Chiral nanosurfaces for enhancement of local electromagnetic field

The ability of plasmonic nanosurfaces to produce strong electromagnetic fields in their vicinity upon illumination can be used to enhance effects, such as those originating from chirality (lack of mirror symmetry) of molecules. We numerically investigate chiral nanosurfaces composed of plasmonic nanobars with varying packing densities. We identify the optimum illumination conditions for maximal field enhancement. Under these illumination conditions, the optical chirality near the surface exceeds the optical chirality of the incident light by almost an order of magnitude in a large area (200 nm × 200 nm) near the surface. Our simulations prove the nanosurfaces to be promising candidates for enhancement of chiral-optical effects.</p

Surface enhanced Raman scattering of crystal violet

Despite the ubiquity of Raman spectroscopy, fluorescence, poor signal strength and photobleaching pose a significant challenge to researchers in the biomedical field. Here, we demonstrate a 17-fold signal enhancement in Raman spectra of crystal violet via surface-enhanced Raman scattering (SERS). The SERS substrate was fabricated by electron beam lithography (EBL); the nanostructured surface was an array of G-shaped elements made of Au on SiO2/Si. In addition to the SERS spectra, finite-difference time-domain simulations were performed to illustrate the distribution of electric-field hot-spots on the SERS substrate. The electric-field hot-spots were prominent at the vertices and edges of the nanostructured G-shaped motifs. The results presented here demonstrate that EBL is a high-end choice for SERS substrate fabrication that opens the way for more complex Raman spectroscopies, for instance involving nonlinear optics or chiral analytes

Plasmonic enhancement in BiVO4 photonic crystals for efficient water splitting.

Photo-electrochemical water splitting is a very promising and environmentally friendly route for the conversion of solar energy into hydrogen. However, the solar-to-H2 conversion efficiency is still very low due to rapid bulk recombination of charge carriers. Here, a photonic nano-architecture is developed to improve charge carrier generation and separation by manipulating and confining light absorption in a visible-light-active photoanode constructed from BiVO4 photonic crystal and plasmonic nanostructures. Synergistic effects of photonic crystal stop bands and plasmonic absorption are observed to operate in this photonic nanostructure. Within the scaffold of an inverse opal photonic crystal, the surface plasmon resonance is significantly enhanced by the photonic Bragg resonance. Nanophotonic photoanodes show AM 1.5 photocurrent densities of 3.1 ± 0.1 mA cm(-2) at 1.23 V versus RHE, which is among the highest for oxide-based photoanodes and over 4 times higher than the unstructured planar photoanode.UK Engineering and Physical Science Research Council. Grant Numbers: EP/H00338X/2, EP/G060649/1 European Community's Seventh Framework Programme. Grant Number: FP7/2007–2013 CARINHYPH project. Grant Number: 310184 Minstry of Science and Technology of Taiwan. Grant Number: 102-2218-E-006-014-MY2 Christian Doppler Research Association OMV Group, a Marie Curie Intra-European Fellowship. Grant Number: FP7-PEOPLE-2011-IEF 298012 ERC. Grant Number: 320503This is the final published version currently under embargo. This will be updated once the publisher has granted a CC BY license

Threading plasmonic nanoparticle strings with light

This work is licensed under a Creative Commons Attribution 4.0 International License.-- et al.Nanomaterials find increasing application in communications, renewable energies, electronics and sensing. Because of its unsurpassed speed and highly tuneable interaction with matter, using light to guide the self-assembly of nanomaterials can open up novel technological frontiers. However, large-scale light-induced assembly remains challenging. Here we demonstrate an efficient route to nano-assembly through plasmon-induced laser threading of gold nanoparticle strings, producing conducting threads 12±2nm wide. This precision is achieved because the nanoparticles are first chemically assembled into chains with rigidly controlled separations of 0.9nm primed for re-sculpting. Laser-induced threading occurs on a large scale in water, tracked via a new optical resonance in the near-infrared corresponding to a hybrid chain/rod-like charge transfer plasmon. The nano-thread width depends on the chain mode resonances, the nanoparticle size, the chain length and the peak laser power, enabling nanometre-scale tuning of the optical and conducting properties of such nanomaterials.We acknowledge financial support from EPSRC grants EP/G060649/1, EP/K028510/1 and EP/L027151/1, ERC grants LINASS 320503 and ASPiRe 240629, and project FIS2010-19609-C02-01 from the Spanish Ministry of Science and Innovation. J.S.B. acknowledges the School of Physical Science, University of Cambridge, for the funding of the transmission electron microscope. S.K. acknowledges funding from the Biochemical Society (Krebs Memorial Scholarship) and the Cambridge Commonwealth Trust.Peer Reviewe

Cu/Ag Sphere Segment Void Array as Efficient Surface Enhanced Raman Spectroscopy Substrate for Detecting Individual Atmospheric Aerosol

Surface enhanced Raman spectroscopy (SERS) shows great promise in studying individual atmospheric aerosol. However, the lack of efficient, stable, uniform, large-array, and low-cost SERS substrates constitutes a major roadblock. Herein, a new SERS substrate is proposed for detecting individual atmospheric aerosol particles. It is based on the sphere segment void (SSV) structure of copper and silver (Cu/Ag) alloy. The SSV structure is prepared by an electrodeposition method and presents a uniform distribution, over large 2 cm 2 arrays and at low cost. The substrate offers a high SERS enhancement factor (due to Ag) combined with lasting stability (due to Cu). The SSV structure of the arrays generates a high density of SERS hotspots (1.3 × 10 14/cm 2), making it an excellent substrate for atmospheric aerosol detection. For stimulated sulfate aerosols, the Raman signal is greatly enhanced (&gt;50 times), an order of magnitude more than previously reported substrates for the same purpose. For ambient particles, collected and studied on a heavy haze day, the enhanced Raman signal allows ready observation of morphology and identification of chemical components, such as nitrates and sulfates. This work provides an efficient strategy for developing SERS substrate for detecting individual atmospheric aerosol. </p