1O2-activatable Eu3+-afterglow nanoprobe for highly sensitive detection of porphyria in whole blood

High-sensitivity detection of porphyrin in blood is very important for the early diagnosis and treatment of porphyria.Based on the advantages of longer luminescence lifetime and lower background interference,organic afterglow molecular porphyrin detection probes were developed,but these probes show poor water solubility and insufficient luminescence intensity.Herein,we present an afterglow nanoprobe(Eu-NP) for porphyria detection in whole blood.The luminescent substance(europium complex) and the...     

Sensitive and fast response ethanol chemical sensor based on as-grown Gd2O3 nanostructures

Well crystalline gadolinium oxide(Gd2O3) nanostructures were grown by annealing the hydrothermally as-prepared nanostructures without using any template. Microscopic studies of Gd2O3 nanostructures were recorded along the [111] direction due to the clearly resolved interplanar distance d(222)~0.31 nm of the cubic crystal structure Gd2O3. Sensing mechanism of Gd2O3 as efficient electron mediator for the detection of ethanol was explored. As-fabricated sensor demonstrated the high-sensitivity of ~0.266 μAm/M/cm2 with low detection limit(~52.2 μmol/L) and correlation coefficient(r2, 0.618). To the best of our knowledge, this was the first report for the detection of ethanol using as-grown(at 1000 oC) Gd2O3 nanostructures by simple and reliable I-V technique and rapid assessment of the reaction kinetics(in the order of seconds). The low cost of the starting reagents and the simplicity of the synthetic route made it a promising chemical sensor for the detection of various toxic analytes, which are not environmentally safe.     

Synthesis and fluorescent properties of a novel europium（III） complex with terpyridine-capped poly（ethylene glycol）

Terpyridine-capped poly(ethylene glycol) (PEG) was synthesized as a novel polymeric ligand and rare earth complex was prepared from Eu(NO3)3 and the telechelic macromolecules. The structure of the complex was characterized by 1H NMR, FT-IR, UV-vis and fluores-cence spectroscopy. Strong fluorescent emission of the complex was observed at 593 and 616 nm upon the excitation of 300 nm. The fluo-rescent emission was quenched upon addition of trace amount of diethyl chlorophosphate (DCP). And the observed Ksv values for DCP were measured to be 0.568×103 and 0.89×103 L/mol for quenching at 593 and 616 nm, which indicated the detection limit for DCP was about 0.014 mmol/L. These results showed that the terpyridine-lanthanide complex could be an effective chemosensor with a potential application in the detection of organophosphates.     

Novel luminescent europium-centered hybrid material covalently grafted with organically modified titania via 2-substituted imidazophenanthroline for fluorescence sensing

By employing a rational approach,we prepared a novel kind of luminescent europium-centered hybrid material named Eu(tta)_3NCP-TiO_2.The resulting material was characterized by FT-IR spectra,SEM,X-ray diffraction,thermogravimetric analysis,and photoluminescence spectra.The hybrid material features the combined advantages of the europium complex and the titania host,exhibiting not only good thermostability,but also long luminescence lifetime.Owing to the excellent luminescence of this material,the application in detecting organic small molecule solvents and metal ions was explored systematically.Significantly,Eu(tta)_3 NCP-TiO_2 exhibits superior detection for nitrobenzene molecule and Cu~(2+) ion in DMF(N,N-dimethylformamide) medium.Furthermore,the limit of detection(LOD) of Eu(tta)_3 NCP-TiO_2 for nitrobenzene and Cu~(2+) ion can be counted as 5.593× 10~(-5) and 9.566 ×10~(-5) mol/L,respectively.The results demonstrate that Eu(tta)_3 NCP-TiO_2 can serve as an efficient fluorescence probe for the detection of sensing of nitrobenzene and Cu~(2+) ion.     

Application of graphite screen printed electrode modified with dysprosium tungstate nanoparticles in voltammetric determination of epinephrine in the presence of acetylcholine

The current work focuses on the development of a sensitive and selective electrochemical device based on a graphite screen printed electrode modified with Dy_2(WO_4)_3 nanoparticles(DWO/SPE) for the analysis of epinephrine in samples also containing acetylcholine. The study proves that the sensor has excellent electron-mediating behavior in the oxidation of epinephrine in a 0.1 mol/L phosphate buffer solution(PBS)(pH 7.0). The application of the DWO/SPE in differential pulse voltammetry(DPV) is found to lead to distinct response for the oxidation of epinephrine and acetylcholine, with the potentials of the epinephrine and acetylcholine peaks(△E_p) to be 550 mV apart. The detection limits of the method for epinephrine and acetylcholine are 0.5 and 0.7 μmol/L(S/N = 3) and the responses are found to be linear in the concentration ranges of 1.0-900.0 μmol/L and 1.0-1200.0 μmol/L in a PBS buffer(pH = 7.0)respectively. The modified electrode was used for the detection of epinephrine and acetylcholine in real samples and found to produce satisfactory results. These results can be a proof that Dy_2(WO_4)_3 nanoparticles can find promising applications in electrochemical sensors to be used for the analysis of(bio)chemical species.     

IFE based nanosensor composed of UCNPs and Fe(Ⅱ)-phenanthroline for detection of hypochlorous acid and periodic acid

Oxidizing CIO^-and IO₄^-exist widely in environment and are closely related to the health of organisms.Accordingly,fast,sensitive,and direct detection of the two species is significant.Using IFE in UCNPs@PAA and Fe(Ⅱ)-phenanthroline system,an elegant ratiometric fluorescent nanosensor,without noble metal nanoparticle,was designed for the detection of CIO^-and IO₄^-.Fe(Ⅱ)-phenanthroline complex is used as fluorescent absorber,which can...     

Study on determination method of iron content in galvanized coating of zinc-iron alloy

The iron content in the galvanized coating of zinc-iron alloy was determined by atomic absorption spectrometry and two kinds of X-ray fluorescence(XRF) methods.Results show that the chemical method exhibits the highest accuracy.However, this method presents low detection efficiency and is thus unsuitable for production quality control.Fundamental parameter and empirical coefficient methods in XRF can be used for the quality control of iron content in the galvanized coating of zinc-iron alloys.Th...     

Preparation and Fluorescence Properties of Polymethyl Methacrylate Resin Incorporated with Sodium Tris （Pyridine Dicarboxylato）Europate

Based on the strong fluorescence and the highly thermal stability of sodium tris (pyridine dicarboxylato)eruopate(Na3Eu(DPA)3),polymethyl methacrylate(PMMA)composite material incorporated with the complex,PMMA:Na3Eu(DPA)3,was prepared at 250℃，The fluorescence behavior of PMMA:Na3Eu(DPA)3material was examined,The results show that the composite material keeps the luminescent characteristics of the Eu^3 chelate after PMMA is incorporated with Na3Eu(PDA)3,and strong orange-red emission of the composite wsa observed.The fluorescence intensity of the composite material increases with the increase of the weight ratio of Na3Eu(PDA)3to PMMA,but the relationship is not linear.     

A fluorescent probe based on a spiropyran for sensitive detection of Ce~(3+) ion

A spiropyran-based probe was developed.It serves as a fluorescence turn-on probe for selective detection of Ce~(3+) in both ethanol and aqueous(water/ethanol,1:9 or 9:1,v/v) media.Ce~(3+) can induce photochromism of the probe though the probe exhibits negligible photochromic property by itself.The probe is sensitive to Ce~(3+) and the detection limit reaches 1.7 μmol/L.It exhibits a high selectivity for Ce~(3+)ion over other common metal cations including Li~+,Na~+,Ag~+,Sr~(2+),Ni~(2+),Co~(2+),Hg~(2+),Zn~(2+),Cr~(3+),Al~(3+),Fe~(3+) and Bi~(3+) and lanthanide ions Nd~(3+),Yb~(3+) and La~(3+).The probe may be used for quantitative determination of the concentration of Ce~(3+) ion in a range of 1-10 μmol/L and for application to environmental water samples.Sensing mechanism of the probe towards Ce~(3+) ion is proposed.     

Inclusion Characterization in High Strength Low Alloy Steel for Pipeline Application

In this work several methods including sulphur printing,modified spark spectrum analysis and SPEED-SEM-EDX methods were used to study the morphology,composition and distribution of inclusions in pipeline steel.The procedure for the last-mentioned method includes:metal sample preparation using Selective Potentiostatic Etching by Electrolytic Dissolution (SPEED) together with inclusion observation and detection using SEM-EDX equipment.The results of sulphur printing and spark spectrum analysis showed that there was a well-defined centerline containing relatively high concentrations of sulphur in the steel slab studied in this work.The results of SEM study showed that most inclusions found in the steel samples were globular in morphology,and roughly 2-5 micrometers in size.The inclusions were rich in sulphur and manganese.Some inclusions with a bright globular shape contained Al,Ca,Mn and S,and were likely composed of MnS,CaS and calcium aluminate.It was concluded that sulphur printing is a convenient and inexpensive method for inclusion analysis,Spark Spectrum Analysis provides a complete and self-contained technique for inclusion detection,and the SPEED-SEM-EDX procedure is best suited for in-situ and three-dimensional observation of inclusions.     

Energy transfer and luminescent properties of Tb3+ and Tb3+, Yb3+ doped CNGG phosphors

In this work,calcium niobium gallium garnet(Ca₃ Nb_1.6875Ga_3.1875O₁₂-CNGG) ceramic samples singledoped with Tb³⁺ and co-doped with Tb³⁺ and Yb³⁺ ions were sintered by the solid-state reaction method.The structural characterization of the samples was carried out by X-ray diffraction measurements.The optimal concentration of Tb³⁺ ions corresponding to the maximum luminescence in the green spectral range in CNGG:...     

A dual-stimuli-responsive intelligent layered lanthanide hydroxide for application in information security and latent fingerprint identification

With the rapid changes in the field of information, the research and development of optical storage materials with high security and large storage capacity are particularly important in the development of contemporary society. However, conventional memory materials with static fluorescent outputs have the disadvantages of easy simulation and forgery, which limits their practical application in the protection of confidential information. In this research, a dual-stimuli-responsive intelligent fluorescent material based on Tb³⁺ and Eu³⁺ ions doped layered lanthanide hydroxide (LYH:Eu_xTb_1–xDPA) was fabricated, which can realize reversible multi-color luminescence conversion (from green to red) by varying the pH and temperature. Combined with the Morse code and security pattern, the multiple encryption and decryption of confidential information and anti-counterfeiting can also be realized. Therefore, the obtained intelligent fluorescent material has a great application prospect for information security. In addition, due to the excellent color tunability, the material can provide the possibility to obtain potential fingerprints with high contrast and no background interference on different color substrates. The unique dual-stimuli-responsive behavior of this material provides more ingenious design inspiration for the design of multi-color intelligent fluorescent devices.     

Structure and luminescence properties of color-tunable phosphor Sr2La3(SiO4)3F:Tb3+,Sm3+

A series of single-phase and color-tunable phosphors Sr₂La₃(SiO₄)₃F:0.15Tb³⁺,xSm³⁺(SLSOF:0.15Tb³⁺,xSm³⁺) was prepared using solid-state route.The X-ray diffraction(XRD) was used to characterize the phase of the as-prepared samples.The synthesized phosphors have apatite-type structure without other impurities.Sm³⁺ and Tb³⁺ ions substitute La³⁺ into the lattice and form a single...     

EXAFS investigation and luminescent properties of nanosized Tb: Lu2O3 phosphors

Nanosized terbium doped Lu2O3 phosphors were synthesized via a modified co-precipitation processing.The as-prepared Tb:Lu2O3 phosphors was consisted of well crystallized nanosized sphere particles with a diameter of about 30 nnx Local structure of Tb ions in Lu2O3 lattice was investigated by an analytical approach based on Fourier transformation of the extended X-ray absorption fine structure(EXAFS) data.X-ray near edge structure (XANES) spectra suggested that all Tb ions doped were tervalonce.EXAFS results indicated that Tb ions have entered the Lu2O3 cubic lattice by means of solid solution.The coordination number and first shell Tb-O distance dropped with the increasing of Tb concentration.Emission spectra of the phosphors was shown to be typical for Tb3+ with main components at 542,550 and 490 nm,derived from irradiative relaxation of 5D4 level.The emission intensity decreased severely with the increasing of Tb concentration from 1 mol.% to 15 tool.%,suggesting a significant concentration quenching above 1 mol.% Tb.The reduction of emission intensity was interpreted by higher distortion derived relaxation among the surface state resident Tb3+ ions.     

Fluorescence enhancement of Tb（Ⅲ） complex with a new β-diketone ligand by 1,10-phenanthroline

A novel β-diketone, 1-(3,4,5-trisbenzyloxy)benzoyl-5-benzoyl acetylacetone (TBAA), and its corresponding binary Tb(III) complex Tb(TBAA)₃·2H₂O and ternary complex Tb(TBAA)₃Phen with 1,10-phenanthroline (Phen) were prepared. The ligand was characterized based on elemental analysis, FT-IR, and ¹H NMR. The complexes were characterized with elemental analysis, FT-IR and thermogravimetry and derivative thermogravimetry (TG-DTG). Photoluminescence measurements indicated that the energy absorbed by the organic ligand was efficiently transferred to the central Tb³⁺ ions, and the complex showed intense and characteristic emissions due to the ⁵D₄→ ⁷F_J transitions of the central Tb³⁺ ions. Both complexes showed longer fluorescence lifetimes. After the introduction of the second ligand Phen group, the relative emission intensities and fluorescence lifetimes of the ternary complex Tb(TBAA)₃Phen enhanced more obviously than that of the binary complex Tb(TBAA)₃·2H₂O. This indicated that the presence of the ligand TBAA and the second ligand Phen could sensitize fluorescence intensities of Tb(III) ions, and the introduction of Phen group resulted in the enhancement of the fluorescence properties of the Tb(III) ternary rare earth complex.     

Synthesis,photoluminescence properties and thermal investigation by TG-MS of RE(DAS)_3·xH_2O(RE=Eu~(3+),Tb~(3+))

Rare earth(Ⅲ) diphenyl-4-amine sulfonates(RE(DAS)_3·xH_2O,RE=Eu~(3+),Tb~(3+))phosphors were synthesized by precursor method from barium diphenyl-4-amine sulfonate and rare earth sulfates.FTIR,TG/DSC coupled to mass spectrometry(TG/DSC/MS),X-ray powder diffraction(XPD),scanning electron microscopy(SEM) and photo luminesce nce(PL) spectroscopy were utilized to structurally and morphologically characterize the samples.Thermal decomposition of Eu(DAS)_3·7H_2O and Tb(DAS)_3·2H_2O at 973 K under dynamic air atmosphere results in crystalline Eu_2O_2SO_4 and Tb_2O_2SO_4 materials,respectively.Accordingly,MS spectra reveal the liberation of thermal decomposition products of precursors,largely as CO_2,NO_2 and SO_2 gases.The diphenyl-4-amine sulfonate(DAS) ligand demonstrats a good stabilizing property for Eu~(3+) and Tb~(3+) ions.The Eu(DAS)_3·7H_2O and Tb(DAS)_3·2H_2O compounds display efficient red and green emissions,under UV excitation,arising from the ~5D_0→~7F_J(J=0-4) and ~5D_4→~7F_J(J=0-6) transitions of the Eu~(3+) and Tb~(3+) ions,respectively.     

Synthesis, crystal structure and characterization of one-dimension complex constructed by terbium（III） and 2-iodobenzoate

The complex of [Tb(2-IBA)₃(H₂O)₂]_n (2-IBA=2-iodobenzoate)was prepared by solvent method from TbCl₃·6H₂O and 2-iodobenzoic acid. The crystal structure was determined with X-ray single-crystal diffraction. The X-ray diffraction analysis indicated that the title complex crystallized in triclinic crystal system and Pī space group. The Tb³⁺ ion was coordinated by six oxygen atoms from five 2-IBA ligands and two oxygen atoms from two water molecules, giving a distorted square-antiprism polyhedral geometry. The carboxyl groups were bonded to the Tb³⁺ ions with bidentate-bridging and bidentate-chelating coordination modes. The adjacent Tb³⁺ ions were linked by two bidentate-bridging 2-IBA ligands, forming 1-D chain structure. The fluorescence spectrum of the complex showed four main peaks at 489, 543, 587, and 618 nm, corresponding to ⁵D₄→⁷F_J (J=6?3) transition emissions of the Tb³⁺ ion, respectively.     

Preparation and characterization of NaYF_4:Er~(3+),Tm~(3+)@NaYF_4:Ce~(3+),Tb~(3+) microcrystals with dual-mode emissions at the single-particle level

Under hydrothermal environment,we synthesized lanthanide ions doped sodium yttrium fluoride(NaYF_4:Er,Tm@NaYF_4:Ce,Tb) luminescent microcrystals via an epitaxial growth technique.The structure and morphology of these microcrystals were examined by SEM,TEM,EDS and XRD measurements.These particles show dual-mode emissions with red upconversion(UC) and green down conversion(DC) as single particles level.The mean length and diameter of these microparticles increase from 0.43 to2.26 μm and from 1.33 to 1.86 μm,respectively.Most interestingly,the photoluminescence properties of NaYF_4:Er,Tm@NaYF_4:Ce,Tb phosphor crystals are highly dependent on the crystallite size.The microcrystals fluoresce emit dual-mode emissions when they are solid or dispersed in solvents.Benefiting its intensive fluorescence and uniform morphology,these materials hold great potential for security and anti-counterfeiting applications.     

Luminescence properties and energy transfer of host sensitized CaMoO4：Tb^3＋ green phosphors

A series of CaMoO 4 :xTb 3+(x=0.01,0.03,0.05,0.07,0.09,0.15 and 0.20) phosphors in pure phase were prepared via high temperature solid-state reaction approach.The crystal structure of the phosphors was investigated by X-ray diffraction(XRD),and the optical properties were investigated by Fourier transform infrared spectroscopy(FT-IR),ultraviolet-visible spectroscopy(UV-Vis) and photoluminescence(PL) spectroscopy.The PL spectra illustrated that these phosphors could be efficiently excited by the charge transfer band of the host and the energy transfer efficiency from the host to the doped activator reached 60% when the doping concentration of the activator Tb 3+ was 20 mol.%.The concentration quenching occurred at x=10 mol.%,from which the critical distance of activator was calculated to be about 1.14 nm.The CIE coordinates were estimated to be close to the standard green value.The host sensitized samples had potential application as green phosphors.