Dopant Ions Research Articles

Deciphering the piezoelectric and conductive mechanisms of Nb-doped Bi3Ti1.5W0.5O9 high-temperature piezoelectric ceramics

The study utilizes Bi3Ti(1.5-x)NbxW0.5O9 (BTW-xNb, x=0.00, 0.01, 0.02, 0.04, 0.06) bismuth layered piezoelectric ceramics synthesized via a conventional solid-phase reaction process. This is the study to investigate the impact of B-site Nb ion doping on the structural and electrical properties of BTW-xNb ceramic. The results show that all ceramics have a single bismuth layer structure, with reduced lattice distortion according to Rietveld refinement findings. The presence of oxygen vacancies in the ceramic is the main factor that affects the high temperature conductivity of the samples. The XPS results, the increase in the activation energy of AC and DC conductivity confirm that doping with Nb5+ ions reduces oxygen vacancy concentration. The ceramics with the highest overall electrical performance are the BTW-0.02 Nb ceramics. Notably, the DC resistivity at 500 °C was enhanced from 9.16 × 105 Ω·cm (x = 0.00) to 8.24 × 106 Ω·cm. The TC was enhanced from 730 °C(undoped) to 743 °C. At 500 °C, tanδ decreases from 21.1 % to 8.2 %. The ceramic's increased resistivity increases the polarization voltage, resulting in more complete polarization. The d33 is increased from 7.5 pC/N (undoped) to 13 pC/N. Furthermore, the piezoelectric properties remain stable up to 700°C, suggesting that the material has considerable potential for use at elevated temperatures.

Mechanisms of enhanced performance in Zr4+/Ta5+ codoped rutile-TiO2 ceramics via broadband dielectric spectroscopy.

Aliovalent dopant codoped rutile-TiO2 materials have garnered attention due to their excellent performance properties, characterized by low loss tangent (tanδ), high dielectric permittivity (ε'), and stable ε' over a broad temperature range. This performance is primarily due to the electron-pinned defect-dipoles (EPDDs) of the complex defects [Formula: see text]Ti3+-[Formula: see text]Ti3+BTi. Notably, the excellent dielectric properties in ZrxTa2.5%Ti0.975-xO2 (Zr-TTO) ceramics can be achieved using the traditional mixed oxide method without the EPDDs, due to the absence of A3+ (acceptor doping ions). Instead, the existence of localized free electrons and oxygen vacancies ([Formula: see text]) in Zr-TTO structures, due to doping ions and the sintering process, was confirmed by X-ray photoelectron and Raman spectroscopies. These ceramics exhibited ε'~ 2 × 104 and tanδ < 0.03 at 1kHz and 25°C in the 2.5-10%Zr-TTO samples. Moreover, all ceramics demonstrated a maximum ε' change (∆ε') of less than ±15% over the temperature range suitable for X7R and X8R type ceramic capacitors. Significantly, the change in ε' related to relative humility was calculated to be less than ±0.5% over the range of 50-95% RH, indicating the environmental stability of the dielectric properties, which is essential for capacitor applications. Investigations suggested that at least four mechanisms contributed to this system: the intrinsic effect of ionic polarization, Ti4+ · e- -[Formula: see text]- Ti4+ · e- and Ti4+ · e- - [Formula: see text] defects, interfacial polarization at insulating grain boundaries, and non-Ohmic contact between the surface sample and the metal electrode.

Theoretical Study of the Co‐doping Effects at Sr and Fe Sites on the Magnetic and Optical Properties of SrFe12O19

For the first time, the magnetic and optical (bandgap) properties of co‐doped Mg/Dy, Al/Dy, and Mn/Nd (SFO) at Sr and Fe sites are investigated using a microscopic model and the Green's function theory. It is shown that the co‐doping at both Sr and Fe sites can change the behavior of the magnetization which decreases by transition metal or nonmagnetic ion doping at the Fe site (with doping ions larger than the host Fe ions), but by additive co‐doping at the Sr site with rare‐earth ion (which ionic radius is smaller than that of Sr) the magnetization increases with increasing the co‐doping concentration. The bandgap energy decreases in the co‐doped SFO. The mechanism of this co‐doping effect is explained on microscopic level. It is due to the changes of the spin‐exchange interaction constants at the doped sites caused by the appearance of different strain by the doping with two ions. The theoretical results are compared with the existing experimental data and are in good qualitative agreement.

Boosting low-temperature NH3-SCR performance via mixed-valence cobalt dual active sites

Nitrogen oxides (NOx) have become a critical environmental concern, necessitating the development of highly efficient catalysts for temperature which is lower than 300 °C. Selective catalytic reduction with NH3 (NH3-SCR) is a process where ammonia is the reducing agent for selective catalytic reduction of nitrogen oxides in exhaust gases. The mechanism-property relationship between catalytic active sites and low-temperature denitrification efficiency, however, remains unclear. In this study, we synthesized a series of cobalt-modified nanoparticle catalysts using a scalable citric acid sol-gel method and conducted comprehensive characterizations. Our findings indicate that an optimal cobalt doping rate significantly enhances catalytic activity due to the synergistic effects of reduced nanoparticle size and the dual active sites of Co0/Co2+. Specifically, at a cobalt doping ratio of 1.0, the catalyst demonstrates peak SCR activity, achieving 85.5% NOₓ conversion at 120 °C and complete conversion at 150 °C. These cobalt-modified nanoparticle catalysts feature high deposition of doped Co ions on their surfaces, predominantly as metallic cobalt and CoOx nanoclusters. Compared to undoped samples, the cobalt-doped nanoparticle catalysts exhibit a greater specific surface area, increased acidity, enhanced chemisorbed oxygen, and improved redox properties, all contributing to superior denitrification efficacy. Additionally, Density Functional Theory (DFT) calculations provide assertive evidence into the reaction mechanism, showing that Co2+ sites effectively adsorb and activate NH₃, while Co0 sites are crucial for NO adsorption and activation. The synergistic interaction between Co2+ and Co0 facilitates NN coupling, enhancing overall reaction efficiency. These findings underscore the potential of cobalt-modified catalysts for practical industrial applications, offering robust performance over a wide temperature range and meeting stringent environmental regulations.

Efficient photocatalytic degradation of microplastics by constructing a novel Z-scheme Fe-doped BiO2−x/BiOI heterojunction with full-spectrum response: Mechanistic insights and theory calculations

Recently, microplastics (MPs) have garnered significant attention as a challenging emerging pollutant to address. Here, a full-spectrum light-driven Fe-doping BiO2−x/BiOI (FBI) Z-scheme heterojunction was constructed for efficiently degrading MPs in waters. Compared with BiO2−x, Fe doping BiO2−x, and BiOI, the optimal photocatalyst (40-FBI) can cause deep cracks in the polyethylene terephthalate (PET) within 10 h under the irradiation of full-spectrum light. Meanwhile, FT-IR characterization revealed that the absorption peak intensities of the C-O group, CO group, -CH stretching vibration, and -OH group on the MPs surface gradually increased with degradation time. A series of experiments and theory calculations revealed that the introduction of Fe creates impurity levels, accelerating the separation of photo-generated carriers and reducing the work function of BiO2−x, thereby enhancing the transport of photo-generated carriers between Z-scheme heterojunctions. This study offers a valuable idea for designing an efficient photocatalyst by simultaneously introducing ion doping and constructing heterojunctions for enhancing MPs degradation.

Electronic structure engineering of NiFe hydroxide nanosheets via ion doping for efficient OER electrocatalysis

Nickel-iron layered double hydroxides (NiFe-LDH) with tunable catalytic properties have shown promise as an outstanding alternative to ruthenium iridium oxide for the oxygen evolution reaction (OER). However, the intrinsic activity of such electrocatalysts is suboptimal, and a considerable gap remains in understanding the working mechanism. To address this issue, we employ a convenient corrosion method to synthesize Mo-modified nickel–iron hydroxide (Mo-NiFeOxHy) ultrathin nanosheets. Mo-NiFeOxHy demonstrates excellent OER activity, requiring only 216 mV at a current density of 10 mA cm−2, with enhanced stability. Theoretical calculations reveal that the Mo doping induces material distortion, shifting the d-band center closer to the Fermi level, which accelerates the kinetic rate and catalytic activity. In situ Raman experiments show that doping with Mo promotes the rapid formation of high-oxidation-state transition metal hydroxide species, further enhancing the catalytic properties of Mo-NiFeOxHy in OER. This work provides a novel strategy to tailor the structure and composition of NiFe-based electrocatalysts, demonstrating a great potential to break barriers in OER.

Single activator doped fluoride nanoparticles for X-ray excited high-resolution and delayed flexible nonplanar imaging

Lanthanide doped fluoride nanoparticles (NPs) exhibit adjustable X-ray excited optical/persistent luminescence (XEOL/XEPL) and possessing extensive potential in XEPL-based delay imaging. However, the high-resolution and delayed XEPL-based delay imaging always requires strict introduction of sensitized or heterovalent ions and the construction of complex structures for excellent XEPL performance of lanthanide-doped fluoride NPs, which is attributed to a lack of effective and convenient strategies. Here we show that the intense XEPL strength was obtained by single Tb3+ activated ion doping and simple CsY2F7@NaYF4 core/shell structure for X-ray excited high-resolution and delayed flexible nonplanar imaging. The strict introduction and control of sensitized or heterovalent ions, and the construction of intricate multilayer nanostructure are avoided. In addition, we enable the NPs to achieve high and long-term XEPL performance by simply thermal processing strategy. We successfully mixed minimized amount of the NPs into flexible film to create a scintillation screen which consequently exhibit high surface smoothness, environmental stability, and transparency. Our results demonstrate high resolution delayed imaging of the NPs integrated flexible film for the interior of nonplanar objects. The spatial resolution of 14.3 lp mm−1 is substantially higher than the typical spatial resolutions required for medical CT scans (2 lp mm−1) and X-ray imaging (3.5 lp mm−1). These findings will promote the development of advanced delayed X-ray nonplanar imaging applications.

Lithium-doped ZrO2 nanoparticles for SERS-based norfloxacin drug detection

Surface-enhanced Raman scattering (SERS) spectroscopy is a highly specific and ultrasensitive analytical technique; thus, it is an ideal candidate for therapeutic drug monitoring. However, SERS measurements of drugs in a sample are inevitably affected by the environment. In this study, we synthesized ZrO2 nanoparticles (NPs) doped with the first group of elements (Li, Na, and K) in the main block and evaluated their SERS performance. The results showed that Li-ion doping could significantly enhance the SERS effect, and the degree of enhancement depended on the type and concentration of the doped ions. Compared with the highly stable ZrO2, Li ion-doped ZrO2 (Li-ZrO2) exhibited a significant increase in SERS activity. In particular, 1 % Li-ZrO2 NPs exhibited excellent SERS enhancement with an enhancement factor (EF) of 2.60 × 104, which was attributed to the decreased band gap and improved the charge transfer (CT) process after Li ion doping. The adsorption capacity of the Li-ZrO2 NPs for norfloxacin (NOR) molecules was gradually saturated with time. In addition, both acidic and alkaline conditions were unfavorable for NOR detection by the substrate. The SERS intensity exhibited a linear relationship within the NOR concentration range of 10−3–10–6 mol/L, and approximately 97.51 % of the active ingredients were detected, with a competitive detection limit of 10−6 mol/L. Furthermore, NOR detection is cost-effective and time-efficient, and the results of our study can aid in the research process and support practical applications. The proposed study provides a guidance for improving the SERS activity of semiconductors for sensing.

Upconversion enhancement and temperature sensing studies in Li+ ions incorporated GdPO4:Tm3+/Yb3+ phosphor

The GdPO4:Tm3+/Yb3+ phosphor codoped with various concentrations of Li + ions were synthesized for upconversion emission and optical thermometry studies. Excitation using 980 nm laser diode results in three upconversion (UC) emission bands with centre wavelengths of 478, 648 and 692 nm. These bands are originated from 1G4→3H6, 1G4→3F4, and 3F3→3H6 transitions of the Tm3+ ion, respectively. Li+ ions modified the local crystal symmetry around dopant ions, resulting enhanced UC emissions. The lifetime of the 1G4 level of Tm3+ ion was studied using a 980 nm laser excitation. The temperature sensing performances of GdPO4:Tm3+/Yb3+ and GdPO4:Tm3+/Yb3+/Li+ based on fluorescence intensity ratio (FIR) technique were evaluated in the temperature range 301–713 K under 980 nm excitation. Non-thermally coupled levels 3F3 (692 nm) and 1G4 (478, 648 nm) were utilized for FIR estimation. A maximum absolute sensitivity of 6.28 × 10−3 K−1 at 653 K and 18.71 × 10−3 K−1 at 713 K were observed for Li + undoped and codoped phosphors respectively. The result indicates that codoping of Li + ions improved the UC emission as well as optical thermometry. Moreover, CIE colour coordinates and anti-counterfeiting application were also exhibited.

Red luminescence CaSiO3:Eu3+ eco-friendly nontoxic phosphor derived from biomass for display and latent finger print applications

Red luminescent Eu3+ activated CaSiO3 phosphor has been prepared by facile green synthesis hydrothermal route using biomass. Future technologies will be required to synthesize on a massive scale using quick, easy, and affordable ways. The current study deals with the preparation of CaSiO3:Eu3+ using egg shell and rice husk ash. The synthesized powders had a single phased monoclinic structure with space group P1 21/C1. It has been found that addition of Eu3+ ion dopant causes decrease in the optical energy band gap. The phosphor exhibits the intense peak at 612 nm corresponds to 5D0 → 7F2 of the Eu3+ anions upon excitation at 392 nm. The lifetimes ranged from 1.90 to 3.53 ms. With an increase in Eu3+ concentration, emission was tuned towards the red area of the CIE diagram. In order to detect hidden fingerprints on flat surfaces using the powder dusting approach, the CaSiO3:Eu3+ effectiveness was also evaluated. The nontoxicity of CaSiO3:Eu3+ was validated by carrying out a cell viability test on MG 63 cell lines. These outcomes demonstrated that the luminescent CaSiO3:Eu3+ can be used as potential material for display, security encoding, and latent fingerprint applications.

Constructing electrochemically stable single crystal Ni-rich cathode material via modification with high valence metal oxides

Single crystal Ni-rich cathode materials (SCNCM) are a good supplement in the market of nickel-based materials due to their safety and excellent electrochemical performance. However, the challenges of cation mixing, phase change during charge/discharge, and low thermal stability remain unresolved in single crystal particles. To address these issues, SCNCM are rationally modified by incorporating transition metal (TM) oxides, and the influence of metal ions with different valence states on the electrochemical properties of SCNCM is methodically explored through experimental results and theoretical calculations. Enhanced structural stability is demonstrated in SCNCM after the modifications, and the degree of improvement in the matrix materials varies depending on the valence state of doped TM ions. The highest structural stability is found in WO3-modified SCNCM, due to the smaller effective ion radii, higher electro-negativity, stronger W–O bond, and efficient suppression of oxygen vacancy generation. As a result, WO3-modified SCNCM have outstanding cycle performance, with a capacity retention rate of 90.2% after 200 cycles. This study provides an insight into the design of advanced SCNCM with enhanced reversibility and cyclability.

Significantly Enhanced Electromagnetic Wave Absorption Performances and Corresponding Mechanism of LaMn1-xFexO3 Perovskites

Improving the performance of LaMnO3 perovskite is essential to make it an efficient and ultra-light electromagnetic wave (EMW) absorbing material. In this work, LaMn1-xFexO3 powders (x = 0, 0.1, 0.2, 0.3, 0.4, 0.5) were synthesized by controlling the doping of Fe3+ ions at the B-site using the citric acid-assisted sol-gel method. The effects of Fe3+ ions doping content on crystal structures, magnetic properties and EMW absorption performances were investigated. The obtained LMFO-4 sample exhibited a minimal reflection loss of -54.99 dB at 13.68 GHz, with an adequate absorption bandwidth (RL < -10 dB) spanning 4.56 GHz (11.6∼16.16 GHz) at a matching layer thickness of 2.0 mm. The exceptional EMW absorption performances could be attributed to the Jahn-Teller effect, the double-exchange interactions and the magnetic interactions of Mn and Fe ions. Furthermore, the Computer Simulation Technology (CST) simulations demonstrated that the Radar Cross Section (RCS) value of LMFO-4 was lower than -25.10 dBm2 across angles ranging from -90° to 90° with a thickness of 2.0 mm, indicating the remarkable radar wave attenuation ability. These insights provided valuable guidance for advancing perovskite-based materials tailored for efficient and ultra-light electromagnetic wave absorption applications.

Crystal structure and spectral tuning of Eu2+/Eu3+ co-activated Na2Ba1-xSrxCa(PO4)2 phosphors with high thermal stability

The coupling of UV LED chips with phosphors to produce white or color-tunable light is still a challenge. In this work, we propose a simple rare earth occupation site engineering method to adjust the valence of doped Eu ions. Based on the Ba2+ substituted by Sr2+, new Eu2+/Eu3+ co-activated Na2Ba1-xSrxCa(PO4)2 (NB1-xSxCP) phosphors were designed and successfully synthesized. In NB1-xSxCP, the Ba2+/Sr2+ site is occupied by Eu2+, while the Ca2+ site is occupied by Eu3+. The coupled broad blue 448 nm and sharp red 619 nm luminescence under 321 nm excitation has demonstrated the coexistence of Eu2+ and Eu3+. This double emission phenomenon is studied in terms of the fluorescence lifetime as well as lattice distortion induced by the substitution ions. With the increased substitution of Sr, the luminescence of NB1-xSxCP:0.03Eu2+/3+ can be tuned from blue to red crossing the warm-white region. When x = 0.3, the chromaticity coordinates is located at (0.3779, 0.2495). The integrated intensity of Na2Ba0.7Sr0.3Ca(PO4)2:0.03Eu2+/3+ at 150℃ remains 90.9 % of that at room temperature, while the chromaticity shift (ΔE) can be calculated as 15 ×10−3. The Eu2+/Eu3+ co-activated NB1-xSxCP is a potential candidate for single-phase color-tunable phosphors used for light-tunable applications due to the combining contributions from both Eu3+ and Eu2+ ions.

Navigating Challenges and Promises for Next‐Generation CsPbIBr2 Perovskite Solar Cells: A Review

AbstractGiven the increasing demand for electricity due to modernization and population growth, there is an urgent need to develop renewable energy conversion technologies such as photovoltaics. Among these technologies, CsPbIBr2, an all‐inorganic lead halide‐based perovskite, has shown promise due to its thermal stability, phase stability, and ease of fabrication. However, challenges remain, particularly in addressing device hysteresis and stability. Novel materials and optimized device designs could help overcome these challenges. This comprehensive review discusses strategies such as interface engineering, film quality improvement, compositional engineering, defect passivation, band alignments, and metal ion doping to enhance the performance of CsPbIBr2‐based perovskite films and, in turn, their potential for photovoltaic applications.

Effect of Rare Earth Ion Doping on the Performance of Lithium-Rich Cathode Materials for Lithium-Ion Batteries

Lithium-rich layered oxide cathode materials have the advantages of a high voltage and a high specific capacity. Their commercial applications have however been impeded by some disadvantages such as low initial coulombic efficiency and low cycle life. To overcome these issues, rare earth ion-doped lithium-rich layered oxide cathode materials are investigated in this work. The irreversible release of O2- in Li2MnO3 is suppressed by rare earth ions doping, which enhanced the initial coulombic efficiency of the materials. Meanwhile, the rare-earth ion radius used for doping is larger than the Mn4+ radius, which enlarges the (003)-crystalline plane spacing, resulting in a significant enhancement of the rate performance of the material.

Achieving efficient self-trapped excitons emission by suppressing defect level in Sb3+ doped metal halide

The field of metal halide engineering has made considerable progress, yet additional studies are needed to completely grasp the intriguing principles that govern their luminescence. In this work, we report a novel zero-dimensional (0D) organic-inorganic metal halide hybrid (OIMH) (C3H12N2)2InCl7 (C3H12N2 = 1,3-propane diamine cation) and reveal its interesting luminescent properties through experimental research and theoretical calculations. The photoluminescence (PL) of (C3H12N2)2InCl7 is a synergistic combination of intrinsic self-trapped exciton (STE) emission and defect-bound exciton (DBE) emission. Doping with Sb3+ induces several changes in (C3H12N2)2InCl7, including defect passivation, a reduction in the band gap, and structural shrinkage. These modifications result in a transition of PL centers to external STE emission, with the photoluminescence quantum yield (PLQY) increasing from 4.44 % to 68.70 %. Our work proposes, for the first time, the synergistic emission of STE and DBE and reveals the effect of metal ion doping, providing new insights into the mechanisms of materials exhibiting multifunctional exciton emission.

Study on the mechanism of ROS-induced oxidative stress injury and the broad-spectrum antimicrobial performance of nickel ion-doped V6O13 powder

In this study, pure V6O13 and nickel ion-doped V6O13 powders were synthesized by a simple hydrothermal-calcination method, and their broad-spectrum antimicrobial properties and mechanisms were investigated. The crystal structure, morphology, and chemical state of the powders were thoroughly analyzed by XRD, SEM, TEM, XPS, and UV–Vis. Their antimicrobial properties and mechanisms were evaluated by the ring of inhibition, bio-SEM, live-dead cell staining, ROS detection, and protein leakage experiments. The results showed that nickel ion doping modulated the oxygen defects of V6O13, generating more reactive oxygen species and leading to more severe oxidative stress, resulting in a broad-spectrum and highly efficient antimicrobial effect. This study also revealed the antimicrobial mechanism based on oxygen defect -induced ROS production, which caused cellular oxidative stress damage, leading to leakage of intracellular substances and cell death. This study not only demonstrates the potential of V6O13 as an efficient antimicrobial agent but also provides a strong experimental basis and theoretical support for the engineering design and optimization of novel antimicrobial materials by modulating material defects through ion doping.

Metal-doped amorphous microporous carbon for isotope separation: Pore size modulation and selective deuterium adsorption

Efficient hydrogen isotope separation is crucial for applications in energy production and advanced scientific research, but separation of these poses significant challenges. In this study, we developed amorphous microporous carbon (AMC) derived from a zeolite template and explored hydrogen isotope separation using quantum sieving. Thermal desorption spectroscopy (TDS) technique was used to evaluate the selectivity of hydrogen (H2) and deuterium (D2) isotope separation. The doping of metal ions, such as Ca2⁺, Mg2⁺, Ni2⁺, and Cu2⁺, in the porous carbon modulates the physicochemical properties of the pores. The metal-doped carbon samples demonstrated D2vs H2 selectivity (SD2/H2) of over 10, compared to the pristine carbon's SD2/H2 of less than 8. Density functional theory (DFT) calculation infers that pore modulation through metal doping enhanced the binding affinity of materials towards D2 resulting in increased separation selectivity compared to pristine carbon samples. This approach not only boosts separation efficiency but also provides a scalable and cost-effective solution for industrial applications.

Exploring novel magnetic behaviors in cobalt-doped magnetite synthesized by plasma arc discharge method

Magnetite, a naturally occurring iron oxide, has been widely studied due to its potential applications in various fields. Doping magnetite with foreign ions can significantly alter its structural and magnetic properties. This study aimed to investigate the effects of Co2+ ion doping on the structural and magnetic properties of magnetite. The work introduces cobalt-substituted iron ferrites synthesized using a novel plasma arc discharge (PAD) method and systematically explores how cobalt content affects magnetic properties, aiming to optimize the material for enhanced performance. A series of CoxFe1-xFe2O4 (x=0, 0.1, 0.2, 0.3, and 0.5) ferrites with varying Co2+ concentrations (x=0, 0.1, 0.2, 0.3, and 0.5) were synthesized using a PAD method. The synthesized materials were characterized using X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). Magnetic properties were evaluated through magnetic hysteresis loops and permeability spectra. XRD analysis confirmed the formation of a nanostructured spinel-type oxide in all samples. FESEM images revealed ultra-fine particles with a homogeneous composition and narrow size distribution. The optimal combination of magnetic properties was achieved at a Co2+ concentration of x=0.1, which exhibited a high saturation magnetization, low coercivity, moderate effective anisotropy constant, and a relatively high magnetic permeability at 5 MHz. The results demonstrate that Co2+ ion doping can effectively tailor the structural and magnetic properties of magnetite. The optimized composition (x=0.1) offers promising potential for applications requiring a balance of high magnetization and low coercivity.

Synthesis, Structure and Luminescence Properties of Mn-doped MgAl2O4 Red-Emitting Phosphors with Varying Sintering Temperature.

Oxide matrix red-emitting phosphors are deemed as excellent color converters for white light emitting diodes (WLEDs) and laser diodes (LDs). Manganese-doped MgAl2O4 powder was synthesized by a solid-state reaction method at different sintering temperatures. Microstructure shows that grain size is mainly in the range of 0.2-5μm, and grain agglomeration occurs with increased sintering temperature. XPS analysis indicates that the doped Mn ion exhibits a valence state of + 4 within the MgAl2O4 matrix. The diffraction peak of the phosphors is shifted by the sintering temperature, which affects lattice constant. Upon excitation by 300nm ultraviolet light, the samples emit asymmetric broadband red light within the range of 620-720nm, attributed to Mn4+ ion's transition from 2Eg to 4A2g states. With the increasing temperature, the main emission peak shifts from 677nm to 650nm, ascribed to the change in energy level (2Eg) resulting from the reduction of Al2O3 phase. Crystal field theory confirmed that Mn4+ ions are within a strong crystal field environment created by MgAl2O4 matrix. By affecting particle size and crystallinity, the sintering temperature influences the fluorescence lifetime of the Mn4+ ion. Notably, these red-emitting phosphors exhibits remarkable thermal stability as their emission intensity remains approximately at 58% of initial intensity even at elevated temperature (435K). Consequently, Mn4+: MgAl2O4 red-emitting phosphors with high thermal stability render them promising candidates for WLED applications.