BO3 Units Research Articles

Tunable green-blue luminescence of Dy2O3 doped borosilicate glasses for optoelectronic devices

The optical-structural correlated properties of the 40B2O3−40SiO2−10V2O5−(10−x)Fe2O3−xDy2O3 system, where 2, 4, and 6 mol%, were studied. Differential scanning calorimetry (DSC) and X-ray diffraction (XRD) confirmed the glassy and amorphous nature of the samples. Adding Dy2O3 promoted the formation of bridging oxygens (upto 4 mol%) by converting BO3 into BO4 units, however, above 4 mol% Dy2O3 act as a modifier. The optical band gap increased from 3.70 to 4.01 eV, while the refractive index decreased from 2.23 to 2.16. The CIE coordinates indicated that the emission spectra fall within the green-blue region. The as-prepared sample exhibited the highest correlated colour temperature value above 5000 K, suggesting its suitability for cool light-emitting diodes sensitive to human vision. These glasses have potential applications in light-emitting diodes and optoelectronic devices.

Investigation of the optical and radiation shielding parameters of erbium-doped zinc sodium tungsten borate glass using MCNP5 simulations

Abstract This study explores the potential of (20Na2O+25ZnO+10WO3+(60-x)B2O3+xEr2O3 where x = 0.1, 0.5, 0.7, and 1 mol%) glass for optical and radiation shielding applications, fabricated using the melt quenching method. Optical, structural, and radiation shielding properties were analyzed using UV–visible spectroscopy, XRD, FTIR, MCNP5, and Phy-X/PSD software. Results show a 9.01% decrease in refractive index from 2.22 to 2.02 and a significant increase in band gap energy from 2.29 eV to 3.12 eV with increasing Er2O3 content. The addition of Er3+ ions convert BO3 units into BO4 units, creating a denser glass network. The linear attenuation coefficient ( LAC ) increased in BTEr1 glass to 0.676 cm−1, compared to 0.607 cm−1 for BTEr0.1 glass, reflecting an approximate rise of 11.5% in LAC . The BTEr1 glass shows enhanced radiation shielding, with a 10.25% reduction in the half-value layer (HVL) from 1.15 cm in BTEr0.1 to 1.03 cm in BTEr1 at 0.284 MeV, and a further reduction of 8.17% from 4.77 cm in BTEr0.1 to 4.42 cm in BTEr1 at 2.506 MeV for 0.1 and 1 mol% Er2O3 level in the BTEr glass. The BTEr glass enhances light transmission in the visible spectrum and increases glass stability with Er2O3 addition , making it suitable for advanced optical applications. Additionally, its improved photon radiation shielding properties make it a promising candidate for radiation protection.

A multi-function glass shield for neutrons and gamma rays of boron- and bismuth-reinforced silicate glass

A successful attempt to produce a multi-function glass shield for attenuating neutrons and gamma rays by reinforcing a silicate glass network with boron and bismuth has been accomplished. A composition of 20SiO2-80Na2O (BSiBi0) was proposed to be used as a host glass network and prepared using the melt/annealing techniques. The low concentration of SiO2 in BSiBi0 was not sufficient to form a stable glass network. Then, the proposed BSiBi0 was modified with 10, 20, 30, and 40 mol% of each of B2O3 and Bi2O3 (BSiBi1, BSiBi2, BSiBi3, and BSiBi4) simultaneously. The structural effects of adding B3+ and Bi3+ were studied through X-ray diffraction, density, and FTIR, which all showed enhancement of glass forming ability, a former role of Bi3+ ions, and crowded the glass network by BO4 units. The derived structural parameters -\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$-$$\\end{document} molar volume, mean silicon – silicon separation, mean boron – boron separation, oxygen packing density, packing density, and number of bridging/non-bridging oxygen -\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$-$$\\end{document} were extensively discussed to explore the impact of B3+ and Bi3+ on the formed network. The richness of the proposed host glass network by B3+ and Bi3+ enhanced its thermal stability. The obtained elastic properties by ultrasonic measurements reflect the increase of the glass rigidity with increasing concentrations of B3+ and Bi3+ ions. The obtained glasses have high visible light transparency and almost complete UV absorption. The measured shielding parameters against two types of neutron energies (total slow and slow) and a wide range of gamma rays’ energies showed a significant improvement in the shielding efficiency of the considered glasses. The total slow neutrons, slow neutrons, and gamma rays’ attenuation abilities were improved by 22.9, 135.5, and 73.8 -\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$-$$\\end{document} 199.5%. High thermal stability, elasticity, visible light transparency, and neutrons and gamma rays’ attenuation performance features give the produced glasses, especially BSiBi4 glass, preference as shielding materials in nuclear fields.

Structural, vibrational, and luminescent properties of pure and Ce-doped magnesium lithium aluminoborate glass

The objective of this work was to study the properties of new vitreous samples of pure BAlMgLi and Ce-doped BAlMgLi produced by the melt-quenching method. The structural and vibrational characteristics of the samples were analyzed using x-ray diffraction (XRD), vibrational Raman spectroscopy, and vibrational Fourier transform infrared spectroscopy (FTIR). Optically stimulated luminescence (OSL) and thermoluminescence (TL) techniques were also used to identify whether the samples showed a response to ionizing radiation. XRD analyses confirmed the predominance of the amorphous phase of the samples. The Raman spectra revealed that the atomic bonds present in the material matrix are of the pyroborate and metaborate type, enabling stretching vibrations in isolated BO4 and/or Al–O or Al–O–B units. The band at approximately 810 cm−1 is characteristic of the formation of the boroxol ring, indicating that the presence of other elements in the matrix does not affect its glassy characteristics. The FTIR analyses reinforce the results found by Raman spectroscopy, because bands characteristic of low hygroscopic glasses were observed, due to the conversion of BO3 units into BO4 in triborate, tetraborate, and pentaborate groups. This conversion is due to dopant entrainment, which contributes to the high optical transparency of the samples. Their OSL and TL signals were reproducible with intensities dependent on the dopant concentration and radiation dose, with the most intense emissions resulting from 0.5% Ce concentrations.

Effect of replacing B2O3 with CuO on the structural, optical absorption, thermal, mechanical, and gamma-ray shielding properties of B2O3–Bi2O3–K2O glass

This paper delves into the effect of replacing B2O3 with CuO on the structural, optical absorption, thermal, mechanical, and gamma(γ)-ray shielding properties of four CKB glasses formulated as (65-y)B2O3–15Bi2O3–20K2O-yCuO (where y = 0, 0.3, 0.6, and 1.2 mol%). The glasses were created using the melt-quenching technique, and their non-crystalline structure was verified by X-ray diffraction (XRD) analysis. Fourier-transform infrared (FTIR) spectroscopy identified several structural groups, predominantly consisting of BO3, BO4 units, and B–O–B linkages. Thermal properties, assessed via Differential Scanning Calorimetry (DSC), indicated that the glass transition temperature was highest for the 0.3 mol% CuO sample (CKB0.3), demonstrating enhanced thermal stability in comparison to other compositions. Density measurements correlated positively with CuO concentration, peaking at 1.2 mol%, while molar volume, boron molar volume, oxygen packing density, and boron-boron separation distances showed a decreasing trend with increased CuO concentration. UV–Vis absorption spectroscopy indicated a decline in the optical energy gap and an increase in Urbach energy, attributed to the conversion of BO3 into BO4 units in the glass matrix. Mechanical properties, evaluated using the Makishima-Mackenzie model, demonstrated enhancements in elastic moduli and micro-hardness with rising CuO concentration. The γ-ray shielding properties (γ-RPs) were examined at energies of 0.662, 1.173, and 1.333 MeV, revealing that both the linear attenuation coefficient and effective atomic number reached their maximum values at 1.2 mol% CuO (CKB1.2). While CKB1.2 exhibited excellent mechanical and γ-ray shielding performance, CKB0.3 excelled in thermal stability and demonstrated γ-ray shielding efficiency comparable to CKB1.2. This suggests that CKB0.3 is a promising candidate for radiation shielding applications requiring a balanced combination of thermal stability and effective γ-ray attenuation properties, particularly at 0.662 MeV.

Effect of low concentrations of WO3 on synthesis, structural, physical, optical, neutron attenuation, and charged particle absorption properties of B2O3+Na2O+BaO glassy composites

This study presents the physical, optical, and radiation shielding attributes of 75B2O3+5Na2O+(20-x)BaO+xWO3 glasses, with the aim of producing effective transparent and light shields. The well-known melting-and-quenching technique was used to prepare the transparent glasses for x = 0; 03; 10 mol%). The glasses were characterized by determining their density, molar volume, optical transmittance, bandgap, refractive index, dielectric constant, reflection loss, molar refraction charged radiation stopping powers, projected range, fast neutron removal cross section and thermal neutron total cross-section. All the estimated parameters showed variations with glass stoichiometry. The addition of WO3 triggered the BO4 → BO3 unit transformation which prompted the variations in the physical and optical parameters of the glasses. The optical transparency in the visible region and density of the glasses decreased with WO3 concentration while the molar volume increased. For electrons, the stopping powers were in the range, 1.436–11.76 cm2/g, 1.433–11.66 cm2/g, and 1.426–11.44 cm2/g, for BNB-W00, BNB-W03, and BNB-W10, respectively. For protons, alpha particles, and carbon ions, the mass stopping powers increased with WO3 content. Based on projected range data, particles with greater energy per nucleon penetrated the glasses deeper and the WO3- rich glasses had higher transmissivity for charged radiation. Compared to some existing neutron moderators, the investigated glasses displayed higher fast neutron cross-sections. The studied glasses can function well as barriers to moderate fast neutrons, attenuate thermal neutrons, and absorbed charged radiation.

Physical, optical, spectroscopic features of Li2B4O7-Bi2O3-Sb2O3 glass system reinforced with molybdenum ions

To comprehend the physical, optical and spectroscopic properties of a novel multicomponent glass system with compositional formula 60Li2B4O7-30Bi2O3-(10-x)Sb2O3-xMoO3 (x = 0, 2.5, 5, 7.5 and 10 mol%) has been synthesized by melt quench process. The lack of intense peaks in the XRD confirmed the glassy nature of the prepared samples. On Substitution of Sb2O3 with MoO3 in lithium tetraborate-bismuthate glasses, a linear decrease in the density and an increase in the molar volume has been noticed. Physical parameters like oxygen packing density, oxygen molar volume and packing density have been computed. Optical energy bandgap evaluated from UV–Visible absorption spectra, declined with increase of MoO3. Refractive indices exhibited opposite trend with optical energy bandgap and opens applications for non-linear optical devices. Vibrational modes in the as-prepared glasses have been identified by FTIR and Raman spectra. With increase in MoO3 content, Mo6+ ions transformed to Mo5+ units which in turn converted BO4 to BO3 units as confirmed by FTIR and Raman spectroscopies.

Structural Properties of Al-Li-Zn Borate Glass Activated with Dysprosium (Dy3+) for Radiation Dosimeter

This study explores the properties of Al-Li-Zn glass doped with dysprosium ions as a potential radiation dosimeter. The glass was prepared using the novel quenching technique, and various characterisations were performed to evaluate its properties. X-ray diffraction (XRD) analysis confirmed the amorphous phases in the glass. UV-vis spectroscopy revealed a noticeable absorption peak in the visible region, characteristic of the dysprosium ions. PL spectra luminous peaks at 348 nm (yellow), 529 nm (green), and 625 nm (orange hue), which corresponded to the 4H15/2 → 6P7/2, 4F9/2 → 6H15/2, 4F9/2 → 6H15/2, and 4F9/2 → 6H13/2 transitions in 1.5 and 2.5 dysprosium ions respectively. Significant decrease in Tg from 257°C in the undoped sample to 101°C in the doped sample, Tm of the doped sample dropped from 862°C to 815°C and Tc of the doped sample dropped from 756°C to 444°C, suggesting a reduced crystallisation threshold. FTIR analysis demonstrated that OH groups displayed peaks within the 2200 to 4000 cm range. Stretching vibrations of BO3 units occurred between 1200 and 1600. Stretching vibrations of BO4 units were observed between 800 and 1200; these show that the presence of Dy3+ and zinc oxide altered the arrangement of the glass structure, causing a transformation from B03 groups to B04 groups. This transformation leads to defects in a stable trap environment suitable for thermoluminescence phenomena. Considering its properties and optical characteristics, the samples with 1.5 and 2.5 mol % of Dy3+ showed remarkable thermoluminescence properties, suggesting its suitable use as a dosimeter to gauge radiation exposure. The glass demonstrates stability and absorption capability, making it worth considering for radiation detection applications.

Utilizing bypass cement dust in the production of radiation shielding bismuth borate glass

Using the melting-quench technique, a new method for removing bypass cement dust (BCD) was developed in this study using an active environmental glassy system with the chemical formula (65–x)B2O3–5Li2O–5CdO–25BCD–xBi2O3, where x varied from 0 to 30 mol%. A glass density of 3.137 g/cm³ is attained without bismuth, while a density of 5.345 g/cm³ is obtained with 30 mol% Bi2O3. The unit peaks BO3 and BO4 in the FTIR spectra signify the presence of the BLCDBi-series structure. Elevated Bi2O3 concentrations augment BO4 units. Defects influence the optical absorbance of glass within the wavelength range of 190–1000 nm. These defects in the glass network are created by silicon electrons, silicon hole centers, and BCD as well as Bi3+ or Bi6+ after the addition of bismuth oxide to the glassy system. Eg values were found to decrease as Bi2O3 concentration increased, whereas EU and n values exhibited the opposite behavior. A gamma spectroscopy system and the Phy-X/PSD software are used to calculate the linear attenuation coefficient (LAC), mass attenuation coefficient (MAC), half-value layer (HVL), tenth-value layer (TVL), effective atomic number (Zeff), and effective electron density (Neff) of samples. In addition, the Phy-X/PSD software demonstrated good agreement between experimental and theoretical interpretations. Overall, the results showed that the BLCDBi-30 sample is suitable for use in radiation protection.

Effect of Dy3+ ions on physical, structural and thermal properties of ZnNaPbB glasses

In this report, inspired by the excellent spectroscopic characteristics of dysprosium (Dy3+) ions doped borate glasses, a series with the composition (70-x)B2O3-10ZnO-10PbO-10Na2CO3-xDy2O3 (here ‘x’ have the values as 0.1, 0.5, 1.0, 1.5 and 2.0 in mol % ) was made using the melt quenching process and named as ZnNaPbBDy0.1 to ZnNaPbBDy2.0. Here we study the physical, structural and thermal properties of Dy3+ ions doped Zinc Sodium Lead Borate (ZnNaPbB) glasses through different characterization techniques like Fourier transform infrared (FT-IR), Raman spectroscopy, Differential scanning calorimetry (DSC) and decay spectroscopy. Several physical parameters were evaluated to assess the effect of Dy3+ inclusion. FT-IR and Raman spectra confirm the presence of BO3 and BO4 structural units. The data recorded by DSC spectra have been used to predict the glass transition temperature (Tg). The nature of decay spectra was estimated which diverges from exponential to non-exponential at higher concentrations. The decay spectral data is used to calculate the experimental lifetimes for all the glass samples. The Inoakutti Hirayama (I-H) model and Dexter’s plot are used to confirm the type of interaction between the donor and acceptor Dy3+- Dy3+ ions is dipole–dipole in nature that is responsible for the emission intensity quenching with concentration. All the above results might be advantageous for variety of applications in photonic devices.

Investigation on luminescent characteristics of Tb3+/Dy3+co-doped boro-phosphate glass for cool white LED and radiation shielding applications

The Tb3+/Dy3+ co-doped Boro-Phosphate Glass (BPANZDyTb) was produced (40 B2O3 + 39P2O5 + 5 Al2O3 + 5 NaF + 10 ZnO + 0.5 Tb2O3 + 0.5 Dy2O3) using melt-quenching technique. X-ray diffraction measurements, Raman, and Fourier Transform Infrared were used to evaluate the structural behavior of the prepared glass. Powder-XRD spectra, in the 10–90° range showed that the prepared glass was amorphous. FTIR analysis reveals that the network contains a variety of structural groups, including B-O-B, BO4, BO, P-O, PO2, P-O-B, and PO4 units. The UV–visible diffuse reflectance spectroscopy was used to record and study the optical linear properties of Tb3+/Dy3+ co-doped Boro-Phosphate Glass (BPANZDyTb). The photoluminescence excitation peak was obtained at 348 nm. The emission peaks were located at 484 nm (4F9/2 → 6H15/2 → blue), 576 nm (4F9/2 → 6H13/2 → yellow), and 662 nm (4F9/2 → 6H11/2 → red). Tb3+ ions are located at 412 nm (5D3 → 7F5), 441 nm (5D3 → 7F4), 546 nm (5D4 → 7F5), and 625 nm (5D4 → 7F3). The result of CIE 1931 chromaticity coordinates indicate that the prepared glass is suitable material for cold white light emitting diode applications due to its color coordinates x = 0.3106 and y = 0.3240 and correlated color temperature (CCT) values about 6768 K. The gamma-ray parameters such as half-value layer (HVL), mass attenuation coefficient (μ/ρ), mean free path (MFP), and effective atomic number (Zeff) of the BPANZDyTb glass were studied using Phy-X software. The results of the gamma-ray parameter show that the Dy3+ ions and Tb3+ ions co-doped BoroPhosphate glass is an appropriate material for radiation shielding applications.

Compositional impacts of high CdO content on the structure and radiation shielding efficiency of CoO–Na2O–B2O3 glass system

Here, this study investigated the structural changes and radiation shielding efficiency of a borate glass host modified by varying cadmium oxide (CdO) concentrations. The glass composition consisted of boron oxide (B2O3; 80:56 mol%), sodium oxide (Na2O; 19.6 mol%), and cobalt oxide (CoO; 0.4 mol%), with cadmium oxide (CdO; 0:24 mol%). The glass structure was analyzed utilizing mass density and FT-infrared spectroscopy (FTIR) in the 400 to 1600 cm−1 range, while radiation shielding properties were investigated utilizing the online Phy-X software in the 0.284–1.333 MeV energy window. Notably, the addition of CdO significantly impacted the glass density, increasing it by approximately 93 % as the added CdO concentration rose from 0 to 24 mol% (i.e., from 2.507 g/cm3 to 4.849 g/cm3). FTIR analysis revealed a concurrent increase in BO4 structural units with increasing CdO/B2O3 ratios. This observation was supported by the calculated N4BO4/(BO3+BO4) ratio, which increased from 40.73% for the CdO-free sample to 52.00% for the highest CdO content. This increase in BO4 units, denser than BO3 units, explains the observed density increase. Conversely, the concentration of non-bridging oxygens decreased from 10.14% to 4.34% with increasing CdO contents, indicating a more tightly packed glass network. Radiation shielding studies demonstrated that increasing CdO concentration from 0 to 24 mol% enhanced the shielding efficiency, evidenced by a decrease in the half-value layer parameter (HVL). The radiation protection efficacy (RPE) also increased from 0.214 to 0.426 for the CdO-free sample to the sample containing 24 mol% CdO at the investigated energy level. This finding highlights the superior shielding capability of the CdO-rich sample. Furthermore, the transmission factor (TF) was investigated for a constant thickness of 0.75 cm for glasses. The CdO-rich sample exhibited a lower TF compared to the CdO-free sample, particularly at lower energies. This finding confirms that, for a given thickness and energy, raising the cadmium oxide content in the current composition leads to an observed mitigation in the transmitted radiation.

Influence of La3+ ions on the structural, elastic, optical, and radiation shielding properties of Cr2O3-Doped heavy metal glasses

This study investigates the effect of La³⁺ rare earth ions on the structural, elastic, optical, and radiation shielding features of heavy metal borate glass (B₂O₃-PbO) doped with Cr₂O₃. Density measurements and FT-IR spectra analysis revealed the role of La3+ ions as a network modifier, where successive additions of La2O3 content led to a gradual increase in the density and an increase in the non-bridging oxygen content resulting from the structural transformation between the BO4 and BO3 units. The significant improvement in the elastic modulus and microhardness factor moduli was confirmed by calculating the change in ultrasonic velocities through the glassy system. The structural modifications induced by La³⁺ ions narrowed the band gap and increased the Urbach energy, indicating higher disorder within the glass network. The linear refractive indices increased due to increased optical basicity and electronic polarization. Optical absorption results showed that Cr⁶⁺/Cr³⁺ ions occupy octahedral/tetrahedral sites, with the tendency for Cr³⁺ cations to occupy more octahedral sites with increasing La₂O₃ content. The produced samples showed a greenish-yellow color caused by the absorption band centered at ∼415 nm associated with the electronic transition ⁴A₂g(F)→2Eg(G). The ligand field effect highlighted the significance of La³⁺ cations in increasing the crystalline field intensity surrounding Cr³⁺ cations and reducing the nephelauxetic ratio, signifying enhanced covalent character between Cr³⁺ cations and neighboring ions. Moreover, the radiation shielding capabilities of the glassy system were analyzed and compared with standard shielding materials, confirming superior shielding performance in samples with the highest La₂O₃ content.

Heptanuclear Cadmium Borovanadate Containing a Sandwich-Type Anionic Partial Structure {B20V12} as a Heterogeneous Photocatalyst for the Reduction of CO2 into CH4.

The novel heptanuclear cadmium borovanadate [Cd(en)3]{[Cd(H2O)(en)]6[B20V12O60(OH)2]}·8H2O (en = ethylenediamine) has been prepared under hydrothermal condition. It exhibits a 2D layered architecture that is built up from the [Cd(H2O)(en)]2+ coordination cations and new sandwich-type borovanadate anions [B20V12O60(OH)2]14- constructed by BO3, BO4, BO3(OH), and VO5 units. It features the first heptanuclear cadmium borovanadate containing the single valence of V4+ cations and unique B/V ratio (B/V = 20/12). Its thermal, magnetic, XPS, and optical properties have been systematically studied. The Eg (2.60 eV), EVB (1.69 eV), and ECB (-0.91 eV) were well determined by the UV-vis diffuse reflectance spectrum, UPS curve, and the formula ECB = EVB - Eg, respectively. The photocatalytic experiments revealed that the borovanadate could be selected as an effective and stable heterogeneous catalyst for the reduction of CO2 to CH4 by means of visible light (the amount for CH4 gas could reach 50.57 μmol·g-1·h-1 when the reaction time was 3 h). The recycling experiment and photocatalytic mechanism were also well investigated and established in detail.

Structural, thermal and X-ray photoelectron spectroscopic properties of boro-tellurite based quaternary glass system

The structural, functional and thermal properties of the TeZnCaB glass system were investigated in this work. The thermal properties of the glass system were studied using DSC (differential scanning calorimetry), and the glass transition temperature (Tg) decreased from 470 °C to 438 °C with increasing TeO2 concentration. The vibrational and bending modes of the TeZnCaB glass samples were depicted by Raman spectroscopy analysis. FTIR (Fourier-transform infrared spectroscopy) was performed to investigate the functional groups of TeO2 and B2O3 in the samples. The TeZnCaB glass samples consist of TeO3, TeO4, BO4 and BO3 structural units. XPS (X-ray photoelectron spectroscopy) was investigated to reveal information about the chemical environment and the creation of NBO (non-bridging oxygen) and BO (bridging oxygen) for the different glass systems. The high-resolution Te3d spectrum confirms the presence of various tellurium-based structural units such as TeO4, TeO3, and TeO3+1. The deconvolution of B1s spectra confirmed the existence of two forms of boron (B) such as BO4 (four coordination) and BO3 (three coordination) in the TeZnCaB glass system.

Flux Synthesis of Alkaline-Earth Lanthanide Borates as Potential Nuclear Waste Forms.

Neodymium is typically considered the best surrogate for trivalent americium and can be used to identify Am3+ containing materials that are likely to form. We have explored the alkaline-earth lanthanide borate phase space using alkaline-earth halide/carbonate fluxes. This resulted in the synthesis of new compounds AE5Ln(BO3)4X (AE = Ca, Sr; Ln = Pr, Nd, Eu, Tb; X = Cl, Br) and AE3Ln2(BO3)4 (AE = Sr, Ba; Ln = Pr, Nd) as well as the synthesis of two compounds of Ba8Ln2(BO3)6(B2O5) (Ln = Eu, Tb) crystallizing in a new structure type. Ba8Ln2(BO3)6(B2O5) crystallizes in the space group P21/n with lattice parameters a = 8.6002(3) Å, b = 7.9245(3) Å, c = 17.6697(7) Å, and β = 91.3560(10)° for the Eu analogue, and the structure contains isolated LnO8 polyhedra connected into a framework by BO3 and B2O5 units. The fluorescence emission spectra of AE5Ln(BO3)4X (AE = Ca, Sr; Ln = Eu, Tb; X = Cl, Br) and Ba8Ln2(BO3)6(B2O5) (Ln = Eu, Tb) are reported.

Effect of Bismuth on Physical and Spectroscopic Properties of ZnO-Li2B4O7-TbF3 Glasses

The effect of Bismuth on zinc-lithium tetra borate glasses were discussed based on structural, physical, and spectroscopic properties. Glass systems of Bi2O3-ZnO-Li2B4O7-TbF3 [BZLT] were cast by melt-quench process. Transparent glasses were analysed by diffracted Roentgen X-rays. Peak free and broad nature X-ray diffraction revealed the amorphous arrangement prevailing in these glasses. Density was estimated using the Archimedes principle. Bismuth grossly affected the density of BZLT glasses by increasing its value 2.722 gm/cc [BZLT-0] to 4.6739 gm/cc [BZLT-40]. Optical absorption provides valuable information about optical band gap energy and Urbach energy and some of its derived physical quantities. The effect of bismuth is felt in decreased Eopt values [3.312 eV in BZLT-0] [2.619 eV in BZLT-40] in BZLT glasses. Bismuth altered the structure of the borate network by forming non-bridging oxygens which in turn reduced the band gap energy by large margin (ΔEopt = 0.693 eV). Fourier transform infrared spectroscpy and Raman studies revealed the presence of several triangular BO3 and tetrahedral BO4 and BiO3 units and also the existence of metal cation vibrations and supported the large deviations in the optical bandgap energies. Election paramagnetic resonance studies support the presence of Tb3+ ions and absence of Tb4+ions in BZLT glasses.

Impact of SnO2 doping on spectroscopic characteristics of the SnO2-Na2O-CoO-B2O3 borate glass matrix

The role of tin oxide (SnO2) on the structure-optical features of borate glasses containing low cobalt oxide impurities was studied. The study was carried out on a glass system [x SnO2 – (80-x) B2O3 – 19.5 Na2O – 0.5 CoO]; x = 0.0, 0.5, 1.0, 2.0 and 3.0 mol%. Glass synthesis was carried out by the melt-quench technique. Structure and optical absorption spectroscopy were carried out to explore the optical transitions of Co cations inside the present glass matrix. The obtained results indicate that, with the further addition of SnO2 content, the molar volume decreased from 31.675 cm3/mol to 29.147 cm3/mol. FTIR studies indicated the basic structural units of trigonal BO3 units and BO4 tetrahedra. Herein also, additional contents of tin oxide increased the nonbridging oxygen contents. The reason behind such increment is attributed to the existence of Sn4+ ions in octahedral coordination acting as network modifiers. Optical absorption spectra indicated the existence of Co ions in both Co2+ and Co3+ oxidation states. Moreover, the existence of significant SnO2 concurred with the significant blue shift in the visible absorption bands and red shift in near infrared absorption bands. The positions absorption bands of Co ions were analyzed in the context of ligand field parameters determinations. The obtained data of the crystal field splitting parameter (10Dqt) showed decreased values from 3451 cm−1 to 3364 cm−1 with more SnO2 addition. While Racah parameter B values were also, attained showing increased values from 967 cm−1 to 985 cm−1 when additional SnO2 is added. Further, the impacted role of SnO2 addition on the structural and optical properties of the present glasses was finally estimated.

Evaluating the role of Er3+ ion on the structural, optical and thermal properties of CaO–ZrO2–Y2O3–B2O3–SiO2 glasses

The present work is involved in synthesizing, characterizing, and evaluating the role of Er3+ ion on structural, optical, and thermal properties of 20CaO–10ZrO2–10Y2O3-30 B2O3-(30-x)SiO2-xEr2O3 (x = 0.3, 0.6, 1.0, and 1.5 mol%) compositions. The as-synthesized samples are characterized by various experimental techniques such as XRD, FTIR, Raman, UV visible spectroscopy, and DSC to study their suitability for optoelectronic applications. The density of glasses increases, whereas the molar volume decreases with the doping of Er2O3 in place of SiO2. The amorphous nature of the prepared samples is confirmed by the X-ray diffraction pattern. FTIR and Raman spectra confirm the presence of BO4 and BO3 structural units in the prepared glass samples. The UV–visible absorption spectra show 4G9/2, 4G11/2, 2G9/2, 4F5/2, 4F7/2, 2H11/2, and 4F9/2 transitions with the Er2O3 doping. The optical band gap increases from 3.25 to 3.61 eV, whereas the refractive index decreases from 2.33 to 2.24 with increasing doping of Er2O3, except for the SE-1.5 glass sample. The molar refraction decreases with Er2O3 doping. The glass transition temperature increases from 472 to 512 °C with Er2O3 doping in place of SiO2, except for the SE-1.5 glass. SE-0.3 glass shows the highest thermal stability, while SE-1.5 glass shows the lowest thermal stability. Therefore, these glasses can be considered for application in optoelectronics.

Physical, optical, thermal, structural and mechanical properties of alkaline earth borate glasses

Binary alkaline earth borate glasses were synthesized via the melt quenching technique. The density and molar volume of the resultant glasses were determined experimentally. The glass optical basicity has been found to increase with the glass polarizability. The optical properties of the glasses were comprehensively analyzed, revealing a shift in the cutoff wavelength towards longer wavelengths with increasing glass optical basicity. Additionally, the optical band gap (Eg) was estimated. Structural investigations unveiled an increase in the abundance of BO4 units as the glass optical basicity increased. Furthermore, the glass transition temperature was observed to decrease with decreasing cation field strength. Glass packing density and B2O3 packing factor were calculated to assess structural variations. The longitudinal and shear velocities were determined using the pulse echo technique, providing insights into the elastic moduli of the glasses. The Makishima and Mackenzie approach was employed to predict the elastic moduli, yielding results in good agreement with experimental data. This comprehensive analysis sheds light on the relationship between composition, structure, and mechanical properties of binary alkaline earth borate glasses, offering valuable insights for potential applications.