Absorption Spectra Research Articles

Influence of La3+ doping on structural and optical properties of SrCeO3 perovskite

The SrCe1-xLaxO3 (x = 0.0, 0.02, 0.4, 0.6, and 0.10) perovskite materials have been successfully synthesized by auto-combustion method and calcined at 1100°C. The XRD patterns reveal a highly crystalline orthorhombic crystal structure with a Pnma space group in all samples. The TEM micrograph shows a spherical morphology of the 10 mol% La3+ doped SrCeO3 perovskite sample alongwith the SAED pattern confirming its highly crystalline nature. The incorporation of La3+ ion in the SrCeO3 perovskite has been confirmed by the Raman and Fourier transform infrared (FTIR) measurements. The UV–vis absorption spectra at room temperature show various bands, with a strong absorption band observed below 400 nm. The optical band gap of the undoped and La3+ doped samples have been calculated and it is smaller for the La3+ doped perovskite samples than that of the undoped perovskite sample. Therefore, the La3+ doped SrCeO3 perovskite may be applicable for optoelectronic applications.

WO3@MOF heterostructure in-situ transformed and deposited on La-Bi2WO6-BiFeWOx composite with enhanced photocatalytic performance for degradation of harmful and toxic substances produced by tobacco

Nowadays, tobacco is widely cultivated, and there are millions of people who smoke around the world. The cultivation of tobacco, along with the handling of cigarettes and the consumption of tobacco products, can produce numerous harmful and toxic substances. Many researchers are working diligently to eliminate these harmful and toxic substances. However, the results have been minimal. In this paper, we successfully prepared a novel La-Bi2WO6-BiFeWOx-WO3@MOF using hydrothermal and in-situ transformation methods. All samples were thoroughly investigated using various characterization techniques, including XRD, SEM, TEM, XPS, UV–Vis absorption spectra, transient photocurrent responses, and electron spin resonance. Furthermore, La-Bi2WO6-BiFeWOx-WO3@MOF was utilized as a catalyst for the degradation of harmful and toxic substances produced by tobacco, including phenol, nicotine, benzopyrene, and nitrosamines. The results indicate that La-Bi2WO6-BiFeWOx-WO3@MOF exhibits efficient separation and transfer of photo-generated electron-hole pairs under visible light irradiation. La-Bi2WO6-BiFeWOx-WO3@MOF also exhibits excellent photocatalytic activity, efficiently degrading phenol (98.62%), nicotine (92.41%), benzopyrene (81.74%), and nitrosamine (98.23%). Furthermore, the effects of varying catalyst dosage, phenol concentration, and pH values, as well as the degradation of nicotine, benzopyrene, and nitrosamine by La-Bi2WO6-BiFeWOx-WO3@MOF, were also investigated. The main active radicals are ·OH and ·O2– during the degradation process. Finally, a potential degradation mechanism for phenol, nicotine, benzopyrene, and nitrosamine by La-Bi2WO6-BiFeWOx-WO3@MOF is proposed.

Local symmetry distortions during f-f transitions in HoAl3(BO3)4 single crystal

The polarized absorption spectra of the HoAl3(BO3)4 single crystal were studied in the region of f–f transitions 5I8→5F5, 5S2 + 5F4, 5F3 and 5F2 inside the 4f shell of the holmium ion as a function of temperature in the range of 5–90 K. In a number of absorption lines the splitting which are not provided by the local point group D3 symmetry of holmium ion in the crystal are found. This phenomenon is explained by local changes in the structure in both the excited and ground states of holmium under the influence of a perturbation caused by a photon. This perturbation mixes the ground and excited states and changes the interaction of the atom with its environment. It was also shown that the magnitude of the splitting depends on the polarization of the incident light and on the temperature of the sample.

Molten-salt-chemistry-assisted synthesis of heterostructured g-C3N4/BiOI nanocomposites with enhanced sunlight absorption properties for efficient solar-to-chemical energy conversion

The g-C3N4 nanosheets coupled BiOI (g-C3N4/BiOI) nanocomposites with unique heterojunction structure and excellent wide-spectrum sunlight absorption properties have been developed via molten-salt-chemistry-assisted strategy. The heterostructured g-C3N4/BiOI shows enhanced solar to the thermal effect, improved electron mobility and carrier lifetime for efficient photocatalytic dye degradation. The engineered g-C3N4/BiOI catalyst exhibits outstanding photocatalytic activity for methyl orange (MO) removal with 100 % degradation conversion and excellent stability under solar light irradiation, which is respectively 2.69 and 1.27 times higher than those of g-C3N4 and BiOI counterparts. The broad scope toward other dyes degraded by g-C3N4/BiOI and the generality of the molten-salt-chemistry-assisted strategy for synthesizing g-C3N4/BiOCl and g-C3N4/BiOBr with considerable photodegradation efficiency are proved. The analysis of kinetic behaviors, electron spin resonance, and nanosecond transient absorption spectra for structure-activity relationship, key intermediate of •O2− species, and excited state lifetime of g-C3N4/BiOI heterojunction material in the photocatalytic MO degradation processes are also demonstrated.

Development of 2D Ir-DMG nanosheets as a colorimetric sensor probe for Ni (II) sensing and a highly sensitive, reliable, and portable colorimetric sensor device for environmental analysis

The era of nanomaterials made a revolutionary change in colorimetric sensing with ultra-high sensitivity, improved reactivity, and enhanced photoactivity. The first-ever novel 2D metal–organic nanosheets were synthesized using IrCl3 and Dimethylglyoxime (DMG) by probe ultrasonication (PUS) followed by a solvothermal wet-chemical approach. This material has shown a rapid color change from yellow to crimson red with Ni (II) after the formation of complex. The UV–visible absorption spectra are the conventional methodology for colorimetric sensors and here, it was given a perfect linear relationship with an R2 of 0.99 and an LOD of 1.60 µM (0.1 ppm). The average calculated molar extinction coefficient for this system was 1889.30 M−1 cm−1. This is comparatively high absorptivity value. In addition, a novel Arduino-based colorimetric sensor device and corresponding software were developed under the name of “Chrom Metrics”. This Arduino device is unique since it can sense all wavelengths and the combined RGB delta E values. Therefore, it can provide more information/rationale for colorimetry than other devices/methods. The same Ir-DMG & Ni (II) system showed a perfect linear relationship with an R2 of 0.98 and a LOD of 0.85 µM (0.05 ppm) by the data obtained from this sensor device. Thus, this new device is easier and more accurate, highly efficient, rapid, highly selective, and sensitive.

Synthesis, spectroscopic characterization, DFT analysis, antibacterial, antifungal, antioxidant, molecular docking, and ADME study of 3,4-dihydro-2H-napthalen-1-one tagged chalcone derivatives

Chalcone derivatives were synthesized from 3,4-dihydro-2H-naphthalen-1-one using a base-catalyzed Claisen-Schmidt reaction and characterized by FT-IR, ¹H NMR, and ¹³C NMR spectroscopy. Density functional theory (DFT) with the B3LYP/6-311G(d,p) basis set was employed to explore the structural, electronic, and quantum properties of the compounds. Simulated electronic absorption spectra for compounds 3c and 3e in gas phase, DMSO, and DCM were generated using time-dependent DFT (TD-DFT). Compound 3c's first singlet excited state shifted from 376.10 nm in the gas phase to 390.08 nm in DMSO, while compound 3e shifted from 381.58 nm to 383.54 nm in DMSO. Experimental absorption values matched the theoretical predictions, with higher oscillator strengths in DMSO and DCM indicating solvent-enhanced transition probabilities. The antimicrobial activity of the chalcones was evaluated against four bacterial strains (E. coli, B. subtilis, S. aureus, and Streptococcus spp.) and four fungal strains (R. oryzae, P. chrysogenum, A. niger, and C. albicans). Compounds 3d and 3f showed strong antibacterial activity with MIC values of 3.9 µg/mL and moderate antifungal activity. Antioxidant properties were assessed using DPPH and hydroxyl radical assays, with compound 3d demonstrating 75.8 % and 76.4 % scavenging activity for OH and DPPH radicals, respectively. ADME studies were conducted to evaluate pharmacokinetics, and molecular docking studies revealed strong binding affinities. Compounds 3a and 3e had docking scores of -8.7 kcal/mol with the E. coli protein (PDB ID: 1KZN), while 3d and 3f performed best against B. subtilis (PDB ID: 1BAG) and S. aureus gyrase (PDB ID: 2XCT), with scores of -9.1 and -8.3 kcal/mol, respectively. Molecular dynamics simulation of compound 3d with 1BAG over 100 ns confirmed stable binding. These findings suggest chalcone derivatives have strong potential for pharmaceutical development.

ZnS and Reduced Graphene Oxide Nanocomposite-Based Non-Enzymatic Biosensor for the Photoelectrochemical Detection of Uric Acid.

In this work, we report a study of a zinc sulfide (ZnS) nanocrystal and reduced graphene oxide (RGO) nanocomposite-based non-enzymatic uric acid biosensor. ZnS nanocrystals with different morphologies were synthesized through a hydrothermal method, and both pure nanocrystals and related ZnS/RGO were characterized with SEM, XRD and an absorption spectrum and resistance test. It was found that compared to ZnS nanoparticles, the ZnS nanoflakes had stronger UV light absorption ability at the wavelength of 280 nm of UV light. The RGO significantly enhanced the electron transfer efficiency of the ZnS nanoflakes, which further led to a better photoelectrochemical property of the ZnS/RGO nanocomposites. The ZnS nanoflake/RGO nanocomposite-based biosensor showed an excellent uric acid detecting sensitivity of 534.5 μA·cm-2·mM-1 in the linear range of 0.01 to 2 mM and a detection limit of 0.048 μM. These results will help to improve non-enzymatic biosensor properties for the rapid and accurate clinical detection of uric acid.

FABRICATION AND CHARACTERIZATION OF BISMUTH TELLURIDE THIN FILMS BY THERMAL EVAPORATION TECHNIQUE

An interest in the study of the structural and optical properties of topological insulators, led to the selection of Bismuth telluride thin films. Among the topological insulators, Bismuth telluride is one of the promising materials that exhibit applications in the field of thermoelectric power generation. The films were prepared using the thermal evaporation method under vacuum conditions of [Formula: see text] mbar on glass substrates maintained at a temperature of 120∘C. The thickness of the film samples ranges from 400 Å to 1400 Å. Pure phases of Bi2Te3 with a rhombohedral structure are confirmed using X-ray Diffraction. The crystallite size was calculated using Debye–Scherrer’s formula. Structural morphology and compositions are examined using SEM and EDAX. The UV–Vis study reflects the optical behavior of the thin film samples. The absorption spectra gives the direct and allowed transition band gap of the Bi2Te3 thin film samples for various thicknesses. The band gap decreases with the increase in the thickness of the Bi2Te3 thin films, suggesting that the material has significant absorption towards the visible spectrum. The Photoluminescence (PL) emissions for Bi2Te3 thin film samples of various thicknesses are examined and analysed. Raman study reveals the presence of two active modes.

Moisture‐resistant nitroaromatic explosive gas sensor based on hydrophilic pentiptycene polymer

AbstractThe detection of explosive materials, particularly nitroaromatic compounds such as 2,4,6‐trinitrotoluene (TNT), is critical for public safety and national security. Existing detection methods often require complex instrumentation, limiting their applicability for real‐time or in‐field use. Fluorescent sensors, which offer rapid and sensitive detection through fluorescence quenching, present a promising alternative. This study evaluates the performance of two pentiptycene‐based polymers, P‐1 and P‐2, in detecting explosive vapors, with a specific focus on their behavior under high‐humidity conditions. P‐2, modified with triethylene glycol groups, demonstrated significantly increased hydrophilicity compared to the commonly studied P‐1, as confirmed by contact angle measurements. Spectroscopic analysis revealed a blue shift in P‐2's UV–Vis absorption and photoluminescence spectra, indicating electronic property changes due to structural modifications. The enhanced hydrophilicity of P‐2 enabled it to maintain stable sensing performance under moist conditions, showing less than a 10% reduction in sensitivity, compared to the 20% decrease observed in P‐1. This superior moisture resistance suggests that P‐2 is a more robust and practical sensor for explosive detection in environments with variable humidity levels.

Environmentally friendly, high near-infrared reflection green pigments for thermal insulation

In this paper, TiO2 and MgAl-LDHs were coated on yellow pigment hydroxyl iron oxide (FeOOH) with sol-gel and hydrothermal synthesis method respectively to prepare loaded yellow pigment (FT8M0.25). Then, phthalocyanine blue (CuPc) was combined with FT8M0.25 to prepare composite green pigment (FT8M0.25Px). The results indicate the FT8M0.25Px has the structural characteristics of hydrotalcites and CuPc. The surface of FeOOH pigment has a clear TiO2 coating layer and MgAl-LDHs flake structure. KPFM analysis indicate that there is electron transfer between the interfaces of pigments. According to the analysis of color performance and near-infrared reflectance (NIR), the FT8M0.25P0.13 (a*=-12.98) is greener than that of Cr2O3 (a*=-6.65). The NIR of FT8M0.25P0.13 is as high as 73.54 %. The visible light absorption spectrum characteristics determine the color of the pigments, and there is electron transfer between the interfaces of each group. The formation of multi-level interfaces and the resulting multiple light reflections increase the reflectivity of the pigment. The developed coating achieved a considerable temperature difference of 20 °C before and after the coating surface with excellent photostability and reusability, which makes it possible for pigments to replace chromium containing pigments and be used as energy-saving cold pigments.

Study in the Extreme UV Range of the Spectral Transmission of Nickel Plasma Created under the Effect of an X-Ray Pulse of the Z-Pinch

Spectral properties of the high-temperature plasma obtained by exposing a nickel layer to a source of high-power X-ray radiation (a power of 6–10 TW with a duration of 7–10 ns) based on a Z-pinch, formed during implosion of tungsten multi-wire arrays at the Angara-5-1 facility, are studied. In this case, the Z-pinch radiation heats the target and turns it into the hot plasma, and the same radiation probes the target plasma to determine the spectral dependence of the transmission of this plasma. An original scheme is proposed for measuring the incident, transmitted and self-emission of a target simultaneously in one experiment in the frame mode using a grazing incidence diffraction spectrograph. Using laser shadow imaging, experimental data are obtained on the velocity of the plasma expansion on the irradiated and back sides of the target, which reached 100 km/s. Targets made of thin Ni layers deposited on a mylar film are studied. An irradiationinduced multiple increase in the transmission of the target plasma in the EUV range is observed compared to the transmittance of the target in the cold state. The dependence of the absorption spectrum of the plasma and the accompanying self-radiation of the target on the power and shape of the heating pulse is studied. The measurement results are compared with numerical calculations performed using the RALEF-2D two-dimensional radiation code, which has been repeatedly used previously to simulate similar experiments. The shape of the spectral dependence of the transmission in the experiment and calculation is similar in the range of ∼30–200 Å, but the model plasma transmission (∼0.8–0.9) is higher than that obtained using a spectrograph and X-ray multi-frame photography (∼0.5–0.6).

Phenomenology of a Rydberg impurity in an ideal Bose-Einstein condensate

We investigate the absorption spectrum of a Rydberg impurity immersed in and interacting with an ideal Bose-Einstein condensate. Here, the impurity-bath interaction range can greatly exceed the mean interparticle distance; this discrepancy in length scales challenges the assumptions underlying the universal aspects of impurity atoms in dilute bosonic environments. Our analysis finds three distinct parameter regimes, each characterized by a unique spectral response. In the low-density regime, we find that the Rydberg impurity is dressed by the surrounding bath similarly to the known Bose polaron. Transitioning to intermediate densities, the impurity response, given by sharp quasiparticle peaks, fragments into an intricate pattern bearing the hallmarks of a diverse molecular structure. Finally, at high density, a universal Gaussian response emerges as the statistical nature of the bath dominates its quantum dynamics. We complement this analysis with a study of an ionic impurity, which behaves equivalently. Our exploration offers insights into the interplay between interaction range, density, and many-body behavior in impurity systems. Published by the American Physical Society 2024

Optical absorption spectrum reveals gaseous chlorine in anti-resonant hollow core fibers

We have observed unexpected spectral attenuation of ultraviolet light in freshly drawn hollow core optical fibers. When the fiber ends are left open to atmosphere, this loss feature dissipates over time. The loss matches the absorption spectrum of gaseous (molecular) chlorine and, given enough time, the transmission spectrum of the fiber recovers to that expected from the morphological structure of the fiber. Our measurements indicate an initial chlorine concentration of 0.45 µmol/cm3 in the hollow core, equivalent to 1.1 mol% Cl2 at atmospheric pressure.

Optical properties of CdO thin films

Cadmium Oxide thin films were deposited on glass substrate by spray pyrolysis technique at different temperatures (300,350,400, 500)oC. The optical properties of the films were studied in this work. The optical band-gap was determined from absorption spectra, it was found that the optical band-gap was within the range of (2.5-2.56)eV also width of localized states and another optical properties.

Templating Iron(III) Oxides on DNA Molecules.

Fe(III) oxides were prepared as free nanoparticles and on DNA templates via the precipitation of Fe(III) salts with NaOH in the presence/absence of DNA. Through control of the pH and temperature, FeOOH and Fe2O3 were synthesised. The formation of templated materials FeOOH/DNA and Fe2O3/DNA was confirmed using UV-Vis absorption and FTIR spectra. The direct optical gap of Fe2O3/DNA was estimated as 3.2 eV; the absorption by FeOOH/DNA and Fe2O3/DNA at longer wavelengths is weaker, but consistent with indirect gaps near 2 eV. X-ray photoelectron spectra confirmed the presence of Fe(III) and DNA in the templated samples. Analysis of the X-ray diffraction patterns of both templated and non-templated FeOOH and Fe2O3 demonstrated that the materials were the α-FeOOH and α-Fe2O3 polymorphs with crystallite diameters of the DNA-templated materials estimated as 7.6 nm and 6.8 nm. Transmission electron microscopy showed needle-like crystals of both FeOOH and Fe2O3, but the Fe2O3 contains some globular structures. In contrast, the morphology of FeOOH/DNA and Fe2O3/DNA consists of needle-like crystallites of the respective oxides organised into complex dendritic structures with a length on the 10 μm scale formed by the DNA molecules. Finally, scanned conductance microscopy provided evidence for the conductivity of the FeOOH/DNA after alignment via molecular combing on an Si/SiO2 substrate. Fe2O3/DNA did not exhibit any detectable conductivity.

Structural and Optical Properties of SnS2:Cu Thin films prepared by chemical Spbay Pyrolysis

Thin filis have been prepared from the tin disulphide (SnS2 ), the pure and the doped with copper (SnS2:Cu) with a percentages (1,2,3,4)% by using ahemical spray pyrolysis techniqee on substrate of glass heated up to(603K)and sith thicknesses (0.7±0.02)?m ,after that the films were treated thermally with a low pressure (10-3mb) and at a temperature of (473K) for one hour. The influence of both doping with copper and the thermal treatment on some of the physical characteristics of the prepared films(structural and optical) was studied. The X-ray analysis showed that the prepared films were polycrystalline Hexagonal type. The optical study that included the absorptance and transmitance spectra in the weavelength range (300-900)nm demonstrated that the value of absorption coefficient (?) was greater than (104 cm-1) for the pure and doped films and that the electronic transitions at the fundamental absorption edge were of the indirect kind whether allowed or forbidden and the value of the optical energy gap in the case of the indirect transition, the allowed decreased from (2 eV) to (1.8,1.7,1.5,1.2)eV at the doping percentages (1,2,3,4)% respectively, also it was found that the value of energy gap for the pure and doped films increased after annealing. Tthe absorption and transmission spectra were used to find the optical constant including refractive index(n), extinction coefficient (k), imaginary and real part of dielectric constant (?1 &?2) , and it was found that all the optical constant was affected by changing the doping percentages; in addition to being affected after treating the films thermally

CdWO4 Sub‐1 nm Nanowires for Visible‐light CO2 Photoreduction

Quantum size effect usually causes energy level splitting and band broadening as material size decreases. However, this may change again by the surface adsorbents, doping and defects, which rarely attracts much attention. Herein, CdWO4 sub‐1 nm nanowires (SNWs) with oleylamine adsorption, PO43‐‐doping and oxygen defects are synthesized by combining Cd(CH3COO)2, H3PW12O40 (PW12) and oleylamine (abbreviated as PO43‐‐CdWO4‐X SNWs). Compared with bulk CdWO4, they exhibit unexpected absorption spectra (extended from 292 nm to 453 nm) and bandgap (reduced from 4.25 eV to 2.74 eV), thus bringing remarkable visible‐light CO2 photoreduction activity. Under 410 nm LED light irradiation, PO43‐‐CdWO4‐40 SNWs exhibit the highest photocatalytic performance with a CO2‐to‐CO generation rate of 1685 µmol g‐1 h‐1. Density functional theory (DFT) calculations demonstrate the adsorbed oleylamine raises the valence band and enhances the adsorption of reaction substrate and intermediates, thus decreasing their reduction energy barriers. Furthermore, PO43‐‐doping and oxygen defects will generate defect energy band below the conduction band of PO43‐‐CdWO4‐40 SNWs, resulting in remarkable visible light absorption and superior photocatalytic CO2 reduction performance. This work highlights the significant impacts of surface adsorbents, doping and defects on the physicochemical and catalytic properties of sub‐nano materials.

Transformation Dynamics of Nanosized Bi Films into Semiconductor Films of Bismuth Oxide in the Cold Plasma Device

This work proposes an original method that reveals the transformation dynamics of nanosized Bi films into semiconductor films of bismuth oxide (Bi2O3) and the factors affecting the low‐energy cold plasma on the electro‐optical properties of Bi2O3. In the plasma microreactor with a photosensitive GaAs:Cr electrode, the transformed Bi films 400–1100 nm thick are analyzed by X‐ray diffraction to determine the crystal structure of Bi2O3 and by an electron probe microanalyzer to explore the evolution of the composition. The morphological properties of the Bi films exposed to electron–ion flow are examined by processing the scanning electron microscope images. It is found that as a result of the combined effect of photoactive illumination, charged particles, and active plasma components: 1) an absorption spectrum of a new substance is formed in the range λ = 330–1100 nm; 2) the optical width of the bandgap of the resulting substance is Eg ≈ 3 eV, which satisfactorily coincides with the width of the bandgap of Bi2O3; and 3) to overcome the potential barrier and formation of semiconducting Bi2O3 film energy is required, which is provided by the combined kinetic energy of electrons and negatively charged oxygen ions bombarding on the Bi film.

Magnetic field-engineered optical nonlinearity in germanene nanotubes

Abstract The linear and nonlinear optical properties of germanene nanotubes (GeNTs) under the influence of magnetic fields are investigated through theoretical analysis. By employing a tight-binding model beyond the Dirac cone approximation, the electronic band structure, density of states, dipole matrix elements, and third-order nonlinear optical susceptibilities are calculated. The application of a magnetic field induces a Zeeman splitting of the energy levels, breaking the band degeneracy. Consequently, the dipole matrix elements exhibit a magnetic field dependence, altering the intensity and number of allowed transitions. In the infrared and ultraviolet energy regions, the linear optical absorption spectrum displays the splitting of peaks into dual neighboring peaks, with the splitting distance linearly dependent on the magnetic field strength. The third-order nonlinear optical susceptibilities, χTHG(3)3ω and χIDIR(3)ω, reveal the emergence of multiple resonance peaks in different energy regions due to two-photon and three-photon absorption processes. The magnetic field significantly influences the number, position, and height of these optical peaks, enabling effective control over the nonlinear optical response. By investigating the scaled energy (E/E_g) dependence, a universal behavior is observed for the three- and two photon resonance peaks, where their positions remain constant, but their peak intensities are significantly enhanced under the influence of the magnetic field. These findings demonstrate the potential of GeNTs as tunable nonlinear optical materials, with the magnetic field serving as an effective parameter for engineering their optical properties for various applications in optoelectronics, photonics, and related fields.

Harnessing spectrophotometry resolution power for determining ternary mixture for respiratory disorders treatment in their pharmaceutical formulation.

A ternary mixture incorporating Hydroxyzine hydrochloride (HYX), Ephedrine hydrochloride (EPH) and Theophylline (THP) frequently prescribed for the treatment of respiratory diseases. Herein, two spectrophotometric methods are designated and applied to resolve these three components in their mixture. Method A is ratio-subtraction combined with derivative spectrophotometry, where THP can be determined directly at its λmax 271 nm (neither HYX or EPH interfere), then for determination of HYX and EPH, the ternary mixture was divided by 22 μg/mL of THP and after subtraction of the plateau region, HYX can be determined directly at its λmax 234.2 nm (absence of EPH intervention). Finally, the third derivative (3D) spectrophotometric approach was utilized to estimate EPH by detecting the peak amplitude at 222 nm with Δλ = 4 and a scaling factor 100. Principal Component Regression (PCR) and Partial Least Squares (PLS), two multivariate calibration approaches, were applied effectively in Method B. This method effectively quantified the mixture under investigation by using the absorption spectra obtained from suitable solutions of the three components in the 210-230 nm region. The calibration models were evaluated using cross-validation with PCR and PLS, producing statistical characteristics that demonstrate the effectiveness of the calibration models. Synthetic and pharmaceutical preparations were also used to conduct external validation. In pharmaceutical formulation, these methods were successfully applied to analyze HYX, EPH, and THP without overlap from formulation's excipients. Moreover, the study's findings were statistically contrasted with those of earlier reported HPLC method. Appraisal approaches were used to determine whether the new spectrophotometric methods had an adverse environmental impact involving the Green Analytical Procedure Index (GAPI) and the AGREE (Analytical Greenness). These evaluations delivered information about the methods' eco-friendliness and sustainability, proving that they are in line with ecologically attributed practices. Furthermore, the Blue Applicability Grade Index (BAGI) was utilized to identify and verify the feasibility and practicality of the suggested approaches.