Magnesium ferrite nanoparticles as a magnetic sorbent for the removal of Mn2+, Co2+, Ni2+ and Cu2+ from aqueous solution

The aim of this research was to prepare magnesium ferrite (MgFe₂O₄) magnetic nanoparticles and to investigate their sorption characteristics towards Mn²⁺, Co²⁺, Ni²⁺, Cu²⁺ ions in aqueous solution. MgFe₂O₄ was synthesized by glycine-nitrate combustion method and was characterized by low crystallinity with crystallite size of 8.2?nm, particle aggregates of 13–25?nm, BET surface area of 14?m²/g and pore size of 8.0?nm. Sorption properties of MgFe₂O₄ towards Mn²⁺, Co²⁺, Ni²⁺, Cu²⁺ ions were studied using one-component model solutions and found to be dependent on metal ions concentration, contact time, pH and conditions of regeneration experiment. The highest sorption capacity of MgFe₂O₄ was detected towards Co²⁺ (2.30?mmol?g¹) and Mn²⁺ (1.56?mmol?g^?1) and the lowest towards Ni²⁺ (0.89?mmol?g^?1) and Cu²⁺ (0.46?mmol?g^?1). It was observed that sorption equilibrium occurs very quickly within 20–60?min. The pH_zpc of sorbent was calculated to be 6.58. At studied pH interval (3.0–7.0) the sorption capacity of MgFe₂O₄ was not significantly affected. Regeneration study showed that the metal loaded sorbent could be regenerated by aqueous solution of 10^?3 M MgCl₂ at pH 6.0 within 120?min of contact time. Regeneration test suggested that MgFe₂O₄ magnetic sorbent can be efficiently used at least for four adsorption-desorption cycles. The high sorption properties and kinetics of toxic metal ion sorption indicates good prospects of developed sorbent in practice for wastewater treatment.     

Structural,morphological, and magnetic properties of ZnxCo1-xFe2O4 (0 ≤ x ≤ 1) prepared using a chemical co-precipitation method

In the present study, the chemical co-precipitation technique was adopted to synthesize Zn_xCo_1-xFe₂O₄ (ZCF) (0?≤ x?≤?1) ferrites. The thermogravimetric-differential thermal analysis results revealed that above 405?°C, the precursor had decomposed and ferrite formation had occurred. The structure and morphology of the prepared ferrite nanoparticles were investigated using X-ray diffraction, Fourier transform infrared spectroscopy, and field emission scanning electron microscopy (FE-SEM). The synthesized polycrystalline nanoparticles had a cubic spinel structure and the crystallite size was in the range of 6.09–12.98?nm. The prepared ferrites appeared as nearly spherical nanoparticles with a particle size in between 0.13 and 0.23?µm, as confirmed using FE-SEM. The elemental composition was determined using the energy-dispersive X-ray spectroscopy technique. The influence of the Zn-substituted cobalt ferrites (ZCF) on the structural, morphological, and magnetic properties were studied. The magnetic properties of the ZCF samples such as saturation magnetization, remanence magnetization, and coercivity measured at room temperature were 0.387–2.065?emu/g, 0.057–1.282?emu/g, and 60–1834?Oe, respectively. It was confirmed from the nature of the hysteresis loops that the given ZCF samples can be considered as a soft magnetic material.     

Structural,magnetic and magnetostrictive properties of Co1-xLixFe2O4 synthesized by cathode materials of spent Li-ion batteries

In this study, we investigated the effects of substituting Li⁺ for Co²⁺ at the B sites of the spinel lattice on the structural, magnetic and magnetostrictive properties of cobalt ferrites. The Li⁺ substituted cobalt ferrites, Co_1-xLi_xFe₂O₄, with x varying from 0 to 0.7 in 0.1 increments, were synthesized with a sol-gel auto-combustion method using the cathode materials of spent Li-ion batteries. X-ray diffraction analysis revealed that all the Co_1-xLi_xFe₂O₄ nanopowders had a single-phase spinel structure and the lattice parameters decreased with increasing Li⁺ content, which can be proved by slight shifts towards higher diffraction angle values of the (311) peak. Field emission scanning electron microscopy was used to observe the fractured inner surface of the sintered cylindrical rods and the increased porosity resulted in a decreased magnetostriction. The oxidation states of Co and Fe in the cobalt ferrite samples were examined by X-ray photoelectron spectroscopy. High resolution transmission electron microscopy micrographs showed that most particles were roughly spherical and with sizes of 25–35?nm. Li⁺ substitution had a strong effect on the saturation magnetization and coercivity, which were characterized with a vibrating sample magnetometer. The Curie temperature was reduced due to the decrease in magnetic cations and the weakening of the exchange interactions. The magnetostrictive properties were influenced by the incorporation of Li⁺ at the B sites of the spinel structure and correlated with the changes in porosity, magnetocrystalline anisotropy and the cation distribution.     

Cathodoluminescence and thermoluminescence of ZnB2O4:Eu3+ phosphors prepared via wet-chemical synthesis

In present work, a series of Eu doped zinc borate, ZnB₂O₄, phosphors prepared via wet chemical synthesis and their structural, surface morphology, cathodoluminescence (CL) and thermoluminescence (TL) properties have been studied. Phase purity and crystal structure of as-prepared samples are confirmed by X-ray diffraction measurements (XRD) and they were well consistent with PDF card No. 39-1126, indicating the formation of pure phase. The thermoluminescence (TL) behaviors of Eu activated ZnB₂O₄ host lattice are studied for various beta doses ranging from 0.1 to 10?Gy. The high-temperature peak of Eu activated sample located at 192?°C exhibited a linear dose response in the range of 0.1–10?Gy. Initial rise (IR) and peak shape (PS) methods were used to determine the activation energies of the trapping centres. The effects of the variable heating rate on TL behaviour of Eu activated ZnB₂O₄ were also studied. When excited using an electron beam induced light emission (i.e cathodoluminescence, CL) at room temperature (RT), the as-prepared phosphors generate reddish-orange color due to predominant emission peaks of Eu³⁺ ions located at 576–710?nm assigned to the ⁵D₀→⁷F_J (J=1,2,3, and 4) transitions. The maximum CL intensity for Eu³⁺ ions at 614?nm with transition ⁵D₀→⁷F₂ was reached Eu³⁺ concentration of 5?mol%; quenching occurred at higher concentrations. Strong emission peak for Eu³⁺ ions at 614?nm with transition ⁵D₀→⁷F₂ is observed. The CL experimental data indicate that ZnB₂O₄:Eu³⁺ phosphor as an orange-red emitting phosphor may be promising luminescence materials for the optoelectronic applications.     

Color-tunable up-conversion luminescence of Zn(AlxGa1-x)2O4:Yb3+,Tm3+,Er3+ powders

Color-tunable up-conversion powder phosphors Zn(Al_xGa_1-x)₂O₄: Yb³⁺,Tm³⁺,Er³⁺ were synthesized via high temperature solid-state reaction. Also, the morphological and structural characterization, up-conversion luminescent properties were all investigated in this paper. In brief, under the excitation of a 980?nm laser, all powders have same emission peaks containing blue emission at 477?nm (attributed to ¹G₄→³H₆ transition of Tm³⁺ ions), green emission at 526?nm and 549?nm (attributed to ²H_11/2→ ⁴I_15/2 and ⁴S_3/2→⁴I_15/2 transition of Er³⁺ ions respectively), red emission at about 659?nm and 694?nm (attributed to ⁴F_9/2→⁴I_15/2 transition of Er³⁺ ions and ³F₃→³H₆ transition of Tm³⁺ ions, respectively), which are not changed after the doping of Al³⁺ ions. However, the doping of Al³⁺ ions can enhance the up-conversion luminescent intensity and efficiency, while the emission color of as-prepared powder phosphors can be tunable by controlling the doping amount of Al³⁺ ions. Taking Zn(Al_0.5Ga_0.5)₂O₄:Yb,Tm,Er as the cut-off value, the emissions have clear blue-shift firstly and then show obvious red-shift with the increasing doping of Al³⁺ ions. Stated thus, pink emission in ZnAl₂O₄:Yb,Tm,Er, purplish pink emission in ZnGa₂O₄:Yb,Tm,Er and Zn(Al_0.9Ga_0.1)₂O₄:Yb,Tm,Er, purple emission in Zn(Al_0.1Ga_0.9)₂O₄:Yb,Tm,Er and Zn(Al_0.3Ga_0.7)₂O₄:Yb,Tm,Er, purplish blue emission in Zn(Al_0.7Ga_0.3)₂O₄:Yb,Tm,Er, blue emission in Zn(Al_0.5Ga_0.5)₂O₄:Yb,Tm,Er can be observed, which confirm the potential applications of as-prepared Zn(Al_xGa_1-x)₂O₄:Yb³⁺,Tm³⁺,Er³⁺ powder phosphors in luminous paint, infrared detection and so on.     

Rietveld refinement,Raman, optical,dielectric, Mössbauer and magnetic characterization of superparamagnetic fcc-CaFe2O4 nanoparticles

This article describes synthesis of superparamagnetic fcc-CaFe₂O₄ nanoparticles by a metal nitrate-citrate monohydrate sol–gel route and characterization using X-ray diffractometry, Raman spectroscopic, UV–Vis–NIR optical absorption spectroscopic, Mössbauer spectroscopy, dielectric and SQUID magnetometry measurements. Rietveld refinement of the X-ray diffraction pattern and observation of active A_1?g, T_2?g & E_g modes in the Raman spectrum confirmed formation of single phase CaFe₂O₄ nanoparticles in the spinel ferrite type fcc structure without impurity. Mössbauer and Rietveld data analysis revealed that nanocrystalline CaFe₂O₄ is dominantly an inverse ferrite in which 85% Ca atoms preferentially occupy the octahedral site in the fcc symmetry and the Fe ions are in high spin Fe⁺³ state. Nanocrystalline CaFe₂O₄ significantly absorbs optical light below 500?nm and the direct band gap energy is estimated to ~1.83?eV, which is higher than 1.26?eV reported for orthorhombic CaFe₂O₄. Temperature and field dependent magnetic studies showed that fcc-CaFe₂O₄ nanoparticles exhibit superparamagnetism at room temperature with high saturation magnetization of 1.07μ_B. The blocking temperature is ~53?K at 1000?Oe and ~72?K at 500?Oe clearly shows lowering of blocking temperature at higher magnetic field. Interestingly below the blocking temperature at 20?K, CaFe₂O₄ nanoparticles behave as non collinear soft-ferrimagnetic material with a saturation magnetization of 1.16 μ_B, coercivity of 150?Oe and remanence of 4.45?emu/g. The magnetic momenta of Fe⁺³ ions residing at the octahedral sub-lattice are canted at ~25?°.     

Structural,dielectric and magnetic properties of (ZnFe2O4/Polystyrene) nanocomposites synthesized by micro-emuslion technique

This work aims to study the effect of polymer on the structure, magnetic and dielectric properties of spinel ferrite composite. Nanocomposites based on polystyrene (PST)/ZnFe₂O₄ were synthesized by using the micro-emulsion method. The novel composites with PST to ZnFe₂O₄ ratios (4:0, 4:1, 4:2, 4:3, 4:4, 0:4) were analyzed by X-ray diffractometer (XRD) which confirms the spinel structure of ZnFe₂O₄ with an average crystallite size of 15.3 nm for pure ZnFe₂O₄ and decreases by increasing the polystyrene concentration. Field Emission Scanning Electron Microscopy (FESEM) gave the optimized results of surface morphology and the crystallite size which are in accordance with XRD data. Fourier Transform Infrared (FTIR) spectra show two main broad metal–oxygen bands corresponding to the intrinsic stretching vibrations of the metal at the tetrahedral site (observed between 837.9 and 1034.3 cm⁻¹) and traces of organic materials were observed at 1499.2 and 1766.4 cm⁻¹, which are associated with CO and CC stretching vibration respectively. O–H stretch of COOH weak acid of the carboxyl group was found at 2978.7 cm^-1. The composite with equal ZnFe₂O₄ to PST ratio (4:4) shows that real part of dielectric constant is independent of frequency at lower frequencies of an applied electric field. The resonance type behaviour was observed at higher frequency (2.5 GHz) which shows the material is excellent for dispersion of electric part of microwaves. The magnetization for pure ferrite (ZnFe₂O₄) at 15000 Oe was found to be 1.49 emu/g which decreases to 0.54 emu/g for the composite with the equal ferrite to polystyrene ratio. Based on their dielectric and magnetic characterization, these composites are considered suitable candidates to employ as microwave absorbing materials.     

Synthesis,structure and luminescent properties of Eu3+ doped Ca3LiMgV3O12 color-tunable phosphor

A new vanadate Ca₃LiMgV₃O₁₂ and its Eu³⁺-doped counterparts were synthesized. Rietveld confinement result of Ca₃LiMgV₃O₁₂ host indicates that it belongs to cubic space group Ia-3d with parameters of a =?12.4300?Å, V =?1920.49?ų, Z?=?8. Under UV excitation, pure Ca₃LiMgV₃O₁₂ exhibits a bluish-green broadband emission at 490?nm, while Eu³⁺ doped Ca₃LiMgV₃O₁₂ shows one bluish-green broad band with a series of red sharp peaks, which originate from the V⁵⁺-O^2- charge transfer and the Eu³⁺ intra-4f transitions, respectively. The occurrence of VO₄→Eu³⁺ energy transfer is confirmed by decay lifetime analysis and time-resolved emission spectra. It is found that emitting color varies from bluish-green to orange-red with increasing Eu³⁺ concentration. VO₄ bluish-green and Eu³⁺ red emission shows different thermal quenching response with increasing temperature, due to their different activation energy.     

Atomic hydrogenation-induced paramagnetic-ferromagnetic transition in zinc ferrite

A paramagnetic-ferromagnetic transition was observed in normal spinel zinc ferrite (ZnFe₂O₄) during atomic hydrogenation at room temperature. Magnetic measurements showed enhanced ferromagnetic property with increasing hydrogenation time. The hydrogenated ZnFe₂O₄ has normal spinel structure according to X-ray diffraction (XRD) and Raman analyses. Iron hydride was found from the XRD and X-ray absorption fine structure results. No A–B site ions exchange was observed in the x-ray absorption spectra while the atomic distances of Fe–O, Zn–O, Fe–Fe, Zn–Zn and Fe–Zn coordinations were reduced. A hybrid of Fe²⁺ and Fe³⁺ in hydrogenated ZnFe₂O₄ can be further revealed through deconvolution of x-ray absorption near edge structure. The paramagnetic-ferromagnetic transition and enhanced ferromagnetic property were mainly due to the formation of iron hydride and the B-site super-exchange interactions of Fe²⁺ and Fe³⁺.     

Synthesis of Li+-ion activated NaYF4: Er3+/Yb3+ phosphors via a modified solid-state process for latent fingerprint detection

Li⁺-ion codoped NaYF₄: Er³⁺/Yb³⁺ phosphors (β-NaYF₄) with a hexagonal structure were synthesized via a modified solid-state route. High-speed planetary ball milling and solid-liquid mixing were simultaneously used to overcome the drawbacks of high synthesis temperatures in conventional routes. A pure β-NaYF₄ phase was obtained through calcination at 600?°C for 3?h. Increases in the codoping content of Li⁺ ion caused a slight shift in X-ray diffraction peak positions toward high angles owing to the distortion of the local crystal field. Field emission scanning electron microscope images showed agglomerated spherical particles of approximately 0.7?µm with narrow size distribution. The upconversion properties of β-NaYF₄ codoped with Li⁺-ion were explored. Two emission bands in the green regions (520?nm and 545?nm) and one emission band in the red region (615?nm) were observed owing to the ²H_11/2→⁴I_15/2, ⁴S_3/2→⁴I_15/2, and ⁴F_9/2→⁴I_15/2 transitions of Er³⁺, respectively. Codoping with 6?mol% Li⁺ increased the upconversion intensity by three times, which was explained using the energy level diagram. The present phosphors with improved upconversion properties were utilized for latent fingerprint detection on smooth surfaces of regularly used polymer sheets, glass substrates, and compact discs. Using the present phosphors, the base elements with three-level features, such as sharp ridges, valleys, ridge flow, bifurcation, ridge shapes, and dots, were observed on all hydrophilic and hydrophobic surfaces. The prepared phosphors exhibited promising characteristics to detect the features of fingerprint impression for individual identification in forensic applications.     

Spectral pure RGB up-conversion emissions in self-assembled Gd2O3: Yb3+, Er3+/Ho3+/Tm3+ 3D hierarchical architectures

Self-assembled three-dimensional Yb³⁺(Ln = Er, Ho, Tm) co-doped Gd₂O₃ up-converted (UC) phosphors were synthesized by a facile co-precipitation method, and their morphologies and microstructures were investigated by scanning electron microscope (SEM) and transmission electron microscope (TEM) analysis. Under the excitation at 980 nm, spectral pure three primary colors red, green and blue (RGB) emissions were respectively achieved in Yb³⁺/Er³⁺, Yb³⁺/Ho³⁺ and Yb³⁺/Tm³⁺ co-doped Gd₂O₃ phosphors, in which spectral color purities were tuned by adjusting the doping concentration, annealing temperature, excitation power density and the pulse-width of 980 nm laser. These results provide deeper insights into modulating spectral color purities of up-converted emission, and the potential applications of spectrally pure RGB up-converted materials in fingerprint recognition and multi-color printing were also investigated.     

Toughening of MgAl2O4 spinel/ Si3N4 nanocomposite fabricated by spark plasma sintering

The main objective of this work is to compare the hardness, fracture toughness, and optical transparency of MgAl₂O₄ spinel (magnesium aluminate), MgAl₂O₄ spinel/ Si₃N₄ nanocomposite, and the heat-treated spinel/Si₃N₄ nanocomposite. For this purpose, the commercial spinel nanopowder and the laboratory-made spinel/ Si₃N₄ nanocomposite powder were sintered using spark plasma sintering (SPS). A heat treatment at 1000?°C for 4?h was carried out on the as-sintered nanocomposite. The field emission scanning electron microscopy (FESEM), Energy dispersive X-ray (EDX) mapping, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Nanoindentation, and Vickers microhardness analyses were used to determine microstructure, elemental analysis, functional group, hardness, and indentation toughness of the samples. The results showed that the hardness and toughness of the heat-treated sample are more than those of the as-SPSed nanocomposite as much as 15.7% and 25.7%, respectively. Also, the values of optical transmission of the nanocomposite sample in the visible range (400–800?nm) and infrared region (800–2000?nm) were lower than those of pure spinel.     

Nanocrystalline/Nanosized Ni1−γFe2+γO4 Ferrite Obtained by Contamination with Fe During Milling of NiO–Fe2O3 Mixture. Structural and Magnetic Characterization

The nanocrystalline nickel ferrite (NiFe₂O₄) was synthesized by reactive milling starting from equimolar mixture of oxides. The iron contamination during milling leads to a solid state reaction between Fe and NiFe₂O₄ spinel. This reaction starts for a milling time longer than 30 h. A mixed nickel–iron ferrite (Ni_1?γFe_2+γO₄) and elemental Ni are obtained. The evolution of the nickel–iron mixed ferrite during milling and its properties were investigated using X‐ray diffraction, Fourier Transform Infrared Spectroscopy (FTIR), Laser Particles Size Analyzer and magnetic measurements. Annealing treatment (350°C/4 h in vacuum) is favorable to the reaction between phases. Replacement of Ni²⁺ cations by iron cations provided by contamination leads to the increase of lattice parameter value of the spinel structure. The magnetization of the nickel–iron mixed ferrite newly formed is larger than the nickel ferrite magnetization (13.6 μ_B/f.u. and 6.22 μ_B/f.u., respectively), due to the magnetic moment of Fe²⁺ cation which is double as compared to the Ni²⁺ cation. Magnetization of the milled samples decreases during milling due to the structural changes induced by milling in the nickel–iron mixed ferrite. The annealing induces a reordering of the cations which leads to a larger magnetization.     

Preparation and mid-infrared 2.7 µm luminescence property of high content Er3+-doped (Y0.9La0.1)2O3 transparent ceramics pumped at 980 nm

High content Er³⁺ doped (Y_0.9La_0.1)₂O₃ transparent ceramics have been prepared by conventional ceramic process. Absorption spectra, mid-infrared, up-conversion and near-infrared emission spectra of Er³⁺ pumped at 980 nm have been investigated. The mechanisms of energy transfer processes have been discussed. Large values of Judd–Ofelt parameter Ω₂ (5.73 × 10^–20 cm²) and spectral quality factor X (3.71) have been obtained. The greatly enhanced green up-conversion emission in the high Er³⁺ doped sample is considered important for the applications in up-converters. The much enhanced mid-infrared 2.7 µm and up-conversion emissions, as well as the depressed near-infrared 1.5 µm emission demonstrate the efficient population inversion of Er³⁺:⁴I_11/2 → ⁴I_13/2 in high Er³⁺-doped ceramics for the 2.7 µm emission. These results suggest that high Er³⁺-doped (Y_0.9La_0.1)₂O₃ transparent ceramics are promising host materials for the applications of mid-infrared lasers and infrared-to-visible up-converters.     

Synthesis and acetone gas sensing properties of Ag activated hollow sphere structured ZnFe2O4

Sheet stacked ZnFe₂O₄ hollow spheres have been synthesized through a simple hydrothermal method using Zn(CH₃COO)₂ and Fe(NO₃)₃ as Zn and Fe sources, respectively. Then a series of Ag activated ZnFe₂O₄ composites are prepared. XRD patterns demonstrate that the as-synthesized powders are pure ZnFe₂O₄. FE-SEM images exhibit that the as-synthesized Ag-ZnFe₂O₄ particles are spherical with the diameter of 800–1000?nm. TEM images demonstrate that the as-synthesized Ag-ZnFe₂O₄ are hollow sphere structure. The gas sensing tests show that 0.25?wt% Ag-ZnFe₂O₄ has the highest responses to 100?ppm acetone vapor at 175?°C, and response time and recovery time are 17 and 148?s respectively. In addition, 0.25?wt% Ag-ZnFe₂O₄ has a good selectivity to acetone. Ag activated ZnFe₂O₄ composites exhibit excellent acetone gas sensing properties and gives potential for the detection of acetone vapor in the application of practical industrial processes and health control.     

Observation of low- and high-temperature CuFe2O4 phase at 1100 °C: The influence of Fe3+ ions on CuFe2O4 structural transformation

Samples containing CuFe₂O₄ and CuO nanoparticles were synthesized by coprecipitation method and subjected to thermal treatment at 300?°C, 500?°C, 700?°C, 900?°C and 1100?°C. Depending on the synthesis conditions, high-temperature treatment of the prepared samples brought to the formation of CuFe₂O₄ with a tetragonal or cubic structure, which was confirmed by X-ray diffraction analysis. The influence of formation mechanism onto the crystallite sizes of nanoparticles and structural transformation of CuFe₂O₄ is discussed. For the first time it was shown that variations of the initial amount of Fe³⁺and Cu²⁺ ions precursors resulted in the formation of low- and high-temperature CuFe₂O₄ phase at the same annealing temperature, 1100?°C.     

Effect of Sr2+ and Ba2+ doping on structural stability and mechanical properties of La2NiO4+δ

Structural and mechanical Characterizations of La_1.8M_0.2NiO_4+δ (M: Sr and Ba) prepared by low frequency ultra-sound assisted synthesis technique and sintered at different temperatures were studied. HRTEM and XRD analyses showed the uniform shape of calcined nanocrystalline powders with the particle size of less than 100?nm with mixed phases, which were refined by Rietveld method using orthorhombic (Fmmm) and tetragonal (F4/mmm) structures. Sintering La_1.8Sr_0.2NiO_4+δ and La_1.8Ba_0.2NiO_4+δ compacted discs at temperatures higher than 1300?°C and 1250?°C, respectively, resulted in appearance of extra peaks close to a monoclinic phase. Doping La₂NiO_4+δ with Sr²⁺ and Ba²⁺ did not affect its sinterability and average grain size significantly, however, Ba²⁺ improved the elastic modulus and microhardness, while Sr²⁺ improved the fracture toughness.     

Crystal structure,impedance and broadband dielectric spectra of ordered scheelite-structured Bi(Sc1/3Mo2/3)O4 ceramic

Bi(Sc_1/3Mo_2/3)O₄ ceramics were prepared via solid state reaction method. It crystallized with an ordered scheelite-related structure (a?=?16.9821(9)?Å, b?=?11.6097(3)?Å, c?=?5.3099(3)?Å and β?=?104.649(2)°) with a space group C12/C1, in which Bi³⁺, Sc³⁺ and Mo⁶⁺ are ?8, ?6 and ?4 coordinated, respectively. Bi(Sc_1/3Mo_2/3)O₄ ceramics were densifiedat 915?°C, giving a permittivity (ε_r) ～24.4, quality factor (Qf, Q?=?1/dielectric loss, f?=?resonant frequency) ～48, 100?GHz and temperature coefficient of resonant frequency (TCF)?～??68?ppm/°C. Impedance spectroscopy revealed that there was only a bulk response for conductivity with activation energy (E_a) ～0.97?eV, suggesting the compound is electrically and chemically homogeneous. Wide band dielectric spectra were employed to study the dielectric response of Bi(Sc_1/3Mo_2/3)O₄ from 20?Hz to 30?THz. ε_r was stable from 20?Hz to the GHz region, in which only ionic and electron displacive polarization contributed to the?ε_r.     

Influential diamagnetic magnesium (Mg2+) ion substitution in nano-spinel zinc ferrite (ZnFe2O4): Thermal,structural, spectral,optical and physisorption analysis

Nano-spinel zinc ferrites (ZnFe₂O₄) with substitution of diamagnetic magnesium (Mg²⁺) ions were synthesized using solution-gelation (sol-gel) self ignition route. The thermal, structural, spectral, optical and N₂-physisorption properties of the prepared Zn–Mg ferrite nanoparticles were analyzed by standard characterization techniques. The temperature dependent spinel phase formation and percentage weight loss was studied by thermogravimetric and differential thermal analysis (TG-DTA). The analysis of the room temperature X-ray diffraction (XRD) patterns showed the formation of cubic spinel structure with single phase in the Zn–Mg ferrites. The crystallite size decreasing from 27 nm to 20 nm with Mg²⁺ substitution confirmed the nanocrystalline formation of the Zn–Mg ferrites. The two characteristics vibrational modes of interstitial sub-lattice sites corresponding to the spinel structure were observed within the desired wavelength range of the FT-IR spectra. The optical band gap values estimated from the UV–Visible data analysis is found to be in the scope of 1.96 eV–2.39 eV. The photoluminescence (PL) spectra showed the broader emission band in the visible region (around 525 nm) for all the samples of Zn–Mg ferrites. The BET isotherms were recorded by the N₂ adsorption-desorption and the surface area, pore volume, average pore radius etc surface parameters were deduced. The BET surface area and average pore radius values were obtained in the range of 5.6–24.8 m²/gm and 2.61–4.52 nm respectively.     

Energy transfer and photoluminescent analysis of a novel color-tunable Ba2Y1-xV3O11:xSm3+ nanophosphor for single-phased phosphor-converted white LEDs

Metal nitrates are used to synthesize a series of novel Ba₂Y_1-xV₃O₁₁:xSm³⁺ nanophosphors via urea-assisted solution combustion route. X-ray diffraction (XRD), diffuse reflectance (DR), transmission electron microscopy (TEM) and photoluminescence (PL) spectroscopy were employed to analyse the structure, morphology, photoluminescent behaviour and energy transfer mechanism. Rietveld analysis over Ba₂Y_0.98Sm_0.02V₃O₁₁ showed that Y³⁺ ions can be well-replaced by trivalent samarium ions without resulting any major alteration in the crystal structure of host lattice. Furthermore, the lattice parameters were determined for both the host as well as the doped composition. The Scherrer equation yielded an average particle size of 44?nm, which in turn was further confirmed by TEM micrographs. The optical band-gap of the host (3.92?eV) was calculated from the diffuse reflectance spectra. Moreover, the photoluminescence spectral studies showed that under near ultra-violet (NUV) excitation of 340?nm, our nanophosphor powder exhibits the characteristic emission peaks of trivalent samarium along with the emission of VO₄^3? (501?nm) group. The excitation energy transfer from vanadate group to Sm³⁺ produced a systematic color tunablity in white region itself. The optimum Sm³⁺ concentration for better luminescence was found to be 2?mol%. The critical distance for energy transfer was calculated to be 29.02?Å, which in turn assisted to shortlist the mechanism responsible for luminescence-quenching (dipole-dipole) arising from the over-doping of the activator. The photoluminescence decay curves revealed the decay kinetics of ⁴G_5/2 electronic state. Finally, the calculation of CIE color coordinates from emission spectra in MATLAB program unveiled a somewhat white-light emitter which may find potential applications in phosphor-converted white light emitting diodes (PC-WLED) under near-ultraviolet (NUV) excitation.