skip to main content


Title: Broadband Nanoscale Surface‐Enhanced Raman Spectroscopy by Multiresonant Nanolaminate Plasmonic Nanocavities on Vertical Nanopillars
Abstract

Surface‐enhanced Raman spectroscopy (SERS) has become a sensitive detection technique for biochemical analysis. Despite significant research efforts, most SERS substrates consisting of single‐resonant plasmonic nanostructures on the planar surface suffer from limitations of narrowband SERS operation and unoptimized nano‐bio interface with living cells. Here, it is reported that nanolaminate plasmonic nanocavities on 3D vertical nanopillar arrays can support a broadband SERS operation with large enhancement factors (>106) under laser excitations at 532, 633, and 785 nm. The multi‐band Raman mapping measurements show that nanolaminate plasmonic nanocavities on vertical nanopillar arrays exhibit broadband uniform SERS performance with diffraction‐limited resolution at a single nanopillar footprint. By selective exposure of embedded plasmonic hotspots in individual metal–insulator–metal (MIM) nanogaps, nanoscale broadband SERS operation at the single MIM nanocavity level with visible and near‐infrared (vis–NIR) excitations is demonstrated. Numerical studies reveal that nanolaminate plasmonic nanocavities on vertical nanopillars can support multiple hybridized plasmonic modes to concentrate optical fields across a broadband wavelength range from 500 to 900 nm at the nanoscale.

 
more » « less
NSF-PAR ID:
10369482
Author(s) / Creator(s):
 ;  ;  ;  ;  ;  ;  ;  
Publisher / Repository:
Wiley Blackwell (John Wiley & Sons)
Date Published:
Journal Name:
Advanced Functional Materials
Volume:
32
Issue:
32
ISSN:
1616-301X
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract

    Two‐dimensional transition metal dichalcogenides (TMDs)/graphene van der Waals (vdW) heterostructures integrate the superior light–solid interaction in TMDs and charge mobility in graphene, and therefore are promising for surface‐enhanced Raman spectroscopy (SERS). Herein, a novel TMD (MoS2and WS2) nanodome/graphene vdW heterostructure SERS substrate, on which an extraordinary SERS sensitivity is achieved, is reported. Using fluorescent Rhodamine 6G (R6G) as probe molecules, the SERS sensitivity is in the range of 10−11to 10−12mon the TMD nanodomes/graphene vdW heterostructure substrates using 532 nm Raman excitation, which is comparable to the best sensitivity reported so far using plasmonic metal nanostructures/graphene SERS substrates, and is more than three orders of magnitude higher than that on single‐layer TMD and graphene substrates. Density functional theory simulation reveals enhanced electric dipole moments and dipole–dipole interaction at the TMD/graphene vdW interface, yielding an effective means to facilitate an external electrostatic perturbation on the graphene surface and charge transfer. This not only promotes chemical enhancement on SERS, but also enables electromagnetic enhancement of SERS through the excitation of localized surface plasmonic resonance on the TMD nanodomes. This TMD nanodome/graphene vdW heterostructure is therefore promising for commercial applications in high‐performance optoelectronics and sensing.

     
    more » « less
  2. Metallic nanostructures supporting surface plasmon modes can concentrate optical fields, and enhance luminescence processes from the metal surface at plasmonic hotspots. Such nanoplasmonic metal luminescence contributes to the spectral background in surface-enhanced Raman spectroscopy (SERS) measurements and is helpful in bioimaging, nano-thermometry, and chemical reaction monitoring applications. Despite increasing interest in nanoplasmonic metal luminescence, little attention has been paid to investigating its dependence on voltage modulation. Also, the hyphenated electrochemical surface-enhanced Raman spectroscopy (EC-SERS) technique typically ignores voltage-dependent spectral background information associated with nanoplasmonic metal luminescence due to limited mechanistic understanding and poor measurement reproducibility. Here, we report a combined experiment and theory study on dynamic voltage-modulated nanoplasmonic metal luminescence from hotspots at the electrode-electrolyte interface using multiresonant nanolaminate nano-optoelectrode arrays. Our EC-SERS measurements under 785 nm laser excitation demonstrate that short-wavenumber nanoplasmonic metal luminescence associated with plasmon-enhanced electronic Raman scattering (PE-ERS) exhibits a negative voltage modulation slope (up to ≈30 % V-1) in physiological ionic solutions. Furthermore, we have developed a phenomenological model to intuitively capture plasmonic, electronic, and ionic characteristics at the metal-electrolyte interface to understand the observed dependence of the PE-ERS voltage modulation slope on voltage polarization and ionic strength. The current work represents a critical step toward the general application of nanoplasmonic metal luminescence signals in optical voltage biosensing, hybrid optical-electrical signal transduction, and interfacial electrochemical monitoring. 
    more » « less
  3. Abstract

    Diatoms are single‐celled algae that biologically fabricate nanostructured silica shells with ordered pore arrays called frustules that resemble a 2D photonic crystal. A monolayer ofPinnulariafrustules isolated from cell culture is deposited on a glass substrate and then conformally coated with silver nanoparticles (AgNPs) to serve as a nanostructured thin film for ultrathin layer chromatography (UTLC). Malachite green and Nile red are resolved in toluene mobile phase and the separated analytes are profiled micro‐Raman spectroscopy, where plasmonic AgNPs provide surface‐enhanced Raman scattering (SERS). The AgNP‐diatom frustule monolayer improves SERS detection of malachite green by an average factor of 1.8 ± 0.1 over the plasmonic AgNP layer on glass. Analysis of hot spots on the AgNP‐diatom frustule monolayer reveals that nearly 20% of the SERS active area intensifies the SERS signal at least tenfold over the SERS signal for AgNP on glass. Diatom‐SERS enhancement is attributed to guided‐mode resonances of the Raman laser source, which in turn further enhances the localized surface plasmonic resonance from AgNPs. Overall, the AgNP‐diatom frustule monolayer thin film is a new functional material that uniquely enables separation of analytes by UTLC, quantitative SERS detection of separated analytes, and photonic enhancement of the SERS signals.

     
    more » « less
  4. Abstract

    Gradient plasmonic nanostructures are produced by a straightforward and powerful fabrication strategy—deposition on curved nanomask (DCNM), a physical vapor deposition on a curved mask substrate covered with a monolayer of close‐packed nanospheres. The feasibility of the DCNM strategy is demonstrated by producing well‐ordered Ag gradient single/double nanotriangle (NT) arrays with continuously adjustable color, extinction, localized surface plasmon resonance wavelength, and surface enhanced Raman scattering (SERS). The plasmonic property and the structure gradient are controlled by the size of the mask and the curvature of the curved substrate, as well as the deposition configuration. A plasmonic library of the single/double NT arrays is easily established in a single fabrication. The DCNM strategy can in principle produce a wide range of gradient nanostructures and further be used for flexible components in optical devices, tunable plasmonic SERS sensors, as well as high‐throughput screening of nanostructures.

     
    more » « less
  5. Herein, deep learning (DL) is used to predict the structural parameters of Ag nanohole arrays (NAs) for spectrum‐driving and color‐driving plasmonic applications. A dataset of transmission spectra and structural parameters of NAs is generated using finite‐difference time‐domain (FDTD) calculations and is converted to vivid structural colors using the corresponding transmission spectrum. A bidirectional neural network is used to train the transmission spectrum and structural color together. The accuracy of predicting the structural parameters using a desired spectrum is tested and found to be up to 0.99, with a determination coefficient of reproducing the desired spectrum and color to be 0.97 and 0.96, respectively. These values are higher compared to those when only training for spectrum, but requiring less training time. This strategy is able to inverse design the NAs in less than 1 s to maximize surface‐enhanced Raman scattering (SERS) enhancement by matching transmission resonance and laser excitation wavelength, and accurately regenerate colored images in 7.5 s, allowing for nanoscale printing at a resolution of approximately 100 000 dots in−1. This work has important implications for the efficient design of nanostructures for various plasmonic applications, such as plasmonic sensors, optical filters, metal‐enhanced fluorescence, SERS, and super‐resolution displays.

     
    more » « less