Search Results (44)

We provide an approach to detect a nitrogen-vacancy (NV) center, which might be a defect in a diamond nanomembrane, using a dual-coupling optomechanical system. The NV center modifies the energy-level structure of a dual-coupling optomechanical system through dressed states arising from its interaction with the mechanical membrane. Thus, we study the photon blockade in the cavity of a dual-coupling optomechanical system in which an NV center is embedded in a single-crystal diamond nanomembrane. The NV center significantly influences the statistical properties of the cavity field. We systematically investigate how three key NV center parameters affect photon blockade: (i) its coupling strength to the mechanical membrane, (ii) transition frequency, and (iii) decay rate. We find that the NV center can shift, give rise to a new dip, and even suppress the original dip in a bare quadratic optomechanical system. In addition, we can amplify the effect of the NV center on photon statistics by adding a gravitational potential when the NV center has little effect on photon blockade. Therefore, our study provides a method to detect diamond nanomembrane defects in a dual-coupling optomechanical system. Full article

This article presents a comprehensive overview of recent advancements in photonic crystal fiber (PCF)-based sensors, with a particular focus on the surface plasmon resonance (SPR) phenomenon for biosensing. With their ability to modify core and cladding structures, PCFs offer exceptional control over light guidance, dispersion management, and light confinement, making them highly suitable for applications in refractive index (RI) sensing, biomedical imaging, and nonlinear optical phenomena such as fiber tapering and supercontinuum generation. SPR is a highly sensitive optical phenomenon, which is widely integrated with PCFs to enhance detection performance through strong plasmonic interactions at metal–dielectric interfaces. The combination of PCF and SPR technologies has led to the development of innovative sensor geometries, including D-shaped fibers, slotted-air-hole structures, and internal external metal coatings, each optimized for specific sensing goals. These PCF-SPR-based sensors have shown promising results in detecting biomolecular targets such as excess cholesterol, glucose, cancer cells, DNA, and proteins. Furthermore, this review provides an in-depth analysis of key design parameters, plasmonic materials, and sensor models used in PCF-SPR configurations, highlighting their comparative performance metrics and application prospects in medical diagnostics, environmental monitoring, and chemical analysis. Thus, an exhaustive analysis of various sensing parameters, plasmonic materials, and sensor models used in PCF-SPR sensors is presented and explored in this article. Full article

(1) Background: DNA damage is of great importance in the understanding of the effects of ionizing radiation. Various types of DNA damage can result from exposure to ionizing radiation, with clustered types considered the most important for radiobiological effects. (2) Methods: The code RITRACKS (Relativistic Ion Tracks), a program that simulates stochastic radiation track structures, was used to simulate DNA damage by photons and ions spanning a broad range of linear energy transfer (LET) values. To perform these simulations, the transport code was modified to include cross sections for the interactions of ions or electrons with DNA and amino acids for ionizations, dissociative electron attachment, and elastic collisions. The radiochemistry simulations were performed using a step-by-step algorithm that follows the evolution of all particles in time, including reactions between radicals and DNA structures and amino acids. Furthermore, detailed DNA damage events, such as base pair positions, DNA fragment lengths, and fragment yields, were recorded. (3) Results: We report simulation results using photons and the ions ¹H⁺, ⁴He²⁺, ¹²C⁶⁺, ¹⁶O⁸⁺, and ⁵⁶Fe²⁶⁺ at various energies, covering LET values from 0.3 to 164 keV/µm, and performed a comparison with other codes and experimental results. The results show evidence of DNA protection from damage at its points of contacts with histone proteins. (4) Conclusions: RITRACKS can provide a framework for studying DNA damage from a variety of ionizing radiation sources with detailed representations of DNA at the atomic scale, DNA-associated proteins, and resulting DNA damage events and statistics, enabling a broader range of future comparisons with experiments such as those based on DNA sequencing. Full article

To revolutionize the photochemical efficiency of quantum dots sensitized solar cells (QDSSCs) devices, herein, a passivation of the cells with multilayer material has been developed for heterojunctions TiO₂/NiS/MnS/HI-30/Pt devices. In this study, NiS and MnS were deposited on a photoanode for the first time as passivated photon absorbers at room temperature. The adoption of NiS as a passisvative layer could tailor the active surface area and improve the photochemical properties of the newly modified cells. The vibrational shifts obtained from the Raman spectra imply that the energy change is influenced by the surface effect, giving rise to better electronic conductivity. The electrochemical stability and durability test for the N/M-3 device slows down and remains at 8.88% of its initial current after 3500 s, as compared to the N/M-1 device at 7.20%. The disparity in charge recombination implies that both the outer and inner parts of the nanoporous material are involved in the photogeneration reaction. The hybridized N/M-3 cell device reveals the highest current density with a low potential onset, indicating that power conversion occurs more easily because photons tend to be adsorbed easily on the surface of the MnS. The Nyquist plot for N/M-1 and N/M-3 promotes the faster transport of electrolytic ions across the TiO₂/NiS/MnS, providing a good interaction for the electrolyte. The I-J Value of 9.94% shows that the passivation with the NiS layer promotes electron transport and enhances the performance of the modified cells. The passivation of the TiO₂ layer with NiS attains a better power conversion efficiency among the scant studies so far on the surface passivation of QDSCs. Full article

Investigation of chiroptical polymers in the solution phase is paramount for designing supramolecular architectures for photonic or biomedical devices. This work is devoted to the case study of poly(propylene oxide) (PPO) optical activity in several solvents: benzonitrile, carbon disulfide, chloroform, ethyl acetate, and p-dioxane. To attain information on the interactions in these systems, rheological testing was undertaken, showing distinct variations of the rheological parameters as a function of the solvent type. These aspects are also reflected in the refractive index dispersive behavior, from which linear and non-linear optical properties are extracted. To determine the circular birefringence and specific rotation of the PPO solutions, the alternative method of the channeled spectra was employed. The spectral data were correlated with the molecular modeling of the PPO structural unit in the selected solvents. Density functional theory (DFT) computational data indicated that the torsional potential energy—related to the O1-C2-C3-O4 dihedral angle from the polymer repeating unit—was hindered in solvation environments characterized by high polarity and the ability to interact via hydrogen bonding. This was in agreement with the optical characterization of the samples, which indicated a lower circular birefringence and specific rotation for the solutions of PPO in ethyl acetate and p-dioxane. Also, the shape of optical rotatory dispersion curves was slightly modified for PPO in these solvents compared with the other ones. Full article

We investigate the impact of asymmetric fermionic dark matter (DM) on the thermal evolution of neutron stars (NSs), considering a scenario where DM interacts with baryonic matter (BM) through gravity. Employing the two-fluid formalism, our analysis reveals that DM accrued within the NS core exerts an inward gravitational pull on the outer layers composed of BM. This gravitational interaction results in a noticeable increase in baryonic density within the core of the NS. Consequently, it strongly affects the star’s thermal evolution by triggering the early onsets of the direct Urca (DU) processes, causing enhanced neutrino emission and rapid star cooling. Moreover, the photon emission from the star’s surface is modified due to a reduction in radius. We demonstrate the effect of DM gravitational pull on nucleonic and hyperonic DU processes that become kinematically allowed even for NSs of low mass. We then discuss the significance of observing NSs at various distances from the Galactic center. Given that the DM distribution peaks toward the Galactic center, NSs within this central region are expected to harbor higher fractions of DM, potentially leading to distinct cooling behaviors. Full article

One aim of personalized medicine is to use continuous or on-demand monitoring of metabolites to adjust prescription dosages in real time. Surface-enhanced spatially offset Raman spectroscopy (SESORS) is an optical technique capable of detecting surface-enhanced Raman spectroscopy (SERS)-active targets under a barrier, which may enable frequent metabolite monitoring. Here we investigate how the intensity of the signal from SERS-active material varies spatially through tissue, both experimentally and in a computational model. Implant-sized, SERS-active hydrogel was placed under different thicknesses of contiguous tissue. Emission spectra were collected at the air-tissue boundary over a range of offsets from the excitation site. New features were added to the Monte Carlo light-tissue interaction model to modify the optical properties after inelastic scattering and to calculate the distribution of photons as they exit the model. The Raman signals were detectable through all barrier thicknesses, with strongest emission for the case of 0 mm offset between the excitation and detector. A steep decline in the signal intensities occurred for offsets greater than 2 mm. These results did not match published SORS work (where targets were much larger than an implant). However, the model and experimental results agree in showing the greatest intensities at 0 mm offset and a steep gradient in the intensities with increasing offset. Also, the model showed an increase in the number of photons when the new, longer wavelengths were used following the Stokes shift for scattering and the graphical display of the exiting photons was helpful in the determination and confirmation of the optimal offset. Full article

Radiation has become an essential part in medicine and researchers are constituently investigating radiation shielding materials that are suitable for different medical applications. Glass, due to its properties, has been considered an excellent radiation shield for such applications. One of the most common glasses used as a radiation shield is the ZnO-Bi₂O₃-B₂O₃-SiO₂ anti-radiation glass. Heavy metal oxides have many desirable properties such as high density, transparency to visible light, stability in air and water, high interaction cross section, high infrared transparency, and good absorption of radiation, which make them desirable to be used as modifiers with anti-radiation glass. Research has been focusing on environmentally friendly shielding material which leads to non-lead modifiers such as Na₂O, Al₂O₃, MgO, TiO₂, SrO, Sb₂O₃, and BaO, which have become more desired than PbO. So far, ZnO-Bi₂O₃-B₂O₃-SiO₂’s photon shielding properties have been studied experimentally with the addition of BaO at certain energies only. In this work, different heavy metal oxides are added as modifiers to ZnO-Bi₂O₃-B₂O₃-SiO₂ glass in order to investigate theoretically their effects on the shielding properties of the glass at a wide range of photon and neutron energies. Simulation is cost- and time-effective when it comes to investigating different compositions of glass and different modifiers with different weight percentages at any energy range for any type of radiation. Simulation could be considered the first step in order to identify the best mixture with the best weight fractions prior to any experimental investigations of other desired properties based on the needed application. In this work, the photon- and neutron-shielding capabilities of the ZnO-Bi₂O₃-B₂O₃-SiO₂ anti-radiation glass is investigated with different weight fractions of heavy metal oxides at wide photon and neutron energy ranges. Geant4, which is a Monte Carlo-based powerful toolkit, is used to find the mass attenuation coefficients (µm) of photons, as well as the effective removal cross sections (ΣR) of neutrons, of all the investigated samples in the studied energy range. Full article

We propose and demonstrate dendrimer-based coatings for a sensitive biochip surface that enhance the high-performance sorption of small molecules (i.e., biomolecules with low molecular weights) and the sensitivity of a label-free, real-time photonic crystal surface mode (PC SM) biosensor. Biomolecule sorption is detected by measuring changes in the parameters of optical modes on the surface of a photonic crystal (PC). We describe the step-by-step biochip fabrication process. Using oligonucleotides as small molecules and PC SM visualization in a microfluidic mode, we show that the PAMAM (poly-amidoamine)-modified chip’s sorption efficiency is almost 14 times higher than that of the planar aminosilane layer and 5 times higher than the 3D epoxy-dextran matrix. The results obtained demonstrate a promising direction for further development of the dendrimer-based PC SM sensor method as an advanced label-free microfluidic tool for detecting biomolecule interactions. Current label-free methods for small biomolecule detection, such as surface plasmon resonance (SPR), have a detection limit down to pM. In this work, we achieved for a PC SM biosensor a Limit of Quantitation of up to 70 fM, which is comparable with the best label-using methods without their inherent disadvantages, such as changes in molecular activity caused by labeling. Full article

An electromagnetic (EM) wave is a form of continuous energy, of which both the frequency and the amplitude are parts, as shown in a recent report. All the facts relating to the photoelectric effect are explained by the new modified EM wave concept. Since the photon concept is not able to explain the intensity effect and the ejection direction clearly, it cannot be used to explain nonlinear optical phenomena clearly. The current understanding of the interaction process between orbital electrons and light may not be realistic. In this work, the electron transition process is explained with the new modified EM wave concept. The orbital electrons of a material rotate circularly by the sinusoidal fields of the EM waves. In this way, the electrons absorb light energy as rotational kinetic energy. During the first rotational cycle, the electrons with large enough radii face different potential barriers in neighboring orbits. Consequently, the electrons’ speed is obstructed, and the electrons move behind their natural places (phase); in other words, the electrons cannot follow the required phase of EM waves. Thus, sufficient energetic electrons are scattered from their orbit. The high-intensity EM waves reach the inner orbits of the targeted atom and transit electrons from different orbits. The light can regenerate through processes with different frequencies. The frequency of the regenerated light can be higher than that of primary light, depending on the energy (frequency and amplitude) of the primary light. The results of previous reports match the prediction of the new concept of EM waves. The new wave concept may be able to explain all photonic behaviors of light clearly. Full article

The development of a highly efficient, visible-light responsive catalyst for environment purification has been a long-standing exploit, with obstacles to overcome, including inefficient capture of near-infrared photons, undesirable recombination of photo-generated carriers, and insufficient accessible reaction sites. Hence, novel carbon quantum dots (CQDs) modified PbBiO₂I photocatalyst were synthesized for the first time through an in-situ ionic liquid-induced method. The bridging function of 1-butyl-3-methylimidazolium iodide ([Bmim]I) guarantees the even dispersion of CQDs around PbBiO₂I surface, for synchronically overcoming the above drawbacks and markedly promoting the degradation efficiency of organic contaminants: (i) CQDs decoration harness solar photons in the near-infrared region; (ii) particular delocalized conjugated construction of CQDs strength via the utilization of photo-induced carriers; (iii) π–π interactions increase the contact between catalyst and organic molecules. Benefiting from these distinguished features, the optimized CQDs/PbBiO₂I nanocomposite displays significantly enhanced photocatalytic performance towards the elimination of rhodamine B and ciprofloxacin under visible/near-infrared light irradiation. The spin-trapping ESR analysis demonstrates that CQDs modification can boost the concentration of reactive oxygen species (O₂^•−). Combined with radicals trapping tests, valence-band spectra, and Mott–Schottky results, a possible photocatalytic mechanism is proposed. This work establishes a significant milestone in constructing CQDs-modified, bismuth-based catalysts for solar energy conversion applications. Full article

Background: In addition to their great optical properties, nanodiamonds (NDs) have recently proved useful for two-photon-excited photodynamic therapy (TPE-PDT) applications. Indeed, they are able to produce reactive oxygen species (ROS) directly upon two-photon excitation but not with one-photon excitation; Methods: Fluorescent NDs (FNDs) with a 100 nm diameter and detonation NDs (DNDs) of 30 nm were compared. In order to use the gems for cancer-cell theranostics, they were encapsulated in a bis(triethoxysilyl)ethylene-based (ENE) periodic mesoporous organosilica (PMO) shell, and the surface of the formed nanoparticles (NPs) was modified by the direct grafting of polyethylene glycol (PEG) and amino groups using PEG-hexyltriethoxysilane and aminoundecyltriethoxysilane during the sol–gel process. The NPs’ phototoxicity and interaction with MDA-MB-231 breast cancer cells were evaluated afterwards; Results: Transmission electronic microscopy images showed the formation of core–shell NPs. Infrared spectra and zeta-potential measurements confirmed the grafting of PEG and NH₂ groups. The encapsulation of the NDs allowed for the imaging of cancer cells with NDs and for the performance of TPE-PDT of MDA-MB-231 cancer cells with significant mortality. Conclusions: Multifunctional ND@PMO core–shell nanosystems were successfully prepared. The NPs demonstrated high biocompatibility and TPE-PDT efficiency in vitro in the cancer cell model. Such systems hold good potential for two-photon-excited PDT applications. Full article

Owing to the localized plasmon resonance of an ensemble of interacting plasmonic nanoparticles (NPs), there has been a tremendous drive to conceptualize complex optical nanocircuits with versatile functionalities. In comparison to modern research, there is still not a sufficient level of sophistication to treat the nanostructures as lumped circuits that can be adjusted into complex systems on the basis of a metatronic touchstone. Here, we present the design, assembly, and characterization of single relatively complex photonic nanocircuits by accurately positioning several metallic and dielectric nanoparticles acting as modular lumped elements. In this research, Au NPs along with silica NPs were used to compare the proficiency and precision of our lumped circuit model analytically. On increasing the size of an individual Au NP, the spectral peak resonance not only modifies but also causes more scattering efficiency which increases the fringe capacitance linearly and decreases the nanoinductance of lumped circuit element. The NPs-based assembly induced the required spectral resonance ascribed by simple circuit methods and are depicted to be actively reconfigurable by tuning the direction or polarization of input signals. Our work demonstrates a vital step toward developing the modern modular designing tools of complex electronic circuits into nanophotonic-related applications. Full article

The emission of characteristic lines after X-ray excitation is usually explained as the consequence of two independent and consecutive physical processes: the photoelectric ionization produced by incoming photons and the successive spontaneous atomic relaxation. However, the photoelectric effect is not the only ionization mechanism driven by incoming photons. It has been recently shown that Compton ionization is another possible process that contributes not negligibly to the ionization of the L and M shells. In addition, the secondary electrons from these two interactions, photoelectric and Compton, are also able to ionize the atom by means of so-called impact ionization. Such a contribution has been recently described, showing that it can be relevant in cases of monochromatic excitation for certain lines and elements. A third mechanism of line modification is the so-called self-enhancement produced by absorption of the tail of Lorentzian distribution of the characteristic line, which mainly modifies the shape of the lines but also produces an intensity increase. The four effects contribute to the formation of the characteristic line and must be considered to obtain a precise picture in terms of the shell and the element. This work furnishes a review of these contributions and their formal theoretical descriptions. It gives a complete picture of the photon kernel, describing the emission of characteristic X-rays comprising the main photoelectric contribution and the three effects of lower extent. All four contributions to the characteristic X-ray line must be followed along successive photon interactions to describe multiple scattering using the Boltzmann transport equation for photons. Full article

Ions with multiple inner-shell vacancies frequently arise due to their interaction with different targets, such as (intense) light pulses, atoms, clusters or bulk material. They are formed, in addition, if highly charged ions approach surfaces and capture electrons at rather large distances. To explore the interaction of such hollow ions and their subsequent relaxation, photon spectra in different frequency regions have been measured and compared to calculations. To support these and related measurements, we here show within the framework of the Jena Atomic Calculator (Jac) how (additional) electrons in outer shells modify photon emission and lead to characteristic shifts in the observed spectra. Further, for highly charged Ar ions in KL${}^m(m=1\dots 8)$ configurations, we analyze the mean relaxation time for their stabilization into the different ground configurations. These examples demonstrate how a powerful and flexible toolbox such as Jac will be useful (and necessary) in order to model the photon and electron emission of ions as they occur not only near surfaces but also in astro-, atomic and plasma physics. Full article