Resonance Positions Research Articles

Characterization and alignment of a resonant cavity beam position monitor for the Compact LInear Collider (CLIC) project at CERN

Beam diagnostic devices are essential tools to sense the properties of the beam in particle accelerators. Beam Position Monitors (BPMs) are used to detect the transverse beam spatial coordinates. A large number of high-resolution resonant cavity BPMs, operating at 14GHz, are proposed to monitor the orbit of the two main beam linacs of the CLIC project. This paper discusses innovative calibration techniques on a dedicated test bench in the frame of the PACMAN project. The particular location of the electromagnetic center of the resonant cavity BPM is detected utilizing a stretched-wire measurement approach. Measurements, RF characterization and final fiducialization of the BPM electrical offset are treated with details. Initial studies through EM simulations of the cavity BPM are covered. The presented experimental results prove the feasibility of the alignment methodology with nanometric resolution.

Saturable absorption and negative nonlinear refraction index evolution in silver nanoparticles colloids

In this paper, silver nanoparticles colloids in deionized water with evolution from spherical to disk and decahedral shapes, and average size between ∼10–50 nm, were synthesized controlling the reaction conditions. The samples were irradiated using a cool-white light-emitting diode source for several hours, which allowed the tailoring of the position of the surface plasmon resonance from 408 nm to 495 nm. The nonlinear optical properties of silver nanoparticles colloids were investigated by the Z-scan technique and femtosecond laser pulses @ 800 nm. The nonlinear absorption obtained by an open aperture Z-scan setup showed a saturable absorption effect, while the nonlinear refraction index measured by a close aperture setup revealed a negative lens-like (self-defocusing) behavior in all samples. Measured effective nonlinear absorption ranged from −5.26×10−9 to −1.03×10−9 cm/W, while nonlinear refractive index was −2.47×10−13 to −1.48×10−13 cm2/W. We found that as the silver nanoparticles shape is modified from quasi-spherical to disk and decahedral, and its size is increased, the linear absorption and the absolute values of the effective nonlinear absorption and nonlinear refractive index decreased. We also found that the nonlinear optical response is more sensitive to size and morphology than the linear optical response.

Dendric nanostructures for SARS-CoV-2 proteins detection based on surface enhanced infrared absorption spectroscopy.

Infrared spectroscopy is a non-destructive and rapid characterization tool that can distinguish different viral proteins by spectral details. However, traditional infrared spectroscopy has insufficient absorption signal intensity contrast when measuring low-concentration samples. In this work, surface enhanced infrared absorption (SEIRA) spectroscopy is proposed by deploying a novel nanostructure array as SEIRA substrates. An array of gold dendric nanostructures are designed and fabricated with a precision resonance control to achieve surface enhancement covering a broadband molecular "finger-print" region. The spectral positions of the multiple resonances accurately correspond to the characteristic absorption peaks of the SARS-CoV-2 proteins. An approach for SARS-CoV-2 protein detection based on SEIRA spectroscopy is then proposed. A low concentration detection of 40 μg/ml diluted SARS-CoV-2 nucleocapsid protein is experimentally demonstrated and the enhancement factor (EF) achieved is in good agreement with simulation results. The SEIRA methodology based on broadband resonance nanostructure design provides a systematic approach for sensitive, non-destructive and rapid protein molecular detection, which could be extended to various kind of molecular characterization and biomedical diagnostics.

High resolution UV spectral imaging and bio-detection with magnetic dipole quasi-BIC resonant dielectric metasurfaces

In this paper, we designed a ring-shaped metasurface based on diamond material that response in ultraviolet band, and with which the BIC mode is obtained by breaking the symmetry of its structural units. We show that only when the radiation rate of the magnetic dipole resonance of the BIC mode is equal to the dissipation loss brought by the surface covering material, the interaction between light and matter is maximally enhanced. The absorptivity of the film material is enhanced by an order of magnitude. The simulation results show that there is a linear relationship between the resonant positions of the structure and the scaling factor S varying structure sizes. When the metasurface is covered with a single DNA film, changes differently due to the absorption of the DNA. The reflection information of the system is further converted into ultraviolet absorption of DNA. Then the multiple absorption peaks form the absorption spectrum of DNA molecules. By Arranging the different scaling factor metasurface pixels on a same substrate we can obtain a specific absorption image. The absorptivity of DNA leads to the difference in brightness and darkness of the metasurface pixels, which can be processed into gray-scale images that give out the specific fingerprint information of the DNA. So, we realized calibration and analysis of DNA without spectroscopic measurements in the ultraviolet band now. The metasurface device can effectively detect the contamination of DNA by other biomolecules such as RNA. This work has great significance in promoting the application of metasurfaces in the field of biological detection and demonstrates that a specially designed metasurface can be applied in nucleic acid detection.

Spectroscopic signatures of states in the continuum characterized by a joint experimental and theoretical study of pyrrole.

We report a combined experimental and theoretical investigation of electron-molecule interactions using pyrrole as a model system. Experimental two-dimensional electron energy loss spectra (EELS) encode information about the vibrational states of the molecule as well as the position and structure of electronic resonances. The calculations using complex-valued extensions of equation-of-motion coupled-cluster theory (based on non-Hermitian quantum mechanics) facilitate the assignment of all major EELS features. We confirm the two previously described π resonances at about 2.5 and 3.5eV (the calculations place these two states at 2.92 and 3.53eV vertically and 2.63 and 3.27eV adiabatically). The calculations also predict a low-lying resonance at 0.46eV, which has a mixed character-of a dipole-bound state and σ* type. This resonance becomes stabilized at one quanta of the NH excitation, giving rise to the sharp feature at 0.9eV in the corresponding EELS. Calculations of Franck-Condon factors explain the observed variations in the vibrational excitation patterns. The ability of theory to describe EELS provides a concrete illustration of the utility of non-Hermitian quantum chemistry, which extends such important concepts as potential energy surfaces and molecular orbitals to states embedded in the continuum.

Matrix-Specific Effects on Caffeine and Chlorogenic Acid Complexation in a Novel Extract of Whole Coffea arabica Coffee Cherry by NMR Spectroscopy.

Coffee cherry is a rich source of caffeine and chlorogenic acids. In this study we investigate the structural analysis of caffeine-enriched whole coffee cherry extracts, CEWCCE by using 1H and 13C NMR spectroscopy. The changes in 1H chemical shift data in NMR spectra of CEWCCE compared to pure caffeine indicated the formation of complexes between caffeine and chlorogenic acids in aqueous solution. The effect of complexation on the peak position of caffeoylquinic acid and caffeine resonance with increasing addition of caffeine was investigated. 2D NOESY experiments show the presence of cross-peaks that are due to the proximity of chlorogenic acid and caffeine molecules in stable complexes in protic solvents. The quantification data of caffeine by 1H qNMR was found to be in close agreement with the data obtained by HPLC analysis.

Whispering gallery modes of a triatomic photonic molecule

In this paper, we present the results of numerical simulations of the optical spectra of a three-sphere photonic molecule. The configuration of the system was continuously modified from linear to triangular, in-plane with the fundamental mode excited in one of the spheres and perpendicular to it. We found the relative insensitivity of the spectra to the in-plane deviation from the linear arrangement up to about 110°. For larger angles, the spectra show significant modification consisting of the major spectral peaks splitting and shifting. On the contrary, the spectra are quite sensitive to out-of-plane molecule deviation, even at small angles. Thus, the spectra of photonic molecules can be modified by changing the mutual positions of the constituent resonators, which can be useful in reconfigurable photonic devices.

Tunable broadband transmittance and Faraday effect in a magnetophotonic nanostructure with gradient thickness.

We propose a magnetic photonic crystal (MPC) nanostructure with a gradient thickness of the magnetic layer. Such a nanostructure exhibits on-the-fly adjustment of optical and magneto-optical (MO) properties. Spatial displacement of the input beam allows tuning of the spectral position of the defect mode resonance in the bandgap of both transmission and magneto-optical spectra. Meanwhile, by varying the diameter of the input beam or its focus one can control the resonance width in both optical and magneto-optical spectra.

A Study of the Lossy Mode Resonances during the Synthesis Process of Zinc Telluride Films.

Films of zinc telluride (ZnTe) were deposited on the surface of a chemically thinned section of an optical fiber by metalorganic chemical vapor deposition. The boundary values of temperatures and the concentration ratios of the initial tellurium and zinc precursors at which the synthesis of ZnTe coatings is possible are determined. The influence of the position of the thinned part of the optical fiber in the reactor on the growth rate of films on the side surface of the fiber was studied, on the basis of which, the parameters of the deposition zone were determined. By placing a section of an optical fiber with an etched cladding in the center of this zone, sensitive elements for refractometers were created. The principle of their operation is based on the dependence of the spectral position of the lossy mode resonance (LMR) maximum on the refractive index (RI) of the external medium. It has been found that even thin films deposited on a light guide in a continuous process have cracks. It is shown that the interruption of the deposition process makes it possible to avoid the appearance of defects in the zinc telluride layers even with the repeated deposition of the sensor. The sensitivity of the spectral position of the LMR to changes in the RI of aqueous sodium chloride solutions in the range from 1.33 to 1.35 for the first transverse electric and transverse magnetic LMRs was 6656 and 6240 nm per refractive index unit, respectively.

Extinction by plasmonic nanoparticles in dispersive and dissipative media.

Extinction of small metallic spheres has been well understood through the classical Mie theory when the host medium is dispersive and transparent. However, the role of host dissipation on the particulate extinction remains a competition between the enhancing and reducing effects on the localized surface plasmonic resonance (LSPR). Here, using a generalized Mie theory, we elaborate on the specific influence mechanisms of host dissipation on the extinction efficiency factors of a plasmonic nanosphere. To this end, we isolate the dissipative effects by comparing the dispersive and dissipative host with its dissipationless counterpart. As a result, we identify the damping effects of host dissipation on the LSPR including the resonance widening and amplitude reducing. The resonance positions are shifted by host dissipation, which cannot be predicted by the classical Fröhlich condition. Finally, we demonstrate that a wideband extinction enhancement due to host dissipation can be realized away from the positions of the LSPR.

Suppressing the spectral shift of a polarization-independent nanostructure with multiple resonances.

Resonances are the cornerstone of photonic applications in many areas of physics and engineering. The spectral position of a photonic resonance is dominated by the structure design. Here, we devise a polarization-independent plasmonic structure comprising nanoantennas with two resonances on an epsilon-near-zero (ENZ) substrate in order to loosen this correlation to obtain less sensitivity to geometrical perturbations of the structure. Compared with the bare glass substrate, the designed plasmonic nanoantennas on an ENZ substrate exhibit a nearly three-fold reduction only in the resonance wavelength shift near the ENZ wavelength as a function of antenna length.

Observation of the p -wave shape resonance in atom-molecule collisions

Partial wave resonances are quasi-bound states that are formed by tunneling through the centrifugal barrier. Such states are important to collisions that deviate from the Langevin limit where direct collision path is suppressed due to quantum symmetry or a potential barrier. In such a case, quantum resonances play a major role in the dynamics at low temperatures where scattering process can be described mainly by the resonance contribution. Here we present the first observation of the lowest-lying partial wave resonance in the Penning ionization collisions between metastable neon and rovibrationally ground state HD molecules. We observe the resonance at an energy of $k_B\times$22mK taking advantage of the phase space correlation similar to atomic delta kick cooling. We show that the $p$-wave resonance position is particularly sensitive to the leading term of the van der Waals interaction. We also measure shape resonance at a higher angular momentum state, $l=6$, allowing us to disentangle and probe the short and the long parts of the intermolecular interaction.

Concave gold nano-arrows (AuCNAs) for efficient catalytic reduction of 4-nitrophenol

Anisotropic gold nanostructures have attracted great attention in different fields including catalysis. Thermodynamically driven selective surface growth offers a reliable and reproducible method for anisotropic gold nanoparticle synthesis with specific morphologies. Herein, monocrystalline concave gold nano-arrows (AuCNAs) are prepared by the over-growth method using Au nanorods (AuNRs) as seeds. The as-prepared AuCNAs consist of a biconical head and four concave structures. Interestingly, silver ions (Ag+) concentration significantly affects the product morphology by tuning the peak positions of surface plasmon resonance (SPR), aspect ratio, arrow, and concave morphology of AuCNAs. The position of longitudinal SPR peaks is observed at 810, 805 and 782 nm at [Ag+]/[Au3+] molar ratios of 1:2, 1:1, and 2:1, respectively. Diameters and lengths of AuCNAs varied from 25 nm to 36 nm; 104 nm, 78 nm, and 120 nm, respectively. Additionally, the AuCNAs are applied for the catalytic reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) in presence of excess NaBH4. Compared to gold nanorods (AuNRs), the prepared AuCNAs catalyst shows excellent catalytic activity, demonstrating that concave structures and sharp corners significantly enhance the catalytic activity. The value of pseudo-first-order reaction kinetic constants (kapp) increased from 0.0051 to 0.0195 s−1 with increasing catalyst valume from 7.5 to 37.5 μL. The highest normalized reaction rate constant (Knor) and turnover frequency (TOF) reach 5.84 × 104 min−1 mmol−1 and 443.47 h−1, respectively, at [Ag+]/[Au3+] ratio of 1:1 in AuCNAs catalyst. This study expands catalytic applications of anisotropic gold nanostructures and widens their potential application areas, such as surface plasmon exciton photonics, biomedical photonics, and photocatalysis.

Determination of the 2s22p5−2s2p6 transition energy in fluorine-like nickel utilizing a low-lying dielectronic resonance

High precision spectroscopy of the low-lying dielectronic resonances in fluorine-like nickel ions were determined by employing the merged electron-ion beam at the heavy-ion storage ring CSRm. The measured dielectronic resonances are identified by comparing with the most recent relativistic calculation utilizing the FAC code. The first resonance at about 86 meV due to the dielectronic recombination via (2s2p6[2S1/2]6s)J=1 intermediate state was recognized. The experimental determination of the resonance position at 86 meV reaches an uncertainty of 4 meV, which allows precise determination of the 2s22p5[2P3/2] - 2s2p6[2S1/2] transition energy. The Rydberg binding energy of the 6s electron in the (2s2p6[2S1/2]6s)J=1 state is calculated by the multi-configurational Dirac-HartreeFock and stabilization methods. The determined transition energies are 149.056(4)exp(10)theo and 149.032(4)exp(6)theo, respectively. Moreover, the transition energy has also been calculated by fully relativistic and ab initio approaches. Individual theoretical contributions are evaluated by employing the core-Hartree and Kohn-Sham screening potentials, respectively. High-order QED and correlation effects contribute prominently to the total transition energy. The present DR precision spectroscopy study at the CSRm paves the way for future precision measurements of atomic energy levels with heavier highly charged ions.

Phase-Selective Four-Wave Mixing of Resonant Plasmonic Nanoantennas

Metallic nanoantennas are key components of a wide range of optical techniques that exploit their plasmonic response for signal amplification and extremely sensitive detection. For nonlinear techniques, the higher-order plasmonic response of a nanoantenna can be predicted by the product of the nanoantenna’s linear susceptibilities, known as Miller’s rule, provided that the spatial field distributions at the fundamental and the nonlinear frequencies are the same. Here, we show that Miller’s rule also holds for ultra-broadband excitation pulses and that it can be utilized to predict the frequency dependence of the near-degenerate four-wave mixing (ND-FWM) intensities generated by individual resonant plasmonic nanoantennas. Importantly, this implies that the nanoantenna’s nonlinear response can be deterministically controlled and further optimized by varying the spectral phase of the laser pulse. We demonstrate this by measuring the chirp dependence of the ND-FWM signal and observe an enhancement of up to 60% depending on the position of the plasmon resonance with respect to the laser spectrum, in agreement with model predictions. Finally, we exploit this phase control for chirp-selective confocal imaging of resonant nanoantennas. Our findings may help improve the sensitivity of nonlinear techniques such as plasmon-enhanced coherent anti-Stokes Raman scattering.

In Situ Monitoring of Layer-by-Layer Assembly Surface Modification of Nanophotonic-Microfluidic Sensor.

An elaboration of the photonic based sensors is the most promising direction in modern analytical chemistry from the point of view of real clinical applications. The highest sensitivity is demonstrated by sensors based on photonic integrated circuits (PICs). This type of sensor has been recently successfully combined with microfluidics, which decreased the analyte volume for analysis down to microliter units. The most significant disadvantage regarding these photonic sensors is low specificity. One of the methods that could be useful for such type of problem is the layer by layer (LBL) assembly. The peculiarity of a PIC based sensor is the ability to precisely control surface modification by using measurements of a minimum resonance position shift. The bovine serum albumin (BSA) and tannic acid (TA) molecules were selected for LBL assembly because on one side they form a stable LBL assembly film based on hydrogen bonds, while the other side of both TA and BSA molecules can be used for conjugation with target molecules. A microring resonator (MRR) and a Mach-Zehnder interferometer (MZI) based on a silicon nitride platform combined with a microfluidic system were elaborated and used for monitoring the LBL film assembly. Obtained results have a good correlation with measurements carried out by atom force microscopy. Thus, the ability of using PIC based sensors for in situ control of surface modification was demonstrated and can be considered in point-of-care (POC) devices that have a very good perspective for both early pathological state diagnosis and evaluation of treatment efficiency.

Investigation of electron-induced scattering resonances using a multiconfigurational polarization propagator and a complex absorbing potential

We develop a method based on the polarization propagator (PP) combined with the complex absorbing potential (CAP) technique to study metastable resonances induced by electron impact. We use a CASSCF wavefunction corresponding to the ground state of the anion as the initial state for the PP. The perturbation of the Hamiltonian by the CAP allows for complex eigenvalues that represent the continuum states including the resonance buried in the continuum. The artifacts due to the CAP are eliminated using the Padé extrapolation method. We apply our method to study the 2P Be− atomic shape resonance, and 2Πg N2− and 2Π CO− molecular shape resonances. Our estimated resonance positions and widths for the resonances are in agreement with the previously reported values. Overall, this method is a powerful and computationally tractable tool for the study of resonances.

Silver particles embedded in silicon: The fabrication process and their application in surface enhanced Raman scattering (SERS)

The formation of hybrid structures for creating sensitive sensors is a difficult task. In this study, we developed a facile technique of semiconductor technology to fabricate hybrid structures based on SiO2/embeddedAg/Si and embeddedAg/Si for a surface-enhanced Raman scattering. Herein, our hybrid structures were created in one technological cycle, which consists of the reduction of silver nitrate salt from a solution on the silicon surface and subsequent high-temperature annealing at 1000 °C. In addition, it allows not only to preserve the plasmonic properties of Ag particles on the Si surface but also to protect them from further external influences by coating them with a SiO2 layer. Also, the basis for creating such hybrid structures is the performed numerical calculations of the position of a localized surface plasmon resonance as a function of the geometry of structures. Furthermore, the theoretical full-wave electromagnetic modeling of Raman scattering in an embedded Ag/Si structure showed the presence of enhancement regions “hot spots” at sharp corners with a maximum enhancement factor of 106. Finally, surface-enhanced Raman scattering spectroscopy of such structures showed reliable detection of the methyl orange from an aqueous solution at a concentration of 10-5M.

The effect of structure parameters and static electric field on the nonlinear optical properties of triple InGaAs/GaAs quantum well

Optical properties of InxGa1-xAs/GaAs triple QW are studied for different quantum well thicknesses and external electric fields. The effective mass approximation is used to calculate the band alignment of the structure. The finite difference method (FDM) is applied to solve the 1D- Schrödinger equation. Intersubband energies and the total optical absorption coefficients (TOACs) and total relative refractive index changes (RRICs) are numerically calculated under the applied external electric field. The structure parameters and applied electric field cause the separation of the energy levels and variation of the dipole moment matrix elements. These separations are responsible for the resonant peak shifts. It is shown that the varied structure parameters and external electric field cause red or blue shifts in the resonant peak position of TOAC and RRIC coefficients.

Super-Resolution Displacement Spectroscopic Sensing over a Surface "Rainbow".

Subwavelength manipulation of light waves with high precision can enable new and exciting applications in spectroscopy, sensing, and medical imaging. For these applications, miniaturized spectrometers are desirable to enable the on-chip analysis of spectral information. In particular, for imaging-based spectroscopic sensing mechanisms, the key challenge is to determine the spatial-shift information accurately (i.e., the spatial displacement introduced by wavelength shift or biological or chemical surface binding), which is similar to the challenge presented by super-resolution imaging. Here, we report a unique "rainbow" trapping metasurface for on-chip spectrometers and sensors. Combined with super-resolution image processing, the low-setting 4× optical microscope system resolves a displacement of the resonant position within 35 nm on the plasmonic rainbow trapping metasurface with a tiny area as small as 0.002 mm2. This unique feature of the spatial manipulation of efficiently coupled rainbow plasmonic resonances reveals a new platform for miniaturized on-chip spectroscopic analysis with a spectral resolution of 0.032 nm in wavelength shift. Using this low-setting 4× microscope imaging system, we demonstrate a biosensing resolution of 1.92 × 109 exosomes per milliliter for A549-derived exosomes and distinguish between patient samples and healthy controls using exosomal epidermal growth factor receptor (EGFR) expression values, thereby demonstrating a new on-chip sensing system for personalized accurate bio/chemical sensing applications.