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

Authors
Lee, HaemiNam, Sang HwanJung, Yu JinPark, SojeongKim, Jung-MuSuh, Yung DougLim, 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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