Search Results (837)

Water electrolysis using electricity generated from renewable sources is a promising approach for producing green hydrogen. However, this process requires the development of electrocatalysts that are not only highly active and durable but also low-cost. Considerable efforts are being directed toward discovering and optimizing such materials, and this study contributes to the ongoing research in this area. In this work, three novel LaMnO₃ perovskite–graphene oxide hybrids—namely LaMnO₃/GO, Ag-doped LaMnO₃/GO, and Pd-doped LaMnO₃/GO—were synthesized and investigated for their electrocatalytic activity in water electrolysis under strongly alkaline conditions. To the best of our knowledge, these hybrid materials have not been previously reported in the context of electrocatalytic water splitting. Among the electrodes fabricated and tested for the hydrogen evolution reaction (HER), the one based on a catalyst ink containing Pd-doped LaMnO₃/GO mixed with carbon black showed the best performance, achieving a low overpotential of 0.385 V at a current density of −10 mA/cm². It also demonstrated good stability in the alkaline electrolyte and exhibited a Tafel slope of 0.34 V. These findings highlight the potential of the studied materials as effective and previously unreported electrocatalysts for water splitting. Full article

The catalytic removal of toluene, a representative aromatic volatile organic compound (VOC), requires efficient and stable catalysts. This study systematically investigated the effect of B-site doping with transition metals (Fe, Cu, and Ni) on the catalytic performance of LaMnO₃ perovskite for toluene oxidation. The LaMn_0.5X_0.5O₃ catalysts were synthesized via a sol–gel method and evaluated. The LaMn_0.5Ni_0.5O₃ catalysts exhibited the optimal catalytic performance, achieving toluene conversion temperatures of 243 °C at 50% conversion (T₅₀) and 296 °C at 90% conversion (T₉₀). Comprehensive characterization revealed that Ni doping effectively refined the catalyst’s microstructure (grain size decreased to 19.21 nm), increased the concentration of surface-active oxygen species (142.7%), elevated the Mn⁴⁺/Mn³⁺ ratio to 0.65, and enhanced lattice oxygen mobility. These modifications collectively contributed to its outstanding catalytic activity. The findings demonstrate that targeted B-site doping, particularly with Ni, is a promising strategy for engineering efficient perovskite catalysts for VOC abatement. Full article

Transition metal (TM)-doped zinc oxide (ZnO) and zirconium dioxide (ZrO₂) nanocrystals exhibit complex correlations between crystal structure, defect chemistry, vibrational properties, and magnetic behavior that are strongly governed by synthesis route and dopant incorporation mechanisms. This review critically summarizes recent progress on Fe-, Mn-, and Co-doped ZnO and ZrO₂ nanocrystals synthesized by wet chemical, hydrothermal, and microwave-assisted hydrothermal methods, with emphasis on synthesis-driven phase evolution and apparent solubility limits. ZnO and ZrO₂ are treated as complementary host lattices: ZnO is a semiconducting, piezoelectric oxide with narrow solubility limits for most 3d dopants, while ZrO₂ is a dielectric, polymorphic oxide in which transition metal doping may stabilize tetragonal or cubic phases. Structural and microstructural studies using X-ray diffraction, electron microscopy, Raman spectroscopy, and Mössbauer spectroscopy demonstrate that at low dopant concentrations, TM ions may be partially incorporated into the host lattice, giving rise to diluted or defect-mediated magnetic behavior. When solubility limits are exceeded, nanoscopic secondary oxide phases emerge, leading to superparamagnetic, ferrimagnetic, or spin-glass-like responses. Magnetic measurements, including DC magnetization and AC susceptibility, reveal a continuous evolution from paramagnetism in lightly doped samples to dynamic magnetic states characteristic of nanoscale magnetic entities. Vibrational spectroscopy highlights phonon confinement, surface optical phonons, and disorder-activated modes that sensitively reflect nanocrystal size, lattice strain, and defect populations, and often correlate with magnetic dynamics. Rather than classifying these materials as diluted magnetic semiconductors, this review adopts a synthesis-driven and correlation-based framework that links dopant incorporation, local structural disorder, vibrational fingerprints, and magnetic response. By emphasizing multi-technique characterization strategies required to distinguish intrinsic from extrinsic magnetic contributions, this review provides practical guidelines for interpreting magnetism in TM-doped oxide nanocrystals and outlines implications for applications in photocatalysis, sensing, biomedicine, and electromagnetic interference (EMI) shielding. Full article

The development of lithium-ion batteries necessitates cathode materials that possess excellent mechanical and thermal properties in addition to electrochemical performance. As a prominent functional ceramic, the properties of spinel LiMn₂O₄ are governed by its atomic-level structure. This study systematically investigates the impact of Ni doping concentration on the mechanical and thermal properties of spinel LiNi_xMn_2−xO₄ via first-principles calculations combined with the bond valence model. The results suggest that when x = 0.25, the LiNi_xMn_2−xO₄ shows excellent mechanical properties, including a high bulk modulus and hardness, due to the favorable ratio of bond valence to bonds length in octahedra. Furthermore, this optimized composition shows a lower thermal expansion coefficient. Additionally, Ni doping concentration has a very minimal influence on the maximum tolerable temperature of the cathode material during rapid heating. Therefore, from the perspective of mechanical and thermal properties, this composition could be beneficial for improving the cycling life of the battery, since comparatively inferior mechanical properties and a higher thermal expansion coefficient make it prone to microcrack formation during charge–discharge cycles. Full article

In this study, Ni/Mn-doped cobalt–reduced graphene oxide (Co-RGO) composites were successfully synthesized as advanced electrode materials for supercapacitors. The structural and morphological properties of the composites were characterized using FTIR, XRD, SEM, TEM, and UV–Vis spectroscopy. Their electrochemical performance was evaluated through electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic charge–discharge (GCD). Among the prepared samples, Co-RGO doped with Ni/Mn at a 40:10 ratio exhibited the most outstanding capacitive behavior, achieving a specific capacitance of 7414 F g⁻¹ at a current density of 10 A g⁻¹, along with a high energy density of 565 Wh kg⁻¹ and a power density of 4998 W kg⁻¹. The high capacitance arises from faradaic pseudocapacitive reactions rather than electric double-layer capacitance, eliminating the need for a large surface area. These results confirm that Ni doping significantly enhances pseudocapacitance and conductivity in the Co-RGO matrix, making Ni/Mn (40:10)–Co-RGO a potential material for advanced energy storage systems. Full article

This paper explores the feasibility of producing manganese- and lead-doped luminescent materials from phosphogypsum. For the first time, orange- and red-emitting ultraviolet pigments were obtained using a sulfide matrix reduced from phosphogypsum. The resulting materials were characterized using X-ray diffraction (XRD), transmission electron microscopy, Fourier transform infrared spectroscopy, elemental analysis, and X-ray photoelectron spectroscopy (XPS). Doping with manganese or lead cations is shown to produce luminophores whose luminescence shifts from orange to red–orange under UV radiation as lead cations replace manganese cations in the CaS:Mn_1-xPb_x solid solution. A sharp increase in red luminescence intensity was observed for CaS: Mn luminophores when they were irradiated with short-wavelength ultraviolet radiation. These results open up broad possibilities for using phosphogypsum, a high production volume (HPV) chemical waste product, to produce highly innovative products. Full article

To address the issues of hydrophobicity, easy fouling, and limited application of polyvinylidene fluoride (PVDF) membranes in water treatment processes, this study prepared Cu-MnO₂/GO/PVDF catalytic membranes via the immersion precipitation phase inversion method. Graphene oxide (GO) was incorporated to facilitate the construction of good water channels, while copper-doped manganese dioxide (Cu-MnO₂) was added to enhance catalytic activity. The structure, morphology, and performance of the membranes were characterized comprehensively. Results showed that Cu-MnO₂ was well interspersed between GO sheets, thereby increasing membrane surface roughness, effective filtration area, and hydrophilicity. The best catalytic membrane CM-5 exhibited the highest pure water flux (1391.20 L·m⁻²·h⁻¹) and methyl blue (MBE) rejection rate (98.06%), and it also displayed excellent reusability and stability. EPR tests confirmed the generation of HO· and HOO· in the Fenton-like system, which mediated dye degradation. The Cu-MnO₂/GO/PVDF catalytic membrane demonstrated excellent hydrophilicity, antifouling properties, and catalytic efficiency, thus providing a viable solution for dye wastewater treatment. Full article

The effect of Mn-doped zinc ferrite nanoparticles at a low volume concentration (1 × 10⁻⁴) on structural changes in the nematic liquid crystals 6CHBT and 5CB, induced by weak magnetic fields, was investigated using surface acoustic wave (SAW) and light transmission (LT) techniques. Structural changes caused by the applied magnetic field, in both increasing and decreasing modes, as well as after pulsed changes, were examined by measuring the responses of SAW attenuation and LT using a linearly polarized laser beam. The influence of nanoparticle shape (rods, needles, and clusters) and temperature on the structural changes was investigated. A shift in the threshold field and the transition temperature was observed. In addition, the magnetic properties of the individual samples in powder form were examined using M–H curves, M–T curves, and XRD patterns. The results obtained from all measurements are compared, and the effectiveness of each technique, considering the influence of nanoparticle shape and suspension stability, was evaluated. Full article

FeCoNiCu(Cr, Mn, La, Ce)-Al high-entropy alloys (HEAs) were prepared via a combined centrifugal casting–self-propagating high-temperature synthesis process to serve as multifunctional catalyst precursors. The findings indicated that even with aluminum content reaching 50 wt %, the typical bcc structure inherent to HEAs was preserved. Doping additions (Cr, Mn, La, and Ce) led to pronounced microstructural changes, including alterations in morphology, porosity, and elemental distribution, while the primary phase constituents of the FeCoNiCuAl-based alloys remained consistent. It was found that La and Ce exhibited poor bulk incorporation into the HEAs, evidenced by a low surface content. Aluminum leaching and hydrogen peroxide stabilization converted these precursors into catalysts. These catalysts demonstrated high activity in the deep oxidation of propane and CO. The FeCoNiCu catalyst achieved the best results for CO oxidation, reaching 100% CO conversion at 250 °C. For propane oxidation, the FeCoNiCuCrMn catalyst was the most active, yielding 100% CO conversion at 300 °C and 97% propane conversion at 400 °C. Full article

Doping lead-free halide perovskite nanocrystals with trivalent lanthanide ions has emerged as a promising strategy for engineering their optical properties in various photonic applications. Here, we report the design and synthesis of a series of lead-free double halide perovskite (Cs₂Na(In/Y/Gd)Cl₆) nanocrystals co-doped with a pair of different lanthanides (e.g., Tb³⁺, Dy³⁺, and Eu³⁺) as emission centers, and ns² ions (Sb³⁺ or Bi³⁺) as sensitizers. The tunability of the delayed photoluminescence spectral density was achieved through the selective excitation of lanthanide dopants either via ligand-to-metal charge transfer (e.g., Eu³⁺) or via ns² ion s-p transitions (e.g., Dy³⁺ or Tb³⁺). The intensities of the narrow lanthanide f-f emission bands can, therefore, be tuned by modulating the excitation wavelength and/or dopant ratio, allowing for the accurate engineering of the emission color coordinates and spectral density. We also demonstrated time-resolved tuning of the photoluminescence spectral density for the investigated nanocrystal host lattices co-doped with transition-metal (Mn²⁺) and lanthanide ions, owing to a large difference between the decay dynamics for Mn²⁺ d-d and lanthanide f-f transitions. The rational co-doping of double halide perovskite nanocrystals reported in this work provides a new strategy for generating pre-designed multilevel luminescent signatures for protection against counterfeiting. Full article

Layered transition-metal oxides are among the most promising sodium-ion battery cathodes owing to their high specific capacities and structurally tunable frameworks. However, the prototypical P2-Na_0.67Ni_0.33Mn_0.67O₂ (NM) undergoes an irreversible P2 → O2 phase transition at high voltages, accompanied by severe lattice strain and capacity fade, which hinders practical deployment. Here, we propose a cooperative regulation strategy that couples Zn/Al co-doping with Na enrichment, and successfully synthesize P2-Na_0.80Ni_0.14Zn_0.14Mn_0.58Al_0.14O₂ (NMZA-N14). The optimized NMZA-N14 delivers an initial discharge capacity of 125 mAh g⁻¹ at 0.1C and demonstrates exceptional cycling and rate performance, retaining 98.6% of its capacity after 100 cycles at 0.2C and 93.6% after 200 cycles at 1C. Kinetic analyses indicate a higher Na⁺ diffusion coefficient and a lower charge-transfer resistance in NMZA-N14, evidencing substantially accelerated ion transport. In situ X-ray diffraction further reveals a reversible P2 → OP4 phase transition in the high-voltage regime with a unit-cell volume change of only ~2.27%, thereby avoiding the irreversible structural degradation observed in NM. This synergistic modulation markedly enhances structural stability and electrochemical kinetics, providing a viable pathway for the rational design of high-performance sodium-ion battery cathodes. Full article

Mn⁴⁺-doped fluoride red phosphors are widely used in white LED lighting and display applications due to their excellent luminescent properties. However, their synthesis relies heavily on highly toxic aqueous hydrofluoric acid, which not only causes severe environmental and soil/water pollution but also makes it difficult to control the microstructure of the products due to the rapid reaction rate. In this study, low-melting-point NH₄HF₂ was used as the molten salt, with KMnO₄ and MnF₂ as manganese sources, to synthesize the red phosphor K₃AlF₆: Mn⁴⁺ via the molten salt method. After the reaction, impurities such as NH₄HF₂ were removed by washing with a dilute H₂O₂ solution. The microstructure, photoluminescence properties, thermal quenching behavior, and application in warm white light-emitting diodes (W-LEDs) of the K₃AlF₆: Mn⁴⁺ phosphors were investigated. The results indicate that the phosphors prepared by this method consist of a single pure phase. By adjusting the molten salt content, the morphology of the product can be transformed from nanoparticle-like to nanorod-like structures. All products exhibit the characteristic red emission of Mn⁴⁺ under blue and violet light excitation, with the optimally doped sample achieving an internal quantum efficiency (IQE) of 69% under blue light excitation. The combination of the obtained K₃AlF₆: Mn⁴⁺ with the yellow phosphor YAG enabled the fabrication of W-LEDs. These W-LEDs achieved a color rendering index (Ra) of 86.8, a luminous efficacy (LE) of 77 lm/W, and a correlated color temperature (CCT) of 3690 K, along with excellent color stability under operating conditions. Full article

KY₃F₁₀:Yb³⁺, Tm³⁺ upconversion microparticles (UCMPs) with varying Mn²⁺ doping concentrations were synthesized via a hydrothermal method. Under 980 nm laser excitation, the sample with 3 mol% Mn²⁺ doping demonstrated markedly enhanced luminescence performance, exhibiting a significant intensity increase compared to undoped samples. The as-synthesized UCMPs were successfully incorporated into an anti-counterfeiting ink. Target information was encrypted using a hash function to generate a QR code, which was then screen-printed onto substrate materials. Under 980 nm laser irradiation, the printed QR code exhibited visible blue fluorescence with high stability, confirming its anti-counterfeiting capability. Furthermore, an image recognition system for anti-counterfeiting, based on a hybrid Convolutional Neural Network-Bidirectional Long Short-Term Memory (CNN-BiLSTM) architecture, was developed on the Matlab platform. The system achieved 100% recognition accuracy for the luminescent QR code patterns, providing valuable insights for the development of deep learning-based image anti-counterfeiting technologies. Full article

A-site-ordered quadruple perovskite manganites, AMn₇O₁₂, show many interesting physical phenomena, including orbital and spin modulations, spin-induced multiferroic properties, and competitions between different magnetic ground states. Doping with Cu²⁺ can result in colossal magnetoresistance properties, ferrimagnetism, and additional structural modulations producing electric–dipole helicoidal textures. Many previous works have focused on large-concentration doping, reaching ACu₃Mn₄O₁₂ compositions. Small-concentration doping has been investigated in a limited number of systems, e.g., in BiCu_xMn_7−xO₁₂. In this work, we investigated solid solutions of NdCu_xMn_7−xO₁₂ with x = 0.1, 0.2, and 0.3, prepared at 6 GPa and 1500 K. Specific heat measurements detected three magnetic transitions at x = 0 (at T_N3 = 9 K, T_N2 = 12 K, and T_N1 = 84 K) and two transitions at x = 0.1 (at T_N2 = 10 K and T_N1 = 78 K), while only one transition was found at x = 0.2 (T_N1 = 72 K) and x = 0.3 (T_N1 = 65 K). Differential scanning calorimetry (DSC) measurements showed sharp and strong peaks near T_OO = 664 K at x = 0, corresponding to an orbital-order (OO) structural transition from I2/m to Im-3 symmetry. DSC anomalies were significantly broadened and their intensities were significantly reduced at x = 0.1–0.3, and structural transitions were observed near T_OO = 630 K at x = 0.1, T_OO = 600 K at x = 0.2, and T_OO = 570 K at x = 0.3. The x = 0.1 sample clearly showed double-peak features on the DSC curves near T_OO because of the presence of two close phases. High-resolution synchrotron powder X-ray diffraction studies gave strong evidence that phase separation phenomena took place in the x = 0.1–0.3 samples, where two I2/m phases with an approximate ratio of 1:1 were present (e.g., a = 7.47143 Å, b = 7.36828 Å, c = 7.46210 Å, and β = 90.9929° for one phase and a = 7.46596 Å, b = 7.37257 Å, c = 7.45756 Å, and β = 90.9328° for the second phase at x = 0.3). The Curie–Weiss temperature changed from negative (for x = 0, 0.1, and 0.2) to positive (for x = 0.3). T_OO, T_N1, the Curie–Weiss temperature, and magnetization (at 5 K and 70 kOe) changed almost linearly with x. Full article