准粒子
物理
凝聚态物理
超导电性
对称性破坏
电荷密度波
量子力学
作者
Hong Li,Huaizhou Zhao,Brenden R. Ortiz,Yuzki M. Oey,Ziqiang Wang,Stephen D. Wilson,Ilija Zeljkovic
出处
期刊:Nature Physics
[Springer Nature]
日期:2023-02-09
卷期号:19 (5): 637-643
被引量:8
标识
DOI:10.1038/s41567-022-01932-1
摘要
Kagome metals AV3Sb51 (where the A can stand for K, Cs or Rb) display a rich phase diagram of correlated electron states, including superconductivity2–4 and density waves5–7. Within this landscape, recent experiments have revealed signs of a transition below approximately 35 K attributed to an electronic nematic phase that spontaneously breaks the rotational symmetry of the lattice8. Here we show that the rotational symmetry breaking initiates universally at a high temperature in these materials, towards the 2 × 2 charge density wave transition temperature. We do this via spectroscopic-imaging scanning tunnelling microscopy and study the atomic-scale signatures of the electronic symmetry breaking across several materials in the AV3Sb5 family: CsV3Sb5, KV3Sb5 and Sn-doped CsV3Sb5. Below a substantially lower temperature of about 30 K, we measure the quantum interference of quasiparticles, a key signature for the formation of a coherent electronic state. These quasiparticles display a pronounced unidirectional feature in reciprocal space that strengthens as the superconducting state is approached. Our experiments reveal that high-temperature rotation symmetry breaking and the charge ordering states are separated from the superconducting ground state by an intermediate-temperature regime with coherent unidirectional quasiparticles. This picture is phenomenologically different compared to that in high-temperature superconductors, shedding light on the complex nature of rotation symmetry breaking in AV3Sb5 kagome superconductors. The charge density wave state in kagome superconductors is not fully understood. Now, evidence suggests that the rotational symmetry of the lattice is broken before coherence of unidirectional quasiparticles is established at a lower temperature.
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