| Literature DB >> 28272897 |
Patrick W Granitzka1,2, Emmanuelle Jal1, Loïc Le Guyader1,3, Matteo Savoini4, Daniel J Higley1, Tianmin Liu1, Zhao Chen1, Tyler Chase1, Hendrik Ohldag, Georgi L Dakovski, William F Schlotter, Sebastian Carron, Matthias C Hoffman, Alexander X Gray5, Padraic Shafer6, Elke Arenholz6, Olav Hellwig7, Virat Mehta7, Yukiko K Takahashi8, Jian Wang8, Eric E Fullerton9, Joachim Stöhr1, Alexander H Reid1, Hermann A Dürr1.
Abstract
Light-matter interaction at the nanoscale in magnetic materials is a topic of intense research in view of potential applications in next-generation high-density magnetic recording. Laser-assisted switching provides a pathway for overcoming the material constraints of high-anisotropy and high-packing density media, though much about the dynamics of the switching process remains unexplored. We use ultrafast small-angle X-ray scattering at an X-ray free-electron laser to probe the magnetic switching dynamics of FePt nanoparticles embedded in a carbon matrix following excitation by an optical femtosecond laser pulse. We observe that the combination of laser excitation and applied static magnetic field, 1 order of magnitude smaller than the coercive field, can overcome the magnetic anisotropy barrier between "up" and "down" magnetization, enabling magnetization switching. This magnetic switching is found to be inhomogeneous throughout the material with some individual FePt nanoparticles neither switching nor demagnetizing. The origin of this behavior is identified as the near-field modification of the incident laser radiation around FePt nanoparticles. The fraction of not-switching nanoparticles is influenced by the heat flow between FePt and a heat-sink layer.Entities:
Keywords: FePt; X-ray scattering; magnetic switching; pump−probe; ultrafast magnetism
Year: 2017 PMID: 28272897 DOI: 10.1021/acs.nanolett.7b00052
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189