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Amplified Circular Photogalvanic Effect in a Strongly Electron–Phonon-Coupled Topological Material

  • Md Shafayat Hossain*
  • , Xiaoxiong Liu*
  • , Zi Jia Cheng
  • , Qi Zhang
  • , Premakumar Yanda
  • , Satya N. Guin
  • , Nitesh Kumar
  • , Chandra Shekhar
  • , Zhiwei Wang
  • , Yongkai Li
  • , Byunghoon Kim
  • , Tyler A. Cochran
  • , Maksim Litskevich
  • , Yu Xiao Jiang
  • , Xian P. Yang
  • , Song Bo Zhang
  • , Yugui Yao
  • , Luis Balicas
  • , Claudia Felser
  • , Titus Neupert
  • M. Zahid Hasan*
*此作品的通讯作者
  • University of California at Los Angeles
  • University of California
  • Princeton University
  • Southern University of Science and Technology
  • Max Planck Institute for Chemical Physics of Solids
  • Beijing Institute of Technology
  • CAS - Institute of Physics
  • University of Science and Technology of China
  • National High Magnetic Field Laboratory
  • Florida State University
  • University of Zurich

科研成果: 期刊稿件文章同行评审

摘要

Berry curvature physics is responsible for the anomalous electromagnetic responses in solids. One such response is the circular photogalvanic effect (CPGE), typically observed in systems with pronounced Berry curvature─such as flat-band systems or topological semimetals featuring band crossings near the Fermi level, where Berry curvature exhibits sharp discontinuities. To maximize CPGE, one must develop the ability to tune their electronic band dispersion without introducing disorder, which is a challenging endeavor. Here, we demonstrate that it is possible to maximize the CPGE response in a topological material by a fundamentally different approach: controlling the proximity of a given system to a symmetry-breaking phase transition that induces a reconstruction of the electronic band structure. Through measurements of the longitudinal circular photogalvanic effect in the Weyl semimetal (TaSe4)2 I, we show that the circular photogalvanic effect can be amplified by a dramatic factor of 2 by tuning the proximity of this compound to charge density wave order. The first-principles calculations we present here show that this enhancement arises from the development of the CDW order parameter and the divergence of the associated relaxation time near the critical temperature. Therefore, this work provides a paradigm for boosting CPGE responses in solids─not by engineering band structure alone but by exploiting critical fluctuations near phase transitions in topological materials.

源语言英语
页(从-至)40354-40363
页数10
期刊ACS Nano
19
47
DOI
出版状态已出版 - 2 12月 2025
已对外发布

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