Energy Shift Research Articles

Electron-induced hydrogen desorption from selected polymers (polyacetylene, polyethylene, polystyrene, and polymethyl-methacrylate)

Elastic Peak Electron Spectroscopy, abbreviated as EPES, involves the analysis of the line shape found in the elastic peak. The reduction in the energy of electrons within the elastic peak is a result of energy being transferred to the target atoms, a phenomenon referred to as recoil energy. EPES distinguishes itself among electron spectroscopies by its unique ability to identify hydrogen in polymers and hydrogenated carbon-based materials. This distinctiveness is particularly notable because lighter elements demonstrate more pronounced energy shifts. The detection of hydrogen in polymers entails measuring the energy difference between the positions of the carbon (or carbon+oxygen) elastic peak and the hydrogen elastic peak. This difference tends to increase as the kinetic energy of the incident electrons rises. Concerning hydrogen peak intensity, electron beam-induced damage represents a critical aspect of EPES, as hydrogen desorbs under electron irradiation. In this study, the Monte Carlo method was employed to simulate EPES spectra involving electrons interacting with polyacetylene (C2H2), polyethylene (C2H4), polystyrene (C8H8), and polymethyl-methacrylate (C5H8O2) and to evaluate electron-induced hydrogen desorption from these polymers.

One-Dimensional Magnetic Conduction Channels across Zigzag Graphene Nanoribbon/Hexagonal Boron Nitride Heterojunctions.

We examine the electronic structure of recently fabricated in-plane heterojunctions of zigzag graphene nanoribbons embedded in hexagonal boron nitride. We focus on hitherto unexplored interface configurations in which both edges of the nanoribbon are bonded to the same chemical species, either boron or nitrogen atoms. Using ab initio and mean-field Hubbard model calculations, we reveal the emergence of one-dimensional magnetic conducting channels at these interfaces. These channels originate from the energy shift of the magnetic interface states that is induced by charge transfer between the nanoribbon and hexagonal boron nitride. We further address the response of these heterojunctions to external electric and magnetic fields, demonstrating the tunability of energy and spin splittings in the electronic structure. Our findings establish that zigzag graphene nanoribbon/hexagonal boron nitride heterojunctions are a suitable platform for exploring and engineering spin transport in the atomically thin limit, with potential applications in integrated spintronic devices.

Investigations of structural, photoluminescence, colorimetric, lifetime, and luminous efficiency of Tb3+ and Sm3+ co-doped calcium tungstate for WLEDs

Structure, photoluminescence, colorimetric, and thermoluminescence analysis of Ca1-x-yTb2x/3Sm2y/3WO4; x = 0.01; y = 0.01–0.05 ceramics are reported in this manuscript. The materials are made by the use of the solid-state method. Reitveld refinements of the obtained X-ray diffraction patterns are done by using the Fullprof Suite software. The obtained results denoted that the synthesized materials have a tetragonal structure and I41/a space group. Energy bandgaps are found in the UV–visible absorbance spectra. Photoluminescence investigations of the phosphors are done. The critical quenching concentrations of the phosphor are found to be x = 0.01; and y = 0.04. Moreover, the critical distance of energy shift with the adjacently presented ions is computed. Dexter’s theory is employed to elucidate that the dipole-dipole electronic interactions are the imperative reasons for the transfer of energy in the phosphor. The white color of emission is achieved for x = 0.01, y = 0.04 Tb, and Sm doped CaWO4 material. Moreover, great values in color purity, correlated color temperature, color rendering index as well as luminous efficiency of radiation are obtained from the CIE Chromaticity coordinates. Quantum yield efficiency of x = 0.01, y = 0.04 Tb & Sm codoped CaWO4 is measured. Photoluminescence decay analysis of all the samples is done to study the long-after glow properties and also the average lifetime values are evaluated. This is an indication of the suitable usage of the prepared materials in the white light-emitting diodes. Concentration as well as dose-dependent Thermoluminescence spectroscopy is investigated thoroughly. Kinetic parameters are calculated by deconvoluting the spectra of x = 0.01; y = 0.01 Tb & Sm codoped CaWO4 irradiated with 15 min of UV excitation dose. These results are denoted by high trap depth, second-order kinetics, and low UV dosimetry of the phosphor.

Saudi Arabia’s Journey toward a Renewable Future

Recent statistics indicate that as of 2023, the global renewable energy capacity has reached new heights, with Saudi Arabia significantly contributing to this growth through its strategic initiatives. The kingdom is particularly focusing on harnessing solar power, given its abundant sunlight, and is also exploring wind energy, leveraging its vast desert landscapes. These efforts are part of Saudi Arabia’s broader strategy to become a global leader in renewable energy. This paper provides a detailed exploration of Saudi Arabia’s ambitious journey from a fossil-fuel-dominated energy sector to a more sustainable, renewable-energy-driven future. Anchored in the broader context of global energy trends, the study emphasizes the critical shift toward renewable resources, with a particular focus on Saudi Arabia’s unique position in this global movement. Key to this transition is Saudi Arabia’s Vision 2030, a strategic framework that guides the country’s renewable energy policies and initiatives. A comprehensive review of these policies, including other governmental and international collaborations that support renewable energy development, is offered. The current state of renewable energy in Saudi Arabia is assessed, including an overview of existing projects and production statistics. The paper also explores emerging technologies such as energy storage systems and smart grid solutions, emphasizing their role in Saudi Arabia’s energy transition. An impact assessment is conducted to understand the environmental, economic, and social effects of this energy shift. The paper also includes a comparative analysis of other countries’ renewable energy transitions, extracting lessons and best practices applicable to the Saudi context. Strategic recommendations and reflections on Saudi Arabia’s future role in the global energy landscape are provided for stakeholders in energy policy, environmental planning, and sustainable development.

Observation of energetic ion anisotropy using neutron diagnostics in the Large Helical Device

Energetic ion anisotropy was observed by tangential sightline compact neutron energy spectrometers (CNESs) in tangential neutral beam heated deuterium plasmas in Large Helical Device. Significant upper and lower energy shifts in D–D neutron energy from 2.45 MeV were measured according to the beam ion injection directions and CNES sightline using a conventional liquid scintillation detector with the unfolding technique and a novel Cs2LiYCl6:Ce with a 7Li-enrichment (CLYC7) scintillation detector without unfolding. The observed neutron energy spectrum was compared with that predicted by a numerical simulation based on orbit following models. Numerical simulation revealed that the Doppler shift in D–D neutron energy results from energetic ion anisotropy.

Radiative impacts of cloud hydrometeors on the radial movement of the maximum wind of Typhoon Rammasun (2014)

This study aimed to investigate the radiative impacts of cloud hydrometeors on the radial movement of the maximum wind of Typhoon Rammasun (2014), as indicated by the radial shift in the maximum symmetric rotational kinetic energy (Kψsmax). The sensitivity experiments conducted using the Weather Research and Forecasting (WRF) model indicated that the radial movement of Kψsmax remains unaffected by the radiative impacts of cloud water, raindrops, snow, and graupel. However, eliminating the radiative impacts of cloud ice produced a 10-h pause in Kψsmax and contraction of its radius, which eventually led to a delay in rapid intensification, resulting in a 13% reduction in intensity peak. The analysis reveals that removal of the radiative impacts of cloud ice induced the instability in the lower troposphere and enhanced the dissipation as well as the conversion from Kψs to asymmetric rotational kinetic energy (Kψa). This significantly reduced the Kψs tendency by offsetting the conversion from symmetric divergent kinetic energy (Kχs) to Kψs and Kψs flux convergence.

GeC/SnSe2 van der waals heterostructure: A promising direct Z-scheme photocatalyst for overall water splitting with strong optical absorption, high solar-to-hydrogen energy conversion efficiency and superior catalytic activity

To alleviate the energy crisis and achieve green energy conversion, the heterojunctions that can be applied to the photocatalytic decomposition of water have attracted attention. In this paper, we design a novel two-dimensional GeC/SnSe2 heterostructure and investigate in detail the structural stability, electronic characteristics, photocatalytic activity and optical behavior as well as the effects due to the applied strain based on the first-principles. Firstly, the most stable γ-stacking mode is determined by combining energy comparison, thermodynamic and dynamic studies. Second, the analysis of electronic properties demonstrates that the GeC/SnSe2 heterostructure exhibits a type-II energy band arrangement and a direct Z-scheme photocatalytic mechanism. This pivotal aspect enhances the separation of photogenerated carriers at the interface and facilitates the active participation of the most proficient materials in oxidation-reduction processes during photocatalytic hydrolysis reactions. The hydrolysis reaction's Gibbs free energy shift demonstrates the GeC/SnSe2 heterostructure's superior photocatalytic activity in neutral and alkaline environments and can spontaneously carry out the overall hydrolysis reaction, and this outstanding ability is not affected by the −4% to 4% strain range. In addition, the GeC/SnSe2 heterostructure has outstanding solar-to-hydrogen efficiency (58.18%) and excellent light absorption capability (up to 4×105cm−1) within visible light. The implications of these discoveries point towards the direct Z-scheme GeC/SnSe2 heterostructure holds promise as an excellent candidate for photocatalytic water splitting applications.

Impact of Single-Melamine Tautomerization on the Excitation of Molecular Vibrations in Inelastic Electron Tunneling Spectroscopy.

Vibrational quanta of melamine and its tautomer are analyzed at the single-molecule level on Cu(100) with inelastic electron tunneling spectroscopy. The on-surface tautomerization gives rise to markedly different low-energy vibrational spectra of the isomers, as evidenced by a shift in mode energies and a variation in inelastic cross sections. Spatially resolved spectroscopy reveals the maximum signal strength on an orbital nodal plane, excluding resonant inelastic tunneling as the mechanism underlying the quantum excitations. Decreasing the probe-molecule separation down to the formation of a chemical bond between the melamine amino group and the Cu apex atom of the tip leads to a quenched vibrational spectrum with different excitation energies. Density functional and electron transport calculations reproduce the experimental findings and show that the shift in the quantum energies applies to internal molecular bending modes. The simulations moreover suggest that the bond formation represents an efficient manner of tautomerizing the molecule.

Interlayer Interaction of Excitons and Magnons in Graphene/WS2/Néel‐Type Manganese Phosphorus Trichalcogenide Heterostructures

Abstract2D materials, particularly 2D semiconductors, and layered antiferromagnetic (AFM) compounds, exhibit rich light‐matter coupling phenomena in low‐dimensional systems. In this work, the occurrence of interlayer exciton–magnon coupling (EMC) is observed in Néel‐type AFM of MnPX3 (X = S or Se) and monolayer (1L) WS2 heterostructures. The energy of neutral exciton in 1L WS2 can be tuned by the adjacent AFM order, resulting in an additional energy shift of 10–14 meV. Furthermore, by filtering the photoluminescence spectrum with graphene and conducting magnetic measurements, the correlation is elucidated between the interlayer EMC and AFM transition process. In MnPS3, this coupling behavior exhibits sensitivity to the changes of magnetic structures, manifesting with a correlated length ξ of 8.34 Å at temperatures higher than Néel temperature (TN). The decoupling process in WS2/MnPS3 heterostructure below 50 K is originated from a weak out‐of‐plane ferromagnetic order, confirming the presence of an XY‐type magnetic phase transition in MnPS3 at sub‐TN temperature. This study provides a fundamental understanding of EMC and its potential applications in the integration of optical and magnetic devices.

Dimensional regularization and two-loop vacuum polarization operator: Master integrals, analytic results, and energy shifts

We present a complete reevaluation of the irreducible two-loop vacuum-polarization correction to the photon propagator in quantum electrodynamics, i.e. with an electron-positron pair in the fermion propagators. The integration is carried out by reducing the integrations to a limited set of master integrals, which are calculated using integration-by-parts identities. Dimensional regularization is used in D=4−2ε dimensions, and on-mass shell renormalization is employed. The one-loop effect is given to order ε, to be combined with the 1/ε divergence of the two-loop amplitude. Master integrals are given. Final evaluations of two-loop energy shifts for 1S, 2S, and 2P states are done analytically, and results are presented, with an emphasis on muonic hydrogen. For relativistic Dirac-Coulomb reference states, higher-order coefficients are obtained for the Zα-expansion. We compare the results obtained to the existing literature. Published by the American Physical Society 2024

Signal oscillations in helium scattering by bismuth atoms in the low energy range

Low Energy Ion Scattering (LEIS) analysis of bismuth selenide (Bi2Se3), a strong 3D topological insulator, revealed oscillations of the detected signal in dependence on primary ion beam energy. Bismuth is a part of the group of elements where oscillatory behaviour was already noticed, such as gallium, indium, or lead. Generally, it is ascribed to quasi-resonant charge exchange processes between primary ion and target atom. Moreover, clear differences exist between data for target atoms in elemental form and for atoms in compound form. A study of Bi signal yields in different material forms was performed for primary He+ projectiles within the energy range from 0.50 to 6.00 keV. A foil of pure Bi, Bi2Se3, Bi2O3 and thin Bi films deposited on several substrates (SiO2, CuOx) by Molecular Beam Epitaxy were analysed. The energy shift in the position of oscillations was observed when the oxygen atoms were present at the surface and bonded to Bi atoms. A description of the Bi ion yield variation is provided to facilitate the quantification process in LEIS.

Atomic-Scale Interface for Pt Nanoparticles on SrTiO3 (001).

The interfacial structure formed by Pt nanoparticles grown epitaxially on a SrTiO3 (001) surface by pulsed laser deposition was studied by X-ray standing-wave (XSW) excited core-level photoelectron emission. The XSW-generated 3D atomic map of the Pt and interfacial oxygens for the oxidized Pt/SrTiO3 interface differs significantly from that of the as-deposited interface. After oxidation, the Pt atoms shifted upward and their atomic occupation at fcc-like sites evolved as the oxidation temperature increased. Interfacial oxygen atoms were differentiated from bulk O atoms by the chemical shift in the binding energy of their 1s electrons. After oxidation, the interfacial oxygen atoms rearranged to form a TiO2 bilayer at the interface. These results provide a more complete description of the strong metal-support interaction process at the interface.

Effects of higher-order Casimir-Polder interactions on Rydberg atom spectroscopy

In the extreme near field, when the spatial extension of the atomic wavefunction is no longer negligible compared to the atom-surface distance, the dipole approximation is no longer sufficient to describe Casimir-Polder interactions. Here we calculate the higher-order, quadrupole and octupole, contributions to Casimir-Polder energy shifts of Rydberg atoms close to a dielectric surface. We subsequently investigate the effects of these higher-order terms in thin-cell and selective reflection spectroscopy. Beyond its fundamental interest, this regime of extremely small atom surface separations is relevant for quantum technology applications with Rydberg or surface-bound atoms interfacing with photonic platforms. Published by the American Physical Society 2024

Monitoring underground hydrogen storage migration and distribution using time-lapse acoustic waveform inversion

The ongoing global energy shift from fossil fuels to renewable sources highlights the importance of underground hydrogen storage (UHS) as a sustainable mechanism to counterbalance the seasonal inconsistencies of renewable energy. Comparable to geological CO2 sequestration, UHS necessitates precise subsurface imaging and a thorough understanding of hydrogen behavior within geological formations, including its location and migration patterns. Since direct subsurface measurement is unattainable, there is a pronounced need for robust subsurface characterization and monitoring techniques. This research focuses on UHS feasibility in enduring storage scenarios, employing seismic monitoring strategies adapted from CO2 storage practices. Specifically, we integrate Continuous Active Source Seismic Monitoring (CASSM) and Time-Lapse Full Waveform Inversion (TLFWI) to scrutinize UHS. The study employs synthetic crosshole surveys that initially model the coexistence of hydrogen and water within fractured reservoirs, aiming to pinpoint hydrogen-related velocity alterations in acoustic waveforms. Subsequently, we utilize a time-lapse synthetic model of hydrogen injection to emulate CASSM observations. Utilizing TLFWI in conjunction with White's model, we successfully process the CASSM data to discern and quantify temporal variations in velocity and saturation, which effectively maps the spatial and temporal distribution of mobile hydrogen. The results affirm the capabilities of TLFWI and CASSM as proficient monitoring systems for UHS. This study aspires to offer a dependable methodology for the administration of large-scale and long-term geological hydrogen storage.

Quantum time dilation in a gravitational field

According to relativity, the reading of an ideal clock is interpreted as the elapsed proper time along its classical trajectory through spacetime. In contrast, quantum theory allows the association of many simultaneous trajectories with a single quantum clock, each weighted appropriately. Here, we investigate how the superposition principle affects the gravitational time dilation observed by a simple clock – a decaying two-level atom. Placing such an atom in a superposition of positions enables us to analyze a quantum contribution to a classical time dilation manifest in spontaneous emission. In particular, we show that the emission rate of an atom prepared in a coherent superposition of separated wave packets in a gravitational field is different from the emission rate of an atom in a classical mixture of these packets, which gives rise to a quantum gravitational time dilation effect. We demonstrate that this nonclassical effect also manifests in a fractional frequency shift of the internal energy of the atom that is within the resolution of current atomic clocks. In addition, we show the effect of spatial coherence on the atom's emission spectrum.

Development of non-destructive isotope measurement of the natural galena (PbS) using negative muon beams

In Earth and planetary science, Pb isotopic composition is well known to play a key role in deciphering the origin and evolution of materials because they provide unique chronological and/or indigenous regional information as a radiogenic daughter nuclide from U and Th. To determine such an isotopic composition, mass spectrometers have been widely used over several decades, which requires a destructive/consuming treatment such as sputtering, laser ablation and thermal ionization. Here, we first report the non-destructive Pb isotopic measurement of natural galena (PbS) using the energy shift of muon-induced characteristic X-rays. The observed Pb isotopic composition of the natural galena is in good agreement with that obtained by conventional mass spectrometry. Such a muon-based Pb isotopic analysis method is expected to be applied to identify the production area of archaeological artefacts (e.g. bronze products), where non-destructive analysis is highly desirable compared to conventional mass spectrometry.

Experimental investigation of electrostatic capture of 1+ ions in charge breeder electron cyclotron resonance ion source plasma

We present comprehensive experimental data demonstrating that the capture process of the 1+ ions in charge breeder electron cyclotron resonance ion sources (ECRIS) is dominated by electrostatic deceleration by the ambipolar plasma potential, not by cumulative small-angle scattering of the incident ions in ion–ion collisions as postulated previously. To achieve this we varied the plasma potential of an ECRIS charge breeder by adjusting the microwave power applied to sustain the helium discharge and measured the corresponding shift in the optimum injection energy of the 1+ ions. The experiment was repeated with sodium, potassium, and cesium ions. It is shown that the optimum injection energy does not depend on the incident ion mass, which contradicts the collisional drag model. Conversely, the optimum injection energy (in eV) shifts in unison with the plasma potential (in V), which provides strong evidence for the electrostatic deceleration hypothesis.

Tailoring the functional properties of LSMO-BTO nanocomposites: A sol-gel synthesis approach and comprehensive characterization

In this study, the sol-gel synthesis technique was harnessed to craft nanocomposites of (1-x)La0.7Sr0.3MnO3-(x)BTO with x values of 0.4, 0.6, and 0.8. The attributes of these meticulously engineered materials were exhaustively explored using a diverse suite of characterization methods. X-ray diffraction analysis irrefutably confirmed the phase purity of the perovskite structure, emphasizing the synthesis's precision. Furthermore, Diffuse Reflectance Spectroscopy shed light on the optical properties of the nanocomposites, revealing a significant shift in bandgap energy that correlated directly with the BTO concentration. Specifically, an increment in BTO concentration resulted in a systematic expansion of the bandgap from 1.51 eV to 1.44 eV. For an in-depth analysis of the magnetic characteristics of the composites, Vibrating Sample Magnetometry was utilized. The magnetic analysis identified a conspicuous reduction in saturation magnetization, highlighting the complex interplay between the composite components at the nanoscale. Additionally, the dielectric properties were rigorously investigated through dielectric measurements, which unveiled a notable increase in the dielectric constant, accompanied by the emergence of novel relaxation behaviors. This finding indicates that adjusting the BTO content within the nanocomposites not only modifies their dielectric properties but also provides a method for fine-tuning their functional performance.

NC Loaded PtM Alloy from M-NC with Ultralow Pt Loading for Oxygen Reduction Reaction

Developing low Pt or non-precious metal catalysts for oxygen reduction reaction (ORR) has becoming necessary in recent years. Herein, PtM alloy anchored on nitrogen-doped carbon (PtM/NC, M=Fe, Co) catalyst with ultralow Pt loading (∼1 wt%) is prepared from the simple two-process pyrolysis, namely from C to M-NC then to PtM/NC. The as-prepared PtM/NC (M=Fe, Co) shows an excellent ORR catalytic performance with the peak potential and half-wave potential of 0.901 and 0.870 V for PtFe/NC, 0.868 and 0.845 V for Pt3Co/NC. The ORR on PtM/NC (M=Fe, Co) is a mainly direct 4-electron reaction pathway (3.75–3.90) in alkaline solution. Moreover, they possess good methanol tolerance and stability. Synergistic effect of Pt and M together with N species result in the excellent ORR catalytic activity of PtM/NC (M=Fe, Co). The negative shift of Pt binding energy caused by both lattice contraction and electron orbital coupling from M is beneficial for reducing the d-band center of Pt, weakening the oxygen binding energy and enhancing the ORR intrinsic activity of Pt. The strong interactions between NC and PtM alloy are beneficial for anchoring PtM nanoparticles, promoting the stability of catalyst. This work provides a new strategy for preparing ultralow Pt loading catalysts.

Surface chemistry of ion beam modified native titania/Ti interfaces examined using X-ray photoelectron spectroscopy

It is often assumed in X-ray Photoelectron Spectroscopy that binding energy shifts are synonymous with changes in the chemical state of an atom and the chemical state can be described in terms of oxidation state and stoichiometry of the elements in a material that correlates with photoemission peaks. However, when an atom is bonded into a crystal lattice, the shapes and binding energy of photoemission may not match the expected stoichiometry when measured by XPS, even though shifts in binding energy suggest new oxidation states. In this work, a set of experiments is presented, in which Ar+ and He+ ions of different energies modify the native oxide on a titanium foil which yields XPS spectra that are not easily open to analysis by conventional peak models. In the course of analyzing these complex photoemission data by linear algebraic methods, the prospect emerged that XPS is suggesting that sputtering a native oxide may be providing insight into structural perturbation in addition to the stoichiometry-type changes to the native oxide.