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J. Kimak

Publications and source records attributed to J. Kimak.

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Disentangling magnetic and optical contributions in ultrafast dynamics of antiperovskite non-collinear antiferromagnets

Non-collinear antiferromagnets are a class of spin-polarized antiferromagnets in which chiral spin textures give rise to Berry-curvature-driven phenomena, such as the anomalous Hall effect (AHE), without net magnetization. We investigate the properties of thin films of antiperovskite non-collinear antiferromagnetic metals Mn3NiN and Mn3GaN using pump-probe experiments. In both materials, we observe a strong dependence of pump-polarization-independent dynamics, induced by femtosecond laser pulses, on the angle between the sample normal and the direction of probe propagation. In Mn3NiN, where the presence of a sizable AHE indicates the {\Gamma}4g phase, the measured magnetooptical (MO) signals acquire an additional, strong dependence on the external magnetic field when the probe pulses are incident at nonzero angles. In contrast, in Mn3GaN, where the absence of AHE indicates the {\Gamma}5g phase, the measured signals do not depend on the magnetic field. Using probe-polarization-resolved measurements combined with full optical modeling based on Yeh's formalism, we quantitatively separate magnetic and non-magnetic contributions to the measured signals. We show that in Mn3NiN, the observed magnetic field dependence results from field-controlled redistribution of magnetic domain populations, enabled by their piezomagnetic moments and detected by a Kerr-like MO effect, while this effect is absent in Mn3GaN. Temperature-dependent measurements reveal a change from single-step to two-step quenching dynamics with increasing temperature in Mn3NiN. This behavior contrasts with the nearly temperature-independent quenching dynamics reported for the non-collinear antiferromagnetic Heusler compound Mn3Sn, but resembles the crossover from type-I to type-II demagnetization dynamics in metallic ferromagnets.

cond-mat.mtrl-sci

Ultrafast control of spin order by linearly polarized light in noncollinear antiferromagnetic metals

The non-thermal optical control of magnetic order offers a promising route to ultrafast, energy-efficient information technologies. Although optical manipulation of magnetism in metals has been extensively studied, experimentally demonstrated effects have so far been limited to heat-driven dynamics or helicity-dependent mechanisms. Here, we report ultrafast non-thermal control of spin order in noncollinear antiferromagnetic Mn-based antiperovskite nitrides Mn3NiN and Mn3GaN, driven solely by the polarization orientation of linearly polarized femtosecond laser pulses. Using time-resolved magneto-optical pump-probe experiments based on the Voigt effect, we observe sub-picosecond changes in magnetic order followed by picosecond relaxation. The magneto-optical response depends on the relative orientation of the pump and probe polarization planes, with linear-polarization dependence reaching up to 95%, a value unprecedented in metallic magnets. This phenomenon is observed in two different materials and persists over a wide range of excitation wavelengths, fluences, and temperatures, demonstrating its robustness. Symmetry analysis and microscopic modeling indicate that optically induced torques alone cannot fully explain the observed dynamics. We therefore propose laser-induced formation of transient spin-spiral states as a possible excitation mechanism.

cond-mat.mtrl-sci