RESUMEN

We demonstrate the use of white-light spectral interferometry as an effective technique involving only linear optical interactions and a partially coherent light source to measure the complex transmission response function of optical resonance and to determine the corresponding variation in the refractive index relative to a reference. We also discuss experimental arrangements to increase the accuracy and sensitivity of the technique. The superiority of the technique over single-beam absorption measurements is demonstrated by the accurate determination of the response function of the chlorophyll-a solution. The technique is then applied to chlorophyll-a solutions of varying concentrations and gold nanocolloids to characterize inhomogeneous broadening. Results on the inhomogeneity of gold nanocolloids are also supported by transmission electron micrographs, showing distributions of the size and shape of the constituent gold nanorods.

RESUMEN

One of the most straightforward methods to actively control optical functionalities of metamaterials is to apply mechanical strain deforming the geometries. These deformations, however, leave symmetries and topologies largely intact, limiting the multifunctional horizon. Here, we present topology manipulation of metamaterials fabricated on flexible substrates by mechanically closing/opening embedded nanotrenches of various geometries. When an inner bending is applied on the substrate, the nanotrench closes and the accompanying topological change results in abrupt switching of metamaterial functionalities such as resonance, chirality, and polarization selectivity. Closable nanotrenches can be embedded in metamaterials of broadband spectrum, ranging from visible to microwave. The 99.9% extinction performance is robust, enduring more than a thousand bending cycles. Our work provides a wafer-scale platform for active quantum plasmonics and photonic application of subnanometer phenomena.

RESUMEN

Various material properties change considerably when material is thinned down to nanometer thicknesses. Accordingly, researchers have been trying to obtain homogeneous thin films with nanometer thickness but depositing homogeneous few nanometers thick gold film is challenging as it tends to form islands rather than homogenous film. Recently, studies have revealed that treating the substrate with an organic buffer, (3-mercaptopropyl) trimethoxysilane (MPTMS) enables deposition of ultra-thin gold film having thickness as low as 5 nm. Different aspects of MPTMS treatment for ultra-thin gold films like its effect on the structure and optical properties at visible wavelengths have been investigated. However, the effect of the MPTMS treatment on electrical conductivity of ultra-thin gold film at terahertz frequency remains unexplored. Here, we measure the complex conductivity of nanometer-thick gold films deposited onto an MPTMS-coated silicon substrate using terahertz time-domain spectroscopy. Following the MPTMS treatment of the substrate, the conductivity of the films was found to increase compared to those deposited onto uncoated substrate for gold films having the thickness less than 11 nm. We observed 5-fold enhancement in the conductivity for a 7 nm-thick gold film. We also demonstrate the fabrication of nanoslot-antenna arrays in 8.2-nm-thick gold films. The nanoslot-antenna with MPTMS coating has resonance at around 0.5 THz with an electric field enhancement of 44, whereas the nanoslot-antenna without MPTMS coating does not show resonant properties. Our results demonstrate that gold films deposited onto MPTMS-coated silicon substrates are promising advanced materials for fabricating ultra-thin terahertz plasmonic devices.

RESUMEN

Low-power laser pulses of 6 ns duration (1064 nm wavelength) have been used to create plasma in an aqueous solution of plasmid DNA (pUC19). Thermal energy electrons and •OH radicals in the plasma induce strand breakages in DNA, including double strand breaks and possible base oxidation/base degradation. The time evolution of these modifications shows that it takes barely 30 s for damage to DNA to occur. Addition of physiologically relevant concentrations of a salt (NaCl) significantly inhibits such damage. We rationalize such inhibition using simple electrostatic considerations. The observation that DNA damage is induced by plasma-induced photolysis of water suggests implications beyond studies of DNA and opens new vistas for using simple nanosecond lasers to probe how ultralow energy radiation may affect living matter under physiological conditions.

Asunto(s)

Roturas del ADN de Doble Cadena/efectos de los fármacos , ADN/química , Nanoestructuras/química , Sodio/química , ADN/efectos de la radiación , Roturas del ADN de Doble Cadena/efectos de la radiación , Electrones , Radical Hidroxilo , Rayos Láser , Luz , Oxidación-Reducción , Fotólisis , Cloruro de Sodio/química , Electricidad Estática , Agua/química

RESUMEN

We report on the interplay between strong coupling and radiative damping of strongly coupled excitons (Xs) and surface plasmon polaritons (SPPs) in a hybrid system made of J-aggregates and metal nanostructures. The optical response of the system is probed at the field level by angle-resolved spectral interferometry. We show that two different energy transfer channels coexist: coherent resonant dipole-dipole interaction and an incoherent exchange due to the spontaneous emissions of a photon by one emitter and its subsequent reabsorption by another. The interplay between both pathways results in a pronounced modification of the radiative damping due to the formation of super- and subradiant polariton states. This is confirmed by probing the ultrafast nonlinear response of the polariton system and explained within a coupled oscillator model. Such a strong modification of the radiative damping opens up interesting directions in coherent active plasmonics.

RESUMEN

We demonstrate adiabatic nanofocusing of few-cycle light pulses using ultrasharp and ultrasmooth single-crystalline gold tapers. We show that the grating-induced launching of spectrally broad-band surface plasmon polariton wavepackets onto the shaft of such a taper generates isolated, point-like light spots with 10 fs duration and 10 nm diameter spatial extent at its very apex. This nanofocusing is so efficient that nanolocalized electric fields inducing strong optical nonlinearities at the tip end are reached with conventional high repetition rate laser oscillators. We use here the resulting second harmonic to fully characterize the time structure of the localized electric field in frequency-resolved interferometric autocorrelation measurements. Our results strongly suggest that these nanometer-sized ultrafast light spots will enable new experiments probing the dynamics of optical excitations of individual metallic, semiconducting, and magnetic nanostructures.

RESUMEN

A direct measurement of the superconducting energy gap by point contact spectroscopy in nanostructured Nb films shows that the gap decreases with a reduction in the average particle size. The superconducting T(c), obtained from transport and magnetic measurements, also decreases with size and scales with the energy gap. The size dependence of the superconducting properties in this intermediate coupling type II superconductor is therefore governed by changes in the electronic density of states rather than by phonon softening. Consistent with the Anderson criterion, no T(c) was observed for sizes below 8 nm.

RESUMEN

The application of semiconductor quantum dots in important new areas such as random lasing and quantum-information processing requires knowledge of the coherence of the optical emission from such systems. We report the first direct experimental estimation of the coherence in the light emitted by a nanoparticle ensemble. The photoluminescence from a two-phase nanocomposite CdS-ZnO thin film (with a characteristic grain size of 2-3 nm for both the chemical phases) possesses an appreciable degree of spatial and temporal coherence at room temperature. The degree of spatial coherence was estimated from the classical Young's double slit experiment. We also discuss a simple technique for estimating the degree of spectral coherence of the photoluminescence from thin films.