needed. Here, the authors perform two types of X-ray spectroscopy to investigate the 5 f electronic states of the uranium atom, finding unusual features for the pressure dependence of the 5 f electron count.

Details

Title
Investigating the electronic states of UTe2 using X-ray spectroscopy
Author
Wilhelm, Fabrice 1   VIAFID ORCID Logo  ; Sanchez, Jean-Pierre 2 ; Braithwaite, Daniel 2   VIAFID ORCID Logo  ; Knebel, Georg 2   VIAFID ORCID Logo  ; Lapertot, Gérard 2   VIAFID ORCID Logo  ; Rogalev, Andrei 1 

 European Synchrotron Radiation Facility (ESRF), CS 40220, Grenoble Cedex 9, France (GRID:grid.5398.7) (ISNI:0000 0004 0641 6373) 
 Univ. Grenoble Alpes, Grenoble INP, CEA, IRIG-Pheliqs, Grenoble, France (GRID:grid.5676.2) (ISNI:0000000417654326) 
Pages
96
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
23993650
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2811431024
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.