DNA-based Self-Assembly of Chiral Plasmonic Nanostructures with Tailored Optical Response

TL;DR

This paper demonstrates how DNA origami can be used to assemble plasmonic nanostructures with precise control, resulting in materials with tailored optical properties like giant circular dichroism in the visible spectrum.

Contribution

It introduces a method to create complex 3D plasmonic nanostructures with nanometer precision using DNA self-assembly, enabling customizable optical responses.

Findings

Achieved 2 nm spatial accuracy in nanoparticle placement

Generated giant circular dichroism and optical rotary dispersion

Tuned optical response across the visible spectrum by changing nanoparticle composition

Abstract

Surface plasmon resonances generated in metallic nanostructures can be utilized to tailor electromagnetic fields. The precise spatial arrangement of such structures can result in surprising optical properties that are not found in any naturally occurring material. Here, the designed activity emerges from collective effects of singular components equipped with limited individual functionality. Top-down fabrication of plasmonic materials with a predesigned optical response in the visible range by conventional lithographic methods has remained challenging due to their limited resolution, the complexity of scaling, and the difficulty to extend these techniques to three-dimensional architectures. Molecular self-assembly provides an alternative route to create such materials which is not bound by the above limitations. We demonstrate how the DNA origami method can be used to produce plasmonic materials with a tailored optical response at visible wavelengths. Harnessing the assembly power of 3D DNA origami, we arranged metal nanoparticles with a spatial accuracy of 2 nm into nanoscale helices. The helical structures assemble in solution in a massively parallel fashion and with near quantitative yields. As a designed optical response, we generated giant circular dichroism and optical rotary dispersion in the visible range that originates from the collective plasmon-plasmon interactions within the nanohelices. We also show that the optical response can be tuned through the visible spectrum by changing the composition of the metal nanoparticles. The observed effects are independent of the direction of the incident light and can be switched by design between left- and right-handed orientation. Our work demonstrates the production of complex bulk materials from precisely designed nanoscopic assemblies and highlights the potential of DNA self-assembly for the fabrication of plasmonic nanostructures.