Linearly polarized light-induced magnetism in bilayer MoSe₂

Light-induced symmetry breaking offers a powerful route to manipulate material properties by driving them into non-equilibrium states. Here, we demonstrate that a linearly polarized light transiently breaks time-reversal symmetry in bilayer MoSe2, a nominally non-magnetic van der Waals system. Combined ultrafast measurements and first-principles simulations reveal that linearly polarized excitation launches interlayer-coupled coherent phonons through a displacive mechanism. Time-resolved Faraday rotation measurements confirm that the excitation of two coherent phonons by a linearly polarized light is responsible for breaking time-reversal symmetry. Remarkably, the subsequent beating between the interlayer breathing mode and the in-plane Se-stretching mode, together with asymmetric charge redistribution, phonon dissipation, and spin-layer locking, generates an effective oscillating magnetization. Our findings uncover a new light-induced pathway for interlayer phonon coupling, revealing hidden non-equilibrium functionalities of van der Waals crystals. Our results establish a foundation for light-controlled functionality in stacked two-dimensional systems, advancing the emerging paradigm of materials-on-demand. Light can be used to drive transient changes in a materials phase; in some cases, breaking material symmetries, in others restoring them. Here, using time resolved Faraday rotation measurements, Seo et al demonstrate that linear polarised light can break time reversal symmetry, leading to a transient magnetization in MoSe2.

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Publication Details

Journal
Nature Communications
Published
2026-10-05
DOI
https://doi.org/10.1038/s41467-026-77987-y
Primary Topic
2D Materials and Applications
Type
article
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article

Linearly polarized light-induced magnetism in bilayer MoSe₂

Meenkyo Seo, Dongbin Shin, Dong Eon Kim, Hanbyul Kim
Nature Communications
2D Materials and Applications
article

Linearly polarized light-induced magnetism in bilayer MoSe₂

Meenkyo Seo, Dongbin Shin, Dong Eon Kim, Hanbyul Kim
article en

Abstract

Light-induced symmetry breaking offers a powerful route to manipulate material properties by driving them into non-equilibrium states. Here, we demonstrate that a linearly polarized light transiently breaks time-reversal symmetry in bilayer MoSe2, a nominally non-magnetic van der Waals system. Combined ultrafast measurements and first-principles simulations reveal that linearly polarized excitation launches interlayer-coupled coherent phonons through a displacive mechanism. Time-resolved Faraday rotation measurements confirm that the excitation of two coherent phonons by a linearly polarized light is responsible for breaking time-reversal symmetry. Remarkably, the subsequent beating between the interlayer breathing mode and the in-plane Se-stretching mode, together with asymmetric charge redistribution, phonon dissipation, and spin-layer locking, generates an effective oscillating magnetization. Our findings uncover a new light-induced pathway for interlayer phonon coupling, revealing hidden non-equilibrium functionalities of van der Waals crystals. Our results establish a foundation for light-controlled functionality in stacked two-dimensional systems, advancing the emerging paradigm of materials-on-demand. Light can be used to drive transient changes in a materials phase; in some cases, breaking material symmetries, in others restoring them. Here, using time resolved Faraday rotation measurements, Seo et al demonstrate that linear polarised light can break time reversal symmetry, leading to a transient magnetization in MoSe2.

Nature CommunicationsVol. 17(1)
Pohang University of Science and Technology (KR), Gwangju Institute of Science and Technology (KR), Korea Foundation for Max Planck POSTECH (KR), Max Planck Institute for the Structure and Dynamics of Matter (DE)
Openalex Percentile: Top 26%
2D Materials and Applications
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Linearly polarized light-induced magnetism in bilayer MoSe₂ — Meenkyo Seo, Dongbin Shin, et al. · Nature Communications (2026) | TGRS Research Map | TGRS