DNA-mediated control of Au shell nanostructure and controlled intra-nanogap for a highly sensitive and broad plasmonic response range
- Authors
- Lee, Haemi; Nam, Sang Hwan; Jung, Yu Jin; Park, Sojeong; Kim, Jung-Mu; Suh, Yung Doug; Lim, Dong-Kwon
- Issue Date
- 2015
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- JOURNAL OF MATERIALS CHEMISTRY C, v.3, no.41, pp.10728 - 10733
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF MATERIALS CHEMISTRY C
- Volume
- 3
- Number
- 41
- Start Page
- 10728
- End Page
- 10733
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/96278
- DOI
- 10.1039/c5tc01915j
- ISSN
- 2050-7526
- 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.
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Collections - Graduate School > KU-KIST Graduate School of Converging Science and Technology > 1. Journal Articles
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