Dynamics of the dispersion interaction in an energy transfer system

On the propagation of resonant radiation through an optically dense system, photon capture is commonly followed by one or more near-field transfers of the resulting optical excitation. The process invokes secondary changes to the local electronic environment, shifting the electromagnetic interactions between participant chromophores and producing modified intermolecular forces. From the theory it emerges that energy transfer, when it occurs between chromophores with electronically dissimilar properties, can itself generate significant changes in the intermolecular potentials. This report highlights specific effects that can be anticipated when laser light propagates across an interface between differentially absorbing components in a model energy transfer system.     

Optical characterization of chiral plasmonic nanostructures

Chiral plasmonic nanomaterials can have circular dichroism and optical rotatory dispersion effects orders of magnitude larger than those observed in ordinary chiral molecules. Understanding this fascinating class of materials has proved challenging and has motivated several research groups to develop entirely new experimental techniques for characterizing chirality driven optical properties. In this review, we first describe the classical method of circular dichroism which measures linear, far-field responses from an ensemble population. We then go on to describe several of the more recently developed methods to probe chiral nanostructures as they expand into the domains of non-linear, near-field, and single particle measurements including spatially and spectrally resolved techniques.     

Cantilever tip near-field surface-enhanced Raman imaging of tris(bipyridine)ruthenium(II) on silver nanoparticles-coated substrates

The near-field surface-enhanced Raman scattering (SERS) and surface-enhanced fluorescence (SEF) images of tris(bipyridine)ruthenium(II) adsorbed on a silver nanoparticles-coated substrate were obtained with a scanning near-field optical microscope (SNOM, or near-field scanning optical microscopy, NSOM) using a cantilever tip. In comparison with the most widely used fiber tip for SNOM, the cantilever tip has higher optical throughput and better thermal stability, making it more suitable for detecting the extremely low Raman signal in the near-field spectroscopic investigations. Our preliminary results show that the near-field SERS with the higher spatial resolution can provide richer fingerprint information than the far-field SERS. A comparison of the two types of images shows that there are more SERS than SEF hot spots, and the two types of hot spots do not overlap. More surprisingly, the near-field SERS spectra differ from the far-field SERS spectra obtained on the same sample in the band frequency and relative intensities of some major Raman bands, and some IR-active bands were observed with the near-field mode. These results are explained mainly by the electric field gradient effect and heterogeneous polarization character that operate only in the near-field SERS.     

Scanning thermal microscopy techniques for polymeric thin films using temperature contrast mode to measure thermal diffusivity and a novel approach in conductivity contrast mode to the mapping of thermally conductive particles

Advances in production are leading to increasing use of polymeric thin films in applications such as automotive bearings. Two approaches have been developed to study the thermophysical properties of these thin films: The first technique based on Flash theory uses a scanning thermal microscopy (SThM) tip in temperature contrast mode to measure thermal diffusivity over a nano-scale area. The SThM tip is in contact with the upper surface of the film to detect a heat pulse delivered by a microelectromechanical heater platform from the lower surface. The second technique is a conductivity contrast mode SThM based approach for measuring the size and distribution of thermally conducting particles in thin film polymeric coatings. Topographical and thermal conductivity data are combined to produce a “correlation analysis value” 3D particle map of the coating. Good practice and a case study are highlighted.     

Some features of luminescent properties of PbS suspensions,stabilized by high‐molecular polyvinylpyrrolidone

The results of the investigations of optical and luminescent properties of PbS suspensions stabilized by high‐molecular polyvinylpyrrolidone are described. Suspensions prepared by liquid colloidal method from sodium sulfide and lead nitrate demonstrate strong luminescence in near infrared spectral range at the excitation by visual light with different wavelengths. It was proposed that Förster resonant energy transfer plays the important role in luminescence properties of closed packed PbS particles. The model, which describes the observed luminescent properties of the suspensions PbS‐stabilized high‐molecular polymer, is proposed. The combination of very wide spectral range of excitation of the luminescence with rather narrow range of light radiation in near infrared spectral range determine wide perspectives of the materials in solar luminescent concentrators and photodetectors. Copyright © 2015 John Wiley & Sons, Ltd.     

Nonadiabatic photodissociation process using an optical near field

We demonstrated the deposition of nanometric Zn dots using photodissociation with gas-phase diethylzinc and an optical near field under nonresonant conditions. To explain the experimental results, we proposed an exciton-phonon polariton model, and discuss the quantitative experimental dependence of the deposition rate on the optical power and photon energy based on photodissociation involving multiple-step excitation via molecular vibration modes. The physical basis of this process, which seems to violate the Franck-Condon principle, is the optically nonadiabatic excitation of the molecular vibration mode due to the steep spatial gradient of the optical near-field energy.     

Synthesis and second-order nonlinear optical properties of new chromophores containing benzimidazole, thiophene, and pyrrole heterocycles

A new series of thermally stable benzimidazole-based nonlinear optical (NLO) chromophores 4 and 5 have been developed. These chromophores possess a thienylpyrrolyl π-conjugated system attached to functionalized benzimidazole heterocycles. This feature leads to robust chromophores with excellent solvatochromic properties, high thermal stabilities and good molecular optical nonlinearities.     

Optimizing Gold Nanoparticle Cluster Configurations (n ≤ 7) for Array Applications

Nanoparticle cluster arrays (NCAs) are novel electromagnetic materials whose properties depend on the size and shape of the constituent nanoparticle clusters. A rational design of NCAs with defined optical properties requires a thorough understanding of the geometry dependent optical response of the building blocks. Herein, we systematically investigate the near- and far-field responses of clusters of closely packed 60 nm gold nanoparticles (n ≤ 7) as a function of size and cluster geometry through a combination of experimental spectroscopy and generalized Mie Theory calculations. From all of the investigated cluster configurations, nanoparticle trimers with D(3h) geometry and heptamers in D(6h) geometry stand out due to their polarization insensitive responses and high electric (E-) field intensity enhancement, making them building blocks of choice in this size range. The near-field intensity maximum of the D(6h) heptamer is red-shifted with regard to the D(3h) trimer by 125 nm, which confirms the possibility of a rational tuning of the near-field response in NCAs through the choice of the constituent nanoparticle clusters. For the nanoparticle trimer we investigate the influence of the cluster geometry on the optical response in detail and map near- and far-field spectra associated with the transition of the cluster configuration from D(3h) into D(∞h).     

Single and dual beam optical switching of resonance energy transfer

Through photonic mechanisms based on near-field coupling, laser radiation can engage with resonant energy transfer in a variety of suitably designed materials and molecular structures. Energy that has been acquired, through the initial absorption of resonant laser light, undergoes transfer between chromophores only on the throughput of off-resonant light, the process known as laser-assisted resonance energy transfer. The comprehensive results that are presented here extend and generalize the theory for both single and dual beam configurations, producing results that are applicable to media of various types including doped crystals, heterogeneous multichromophore solids, and solutions. The detailed principles, here explained in terms of both energetics and optical selection rule criteria, are specifically illustrated for a variety of materials. It is shown how general application of the theory can facilitate the elucidation of experiments, by clearly interpreting the effects of laser polarization manipulation. On further analysis of the photophysical mechanisms it is also demonstrated that such effects represent an entirely practicable basis for optical switching and logic gate operation. The additional polarization selectivity afforded by a two-beam setup proves to allow the most complete system control. With such a configuration, there is considerable promise for the realization of new optically driven logic and molecular devices.     

Nanostructured optical fibre arrays for high-density biochemical sensing and remote imaging

Optical fibre bundles usually comprise a few thousand to tens of thousands of individually clad glass optical fibres. The ordered arrangement of the fibres enables coherent transmission of an image through the bundle and therefore enables analysis and viewing in remote locations. In fused bundles, this architecture has also been used to fabricate arrays of various micro to nano-scale surface structures (micro/nanowells, nanotips, triangles, etc.) over relatively large areas. These surface structures have been used to obtain new optical and analytical capabilities. Indeed, the imaging bundle can be thought of as a “starting material” that can be sculpted by a combination of fibre drawing and selective wet-chemical etching processes. A large variety of bioanalytical applications have thus been developed, ranging from nano-optics to DNA nanoarrays. For instance, nanostructured optical surfaces with intrinsic light-guiding properties have been exploited as surface-enhanced Raman scattering (SERS) platforms and as near-field probe arrays. They have also been productively associated with electrochemistry to fabricate arrays of transparent nanoelectrodes with electrochemiluminescent imaging properties. The confined geometry of the wells has been loaded with biosensing materials and used as femtolitre-sized vessels to detect single molecules. This review describes the fabrication of high-density nanostructured optical fibre arrays and summarizes the large range of optical and bioanalytical applications that have been developed, reflecting the versatility of this ordered light-guiding platform.     

Resonant Raman spectroscopic study of biphenyl glutarate diacetylene polymer

The resonantly enhanced Raman spectra of biphenyl glutarate diacetylene polymer chains in fully radiation polymerized and partially thermally polymerized samples are reported. Details of the resonant enhancement in the region of the polymer electronic absorption were studied in partially polymerized samples. The role of defects in producing fluorescent emission and in broadening the optical absorption for radiation polymerized samples is briefly discussed.     

Macroscopic Change in Luminescent Color by Thermally Driven Sliding Motion in [3]Rotaxanes

Systematic investigation of rotaxane structures has revealed a rational design for thermally driven switching of their macroscopic properties. At low temperature, the luminophore is insulated by the macrocycles and displays monomer emission, whereas at high temperature, the luminophore is exposed owing to a change in the macrocyclic location distribution and interacts with external molecules, affording a thermally driven luminescent color change with high reversibility and responsiveness. This macroscopic switching through efficient thermal sliding was made possible by appropriate tuning of both the macrocycle–luminophore interactions within the rotaxane and the coupling between the excited luminophore and external molecules in an exciplex. The ability to switch properties by a simple and clean thermal stimuli should expand the utilization of rotaxanes as components of thermally driven molecular systems.     

Nanomanipulation using near field photonics

In this article we review the use of near-field photonics for trapping, transport and handling of nanomaterials. While the advantages of traditional optical tweezing are well known at the microscale, direct application of these techniques to the handling of nanoscale materials has proven difficult due to unfavourable scaling of the fundamental physics. Recently a number of research groups have demonstrated how the evanescent fields surrounding photonic structures like photonic waveguides, optical resonators, and plasmonic nanoparticles can be used to greatly enhance optical forces. Here, we introduce some of the most common implementations of these techniques, focusing on those which have relevance to microfluidic or optofluidic applications. Since the field is still relatively nascent, we spend much of the article laying out the fundamental and practical advantages that near field optical manipulation offers over both traditional optical tweezing and other particle handling techniques. In addition we highlight three application areas where these techniques namely could be of interest to the lab-on-a-chip community, namely: single molecule analysis, nanoassembly, and optical chromatography.     

Mechanical properties of single motor molecules studied by three-dimensional thermal force probing in optical tweezers.

A new method combining three-dimensional (3D) force measurements in an optical trap with the analysis of thermally induced (Brownian) position fluctuations of a trapped probe was used to investigate the mechanical properties of a single molecule, the molecular motor kinesin. One kinesin molecule attached to the probe was bound in a rigorlike state to one microtubule. The optical trap was kept weak to measure the thermal forces acting on the probe, which were mainly counterbalanced by the kinesin tether. The stiffness of kinesin during stretching and compression with respect to its backbone axis were measured. Our results indicate that a section of kinesin close to the motor domain is the dominating element in the flexibility of the motor structure. The experiments demonstrate the power of 3D thermal fluctuation analysis to characterize mechanical properties of individual motor proteins and indicate its usefulness to study single molecule in general     

Systems of small metal particles: Optical properties and their structure dependences

Experiments on small particles usually require samples containing large numbers of particles. The properties of such samples are determined both by the properties of the individual particle and by collective effects, if particles are packed closely together. Collective optical effects strongly depend on the topography of the samples. It is shown that they can be classified according to the effective local electromagnetic field. Recent experiments and calculations are presented for optical extinction spectra in the spectral region of plasmon polariton excitations, which clearly show the different behaviour of effective medium-like samples and of samples containing particle aggregates.     

Spectroscopic characterizations of molecularly linked gold nanoparticle assemblies upon thermal treatment

The understanding of surface properties of core-shell type nanoparticles is important for exploiting the unique nanostructured catalytic properties. We report herein findings of a spectroscopic investigation of the thermal treatment of such nanoparticle assemblies. We have studied assemblies of gold nanocrystals of approximately 2 nm core sizes that are capped by alkanethiolate shells and are assembled by covalent or hydrogen-bonding linkages on a substrate as a model system. The structural evolution of the nanoparticle assemblies treated at different temperatures was probed by several spectroscopic techniques, including UV-visible, Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS). The results show that the capping/linking shell molecules can be effectively removed to produce controllable surface and optical properties. The data further revealed that the thermally induced evolution of the surface plasmon resonance property of gold nanoparticles is dependent on the chemical nature of the linker molecule. The spectral evolution is discussed in terms of changes in particle size, interparticle distance, and dielectric medium properties, which has important implications for controlled preparation and thermal processing of core-shell nanostructured metal catalysts.     

Raman-spectroscopy and -imaging with surface-plasmon polaritons

We report on surface plasmon field—enhanced Raman imaging investigations of Langmuir—Blodgett multilayer assemblies of cadmium arachidate. This new method is a combination of Plasmon surface polariton field—enhanced Raman scattering with an optical multichannel detection scheme. The imaging capabilities of a CCD—camera are used to spatially resolve the Raman—spectral information of a heterogenous sample.     

Effect of the internal field on the IR absorption spectra of small particles in the case of 3D, 2D, and 1D size confinement

The spectral properties of composite materials based on small particles under 1D, 2D, and 3D size confinement are described using a combination of dispersive internal field and effective media theory approaches. Calculations performed for a number of crystalline materials have shown that the peak position and intensity of the vibrational band of the material under conditions of 1D, 2D, and 3D size confinement are changed, whereas the bandwidth of the band remains the same. In the case of 3D confinement, the peak position of the spectrum of isolated "mesoparticles" (epsilon(meso)(2)) appears to be very close to the intrinsic frequency of the lattice vibrations, calculated from the elastic constants of this crystal, as well as to the Fr?hlich's frequency. The largest shift (Deltanu) of the peak frequency, nu(max), from the bulk value is obtained in the case of 1D confinement when the peak position is practically coincident with the frequency of the longitudinal optical phonon (nu(LO)). These shifts are the result of intermolecular interactions, including both resonant and induced resonant dipole-dipole interactions.