<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(5)</volume><submitter>Wang X</submitter><pubmed_abstract>Anisotropy has played a critical role in many material systems, but its controllable creation and modulation have been a long-lasting challenge for the scientific communities. Polarization-addressed anisotropy appears more attractive among all approaches due to its excellent controllability, simplicity, and accuracy, but only a limited number of material systems are applicable for such a concept, which are largely focused on oriented growth. Here, we establish a polarization-dependent anisotropic etching system made of Au@oligomer core-shell nanoparticles (NPs). As the oligomer coatings can be photochemically degraded via two-photon photolithography, the plasmonic near-field enhancement supported by the Au NP cores renders much faster degradation of the oligomer shells along the polarization, resulting in anisotropic Au@oligomer hybrid NPs. Such shape anisotropy leads to polarization-dependent photoluminescence with embedded dyes of methylene blue, which can be used as single-particle-based polarization detector. The oligomer lobes capped at the sides of the Au NP can also function as a protection agent for anisotropic photochemical growth of Au NPs, which evolve into Au nanorods and mushrooms with controlled irradiation time. Such polarization-directed etching of oligomer shells has unique advantages of high local-selectivity, controllability, and versatility for on-chip nanofabrication, which opens many new opportunities for integrated nanophotonic devices.</pubmed_abstract><journal>Nanophotonics (Berlin, Germany)</journal><pagination>1003-1009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11501720</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Polarization-controlled anisotropy in hybrid plasmonic nanoparticles.</pubmed_title><pmcid>PMC11501720</pmcid><pubmed_authors>Zhou L</pubmed_authors><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Dou Z</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Ding T</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Deng F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polarization-controlled anisotropy in hybrid plasmonic nanoparticles.</name><description>Anisotropy has played a critical role in many material systems, but its controllable creation and modulation have been a long-lasting challenge for the scientific communities. Polarization-addressed anisotropy appears more attractive among all approaches due to its excellent controllability, simplicity, and accuracy, but only a limited number of material systems are applicable for such a concept, which are largely focused on oriented growth. Here, we establish a polarization-dependent anisotropic etching system made of Au@oligomer core-shell nanoparticles (NPs). As the oligomer coatings can be photochemically degraded via two-photon photolithography, the plasmonic near-field enhancement supported by the Au NP cores renders much faster degradation of the oligomer shells along the polarization, resulting in anisotropic Au@oligomer hybrid NPs. Such shape anisotropy leads to polarization-dependent photoluminescence with embedded dyes of methylene blue, which can be used as single-particle-based polarization detector. The oligomer lobes capped at the sides of the Au NP can also function as a protection agent for anisotropic photochemical growth of Au NPs, which evolve into Au nanorods and mushrooms with controlled irradiation time. Such polarization-directed etching of oligomer shells has unique advantages of high local-selectivity, controllability, and versatility for on-chip nanofabrication, which opens many new opportunities for integrated nanophotonic devices.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-04T02:17:04.799Z</modification><creation>2025-04-04T02:17:04.799Z</creation></dates><accession>S-EPMC11501720</accession><cross_references><pubmed>39634475</pubmed><doi>10.1515/nanoph-2021-0691</doi></cross_references></HashMap>