High-Verdet Constant and Low-Optical Loss Tb3+ Doped Magnetite Nanoparticles.

Magneto-optical (MO) polymer nanocomposites have emerged as alternatives to conventional MO crystals, particularly in nanophotonics applications, thanks to their better processing flexibility and superior Verdet constants. However, a higher Verdet constant commonly comes with excessive optical loss due to increased absorption and scattering, resulting in a constant or reduced figure-of-merit (FOM) defined as the Verdet constant over optical loss. By doping magnetite (Fe3O4) nanoparticles with Tb3+ ions, we report a new strategy to enhance the Verdet constant without increasing the optical loss. The Fe3O4:Tb3+ nanocomposite is one of a kind that simultaneously achieves a state-of-the-art Verdet constant of 5.6 × 105 °/T·m and a state-of-the-art FOM of 31°/T in the near-infrared region.

A Novel Low-Density-Biomass-Carbon Composite Coated with Carpet-like and Dandelion-Shaped Rare-Earth-Doped Cobalt Ferrite for Enhanced Microwave Absorption.

A novel low-density composite for the absorption of microwaves was prepared by loading La-doped spinel cobalt ferrite (La-CFO) onto biomass carbon (BC) derived from corn stalks using a hydrothermal method. This composite (La-CFO@BC) not only maintained the advantageous properties of low density and abundant porosity, but also exhibited a unique morphology, with La-CFO displaying a carpet-like structure interspersed with dandelion-shaped particles. The incorporation of La-CFO effectively tuned the electromagnetic parameters of the composite, thereby improving its impedance-matching attributes and its ability to absorb microwave radiation. At a frequency of 12.8 GHz for electromagnetic waves and with a thickness of 2.5 mm, La-CFO@BC demonstrated remarkable performance in microwave absorption, attaining a noteworthy minimum reflection (RLmin) of -53.2 dB and an effective absorption bandwidth (EAB) of 6.4 GHz. Furthermore, by varying the thickness of the La-CFO@BC within the range of 1.0 to 5.5 mm, the EAB could be broadened to 13.8 GHz, covering the entire X-band, the entire Ku-band, and a substantial portion of the C-band. This study demonstrated that La-CFO@BC was a promising alternative for electromagnetic wave attenuation, which offered superior performance in microwave absorption.

Green Synthesis of Er-Doped ZnO Nanoparticles: An Investigation on the Methylene Blue, Eosin, and Ibuprofen Removal by Photodegradation.

We present a study on the green synthesis of undoped and Er-doped ZnO compounds using Mangifera indica gum (MI). A set of tests were conducted to assess the structure of the material. The tests included X-ray diffraction, Raman, and Fourier-transform infrared spectroscopy. Optical properties were studied using diffuse reflectance and photoluminescence. Morphological and textural investigations were done using SEM images and N2 adsorption/desorption. Furthermore, photocatalytic tests were performed with methylene blue (MB), yellow eosin (EY), and the pharmaceutical drug ibuprofen (IBU) under UV irradiation. The study demonstrated that replacing the stabilizing agent with Mangifera indica gum is an effective method for obtaining ZnO nanoparticles. Additionally, the energy gap of the nanoparticles exhibits a slight reduction in value. Photoluminescence studies showed the presence of zinc vacancies and other defects in both samples. In the photocatalytic test, the sample containing Er3+ exhibited a degradation of 99.7% for methylene blue, 81.2% for yellow eosin, and 52.3% for ibuprofen over 120 min. In the presence of methyl alcohol, the degradation of MB and EY dyes is 16.7% and 55.7%, respectively. This suggests that hydroxyl radicals are responsible for the direct degradation of both dyes. In addition, after the second reuse, the degradation rate for MB was 94.08%, and for EY, it was 82.35%. For the third reuse, the degradation rate for MB was 97.15%, and for EY, it was 17%. These results indicate the significant potential of the new semiconductor in environmental remediation applications from an ecological synthesis.

Blue-red emission color change from a heavily-doped Eu@MOF composite: Synthesis, characterization and application for 2,4,6-trinitrophenol sensing.

2,4,6-trinitrophenol (TPA) natural degradation is nearly impossible and its accumulation threatens ecosystem. Optical sensing is an attractive detection method for TPA with low demand of equipment and data processing, but still needs to be improved. This work was dedicated to increasing probe-loading content so as to improve sensing sensitivity. Three probes derived from Eu(III)-benzimidazole were designed, with their active H atoms replaced by alkyl groups to eliminate the hydrogen bond with supporting host and thus to improve probe-loading content. Their molecular structure, absorption, emission, and excitation spectra were discussed to confirm their sensing potential to TPA. Then these three probes were loaded into host (bio-MOF-1) via ionic exchange method, which was confirmed by XRD, N2 adsorption/desorption, ICP, and SEM. The loading content and sensing performance of these three probes in bio-MOF-1 were compared. It was found that the elimination of active H atoms indeed increased probe loading content from 44% to 78%, with sensing coefficient increased from 0.010 µM-1 to 0.029 µM-1. A ratiometric sensing towards TPA was observed, with blue emission from bio-MOF-1 host increased and red emission from Eu(III) probe decreased, which was detectable by naked eyes. Linear working equations were fitted with high selectivity.

Experimental Demonstration of a Magnetically Induced Warping Transition in a Topological Insulator Mediated by Rare-Earth Surface Dopants.

Magnetic topological insulators constitute a novel class of materials whose topological surface states (TSSs) coexist with long-range ferromagnetic order, eventually breaking time-reversal symmetry. The subsequent bandgap opening is predicted to co-occur with a distortion of the TSS warped shape from hexagonal to trigonal. We demonstrate such a transition by means of angle-resolved photoemission spectroscopy on the magnetically rare-earth (Er and Dy) surface-doped topological insulator Bi2Se2Te. Signatures of the gap opening are also observed. Moreover, increasing the dopant coverage results in a tunable p-type doping of the TSS, thereby allowing for a gradual tuning of the Fermi level toward the magnetically induced bandgap. A theoretical model where a magnetic Zeeman out-of-plane term is introduced in the Hamiltonian governing the TSS rationalizes these experimental results. Our findings offer new strategies to control magnetic interactions with TSSs and open up viable routes for the realization of the quantum anomalous Hall effect.

An Ultrafast and Room-Temperature Strategy for Kilogram-Scale Synthesis of Sub-5 nm Eu3+ -doped CaMO4 Nanocrystals with a Photoluminescence Quantum Yield Exceeding 85.

Rare earth-doped metal oxide nanocrystals have a high potential in display, lighting, and bio-imaging, owing to their excellent emission efficiency, superior chemical, and thermal stability. However, the photoluminescence quantum yields (PLQYs) of rare earth-doped metal oxide nanocrystals have been reported to be much lower than those of the corresponding bulk phosphors, group II-VI, and halide-based perovskite quantum dots because of their poor crystallinity and high-concentration surface defects. Here, an ultrafast and room-temperature strategy for the kilogram-scale synthesis of sub-5 nm Eu3+ -doped CaMoO4 nanocrystals is presented, and this reaction can be finished in 1 min under ambient conditions. The absolute PLQYs for sub-5 nm Eu3+ -doped CaMoO4 nanocrystals can reach over 85%, which are comparable to those of the corresponding bulk phosphors prepared by the high-temperature solid state reaction. Moreover, the as-produced nanocrystals exhibit a superior thermal stability and their emission intensity unexpectedly increases after sintering at 600 °C for 2 h in air. 1.9 kg of Eu3+ -doped CaMoO4 nanocrystals with a PLQY of 85.1% can be obtained in single reaction.

Phase Stability and Dual-Mode Photoluminescence Modulation in Er-Doped Lead Zirconate Titanate Antiferroelectrics.

The electric-field-modulation (E-modulation) of photoluminescence (PL) properties in bulk ceramics has attracted tremendous interest due to its potential application in optical data storage and communication devices. One promising approach of reversibly and largely modulating the PL intensity has been proposed in rare-earth Er3+-doped Pb0.96La0.04Zr0.9Ti0.1O3 (PLZT) antiferroelectrics (AFEs) based on the unique E-dependent antiferroelectric-ferroelectric (AFE-FE) phase transition. However, the AFE phase stability of PLZT doped with various Er contents and their E-modulated PL properties have not been systematically investigated. In this paper, the intrinsic AFE phase of PLZT-Er is found to be stabilized in the high-temperature and high-E regions with increasing Er3+ content. The enhanced AFE nature caused by increasing Er doping leads to a larger E-dependent PL tunability (∼35%). Moreover, the ceramics exhibit the characteristics of both upconversion and downconversion PL (UCPL and DCPL) effects. Based on the excellent E-dependent dual-mode PL tunability, an optoelectronic device named the optical latch is demonstrated, where an electric signal can be used to trigger a notable intensity change in both the UCPL and DCPL modes. This reversible E-dependent dual-mode capability in PLZT-Er sheds light on a feasible approach to optoelectronic applications.

Rare Earth Doping Engineering Tailoring Advanced Oxygen-Vacancy Co3 O4 with Tunable Structures for High-Efficiency Energy Storage.

Co3 O4  with high theoretical capacitance is a promising electrode material for high-end energy applications, yet the unexcited bulk electrochemical activity, low conductivity, and poor kinetics of Co3 O4  lead to unsatisfactory charge storage capacity. For boosting its energy storage capability, rare earth (RE)-doped Co3 O4  nanostructures with abundant oxygen vacancies are constructed by simple, economical, and universal chemical precipitation. By changing different types of RE (RE = La, Yb, Y, Ce, Er, Ho, Nd, Eu) as dopants, the RE-doped Co3 O4  nanostructures can be well transformed from large nanosheets to coiled tiny nanosheets and finally to ultrafine nanoparticles, meanwhile, their specific surface area, pore distribution, the ratio of Co2+ /Co3+ , oxygen vacancy content, crystalline phase, microstrain parameter, and the capacitance performance are regularly affected. Notably, Eu-doped Co3 O4  nanoparticles with good cycle stability show a maximum specific capacitance of 1021.3 F g-1 (90.78 mAh g-1 ) at 2 A g-1 , higher than 388 F g-1 (34.49 mAh g-1 ) of pristine Co3 O4  nanosheets. The assembling asymmetric supercapacitor delivers a high energy density of 48.23 Wh kg-1  at high power density of 1.2 kW kg-1 . These findings denote the significance and great potential of RE-doped Co3 O4  in the development of high-efficiency energy storage.

Improved Thermoelectric Properties of SrTiO3 via (La, Dy and N) Co-Doping: DFT Approach.

This work considers the enhancement of the thermoelectric figure of merit, ZT, of SrTiO3 (STO) semiconductors by (La, Dy and N) co-doping. We have focused on SrTiO3 because it is a semiconductor with a high Seebeck coefficient compared to that of metals. It is expected that SrTiO3 can provide a high power factor, because the capability of converting heat into electricity is proportional to the Seebeck coefficient squared. This research aims to improve the thermoelectric performance of SrTiO3 by replacing host atoms by La, Dy and N atoms based on a theoretical approach performed with the Vienna Ab Initio Simulation Package (VASP) code. Here, undoped SrTiO3, Sr0.875La0.125TiO3, Sr0.875Dy0.125TiO3, SrTiO2.958N0.042, Sr0.750La0.125Dy0.125TiO3 and Sr0.875La0.125TiO2.958N0.042 are studied to investigate the influence of La, Dy and N doping on the thermoelectric properties of the SrTiO3 semiconductor. The undoped and La-, Dy- and N-doped STO structures are optimized. Next, the density of states (DOS), band structures, Seebeck coefficient, electrical conductivity per relaxation time, thermal conductivity per relaxation time and figure of merit (ZT) of all the doped systems are studied. From first-principles calculations, STO exhibits a high Seebeck coefficient and high figure of merit. However, metal and nonmetal doping, i.e., (La, N) co-doping, can generate a figure of merit higher than that of undoped STO. Interestingly, La, Dy and N doping can significantly shift the Fermi level and change the DOS of SrTiO3 around the Fermi level, leading to very different thermoelectric properties than those of undoped SrTiO3. All doped systems considered here show greater electrical conductivity per relaxation time than undoped STO. In particular, (La, N) co-doped STO exhibits the highest ZT of 0.79 at 300 K, and still a high value of 0.77 at 1000 K, as well as high electrical conductivity per relaxation time. This renders it a viable candidate for high-temperature applications.

Achieving Giant Piezoelectricity and High Property Uniformity Simultaneously in a Relaxor Ferroelectric Crystal through Rare-Earth Element Doping.

The low uniformity in properties of relaxor ferroelectric crystals is a long-standing issue in the ferroelectric community, which limits the available volume of the entire crystal boule. The aim of this study is to develop a relaxor ferroelectric crystal with improved property uniformity and excellent piezoelectricity. To this end, Pb(In1/2 Nb1/2 )O3 -Pb(Mg1/3 Nb2/3 )O3 -PbTiO3 is doped with Nd2 O3 (Nd-PIN-PMN-PT) to improve the crystal performance. Along the crystal boule, the piezoelectric coefficient d33 varies from 2800 to 3500 pC N-1 , and the dielectric constant ranges from 8400 to 9800, with variations of 25% and 16%, respectively. Such high property uniformity results in over 75% available volume of the crystal boule, compared to 30-50% for undoped crystals grown by Bridgman method. At the electric field of 1 kV cm-1 , the converse piezoelectric response is up to 4780 pm V-1 . In addition, its Curie temperature (TC ) and coercive field (EC ) are above 150 °C and 3 kV cm-1 , respectively. Compared with Pb(Mg1/3 Nb2/3 )O3 -PbTiO3 crystal (d33 : 1500 pC N-1 , TC : 135 °C, EC : 2.3 kV cm-1 ), the larger piezoelectricity, the higher TC and EC , and improved uniformity make Nd-PIN-PMN-PT crystals promising candidates for advanced piezoelectric applications.

Collaborative influence of morphology tuning and RE (La, Y, and Sm) doping on photocatalytic performance of nanoceria.

Tuning morphology and doping additional rare earth (RE) cations are potential techniques to promote the photocatalytic performance of ceria (CeO2), evaluating the collaborative effects of morphology and RE dopants is significant for producing high active ceria-based catalysts. So in this work, cubic, polyhedral and rod-like nanoceria doped with 10 mol % La (lanthanum), Y (yttrium), or Sm (samarium) were synthesized by a facile template-free hydrothermal method. Phases, morphologies, oxygen vacancies (OVs) concentration, energy band structure, photo-carriers separation/recombination, and photodegradation ratio toward methylene blue (MB) dye of as prepared ceria were studied. Results show that doped CeO2 maintains a similar morphology structure with un-doped sample and the band gap narrows slightly. Y-doped nanoceria, with an improved separation and a reduced recombination of photo-excited electrons (e-) and holes (h+), owns a higher MB photodegradation ratio than that of samples doping with La or Sm, which is measured as 79.04, 84.43, and 85.59% for Y-doped cubic, polyhedral, and rod-like CeO2. The collaborative influence of morphology tuning and RE (La, Y, and Sm) doping on photocatalytic performance of nanoceria includes the effects of doped elements and the formation of OVs. The elevation of OVs concentration as well as the separation efficiency of photo-generated e-/h+ are suggested to further enhance the photocatalytic performance of ceria.

White-light emission in Yb3+/Er3+/Tm3+- and Yb3+/Er3+/Tm3+/Ho3+-dopedα-NiMoO4nanoparticles.

Yb3+/Er3+/Tm3+- and Yb3+/Er3+/Tm3+/Ho3+-dopedα-NiMoO4nanoparticles were synthesized using a microwave hydrothermal method and studied for white-light emission under 980 nm laser diode excitation. White upconversion (UC) light was successfully obtained with the appropriate control of blue, green, and red emissions by successfully tuning the Er3+and Ho3+concentrations in Yb3+/Er3+/Tm3+- and Yb3+/Er3+/Tm3+/Ho3+-dopedα-NiMoO4, respectively. In addition, the white color emission was shown by the CIE chromaticity coordinates of samples. The energy transfer mechanisms are explained in detail based on the emission spectra and pump power density-dependent UC luminescence intensity in rare earth (Yb3+/Er3+/Tm3+and Yb3+/Er3+/Tm3+/Ho3+)-dopedα-NiMoO4nanoparticles. The results indicate that Yb3+/Er3+/Tm3+- and Yb3+/Er3+/Tm3+/Ho3+-dopedα-NiMoO4nanoparticles can be good candidates for white-light devices.

Preparation of Zr/Y co-doped TiO2 photocatalyst and degradation performance of hydroquinone.

In this paper, Y-ZrO2-TiO2 photocatalyst was prepared by sol-gel method, the titanium source was tetrabutyl titanate, and the precursors were zirconium nitrate pentahydrate and yttrium nitrate hexahydrate. For the photocatalytic effect of Y-ZrO2-TiO2 to hydroquinone, these effects were investigated: doping ratios of Zr/Y, calcination conditions, pH, etc. And the materials were characterized by XRD, TEM-EDS, XPS, PL, ESR, etc. The results showed that the optimum preparation conditions of Y-ZrO2-TiO2 photocatalyst were as follows: the molar ratio of doping was Ti: Zr: Y = 100:6:0.5, the calcination temperature was 500 °C, and the calcination time was 2 h; the optimum reaction conditions were as follows: the dosage of Y-ZrO2-TiO2 was 1 g/L, and pH value was 6.96. The degradation rate of hydroquinone under 365-nm UV lamp for 50 min could reach 96.58%, while the degradation rates of pure TiO2, Y-TiO2, and ZrO2-TiO2 under the same conditions were 33.95%, 79.55%, and 90.30%, respectively. It can be seen that the addition of elements Zr and Y improves the photocatalytic performance of TiO2.

Construction multifunctional nanozyme for synergistic catalytic therapy and phototherapy based on controllable performance.

Advances in nanozyme involve an efficient catalytic process, which has demonstrated great potential in tumor therapy. The key to improving catalytic therapy is to solve the limitation of the tumor microenvironment on Fenton reaction. In this work, Prussian blue nanoparticles doped with different rare earth ions (Yb3+, Gd3+, Tm3+) were screened to perform synergistic of photothermalandcatalytictumortherapy. The optimized catalytic performance can be further enhanced through photothermal effect to maximize the Fenton reaction to solve the limitation of the tumor microenvironment. Yb-PB, with the optimal photothermal and catalytic performance, was screened out. In order to avoid the scavenging effect of glutathione (GSH) on ·OH in tumor cells and the reaction with a bit H2O2 in normal cells, GSH targeted polydopamine (PDA) was wrapped on the surface of Yb-PB to obtain Yb-PB@PDA. It was found that enough hydroxyl radicals (·OH) can be generated even if at high GSH concentration and the NIR irradiation can help produce more ·OH. Cell fluorescence imaging (FOI) and in vivo magnetic resonance imaging (MRI) experiments showed the potential application in FOI/MRI dual-mode imaging guided therapy. In vivo anti-tumor experiments showed that Yb-PB@PDA has a satisfactory anti-cancer effect through the combined effect of catalytic/photothermal therapy. Thus, a multifunctional nanozyme for tumor therapy is constructed.

The Electrical and Thermal Transport Properties of La-Doped SrTiO3 with Sc2O3 Composite.

Donor-doped strontium titanate (SrTiO3) is one of the most promising n-type oxide thermoelectric materials. Routine doping of La at Sr site can change the charge scattering mechanism, and meanwhile can significantly increase the power factor in the temperature range of 423-773 K. In addition, the introduction of Sc partially substitutes Sr, thus further increasing the electron concentration and optimizing the electrical transport properties. Moreover, the excess Sc in the form of Sc2O3 composite suppresses multifrequency phonon transport, leading to low thermal conductivity of κ = 3.78 W·m-1·K-1 at 773 K for sample Sr0.88La0.06Sc0.06TiO3 with the highest doping content. Thus, the thermoelectric performance of SrTiO3 can be significantly enhanced by synergistic optimization of electrical transport and thermal transport properties via cation doping and composite engineering.

Highly Enhanced OER Performance by Er-Doped Fe-MOF Nanoarray at Large Current Densities.

Great expectations have been held for the electrochemical splitting of water for producing hydrogen as a significant carbon-neutral technology aimed at solving the global energy crisis and greenhouse gas issues. However, the oxygen evolution reaction (OER) process must be energetically catalyzed over a long period at high output, leading to challenges for efficient and stable processing of electrodes for practical purposes. Here, we first prepared Fe-MOF nanosheet arrays on nickel foam via rare-earth erbium doping (Er0.4 Fe-MOF/NF) and applied them as OER electrocatalysts. The Er0.4 Fe-MOF/NF exhibited wonderful OER performance and could yield a 100 mA cm-2 current density at an overpotential of 248 mV with outstanding long-term electrochemical durability for at least 100 h. At large current densities of 500 and 1000 mA cm-2, overpotentials of only 297 mV and 326 mV were achieved, respectively, revealing its potential in industrial applications. The enhancement was attributed to the synergistic effects of the Fe and Er sites, with Er playing a supporting role in the engineering of the electronic states of the Fe sites to endow them with enhanced OER activity. Such a strategy of engineering the OER activity of Fe-MOF via rare-earth ion doping paves a new avenue to design other MOF catalysts for industrial OER applications.

The Effects of La Doping on the Crystal Structure and Magnetic Properties of Ni2In-Type MnCoGe1-xLax (x = 0, 0.01, 0.03) Alloys.

In this experiment, a series of MnCoGe1-xLax (x = 0, 0.01, 0.03) alloy samples were prepared using a vacuum arc melting method. The crystal structure and magnetic properties of alloys were investigated using X-ray diffraction (XRD), Rietveld method, physical property measurement system (PPMS), and vibrating sample magnetometer (VSM) analyses. The results show that all samples were of high-temperature Ni2In-type phases, belonging to space group P63/mmc (194) after 1373 K annealing. The results of Rietveld refinement revealed that the lattice constant and the volume of MnCoGe1-xLax increased along with the values of La constants. The magnetic measurement results show that the Curie temperatures (TC) of the MnCoGe1-xLax series alloys were 294, 281, and 278 K, respectively. The maximum magnetic entropy changes at 1.5T were 1.64, 1.53, and 1.56 J·kg-1·K-1, respectively. The respective refrigeration capacities (RC) were 60.68, 59.28, and 57.72J·kg-1, with a slight decrease along the series. The experimental results show that the doping of La results in decreased TC, basically unchanged magnetic entropy, and slightly decreased RC.

Graphene oxide@Ce-doped TiO2 nanoparticles as electrocatalyst materials for voltammetric detection of hazardous methyl parathion.

A sensitive voltammetric sensor has been developed for hazardous methyl parathion detection (MP) using graphene oxide@Ce-doped TiO2 nanoparticle (GO@Ce-doped TiO2 NP) electrocatalyst. The GO@Ce-doped TiO2 NPs were prepared through the sol-gel method and characterized by various physicochemical and electrochemical techniques. The GO@Ce-doped TiO2 NP-modified glassy carbon electrode (GCE) addresses excellent electrocatalytic activity towards MP detection for environmental safety and protection. The developed strategy of GO@Ce-doped TiO2 NPs at GCE surfaces for MP detection achieved excellent sensitivity (2.359 µA µM-1 cm-2) and a low detection limit (LOD) 0.0016 µM with a wide linear range (0.002 to 48.327 µM). Moreover, the fabricated sensor shows high selectivity and long-term stability towards MP detection; this significant electrode further paves the way for real-time monitoring of environmental quantitative samples with satisfying recoveries.

A study on the spectral, microstructural, and magnetic properties of Eu-Nd double-substituted Ba0.5Sr0.5Fe12O19 hexaferrites synthesized by an ultrasonic-assisted approach.

In this study, an examination on the spectral, microstructural, and magnetic characteristics of Eu-Nd double-substituted Ba0.5Sr0.5Fe12O19 hexaferrites (Ba0.5Sr0.5NdxEuxFe12-2xO19 (x = 0.00-0.05) HFs) fabricated by an ultrasonic-assisted approach has been presented. An UZ SONOPULS HD 2070 ultrasonic homogenizer with frequency of 20 kHz and power of 70 W was used. The chemical bonding, structure and the morphology of the products were evaluated by Fourier-Transform Infrared (FT-IR) Spectroscopy, XRD (X-ray diffraction), scanning and transmission electron microscopy and techniques. The textural properties of the prepared nanomaterials were examined by using the Brunauer-Emmett-Teller (BET) method. The magnetic properties were studied using a vibrating sample magnetometer (VSM) at room temperature (RT) and low temperature 10 K. The magnitudes of various magnetic parameters including Ms (saturation magnetization), Mr (remanence) and Hc (coercivity) were estimated and evaluated. The M-H loops revealed the hard ferrimagnetic nature for all products at both temperatures. The Ms and Mr values showed a decreasing tendency with increasing degree of Eu3+ and Nd3+ substitutions whereas Hc values displayed an increasing trend. At RT, Ms, Mr and Hc values lie in the ranges of 63.0-68.8 emu·g-1, 24.6-39.2 emu·g-1 and 2252.4-2782.1 Oe, respectively. At 10 K, the values of Ms, Mr and Hc lie between 87.5-97.1 emu·g-1, 33.5-40.1 emu·g-1 and 2060.6-2417.2 Oe, respectively. The observed magnetic properties make the prepared products promising candidates to be applied in the recording media.

Fabrication of luminescent TiO2:Eu3+ and ZrO2:Tb3+ encapsulated PLGA microparticles for bioimaging application with enhanced biocompatibility.

Rare earth is of great interest because of their unique optical properties, especially the rich luminescent spectra. In this study, we developed a facile one-pot microwave-assisted synthesis of luminescent Eu3+ doped TiO2 nanoparticles and Tb3+ doped ZrO2 nanoparticles. As a result, the emitting centers (Eu3+ and Tb3+) were all well dispersed in the amorphous host oxide materials, leading to high luminescence. The obtained TiO2:Eu3+ and ZrO2:Tb3+ nanoparticles were then encapsulated into PLGA microparticles for bio-applications. These luminescent microparticles were then proven to be highly stable, biocompatible and of low cytotoxicity. We successfully demonstrated the bioimaging of live cells using the red-luminescent TiO2:Eu3+ nanoparticles and green-luminescent ZrO2:Tb3+ nanoparticles embedded PLGA microparticles. The microwave-assisted synthetic methodology can be further developed to be general method to prepare oxide nanoparticles.