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自组装等离子体单层中的面内表面晶格和高阶共振:从衬底支撑薄膜到独立薄膜

In-Plane Surface Lattice and Higher Order Resonances in Self-Assembled Plasmonic Monolayers: From Substrate-Supported to Free-Standing Thin Films.

作者信息

Volk Kirsten, Fitzgerald Joseph P S, Karg Matthias

机构信息

Institut für Physikalische Chemie I: Kolloide und Nanooptik , Heinrich-Heine-Universität Düsseldorf , Universitätsstr. 1 , D-40225 Düsseldorf , Germany.

出版信息

ACS Appl Mater Interfaces. 2019 May 1;11(17):16096-16106. doi: 10.1021/acsami.9b03197. Epub 2019 Apr 16.

Abstract

Periodic arrays of plasmonic nanostructures are able to strongly confine light at the nanometer scale because of surface lattice resonances. These resonances are the result of electromagnetic coupling between single-particle localized surface plasmon resonances and Bragg resonances of the periodic lattice. Here, we investigate the effect of a finite size refractive index environment on the formation of surface lattice resonances by increasing the thickness of a polymer coating in nanometer-scale increments. Wet-chemically synthesized, spherical silver and gold nanoparticles with soft hydrogel shells are self-assembled into macroscopic, hexagonally ordered arrays on glass substrates using an interface-assisted approach. The resulting periodic plasmonic monolayers are subsequently coated by a polymer matching closely the refractive index of the glass support. The optical response of the plasmonic arrays is studied using far-field extinction spectroscopy and supported by numerical simulations. We show the formation of surface lattice resonances as well as higher order resonances in finite thickness polymer coatings. The resonance positions are determined by the interparticle spacing as well as the plasmonic material. Additionally, we demonstrate that a coating thickness of 450 nm is sufficient to support strong in-plane surface lattice resonances. This enables us to prepare macroscopic, free-standing polymer films with embedded plasmonic nanoparticle arrays, which feature strong surface lattice resonances.

摘要

由于表面晶格共振,等离子体纳米结构的周期性阵列能够在纳米尺度上强烈限制光。这些共振是单粒子局域表面等离子体共振与周期性晶格的布拉格共振之间电磁耦合的结果。在这里,我们通过以纳米级增量增加聚合物涂层的厚度,研究有限尺寸折射率环境对表面晶格共振形成的影响。使用界面辅助方法,将具有软水凝胶壳的湿化学合成球形银和金纳米颗粒自组装成玻璃基板上的宏观六边形有序阵列。随后,通过紧密匹配玻璃载体折射率的聚合物对所得的周期性等离子体单层进行涂层。使用远场消光光谱研究等离子体阵列的光学响应,并通过数值模拟进行支持。我们展示了在有限厚度聚合物涂层中表面晶格共振以及高阶共振的形成。共振位置由粒子间间距以及等离子体材料决定。此外,我们证明450nm的涂层厚度足以支持强面内表面晶格共振。这使我们能够制备具有嵌入式等离子体纳米颗粒阵列的宏观独立聚合物薄膜,其具有强表面晶格共振。

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