Optical binding of metal nanoparticles (NPs) provides a promising way to create tunable photonic materials and devices, where the ultrastrong interparticle interaction is generally attributed to the localized surface plasmon resonances of NPs. Here, it is revealed that the optical binding of metal NPs can be self‐reinforced by the plasmonic surface lattice resonances (PSLRs) associated with the discrete NP arrays. Through simulations and experiments, it is demonstrated that PSLRs can spontaneously arise in optically bound gold NP chains with just a few NPs when they are relatively large, e.g., 150 nm in diameter. Additionally, the PSLRs are enhanced by increasing the chain length, leading to stronger optical binding stiffness. These results reveal a previously unidentified factor that contributes to the ultrastrong optical binding of metal NPs. More importantly, this study presents a prospect for building freestanding and reconfigurable NP arrays that naturally support PLSRs for sensing and other applications.
A top‐down lithographic patterning and deposition process is reported for producing nanoparticles (NPs) with well‐defined sizes, shapes, and compositions that are often not accessible by wet‐chemical synthetic methods. These NPs are ligated and harvested from the substrate surface to prepare colloidal NP dispersions. Using a template‐assisted assembly technique, fabricated NPs are driven by capillary forces to assemble into size‐ and shape‐engineered templates and organize into open or close‐packed multi‐NP structures or NP metamolecules. The sizes and shapes of the NPs and of the templates control the NP number, coordination, interparticle gap size, disorder, and location of defects such as voids in the NP metamolecules. The plasmonic resonances of polygonal‐shaped Au NPs are exploited to correlate the structure and optical properties of assembled NP metamolecules. Comparing open and close‐packed architectures highlights that introduction of a center NP to form close‐packed assemblies supports collective interactions, altering magnetic optical modes and multipolar interactions in Fano resonances. Decreasing the distance between NPs strengthens the plasmonic coupling, and the structural symmetries of the NP metamolecules determine the orientation‐dependent scattering response.
more » « less- Award ID(s):
- 2309043
- NSF-PAR ID:
- 10503490
- Publisher / Repository:
- Advanced Materials
- Date Published:
- Journal Name:
- Advanced Materials
- Volume:
- 35
- Issue:
- 33
- ISSN:
- 0935-9648
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1002/adma.202301323
