3D stacking of plasmonic nanostructures is achieved using a solvent-assisted nanotransfer printing (S-nTP) technique to provide extremely dense and regular hot spot arrays for highly sensitive surface-enhanced Raman spectroscopy (SERS) analysis. Moreover, hybrid plasmonic nanostructures obtained by printing the nanowires on a continuous metal film or graphene surface show significantly intensified SERS signals due to vertical plasmonic coupling.
Plasmonic metal nanostructures have shown great potential in sensing, photovoltaics, imaging and biomedicine, principally due to the enhancement of local electric field by light-excited surface plasmons, i.e., collective oscillation of conduction band electrons. Thin films of nanoporous gold have received a great deal of interest due to the unique 3-dimensional bicontinuous nanostructures with high specific surface area. However, in the form of semi-infinite thin films, nanoporous gold exhibits weak plasmonic extinction and little tunability in the plasmon resonance, because the pore size is much smaller than the wavelength of light. Here we show that by making nanoporous gold in the form of disks of sub-wavelength diameter and sub-100 nm thickness, these limitations can be overcome. Nanoporous gold disks not only possess large specific surface area but also high-density, internal plasmonic "hot-spots" with impressive electric field enhancement, which greatly promotes plasmon-matter interactions as evidenced by spectral shifts in the surface plasmon resonance. In addition, the plasmonic resonance of nanoporous gold disks can be easily tuned from 900 to 1850 nm by changing the disk diameter from 300 to 700 nm. Furthermore, nanoporous gold disks can be fabricated as either bound on a surface or as non-aggregating colloidal suspension with high stability.
Near-infrared (NIR) absorption spectroscopy provides molecular and chemical information based on overtones and combination bands of the fundamental vibrational modes in the infrared wavelengths. However, the sensitivity of NIR absorption measurement is limited by the generally weak absorption and the relatively poor detector performance compared to other wavelength ranges. To overcome these barriers, we have developed a novel technique to simultaneously obtain chemical and refractive index sensing in 1-2.5 μm NIR wavelength range on nanoporous gold (NPG) disks, which feature high-density plasmonic hot-spots of localized electric field enhancement. For the first time, surface-enhanced near-infrared absorption (SENIRA) spectroscopy has been demonstrated for high sensitivity chemical detection. With a self-assembled monolayer (SAM) of octadecanethiol (ODT), an enhancement factor (EF) of up to ∼10(4) has been demonstrated for the first C-H combination band at 2400 nm using NPG disk with 600 nm diameter. Together with localized surface plasmon resonance (LSPR) extinction spectroscopy, simultaneous sensing of sample refractive index has been achieved for the first time. The performance of this technique has been evaluated using various hydrocarbon compounds and crude oil samples.
A novel laser rapid thermal annealing (LRTA) technique is reported to tune the plasmonic resonance of disk-shaped nanoporous gold (NPG) nanoparticles for the first time. LRTA alters both the external and internal geometrical parameters of NPG nanoparticles at temperatures significantly lower than the melting temperature of bulk gold or non-porous gold nanoparticles. With increasing annealing laser intensity, the average pore size increases, while the mean disk diameter decreases. These morphological changes lead to blueshifting of the localized surface plasmon resonance (LSPR), which subsequently fine-tunes the SERS performance by better aligning the excitation laser and Raman scattering wavelengths with the LSPR peak. This technique can provide an effective means to optimize NPG nanoparticles for various plasmonic applications such as photothermal conversion, light-gated molecular release, and molecular sensing.
We report electron beam lithography (EBL) based fabrication and different modeling techniques for disk-shaped nanoporous gold nanoparticles (NPG disk). The EBL technique can provide large area 2D patterns of regularly or randomly distributed nanodisks with narrow size distribution and flexible interdisk (center to center) distance. Such flexibility is essential to obtain quasi-single NPG disk response, which typically peaks in the near-infrared (NIR) spectrum beyond 1 μm, from ensemble measurements by common UV/vis/NIR spectrometers instead of a specialized NIR spectroscopic microscope. NPG disks of 200 to 500 nm diameter and 50 nm thickness have been fabricated and characterized. To model the NPG disk and calculate its plasmonic properties, two different modeling approaches have been developed. A model based on the Bruggeman effective medium theory (B-EMT model) requires little information about the nanoporous structure. In contrast, the nanoporous model (NP model) retains the essential nanoporous structural features of NPG disk. To evaluate the performance of these models, simulated extinction spectra have been compared to the experimental data. Both the B-EMT and NP models perform well to estimate the far-field plasmon resonance peak position. However, to obtain the accurate information about the plasmon peak width/plasmon lifetime and near-field plasmonic hot-spots formation within the nanopores, the NP model is essential since the B-EMT model lacks the nanoporous network.
We report the experimental observation and numerical modeling study of far-field plasmonic coupling (FFPC) in 2-dimensional polycrystalline plasmonic arrays consisting of “single crystalline” domains of a random size and orientation.
Certain noble metal nanostructures as heterogeneous photocatalysts have drawn significant attention in the recent past because of their unique optical properties which lead to the excitation of localized surface plasmon resonance (LSPR). The LSPR concentrates electromagnetic fields to the surfaces and its relaxation processes can convert photon energy to energetic charge carriers or heat, which can be subsequently harvested to enhance surface catalysis. Here, we report the catalytic performance of a novel plasmonic nanostructure, disk-shaped nanoporous gold (NPG) nanoparticles or simply NPG disks, using a well-tested reduction pathway of resazurin to resorufin. We show that the catalytic reaction rate of NPG disks is enhanced by 10-fold upon external light illumination because of the excitation of LSPR. The plasmon-enhanced catalytic reaction follows a linear-to-superlinear transition in the rate dependence on the input light power. In addition, the light input results in a room temperature reaction rate equivalent to that of an ambient temperature of 70 °C. Together, the results support that hot charge carriers play the dominant role in the enhancement.
A multi-point, side-firing design enables an optical fiber to output light at multiple desired locations along the fiber body. This provides advantages over traditional end-to-end fibers, especially in applications requiring fiber bundles such as brain stimulation or remote sensing. This paper demonstrates that continuous wave (CW) laser micro-ablation can controllably create conical-shaped cavities, or side windows, for outputting light. The dimensions of these cavities determine the amount of firing light and their firing angle. Experimental data show that a single side window on a 730 μm fiber can deliver more than 8 % of the input light. This was increased to more than 19 % on a 65 μm fiber with side windows created using femtosecond (fs) laser ablation and chemical etching. Fine control of light distribution along an optical fiber is critical for various biomedical applications such as light activated drug-release and optogenetics studies.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.