Real-time density functional theory reveals laser-induced spin dynamics in altermagnets, suggesting new spintronic applications.
Altermagnetism (AM), an unconventional spin-ordered phase, presents a unique platform for exploring ultrafast spin manipulation. However, the mechanisms underlying laser-driven spin dynamics in low-dimensional altermagnets remain largely unclear. Using real-time time-dependent density functional theory, we investigate laser-induced spin dynamics in d-wave AM V₂Se₂O-based crystals. Our results show that momentum-dependent spin transfer in them can be selectively excited by laser polarization, generating a transient net magnetization via anisotropic optical intersite spin transfer. Compared with K-intercalated bulk KV₂Se₂O, deintercalated bulk and monolayer V₂Se₂O exhibit a much larger laser-induced net magnetization, which is attributed to the K-intercalation controlled electronic reconstruction and the consequent suppression of spin-relaxation channels. These results establish dimensionality and K-intercalation as practical knobs to tailor ultrafast spin responses, highlighting altermagnets as viable candidates for ultrafast spintronic applications.
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Huo et al. (2026) studied this question.
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