Unraveling the Near- and Far-Field Relationship of 2D Surface-Enhanced Raman Spectroscopy Substrates Using Wavelength-Scan Surface-Enhanced Raman Excitation Spectroscopy

2017 ◽  
Vol 121 (27) ◽  
pp. 14737-14744 ◽  
Author(s):  
Dmitry Kurouski ◽  
Nicolas Large ◽  
Naihao Chiang ◽  
Anne-Isabelle Henry ◽  
Tamar Seideman ◽  
...  
2020 ◽  
Author(s):  
Won-Geun Kim ◽  
Jongmin Lee ◽  
Vasanthan Devaraj ◽  
Minjun Kim ◽  
Hyuk Jeong ◽  
...  

Abstract Plasmonic nanoparticle clusters promise to support various, unique artificial electromagnetisms at optical frequencies, realizing new concept devices for diverse nanophotonic applications. However, the technological challenges associated with the fabrication of plasmonic clusters with programmed geometry and composition remain unresolved. Here, we present a freeform fabrication of hierarchical plasmonic clusters (HPCs) based on omnidirectional guiding of evaporative self-assembly of gold nanoparticles (AuNPs) with the aid of 3D printing. Our method offers a facile, universal route to shape the multiscale features of HPCs in three-dimensions, leading to versatile manipulation of both far-field and near-field characteristics. Various functional nanomaterials can be effectively coupled to plasmonic modes of the HPCs by simply mixing with AuNP ink. We demonstrate in particular an ultracompact surface-enhanced Raman spectroscopy (SERS) platform to detect M13 viruses and their mutations from femtolitre volume, sub-100pM analytes. This SERS microplatform could pave the way towards simple, innovative detection methods of diverse pathogens, which is in high demand for handling pandemic situations. We expect our method to freely design and realize nanophotonic structures beyond the restrictions of traditional fabrication processes. Plasmonic nanoparticle clusters have attracted great attention due to the unique capability to manipulate electromagnetic fields at the sub-wavelength scale1–5. Ensembles of metallic nanoparticles generate various electromagnetisms at optical frequencies such as artificial magnetism6–10 and Fano-like interference11–13 and a strong field localization in the structure14–16. These unique properties are geometry-dependent and lead to a broad range of applications in sensing16,17, surface-enhanced spectroscopies18–22, nonlinear integrated photonics23,24, and light harvesting25,26. Traditionally, plasmonic clusters with tailored size and geometry are fabricated on substrates by top-down processes such as electron-beam lithography4,5 or focused-ion beam milling27,28. These approaches suffer from low throughput and are generally limited to in-plane fabrication. Alternatively, the self-assembly of colloids has been proposed as a versatile, high-throughput, and cost-effective route. A number of clever methods based on chemical linking (e.g., DNA origami)29–30 and/or convective assembly on lithographically structured templates25,26,31 have been devised to construct 2D or 3D plasmonic clusters. The shape formation, however, is mostly constrained by the thermodynamic impetus and/or template geometry. A significant challenge would be overcome these restrictions and expand structural design freedom in the fabrication of plasmonic cluster architectures with symmetry-breaking geometries. In this work, we develop a freeform, programmable 3D assembly of of hierarchical plasmonic clusters (HPCs). By exploiting micronozzle 3D printing, we demonstrate highly localized, omnidirectional meniscus-guided assembly of metallic nanoparticles, constructing a freestanding HPC with a tailored geometry that can control the far-field character. Our approach also allows versatile manipulation and exploitation of the near-field interaction in the HPC by a facile heterogeneous nanoparticle mixing. We demonstrate that 3D-printed HPCs can be utilized as an ultracompact surface-enhanced Raman spectroscopy (SERS) platform to detect M13 viruses and their mutations from femtolitre volume, sub-100pM analytes.


2019 ◽  
Vol 55 (60) ◽  
pp. 8824-8827 ◽  
Author(s):  
Jie Wei ◽  
Yu-Jin Zhang ◽  
Si-Na Qin ◽  
Wei-Min Yang ◽  
Hua Zhang ◽  
...  

A gap-mode configuration was developed for the in situ SERS study of the structure–activity relationship of Au@Pd core–shell nanocatalysts, which show much better performance in the selective oxidation of benzyl alcohol compared to Pd.


2017 ◽  
Author(s):  
Caitlin S. DeJong ◽  
David I. Wang ◽  
Aleksandr Polyakov ◽  
Anita Rogacs ◽  
Steven J. Simske ◽  
...  

Through the direct detection of bacterial volatile organic compounds (VOCs), via surface enhanced Raman spectroscopy (SERS), we report here a reconfigurable assay for the identification and monitoring of bacteria. We demonstrate differentiation between highly clinically relevant organisms: <i>Escherichia coli</i>, <i>Enterobacter cloacae</i>, and <i>Serratia marcescens</i>. This is the first differentiation of bacteria via SERS of bacterial VOC signatures. The assay also detected as few as 10 CFU/ml of <i>E. coli</i> in under 12 hrs, and detected <i>E. coli</i> from whole human blood and human urine in 16 hrs at clinically relevant concentrations of 10<sup>3</sup> CFU/ml and 10<sup>4</sup> CFU/ml, respectively. In addition, the recent emergence of portable Raman spectrometers uniquely allows SERS to bring VOC detection to point-of-care settings for diagnosing bacterial infections.


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