Information

Press Release

Chiral superconductivity in UTe2 probed by anisotropic low-energy excitations

Release:Jun 1, 2023 Update:Jun 1, 2023
  • Headline
  • Press Release

Kota Ishihara, Assistant Professor, Kenichiro Hashimoto, Associate Professor, Takasada Shibauchi, Professor, the Department of Advanced Materials Science, the Graduate School of Frontier Sciences (GSFS); and Yuta Mizukami, Associate Professor, the Tohoku University (Assistant Professor, the GSFS, at the time of the project) led the research project.

Abstract

Chiral spin-triplet superconductivity is a topologically nontrivial pairing state with broken time-reversal symmetry, which can host Majorana quasiparticles. The heavy-fermion superconductor UTe2 exhibits peculiar properties of spin-triplet pairing, and the possible chiral state has been actively discussed. However, the symmetry and nodal structure of its order parameter in the bulk, which determine the Majorana surface states, remains controversial. Here we focus on the number and positions of superconducting gap nodes in the ground state of UTe2. Our magnetic penetration depth measurements for three field orientations in three crystals all show the power-law temperature dependence with exponents close to 2, which excludes single-component spin-triplet states. The anisotropy of low-energy quasiparticle excitations indicates multiple point nodes near the ky- and kz-axes in momentum space. These results can be consistently explained by a chiral B3u + iAu non-unitary state, providing fundamentals of the topological properties in UTe2.    

Article

〈Publication〉    Nature Communications (May 23, 2023)
〈Title〉    Chiral superconductivity in UTe2 probed by anisotropic low-energy excitations
〈Authors〉    Kota Ishihara*, Masaki Roppongi, Masayuki Kobayashi, Kumpei Imamura, Yuta Mizukami, Hironori Sakai, Petr Opletal, Yoshifumi Tokiwa, Yoshinori Haga, Kenichiro Hashimoto, and Takasada Shibauchi*
〈DOI〉    10.1038/s41467-023-38688-y
〈URL〉    https://www.nature.com/articles/s41467-023-38688-y

  • X
  • Facebook
  • LINE