Advanced Functional Materials
Advanced Functional Materials
5 years ago

Surface Energy-Controlled SERS Substrates for Molecular Concentration at Plasmonic Nanogaps

Surface Energy-Controlled SERS Substrates for Molecular Concentration at Plasmonic Nanogaps
Xiaofei Xiao, ChaeWon Mun, Dong-Ho Kim, Sung-Gyu Park, Stefan A. Maier, Sunho Kim, Avi Braun, Vincenzo Giannini
Positioning probe molecules at electromagnetic hot spots with nanometer precision is required to achieve highly sensitive and reproducible surface-enhanced Raman spectroscopy (SERS) analysis. In this article, molecular positioning at plasmonic nanogaps is reported using a high aspect ratio (HAR) plasmonic nanopillar array with a controlled surface energy. A large-area HAR plasmonic nanopillar array is generated using a nanolithography-free simple process involving Ar plasma treatment applied to a smooth polymer surface and the subsequent evaporation of metal onto the polymer nanopillars. The surface energy can be precisely controlled through the selective removal of an adsorbed self-assembled monolayer of low surface-energy molecules prepared on the plasmonic nanopillars. This process can be used to tune the surface energy and provide a superhydrophobic surface with a water contact angle of 165.8° on the one hand or a hydrophilic surface with a water contact angle of 40.0° on the other. The highly tunable surface wettability is employed to systematically investigate the effects of the surface energy on the capillary-force-induced clustering among the HAR plasmonic nanopillars as well as on molecular concentration at the collapsed nanogaps present at the tops of the clustered nanopillars. Molecular concentration at the electromagnetic hot spots is achieved using surface-enhanced Raman spectroscopy (SERS) substrates with controlled surface energies. The surface energies of the high aspect ratio plasmonic nanostructures are precisely controlled via the selective removal of low-surface energy chemicals that is chemisorbed onto the structures.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/adfm.201703376

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