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Self-template construction of honeycomb-like mesoporous YPO4:Ln3+ (Ln?=?Eu, Tb) phosphors with tuneable luminescent properties
摘要： Rare earth (RE)-based phosphors with mesoporous structure that can improve the absorption and utilization of light have attracted much attention recently. Herein, we develop a novel and facile self-template strategy to synthesize honeycomb-like mesoporous YPO4:Ln3+ (Ln = Eu, Tb) phosphors using Y4O(OH)9NO3: Ln3+ as the precursor through a simple H3PO4 etching process. The maximum specific surface area of the mesoporous YPO4:Ln3+ phosphors can reach 406 m2 g?1. The influence of mesoporous structure, crystallinity, and the concentration of rare earth ions on the photoluminescence performance of mesoporous YPO4:Ln3+ phosphors was investigated. The results of fluorescence measurements indicate the mesoporous YPO4:Ln3+ phosphors exhibit better photoluminescence performance after calcination at 900 °C due to the large surface area and high crystallinity. The optimum doped concentrations of Eu3+ and Tb3+ ions are 0.12 and 0.08, respectively, and the concentration quenching occurs among nearest-neighbor ions. This work provide a new sight on preparation of phosphors for white light-emitting diodes lamps.
关键词： Mesostructure,Ultrahigh specific surface area,Temperature dependent luminescence,Self-template strategy
更新于2025-11-14 17:15:25
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Luminescence properties in relation to controllable morphologies of Ba <sub/>3</sub> [Ge <sub/>2</sub> B <sub/>7</sub> O <sub/>16</sub> (OH) <sub/>2</sub> ](OH)(H <sub/>2</sub> O):Eu <sup>3+</sup> and its thermal conversion product Ba <sub/>3</sub> Ge <sub/>2</sub> B <sub/>6</sub> O <sub/>16</sub> :Eu <sup>3+</sup>
摘要： Luminescence properties in relation to controllable morphologies of Ba3[Ge2B7O16(OH)2](OH)(H2O):Eu3+ and its thermal conversion product Ba3Ge2B6O16:Eu3+ were investigated. Three types of morphologies of Eu3+-doped Ba3[Ge2B7O16(OH)2](OH)(H2O) phosphors were obtained via hydrothermal reactions by different kinds of raw materials. In addition, Ba3Ge2B6O16:Eu3+ phosphors were obtained by calcining the precursor Ba3[Ge2B7O16(OH)2](OH)(H2O):Eu3+. The structure and morphology of the obtained samples were characterized by XRD, EDS, FT-IR, TG-DTA, SEM and HRTEM. Herein, the effects of the synthesis parameters, including the reaction temperature, boron sources and the dosage, doping of rare earth on the photoluminescence (PL) properties of Ba3[Ge2B7O16(OH)2](OH)(H2O) were investigated in detail. The lifetime and absolute quantum yield (QY) of different morphologies of Ba3[Ge2B7O16(OH)2](OH)(H2O):Eu3+ were also measured. The PL properties of the Ba3Ge2B6O16:Eu3+ phosphor prepared by the precursor calcination method compared with those prepared by the high-temperature solid-state method are discussed.
关键词： Morphologies,Eu3+ doping,Hydrothermal,Borogermanates,Phosphors,Luminescence
更新于2025-11-14 17:04:02
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Simultaneous enhancement of red upconversion luminescence and CT contrast of NaGdF <sub/>4</sub> :Yb,Er nanoparticles <i>via</i> Lu <sup>3+</sup> doping
摘要： To date, lanthanide-doped upconversion nanoparticles (UCNPs) have been widely reported as a promising CT contrast agent because they have high atomic numbers and big X-ray attenuation coefficient values. However, it is still a challenge to fabricate a simple multimodal imaging probe with improved image quality for early cancer diagnosis in clinical medicine. Herein, ultra-small, uniform and monodisperse β-NaGdF4:Yb,Er,X% Lu (X = 0, 1, 2.5, 4, 6, 7.5) UCNPs were prepared through a solvothermal method with high-level modulation of both the phase and morphology. Meanwhile, a remarkably enhanced red upconversion luminescence (UCL) in the β-NaGdF4:Yb,Er,X% Lu NPs was successfully realized via Lu3+ doping. It is found that as the content of Lu3+ increases from 0 to 7.5 mol%, the UCL intensity of the red emission first increases and then decreases, with the optimum doping content of Lu3+ ions of 2.5 mol%. The red UCL enhancement is ascribed to the change of the Yb–Er interionic distance controlling the Yb–Er energy transfer rate and the distortion of the local environment of Er3+ ions influencing the 4f–4f transition rates of Er3+ ions, which has been further confirmed by the experimental check of the crystallographic phase and by photoluminescence spectroscopy employing Eu3+ as the structural probe, respectively. More importantly, after being modified with the HS-PEG2000-NH2 ligand, the NH2-PEGylated-NaGdF4:Yb,Er,X% Lu NPs exhibited low cytotoxicity, high biocompatibility, and remarkably enhanced contrast performance in in vitro UCL and in vivo CT imaging. On the basis of our findings, the as-obtained functionalized UCNPs could be considered as a promising versatile dual-mode imaging probe for bioimaging, tumor diagnosis, and cancer therapy.
关键词： red luminescence enhancement,Lu3+ doping,upconversion nanoparticles,multimodal imaging,CT contrast
更新于2025-11-14 17:04:02
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Tuneable Emission of Polyhedral Oligomeric Silsesquioxane‐ Based Nanostructures Self‐Assembled in the Presence of Europium(III) Ions: Reversible trans‐to‐cis Isomerization
摘要： Hybrids nanostructures with switchable and reversible “blue-red-green” emission were efficiently synthesized. The Polyhedral Oligomeric Silsesquioxane (POSS) behaves as a directional nano-cage for the terpyridine-based organic ligands allowing an easy complexation of Europium (III) cations. The complexes were characterized via UV-Vis and fluorescence spectroscopies and the stoichiometry was also confirmed via 1H NMR investigation. The octafunctionalized nano-cages allow forming novel self-assembled 3D architectures in presence of the lanthanide cation displaying a red-emission of particular intensity especially in solid state. The presence of an alkenyl group bridging the inorganic core to the organic moiety was employed to tune the emission properties via trans-cis isomerization of the double bond. In the case of O-POSS nanocages this isomerization was monitored also in presence of Eu(III) cations and was accompanied by an evident modification of the colour which passed from blue (trans-O-POSS) to red (Eu@trans-O-POSS) and finally to green (cis-O-POSS) as consequence of the release of the metal cations. This behaviour, together with the easy dispersion of the dry powder and the possibility of coating it as a film in presence of small amount of solvent, makes the emitting solid promising for applications in materials science.
关键词： europium,luminescence,silsesquioxanes,isomerization,self-assembly
更新于2025-11-14 15:32:45
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Synthesis and spectral luminescent properties of 4,4′,4′′,4′′′-tetra(tert-butyl)-5,5′,5′′,5′′′-tetrakis(phenylsulfanyl)phthalocyanines and their sulfo acids
摘要： Magnesium and zinc complexes of 4,4′,4′′,4′′′-tetra(tert-butyl)-5,5′,5′′,5′′′-tetrakis(phenylsulfanyl)phthalocyanine were synthesized. The corresponding sulfo acids were prepared by sulfochlorination and further hydrolysis. Spectral luminescent properties of the synthesized phthalocyanine derivatives were studied. Introduction of sulfo groups resulted in a bathochromic shift of Q-band in the spectra recorded in DMF and pyridine regardless of the metal nature as well as in a hypsochromic shift in sulfuric acid.
关键词： metal complexes,phthalocyanines,sulfo acids,luminescence
更新于2025-11-14 15:32:45
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Growth, Luminescence and Scintillation Characterization of Disodium Di-tungstate (Na2W2O7) Crystal Scintillator
摘要： A single crystal of Na2W2O7 was grown by using the conventional Czochralski technique. The crystal structure of the grown sample was veri?ed by using a powder X-ray di?raction (XRD) analysis. The luminescence, as well as scintillation, properties of the crystals were evaluated at room temperature. The emission spectra of the crystal were obtained by irradiating the sample with X-ray and proton sources. The trap level of the grown crystal was studied from 325 K to 500 K, and di?erent kinematic parameters were calculated. The scintillation properties such as; energy resolution, light yield, ?uorescence decay time and α/β ratio of the crystal, were studied by using γ- (662 keV from 137Cs) and α- (5.4 MeV from 241Am) sources. The luminescence and the scintillation results revealed that the Na2W2O7 crystal would be a good material for the dark matter search and for high-energy physics experiment.
关键词： Czochralski technique,Na2W2O7,Dark matter search,Luminescence and scintillation
更新于2025-11-14 15:30:11
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Photoluminescent behaviour of Ce3+ ions in mixed fluoride structures
摘要： Investigations were done to modify the photoluminescence (PL) spectra of a cerium (Ce3+) doped strontium fluoride (SrF2:Ce3+) phosphor for better sensitization for solar cell application. For optimum sensitization it is needed that Ce3+ emission overlaps with Lanthanide (Ln3+) ions’ excitation energy ranges. SrF2:Ce3+ emission, however, does not overlap well with different 4f-4f Ln3+ ions’ excitation ranges. The PL behavior of Ce3+ in Sr1-xMxF2:Ce3+ (where M = Ca, Ba, Mg, La) was therefore investigated. Noticeable changes were observed in the shape of the excitation and emission spectra of Ce3+. The Sr0.49Ba0.50Ce0.01F2 phosphor produced a significant red shift with a broad emission band. The excitation spectrum of this sample was blue shifted if compared to the singly doped sample.
关键词： fluoride structure,XPS,luminescence,Ce3+
更新于2025-11-14 15:28:36
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Luminescence Tuning of Layered Rare-Earth Hydroxides (LRHs, R = Tb, Y) Composites with 3-Hydroxy-2-naphthoic Acid and Application to the Fluorescent Detection of Al <sup>3+</sup>
摘要： Tunable luminescence (quenching or blue shift) of HNA/OS-LRH composites (HNA is 3-hydroxy-2-naphthoic acid; OS is the anionic surfactant of 1-octanesulfonic acid sodium; LRHs are layered rare-earth hydroxides, R = Tb3+, Y3+) in the solid state and delaminated state is reported, which is utilized as an effective fluorescent probe for detecting metal ions. HNA/OS species are intercalated into LRH layers to generate composites of HNAxOS1?x-LTbH (x = 0.10, 0.15, 0.20 , 0.25) and HNAyOS1?y-LYH (y = 0.05, 0.10, 0.15, 0.20, 0.25, 0.30). In the solid state, LYH composites exhibit green emissions (from 493 to 504 nm) with a large blue shift in comparison to the 542 nm emission of free HNA? anions, while in the delaminated state in formamide (FM), the composites display blue emission (480 nm) relative to the green emission (512 nm) of an HNA soltuion in FM. However, LTbH composites display coquenched luminescence in both the solid state and delaminated state. Also, HNA0.25OS0.75-1:1-LYH, HNA0.25OS0.75-1:2-LYH, and HNA0.05OS0.95-1:1-LYH (1:1 and 1:2 are HNA:NaOH molar ratios) show significantly elongated fluorescence lifetimes of 15.35, 14.37, and 12.72 ns, respectively, in comparison with free HNA-Na (6.44 ns), and their quantum yields of 23.40%, 21.97%, and 22.31%, respectively, are much larger than that of free HNA-Na (4.86%). The LTbH composite (HNA0.25OS0.75-1:1-LTbH) has also a relatively higher quantum yield of 12.46%. The HNA0.25OS0.75-1:1-LYH colloid exhibits excellent recognition selectivity for Al3+ over other metal ions (Mg2+, Co2+, Ni2+, Cu2+, Zn2+, Pb2+, Cd2+, and Hg2+) with distinct fluorescence sensitization. It shows an intense change in its fluorescence emission when it is bound to Al3+ ions, giving a lower detection limit of 6.32 × 10?6 M. This is novel research on the fluorescence chemosensing of LRH composites.
关键词： Layered rare-earth hydroxides,Fluorescent detection,Chemosensing,Luminescence tuning,Al3+ ions
更新于2025-11-14 15:28:36
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Near-infrared-light-triggered photoelectrochemical biosensor for detection of alpha-fetoprotein based on upconversion nanophosphors
摘要： A novel photoelectrochemical (PEC) biosensor based on hybrids of NaYF4:Yb, Tm， zinc oxide (ZnO) and cadmium sulfide (CdS) was constructed to detect alpha-fetoprotein (AFP), which possesses the advantages of low background noise and non-damage to the biological substance. Herein, we prepared NaYF4:Yb,Tm/ZnO/CdS composite film electrode by pulsed laser deposition. The selected materials of ZnO and CdS can make full use of the upconversion luminescence (~360nm, ~480nm) of NaYF4:Yb,Tm nanophosphors under 980nm laser excitation. Meanwhile, an effective matching of energy levels between the conduction bands of CdS and ZnO can prompt photoelectrochemical performance of the electrode. The biosensor shows ultrasensitive detection of AFP with a wide linear range from 0.01 ng mL-1 to 200 ng mL-1 and a low detection limit of 5 pg mL-1. Therefore, the proposed PEC biosensor based on upconversion nanophosphors is potentially attractive for achieving excellent photoelectrochemical biosensor for detection of other cancer markers in clinical analysis.
关键词： photoelectrochemical,pulsed laser deposition,upconversion luminescence,near-infrared light-triggered biosensor
更新于2025-11-14 15:27:09
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KMnF3:Yb3+,Er3+ Core-Active-Shell Nanoparticles with Broadband Down-Shifting Luminescence at 1.5 μm for Polymer-Based Waveguide Amplifiers
摘要： In this study, we prepared cubic-phase oleic-acid-coated KMnF3: Yb3+,Er3+ nanoparticles (NPs) and NaYF4:Yb3+,Er3+ NPs, which were about 23 nm. From the down-shifting emissions spectra of the two NPs obtained by 980 nm excitation, we observed the fact that the KMnF3: 18%Yb3+,1%Er3+ NPs were a luminescent material with a broadband near-infrared emission of 1.5 μm, and full-width at half-maximum (FWHM) of 55 cm?1, which was wider than that of the NaYF4: 18%Yb3+,1% NPs. Therefore, we believe that the oleic-acid-coated KMnF3:Yb3+,Er3+ NPs have great potential in fabricating broadband waveguide ampli?ers. Through epitaxial growth of a KMnF3: Yb3+ active-shell on the core NPs, we compounded KMnF3:Yb3+,Er3+@KMnF3:Yb3+ core-active-shell NPs whose 1.5-μm infrared emissions intensity was 3.4 times as strong as that of the core NPs. In addition, we manufactured waveguide ampli?ers using KMnF3:18%Yb3+,1%Er3+@KMnF3:2%Yb3+ NPs as the core materials of the waveguide ampli?ers. When the input signal power was 0.2 mW and the pump power was 200 mW, we achieved a relative gain of 0.6 dB at 1534 nm in a 10-mm long waveguide.
关键词： broadband,1.5 μm,KMnF3:Yb3+,Er3+ core-shell nanoparticles,polymer-based waveguide ampli?ers,down-shifting luminescence
更新于2025-11-14 15:27:09