Ceramic Route Research Articles

Arresting of efflorescence in ceramic tiles developed using caustic alumina industry waste (red mud).

Conversion of caustic red mud (RM, Alumina industry waste) into building materials becoming one of the viable solution for its large scale utilization. The building materials developed using RM often results in efflorescence due to its high alkalinity, which is detrimental for the structural integrity of the buildings. The X-ray shielding tiles developed through ceramic route using the mixtures of RM, BaSO4 and kaolin clay also suffers from severe Na2SO4 efflorescence when sintered above 1000°C. The XRD analysis confirms the formation of Na2SO4 through the solid-state reaction that occurs between BaSO4, Na2Fe2Ti6O16 and NaAlSiO4 at above 1000°C. The formation of Na2SO4 was reduced by adding KOH with the mixtures, which reacts with RM and BaSO4 and form stable K3NaS2O8 and KAlSiO4 phases, as revealed through Rietveld refinement. Eventually, the wt% of Na2SO4 was found to decrease from 3.2% to 0.2% while adding 8% of KOH. Subsequently, the efflorescence has decreased from 90% to 2%. Moreover, the KOH addition assist to increase the density of the shield from 2.8g/cc to 3.6g/cc. It eventually increases both the mechanical strength and X-ray attenuation characteristics of the shield. The flexural strength of the tile has increased from 16.46N/mm2 to 19.46N/mm2 while adding 8% KOH. The 15mm thick tile possess the attenuation equivalent to 2mm lead at 100kV.

Design and Simulation of Circular Dielectric Resonator Antenna and Investigation of Structure, Microstructure, and Dielectric Properties of Mn‐Modified Sr2SnO4

Samples with compositions of Sr2Sn1−xMnxO4(SSM) with 0 ≤ x ≤ 0.10 are prepared by conventional ceramic route via heat treatment at 1350 °C. Phase and crystal structure analysis is studied using X‐ray diffraction and Rietveld refinement to confirm the crystallization of samples in the tetragonal structure under space group I4/mmm. The size‐strain plot method is employed to identify the role of Mn on crystallite size/microstrain/dislocation density. The scanning electron microscope and energy‐dispersive X‐ray spectroscopy analysis confirm a significant change in the grain size and compositional homogeneity of all samples with Mn‐doping. Dielectric properties of samples are explained in terms of interfacial and orientation polarization of dipoles . Modulus studies show the exclusion of electrode contribution from the electrical properties. The single‐segment circular dielectric resonator antenna is designed with the help of experimental dielectric parameters and showed two major resonant frequencies at 3.6 and 6.7 GHz. The reduction in the S11 parameter and −10 dB reflection coefficient bandwidth with Mn‐doping observed due to overlapping of the E‐field line suggests the application in patch array antenna for radar and satellite communication applications. This study also enables to explore Sr2SnO4‐based Ruddlesden Popper oxide for antenna and mm‐wave communication applications.

Synthesis and shrinkage resistance of precursor ceramic microspheres aerogel composed of curled molecular chains via polymer-derived ceramics route

Structural damage and shrinkage cracking were exhibited during the pyrolysis of ceramic aerogels prepared by the polymer-derived ceramics (PDCs) route. Herein, the shrinkage of the ceramic precursor during the pyrolysis was offset by utilizing curled molecular chains to store strain in advance. Microspheres composed of curled molecular chains were prepared using polysilazane (PSZ) as a precursor. The microspheres were linked into a three-dimensional skeleton and further fabricated into precursor ceramic microspheres aerogel (PSZ/MCMSA) with shrinkage resistance. The morphology, thermal insulation, and shrinkage resistance properties of the material were tested. The results indicated that PSZ/MCMSA exhibited outstanding thermal insulation and shrinkage resistance properties. The shrinkage of the precursor ceramic microspheres (PSZ/MCMS) was offset by the strain stored through the curled PSZ molecular chains in the PSZ/MCMS. In addition, the microsphere skeleton structural supporting and gas escape channels were formed during the sintering, and the shrinkage resistance of the precursor ceramic aerogel was further enhanced.

Ball milling and annealing effect in structural and magnetic properties of copper ferrite by ceramic synthesis

This study aims to better understand the relationship between the microstructure and magnetic properties of copper ferrite, which is an inverse spinel that present a body-centered tetragonal structure associated with a remarkable Jahn–Teller (JT) effect. For this goal, a sample has been synthesized by the ceramic route from a stoichiometric mixture of high-purity CuO and Fe2O3 powders activated mechanically in a high-energy planetary ball mill. This sample was calcined in air furnace at 1000 ºC for 6 h. As synthetized sample with a cubic structure was divided into two parts and one of them was annealed at 650 ºC for 3 h and slowly cooled to room temperature to obtain a pure tetragonal spinel sample. Furthermore, these two samples were subjected to the same processes of severe plastic deformation by milling for up to 70 h and subsequent annealing at temperatures ranging between 300 and 600 ºC to obtain samples with a mixture of phases in different proportions. For the cubic one, there is no change in its structure due to milling, always remaining 100 % cubic, and the evolution in the saturation magnetization was related to the changes in the density of defects present. On the other hand, copper cations are always found in the octahedral sites of spinel with a tetragonal structure. The small decrease in the degree of inversion to 0.95 induced by milling in this sample is capable of breaking the JT distortion, giving rise to the appearance of a cubic phase. This work demonstrates how the structure, microstructure, defects like stacking faults and deformation twins, and degree of inversion of the different phases are related to changes in magnetic properties.

Curvature-ordered biomimetic helical ceramic composite fiber aerogel with shrinkage resistance, thermal insulation properties, and mechanical properties

Ceramic aerogel with high porosity and low thermal conduction was widely used in the field of thermal insulation. However, shrinkage and structural damage were produced by the ceramic precursors during pyrolysis. The shrinkage and mechanical properties of ceramic aerogels required to be improved. Herein, inspired by spiral grass and passionflower, curvature-ordered ceramic fiber aerogels were prepared by electrostatic spinning combined with polymer-derived ceramics (PDCs) route. Shrinkage resistance properties, thermal insulation properties, and mechanical properties of ceramic fiber aerogels were investigated. The shrinkage resistance property of aerogels was improved by the tensile deformation of helical fibers during pyrolysis. The path of heat transfer was extended through the helical fibers and heat conduction was reduced. The gas was confined in a porous network formed by helical fibers that lapped over each other, and thermal convection was minimized. Thermal radiation was attenuated due to reflection and scattering at the core-shell interface of the helical fibers. The mechanical properties of the aerogel were enhanced by the helical structure of the fibers and the stress diffusion mechanism. The tensile and compressive properties of the spiral ceramic aerogel were improved through the curvature structure by about 6 MPa and 3 MPa, respectively. The results showed that the helical ceramic composite fiber aerogel with ordered curvature exhibited shrinkage resistance, thermal insulation, and mechanical properties.

A single phased full color emitting pyrochlore type phosphor La2Y0.66Sn0.66Sb0.66O7: Bi3+, Eu3+ for white light emitting diode applications (WLEDs)

The phosphor converted white light emitting diodes (pc-WLEDs) are advancing rapidly in replacing the conventional fluorescent and incandescent light sources. However, the current technology of pc-WLEDs limits their large scale indoor lighting applications due to their high correlated color temperature (CCT) and poor color rendering index (CRI). In this work, a single phased full color emitting phosphor in the pyrochlore oxide system, La2Y0.66Sn0.66Sb0.66O7: Bi3+, Eu3+ has been developed by the high temperature ceramic route. The developed phosphors are characterized by powder X-ray diffraction, luminescence and lifetime measurements. Upon near UV excitation wavelength, the singly doped phosphor, La2Y0.66Sn0.66Sb0.66O7: Bi3+ show intense blue green light in the wavelength region 400–600 nm due to the characteristic transitions (3P1 → 1S0) of Bi3+. The emission spectral analysis suggests that there exist two luminescence centers of Bi3+ due to occupation of different crystallographic sites in the pyrochlore lattice of La2Y0.66Sn0.66Sb0.66O7. The deficit of red component in the emission spectra is overcome by the Eu3+ co-doping in the system, La2Y0.66Sn0.66Sb0.66O7: Bi3+, Eu3+ which results in the full color emission covering the visible spectral range up to 700 nm with broad peaks along with sharp narrow characteristic peaks of Eu3+. The full color emission of the La2Y0.66Sn0.66Sb0.66O7: 0.04Bi3+, yEu3+ phosphors can be tuned by adjusting the suitable Eu3+ dopant concentration and using appropriate energy transfer from Bi3+ to Eu3+. The full color emitting phosphor, La2Y0.66Sn0.66Sb0.66O7:0.04Bi3+, 0.06Eu3+ can be realized with the color coordinates (0.30, 0.36), and correlated color temperature (4383K). All these results demonstrate that La2Y0.66Sn0.66Sb0.66O7:xBi3+, yEu3+ are potential single phased full color emitting phosphors for the development of pc-WLEDs.

Deep-sea glass sponges-like hollow porous ceramic fiber aerogel: Fabrication, anti-shrinkage and thermal insulation

Ceramic aerogels prepared using the polymer-derived ceramics (PDCs) route were extensively applied in the thermal insulation field with lightweight and high-temperature resistance. However, ceramic aerogels were susceptible to weight loss and volume shrinkage at high temperatures, leading to the collapse of the aerogel structure and a reduction in thermal insulation performance. In this paper, inspired by the skeletal structure of deep-sea glass sponges, hollow porous MHP-SiC-CA ceramic fiber aerogel was prepared by electrostatic spinning. The anti-shrinkage property of ceramic fiber aerogel was improved through the circular and spindle-shaped pores on the surface of hollow fibers. The gas-solid phase interface was increased by the abundant nanopore structure, leading to enhanced reflection and refraction of thermal radiation within the aerogel. The heat conduction and heat convection of the aerogel were reduced with the hollow and porous structure. The results presented that the ceramic fiber aerogel exhibited excellent anti-shrinkage properties, high specific strength, and ultra-low thermal conductivity. The material was expected to provide novel perspectives for the development of ceramic fiber aerogels applicable to ultra-high-temperature environments.

Strong magnetoelectric coupling in novel Na0.5Bi0.5TiO3–BaFe12-2xCoxTixO19 multiferroic composite

Multiferroic composites of sol-gel synthesized Sodium Bismuth Titanate (Na0.5Bi0.5TiO3) and Co–Ti substituted Barium Hexaferrite (BaFe12-2xCoxTixO19; x = 0.0, 0.5, 1.0, 1.5 and 2.0) in the ratio 3:1 was synthesized through ceramic route. Successful formation of R3c rhombohedral and P63/mmc hexagonal phases corresponding to Na0.5Bi0.5TiO3 and BaFe12-2xCoxTixO19 respectively was confirmed from the XRD and Rietveld refinement pattern. The frequency and temperature dependence of dielectric constant and loss of the composite systems exhibited typical dispersion behaviour which could be understood using the Maxwell-Wagner model. Substituted samples showed enhanced dielectric behaviour where dielectric constant was observed to increase while loss tangent decreased. Using the Universal Jonscher's Power law (JPL), conductivition mechanisms of the composite systems were studied from the ac conductivity behaviour which revealed that the x = 0.0 sample followed Non-overlapping Small Polaron Tunnelling (NSPT) model while the remaining samples followed the Correlated Barrier Hopping (CBH) model. The complex impedance and Nyquist plot analysis showed the enhancement of resistive property in the x≠0 systems. Magnetic hysteresis loop measurements were conducted, and the associated parameters were determined with the assistance of the Law of Approach to Saturation (LAS). Favourable reduction in the magnetic anisotropy was observed indicating the disturbance of magnetic spin structure in the hexaferrite phase. The P-E loops established the novel room temperature multiferroic nature of the composite systems. Significant magnetoelectric coupling was detected at room temperature in all samples, with the x = 0.5 sample exhibiting the highest value of approximately 59.81 mV/cmOe. These desirable properties suggest that the composites may find future device applications as in magnetically tunable energy harvesting devices and self-powered magnetoelectric sensors in the future.

Macroporous polymer-derived ceramics produced by standard and additive manufacturing methods: How the shaping technique can affect their high temperature thermal behavior

This work proposes the processing of porous ceramic lattices via three polymer-derived ceramic routes, namely powder bed fusion and infiltration, fused filament fabrication and replica, and a direct replica of a foamed polymer. A common feature in the processing of these lattices is the use of the same polysilazane as the preceramic source for the Si-C-N-O network that builds up during ceramization.We adopted rotated cube, honeycomb and randomized cellular geometries as a matter of comparison for thermal exchange when an air flow is forced through the structures up to 1050 °C. The three procedural pathways are discussed in their limitations regarding geometry, polymer-to-ceramic conversion, high-temperature heat exchange performance and durability. In this regard, while rotated cube geometry results in the best thermal exchange and highest pressure drop, we show a correlation between chemical composition and high temperature oxidation of the Si-C-N-O network, possibly attributed to the selection of the processing routes.

Microwave assisted cobalt nickel ferrite as exhaust thrust sensor and EMI shield

Spinel ferrites have garnered an increasing share of attention in recent decades. The fact that these substances are employed in a wide range of applications, such as electromagnetic interference interference (EMI) shielding and sensor technology. Exhaust thrust sensors have an increasing demand in exhaust air circulator of automobile engine. In the present article Co0.5Ni0.5Fe2O4 (CNF) is synthesized by ceramic route and are sintered using microwaves. The structural, optical, magnetic and morphology are studied using X-ray diffraction, Ultraviolet (UV) visible, Vibrating sample magnetometer (VSM) and scanning electron microscopy (SEM). The magnetic initial permeability as a function of temperature has exhibited quasi single domain grain behaviour. Large stress response and exhaust pressure sensitivity are noticed for the bulk as well as micro inductor fabricated suggesting a plausible application as exhaust thrust sensor applications. The CNF exhibits a high total shielding effectiveness of 55.96 dB, suggesting that almost 99.999% of incoming electromagnetic radiation is effectively reduced by this material. Spinel ferrite CNF have excellent electromagnetic shielding in microwave region and making it very useful for military (radar and stealth) and electronic industries.

Strengthened and toughened SiHfBCN-based high-temperature resistant adhesive with SiC NWs

To further improve the performance of binders, a SiHfBCN-based high-temperature resistant adhesive was successfully synthesized by Polymer-Derived Ceramics (PDC) route using TiB2, Polysiloxane (PSO) and short SiC nanowires as fillers. The effect of short SiC nanowires on the adhesive strength at room temperature and high temperature, as well as the reinforcing mechanism was studied. Compared with the adhesive without SiC nanowires, after curing (at 170 °C) and pyrolysis (at 1000 °C) in air, the appropriate adding of SiC nanowires upgrades the room temperature and high temperature (at 1000 °C in air) adhesive strength to (12.50 ± 0.67) MPa (up by about 32%) and (13.11 ± 0.79) MPa (up by about 106%), respectively. Attractively, under the synergistic impact of the nanowire bridging, nanowire breaking, nanowire drawing and crack deflection, the optimized adhesive exhibits multi-stage fracture, causing the increscent fracture displacement.

Tailoring crystal structure of high-entropy carbides in Si-based ceramic nanocomposites through precursor engineering

High-entropy carbides with tunable crystallization and growth have been demonstrated using single-source precursor derived ceramic route. The in situ nanocrystallization of high-entropy carbide phases, (Ta0.2W0.2V0.2Mo0.2Nb0.2)SiδC and (Ta0.167W0.167V0.167Mo0.167Nb0.167Si0.167)C in amorphous Si-based ceramic matrices was achieved by using polysiloxanes and polycarbosilanes as polymer precursors respectively. The results exemplify a prominent role of the architectures of the polymeric precursors in controlling the structural features of these ceramics at various length scales. In particular, it was observed that high-entropy carbides with rock salt and zinc blende crystal structures were formed when polysiloxanes and polycarbosilanes with different backbone structure were used as polymeric precursors respectively. This is attributed to the thermodynamics of nucleation of the carbidic phases in these nanocomposites. Furthermore, the precursor architecture that dictates free carbon content, influenced nanostructural features and porosity in the material. Therefore, engineering such compositionally complex phases is feasible by selecting suitable polymeric precursors.

Effects of La-Mn co-substitution on the structure and magnetic properties of M-type strontium hexaferrite

Research into enhancing the magnetic properties of permanent ferrite using ion substitution techniques has continued, particularly concerning replacing commercially available La-Co co-substitution ferrite with larger magnetic anisotropy and lower prices. Mn ions with larger magnetic moments have become one of the options. In this work, Sr1-xLaxFe11.6-xMnxO19 (0 ≤ x ≤ 0.5) with equal substitution of La-Mn was synthesized by the conventional ceramic route. X-ray diffraction analyses indicated that the upper limit of La-Mn concentration was 0.4. The lattice constant a increases and c decreases with increasing La-Mn concentrations. With the increase of La-Mn concentrations, Ms reaches the highest value of 80.52 emu/g (x = 0.2) at 300 K. As evidenced by Raman spectroscopy, the substitution sites of Mn ions in the ferrite lattice altered with the substitution concentration, and the substitution tendency was 4f2 > 12 k + 2a > 4f1. In addition, La-Mn substitution affects the inherent magnetic properties such as HA and Tc of the samples, which has a reference for further improvement of permanent ferrites.

Sites and Mobility of Lithium along the Li1+xTi2-xInx(PO4)3 (0 ≤ x ≤ 2) Series Deduced by XRD, NMR, and Impedance Spectroscopy.

The structure and Li conductivity has been investigated in the Li1+xTi2-xInx(PO4)3 (0 ≤ x ≤ 2) series prepared by the ceramic route at 900 °C. The XRD patterns of 0 ≤ x ≤ 0.2 samples show the presence of rhombohedral (S.G. R3̅c); those of 0.2 ≤ x ≤ 1 samples display both rhombohedral and orthorhombic (S.G. Pbca), and 1 ≤ x ≤ 2 samples exhibit only monoclinic (S.G. P21/n) phases. At intermediate compositions, the secondary LiTiPO5 phase was detected. The Rietveld analysis of XRD patterns was used to deduce unit-cell parameters, chemical composition, and percentage of phases. The amount of In3+, deduced from structural refinements of three phases, was confirmed by 31P MAS NMR spectroscopy. The Li mobility was investigated by 7Li MAS NMR and impedance spectroscopies. The Li conductivity increased with the Li content in rhombohedral but decreased in orthorhombic, increasing again in monoclinic samples. The maximum conductivity was obtained in the rhombohedral x = 0.2 sample (σb = 1.9 × 10-3 S·cm-1), with an activation energy Eb = 0.27 eV. In this composition, the overall Li conductivity was σov = 1.7 × 10-4 S·cm-1 and Eov = 0.32 eV, making this composition a potential solid electrolyte for all-solid-state batteries. Another maximum conductivity was detected in the monoclinic x ∼ 1.25 sample (σov = 1.4 × 10-5 S·cm-1), with an activation energy Eov = 0.39 eV. Structural models deduced with the Rietveld technique were used to analyze the conduction channels and justify the transport properties of different Li1+xTi2-x Inx(PO4)3 phases.

Effect of La3+and Al3+ doping on the crystal structure and magnetic properties of strontium hexaferrites

Modification of crystal structure and magnetic properties of M-type strontium hexaferrites (SrM) doped with foreign ions (Al3+, La3+) was studied, focusing on the distortion of the lattice. Incorporation of Al3+ ions contracted the lattice of SrM and hardened lattice vibration modes with lattice disorders. X-ray diffraction examined the lattice distortion of FeO5 trigonal bipyramidal sites (TBP) revealing that off-center displacement (z0) was reduced to z0 = 0 by heavy Al3+ doping. This reduction of z0 was attributed to stabilization of single-well potential in the positioning of Fe3+ ions in TBP. Furthermore, La3+ doping led to a more significant contraction of the lattice and restored a non-zero off-center displacement of Fe3+ ion in TBP. The polycrystalline ceramics with high coercivity exceeding 21 kOe through the conventional ceramic processing route with concomitant La3+ and Al3+ doping.

Polymer-derived Biosilicate-C composite foams: In-vitro bioactivity, biocompatibility and antibacterial activity

Biosilicate/carbon composites were fabricated in the form of highly porous foams by the polymer-derived ceramic route, and their biological response was analysed. Two different commercial silicone polymers (a poly-methyl-siloxane, MK, and a polymethyl-phenyl-silsesquioxane, H44) were considered as a silica source, mixed with active fillers yielding Na2O, CaO and P2O5. The samples were heat treated either in air or in N2 atmosphere to obtain products resembling the known Biosilicate® glass-ceramic, with or without free carbon. All fabricated samples exhibited acellular in-vitro bioactivity upon immersion in SBF as well as antibacterial activity against S. aureus and E. coli. Direct contact cell viability test, assessed by using a WST-8 assay, indicated that both carbon-containing and carbon-free samples were cytocompatible.

Effect of La, Zr Doping on the Structural and Electrical Conduction Behaviour of BiFeO<sub>3</sub>-BaTiO<sub>3</sub> Ceramics

<p>This study presents a comprehensive investigation of the crystal structure and DC conduction mechanism of [(Ba<sub>0.7-x</sub> La<sub>x</sub>) Bi<sub>0.3</sub>][(Ti<sub>0.5</sub> Zr<sub>0.2</sub>) Fe<sub>0.3</sub>]O<sub>3</sub> with x = 0.00, 0.01, 0.03, 0.05 employing X-ray diffraction (XRD) and electrical conductivity measurements. Various compositions were synthesized through the solid-state ceramic route. XRD was used to investigate phase formation. Analysis of XRD data suggested a structural transition from cubic to tetragonal for x ≥ 0.01. The average crystallite size first increases for x = 0.01 and then decreases for x ≥ 0.03. The temperature-dependent electrical conductivity measurements were investigated over a wide temperature range which revealed distinct conductivity mechanisms governing the material's transport properties. The activation energy (E<sub>a</sub>) has been estimated from temperature-dependent DC conductivity. Overall, this study provides valuable insights into the correlation between crystal structure and electrical properties in [(Ba<sub>0.7-x</sub> La<sub>x</sub>) Bi<sub>0.3</sub>][(Ti<sub>0.5</sub> Zr<sub>0.2</sub>) Fe<sub>0.3</sub>]O<sub>3</sub>, offering significant implications for its potential applications in electronic and optoelectronic devices requiring tailored conductivity characteristics.</p>

Exploration of Griffiths phase, spin glass behaviour and memory effect in a frustrated Al2MnCoO7 pyrochlore compound

Al2MnCoO7 pyrochlore compound has been synthesized following the multistep solid-state ceramics route. The compound exhibits a monoclinic structure, which was confirmed through the X-ray diffraction pattern analysis. The magnetization measurements in both zero-field-cooled (ZFC) and field-cooled (FC) modes indicate that the compound undergoes a phase transition from paramagnetic (PM) to antiferromagnetic (AFM) state at the Néel transition temperature TN ∼31 K. Notably, below TN, there is a substantial discrepancy between the ZFC and FC curves, which can be ascribed to the existence of competing ferromagnetic (FM) and AFM interactions, resulting in a glassy behaviour. Additionally, the compound demonstrates a Griffiths phase above TN, signifying the presence of ferromagnetic clusters within the PM region of the material. The spin-glass behaviour is confirmed by the shift of maxima towards higher temperatures with increasing frequency in the ac susceptibility measurement. The memory effect also confirms the spin-glass nature of the compound. The Arrott's plots confirmed that the magnetic phase transition in the material to be a second-order type. Additionally, the material exhibited a maximum magnetic entropy change (−ΔS) value of 1.08 J/kg.K and a relative cooling power of 36.60 J/kg under an applied magnetic field of 5 T.

Greener solvents for the processing of preceramic polycarbosilane: application in the preparation of B4C/SiC composites.

The innovation introduced in this study consists of replacing toluene with safer solvents such as cyclopentane or diethyl ether in the processing of a preceramic polycarbosilane (allylhydridopolycarbosilane, AHPCS) and assessing its impact on the functionalisation of B4C powders to produce B4C/SiC composites. Fourier-transform infrared (FT-IR) with ATR and nuclear magnetic resonance (NMR) spectroscopy revealed no major modification in the polymer structure. SEC/MALS analysis showed a slight change in the number-average molar mass of the polymer regardless of the functionalisation solvent used in correlation with a slight decrease in the polymer ceramic yield due to oligomer loss. The thermal behaviour of the preceramic polymer investigated via mass spectrometry remained unaffected by the solvent change. The search for polymer residues after distillation highlighted the recyclability of both the functionalisation solvent and the polymer, despite a slight increase in the molar mass of the polymer. Finally, the sinterability of B4C/AHPCS samples was studied with the preparation of B4C/SiC composites via a polymer-derived ceramic (PDC) route and spark plasma sintering (SPS). The effect of the solvent on the microstructure and relative density of the specimens (>92%) is negligible. The specimens retain a fine and homogeneous phase distribution despite process modification. The results highlight the approach developed to use greener solvents for the chemical synthesis of functionalised ceramics and represent a step towards the generalisation of more environmentally friendly processes.

Enhancing the inherent NIR photoluminescence in SrLaLiTeO6 through Cr3+-Yb3+ co-substitution for high performance pc-LEDs.

Until now, double perovskite tellurates have not been reported to exhibit inherent NIR photoluminescence. Therefore, the current study's revelation of inherent NIR luminescence in SrLaLiTeO6 double perovskite centered at 970 nm under 340 nm excitation is particularly intriguing. This phenomenon is attributed to the photoluminescence of Te4+ ions. This study also examines the NIR luminescence of Cr3+-Yb3+ co-doped SrLaLiTeO6. The host and SrLaLiTeO6:3%Cr3+, y%Yb3+ (y = 1, 2, 4, 6, 8, 10 mol%) were synthesized using the solid-state ceramic route. The successful incorporation of Cr3+ and Yb3+ ions into the host lattice was confirmed through XRD, Raman, and diffuse reflectance spectral analyses. Under 270 nm excitation, the photoluminescence (PL) of SrLaLiTeO6:Cr3+ exhibits a blueshift of the PL band to 965 nm due to the 4T2(4F) → 4A2g(4F) emission component of Cr3+ ions. The excited-state lifetime of SrLaLiTeO6:0.5%Cr3+ was measured at 36 μs, but this decreased to 26 μs as the Cr3+ concentration reached 10 mol%, primarily due to the enhancement of non-radiative energy transfer between Cr3+ ions. Incorporating Yb3+ into the system results in additional spectral lines with an enhanced intensity in the range of 970 nm to 1125 nm when excited at 270 nm. These emission lines correspond to the 2F5/2 → 2F7/2 transitions of Yb3+ ions, indicating an efficient energy transfer from Cr3+ to Yb3+. Furthermore, the study also reveals that Yb3+ emission is observed even without Cr3+ ions in SrLaLiTeO6 under 340 nm excitation, suggesting the possibility of energy transfer from the host to Yb3+ ions. The thermal stability and crystal field parameters of the synthesized phosphors are also explained in detail. To explore the potential of these phosphors in practical applications, phosphor-converted NIR LEDs were fabricated using SrLaLiTeO6, SrLaLiTeO6:3% Cr3+, and SrLaLiTeO6:3% Cr3+, 1%Yb3+.