Surface plasmon resonance

About: Surface plasmon resonance is a research topic. Over the lifetime, 24909 publications have been published within this topic receiving 810976 citations. The topic is also known as: Surface plasmon resonance & SPR (technology).

Size dependent surface plasmon resonance broadening in non-spherical nanoparticles: Single gold nanorods

Abstract: The spectral response of metallic nanoparticles is dominated by the Localized Surface Plasmon Resonance (LSPR). While its spectral position is well understood, measuring and interpreting the LSPR linewidth evolution with shape and size is still an important issue for both fundamental investigations and applications. It needs the use of single particle experiments on nanoparticles with a well controlled environment, to avoid inhomogeneous broadening and/or spurious effects. The dominant effect related to size reduction is an increase of the surface contribution to the linewidth of the LSPR, due to the quantum confinement of the electrons.

Plasmon-driven reaction controlled by the number of graphene layers and localized surface plasmon distribution during optical excitation

Abstract: Graphene-plasmonic hybrid platforms have attracted an enormous amount of interest in surface-enhanced Raman scattering (SERS); however, the mechanism of employing graphene is still ambiguous, so clarification about the complex interaction among molecules, graphene, and plasmon processes is urgently needed. We report that the number of graphene layers controlled the plasmon-driven, surface-catalyzed reaction that converts para-aminothiophenol (PATP)-to-p,p′-dimercaptoazobenzene (DMAB) on chemically inert, graphene-coated, silver bowtie nanoantenna arrays. The catalytic reaction was monitored by SERS, which revealed that the catalytic reaction occurred on the chemical inertness monolayer graphene (1G)-coated silver nanostructures. The introduction of 1G enhances the plasmon-driven surface-catalyzed reaction of the conversion of PATP-to-p,p′-DMAB. The chemical reaction is suppressed by bilayer graphene. In the process of the catalytic reaction, the electron transfer from the PATP molecule to 1G-coated silver nanostructures. Subsequently, the transferred electrons on the graphene recombine with the hot-hole produced by the localized surface plasmon resonance of silver nanostructures. Then, a couple of PATP molecules lost electrons are catalyzed into the p,p′-DMAB molecule on the graphene surface. The experimental results were further supported by the finite-difference time-domain method and quantum chemical calculations. The introduction of a graphene coating on metal nanostructures can help control the efficiency of plasmon-driven chemical reactions. Xiang-heng Xiao and co-workers from China used an array of silver bowtie nanoantennas to perform a surface-enhanced photocatalytic reaction and convert para-aminothiophenol (PATP) into p,p′-dimercaptoazobenzene under optical excitation. The conversion was enhanced when the nanoantennas were coated with monolayer graphene, whereas it was suppressed when they were coated with bilayer graphene. The reaction was monitored in situ by capturing and analysing surface-enhanced Raman spectra. The enhanced reaction rate is thought to stem from the efficient transport of electrons from the PATP molecules to the nanoantennas coated with monolayer graphene and their subsequent recombination with hot-holes. Quantum chemical calculations and finite-difference time-domain modelling confirmed this scenario.

Tailoring the sensing capabilities of nanohole arrays in gold films with Rayleigh anomaly-surface plasmon polaritons.

Abstract: Surface plasmon polaritons (SPPs) and diffraction effects such as Rayleigh anomalies (RAs) play key roles in the transmission of light through periodic subwavelength hole arrays in metal films. Using a combination of theory and experiment we show how refractive index (RI) sensitive transmission features arise from hole arrays in thin gold films. We show that large transmission amplitude changes occur over a narrow range of RI values due to coupling between RAs and SPPs on opposite sides of the metal film. Furthermore, we show how to predict, on the basis of a relatively simple analysis, the periodicity and other system parameters that should be used to achieve this “RA-SPP” effect for any desired RI range.

Nonlinear excitation of surface plasmon polaritons by four-wave mixing.

Abstract: We demonstrate nonlinear excitation of surface plasmons on a gold film by optical four-wave mixing. Two excitation beams of frequencies omega(1) and omega(2) are used in a modified Kretschmann configuration to induce a nonlinear polarization at a frequency of omega(4wm)=2omega(1)-omega(2), which gives rise to surface plasmon excitation at a frequency of omega(4wm). We observe a characteristic plasmon dip at the Kretschmann angle and explain its origin in terms of destructive interference. Despite a nonvanishing bulk response, surface plasmon excitation by four-wave mixing is dominated by a nonlinear surface polarization. To interpret and validate our results, we provide a comparison with second-harmonic generation.

Suppression Of The Plasmon Resonance In Au/cds Colloidal Nanocomposites

Abstract: The nature of exciton-plasmon interactions in Au-tipped CdS nanorods has been investigated using femtosecond transient absorption spectroscopy. The study demonstrates that the key optoelectronic properties of composite heterostructures comprising electrically coupled metal and semiconductor domains are substantially different from those observed in systems with weak interdomain coupling. In particular, strongly coupled nanocomposites promote mixing of electronic states at semiconductor-metal domain interfaces, which causes a significant suppression of both plasmon and exciton excitations of carriers.