<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Mishra K</submitter><funding>Dutch Research Council (NWO)</funding><funding>Svenska Forskningsr?det Formas</funding><funding>H2020 Future and Emerging Technologies</funding><funding>Knut och Alice Wallenbergs Stiftelse</funding><funding>Swedish Foundation for International Cooperation in Research and Higher Education</funding><funding>European Cooperation in Science and Technology</funding><funding>Vetenskapsr?det</funding><pubmed_abstract>Magnetic memory combining plasmonics and magnetism is poised to dramatically increase the bit density and energy efficiency of light-assisted ultrafast magnetic storage, thanks to nanoplasmon-driven enhancement and confinement of light. Here we devise a new path for that, simultaneously enabling light-driven bit downscaling, reduction of the required energy for magnetic memory writing, and a subtle control over the degree of demagnetization in a magnetophotonic surface crystal. It features a regular array of truncated-nanocone-shaped Au-TbCo antennas showing both localized plasmon and surface lattice resonance modes. The ultrafast magnetization dynamics of the nanoantennas show a 3-fold resonant enhancement of the demagnetization efficiency. The degree of demagnetization is further tuned by activating surface lattice modes. This reveals a platform where ultrafast demagnetization is localized at the nanoscale and its extent can be controlled at will, rendering it multistate and potentially opening up so-far-unforeseen nanomagnetic neuromorphic-like systems operating at femtosecond time scales controlled by light.</pubmed_abstract><journal>Nano letters</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9756331</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ultrafast Demagnetization Control in Magnetophotonic Surface Crystals.</pubmed_title><pmcid>PMC9756331</pmcid><funding_grant_id>2015.0060</funding_grant_id><funding_grant_id>KO2016-6889</funding_grant_id><funding_grant_id>2019-03581</funding_grant_id><funding_grant_id>2017-04828</funding_grant_id><funding_grant_id>CA17123</funding_grant_id><funding_grant_id>2021-01390</funding_grant_id><funding_grant_id>737093</funding_grant_id><pubmed_authors>Kapaklis V</pubmed_authors><pubmed_authors>Ciuciulkaite A</pubmed_authors><pubmed_authors>Kimel AV</pubmed_authors><pubmed_authors>Rowan-Robinson RM</pubmed_authors><pubmed_authors>Kirilyuk A</pubmed_authors><pubmed_authors>Davies CS</pubmed_authors><pubmed_authors>Dmitriev A</pubmed_authors><pubmed_authors>Mishra K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultrafast Demagnetization Control in Magnetophotonic Surface Crystals.</name><description>Magnetic memory combining plasmonics and magnetism is poised to dramatically increase the bit density and energy efficiency of light-assisted ultrafast magnetic storage, thanks to nanoplasmon-driven enhancement and confinement of light. Here we devise a new path for that, simultaneously enabling light-driven bit downscaling, reduction of the required energy for magnetic memory writing, and a subtle control over the degree of demagnetization in a magnetophotonic surface crystal. It features a regular array of truncated-nanocone-shaped Au-TbCo antennas showing both localized plasmon and surface lattice resonance modes. The ultrafast magnetization dynamics of the nanoantennas show a 3-fold resonant enhancement of the demagnetization efficiency. The degree of demagnetization is further tuned by activating surface lattice modes. This reveals a platform where ultrafast demagnetization is localized at the nanoscale and its extent can be controlled at will, rendering it multistate and potentially opening up so-far-unforeseen nanomagnetic neuromorphic-like systems operating at femtosecond time scales controlled by light.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T08:55:45.922Z</modification><creation>2025-04-04T08:55:45.922Z</creation></dates><accession>S-EPMC9756331</accession><cross_references><pubmed>36321690</pubmed><doi>10.1021/acs.nanolett.2c00769</doi></cross_references></HashMap>