Resonance Absorption Research Articles

Low-nuclearity CuZn ensembles on ZnZrOx catalyze methanol synthesis from CO2

Metal promotion could unlock high performance in zinc-zirconium catalysts, ZnZrOx, for CO2 hydrogenation to methanol. Still, with most efforts devoted to costly palladium, the optimal metal choice and necessary atomic-level architecture remain unclear. Herein, we investigate the promotion of ZnZrOx catalysts with small amounts (0.5 mol%) of diverse hydrogenation metals (Re, Co, Au, Ni, Rh, Ag, Ir, Ru, Pt, Pd, and Cu) prepared via a standardized flame spray pyrolysis approach. Cu emerges as the most effective promoter, doubling methanol productivity. Operando X-ray absorption, infrared, and electron paramagnetic resonance spectroscopic analyses and density functional theory simulations reveal that Cu0 species form Zn-rich low-nuclearity CuZn clusters on the ZrO2 surface during reaction, which correlates with the generation of oxygen vacancies in their vicinity. Mechanistic studies demonstrate that this catalytic ensemble promotes the rapid hydrogenation of intermediate formate into methanol while effectively suppressing CO production, showcasing the potential of low-nuclearity metal ensembles in CO2-based methanol synthesis.

Optical design and bandgap engineering in ultrathin multiple quantum well solar cell featuring photonic nanocavity

AbstractUltrathin solar cells are efficient and captivating devices with unique technological and scientific features in terms of minimal material consumption, fast fabrication processes, and good compatibility with semi‐transparent applications. Such photovoltaic (PV) technologies can enable effective synergy between optical and electronic confinements with large tuning capabilities of all the optoelectronic characteristics. In this work, the implications of the optical design and the bandgap engineering in ultrathin hydrogenated amorphous Si/Ge multiple quantum well (MQW) solar cells featuring photonic nanocavity are analyzed based on experimental measurements and optoelectronic modelling. By changing the period thicknesses and the positions of QWs inside the deep‐subwavelength nanophotonic resonator, the spatial and spectral distributions of the optical field and the local absorption are strongly affected. This leads to a modulation of the absorption resonance condition, the absorption edge and the resulting photocurrent outputs. Because of quantum confinement effect, the change of MQW configurations with different individual QW periods while keeping similar total thickness of about 20 nm alters both the bandgap energy and the band offset at the QW/barrier heterojunctions. This in turn controls the photovoltage as well as the carrier collection efficiency in solar cells. The highest open circuit voltage and fill factor values are achieved by employing MQW device configuration with 2.5 nm‐thin QWs. A record efficiency above 5.5% is reached for such emerging ultrathin Si/Ge MQW solar cell technology using thinner QWs with sufficient number, because of the optimum trade‐off between all the optoelectronic characteristic outputs. The presented design rules for opaque ultrathin solar cells with quantum‐confined nanostructures integrated in a photonic nanocavity can be generalized for the engineering of relevant multifunctional semitransparent PV devices.

Smartphone-Integrated resorcinarene macrocycle capped silver nanoparticles (RMF-AgNPs) probe for enhanced La(III) detection in diverse environments

The demand for precise and responsive detection of Lanthanum (La(III)) is critical in key areas such as environmental monitoring, biomedical research, and industrial processes, underscoring the need for advanced sensor technologies. This research reports an efficient and cost-effective preparation of resorcinarene macrocycle framework (RMF) capped silver nanoparticles (RMF-AgNPs). These nanoparticles were then applied as a novel sensor for La(III), demonstrating dual functionality: they act as a colorimetric sensor and a paper-based probe. Unique in its class, the sensor excels in detecting La(III) at ultra-low concentrations, unaffected by other ions, and undergoes a significant color transition from yellow to grey in response to La(III) presence. This change is linked to the localized surface plasmon resonance (LSPR) absorbance alteration. Extensive analytical methods like FTIR, XPS, AFM, FESEM, DLS, Zeta potential, and UV–Vis spectroscopy confirmed that the sensor operates by aggregating nanoparticles induced by La(III). Adding to its practicality, we incorporated a smartphone interface with the paper-based sensor, enhancing its utility for on-the-spot, real-time detection. The sensor's efficacy was validated across various samples, including soil, rock, urine, drinking water, and industrial effluent, showing its versatility. With detection limits of 15 nM (colorimetric) and 280 nM (paper-based), and linear dynamic ranges from 0.05 to 100 µM and 0.5–100 µM respectively, this sensor marks a significant advancement, effectively bridging lab-based detection with field application needs.

High-resolution spectroscopy of liquid water with dispersive atomic vapor prism cell

This article presents an experimental demonstration of a spectroscopic method based on the dispersion of the scattering spectrum from laser-illuminated liquid water collected through a rubidium atomic vapor prism cell. Resonant absorption at 780 nm suppresses Mie/Rayleigh scattering and the steep gradients in refractive index near the 780 nm absorption lines separate Brillouin scattering from Raman scattering in liquid water. The opposing spatial displacements of the Stokes and Anti-Stokes shifted Brillouin peaks yield a measurement of their spectral shifts and thus the temperature or salinity of the water. Performance of the prism cell was mapped with a frequency tunable laser for frequency offsets from the center of the rubidium absorption feature of between −15 GHz and 15 GHz and at rubidium cell temperatures between 148 °C and 177 °C. The experimental results are compared with a numerical model and show good agreement with the scattering peak displacements within experimental uncertainties of probe frequency and cell temperature. In the present configuration, the minimum detectable frequency shift is estimated to be 15.5 MHz. Experiments were conducted in water demonstrating the utility of this method for the measurement of water temperature. Liquid water LiDAR was suggested as one of the possible applications for this method and several ways to improve the experimental setup and cell temperature stability were identified.

Research on noise reduction methods for indoor substations based on resonant sound absorption

Aiming to reduce the impact of substation noise on the lives of surrounding residents, improving the low and middle frequencies acoustic performance of traditional resistive mufflers in indoor substations is significant. The paper is based on the resonance sound absorption mechanism, and for the first time applies multi-frequency resonance noise reduction technology to the research field of indoor substation noise control, proposing a multi-frequency resonant muffling structure. The acoustic performance of the proposed muffler unit is investigated through theoretical and numerical analysis. The measured noise data of the indoor substation is used as sound excitation in the numerical analysis. The results show that at frequencies of 100 Hz, 200 Hz, 300 Hz, 400 Hz, and 500 Hz, the noise in indoor substations is significantly reduced by the multi-frequency resonant muffling structure. The paper provides references for the application of multi-frequency resonant mufflers in the field of noise control of indoor substations.

A four-band coherent perfect absorber of borophene metamaterial operating in the communication band

We propose a coherent perfect absorber based on a borophene metamaterial grating structure. Based on the theoretical analysis of the temporal coupled mode theory and the numerical results of the finite-difference time-domain simulations, the transmission characteristics of the system are investigated. The dynamic tunability of the absorption intensity and resonance wavelength is realized by adjusting the phase difference of the coherent incident beams and carrier density of borophene. Moreover, by optimizing the parameters, the coherent perfect absorption peak (99.99%) is obtained near the wavelength of 1550 nm, that is, the third communication window. Meanwhile, the structure can be operated in ultra-thin gratings as low as 6 nm and angle tolerances as large as 45°, which provides the possibility for applications in highly integrated and wide-angle tolerated devices.

Resonant Absorption of Magnetohydrodynamic Body Modes under Photospheric Conditions

Observations reveal that surface and body modes exist in solar pores under photospheric conditions. While the effects of resonant absorption on photospheric surface modes are well established, its effect on body modes is not known yet. In this paper, we investigate resonant absorption for the body modes under photospheric conditions. We numerically solve the dispersion relation induced by thin boundary approximation and obtain the wave dispersion curves and damping rates of three arbitrarily chosen body modes for sausage and kink waves, respectively. The results show that resonant absorption for the body modes is weaker than for the slow surface modes in both cusp and Alfvén continua. The damping behavior of body modes is similar to slow surface modes while the higher body mode has stronger resonant absorption.

Horizontally polarized kink oscillations supported by solar coronal loops in an asymmetric environment

Context. Kink oscillations are ubiquitously observed in solar coronal loops, and understanding them is crucial in the contexts of coronal seismology and atmospheric heating. Aims. We studied kink modes supported by a straight coronal loop embedded in an asymmetric environment using 3D magnetohydrodynamic simulations. Methods. We implemented the asymmetric effect by setting different exterior densities below and above the loop interior and initiated the simulation using a kink-like velocity perturbation perpendicular to the loop plane, mimicking the frequently measured horizontally polarized kink modes. Results. We find that the external velocity fields show fan-blade structures propagating in the azimuthal direction as a result of the successive excitation of higher azimuthal Fourier modes. Resonant absorption and phase-mixing can still occur despite an asymmetric environment, leading to the development of small-scale structures at loop boundaries. These small-scale structures nonetheless develop asymmetrically at the upper and lower boundaries due to the different gradients of the Alfvén speed. Conclusions. These findings enrich our understanding of kink modes in coronal loops embedded within an asymmetric environment, providing insights that will be helpful for future high-resolution observations.

Raman time-delay in attosecond transient absorption of strong-field created krypton vacancy

Strong field ionization injects a transient vacancy in the atom which is entangled to the outgoing photoelectron. When the electron is finally detached, the ion is populated at different excited states with part of coherence information lost. The preserved coherence of matter after interacting with intense short pulses has important consequences on the subsequent nonequilibrium evolution and energy relaxation. Here we employ attosecond transient absorption spectroscopy to measure the time-delay of resonant transitions of krypton vacancy during their creation. We have observed that the absorptions by the two spin-orbit split states are modulated at different paces when varying the time-delay between the near-infrared pumping pulse and the attosecond probing pulse. It is shown that the coupling of the ions with the remaining field leads to a suppression of ionic coherence. Comparison between theory and experiments uncovers that coherent Raman coupling induces time-delay between the resonant absorptions, which provides insight into laser-ion interactions enriching attosecond chronoscopy.

Correlating Structure with Spectroscopy in Ascorbate Peroxidase Compound II.

Structural and spectroscopic investigations of compound II in ascorbate peroxidase (APX) have yielded conflicting conclusions regarding the protonation state of the crucial Fe(IV) intermediate. Neutron diffraction and crystallographic data support an iron(IV)-hydroxo formulation, whereas Mössbauer, X-ray absorption (XAS), and nuclear resonance vibrational spectroscopy (NRVS) studies appear consistent with an iron(IV)-oxo species. Here we examine APX with spectroscopy-oriented QM/MM calculations and extensive exploration of the conformational space for both possible formulations of compound II. We establish that irrespective of variations in the orientation of a vicinal arginine residue and potential reorganization of proximal water molecules and hydrogen bonding, the Fe-O distances for the oxo and hydroxo forms consistently fall within distinct, narrow, and nonoverlapping ranges. The accuracy of geometric parameters is validated by coupled-cluster calculations with the domain-based local pair natural orbital approach, DLPNO-CCSD(T). QM/MM calculations of spectroscopic properties are conducted for all structural variants, encompassing Mössbauer, optical, X-ray absorption, and X-ray emission spectroscopies and NRVS. All spectroscopic observations can be assigned uniquely to an Fe(IV)═O form. A terminal hydroxy group cannot be reconciled with the spectroscopic data. Under no conditions can the Fe(IV)═O distance be sufficiently elongated to approach the crystallographically reported Fe-O distance. The latter is consistent only with a hydroxo species, either Fe(IV) or Fe(III). Our findings strongly support the Fe(IV)═O formulation of APX-II and highlight unresolved discrepancies in the nature of samples used across different experimental studies.

Inorganic-Organic Hybrid Layered Semiconductor AgSePh: Quasi-Solution Synthesis, Optical Properties, and Thermolysis Behavior.

Two-dimensional inorganic-organic hybrid layered semiconductors are actively studied because of their naturally formed multiquantum well (MQW) structures and associated optical, photoelectric, and quantum optics characteristics. Silver benzeneselenolate (AgSePh, Ph = C6H5) is a new member of such hybrid layered materials, but has not fully been exploited. Herein, we present a quasi-solution method to prepare high quality free-standing AgSePh flake-like microcrystals by reacting diphenyl diselenide (Ph2Se2) with silver nanoparticles. The resultant AgSePh microflakes exhibit room-temperature (RT) resolvable MQW-induced quasi-particle quantization and interesting optical properties, such as three distinct excitonic resonance absorptions X1 (2.67 eV), X2 (2.71 eV), and X3 (2.83 eV) in the visible region, strong narrow-line width blue photoluminescence at ∼2.64 eV (470 nm) from the radiative recombination of the X1 exciton state, and a large exciton binding energy (∼0.35 eV). Furthermore, AgSePh microcrystals show high stability under water, oxygen, and heat environments, while above 220 °C, they will thermally decompose to silver and Ph2Se2 as evidenced by a combination of thermogravimetry and differential scanning calorimetry and pyrolysis-coupled gas chromatography-mass spectrometry studies. Finally, a comparison is extended between AgSePh and other metal benzeneselenolates, benzenethiolates, and alkanethiolates to clarify differences in their solubility, decomposition/melting temperature, and pyrolytic products.

Band gap, ferromagnetic resonance and strong microwave absorption of BaFe12-2xZnxSnxO19 compounds and enhanced dielectric loss in BaFe12-2xZnxSnxO19/carbon nano tube composites

The forbidden bandgap energy, magnetic properties, natural ferromagnetic resonance and microwave absorption are studied on the Zn2+ and Sn4+ doped BaFe12-2xZnxSnxO19. The forbidden band gap of BaFe12-2xZnxSnxO19 increases with the increasing doping content x from 1.80 eV up to 1.97 eV. The coercive field, the anisotropy field and the magnetocrystalline constant of BaFe12-2xZnxSnxO19 decreases with the increasing doping. The natural ferromagnetic resonance is observed. The high permeability, accompanied with the ferromagnetic resonance, enables strong microwave absorption. BaFe10.4Zn0.8Sn0.8O19 has a wide effective microwave absorption bandwidth (RL≤-10dB) of 6 GHz with the material thickness below 2.5 mm in 11.4–17.4 GHz. The dielectric loss has little contribution to the excellent microwave absorption of BaFe12-2xZnxSnxO19. The BaFe12-2xZnxSnxO19/carbon nanotube (CNT) composites significantly increase the permittivity. The high dielectric loss and the high magnetic loss further improve the microwave absorption. With a very thin thickness of 1.8 mm, BaFe10.4Zn0.8Sn0.8O19/CNT has a bandwidth of 7.1 + GHz of 10.9–––18 + GHz. With the material thickness thinner than 3 mm, BaFe12-2xZnxSnxO19/CNT composites have very broad effective microwave absorption bandwidth of 11.4+, 10.7 and 10.7 GHz, with x = 0.6, 0.8 and 1.0, respectively. It illustrates that both BaFe10.4Zn0.8Sn0.8O19 and BaFe12-2xZnxSnxO19/CNT composites are very promising microwave absorbers.

Three-Dimensional Full-Core BEAVRS Using OpenMOC with Transport Equivalence

Using an optimized implementation of the three-dimensional (3D) method of characteristics for neutron transport, along with a novel equivalence method for transport calculations that was designed to correct self-shielding errors from neglecting the angular dependence of resonant group absorption, a 3D full-core light water reactor hybrid stochastic-deterministic eigenvalue calculation was achieved. This paper presents the optimizations developed and compares the transport solutions obtained. For the statepoint, run times near 10 000 CPU hours are achieved—improving on previous works by an order of magnitude—with near 1% error on pin fission to 238U capture ratios and a few dozen pcms on the eigenvalue.

Selective detection of thallium by prussian blue-coated gold nano-colorimetric probe

Thallium as a highly dispersed and toxic heavy metal element, is distributed in soil and water due to a result of industrial activities. Thallium is extremely accumulative, which not only makes it harmful to the environment, but also enriches in living organisms and eventually poses a serious threat to human health. In order to detect thallium ions in water quickly and effectively, a PB@AuNPs nano-colorimetric probe based on gold nanoparticles coated with soluble prussian blue was proposed and characterized by UV–visible photometer, dynamic light scattering particle size distribution, Fourier transform infrared spectroscopy and X-ray diffraction. When Tl+ ions were present in the test sample, PB@AuNPs tended to adsorb Tl+ in the system and agglomerated, which exhibited a remarkable color change from wine red to blue. Meanwhile, the intensity and displacement of surface plasmon resonance (SPR) absorption peak changed. PB@AuNPs nanoprobe exhibited a 0.67 μM of limit of detection (LOD) for UV–vis spectra under the optimal pH being 6 with a good linear relationship between the absorbance ratios and the concentrations of Tl+ ions in the range of 10.0 ∼ 30.0 μM, y = 0.04239 x − 0.07483, R2 = 0.99137. The results showed that PB@AuNPs nanoprobe had high selectivity and good anti-interference, which could be used in the detection of actual water samples.

Electronic structure of superconducting VN(111) films

Vanadium nitride (VN) is a transition-metal nitride with remarkable properties that have prompted extensive experimental and theoretical investigations in recent years. However, there is a current paucity of experimental research investigating the temperature-dependent electronic structure of single-crystalline VN. In this study, high-quality VN(111) films were successfully synthesized on α\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\alpha$$\\end{document}-Al2\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_2$$\\end{document}O3\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_3$$\\end{document}(0001) substrates using magnetron sputtering. The crystal and electronic structures of the VN films were characterized by a combination of high-resolution X-ray diffraction, low-energy electron diffraction, resonant soft X-ray absorption spectroscopy, and ultraviolet photoelectron spectroscopy. The electrical transport measurements indicate that the superconducting critical temperature of the VN films is around 8.1 K. Intriguingly, the temperature-dependent photoelectron spectroscopy measurements demonstrate a weak temperature dependence in the electronic structure of the VN films, which is significant for understanding the ground state of VN compounds.

Enhancement of spin to charge conversion efficiency at the topological surface state by inserting normal metal spacer layer in the topological insulator based heterostructure

In this study, we report efficient spin to charge conversion (SCC) in the topological insulator (TI) based heterostructure (BiSbTe1.5Se1.5/Cu/Ni80Fe20) by using spin-pumping technique, where BiSbTe1.5Se1.5 is the TI and Ni80Fe20 is the ferromagnetic (FM) layer. The SCC, characterized by inverse Edelstein effect length (λIEE) in the TI material, gets altered with an intervening Copper (Cu) layer, and it depends on the interlayer thickness. The introduction of Cu layer at the interface of TI and FM metal provides a new degree of freedom for tuning the SCC efficiency of the topological surface states. The significant enhancement of the measured spin-pumping voltage and the increased linewidth of ferromagnetic resonance absorption spectra due to the insertion of Cu layer at the interface indicate a reduction in spin memory loss at the interface that resulted from the presence of exchange coupling between the surface states of TI and the local moments of FM metal. The temperature dependence (from 8 to 300 K) of the evaluated λIEE data for all the trilayer systems, TI/Cu/FM with different Cu thicknesses, confirms the effect of exchange coupling between the TI and FM layer on the SCC efficiency of the topological surface state. This study offers promising ways for designing more efficient spin-charge conversion devices of the TI-based heterostructure by controlling the interface effects.

Near-Unity Light-Matter Interaction in Mid-Infrared van der Waals Metasurfaces.

Accessing mid-infrared radiation is of great importance for a range of applications, including thermal imaging, sensing, and radiative cooling. Here, we study light interaction with hexagonal boron nitride (hBN) nanocavities and reveal strong and tunable resonances across its hyperbolic transition. In addition to conventional phonon-polariton excitations, we demonstrate that the high refractive index of hexagonal boron nitride outside the Reststrahlen band allows enhanced light-matter interactions in deep subwavelength (<λ/15) nanostructures across a broad 7-8 μm range. Emergence and interplay of Fabry-Perot and Mie-like resonances are examined experimentally and theoretically. Near-unity absorption and high quality (Q ≥ 80) resonance interaction in the vicinity of the hBN transverse optical phonon is further observed. Our study provides avenues to design highly efficient and ultracompact structures for controlling mid-infrared radiation and accessing strong light-matter interactions with hBN.

Simulation of laser-induced ionization in wide bandgap solid dielectrics with a particle-in-cell code.

Modeling the laser-plasma interaction within solids is crucial in controlling ultrafast laser processing of dielectrics, where the pulse propagation and plasma formation dynamics are highly intricate. This is especially important when dealing with nano-scale plasmas where specific phenomena of plasma physics, such as resonance absorption, can significantly impact the energy deposition process. In this article, we report on adapting of a Particle-In-Cell code, EPOCH, to model the laser-plasma interaction within solids. This is performed by implementing a background permittivity and by developing and validating adapted field ionization and impact ionization modules. They are based on the Keldysh ionization theory and enable the modeling of ionization processes within solids. The implementation of these modules was validated through comparisons with a hydrodynamic code and existing literature. We investigate the necessary number of super-particles per cell to model realistic ionization dynamics. Finally, we apply the code to explore the dynamics of plasma formation in the regime of of quantized structuring of transparent films. Our study elucidates how a stack of nano-plasma layers can be formed by the interference of a pulse with its reflection on the exit surface of a high refractive index material.

Light erasable surface-enhanced Raman scattering substrates based on the metallic molybdenum dioxide nanospheres

Surface-enhanced Raman scattering (SERS) is a powerful label-free technique for the identification of molecules and molecular structures at extremely low concentrations. However, in most cases, the analytes will remain on SERS substrates, making the substrate a disposable consumable. Here, we propose a light erasable SERS substrate based on the metallic molybdenum dioxide (MoO2) nanospheres. The MoO2 nanospheres present a remarkable localized surface plasmon resonance (LSPR) absorption peak centered at 800 nm. Profiting from the local field magnification induced by the LSPR, MoO2 exhibits excellent SERS detection sensitivity towards rhodamine 6 G (R6G), rhodamine B (RhB), methyl blue (MB), crystal violet (CV) and Malachite Green (MG), with a detection limit of 10−7 M and a maximum enhancement factor up to 5.4 × 104. Moreover, the metallic MoO2 nanospheres possess a high photothermal conversion efficiency of 70.1% and good photothermal stability. The temperature of the MoO2 surface can reach 438 °C under 808 nm laser irradiation with a power density of 2.5 W cm−2, exceeding the decomposition temperature of most organic molecules. Thus, the residual probe molecules can be completely removed from the MoO2 substrate in less than 7.5 min under laser irradiation without compromising its SERS sensitivity and reproducibility. We anticipate our work will pave a new avenue for the development of reusable and highly sensitive SERS substrates.

Increasing contrast in water-embedded particles via time-gated mid-infrared photothermal microscopy.

The transient dynamics of photothermal signals provide interesting insights into material properties and heat diffusion. In a mid-infrared (mid-IR) photothermal microscope, the imaging contrast in a standard amplitude imaging can decrease due to thermal diffusion effects. It is shown that contrast varies for poly-methyl 2-methylpropenoate (PMMA) particles of different sizes when embedded in an absorbing medium of water (H2O) based on levels of heat exchange under the water absorption resonance. Using time-resolved boxcar (BC) detection, analysis of the transient thermal dynamics at the bead-water interface is presented, and the time decay parameters for 500 nm and 100 nm beads are determined. Enhanced (negative) imaging contrast is observed for less heat exchange between the water and bead, as in the case for the 100 nm bead. For the 500 nm bead, boxcar imaging before heat exchange starts occurring, leads to an increase of the imaging contrast up to a factor of 1.6.