Search Results (887)

Ultrafast spin dynamics is a core research focus for advancing ultrafast spintronic devices, yet its accurate quantitative probing remains a challenge with conventional time-resolved techniques. Herein, we employ double-pump optical pump–terahertz emission spectroscopy (OPTE) to investigate the ultrafast spin dynamics of a Pt/Gd₁₉(Co_0.8Fe_0.2)₈₁/Ta ferrimagnetic rare-earth–transition-metal heterostructure. Experimental measurements resolve a single-step ultrafast demagnetization process with a characteristic time of ~0.42 ± 0.02 ps, followed by two-stage magnetic recovery involving a fast relaxation and a slow relaxation process. The fast and slow recovery time constants show a distinct positive dependence on the control pump fluence, increasing from 2.49 ± 0.11 ps to 3.28 ± 0.03 ps and 57.36 ± 11.28 ps to 164.96 ± 1.61 ps, respectively, as the pump fluence rises from 0.80 to 1.19 mJ/cm². The ~0.42 ps demagnetization timescale is consistent with that of 3d transition metals, indicating the transient magnetic response of the low-Gd-concentration heterostructure is dominated by the CoFe sublattice. Our findings validate that OPTE is an effective approach for the quantitative characterization of electron–lattice–spin coupling processes in spin-based heterostructures and provide critical experimental insights for controllable manipulation of ultrafast spin dynamics, laying a foundation for the design of ultrafast terahertz spintronic devices. Full article

Spin-exchange relaxation-free (SERF) atomic magnetometers have emerged as highly promising candidates for ultra-weak magnetic field detection, particularly in biomagnetic imaging, owing to their exceptional sensitivity, amenability to miniaturization, and near-room-temperature operation. While current miniaturized magnetometers typically employ laser chips with fixed optical power, the quantitative impact of laser power on critical performance metrics remains to be fully elucidated. This study systematically investigates the influence of laser power on sensitivity, bandwidth, and dynamic range by incorporating considerations of power broadening, saturation absorption, and noise constraints. A miniaturized probe, integrated with an actively controlled vertical-cavity surface-emitting laser (VCSEL), was developed for experimental validation. Theoretical and experimental results consistently demonstrate that as optical power increases, sensitivity exhibits a non-monotonic dependence, whereas both bandwidth and dynamic range manifest a monotonic upward trend, aligning well with theoretical simulations. The optimized sensor achieved a peak sensitivity of 16 fT/√Hz at 300 μW, while the bandwidth and dynamic range reached 230 Hz and ±5.4 nT at 500 μW, respectively. This work establishes a robust theoretical and experimental framework for the comprehensive performance optimization of laser-integrated miniaturized atomic magnetometers. Full article

In this work, a comprehensive first-principles investigation of the electronic, magnetic, and optical properties of pristine and Fe-, Co-, and Ni-doped MoS₂ monolayers is presented within the framework of density functional theory. Substitutional transition-metal doping at the Mo site is shown to induce spin-polarized impurity states within the pristine band gap, leading to significant modifications of the electronic structure, including metallic, semimetallic, or half-metallic behavior depending on the dopant species. The calculated spin-resolved band structures and projected density of states reveal a strong hybridization between the dopant $3d$ orbitals and the Mo-$4d$/S-$3p$ states, giving rise to sizable magnetic moments and dopant-dependent exchange splitting. When spin–orbit coupling is included, the combined effect of exchange interactions and relativistic effects leads to an effective valley splitting at the K and $K^{\prime }$ points, whose magnitude and sign depend sensitively on the chemical nature of the dopant. Optical properties are analyzed within a linear-response framework, showing pronounced dopant-induced modifications of the optical spectra. While the pristine monolayer exhibits well-defined excitonic features, transition-metal substitution introduces low-energy optical transitions associated with impurity-related states. Consequently, the exciton binding energies estimated from the difference between the electronic and optical gaps are interpreted as effective measures of dopant-induced perturbations to optical transitions, rather than as quantitative many-body excitonic binding energies in the strict sense. These results provide microscopic insight into the interplay between magnetism, spin–orbit coupling, and optical response in doped MoS₂ monolayers, highlighting the potential of transition-metal substitution as a route to engineer spin- and valley-dependent phenomena in two-dimensional materials. Full article

The technological promise of nonlinear optical (NLO) compounds has stimulated intense interest in optoelectronic devices, data storage, photonics, and anticancer therapy. Thiosemicarbazone ruthenium materials are of growing interest because of their tunable ligand framework and coordination sphere, allowing fine control over geometry, electronics, and functional properties. Here, we report an N-substituted salicylaldehyde thiosemicarbazone ligand and a series of octahedral Ru(III) complexes bearing triphenylphosphine or triphenylarsine and halide (Cl, Br) co-ligands. The complexes were characterized by elemental analysis, FT-IR, UV–Vis, EPR, mass spectrometry, and magnetic susceptibility measurements, which together confirm NS-chelation to a low-spin Ru(III) center in a distorted octahedral environment. Their photophysical and NLO responses were assessed by UV–Vis spectroscopy and powder second-harmonic generation measurements (Kurtz–Perry method), revealing promising NLO behavior. In parallel, antioxidant activity and in vitro anticancer effects against HeLa cells were evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical-scavenging and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cytotoxicity assays. These results provide insight into ligand-controlled structure–activity relationships, in which the halide (Cl/Br) and ancillary triarylphosphine co-ligands regulate electronic interactions and lipophilicity and ultimately increase biological performance, underscoring the dual materials and medicinal potential of these Ru(III) complexes. Full article

To overcome the physical constraints during the miniaturization of conventional semiconductor devices, spintronics is playing an increasingly prominent role. The Rashba effect, characterized by spin–momentum locking, has emerged as a promising solution to address challenges. Two-dimensional (2D) Janus transition metal dichalcogenides (TMDCs) break spatial inversion symmetry, creating favorable conditions for the Rashba effect. Based on first-principles calculations, 2D Janus materials XMoYZ₂ (X = S/Se/Te; Y = Si/Ge; Z = N/P) were investigated, with strain, external electric field and charge doping employed to modulate the Rashba effect. The strain results reveal that the Rashba constants of XMoYZ₂ increase significantly with compressive strain. Specifically, after applying uniaxial strain, the Rashba constant of TeMoSiP₂ is enhanced to ~2.2 times its initial value. Compressive strain reduces atomic spacing, enhances orbital overlap, and increases spin–orbit coupling (SOC) strength. All the TeMoYZ₂ materials exhibit significant anisotropy under uniaxial strain, which is favorable for spin-oriented transport. SeMoGeP₂ shows an almost linear Rashba constant–electric field correlation, while TeMoGeP₂ and TeMoSiP₂ show non-monotonic variation. The Rashba constant of TeMoSiP₂ can be enhanced to ~2.7 times its intrinsic value under either positive or negative applied electric fields. Charge doping induces negligible changes in the SOC effect. Finally, the optical absorption properties of TeMoGeP₂, TeMoSiN₂, and TeMoSiP₂ were investigated. This study clarifies the mechanism underlying the enhancement of Rashba constants in XMoYZ₂ materials, enriching the research landscape of spintronics. Full article

Ceramic-polymer nanocomposites combine the respective advantages of ceramics and polymers, boasting superior mechanical flexibility, thermal stability, optical transparency, and electrical conductivity, enabling their wide use in cutting-edge fields like medicine, aerospace, optoelectronic devices, and energy storage components. Notably, ceramic-polymer nanocomposites are a promising, widely recognized strategy for developing high-energy-density, low-dielectric-loss, and flexible capacitors, due to the ceramic phase’s intrinsic high dielectric constant, which enhances dielectric capability, and the polymer phase’s high breakdown strength and mechanical flexibility. Ultimately, ceramic-polymer nanocomposites can reach an optimal dielectric performance. In this study, polyvinylidene fluoride (PVDF) was used as the matrix material and barium titanate (BaTiO₃) as the reinforcing phase within the composite structure. The BaTiO₃ ceramic particles were incorporated into PVDF via spin-coating technology, with composite formulations prepared at different concentrations (0.5 wt%, 1.0 wt%, 1.5 wt%, 2.0 wt%, 2.5 wt%, 3.0 wt%). A series of key parameters were measured and compared, such as the dielectric constant, breakdown strength, and energy storage density, of the BT/PVDF nanocomposite. The results indicated that the BT/PVDF nanocomposite with the optimal low BaTiO₃ content demonstrates remarkable performance, achieving a breakdown strength (E_b) of 500 MV/m and an effective energy storage density of 15.5 J/cm³. This represents an improvement over conventional uniformly high-filler films. Full article

We investigate the optical response properties of an atom-assisted spinning optomechanical system, in which a spinning optical resonator is coupled simultaneously to a two-level atomic ensemble and a mechanical resonator driven by a weak pump field. Remarkably, we demonstrate that by simply reversing the rotation direction, the system can be switched between a low-absorption electromagnetic and optomechanically induced transparency state and a high-absorption state, constituting a form of non-reciprocal optical control at the quantum level. Furthermore, by tuning the phase difference between the mechanical pump and the probe field, direction-dependent switching between absorption and gain is achieved. These non-reciprocal effects originate from the Sagnac-induced frequency shift in the optical mode, which leads to distinct optomechanical and atom–cavity couplings for opposite spinning directions. We also show that the absorption spectrum can be modulated by the angular velocity and the atomic number. Our results indicate that the optical properties of the hybrid system can be manipulated via the angular velocity, phase difference, and atom number, with potential applications in chiral photonic communications. Full article

The photocatalytic efficacy of metallic silver nanoparticle/zinc oxide (Ag-NPs/ZnO) composite thin films, COMP-Ag_x, with varying silver concentrations (0 mol% ≤ x ≤ 100 mol%), is investigated for the degradation of methyl orange (MO). The films were spin-coated on a silica glass surface at 600 °C utilizing the molecular precursor method (MPM). The XRD spectra of these composite thin films revealed three significant peaks corresponding to the diffraction planes of (0 0 2), (1 0 0), and (1 0 1), indicative of the formation of ZnO crystallites in diverse orientations, in conjunction with an additional signal for cubic Ag crystals. The magnitude of the ZnO peaks diminishes as the mol% of silver increases. The images from the SEM confirm the integration of Ag-NPs into the ZnO matrix. The UV/Vis absorption spectra exhibit a 410 nm surface plasmon resonance (SPR) peak for composite Ag-NP/ZnO thin films. The absorption spectra of ZnO and Ag-NP/ZnO composite thin films demonstrate the band gap of ZnO to be 3.4 eV, while the band gaps of the composite thin films nearly approximate that of ZnO. The decomposition rates of the MO solution indicate that composite thin films function effectively under visible irradiation compared to pure ZnO. The optical properties indicated that the SPR of Ag-NPs contributed to the visible responsiveness of the composite thin films. The SPR demonstrate significant visible light responsiveness and essential characteristics during photoexcited electron transfer from the Ag-NPs to the ZnO conduction band. Full article

Dental wear provides valuable evidence for reconstructing past human behaviour, including diet abrasiveness and non-masticatory activities such as the use of teeth as a “third hand”. This study investigates activity-induced dental modifications (AIDMs) in two adult human skeletons recovered from a 15th–19th-century necropolis at the St. Athanasius Church in Niculițel (Tulcea County, Romania). Dental remains and associated dental calculus were examined using low- and high-magnification optical microscopy and scanning electron microscopy (SEM). Well-polished grooves with parallel striations were identified on the incisor crowns, consistent with repetitive extra-masticatory activities related to fibre drafting during spinning and textile production. Dental calculus analysis revealed the presence of plant and animal fibres, providing direct micro-contextual evidence for textile-related practices. These results offer new insights into the use of teeth as tools and contribute to the reconstruction of textile-related craft activities during the Ottoman and early modern periods in southeastern Europe. Full article

We reviewand update schemes for different measurements using STA-mediated guided interferometry with a single trapped particle. STA stands for “shortcuts to adiabaticity”, a set of techniques to achieve the results of adiabatic dynamics in shorter times. In the first scheme we presented a protocol aimed at detecting weak unknown forces. It consisted of a single ion trapped in a harmonic potential and driven by time-and-spin-dependent forces generated via off-resonant lasers. Our approach provided stability and the independence of the results on the motional states for the small-oscillations regime. We could, also, design faster-than-adiabatic processes with sensitivity control. However, it required a rotation of the trapping potential at the moment the experiment starts. A much more practical and broadly applicable design was then developed, where no rotation is involved. Here, a single atom is driven by two moving spin-dependent trapping potentials where we guide the arms of the interferometer via shortcuts to adiabatic paths. In this paper, in addition to a brief review of these two previous proposals, we revisit the first scheme and present a new protocol where the spin-dependent driving force is generated via a “shaken” optical lattice. This opens the possibility for additional interferometric measurements beyond an unknown force, for example, the mass of the trapped ion, while still preserving the advantages of the previously proposed method. Full article

This work investigates the use of two photoactive polymers, functionalized with quantum dots (QDs) (ZnS and CdTe/ZnS), to develop optical sensing hydrogel films through their interactions. It examines their responses to light stimulation for potential biological applications. The optical and morphological properties of the films were studied, revealing photoactive surfaces. The photoactive copolymers were synthesized based on poly(maleic anhydride-alt-2-methyl-2-butene), P(MAn-alt-2MB), and poly(maleic anhydride-alt-1-octadecene), P(MAn-alt-OD), by attaching the photochromic agent, 1-(2-hydroxyethyl)-3,3-dimethylindoline-6-nitrobenzo pyran (SP). Subsequently, QD nanoparticles (ZnS or CdTe/ZnS NPs) were incorporated into the polymer solutions in the presence of a crosslinker agent, and were then spin-coated onto glass substrates under suitable conditions to produce porous-patterned films. These films were created using a one-step bio-inspired process called the breath figure (BF) method. SEM images of QD-containing samples show a photoactive porous surface resulting from a synergistic interaction between the components. The reversibility of these macroscopic properties results from photoinduced transformations at the molecular level. The light-emitting properties of the films were characterized by blue and violet fluorescence under UV light. Advances in film-forming techniques enable the creation of functional structures with important applications, such as microstructured hydrogel films for biological uses. Full article

ZnO and ZnO:5%B nanoparticles produced by sol–gel synthesis exhibit a single-phase wurtzite structure. X-ray diffraction (XRD) investigation reveals crystallite sizes in the range of $32.37–39.63$ nm and microstrain values on the order of $(1.98–8.03)\times {10}^{-4}$, despite the Uniform Stress Deformation Model (USDM) indicating the presence of considerable tensile stress. Significant band-tail states are introduced via boron doping, resulting in Urbach energies ranging from $110$ to $193$ meV and a narrowed optical band gap of $3.216$ eV. With a refractive index range of $2.05–2.71$, the material exhibits tunable optical characteristics. Violet and blue emissions originating predominantly from zinc interstitials (Znᵢ) and zinc vacancies (V_Zn) dominate the photoluminescence spectra, while oxygen interstitial-related contributions remain relatively weak. A high spin density is confirmed by electron spin resonance measurements, which reveal a strong defect-related signal at $g\approx 2.294$. The formation of Znᵢ/V_Zn defect centers due to charge compensation and ionic size mismatch induced by B³⁺ substitution for Zn²⁺ significantly modifies the band-edge states and optical constants. These defect-engineered properties render the material promising for applications in ultraviolet (UV) photodetectors, transparent conducting oxides, and electron transport layers in organic photovoltaic devices. Full article

We report the development of a high-power, cost-effective, and rapidly tunable laser system optimized for rubidium optical pumping in spin-exchange optical pumping (SEOP) applications. The system combines a spectrally narrowed diode laser bar with a low-cost yet high-stability thermal-management architecture based on consumer-grade CPU liquid-cooling components. Wavelength narrowing and fast tuning are achieved by linearly translating a chirped volume Bragg grating (CVBG), providing mode-hop-free, continuous wavelength control without relying on slow thermal tuning mechanisms. Long-term wavelength stability is ensured through a terminal proportional–integral–derivative (PID) feedback loop that locks the laser directly to the rubidium absorption spectrum in the pumping cell, rather than to an internal reference. Operating near 795 nm, the laser delivers up to 40 W of optical power with a measured linewidth of approximately 0.15 nm. The system supports rapid wavelength agility over a continuous tuning range of $794.73\pm 0.24$ nm and exhibits stable spectral performance during extended operation. Owing to its compact design, fast response, and substantially lower cost than conventional volume-grating-based systems, this laser architecture provides a practical and scalable solution for SEOP and other precision atomic and spectroscopic applications that require high power, a narrow linewidth, and robust wavelength stability. Full article

In this study, the synergistic effects of Fe doping and oxygen vacancies on the structural, electronic, and optical properties of Bi₄O₅Br₂, as well as their influence on the photocatalytic CO₂ reduction mechanism, were systematically explored through first-principles calculations. The results reveal that Fe-doped, oxygen-defective, and Fe–Vo co-modified Bi₄O₅Br₂ systems exhibit excellent thermodynamic and dynamic stability. Oxygen vacancies introduce defect states near the Fermi level, narrowing the band gap and enhancing charge localization and CO₂ adsorption, while Fe doping induces strong spin polarization and introduces Fe 3d impurity levels that effectively couple with O 2p orbitals, promoting charge transfer and visible-light absorption. The coexistence of Fe dopants and oxygen vacancies produces a significant synergistic effect, forming a continuous energy-level bridge that enhances charge separation and broadens the light absorption range. Gibbs free energy analyses further demonstrate that the Fe–Vo–BOB system exhibits the lowest energy barriers and the most favorable thermodynamics for CO₂-to-CO conversion. This study provides deep insight into the defect–dopant synergy in Bi₄O₅Br₂ and offers valuable theoretical guidance for engineering highly efficient visible-light-driven photocatalysts in solar energy conversion and environmental remediation. Full article

Interfacial coupling between CoFe₂O₄ (CFO) nanoparticles and oxidatively functionalized multi-walled carbon nanotubes (MWCNTs) enables controlled modulation of structural, optical, and spin dynamic properties in CFO–MWCNT nanocomposites. The solvothermal synthesis promotes nucleation of CFO on –COOH/–OH functional groups, ensuring uniform anchoring along the nanotube surface. X-ray diffraction confirms a cubic spinel phase with lattice expansion from 8.385 Å to 8.410 Å and crystallite growth from 18 nm to 25 nm, reflecting strain transfer and partial nanoparticle coalescence at the carbon interface. The observed bandgap narrowing from 2.72 eV to 2.50 eV, confirmed via Tauc plot analysis, is attributed to localized defect states induced by charge delocalization and orbital hybridization at the interface of the CFO–MWCNT boundary. DC magnetometry reveals a reduction in saturation magnetization from 46 emu/g to 35 emu/g due to diamagnetic dilution and interfacial spin canting, while coercivity decreases from 852 Oe to 841 Oe, indicating modified pinning and domain-wall dynamics associated with exchange-coupled interfaces. Ferromagnetic resonance measurements show a resonance field shift from 3495 G to 3500 G and an increase in the Landé g-factor from 1.97 to 2.00, signifying altered spin–orbit coupling and enhanced local magnetic perturbations. The spin–lattice relaxation time increases from 1.41 ns to 1.59 ns, demonstrating suppressed phonon-mediated relaxation and improved spin coherence across the hybrid network. Spin density rises from 3.72 × 10²² to 4.58 × 10²² spins/g, confirming an increase in unpaired electrons generated by orbital asymmetry at the interface. The anisotropy field and effective magnetocrystalline anisotropy constant exhibit pronounced modulation, evidencing strengthened exchange stiffness and altered Co²⁺/Fe³⁺ superexchange pathways. These results establish CFO-MWCNT nanocomposites as tuneable platforms for spintronic logic elements, high-frequency microwave attenuation, and magneto-optical device architectures. Full article