Red-shift Phenomenon Research Articles

A dual-mode optical thermometry of Ca2Al2SiO7:Tb3+/K+ phosphors based on the redshift of f-d transition adsorption edge

This study presents the synthesis of Ca2Al2SiO7: xTb3+ and Ca2Al2SiO7: 0.09 Tb3+/yK + phosphors via the solid-state reaction method for temperature sensing applications. The results show that the materials synthesized exhibit a tetragonal gehlenite crystal structure with space group P4‾ 21m, where Ca2+ sites are substituted by Tb3+/K+ ions as confirmed by refinement analysis. Concentration quenching is attributed to the energy transfer mechanism between Tb3+ ions, possibly involving electron exchange and dipole-dipole interactions. A redshift phenomenon is observed in the f-d transition absorption edge, which is crucial for dual-mode thermometry of excitation intensity ratio (EIR) and single band ratio (SBR) thermometry. Based on EIR thermometry, the sample Ca2Al2SiO7:0.09 Tb3+/0.13 K+ showed a higher sensitivity with Sr value of 0.65 % K−1@298 K and a lower temperature uncertainty δT value of 0.77 K@298 K, compared to Ca2Al2SiO7:0.09 Tb3+ (Sr value of 0.59 % K−1@298 K and δT value of 0.85 K). Considering practical applications, a single band ratio (SBR) thermometry was constructed for Ca2Al2SiO7:0.09 Tb3+/0.13 K+ under two excitation wavelengths of 265 nm and 284 nm, yielding the Sr value of 0.743 % K−1@298 K and a δT value of 0.67 K@ 298 K. These results indicate the strong potential of Ca2Al2SiO7: Tb3+/K+ phosphors for dual-mode optical thermometry, offering high sensitivity and accuracy.

Temperature dependence of Ce luminescence characteristics in LaBr3: Ce crystal

Despite the large interest in the scintillation properties of LaBr3:Ce, a detailed understanding of the underlying mechanism of temperature-dependence properties of Ce luminescence remains elusive. This study introduces a self-designed spectral apparatus to explore these properties in LaBr3:5%Ce. We observed a redshift phenomenon and band changes in the emission peak bands, indicating a reduction of the bond length between Ce and the host with increasing temperature. Moreover, the probability of low-energy peak emission decreases and the probability of high-energy peak emission increases, with increasing temperature was observed, suggesting a correlation with the proximity of Ce's 4f energy level to the valence band. Utilizing intensity parameters from the spectra, we identified the impact of temperature on LaBr3:Ce's self-absorption effect, revealing a significant self-absorption effect at the high-energy peak for the first time. A simple self-absorption model indicated that, despite high quantum efficiency of Ce, the overall self-absorption is minimal, establishing a correlation between the self-absorption coefficient of the high-energy peak and overall absorption. This research offers insights for developing radiation-resistant high-temperature luminescent devices and advances the field of high-temperature luminescent materials.

Friction-Induced Near-Infrared Emission and Its Mechanism.

Triboluminescence (TL) is an optical phenomenon in which light is emitted from the surface of a material when subjected to pressure or shear forces. Due to its potential applications in non-destructive testing, radiation sources, and spectroscopic probes, TL has garnered increasing attention over the past two decades. However, experimental observations in the infrared spectrum remain limited, and its emission mechanism has not yet been fully understood. In this study, significant emission in the near-infrared spectrum was experimentally observed from the tribo-pairs of Cr/YSZ and quartz/YSZ. The results indicate that the Tribo-Induced Near-Infrared Light Emission consists of three peaks, in which the 780 nm peak is related to the electronic transition between the 3d5/2 and 3d3/2 orbitals of Y3+ ions, while the 880 nm and 990 nm peaks can be attributed to hole centers and T-type centers in the intrinsic defects of YSZ, respectively. Additionally, experiments reveal that the Cr/YSZ tribo-pair exhibits a redshift of 11-18 nm at the 780 nm peak compared to the quartz/YSZ tribo-pair. To explain the cause of the redshift phenomenon, X-ray photoelectron spectroscopy and UV-Vis absorption spectroscopy were used to measure the energy level spacing between the 3d5/2 and 3d3/2 orbitals of Y3+ and the bandgap width of YSZ before and after friction, respectively. We found that the bandgap width of the doped YSZ decreases after friction, which is often accompanied by a reduction in the energy level spacing between the 3d5/2 and 3d3/2 orbitals of Y3+. The extent of the reduction in energy level spacing varies with different dopants, leading to the redshift phenomenon.

Analysis of alternatives to the accelerating expansion of the Universe

Observations from the James Webb Space Telescope (JWST) in recent years pose serious challenges to standard cosmology. Such a situation prompts to reconsider the models presented as alternatives to the Lambda-Cold Dark Matter (ΛCDM) model. In this work, a number of such models are considered, including models related to modifying gravity, models related to intrinsic luminosity of supernovae type Ia (SNe Ia), and models related to red shift. The accelerated expansion of the Universe is associated with the red shift of distant objects, and standard cosmology assumes that this red shift is caused by cosmological expansion. In this paper, we consider the alternative possibility that the red shift of distant objects may also be due to the phenomenon of red shift of light in the intergalactic and interstellar media.

Photoelectrocatalytic property and DFT calculations of TiO2 with broadened infrared light absorption by Gd2O3:Er3+

In this paper, erbium-doped gadolinium oxide rare earth oxide nanoparticles (Gd2O3:Er3+) with good light absorption capacity from the visible to the infrared region were prepared by polyol method, and then compounded with TiO2 by hydrothermal method. SEM, TEM, XPS, UV–vis and electrochemical workstation were used to study the morphology, structure, UV–vis light absorption and photoelectrochemical (PEC) properties of Gd2O3:Er3+/TiO2. The results showed that the Gd2O3:Er3+ spherical nanoparticles with a particle size of about 15 nm were uniformly distributed on the surface of the TiO2 nanorod array, and the Gd2O3:Er3+/TiO2 nanocomposites had good light absorption capacity in the infrared region. Furthermore, the photocurrent densities of Gd2O3/TiO2 and Gd2O3:Er3+/TiO2 were 2.08 and 2.75 times higher than those of TiO2, respectively, manifesting that the broadening of infrared light absorption can improve the PEC property of TiO2. Meanwhile, the DFT calculation results showed that the energy band of Gd2O3:Er3+/TiO2 was significantly narrower than that of TiO2, indicating that Gd2O3:Er3+/TiO2 had a redshift phenomenon of UV–vis absorption. The calculation results of state density showed that the f orbital of Gd2O3:Er3+ intersected with the d orbital of TiO2, indicating that there is an electron transfer between Gd2O3:Er3+ and TiO2.

Constraint on the Cosmic Curvature in a Model with the Schwarzschild–de Sitter Metric from Supernovae and Gamma-Ray Burst Observational Data

In developing his cosmological model of 1917, de Sitter theoretically predicted the phenomenon of cosmological redshift (the de Sitter effect), which he did long before the discovery of this phenomenon in observations. The de Sitter effect is gravitational by its nature, as it is due to differences between the coordinate systems of the observer and the distant source. However, the relationship between the redshift and distance derived from the de Sitter metric is at odds with observations, since this relationship is nonlinear (quadratic) for small redshifts, while the observed relationship between the same quantities is strictly linear. This paper discusses the possibility that cosmological redshift is gravitational by its nature, as in de Sitter’s 1917 model. At the same time, here, as in de Sitter’s model, an elliptical space is used, the main characteristic of which is the identification of its antipodal points. But, unlike de Sitter’s model, here, in order to ensure strict linear dependence of the redshift on distance, the origin of the reference system is transferred to the observer’s antipodal point. The Schwarzschild–de Sitter metric used in this model allows you to estimate the curvature of space from observational data. To achieve this, a theoretical Hubble diagram is built within the framework of the model with the Schwarzschild–de Sitter metric, which is compared with observations from the Pantheon+ catalogue of type Ia supernovae and the Amati catalogue of gamma-ray bursts in the redshift range of 0<z<8. As a result of this comparison, we found that the lower estimate of the radius of curvature of space was quite large: 2.4×1015 Mpc. This means that the observational data indicate a negligible curvature of space.

A four core fiber temperature and strain dual parameter sensor based on T-shaped taper

A four core fiber temperature and strain dual parameter sensor based on T-shaped taper is proposed and prepared. The sensor is composed of single-mode fiber (SMF), multi-mode fiber (MMF), and four core fiber (FCF). Among them, MMF plays a role in beam expansion, and FCF is tapered and fused with SMF to form a T-shaped taper structure, thereby preparing a sensor based on Mach Zehnder interference principle. When the external environmental temperature and strain change, due to thermal effect and elastic optical effect, the refractive index of the FCF cladding and fiber core changes differently, resulting in shift in the interference spectrum. Based on the temperature and strain sensitivity at different interference valleys, the temperature and strain dual parameter matrix equation of the sensor can be obtained. The experimental results indicate that when the temperature rises within the range of 30 ℃ to 90 ℃, the sensor spectrum shows a red shift phenomenon, and the maximum temperature sensitivity can reach 55 pm/ ℃. When the strain increases within the range of 0 με∼ 2000 με, the transmission spectrum of the sensor exhibits a blue shift phenomenon, and the maximum strain sensitivity can reach −2.6 pm/ με. Finally, based on the experimental results, the matrix equation for dual parameter sensing can be obtained. This sensor is easy to manufacture and has high sensitivity. It can measure sensing parameters normally in micro magnetic and micro electric field environments.

Triaxial strain enhanced thermoelectric performance and conversion efficiency in Tl3TaSe4

Thermoelectric (TE) materials have garnered significant attention due to their potential in converting waste heat into useful electrical energy. Strain engineering has emerged as a promising strategy for tailoring the properties of materials, offering opportunities to optimize TE performance. In this study, we employ first-principles calculations to investigate the electronic and thermal transport properties of cubic Tl3TaSe4 under triaxial strain. Our results demonstrate that tensile strain can reduce the effective mass of carriers and contribute to high carrier mobility. The phonon calculation and AIMD simulation reveal excellent dynamic stability and thermal stability of Tl3TaSe4 both with and without strain. The red shift phenomenon of phonon vibration modes and the higher portion of phonon DOS in the low frequency region indicate that tensile strain enhances the anharmonicity of Tl3TaSe4. In addition, triaxial tensile strain can effectively reduce the heat capacity, group velocity, and phonon lifetime, while enhancing the anharmonicity of Tl3TaSe4, which contributes to the lower κl. Compared to the condition without strain, the room temperature κl of Tl3TaSe4 under 1 % and 2 % tensile strain is reduced by about 43 % and 79 %, respectively. Furthermore, the tensile strain exhibits a positive enhancement effect on the ZT value of Tl3TaSe4. At 700 K, the optimal ZT values of p-type and n-type Tl3TaSe4 under 2 % tensile strain are 1.31 and 0.94, respectively, which are three times higher than that of 0.4 and 0.33 without strain. Finally, the TE conversion efficiency of Tl3TaSe4 under 2 % tensile strain is 6.8 %, which is higher than BiCuSeO and α-Cu2+xSe, and comparable to SnSe. Our results demonstrate the effectiveness of triaxial tensile strain in enhancing the phonon scattering, reducing the κl, and improving the TE properties of Tl3TaSe4.

Tunable Band Alignment and Optoelectronic Structure of Cu2Se/PtX2 (X=Se,Te) Heterostructures: under Strain and Electric Field

Two-dimensional (2D) material-based van der Waals heterostructures (vdWHs) are an emerging strategy for regulating the electronic properties of two-dimensional materials. This study investigated the effects of a vertical electric field and strain on the band alignment transition and optoelectronic properties of Cu2Se/PtSe2 (PtTe2) vdWHs using density functional theory calculations. Cu2Se/PtSe2 vdWHs exhibited type-I to type-II band alignment transformation under an in-plane strain, interlayer distance, and electric field of 2%, 2.40 Å, and -0.40 V/Å, respectively. Moreover, Cu2Se/PtTe2 vdWH demonstrated a rich transition of types I, II, and III band alignments with in-plane strain. The absorption spectra of Cu2Se/PtSe2 (PtTe2) vdWHs show a certain degree of blue and red shift phenomenon upon the application of strain and electric fields. The predicted power conversion efficiencies at 3% in-plane strain with an interlayer distance of 3.40 Å for Cu2Se/PtSe2 (PtTe2) vdWHs were observed to be as high as 22.58% (19.80%). Thus, our work demonstrated that both strain and electric field can effectively and flexibly control the electronic properties of Cu2Se/PtSe2 (PtTe2) vdWHs, making them a promising candidate material for applications in photodetectors and field-effect transistors.

Enhanced Photocatalytic Degradation of Rhodamine B Using ZnO Microspheres Decorated with Ag Nanoparticles

Zinc oxide (ZnO) has demonstrated significant potential as a photocatalyst for the wastewater treatment. However, its wide bandgap leads to inefficient light utilization and rapid carrier recombination, which inhibits its photocatalytic activity. To overcome these limitations, we employed a hydrothermal method to synthesize Ag/ZnO composite microspheres with different concentrations of Ag nanoparticles. By utilizing Ag complexed with ZnO, the Ag/ZnO composite photocatalysts were made to have a narrower bandgap and a broadened light response range, as well as the red-shift phenomenon at the absorption edge. In addition, Ag nanoparticles can act as electron traps to efficiently capture electrons and minimize the recombination of photoexcited carriers for improved photocatalytic performance. Compared with other concentrations of ZnO microspheres and pure ZnO microspheres, the 5% Ag/ZnO composite microspheres exhibited excellent degradation performance when exposed to a xenon lamp, with 90.1% degradation of rhodamine B (RhB) solution in 100[Formula: see text]min. Incorporating trapping agents in experimental studies has indicated that the RhB degradation process is significantly influenced by •O[Formula: see text], while the impact of •OH and h[Formula: see text] were relatively weak. Thus, Ag/ZnO nanocomposites hold great promise as materials for use in wastewater treatment.

Energy transfer and a novel SBR thermometry of SrY2O4:Sm3+/Eu3+ phosphor based on redshift of charge transfer band edge

In this study, a solid-state reaction was employed to synthesize SrY2O4: Sm3+, SrY2O4: Eu3+ and SrY2O4: Sm3+/Eu3+ phosphors. An intriguing redshift phenomenon from charge transfer band (CTB) edge was investigated for single-band ratiometric (SBR) thermometry applications. The phosphors synthesized exhibited an orthogonal CaFe2O4 structure with Pnam (62) space group. The Y3+ sites from host lattice were most likely to be replaced by Sm3+/Eu3+ ions. The sample of SrY2O4: 0.03 Sm3+/0.3Eu3+ showed a large degree of agglomeration with elongated particles, having an average size of approximately 4 μm. The energy bandgap decreased due to increased surface imperfections, resulting in enhanced defect level concentration. The dipole-dipole interaction could be used to explain energy transfer (ET) of Sm3+-Sm3+ and Sm3+-Eu3+. Furthermore, the energy transfer (ET) efficiency of Sm3+→Eu3+ in Sr2YO4 reached 77.7 %. The sample exhibited a good thermal stability (90.956 %@423 K) with Ea of 0.31 eV, which was an important parameter for broadening thermometry range. A thermometry strategy utilized this redshift phenomenon from CTB edge with anti-thermal quenching behavior and other peaks or bands with thermal quenching was therefore proposed. The high Sr value of 1.533 % K−1@298 K provides a great potential for optical thermometry application, contributing significantly to the advancement of single band ratiometric thermometry technologies.

Boron-Catalyzed C1 Copolymerization of Arsonium and Sulfoxonium Ylides toward Unrepresented Structures and Fluorescence Properties.

The first synthesis of well-defined poly(methylene-co-1,1-diphenylpropenenylene) (C1-co-C1'), equivalent to poly(ethylene-co-diphenylbutadiene) copolymers was accomplished by C1 copolymerization of novel diphenylpropenyl triphenyl arsonium ylides (Ph2AY) and dimethylsulfoxonium methylide (Me2SY) using B-thexylborepane as initiator. All polymerization conditions, including feed ratio, temperature, and reaction time, were optimized. A series of photoluminescent poly(ethylene-co-diphenylbutadiene)s were synthesized at different feed ratios, opening a new synthetic horizon for poly(ethylene-co-disubstitutedbutadiene) copolymers. Notably, a new C1 segment, arising from a double bond rearrangement, was confirmed by NMR, resulting in an unprecedented two-monomer three-structure random terpolymer. An unexpected red-shift phenomenon in the fluorescence spectra was observed with increasing the ratio of Ph2AY in the copolymer. This shift is attributed to the aggregation of diphenylbutadiene segment, similar to through-space conjugation (TSC), likely induced by a decrease in the crystallinity of copolymers. Furthermore, another disubstituted allylic triphenyl arsonium ylides, (E)-2-phenylbutenyl triphenyl arsonium ylide (MePhAY) was also synthesized and investigated. These additional compounds expand the knowledge and the potential applications of such copolymerization techniques in advanced materials.

Four-band terahertz perfect-absorption and high-sensitivity sensor based on tunable Dirac semimetal

In this paper, we designed a dynamically tunable four-band perfect sensor based on bulk Dirac semimetal (BDS). The sensor comprises a top BDS layer, a bottom Au layer, and an intermediate dielectric layer. Four resonant modes with >98 % absorption are achieved in the range of 9–11.8 THz. Due to the rotationally symmetric design, the sensor is polarization insensitive. The formation mechanism of perfect absorption is explained using the principles of impedance matching. We also determined the effects of structural parameters and Fermi energy of the BDS on the absorption spectra. We explain the blue-shift and red-shift phenomena of the resonant frequency based on equivalent circuits. Additionally, we define the refractive index sensitivity (S) and find that the maximum sensitivity is 516 GHz/RIU. Due to these excellent properties, our design provides a way of thinking about actively tunable terahertz sensors and expands their application scope.

Highly active ZnO/Fe3+-TiO2 photocatalysts for visible-light photodegradation application and its colour change behaviour by d-d transition

Highly active novel ZnO/Fe-TiO2 composite catalysts with p-n junction heterostructure have been fabricated by adding commercial ZnO and sol–gel derived Fe-TiO2 nano-powders controlled by grinding and drying. This work reported that doped Fe (III) with TiO2 form a p-type semiconductor and whereas ZnO is an n-type semiconductor. The slight variation of electronegativity between ZnO and TiO2 causes a strong rectifying action for the formation of an interface between ZnO and Fe-TiO2. The occurrence of red shift phenomenon in absorption spectrum of the samples suggest the outcome of d-d transition of Fe3+ (2T2g → 2A2g, 2T1g) and the charge transfer transition between interacting Fe3+ ions (Fe3+ + Fe3+ → Fe4+ + Fe2+). These Fe3+ 3d states in addition to oxygen vacancies and Ti3+ centers create band states, thereby favouring the electronic transition to these levels and resulting in narrowing of TiO2 band gap. A direct confirmation is the increase of Urbach energy with the lowering in the band gap of ZnO/Fe-TiO2.The crystal field splitting of d orbitals (5 degenerate orbitals) of Fe3+ and the approach of free ligand ions which split into two sets and Fe3+ ligand field transition is discussed schematically. The photocatalytic activities of these heterostructure photocatalysts were evaluated by degrading toxic cationic organic dyes such as Methylene Blue (MB) and Malachite Green Oxalate (MG) under visible light. The mechanism of photocatalysis has been recommended which is based on the relative band structure of the semiconductor and integrated heterostructure. The formation of a spike barrier in the CB at the interface gives rise to trap sites that capture the migration of charge carriers and occurs recombination of electron-hole pair at higher Fe(III) doping concentration. The dark adsorption property of the catalysts sample has been also studied.

Reevaluating Cosmic Origins: A Critical Analysis of Relic Radiation and Cosmometric Assumptions in Big Bang Cosmology

This article presents a critical examination of two key aspects of Big Bang cosmology: the nature and observability of cosmic microwave background (CMB) radiation and geometric inconsistencies or “cosmometric contradictions” within established approaches to cosmology. By dissecting the conventional interpretation of the CMB as relic radiation from a primordial fireball, we uncover that the standard model’s reliance on a spatially homogeneous fluid to represent radiation and matter underestimates the propagation of radiation and leads to the conclusion that the observability of the CMB contradicts its purported origins. Treating free radiation as if it expanded with the universe while disregarding that it escapes from its source at the speed of light is termed here as the “relic radiation blunder”. Furthermore, we delve into the cosmometric contradiction, highlighting how the calculated distances in standard cosmology imply a universe that exceeds the spatial limitations of its own foundational premise. This makes it evident that standard cosmology is not a unitary theory but involves models with conflicting spatial extensions. The analysis suggests a need for a revised understanding of redshift phenomena and cosmic expansion. It advocates for a reassessment of the underpinnings of cosmology, urging the scientific community to consider alternative frameworks that reconcile these critical inconsistencies. This work challenges the inviolable core of established cosmological theory, calling for a paradigm shift to foster foundational advances in our understanding of the universe.

A Bifunctional Three-Dimensional Zn(II) Metal-Organic Framework with Strong Luminescence and Adsorption Cr(VI) Properties.

The mixed ligand 3-amino-1,2,4-triazole (Hatz) and terephthalic acid (H2pta) reacted with Zn(NO3)2·6H2O to synthesize a three-dimensional binuclear Zn(II) metal-organic framework: {[Zn2·(atz)2·(pta)]·3H2O}n (3D-Zn-MOF). This 3D-Zn-MOF has two different types of pores (4.5 × 4.5 Å2, 5.7 × 5.7 Å2). The crystalline 3D-Zn-MOF could be prepared into nanomaterials (3D-N-Zn-MOF) with particles of approximately 100 nm by a cell fragmentation apparatus. Compared with the solid-state luminescence of Hatz and H2pta, it was found that 3D-N-Zn-MOF exhibited strong luminescence performance and significant red-shift phenomenon. Due to the decrease in electronegativity and rigidity of ligands, as well as the effect of ligand metal charge transfer (LMCT), the fluorescence lifetime and quantum yield of 3D-ZN-N-MOF were 2.7241 ns and 3.02%, respectively. The maximum experimental adsorption capacity of 3D-N-Zn-MOF could reach 125.52 mg/g, which was superior to the majority of MOF adsorbents under the optimal adsorption conditions (25 °C, pH = 7, and the adsorbent concentration is 0.2000 g/L). The thermodynamic analysis of adsorption showed that the adsorption of Cr(VI) by 3D-N-Zn-MOF was a spontaneous (△G < 0) and exothermic (△H < 0) process. It could be found that 3D-N-Zn-MOF was a bifunctional material with potential applications by comprehensive analysis of the fluorescence and adsorption Cr(VI) performance.

Review on Minimally Extended Varying Speed of Light Model

It is known that dimensional constants, such as ℏ, c, G, e, and k, are merely human constructs whose values and units vary depending on the chosen system of measurement. Therefore, the time variations in dimensional constants lack operational significance due to their dependence on these dimensional constants. They are well structured and represent a valid discussion. However, this fact only becomes a meaningful debate within the context of a static or present Universe. As theoretically and observationally well established, the current Universe is undergoing accelerated expansion, wherein dimensional quantities, like the wavelength of light, also experience redshift phenomena elongating over cosmic time. In other words, in an expanding Universe, dimensional quantities of physical parameters vary with cosmic time. From this perspective, there exists the possibility that dimensional constants, such as the speed of light, could vary with the expansion of the Universe. In this review paper, we contemplate under what circumstances the speed of light may change or remain constant over cosmic time and discuss the potential for distinguishing these cases observationally.

A study on the electromagnetic mechanism of a flexible terahertz toroidal dipole metasurfaces

We have designed and fabricated metasurfaces structures generated toroidal dipole phenomenon by fabricating periodic metal pattern on polyimide substrate. The metasurfaces structure consists of two symmetric split rings along the Y-axis. The impact of structural parameters, gap, and SR, on the electromagnetic characteristics of metasurfaces at terahertz frequencies was investigated. An increase in gap results in a blue shift phenomenon in the amplitude transmission spectrum, while an increase in SR leads to a red shift phenomenon in the amplitude transmission spectrum. The intrinsic mechanism of the toroidal resonance is investigated more deeply by calculating the multipole scattering power and Q-factor. Q-factor values of 2.3 and 9.5 were obtained at low and high frequencies, respectively. Terahertz toroidal dipole metasurfaces made on flexible substrates like this have the potential for applications in terahertz functional devices, such as sensors and tuners.

First-principles study of the effect of alkaline-earth metal doping on the intrinsic MoSe2 photovoltaic properties

In this study, the effect of alkaline-earth metal element doping on the photoelectric properties of intrinsic MoSe2 is systematically investigated based on the first-principles approach, and it is believed that the findings of this work will give some theoretical guidance for future research on MoSe2 doping modification. The results show that all the doping systems exhibit good stability, and Be atom doping has the lowest formation energy value, making the doping easier to produce. The doping of alkaline-earth metal elements resulted in some lattice distortion of MoSe2. Intrinsic MoSe2 is a semiconductor with a direct bandgap of 1.498[Formula: see text]eV, and the doping of alkaline-earth metal elements causes the bandgap value to decrease in each system, and the bandgap is the smallest when Be is doped. All doped systems exhibit P-type conducting properties. Compared with the intrinsic MoSe2, all doped systems have their conduction band fraction moved to the low-energy direction overall, and new density of states peaks appear near the Fermi energy level. These state density peaks mainly originate from the results contributed by the s-orbitals of each doping system Mo-4d, Se-4p, and each dopant atom. The analysis of the work function reveals that the work function of each doped system is smaller than the intrinsic MoSe2, then the energy required for the occurrence of electron leaps is reduced, which improves the electron mobility of the doped system. The Mulliken Population analysis shows that stable chemical bonds are formed between the doped alkaline-earth metal elements and the surrounding Se atoms. The examination of the optical characteristics demonstrated that, in comparison to the intrinsic MoSe2, all doped systems’ greatest dielectric absorption peaks were attenuated and moved toward the low-energy region; the doping of alkaline-earth metal elements broadened the light absorption edge of the intrinsic MoSe2. The absorption peaks of each doping system are shifted toward the low-energy region with the red-shift phenomenon, and the light absorption is good in the ultraviolet region.

Using Planar Metamaterials to Design a Bidirectional Switching Functionality Absorber—An Ultra-Wideband Optical Absorber and Multi-Wavelength Resonant Absorber

This study aimed to investigate a bidirectional switching functionality absorber, which exhibited an ultra-wideband characteristic in one direction, while in the other direction it demonstrated the absorption of three different resonant wavelengths (frequencies). The fully layered planar structure of the absorber consisted of Al2O3, Zr, yttria-stabilized zirconia (YSZ), Zr, YSZ, Al, YSZ, and Al. The simulations were conducted using the COMSOL Multiphysics® simulation software (version 6.1) for analyses, and this study introduced three pivotal innovations. Firstly, there had been scarce exploration of YSZ and Zr as the materials for designing absorbers. The uses of YSZ and Zr in this context were a relatively uncharted territory, and our research endeavored to showcase their distinctive performance as absorber materials. Secondly, the development of a planar absorber with multifunctional characteristics was a rarity in the existing literature. This encompassed the integrations of an ultra-wideband optical absorber and the creation of a multi-wavelength resonant absorber featuring three resonant wavelengths. The design of such a multi-wavelength resonant absorber holds promise for diverse applications in optical detection and communication systems, presenting novel possibilities in related fields. Lastly, a notable discovery was demonstrated: a discernible redshift phenomenon in the wavelengths of the three resonant peaks when the thickness of YSZ, serving as the material of resonant absorber layer, was increased.