Abstract

A recently proposed exchange-correlation functional within density functional theory, which ensures that the exchange-correlation magnetic field is source-free, is shown to give non-zero internal spin–torque. This spin–torque is identically zero for all conventional local and semi-local functionals. Extension of this source-free functional to the time domain is used to study the effect of the internal spin–torque on the laser induced spin-dynamics in bulk Co, Ni and interfaces of these metals with Pt. It is shown that the internal spin–torque contributes significantly to spin-dynamics only when the magneto crystalline anisotropy energy is small, as in the case of cubic bulk materials. For surfaces or interfaces, where the anisotropy energy is large, these torques are too small to cause any significant precession of spins in early times (<100 fs). Furthermore, it is shown that the spin-dynamics caused by the internal spin–torque is slow compared to the inter-site spin transfer and spin–orbit mediated spin-flips.

Highlights

  • IntroductionThe possibility of controlling electronic spins by light offers a future of highly efficient devices and fast (sub femtosecond) memory storage

  • The possibility of controlling electronic spins by light offers a future of highly efficient devices and fast memory storage

  • We find that for bulk systems (Ni and Co), where SO induced anisotropy is very small i.e. magneto crystalline anisotropy (MCA) energy is only 2 μeV/atom, internal torques on spins lead to canting of spins about the easy axis an effect which cannot be described by conventional functionals like ALSDA

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Summary

Introduction

The possibility of controlling electronic spins by light offers a future of highly efficient devices and fast (sub femtosecond) memory storage. In light of this a large amount of research is being devoted to the study of laser induced dynamics of spins: spin-injection [1–5], spin transfer torque [6–9] across tailored interfaces, all-optical switching [10–12], ultra-fast demagnetization [13–26] to name but a few examples. Ab-initio methods for treating this laserinduced spin-dynamics is the non-collinear spin-polarized extension of time-dependent density functional theory (TD-DFT).

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