We demonstrate that a nanostructured metal thin film can achieve enhanced transmission efficiency and sharp resonances and use a large-scale and high-throughput nanofabrication technique for the plasmonic structures. The fabrication technique combines the features of nanoimprint and soft lithography to topographically construct metal thin films with nanoscale patterns. Metal nanogratings developed using this method show significantly enhanced optical transmission (up to a one-order-of-magnitude enhancement) and sharp resonances with full width at half maximum (FWHM) of ~15nm in the zero-order transmission using an incoherent white light source. These nanostructures are sensitive to the surrounding environment, and the resonance can shift as the refractive index changes. We derive an analytical method using a spatial Fourier transformation to understand the enhancement phenomenon and the sensing mechanism. The use of real-time monitoring of protein-protein interactions in microfluidic cells integrated with these nanostructures is demonstrated to be effective for biosensing. The perpendicular transmission configuration and large-scale structures provide a feasible platform without sophisticated optical instrumentation to realize label-free surface plasmon resonance (SPR) sensing.
Artificial and engineered nanostructures expand the degrees of freedom with which one can manipulate the intricate interplay of light and matter. Certain nanostructural arrangements in the excited state enable the efficient electromagnetic coupling of propagating light with localized fields. Here, we demonstrate that light transmitted through a nanostructured metal thin film without any apertures can be significantly enhanced. Distinct asymmetric Fano resonances are observed in the zero-order transmission spectra using an incoherent light source. The transmission efficiency surpasses that of a metal thin film with the same area and thickness at the resonance maxima. The transmission minima and the sharp resonance maxima bear a strong resemblance to the extraordinary optical transmission observed in sub-wavelength nanohole array structures The resonance wavelength closely matches the nanostructural periodicity. The sensitivity of the resonances to the surrounding medium and the transmission efficiency demonstrate the potential for use in energy harvesting, imaging, optical processing and sensing applications.
We have demonstrated a novel platform of quantum dots (QDs) core-shell conjugated graphene oxide (GO) biosensor for effective protein detection. The advantage in making core shell nanostructure allows preserving stable QDs, by improving quantum yield, and lowering the toxicity of the core. Both QDs and GO are efficient nanoparticle systems that can potentially be used for drug delivery, diagnosis, and biosensors scaffolds. However, our study indicates that the conjugation between these two nanoparticle systems makes their properties even more effective. The change in fluorescent intensity through fluorescence resonance energy transfer from quantum dots to GO produced a novel method for detection of the target and allows for the optimization of the recognition limit of Bovine serum albumin (BSA) due to efficient fluorescence resonance energy transfer as observed through time resolved relaxation spectroscopy. It is observed that the quenching of photoluminescence peak of QDs due to GO shell produced an applicable strategy and could be conveniently extended for detection of other biomolecules. We obtained significantly enhanced spectral signal through successful conjugation of GO with CdSe/CdS core shell, which can potentially be used for the detection of biomolecules with high sensitivity and selectivity. Our study underlines the efficiency of QD conjugated GO core shell in spectral detection of proteins even at very low concentration (0.25 mmol).
Combining two materials in a nanoscale level can create a composite with new functionalities and improvements in their physical and chemical properties. Here we present a high-throughput approach to produce a nanocomposite consisting of metal nanoparticles and semiconductor oxide nanostructures. Volmer-Weber growth, though unfavorable for thin films, promotes nucleation of dense and isolated metal nanoparticles on crystalline oxide nanostructures, resulting in new material properties. We demonstrate such a growth of Au nanoparticles on SnO 2 nanostructures and a remarkable sensitivity of the nanocomposite for detecting traces of analytes in surface enhanced Raman spectroscopy. Au nanoparticles with tunable size enable us to modify surface wettability and convert hydrophilic oxide surfaces into super-hydrophobic with contact angles over 150°. We also find that charge injection through electron beam exposure shows the same effect as photo-induced charge separation, providing an extra Raman enhancement up to an order of magnitude.Metal nanoparticles or nanostructures can interact with the electromagnetic field at optical frequencies. A unique physical property in these nanoparticles is the strong field enhancement associated with localized plasmon excitation, which inspires development of novel devices in applications such as energy harvesting, chemical, and biological sensing. Among them, surface enhanced Raman spectroscopy (SERS) is an analytical technique with high sensitivity that enables the detection of chemical or biological analytes in trace amount far below the limit of the conventional Raman spectroscopy. The enhancement of electromagnetic fields amplifies Raman scattering signals of analytes adsorbed on rough metal surfaces, especially on the rough surfaces generated by noble metal nanostructures. The excitation of localized surface plasmon resonances (LSPRs) in the noble metals is generally considered as the main mechanism of SERS. Theoretical calculations revealed that the electromagnetic enhancement factor can be up to ~10 10 -10 12 1 , reaching the level high enough for single-molecule detection. Therefore, SERS can significantly improve the sensitivity of the conventional Raman spectrometers and provides an accessible and flexible tool to emerging portable and mobile demands in applications such as medical diagnostics, environmental monitoring, food safety, national security, and rapid screening.Noble metal nanoparticles typically exhibit SERS enhancement at sharp edges or gaps between metallic protrusions, called hot spots. Hot spots concentrate electromagnetic radiation energy within small areas, which account for the majority of the Raman scattering signals from SERS. Because the near-field behavior dominates the concentrated electromagnetic radiation in the hot spots, the field strength, as well as associated SERS enhancement, decreases rapidly within the distance of a few nanometers. Hot spots between the nanostructure gaps should be sufficiently small 2-4 . And high-density hot spots are desire...
Utilizing ultraviolet photochemical reduction of gold(III) chloride trihydrate (HAuCl4), a new kind of synthesis of a highly dense gold nanoparticle film on a p-type silicon wafer was conducted. Through scanning electron microscopy and atomic force microscopy, the gold nanoparticle film was confirmed to be 90 nm thick, with an average gold nanoparticle size of 125 nm in diameter. To explore applications in surface enhanced Raman spectroscopy (SERS), a protein model of streptavidin and pegylated biotin functionalized to the surface of gold nanoparticle films was employed. Observations indicate that there was a proximity induced excitation of localized surface plasmons due to the densely packed gold nanoparticle film. Excitation of the localized surface plasmons leading to hot spots of SERS activity on the gold nanoparticle film allowing it to act as an eco-friendly and highly sensitive SERS substrate for biomedical diagnostic applications.
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