Issue 41, 2015

DNA-mediated control of Au shell nanostructure and controlled intra-nanogap for a highly sensitive and broad plasmonic response range

Abstract

We report DNA-mediated simple synthetic methods to obtain anisotropic plasmonic nanostructures with a tailorable intra-nanogap distance ranging from 0.9 to 4.0 nm. Anisotropic half-shell structures with sub-1.0 nm intra-nanogaps showed a wavelength-independent surface-enhanced Raman scattering (SERS) intensity and a highly sensitive SERS response to NIR light. We found that the reaction conditions such as pH and NaCl concentration are responsible for the resulting shell structures and intra-nanogap distances. Three noticeable plasmonic nanostructures [i.e., half-shell with sub-1.0 nm nanogaps, closed-shell with a wide nanogap (2.1 nm) and star-shaped with an irregular nanogap (1.5–4.0 nm)] were synthesized, and solution-based and single particle-based Raman measurements showed a strong relationship between the plasmonic structures and the SERS intensity. An understanding of DNA-mediated control for nanogap-engineered plasmonic nanostructures and studies of SERS-activity relationships using single particle-correlated measurements can provide new insights into the design of new plasmonic nanostructures and SERS-based biosensing applications.

Graphical abstract: DNA-mediated control of Au shell nanostructure and controlled intra-nanogap for a highly sensitive and broad plasmonic response range

Supplementary files

Article information

Article type
Paper
Submitted
28 Jun 2015
Accepted
23 Jul 2015
First published
24 Jul 2015

J. Mater. Chem. C, 2015,3, 10728-10733

Author version available

DNA-mediated control of Au shell nanostructure and controlled intra-nanogap for a highly sensitive and broad plasmonic response range

H. Lee, S. H. Nam, Y. J. Jung, S. Park, J. Kim, Y. D. Suh and D. Lim, J. Mater. Chem. C, 2015, 3, 10728 DOI: 10.1039/C5TC01915J

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