Coherent Spin Pumping Originated from Sub-Terahertz Néel Vector Dynamics in Easy Plane α-Fe2O3/Pt
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arXiv
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| Autori principali: | , , , , , , , |
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| Natura: | Preprint |
| Pubblicazione: |
2025
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| _version_ | 1866914206018699264 |
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| author | Fritjofson, Gregory Regmi, Atul Hanson-Flores, Jacob Michel, Justin Tang, Junyu Yang, Fengyuan Cheng, Ran Del Barco, Enrique |
| author_facet | Fritjofson, Gregory Regmi, Atul Hanson-Flores, Jacob Michel, Justin Tang, Junyu Yang, Fengyuan Cheng, Ran Del Barco, Enrique |
| contents | We present a thorough study of spin-to-charge current interconversion in bulk and thin films of (0001) α-Fe2O3 /Pt heterostructures by means of all-optical polarization-controlled microwave excitation at sub-Terahertz frequencies. Our results demonstrate that coherent spin pumping is generated through excitations of both the acoustic and optical modes of antiferromagnetic resonance, provided that the corresponding selection rules are met for the relative orientation between the microwave magnetic field h_ac and the magnetic moment m_0 of the Hematite. In particular, our results unanimously show that while a microwave field with h_ac perpendicular to m_0 pumps a net spin angular momentum from the acoustic mode, spin pumping from the optical mode is only enabled when h_ac parallel to m_0, as expected from the selection rules imposed by the Neel vector dynamics. Our results support the current understanding of spin mixing conductance in antiferromagnetic/non-magnetic interfaces, contrary to recent reports where the absence of spin pumping from the optical mode in Hematite was interpreted as a cancellation effect between the diagonal and off-diagonal components of the spin mixing conductance. We also provide an explanation for the previously reported observations and show how the optical spin pumping actually vanishes for thin films, which we speculate being either due to an increased level of inhomogeneities or to insufficient film thickness for the optical mode to fully realize. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2502_11281 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Coherent Spin Pumping Originated from Sub-Terahertz Néel Vector Dynamics in Easy Plane α-Fe2O3/Pt Fritjofson, Gregory Regmi, Atul Hanson-Flores, Jacob Michel, Justin Tang, Junyu Yang, Fengyuan Cheng, Ran Del Barco, Enrique Mesoscale and Nanoscale Physics Materials Science We present a thorough study of spin-to-charge current interconversion in bulk and thin films of (0001) α-Fe2O3 /Pt heterostructures by means of all-optical polarization-controlled microwave excitation at sub-Terahertz frequencies. Our results demonstrate that coherent spin pumping is generated through excitations of both the acoustic and optical modes of antiferromagnetic resonance, provided that the corresponding selection rules are met for the relative orientation between the microwave magnetic field h_ac and the magnetic moment m_0 of the Hematite. In particular, our results unanimously show that while a microwave field with h_ac perpendicular to m_0 pumps a net spin angular momentum from the acoustic mode, spin pumping from the optical mode is only enabled when h_ac parallel to m_0, as expected from the selection rules imposed by the Neel vector dynamics. Our results support the current understanding of spin mixing conductance in antiferromagnetic/non-magnetic interfaces, contrary to recent reports where the absence of spin pumping from the optical mode in Hematite was interpreted as a cancellation effect between the diagonal and off-diagonal components of the spin mixing conductance. We also provide an explanation for the previously reported observations and show how the optical spin pumping actually vanishes for thin films, which we speculate being either due to an increased level of inhomogeneities or to insufficient film thickness for the optical mode to fully realize. |
| title | Coherent Spin Pumping Originated from Sub-Terahertz Néel Vector Dynamics in Easy Plane α-Fe2O3/Pt |
| topic | Mesoscale and Nanoscale Physics Materials Science |
| url | https://arxiv.org/abs/2502.11281 |