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This paper presents the synthesis and characterization of graphene–polymer composites, focusing on their mechanical and antibacterial properties. Graphene flakes were obtained via an electrochemical method and integrated into polyamide 6 (PA6) matrices using melt intercalation. Various characterization techniques confirmed the quality of the graphene flakes, including X-ray diffraction (XRD), Raman spectroscopy, and infrared (IR) spectroscopy, as well as scanning and transmission electron microscopy (SEM and TEM) imaging. Mechanical tests showed an increase in the elastic modulus with graphene incorporation, while the impact strength decreased. The SEM analysis highlighted the dispersion of the graphene flakes within the composites and their impact on fracture behavior. Antimicrobial tests demonstrated significant antibacterial properties of the composites, attributed to both oxidative stress and mechanical damage induced by the graphene flakes. The results suggest promising applications for graphene–polymer composites in advanced antimicrobial materials. [ABSTRACT FROM AUTHOR]

Aluminum garnets display exceptional adaptability in incorporating mismatching elements, thereby facilitating the synthesis of novel materials with tailored properties. This study explored Ce3+-doped Tb3Al5−xScxO12 crystals (where x ranges from 0.5 to 3.0), revealing a novel approach to control luminescence and photoconversion through atomic size mismatch engineering. Raman spectroscopy confirmed the coexistence of garnet and perovskite phases, with Sc substitution significantly influencing the garnet lattice and induced A1g mode softening up to Sc concentration x = 2.0. The Sc atoms controlled sub-eutectic inclusion formation, creating efficient light scattering centers and unveiling a compositional threshold for octahedral site saturation. This modulation enabled the control of energy transfer dynamics between Ce3+ and Tb3+ ions, enhancing luminescence and mitigating quenching. The Sc admixing process regulated luminous efficacy (LE), color rendering index (CRI), and correlated color temperature (CCT), with adjustments in CRI from 68 to 84 and CCT from 3545 K to 12,958 K. The Ce3+-doped Tb3Al5−xScxO12 crystal (where x = 2.0) achieved the highest LE of 114.6 lm/W and emitted light at a CCT of 4942 K, similar to daylight white. This approach enables the design and development of functional materials with tailored optical properties applicable to lighting technology, persistent phosphors, scintillators, and storage phosphors. [ABSTRACT FROM AUTHOR]

Silver phosphate and its composites have been attracting extensive interest as photocatalysts potentially effective against pathogenic microorganisms. The purpose of the present study was to investigate the mechanism of bactericidal action on cells of opportunistic pathogens. The Ag3PO4/P25 (AGP/P25) and Ag3PO4/HA (HA/AGP) powders were prepared via a co-precipitation method. Thereafter, their antimicrobial properties against Enterococcus faecalis, Staphylococcus epidermidis, and Staphylococcus aureus (clinical and reference strains) were analyzed in the dark and after exposure to visible light (VIS). The mechanism leading to cell death was investigated by the leakage of metabolites and potassium ions, oxidative stress, and ROS production. Morphological changes of the bacterial cells were visualized by transmission electron microscopy (TEM) and scanning transmission electron microscopy with energy-dispersive X-ray spectroscopy (SEM EDS) analysis. It has been shown that Ag3PO4-based composites are highly effective agents that can eradicate 100% of bacterial populations during the 60 min photocatalytic inactivation. Their action is mainly due to the production of hydroxyl radicals and photogenerated holes which lead to oxidative stress in cells. The strong affinity to the bacterial cell wall, as well as the well-known biocidal properties of silver itself, increase undoubtedly the antimicrobial potential of the Ag3PO4-based composites. [ABSTRACT FROM AUTHOR]

Four highly bioactive glasses in a binary SiO2–CaO system are prepared following a sol−gel method using Ca(OH)2 as a calcium precursor. In the synthesis of glass according to the modified Stöber method, Ca(OH)2 suspended in polyethylene glycol allows the elimination of the presence of calcite and the increase of ammonia concentration causes formation of spherical particles with different sizes in the range of 26–266 nm. The relation among the size and properties, including bioactivity, of the glass particles is evaluated. New glasses that vary in composition (10–25 wt% CaO), porosity (15–113 m2 g−1), and hydroxyl groups content greatly enhance the formation process of hydroxyapatite (HA) in simulated physiological fluids. For all glasses, superior apatite‐mineralization ability in time as short as 2 h in the physiological‐like buffer is achieved, thus exceeding the bioactivity of the known bioactive glasses, including 45S5 glass (Bioglass). The assessment of the safety and toxicity profile of the obtained glasses is verified in a wide range of concentrations (1–1000 µg mL−1) against human dermal fibroblasts and MC3T3 mouse osteoblast precursors, but also to human erythrocytes by determining hemocompatibility. Two glasses of different sizes, 73 and 266 nm, are promising and warrant further research. [ABSTRACT FROM AUTHOR]

Catalytic combustion of hazardous particulate matter (soot) generated by automobile engines is a primary method of their elimination. Ruthenium-based catalysts are a promising alternative for traditional noble metal (Pt, Pd) based systems; however, their relatively poor thermal stability hinders wide applications. In this study, we synthesized a novel, highly active, and stable catalyst for soot oxidation containing bimetallic RuRe nanoparticles supported on TiO2. The RuRe NPs were synthesized by colloidal, microwave-assisted polyol method and deposited on rutile or anatase TiO2. The effect of rhenium content and the nature of TiO2 support on the performance of RuRe nanoparticles (NPs) in the soot oxidation under air atmosphere was investigated. Bimetallic RuRe/TiO2 nanocatalysts exhibited higher activity in the soot oxidation than Ru/TiO2 systems, and the rutile supported 2 wt% Ru–0.4 wt% Re nanocatalyst (Ru/Re atomic ratio of 9:1) showed the best catalytic performance (T50 = 340 °C and T90 < 400 °C). All studied nanocatalysts were stable under reaction conditions in the consecutive catalytic tests. The exceptional catalytic performance of bimetallic RuRe NPs is explained by the synergy effect between ruthenium, rhenium, and TiO2. [ABSTRACT FROM AUTHOR]

We report on the magnetocaloric and thermoelectric properties of CeCrGe3. The compound crystallizes in the BaNiO3-type crystal structure (space group P63/mmc, no. 194, hP10) and undergoes paramagnetic to ferromagnetic phase transition at 70 K, close to the temperature of nitrogen condensation. The transition is found to be second order in nature as evidenced from the Arrott plot analysis. The reversible magnetocaloric effect was observed at low temperature with the magnetic entropy change reaching ΔSm = −2.2 J/(kg K) around 70 K in a magnetic field change of 5 T, with the relative cooling power of RCP = 57 J/kg and the adiabatic temperature change of ΔTad = 0.8 K. The electrical resistivity of CeCrGe3 shows a metalliclike behavior up to 900 K. The Seebeck coefficient remains positive from 2 K up to 900 K and reveals a broad maximum with Smax = 18 μV/K at 300 K. The thermal conductivity near room temperature is of the order of 5.3 W/(m K), resulting in a small value of thermoelectric figure of merit ZT = 0.005. [ABSTRACT FROM AUTHOR]

Abstract: Single crystals of α-Sm3+:Na3Y(VO4)2 have been grown by the flux growth method. The absorption (300K) fluorescence (4.2 and 300K) and excitation (7 and 300K) spectra as well as the fluorescence dynamics of the Sm3+-doped title crystals are presented and analyzed in detail. The energy transfer between Sm3+–Sm3+ as well as from VO4 3− to Sm3+ were studied in detail. A Judd–Ofelt intensity analysis of the absorption (300K) spectrum has been applied for determination of Ω λ parameters which in turn have been used in calculation of the radiative transition probability factor (A), fluorescence branching ratios (β), natural (radiative) lifetime of the 4G(4)5/2 level of Sm3+ and emission cross-section (σ em ). For the first time very large lifetimes of the Sm3+ fluorescence level have been observed. [Copyright &y& Elsevier]

Looking for upconverting biocompatible nanoparticles, we have prepared by the sol–gel method, silica–calcia glass nanopowders doped with different concentration of Tm3+ and Yb3+ ions (Tm3+ from 0.15 mol% up to 0.5 mol% and Yb3+ from 1 mol% up to 4 mol%) and characterized their structure, morphology, and optical properties. X-ray diffraction patterns indicated an amorphous phase of the silica-based glass with partial crystallization of samples with a higher content of lanthanides ions. Transmission electron microscopy images showed that the average size of particles decreased with increasing lanthanides content. The upconversion (UC) emission spectra and fluorescence lifetimes were registered under near infrared excitation (980 nm) at room temperature to study the energy transfer between Yb3+ and Tm3+ at various active ions concentrations. Characteristic emission bands of Tm3+ ions in the range of 350 nm to 850 nm were observed. To understand the mechanism of Yb3+–Tm3+ UC energy transfer in the SiO2–CaO powders, the kinetics of luminescence decays were studied. [ABSTRACT FROM AUTHOR]

We report on the magnetocaloric and thermoelectric properties of CeCrGe3. The compound crystallizes in the BaNiO3-type crystal structure (space group P63/mmc, no. 194, hP10) and undergoes paramagnetic to ferromagnetic phase transition at 70 K, close to the temperature of nitrogen condensation. The transition is found to be second order in nature as evidenced from the Arrott plot analysis. The reversible magnetocaloric effect was observed at low temperature with the magnetic entropy change reaching ΔSm = −2.2 J/(kg K) around 70 K in a magnetic field change of 5 T, with the relative cooling power of RCP = 57 J/kg and the adiabatic temperature change of ΔTad = 0.8 K. The electrical resistivity of CeCrGe3 shows a metalliclike behavior up to 900 K. The Seebeck coefficient remains positive from 2 K up to 900 K and reveals a broad maximum with Smax = 18 μV/K at 300 K. The thermal conductivity near room temperature is of the order of 5.3 W/(m K), resulting in a small value of thermoelectric figure of merit ZT = 0.005. [ABSTRACT FROM AUTHOR]

Aluminum garnets display exceptional adaptability in incorporating mismatching elements, thereby facilitating the synthesis of novel materials with tailored properties. This study explored Ce 3+ -doped Tb 3 Al 5-x Sc x O 12 crystals (where x ranges from 0.5 to 3.0), revealing a novel approach to control luminescence and photoconversion through atomic size mismatch engineering. Raman spectroscopy confirmed the coexistence of garnet and perovskite phases, with Sc substitution significantly influencing the garnet lattice and induced A 1g mode softening up to Sc concentration x = 2.0. The Sc atoms controlled sub-eutectic inclusion formation, creating efficient light scattering centers and unveiling a compositional threshold for octahedral site saturation. This modulation enabled the control of energy transfer dynamics between Ce 3+ and Tb 3+ ions, enhancing luminescence and mitigating quenching. The Sc admixing process regulated luminous efficacy (LE), color rendering index (CRI), and correlated color temperature (CCT), with adjustments in CRI from 68 to 84 and CCT from 3545 K to 12,958 K. The Ce 3+ -doped Tb 3 Al 5-x Sc x O 12 crystal (where x = 2.0) achieved the highest LE of 114.6 lm/W and emitted light at a CCT of 4942 K, similar to daylight white. This approach enables the design and development of functional materials with tailored optical properties applicable to lighting technology, persistent phosphors, scintillators, and storage phosphors.