The magnetization of a nonmagnetic semiconductor by femtosecond light pulses is crucial to achieve an all-optical control of the spin dynamics in materials and to develop faster memory devices. However, the conditions for its detection are largely unknown. In this paper, we identify the criteria for the observation of ultrafast magnetization and critically discuss the difficulties hindering its experimental detection. We show that ultrafast magnetization of a nonmagnetic semiconductor can be observed in compounds with very localized conduction band states and more delocalized valence bands, such as in the case of a p-d charge transfer gap. By using constrained and time-dependent density functional theory simulations, we demonstrate that a transient ferrimagnetic state can be induced in diamagnetic semiconductor ${\mathrm{V}}_2{\mathrm{O}}_5$ via ultrafast pulses at realistic fluences. The ferrimagnetic state has opposite magnetic moments on vanadium (conduction) and oxygen (valence) states. Our methodology outruns the case of ${\mathrm{V}}_2{\mathrm{O}}_5$ as it identifies the key requirements for a computational screening of ultrafast magnetism in nonmagnetic semiconductors.

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• Magnetism
• Ultrafast magnetic effects
• Ultrafast phenomena