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Planar assemblies of plasmonic nanoparticles have provided opportunities in various fields. This study exploits the self-assembly of gold nanorods (AuNRs) into planar, layered chiral superstructures (dodecamer) using DNA origami technology. Due to the collective plasmonic coupling modes, the dodecamers exhibit g-factors of up to +0.06, which is 4–5 times higher than those of the dextrodimers. The chiroptical property of the superstructures proved to be strongly size-dependent, exhibiting enhanced g-factors with increasing the size of AuNRs. Moreover, by excluding the averaging and close-to-racemic effects in the ensemble colloids, circular differential scattering (CDS) and circularly polarized luminescence (CPL) were studied at the single-particle level, revealing the essential role of the structural chirality of superstructure in correlating single-particle scattering with nearby dye emission. The observed correlated CDS and CPL show g-factors up to −0.17 and −0.6, respectively. These results highlight the potential of DNA origami-directed plasmonic assemblies for nanoscale chirality engineering, with applications in biosensing, chiral photonics, and metamaterials.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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