The modulation instability development of intensive surface plasmon–polariton waves in a thin metal film is studied. It is shown both analytically and numerically that the modulation‐instability effect can give rise to spatial redistribution and longitudinal localization of surface plasmon–polariton wave energy on the subwavelength scale. Analytical expressions for the driving parameters of the modulation instability process ? nonlinearity and dispersion ? are derived. The impact of the film thickness and dielectric permittivities of constituents on the dynamics of surface plasmon–polariton wave transformation is considered. Numerical simulations show that in the layer structure comprising a silver film of subwavelength thickness a train of subpicosecond optical pulses with high repetition rate can be generated.
The non‐centrosymmetric polar tetragonal (P 41) barium antimony tartrate trihydrate, Ba[Sb2((+)C4H2O6)2]·3H2O, was found to be an attractive novel semi‐organic crystal manifesting numerous χ (2)‐ and χ (3)‐nonlinear optical interactions. In particular, with picosecond single‐ and dual‐wavelength pumping SHG and THG via cascaded parametric four‐wave processes were observed. High‐order Stokes and anti‐Stokes lasing related to two SRS‐promoting vibration modes of the crystal, with ωSRS1 ≈ 575 cm?1 and ωSRS2 ≈ 2940 cm?1, takes place. Basing on a spontaneous Raman investigation an assignment of the two SRS‐active vibration modes is discussed.
The optical properties and sensing performances of the molecular sensors based on plasmonic Fano‐resonance (PFR) nanostructures have been numerically investigated in detail. The on‐resonance sensor, in which the Fano‐resonance position is overlapping with the absorption‐band of the detected molecules perfectly, reveals a powerful ability to detect the molecules with a low concentration or thin thickness. By the bias‐modulation of a single‐layer graphene, the Fano‐resonance position of the nanostructures can be tuned effectively. On being modulated properly, the PFR sensor shows an ultrahigh performance because of the unprecedentedly high overlap of the Fano‐resonance position with the absorption‐band of molecules, which is enabling superior signal strength in the molecular detections based on their vibrational fingerprints. Our proposed strategy may enable the development of dynamic sensors and open exciting prospects for bio‐sensing.
Following the Dirac‐Frenkel time‐dependent variational principle, transient dynamics of a one‐dimensional Holstein polaron with diagonal and off‐diagonal exciton‐phonon coupling in an external electric field is studied by employing the multi‐D2Ansatz, also known as a superposition of the usual Davydov D2 trial states. Resultant polaron dynamics has significantly enhanced accuracy, and is in perfect agreement with that derived from the hierarchy equations of motion method. Starting from an initial broad wave packet, the exciton undergoes typical Bloch oscillations. Adding weak exciton‐phonon coupling leads to a broadened exciton wave packet and a reduced current amplitude. Using a narrow wave packet as the initial state, the bare exciton oscillates in a symmetric breathing mode, but the symmetry is easily broken by weak coupling to phonons, resulting in a non‐zero exciton current. For both scenarios, temporal periodicity is unchanged by exciton‐phonon coupling. In particular, at variance with the case of an infinite linear chain, no steady state is found in a finite‐sized ring within the anti‐adiabatic regime. For strong diagonal coupling, the multi‐ Anstaz is found to be highly accurate, and the phonon confinement gives rise to exciton localization and decay of the Bloch oscillations.
A theory of dielectric response of water under nanoscale confinement was long overdue. This work addresses the problem by establishing a relation between dielectric response and hydrogen‐bond frustration subsumed in a non‐Debye polarization term. The results hold down to the single‐molecule contribution and are validated vis‐à‐vis experimental measurements on a system where dielectric modulation entails removal of a single water molecule. The frustrated dielectric response down to molecular scales is assessed by contrasting two enantiomeric ligands in association with the same protein, with the complexes differing in the removal of a single interfacial water molecule.
A new model of nonlinear electrodynamics with three parameters is suggested and investigated. It is shown that if the external constant magnetic field is present the phenomenon of vacuum birefringence takes place. The indices of refraction for two polarizations of electromagnetic waves, parallel and perpendicular to the magnetic induction field are calculated. The electric field of a point‐like charge is not singular at the origin and the static electric energy is finite. We have calculated the static electric energy of point‐like particles for different parameters of the model. The canonical and symmetrical Belinfante energy‐momentum tensors and dilatation current are obtained. We demonstrate that the dilatation symmetry and dual symmetry are broken in the model suggested.
The properties of the superconducting and the anomalous normal state were described by using the Eliashberg method. The pairing mechanism was reproduced with the help of the Hamiltonian, which models the electron‐phonon and the electron‐electron‐phonon interaction (EEPh). The set of the Eliashberg equations, which determines the order parameter function (φ), the wave function renormalization factor (Z), and the energy shift function (χ), was derived. It was proven that for the sufficiently large values of the EEPh potential, the doping dependence of the order parameter () has the analogous course to that observed experimentally in cuprates. The energy gap in the electron density of states is induced by Z and χ ‐ the contribution from φ is negligible. The electron density of states possesses the characteristic asymmetric form and the pseudogap is observed above the critical temperature.
Uniform, graded and spaced arrays of 3 μm triangular antidots in pulsed laser deposited YBa2Cu3O7 (YBCO) superconducting thin films are compared by examining the improvements in the critical current density they produced. The comparison is made to establish the role of their lithographically defined (non‐)uniformity and the effectiveness to control and/or enhance the critical current density. It is found that almost all types of non‐uniform arrays, including graded ones enhance over the broad applied magnetic field and temperature range due to the modified critical state. Whereas uniform arrays of antidots either reduce or produce no effect on compared to the original (as‐deposited) thin films.
We consider a universe with a bulk viscous cosmic fluid, in a flat Friedmann‐Lemaitre‐Robertson‐Walker geometry. We derive the conditions for the existence of inflation, and those which at the same time prevent the occurrence of self‐reproduction. Our theoretical model gives results which are in perfect agreement with the most recent data from the PLANCK surveyor.
Nonlinear wave mixing in mesoscopic silicon structures is a fundamental nonlinear process with broad impact and applications. Silicon nanowire waveguides, in particular, have large third‐order Kerr nonlinearity, enabling salient and abundant four‐wave‐mixing dynamics and functionalities. Besides the Kerr effect, in silicon waveguides two‐photon absorption generates high free‐carrier densities, with corresponding fifth‐order nonlinearity in the forms of free‐carrier dispersion and free‐carrier absorption. However, whether these fifth‐order free‐carrier nonlinear effects can lead to six‐wave‐mixing dynamics still remains an open question until now. Here we report the demonstration of free‐carrier‐induced six‐wave mixing in silicon nanowires. Unique features, including inverse detuning dependence of six‐wave‐mixing efficiency and its higher sensitivity to pump power, are originally observed and verified by analytical prediction and numerical modeling. Additionally, asymmetric sideband generation is observed for different laser detunings, resulting from the phase‐sensitive interactions between free‐carrier six‐wave‐mixing and Kerr four‐wave‐mixing dynamics. These discoveries provide a new path for nonlinear multi‐wave interactions in nanoscale platforms.
Single neutral atom mechanics is controllable by focused, high‐intensity optical vortices. The intensity‐dependent, laser‐driven motion of the atom's active electrons subsumes to a net transfer of the orbital angular momentum of the light to the neutral atom. The ponderomotive force on these electrons translates so into an unbounded or a bounded radial drift of the atom depending on its initial kinetic energy, as set by the temperature. Appropriate combination of laser beams results in sub‐wavelength, dynamical radial traps for tweezing atoms controllably, an effect that can be exploited for atom guiding, structuring, and lithographic applications.
Defects and frequently used defect models of solids are reviewed. Signatures for identifying the disorder from x‐ray and neutron scattering data are given. To give illustrative examples how technologically important defects contribute to x‐ray and neutron scattering numerical method able to treat non‐periodical solids possessing several simultaneous defect types is given for simulating scattering in nanosize disordered clusters. The approach takes particle size, shape, and defects into account and isolates element specific signals. As a case study a statistical approximation model for lead‐zirconate titanate [Pb(ZrxTi)O3, PZT] is introduced. PZT is a material possessing several defect types, including substitutional, displacement and surface defects. Spatial composition variation is taken into account by introducing a model in which the edge lengths of each cell depend on the distribution of Zr and Ti ions in the cluster. Spatially varying edge lengths and angles is referred to as microstrain. The model is applied to compute the scattering from ellipsoid shaped PZT clusters and to simulate the structural changes as a function of average composition. Two‐phase co‐existence range, the so called morphotropic phase boundary composition is given correctly. The composition at which the rhombohedral and tetragonal cells are equally abundant was . Selected x‐ray and neutron Bragg reflection intensities and line shapes were simulated. Examples of the effect of size and shape of the scattering clusters on diffraction patterns are given and the particle dimensions, computed through Scherrer equation, are compared with the exact cluster dimensions. Scattering from two types of 180° domains in spherical particles, one type assigned to Ti‐rich PZT and the second to the MPB and Zr‐rich PZT, is computed. We show how the method can be used for modelling polarization reversal.
In this article a particular solution of Heun equation is derived by making use of the Nikiforov‐Uvarov (NU) method which provides exact solutions for general hypergeometric equation and eigenvalues together with eigenfunctions of the Heun equation for this particular solution are obtained. One to one correspondence (isomorphism) of the aforesaid equation with the radial Schrödinger equation is emphasized and also physical counterparts of the parameters in this equation are put forward by introducing solutions for two different potential functions (Hulthen and Woods‐Saxon potentials).
A possible scenario of the Lorentz symmetry violation is discussed based on the arising of geometric quantum phases yielded by the effects of the Lorentz symmetry violation in the CPT‐even gauge sector of Standard Model Extension. Analogues of the Anandan quantum phase and the scalar Aharonov‐Bohm effect for a neutral particle [J. Anandan, Phys. Lett. A 138 , 347 (1989)] are obtained from the parity‐odd sector of the tensor . Moreover, we build quantum holonomies associated with the analogue of the Anandan quantum phase and discuss a possible analogy with the geometric quantum computation [A. Ekert et al., J. Mod. Opt. 47 , 2501 (2000)].
The ferroelectric domain structures of periodically poled KTiOPO4 and two‐dimensional short range ordered poled LiNbO3 crystals are determined non‐invasively by interferometric measurements of the electro‐optically induced phase retardation. Owing to the sign reversal of the electro‐optical coefficients upon domain inversion, a π phase shift is observed for the inverted domains. The microscopic setup provides diffraction‐limited spatial resolution allowing us to reveal the nonlinear and electro‐optical modulation patterns in ferroelectric crystals in a non‐destructive manner and to determine the poling period, duty cycle and short‐range order as well as detect local defects in the domain structure. Conversely, knowing the ferroelectric domain structure, one can use electro‐optical microscopy so as to infer the distribution of the electric field therein.
This article presents a novel III‐V on silicon laser. This work exploits the phenomenon that a passive silicon cavity, side‐coupled to a III‐V waveguide, will provide high and narrow‐band reflectivity into the III‐V waveguide: the resonant mirror. This results in an electrically pumped laser with a threshold current of 4 mA and a side‐mode suppression ratio up to 48 dB.
In the paper, for the Kerr field, we prove that Chandrasekhar's Dirac Hamiltonian and the self‐adjoint Hamiltonian with a flat scalar product of the wave functions are physically equivalent. Operators of transformation of Chandrasekhar's Hamiltonian and wave functions to the η representation with a flat scalar product are defined explicitly. If the domain of the wave functions of Dirac's equation in the Kerr field is bounded by two‐dimensional surfaces of revolution around the z axis, Chandrasekhar's Hamiltonian and the self‐adjoint Hamiltonian in the η representation are Hermitian with equality of the scalar products, .
Monocrystalline titanium dioxide (TiO2) micro‐spheres support two orthogonal magnetic dipole modes at terahertz (THz) frequencies due to strong dielectric anisotropy. For the first time, we experimentally detected the splitting of the first Mie mode in spheres of radii m through near‐field time‐domain THz spectroscopy. By fitting the Fano lineshape model to the experimentally obtained spectra of the electric field detected by the sub‐wavelength aperture probe, we found that the magnetic dipole resonances in TiO2 spheres have narrow linewidths of only tens of gigahertz. Anisotropic TiO2 micro‐resonators can be used to enhance the interplay of magnetic and electric dipole resonances in the emerging THz all‐dielectric metamaterial technology.
The broadband enhancement of single‑photon emission from nitrogen‐vacancy centers in nanodiamonds coupled to a planar multilayer metamaterial with hyperbolic dispersion is studied experimentally. The metamaterial is fabricated as an epitaxial metal/dielectric superlattice consisting of CMOS‐compatible ceramics: titanium nitride (TiN) and aluminum scandium nitride (AlxSc1‐xN). It is demonstrated that employing the metamaterial results in significant enhancement of collected single‑photon emission and reduction of the excited‐state lifetime. Our results could have an impact on future CMOS‐compatible integrated quantum sources.
The threshold, temporal behavior, and conversion efficiency of stimulated Brillouin scattering (SBS) and stimulated Raman scattering (SBS) in three liquids (benzene, hexane, and dimethyl sulfoxide) and two crystals (calcite and barium nitrate) have been investigated under three largely different spectral linewidth conditions. Pumped with 532‐nm and nanosecond duration laser pulses of ≤ 0.01 cm?1 linewidth, only SBS can be generated in all tested liquids with a high nonlinear reflectivity. However when the pump spectral linewidth is ～0.07 cm?1 or ～0.8 cm?1, both SBS and SRS can be observed in benzene while only SRS can be generated in dimethyl sulfoxide; in all these cases SRS is the dominant contribution to the stimulated scattering but the efficiency values are drastically decreased due to the self‐termination behavior of SRS in liquids, which arises from the thermal self‐defocusing of both pump beam and SRS beam owing to Stokes‐shift related opto‐heating effect. In contrast, for SRS process in the two crystals, the thermal self‐defocusing influence is negligible benefitting from their much greater thermal conductivity, and a higher conversion efficiency of SRS generation can be retained under all three pump conditions.
下载免费PDF全文