RESUMEN
High-efficiency energy transfer (ET) from Sm3+ to Eu3+ leads to dominant red emission in Sm3+, Eu3+ co-doped single-phase cubic CeO2 phosphors. In this work, a series of Sm3+ singly and Sm3+/Eu3+ co-doped CeO2 cubic phosphors was successfully synthesized by solution combustion followed by heat treatment at 800 °C in air. The crystal structure, morphology, chemical element composition, and luminescence properties of the obtained phosphors were investigated using X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and photoluminescence analysis. Under 360 nm excitation, the Sm3+ singly doped CeO2 phosphor emitted strong yellow-red light at 573 nm (4G5/2-6H5/2) and 615 nm (4G5/2-6H7/2). Meanwhile, the CeO2:Sm3+, Eu3+ phosphors showed the emission characteristic of both Sm3+ and Eu3+, with the highest emission intensity at 631 nm. The emission intensity of Sm3+ decreased with increasing Eu3+ content, suggesting the ET from Sm3+ to Eu3+ in the CeO2:Sm3+, Eu3+ phosphors. The decay kinetics of the 4G5/2-6H5/2 transition of Sm3+ in the CeO2:Sm3+, Eu3+ phosphors were investigated, confirming the high-efficiency ET from Sm3+ to Eu3+ (reached 84%). The critical distance of energy transfer (RC = 13.7 Å) and the Dexter theory analysis confirmed the ET mechanism corresponding to the quadrupole-quadrupole interaction. These results indicate that the high-efficiency ET from Sm3+ to Eu3+ in CeO2:Sm3+, Eu3+ phosphors is an excellent strategy to improve the emission efficiency of Eu3+.
RESUMEN
The weak emission intensity of rare-earth element-doped dual-mode materials leads to low-sensor sensitivity, which is a challenge in optical sensor applications. The present work achieved high-sensor sensitivity and high green color purity based on the intense green dual-mode emission of Er/Yb/Mo-doped CaZrO3 perovskite phosphors. Their structure, morphology, luminescent properties, and optical temperature sensing properties have been investigated in detail. Phosphor shows a uniform cubic morphology with an average size of approximately 1 µm. Rietveld refinement confirms the formation of single-phase orthorhombic CaZrO3. Under the excitation of 975 and 379 nm, the phosphor emits pure green up and down-conversion (UC and DC) emission at 525/546 nm corresponding to 2H11/2/4S3/2-4I15/2 transitions of Er3+ ions, respectively. Intense green UC emissions were achieved because of energy transfer (ET) from the high-energy excited state of Yb3+-MoO42- dimer to the 4F7/2 level of Er3+ ion. Furthermore, the decay kinetics of all obtained phosphors confirmed ET efficiency from Yb3+-MoO42- dimer to Er3+ ions, leading to strong green DC emission. Moreover, the DC of the obtained phosphor shows that a sensor sensitivity value of 0.697% K-1 at 303 K is higher than the UC (0.667% K-1 at 313 K) because the thermal effect generated by the DC excitation source light is ignored compared with UC luminescence. CaZrO3:Er-Yb-Mo phosphor shows intense green dual-mode emission with high green color purity, 96.50% of DC and 98% of UC emissions, and high sensitivity, making it suitable for optoelectronic devices and thermal sensor applications.
RESUMEN
This article reports on the first attempt of a systematic study on the synthesis of carbon dots (C-dots) for the potential applications in labeling and detection of molybdenum ion (Mo6+ ). Carbon dots (C-dots) were synthesized directly via a simple hydrothermal method using lemon juices as carbon precursor with different temperatures to control the luminescence of C-dots. The obtained C-dots had strong green light emission and the ability to use its luminescence properties as probes for Mo6+ detection application, which is based on Mo6+ induced luminescence quenching of C-dots. This analysis system exhibits strong sensitivity and good selectivity for Mo6+ ion, and a detection limit as low as 20 ppm is achieved. These results suggest that the present C-dots have potential application in optoelectronic, labeling and luminescent probing of Mo6+ ions.
Asunto(s)
Citrus/química , Colorantes Fluorescentes/química , Molibdeno/análisis , Puntos Cuánticos/química , Carbono/química , Jugos de Frutas y Vegetales , Humanos , Mediciones Luminiscentes/métodos , Microscopía Electrónica de Transmisión , Molibdeno/sangre , Sensibilidad y Especificidad , Espectrofotometría Infrarroja , Temperatura , Difracción de Rayos XRESUMEN
This paper reports a novel way for the synthesis of a europium (Eu)-doped fluor-hydroxyapatite (FHA) nanostructure to control the luminescence of hydroxyapatite nanophosphor, particularly, by applying optimum fluorine concentrations, annealed temperatures and pH value. The Eu-doped FHA was made using the co-precipitation method followed by thermal annealing in air and reducing in a H2 atmosphere to control the visible light emission center of the nanophosphors. The intensities of the OH- group decreased with the increasing fluorine concentrations. For the specimens annealed in air, the light emission center of the nanophosphor was 615 nm, which was emission from the Eu3+ ion. However, when they were annealed in reduced gas (Ar + 5% H2 ), a 448 nm light emission center from the Eu2+ ion of FHA was observed. The presence of fluorine in Eu-doped FHA resulted in a significant enhancement of nanophosphor luminescence, which has potential application in light emission and nanomedicine.