Influence of Yb Concentration on the Optical Properties of CaF2 Transparent Ceramics Codoped with Er and Yb

Er, Yb:CaF₂ nanoparticles with different Yb concentrations were synthesized by a coprecipitation method using nitrates as raw materials. X‐ray powder diffraction and transmission electron microscopy analysis showed that the nanoparticles were single fluorite phase and the nanoparticle size was found to decrease with increasing Yb concentrations. The obtained nanoparticles were hot‐pressed at 800°C under 30 MPa under vacuum environment to fabricate Er, Yb:CaF₂ transparent ceramics. The influence of Yb ion concentrations on the optical transmission, microstructure, and luminescence properties of Er, Yb:CaF₂ transparent ceramics were investigated. The addition of Yb ions was found effectively to reduce grain size and has a positive effect on improving the optical transmission of Er, Yb:CaF₂ transparent ceramics. The highest transmittance in the near‐infrared spectral region of the Er, Yb:CaF₂ transparent ceramic reached about 90%. The green, red, and near‐infrared emission intensities were found to increase with increasing Yb concentration.     

Fabrication and microstructure characterizations of transparent Er:CaF2 composite ceramic

A novel layered transparent Er:CaF₂ composite ceramic was proposed in the present study. Er:CaF₂ nanoparticles were synthesized by a chemical coprecipitation method. The crystal structures and morphologies of synthesized nanoparticles were performed by X-ray diffraction (XRD) and field emission scanning electron microscope (FE-SEM) measurements, respectively. Transparent composite ceramic was fabricated by the combination of multistep dry pressing and hot-pressed sintering method without any sintering aids or binders. The average grain size of 2% Er-doped and 5% Er-doped layers were about 30 and 55 μm, respectively. The thickness of interfacial between two different Er-doped layers was 150-200 μm. For a 1.5 mm thickness transparent Er:CaF₂ composite ceramic, the optical transmittance reached 44.9% at 500 nm and 53.6% at 1200 nm. The luminescence spectra and thermal conductivities of transparent ceramic specimens were also discussed.     

Fabrication and upconversion luminescence properties of Er:SrF2 transparent ceramics compared with Er:CaF2

SrF₂ transparent ceramic is a promising upconversion material due to the low phonon energy. The effect of different sintering temperatures on Er:SrF₂ transparent ceramics was investigated. The suitable sintering temperature for Er:SrF₂ transparent ceramics was 900 °C by hot-pressed sintering in this study. High quality of Er:SrF₂ transparent ceramics with different doping concentrations were obtained. The upconversion luminescence spectra and decay behavior were compared between Er:SrF₂ and Er:CaF₂ transparent ceramics with different Er³⁺ doping concentration. The green emission of 5 at.% Er:SrF₂ ceramic was much stronger than that of 5 at.% Er:CaF₂ ceramic, while the red emission of Er:SrF₂ ceramic was almost the same as that of Er:CaF₂ ceramic. The upconversion luminescence lifetime of Er:SrF₂ transparent ceramics was longer than that of Er:CaF₂.All the results indicated Er:SrF₂ transparent ceramics was a candidate for green fluorescent upconversion materials.     

Fabrication and optical characterizations of Yb,Er codoped CaF2 transparent ceramic

Nanoparticles of Yb, Er codoped calcium fluoride were obtained by a co-precipitation method. Scanning electron microscope (SEM) and X-ray powder diffraction (XRD) analysis showed that the obtained nanoparticles were single fluorite phase with grains size around 30–50 nm. Yb, Er:CaF₂ transparent ceramics were fabricated by hot pressing (HP) the nanoparticles at a temperature of 800 °C in a vacuum environment. For a 2 mm thickness ceramic sample, the transmittance at 1200 nm reached about 83%. Microstructures were characterized using SEM analysis, and the average grain size was about 700 nm. Grain boundaries of the ceramic sample were clean and no impurities were detected. The absorption, upconversion and infrared emission spectra of transparent ceramic sample under 978 nm excitation were measured and discussed.     

Effect of sintering temperature on the microstructure and transparency of Nd,Y:CaF2 ceramics

1 at% Nd, 3 at% Y doped CaF₂ transparent ceramics were obtained by hot pressing at the sintering temperature varing from 500 to 800 °C under vacuum environment with co-precipitated CaF₂ nanopowders. Transmission electron microscopy (TEM) and X-ray diffraction (XRD) analysis showed that the obtained nanoparticles were single fluorite phase with grain size around 26 nm. Scanning electron microscopy (SEM) observations of the Nd, Y: CaF₂ ceramics indicated that the mean grain size of the ceramic sintered at 800 °C was about 748 nm. The influence of the temperature on the grain size, microstructure and optical transmittance was investigated. For the ceramic sintered at 800 °C, the transmittance was 85.49% at the wavelength of 1200 nm. The room temperature emission spectra of Nd: CaF₂ and Nd, Y: CaF₂ ceramics were measured and discussed.     

Effects of Nd Concentration on Microstructure and Optical Properties of Nd: CaF2 Transparent Ceramics

Highly transparent Nd‐doped calcium fluoride (Nd: CaF₂) ceramics with different Nd‐doped concentrations were fabricated by hot‐pressed method using Nd: CaF₂ nanopowders synthesized by coprecipitation method. SEM observations indicated that the average grain size of nanopowders was about 16–30 nm and the average grain size of the ceramics was between 200 nm and 1 μm. The grain boundaries of the ceramics were clean and no pores or impurities were detected. For 2‐mm‐thickness sample, the transmittance of the as‐fabricated 5 at.% Nd: CaF₂ ceramic at 1200 nm was about 85%. The absorption coefficient and emission intensity of the Nd: CaF₂ ceramics were measured and discussed. From the Nd: CaF₂ ceramics fluorescent spectra and the decay curves, it was found that the fluorescent quenching effect became more evident with the increase in the Nd³⁺ ions‐doped concentration.     

Rare‐earth‐doped SiO2‐CaF2 glass ceramic nano‐particle with upconversion properties

Rare‐earth‐doped upconversion nano‐phosphor shows new possibilities in the field of bioimaging because of its unique properties like higher penetration depth, low signal to noise ratio (SNR), good photo stability, and zero auto fluorescence. The oxyfluoride glass system is the combination of both fluoride and oxide where fluoride host offers high optical transparency due to low phonon energy and oxide network offers high physical stability. Thus, in the present work, an attempt has been made to synthesize 1 mol% Er³⁺ doped SiO₂‐CaF₂ glass ceramic nano‐particles through sol‐gel route. The synthesized glass ceramic particles were heat treated at 4 different temperatures starting from 600°C to 900°C.The X‐ray diffraction (XRD) analysis and Transmission electron microscopy (TEM) analysis confirmed the formation of CaF₂ nano‐crystals in the matrix which is 20‐30 nm in size. The vibrational spectroscopic analysis of the glass ceramics sample has been investigated by Fourier transform infrared (FTIR) spectroscopy. The UV‐Visible‐NIR spectroscopy analysis was carried out to analyze the absorption intensity in the near infrared region. Upon 980 nm excitation, the sample shows red emission corresponds to ⁴F_9/2→⁴I_15/2 energy level transition. The prepared nano‐particles showed excellent biocompatibility when tasted on MG‐63 osteoblast cells.     

Fabrication and Characterization of Glass‐Ceramic Fiber‐Containing Cr3 + ‐Doped ZnAl2O4 Nanocrystals

Glass‐ceramic fibers containing Cr³⁺‐doped ZnAl₂O₄ nanocrystals were fabricated by the melt‐in‐tube method and successive heat treatment. The obtained fibers were characterized by electro‐probe micro‐analyzer, X‐ray diffraction, Raman spectrum and high‐resolution transmission electron microscopy. In our process, fibers were precursor at the drawing temperature where the fiber core glass was melted while the clad was softened. No obvious element interdiffusion between the core and the clad section or crystallization was observed in precursor fiber. After heat treatment, ZnAl₂O₄ nanocrystals with diameters ranging from 1.0 to 6.3 nm were precipitated in the fiber core. In comparison to precursor fiber, the glass‐ceramic fiber exhibits broadband emission from Cr³⁺ when excited at 532 nm, making Cr³⁺‐doped glass‐ceramic fiber a promising material for broadband tunable fiber laser. Furthermore, the melt‐in‐tube method demonstrated here may open a new gate toward the fabrication of novel glass‐ceramic fibers.     

Preparation and characterizations of Pr3+:CaF2 transparent ceramics with different doping concentrations

0.2–5.0?at% Pr³⁺-doped CaF₂ transparent ceramics were fabricated by hot-pressed processing for the first time. The phase compositions, microstructure and optical characteristics of the presented transparent ceramics were examined systematically. The average in-line transmittance of Pr:CaF₂ transparent ceramics (2.0?mm thick) with high Pr³⁺ doping concentrations (1.0–5.0?at%) exceeds 86% at the wavelength of 1200?nm. The absorption spectrum manifests that the prepared Pr:CaF₂ transparent ceramics contain some absorption peaks overlapped with emission bands of the commercial InGaN laser diodes. Further, a detailed investigation on the visible emission properties as a function of Pr³⁺ concentrations in CaF₂ transparent ceramics was reported. The emission spectra presented two main characteristic peaks at 496?nm (bluish green) and 656?nm (red) corresponded to the transitions of ³P₀→³H₄ and ³P₀→³F₂ for Pr³⁺ activator ions. With the increase of the Pr³⁺ doping concentrations, the emission intensity and decay lifetimes decreased generally attributed to the concentration quenching effect. Details on energy transfer mechanism of Pr³⁺ in CaF₂ transparent ceramics were demonstrated and discussed.     

Conventional HP sintering of asymmetric hexagonal structure Yb3+-doped Sr5(PO4)3F transparent ceramic without additives

The 2 at.% Yb³⁺:Sr₅(PO₄)₃F (S-FAP) polycrystalline transparent ceramic with asymmetric hexagonal structures has been synthesized by vacuum hot-pressing the nanoparticles prepared via coprecipitation method. X-ray diffraction results of powder and ceramic indicate that their phase peaks are well matched to the crystal structure of S-FAP. The average particle size of 35.5 nm has been exhibited by powder scanning electron microscopy images, and subsequent images of the ceramic cross section and surface morphology revealed a homogenous and compact microstructure with an average grain size of around 220 nm. The relationship between the optical loss caused by the scattering of anisotropic ceramic grains and the optical transmittance of ceramics was revealed in the hexagonal S-FAP transparent ceramics with different thicknesses. The in-line transmittance of hot-pressed ceramics with 1.5-mm thickness achieved 79.95% at 1100-nm wavelength, and the room-temperature absorption and emission spectra of Yb³⁺ in S-FAP polycrystalline ceramic matrix were measured using a spectrofluorometer.     

Enhanced Sunlight Excited 1‐μm Emission in Cr3+–Yb3+ Codoped Transparent Glass‐Ceramics Containing Y3Al5O12 Nanocrystals

Cr³⁺–Yb³⁺ codoped transparent glass‐ceramics containing Y₃Al₅O₁₂ nanocrystals were prepared by heat treatment of as‐prepared glass sample and characterized by X‐ray diffraction and transmission electron microscopy. The efficient energy transfer from Cr³⁺ to Yb³⁺ ions through multi‐phonon‐assisted process was confirmed by the luminescence spectrum and fluorescent lifetime measurements. When excited by the lights from a solar simulator in the wavelength region of 400–800 nm, greatly enhanced near‐infrared emission around 1 μm was achieved from Cr³⁺–Yb³⁺ codoped glass ceramic compared with that from as‐prepared glass and Ce³⁺–Yb³⁺ codoped glass ceramic. These results demonstrate that the Cr³⁺–Yb³⁺ codoped glass ceramic is a promising material for enhancement of the efficiency of solar energy utilization.     

Energy transfer and controllable colors of upconversion emission in Er3+ and Dy3+ co-doped CaF2 transparent ceramics

x at. % Er³⁺, 3 at. % Dy³⁺: CaF₂ transparent ceramics (x=1-5) with good transparency were fabricated by hot-pressed sintering. The phase composition of nanoparticles and transparent ceramics, microstructure, in-line transmittance, upconversion spectra and lifetime of transparent ceramics, as well as energy transfer mechanism between Er³⁺ and Dy³⁺ were investigated. The mean grain sizes of nanoparticles decreased from 33.0 nm to 26.2 nm with the Er³⁺ doping concentration increasing from 1 to 5 at.%. The microstructure of ceramic samples presented nearly dense microstructure and EDS analysis indicated Er³⁺ and Dy³⁺ were uniformly incorporated into CaF₂ lattice. Under 900 nm excitation, the emission intensity for ⁴F_9/2→⁶H_15/2 transition of Dy³⁺ decreased and for ⁴S_3/2→⁴I_15/2 transition of Er³⁺ increased, the lifetime for the ⁴F_9/2 level of Dy³⁺ decreased while the ⁴F_7/2 level of Er³⁺ increased with the raise of Er³⁺ doping concentration. The energy transfer mechanism was proved to be the dipole-dipole interaction. The upconversion luminescence color was tuned from orange through yellow to green by changing the Er³⁺/Dy³⁺ ratio. In addition, the Vickers hardness, fracture toughness, and the thermal conductivity of Er³⁺, Dy³⁺: CaF₂ transparent ceramics were discussed. All the results showed the Dy³⁺ could be used as a sensitizer for Er³⁺: CaF₂ transparent ceramic in the upconversion field.     

Erbium doped Bi2O3-B2O3 glass-ceramics containing Bi3B5O12 and CaF2 nanocrystallites for 1.53 μm fiber lasers

Trivalent erbium ions doped Bi₂O₃-B₂O₃ transparent glass ceramics containing CaF₂ were prepared and characterized through X -ray diffraction, scanning electron microscopy, Fourier transform infrared absorption, optical absorption, and near infrared emission for 1.53 μm fiber lasers. The glass ceramics obtained by applying thermal treatment at 575 °C for 5 h and 575 °C for 10 h contain Bi₃B₅O₁₂ and CaF₂ crystallites. The Judd-Ofelt theory was applied to evaluate various spectroscopic and laser characteristic properties. The NIR emission corresponding to the ⁴I_13/2 → ⁴I_15/2 (∼1.53 μm) transition was studied by exciting the samples at 514.5 nm laser radiation. The stimulated emission cross-sections of ∼1.53 μm luminescence were also obtained applying the Mc Cumber theory. The experimental results confirm that the transparent glass ceramic obtained at a thermal treatment of 575 °C for 10 h is more suitable to design fiber lasers for diverse applications in the fields of industry, medicine and scientific research.     

Application of Judd–Ofelt theory in analyzing Nd3+ doped SrF2 and CaF2 transparent ceramics

Nd³⁺ doped SrF₂ and CaF₂ transparent ceramics were fabricated by vacuum hot-press sintering and the absorption spectra, emission spectra as well as luminescence decays of the samples were measured. Judd-Ofelt (J–O) theory was used to analyze the optical performance of Nd³⁺ in these two isostructural hosts. The Nd: SrF₂ transparent ceramic was found to have smaller line strength, larger radiative lifetime and smaller Ω₂ value (corresponding to more ionic Nd³⁺-ligand bonding and more symmetry of Nd³⁺ environment). These features made it easier for Nd: SrF₂ to realize population inversion and strong emission, thus doing good to laser performance. The strong emission of ⁴F_3/2 → ⁴I_9/2 transition in Nd: SrF₂, which was predicted by J–O theory and demonstrated by luminescence spectrum, made it possible to achieve effective laser output around 900 nm. The intensity parameters and radiative lifetimes of ceramics were found comparable with their corresponding single crystals.     

Samarium‐Doped Oxyfluoride Glass‐Ceramic as a New Fast Erasable Dosimetric Detector Material for Microbeam Radiation Cancer Therapy Applications at the Canadian Synchrotron

There is a special need to develop a dosimetry technique with a large‐dynamic range and high‐spatial resolution to characterize the microstructured X‐ray beams used in microbeam radiation therapy (MRT) for cancer. We report the synthesis and characterization of oxyfluoride glass‐ceramic (SiO₂–Al₂O₃–CaF₂–CaO–SmF₃) plates, which contain trivalent‐samarium‐doped calcium fluoride (CaF₂:Sm³⁺) nanocrystals, for use as a dosimetric detector material, particularly for MRT applications. Our approach utilizes the extent of Sm³⁺→Sm²⁺ valence reduction caused by X‐ray irradiation as a probe of the X‐ray dose delivered; and confocal fluorescent microscopy is used to read out the distribution of valence reduction through the photoluminescence (PL) signal. Our study showed that the Sm³⁺→Sm²⁺ valence reduction takes place in CaF₂ nanocrystals, but not in the glass matrix. The Sm²⁺ shows PL emission predominantly due to the fast 4f⁵5d¹→⁷F₀ transition, which allows us to read out the detector plate at a high scanning speed. Further, our experiments showed that the detection dose range reaches several thousands of grays, and X‐ray dose distribution is detected at a micrometer scale. In addition, the Sm²⁺ signal can be erased either by heating the irradiated sample at a suitable high temperature or by exposing it to UV light; and the erased glass‐ceramic plate is reusable. The new Sm‐doped oxyfluoride glass‐ceramic with CaF₂ nanocrystals reported in this work shows potential for practical use in high‐dose and high‐resolution dosimetry for MRT.     

Gadolinium‐conjugated FA‐PEG‐PAMAM‐COOH nanoparticles as potential tumor‐targeted circulation‐prolonged macromolecular MRI contrast agents

The aim of research is to develop potential tumor‐targeted circulation‐prolonged macromolecular magnetic resonance imaging (MRI) contrast agents without the use of low molecular gadolinium (Gd) ligands. The contrast agents were based on polymer–metal complex nanoparticles with controllable particle size to achieve the active and passive tumor‐targeted potential. In particular, poly (amidoamine) (PAMAM) dendrimer with 32 carboxylic groups was modified with folate‐conjugated poly (ethyleneglycol) amine (FA‐PEG‐NH₂, M_w: 2 k and 4 kDa). FA‐PEG‐PAMAM‐Gd macromolecular MRI contrast agents were prepared by the complex reaction between the carboxylic groups in PAMAM and GdCl₃. The structure of FA‐PEG‐PAMAM‐COOH was confirmed by nuclear magnetic resonance (¹H‐NMR), Fourier transform infrared (FTIR) spectra, and electrospray ionization mass spectra (ESI‐MS). The mass percentage content of Gd (III) in FA‐PEG‐PAMAM‐Gd was measured by inductively coupled plasma‐atomic emission spectrometer (ICP‐AES). The sizes of these nanoparticles were about 70 nm measured by transmission electron microscopy, suggestion of their passive targeting potential to tumor tissue. In comparison with clinically available small molecular Gadopentetate dimeglumine, FA‐PEG‐PAMAM‐Gd showed comparable cytotoxicity and higher relaxation rate, suggestion of their great potential as tumor‐targeted nanosized macromolecular MRI contrast agents due to the overexpressed FA receptor in human tumor cell surfaces. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Novel Er3+/Ho3+‐codoped glass‐ceramic fibers for broadband tunable mid‐infrared fiber lasers

It is well recognized that a widely wavelength‐tunable mid‐infrared (MIR) fiber laser plays an important role in the development of compact and efficient coherent sources in the MIR range. Herein, the optimizing Er/Ho ratio for enhancement of broadband tunable MIR emission covering 2.6‐2.95 μm in the Er³⁺/Ho³⁺‐codoped transparent borosilicate glass‐ceramic (GC) fibers containing NaYF₄ nanocrystals under 980 nm excitation was investigated. Specifically, the obtained GC fibers with controllable crystallization and well fsd‐maintained structures were prepared by the novel melt‐in‐tube approach. Owing to the effective energy transfer between Er³⁺ and Ho³⁺ after crystallization, the 2.7 μm MIR emission was obviously enhanced and the emission region showed a notable extension from 2.6‐2.82 μm to 2.6‐2.95 μm after the addition of Ho³⁺. Importantly, we conducted a theoretical simulation and calculation related to the MIR laser performance, signifying that the GC fiber may be a promising candidate for MIR fiber laser. Furthermore, the melt‐in‐tube approach will provide a versatile strategy for the preparation of diverse optical functional GC fibers.     

Thermal,Structural, and Enhanced Photoluminescence Properties of Eu3+‐doped Transparent Willemite Glass–Ceramic Nanocomposites

The precursor glass in the ZnO–Al₂O₃–B₂O₃–SiO₂ (ZABS) system doped with Eu₂O₃ was prepared by the melt‐quench technique. The transparent willemite, Zn₂SiO₄ (ZS) glass–ceramic nanocomposites were derived from this precursor glass by a controlled crystallization process. The formation of willemite crystal phase, size, and morphology with increase in heat‐treatment time was examined by X‐ray diffraction (XRD) and field‐emission scanning electron microscopy (FESEM) techniques. The average calculated crystallite size obtained from XRD is found to be in the range 18–70 nm whereas the grain size observed in FESEM is 50–250 nm. The refractive index value is decreased with increase in heat‐treatment time which is caused by the partial replacement of ZnO₄ units of ZS nanocrystals by AlO₄ units due to generation of vacancies. Fourier transform infrared (FTIR) reflection spectroscopy was used to evaluate its structural evolution. Vickers hardness study indicates marked improvement of hardness in the resultant glass‐ceramics compared with its precursor glass. The photoluminescence spectra of Eu³⁺ ions exhibit emission transitions of ⁵D₀→⁷F_j (j = 0, 1, 2, 3, and 4) and its excitation spectra show an intense absorption band at 395 nm. These spectra reveal that the luminescence performance of the glass–ceramic nanocomposites is enhanced up to 17‐fold with the process of heat treatment. This enhancement is caused by partitioning of Eu³⁺ ions into glassy phase instead of into the willemite crystals with progress of heat treatment. Such luminescent glass–ceramic nanocomposites are expected to find potential applications in solid‐state red lasers, phosphors, and optical display systems.     

Transmission electron microscopic and optical spectroscopic studies of Ni2+/Yb3+/Er3+/Tm3+ doped dual‐phase glass‐ceramics

Ni²⁺/Yb³⁺/Er³⁺/Tm³⁺ codoped transparent glass‐ceramics (GCs) containing both hexagonal β‐YF₃ and spinel‐like γ‐Ga₂O₃ dual‐phase nanoparticles (NCs) are synthesized by melt‐quenching and subsequent heating procedures. Two techniques of transmission electron microscopy (TEM) nanoanalytics and optical spectroscopy are conjugated to understand the distribution of the rare‐earth ions (REs) and transition metals (TMs) in the nanostructured GCs. It is found that the REs are located predominantly in β‐YF₃, whereas the TMs in γ‐Ga₂O₃ NCs. As a result, energy transfer (ET) between the REs and TMs is considerably suppressed due to the large spatial separation (> 3 nm), but it is enhanced between the REs partitioned in the β‐YF₃ NCs. This has important implications for intended and demanding photoluminescence functions. For example, an ultrabroadband near‐infrared (NIR) emission in the wavelength region of 1000‐2000 nm covering the entire telecommunications window is observed for the first time. Meanwhile, intense upconversion (UC) emissions covering the 3 primary colors and locating in the first biological window can be also recorded under excitation by a single pump source at 980 nm.     

Spectral Properties of Pr3+‐Doped Transparent‐Glass‐Ceramic Containing Ca5(PO4)3F Nanocrystals

A Pr³⁺‐doped transparent oxyfluoride glass‐ceramic containing Ca₅(PO₄)₃F nanocrystals was prepared by melt quenching and subsequent thermal treatment. The crystallization phase and morphology of the Ca₅(PO₄)₃F nanocrystals were investigated by X‐ray diffraction and transmission electron microscope, respectively. The volume fraction of the Ca₅(PO₄)₃F nanocrystals in the glass‐ceramic is about 10% and the fraction of Pr³⁺ ions incorporated into the Ca₅(PO₄)₃F nanocrystals is about 22%. The peak absorption cross sections at 435 and 574 nm increase up to 128% and 132% after crystallization, respectively. The peak stimulated emission cross sections of the ³P₀→³H₄ blue laser channel and ³P₀→³F₂ red laser channel for the glass‐ceramic are 4.95 × 10^?20 and 29.8 × 10^?20 cm², respectively. The spectral properties indicate that the glass‐ceramic is a potential visible laser material.