There has been growing interest in using strong field enhancement and light localization in plasmonic nanostructures to control the polarization properties of light. Various experimental techniques are now used to fabricate twisted metallic nanoparticles and metasurfaces, where strongly enhanced chiral near-fields are used to intensify circular dichroism (CD) signals. In this review, state-of-the-art strategies to develop such chiral plasmonic nanoparticles and metasurfaces are summarized, with emphasis on the most recent trends for the design and development of functionalizable surfaces. The major objective is to perform enantiomer selection which is relevant in pharmaceutical applications and for biosensing. Enhanced sensing capabilities are key for the design and manufacture of lab-on-a-chip devices, commonly named point-of-care biosensing devices, which are promising for next-generation healthcare systems.

Circular dichroism spectroscopy is a technique used to discriminate molecular chirality, which is essential in fields like biology, chemistry, or pharmacology where different chiral agents often show different biological activities. Nevertheless, due to the inherently weak molecular-chiroptical activity, this technique is limited to high concentrations or large analyte volumes. Finding novel ways to enhance the circular dichroism would boost the performance of these techniques. So far, the enhancement of light–matter interaction mediated by plasmons is the most common way to develop chiral plasmonic structures with extraordinarily strong chiroptical responses. However, absorptive losses of metals at optical frequencies has hindered its practical use in many scenarios. In this work, we propose an all-dielectric low-loss chiral metasurface with unit cells built by high-refractive-index crossed-bowtie nanoantennas. These unit cells, built of silicon, strongly increase the chiroptical effect through the simultaneous interaction of their electric and magnetic modes, which in contrast to other recent proposals shows at the same time a high concentration of the electric field in its gap that leads to the presence of hotspots. The proposed structure exhibits a circular dichroism spectra up to 3-fold higher than that of previous proposals that use complex plasmonic or hybrid nanostructures, making it a clear alternative to develop low-loss metasurfaces with potential applications in chiral target sensing/biosensing. For completeness, single triangular shaped and symmetric (achiral) bowtie nanostructures were also studied as possible candidates for a detection up to the single-molecule level due the lack of a circular dichroism background of the nanostructures themselves.

We demonstrate a concept for the giant enhancement of the transverse magneto-optical Kerr effect (TMOKE), with amplitudes reaching the maximum theoretical values of ±1. The concept exploits the strong electromagnetic field localization in ε-near-zero metamaterials to excite surface plasmon resonances with no need of a prism or grating coupler, thus opening routes for magneto-optical devices amenable to miniaturization. A demonstration of the capability of the enhancement mechanism is presented in which giant TMOKE values can be used for sensing and biosensing.

No abstract

Detection of the drug Levodopa (3,4-dihydroxyphenylalanine, L-Dopa) is essential for the medical treatment of several neural disorders, including Parkinson's disease. In this paper, we employed surface-enhanced Raman scattering (SERS) with three shapes of silver nanoparticles (nanostars, AgNS; nanospheres, AgNP; and nanoplates, AgNPL) to detect L-Dopa in the nanoparticle dispersions. The sensitivity of the L-Dopa SERS signal depended on both nanoparticle shape and L-Dopa concentration. The adsorption mechanisms of L-Dopa on the nanoparticles inferred from a detailed analysis of the Raman spectra allowed us to determine the chemical groups involved. For instance, at concentrations below/equivalent to the limit found in human plasma (between 10 −7 -10 −8 mol/L), L-Dopa adsorbs on AgNP through its ring, while at 10 −5 -10 −6 mol/L adsorption is driven by the amino group. At even higher concentrations, above 10 −4 mol/L, L-Dopa polymerization predominates. Therefore, our results show that adsorption depends on both the type of Ag nanoparticles (shape and chemical groups surrounding the Ag surface) and the L-Dopa concentration. The overall strategy based on SERS is a step forward to the design of nanostructures to detect analytes of clinical interest with high specificity and at varied concentration ranges.Sensors 2020, 20, 15 2 of 18 atrazine (ATZ) on Ag nanospheres (AgNP) made it possible to detect picomolar concentrations of ATZ using SERS, whose intensity was higher in solution than in a cast film [7]. This also means that the orientation of ATZ molecules on AgNP is crucial for this ultrasensitive analysis. One may infer that signal enhancement for analytes can be obtained by tailoring the size and shape of the nanoparticles [12][13][14], in addition to the conformation of the analyte adsorbed as in the detection of B-complex vitamins in pharmaceutical samples [15].Such control in nanoparticle shape is afforded through various synthetic routes [16][17][18], then allowing the Localized Surface Plasmon Resonances (LSPR) to be tuned according to the region of best response (excitation) of the analyte [14,18,19]. For example, the near electromagnetic field is higher in nanoprisms (AgNPR), nanostars (AgNS) and nanorods (AgNR) than on spherical nanoparticles (AgNP) [18,19], and the LSPR may be wider to allow excitation down to the near infrared (IR) [18][19][20]. Indeed, Rycenga et al. [21] reported higher SERS activity for three molecules adsorbed on Ag nanocubes (AgNC) than on AgNP due to the wider LSPR for AgNC. Izquierdo-Lorenzo et al. [18] found that AgNPR were more efficient than AgNP for detecting aminoglutethimide used in sport doping owing to field enhancement in the corners of AgNPR, forming interstitial junctions, which are called "hot spots".The adsorption (and orientation, as a consequence) of an analyte can in principle be controlled by: (a) the affinity between analyte and metal; (b) charge of the analyte, which can be modulated via pH; (c) size and shape of the nanoparticles, and (d) metallic surface, wh...

Low-cost, instrument-free colorimetric tests were developed to detect SARS-CoV-2 using plasmonic biosensors with Au nanoparticles functionalized with polyclonal antibodies (f-AuNPs). Intense color changes were noted with the naked eye owing to plasmon coupling when f-AuNPs form clusters on the virus, with high sensitivity and a detection limit of 0.28 PFU mL −1 (PFU stands for plaque-forming units) in human saliva. Plasmon coupling was corroborated with computer simulations using the finite-difference time-domain (FDTD) method. The strategies based on preparing plasmonic biosensors with f-AuNPs are robust to permit SARS-CoV-2 detection via dynamic light scattering and UV−vis spectroscopy without interference from other viruses, such as influenza and dengue viruses. The diagnosis was made with a smartphone app after processing the images collected from the smartphone camera, measuring the concentration of SARS-CoV-2. Both image processing and machine learning algorithms were found to provide COVID-19 diagnosis with 100% accuracy for saliva samples. In subsidiary experiments, we observed that the biosensor could be used to detect the virus in river waters without pretreatment. With fast responses and requiring small sample amounts (only 20 μL), these colorimetric tests can be deployed in any location within the point-of-care diagnosis paradigm for epidemiological control.

The recent development of silver nanostars (Ag-NSs) is promising for improved surface-enhanced sensing and spectroscopy, which may be further exploited if the mechanisms behind the excitation of localized surface plasmon resonances (LSPRs) are identified. Here, we show that LSPRs in Ag-NSs can be obtained with finite-difference time-domain (FDTD) calculations by considering the nanostars as combination of crossed nanorods (Ag-NRs). In particular, we demonstrate that an apparent tail at large wavelengths (λ≳700 nm) observed in the extinction spectra of Ag-NSs is due to a strong dipolar plasmon resonance, with no need to invoke heterogeneity (different number of arms) effects as is normally done in the literature. Our description also indicates a way to tune the strongest LSPR at desired wavelengths, which is useful for sensing applications.

No abstract