Abstract-Launching magnons at the terahertz speed of the spin Seebeck effect

T. Seifert, S. Jaiswal, J. Barker, I. Razdolski, J. Cramer, O. Gueckstock, S. Watanabe, C. Ciccarelli, A. Melnikov, G. Jakob, S.T.B. Goennenwein, G. Woltersdorf, P.W. Brouwer, M. Wolf, M. Kläui, T. Kampfrath

(Submitted on 3 Sep 2017)

https://arxiv.org/abs/1709.00768

Transport of spin angular momentum is an essential operation in spintronic devices. In magnetic insulators, spin currents are carried by magnons and can be launched straightforwardly by heating an adjacent metal layer. Here, we study the ultimate speed of this spin Seebeck effect with 10-fs time resolution in prototypical bilayers of ferrimagnetic yttrium iron garnet and platinum. Upon exciting the metal by a laser pulse, the spin flow is measured using the inverse spin Hall effect and terahertz electrooptic sampling. The spin Seebeck current reaches its peak within ~200 fs, a hallmark of the photoexcited metal electrons approaching a Fermi-Dirac distribution. Analytical modeling shows the spin Seebeck response is virtually instantaneous because the ferrimagnetic spins react without inertia and the metal spins impinging on the interface have a correlation time of only ~4 fs. Novel applications for material characterization, interface probing, spin-noise detection and terahertz spin pumping emerge.

Abstract-Novel electronic ferroelectricity in an organic charge-order insulator investigated with terahertz-pump optical-probe spectroscopy.

• http://www.nature.com/articles/srep20571
• H. Yamakawa
• , T. Miyamoto
• , T. Morimoto
• , H. Yada
• , Y. Kinoshita
• , M. Sotome
• , N. Kida
• , K. Yamamoto
• , K. Iwano
• , Y. Matsumoto
• , S. Watanabe
• , Y. Shimoi
• , M. Suda
• , H. M. Yamamoto
• , H. Mori
•  & H. Okamoto
• In electronic-type ferroelectrics, where dipole moments produced by the variations of electron configurations are aligned, the polarization is expected to be rapidly controlled by electric fields. Such a feature can be used for high-speed electric-switching and memory devices. Electronic-type ferroelectrics include charge degrees of freedom, so that they are sometimes conductive, complicating dielectric measurements. This makes difficult the exploration of electronic-type ferroelectrics and the understanding of their ferroelectric nature. Here, we show unambiguous evidence for electronic ferroelectricity in the charge-order (CO) phase of a prototypical ET-based molecular compound, α-(ET)2I3 (ET:bis(ethylenedithio)tetrathiafulvalene), using a terahertz pulse as an external electric field. Terahertz-pump second-harmonic-generation(SHG)-probe and optical-reflectivity-probe spectroscopy reveal that the ferroelectric polarization originates from intermolecular charge transfers and is inclined 27° from the horizontal CO stripe. These features are qualitatively reproduced by the density-functional-theory calculation. After sub-picosecond polarization modulation by terahertz fields, prominent oscillations appear in the reflectivity but not in the SHG-probe results, suggesting that the CO is coupled with molecular displacements, while the ferroelectricity is electronic in nature. The results presented here demonstrate that terahertz-pump optical-probe spectroscopy is a powerful tool not only for rapidly controlling polarizations, but also for clarifying the mechanisms of ferroelectricity.