<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Boyce AM</submitter><funding>American Society for Engineering Education</funding><funding>Army Research Office</funding><funding>Air Force Office of Scientific Research</funding><funding>Office of Naval Research</funding><pagination>3525-3531</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9101075</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(9)</volume><pubmed_abstract>Actively tunable optical materials integrated with engineered subwavelength structures could enable novel optoelectronic devices, including reconfigurable light sources and tunable on-chip spectral filters. The phase-change material vanadium dioxide (VO&lt;sub>2&lt;/sub>) provides a promising solid-state solution for dynamic tuning; however, previous demonstrations have been limited to thicker and often rough VO&lt;sub>2&lt;/sub> films or require a lattice-matched substrate for growth. Here, sub-10-nm-thick VO&lt;sub>2&lt;/sub> films are realized by atomic layer deposition (ALD) and integrated with plasmonic nanogap cavities to demonstrate tunable, spectrally selective absorption across 1200 nm in the near-infrared (NIR). Upon inducing the phase transition via heating, the absorption resonance is blue-shifted by as much as 60 nm. This process is reversible upon cooling and repeatable over more than ten temperature cycles. Dynamic, ultrathin VO&lt;sub>2&lt;/sub> films deposited by ALD, as demonstrated here, open up new potential architectures and applications where VO&lt;sub>2&lt;/sub> can be utilized to provide reconfigurability including three-dimensional, flexible and large-area structures.</pubmed_abstract><journal>Nano letters</journal><pubmed_title>Actively Tunable Metasurfaces via Plasmonic Nanogap Cavities with Sub-10-nm VO&lt;sub>2&lt;/sub> Films.</pubmed_title><pmcid>PMC9101075</pmcid><funding_grant_id>FA9550-18-1-0326</funding_grant_id><funding_grant_id>N00014-17-1-2589</funding_grant_id><funding_grant_id>W911NF1610471</funding_grant_id><funding_grant_id>FA9550-21-1-0312</funding_grant_id><pubmed_authors>Boyce AM</pubmed_authors><pubmed_authors>Shen Q</pubmed_authors><pubmed_authors>Avila J</pubmed_authors><pubmed_authors>Wheeler VD</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Stewart JW</pubmed_authors><pubmed_authors>Mikkelsen MH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Actively Tunable Metasurfaces via Plasmonic Nanogap Cavities with Sub-10-nm VO&lt;sub>2&lt;/sub> Films.</name><description>Actively tunable optical materials integrated with engineered subwavelength structures could enable novel optoelectronic devices, including reconfigurable light sources and tunable on-chip spectral filters. The phase-change material vanadium dioxide (VO&lt;sub>2&lt;/sub>) provides a promising solid-state solution for dynamic tuning; however, previous demonstrations have been limited to thicker and often rough VO&lt;sub>2&lt;/sub> films or require a lattice-matched substrate for growth. Here, sub-10-nm-thick VO&lt;sub>2&lt;/sub> films are realized by atomic layer deposition (ALD) and integrated with plasmonic nanogap cavities to demonstrate tunable, spectrally selective absorption across 1200 nm in the near-infrared (NIR). Upon inducing the phase transition via heating, the absorption resonance is blue-shifted by as much as 60 nm. This process is reversible upon cooling and repeatable over more than ten temperature cycles. Dynamic, ultrathin VO&lt;sub>2&lt;/sub> films deposited by ALD, as demonstrated here, open up new potential architectures and applications where VO&lt;sub>2&lt;/sub> can be utilized to provide reconfigurability including three-dimensional, flexible and large-area structures.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-04T18:39:30.36Z</modification><creation>2025-02-19T00:55:51.205Z</creation></dates><accession>S-EPMC9101075</accession><cross_references><pubmed>35472261</pubmed><doi>10.1021/acs.nanolett.1c04175</doi></cross_references></HashMap>