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Exchange scaling of ultrafast angular momentum transfer in 4ƒ antiferromagnets

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Windsor,  Yoav William
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Lee,  Sang-Eun
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Zahn,  Daniela
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

Ernst,  A.
Institute for Theoretical Physics, Johannes Kepler University;
Max Planck Institute of Microstructure Physics, Max Planck Society;

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Rettig,  Laurenz
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Windsor, Y. W., Lee, S.-E., Zahn, D., Borisov, V., Thonig, D., Kliemt, K., et al. (2022). Exchange scaling of ultrafast angular momentum transfer in 4ƒ antiferromagnets. Nature Materials, 21(5), 514-517. doi:10.1038/s41563-022-01206-4.


Cite as: https://hdl.handle.net/21.11116/0000-0009-0644-4
Abstract
Ultrafast manipulation of the magnetic state of matter bears great potential for future information technologies. While demagnetisation in ferromagnets is governed by dissipation of angular momentum, materials with multiple spin sublattices, e.g. antiferromagnets, can allow direct angular momentum transfer between opposing spins, promising faster functionality. In lanthanides, 4ƒ magnetic exchange is mediated indirectly through the conduction electrons (the Ruderman-Kittel-Kasuya-Yosida interaction, RKKY), and the effect of such conditions on direct spin transfer processes is largely unexplored. Here, we investigate ultrafast magnetization dynamics in 4ƒ antiferromagnets, and systematically vary the 4ƒ occupation, thereby altering the magnitude of RKKY. By combining time-resolved soft x-ray diffraction with ab-initio calculations, we find that the rate of direct transfer between opposing moments is directly determined by the magnitude of RKKY. Given the high sensitivity of RKKY to the conduction electrons, our results offer a novel approach for fine-tuning the speed of magnetic devices.