4.8 Article

High-Throughput Fabrication of Triangular Nanogap Arrays for Surface-Enhanced Raman Spectroscopy

Journal

ACS NANO
Volume 16, Issue 5, Pages 7438-7447

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c09930

Keywords

nanogaps; lithography; self-assembly; surface-enhanced Raman spectroscopy; nanofabrication

Funding

  1. NTNU [81771118]
  2. Research Council of Norwayvia the Norwegian Micro and Nano-Fabrication Facility, NorFab [245963/F50]
  3. Norwegian PhD Network on Nanotechnology for Microsystem - Research Council of Norway, Division for Science [221860/F60]
  4. DFG Cluster of Excellence e-conversion [EXC 2089/1-390776260]
  5. National Natural Science Foundation of China [22173075, 21933012]
  6. Fundamental Research Funds for the Central Universities [20720200068]

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This paper presents a high-throughput method for fabricating large-area arrays of triangular nanogaps with precise control over the gap size, which can significantly enhance the surface-enhanced Raman spectroscopy (SERS) detection. The method has important implications for practical applications.
Squeezing light into nanometer-sized metallic nanogaps can generate extremely high near-field intensities, resulting in dramatically enhanced absorption, emission, and Raman scattering of target molecules embedded within the gaps. However, the scarcity of low-cost, high-throughput, and reproducible nanogap fabrication methods offering precise control over the gap size is a continuing obstacle to practical applications. Using a combination of molecular self-assembly, colloidal nanosphere lithography, and physical peeling, we report here a high-throughput method for fabricating large-area arrays of triangular nanogaps that allow the gap width to be tuned from similar to 10 to similar to 3 nm. The nanogap arrays function as high-performance substrates for surface-enhanced Raman spectroscopy (SERS), with measured enhancement factors as high as 10(8) relative to a thin gold film. Using the nanogap arrays, methylene blue dye molecules can be detected at concentrations as low as 1 pM, while adenine biomolecules can be detected down to 100 pM. We further show that it is possible to achieve sensitive SERS detection on binary-metal nanogap arrays containing gold and platinum, potentially extending SERS detection to the investigation of reactive species at platinum-based catalytic and electrochemical surfaces.

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