arXiv Analytics

Sign in

arXiv:2411.03754 [cond-mat.mtrl-sci]AbstractReferencesReviewsResources

Magnetic order induced truly chiral phonons in a ferromagnetic Weyl semimetal

Mengqian Che, Jinxuan Liang, Yunpeng Cui, Hao Li, Bingru Lu, Wenbo Sang, Xiang Li, Xuebin Dong, Shuai Zhang, Tao Sun, Enke Liu, Feng Jin, Tiantian Zhang, Luyi Yang

Published 2024-11-06Version 1

Chiral phonons are vibrational modes in a crystal that possess a well-defined handedness or chirality, typically found in materials that lack inversion symmetry. Here we report the discovery of truly chiral phonon modes in the kagome ferromagnetic Weyl semimetal Co3Sn2S2, a material that preserves inversion symmetry but breaks time-reversal symmetry. Using helicity-resolved magneto-Raman spectroscopy, we observe the spontaneous splitting of the doubly degenerate in-plane Eg modes into two distinct chiral phonon modes of opposite helicity when the sample is zero-field cooled below the Curie temperature, without the application of an external magnetic field. As we sweep the out-of-plane magnetic field, this Eg phonon splitting exhibits a well-defined hysteresis loop directly correlated with the material's magnetization. The observed spontaneous splitting reaches up to 1.27 cm-1 at low temperatures and diminishes with increasing temperature, ultimately vanishing at the Curie temperature. Our findings highlight the role of the magnetic order in inducing chiral phonons, paving the way for novel methods to manipulate chiral phonons through magnetization and vice versa. Additionally, our work introduces new possibilities for controlling chiral Weyl fermions using chiral phonons.

Related articles: Most relevant | Search more
arXiv:0712.1247 [cond-mat.mtrl-sci] (Published 2007-12-07)
Pyrometric Measurement of the Temperature of Shocked Molybdenum
arXiv:cond-mat/9911125 (Published 1999-11-09)
Hopping Transport in the Presence of Site Energy Disorder: Temperature and Concentration Scaling of Conductivity Spectra
arXiv:cond-mat/0110086 (Published 2001-10-04)
Effects of temperature and adsorbates on the composition profile of Pt-Rh nanocatalysts : A comparative study