Double resonant plasmonic lattices for Raman studies.

We demonstrate radiation induced enhancement of both the in coupling of Raman excitation wavelength and Raman signal in plasmonic nanoparticle lattices. Rectangular nanoparticle lattices show two independently controllable lattice resonances, which we tune to be resonant with both the Raman excitation wavelength and the Raman transitions of rhodamine 6G molecules. We demonstrate that these narrow and intense resonances produced by the nanoparticle lattices allow for Raman transition specific enhancements. The system allows for independent tuning of both resonance conditions, enabling an efficient and versatile platform for Raman studies of various molecules.

Erbium-doped hybrid waveguide amplifiers with net optical gain on a fully industrial 300 mm silicon nitride photonic platform.

Recently, erbium-doped integrated waveguide devices have been extensively studied as a CMOS-compatible and stable solution for optical amplification and lasing on the silicon photonic platform. However, erbium-doped waveguide technology still remains relatively immature when it comes to the production of competitive building blocks for the silicon photonics industry. Therefore, further progress is critical in this field to answer the industry's demand for infrared active materials that are not only CMOS-compatible and efficient, but also inexpensive and scalable in terms of large volume production. In this work, we present a novel and simple fabrication method to form cost-effective erbium-doped waveguide amplifiers on silicon. With a single and straightforward active layer deposition, we convert passive silicon nitride strip waveguide channels on a fully industrial 300 mm photonic platform into active waveguide amplifiers. We show net optical gain over sub-cm long waveguide channels that also include grating couplers and mode transition tapers, ultimately demonstrating tremendous progress in developing cost-effective active building blocks on the silicon photonic platform.

Measurement of Nanowire Optical Modes Using Cross-Polarization Microscopy.

A method to detect optical modes from vertical InGaAs nanowires (NWs) using cross-polarization microscopy is presented. Light scattered from the optical modes in the NWs is detected by filtering out the polarized direct reflection with a crossed polarizer. A spectral peak and a valley were seen to red-shift with increasing NW diameter in the measured spectra. The peak was assigned to scattering from the TE01 optical mode and the valley was an indication of the HE11 mode, based on finite-element and scattering matrix method simulations. The cross-polarization method can be used to experimentally determine the spectral positions of the TE01 and HE11 optical modes. The modes are significantly more visible in comparison to conventional reflectance measurements. The method can be beneficial in the characterization of NW solar cells, light-emitting diodes and lasers where precise mode control is required.

Scalable fabrication of the graphitic substrates for graphene-enhanced Raman spectroscopy.

We propose direct synthesis of ultra-thin graphitic films on a dielectric substrate using sacrificial Ni catalyst layer, which significantly increases the crystallinity of the photoresist pyrolyzed at the temperature of 800 °C and above. A considerable amount of multilayer graphene in the photoresist film pyrolyzed in the presence of the Ni catalyst gives rise to an enhancement of the Raman signal of dye Sudan III molecules deposited on the substrate. We demonstrate comparable enhancement of the Raman signal from Sudan III molecules deposited on the fabricated graphitic substrate and those deposited on graphene, which was conventionally transferred to the silica substrate.

Atmospheric oxidation and carbon contamination of silver and its effect on surface-enhanced Raman spectroscopy (SERS).

Surface-enhanced Raman spectroscopy (SERS) is considered a highly promising technology for different analytical purposes. The applications of SERS are still quite limited due its relatively poor quantitative repeatability and the fact that SERS is very sensitive to oxidation, which is a challenge especially with silver based SERS substrates. Here, the link between these phenomena is investigated by exposing silver SERS substrates to ambient laboratory air. We show that SERS intensity decreases exponentially after the exposure, which consequently leads to an increasing standard deviation (σ) in intensity. Within a five-hour measurement window, the SERS intensity already drops by 60%, while σ triples from 7% to 21%. The SERS results are supplemented by elemental analysis, which shows that oxidation and atmospheric carbon contamination coincide with the rapid SERS intensity decrease. The results emphasize how sensitive SERS is towards atmospheric contamination and how it can also reduce the measurement repeatability - even if the substrates are exposed to air just for a very short period of time.

High Aspect-Ratio Iridium-Coated Nanopillars for Highly Reproducible Surface-Enhanced Raman Scattering (SERS).

A variety of different gold and silver nanostructures have been proposed over the years as high sensitivity surface-enhanced Raman scattering (SERS) sensors. However, efficient use of SERS has been hindered by the difficulty of realizing SERS substrates that provide reproducible SERS response over the whole active area. Here, we show that atomic layer deposition (ALD) grown iridium can be used to produce highly reliable SERS substrates. The substrates are based on a periodic array of high aspect-ratio iridium coated nanopillars that feature efficient and symmetrically distributed hot spots within the interpillar gaps (gap width<10 nm). We show that the enhancement with the iridium based nanostructures is of significant magnitude and it equals the enhancement of silver based reference substrates. Most notably, we demonstrate that the ordered and well-defined plasmonic nanopillars offer a measurement-to-measurement variability of 5%, which paves the way for truly quantitative SERS measurements.

A solution to the fabrication and tarnishing problems of surface-enhanced Raman spectroscopy (SERS) fiber probes.

Surface enhanced Raman scattering (SERS) fiber probes have enormous potential in optical sensing applications. However, their widespread use has been hindered by two major obstacles: the difficulty of fabricating the required silver nanostructures on optical fibers and the tarnishing of silver, rapidly degrading their sensing properties. Here we propose a solution to these dilemmas by abandoning the use of metallic silver and conventional nanofabrication procedures. Instead, we base our fabrication on chemically stable silver chloride and show that it can be directly grown on the optical fibers without any advanced fabrication equipment. As silver chloride itself is not SERS-active, we demonstrate how to "activate" the probes by turning the crystals into metallic silver nanostructures via photoreduction. We verify that if stored in the non-activated stage, the sensing properties of the structures remain unchanged. Finally, we demonstrate the high sensitivity (signal-to-noise ratio up to 42 ± 3 dB) of the probes in real-time in situ measurements at nanomolar analyte concentrations.

Uniform distribution of Ag particles upon imprinted polymer grating for Raman signal enhancement.

Surface Enhanced Raman Scattering (SERS) is gaining popularity among analytical methods in biosciences and sensor technology since it provides high specificity, non-destructiveness, and the unique fingerprint spectra of the molecules. Historically, glass has been the primary choice as a substrate for SERS, but polymers are attractive due to their plasticity, ease of handling, and their low cost. Herein, the performance of cyclo olefin polymer (COP) as a substrate with 1D subwavelength modulations combined with silver nanoparticles is studied for SERS measurements. These 1D grating structures on polymer are fabricated by hot embossing method followed by deposition of silver nanoparticles (AgNPs) using the drop-casting method. Spatial variations of the substrate surface have been reduced by providing a consistent distribution of hot-spots. We present an analysis of the surface uniformity related to the distribution of Ag particles. We achieve around 8-fold Raman signal enhancements with improved reproducibility in comparison to smooth, unmodulated surfaces with AgNPs. This method of fabrication of SERS substrates is simple and inexpensive compared to the thermal evaporation method (TEM) of metallic layer deposition. It also helps to control the tarnishing effect on metallic surfaces due to silver deposition prior to Raman measurements. This kind of polymer gratings combined with AgNPs have potential applications in medical, biological and chemical sensing, where Raman signal enhancement with high reproducibility is required.

Out-diffused silver island films for surface-enhanced Raman scattering protected with TiO2 films using atomic layer deposition.

We fabricated self-assembled silver nanoisland films using a recently developed technique based on out-diffusion of silver from an ion-exchanged glass substrate in reducing atmosphere. We demonstrate that the position of the surface plasmon resonance of the films depends on the conditions of the film growth. The resonance can be gradually shifted up to 100 nm towards longer wavelengths by using atomic layer deposition of titania, from 3 to 100 nm in thickness, upon the film. Examination of the nanoisland films in surface-enhanced Raman spectrometry showed that, in spite of a drop of the surface-enhanced Raman spectroscopy (SERS) signal after the titania spacer deposition, the Raman signal can be observed with spacers up to 7 nm in thickness. Denser nanoisland films show slower decay of the SERS signal with the increase in spacer thickness. PACS: 78.67.Sc (nanoaggregates; nanocomposites); 81.16.Dn (self-assembly); 74.25.nd (Raman and optical spectroscopy).