Abstract

In this work we combine theory and experiment to study transient magnetic circular dichroism (tr-MCD) in the extreme ultraviolet spectral range (XUV) in bulk Co and CoPt. We use the \emph{ab-initio} method of real-time time-dependent density functional theory (RT-TDDFT) to simulate the magnetization dynamics in the presence of ultrafast laser pulses. From this we demonstrate how tr-MCD may be calculated using an approximation to the excited-state linear-response. We apply this approximation to Co and CoPt and show computationally that element-specific dynamics of the local spin moments can be extracted from the tr-MCD in XUV energy range, as is commonly assumed. We then compare our theoretical prediction for the tr-MCD for CoPt with experimental measurement and find excellent agreement at many different frequencies including the M23M_{2 3}-edge of Co and N67N_{6 7}- and O23O_{2 3}- edges of Pt.

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