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Sample records for strong luminescent emission

  1. Strong Circularly Polarized Luminescence from Highly Emissive Terbium Complexes in Aqueous Solution

    Energy Technology Data Exchange (ETDEWEB)

    Samuel, Amanda; Lunkley, Jamie; Muller, Gilles; Raymond, Kenneth

    2010-03-15

    Two luminescent terbium(III) complexes have been prepared from chiral ligands containing 2-hydroxyisophthalamide (IAM) antenna chromophores and their non-polarized and circularly-polarized luminescence properties have been studied. These tetradentate ligands, which form 2:1 ligand/Tb{sup III} complexes, utilize diaminocyclohexane (cyLI) and diphenylethylenediamine (dpenLI) backbones, which we reasoned would impart conformational rigidity and result in Tb{sup III} complexes that display both large luminescence quantum yield ({phi}) values and strong circularly polarized luminescence (CPL) activities. Both Tb{sup III} complexes are highly emissive, with {phi} values of 0.32 (dpenLI-Tb) and 0.60 (cyLI-Tb). Luminescence lifetime measurements in H{sub 2}O and D{sub 2}O indicate that while cyLI-Tb exists as a single species in solution, dpenLI-Tb exists as two species: a monohydrate complex with one H{sub 2}O molecule directly bound to the Tb{sup III} ion and a complex with no water molecules in the inner coordination sphere. Both cyLI-Tb and dpenLI-Tb display increased CPL activity compared to previously reported Tb{sup III} complexes made with chiral IAM ligands. The CPL measurements also provide additional confirmation of the presence of a single emissive species in solution in the case of cyLI-Tb, and multiple emissive species in the case of dpenLI-Tb.

  2. Grassy Silica Nanoribbons and Strong Blue Luminescence

    Science.gov (United States)

    Wang, Shengping; Xie, Shuang; Huang, Guowei; Guo, Hongxuan; Cho, Yujin; Chen, Jun; Fujita, Daisuke; Xu, Mingsheng

    2016-09-01

    Silicon dioxide (SiO2) is one of the key materials in many modern technological applications such as in metal oxide semiconductor transistors, photovoltaic solar cells, pollution removal, and biomedicine. We report the accidental discovery of free-standing grassy silica nanoribbons directly grown on SiO2/Si platform which is commonly used for field-effect transistors fabrication without other precursor. We investigate the formation mechanism of this novel silica nanostructure that has not been previously documented. The silica nanoribbons are flexible and can be manipulated by electron-beam. The silica nanoribbons exhibit strong blue emission at about 467 nm, together with UV and red emissions as investigated by cathodoluminescence technique. The origins of the luminescence are attributed to various defects in the silica nanoribbons; and the intensity change of the blue emission and green emission at about 550 nm is discussed in the frame of the defect density. Our study may lead to rational design of the new silica-based materials for a wide range of applications.

  3. Luminescent solar concentrators utilizing stimulated emission.

    Science.gov (United States)

    Kaysir, Md Rejvi; Fleming, Simon; MacQueen, Rowan W; Schmidt, Timothy W; Argyros, Alexander

    2016-03-21

    Luminescent solar concentrators (LSCs) are an emerging technology that aims primarily to reduce the cost of solar energy, with great potential for building integrated photovoltaic (PV) structures. However, realizing LSCs with commercially viable efficiency is currently hindered by reabsorption losses. Here, we introduce an approach to reducing reabsorption as well as improving directional emission in LSCs by using stimulated emission. Light from a seed laser (potentially an inexpensive laser diode) passes through the entire area of the LSC panel, modifying the emission spectrum of excited dye molecules such that it is spectrally narrower, at wavelengths that minimize reabsorption to allow net gain in the system, and directed towards a small PV cell. A mathematical model, taking into account thermodynamic considerations, of such a system is presented which identifies key parameters and allows evaluation in terms of net effective output power.

  4. Strong near-infrared luminescence in BaSnO3.

    Science.gov (United States)

    Mizoguchi, Hiroshi; Woodward, Patrick M; Park, Cheol-Hee; Keszler, Douglas A

    2004-08-11

    Powdered samples of the perovskite BaSnO(3) exhibit strong near-infrared (NIR) luminescence at room temperature, following band-gap excitation at 380 nm (3.26 eV). The emission spectrum is characterized by a broad band centered at 905 nm (1.4 eV), tailing on the high-energy side to approximately 760 nm. The Stokes shift is 1.9 eV, and measured lifetimes in the range 7-18 ms depend on preparative conditions. These extraordinary long values indicate that the luminescence involves a defect state(s). At low temperatures, both a sharp peak and a broad band appear in the visible portion of the luminescence spectrum at approximately 595 nm. Upon cooling, the intensity of the NIR emission decreases, while the integrated intensities of the visible emission features increase to approximately 40% of the NIR intensity at 77 K. Room-temperature photoluminescence (PL) is observed across the Ba(1-x)Sr(x)SnO(3) series. As the strontium content increases, the excitation maximum and band gap shift further into the UV, while the intensity of the NIR emission peak decreases and shifts further into the infrared. This combination leads to an unexpectedly large increase in the Stokes shift. The unusual NIR PL in BaSnO(3) may originate from recombination of a photogenerated valence-band hole and an occupied donor level, probably associated with a Sn(2+) ion situated roughly 1.4 eV above the valence-band edge.

  5. Defect-related luminescent materials: synthesis, emission properties and applications.

    Science.gov (United States)

    Zhang, Cuimiao; Lin, Jun

    2012-12-07

    Luminescent materials have found a wide variety of applications, including information displays, lighting, X-ray intensification and scintillation, and so on. Therefore, much effort has been devoted to exploring novel luminescent materials so far. In the past decade, defect-related luminescent materials have inspired intensive research efforts in their own right. This kind of luminescent material can be basically classified into silica-based materials, phosphate systems, metal oxides, BCNO phosphors, and carbon-based materials. These materials combine several favourable attributes of traditional commercially available phosphors, which are stable, efficient, and less toxic, being free of the burdens of intrinsic toxicity or elemental scarcity and the need for stringent, intricate, tedious, costly, or inefficient preparation steps. Defect-related luminescent materials can be produced inexpensively and on a large scale by many approaches, such as sol-gel process, hydro(solvo)thermal reaction, hydrolysis methods, and electrochemical methods. This review article highlights the recent advances in the chemical synthesis and luminescent properties of the defect-related materials, together with their control and tuning, and emission mechanisms (solid state physics). We also speculate on their future and discuss potential developments for their applications in lighting and biomedical fields.

  6. Strongly Enhanced Free-Exciton Luminescence in Microcrystalline CsPbBr3 Films

    Science.gov (United States)

    Kondo, Shin-ichi; Kakuchi, Mitsugu; Masaki, Atsushi; Saito, Tadaaki

    2003-07-01

    The luminescence properties of CsPbBr3 films prepared via the amorphous phase by crystallization are dominated by free-exciton emission, and only a weak trace of emission due to trapped excitons was observed, in contrast to the case of bulk CsPbBr3 crystals. In particular, the films in the microcrystalline state show by more than an order of magnitude stronger free-exciton emission than in the polycrystalline state. The enhanced free-exciton emission is suggestive of excitonic superradiance.

  7. Characterization of a nondestructive beam profile monitor using luminescent emission

    Directory of Open Access Journals (Sweden)

    A. Variola

    2007-12-01

    Full Text Available The LHC (large hadron collider [LHC study group: LHC. The large hadron collider conceptual design; CERN/AC/95-05] is the future p-p collider under construction at CERN, Geneva. Over a circumference of 26.7 km a set of cryogenic dipoles and rf cavities will store and accelerate proton and ion beams up to energies of the order of 7 TeV. Injection in LHC will be performed by the CERN complex of accelerators, starting from the source and passing through the linac, the four booster rings, the proton synchrotron (PS, and super proton synchrotron (SPS accelerators. One of the main constraints on LHC performance is emittance preservation along the whole chain of CERN accelerators. The accepted relative normalized emittance blowup after filamentation is ±7%. To monitor the beam and the emittance blowup process, a study of different prototypes of nonintercepting beam profile monitors has been performed. In this context a monitor using the luminescent emission of gases excited by ultrarelativistic protons (450 GeV was developed and tested in the SPS ring. The results of beam size measurements and their evolution as a function of the machine parameters are presented. The image quality and resolution attainable in the LHC case have been assessed. A first full characterization of the luminescence cross section, spectrum, decay time, and afterglow effect for an ultrarelativistic proton beam is provided. Some significant results are also provided for lead ion beams.

  8. Luminescent Organometallic Nanomaterials with Aggregation-Induced Emission.

    Science.gov (United States)

    Shu, Tong; Wang, Jianxing; Su, Lei; Zhang, Xueji

    2018-07-04

    Recent researches in metal nanoclusters (NCs) have prompted their promising practical applications in biomedical fields as novel inorganic luminophores. More recently, to further improve the photoluminescence (PL) performance of NCs, the aggregation-induced emission (AIE) effect has been introduced to develop highly luminescent metal NCs and metal complex materials. In this review, we start our discussion from recent progresses on AIE materials developments. Then, we address our understandings on the PL properties of thiolated metal NCs. Subsequently, we link thiolated metal NCs with AIE effect. We also highlight some recent advances in synthesizing the AIE-type metal complex nanomaterials. We finally discuss visions and directions for future development of AIE-type metal complex nanomaterials.

  9. Conversion of the luminescence of laser dyes in opal matrices to stimulated emission

    International Nuclear Information System (INIS)

    Alimov, O K; Basiev, T T; Orlovskii, Yu V; Osiko, V V; Samoilovich, M I

    2008-01-01

    The luminescence and laser characteristics of a synthetic opal matrix filled with organic dyes are studied upon excitation by nanosecond laser pulses. The appearance of stimulated emission in a partially ordered scattering medium is investigated. It is shown that if the luminescence spectrum of a dye (oxazine-17) is located far outside the photonic bandgap of the opal matrix, stimulated emission along a preferential direction in the (111) plane is observed when pumping exceeds a threshold even without an external optical cavity. The stimulated emission spectrum is considerably narrower than the luminescence spectrum and consists of several narrow lines located within the dye luminescence band. If the luminescence spectrum of a dye (rhodamine 6G) overlaps with the photonic bandgap of the opal matrix, a different picture is observed. The loss of radiation in the matrix leads to the red shift of the luminescence spectrum, while the stimulated emission as in the case of oxazine-17 lies is observed within the luminescence band. (active media, lasers, and amplifiers)

  10. On the role of non-bridging oxygen centers in the red luminescence emission from silicon nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Borsella, Elisabetta; D' Amato, Rosaria; Fabbri, Fabio [ENEA, C. R. Frascati, via E. Fermi 45, 00044 Frascati, Roma (Italy); Falconieri, Mauro [ENEA, C. R. Casaccia, via Anguillarese 301, 00123 Roma (Italy); Trave, Enrico [Physical Chemistry Department, Universita Ca' Foscari Venezia, Dorsoduro 2137, 30123 Venezia (Italy); Bello, Valentina; Mattei, Giovanni [Physics Department, Universita degli Studi di Padova, Via Marzolo 8, 35131 Padova (Italy); Nie, Yaru; Wang, Dayang [Max Planck Institute of Colloids and Interfaces, 14424 Potsdam (Germany)

    2011-03-15

    The process responsible for visible-near infrared luminescence emission in Si nanostructures has been generating significant controversy for years. The debate has focused on whether light emission is originated by recombination of quantum confined excitons or by defects located at the surface. It is experimentally difficult to distinguish the two contributions since both are size-dependent. Moreover, all the studies were performed on different systems and consequently the comparisons were not free from ambiguities. Here we relate the spectroscopic properties of pyrolytic Si nanocrystals, aged in air, and after complete conversion to amorphous silica by alkali etching-assisted oxidation. The strong resemblance of the spectral and time decay behavior of the red PL emission in both systems (surface oxidized nanocrystalline Si and amorphous silica sample) indicates that this emission is dominated by defects in the silicon oxide. The strongly non-exponential time behavior of the photo-luminescence emission in both systems can be modeled as the sum of exponential decays from the emitting defects, thus ruling out the interpretation in terms of the so-called ''stretched exponential'' decay. Using this model we also obtained the emission energy and inhomogeneous linewidth of the luminescent defects, allowing us to identify them as the non-bridging oxygen hole centers. The emission energy of these defects depends strongly on their physical and chemical environment and can produce a shift apparently due to the size effect. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  11. Characterization of a nondestructive beam profile monitor using luminescent emission

    CERN Document Server

    Variola, A; Ferioli, G

    2007-01-01

    The LHC (large hadron collider) [LHC study group: LHC. The large hadron collider conceptual design; CERN/AC/95-05] is the future p-p collider under construction at CERN, Geneva. Over a circumference of 26.7 km a set of cryogenic dipoles and rf cavities will store and accelerate proton and ion beams up to energies of the order of 7 TeV. Injection in LHC will be performed by the CERN complex of accelerators, starting from the source and passing through the linac, the four booster rings, the proton synchrotron (PS), and super proton synchrotron (SPS) accelerators. One of the main constraints on LHC performance is emittance preservation along the whole chain of CERN accelerators. The accepted relative normalized emittance blowup after filamentation is ±7%. To monitor the beam and the emittance blowup process, a study of different prototypes of nonintercepting beam profile monitors has been performed. In this context a monitor using the luminescent emission of gases excited by ultrarelativistic protons (450 GeV) ...

  12. Excitation and emission spectrometry of stimulated luminescence from quartz and feldspars

    DEFF Research Database (Denmark)

    Bøtter-Jensen, L.; Duller, G.A.T.; Poolton N.R.J.

    1994-01-01

    A new scanning monochromator was designed to investigate the wavelength-resolved luminescence excitation and emission characteristics of quartz and feldspar samples; results are presented together with detailed measurements of the thermal activation energies required for luminescence stimulation...... in feldspar over the wavelength range 400-1000 nm. When coupled to automated dating equipment, we demonstrate that optical characteristics of sample selected for dating can be routinely measured, or more detailed analysis of physical processes can be made....

  13. Tunable colors and white-light emission based on a microporous luminescent Zn(II)-MOF.

    Science.gov (United States)

    He, Hongming; Sun, Fuxing; Borjigin, Tsolmon; Zhao, Nian; Zhu, Guangshan

    2014-03-07

    Metal-organic frameworks (MOFs) are a rapidly growing class of hybrid materials with many multifunctional properties. The permanent porosity plays a central role in the functional properties. In particular, the luminescent MOFs with a permanent porosity have wide applications in guest species recognition and adsorption. In this contribution, we aim to develop tunable colors and white-light luminescence materials by the encapsulation of Ln(3+) species in microporous luminescent MOFs. A semi-rigid trivalent carboxylic acid 1,3,5-tri(4-carboxyphenoxy)benzene (H3TCPB) was selected as the organic building block, not only because it is suitable to construct microporous frameworks, but also by reason of its blue luminescent emission. Under solvothermal reactions, a microporous MOF material, [Zn3(TCPB)2(H2O)2]·2H2O·4DMF (JUC-113, JUC = Jilin University, China), was synthesized, which has a permanent porosity and emits blue light. According to three-primary colors, the guest luminescent species should be Tb(3+) and Eu(3+) owing to their distinctive colors (Tb(3+), green; Eu(3+), red). In addition, the luminescent properties of JUC-113 can be easily tuned by different combinations of the encapsulation amount of Tb(3+) and Eu(3+), obtaining white-light emission materials.

  14. Thermochromic Luminescent Materials and Multi-Emission Bands in d10Clusters.

    Science.gov (United States)

    Gautier, Romain; Latouche, Camille; Paris, Michael; Massuyeau, Florian

    2017-03-30

    Thermochromic luminescent compounds with d 10 metal ions are interesting materials for applications such as sensors or display devices. However, these properties are difficult to predict prior to their synthesis. In this communication, we investigated materials with structural assemblies known to be responsible of distinct luminescence mechanisms and show that they can be interesting potential thermometers. Thus, we compared the synthesis of a zinc halide and a copper halide based compounds which only differ in their ability to create clusters with metallophilic interactions. The compounds synthesized by hydrothermal method have been structurally characterized by Single-crystal X-ray diffraction, Solid-State NMR, FTIR, UV-Visible spectroscopy, thermal analysis and EPR. The photoluminescence properties of the two materials have been characterized at different temperatures. The copper bromide compound shows luminescence thermochromism in a wide spectrum of colors owing to the formation of clusters generating multi-emission bands while the zinc bromide exhibits a single emission band and no thermochromism.

  15. Control of spontaneous emission rate in luminescent resonant diamond particles

    Science.gov (United States)

    Savelev, R.; Zalogina, A.; Kudryashov, S.; Ivanova, A.; Levchenko, A.; Makarov, S.; Zuev, D.; Shadrivov, I.

    2018-01-01

    We study the properties of luminescent diamond particles of different sizes (up to ~1.5 μm) containing multiple NV-centers. We theoretically predict that the average liftetime in such particles is decreased by several times as compared to optically small subwavelength nanodiamonds. In our experiments, samples were obtained by milling the plasma-enhanced chemical vapor deposited diamond film, and characterized by Raman spectroscopy and dark- field spectroscopy methods. Time-resolved luminescence measurements of the excited state of NV-centers showed that their average lifetime varies from 10 to 17 ns in different samples. By comparing this data to the values of the lifetime of the NV-centers in optically small nanodiamonds, known from literature, we confirm a severalfold decrease of the lifetime in resonant particles.

  16. Discernment of lint trash in raw cotton using multivariate analysis of excitation-emission luminescence spectra

    Science.gov (United States)

    Excitation-Emission luminescence spectra of basic (pH 12.5) phosphate buffer solution extracts were used to distinguish among botanical components of trash within seed cotton. All components were separated from whole plants removed from a field in southern New Mexico. Unfolded Principal Component An...

  17. Stimulated luminescence emission from localized recombination in randomly distributed defects

    DEFF Research Database (Denmark)

    Jain, Mayank; Guralnik, Benny; Andersen, Martin Thalbitzer

    2012-01-01

    408–15) which assumes a fixed d → a tunnelling probability for the entire crystal, our model is based on nearest-neighbour recombination within randomly distributed centres. Such a random distribution can occur through the entire volume or within the defect complexes of the dosimeter, and implies...... that the tunnelling probability varies with the donor–acceptor (d–a) separation distance. We first develop an ‘exact kinetic model’ that incorporates this variation in tunnelling probabilities, and evolves both in spatial as well as temporal domains. We then develop a simplified one-dimensional, semi-analytical model...... results in a highly asymmetric TL peak; this peak can be understood to derive from a continuum of several first-order TL peaks. Our model also shows an extended power law behaviour for OSL (or prompt luminescence), which is expected from localized recombination mechanisms in materials with random...

  18. Light emission and luminescence enhancement in Erbium Oxide nanoparticles

    Science.gov (United States)

    Wilkinson, Lynda; Maqbool, Muhammad; Ahmad, Iftikhar

    2011-10-01

    We reports light emission from Erbium Oxide nanoparticles. The nanoparticles, with 45 nm diameter, were obtained in the form of nanopowder. These nanoparticles were characterized for light emission under a 30 mW, 532 nm Nd:YAG laser excitation and a Photoluminescence (PL) system, made by Princeton Instrumentation, with a Pixis brand CCD camera. The nanoparticles were stick on a scotch tape and placed in the PL system. Spectrum of the light emitted from the nanoparticles was obtained and analyzed after subtracting the background spectrum. Two emission peaks were observed around 554 nm and 820 nm. The green emission at 554 nm was obtained as a result of ^2H11/2 ->^4I15/2 transition, and the near infrared emission from ^4I9/2->^4I15/2 transition. The process was also repeated in vacuum and it was found that the green emission enhances tremendously, showing the importance of Erbium Oxide nanoparticles optical and biophotonics applications.

  19. Hybrid silica luminescent materials based on lanthanide-containing lyotropic liquid crystal with polarized emission

    Energy Technology Data Exchange (ETDEWEB)

    Selivanova, N.M., E-mail: natsel@mail.ru [Kazan National Research Technological University, 68 Karl Marx Str., Kazan 420015 (Russian Federation); Vandyukov, A.E.; Gubaidullin, A.T. [A.E. Arbuzov Institute of Organic and Physical Chemistry of the Kazan Scientific Center of the Russian Academy of Sciences, 8 Acad. Arbuzov Str., Kazan 420088 (Russian Federation); Galyametdinov, Y.G. [Kazan National Research Technological University, 68 Karl Marx Str., Kazan 420015 (Russian Federation)

    2014-11-14

    This paper represents the template method for synthesis of hybrid silica films based on Ln-containing lyotropic liquid crystal and characterized by efficient luminescence. Luminescence films were prepared in situ by the sol–gel processes. Lyotropic liquid crystal (LLC) mesophases C{sub 12}H{sub 25}O(CH{sub 2}CH{sub 2}O){sub 10}H/Ln(NO{sub 3}){sub 3}·6H{sub 2}O/H{sub 2}O containing Ln (III) ions (Dy, Tb, Eu) were used as template. Polarized optical microscopy, X-ray powder diffraction, and FT-IR-spectroscopy were used for characterization of liquid crystal mesophases and hybrid films. The morphology of composite films was studied by the atomic force microscopy method (AFM). The optical properties of the resulting materials were evaluated. It was found that hybrid silica films demonstrate significant increase of their lifetime in comparison with an LLC system. New effects of linearly polarized emission revealed for Ln-containing hybrid silica films. Polarization in lanthanide-containing hybrid composites indicates that silica precursor causes orientation of emitting ions. - Highlights: • We suggest a new simple approach for creating luminescence hybrid silica films. • Ln-containing hybrid silica films demonstrate yellow, green and red emissions. • Tb(III)-containing hybrid film have a high lifetime. • We report effects of linearly polarized emission in hybrid film.

  20. Water-Triggered Luminescent "Nano-bombs" Based on Supra-(Carbon Nanodots)

    NARCIS (Netherlands)

    Lou, Q.; Qu, S.; Jing, P.; Ji, W.; Li, D.; Cao, J.; Zhang, H.; Liu, L.; Zhao, J.; Shen, D.

    2015-01-01

    Novel luminescent "nano-bombs" based on a self-assembled system of carbon-nanodots, termed supra-CDs, are developed. The luminescence of these luminescent "nano-bombs" depends strongly on water contact; they show weak emission in toluene and decompose in contact with water, resulting in strong

  1. Efficient three-photon luminescence with strong polarization dependence from a scintillating silicate glass co-doped with Gd3+ and Tb3+.

    Science.gov (United States)

    Li, Guang-Can; Zhang, Cheng-Yun; Deng, Hai-Dong; Liu, Guang-Yin; Lan, Sheng; Qian, Qi-; Yang, Zhong-Min; Gopal, Achanta Venu

    2013-03-11

    Efficient three-photon luminescence (3PL) from a scintillating silicate glass co-doped with Gd(3+) and Tb(3+) was generated by using a focused femtosecond laser beam at 800 nm. Four emission bands centered at 496, 541, 583, and 620 nm were identified as the electronic transitions between the energy levels of Tb(3+) followed by three-photon absorption (3PA) in Gd(3+) and Tb(3+) and the resonant energy transfer from Gd(3+) to Tb(3+). More interestingly, a strong polarization dependence of the 3PL was observed and it is ascribed to the polarization dependent 3PA in Gd(3+) and Tb(3+) and/or the angular distribution of photogenerated electrons in the glass.

  2. Bismuth Complexes in Phenylazomethine Dendrimers: Controllable Luminescence and Emission in the Solid State.

    Science.gov (United States)

    Kambe, Tetsuya; Watanabe, Aiko; Imaoka, Takane; Yamamoto, Kimihisa

    2016-10-10

    Dendritic phosphors were obtained by the stepwise integration of BiCl 3 in phenylazomethine dendrimers. The bismuth-coordinated phenylazomethines displayed photoluminescence at 500-800 nm, and the intensity could be tuned by changing the stoichiometry of BiCl 3 and the dendrimer. This phosphor did not show serious luminescence quenching even though the local concentration of BiCl 3 in the dendrimer was as high as 20 M, and luminescence was also observed in the solid state. The absorption and emission properties could be reversibly switched by addition of a Lewis base or under electrochemical redox control, which induced the reversible complexation of BiCl 3 in the dendrimer. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Three-coordinate gold(I) N-heterocyclic carbene complexes: a new class of strongly luminescent derivatives.

    Science.gov (United States)

    Visbal, Renso; López-de-Luzuriaga, José M; Laguna, Antonio; Gimeno, M Concepción

    2014-01-07

    A selected group of cationic three-coordinate Au(I)-NHC complexes of the form [Au(NHC)(dppbz)]OTf have been prepared from a commercially available bidentate phosphine. All complexes have been fully characterised by NMR and mass spectroscopy. The [Au(NHC)](+) fragment shows a pronounced tendency to form linear complexes which is confirmed by the molecular structure of [Au(IPr)(dppbz)]OTf in the solid state. The complexes are brightly luminescent and present very high quantum yield values in the solid state. The assignments of the electronic transitions involved in the emissions are of a phosphorescent nature and it is proposed that the origin of the emissions is derived from the ligand (dppbz) to metal-ligand (Au-NHC) charge-transfer (LML'CT) transition.

  4. Long-lived luminescent soft materials of hexanitratosamarate(III) complexes with orange visible emission.

    Science.gov (United States)

    Tang, Ning; Zhao, Ying; He, Ling; Yuan, Wen-Li; Tao, Guo-Hong

    2015-05-21

    Sm(III)-based ionic liquids incorporating hexanitratosamarate(III) anions were obtained and fully characterized as novel Sm(III)-containing organic complexes. The structure of the ionic liquids was determined by single-crystal X-ray diffraction (1: monoclinic system C2/c space group with cell parameters: a = 19.5624(4) Å, b = 10.11895(18) Å, c = 33.2256(6) Å, β = 101.2912(18)°, Z = 8). The central Sm(III) ion is 12-coordinated by six bidentate nitrate ligands with twelve oxygen donors to form a [Sm(NO3)6](3-) anion. The low melting point, high thermostability and wide liquid range of these ionic liquids were determined in detail. All the complexes 1-5 display orange luminescence, rather than red luminescence as in most Sm(III)-containing organic complexes. Three characteristic monochromatic bands and an intense emission, derived from (4)G5/2→(6)HJ (J = 5/2, 7/2, and 9/2) intraconfigurational f-f transitions, were revealed. All these complexes exhibit long luminescence lifetimes.

  5. Spatial-resolved cathode luminescence study of S-doped ZnO particles for the luminescence of UV, green and orange band emission

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Yuanping, E-mail: ypsun@ytu.edu.cn [Institute of Science and Technology for Opto-electronic Information, Yantai University, Shandong 264005 (China); Guo, Hongying; Jiang, Feihong; Yuan, Run; Zhang, Jun [Institute of Science and Technology for Opto-electronic Information, Yantai University, Shandong 264005 (China); Zeng, Xionghui; Zhou, Taofei; Qiu, Yongxin; Zhang, Baoshun; Xu, Ke; Yang, Hui [Suzhou Institute of Nano-tech and Nano-bionics, Chinese Academy of Sciences, Suzhou 215123 (China)

    2013-10-15

    The hexagonal bi-pillar structures of undoped and sulfur-doped ZnO particles have been synthesized by hydrothermal method to study the relationship between UV and long wavelength emissions, green emission (GE) and orange emission (OE) bands. A room temperature photoluminescence comparison between undoped and sulfur-doped ZnO shows an increase of long wavelength emission, that is presumably due to an increase of defects in doped ZnO. Spatial cathode luminescence (CL) analysis on a single ZnO particle shows a competitive behavior between GE and OE bands. The long wavelength emissions in ZnO are all related to Zn vacancies. GE will dominate if the Zn vacancy-related oxygen stays at lattice point; otherwise OE will dominate if this oxygen atom leaves lattice point to form a interstitial atom.

  6. Anomalous radon emission as precursor of medium to strong earthquakes

    Science.gov (United States)

    Zoran, Maria

    2016-03-01

    Anomalous radon (Rn222) emissions enhanced by forthcoming earthquakes is considered to be a precursory phenomenon related to an increased geotectonic activity in seismic areas. Rock microfracturing in the Earth's crust preceding a seismic rupture may cause local surface deformation fields, rock dislocations, charged particle generation and motion, electrical conductivity changes, radon and other gases emission, fluid diffusion, electrokinetic, piezomagnetic and piezoelectric effects as well as climate fluctuations. Space-time anomalies of radon gas emitted in underground water, soil and near the ground air weeks to days in the epicentral areas can be associated with the strain stress changes that occurred before the occurrence of medium and strong earthquakes. This paper aims to investigate temporal variations of radon concentration levels in air near or in the ground by the use of solid state nuclear track detectors (SSNTD) CR-39 and LR-115 in relation with some important seismic events recorded in Vrancea region, Romania.

  7. Thallium and manganese complexes involved in the luminescence emission of potassium-bearing aluminosilicates

    Energy Technology Data Exchange (ETDEWEB)

    Gomez-Gonzalez, Miguel A., E-mail: miguel.gomez@mncn.csic.es [Museo Nacional de Ciencias Naturales, CSIC, Jose Gutierrez Abascal 2, Madrid E-28006 (Spain); Garcia-Guinea, Javier, E-mail: guinea@mncn.csic.es [Museo Nacional de Ciencias Naturales, CSIC, Jose Gutierrez Abascal 2, Madrid E-28006 (Spain); Garrido, Fernando, E-mail: fernando.garrido@mncn.csic.es [Museo Nacional de Ciencias Naturales, CSIC, Jose Gutierrez Abascal 2, Madrid E-28006 (Spain); Townsend, Peter D., E-mail: pdtownsend@gmail.com [School of Science and Technology, University of Sussex, Brighton BN1 9QH (United Kingdom); Marco, Jose-Francisco, E-mail: jfmarco@iqfr.csic.es [Instituto de Química-Física Rocasolano, CSIC, Calle Serrano 119, Madrid E-28006 (Spain)

    2015-03-15

    The luminescence emission at 285 nm in natural K-feldspar has been studied by Russian groups and associated with thallium ions in structural positions of K{sup +} sites as artificially thallium-doped feldspars display the same emission band. Here attention is focussed on spectra of CL emission bands centered near 285 and 560 nm from paragenetic adularia, moscovite and quartz micro-inclusions. With accesorial thallium they show clear resemblances to each other. Associated sedimentary and hydrothermal aluminosilicate samples collected from Guadalix (Madrid, Spain) were analyzed with a wide range of experimental techniques including Environmental Scanning Electron Microscopy (ESEM) with an attached X-Ray Energy-Dispersive Spectrometer (EDS) and a cathodoluminescence probe (CL) and Electron Probe Microanalysis (EPMA), X-Ray Fluorescence Spectrometry (XRF), Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES), Differential and Thermogravimetric Analyses (DTA-TG), radioluminescence (RL), Mössbauer spectroscopy and X-Ray Photoelectron Spectrometry (XPS). The luminescence emission bands at 285 and 560 nm seem to be associated with hydrous thallium–manganese complexes bonded to potassium-bearing aluminosilicates since various minerals such as K-feldspar, moscovite and quartz micro-inclusions display similar CL spectra, accesorial thallium and hydroxyl groups. The presence of iron introduces a brown color which is attributed to submicroscopic iron oxides detectable in the optical and chemical microanalysis, but this does not contribute to the luminescence emission. The XPS Mn 2p spectrum of the adularia sample at room temperature is composed of a spin–orbit doublet plus clear shake-up satellite structure ∼4 eV above the main photoemision lines and is consistent with Mn{sup 2+} in good agreement with the observed luminescence emission at 560 nm for aluminosilicates produced by a {sup 4}T1({sup 4}G)→{sup 6}A1({sup 6}S) transition in tetrahedrally

  8. Luminescent emission of LiF: Mg, Ti exposed to UV radiation

    International Nuclear Information System (INIS)

    Estrada G, A.; Castano M, V.M.; Cruz Z, E.; Garcia F, F.

    2002-01-01

    It was investigated the luminescent emission stimulated by heat (Tl) of LiF: Mg, Ti crystals which were exposed to UV radiation coming from a mercury lamp. Since this crystal depends on the thermal history, it has been used a thermal treatment consisting of a baking at 380 C during one hour for each reading and they were irradiated with UV. The brilliance curves between 5 and 840 minutes of exposure in the face of UV light were obtained. An important loss in the response, starting from 150 minutes of irradiation was observed. Also the relative intensity of the brilliance curve decay when the crystals being stored in darkness and room temperature conditions, which is according to the results in the literature about. (Author)

  9. Ionising radiation effect on the luminescence emission of inorganic and biogenic calcium carbonates

    Energy Technology Data Exchange (ETDEWEB)

    Boronat, C. [CIEMAT, Av. Complutense 40, Madrid 28040 (Spain); Correcher, V., E-mail: v.correcher@ciemat.es [CIEMAT, Av. Complutense 40, Madrid 28040 (Spain); Virgos, M.D. [CIEMAT, Av. Complutense 40, Madrid 28040 (Spain); Garcia-Guinea, J. [CSIC, Museo Nacional Ciencias Naturales, José Gutiérrez Abascal 2, Madrid 28006 (Spain)

    2017-06-15

    Highlights: • Aragonite and biogenic Ca-carbonates could be used as a TL dosimeters. • TL can be employed for retrospective dosimetry purposes. • Calcium carbonates show an acceptable ionizing radiation sensitivity. • The stability of the radiation–induced TL remains, at least, till 700 h. - Abstract: As known, the luminescence emission of mineral phases could be potentially employed for dosimetric purposes in the case of radiological terrorism or radiation accident where conventional monitoring is not available. In this sense, this paper reports on the thermo- (TL) and cathodoluminescence (CL) emission of both biogenic (common periwinkle – littorina littorera – shell made of calcite 90% and aragonite 10%) and inorganic (aragonite 100%) Ca-rich carbonates previously characterized by X-ray diffraction and Raman spectroscopy. Whereas the aragonite sample displays the main CL waveband peaked in the red region (linked to point defects), the more intense emission obtained from the common periwinkle shell appears at higher energies (mainly associated with structural defects). The UV-blue TL emission of the samples, regardless of the origin, displays (i) an acceptable ionizing radiation sensitivity, (ii) linear dose response in the range of interest (up to 8 Gy), (iii) reasonable stability of the TL signal after 700 h of storage with an initial decay of ca. 88% for the mineral sample and 60% for the biogenic sample and maintaining the stability from 150 h onwards. (iv) The tests of thermal stability of the TL emission performed in the range of 180–320 °C confirm a continuum in the trap system.

  10. Ionising radiation effect on the luminescence emission of inorganic and biogenic calcium carbonates

    International Nuclear Information System (INIS)

    Boronat, C.; Correcher, V.; Virgos, M.D.; Garcia-Guinea, J.

    2017-01-01

    Highlights: • Aragonite and biogenic Ca-carbonates could be used as a TL dosimeters. • TL can be employed for retrospective dosimetry purposes. • Calcium carbonates show an acceptable ionizing radiation sensitivity. • The stability of the radiation–induced TL remains, at least, till 700 h. - Abstract: As known, the luminescence emission of mineral phases could be potentially employed for dosimetric purposes in the case of radiological terrorism or radiation accident where conventional monitoring is not available. In this sense, this paper reports on the thermo- (TL) and cathodoluminescence (CL) emission of both biogenic (common periwinkle – littorina littorera – shell made of calcite 90% and aragonite 10%) and inorganic (aragonite 100%) Ca-rich carbonates previously characterized by X-ray diffraction and Raman spectroscopy. Whereas the aragonite sample displays the main CL waveband peaked in the red region (linked to point defects), the more intense emission obtained from the common periwinkle shell appears at higher energies (mainly associated with structural defects). The UV-blue TL emission of the samples, regardless of the origin, displays (i) an acceptable ionizing radiation sensitivity, (ii) linear dose response in the range of interest (up to 8 Gy), (iii) reasonable stability of the TL signal after 700 h of storage with an initial decay of ca. 88% for the mineral sample and 60% for the biogenic sample and maintaining the stability from 150 h onwards. (iv) The tests of thermal stability of the TL emission performed in the range of 180–320 °C confirm a continuum in the trap system.

  11. Intervalence charge transfer luminescence: Interplay between anomalous and 5d − 4f emissions in Yb-doped fluorite-type crystals

    Energy Technology Data Exchange (ETDEWEB)

    Barandiarán, Zoila, E-mail: zoila.barandiaran@uam.es; Seijo, Luis [Departamento de Química, Universidad Autónoma de Madrid, 28049 Madrid (Spain); Instituto Universitario de Ciencia de Materiales Nicolás Cabrera, Universidad Autónoma de Madrid, 28049 Madrid (Spain)

    2014-12-21

    In this paper, we report the existence of intervalence charge transfer (IVCT) luminescence in Yb-doped fluorite-type crystals associated with Yb{sup 2+}–Yb{sup 3+} mixed valence pairs. By means of embedded cluster, wave function theory ab initio calculations, we show that the widely studied, very broad band, anomalous emission of Yb{sup 2+}-doped CaF{sub 2} and SrF{sub 2}, usually associated with impurity-trapped excitons, is, rather, an IVCT luminescence associated with Yb{sup 2+}–Yb{sup 3+} mixed valence pairs. The IVCT luminescence is very efficiently excited by a two-photon upconversion mechanism where each photon provokes the same strong 4f{sup 14}–1A{sub 1g}→ 4f{sup 13}({sup 2}F{sub 7/2})5de{sub g}–1T{sub 1u} absorption in the Yb{sup 2+} part of the pair: the first one, from the pair ground state; the second one, from an excited state of the pair whose Yb{sup 3+} moiety is in the higher 4f{sup 13}({sup 2}F{sub 5/2}) multiplet. The Yb{sup 2+}–Yb{sup 3+} → Yb{sup 3+}–Yb{sup 2+} IVCT emission consists of an Yb{sup 2+} 5de{sub g} → Yb{sup 3+} 4f{sub 7/2} charge transfer accompanied by a 4f{sub 7/2} → 4f{sub 5/2} deexcitation within the Yb{sup 2+} 4f{sup 13} subshell: [{sup 2}F{sub 5/2}5de{sub g},{sup 2}F{sub 7/2}] → [{sup 2}F{sub 7/2},4f{sup 14}]. The IVCT vertical transition leaves the oxidized and reduced moieties of the pair after electron transfer very far from their equilibrium structures; this explains the unexpectedly large band width of the emission band and its low peak energy, because the large reorganization energies are subtracted from the normal emission. The IVCT energy diagrams resulting from the quantum mechanical calculations explain the different luminescent properties of Yb-doped CaF{sub 2}, SrF{sub 2}, BaF{sub 2}, and SrCl{sub 2}: the presence of IVCT luminescence in Yb-doped CaF{sub 2} and SrF{sub 2}; its coexistence with regular 5d-4f emission in SrF{sub 2}; its absence in BaF{sub 2} and SrCl{sub 2}; the quenching of

  12. Thermal quenching of luminescence processes in feldspars

    DEFF Research Database (Denmark)

    Poolton, N.R.J.; Bøtter-Jensen, L.; Duller, G.A.T.

    1995-01-01

    of these processes is, in general, thermally dependent, and leads either to enhancement or quenching of the luminescence with increasing temperature. Previous studies have measured the combined thermal activation characteristics of all three processes, and show a strong dependence on stimulation energy....... In this article, an initial attempt is made to isolate only the recombination part of the luminescence cycle, and determine its thermal characteristics separately. A Variety of luminescence transitions are examined in a range of both alkali and plagioclase feldspars; three distinct emission types are identified...... of the defect. The third category is the most difficult to analyse since it involves irreversible changes in the luminescence characteristics with increasing temperature; we consider these to be due to thermally-induced destruction or creation of luminescence centres. Most of the alkali and plagioclase...

  13. New AIE-active pyrimidine-based boronfluoride complexes with high solid-state emission and reversible mechanochromism luminescence behavior.

    Science.gov (United States)

    Qi, Fen; Lin, Jianjian; Wang, Xiaoqing; Cui, Peng; Yan, Hui; Gong, Shuwen; Ma, Chunlin; Liu, Zhipeng; Huang, Wei

    2016-04-25

    A new family of pyrimidine-based BF2 complexes () with aggregation-induced emission (AIE) and mechanochromic luminescence properties were developed. These compounds exhibit intense fluorescence in their aggregation/solid-state resulting from their large Stokes shift and AIE. X-ray crystallographic analysis shows that the weak intermolecular interactions by fixing the molecular conformations of are responsible for the intense fluorescence in solid-state. In addition to their pronounced AIE behaviour, also exhibits a reversible chromic response to grinding, and a distinct red-shift of emission is observed. The high solid-state luminescence and grinding-stimuli response properties of these compounds make them potential candidates for smart materials.

  14. Dual luminescence in solid CuI(piperazine): hypothesis of an emissive 1-D delocalized excited state.

    Science.gov (United States)

    Maini, L; Braga, D; Mazzeo, P P; Maschio, L; Rérat, M; Manet, I; Ventura, B

    2015-08-07

    Solid [CuI(piperazine)0.5]∞, characterized by a structure with an infinite double chain of CuI, presents an unexpected dual luminescence. The short copper-copper distances allow the existence of both cluster-centered and 1-D delocalized electronic transitions, as emerged from theoretical calculations. Beyond the more common cluster-centered emission a higher energy band, which differs in lifetime and in temperature dependence, is observed.

  15. Luminescence emission spectra of several Al2O3 TL materials

    International Nuclear Information System (INIS)

    Petoe, A.

    1996-01-01

    The paper reports on the radioluminescence (RL) and the thermoluminescence (TL) emission characteristics of several aluminium-oxide dosimeter materials: 'pure' a-Al 2 O 3 (corundum), Al 2 O 3 :C (TLK-500), Al 2 O 3 :Si, Ti, and Al 2 O 3 :Mg, Y. The general feature of the RL spectra is a strong emission line at 695 nm caused by the Cr 3+ impurity, and a wide UV band around 310 nm, which is related to F + -centres. A further emission appears around 420 nm in all of the 'doped' materials. However, the origin of this band is not the same an all phosphors: in Al 2 O 3 :Si, Ti it is associated with Ti 3+ , while in the other two samples it is more likely to be due to F-centres. Al 2 O 3 :Mg, Y shows several more emission lines between 450 and 600 nm, which increase with increasing dopant concentration and therefore these are attributed to Y 3+ impurity. The most obvious feature of the TL emission spectra is the lack of the 310 nm band. Apart from this, all the other emission bands found in the RL are clearly identifiable, and show the same intensity ratios. Corundum shows three major TL peaks at 90, 180 and 350 o C, all of them featuring the Cr 3+ emission. The two glow peaks of Al 2 O 3 :Si, Ti at 120 and 270 o C exhibit the same emission spectra: a strong Cr 3+ line and a somewhat weaker band around 410-420 nm. It is remarkable, that in Al 2 O 3 :C and in Al 2 O 3 :Mg, Y the different glow peaks have different emission spectra. In Al 2 O 3 :C the low temperature, 120 o C peak emits the Cr 3+ line, while the main dosimetry peak at 180 o C exhibits only the 410-420 nm band. On the other hand, in Al 2 O 3 :Mg, Y this blue band appears only in a separated glow peak around 270 o C, while the other three glow peaks at 120, 180 and 350 o C show the Cr 3+ and Y 3+ related emission lines. The detailed knowledge of the RL and TL emission spectra of different Al 2 O 3 TL dosimeters can be used to improve the performance of routine dosimetry work. (author)

  16. luminescence properties

    Indian Academy of Sciences (India)

    EDX analysis were taken with LEO 440 model scanning electron microscope using an accelerating voltage of 20 kV. The excitation and emission spectra of phosphors were recorded by Perkin Elmer LS 45 model luminescence spec- trophotometer with xenon lamp. Thermoluminescence (TL) glow curves of phosphors were.

  17. All-in-One: Achieving Robust, Strongly Luminescent and Highly Dispersible Hybrid Materials by Combining Ionic and Coordinate Bonds in Molecular Crystals.

    Science.gov (United States)

    Liu, Wei; Zhu, Kun; Teat, Simon J; Dey, Gangotri; Shen, Zeqing; Wang, Lu; O'Carroll, Deirdre M; Li, Jing

    2017-07-12

    Extensive research has been pursued to develop low-cost and high-performance functional inorganic-organic hybrid materials for clean/renewable energy related applications. While great progress has been made in the recent years, some key challenges remain to be tackled. One major issue is the generally poor stability of these materials, which originates from relatively fragile/weak bonds between inorganic and organic constituents. Herein, we report a unique "all-in-one" (AIO) approach in constructing robust structures with desired properties. Such approach allows formation of both ionic and coordinate bonds within a molecular cluster, which greatly enhances structural stability while maintaining the molecular identity of the cluster and its high luminescence. The novel AIO structures are composed of various anionic (Cu m I m+n ) n- clusters and cationic N-ligands. They exhibit high luminescence efficiency, significantly improved chemical, thermal and moisture stability, and excellent solution processability. Both temperature dependent photoluminescence experiments and DFT calculations are performed to investigate the luminescence origin and emission mechanism of these materials, and their suitability as energy-saving LED lighting phosphors is assessed. This study offers a new material designing strategy that may be generalized to many other material classes.

  18. Oxide/polymer nanocomposites as new luminescent materials

    Science.gov (United States)

    Vollath, D.; Szabó, D. V.; Schlabach, S.

    2004-06-01

    It is demonstrated that nanocomposites, consisting of an electrically insulating oxide core and PMMA coating exhibit strong luminescence. This luminescence is connected to the interface, where PMMA is bond via a carboxylate bonding to the surface. In this case, luminescence is originated at the carbonyl group of the coating polymer. With decreasing particle size, this emission shows a blue shift, following a law inversely the ones found for quantum confinement systems. For semi-conducting oxides, such as ZnO, this interface related emission is found additionally to quantum confinement phenomena.

  19. <strong>Potential for reduction of methane emissions from dairy cowsstrong>

    DEFF Research Database (Denmark)

    Johannes, Maike; Hellwing, Anne Louise Frydendahl; Lund, Peter

    2010-01-01

    Methane is a gas cows naturally produce in the rumen. However, it is also a potential greenhouse gas. Therefore, there is a certain interest from an environmental point of view to reduce methane emissions from dairy cows. Estimates from earlier studies indicate that there is a potential to reduce...... methane production by 10 to 25% by changing the feeding strategies. Several feedstuffs influence methane production, such as additional fat. The increase of the concentrate proportion can potentially decrease methane by decreasing the rumen degradability of the diet or by changing the rumen fermentation...

  20. The Design of Dual-Emissive Composite Material [Zn2(HL)3]+@MOF-5 as Self-Calibrating Luminescent Sensors of Al3+Ions and Monoethanolamine.

    Science.gov (United States)

    Wu, Meng-Meng; Wang, Jiao-Yang; Sun, Rui; Zhao, Cui; Zhao, Jiong-Peng; Che, Guang-Bo; Liu, Fu-Chen

    2017-08-21

    Introducing another chromophore into a luminescent MOF is a potential way to assembling novel dual-emissive luminescent materials. Putting the chromophore, for which luminescence can be enhanced by Zn 2+ ion, into MOF-5 by the "bottle around ship" strategy is a simple but efficient synthesis method to realize such dual-emissive materials. According to this strategy, a novel dual-emissive luminescent composite material [Zn 2 (HL) 3 ] + @MOF-5 was constructed by loading the [La 3 (HL) 2 L 2 (NO 3 ) 3 H 2 O] (1) (H 2 L = 7,7'-(ethane-1,1'-diyl)8-hydro-quinoline) into MOF-5, in which the [Zn 2 (HL) 3 ] + anions were transformed from 1 with the existence of Zn 2+ . The dual-emissive composite materials show excellent luminescence with two emissions of MOF-5 at 410 nm and [Zn 2 (HL) 3 ] + at 524 nm. Furthermore, by combining characteristics of MOF-5 and the guest chromophore, the composite material is highly selectively sensitive toward Al 3+ and monoethanolamine, which makes [Zn 2 (HL) 3 ] + @MOF-5 a potential self-calibrated fluorescence sensor.

  1. Electromagnetic emission of a strongly charged oscillating droplet

    Science.gov (United States)

    Grigor'ev, A. I.; Kolbneva, N. Yu.; Shiryaeva, S. O.

    2016-08-01

    Analytical expressions for electric field in the vicinity of an oscillating strongly charged droplet of nonviscous conducting liquid and intensity of electromagnetic radiation are derived in the linear approximation with respect to perturbation amplitude of the droplet surface. Order-of-magnitude estimations of the radiation intensity are presented. The intensity of electromagnetic radiation of a ball lightning that can be simulated using a charged droplet is not related to the surface oscillations.

  2. A Sample of Quasars with Strong Nitrogen Emission Lines from the Sloan Digital Sky Survey

    DEFF Research Database (Denmark)

    Jiang, Linhua; Fan, Xiaohui; Vestergaard, Marianne

    2008-01-01

    We report on 293 quasars with strong NIV] lambda 1486 or NIII] lambda 1750 emission lines (rest-frame equivalent width > 3 \\AA) at 1.7......We report on 293 quasars with strong NIV] lambda 1486 or NIII] lambda 1750 emission lines (rest-frame equivalent width > 3 \\AA) at 1.7...

  3. STRONG POLYCYCLIC AROMATIC HYDROCARBON EMISSION FROM z ∼ 2 ULIRGs

    International Nuclear Information System (INIS)

    Desai, Vandana; Soifer, B. T.; Melbourne, Jason; Dey, Arjun; Brand, Kate; Brodwin, Mark; Jannuzi, Buell T.; Le Floc'h, Emeric; Armus, Lee; Teplitz, Harry; Brown, Michael J. I.; Houck, James R.; Weedman, Daniel W.; Ashby, Matthew L. N.; Huang Jiasheng; Smith, Howard A.; Willner, Steve P.; Gonzalez, Anthony

    2009-01-01

    Using the Infrared Spectrograph on board the Spitzer Space Telescope, we present low-resolution (64 ν (24 μm)>0.5 mJy; (2) R - [24]>14 Vega mag; and (3) a prominent rest frame 1.6 μm stellar photospheric feature redshifted into Spitzer's 3-8 μm IRAC bands. Of these, 20 show emission from polycyclic aromatic hydrocarbons (PAHs), usually interpreted as signatures of star formation. The PAH features indicate redshifts in the range 1.5 < z < 3.0, with a mean of (z) = 1.96 and a dispersion of 0.30. Based on local templates, these sources have extremely large infrared luminosities, comparable to that of submillimeter galaxies. Our results confirm previous indications that the rest-frame 1.6 μm stellar bump can be efficiently used to select highly obscured star-forming galaxies at z ∼ 2, and that the fraction of starburst-dominated ULIRGs increases to faint 24 μm flux densities. Using local templates, we find that the observed narrow redshift distribution is due to the fact that the 24 μm detectability of PAH-rich sources peaks sharply at z = 1.9. We can analogously use observed spectral energy distributions to explain the broader redshift distribution of Spitzer-detected ULIRGs that are dominated by an active galactic nucleus (AGN). Finally, we conclude that z ∼ 2 sources with a detectable 1.6 μm stellar opacity feature lack sufficient AGN emission to veil the 7.7 μm PAH band.

  4. Critical view on the luminescence emission of ZnO, ZnO:Eu and ZnO: Eu/Y2O3

    International Nuclear Information System (INIS)

    Robindro Singh, L.; Prasad, Amresh I.; Gogoi, Manashjit

    2013-01-01

    Development of advanced display and lighting technology such as field emission displays and plasma display panels requires phosphor which has a high efficiency and low degradation. Particle sizes and the locations of dopants in the hosts take an important role in the luminescence emission properties of phosphors. ZnO is widely employed in plasma field emission display devices and widely investigated, still lanthanide (Ln 3+ ) ion doped ZnO need more investigations. In ZnO:Eu the lanthanide ions (Eu 3+ ) may occupy either Zn 2+ lattice site or on surface of ZnO crystal. The emissions of Eu 3+ ion on the surface are the characteristic of Eu 2 O 3 , leads to weak luminescence emission. To study such phenomena nanoparticles of ZnO, 2 at % Eu 3+ doped ZnO (ZnO:Eu) and ZnO:Eu covered with yttria matrix were prepared by wet chemical method at low temperature. The prepared nanoparticles were characterized by XRD and TEM. XRD data reveals significant phase segregation of the annealed nanoparticles compared to lower heated samples. This phase segregation of Eu 3+ ion establishes responsible for the decrease luminescence intensity of annealed ZnO:Eu nanoparticles compared to the as-prepared ZnO:Eu nanoparticles. Improvement on luminescence emissions could be achieved only for the as-prepared ZnO:Eu nanoparticles while covered with yttria matrix. Annealing the phosphors crystallization of Y 2 O 3 starts, the Eu 3+ leave ZnO site and enter Y 3+ site in Y 2 O 3 hence contribute luminescence emission. Incorporation the ZnO:Eu nanoparticles in Y 2 O 3 , significantly prevent the phase segregation of europium oxide by allowing it diffuse into the amorphous environment of Y 2 O 3 and thereby enhanced the luminescence for such samples. (author)

  5. Spontaneous electromagnetic emission from a strongly localized plasma flow.

    Science.gov (United States)

    Tejero, E M; Amatucci, W E; Ganguli, G; Cothran, C D; Crabtree, C; Thomas, E

    2011-05-06

    Laboratory observations of electromagnetic ion-cyclotron waves generated by a localized transverse dc electric field are reported. Experiments indicate that these waves result from a strong E×B flow inhomogeneity in a mildly collisional plasma with subcritical magnetic field-aligned current. The wave amplitude scales with the magnitude of the applied radial dc electric field. The electromagnetic signatures become stronger with increasing plasma β, and the radial extent of the power is larger than that of the electrostatic counterpart. Near-Earth space weather implications of the results are discussed.

  6. Luminescent materials: probing the excited state of emission centers by spectroscopic methods

    Science.gov (United States)

    Mihóková, E.; Nikl, M.

    2015-01-01

    We review recent methods employed to study the excited state of rare-earth centers in various luminescent and scintillating materials. The focus is on processes that help determine localization of the excited state within the material band gap, namely photoionization and thermally stimulated ionization. Then the tunneling process between the luminescence center and the trapping state is addressed. We describe the experimental implementation of methods recently developed to study these processes. We report theoretical models helping the data interpretation. We also present application to currently investigated materials.

  7. Using Strong Solar Coronal Emission Lines as Coronal Flux Proxies

    Science.gov (United States)

    Falconer, David A.; Jordan, Studart D.; Davila, Joseph M.; Thomas, Roger J.; Andretta, Vincenzo; Brosius, Jeffrey W.; Hara, Hirosha

    1997-01-01

    A comparison of Skylab results with observations of the strong EUV lines of Fe XVI at 335 A and 361 A from the Goddard Solar EUV Rocket Telescope and Spectrograph (SERTS) flight of 1989 suggests that these lines, and perhaps others observed with SERTS, might offer good proxies for estimating the total coronal flux over important wavelength ranges. In this paper, we compare SERTS observations from a later, 1993 flight with simultaneous cospatial Yohkoh soft X-ray observations to test this suggestion over the energy range of the Soft X-ray Telescope (SXT) on Yohkoh. Both polynomial and power-law fits are obtained, and errors are estimated, for the SERTS lines of Fe XVI 335 A and 361 A, Fe XV 284 A and 417 A, and Mg IX 368 A. It is found that the power-law fits best cover the full range of solar conditions from quiet Sun through active region, though not surprisingly the 'cooler' Mg IX 368 A line proves to be a poor proxy. The quadratic polynomial fits yield fair agreement over a large range for all but the Mg IX line, but the linear fits fail conspicuously when extrapolated into the quiet Sun regime. The implications of this work for the He 11 304 A line formation problem are briefly considered. The paper concludes with a discussion of the value of these iron lines observed with SERTS for estimating stellar coronal fluxes, as observed for example with the EUVE satellite.

  8. Persistent luminescence nanothermometers

    Science.gov (United States)

    Martín Rodríguez, Emma; López-Peña, Gabriel; Montes, Eduardo; Lifante, Ginés; García Solé, José; Jaque, Daniel; Diaz-Torres, Luis Armando; Salas, Pedro

    2017-08-01

    Persistent phosphorescence nanoparticles emitting in the red and near-infrared spectral regions are strongly demanded as contrast nanoprobes for autofluorescence free bioimaging and biosensing. In this work, we have developed Sr4Al14O25:Eu2+, Cr3+, Nd3+ nanopowders that produce persistent red phosphorescence peaking at 694 nm generated by Cr3+ ions. This emission displays temperature sensitivity in the physiological temperature range (20-60 °C), which makes these nanoparticles potentially useful as fluorescence (contactless) nanothermometers operating without requiring optical excitation. Nd3+ ions, which act as shallow electron traps for the red Cr3+ persistent emission, also display infrared emission bands, extending the fluorescence imaging capability to the second biological window. This unique combination of properties makes these nanoparticles multifunctional luminescent probes with great potential applications in nanomedicine.

  9. Luminescent materials: probing the excited state of emission centers by spectroscopic methods

    Czech Academy of Sciences Publication Activity Database

    Mihóková, Eva; Nikl, Martin

    2015-01-01

    Roč. 26, č. 1 (2015), s. 1-17 ISSN 0957-0233 R&D Projects: GA ČR GA13-09876S Grant - others:AVČR(CZ) M100101212 Institutional support: RVO:68378271 Keywords : luminescence * rare- earth ions * ionization * tunneling * scintillators Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.492, year: 2015

  10. Controlling intermolecular aurophilicity in emissive dinuclear Au(I) materials and their luminescent response to ammonia vapour.

    Science.gov (United States)

    Roberts, Ryan J; Le, Debbie; Leznoff, Daniel B

    2015-10-01

    The concept that hydrogen bonding cations can reduce the coulombic repulsion inherent to anionic gold species and thereby trigger aurophilicity is realized with three new photoluminescent compounds of the form [Q]2[Au2(i-mnt)2] (i-mnt = (CN)2C[double bond, length as m-dash]CS2(2-), Q = 3,5-dimethylpyrazolium, piperidinium). These compounds illustrate unprecedented supramolecular aurophilicity between the anions, the emission of which is significantly red-shifted compared to zero-dimensional analogues, a direct result of the aurophilic network. The piperidinium salt exhibits a vapochromic/luminescent response to ammonia, inducing a change in colour of the reflectance and emission from red to yellow. These results demonstrate the ability to rationally control the formation of supramolecular metallophilic networks via the incorporation of hydrogen bonding cations.

  11. Strong blue excitonic emission from CdS nanocrystallites prepared by LB technique

    International Nuclear Information System (INIS)

    Mandal, P.; Talwar, S.S.; Major, S.S.; Srinivasa, R.S.

    2009-01-01

    CdS nanocrystallites formed in ordered fatty acid LB multilayers exhibited strong surface states emission ∝550 nm and weak excitonic emission ∝400 nm. Treatment with aqueous CdCl 2 resulted in the suppression of surface states emission and enhancement of the blue excitonic emission. Subsequent annealing in air at 200 C caused an order of magnitude enhancement of excitonic emission. The growth of nanocrystallites during annealing as seen from the red-shift of excitonic absorption and emission is suppressed by the CdCl 2 treatment. The hindered growth of nanocrystallites, the significant enhancement of excitonic emission from CdS, and the suppression of surface states emission are attributed to surface passivation of CdS nanocrystallites by surface oxide formation. (orig.)

  12. Luminescent sensitization and blue shift emission of Ir(ppy){sub 2}(VPHD) by copolymerization with MMA

    Energy Technology Data Exchange (ETDEWEB)

    An Baoli, E-mail: blan@staff.shu.edu.cn [Department of Chemistry, College of Science, Shanghai University, Shanghai 200444 (China); Dai Fanzeng; Zhang Yanling; Song Jian; Huang, Xiao-Di [Department of Chemistry, College of Science, Shanghai University, Shanghai 200444 (China); Xu, Jia-Qiang, E-mail: xujiaqiang@shu.edu.cn [Department of Chemistry, College of Science, Shanghai University, Shanghai 200444 (China); State Key Laboratory of Transducer Technology, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050 (China)

    2011-08-15

    Ir(ppy){sub 2}(VPHD) (ppy=2-phenyl pyridine, VPHD=6-(4-vinylphenyl)-2,4-hexanedione) was copolymerized with methyl methacrylate (MMA). The copolymer had high quantum yield of 52.3{+-}0.5% in dilute ethyl acetate solution, and the yield increased around 45% than that of the iridium monomer. The maximum emission peaks for the copolymers shifted from 515 to 489 nm while the iridium complex content was less than 0.005 mol% in the feed. The blue emission at 489 nm and the green emission at 520 nm were analyzed by Lorenz function. They are attributed to {sup 1}MLCT and {sup 3}MLCT emissions, respectively. - Highlights: > PMMA-Ir(ppy){sub 2}(VPHD) as luminescent material with high yield of 53%. > The blue color emission at 489 nm from {sup 1}MLCT in conformity with Lorenz function. > The quantum yield for the copolymer increases 45% than that of the iridium monomer. > The {sup 3}MLCT Ex. intensity versus the monomer concentration is in conformity with Boltzmann function.

  13. The red, white and blue of quartz luminescence: A comparison of D{sub e} values derived for sediments from Australia and Indonesia using thermoluminescence and optically stimulated luminescence emissions

    Energy Technology Data Exchange (ETDEWEB)

    Westaway, K.E. [Department of Environment and Geography, Faculty of Science, Macquarie University, NSW 2109 (Australia)], E-mail: kira@els.mq.edu.au

    2009-05-15

    Heated quartz, including quartz from volcanic provinces, commonly displays different luminescence characteristics compared with the same mineral in non-volcanic contexts. These differing properties demand thorough investigations into the most suitable dating techniques for samples composed of quartz grains with different origins. In cave settings, independent techniques such as radiocarbon and U-series can prove useful for validating results, but further insights may be gained by comparing the results obtained for quartz using different luminescence emissions. Twenty-two quartz samples have been selected from five areas (Australia, Timor, Flores, Java and Sulawesi) for comparison of the red and blue emissions. The dual-aliquot regenerative-dose protocol was used to estimate the equivalent dose (D{sub e}) associated with the light-sensitive red thermoluminescence while the single aliquot regenerative-dose protocol was used to measure the D{sub e} values for single grains and single aliquots, which were optically stimulated by green or blue light, respectively. The results obtained from the red thermoluminescence and optically stimulated luminescence measurements display good agreement with independent dating techniques (within {approx}20%). However, the blue emissions exhibit a thermally unstable component, which causes a large underestimation in palaeodoses (on average {approx}80%) and an age limit of {approx}25 ka, while the red emissions are more thermally stable over geological timescales but produce an overestimation in red TL ages (by {approx}13 ka) and low precision (typically {approx}24%). These results can be correlated to three different quartz groups, which have been divided according to their luminescence emissions.

  14. Hormonal control of luminescence from lantern shark (Etmopterus spinax) photophores.

    Science.gov (United States)

    Claes, Julien M; Mallefet, Jérôme

    2009-11-01

    The velvet belly lantern shark (Etmopterus spinax) emits a blue luminescence from thousands of tiny photophores. In this work, we performed a pharmacological study to determine the physiological control of luminescence from these luminous organs. Isolated photophore-filled skin patches produced light under melatonin (MT) and prolactin (PRL) stimulation in a dose-dependent manner but did not react to classical neurotransmitters. The alpha-melanocyte-stimulating hormone (alpha-MSH) had an inhibitory effect on hormonal-induced luminescence. Because luzindole and 4P-PDOT inhibited MT-induced luminescence, the action of this hormone is likely to be mediated through binding to the MT2 receptor subtype, which probably decreases the intracellular concentration of cyclic AMP (cAMP) because forskolin (a cAMP donor) strongly inhibits the light response to MT. However, PRL seems to achieve its effects via janus kinase 2 (JAK2) after binding to its receptor because a specific JAK2 inhibitor inhibits PRL-induced luminescence. The two stimulating hormones showed different kinetics as well as a seasonal variation of light intensity, which was higher in summer (April) than in winter (December and February). All of these results strongly suggest that, contrary to self-luminescent bony fishes, which harbour a nervous control mechanism of their photophore luminescence, the light emission is under hormonal control in the cartilaginous E. spinax. This clearly highlights the diversity of fish luminescence and confirms its multiple independent apparitions during the course of evolution.

  15. The CO/NOx emissions of swirled, strongly pulsed jet diffusion flames

    KAUST Repository

    Liao, Ying-Hao

    2014-05-28

    The CO and NOx exhaust emissions of swirled, strongly pulsed, turbulent jet diffusion flames were studied experimentally in a coflow swirl combustor. Measurements of emissions were performed on the combustor centerline using standard emission analyzers combined with an aspirated sampling probe located downstream of the visible flame tip. The highest levels of CO emissions are generally found for compact, isolated flame puffs, which is consistent with the quenching due to rapid dilution with excess air. The imposition of swirl generally results in a decrease in CO levels by up to a factor of 2.5, suggesting more rapid and compete fuel/air mixing by imposing swirl in the coflow stream. The levels of NO emissions for most cases are generally below the steady-flame value. The NO levels become comparable to the steady-flame value for sufficiently short jet-off times. The swirled coflow air can, in some cases, increase the NO emissions due to a longer combustion residence time due to the flow recirculation within the swirl-induced recirculation zone. Scaling relations, when taking into account the impact of air dilution over an injection cycle on the flame length, reveal a strong correlation between the CO emissions and the global residence time. However, the NO emissions do not successfully correlate with the global residence time. For some specific cases, a compact flame with a simultaneous decrease in both CO and NO emissions compared to the steady flames was observed. © Copyright © Taylor & Francis Group, LLC.

  16. Enhancing and quenching luminescence with gold nanoparticle films: the influence of substrate on the luminescent properties

    International Nuclear Information System (INIS)

    Guidelli, Eder José; Baffa, Oswaldo; Ramos, Ana Paula

    2016-01-01

    Gold nanoparticle (AuNP) films were sputtered over glass and aluminum substrates to enhance optically stimulated luminescence (OSL), a luminescent technique employed for radiation detection, from x-ray irradiated NaCl nanocrystals. The AuNP films deposited over glass led to enhanced-OSL emission, whereas the AuNP films deposited on aluminum substrates quenched the OSL emission. The enhanced-OSL intensity is proportional to the optical density of the film's plasmon resonance band at the stimulation wavelength. For the case of the AuNP/aluminum films, the luminescence quenching diminishes, and OSL intensity partially recovers upon increasing the distance between the AuNPs and the aluminum substrates, and between the luminescent nanocrystals and the AuNP films. These results suggest that plasmonic interactions between the emitter nanocrystals, the localized surface plasmons (LSP) of the AuNPs, and the substrate are responsible for the OSL enhancement and quenching. In this sense, the substrate dictates whether LSP relaxation occurs by radiative or non-radiative transisitions, leading to enhanced or quenched OSL, respectively. Therefore, besides showing that AuNP films can enhance and/or tune the sensitivity of luminescent radiation detectors, and demonstrating OSL as a new technique to investigate mechanisms of plasmon-enhanced luminescence, these results bring insights on how substrates strongly modify the optical properties of AuNP films. (paper)

  17. Luminescence property and emission enhancement of YbAlO3:Mn4+ red phosphor by Mg2+ or Li+ ions

    Science.gov (United States)

    Cao, Renping; Luo, Wenjie; Xu, Haidong; Luo, Zhiyang; Hu, Qianglin; Fu, Ting; Peng, Dedong

    2016-03-01

    YbAlO3:Mn4+, YbAlO3:Mn4+, Li+, and YbAlO3:Mn4+, Mg2+ phosphors are synthesized by high temperature solid-state reaction method in air. Their crystal structures and luminescence properties are investigated. Photoluminescence excitation (PLE) spectrum monitored at 677 nm contains broad PLE band with three PLE peaks located at ∼318, 395, and 470 nm within the range 220-600 nm. Emission spectra with excitation 318 and 470 nm exhibit three emission band peaks located at ∼645, 677, and 700 nm in the range of 610-800 nm and their corresponding chromaticity coordinates are about (x = 0.6942, y = 0.3057). The possible luminous mechanism of Mn4+ ion is analyzed by the simple energy level diagram of Mn4+ ion. The optimum Mn4+-doped concentration in YbAlO3:Mn4+ phosphor is about 0.4 mol% and the luminescence lifetime of YbAlO3:0.4%Mn4+ phosphor is ∼0.59 ms. Emission intensity of YbAlO3:0.4%Mn4+ phosphor can be enhanced ∼6 times after Mg2+ ion is co-doped and it is ∼2 times when Li+ ion is co-doped. The content in the paper is useful to research new Mn4+-doped luminescence materials and improve luminescence property of other Mn4+-doped phosphors.

  18. Stable luminescent metal-organic frameworks as dual-functional materials to encapsulate ln(3+) ions for white-light emission and to detect nitroaromatic explosives.

    Science.gov (United States)

    Xie, Wei; Zhang, Shu-Ran; Du, Dong-Ying; Qin, Jun-Sheng; Bao, Shao-Juan; Li, Jing; Su, Zhong-Min; He, Wen-Wen; Fu, Qiang; Lan, Ya-Qian

    2015-04-06

    A stable porous carbazole-based luminescent metal-organic framework, NENU-522, was successfully constructed. It is extremely stable in air and acidic/basic aqueous solutions, which provides the strategy for luminescent material encapsulation of Ln(3+) ions with tunable luminescence for application in light emission. More importantly, Ln(3+)@NENU-522 can emit white light by encapsulating different molar ratios of Eu(3+) and Tb(3+) ions. Additionally, Tb(3+)@NENU-522 is found to be useful as a fluorescent indicator for the qualitative and quantitative detection of nitroaromatic explosives with different numbers of -NO2 groups, and the concentrations of complete quenching are about 2000, 1000, and 80 ppm for nitrobenzene, 1,3-dinitrobenzene, and 2,4,6-trinitrophenol, respectively. Meanwhile, Tb(3+)@NENU-522 displays high selectivity and recyclability in the detection of nitroaromatic explosives.

  19. Luminescence Instrumentation

    DEFF Research Database (Denmark)

    Jain, Mayank; Bøtter-Jensen, Lars

    2014-01-01

    This chapter gives an introduction to instrumentation for stimulated luminescence studies, with special focus on luminescence dating using the natural dosimeters, quartz and feldspars. The chapter covers basic concepts in luminescence detection, and thermal and optical stimulation, and reference...

  20. Strongly emissive plasma-facing material under space-charge limited regime: Application to emissive probes

    Czech Academy of Sciences Publication Activity Database

    Cavalier, Jordan; Lemoine, N.; Bousselin, G.; Plihon, N.; Ledig, J.

    2017-01-01

    Roč. 24, č. 1 (2017), č. článku 013506. ISSN 1070-664X Institutional support: RVO:61389021 Keywords : plasma * tokamak * emissive probes Subject RIV: BL - Plasma and Gas Discharge Physics OBOR OECD: Fluids and plasma physics (including surface physics) Impact factor: 2.115, year: 2016 http://dx. doi . org /10.1063/1.4973557

  1. Redox-Triggered Bonding-Induced Emission of Thiol-Functionalized Gold Nanoclusters for Luminescence Turn-On Detection of Molecular Oxygen.

    Science.gov (United States)

    Ao, Hang; Feng, Hui; Zhao, Mengting; Zhao, Meizhi; Chen, Jianrong; Qian, Zhaosheng

    2017-11-22

    Most optical sensors for molecular oxygen were developed based on the quenching effect of the luminescence of oxygen-sensitive probes; however, the signal turn-off mode of these probes is undesirable to quantify and visualize molecular oxygen. Herein, we report a novel luminescence turn-on detection strategy for molecular oxygen via the specific oxygen-triggered bonding-induced emission of thiol-functionalized gold nanoclusters. Thiol-functionalized gold nanoclusters were prepared by a facile one-step synthesis, and as-prepared gold nanoclusters possess significant aggregation-induced emission (AIE) property. It is the first time to discover the oxygen-triggered bonding-induced emission (BIE) behavior of gold nanoclusters, which results in disulfide-linked covalent bonding assemblies with intensely red luminescence. This specific redox-triggered BIE is capable of quantitatively detecting dissolved oxygen in aqueous solution in a light-up manner, and trace amount of dissolved oxygen at ppb level is achieved based on this detection method. A facile and convenient test strip for oxygen detection was also developed to monitor molecular oxygen in a gas matrix. Covalent bonding-induced emission is proven to be a more efficient way to attain high brightness of AIEgens than a physical aggregation-induced emission process, and provides a more convenient and desirable detection method for molecular oxygen than the previous sensors.

  2. Luminescent pincer platinum(II) complexes with emission quantum yields up to almost unity: photophysics, photoreductive C-C bond formation, and materials applications.

    Science.gov (United States)

    Chow, Pui-Keong; Cheng, Gang; Tong, Glenna So Ming; To, Wai-Pong; Kwong, Wai-Lun; Low, Kam-Hung; Kwok, Chi-Chung; Ma, Chensheng; Che, Chi-Ming

    2015-02-09

    Luminescent pincer-type Pt(II)  complexes supported by C-deprotonated π-extended tridentate RC^N^NR' ligands and pentafluorophenylacetylide ligands show emission quantum yields up to almost unity. Femtosecond time-resolved fluorescence measurements and time-dependent DFT calculations together reveal the dependence of excited-state structural distortions of [Pt(RC^N^NR')(CC-C6 F5 )] on the positional isomers of the tridentate ligand. Pt complexes [Pt(R-C^N^NR')(CC-Ar)] are efficient photocatalysts for visible-light-induced reductive CC bond formation. The [Pt(R-C^N^NR')(CC-C6 F5 )] complexes perform strongly as phosphorescent dopants for green- and red-emitting organic light-emitting diodes (OLEDs) with external quantum efficiency values over 22.1 %. These complexes are also applied in two-photon cellular imaging when incorporated into mesoporous silica nanoparticles (MSNs). © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Existence of a virtual cathode close to a strongly electron emissive wall in low density plasmas

    Energy Technology Data Exchange (ETDEWEB)

    Tierno, S. P., E-mail: sp.tierno@upm.es; Donoso, J. M.; Domenech-Garret, J. L.; Conde, L. [Department of Applied Physics, E.T.S.I. Aeronáutica y del Espacio. Universidad Politécnica de Madrid, 28040 Madrid (Spain)

    2016-01-15

    The interaction between an electron emissive wall, electrically biased in a plasma, is revisited through a simple fluid model. We search for realistic conditions of the existence of a non-monotonic plasma potential profile with a virtual cathode as it is observed in several experiments. We mainly focus our attention on thermionic emission related to the operation of emissive probes for plasma diagnostics, although most conclusions also apply to other electron emission processes. An extended Bohm criterion is derived involving the ratio between the two different electron densities at the potential minimum and at the background plasma. The model allows a phase-diagram analysis, which confirms the existence of the non-monotonic potential profiles with a virtual cathode. This analysis shows that the formation of the potential well critically depends on the emitted electron current and on the velocity at the sheath edge of cold ions flowing from the bulk plasma. As a consequence, a threshold value of the governing parameter is required, in accordance to the physical nature of the electron emission process. The latter is a threshold wall temperature in the case of thermionic electrons. Experimental evidence supports our numerical calculations of this threshold temperature. Besides this, the potential well becomes deeper with increasing electron emission, retaining a fraction of the released current which limits the extent of the bulk plasma perturbation. This noninvasive property would explain the reliable measurements of plasma potential by using the floating potential method of emissive probes operating in the so-called strong emission regime.

  4. Existence of a virtual cathode close to a strongly electron emissive wall in low density plasmas

    Science.gov (United States)

    Tierno, S. P.; Donoso, J. M.; Domenech-Garret, J. L.; Conde, L.

    2016-01-01

    The interaction between an electron emissive wall, electrically biased in a plasma, is revisited through a simple fluid model. We search for realistic conditions of the existence of a non-monotonic plasma potential profile with a virtual cathode as it is observed in several experiments. We mainly focus our attention on thermionic emission related to the operation of emissive probes for plasma diagnostics, although most conclusions also apply to other electron emission processes. An extended Bohm criterion is derived involving the ratio between the two different electron densities at the potential minimum and at the background plasma. The model allows a phase-diagram analysis, which confirms the existence of the non-monotonic potential profiles with a virtual cathode. This analysis shows that the formation of the potential well critically depends on the emitted electron current and on the velocity at the sheath edge of cold ions flowing from the bulk plasma. As a consequence, a threshold value of the governing parameter is required, in accordance to the physical nature of the electron emission process. The latter is a threshold wall temperature in the case of thermionic electrons. Experimental evidence supports our numerical calculations of this threshold temperature. Besides this, the potential well becomes deeper with increasing electron emission, retaining a fraction of the released current which limits the extent of the bulk plasma perturbation. This noninvasive property would explain the reliable measurements of plasma potential by using the floating potential method of emissive probes operating in the so-called strong emission regime.

  5. Mechanically induced strong red emission in samarium ions doped piezoelectric semiconductor CaZnOS for dynamic pressure sensing and imaging

    Science.gov (United States)

    Wang, Wei; Peng, Dengfeng; Zhang, Hanlu; Yang, Xiaohong; Pan, Caofeng

    2017-07-01

    Piezoelectric semiconductor with optical, electrical and mechanical multifunctions has great potential applications in future optoelectronic devices. The rich properties and applications mainly encompass the intrinsic structures and their coupling effects. Here, we report that lanthanide ions doped piezoelectric semiconductor CaZnOS:Sm3+ showing strong red emission induced by dynamic mechanical stress. Under moderate mechanical load, the doped piezoelectric semiconductor exhibits strong visible red emission to the naked eyes even under the day light. A flexible dynamic pressure sensor device is fabricated based on the prepared CaZnOS:Sm3+ powders. The mechanical-induced emission properties of the device are investigated by the optical fiber spectrometer. The linear characteristic emissions are attributed to the 4G5/2→6H5/2 (566 nm), 4G5/2→6H7/2 (580-632 nm), 4G5/2→6H9/2 (653-673 nm) and 4G5/2→6H11/2 (712-735 nm) f-f transitions of Sm3+ ions. The integral emission intensity is proportional to the value of applied pressure. By using the linear relationship between integrated emission intensity and the dynamic pressure, the real-time pressure distribution is visualized and recorded. Our results highlight that the incorporation of lanthanide luminescent ions into piezoelectric semiconductors as smart materials could be applied into the flexible mechanical-optical sensor device without additional auxiliary power, which has great potential for promising applications such as mapping of personalized handwriting, smart display, and human machine interface.

  6. Emission of strong Terahertz pulses from laser wakefields in weakly coupled plasma

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Divya, E-mail: dsingh@rajdhani.du.ac.in [PWAPA Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110 016 (India); Department of Physics & Electronics, Rajdhani College, University of Delhi, Raja Garden, Ring Road, New Delhi 110015 (India); Malik, Hitendra K. [PWAPA Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110 016 (India)

    2016-09-01

    The present paper discusses the laser plasma interaction for the wakefield excitation and the role of external magnetic field for the emission of Terahertz radiation in a collisional plasma. Flat top lasers are shown to be more appropriate than the conventional Gaussian lasers for the effective excitation of wakefields and hence, the generation of strong Terahertz radiation through the transverse component of wakefield.

  7. Strong coupling and stimulated emission in single parabolic quantum well microcavity for terahertz cascade

    International Nuclear Information System (INIS)

    Tzimis, A.; Savvidis, P. G.; Trifonov, A. V.; Ignatiev, I. V.; Christmann, G.; Tsintzos, S. I.; Hatzopoulos, Z.; Kavokin, A. V.

    2015-01-01

    We report observation of strong light-matter coupling in an AlGaAs microcavity (MC) with an embedded single parabolic quantum well. The parabolic potential is achieved by varying aluminum concentration along the growth direction providing equally spaced energy levels, as confirmed by Brewster angle reflectivity from a reference sample without MC. It acts as an active region of the structure which potentially allows cascaded emission of terahertz (THz) light. Spectrally and time resolved pump-probe spectroscopy reveals characteristic quantum beats whose frequencies range from 0.9 to 4.5 THz, corresponding to energy separation between relevant excitonic levels. The structure exhibits strong stimulated nonlinear emission with simultaneous transition to weak coupling regime. The present study highlights the potential of such devices for creating cascaded relaxation of bosons, which could be utilized for THz emission

  8. Characteristics of electron emission from PZT ferroelectric cathode under strong accelerating field

    Energy Technology Data Exchange (ETDEWEB)

    Hayashi, Yasushi [Department of Energy Sciences, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama (Japan)]. E-mail: hayashi@es.titech.ac.jp; Hotta, Eiki [Department of Energy Sciences, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama (Japan); Flechtner, Donald [High Voltage Laboratory, Cornell University, Ithaca, NY (United States)

    2002-02-07

    We have studied emission characteristics of a PZT ferroelectric cathode under the influence of a strong accelerating field by varying the triggering conditions. The beam current pulse reveals a rising and a steady phase. In the rising phase, the time variation of the beam current is found to be linearly dependent on both the trigger voltage and the diode voltage at the time when the current starts. In the steady phase, field emission characteristics are observed. The results show that the diode voltage is not only accelerating the emitted electrons but also assisting the electron emission from the ferroelectric cathode. An empirical model is proposed and is found to yield a reasonable beam current pulse when the electric field on the surface of the cathode is uniformly distributed. It also provides us with a new possibility to diagnose the emission process of a ferroelectric electron gun. (author)

  9. Optically stimulated luminescence emission spectra from feldspars as a function of sample temperature

    DEFF Research Database (Denmark)

    Duller, G.A.T.; Bøtter-Jensen, L.

    1997-01-01

    samples have been measured at various sample temperatures. A small but consistent shift of the peak emission wavelength to shorter wavelengths at higher temperatures is observed. However, the magnitude of this shift is sufficiently small that it will not affect measurements of the thermal activation...... energy. A systematic difference is observed between the thermal activation energies measured when using different emission wavelengths. In particular, the thermal activation energy of the emission at 400 nm is typically 0.11 eV, while that at 570 nm from the same samples is 0.03-0.05 eV. Several possible...

  10. Luminescence properties of red-emission Mg4 Nb2 O9:Eu3+ phosphor.

    Science.gov (United States)

    Cao, Renping; Cao, Chunyan; Yu, Xiaoguang; Qiu, Jianrong

    2015-03-01

    Red-emitting Mg4 Nb2 O9 :Eu(3+) phosphor is synthesized via a solid-state reaction method in air, and its crystal structure and luminescence are investigated. The phosphor can be excited efficiently by ~ 395 nm light, coupled well with a ~ 395 nm near-ultraviolet chip and emits red light at ~ 613 nm with sharp spectra due to (5) D0  → (7)  F2 transition of the Eu(3+) ion. Mg4 Nb2 O9 :Eu(3+) phosphor sintered at 1350 ºC shows Commission international de I'Eclairage (CIE) chromaticity coordinates of x = 0.6354, y = 0.3592, and is a potential red-emitting phosphor candidate for white light-emitting diodes (W-LEDs) under ~ 395 nm near-ultraviolet LED chip excitation. Copyright © 2014 John Wiley & Sons, Ltd.

  11. Method of measuring luminescence of a material

    Science.gov (United States)

    Miller, Steven D.

    2015-12-15

    A method of measuring luminescence of a material is disclosed. The method includes applying a light source to excite an exposed material. The method also includes amplifying an emission signal of the material. The method further includes measuring a luminescent emission at a fixed time window of about 10 picoseconds to about 10 nanoseconds. The luminescence may be radio photoluminescence (RPL) or optically stimulated luminescence (OSL).

  12. Radiation luminescence of polymers - emission behaviour of aromatic compounds incorporated in synthetic rubbers

    International Nuclear Information System (INIS)

    Kawanishi, Shunichi; Hagiwara, Miyuki

    1986-01-01

    For a deep understanding of a radiation protection mechanism of some aromatic compounds on synthetic polymers, their optical emission behavior under electron irradiation was studied. The fluorescence light was led out of an irradiation room through a wave guide and detected by a photomultiplier so that less noisy spectrum was obtained. Acenaphthene or acenaphthylene was added to the synthetic rubbers such as ethylene propylene diene terpolymer, styrene butadiene rubber and cis-1,4-polybutadiene. The intensities of optical emission induced by electron beams changed from polymer to polymer, while those by ultraviolet lights were independent of the kind of polymers. The dependence of emission intensity on polymers under electron irradiation was estimated to show the fact that the radiation excited energy transfers occur from the polymer matrix to the additives and that an efficiency of the energy transfer is dependent on kinds of polymers. (author)

  13. Sensitisation of visible and NIR lanthanide emission by InPZnS quantum dots in bi-luminescent hybrids

    NARCIS (Netherlands)

    Molloy, Jennifer K.; Lincheneau, Christophe; Karimdjy, Maria Moula; Agnese, Fabio; Mattera, Lucia; Gateau, Christelle; Reiss, Peter; Imbert, Daniel; Mazzanti, Marinella

    2016-01-01

    The synthesis of stable hybrid nanoparticles combining InPZnS@ZnSe/ZnS quantum dots (QDs) and grafted lanthanide complexes has been performed using two different approaches in organic and aqueous media. The final bi-luminescent hybrids exhibit Ln(III) (Ln = Eu and Yb) centred luminescence upon QD

  14. A highly emissive inorganic hexamolybdenum cluster complex as a handy precursor for the preparation of new luminescent materials.

    Science.gov (United States)

    Efremova, O A; Shestopalov, M A; Chirtsova, N A; Smolentsev, A I; Mironov, Y V; Kitamura, N; Brylev, K A; Sutherland, A J

    2014-04-28

    The synthesis and characterisation of a new, highly luminescent inorganic cluster complex, (Bu4N)2[Mo6I8(NO3)6], are described. The complex possesses labile nitrato ligands and is therefore a useful precursor for the design of new luminescent materials. To exemplify this, functionalised polystyrene beads have been utilised as "polymeric ligands" to immobilise the molybdenum cluster complex.

  15. The luminescent concentrator. Stability issues

    Energy Technology Data Exchange (ETDEWEB)

    Slooff, L.H.; Budel, T.; Burgers, A.R.; Bakker, N.J. [ECN Solar Energy, P.O.Box 1, 1755 ZG Petten (Netherlands); Buechtemann, A.; Danz, R. [Fraunhofer-Institute for Applied Polymer Research, Geiselbergstr.69, D-14476 Golm (Germany); Meyer, T.; Meyer, A. [Solaronix SA, Rue de l' Ouriette 129, CH-1170 Aubonne (Switzerland)

    2007-08-15

    One of the major challenges in the research on luminescent concentrators is the lifetime of the luminescent polymer plates. There are some commercial plates available, but data on lifetime are very limited, especially when dedicated to applications like the luminescent concentrator. In this paper we report stability experiments on luminescent concentrator plates, aged under continuous white light illumination, outdoor conditions and high intensity monochromatic illumination. The results show that the lifetime strongly depends on the organic luminescent dye in the plate. The best materials exhibit an initial decrease in performance of about 20% and then remain more or less stable. It is shown that the degradation is not caused by UV illumination.

  16. Strong water absorption in the dayside emission spectrum of the planet HD 189733b.

    Science.gov (United States)

    Grillmair, Carl J; Burrows, Adam; Charbonneau, David; Armus, Lee; Stauffer, John; Meadows, Victoria; van Cleve, Jeffrey; von Braun, Kaspar; Levine, Deborah

    2008-12-11

    Recent observations of the extrasolar planet HD 189733b did not reveal the presence of water in the emission spectrum of the planet. Yet models of such 'hot-Jupiter' planets predict an abundance of atmospheric water vapour. Validating and constraining these models is crucial to understanding the physics and chemistry of planetary atmospheres in extreme environments. Indications of the presence of water in the atmosphere of HD 189733b have recently been found in transmission spectra, where the planet's atmosphere selectively absorbs the light of the parent star, and in broadband photometry. Here we report the detection of strong water absorption in a high-signal-to-noise, mid-infrared emission spectrum of the planet itself. We find both a strong downturn in the flux ratio below 10 microm and discrete spectral features that are characteristic of strong absorption by water vapour. The differences between these and previous observations are significant and admit the possibility that predicted planetary-scale dynamical weather structures may alter the emission spectrum over time. Models that match the observed spectrum and the broadband photometry suggest that heat redistribution from the dayside to the nightside is weak. Reconciling this with the high nightside temperature will require a better understanding of atmospheric circulation or possible additional energy sources.

  17. Strong geologic methane emissions from discontinuous terrestrial permafrost in the Mackenzie Delta, Canada.

    Science.gov (United States)

    Kohnert, Katrin; Serafimovich, Andrei; Metzger, Stefan; Hartmann, Jörg; Sachs, Torsten

    2017-07-19

    Arctic permafrost caps vast amounts of old, geologic methane (CH 4 ) in subsurface reservoirs. Thawing permafrost opens pathways for this CH 4 to migrate to the surface. However, the occurrence of geologic emissions and their contribution to the CH 4 budget in addition to recent, biogenic CH 4 is uncertain. Here we present a high-resolution (100 m × 100 m) regional (10,000 km²) CH 4 flux map of the Mackenzie Delta, Canada, based on airborne CH 4 flux data from July 2012 and 2013. We identify strong, likely geologic emissions solely where the permafrost is discontinuous. These peaks are 13 times larger than typical biogenic emissions. Whereas microbial CH 4 production largely depends on recent air and soil temperature, geologic CH 4 was produced over millions of years and can be released year-round provided open pathways exist. Therefore, even though they only occur on about 1% of the area, geologic hotspots contribute 17% to the annual CH 4 emission estimate of our study area. We suggest that this share may increase if ongoing permafrost thaw opens new pathways. We conclude that, due to permafrost thaw, hydrocarbon-rich areas, prevalent in the Arctic, may see increased emission of geologic CH 4 in the future, in addition to enhanced microbial CH 4 production.

  18. Luminescence of neutron irradiated amorphous SiO2. The 1.9 and 2.2 eV emission bands

    International Nuclear Information System (INIS)

    Mervic, A.; Guzzi, M.; Lucchini, G.; Spinolo, G.

    1992-01-01

    Experimental results on the 1.9 and 2.2 eV luminescence bands in neutron irradiated amorphous silica are reported. All the four types in which silicas are usually classified (natural and synthetic, both dry and wet) are considered. Photoluminescence spectra in the 80 to 650 K temperature range, photoluminescence excitation spectra at 80 and 300 K, and spectrally resolved thermally stimulated luminescence are measured. The comparison of the intensity of the 1.9 eV band in the different types of silicas allows us to support one of the models recently proposed for the structure of the emitting center. A first systematic description of the main properties of the 2.2 eV emission band is given. (orig.)

  19. Directed emission of CdSe nanoplatelets originating from strongly anisotropic 2D electronic structure

    Science.gov (United States)

    Scott, Riccardo; Heckmann, Jan; Prudnikau, Anatol V.; Antanovich, Artsiom; Mikhailov, Aleksandr; Owschimikow, Nina; Artemyev, Mikhail; Climente, Juan I.; Woggon, Ulrike; Grosse, Nicolai B.; Achtstein, Alexander W.

    2017-12-01

    Intrinsically directional light emitters are potentially important for applications in photonics including lasing and energy-efficient display technology. Here, we propose a new route to overcome intrinsic efficiency limitations in light-emitting devices by studying a CdSe nanoplatelets monolayer that exhibits strongly anisotropic, directed photoluminescence. Analysis of the two-dimensional k-space distribution reveals the underlying internal transition dipole distribution. The observed directed emission is related to the anisotropy of the electronic Bloch states governing the exciton transition dipole moment and forming a bright plane. The strongly directed emission perpendicular to the platelet is further enhanced by the optical local density of states and local fields. In contrast to the emission directionality, the off-resonant absorption into the energetically higher 2D-continuum of states is isotropic. These contrasting optical properties make the oriented CdSe nanoplatelets, or superstructures of parallel-oriented platelets, an interesting and potentially useful class of semiconductor-based emitters.

  20. Luminescent phosphor materials

    International Nuclear Information System (INIS)

    Jamieson, P.B.

    1980-01-01

    The invention relates to luminescent phosphors and in particular those phosphors which emit ultra-violet radiation when struck by X-rays. The formula of the phosphor is Lasub(1-x-y-z-a)Gdsub(x)Cesub(y)Tbsub(z)Thsub(a)XO 4 in which X represents phosphorus atoms, arsenic atoms or a mixture of phosphorus and arsenic atoms, x is 0.01 to 0.50 and preferably 0.05 to 0.30, y is 0 or up to 0.50, z is 0 or up to 0.10 and preferably 0 or up to 0.02, a is 0 or up to 0.02, and when X represents phosphor atoms alone y + z + a is at least 0.01. The phosphors emit strong ultra-violet radiation when irradiated by X-rays and so can be used in intensifying screens particularly where the photographic material is UV radiation sensitive. In this case the overall emission should be in the 250-400 nm wavelength range. Another use is in the emission coating of cathode ray tubes. Details of the characteristics of various compositions are given with examples of preparation and emission spectra. (UK)

  1. Hydrothermal synthesis, crystal structure and luminescence property ...

    Indian Academy of Sciences (India)

    3.4 Luminescence properties of 1. The solid state luminescence property of 1 along with free ligand was investigated at room temperature. On photoexcitation at 365 nm, a characteristic peak at. 583 nm was observed in the emission spectrum of. 1 (figure 6). The yellow luminescence observed at. 583 nm is possibly due to ...

  2. How far are luminescence properties predictable?

    NARCIS (Netherlands)

    Blasse, G.

    Our knowledge of the luminescence of isolators has increased considerably during the past decade. As a consequence it has become possible to understand the luminescence of technically important phosphors and even to predict efficient luminescent materials. We first illustrate how emission spectra of

  3. Laser based imaging of time depending microscopic scenes with strong light emission

    Science.gov (United States)

    Hahlweg, Cornelius; Wilhelm, Eugen; Rothe, Hendrik

    2011-10-01

    Investigating volume scatterometry methods based on short range LIDAR devices for non-static objects we achieved interesting results aside the intended micro-LIDAR: the high speed camera recording of the illuminated scene of an exploding wire -intended for Doppler LIDAR tests - delivered a very effective method of observing details of objects with extremely strong light emission. As a side effect a schlieren movie is gathered without any special effort. The fact that microscopic features of short time processes with high emission and material flow might be imaged without endangering valuable equipment makes this technique at least as interesting as the intended one. So we decided to present our results - including latest video and photo material - instead of a more theoretical paper on our progress concerning the primary goal.

  4. Relativistic quantum dynamics in strong fields: Photon emission from heavy, few-electron ions

    International Nuclear Information System (INIS)

    Fritzsche, S.; Stoehlker, T.

    2005-03-01

    Recent progress in the study of the photon emission from highly-charged heavy ions is reviewed. These investigations show that high-Z ions provide a unique tool for improving the understanding of the electron-electron and electron-photon interaction in the presence of strong fields. Apart from the bound-state transitions, which are accurately described in the framework of quantum electrodynamics, much information has been obtained also from the radiative capture of (quasi-) free electrons by high-Z ions. Many features in the observed spectra hereby confirm the inherently relativistic behavior of even the simplest compound quantum systems in nature. (orig.)

  5. Increasing fluorescent concentrator light collection efficiency by restricting the angular emission characteristic of the incorporated luminescent material: the 'Nano-Fluko' concept

    Science.gov (United States)

    Goldschmidt, J. C.; Peters, M.; Gutmann, J.; Steidl, L.; Zentel, R.; Bläsi, B.; Hermle, M.

    2010-05-01

    Fluorescent concentrators concentrate both diffuse and direct radiation without requiring tracking of the sun. In fluorescent concentrators, luminescent materials embedded in a transparent matrix absorb sunlight and emit radiation with a different wavelength. Total internal reflection traps the emitted light and guides it to solar cells attached to the concentrator's edges. The escape cone of total internal reflection, however, limits the light collection efficiency. Spectrally selective photonic structures, which transmit light in the absorption range of the luminescent material and reflect the emitted light, reduce these losses. In this paper, we review different realizations of such structures and show that they increase collection efficiency by 20%. However, light emitted into steep angles in respect to the front surface, which would be lost without the photonic structures, has a very long effective path inside the concentrator until it reaches a solar cell. Therefore it suffers from path length dependent losses. We discuss how emission into the unfavorable directions can be suppressed by integrating the luminescent material into photonic structures, thus reducing these losses. We present possible realizations both for the concentrator design and for the solar cells used in such systems.

  6. An aggregation-induced emissive NIR luminescent based on ESIPT and TICT mechanisms and its application to the detection of Cys

    Science.gov (United States)

    Li, Renjie; Yan, Liqiang; Wang, Zhongwei; Qi, Zhengjian

    2017-05-01

    A series of red to near-infrared (NIR) emissive organic compound 1-3 based on the 2‧-hydroxyacetophenone derivatives were synthesized through a mild condensation reaction, which exhibit typical AIE properties and long fluorescence lifetime in an aggregated state. Compound 2 displays the highest quantum yield (Φf) of 0.49 among the reported organic compound with an emission maximum (λem) 700 nm. Comparison between the bright emissive compound 2 and the weak fluorescence compounds 1 and 3 clearly gives evidence that a subtle structure modification can arouse great property changes, which is instructive in designing new high-efficiency organic luminescent materials. In demonstration of the potential application of these new fluorescence dyes, Probe 4 that is capable of unique detecting Cys in water media is also reported.

  7. The first detection of neutral hydrogen in emission in a strong spiral lens

    Science.gov (United States)

    Lipnicky, Andrew; Chakrabarti, Sukanya; Wright, Melvyn C. H.; Blitz, Leo; Heiles, Carl; Cotton, William; Frayer, David; Blandford, Roger; Shu, Yiping; Bolton, Adam S.

    2018-05-01

    We report H I observations of eight spiral galaxies that are strongly lensing background sources. Our targets were selected from the Sloan WFC (Wide Field Camera) Edge-on Late-type Lens Survey (SWELLS) using the Arecibo, Karl G. Jansky Very Large Array, and Green Bank telescopes. We securely detect J1703+2451 at z = 0.063 with a signal-to-noise ratio of 6.7 and W50 = 79 ± 13 km s-1, obtaining the first detection of H I emission in a strong spiral lens. We measure a mass of M_{H I} = (1.77± 0.06^{+0.35}_{-0.75})× 10^9 M_{⊙} for this source. We find that this lens is a normal spiral, with observable properties that are fairly typical of spiral galaxies. For three other sources, we did not secure a detection; however, we are able to place strong constraints on the H I masses of those galaxies. The observations for four of our sources were rendered unusable due to strong radio frequency interference.

  8. The First Detection of Neutral Hydrogen in Emission in a Strong Spiral Lens

    Science.gov (United States)

    Lipnicky, Andrew; Chakrabarti, Sukanya; Wright, Melvyn C. H.; Blitz, Leo; Heiles, Carl; Cotton, William; Frayer, David; Blandford, Roger; Shu, Yiping; Bolton, Adam S.

    2018-02-01

    We report H I observations of eight spiral galaxies that are strongly lensing background sources. Our targets were selected from the Sloan WFC (Wide Field Camera) Edge-on Late-type Lens Survey (SWELLS) using the Arecibo, Karl G. Jansky Very Large Array, and Green Bank telescopes. We securely detect J1703+2451 at z = 0.063 with a signal-to-noise of 6.7 and W50 = 79 ± 13 km s-1, obtaining the first detection of H I emission in a strong spiral lens. We measure a mass of M_{H I}= (1.77± 0.06^{+0.35}_{-0.75})× 10^9 {M}_{\\odot} for this source. We find that this lens is a normal spiral, with observable properties that are fairly typical of spiral galaxies. For three other sources we did not secure a detection; however, we are able to place strong constraints on the H I masses of those galaxies. The observations for four of our sources were rendered unusable due to strong radio frequency interference.

  9. White light emission from radical carbonyl-terminations in Al2O3-SiO2 porous glasses with high luminescence quantum efficiencies

    International Nuclear Information System (INIS)

    Hayakawa, Tomokatsu; Hiramitsu, Ai; Nogami, Masayuki

    2003-01-01

    Development of white phosphors with highly emissive, stable, and less toxic characteristics has been important for display and lighting technology. In this letter, it is shown that sol-gel-derived glasses of aluminosilicate composition, followed by a heat treatment in air at low temperatures around 500 deg. C, exhibit two intense, visible photoluminescence bands: One is due to point defects in these glasses and the other comes from radical carbonyl-terminations on the surface of pores. The photoluminescence provides a white light with high luminescence quantum efficiency (∼66.5%) under long-wavelength ultraviolet excitation

  10. Engineering light emission of two-dimensional materials in both the weak and strong coupling regimes

    Science.gov (United States)

    Brotons-Gisbert, Mauro; Martínez-Pastor, Juan P.; Ballesteros, Guillem C.; Gerardot, Brian D.; Sánchez-Royo, Juan F.

    2018-01-01

    Two-dimensional (2D) materials have promising applications in optoelectronics, photonics, and quantum technologies. However, their intrinsically low light absorption limits their performance, and potential devices must be accurately engineered for optimal operation. Here, we apply a transfer matrix-based source-term method to optimize light absorption and emission in 2D materials and related devices in weak and strong coupling regimes. The implemented analytical model accurately accounts for experimental results reported for representative 2D materials such as graphene and MoS2. The model has been extended to propose structures to optimize light emission by exciton recombination in MoS2 single layers, light extraction from arbitrarily oriented dipole monolayers, and single-photon emission in 2D materials. Also, it has been successfully applied to retrieve exciton-cavity interaction parameters from MoS2 microcavity experiments. The present model appears as a powerful and versatile tool for the design of new optoelectronic devices based on 2D semiconductors such as quantum light sources and polariton lasers.

  11. STRONG FIELD EFFECTS ON EMISSION LINE PROFILES: KERR BLACK HOLES AND WARPED ACCRETION DISKS

    International Nuclear Information System (INIS)

    Wang Yan; Li Xiangdong

    2012-01-01

    If an accretion disk around a black hole is illuminated by hard X-rays from non-thermal coronae, fluorescent iron lines will be emitted from the inner region of the accretion disk. The emission line profiles will show a variety of strong field effects, which may be used as a probe of the spin parameter of the black hole and the structure of the accretion disk. In this paper, we generalize the previous relativistic line profile models by including both the black hole spinning effects and the non-axisymmetries of warped accretion disks. Our results show different features from the conventional calculations for either a flat disk around a Kerr black hole or a warped disk around a Schwarzschild black hole by presenting, at the same time, multiple peaks, rather long red tails, and time variations of line profiles with the precession of the disk. We show disk images as seen by a distant observer, which are distorted by the strong gravity. Although we are primarily concerned with the iron K-shell lines in this paper, the calculation is general and is valid for any emission lines produced from a warped accretion disk around a black hole.

  12. Luminescence nanothermometry

    Science.gov (United States)

    Jaque, Daniel; Vetrone, Fiorenzo

    2012-07-01

    The current status of luminescence nanothermometry is reviewed in detail. Based on the main parameters of luminescence including intensity, bandwidth, bandshape, polarization, spectral shift and lifetime, we initially describe and compare the different classes of luminescence nanothermometry. Subsequently, the various luminescent materials used in each case are discussed and the mechanisms at the root of the luminescence thermal sensitivity are described. The most important results obtained in each case are summarized and the advantages and disadvantages of these approaches are discussed.The current status of luminescence nanothermometry is reviewed in detail. Based on the main parameters of luminescence including intensity, bandwidth, bandshape, polarization, spectral shift and lifetime, we initially describe and compare the different classes of luminescence nanothermometry. Subsequently, the various luminescent materials used in each case are discussed and the mechanisms at the root of the luminescence thermal sensitivity are described. The most important results obtained in each case are summarized and the advantages and disadvantages of these approaches are discussed. This work was supported by the Universidad Autónoma de Madrid and Comunidad Autónoma de Madrid (Project S2009/MAT-1756), by the Spanish Ministerio de Educacion y Ciencia (MAT2010-16161) and by Caja Madrid Foundation.

  13. Tuneable luminescence properties of EDTA-assisted ZnS:Mn nanocrystals from a yellow-orange to a red emission band.

    Science.gov (United States)

    Viswanath, R; Bhojya Naik, H S; Arun Kumar, G; Suresh Gowda, I K; Yallappa, S

    2017-11-01

    Luminescence technology has been improved with the help of semiconductor nanoparticles that possess novel optical and electrical properties compared with their bulk counterpart. The aim of this study was to design semiconductor nanocrystals in their pure (ZnS) or doped form (ZnS:Mn) with different concentrations of Mn 2+ ions by a wet chemical route stabilized by ethylenediamine tetra-acetic acid (EDTA) and to evaluate their luminescence properties. The nanocrystals were characterized by physicochemical techniques such as X-ray diffraction (XRD), High-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SEAD), EDS, and ultraviolet (UV)-visible light and photoluminescence (PL) studies. These results showed the presence of cubic phase and spherically shaped nanocrystals. A blue shift with respect to their bulk counterpart was observed. PL emission spectra were observed with a fixed blue peak and the yellow-orange bands were red shifted towards the red region under the same excitation wavelength. The orange-red bands were attributed to the radiation transition of electrons in 3d5 unfilled shells of Mn 2+ ions [ 4 T 1 ( 4 G)- 6 A 1 ( 6 S)]; the ZnS matrix varied with Mn 2+ concentration. Shift and increase in the intensity of the PL and absorption bands were observed with increase in Mn content. The study showed that Mn 2+ -doped ZnS nanocrystal emission bands can be tuned from the yellow-orange to the red regions under a controlled synthesis process and could be used as promising luminescent emitters in the biology field upon functionalization with suitable materials. Further studies on construction with various other materials will be useful for practical applications. Copyright © 2017 John Wiley & Sons, Ltd.

  14. Hard X-ray PhotoEmission Spectroscopy of strongly correlated systems

    Science.gov (United States)

    Panaccione, Giancarlo; Offi, Francesco; Sacchi, Maurizio; Torelli, Piero

    2008-06-01

    Hard X-ray PhotoEmission Spectroscopy (HAXPES) is a new tool for the study of bulk electronic properties of solids using synchrotron radiation. We review recent achievements of HAXPES, with particular reference to the VOLPE project, showing that high energy resolution and bulk sensitivity can be obtained at kinetic energies of 6-8 keV. We present also the results of recent studies on strongly correlated materials, such as vanadium sesquioxide and bilayered manganites, revealing the presence of different screening properties in the bulk with respect to the surface. We discuss the relevant experimental features of the metal-insulator transition in these materials. To cite this article: G. Panaccione et al., C. R. Physique 9 (2008).

  15. Spontaneous emission spectra and quantum light-matter interactions from a strongly coupled quantum dot metal-nanoparticle system

    DEFF Research Database (Denmark)

    Van Vlack, C.; Kristensen, Philip Trøst; Hughes, S.

    2012-01-01

    the dot to the detector, we demonstrate that the strong-coupling regime should be observable in the far-field spontaneous emission spectrum, even at room temperature. The vacuum-induced emission spectra show that the usual vacuum Rabi doublet becomes a rich spectral triplet or quartet with two of the four...

  16. Highly stable colloidal TiO2 nanocrystals with strong violet-blue emission

    International Nuclear Information System (INIS)

    Ghamsari, Morteza Sasani; Gaeeni, Mohammad Reza; Han, Wooje; Park, Hyung-Ho

    2016-01-01

    Improved sol–gel method has been applied to prepare highly stable colloidal TiO 2 nanocrystals. The synthesized titania nanocrystals exhibit strong emission in the violet-blue wavelength region. Very long evolution time was obtained by preventing the sol to gel conversion with reflux process. FTIR, XRD, UV–vis absorption, photoluminescence and high resolution transmission electron microscope (HRTEM) were used to study the optical properties, crystalline phase, morphology, shape and size of prepared TiO 2 colloidal nanocrystals. HRTEM showed that the diameter of TiO 2 colloidal nanocrystals is about 5 nm. Although the PL spectra show similar spectral features upon excitation wavelengths at 280, 300 and 350 nm, but their emission intensities are significantly different from each other. Photoluminescence quantum yield for TiO 2 colloidal nanocrystals is estimated to be 49% with 280 nm excitation wavelength which is in agreement and better than reported before. Obtained results confirm that the prepared colloidal TiO 2 sample has enough potential for optoelectronics applications.

  17. BG2003 luminescent spectrograph

    International Nuclear Information System (INIS)

    Li Huhou

    2004-01-01

    A new equipment for luminescent spectrograph has been created. The prototype is named BG2003. It is qualified for running. Dating with selected frequency optical luminescence means that the wavelength of the stimulating source and the emission photons can be selected. Then, one can use this equipment to do the separation of the minerals in the fine grains sample for the fine grains dating technique. And also it may be effective to resolve many problems for the minerals authentication. A new optical separate technique will be created and developed in mineralogy. (authors)

  18. Luminescence dating

    International Nuclear Information System (INIS)

    Rieser, U.

    2013-01-01

    The luminescence techniques have evolved over the last 40 years to a powerful dating instrument in archaeology and geoscience. Depending on how the luminescence is stimulated, one distinguishes the phenomena of thermoluminescence (TL), optically stimulated luminescence (OSL) and infrared stimulated luminescence (IRSL). Each of these phenomena has its specific potential for dating various archaeological materials in the time range from medieval back to palaeolithic periods, or, speaking in geological terms, for dating of Holocene and late Pleistocene objects. The OSL and IRSL techniques are sometimes treated together as 'optical dating'. The luminescence techniques differ from other major dating techniques, such as 14 C, essentially by their applicability to inorganic materials, their wide age-range from about 100 years to more than 100,000 years and the kind of datable events which are the last exposure to heat or to light. (author). 10 refs., 3 figs.

  19. Luminescence dating

    International Nuclear Information System (INIS)

    Rieser, U.

    2009-01-01

    The luminescence techniques have evolved over the last 40 years to a powerful dating instrument in archaeology and geoscience. Depending on how the luminescence is stimulated, one distinguishes the phenomena of thermoluminescence (TL), optically stimulated luminescence (OSL) and infrared stimulated luminescence (IRSL). Each of these phenomena has its specific potential for dating various archaeological materals in the time range from medieval back to palaeolithic periods, or, speaking in geological terms, for dating of Holocene and late Pleistocene objects. The OSL and IRSL techniques are sometimes treated together as 'optical dating'. The luminescence techniques differ from other major dating techniques, such as 14 C, essentially by their applicability to inorganic materials, their wide age-range from about 100 years to more than 100,000 years and the kind of datable events which are the last exposure to heat or to light. (author). 10 refs., 3 figs.

  20. Luminescence dating

    International Nuclear Information System (INIS)

    Rieser, U.

    2012-01-01

    The luminescence techniques have evolved over the last 40 years to a powerful dating instrument in archaeology and geoscience. Depending on how the luminescence is stimulated, one distinguishes the phenomena of thermoluminescence (TL), optically stimulated luminescence (OSL) and infrared stimulated luminescence (IRSL). Each of these phenomena has its specific potential for dating various archaeological materials in the time range from medieval back to palaeolithic periods, or, speaking in geological terms, for dating of Holocene and late Pleistocene objects. The OSL and IRSL techniques are sometimes treated together as 'optical dating'. The luminescence techniques differ from other major dating techniques, such as 14 C, essentially by their applicability to inorganic materials, their wide age-range from about 100 years to more than 100,000 years and the kind of datable events which are the last exposure to heat or to light. (author). 10 refs., 3 figs.

  1. Luminescence from metals and insulators

    International Nuclear Information System (INIS)

    Crawford, O.H.

    1985-01-01

    The term luminescence is normally applied to light emission that is not explainable by the mechanisms discussed by the other speakers in this meeting. Specifically, it is not transition radiation, surface plasmon radiation, or bremsstrahlung. One normally thinks of luminescence as arising from one-electron transitions within a medium. This talk consists of an overview of luminescence from condensed matter under irradiation by either energetic particles or photons. The author begins with organic molecules, where luminescence is best understood, and then discusses inorganic insulators and metals. Finally, the dependence of yield upon projectile species and velocity is discussed, and predictions are made concerning the relative effectiveness of electrons, protons, and hydrogen atoms in exciting luminescence

  2. Boron clusters in luminescent materials.

    Science.gov (United States)

    Mukherjee, Sanjoy; Thilagar, Pakkirisamy

    2016-01-21

    In recent times, luminescent materials with tunable emission properties have found applications in almost all aspects of modern material sciences. Any discussion on the recent developments in luminescent materials would be incomplete if one does not account for the versatile photophysical features of boron containing compounds. Apart from triarylboranes and tetra-coordinate borate dyes, luminescent materials consisting of boron clusters have also found immense interest in recent times. Recent studies have unveiled the opportunities hidden within boranes, carboranes and metalloboranes, etc. as active constituents of luminescent materials. From simple illustrations of luminescence, to advanced applications in LASERs, OLEDs and bioimaging, etc., the unique features of such compounds and their promising versatility have already been established. In this review, recent revelations about the excellent photophysical properties of such materials are discussed.

  3. Sub-10 nm lanthanide doped BaLuF{sub 5} nanocrystals: Shape controllable synthesis, tunable multicolor emission and enhanced near-infrared upconversion luminescence

    Energy Technology Data Exchange (ETDEWEB)

    Rao, Ling [School of Materials Science and Engineering, Key Laboratory of Low-dimensional Materials and Application Technology (Ministry of Education), Xiangtan University, Xiangtan 411105 (China); Lu, Wei [Department of Applied Physics and Materials Research Center, The Hong Kong Polytechnic University (Hong Kong); Wang, Haibo; Yi, Zhigao [School of Materials Science and Engineering, Key Laboratory of Low-dimensional Materials and Application Technology (Ministry of Education), Xiangtan University, Xiangtan 411105 (China); Zeng, Songjun, E-mail: songjunz@hunnu.edu.cn [College of Physics and Information Science and Key Laboratory of Low-dimensional Quantum Structures and Quantum Control of the Ministry of Education, Hunan Normal University, Changsha 410081 (China); Li, Zheng, E-mail: zhengli58@gmail.com [School of Materials Science and Engineering, Key Laboratory of Low-dimensional Materials and Application Technology (Ministry of Education), Xiangtan University, Xiangtan 411105 (China)

    2015-04-15

    Highlights: • Sub-10 nm cubic phase BaLuF{sub 5} nanocrystals were synthesized by a hydrothermal method for the first time. • Tunable multicolor from yellow to yellow-green was achieved by controlling Gd{sup 3+} content in BaLuF{sub 5}:Yb/Er system. • Intense near-infrared upconversion luminescence in BaLuF{sub 5}:Gd/Yb/Tm nanocrystal. • The enhancement near-infrared luminescence can be realized by adjusting the content of Gd{sup 3+} in BaLuF{sub 5}:Gd/Yb/Tm system. - Abstract: In this study, sub-10 nm BaLuF{sub 5} nanocrystals with cubic phase structure were synthesized by a solvothermal method using oleic acid as the stabilizing agent. The as-prepared BaLuF{sub 5} nanocrystals were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), and analyzed by the upconversion (UC) spectra. The TEM results reveal that these samples present high uniformity. Compared with Gd-free samples, the size of BaLuF{sub 5}:Yb/Er doped with 10% Gd{sup 3+} decreased to 5.6 nm. In addition, BaLuF{sub 5}:Yb/Tm/Gd upconversion nanoparticles (UCNPs) presented efficient near-infrared (NIR)-NIR UC luminescence. Therefore, it is expected that these ultra-small BaLuF{sub 5} nanocrystals with well-controlled shape, size, and UC emission have potential applications in biomedical imaging fields.

  4. Problems related to stimulated electromagnetic emissions, strong turbulence and ionospheric modification

    International Nuclear Information System (INIS)

    Goodman, S.

    1993-05-01

    Optical pumping of the ionospheric plasma by high-frequency radio waves produces a state of turbulence. Several consequences of the pumping are considered in this thesis. At reflection altitude the plasma is thought to be dominated by parametric instabilities and strong turbulence; these are both encapsulated in the so called Zakharov equations. The Zakharov equations are derived and generalised from kinetic theory. Limits of validity, corrections to the ion sound speed,effective ponderomotive force, nonlinear damping and other generalisation are included. As an example of the difference a kinetic approach makes, the threshold for parametric instabilities is seen to be lowered in a kinetic plasma. Mostly relevant to the upper hybrid layer is the recent discovery in the pumping experiments of stimulated electromagnetic emissions (SEE). In particular one feature of SEE which occurs around the cyclotron harmonics and depends on density striations is investigated. The observed frequency of emission, dependency on striations, time evolution and cutoff frequency below which the feature does not occur, are explained. Two theoretical approaches are taken. The first is a parametric three wave decay instability followed by a nonlinear mixing to produce SEE. Thresholds for the instability are well within experimental capacity. The second, less orthodox, approach, is a finite amplitude model. The finite amplitude model goes beyond the traditional parametric approach by being able to predict radiated power output. Miscellaneous aspects of a turbulent ionosphere are also examined. The dependency of the scattering cross section of a turbulent plasma upon higher order perturbations is considered. In a turbulent plasma, density gradients steeper than characteristic plasma scales may develop. The case of calculating the dielectric permittivity for a linear gradient of arbitrary steepness is considered

  5. Luminescent solutions and powders of new samarium complexes with N,N',O,O'-chelating ligands

    Science.gov (United States)

    Kharcheva, Anastasia V.; Nikolskiy, Kirill S.; Borisova, Nataliya E.; Ivanov, Alexey V.; Reshetova, Marina D.; Yuzhakov, Viktor I.; Patsaeva, Svetlana V.

    2016-04-01

    Imaging techniques in biology and medicine are crucial tools to obtain information on structural and functional properties of living cells and organisms. To fulfill the requirements associated with application of these techniques it appears necessary to design markers with specific characteristics. Luminescent complexes of trivalent lanthanide ions with chelating ligands are of increasing importance in biomedical applications because of their millisecond luminescence lifetime, narrow emission band, high signal-to-noise ratio and minimal photodamage to biological samples. In order to extend the available emission wavelength range the luminescent samarium chelates are highly desirable. In this study the ligands with diamides of 2,2'-bipyridin-6,6'-dicarboxylic acid were used to improve photophysical characteristics of samarium complexes. We report the luminescence characteristics of samarium complexes with novel ligands. All complexes exhibited the characteristic emission of Sm (III) ion with the lines at 565, 597, 605, 645 and 654 nm, the intensity strongly depended on the ligand. Absorption and luminescence excitation spectra of Sm (III) complexes showed main peaks in the UV range demonstrating lanthanide coordination to the ligand. The absolute lumenescence quantum yield was measured for solutions in acetonitrile with excitation at 350 nm. The largest luminescence quantum yield was found for the samarium complex Bipy 6MePy Sm (3%) being much higher that for samarium complexes reported in the literature earlier. These results prove as well that samarium chelates are potential markers for multiparametric imaging techniques.

  6. Very Strong TeV Emission as $\\gamma$-Ray Burst Afterglows

    CERN Document Server

    Totani, T

    1998-01-01

    Gamma-ray bursts (GRBs) and following afterglows are considered to be produced by dissipation of kinetic energy of a relativistic fireball and radiation process is widely believed as synchrotron radiation or inverse Compton scattering of electrons. We argue that the transfer of kinetic energy of ejecta into electrons may be inefficient process and hence the total energy released by a GRB event is much larger than that emitted in soft gamma-rays, by a factor of \\sim (m_p/m_e). We show that, in this case, very strong emission of TeV gamma-rays is possible due to synchrotron radiation of protons accelerated up to \\sim 10^{21} eV, which are trapped in the magnetic field of afterglow shock and radiate their energy on an observational time scale of \\sim day. This suggests a possibility that GRBs are most energetic in TeV range and such TeV gamma-rays may be detectable from GRBs even at cosmological distances, i.e., z gives a quantitative explanation for the famous long-duration GeV photons detected from GRB940217. ...

  7. Luminescent emission of LiF: Mg, Ti exposed to UV radiation; Emision luminiscente del LiF: Mg, Ti expuesto a la radiacion UV

    Energy Technology Data Exchange (ETDEWEB)

    Estrada G, A. [Estudiante de Facultad de Ciencias, UNAM, Circuito Exterior, 04500 Mexico D.F. (Mexico); Castano M, V.M. [Centro de Fisica Aplicada y Tecnologia Avanzada, UNAM, Campus Juriquilla, Queretaro (Mexico); Cruz Z, E.; Garcia F, F. [Instituto de Ciencias Nucleares UNAM, A.P. 70-543 Mexico D.F. (Mexico)

    2002-07-01

    It was investigated the luminescent emission stimulated by heat (Tl) of LiF: Mg, Ti crystals which were exposed to UV radiation coming from a mercury lamp. Since this crystal depends on the thermal history, it has been used a thermal treatment consisting of a baking at 380 C during one hour for each reading and they were irradiated with UV. The brilliance curves between 5 and 840 minutes of exposure in the face of UV light were obtained. An important loss in the response, starting from 150 minutes of irradiation was observed. Also the relative intensity of the brilliance curve decay when the crystals being stored in darkness and room temperature conditions, which is according to the results in the literature about. (Author)

  8. Strong Correlation Between Isoprene Emission and Gross Photosynthetic Capacity During Leaf Phenology of the Tropical Tree Species Hymenaea courbaril

    Science.gov (United States)

    Kuhn, U.; Rottenberger, S.; Biesenthal, T.; Wolf, A.; Schebeske, G.; Ciccioli, P.; Kesselmeier, J.

    2004-12-01

    Composition and amount of volatile organic compound (VOC) emission of the tropical tree species Hymenaea courbaril was studied under different developmental stages at a remote Amazonian rainforest site. The different stages covered young leaves (= grown full in size, but not fully turgescent) in the end of the dry season, mature leaves in the end of dry and wet season, and senescent leaves in the end of dry season. Though the diel isoprene emissions pattern could adequately be modelled by a current isoprene algorithm, the basal emission capacity of isoprene changed considerably over the course of leaf development. The inadequacy of using one single standard emission factor to represent the VOC emission capacity of tropical vegetation for an entire seasonal cycle is obvious. A strong linear correlation between the isoprene emission capacity and the gross photosynthetic capacity (GPmax) covering all developmental stages and seasons was observed. Hence, basic leaf photosynthetic activity may offer a valuable basis to model the seasonal variation of isoprene emission, especially in tropical regions where the environmental conditions vary less than in temperate regions. Of special interest was the light dependent monoterpene emission found exclusively in the period between bud break and leave maturity. The finding of this temporary emergence of monoterpene emission may be of general interest in understanding both the ecological functions of isoprenoid production and the regulatory processes involved.

  9. Strong Photonic-Band-Gap Effect on the Spontaneous Emission in 3D Lead Halide Perovskite Photonic Crystals.

    Science.gov (United States)

    Zhou, Xue; Li, Mingzhu; Wang, Kang; Li, Huizeng; Li, Yanan; Li, Chang; Yan, Yongli; Zhao, Yongsheng; Song, Yanlin

    2018-03-25

    Stimulated emission in perovskite-embedded polymer opal structures is investigated. A polymer opal structure is filled with a perovskite, and perovskite photonic crystals are prepared. The spontaneous emission of the perovskite embedded in the polymer opal structures exhibits clear signatures of amplified spontaneous emission (ASE) via gain modulation. The difference in refractive-index contrast between the perovskite and the polymer opal is large enough for retaining photonic-crystals properties. The photonic band gap has a strong effect on the fluorescence emission intensity and lifetime. The stimulated emission spectrum exhibits a narrow ASE rather than a wide fluorescence peak in the thin film. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Luminescence of tartrate bridged dinuclear 2,2'-bipyridine platinum(ii) complexes: emission color controlled by intra- and inter-molecular interactions in the solid state.

    Science.gov (United States)

    Ohno, Keiji; Tanuma, Honami; Kusano, Yukiko; Kaizaki, Sumio; Nagasawa, Akira; Fujihara, Takashi

    2017-06-13

    Novel dinuclear Pt II complexes with a chiral (l-) and an achiral (meso-) tartrate [{Pt II (bpy)} 2 (μ-x-tart)] (bpy: 2,2'-bipyridine; tartH 2 2- : tartrate; x = l (1), meso (2)) and with a racemic (dl-) tartrate [{Pt II (bpy)} 2 (μ-d-tart)][{Pt II (bpy)} 2 (μ-l-tart)] (3) were synthesized, and the influence of their stereochemistry on their molecular and crystal structures affecting their luminescence was discussed. Effects of the dinuclearity on the structures and luminescence were revealed by comparison with those of a novel racemic mononuclear complex [Pt II (bpy)(d-tartH 2 )][Pt II (bpy)(l-tartH 2 )] (4). The X-ray crystallography showed the crystallization of 1 in two polymorphs, namely monoclinic 3[1·6H 2 O] (1α) and triclinic 2[1·6H 2 O] (1β), and those of other complexes in monoclinic hydrate crystals 2·12.5H 2 O, 3·4H 2 O, and 4·H 2 O. The chiral complexes in 1α, 1β, and 3·4H 2 O showed clamshell-like structures with Pt-Pt and π-π interactions, while the achiral complex in 2·12.5H 2 O displayed a twisted form without intramolecular interactions. The complexes in 1α were assembled in a right-handed helical arrangement through significant Pt-Pt interactions, and those in 1β and 3·4H 2 O were stacked in one-dimensional columns through significant and slight π-π interactions, respectively. The complex in 2·12.5H 2 O constructed an intermolecular dimer through Pt-Pt interactions with its adjacent complex. The crystal structure of 4·H 2 O displayed a three-dimensional network architecture through π-π interactions and hydrogen bonding. These crystals exhibited luminescence depending on their molecular and crystal structures (λ max nm = 535 (4·H 2 O), 569 (3·4H 2 O), 621 (2·12.5H 2 O), 649 (1β), and 656 (1α)). The formations of intermolecular dimers and clamshell-like structures through Pt-Pt interactions in 2·12.5H 2 O and in 3·4H 2 O, respectively, lead to red-shifts in emissions compared to 4·H 2 O, and further low

  11. Strong mutagenic effects of diesel engine emissions using vegetable oil as fuel.

    Science.gov (United States)

    Bünger, Jürgen; Krahl, Jürgen; Munack, Axel; Ruschel, Yvonne; Schröder, Olaf; Emmert, Birgit; Westphal, Götz; Müller, Michael; Hallier, Ernst; Brüning, Thomas

    2007-08-01

    Diesel engine emissions (DEE) are classified as probably carcinogenic to humans. In recent years every effort was made to reduce DEE and their content of carcinogenic and mutagenic polycyclic aromatic compounds. Since 1995 we observed an appreciable reduction of mutagenicity of DEE driven by reformulated or newly designed fuels in several studies. Recently, the use of rapeseed oil as fuel for diesel engines is rapidly growing among German transportation businesses and agriculture due to economic reasons. We compared the mutagenic effects of DEE from two different batches of rapeseed oil (RSO) with rapeseed methyl ester (RME, biodiesel), natural gas derived synthetic fuel (gas-to-liquid, GTL), and a reference diesel fuel (DF). The test engine was a heavy-duty truck diesel running the European Stationary Cycle. Particulate matter from the exhaust was sampled onto PTFE-coated glass fibre filters and extracted with dichloromethane in a soxhlet apparatus. The gas phase constituents were sampled as condensates. The mutagenicity of the particle extracts and the condensates was tested using the Salmonella typhimurium/mammalian microsome assay with tester strains TA98 and TA100. Compared to DF the two RSO qualities significantly increased the mutagenic effects of the particle extracts by factors of 9.7 up to 59 in tester strain TA98 and of 5.4 up to 22.3 in tester strain TA100, respectively. The condensates of the RSO fuels caused an up to factor 13.5 stronger mutagenicity than the reference fuel. RME extracts had a moderate but significant higher mutagenic response in assays of TA98 with metabolic activation and TA100 without metabolic activation. GTL samples did not differ significantly from DF. In conclusion, the strong increase of mutagenicity using RSO as diesel fuel compared to the reference DF and other fuels causes deep concern on future usage of this biologic resource as a replacement of established diesel fuels.

  12. Spectroscopic studies on the lanthanide sensitized luminescence and chemiluminescence properties of fluoroquinolone with different structure

    Science.gov (United States)

    Sun, Chunyan; Ping, Hong; Zhang, Minwei; Li, Hongkun; Guan, Fengrui

    2011-11-01

    Lanthanide sensitized luminescence and chemiluminescence (CL) are of great importance because of the unique spectral properties, such as long lifetime, large Stokes shifts, and narrow emission bands characteristic to lanthanide ions (Ln 3+). With the fluoroquinolone (FQ) compounds including enoxacin (ENX), norfloxacin (NFLX), lomefloxacin (LMFX), fleroxacin (FLRX), ofloxacin (OFLX), rufloxacin (RFX), gatifloxacin (GFLX) and sparfloxacin (SPFX), the luminescence and CL properties of Tb 3+-FQ and Eu 3+-FQ complexes have been investigated in this contribution. Ce 4+-SO 32- in acidic conditions was taken as the CL system and sensitized CL intensities of Tb 3+-FQ and Eu 3+-FQ complexes were determined by flow-injection analysis. The luminescence and CL spectra of Tb 3+-FQ complexes show characteristic peaks of Tb 3+ at 490 nm, 545 nm, 585 nm and 620 nm. Complexes of Tb 3+-ENX, Tb 3+-NFLX, Tb 3+-LMFX and Tb 3+-FLRX display relatively strong emission intensity compared with Tb 3+-OFLX, Tb 3+-RFX, Tb 3+-GFLX and Tb 3+-SPFX. Quite weak peaks with unique characters of Eu 3+ at 590 nm and 617 nm appear in the luminescence and CL spectra of Eu 3+-ENX, but no notable sensitized luminescence and CL of Eu 3+ could be observed when Eu 3+ is added into other FQ. The distinct differences on emission intensity of Tb 3+-FQ and Eu 3+-FQ might originate from the different energy gap between the triplet levels of FQ and the excited levels of the Ln 3+. The different sensitized luminescence and CL signals among Tb 3+-FQ complexes could be attributed to different optical properties and substituents of these FQ compounds. The detailed mechanism involved in the luminescence and CL properties of Tb 3+-FQ and Eu 3+-FQ complexes has been investigated by analyzing the luminescence and CL spectra, quantum yields, and theoretical calculation results.

  13. Unprecedentedly strong and narrow electromagnetic emissions stimulated by high-frequency radio waves in the ionosphere.

    Science.gov (United States)

    Norin, L; Leyser, T B; Nordblad, E; Thidé, B; McCarrick, M

    2009-02-13

    Experimental results of secondary electromagnetic radiation, stimulated by high-frequency radio waves irradiating the ionosphere, are reported. We have observed emission peaks, shifted in frequency up to a few tens of Hertz from radio waves transmitted at several megahertz. These emission peaks are by far the strongest spectral features of secondary radiation that have been reported. The emissions are attributed to stimulated Brillouin scattering, long predicted but hitherto never unambiguously identified in high-frequency ionospheric interaction experiments. The experiments were performed at the High-Frequency Active Auroral Research Program (HAARP), Alaska, USA.

  14. Zinc-coordinated MOFs complexes regulated by hydrogen bonds: Synthesis, structure and luminescence study toward broadband white-light emission

    Science.gov (United States)

    Duan, Hui; Dan, Wenyan; Fang, Xiangdong

    2018-04-01

    Two new compounds, namely {[Zn(apc)2]·H2O}n (1) and [Zn(apc)2(H2O)2] (2), have been designed and synthesized with a multi-functional ligand 2-aminopyrimidine-5-carboxylic acid (Hapc). Both compounds were characterized by single crystal X-ray diffraction analysis (SC-XRD), elemental analysis (EA), infrared spectroscopy (IR), and thermogravimetric analysis (TG). In solid-state structures, 1 features a two-fold interpenetrating pillared-layer 3D framework with point symbol {83}2{86}, referring to tfa topology; while 2 exhibits a 3D framework based on super unit of Zn(apc)2(H2O)2 interconnected via hydrogen bonds. Furthermore, the luminescent properties of 1 and 2 were discussed.

  15. Controlling light emission in luminescent solar concentrators through use of dye molecules aligned in a planar manner by liquid crystals

    Energy Technology Data Exchange (ETDEWEB)

    Verbunt, Paul P.C.; Kaiser, Anton; Hermans, Ko; Broer, Dirk J.; Debije, Michael G. [Polymer Technology Chemical Engineering and Chemistry, Eindhoven University of Technology (Netherlands); Bastiaansen, Cees W.M. [Polymer Technology Chemical Engineering and Chemistry, Eindhoven University of Technology (Netherlands); School of Engineering and Materials Science, Queen Mary University of London (United Kingdom)

    2009-09-09

    A luminescent solar concentrator (LSC) is a potential low-cost enhancement of the standard large-area silicon photovoltaic panels for the generation of electricity from sunlight. In this work, guest-host systems are investigated using anisotropic fluorescent dyes and liquid crystal mesogens to control the direction of emitted light in the LSC. It is determined that up to 30% more light is emitted from the edge of an LSC waveguide with planar dye alignment parallel to the alignment direction than from any edge of an LSC with no alignment (isotropic). The aligned samples continue to show dichroic performance after additions of both edge mirrors and rear scattering layer. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  16. Excited-state intramolecular proton transfer (ESIPT) emission of hydroxyphenylimidazopyridine: computational study on enhanced and polymorph-dependent luminescence in the solid state.

    Science.gov (United States)

    Shigemitsu, Yasuhiro; Mutai, Toshiki; Houjou, Hirohiko; Araki, Koji

    2012-12-13

    Although 2-(2'-hydroxyphenyl)imidazo[1,2-a]pyridine (HPIP) is only weakly fluorescent in solution, two of its crystal polymorphs in which molecules are packed as stacked pairs and in nearly coplanar conformation exhibit bright excited-state intramolecular proton transfer (ESIPT) luminescence of different colors (blue-green and yellow). In order to clarify the enhanced and polymorph-dependent luminescence of HPIP in the solid state, the potential energy surfaces (PESs) of HPIP in the ground (S(0)) and excited (S(1)) states were analyzed computationally by means of ab initio quantum chemical calculations. The calculations reproduced the experimental photophysical properties of HPIP in solution, indicating that the coplanar keto form in the first excited (S(1)) state smoothly approaches the S(0)/S(1) conical intersection (CI) coupled with the twisting motion of the central C-C bond. The S(1)-S(0) energy gap of the keto form became sufficiently small at the torsion angle of 60°, and the corresponding CI point was found at 90°. Since a minor role of the proximity effect was indicated experimentally and theoretically, the observed emission enhancement of the HPIP crystals was ascribed to the following two factors: (1) suppression of efficient radiationless decay via the CI by fixing the torsion angle at the nearly coplanar conformation of the molecules in the crystals and (2) inhibition of excimer formation resulting from the lower excited level of the S(1)-keto state compared to the S(0)-S(1) excitation energy in the enol form. However, the fluorescence color difference between the two crystal polymorphs having slightly different torsion angles was not successfully reproduced, even at the MS-CASPT2 level of theory.

  17. Kinetics of infrared stimulated luminescence from feldspars

    DEFF Research Database (Denmark)

    Jain, Mayank; Sohbati, Reza; Guralnik, Benny

    2015-01-01

    thermal and optical, of the infrared stimulated luminescence signal from feldspar. Based on the application of this model, it is concluded that different infra-red stimulated luminescence emissions (UV, blue, yellow and far-red) follow the same kinetics, and, therefore, involve participation of the same...... in feldspar. © 2015 Elsevier Ltd. All rights reserved....

  18. Sequential Growth of Uniform β-NaYF4@β-NaLnF4 (Ln = Y, Lu, Yb Microcrystals with Luminescent Properties of Multicolor Tuning and Dual-Mode Emission

    Directory of Open Access Journals (Sweden)

    Dandan Ju

    2017-12-01

    Full Text Available We synthesized the uniform core-shell microstructured compounds with hexagonal phase NaYF4:Er/Yb microrods as the core and hexagonal phase NaLnF4 (NaYbF4, NaLuF4:Yb/Tm, NaYF4:Yb/Er, NaYF4:Eu as the shell based on the hydrothermal reaction. These microscale core-shell structures provided a platform for the spatially confining optical process while possessing high luminescence efficiency. The thickness of the shell could be controlled by adjusting the amounts of shell precursor, which significantly affected the intensity of the shell dopant ions emission and the emission color of core-shell upconversion luminescence (UCL. The uniform NaYF4@NaLnF4 (Ln = Y, Lu, Yb microrods, with a series of rare-earth ions doped into the core and shell layer at various doping concentrations, achieved color-tuning of the upconversion (UC emission and dual-mode emission at the single-microcrystal level, thus allowing the efficient utilization of core-shell microcrystals in the photonics and security labeling. This study suggests a new class of luminescent materials in the microscopic field.

  19. Resonance-shifting luminescent solar concentrators

    Energy Technology Data Exchange (ETDEWEB)

    Giebink, Noel Christopher; Wiederrecht, Gary P; Wasielewski, Michael R

    2014-09-23

    An optical system and method to overcome luminescent solar concentrator inefficiencies by resonance-shifting, in which sharply directed emission from a bi-layer cavity into a glass substrate returns to interact with the cavity off-resonance at each subsequent reflection, significantly reducing reabsorption loss en route to the edges. In one embodiment, the system comprises a luminescent solar concentrator comprising a transparent substrate, a luminescent film having a variable thickness; and a low refractive index layer disposed between the transparent substrate and the luminescent film.

  20. Resonance-shifting luminescent solar concentrators

    Energy Technology Data Exchange (ETDEWEB)

    Giebink, Noel Christopher; Wiederrecht, Gary P.; Wasielewski, Michael R.

    2018-01-23

    An optical system and method to overcome luminescent solar concentrator inefficiencies by resonance-shifting, in which sharply directed emission from a bi-layer cavity into a glass substrate returns to interact with the cavity off-resonance at each subsequent reflection, significantly reducing reabsorption loss en route to the edges. In one embodiment, the system comprises a luminescent solar concentrator comprising a transparent substrate, a luminescent film having a variable thickness; and a low refractive index layer disposed between the transparent substrate and the luminescent film.

  1. Host-sensitized luminescence of Dy3+, Pr3+, Tb3+ in polycrystalline CaIn2O4 for field emission displays

    International Nuclear Information System (INIS)

    Liu Xiaoming; Pang Ran; Li Qin; Lin Jun

    2007-01-01

    CaIn 2 O 4 :Dy 3+ /Pr 3+ /Tb 3+ blue-white/green/green phosphors were prepared by the Pechini sol-gel process. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), diffuse reflectance, photoluminescence (PL) and cathodoluminescence (CL) spectra as well as lifetimes were utilized to characterize the samples. The XRD results reveal that the samples begin to crystallize at 800 deg. C and pure CaIn 2 O 4 phase can be obtained after annealing at 900 deg. C. The FE-SEM images indicate that the CaIn 2 O 4 :Dy 3+ , CaIn 2 O 4 :Pr 3+ and CaIn 2 O 4 :Tb 3+ samples consist of spherical grains with size around 200-400 nm. Under the excitation of ultraviolet light and low-voltage electron beams (1-5 kV), the CaIn 2 O 4 :Dy 3+ , CaIn 2 O 4 :Pr 3+ and CaIn 2 O 4 :Tb 3+ phosphors show the characteristic emissions of Dy 3+ ( 4 F 9/2 - 6 H 15/2 and 4 F 9/2 - 6 H 13/2 transitions, blue-white), Pr 3+ ( 3 P 0 - 3 H 4 , 1 D 2 - 3 H 4 and 3 P 1 - 3 H 5 transitions, green) and Tb 3+ ( 5 D 4 - 7 F 6,5,4,3 transitions, green), respectively. All the luminescence is resulted from an efficient energy transfer from the CaIn 2 O 4 host lattice to the doped Dy 3+ , Pr 3+ and Tb 3+ ions, and the corresponding luminescence mechanisms have been proposed. - Graphical abstract: The CaIn 2 O 4 :Dy 3+ /Pr 3+ /Tb 3+ blue-white/green/green phosphors were prepared by the Pechini sol-gel process. Under the excitation of ultraviolet light and low-voltage electron beams (1-5 kV), the CaIn 2 O 4 :Dy 3+ , CaIn 2 O 4 :Pr 3+ and CaIn 2 O 4 :Tb 3+ phosphors show the characteristic emissions of Dy 3+ ( 4 F 9/2 - 6 H 15/2 and 4 F 9/2 - 6 H 13/2 transitions, blue-white), Pr 3+ ( 3 P 0 - 3 H 4 , 1 D 2 - 3 H 4 and 3 P 1 - 3 H 5 transitions, green) and Tb 3+ ( 5 D 4 - 7 F 6,5,4,3 transitions, green), respectively. All the luminescence is resulted from an efficient energy transfer from the CaIn 2 O 4 host lattice to the doped Dy 3+ , Pr 3+ and Tb 3+ ions

  2. Uranyl fluoride luminescence in acidic aqueous solutions

    International Nuclear Information System (INIS)

    Beitz, J.V.; Williams, C.W.

    1996-01-01

    Luminescence emission spectra and decay rates are reported for uranyl species in acidic aqueous solutions containing HF or added NaF. The longest luminescence lifetime, 0.269 ± 0.006 ms, was observed from uranyl in 1 M HF + 1 M HClO 4 at 296 K and decreased with increasing temperature. Based on a luminescence dynamics model that assumes equilibrium among electronically excited uranyl fluoride species and free fluoride ion, this long lived uranyl luminescence in aqueous solution is attributed primarily to UO 2 F 2 . Studies on the effect of added LiNO 3 or Na 2 WO 4 ·2H 2 O showed relatively weak quenching of uranyl fluoride luminescence which suggests that high sensitivity determination of the UF 6 content of WF 6 gas should be feasible via uranyl luminescence analysis of hydrolyzed gas samples of impure WF 6

  3. Paradigms and challenges for bioapplication of rare earth upconversion luminescent nanoparticles: small size and tunable emission/excitation spectra.

    Science.gov (United States)

    Sun, Ling-Dong; Wang, Ye-Fu; Yan, Chun-Hua

    2014-04-15

    Rare earth (RE) materials, which are excited in the ultraviolet and emit in the visible light spectrum, are widely used as phosphors for lamps and displays. In the 1960's, researchers reported an abnormal emission phenomenon where photons emitted from a RE element carried more energy than those absorbed, owing to the sequential energy transfer between two RE ions--Yb(3+)-sensitized Er(3+) or Tm(3+)--in the solid state. After further study, researchers named this abnormal emission phenomenon upconversion (UC) emission. More recent approaches take advantage of solution-based synthesis, which allows creation of homogenous RE nanoparticles (NPs) with controlled size and structure that are capable of UC emission. Such nanoparticles are useful for many applications, especially in biology. For these applications, researchers seek small NPs with high upconversion emission intensity. These UCNPs have the potential to have multicolor and tunable emissions via various activators. A vast potential for future development remains by developing molecular antennas and energy transfer within RE ions. We expect UCNPs with optimized spectra behavior to meet the increasing demand of potential applications in bioimaging, biological detection, and light conversion. This Account focuses on efforts to control the size and modulate the spectra of UCNPs. We first review efforts in size control. One method is careful control of the synthesis conditions to manipulate particle nucleation and growth, but more recently researchers have learned that the doping conditions can affect the size of UCNPs. In addition, constructing homogeneous core/shell structures can control nanoparticle size by adjusting the shell thickness. After reviewing size control, we consider how diverse applications impose different requirements on excitation and/or emission photons and review recent developments on tuning of UC spectral profiles, especially the extension of excitation/emission wavelengths and the adjustment

  4. Temperature lags of luminescence measurements in a commercial luminescence reader

    Energy Technology Data Exchange (ETDEWEB)

    Kitis, George [Aristotle University of Thessaloniki, Nuclear Physics Laboratory, 54124 Thessaloniki (Greece); Kiyak, Nafiye G. [ISIK University, Faculty of Science and Arts, Physics Department, Sile, 34980 Istanbul (Turkey); Polymeris, George S., E-mail: gspolymeris@ankara.edu.tr [Ankara University, Institute of Nuclear Sciences, Beşevler, 06100 Ankara (Turkey)

    2015-09-15

    The temperature recorded in thermoluminescence and optically stimulated luminescence equipments is not the temperature of the sample but that of the heating element on which the thermocouple is attached. Depending upon the rate of heating, a temperature difference appears between the samples and the heating element, termed as temperature lag, which could have serious effects on the curve shapes and trapping parameters. In the present work the temperature lag effect is studied in a newly developed luminescence equipment measuring both thermoluminescence and optically stimulated luminescence. It is found that the temperature lag could be large for heating rates above 2 K/s and it is strongly dependent upon the sample holder. A simple approximation method is proposed in order to both predict as well as correct for temperature lag effects in luminescence measurements.

  5. Measurement of fluorescence emission spectrum of few strongly driven atoms using an optical nanofiber.

    Science.gov (United States)

    Das, Manoj; Shirasaki, A; Nayak, K P; Morinaga, M; Le Kien, Fam; Hakuta, K

    2010-08-02

    We show that the fluorescence emission spectrum of few atoms can be measured by using an optical nanofiber combined with the optical heterodyne and photon correlation spectroscopy. The observed fluorescence spectrum of the atoms near the nanofiber shows negligible effects of the atom-surface interaction and agrees well with the Mollow triplet spectrum of free-space atoms at high excitation intensity.

  6. A Strong Limit on the Very-high-energy Emission from GRB 150323A

    Science.gov (United States)

    Abeysekara, A. U.; Archer, A.; Benbow, W.; Bird, R.; Brose, R.; Buchovecky, M.; Bugaev, V.; Connolly, M. P.; Cui, W.; Errando, M.; Falcone, A.; Feng, Q.; Finley, J. P.; Flinders, A.; Fortson, L.; Furniss, A.; Gillanders, G. H.; Hütten, M.; Hanna, D.; Hervet, O.; Holder, J.; Hughes, G.; Humensky, T. B.; Johnson, C. A.; Kaaret, P.; Kar, P.; Kelley-Hoskins, N.; Kertzman, M.; Kieda, D.; Krause, M.; Krennrich, F.; Lang, M. J.; Lin, T. T. Y.; Maier, G.; McArthur, S.; Moriarty, P.; Mukherjee, R.; O’Brien, S.; Ong, R. A.; Park, N.; Perkins, J. S.; Petrashyk, A.; Pohl, M.; Popkow, A.; Pueschel, E.; Quinn, J.; Ragan, K.; Reynolds, P. T.; Richards, G. T.; Roache, E.; Rulten, C.; Sadeh, I.; Santander, M.; Sembroski, G. H.; Shahinyan, K.; Tyler, J.; Wakely, S. P.; Weiner, O. M.; Weinstein, A.; Wells, R. M.; Wilcox, P.; Wilhelm, A.; Williams, D. A.; Zitzer, B.; VERITAS Collaboration; Vurm, Indrek; Beloborodov, Andrei

    2018-04-01

    On 2015 March 23, the Very Energetic Radiation Imaging Telescope Array System (VERITAS) responded to a Swift-Burst Alert Telescope (BAT) detection of a gamma-ray burst, with observations beginning 270 s after the onset of BAT emission, and only 135 s after the main BAT emission peak. No statistically significant signal is detected above 140 GeV. The VERITAS upper limit on the fluence in a 40-minute integration corresponds to about 1% of the prompt fluence. Our limit is particularly significant because the very-high-energy (VHE) observation started only ∼2 minutes after the prompt emission peaked, and Fermi-Large Area Telescope observations of numerous other bursts have revealed that the high-energy emission is typically delayed relative to the prompt radiation and lasts significantly longer. Also, the proximity of GRB 150323A (z = 0.593) limits the attenuation by the extragalactic background light to ∼50% at 100–200 GeV. We conclude that GRB 150323A had an intrinsically very weak high-energy afterglow, or that the GeV spectrum had a turnover below ∼100 GeV. If the GRB exploded into the stellar wind of a massive progenitor, the VHE non-detection constrains the wind density parameter to be A ≳ 3 × 1011 g cm‑1, consistent with a standard Wolf–Rayet progenitor. Alternatively, the VHE emission from the blast wave would be weak in a very tenuous medium such as the interstellar medium, which therefore cannot be ruled out as the environment of GRB 150323A.

  7. Near-infrared luminescence in perovskite BaSnO3 epitaxial films

    Science.gov (United States)

    Takashima, Hiroshi; Inaguma, Yoshiyuki

    2017-08-01

    Strong near-infrared luminescence under ultraviolet excitation was obtained in epitaxially grown BaSnO3 perovskite films. The films were grown on SrTiO3 (001) substrates by pulsed-laser deposition, and the crystallinity of the epitaxial growth was confirmed by X-ray diffraction and reflected high-energy electron diffraction. Near-infrared luminescence of the as-grown film showed a broad emission peak centered at 905 nm. The transparencies of the double-side-polished substrate with and without the film were about 70% at around 550 nm, suggesting that the transparency of the film itself is close to 100%. The preparation of epitaxial thin films with a strong near-infrared luminescence and a high transparency may open up applications for wavelength conversion in solar cells for realizing a higher efficiency.

  8. Point defects and the blue emission in fired quartz at high doses: a comparative luminescence and EPR study

    Energy Technology Data Exchange (ETDEWEB)

    Woda, C.; Schilles, T.; Riser, U.; Mangini, A.; Wagner, G.A

    2002-07-01

    The dose response of the 375 deg/ C, 470 nm TL peak in fired quartz is studied by using thermoluminescence emission spectra and monochromatic glow curves. The blue emission displays a significant sensitivity increase for doses in excess of 1000 Gy, subsequent saturation at 16 kGy and a pre-dose effect over the entire dose range. Comparison with the growth of the known electron paramagnetic resonance centres and radioluminescence emission spectra indicates that the [AlO{sub 4}] centre is the recombination site for the blue emission, whereas the electron trap remains unknown. The sensitivity change seems to be linked to the dose-induced reduction of the [GeO{sub 4}/Li] centre. Possible mechanisms for the observed dose response are discussed. (author)

  9. Thermal dependence of luminescence lifetimes and radioluminescence in quartz

    Energy Technology Data Exchange (ETDEWEB)

    Pagonis, V., E-mail: vpagonis@mcdaniel.edu [McDaniel College, Physics Department, Westminster, MD 21157 (United States); Chithambo, M.L. [Department of Physics and Electronics, Rhodes University, PO BOX 94, Grahamstown 6140 (South Africa); Chen, R. [Raymond and Beverly Sackler School of Physics and Astronomy, Tel-Aviv University, Tel-Aviv 69978 (Israel); Chruścińska, A. [Institute of Physics, Nicholas Copernicus University, 87-100 Toruń (Poland); Fasoli, M. [Department of Materials Science, University of Milano-Bicocca, Via Cozzi 53, 20125 Milano (Italy); Li, S.H. [Department of Earth Sciences, The University of Hong Kong (Hong Kong); Martini, M. [Department of Materials Science, University of Milano-Bicocca, Via Cozzi 53, 20125 Milano (Italy); Ramseyer, K. [Institut für Geologie, Baltzerstrasse 1-3, 3012 Bern (Switzerland)

    2014-01-15

    carried out using a total of seven emission bands between 1.5 and 4.5 eV, and the behavior of these bands was examined as a function of the annealing temperature. An emission band at ∼3.44 eV (360 nm) was found to be strongly enhanced when the annealing temperature was increased to 500 °C, and this band underwent a significant reduction in intensity with further increase in temperature. Furthermore, a new emission band at ∼3.73 eV (330 nm) became apparent for annealing temperatures in the range 600–700 °C. These new experimental results are discussed within the context of the model presented in this paper. -- Highlights: • Analytical model for luminescence lifetimes in quartz with two luminescence centers. • Results from model are in agreement with published experimental data. • Describes variation of lifetimes with annealing and stimulation temperature. • New radioluminescence measurements fitted seven emission bands 1.5–4.5 eV.

  10. Field emission properties and strong localization effect in conduction mechanism of nanostructured perovskite LaNiO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Kamble, Ramesh B., E-mail: rbk.physics@coep.ac.in [Department of Physics, Indian Institute of Science, Bangalore 560012, Karnataka (India); Department of Physics, College of Engineering, Pune 411005, Maharashtra (India); Tanty, Narendra; Patra, Ananya; Prasad, V. [Department of Physics, Indian Institute of Science, Bangalore 560012, Karnataka (India)

    2016-08-22

    We report the potential field emission of highly conducting metallic perovskite lanthanum nickelate (LaNiO{sub 3}) from the nanostructured pyramidal and whisker shaped tips as electron emitters. Nano particles of lanthanum nickelate (LNO) were prepared by sol-gel route. Structural and morphological studies have been carried out. Field emission of LNO exhibited high emission current density, J = 3.37 mA/cm{sup 2} at a low threshold electric field, E{sub th} = 16.91 V/μm, obeying Fowler–Nordheim tunneling. The DC electrical resistivity exhibited upturn at 11.6 K indicating localization of electron at low temperature. Magnetoresistance measurement at different temperatures confirmed strong localization in nanostructured LNO obeying Anderson localization effect at low temperature.

  11. luminescence properties

    Indian Academy of Sciences (India)

    Gd3+, Tb3+ and Lu3+ in MTiO3 (M = Mg and Sr) luminescence properties. 1085. Table 4. Phosphorescence properties of phosphors. Radiation. Radiation. Radiation. Undoped–doped. Phosphors intensity/a.u. colour wavelength (nm) radiation difference. MgTiO3. 600. Yellow. 514. –. MgTiO3:1 %Tb3+. 415. Yellow. 514.

  12. Silver Nanoshell Plasmonically Controlled Emission of Semiconductor Quantum Dots in the Strong Coupling Regime.

    Science.gov (United States)

    Zhou, Ning; Yuan, Meng; Gao, Yuhan; Li, Dongsheng; Yang, Deren

    2016-04-26

    Strong coupling between semiconductor excitons and localized surface plasmons (LSPs) giving rise to hybridized plexciton states in which energy is coherently and reversibly exchanged between the components is vital, especially in the area of quantum information processing from fundamental and practical points of view. Here, in photoluminescence spectra, rather than from common extinction or reflection measurements, we report on the direct observation of Rabi splitting of approximately 160 meV as an indication of strong coupling between excited states of CdSe/ZnS quantum dots (QDs) and LSP modes of silver nanoshells under nonresonant nanosecond pulsed laser excitation at room temperature. The strong coupling manifests itself as an anticrossing-like behavior of the two newly formed polaritons when tuning the silver nanoshell plasmon energies across the exciton line of the QDs. Further analysis substantiates the essentiality of high pump energy and collective strong coupling of many QDs with the radiative dipole mode of the metallic nanoparticles for the realization of strong coupling. Our finding opens up interesting directions for the investigation of strong coupling between LSPs and excitons from the perspective of radiative recombination under easily accessible experimental conditions.

  13. The early-type strong emission-line supergiants of the Magellanic Clouds - A spectroscopic zoology

    Science.gov (United States)

    Shore, S. N.; Sanduleak, N.

    1984-01-01

    The results of a spectroscopic survey of 21 early-type extreme emission line supergiants of the Large and Small Magellanic Clouds using IUE and optical spectra are presented. The combined observations are discussed and the literature on each star in the sample is summarized. The classification procedures and the methods by which effective temperatures, bolometric magnitudes, and reddenings were assigned are discussed. The derived reddening values are given along with some results concerning anomalous reddening among the sample stars. The derived mass, luminosity, and radius for each star are presented, and the ultraviolet emission lines are described. Mass-loss rates are derived and discussed, and the implications of these observations for the evolution of the most massive stars in the Local Group are addressed.

  14. Ion irradiation effect of alumina and its luminescence

    Energy Technology Data Exchange (ETDEWEB)

    Aoki, Yasushi; Yamamoto, Shunya; Naramoto, Hiroshi [Japan Atomic Energy Research Inst., Takasaki, Gunma (Japan). Takasaki Radiation Chemistry Research Establishment; My, N.T.

    1997-03-01

    The luminescence spectra of single crystalline alpha-alumina and ruby which has 0.02% of Cr{sub 2}O{sub 3} as a impurity, induced by 200 keV He{sup +} and Ar{sup +} irradiation were measured at room temperature as a function of irradiation dose. The analysis of the measured spectra showed the existence of three main luminescence features in the wavelength region of 250 to 350 nm, namely anionic color centers, F-center at 411 nm and F{sup +}-center at 330 nm and a band observed around 315 nm. As alpha-alumina was irradiated with He{sup +}, F-center and F{sup +}-center luminescence grew and decayed, but the behaviors of those were different from each other. It seems that a concentration quenching occurred on the F-center luminescence in the dose range above 1x10{sup 14} He/cm{sup 2}. Furthermore, F-center luminescence was strongly suppressed in ruby, compared with that in alumina. On the other hand, the luminescence band around 315 nm appeared only in the early stage of irradiation and did not show its growth part. The dose dependent behavior was similar to that of Cr{sup 3+} emission at 695 nm (R-line) in ruby in both cases of He{sup +} and Ar{sup +} irradiation. Based on the experimental results mentioned above, the processes of defect formation and excitation in alumina in the early stage of ion irradiation will be discussed. (author)

  15. Design, synthesis and characterization of a highly luminescent Eu-complex monomer featuring thenoyltrifluoroacetone and 5-acryloxyethoxymethyl-8-hydroxyquinoline

    Energy Technology Data Exchange (ETDEWEB)

    Xu Cunjin [State Key Laboratory of Chemical Engineering, Department of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027 (China); College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 310036 (China); Li Bogeng, E-mail: bgli@zju.edu.cn [State Key Laboratory of Chemical Engineering, Department of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027 (China); Wan Jintao; Bu Zhiyang [State Key Laboratory of Chemical Engineering, Department of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027 (China)

    2011-08-15

    A multi-functional ligand, 5-acryloxyethoxymethyl-8-hydroxyquinoline (Hamq), was synthesized, which contained a polymerizable C=C double bond for the copolymerization with other vinyl monomers and acted as photon antenna able to transfer energy to Eu{sup 3+} ions effectively. The triplet state energy of Hamq was determined to be 22,370 cm{sup -1} via the phosphorescence spectra of Hamq and its gadolinium complex. The title complex monomer Eu(tta){sub 2}(amq) was prepared by coordination reaction of Hamq with europium isopropoxide and 2-thenoyltrifluoroacetone (Htta) in dry organic solvents under argon atmosphere and characterized by elemental analysis and IR spectrum. The photophysical properties of the complex were studied in detail with UV-vis, luminescence spectra, luminescence lifetime and quantum yield. The complex exhibited nearly monochromatic red emission at 612 nm, a remarkable luminescence quantum yield at room temperature (30.6%) upon ligand excitation and a long {sup 5}D{sub 0} lifetime (389 {mu}s), which indicated that the ligand Hamq could sensitize the luminescence of Eu(III) ion efficiently in Eu(tta){sub 2}(amq), resulting in a strong luminescence of its copolymer poly[MMA-co-Eu(TTA){sub 2}(amq)] under UV excitation. The excellent luminescence properties of the complex made it not only a promising light-conversion molecular device but also an excellent luminescent monomer. - Highlights: >iWe designed and synthesized a highly luminescent Eu-complex monomer. > Quantum yield and lifetime of the complex are 30.6% and 389 {mu}s, respectively. > Excellent luminescence of the complex made it an excellent luminescent monomer.

  16. Metal-enhanced luminescence: Current trend and future perspectives- A review

    Energy Technology Data Exchange (ETDEWEB)

    Ranjan, Rajeev [Laboratory of Bioluminescent Biotechnologies, Department of Biophysics, Institute of Fundamental Biology and Biotechnology, Siberian Federal University, 79 Svobodny Prospect, Krasnoyarsk 660041 (Russian Federation); Esimbekova, Elena N., E-mail: esimbekova@yandex.ru [Laboratory of Bioluminescent Biotechnologies, Department of Biophysics, Institute of Fundamental Biology and Biotechnology, Siberian Federal University, 79 Svobodny Prospect, Krasnoyarsk 660041 (Russian Federation); Institute of Biophysics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok 50/50, Krasnoyarsk 660036 (Russian Federation); Kirillova, Maria A. [Laboratory of Bioluminescent Biotechnologies, Department of Biophysics, Institute of Fundamental Biology and Biotechnology, Siberian Federal University, 79 Svobodny Prospect, Krasnoyarsk 660041 (Russian Federation); Kratasyuk, Valentina A. [Laboratory of Bioluminescent Biotechnologies, Department of Biophysics, Institute of Fundamental Biology and Biotechnology, Siberian Federal University, 79 Svobodny Prospect, Krasnoyarsk 660041 (Russian Federation); Institute of Biophysics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok 50/50, Krasnoyarsk 660036 (Russian Federation)

    2017-06-08

    Optically enhanced biosensing strategies are prerequisites for developing miniature and highly sensitive multiplexed analytical platforms. Such smart biosensing systems are highly promising for use in the fields of biomedicine and environmental monitoring. Optical signal enhancement during bioassays is attributed to the complex opto-electronic interactions of incoming photonic signals at the nanomaterial interface. Research on the use of metals other than gold and silver for such purposes tends to extend the spectral window to observe luminescence enhancement effects. Such manifold increase in luminescence may be explained by the principles of plasmon coupling, directional emission led high collection efficiency, Rayleigh scattering and related opto-electronic events. The present review begins with a mechanistic description of important phenomena associated with metal-induced luminescence enhancement, particularly focusing on the origin of metal-enhanced luminescence. This review further analyses the hybrid nanostructure capabilities responsible for maintaining unique opto-electronic properties during bio-functionalisation. Current research trends in this area, future scope of this field for designing useful bioassays and concluding remarks are then discussed. - Highlights: • Nanomaterials significantly differ from their bulk counterparts. • Strong and pronounced photophysical effects at the metal surface provide opportunities for designing novel biosensors. • Metal-enhanced luminescence increases the quantum yield of luminescent reactions. • Under optimal conditions, plasmon coupling enhances the optical effects at the nanometal surface.

  17. Can we bet on negative emissions to achieve the 2°C target even under strong carbon cycle feedbacks?

    Science.gov (United States)

    Tanaka, K.; Yamagata, Y.; Yokohata, T.; Emori, S.; Hanaoka, T.

    2015-12-01

    Negative emission technologies such as Bioenergy with Carbon dioxide Capture and Storage (BioCCS) play an ever more crucial role in meeting the 2°C stabilization target. However, such technologies are currently at their infancy and their future penetrations may fall short of the scale required to stabilize the warming. Furthermore, the overshoot in the mid-century prior to a full realization of negative emissions would give rise to a risk because such a temporal but excessive warming above 2°C might amplify itself by strengthening climate-carbon cycle feedbacks. It has not been extensively assessed yet how carbon cycle feedbacks might play out during the overshoot in the context of negative emissions. This study explores how 2°C stabilization pathways, in particular those which undergo overshoot, can be influenced by carbon cycle feedbacks and asks their climatic and economic consequences. We compute 2°C stabilization emissions scenarios under a cost-effectiveness principle, in which the total abatement costs are minimized such that the global warming is capped at 2°C. We employ a reduced-complexity model, the Aggregated Carbon Cycle, Atmospheric Chemistry, and Climate model (ACC2), which comprises a box model of the global carbon cycle, simple parameterizations of the atmospheric chemistry, and a land-ocean energy balance model. The total abatement costs are estimated from the marginal abatement cost functions for CO2, CH4, N2O, and BC.Our preliminary results show that, if carbon cycle feedbacks turn out to be stronger than what is known today, it would incur substantial abatement costs to keep up with the 2°C stabilization goal. Our results also suggest that it would be less expensive in the long run to plan for a 2°C stabilization pathway by considering strong carbon cycle feedbacks because it would cost more if we correct the emission pathway in the mid-century to adjust for unexpectedly large carbon cycle feedbacks during overshoot. Furthermore, our

  18. Hydrothermal synthesis, characterization and luminescent ...

    Indian Academy of Sciences (India)

    Home; Journals; Bulletin of Materials Science; Volume 39; Issue 4. Hydrothermal synthesis, characterization and luminescent properties of lanthanide-doped NaLaF 4 nanoparticles. JIGMET LADOL HEENA KHAJURIA SONIKA KHAJURIA ... Keywords. Citric acid; X-ray diffraction; down-conversion emission; energy transfer.

  19. Toxicity Evaluation of Pig Slurry Using Luminescent Bacteria and Zebrafish

    Directory of Open Access Journals (Sweden)

    Wenyan Chen

    2014-07-01

    Full Text Available Biogas slurry has become a serious pollution problem and anaerobic digestion is widely applied to pig manure treatment for environmental protection and energy recovery. To evaluate environmental risk of the emission of biogas slurry, luminescent bacteria (Vibrio fischeri, larvae and embryos of zebrafish (Danio rerio were used to detect the acute and development toxicity of digested and post-treated slurry. Then the ability of treatment process was evaluated. The results showed that digested slurry displayed strong toxicity to both zebrafish and luminescent bacteria, while the EC50 for luminescent bacteria and the LC50 for larvae were only 6.81% (v/v and 1.95% (v/v respectively, and embryonic development was inhibited at just 1% (v/v. Slurry still maintained a high level of toxicity although it had been treated by membrane bioreactor (MBR, while the LC50 of larvae was 75.23% (v/v and there was a little effect on the development of embryos and V. fischeri; the results also revealed that the zebrafish larvae are more sensitive than embryos and luminescent bacteria to pig slurry. Finally, we also found the toxicity removal rate was higher than 90% after the treatment of MBR according to toxicity tests. In conclusion, further treatment should be used in pig slurry disposal or reused of final effluent.

  20. STRONG RESPONSE OF THE VERY BROAD Hβ EMISSION LINE IN THE LUMINOUS RADIO-QUIET QUASAR PG 1416-129

    International Nuclear Information System (INIS)

    Wang, J.; Li, Y.

    2011-01-01

    We report new spectroscopic observations performed in 2010 and 2011 for the luminous radio-quiet quasar PG 1416-129. Our new spectra with high quality cover both Hβ and Hα regions, and show negligible line profile variation within a timescale of one year. The two spectra allow us to study the variability of the Balmer line profile by comparing the spectra with previous ones taken at 10 and 20 years ago. By decomposing the broad Balmer emission lines into two Gaussian profiles, our spectral analysis suggests a strong response to the continuum level for the very broad component, and significant variations in both bulk blueshift velocity/FWHM and flux for the broad component. The new observations additionally indicate flat Balmer decrements (i.e., too strongemission) at the line wings, which is hard to reproduce using recent optically thin models. With these observations we argue that a separate inner optically thin emission-line region might not be necessary in the object to reproduce the observed line profiles.

  1. Faint Object Spectrograph Spectra of the UV Emission Lines in NGC 5558: Detection of Strong Narrow Components

    Science.gov (United States)

    Crenshaw, D. Michael; Boggess, Albert; Wu, Chi-Chao

    1993-01-01

    Ultraviolet spectra of the Seyfert 1 galaxy NGC 5548 were obtained with the Faint Object Spectrograph (FOS) on the Hubble Space Telescope on 1992 July 5, when the UV continuum and broad emission lines were at their lowest ever observed level. The high resolution of the spectra, relative to previous UV observations, and the low state of NGC 5548 allow the detection and accurate measurement of strong narrow components of the emission lines of Ly alpha, C IV 1549, and C III 1909. Isolation of the UV narrow components enables a detailed comparison of narrow-line region (NLR) properties in Seyfert 1 and 2 galaxies, and removal of their contribution is important for studies of the broad-line region (BLR). Relative to the other narrow lines, C IV 1549 is much stronger in NGC 5548 than in Seyfert 2 galaxies, and Mg II 2798 is very weak or absent.

  2. Strongly emissive perovskite nanocrystal inks for high-voltage solar cells

    Science.gov (United States)

    Akkerman, Quinten A.; Gandini, Marina; di Stasio, Francesco; Rastogi, Prachi; Palazon, Francisco; Bertoni, Giovanni; Ball, James M.; Prato, Mirko; Petrozza, Annamaria; Manna, Liberato

    2016-12-01

    Lead halide perovskite semiconductors have recently gained wide interest following their successful embodiment in solid-state photovoltaic devices with impressive power-conversion efficiencies, while offering a relatively simple and low-cost processability. Although the primary optoelectronic properties of these materials have already met the requirement for high-efficiency optoelectronic technologies, industrial scale-up requires more robust processing methods, as well as solvents that are less toxic than the ones that have been commonly used so successfully on the lab-scale. Here we report a fast, room-temperature synthesis of inks based on CsPbBr3 perovskite nanocrystals using short, low-boiling-point ligands and environmentally friendly solvents. Requiring no lengthy post-synthesis treatments, the inks are directly used to fabricate films of high optoelectronic quality, exhibiting photoluminescence quantum yields higher than 30% and an amplified spontaneous emission threshold as low as 1.5 μJ cm-2. Finally, we demonstrate the fabrication of perovskite nanocrystal-based solar cells, with open-circuit voltages as high as 1.5 V.

  3. Persistent luminescence in nitride and oxynitride phosphors: A review

    Science.gov (United States)

    Smet, Philippe F.; Botterman, Jonas; Van den Eeckhout, Koen; Korthout, Katleen; Poelman, Dirk

    2014-09-01

    The research field of persistent luminescence has experienced a strong growth in the past two decades, with a steady development of new materials and applications. Here we give an overview of the recent progress in a specific class of host materials, namely oxynitride and nitride persistent phosphors. These are interesting hosts to explore because of their unique characteristics, such as chemical stability and tunability of the emission over the entire visible range upon doping with divalent europium. To yield persistent luminescence however, co-dopants have to be added or the synthesis conditions have to be adjusted. Specific materials, such as Ca2Si5N8:Eu,Tm and BaSi2O2N2:Eu, are highlighted and their properties are put into the context of emerging applications such as in vivo imaging and pressure sensing via mechanoluminescence. Finally, directions for future research are given.

  4. Luminescence performance of Eu -doped lead-free zinc phosphate ...

    Indian Academy of Sciences (India)

    These glasses were characterized by several spectroscopic techniques at room temperature. All the glasses showed relatively broad fluorescence excitation and luminescence spectra. Luminescence spectra of these glasses exhibit characteristic emission of Eu3+ ion with an intense and most prominent red emission (614 ...

  5. Diffusion Raman et luminescence dans des aerogels de silice purs ou dopes Dy

    Science.gov (United States)

    Guerri, F.; Fabre, F.; Zwick, A.; Bournett, D.

    1994-02-01

    Light scattering studies of pure and Dy doped aerogels are presented. Careful examination of Stokes and anti-Stokes spectra allow the discrimination between Raman and luminescence processes. It is shown that in pure aerogels, scattered intensity is due to Raman processes only, and the density of vibrational states does not exhibit any singularity. The fractal properties of the structure imply modifications not only in the spectral distribution of the low frequency modes (usually labelled phonons and fractons) but alsoin the high frequency one, at least up to 600 cm-1. In Dy-doped dense silica, coupling between electronic and vibronic excitations is evidenced by the presence of anti-Stokes luminescence. In Dy-doped aerogels, the enlarged Dy3+ electronic levels, strongly coupled with vibrational states give rise to emission processes traducing the response of the sample as a whole, rather than resonant Raman scattering or luminescence processes.

  6. Investigation on the preparation and luminescence emission of LaF{sub 3}:Eu{sup 3+}@LaF{sub 3}/SiO{sub 2} core-shell nanostructure

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Jun, E-mail: jun-shao@snnu.edu.cn; Wang, Zhaojin; Wang, Ruibo; Liu, Zhihui; Wang, Linxiao; Guo, Jingxia; Li, Xiaoyi; Zhang, Mingdi; Zhang, Chengyun; Zheng, Hairong, E-mail: hrzheng@snnu.edu.cn

    2017-05-15

    LaF{sub 3}:Eu{sup 3+}, LaF{sub 3}:Eu{sup 3+}@LaF{sub 3}, LaF{sub 3}:Eu{sup 3+}@CeF{sub 3} and LaF{sub 3}:Eu{sup 3+}@SiO{sub 2} nanoparticles were successfully synthesized via hydrothermal route and modified Stöber method. The surface property of LaF{sub 3}:Eu{sup 3+} particle was successfully modified by coating LaF{sub 3} and SiO{sub 2} shell onto the particle, which resulted in the change of the surface property and luminescence emission of LaF{sub 3}:Eu{sup 3+}. It was found that the surface quenchers were decreased and thus the nonradiative pathways were reduced with core/shell structure, which not only enhanced the yellow emission of the sample, but also changed the intensity ratio of the yellow to orange emission. The dependence of the shell property and shell thickness on the luminescence emission spectra were investigated systematically. The current investigation can provide useful information for developing applications in biological imaging, detection, and sensing and other aspects.

  7. Origin of luminescence from ZnO/CdS core/shell nanowire arrays

    Science.gov (United States)

    Wang, Zhiqiang; Wang, Jian; Sham, Tsun-Kong; Yang, Shaoguang

    2014-07-01

    Chemical imaging, electronic structure and optical properties of ZnO/CdS nano-composites have been investigated using scanning transmission X-ray microscopy (STXM), X-ray absorption near-edge structure (XANES) and X-ray excited optical luminescence (XEOL) spectroscopy. STXM and XANES results confirm that the as-prepared product is ZnO/CdS core/shell nanowires (NWs), and further indicate that ZnS was formed on the surface of ZnO NWs as the interface between ZnO and CdS. The XEOL from ZnO/CdS NW arrays exhibits one weak ultraviolet (UV) emission at 375 nm, one strong green emission at 512 nm, and two broad infrared (IR) emissions at 750 and 900 nm. Combining XANES and XEOL, it is concluded that the UV luminescence is the near band gap emission (BGE) of ZnO; the green luminescence comes from both the BGE of CdS and defect emission (DE, zinc vacancies) of ZnO; the IR luminescence is attributed to the DE (bulk defect related to the S site) of CdS; ZnS contributes little to the luminescence of the ZnO/CdS NW arrays. Interestingly, the BGE and DE from oxygen vacancies of ZnO in the ZnO/CdS nano-composites are almost entirely quenched, while DE from zinc vacancies changes little.Chemical imaging, electronic structure and optical properties of ZnO/CdS nano-composites have been investigated using scanning transmission X-ray microscopy (STXM), X-ray absorption near-edge structure (XANES) and X-ray excited optical luminescence (XEOL) spectroscopy. STXM and XANES results confirm that the as-prepared product is ZnO/CdS core/shell nanowires (NWs), and further indicate that ZnS was formed on the surface of ZnO NWs as the interface between ZnO and CdS. The XEOL from ZnO/CdS NW arrays exhibits one weak ultraviolet (UV) emission at 375 nm, one strong green emission at 512 nm, and two broad infrared (IR) emissions at 750 and 900 nm. Combining XANES and XEOL, it is concluded that the UV luminescence is the near band gap emission (BGE) of ZnO; the green luminescence comes from both the

  8. Luminescent screens

    International Nuclear Information System (INIS)

    Lu, C.-I.

    1982-01-01

    Luminescent screens which are useful for such purposes as intensifying screens for radiographs are comprised of a support bearing a layer of finely divided particles of a phosphor dispersed in a cross-linked polymeric matrix formed by heat-curing of a coating composition comprising an unsaturated cross-linkable polymer, a polymerizable acrylic monomer, a thermoplastic polyurethane elastomer, and a heat-activatable polymerization initiator. The phosphor layer includes voids formed by evaporation of an evaporable component which is present in the coating composition from which such layer is formed. (author)

  9. Intrinsic and defect related luminescence in double oxide films of Al–Hf–O system under soft X-ray and VUV excitation

    International Nuclear Information System (INIS)

    Pustovarov, V.A.; Smirnova, T.P.; Lebedev, M.S.; Gritsenko, V.A.; Kirm, M.

    2016-01-01

    Low temperature time-resolved luminescence spectra in the region of 2.5–9.5 eV under soft X-ray excitation as well as time-resolved luminescence excitation spectra in the UV–VUV region (3.7–12 eV) of solid solutions Al x Hf y O 1−x−y thin films were investigated. The values of x and Al/Hf ratio were determined from X-ray photoelectron srectroscopy data. Hafnia films and films mixed with alumina were grown in a flow-type chemical vapor deposition reactor with argon as a carrier gas. In addition, pure alumina films were prepared by the atomic layer deposition method. A strong emission band with the peak position at 4.4 eV and with the decay time in the μs-range was revealed for pure hafnia films. The emission peak at 7.74 eV with short nanosecond decay kinetics was observed in the luminescence spectra for pure alumina films. These emission bands were ascribed to the radiative decay of self-trapped excitons (an intrinsic luminescence) in pure HfO 2 and Al 2 O 3 films, respectively. Along with intrinsic host emission, defect related luminescence bands with a larger Stokes shift were observed. In the emission spectra of the solid solution films (x=4; 17; 20 at%) the intrinsic emission bands are quenched and only the luminescence of defects (an anion vacancies) was observed. Based on transformation of the luminescence spectra and ns-luminescence decay kinetics, as well as changes in the time-resolved luminescence and luminescence excitation spectra, the relaxation processes in the films of solid solution are discussed. - Highlights: • Low temperature time−resolved PL spectra were studied in a broad range (1.5−9.5 eV). • We carried out a luminescent control of point defects (anion vacancies) and self−trapped excitons. • We observed photoluminescence of excitons bound on defects. • We observed changes of photoluminescence properties with varying ratio components.

  10. Cerenkov luminescence tomography based on preconditioning orthogonal matching pursuit

    Science.gov (United States)

    Liu, Haixiao; Hu, Zhenhua; Wang, Kun; Tian, Jie; Yang, Xin

    2015-03-01

    Cerenkov luminescence imaging (CLI) is a novel optical imaging method and has been proved to be a potential substitute of the traditional radionuclide imaging such as positron emission tomography (PET) and single-photon emission computed tomography (SPECT). This imaging method inherits the high sensitivity of nuclear medicine and low cost of optical molecular imaging. To obtain the depth information of the radioactive isotope, Cerenkov luminescence tomography (CLT) is established and the 3D distribution of the isotope is reconstructed. However, because of the strong absorption and scatter, the reconstruction of the CLT sources is always converted to an ill-posed linear system which is hard to be solved. In this work, the sparse nature of the light source was taken into account and the preconditioning orthogonal matching pursuit (POMP) method was established to effectively reduce the ill-posedness and obtain better reconstruction accuracy. To prove the accuracy and speed of this algorithm, a heterogeneous numerical phantom experiment and an in vivo mouse experiment were conducted. Both the simulation result and the mouse experiment showed that our reconstruction method can provide more accurate reconstruction result compared with the traditional Tikhonov regularization method and the ordinary orthogonal matching pursuit (OMP) method. Our reconstruction method will provide technical support for the biological application for Cerenkov luminescence.

  11. Luminescent lanthanide reporters: new concepts for use in bioanalytical applications.

    Science.gov (United States)

    Vuojola, Johanna; Soukka, Tero

    2014-01-23

    Lanthanides represent the chemical elements from lanthanum to lutetium. They intrinsically exhibit some very exciting photophysical properties, which can be further enhanced by incorporating the lanthanide ion into organic or inorganic sensitizing structures. A very popular approach is to conjugate the lanthanide ion to an organic chromophore structure forming lanthanide chelates. Another approach, which has quickly gained interest, is to incorporate the lanthanide ions into nanoparticle structures, thus attaining improved specific activity and a large surface area for biomolecule immobilization. Lanthanide-based reporters, when properly shielded from the quenching effects of water, usually express strong luminescence emission, multiple narrow emission lines covering a wide wavelength range, and exceptionally long excited state lifetimes enabling time-gated luminescence detection. Because of these properties, lanthanide-based reporters have found widespread applications in various fields of life. This review focuses on the field of bioanalytical applications. Luminescent lanthanide reporters and assay formats utilizing these reporters pave the way for increasingly sensitive, simple, and easily automated bioanalytical applications.

  12. Luminescent lanthanide reporters: new concepts for use in bioanalytical applications

    International Nuclear Information System (INIS)

    Vuojola, Johanna; Soukka, Tero

    2014-01-01

    Lanthanides represent the chemical elements from lanthanum to lutetium. They intrinsically exhibit some very exciting photophysical properties, which can be further enhanced by incorporating the lanthanide ion into organic or inorganic sensitizing structures. A very popular approach is to conjugate the lanthanide ion to an organic chromophore structure forming lanthanide chelates. Another approach, which has quickly gained interest, is to incorporate the lanthanide ions into nanoparticle structures, thus attaining improved specific activity and a large surface area for biomolecule immobilization. Lanthanide-based reporters, when properly shielded from the quenching effects of water, usually express strong luminescence emission, multiple narrow emission lines covering a wide wavelength range, and exceptionally long excited state lifetimes enabling time-gated luminescence detection. Because of these properties, lanthanide-based reporters have found widespread applications in various fields of life. This review focuses on the field of bioanalytical applications. Luminescent lanthanide reporters and assay formats utilizing these reporters pave the way for increasingly sensitive, simple, and easily automated bioanalytical applications. (topical review)

  13. The luminescence of barium titanium phosphate, BaTi(PO4)2

    NARCIS (Netherlands)

    Blasse, G.; Dirksen, G.J.

    1979-01-01

    The luminescence of BaTi(PO4)2 is described. The yellow emission is due to titanate octahedra. This compound is one of the exceptional cases where the octahedral titanate luminescence can be described by a simple model.

  14. Bright white upconversion luminescence from Er3+/Tm3+/Yb3+-doped titanate-based glasses prepared by aerodynamic levitation method

    Science.gov (United States)

    Zhang, Minghui; Yu, Jianding; Jiang, Wan; Liu, Yan; Ai, Fei; Wen, Haiqin; Jiang, Meng; Yu, Huimei; Pan, Xiuhong; Tang, Meibo; Gai, Lijun

    2017-10-01

    Aerodynamic levitation method was employed to prepare Er3+/Tm3+/Yb3+-doped titanate-based glasses. DTA results show that the glass performs high thermal stability with the glass transition temperature of 799 °C. The interaction among rare earth ions has been discussed by adjusting the relative concentration. Er3+ ions can quench the upconversion luminescence of Tm3+ ions. Tm3+ ions play a strong role in quenching the emissions of Er3+ and Tm3+ when the content of Tm3+ ions is greater than or equal 0.05. From the view of the ratio of red emission to green emission, Tm3+ ions can improve the red emission of Er3+ ions to some extent in contrast with the green emissions of Er3+ ions. 980 nm incident laser can be efficiently absorbed by Yb3+ ions. The relative intensity of red, green, and blue upconversion luminescence has been tuned to obtain white light. The composition with white upconversion luminescence of the color coordinate (0.291, 0.3292) has been found. Moreover, white upconversion luminescence mechanism is a two-photon process of ET, ESA, and cooperative sensitization. Rare earth ions doped titanate-based glasses with bright upconversion luminescence perform potential applications in color display, back light, et al.

  15. Evidence of organic luminescent centers in sol-gel-synthesized yttrium aluminum borate matrix leading to bright visible emission

    Energy Technology Data Exchange (ETDEWEB)

    Burner, Pauline; Salauen, Mathieu; Ibanez, Alain; Gautier-Luneau, Isabelle [Univ. Grenoble Alpes, Inst NEEL, Grenoble (France); CNRS, Inst NEEL, Grenoble (France); Sontakke, Atul D.; Viana, Bruno [PSL Research University, Chimie ParisTech - CNRS, Institut de Recherche de Chimie Paris (France); Bardet, Michel [Universite Grenoble Alpes, CEA, CNRS, INAC, MEM, Grenoble (France); Mouesca, Jean-Marie; Gambarelli, Serge; Maurel, Vincent [Universite Grenoble Alpes, CEA, CNRS, INAC, SyMMES, Grenoble (France); Barra, Anne-Laure [Laboratoire National des Champs Magnetiques Intenses, UPR CNRS 3228, Universite Grenoble Alpes, Grenoble (France); Ferrier, Alban [PSL Research University, Chimie ParisTech - CNRS, Institut de Recherche de Chimie Paris (France); Sorbonne Universites UPMC Universites Paris 06, Paris (France)

    2017-11-06

    Yttrium aluminum borate (YAB) powders prepared by sol-gel process have been investigated to understand their photoluminescence (PL) mechanism. The amorphous YAB powders exhibit bright visible PL from blue emission for powders calcined at 450 C to broad white PL for higher calcination temperature. Thanks to {sup 13}C labelling, NMR and EPR studies show that propionic acid initially used to solubilize the yttrium nitrate is decomposed into aromatic molecules confined within the inorganic matrix. DTA-TG-MS analyses show around 2 wt % of carbogenic species. The PL broadening corresponds to the apparition of a new band at 550 nm, associated with the formation of aromatic species. Furthermore, pulsed ENDOR spectroscopy combined with DFT calculations enables us to ascribe EPR spectra to free radicals derived from small (2 to 3 rings) polycyclic aromatic hydrocarbons (PAH). PAH molecules are thus at the origin of the PL as corroborated by slow afterglow decay and thermoluminescence experiments. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  16. Synthesis and Features of Luminescent Bromo- and Iodohectorite Nanoclay Materials

    Directory of Open Access Journals (Sweden)

    Hellen Silva Santos

    2017-11-01

    Full Text Available The smectites represent a versatile class of clay minerals with broad usage in industrial applications, e.g., cosmetics, drug delivery, bioimaging, etc. Synthetic hectorite Na0.7(Mg5.5Li0.3[Si8O20](OH4 is a distinct material from this class due to its low-cost production method that allows to design its structure to match better the applications. In the current work, we have synthesized for the first time ever nanoclay materials based on the hectorite structure but with the hydroxyl groups (OH− replaced by Br− or I−, yielding bromohectorite (Br-Hec and iodohectorite (I-Hec. It was aimed that these materials would be used as phosphors. Thus, OH− replacement was done to avoid luminescence quenching by multiphonon de-excitation. The crystal structure is similar to nanocrystalline fluorohectorite, having the d001 spacing of 14.30 Å and 3 nm crystallite size along the 00l direction. The synthetic materials studied here show strong potential to act as host lattices for optically active species, possessing mesoporous structure with high specific surface area (385 and 363 m2 g−1 for Br-Hec and I-Hec, respectively and good thermal stability up to 800 °C. Both materials also present strong blue-green emission under UV radiation and short persistent luminescence (ca. 5 s. The luminescence features are attributed to Ti3+/TiIV impurities acting as the emitting center in these materials.

  17. Luminescence of ions with s2 configuration

    International Nuclear Information System (INIS)

    Steen, A. van der.

    1980-01-01

    Some Bi 3+ -activated oxidic compounds show a red luminescence (e.g. BaSO 4 -Bi 3+ and Ca 2 P 2 O 7 -Bi 3+ ); others show an ultraviolet emission (e.g. LaGaO 3 -Bi 3+ and Ln 2 SO 6 -Bi 3+ (Ln=Y, La, Lu)). This thesis investigates which factors are responsible for these large differences in the position of the emission bands, which factors determine the occurrence of vibrational structure in the luminescence spectra of an s 2 ion and what the influence of the non-radiative processes in the 3 P multiplet is on the luminescence characteristics of the luminescent materials. (Auth.)

  18. Controlled fabrication of luminescent and magnetic nanocomposites

    Science.gov (United States)

    Ma, Yingxin; Zhong, Yucheng; Fan, Jing; Huang, Weiren

    2018-03-01

    Luminescent and magnetic multifunctional nanocomposite is in high demand and widely used in many scales, such as drug delivery, bioseparation, chemical/biosensors, and so on. Although lots of strategies have been successfully developed for the demand of multifunctional nanocomposites, it is not easy to prepare multifunctional nanocomposites by using a simple method, and satisfy all kinds of demands simultaneously. In this work, via a facile and versatile method, luminescent nanocrystals and magnetic nanoparticles were successfully synthesized through self-assembly under vigorous stirring and ultrasonic treatment. These multifunctional nanocomposites are not only water stable but also find wide application such as magnetic separation and concentration with a series of moderate speed, multicolor fluorescence at different emission wavelength, high efficiency of the excitation and emission, and so on. By changing different kinds of luminescent nanocrystals and controlling the amount of luminescent and magnetic nanoparticles, a train of multifunctional nanocomposites was successfully fabricated via a versatile and robust method.

  19. Strong blue and white photoluminescence emission of BaZrO{sub 3} undoped and lanthanide doped phosphor for light emitting diodes application

    Energy Technology Data Exchange (ETDEWEB)

    Romero, V.H. [Centro de Investigaciones en Optica, A. P. 1-948, Leon Gto., 37160 (Mexico); De la Rosa, E., E-mail: elder@cio.mx [Centro de Investigaciones en Optica, A. P. 1-948, Leon Gto., 37160 (Mexico); Salas, P. [Centro de Fisica Aplicada y Tecnologia Avanzada, Universidad Nacional Autonoma de Mexico, A.P. 1-1010, Queretaro, Qro. 76000 (Mexico); Velazquez-Salazar, J.J. [Department of Physics and Astronomy, The University of Texas at San Antonio One UTSA Circle, San Antonio TX 78249 (United States)

    2012-12-15

    In this paper, we report the obtained strong broadband blue photoluminescence (PL) emission centered at 427 nm for undoped BaZrO{sub 3} observed after 266 nm excitation of submicron crystals prepared by hydrothermal/calcinations method. This emission is enhanced with the introduction of Tm{sup 3+} ions and is stronger than the characteristic PL blue emission of such lanthanide. The proposed mechanism of relaxation for host lattice emission is based on the presence of oxygen vacancies produced during the synthesis process and the charge compensation due to the difference in the electron valence between dopant and substituted ion in the host. Brilliant white light emission with a color coordinate of (x=0.29, y=0.32) was observed by combining the blue PL emission from the host with the green and red PL emission from Tb{sup 3+} and Eu{sup 3+} ions, respectively. The color coordinate can be tuned by changing the ratio between blue, green and red band by changing the concentration of lanthanides. - Graphical abstract: Strong blue emission from undoped BaZrO{sub 3} phosphor and white light emission by doping with Tb{sup 3+} (green) and Eu{sup 3+} (red) after 266 nm excitation. Highlights: Black-Right-Pointing-Pointer Blue emission from BaZrO{sub 3} phosphor. Black-Right-Pointing-Pointer Blue emission enhanced with Tm{sup 3+}. Black-Right-Pointing-Pointer White light from BaZrO{sup 3+} phosphor.

  20. Anomalous ULF Emissions and Their Possible Association with the Strong Earthquakes in Sumatra, Indonesia, during 2007-2012

    Directory of Open Access Journals (Sweden)

    Suaidi Ahadi

    2015-03-01

    Full Text Available Eleven strong Sumatran earthquakes, with their epicenter less than 550 km away from the Kototabang (KTB geomagnetic station (2007-2012, were studied to examine the occurrence of anomalous ultra-low frequency emissions (ULF-EM. Anomalous ULF signals, possibly associated with the earthquake’s precursors, were determined by the Welch ratio SZ/SH at 0.06 Hz at the KTB station. These ULF anomalies were then compared with geomagnetic data observed from two reference stations in Darwin and Davao, to prevent misinterpretation of global geomagnetic disturbances as precursors. This study aims to analyze the relationship between earthquake magnitude and hypocenter radius, and seismic index against lead time during ULF-EM anomalies. We used the polarization ratio Welch method in terms of power spectrum density to evaluate the geomagnetic data by overlapping windows and applying fast Fourier transform (FFT. The results showed anomalous variations in onset and lead time, determined using the standard deviation controlling the SZ/SH power pattern. Our positive correlation between lead time of ULF emission and earthquake magnitude as well as between lead time and seismic index. It shows a negative correlation between hypocenter distances to KTB station against lead time.

  1. Strongly transverse-electric-polarized emission from deep ultraviolet AlGaN quantum well light emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Reich, Christoph, E-mail: Christoph.Reich@tu-berlin.de; Guttmann, Martin; Wernicke, Tim; Mehnke, Frank; Kuhn, Christian [Institut für Festkörperphysik, Technische Universität Berlin, Hardenbergstr. 36, Berlin 10623 (Germany); Feneberg, Martin; Goldhahn, Rüdiger [Institut für Experimentelle Physik, Otto-von-Guericke-Universität, Universitätsplatz 2, Magdeburg 39106 (Germany); Rass, Jens; Kneissl, Michael [Institut für Festkörperphysik, Technische Universität Berlin, Hardenbergstr. 36, Berlin 10623 (Germany); Ferdinand-Braun-Institut, Leibniz-Institut für Höchstfrequenztechnik, Gustav-Kirchhoff-Str. 4, Berlin 12489 (Germany); Lapeyrade, Mickael; Einfeldt, Sven; Knauer, Arne; Kueller, Viola; Weyers, Markus [Ferdinand-Braun-Institut, Leibniz-Institut für Höchstfrequenztechnik, Gustav-Kirchhoff-Str. 4, Berlin 12489 (Germany)

    2015-10-05

    The optical polarization of emission from ultraviolet (UV) light emitting diodes (LEDs) based on (0001)-oriented Al{sub x}Ga{sub 1−x}N multiple quantum wells (MQWs) has been studied by simulations and electroluminescence measurements. With increasing aluminum mole fraction in the quantum well x, the in-plane intensity of transverse-electric (TE) polarized light decreases relative to that of the transverse-magnetic polarized light, attributed to a reordering of the valence bands in Al{sub x}Ga{sub 1−x}N. Using k ⋅ p theoretical model calculations, the AlGaN MQW active region design has been optimized, yielding increased TE polarization and thus higher extraction efficiency for bottom-emitting LEDs in the deep UV spectral range. Using (i) narrow quantum wells, (ii) barriers with high aluminum mole fractions, and (iii) compressive growth on patterned aluminum nitride sapphire templates, strongly TE-polarized emission was observed at wavelengths as short as 239 nm.

  2. Studies of positron induced luminescence from polymers

    International Nuclear Information System (INIS)

    Xu, J.; Hulett, L.D. Jr.; Lewis, T.A.; Tolk, N.H.

    1994-01-01

    Light emission from polymers (anthracene dissolved in polystryrene) induced by low-energy positrons and electrons has been studied. Results indicate a clear difference between optical emissions under positron and electron bombardment. The positron-induced luminescence spectrum is believed to be generated by both collisional and annihilation processes

  3. Characterization of donor-acceptor-pair emission in fluorescent 6H-SiC

    DEFF Research Database (Denmark)

    Ou, Yiyu; Jokubavicius, Valdas; Linnarsson, Margareta

    2012-01-01

    luminescence. A dopant concentration difference greater than 4x10(18) cm(-3) is proposed to help achieve intense PL. Angular-dependent PL was observed that was attributed to the Fabry-Perot microcavity interference effect, and a strong luminescence intensity in a large emission angle range was also achieved....... The results indicate that N-B-doped fluorescent SiC is a good wavelength converter in white LED applications....

  4. Quantification of strong emissions of methane in the Arctic using spectral measurements from TANSO-FTS and IASI

    Science.gov (United States)

    Bourakkadi, Zakia; Payan, Sébastien; Bureau, Jérôme

    2015-04-01

    Methane is the second most important greenhouse gas after the carbon dioxide but it is 25 times more effective in contributing to the radiative forcing than the carbon dioxide(1). Since the pre-industrial times global methane concentration have more than doubled in the atmosphere. This increase is generally caused by anthropogenic activities like the massif use and extraction of fossil fuel, rice paddy agriculture, emissions from landfills... In recent years, several studies show that climate warming and thawing of permafrost act on the mobilization of old stored carbon in Arctic causing a sustained release of methane to the atmosphere(2),(3),(4). The methane emissions from thawing permafrost and methane hydrates in the northern circumpolar region will become potentially important in the end of the 21st centry because they could increase dramatically due to the rapid climate warming of the Artic and the large carbon pools stored there. The objective of this study is to evaluate and quantify methane strong emissions in this region of the globe using spectral measurements from the Thermal And Near Infrared Sensor for carbon Observations-Fourier Transform Spectrometer (TANSO-FTS) and the Infrared Atmospheric Sounding Interferometer (IASI). We use also the LMDZ-PYVAR model to simulate methane fluxes and to estimate how they could be observed by Infrared Sounders from space. To select spectra with high values of methane we developed a statistical approach based on the singular value decomposition. Using this approach we can identify spectra over the important emission sources of methane and we can by this way reduce the number of spectra to retrieve by an line-by-line radiative transfer model in order to focus on those which contain high amount of methane. In order to estimate the capacity of TANSO-FTS and IASI to detect peaks of methane emission with short duration at quasi-real time, we used data from MACC (Monitoring Atmospheric Composition and Climate) simulations

  5. Optically stimulated luminescence

    International Nuclear Information System (INIS)

    Espinosa, G.; Bogard, J.S.

    2007-01-01

    Full text: The use of Optically Stimulated Luminescence (OSL) for radiation dosimetry has become increasingly popular in recent years. The OSL method is based on luminescence emitted from semiconductor materials stimulated with specific wavelengths of light, after being exposed to ionizing radiation. The OSL intensity is a function of the radiation dose absorbed by the material. This work complements previous studies by the authors of the thermoluminescence (TL) response by SiO 2 commercial optical fiber exposed to ionizing radiation and provides preliminary results describing some of the material's OSL properties. Linear OSL response to beta radiation dose, along with a consistent shape of the photon emission curve with time, were observed using a green/blue OSL excitation laser. The reproducibility of OSL response after repeated irradiations and the change in intensity with time were also examined. The search and characterization of materials that exhibit this OSL response, in parallel with the continued development of OSL methodology and instrumentation, is an important scientific and commercial issue. (Author)

  6. Regioselective aromatic substitution reactions of cyclometalated Ir(III) complexes: synthesis and photochemical properties of substituted Ir(III) complexes that exhibit blue, green, and red color luminescence emission.

    Science.gov (United States)

    Aoki, Shin; Matsuo, Yasuki; Ogura, Shiori; Ohwada, Hiroki; Hisamatsu, Yosuke; Moromizato, Shinsuke; Shiro, Motoo; Kitamura, Masanori

    2011-02-07

    In this manuscript, the regioselective halogenation, nitration, formylation, and acylation of Ir(tpy)(3) and Ir(ppy)(3) (tpy = 2-(4'-tolyl)pyridine and ppy = 2-phenylpyridine) and the subsequent conversions are described. During attempted bromination of the three methyl groups in fac-Ir(tpy)(3) using N-bromosuccinimide (NBS) and benzoyl peroxide (BPO), three protons at the 5'-position (p-position with respect to the C-Ir bond) of phenyl rings in tpy units were substituted by Br, as confirmed by (1)H NMR spectra, mass spectra, and X-ray crystal structure analysis. It is suggested that such substitution reactions of Ir complexes proceed via an ionic mechanism rather than a radical mechanism. UV-vis and luminescence spectra of the substituted Ir(III) complexes are reported. The introduction of electron-withdrawing groups such as CN and CHO groups at the 5'-position of tpy induces a blue shift of luminescence emission to about 480 nm, and the introduction of electron-donating groups such as an amino group results in a red shift to about 600 nm. A reversible change of emission for the 5'-amino derivative of Ir(tpy)(3), Ir(atpy)(3), between red and green occurs upon protonation and deprotonation.

  7. Strongly turbulent ionizing shock wave as the mechanism for the first neutron emission in the dense plasma focus discharge

    International Nuclear Information System (INIS)

    Kobata, T.

    1987-01-01

    It is well known that high temperature thermo-nuclear plasma of several keV is very difficult to exist in the dense and small radius plasma column. So, at any time the high neutron yield from the dense plasma focus has had the tendency to be explained by the beam target mechanism based on the observation of the high energy beam emissions. However the manner of neutron emission is very complex and different among the devices and from shot to shot. Especially it is difficult to explain the first neutron emission by the beam target mechanism which is coincide with the formation of very dense plasma column. There is the ionizing shock wave in front of the plasma sheet and the gas is fully ionized after the shock wave because the Mach-number against the filling gas is very large, M--100. The thickness of the shock wave is very thin, 1≤0.5 mm for the discharge condition that the speed of the plasma sheet V/sub sh/ is 1--2 x 10/sup 7/ cm/sec and the discharge gas pressure is several Torr. The intensity of the magnetic field penetrated into the shock wave from the back side of the plasma sheet at the last converging phase will be the order of 1 kG. The plasma density in the shock wave will be n=4--9.10/sup 17//cm/sup 3/ because the density jump in the very strong shock limit is 6 times of the base gas density. Then the Alfven speed b=B/sub θ//(4πrho)/sup 1/2/ calculated from these density and magnetic field is 2.4--1.6 x 10/sup 6/ cm/sec. Similarly the sonic speed a= (γkT/m)/sup 1/2/ in the plasma is also the same order, i.e. a=2--4x10/sup 6/ cm/sec, for the temperature of 10--50 eV expected from the shock wave heating

  8. Feldspar, Infrared Stimulated Luminescence

    DEFF Research Database (Denmark)

    Jain, Mayank

    2014-01-01

    This entry primarily concerns the characteristics and the origins of infrared-stimulated luminescence in feldspars.......This entry primarily concerns the characteristics and the origins of infrared-stimulated luminescence in feldspars....

  9. A qubit strongly coupled to a resonant cavity: asymmetry of the spontaneous emission spectrum beyond the rotating wave approximation

    Energy Technology Data Exchange (ETDEWEB)

    Cao, X [Department of Physics and Institute of Theoretical Physics and Astrophysics, Xiamen University, Xiamen, 361005 (China); You, J Q; Nori, F [Advanced Science Institute, RIKEN, Wako-shi 351-0198 (Japan); Zheng, H, E-mail: xfcao@xmu.edu.cn [Department of Physics, Shanghai Jiao Tong University, Shanghai 200240 (China)

    2011-07-15

    We investigate the spontaneous emission (SE) spectrum of a qubit in a lossy resonant cavity. We use neither the rotating-wave approximation nor the Markov approximation. For the weak-coupling case, the SE spectrum of the qubit is a single peak, with its location depending on the spectral density of the qubit environment. Then, the asymmetry (of the location and heights of the two peaks) of the two SE peaks (which are related to the vacuum Rabi splitting) changes as the qubit-cavity coupling increases. Explicitly, for a qubit in a low-frequency intrinsic bath, the height asymmetry of the splitting peaks is enhanced as the qubit-cavity coupling strength increases. However, for a qubit in an Ohmic bath, the height asymmetry of the spectral peaks is inverted compared to the low-frequency bath case. With further increasing the qubit-cavity coupling to the ultra-strong regime, the height asymmetry of the left and right peaks is slightly inverted, which is consistent with the corresponding case of a low-frequency bath. This inversion of the asymmetry arises from the competition between the Ohmic bath and the cavity bath. Therefore, after considering the anti-rotating terms, our results explicitly show how the height asymmetry in the SE spectrum peaks depends on the qubit-cavity coupling and the type of intrinsic noise experienced by the qubit.

  10. Study of optical absorption, visible emission and NIR–vis luminescence spectra of Tm{sup 3+}/Yb{sup 3+}, Ho{sup 3+}/Yb{sup 3+} and Tm{sup 3+}/Ho{sup 3+}/Yb{sup 3+} doped tellurite glasses

    Energy Technology Data Exchange (ETDEWEB)

    Seshadri, M., E-mail: seshumeruva@gmail.com [Institute of Physics, University of Campinas, UNICAMP, P.O. Box 6165, Campinas 13083-970 (Brazil); Barbosa, L.C.; Cordeiro, C.M.B.; Radha, M. [Institute of Physics, University of Campinas, UNICAMP, P.O. Box 6165, Campinas 13083-970 (Brazil); Sigoli, F.A. [Institute of Chemistry, University of Campinas, UNICAMP, P.O. Box 6154, Campinas 13083-970 (Brazil); Ratnakaram, Y.C. [Department of Physics, Sri Venkateswara University, SVU, Tirupat 517502 (India)

    2015-10-15

    Tm{sup 3+}/Yb{sup 3+}, Ho{sup 3+}/Yb{sup 3+} co-doped and Tm{sup 3+}/Ho{sup 3+}/Yb{sup 3+} triply doped TeO{sub 2}–Bi{sub 2}O{sub 3}–ZnO–Li{sub 2}O–Nb{sub 2}O{sub 5} (TBZLN) tellurite glasses were prepared by melt quenching method. Judd–Ofelt intensity parameters (Ω{sub λ}, λ=2, 4 and 6), radiative transition probabilities, branching ratios and radiative lifetimes of Tm{sup 3+}, Ho{sup 3+} ions in co-doped TBZLN glasses were calculated from the optical absorption spectra. Excitation, visible luminescence and decay lifetimes in visible region were also investigated. The stimulated emission and gain cross-sections for the Tm{sup 3+}:{sup 3}F{sub 4}→{sup 3}H{sub 6} (1700 nm) and Ho{sup 3+}:{sup 5}I{sub 7}→{sup 5}I{sub 8} (1956 nm) transitions in co-doped TBZLN glasses have been analyzed and compared with those of other reported glasses. Up-conversion luminescence was observed in TBZLN glasses under 980 nm laser excitation and energy transfer mechanisms have been discussed. Finally, CIE color co-ordinates were calculated and it is observed that the color co-ordinates fall in blue and green regions for Tm{sup 3+}/Yb{sup 3+} and Ho{sup 3+}/Yb{sup 3+} co-doped TBZLN glasses, respectively. A subsequent shift in color co-ordinates from green to greenish-yellow region has been observed with an increase in the concentration (0.1, 0.5 and 1.0 mol%) of Tm{sup 3+} ions in Tm{sup 3+}/Ho{sup 3+}/Yb{sup 3+} triply doped TBZLN glasses. - Highlights: • High degree of covalecy of RE–O bond in co-doped TBZLN glasses was observed. • Tm{sup 3+}:{sup 1}D{sub 2}→{sup 3}F{sub 4} and Ho{sup 3+}:{sup 5}F{sub 4}({sup 5}S{sub 2})→{sup 5}I{sub 8} transitions show high emission cross-section. • Visible and strong 793 nm emission was observed when pumped by 980 nm diode laser. • Triply doped glasses exhibits tunable emission intensity by increasing Tm{sup 3+} ions.

  11. Anti-Stokes shift luminescent materials for bio-applications.

    Science.gov (United States)

    Zhu, Xingjun; Su, Qianqian; Feng, Wei; Li, Fuyou

    2017-02-20

    Anti-Stokes shift luminescence is a special optical process, which converts long-wavelength excitation to short-wavelength emission. This unique ability is especially helpful for bio-applications, because the longer-wavelength light source, usually referring to near infrared light, has a larger penetration depth offering a longer working distance for in vivo applications. The anti-Stokes shift luminescence signal can also be distinguished from the auto-fluorescence of biological tissues, thus reducing background interference during bioimaging. Herein, we summarize recent advances in anti-Stokes shift luminescent materials, including lanthanide and triplet-triplet-annihilation-based upconversion nanomaterials, and newly improved hot-band absorption-based luminescent materials. We focus on the synthetic strategies, optical optimization and biological applications as well as present comparative discussions on the luminescence mechanisms and characteristics of these three types of luminescent materials.

  12. Lanthanide Organic Framework Luminescent Thermometers.

    Science.gov (United States)

    Rocha, João; Brites, Carlos D S; Carlos, Luís D

    2016-10-10

    Metal-organic frameworks (MOFs) are excellent platforms for engineering luminescence properties as their building blocks, metal ions, linkers, and guest ions or molecules, are all potential sources of light emission. Temperature is one of the most important physical properties affecting the dynamics and viability of natural and engineered systems. Because the luminescence of certain lanthanide-bearing MOFs changes considerably with temperature, in the last few years, these materials have been explored as optical thermometers, especially in temperature sensing based on the intensity ratios of two separate electronic transitions. This review discusses the main concepts and ideas assisting the design of such ratiometric thermometers, and identifies the main challenges presented to this nascent field: develop nanothermometers for bio-applications and nanomedicine; understand the energy transfer mechanisms determining the thermal sensitivity; achieve effective primary thermometers; realize multifunctional nanothermometers; integrate Ln 3+ -based thermometers in commercial products. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Selective detection of Fe{sup 3+}, Cr{sup 3+} and Cu{sup 2+} in water using highly luminescent Gd{sub 2}O{sub 3}:Eu{sup 3+} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ghosh, Debasish [Chemical Engineering and Process Development Division, National Chemical Laboratory, Pune 411008 (India); Luwang, Meitram Niraj, E-mail: mn.luwang@ncl.res.in [Chemical Engineering and Process Development Division, National Chemical Laboratory, Pune 411008 (India); Academy of Scientific and Innovative Research (AcSIR), Anusandhan Bhawan, Rafi Marg, New Delhi 110001 (India)

    2016-03-15

    Rod shaped Eu{sup 3+} doped Gd{sub 2}O{sub 3} nanoparticles were synthesised by a simple wet-chemical method followed by high temperature heating at 700 °C. The nanoparticles were characterised by X-ray diffraction (XRD), infra-red (IR), transmission electron microscopy (TEM), x-ray photonelectron spectroscopy (XPS), photoluminescence (PL) studies and lifetime measurement. The particles show strong host sensitised luminescence in water. Luminescence in water is selectively quenched by Fe{sup 3+}, Cr{sup 3+} and Cu{sup 2+} ions. This luminescence quenching phenomenon has been utilised to detect metal ions in synthetic water and environmental water samples. Results obtained by luminescence quenching for environmental water samples are in good agreement with the results obtained from inductively coupled plasma atomic emission spectroscopy (ICP-AES) study.

  14. Spatial variability of nitrous oxide and methane emissions from an MBT landfill in operation: Strong N{sub 2}O hotspots at the working face

    Energy Technology Data Exchange (ETDEWEB)

    Harborth, Peter, E-mail: p.harborth@tu-bs.de [Department of Waste and Resource Management, Leichtweiß-Institute for Hydraulic Engineering and Water Resources, Technische Universität Braunschweig, Braunschweig (Germany); Fuß, Roland [Institute of Climate-Smart Agriculture, Johann Heinrich von Thünen Institute, Braunschweig (Germany); Münnich, Kai [Department of Waste and Resource Management, Leichtweiß-Institute for Hydraulic Engineering and Water Resources, Technische Universität Braunschweig, Braunschweig (Germany); Flessa, Heinz [Institute of Climate-Smart Agriculture, Johann Heinrich von Thünen Institute, Braunschweig (Germany); Fricke, Klaus [Department of Waste and Resource Management, Leichtweiß-Institute for Hydraulic Engineering and Water Resources, Technische Universität Braunschweig, Braunschweig (Germany)

    2013-10-15

    Highlights: ► First measurements of N{sub 2}O and CH{sub 4} emissions from an MBT landfill. ► High N{sub 2}O emissions from recently deposited material. ► N{sub 2}O emissions associated with aeration and the occurrence of nitrite and nitrate. ► Strong negative correlation between CH{sub 4} and N{sub 2}O production activity. - Abstract: Mechanical biological treatment (MBT) is an effective technique, which removes organic carbon from municipal solid waste (MSW) prior to deposition. Thereby, methane (CH{sub 4}) production in the landfill is strongly mitigated. However, direct measurements of greenhouse gas emissions from full-scale MBT landfills have not been conducted so far. Thus, CH{sub 4} and nitrous oxide (N{sub 2}O) emissions from a German MBT landfill in operation as well as their concentrations in the landfill gas (LFG) were measured. High N{sub 2}O emissions of 20–200 g CO{sub 2} eq. m{sup −2} h{sup −1} magnitude (up to 428 mg N m{sup −2} h{sup −1}) were observed within 20 m of the working face. CH{sub 4} emissions were highest at the landfill zone located at a distance of 30–40 m from the working face, where they reached about 10 g CO{sub 2} eq. m{sup −2} h{sup −1}. The MBT material in this area has been deposited several weeks earlier. Maximum LFG concentration for N{sub 2}O was 24.000 ppmv in material below the emission hotspot. At a depth of 50 cm from the landfill surface a strong negative correlation between N{sub 2}O and CH{sub 4} concentrations was observed. From this and from the distribution pattern of extractable ammonium, nitrite, and nitrate it has been concluded that strong N{sub 2}O production is associated with nitrification activity and the occurrence of nitrite and nitrate, which is initiated by oxygen input during waste deposition. Therefore, CH{sub 4} mitigation measures, which often employ aeration, could result in a net increase of GHG emissions due to increased N{sub 2}O emissions, especially at MBT landfills.

  15. Dissolved organic carbon and nitrogen mineralization strongly affect co2 emissions following lime application to acidic soil

    International Nuclear Information System (INIS)

    Shaaban, M.; Peng, Q.; Lin, S.; Wu, Y.

    2014-01-01

    Emission of greenhouse gases from agricultural soils has main contribution to the climatic change and global warming. Dynamics of dissolved organic carbon (DOC) and nitrogen mineralization can affect CO/sub 2/ emission from soils. Influence of DOC and nitrogen mineralization on CO/sub 2/ emissions following lime application to acidic soil was investigated in current study. Laboratory experiment was conducted under aerobic conditions with 25% moisture contents (66% water-filled pore space) at 25 degree C in the dark conditions. Different treatments of lime were applied to acidic soil as follows: CK (control), L (low rate of lime: 0.2g lime / 100 g soil) and H (high rate of lime: 0.5g lime /100g soil). CO/sub 2/ emissions were measured by gas chromatography and dissolved organic carbon, NH4 +-N, NO/sub 3/ --N and soil pH were measured during incubation study. Addition of lime to acidic soil significantly increased the concentration of DOC and N mineralization rate. Higher concentrations of DOC and N mineralization, consequently, increased the CO/sub 2/ emissions from lime treated soils. Cumulative CO/sub 2/ emission was 75% and 71% higher from L and H treatments as compared to CK. The results of current study suggest that DOC and N mineralization are critical in controlling gaseous emissions of CO/sub 2/ from acidic soils following lime application. (author)

  16. Strong soft X-ray emission from a double-stream gas puff target irradiated with a nanosecond Nd:YAG laser

    Energy Technology Data Exchange (ETDEWEB)

    Fiedorowicz, H.; Bartnik, A.; Rakowski, R.; Szczurek, M. [Military Univ. of Technology, Warsaw (Poland). Inst. of Optoelectronics; Daido, H.; Suzuki, M.; Yamagami, S.; Choi, I.W.; Tang, H.J. [Osaka Univ., Suita (Japan). Inst. of Laser Engineering

    2001-07-01

    Soft X-ray emission from a new double-stream gas puff target irradiated with a nanosecond, high-power Nd:YAG laser pulse has been studied. The target was formed by pulsed injection of gas into a hollow gas stream made from helium by using a double-nozzle setup. Strong X-ray emissions near 10 nm from the double-stream krypton/helium, near 11 nm from the xenon/helium, and at 13 nm from the oxygen/helium targets were observed. The emission from the double-stream gas puff target was several times higher as compared to the ordinary gas puff targets, and comparable to the emission from the solid targets irradiated in the same conditions. (orig.)

  17. Understanding the influence of nanoenvironment on luminescence ...

    Indian Academy of Sciences (India)

    The role of the rare-earth ion concentration, crystal size and crystal phase on the up- and downconversion emission of rare-earth ions in oxide nanocrystals and their underlying mechanisms are discussed. It is also found that the luminescence lifetime of the excited state rare-earth ions is sensitive to the particle crystalline ...

  18. luminescence in coloured alkali halide crystals

    Indian Academy of Sciences (India)

    irradiated alkali halide crystals are similar to the luminescence excited by high energy radiation. Ueta et al [11] ... emission, a correlation between the deformation bleaching and mechanoluminescence of coloured alkali ..... [32] V P Zakrevskii, T S Orlova and A V Shuldiner, J. Solid State 37, 675 (1995). [33] C D Clark and ...

  19. Luminescent solutions and films of new europium complexes with chelating ligands

    Science.gov (United States)

    Kharcheva, Anastasia V.; Ivanov, Alexey V.; Borisova, Nataliya E.; Kaminskaya, Tatiana P.; Patsaeva, Svetlana V.; Popov, Vladimir V.; Yuzhakov, Viktor I.

    2015-03-01

    The development of new complexes of rare earth elements (REE) with chelating organic ligands opens up the possibility of purposeful alteration in the composition and structure of the complexes, and therefore tuning their optical properties. New ligands possessing two pyridine rings in their structure were synthesized to improve coordination properties and photophysical characteristics of REE compounds. Complexes of trivalent europium with novel chelating ligands were investigated using luminescence and absorption spectroscopy, as well as atomic force microscopy. Luminescence properties of new compounds were studied both for solutions and films deposited on the solid support. All complexes exhibit the characteristic red luminescence of Eu (III) ion with the absolute lumenescence quantum yield in polar acetonitrile solution varying from 0.21 to 1.45 % and emission lifetime ranged from 0.1 to 1 ms. Excitation spectra of Eu coordination complexes correspond with absorption bands of chelating ligand. The energy levels of the triplet state of the new ligands were determined from the phosphorescence at 77 K of the corresponding Gd (III) complexes. The morphology of films of europium complexes with different substituents in the organic ligands was investigated by atomic force microscopy (AFM). It strongly depends both on the type of substituent in the organic ligand, and the rotation speed of the spin-coater. New europium complexes with chelating ligands containing additional pyridine fragments represent outstanding candidates for phosphors with improved luminescence properties.

  20. Luminescent beam stop

    Energy Technology Data Exchange (ETDEWEB)

    Bryant, Diane; Morton, Simon A.

    2017-10-25

    This disclosure provides systems, methods, and apparatus related to beam stops. In one aspect, a device comprises a luminescent material, a beam stop plate, and an optical fiber. The luminescent material is a parallelepiped having a first side and a second side that are squares and having a third side that is a rectangle or a square. The first side and the second side are perpendicular to the third side. The beam stop plate is attached to the first side of the luminescent material. The optical fiber has a first end and a second end, with the first end of the optical fiber attached to the third side of the luminescent material.

  1. Emission of thermally stimulated luminescence in mixed monocrystals KCl-KBr: Pb2+, KCl: Pb2+ and KBr: Pb2+ exposed at low doses

    International Nuclear Information System (INIS)

    Cruz Z, E.; Ramos B, S.; Melendrez A, R.; Chernov, V.; Piters, T.M.; Barboza F, M.; Hernandez A, J.; Murrieta S, H.

    2002-01-01

    It is reported the behavior of solid solutions of mixed crystals KCl 1-x KBr x doped with divalent lead which were exposed to gamma radiation. The mixtures of KCl-KBr were varied, with x equivalents at 2, 50, 65, and 85 % including the extremes KCl: Pb 2+ and KBr: Pb 2+ . It was maintained a concentration of divalent lead between 20 and 40 ppm in the crystalline lattice. The production of the generated defects by radiation have been correlated with the increase in the brilliance curves depending on the received dose by the mixed doped crystal. It has been used the thermal stimulation (Tl) for obtaining the crystal luminescence depending on the dose until 130 Gy with gammas of cobalt 60. The results shows that this mixed crystalline material of varied composition responds adequately to low doses which indicates that this would be a good detector of ionizing radiation. The results have been correlated with the optical properties of this mixed doped crystal, however it has been found that exists an important loss of luminescence depending on the halogen quantity presents in the mixed crystal. (Author)

  2. Time-resolved luminescence from quartz: An overview of contemporary developments and applications

    Science.gov (United States)

    Chithambo, M. L.; Ankjærgaard, C.; Pagonis, V.

    2016-01-01

    Time-resolved optical stimulation of luminescence has become established as a key method for measurement of optically stimulated luminescence from quartz, feldspar and α-Al2O3:C, all materials of interest in dosimetry. The aim of time-resolved optical stimulation is to separate in time the stimulation and emission of luminescence. The luminescence is stimulated from a sample using a brief light pulse and the emission monitored during stimulation in the presence of scattered stimulating light or after pulsing, over photomultiplier noise only. Although the use of the method in retrospective dosimetry has been somewhat limited, the technique has been successfully applied to study mechanisms in the processes leading up to luminescence emission. The main means for this has been the temperature dependence of the luminescence intensity as well as the luminescence lifetimes determined from time-resolved luminescence spectra. In this paper we review some key developments in theory and applications to quartz including methods of evaluating lifetimes, techniques of evaluating kinetic parameters using both the dependence of luminescence intensity and lifetime on measurement temperature, and of lifetimes on annealing temperature. We then provide an overview of some notable applications such as separation of quartz signals from a quartz-feldspar admixture and the utility of the dynamic throughput, a measure of luminescence measured as a function of the pulse width. The paper concludes with some suggestions of areas where further exploration would advance understanding of dynamics of luminescence in quartz and help address some outstanding problems in its application.

  3. Particulate matter from both heavy fuel oil and diesel fuel shipping emissions show strong biological effects on human lung cells at realistic and comparable in vitro exposure conditions.

    Directory of Open Access Journals (Sweden)

    Sebastian Oeder

    Full Text Available Ship engine emissions are important with regard to lung and cardiovascular diseases especially in coastal regions worldwide. Known cellular responses to combustion particles include oxidative stress and inflammatory signalling.To provide a molecular link between the chemical and physical characteristics of ship emission particles and the cellular responses they elicit and to identify potentially harmful fractions in shipping emission aerosols.Through an air-liquid interface exposure system, we exposed human lung cells under realistic in vitro conditions to exhaust fumes from a ship engine running on either common heavy fuel oil (HFO or cleaner-burning diesel fuel (DF. Advanced chemical analyses of the exhaust aerosols were combined with transcriptional, proteomic and metabolomic profiling including isotope labelling methods to characterise the lung cell responses.The HFO emissions contained high concentrations of toxic compounds such as metals and polycyclic aromatic hydrocarbon, and were higher in particle mass. These compounds were lower in DF emissions, which in turn had higher concentrations of elemental carbon ("soot". Common cellular reactions included cellular stress responses and endocytosis. Reactions to HFO emissions were dominated by oxidative stress and inflammatory responses, whereas DF emissions induced generally a broader biological response than HFO emissions and affected essential cellular pathways such as energy metabolism, protein synthesis, and chromatin modification.Despite a lower content of known toxic compounds, combustion particles from the clean shipping fuel DF influenced several essential pathways of lung cell metabolism more strongly than particles from the unrefined fuel HFO. This might be attributable to a higher soot content in DF. Thus the role of diesel soot, which is a known carcinogen in acute air pollution-induced health effects should be further investigated. For the use of HFO and DF we recommend a

  4. Particulate Matter from Both Heavy Fuel Oil and Diesel Fuel Shipping Emissions Show Strong Biological Effects on Human Lung Cells at Realistic and Comparable In Vitro Exposure Conditions

    Science.gov (United States)

    Dilger, Marco; Paur, Hanns-Rudolf; Schlager, Christoph; Mülhopt, Sonja; Diabaté, Silvia; Weiss, Carsten; Stengel, Benjamin; Rabe, Rom; Harndorf, Horst; Torvela, Tiina; Jokiniemi, Jorma K.; Hirvonen, Maija-Riitta; Schmidt-Weber, Carsten; Traidl-Hoffmann, Claudia; BéruBé, Kelly A.; Wlodarczyk, Anna J.; Prytherch, Zoë; Michalke, Bernhard; Krebs, Tobias; Prévôt, André S. H.; Kelbg, Michael; Tiggesbäumker, Josef; Karg, Erwin; Jakobi, Gert; Scholtes, Sorana; Schnelle-Kreis, Jürgen; Lintelmann, Jutta; Matuschek, Georg; Sklorz, Martin; Klingbeil, Sophie; Orasche, Jürgen; Richthammer, Patrick; Müller, Laarnie; Elsasser, Michael; Reda, Ahmed; Gröger, Thomas; Weggler, Benedikt; Schwemer, Theo; Czech, Hendryk; Rüger, Christopher P.; Abbaszade, Gülcin; Radischat, Christian; Hiller, Karsten; Buters, Jeroen T. M.; Dittmar, Gunnar; Zimmermann, Ralf

    2015-01-01

    Background Ship engine emissions are important with regard to lung and cardiovascular diseases especially in coastal regions worldwide. Known cellular responses to combustion particles include oxidative stress and inflammatory signalling. Objectives To provide a molecular link between the chemical and physical characteristics of ship emission particles and the cellular responses they elicit and to identify potentially harmful fractions in shipping emission aerosols. Methods Through an air-liquid interface exposure system, we exposed human lung cells under realistic in vitro conditions to exhaust fumes from a ship engine running on either common heavy fuel oil (HFO) or cleaner-burning diesel fuel (DF). Advanced chemical analyses of the exhaust aerosols were combined with transcriptional, proteomic and metabolomic profiling including isotope labelling methods to characterise the lung cell responses. Results The HFO emissions contained high concentrations of toxic compounds such as metals and polycyclic aromatic hydrocarbon, and were higher in particle mass. These compounds were lower in DF emissions, which in turn had higher concentrations of elemental carbon (“soot”). Common cellular reactions included cellular stress responses and endocytosis. Reactions to HFO emissions were dominated by oxidative stress and inflammatory responses, whereas DF emissions induced generally a broader biological response than HFO emissions and affected essential cellular pathways such as energy metabolism, protein synthesis, and chromatin modification. Conclusions Despite a lower content of known toxic compounds, combustion particles from the clean shipping fuel DF influenced several essential pathways of lung cell metabolism more strongly than particles from the unrefined fuel HFO. This might be attributable to a higher soot content in DF. Thus the role of diesel soot, which is a known carcinogen in acute air pollution-induced health effects should be further investigated. For the

  5. In vivo X-Ray excited optical luminescence from phosphor-doped aerogel and Sylgard 184 composites

    Science.gov (United States)

    Allison, Stephen W.; Baker, Ethan S.; Lynch, Kyle J.; Sabri, Firouzeh

    2017-06-01

    X-Ray excited optical luminescence (XEOL) is a new and noninvasive diagnostic technique suitable for in situ biochemical imaging and disease detection. The X-Ray excited optical luminescence of phosphor doping in crosslinked silica aerogel and Sylgard 184 hosts was investigated in this study. Composite silica aerogels and Sylgard 184 samples of 5%, 15%, and 50% concentrations by weight of La2O2S:Eu phosphor were prepared and inserted subcutaneously in a Sprague-Dawley rat and excited by X-Ray emission at 70 and 100 kV. A fiber optic bundle positioned within 5 mm of the sample collected the luminescence signal and conveyed it to a photomultiplier detector. The signal intensity scaled with dopant concentration. The time dependence of the predominantly red luminescence consisted of 60 cycle bursts of approximately 8 ms duration. The amplitude was modulated at about 10 Hz with a 60% depth. This indicates the time dependence of the X-Ray source. A simulation showed how to observe phosphor decay between individual burst pulses. The emission from the two types of composite samples was easily detected from the outside of the skin layer. Both Sylgard 184 and crosslinked silica aerogels are biocompatible and bio stable materials that could serve a variety of potential XEOL applications. These very strong signals imply potential for creating new In-vivo sensing applications and diagnostic tools.

  6. Fabrication and luminescent properties of (Y0.99Eu0.01)2O3 transparent nanostructured ceramics

    Science.gov (United States)

    Yavetskiy, R. P.; Dobrotvorskaya, M. V.; Doroshenko, A. G.; Tolmachev, A. V.; Petrusha, I. A.; Turkevich, V. Z.; Tomala, R.; Hreniak, D.; Strek, W.; Baumer, V. N.

    2018-04-01

    (Y0.99Eu0.01)2O3 nanoceramics have been produced by sintering of stable cubic nanopowders under 8 GPa at temperature in the range of 25-500 °C with the use of Low Temperature High Pressure (LTHP) technique. During consolidation step irreversible phase transition from cubic to monoclinic yttria occurs resulting in two-phase nanoceramics with a grain size in the 10-40 nm range. It has been demonstrated that composite nanoceramics possess a high transmittance in the visible and mid IR ranges due to small light scattering on the nanoscale pores and low birefringence due to extremely small grain size. It has been shown that Eu3+ ions act as a luminescent probe in composite (Y0.99Eu0.01)2O3 nanoceramics since their 4f-4f luminescence strongly depends on the crystallographic environment. The luminescence spectra excited in the charge transfer band (CTB) are presented by superposition of emission from europium ions in cubic and monoclinic yttria. A new wide emission band of (Y0.99Eu0.01)2O3 ceramics in the λ = 500-650 nm wavelengths range (λex. = 307 nm) were attributed to luminescence of Eu3+ ions located in perturbed sites at grain boundaries or interfaces.

  7. Luminescence properties of Yb:Nd:Tm:KY3F10 nanophosphor and thermal treatment effects

    International Nuclear Information System (INIS)

    Gomes, Laércio; Linhares, Horácio Marconi da Silva M.D.; Ichikawa, Rodrigo Uchida; Martinez, Luis Gallego; Ranieri, Izilda Marcia

    2015-01-01

    In this work, we present the spectroscopic properties of KY 3 F 10 (KY3F) nanocrystals activated with thulium and codoped with ytterbium and neodymium ions. The most important processes that lead to the thulium upconversion emissions in the blue region were identified. A time-resolved luminescence spectroscopy technique was employed to measure the luminescence decays and to determine the most important mechanisms involved in the upconversion process that populates 1 G 4 (Tm 3+ ) excited states. Analysis of the energy-transfer processes dynamics using selective pulsed-laser excitations in Yb:Nd:Tm, Nd:KY3F nanocrystals shows that the direct energy transfer from Nd 3+ to Tm 3+ ions is the mechanism responsible for the 78% of the blue upconversion luminescence in the Yb:Nd:Tm:KY3F when compared with the Yb:Nd:Tm:KY3F bulk crystal for an laser excitation at 802 nm. An investigation of the 1 G 4 level luminescence kinetic of Tm 3+ in Yb/Nd/Tm system revealed that the luminescence efficiency ( 1 G 4 ) starts with a very low value (0.38%) for the synthesized nanocrystal (as grown) and strongly increases to 97% after thermal treatment at 550 °C for 6 h under argon flow. As a consequence of the thermal treatment at T=550 °C, the contributions of the (Nd×Tm) (Up 1 ) and (Nd×Yb×Tm) (Up 2 ) upconversion processes to the 1 G 4 luminescence are 33% (Up 1 ) and 67% for Up 2 . Up 2 process represented by Nd 3+ ( 4 F 3/2 )→Yb 3+ ( 2 F 7/2 ) followed by Yb 3+ ( 2 F 5/2 )→Tm ( 3 H 4 )→Tm 3+ ( 1 G 4 ) was previously reported as the main mechanism to produce the blue luminescence in Yb:Nd:Tm:YLiF 4 and KY 3 F 10 bulk crystals. Results of X-ray diffraction analysis of nanopowder using the Rietveld method reveled that crystallite sizes remain unchanged (12–14 nm) after thermal treatments with T≤400 °C, while the 1 G 4 luminescence efficiency strongly increases from 0.38% (T=25 °C) to 12% (T=400 °C). Results shown that the Nd 3+ ions distribution has a concentration

  8. Water dispersible, non-cytotoxic, cross-linked luminescent AIE dots: Facile preparation and bioimaging applications

    Science.gov (United States)

    Liu, Meiying; Zhang, Xiqi; Yang, Bin; Deng, Fengjie; Li, Zhen; Wei, Junchao; Zhang, Xiaoyong; Wei, Yen

    2014-12-01

    Fluorescent organic nanoparticles have attracted great current research interest due to their superior properties as compared with small organic dyes and fluorescent inorganic nanoparticles. However, fluorescent organic nanoparticles based on conventional organic dyes often result in significant fluorescence decrease due to the notorious aggregation-caused quenching effect. On the other hand, these fluorescent organic nanoparticles obtained from self-assembly are normally not stable in diluted solution. Therefore, the development of novel fluorescent organic nanoparticles which could overcome these limitations is highly desirable for their practical biomedical applications. In this work, water dispersible, non-cytotoxic and cross-linked luminescent polymeric nanoparticles based on aggregation induced emission dyes were prepared via one pot emulsion polymerization. These cross-linked luminescent polymeric nanoparticles emitted strong red fluorescence and were highly stable in diluted aqueous solution, making them highly potential for various biomedical applications.

  9. Novel Green Luminescent and Phosphorescent Material: Semiconductive Nanoporous ZnMnO with Photon Confinement.

    Science.gov (United States)

    Lee, Sejoon; Lee, Youngmin; Panin, Gennady N

    2017-06-21

    A novel green luminescent and phosphorescent material of semiconductive nanoporous ZnMnO was synthesized by the thermal nucleation of nanopores in the 20-period Zn 0.93 Mn 0.07 O/Zn 0.65 Mn 0.35 O multilayer structure. Nanoporous ZnMnO showed an n-type semiconducting property and exhibited an extremely strong green light emission in its luminescence and phosphorescence characteristics. This arises from the formation of the localized energy level (i.e., green emission band) within the energy band gap and the confinement of photons. The results suggest nanoporous ZnMnO to have a great potential for the new type of semiconducting green phosphors and semiconductor light-emitting diodes with lower thresholds, producing an efficient light emission. In-depth analyses on the structural, electrical, and optical properties are thoroughly examined, and the formation mechanism of nanoporous ZnMnO and the origin of the strong green light emission are discussed.

  10. High coating of Ru(II) complexes on gold nanoparticles for single particle luminescence imaging in cells.

    Science.gov (United States)

    Rogers, Nicola J; Claire, Sunil; Harris, Robert M; Farabi, Shiva; Zikeli, Gerald; Styles, Iain B; Hodges, Nikolas J; Pikramenou, Zoe

    2014-01-18

    Gold nanoparticles are efficiently labelled with a luminescent ruthenium complex, producing 13 and 100 nm diameter, monodisperse red-emissive imaging probes with luminescence lifetimes prolonged over the molecular unit. Single, 100 nm particles are observed in whole cell luminescence imaging which reveals their biomolecular association with chromatin in the nucleus of cancer cells.

  11. Mesoporous upconversion nanoparticles modified with a Tb(III) complex to display both green upconversion and down conversion luminescence for in vitro bioimaging and sensing of temperature

    International Nuclear Information System (INIS)

    Ge, Xiaoqian; Sun, Lining; Liu, Jinliang; Xu, Yanxia; Wei, Zuwu; Shi, Liyi; Dang, Song; Zhang, Hongjie

    2015-01-01

    A new multifunctional nanocomposite is described that displays both upconversion and down conversion luminescence. It is based on upconversion nanoparticles (UCNPs) with a mesoporous coating that is boned with a terbium(III) complex. The modified mesoporous nanocomposite was characterized by transmission electron microscopy, X-ray powder diffraction, nitrogen adsorption-desorption isotherms, and photoluminescence spectra. They display dual (green and red) fluorescence under 980-nm excitation, and green fluorescence under 365-nm excitation. Both emissions can be easily detected by bare eyes. The material has low cytotoxicity and good biocompatibility as proven by the methyl thiazolyltetrazolium (MTT) assay. The nanocomposite was successfully applied to upconversion luminescence based in-vitro confocal imaging of the cytosol of murine macrophage cells (RAW264.7), and this resulted in images of excellent contrast. In addition, the particles display strongly temperature-dependent luminescence in the range from 280 K to 330 K. (author)

  12. A perfectly aligned 63 helical tubular cuprous bromide single crystal for selective photo-catalysis, luminescence and sensing of nitro-explosives.

    Science.gov (United States)

    Yao, Ru-Xin; Hailili, Reshalaiti; Cui, Xin; Wang, Li; Zhang, Xian-Ming

    2015-02-21

    A perfectly aligned 63 helical tubular cuprous bromide single crystal has been synthesized and characterized, which can selectively decompose negatively charged dyes of Methyl Orange (MO) and Kermes Red (KR), and the photocatalytic efficiency is higher than that of nanosized (∼25 nm) TiO2 and ZnO. The direction and magnitude of the dipole moments as well as the band structure were calculated to reveal high photocatalytic efficiency. Moreover, luminescence studies indicate that the CuBr tube materials show very strong yellowish green emissions in the solid state and emulsion even at room temperature, and exhibit extremely high detection sensitivity towards nitro-explosives via fluorescence quenching. Detectable luminescence responses were observed at a very low concentration of 20 ppm with a high quenching efficiency of 94.90%. The results suggest that they may be promising multifunctional materials for photo-catalysis, luminescence and sensing of nitro-explosives.

  13. Towards space based verification of CO2 emissions from strong localized sources: fossil fuel power plant emissions as seen by a CarbonSat constellation

    Directory of Open Access Journals (Sweden)

    T. Krings

    2011-12-01

    Full Text Available Carbon dioxide (CO2 is the most important man-made greenhouse gas (GHG that cause global warming. With electricity generation through fossil-fuel power plants now being the economic sector with the largest source of CO2, power plant emissions monitoring has become more important than ever in the fight against global warming. In a previous study done by Bovensmann et al. (2010, random and systematic errors of power plant CO2 emissions have been quantified using a single overpass from a proposed CarbonSat instrument. In this study, we quantify errors of power plant annual emission estimates from a hypothetical CarbonSat and constellations of several CarbonSats while taking into account that power plant CO2 emissions are time-dependent. Our focus is on estimating systematic errors arising from the sparse temporal sampling as well as random errors that are primarily dependent on wind speeds. We used hourly emissions data from the US Environmental Protection Agency (EPA combined with assimilated and re-analyzed meteorological fields from the National Centers of Environmental Prediction (NCEP. CarbonSat orbits were simulated as a sun-synchronous low-earth orbiting satellite (LEO with an 828-km orbit height, local time ascending node (LTAN of 13:30 (01:30 p.m. LT and achieves global coverage after 5 days. We show, that despite the variability of the power plant emissions and the limited satellite overpasses, one CarbonSat has the potential to verify reported US annual CO2 emissions from large power plants (≥5 Mt CO2 yr−1 with a systematic error of less than ~4.9% and a random error of less than ~6.7% for 50% of all the power plants. For 90% of all the power plants, the systematic error was less than ~12.4% and the random error was less than ~13%. We additionally investigated two different satellite configurations using a combination of 5 CarbonSats. One achieves global coverage everyday but only samples the targets at fixed local times. The other

  14. Cerium luminescence in nd0 perovskites

    International Nuclear Information System (INIS)

    Setlur, A.A.; Happek, U.

    2010-01-01

    The luminescence of Ce 3+ in perovskite (ABO 3 ) hosts with nd 0 B-site cations, specifically Ca(Hf,Zr)O 3 and (La,Gd)ScO 3 , is investigated in this report. The energy position of the Ce 3+ excitation and emission bands in these perovskites is compared to those of typical Al 3+ perovskites; we find a Ce 3+ 5d 1 centroid shift and Stokes shift that are larger versus the corresponding values for the Al 3+ perovskites. It is also shown that Ce 3+ luminescence quenching is due to Ce 3+ photoionization. The comparison between these perovskites shows reasonable correlations between Ce 3+ luminescence quenching, the energy position of the Ce 3+ 5d 1 excited state with respect to the host conduction band, and the host composition. - Graphical abstract: Ce 3+ decay times versus temperature for perovskites with nd 0 B-site cations.

  15. Effects of nanostructuring on luminescence properties of SrS:Ce,Sm phosphor: An experimental and phenomenological study

    Science.gov (United States)

    Yazdanmehr, Mohsen; Sadeghi, Hossein; Tehrani, Masoud Kavosh; Hashemifar, Seyed Javad; Mahdavi, Mohammad

    2018-01-01

    In this work, we employ various experimental techniques to illustrate the effects of nanostructuring on improvement of the luminescence properties of the polycrystalline SrS co-activated by cerium and samarium dopants (SrS : Ce , Sm). The nano and microstructure SrS : Ce , Sm powders were synthesized by the co-precipitation and solid state diffusion methods, respectively, followed by the spark plasma sintering (SPS) process to densify powders into pellet shape. It is observed that the photo-luminescence (PL), radio-luminescence (RL), and optically stimulated luminescence (OSL) emission intensity of the nanostructure samples are significantly improved with respect to the microstructure samples. Moreover, by using an accurate photomultiplier tube, we measured the CW-OSL decay curves of the samples to demonstrate much higher and faster sensitivity of the nanostructure SrS : Ce , Sm for in-flight and online OSL radiation dosimetry. The obtained absorption and emission spectra are used for phenomenology of the electronic band structure of the SrS : Ce , Sm micro and nano-phosphors inside the band gap. The proposed phenomenological electronic structures are then used to clarify the role of Ce3+ and Sm3+ localized energy levels in the luminescence properties of the nano and microstructure samples. It is argued that electronic transitions from the 2T2g state of Ce3+ and the 4G5/2 state of Sm3+ have strong contribution to the PL and RL emission spectra, while in the OSL mechanism, the Sm3+ 4G5/2 state is mainly responsible for electrons trapping.

  16. Magnetic-luminescent spherical particles synthesized by ultrasonic spray pyrolysis

    International Nuclear Information System (INIS)

    Michel, Norma L; Hirata, Gustavo A; Flores, Dora L

    2015-01-01

    The combination of magnetic and luminescent properties in a single particle system, opens-up a wide range of potential applications in biotechnology and biomedicine. In this work, we performed the synthesis of magnetic-luminescent Gd 2 O 3 :Eu 3+ @Fe 2 O 3 particles by ultrasonic spray pyrolysis performed in a tubular furnace. In order to achieve the composite formation, commercial superparamagnetic Fe 3 O 4 nanoparticles were coated with a luminescent Eu 3+ -doped Gd 2 O 3 shell in a low-cost one-step process. The spray pyrolysis method yields deagglomerated spherical shape magneto/luminescent particles. The photoluminescence spectra under UV excitation (λ Exc = 265 nm) of the magnetic Gd 2 O 3 :Eu 3+ @Fe 2 O 3 compound showed the characteristic red emission of Eu 3+ (λ Em = 612 nm). This magneto/luminescent system will find applications in biomedicine and biotechnology. (paper)

  17. Spatially Resolved Patchy Ly α Emission within the Central Kiloparsec of a Strongly Lensed Quasar Host Galaxy at z = 2.8

    Energy Technology Data Exchange (ETDEWEB)

    Bayliss, Matthew B.; Bordoloi, Rongmon [Kavli Institute for Astrophysics and Space Research, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139 (United States); Sharon, Keren; Runnoe, Jessie; Johnson, Traci; Paterno-Mahler, Rachel [Department of Astronomy, University of Michigan, 1085 S. University Avenue, Ann Arbor, MI 48109 (United States); Acharyya, Ayan; Bian, Fuyan; Kewley, Lisa [RSAA, Australian National University, Cotter Road, Weston Creek, ACT 2611 (Australia); Gladders, Michael D. [Kavli Institute for Cosmological Physics, University of Chicago, Chicago, IL 60637 (United States); Rigby, Jane R. [Astrophysics Science Division, NASA Goddard Space Flight Center, 8800 Greenbelt Road, Greenbelt, MD 20771 (United States); Dahle, Hakon [Institute of Theoretical Astrophysics, University of Oslo, P.O. Box 1029, Blindern, NO-0315 Oslo (Norway); Florian, Michael, E-mail: mbayliss@mit.edu [Department of Astronomy and Astrophysics, University of Chicago, Chicago, IL 60637 (United States)

    2017-08-20

    We report the detection of extended Ly α emission from the host galaxy of SDSS J2222+2745, a strongly lensed quasar at z = 2.8. Spectroscopic follow-up clearly reveals extended Ly α in emission between two images of the central active galactic nucleus (AGN). We reconstruct the lensed quasar host galaxy in the source plane by applying a strong lens model to HST imaging and resolve spatial scales as small as ∼200 pc. In the source plane, we recover the host galaxy morphology to within a few hundred parsecs of the central AGN and map the extended Ly α emission to its physical origin on one side of the host galaxy at radii ∼0.5–2 kpc from the central AGN. There are clear morphological differences between the Ly α and rest-frame ultraviolet stellar continuum emission from the quasar host galaxy. Furthermore, the relative velocity profiles of quasar Ly α , host galaxy Ly α , and metal lines in outflowing gas reveal differences in the absorbing material affecting the AGN and host galaxy. These data indicate the presence of patchy local intervening gas in front of the central quasar and its host galaxy. This interpretation is consistent with the central luminous quasar being obscured across a substantial fraction of its surrounding solid angle, resulting in strong anisotropy in the exposure of the host galaxy to ionizing radiation from the AGN. This work demonstrates the power of strong-lensing-assisted studies to probe spatial scales that are currently inaccessible by other means.

  18. Optical spectroscopy and luminescence properties of Ho3+ doped zinc fluorophosphate (ZFP) glasses for green luminescent device applications

    Science.gov (United States)

    Reddy Prasad, V.; Damodaraiah, S.; Ratnakaram, Y. C.

    2018-04-01

    Ho3+ doped zinc fluorophosphate (ZFP) glasses with molar chemical compositions, (60-x) NH4H2PO4+20ZnO+10BaF2+10NaF+xHo2O3 (where x = 0.1, 0.3, 0.5, 1.0 and 1.5 mol%) were prepared by melt quenching technique. These glasses were characterized through physical, structural, optical, excitation, luminescence and decay curve analysis. From the absorption spectra, spectral intensities (fexp and fcal), Judd-Ofelt intensity parameters (Ω2, Ω4 and Ω6), radiative transition probabilities (AT), radiative lifetimes (τR) and branching ratios (βR) were evaluated for all Ho3+ doped ZFP glass matrices. From the photoluminescence spectra, peak stimulated emission cross-sections (σP) were calculated for all Ho3+ doped ZFP glasses. The Ho3+ doped ZFP glasses show strong green emission at 545 nm and red emission at 656 nm under excitation, 450 nm. The measured lifetimes (τmeas) of (5S2)5F4 level of Ho3+ doped ZFP glasses were obtained from decay profiles. The CIE color coordinates of Ho3+ doped ZFP glasses were calculated from emission spectra and 1.0 mol% of Ho3+ doped ZFP glass matrix gives green emission. Hence, these results confirm that the Ho3+ doped ZFP glasses could be considered as a promising candidate for visible green laser applications.

  19. A STRONG EMISSION LINE NEAR 24.8 Angstrom-Sign IN THE X-RAY BINARY SYSTEM MAXI J0556-332: GRAVITATIONAL REDSHIFT OR UNUSUAL DONOR?

    Energy Technology Data Exchange (ETDEWEB)

    Maitra, Dipankar; Miller, Jon M.; Reynolds, Mark T. [Department of Astronomy, University of Michigan, Ann Arbor, MI 48109 (United States); Raymond, John C., E-mail: dmaitra@umich.edu [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States)

    2011-12-10

    We report the discovery of a strong emission line near 24.8 Angstrom-Sign (0.5 keV) in the newly discovered X-ray binary system MAXI J0556-332 with the reflection grating spectrometer (RGS) on board the XMM-Newton observatory. The X-ray light curve morphology during these observations is complex and shows occasional dipping behavior. Here we present time- and rate-selected spectra from the RGS and show that this strong emission line is unambiguously present in all the XMM observations. The measured line center is consistent with the Ly{alpha} transition of N VII in the rest frame. While the spectra contain imprints of absorption lines and edges, there appear to be no other significantly prominent narrow line due to the source itself, thus making the identification of the 24.8 Angstrom-Sign line uncertain. We discuss possible physical scenarios, including a gravitationally redshifted O VIII Ly{alpha} line originating at the surface of a neutron star or an unusual donor with an extremely high N/O abundance (>57) relative to solar that may have produced this comparatively strong emission line.

  20. Luminescence variations in europium-doped silicon-substituted hydroxyapatite nanobiophosphor via three different methods

    Energy Technology Data Exchange (ETDEWEB)

    Thang, Cao Xuan; Pham, Vuong-Hung, E-mail: vuong.phamhung@hust.edu.vn

    2015-07-15

    Highlights: • Europium doped silicon-substituted hydroxyapatite was synthesized by wet chemical synthesis method. • Morphology of nanoparticles depended on the synthesized method. • Photoluminescence intensity of the sample increases with the increasing of Si substitutions, Eu dopants and thermal annealing. - Abstract: This paper reports the first attempt for the synthesis of europium-doped Si-substituted hydroxyapatite (HA) nanostructure to achieve strong and stable luminescence of nanobiophosphor, particularly, by addition of different Eu dopants, Si substitutions, and application of optimum annealing temperatures of up to 1000 °C. The nanobiophosphor was synthesized by the coprecipitation, microwave, and hydrothermal methods. The nanoparticles demonstrated a nanowire to a spindle-like morphology, which was dependent on the method of synthesis. The photoluminescence (PL) intensity of the sample increases with the increase in Si substitutions and Eu dopants. The luminescent nanoparticles also showed the typical luminescence of Eu{sup 3+} centered at 610 nm, which was more efficient for the annealed Eu-doped Si-HA nanoparticles than for the as-synthesized nanoparticles. Among the different synthesis methods, the hydrothermal method reveals the best light emission represented by high PL intensity and narrow PL spectra. These results suggest the potential application of Eu-doped Si-HA in stable and biocompatible nanophosphors for light emission and nanomedicine.

  1. X-RAY EMISSION FROM STRONGLY ASYMMETRIC CIRCUMSTELLAR MATERIAL IN THE REMNANT OF KEPLER'S SUPERNOVA

    Energy Technology Data Exchange (ETDEWEB)

    Burkey, Mary T.; Reynolds, Stephen P.; Borkowski, Kazimierz J.; Blondin, John M., E-mail: reynolds@ncsu.edu [Department of Physics, North Carolina State University, Raleigh NC 27695-8202 (United States)

    2013-02-10

    Kepler's supernova remnant resulted from a thermonuclear explosion, but is interacting with circumstellar material (CSM) lost from the progenitor system. We describe a statistical technique for isolating X-ray emission due to CSM from that due to shocked ejecta. Shocked CSM coincides well in position with 24 {mu}m emission seen by Spitzer. We find most CSM to be distributed along the bright north rim, but substantial concentrations are also found projected against the center of the remnant, roughly along a diameter with position angle {approx}100 Degree-Sign . We interpret this as evidence for a disk distribution of CSM before the supernova, with the line of sight to the observer roughly in the disk plane. We present two-dimensional hydrodynamic simulations of this scenario in qualitative agreement with the observed CSM morphology. Our observations require Kepler to have originated in a close binary system with an asymptotic giant branch star companion.

  2. Luminescence techniques: Instrumentation and methods

    DEFF Research Database (Denmark)

    Bøtter-Jensen, L.

    1997-01-01

    This paper describes techniques, instruments and methods used in luminescence dating and environmental dosimetry in many laboratories around the world. These techniques are based on two phenomena - thermally stimulated luminescence and optically stimulated luminescence. The most commonly used...... luminescence stimulation and detection techniques are reviewed and information is given on recent developments in instrument design and on the stale of the art in luminescence measurements and analysis. (C) 1998 Elsevier Science Ltd. All rights reserved....

  3. Effect of oxygen concentration on singlet oxygen luminescence detection

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Longchao; Lin, Lisheng; Li, Yirong; Lin, Huiyun; Qiu, Zhihai [MOE Key Laboratory of OptoElectronic Science and Technology for Medicine, Fujian Provincial Key Laboratory for Photonics Technology, Fujian Normal University, Fuzhou 350007 (China); Gu, Ying [Department of Laser Medicine, Chinese PLA General Hospital, Beijing 100853 (China); Li, Buhong, E-mail: bhli@fjnu.edu.cn [MOE Key Laboratory of OptoElectronic Science and Technology for Medicine, Fujian Provincial Key Laboratory for Photonics Technology, Fujian Normal University, Fuzhou 350007 (China)

    2014-08-01

    Singlet oxygen ({sup 1}O{sub 2}) is a major phototoxic component in photodynamic therapy (PDT) and its generation is dependent on the availability of tissue oxygen. To examine the effect of oxygen concentration on {sup 1}O{sub 2} detection, two hydrophilic photosensitizer (PS), rose bengal (RB) and meso-metra (N-methyl-4-pyridyl) porphine tetra tosylate (TMPyP) were used as model PS. Irradiation was carried out using 523 nm under hypoxic (2%, 13%), normoxic (21%) and hyperoxic (65%) conditions. The spectral and spatial resolved {sup 1}O{sub 2} luminescence was measured by near-infrared (NIR) photomultiplier tube (PMT) and camera, respectively. Upon the irradiation, the emission signal mainly consisted of background scattering light, PS fluorescence and phosphorescence, and {sup 1}O{sub 2} luminescence. The PS phosphorescence was evidently dependent on the oxygen concentration and PS type, which resulted in the change of emission profile of {sup 1}O{sub 2} luminescence. This change was further demonstrated on {sup 1}O{sub 2} luminescence image. The present study suggests that the low oxygen concentration could affect {sup 1}O{sub 2} luminescence detection. - Highlights: • Both spectral and spatial resolved {sup 1}O{sub 2} luminescence measurements were performed. • Effect of oxygen concentration on {sup 1}O{sub 2} generation was quantitatively evaluated. • Low oxygen concentration could affect {sup 1}O{sub 2} luminescence detection.

  4. Enhanced luminescence and white light emission from Eu(3+) -co-doped K3 Ca2 (SO4 )3 Cl:Dy(3+) phosphor with near visible ultraviolet excitation for white LEDs.

    Science.gov (United States)

    Baig, N; Dhoble, N S; Park, K; Kokode, N S; Dhoble, S J

    2015-06-01

    The luminescent properties of europium (Eu)- and dysprosium (Dy)-co-doped K3 Ca2 (SO4 )3 Cl halosulfate phosphors were analyzed. This paper reports the photoluminescence (PL) properties of K3 Ca2 (SO4 )3 Cl microphosphor doped with Eu and Dy and synthesized using a cost-effective wet chemical method. The phosphors were characterized by X-ray diffraction and scanning electron microscopy. The CIE coordinates were calculated to display the color of the phosphor. PL emission of the prepared samples show peaks at 484 nm (blue), 575 nm (yellow), 594 nm (orange) and 617 nm (red). The emission color of the Eu,Dy-co-doped K3 Ca2 (SO4 )3 Cl halophosphor depends on the doping concentration and excitation wavelength. The addition of Eu in K3 Ca2 (SO4 )3 Cl:Dy greatly enhances the intensity of the blue and yellow peaks, which corresponds to the (4)  F9/2  → (6) H15/2 and (4)  F9/2  → (6) H13/2 transitions of Dy(3+) ions (under 351 nm excitation). The Eu(3+) /Dy(3+) co-doping also produces white light emission for 1 mol% of Eu(3+) , 1 mol% of Dy(3+) in the K3 Ca2 (SO4 )3 Cl lattice under 396 nm excitation, for which the calculated chromaticity coordinates are (0.35, 0.31). Thus, K3 Ca2 (SO4 )3 Cl co-doped with Eu/Dy is a suitable candidate for NUV based white light-emitting phosphors technology. Copyright © 2014 John Wiley & Sons, Ltd.

  5. Luminescence properties of porcelain ceramics relevant to restrospective radiation dosimetry

    DEFF Research Database (Denmark)

    Bøtter-Jensen, L.; Markey, B.G.; Poolton, N.R.J.

    1996-01-01

    When applied to porcelain products, optically stimulated luminescence (OSL) is a potentially viable method for use in dose reconstruction following contamination from nuclear accidents. However, dose sensitivities are highly variable, depending on what type of porcelain is being measured. This ap......When applied to porcelain products, optically stimulated luminescence (OSL) is a potentially viable method for use in dose reconstruction following contamination from nuclear accidents. However, dose sensitivities are highly variable, depending on what type of porcelain is being measured...... to have the highest sensitivities to radiation dose. Moreover, the presence of these phases is easily identifiable by characteristic signatures in the luminescence emission spectra....

  6. Europium enabled luminescent nanoparticles for biomedical applications

    International Nuclear Information System (INIS)

    Syamchand, S.S.; Sony, G.

    2015-01-01

    Lanthanide based nanoparticles are receiving great attention ought to their excellent luminescent and magnetic properties and find challenging biomedical applications. Among the luminescent lanthanide NPs, europium based NPs (Eu-NPs) are better candidates for immunoassay and imaging applications. The Eu-NPs have an edge over quantum dots (QDs) by means of their stable luminescence, long fluorescence lifetime, sharp emission peaks with narrow band width, lack of blinking and biocompatibility. This review surveys the synthesis and properties of a variety of Eu-NPs consolidated from different research articles, for their applications in medicine and biology. The exquisite luminescent properties of Eu-NPs are explored for developing biomedical applications such as immunoassay and bioimaging including multimodal imaging. The biomedical applications of Eu-NPs are mostly diagnostic in nature and mainly focus on various key analytes present in biological systems. The luminescent properties of europium enabled NPs are influenced by a number of factors such as the site symmetry, the metal nanoparticles, metal ions, quantum dots, surfactants, morphology of Eu-NPs, crystal defect, phenomena like antenna effect and physical parameters like temperature. Through this review we explore and assimilate all the factors which affect the luminescence in Eu-NPs and coil a new thread of parameters that control the luminescence in Eu-NPs, which would provide further insight in developing Eu-based nanoprobes for future biomedical prospects. - Highlights: • The review describes 14 major factors that influence the luminescence properties of europium enabled luminescent nanoparticles (Eu-NPs). • Surveys different types of europium containing nanoparticles that have been reported for their biomedical applications. • Eu-NPs are conveniently divided into four different categories, based on the type of the substrates involved. The four categories are (1) virgin Eu-substrate based NPs; (2

  7. Monitoring Temperatures of Tires Using Luminescent Materials

    Science.gov (United States)

    Bencic, Timothy J

    2006-01-01

    A method of noncontact, optical monitoring of the surface temperature of a tire has been devised to enable the use of local temperature rise as an indication of potential or impending failures. The method involves the use of temperature-sensitive paint (or filler): Temperature-sensitive luminescent dye molecules or other luminescent particles are incorporated into a thin, flexible material coating the tire surface of interest. (Alternatively, in principle, the luminescent material could be incorporated directly into the tire rubber, though this approach has not yet been tested.) The coated surface is illuminated with shorter-wavelength light to excite longer-wavelength luminescence, which is observed by use of a charge-coupled-device camera or a photodetector (see Figure 1). If temporally constant illumination is used, then the temperature can be deduced from the known temperature dependence of the intensity response of the luminescence. If pulsed illumination is used, then the temperature can be deduced from the known temperature dependence of the time or frequency response of the luminescence. If sinusoidally varying illumination is used, then the temperature can be deduced from the known temperature dependence of the phase response of the luminescence. Unlike a prior method of monitoring the temperature at a fixed spot on a tire by use of a thermocouple, this method is not restricted to one spot and can, therefore, yield information on the spatial distribution of temperature: in particular, it enables the discovery of newly forming hot spots where damage may be starting. Also unlike in the thermocouple method, the measurements in this method are not vulnerable to breakage of wires in repeated flexing of the tire. Moreover, unlike in another method in which infrared radiation is monitored as an indication of surface temperature, the luminescence measurements in this method are not significantly affected by changes in infrared emissivity. This method has been

  8. Radio emission from the X-ray pulsar Her X-1: a jet launched by a strong magnetic field neutron star?

    Science.gov (United States)

    van den Eijnden, J.; Degenaar, N.; Russell, T. D.; Miller-Jones, J. C. A.; Wijnands, R.; Miller, J. M.; King, A. L.; Rupen, M. P.

    2018-01-01

    Her X-1 is an accreting neutron star (NS) in an intermediate-mass X-ray binary. Like low-mass X-ray binaries (LMXBs), it accretes via Roche lobe overflow, but similar to many high-mass X-ray binaries containing a NS; Her X-1 has a strong magnetic field and slow spin. Here, we present the discovery of radio emission from Her X-1 with the Very Large Array. During the radio observation, the central X-ray source was partially obscured by a warped disc. We measure a radio flux density of 38.7 ± 4.8 μJy at 9 GHz but cannot constrain the spectral shape. We discuss possible origins of the radio emission, and conclude that coherent emission, a stellar wind, shocks and a propeller outflow are all unlikely explanations. A jet, as seen in LMXBs, is consistent with the observed radio properties. We consider the implications of the presence of a jet in Her X-1 on jet formation mechanisms and on the launching of jets by NSs with strong magnetic fields.

  9. Raman scattering and luminescence of high-Tc superconducting oxides

    International Nuclear Information System (INIS)

    Eremenko, V.V.; Gnezdilov, V.P.; Fomin, V.I.; Fugol', I.Ya.; Samovarov, V.N.

    1989-01-01

    Raman and luminescence spectra of high-T c superconducting oxides are summarized, mainly YBa 2 Cu 3 O 7-σ and partly La 2-x Ba x CuO 4-σ . In raman spectra we succeeded to distinguish electron scattering to define the energy gap Δ in the superconducting state. The luminescence spectra are due to the emission of oxygen and interaction with conduction electrons. 70 refs.; 13 figs

  10. Dimensions of luminescent oxidized and porous silicon structures

    Science.gov (United States)

    Schuppler, S.; Friedman, S. L.; Marcus, M. A.; Adler, D. L.; Xie, Y.-H.; Ross, F. M.; Harris, T. D.; Brown, W. L.; Chabal, Y. J.; Brus, L. E.; Citrin, P. H.

    1994-04-01

    X-ray absorption measurements from H-passivated porous Si and from oxidized Si nanocrystals, combined with electron microscopy, ir absorption, α recoil, and luminescence emission data, provide a consistent structural picture of the species responsible for the visible luminescence observed in these samples. The mass-weighted average structures in por-Si are particles, not wires, with dimensions significantly smaller than previously reported or proposed.

  11. Device and method for luminescence enhancement by resonant energy transfer from an absorptive thin film

    Energy Technology Data Exchange (ETDEWEB)

    Akselrod, Gleb M.; Bawendi, Moungi G.; Bulovic, Vladimir; Tischler, Jonathan R.; Tisdale, William A.; Walker, Brian J.

    2017-12-12

    Disclosed are a device and a method for the design and fabrication of the device for enhancing the brightness of luminescent molecules, nanostructures, and thin films. The device includes a mirror, a dielectric medium or spacer, an absorptive layer, and a luminescent layer. The absorptive layer is a continuous thin film of a strongly absorbing organic or inorganic material. The luminescent layer may be a continuous luminescent thin film or an arrangement of isolated luminescent species, e.g., organic or metal-organic dye molecules, semiconductor quantum dots, or other semiconductor nanostructures, supported on top of the absorptive layer.

  12. Kinetics of infrared stimulated luminescence from feldspars

    International Nuclear Information System (INIS)

    Jain, M.; Sohbati, R.; Guralnik, B.; Murray, A.S.; Kook, M.; Lapp, T.; Prasad, A.K.; Thomsen, K.J.; Buylaert, J.P.

    2015-01-01

    We extend the localised transition model based on randomly varying recombination distances (Jain et al., 2012) to include Arrhenius analysis and truncated nearest neighbour distributions. The model makes important predictions regarding a) the physical understanding of the linear intercepts in the Arrhenius analysis for localised recombination systems and b) the relationship between charge depletion and shape of the luminescence decay curves; these predictions are successfully tested by experimental investigations. We demonstrate that this model successfully describes the kinetic behaviour, both thermal and optical, of the infrared stimulated luminescence signal from feldspar. Based on the application of this model, it is concluded that different infra-red stimulated luminescence emissions (UV, blue, yellow and far-red) follow the same kinetics, and, therefore, involve participation of the same electron (dosimetric) trap. The differences in thermal stabilities of the different emissions results from differences in number densities of the recombination sites. The results have implications for understanding the mechanism of the far-red emission, and the spatial distributions of recombination sites in feldspar. - Highlights: • Arrhenius analysis of IRSL based on localized transition model (Jain et al., 2012). • Kinetics of IRSL for the different emission bands. • A new analytical description for IRSL. • Demonstrating that feldspar IRSL is consistent with the predictions of the LTM.

  13. Luminescent properties of (Y,Gd)BO3:Bi3+,RE3+ (RE=Eu, Tb) phosphor under VUV/UV excitation

    International Nuclear Information System (INIS)

    Zeng Xiaoqing; Im, Seoung-Jae; Jang, Sang-Hun; Kim, Young-Mo; Park, Hyoung-Bin; Son, Seung-Hyun; Hatanaka, Hidekazu; Kim, Gi-Young; Kim, Seul-Gi

    2006-01-01

    Bi 3+ - and RE 3+ -co-doped (Y,Gd)BO 3 phosphors were prepared and their luminescent properties under vacuum ultraviolet (VUV)/UV excitation were investigated. Strong red emission for (Y,Gd)BO 3 :Bi 3+ ,Eu 3+ and strong green emission for (Y,Gd)BO 3 :Bi 3+ ,Tb 3+ are observed under VUV excitation from 147 to 200 nm with a much broader excitation region than that of single Eu 3+ -doped or Tb 3+ -doped (Y,Gd)BO 3 phosphor. Strong emissions are also observed under UV excitation around 265 nm where as nearly no luminescence is observed for single Eu 3+ -doped or Tb 3+ -doped (Y,Gd)BO 3 . The luminescence enhancement of Bi 3+ - and RE 3+ -co-doped (Y,Gd)BO 3 phosphors is due to energy transfer from Bi 3+ ion to Eu 3+ or Tb 3+ ion not only in the VUV region but also in the UV region. Besides, host sensitization competition between Bi 3+ and Eu 3+ or Tb 3+ is also observed. The investigated phosphors may be preferable for devices with a VUV light 147-200 nm as an excitation source such as PDP or mercury-free fluorescent lamp

  14. Green luminescence of divalent europium in the hydride chloride EuHCl

    International Nuclear Information System (INIS)

    Kunkel, Nathalie; Kohlmann, Holger; Rudolph, Daniel; Schleid, Thomas; Meijerink, Andries; Rommel, Stefan; Weihrich, Richard

    2015-01-01

    Luminescence properties of divalent europium in the mixed-anion hydride chloride EuHCl were studied for the first time. Olive-green single crystals of EuHCl (PbFCl-type structure: tetragonal, P4/nmm, a = 406.58(3) pm, c = 693.12(5) pm, c/a = 1.705, Z = 2) resulted from the reaction of elemental europium (Eu), sodium hydride (NaH) and sodium chloride (NaCl), while powder samples were prepared from the binary components europium dihydride (EuH 2 ) and dichloride (EuCl 2 ). Low temperature X-ray powder diffraction proved the absence of phase transitions for 12(2) K ≤ T ≤ 295(2) K. Bright green emission was observed under UV-excitation and assigned to the 4f 6 5d 1 -4f 7 transition of divalent europium. Temperature-dependent luminescence absorption and emission, as well as lifetime measurements were carried out on single crystal and powder samples. Surprisingly, only limited concentration quenching was found. Additionally, two emission bands (485 and 510 nm) are observed, whose intensity ratio depends strongly on temperature. In order to explain this behavior for a single Eu 2+ site, we suggest either a dynamical Jahn-Teller effect in the excited 5d 1 state or emission from both a 4f 6 5d 1 state and a trapped exciton state. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  15. The addition of a second lanthanide ion to increase the luminescence of europium(III) macrocyclic complexes

    Energy Technology Data Exchange (ETDEWEB)

    Bromm, A.J. Jr.; Vallarino, L.M. [Virginia Commonwealth Univ., Richmond, VA (United States). Dept. of Chemistry; Leif, R.C. [Newport Instruments, San Diego, CA (United States); Quagliano, J.R. [Los Alamos National Lab., NM (United States)

    1998-12-29

    At present, the microscopic visualization of luminescent labels containing lanthanide(III) ions, primarily europium(III), as light-emitting centers is best performed with time-gated instrumentation, which by virtually eliminating the background fluorescence results in an improved signal to noise ratio. However, the use of the europium(III) macrocycle, Quantum Dye{trademark}, in conjunction with the strong luminescence enhancing effect (cofluorescence) of yttrium(III) or gadolinium(III), can eliminate the need for such specialized instrumentation. In the presence of Gd(III), the luminescence of the Eu(III)-macrocycles can be conveniently observed with conventional fluorescence instrumentation at previously unattainable low levels. The Eu(III) {sup 5}D{sub 0} {r_arrow} {sup 7}F{sub 2} emission of the Eu(III)-macrocycles was observed as an extremely sharp band with a maximum at 619 nm and a clearly resolved characteristic pattern. At very low Eu(III)-macrocycle concentrations, another sharp emission was detected at 614 nm, arising from traces of Eu(III) present in even the purest commercially available gadolinium products. Discrimination of the resolved emissions of the Eu(III)-macrocycle and Eu(III) contaminant should provide a means to further lower the limit of detection of the Eu(III)-macrocycle.

  16. Luminescent molecular rods - transition-metal alkynyl complexes.

    Science.gov (United States)

    Yam, Vivian Wing-Wah; Wong, Keith Man-Chung

    2005-01-01

    A number of transition-metal complexes have been reported to exhibit rich luminescence, usually originating from phosphorescence. Such luminescence properties of the triplet excited state with a large Stoke's shift, long lifetime, high luminescence quantum yield as well as lower excitation energy, are envisaged to serve as an ideal candidate in the area of potential applications for chemosensors, dye-sensitized solar cells, flat panel displays, optics, new materials and biological sciences. Organic alkynes (poly-ynes), with extended or conjugatedπ-systems and rigid structure with linear geometry, have become a significant research area due to their novel electronic and physical properties and their potential applications in nanotechnology. Owing to the presence of unsaturated sp-hybridized carbon atoms, the alkynyl unit can serve as a versatile building block in the construction of alkynyl transition-metal complexes, not only throughσ-bonding but also viaπ-bonding interactions. By incorporation of linear alkynyl groups into luminescent transition-metal complexes, the alkynyl moiety with goodσ-donor,π-donor andπ-acceptor abilities is envisaged to tune or perturb the emission behaviors, including emission energy (color), intensity and lifetime by its role as an auxiliary ligand as well as to govern the emission origin from its direct involvement. This review summarizes recent efforts on the synthesis of luminescent rod-like alkynyl complexes with different classes of transition metals and details the effects of the introduction of alkynyl groups on the luminescence properties of the complexes.

  17. Triple-doped KMnF3:Yb3+/Er3+/Tm3+ nanocubes: four-color upconversion emissions with strong red and near-infrared bands

    Science.gov (United States)

    Wang, Hao; Hong, Xiaodong; Han, Renlu; Shi, Junhui; Liu, Zongjun; Liu, Shujuan; Wang, You; Gan, Yang

    2015-11-01

    Triple-doped (Yb3+/Er3+/Tm3+) KMnF3 nanocubes with uniform sizes of 250 nm were synthesized by a facile hydrothermal route using the oleic acid as the capping agent. It was found that these nanocubes can simultaneously exhibited four-color (blue, green, red and NIR) upconversion emissions under a single 980 nm near-infrared (NIR) laser excitation, which should have potential multicolor in vivo imaging applications. Specifically, the red (660 nm) and NIR (800 nm) peaks, known as two “optical windows” for imaging biological tissues, were strong. The spectral and pump analyses indicated the two-photon processes were responsible for the both red and NIR emissions.

  18. The effects of Tb 3 doping concentration on luminescence properties ...

    Indian Academy of Sciences (India)

    This paper is aimed at explaining the effects of Tb3+ concentration on structure and luminescence properties and clarifying the concentration quenching mechanism of Tb3+. The lattice of BaF2 decreases with the increase of Tb3+ ions concentration. The emission spectrum of BaF2:Tb3+ consists of blue emission band and ...

  19. Luminescence of nanocrystalline ZnSe:Mn2+

    NARCIS (Netherlands)

    Suyver, J.F.; Wuister, S.F.; Kelly, J.J.; Meijerink, A.

    2000-01-01

    The luminescence properties of nanocrystalline ZnSe:Mn^(2+) prepared via an inorganic chemical synthesis are described. Photoluminescence spectra show distinct ZnSe and Mn^(2+) related emissions, both of which are excited via the ZnSe host lattice. The Mn^(2+) emission wavelength and the

  20. Study of the luminescence properties of a natural amazonite

    International Nuclear Information System (INIS)

    Correcher, V.; Garcia-Guinea, J.

    2011-01-01

    Most gemstones, being natural materials (silicates, carbonates, phosphates, etc.), exhibit luminescence emission. This property could be potentially employed for personal dosimetry in the case of radiation accident or radiological terrorism where conventional monitoring has not been established. We, herein, report on the thermoluminescence (TL), radioluminescence (RL) and infra-red stimulated luminescence (IRSL) response of a well-characterised natural amazonite (KAlSi 3 O 8 ) that, due to its bright blue-green colour when polished, is used as a gemstone. The luminescence emission wavelengths, intensities and thermal kinetics of the amazonite luminescence curves reveal that the ultraviolet band measured on amazonite aliquots is similar to other common K-rich feldspars. On this basis, one can conclude (i) association between twinning and the UV-blue TL emission can be related to structural defects located in the twin-domain boundaries where ionic alkali-self-diffusion, irreversible water losses and irreversible dehydroxylation processes can be involved. (ii) Amazonite exhibits a complex structure with several planar defects (twinning and exsolution interphases which can hold hydroxyl groups, water molecules, etc.) and point defects (impurities, Na, Pb, Mn, etc.) that can act as luminescence centres, and in fact, green and red emissions are respectively associated with the presence of Mn and Fe impurities. Finally, (iv) the thermal stability tests performed on the TL emission of the amazonite confirm a continuum in the trap distribution, i.e. progressive changes in the glow curve shape, intensity and temperature position of the maximum peak.

  1. Study of the luminescence properties of a natural amazonite

    Energy Technology Data Exchange (ETDEWEB)

    Correcher, V., E-mail: v.correcher@ciemat.es [CIEMAT, Av. Complutense 22, Madrid 28040 (Spain); Garcia-Guinea, J. [Museo Nacional de Ciencias Naturales, CSIC, C/Jose Gutierrez Abascal 2, Madrid 28006 (Spain)

    2011-09-15

    Most gemstones, being natural materials (silicates, carbonates, phosphates, etc.), exhibit luminescence emission. This property could be potentially employed for personal dosimetry in the case of radiation accident or radiological terrorism where conventional monitoring has not been established. We, herein, report on the thermoluminescence (TL), radioluminescence (RL) and infra-red stimulated luminescence (IRSL) response of a well-characterised natural amazonite (KAlSi{sub 3}O{sub 8}) that, due to its bright blue-green colour when polished, is used as a gemstone. The luminescence emission wavelengths, intensities and thermal kinetics of the amazonite luminescence curves reveal that the ultraviolet band measured on amazonite aliquots is similar to other common K-rich feldspars. On this basis, one can conclude (i) association between twinning and the UV-blue TL emission can be related to structural defects located in the twin-domain boundaries where ionic alkali-self-diffusion, irreversible water losses and irreversible dehydroxylation processes can be involved. (ii) Amazonite exhibits a complex structure with several planar defects (twinning and exsolution interphases which can hold hydroxyl groups, water molecules, etc.) and point defects (impurities, Na, Pb, Mn, etc.) that can act as luminescence centres, and in fact, green and red emissions are respectively associated with the presence of Mn and Fe impurities. Finally, (iv) the thermal stability tests performed on the TL emission of the amazonite confirm a continuum in the trap distribution, i.e. progressive changes in the glow curve shape, intensity and temperature position of the maximum peak.

  2. Increasing lanthanide luminescence by use of the RETEL effect.

    Science.gov (United States)

    Leif, Robert C; Vallarino, Lidia M; Becker, Margie C; Yang, Sean

    2006-08-01

    Luminescent lanthanide complexes produce emissions with the narrowest-known width at half maximum; however, their significant use in cytometry required an increase in luminescence intensity. The companion review, Leif et al., Cytometry 2006;69A:767-778, described a new technique for the enhancement of lanthanide luminescence, the Resonance Energy Transfer Enhanced Luminescence (RETEL) effect, which increases luminescence and is compatible with standard slide microscopy. The luminescence of the europium ion macrocyclic complex, EuMac, was increased by employing the RETEL effect. After adding the nonluminescent gadolinium ion complex of the thenoyltrifluoroacetonate (TTFA) ligand or the sodium salt of TTFA in ethanol solution, the EuMac-labeled sample was allowed to dry. Both a conventional arc lamp and a time-gated UV LED served as light sources for microscopic imaging. The emission intensity was measured with a CCD camera. Multiple time-gated images were summed with special software to permit analysis and effective presentation of the final image. With the RETEL effect, the luminescence of the EuMac-streptavidin conjugate increased at least six-fold upon drying. Nuclei of apoptotic cells were stained with DAPI and tailed with 5BrdUrd to which a EuMac-anti-5BrdU conjugate was subsequently attached. Time-gated images showed the long-lived EuMac luminescence but did not show the short-lived DAPI fluorescence. Imaging of DNA-synthesizing cells with an arc lamp showed that both S phase and apoptotic cells were labeled, and that their labeling patterns were different. The images of the luminescent EuMac and fluorescent DAPI were combined to produce a color image on a white background. This combination of simple chemistry, instrumentation, and presentation should make possible the inexpensive use of the lanthanide macrocycles, Quantum Dyes, as molecular diagnostics for cytological and histopathological microscopic imaging. (c) 2006 International Society for Analytical

  3. Preparation and luminescence properties of SiO2@LaBO3:Eu3+ nanoparticles

    Science.gov (United States)

    Qin, Chuanxiang; Qin, Lin; Chen, Guoqiang; Xu, Haitao; Lin, Tong

    2013-08-01

    Spherical SiO2 particles having a LaBO3:Eu3+ shell have been prepared by coating of silica nanoparticles (size around 130-150 nm) with a LaBO3:Eu3+ sol-gel precursor and subsequent calcination. The SiO2@LaBO3:Eu3+ nanoparticles were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy, and transmission electron microscopy. The XRD and FTIR results revealed that the LaBO3:Eu3+ layer on SiO2 nanoparticles formed an H-LaBO3 crystal phase when calcination at a temperature up to 700 °C. Both excitation and emission properties were characterized. The strong excitation lines at 393 and 465 nm of SiO2@LaBO3:Eu3+ indicated that the core-shell phosphor matched well with the output wavelength of near-UV (350-400 nm) or blue LED (450 nm) chips in phosphor-converted W-LEDs. The emission spectra of the 5D0 → 7F J ( J = 0, 1, 2, 3, and 4) transitions at blue/near-UV light showed strong emission lines around 615 nm which were attributed to the induced electric dipole transition of 5D0 → 7F2. The coating cycles affected the luminescence of SiO2@LaBO3:Eu3+ nanoparticles and their CIE chromaticity coordinate shifted from orange-red to the deep red zone with the increase in the coating cycles (up to 3). The luminescence lifetime of the Eu3+ ions in SiO2@LaBO3:Eu3+ was 2.32 ms. Such a luminescent material may be useful for display and light applications.

  4. Highly luminescent colloidal Eu(3)+-doped KZnF(3) nanoparticles for the selective and sensitive detection of Cu(II) ions.

    Science.gov (United States)

    Sarkar, Shyam; Chatti, Manjunath; Mahalingam, Venkataramanan

    2014-03-17

    This article describes a green synthetic approach to prepare water dispersible perovskite-type Eu3+-doped KZnF3 nanoparticles, carried out using environmentally friendly microwave irradiation at low temperature (85 8C) with water as a solvent. Incorporation of Eu3+ ions into the KZnF3 matrix is confirmed by strong red emission upon ultraviolet (UV) excitation of the nanoparticles. The nanoparticles are coated with poly(acrylic acid) (PAA), which enhances the dispersibility of the nanoparticles in hydrophilic solvents. The strong red emission from Eu3+ ions is selectively quenched upon addition of CuII ions, thus making the nanoparticles a potential CuII sensing material. This sensing ability is highly reversible by the addition of ethylenediaminetetraacetic acid (EDTA), with recovery of almost 90% of the luminescence. If the nanoparticles are strongly attached to a positively charged surface, dipping the surface in a CuII solution leads to the quenching of Eu3+ luminescence, which can be recovered after dipping in an EDTA solution. This process can be repeated for more than five cycles with only a slight decrease in the sensing ability. In addition to sensing, the strong luminescence from Eu3+-doped KZnF3 nanoparticles could be used as a tool for bioimaging.

  5. The propagation of a strong x-ray pulse followed by pulse slowdown and compression, amplified spontaneous emission and lasing without inversion

    Energy Technology Data Exchange (ETDEWEB)

    Sun Yuping; Liu Jicai; Gel' mukhanov, Faris, E-mail: jicai@theochem.kth.s [Department of Theoretical Chemistry, School of Biotechnology, Royal Institute of Technology, S-106 91 Stockholm (Sweden)

    2009-10-28

    We study self-seeded stimulated resonant x-ray Raman scattering and show a 20-fold compression of the strong XFEL pulse propagating through the resonant medium of atomic argon with the frequency (244.3 eV) tuned to the 2p{sub 3/2}-4s resonance. The strong x-ray pulse inverts the medium and produces an extensive ringing tail which widens the power spectrum. Newly created seed field triggers the Stokes channel 3s-2p{sub 3/2} of amplified spontaneous emission. The population inversions are quenched for longer propagation distances where lasing without inversion enhances the Stokes component. The pump pulse also generates weaker Stokes and anti-Stokes fields caused by four-wave mixing. The group velocity is decreased up to 78% of the speed of light in vacuum. (fast track communication)

  6. The propagation of a strong x-ray pulse followed by pulse slowdown and compression, amplified spontaneous emission and lasing without inversion

    International Nuclear Information System (INIS)

    Sun Yuping; Liu Jicai; Gel'mukhanov, Faris

    2009-01-01

    We study self-seeded stimulated resonant x-ray Raman scattering and show a 20-fold compression of the strong XFEL pulse propagating through the resonant medium of atomic argon with the frequency (244.3 eV) tuned to the 2p 3/2 -4s resonance. The strong x-ray pulse inverts the medium and produces an extensive ringing tail which widens the power spectrum. Newly created seed field triggers the Stokes channel 3s-2p 3/2 of amplified spontaneous emission. The population inversions are quenched for longer propagation distances where lasing without inversion enhances the Stokes component. The pump pulse also generates weaker Stokes and anti-Stokes fields caused by four-wave mixing. The group velocity is decreased up to 78% of the speed of light in vacuum. (fast track communication)

  7. Biosensing with Luminescent Semiconductor Quantum Dots

    OpenAIRE

    Sapsford, Kim E.; Pons, Thomas; Medintz, Igor L.; Mattoussi, Hedi

    2006-01-01

    Luminescent semiconductor nanocrystals or quantum dots (QDs) are a recently developed class of nanomaterial whose unique photophysical properties are helping to create a new generation of robust fluorescent biosensors. QD properties of interest for biosensing include high quantum yields, broad absorption spectra coupled to narrow size-tunable photoluminescent emissions and exceptional resistance to both photobleaching and chemical degradation. In this review, we examine the progress in adapti...

  8. A facile synthesis approach and impact of shell formation on morphological structure and luminescent properties of aqueous dispersible NaGdF{sub 4}:Yb/Er upconversion nanorods

    Energy Technology Data Exchange (ETDEWEB)

    Ansari, Anees A., E-mail: aneesaansari@gmail.com [King Saud University, King Abdullah Institute for Nanotechnology (Saudi Arabia); Yadav, Ranvijay; Rai, S. B. [Banaras Hindu University, Department of Physics (India)

    2016-12-15

    A general facile synthesis approach was used for fabrication of highly emissive aqueous dispersible hexagonal phase upconversion luminescent NaGdF{sub 4}:Yb/Er nanorods (core NRs) through metal complex decomposition process. An inert NaGdF{sub 4} and porous silica layers were grafted surrounding the surface of each and every NRs to enhance their luminescence efficiency and colloidal dispersibility in aqueous environment. Optical properties in terms of band gap energy of core, core/shell, and silica-coated core/shell/SiO{sub 2} nanorods were observed to investigate the influence of surface coating, which was gradually decreased after surface coating because of increase crystalline size after growth of inert and silica shells. The inert shell formation before silica surface grafting, upconversion luminescence intensity was greatly improved by about 20 times, owing to the effective surface passivation of the seed core and, therefore, protection of Er{sup 3+} ion in the core from the nonradiative decay caused by surface defects. Moreover, after silica coating, core/shell nanorods shows strong upconversion luminescence property similar to the hexagonal upconversion core NRs. It is expected that these NaGdF{sub 4}:Yb/Er@NaGdF{sub 4}@SiO{sub 2} (core/shell/SiO{sub 2}) NRs including highly upconversion emissive and aqueous dispersible properties make them an ideal materials for various photonic-based potential applications such as in upconversion luminescent bioimaging, magnetic resonance imaging, and photodynamic therapy.

  9. Nitric oxide (NO) emissions from N-saturated subtropical forest soils are strongly affected by spatial and temporal variability in soil moisture

    Science.gov (United States)

    Kang, Ronghua; Dörsch, Peter; Mulder, Jan

    2016-04-01

    Subtropical forests in Southwest China have chronically high nitrogen (N) deposition. This results in high emission rates of N gasses, including N2O, NO and N2. In contrast to N2O, NO emission in subtropical China has received little attention, partly because its quantification is challenging. Here we present NO fluxes in a Masson pine-dominated headwater catchment with acrisols on mesic, well-drained hill slopes at TieShanPing (Chongqing, SW China). Measurements were conducted from July to September in 2015, using a dynamic chamber technique and a portable and highly sensitive chemiluminesence NOx analyzer (LMA-3M, Drummond Technology Inc, Canada). Mean NO fluxes as high as 120 μg N m-2 h-1 (± 56 μg N m-2 h-1) were observed at the foot of the hill slope. Mid-slope positions had intermediate NO emission rates (47 ± 17 μg N m-2 h-1), whereas the top of the hill slope showed the lowest NO fluxes (3 ± 3 μg N m-2 h-1). The magnitude of NO emission seemed to be controlled mainly by site-specific soil moisture, which was on average lower at the foot of the hill slope and in mid-slope positions than at the top of the hill slope. Rainfall episodes caused a pronounced decline in NO emission fluxes in all hill slope positions, whereas the subsequent gradual drying of the soil resulted in an increase. NO fluxes were negatively correlated with soil moisture (r2 = 0.36, p ˂ 0.05). The NO fluxes increased in the early morning, and decreased in the late afternoon, with peak emissions occurring between 2 and 3 pm. The diurnal variation of NO fluxes on mid-slope positions was positively correlated with soil temperature (r2 = 0.9, p ˂ 0.05). Our intensive measurements indicate that NO-N emissions in N-saturated subtropical forests are significant and strongly controlled by local hydrological conditions.

  10. Nitrous Oxide Emissions in a Managed Grassland are Strongly Influenced by CO2 Concentrations Across a Range of Soil Moisture Levels

    Science.gov (United States)

    Brown, Z. A.; Hovenden, M. J.; Hunt, M.

    2017-12-01

    Though the atmosphere contains less nitrous oxide (N2O, 324 ppb) than carbon dioxide (CO2, 400 ppm­), N2O has 298 times the global warming potential of CO2 on a 100-year horizon. Nitrous oxide emissions tend to be greater in moist soils because denitrification is an anaerobic process. The rising concentration of CO2 in the atmosphere reduces plant stomatal aperture, thereby slowing transpiration and water use and leading to higher soil moisture levels. Thus, the rising CO2 concentration could stimulate N2O emissions indirectly via increasing soil moisture. Further, results from field experiments in which CO2 is elevated have demonstrated nitrification is accelerated at elevated CO2 concentrations (eCO2). Hence, N2O emissions could be substantially increased by the impacts of rising CO2 concentrations on plant and ecosystem physiology. However, the scale of this impact could be influenced by the amount of water supplied through irrigation or rainfall since both nitrification and denitrification are sensitive to soil moisture. Here, we use measurements of CO2 and N2O emissions from the TasFACE2 experiment to explore the ways in which the impact of CO2 concentration on greenhouse gas emissions is influenced by water supply in a managed temperate pasture. TasFACE2 is the world's only experiment that explicitly controls soil water availability at three different CO2 concentrations. Application of chemical nitrification inhibitor severely reduces N2O flux from soils regardless of CO2 level, water treatment and time following urea application. This inhibitor reduced soil respiration in plots exposed to ambient CO2 plots but not in eCO2 plots. N2O flux is stimulated by eCO2 but not consistently among watering treatments or seasons. Soil respiration is strongly enhanced by CO2 effect regardless of watering treatment. The results demonstrate that CO2 concentration has a sustained impact on CO2 and N2O flux across a range of water availabilities in this fertilised, ryegrass

  11. Biosynthesis of myristic acid in luminescent bacteria

    International Nuclear Information System (INIS)

    Byers, D.M.

    1987-01-01

    In vivo pulse-label studies have demonstrated that luminescent bacteria can provide myritic acid (14:0) required for the synthesis of the luciferase substrate myristyl aldehyde. Luminescent wild type Vibrio harveyi incubated with [ 14 C] acetate in a nutrient-depleted medium accumulated substantial tree [ 14 C]fatty acid (up to 20% of the total lipid label). Radio-gas chromatography revealed that > 75% of the labeled fatty acid is 14:0. No free fatty acid was detected in wild type cells labeled prior to the development of bioluminescence in the exponential growth phase, or in a dark mutant of V. harveyi (mutant M17) that requires exogenous 14:0 for light emission. The preferential accumulation of 14:0 was not observed when wild type cells were labeled with [ 14 C]acetate in regular growth medium. Moreover, all V. harveyi strains exhibited similar fatty acid mass compositions regardless of the state of bioluminescence. Since earlier work has shown that a luminescence-related acyltransferase (defective in the M17 mutant) can catalyze the deacylation of fatty acyl-acyl carrier protein in vitro, the present results are consistent with a model in which this enzyme diverts 14:0 to the luminescence system during fatty acid biosynthesis. Under normal conditions, the supply of 14:0 by this pathway is tightly regulated such that bioluminescence development does not significantly alter the total fatty acid composition

  12. Luminescence properties of Yb:Nd:Tm:KY{sub 3}F{sub 10} nanophosphor and thermal treatment effects

    Energy Technology Data Exchange (ETDEWEB)

    Gomes, Laércio, E-mail: lgomes@ipen.br [Centro de Lasers e Aplicações, Instituto de Pesquisas Energéticas e Nucleares, IPEN-CNEN/SP, Butantã, P.O. Box 11049, São Paulo, SP o5422-970 (Brazil); Linhares, Horácio Marconi da Silva M.D. [Centro de Lasers e Aplicações, Instituto de Pesquisas Energéticas e Nucleares, IPEN-CNEN/SP, Butantã, P.O. Box 11049, São Paulo, SP o5422-970 (Brazil); Ichikawa, Rodrigo Uchida; Martinez, Luis Gallego [Departamento de Ciências dos Materiais, Instituto de Pesquisas Energéticas e Nucleares (Brazil); Ranieri, Izilda Marcia [Centro de Lasers e Aplicações, Instituto de Pesquisas Energéticas e Nucleares, IPEN-CNEN/SP, Butantã, P.O. Box 11049, São Paulo, SP o5422-970 (Brazil)

    2015-01-15

    In this work, we present the spectroscopic properties of KY{sub 3}F{sub 10} (KY3F) nanocrystals activated with thulium and codoped with ytterbium and neodymium ions. The most important processes that lead to the thulium upconversion emissions in the blue region were identified. A time-resolved luminescence spectroscopy technique was employed to measure the luminescence decays and to determine the most important mechanisms involved in the upconversion process that populates {sup 1}G{sub 4} (Tm{sup 3+}) excited states. Analysis of the energy-transfer processes dynamics using selective pulsed-laser excitations in Yb:Nd:Tm, Nd:KY3F nanocrystals shows that the direct energy transfer from Nd{sup 3+} to Tm{sup 3+} ions is the mechanism responsible for the 78% of the blue upconversion luminescence in the Yb:Nd:Tm:KY3F when compared with the Yb:Nd:Tm:KY3F bulk crystal for an laser excitation at 802 nm. An investigation of the {sup 1}G{sub 4} level luminescence kinetic of Tm{sup 3+} in Yb/Nd/Tm system revealed that the luminescence efficiency ({sup 1}G{sub 4}) starts with a very low value (0.38%) for the synthesized nanocrystal (as grown) and strongly increases to 97% after thermal treatment at 550 °C for 6 h under argon flow. As a consequence of the thermal treatment at T=550 °C, the contributions of the (Nd×Tm) (Up{sub 1}) and (Nd×Yb×Tm) (Up{sub 2}) upconversion processes to the {sup 1}G{sub 4} luminescence are 33% (Up{sub 1}) and 67% for Up{sub 2}. Up{sub 2} process represented by Nd{sup 3+} ({sup 4}F{sub 3/2})→Yb{sup 3+} ({sup 2}F{sub 7/2}) followed by Yb{sup 3+} ({sup 2}F{sub 5/2})→Tm ({sup 3}H{sub 4})→Tm{sup 3+} ({sup 1}G{sub 4}) was previously reported as the main mechanism to produce the blue luminescence in Yb:Nd:Tm:YLiF{sub 4} and KY{sub 3}F{sub 10} bulk crystals. Results of X-ray diffraction analysis of nanopowder using the Rietveld method reveled that crystallite sizes remain unchanged (12–14 nm) after thermal treatments with T≤400 °C, while the

  13. Light-emitting-diode Lambertian light sources as low-radiant-flux standards applicable to quantitative luminescence-intensity imaging

    Science.gov (United States)

    Yoshita, Masahiro; Kubota, Hidehiro; Shimogawara, Masahiro; Mori, Kaneo; Ohmiya, Yoshihiro; Akiyama, Hidefumi

    2017-09-01

    Planar-type Lambertian light-emitting diodes (LEDs) with a circular aperture of several tens of μ m to a few mm in diameter were developed for use as radiant-flux standard light sources, which have been in strong demand for applications such as quantitative or absolute intensity measurements of weak luminescence from solid-state materials and devices. Via pulse-width modulation, time-averaged emission intensity of the LED devices was controlled linearly to cover a wide dynamic range of about nine orders of magnitude, from 10 μ W down to 10 fW. The developed planar LED devices were applied as the radiant-flux standards to quantitative measurements and analyses of photoluminescence (PL) intensity and PL quantum efficiency of a GaAs quantum-well sample. The results demonstrated the utility and applicability of the LED standards in quantitative luminescence-intensity measurements in Lambertian-type low radiant-flux level sources.

  14. SUZAKU OBSERVATION OF STRONG FLUORESCENT IRON LINE EMISSION FROM THE YOUNG STELLAR OBJECT V1647 ORI DURING ITS NEW X-RAY OUTBURST

    International Nuclear Information System (INIS)

    Hamaguchi, Kenji; Grosso, Nicolas; Kastner, Joel H.; Richmond, Michael; Weintraub, David A.

    2010-01-01

    The Suzaku X-ray satellite observed the young stellar object (YSO) V1647 Ori on 2008 October 8 during the new mass accretion outburst reported in 2008 August. During the 87 ks observation with a net exposure of 40 ks, V1647 Ori showed a high level of X-ray emission with a gradual decrease in flux by a factor of 5 and then displayed an abrupt flux increase by an order of magnitude. Such enhanced X-ray variability was also seen in XMM-Newton observations in 2004 and 2005 during the 2003-2005 outburst, but has rarely been observed for other YSOs. The spectrum clearly displays emission from Helium-like iron, which is a signature of hot plasma (kT ∼ 5 keV). It also shows a fluorescent iron Kα line with a remarkably large equivalent width (EW) of ∼600 eV. Such a large EW suggests that a part of the incident X-ray emission that irradiates the circumstellar material and/or the stellar surface is hidden from our line of sight. XMM-Newton spectra during the 2003-2005 outburst did not show a strong fluorescent iron Kα line, so that the structure of the circumstellar gas very close to the stellar core that absorbs and re-emits X-ray emission from the central object may have changed in between 2005 and 2008. This phenomenon may be related to changes in the infrared morphology of McNeil's nebula between 2004 and 2008.

  15. Luminescent Tension-Indicating Orthopedic Strain Gauges for Non-Invasive Measurements Through Tissue

    Science.gov (United States)

    Anker, Jeffrey (Inventor); Rogalski, Melissa (Inventor); Anderson, Dakota (Inventor); Heath, Jonathon (Inventor)

    2015-01-01

    Strain gauges that can provide information with regard to the state of implantable devices are described. The strain gauges can exhibit luminescence that is detectable through living tissue, and the detectable luminescent emission can vary according to the strain applied to the gauge. A change in residual strain of the device can signify a loss of mechanical integrity and/or loosening of the implant, and this can be non-invasively detected either by simple visual detection of the luminescent emission or through examination of the emission with a detector such as a spectrometer or a camera.

  16. Nd sup(3+): YLF luminescence quantum efficiency determination using photoacoustic spectroscopy

    International Nuclear Information System (INIS)

    Vieira, M.M.F.; Franca, E.J.; Bandochi, S.L.; Morato, S.P.

    1990-01-01

    The optical properties of Nd sup(3+):LiYF sub(4) crystals were studied using absorption, emission, excitation and photoacoustic spectroscopies. A new method based on parameters from these spectra was used to determine the luminescence quantum efficiency. This method was applied to four bands centered on 517, 577, 743 and 792 nm. The luminescence quantum efficiency values obtained are presented. (author)

  17. Spectral analysis in microscopy : a study of FRET and single quantum dot luminescence

    NARCIS (Netherlands)

    Frederix, Patrick Louis Theodorus Martin

    2001-01-01

    This thesis deals with the development of new techniques and luminescent markers, to improve the quality of luminescence studies in microscopy. A sensitive spectrograph that can be used for spectrally resolved emission spectroscopy in the microscope is described, including design considerations,

  18. Luminescence of Ce doped oxygen crystalline compounds based on Hf and Ba

    CERN Document Server

    Borisevich, A E; Lecoq, P

    2003-01-01

    The luminescence properties of the Ce-doped hafnium and barium compounds have been investigated to determine their potential as heavy scintillation materials. Compounds have been prepared by solid state synthesis. All of them have shown a bright luminescence attributed to trivalent cerium. Emission bands are peaked in the 425-475nm spectral region at room temperature.

  19. Certain relationships in the luminescence of organophosphors based on metal complexes

    International Nuclear Information System (INIS)

    Zel'tser, L.E.; Talipov, S.T.; Vereshchagina, N.G.

    1986-01-01

    A study has been made of general relationships in the luminescent radiation of organophosphors based on metal complexes and the specific features of chemical and analytical properties of organic analytical reagents in the electronically excited state. Routes have been proposed for activation of emission and for the improvement of metrological characteristics of the luminescence method of analysis

  20. Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure-property relationship of polymorphs.

    Science.gov (United States)

    Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong

    2015-08-01

    Racemic C6-unsubstituted tetrahydropyrimidines (THPs) are a series of fluorophores with a strong aggregation-induced emission (AIE) effect. However, they do not possess the structural features of conventional AIE compounds. In order to understand their AIE mechanism, here, the influences of the molecular packing mode and the conformation on the optical properties of THPs were investigated using seven crystalline polymorphs of three THPs ( 1-3 ). The racemic THPs 1-3 have low-conjugated and highly flexible molecular structures, and hence show practically no emission in different organic solvents. However, the fluorescence quantum yields of their polymorphs are up to 93%, and the maximum excitation ( λ ex ) and emission ( λ em ) wavelengths of the polymorphs are long at 409 and 484 nm, respectively. Single-crystal structures and theoretical calculation of the HOMOs and LUMOs based on the molecular conformations of these polymorphs indicate that the polymorphs with the shortest λ ex and λ em values possess a RS -packing mode ( R - and S -enantiomers self-assemble as paired anti-parallel lines) and a more twisted conformation without through-space conjugation between the dicarboxylates, but the polymorphs with longer λ ex and λ em values adopt a RR / SS -packing mode ( R - and S -enantiomers self-assemble as unpaired zigzag lines) and a less twisted conformation with through-space conjugation between the dicarboxylates. The molecular conformations of 1-3 in all these polymorphs are stereo and more twisted than those in solution. Although 1-3 are poorly conjugated, the radiative rate constants ( k r ) of their polymorphs are as large as conventional fluorophores (0.41-1.03 × 10 8 s -1 ) because of improved electronic conjugation by both through-bond and through-space interactions. Based on the obtained results, it can be deduced that the strong AIE arises not only from the restriction of intramolecular motion but also from enhanced electronic coupling and

  1. THE REST-FRAME OPTICAL SPECTROSCOPIC PROPERTIES OF LY α -EMITTERS AT z  ∼ 2.5: THE PHYSICAL ORIGINS OF STRONG LY α EMISSION

    Energy Technology Data Exchange (ETDEWEB)

    Trainor, Ryan F. [Department of Astronomy, University of California, Berkeley, 501 Campbell Hall, Berkeley, CA 94720 (United States); Strom, Allison L.; Steidel, Charles C. [Cahill Center for Astrophysics, MC 249-17, 1200 E California Boulevard, Pasadena, CA 91125 (United States); Rudie, Gwen C., E-mail: trainor@berkeley.edu [Carnegie Observatories, 813 Santa Barbara Street, Pasadena, CA 91101 (United States)

    2016-12-01

    We present the rest-frame optical spectroscopic properties of 60 faint ( R {sub AB} ∼ 27; L ∼ 0.1 L {sub *}) Ly α -selected galaxies (LAEs) at z  ≈ 2.56. These LAEs also have rest-UV spectra of their Ly α emission line morphologies, which trace the effects of interstellar and circumgalactic gas on the escape of Ly α photons. We find that the LAEs have diverse rest-optical spectra, but their average spectroscopic properties are broadly consistent with the extreme low-metallicity end of the populations of continuum-selected galaxies selected at z  ≈ 2–3. In particular, the LAEs have extremely high [O iii] λ 5008/H β ratios (log([O iii]/H β ) ∼ 0.8) and low [N ii] λ 6585/H α ratios (log([N ii]/H α ) < 1.15). Coupled with a detection of the [O iii] λ 4364 auroral line, these measurements indicate that the star-forming regions in faint LAEs are characterized by high electron temperatures (T{sub e} ≈ 1.8 × 10{sup 4} K), low oxygen abundances (12 + log(O/H) ≈ 8.04, Z{sub neb} ≈ 0.22 Z {sub ⊙}), and high excitations with respect to their more luminous continuum-selected analogs. Several of our faintest LAEs have line ratios consistent with even lower metallicities, including six with 12 + log(O/H) ≈ 6.9–7.4 (Z {sub neb} ≈ 0.02–0.05 Z{sub ⊙}). We interpret these observations in light of new models of stellar evolution (including binary interactions) that have been shown to produce long-lived populations of hot, massive stars at low metallicities. We find that strong, hard ionizing continua are required to reproduce our observed line ratios, suggesting that faint galaxies are efficient producers of ionizing photons and important analogs of reionization-era galaxies. Furthermore, we investigate the physical trends accompanying Ly α emission across the largest current sample of combined Ly α and rest-optical galaxy spectroscopy, including both the 60 KBSS-Ly α LAEs and 368 more luminous galaxies at similar redshifts. We

  2. From Antenna to Assay: Lessons Learned in Lanthanide Luminescence

    Energy Technology Data Exchange (ETDEWEB)

    Moore, Evan; Samuel, Amanda; Raymond, Kenneth

    2008-09-25

    these chromophores as a tool to guide ligand design. Additionally we have investigated chiral IAM ligands that yield Tb(III) complexes possessing both high quantum yield values and strong circularly polarized luminescence (CPL) activity. To efficiently sensitize Eu(III) emission, we have utilized ligands based on the 1-hydroxypyridin-2-one (1,2-HOPO) chelate, which are remarkable since they combine both excellent photophysical properties in addition to exceptional aqueous stabilities. A more compete understanding of this chromophore has been achieved by combining low temperature phosphorescence measurements with the same TD-DFT approach used with the IAM system. Also, Eu(III) complexes with strong CPL activity have been obtained through preparation of chiral 1,2-HOPO ligands. Using the unique spectroscopic properties of Eu(III), we have also undertaken the kinetic analysis of radiative and non-radiative decay pathways for a series of complexes, which has highlighted the importance of the metal ion symmetry on the ensuing photophysical properties. Lastly, the commercial development of a Tb-IAM compound that offers improved performance in the common HTRF platform and has the potential to vastly improve the sensitivity of measurements carried out using this technique is presented.

  3. Influence of emissive hole-transporting materials on the electrical and luminescent performance of highly efficient white light organic light-emitting diodes

    Science.gov (United States)

    Wang, Ching-Wu; Chen, Shih-Fang; Kuo, Wen-Fa

    2002-09-01

    An emissive hole-transporting material with a dopant was proposed for realizing highly efficient and relatively pure white-light organic light-emitting diode (OLED). The device structure included ITO/N, N'-diphenyl-N, N'-bis(1-naphthyl-phenyl)-(1, 1'-biphenyl)-4,4'-diamine (NPB)/NPB doped with 4-Dicyanomethylene-2-methyl-6-[2, 3, 6, 7-tetra-hydro-1H, 5H-behzo[ij]-quinolizin-8-yl)vinyl]-4H-pyran (DCM2) (NPB:DCM2)/bathocuproine (BCP)/tris-(8-hydroxyquinoline) aluminum (Alq3)/Mg/Ag. By appropriately controlling the DCM2 doping concentration as well as thickness of the blue-red-emitting layer of NPB:DCM2, the white-light OLED has a relatively stable white color even the operating voltages change from 9 to 18 V.

  4. Strong Energy-Transfer-Induced Enhancement of Luminescence Efficiency of Eu(2+)- and Mn(2+)-Codoped Gamma-AlON for Near-UV-LED-Pumped Solid State Lighting.

    Science.gov (United States)

    Liu, Lihong; Wang, Le; Zhang, Chenning; Cho, Yujin; Dierre, Benjamin; Hirosaki, Naoto; Sekiguchi, Takashi; Xie, Rong-Jun

    2015-06-01

    A series of Eu(2+)- and Mn(2+)-codoped γ-AlON (Al1.7O2.1N0.3) phosphors was synthesized at 1800 °C under 0.5 MPa N2 by using the gas-pressure sintering method (GPS). Eu(2+) and Mn(2+) ions were proved to enter into γ-AlON host lattice by means of XRD, CL, and EDS measurements. Under 365 nm excitation, two emission peaks located at 472 and 517 nm, resulting from 4f(6)5d(1) → 4f(7) and (4)T1(4G) → (6)A1 electron transitions of Eu(2+) and Mn(2+), respectively, can be observed. Energy transfer from Eu(2+) to Mn(2+) was evidenced by directly observing appreciable overlap between the excitation spectrum of Mn(2+) and the emission spectrum of Eu(2+) as well as by the decreased decay time of Eu(2+) with increasing Mn(2+) concentration. The critical energy-transfer distance between Eu(2+) and Mn(2+) and the energy-transfer efficiency were also calculated. The mechanism of energy transfer was identified as a resonant type via a dipole-dipole mechanism. The external quantum efficiency was increased 7 times (from 7% for γ-AlON:Mn(2+) to 49% for γ-AlON:Mn(2+),Eu(2+) under 365 nm excitation), and color-tunable emissions from blue-green to green-yellow were also realized with the Eu(2+) → Mn(2+) energy transfer in γ-AlON.

  5. Luminescence properties of tetravalent uranium in aqueous solution

    International Nuclear Information System (INIS)

    Kirishima, A.; Kimura, T.; Nagaishi, R.; Tochiyama, O.

    2004-01-01

    The luminescence spectra of U 4+ in aqueous solutions were observed in the UV-VIS region at ambient and liquid nitrogen temperatures. The excitation spectrum indicates that the luminescence is arising from the deexcitation of a 5f electron at the 1 S 0 level and no other emissions of U 4+ in aqueous solutions were detected for other f-f transitions. All the luminescence peaks were assigned to the transitions from 1 S 0 to lower 5f levels. To estimate the luminescence lifetime, luminescence decay curves were measured using time-resolved laser-induced fluorescence spectroscopy. At room temperature, the decay curve indicated that the lifetime was shorter than 20 ns. On the other hand, the frozen sample of U 4+ in aqueous solution at liquid nitrogen temperature showed the same emission spectrum as at room temperature and its lifetime was 149 ns in H 2 O system and 198 ns in D 2 O system. The longer lifetime at liquid nitrogen temperature made it possible to measure the spectrum of U 4+ at the concentration as low as 10 -6 M. The difference in the anion species (ClO 4 - , Cl - , SO 4 2- ) affected the structure of the emission spectrum to some extent. (orig.)

  6. Time-resolved pulse-counting lock-in detection of laser induced fluorescence in the presence of a strong background emission

    International Nuclear Information System (INIS)

    Pelissier, B.; Sadeghi, N.

    1996-01-01

    We describe a time-resolved pulse-counting system well adapted for the detection of continuous laser induced fluorescence (LIF) signals in repetitive phenomena, when a strong background emission is present. It consists of 256 channels coupled to a first in first out memory and interfaced to a 486 DX 33 PC, for data storage. It accepts time-averaged count rates up to 450 kcount/s. Time between channels can be set from 12.5 ns to several μs and the dead time between two consecutive cycles of the physical phenomena is less than 20 ns. In phase with a chopper, which modulates the laser beam, it adds the observed photon signal to the channel memories when the beam is on and substracts it when the beam is stopped, acting like a lock-in amplifier which detect only the modulated part of the signal. The minimum detectivity on the LIF signal is only limited by the shot noise of the plasma induced emission signal. As an application, we studied the time variation of the Ar + *( 2 G 9/2 ) metastable ions, detected by LIF, in two types of plasmas. Their radiative lifetime and collisional quenching frequencies were deduced from their decay rate in the afterglow of a pulsed Helicon reactor. We also observed the evolution of their density in a 455 kHz capacitively coupled argon discharge. copyright 1996 American Institute of Physics

  7. Time-resolved pulse-counting lock-in detection of laser induced fluorescence in the presence of a strong background emission

    Science.gov (United States)

    Pelissier, B.; Sadeghi, N.

    1996-10-01

    We describe a time-resolved pulse-counting system well adapted for the detection of continuous laser induced fluorescence (LIF) signals in repetitive phenomena, when a strong background emission is present. It consists of 256 channels coupled to a first in first out memory and interfaced to a 486 DX 33 PC, for data storage. It accepts time-averaged count rates up to 450 kcount/s. Time between channels can be set from 12.5 ns to several μs and the dead time between two consecutive cycles of the physical phenomena is less than 20 ns. In phase with a chopper, which modulates the laser beam, it adds the observed photon signal to the channel memories when the beam is on and substracts it when the beam is stopped, acting like a lock-in amplifier which detect only the modulated part of the signal. The minimum detectivity on the LIF signal is only limited by the shot noise of the plasma induced emission signal. As an application, we studied the time variation of the Ar+*(2G9/2) metastable ions, detected by LIF, in two types of plasmas. Their radiative lifetime and collisional quenching frequencies were deduced from their decay rate in the afterglow of a pulsed Helicon reactor. We also observed the evolution of their density in a 455 kHz capacitively coupled argon discharge.

  8. The nature of unusual luminescence in natural calcite, CaCO3

    Energy Technology Data Exchange (ETDEWEB)

    Gaft, M.; Nagli, L.; Panczer, G.; Waychunas, G.; Porat, N.

    2008-11-01

    The unusual luminescence of particular varieties of natural pink calcite (CaCO{sub 3}) samples was studied by laser-induced time-resolved luminescence spectroscopy at different temperatures. The luminescence is characterized by intense blue emission under short-wave UV lamp excitation with an extremely long decay time, accompanied by pink-orange luminescence under long wave UV excitation. Our investigation included optical absorption, natural thermostimulated luminescence (NTL) and Laser-Induced Breakdown Spectroscopy (LIBS) studies. Two luminescence centers were detected: a narrow violet band, with {lambda}{sub max} = 412 nm, {Delta} = 45 nm, two decay components of {tau}{sub 1} = 5 ns and {tau}{sub 2} = 7.2 ms, accompanied by very long afterglow, and an orange emission band with {lambda}{sub max} = 595 nm, {Delta} = 90 nm and {tau} = 5 ns. Both luminescence centers are thermally unstable with the blue emission disappearing after heating at 500 C, and the orange emission disappearing after heating at different temperatures starting from 230 C, although sometimes it is stable up to 500 C in different samples. Both centers have spectral-kinetic properties very unusual for mineral luminescence, which in combination with extremely low impurity concentrations, prevent their identification with specific impurity related emission. The most likely explanation of these observations may be the presence of radiation-induced luminescence centers. The long violet afterglow is evidently connected with trapped charge carrier liberation, with their subsequent migration through the valence band and ultimate recombination with a radiation-induced center responsible for the unusual violet luminescence.

  9. Structural and luminescence properties of Mn2+ ions doped calcium zinc borophosphate glasses

    International Nuclear Information System (INIS)

    Wan, Ming Hua; Wong, Poh Sum; Hussin, Rosli; Lintang, Hendrik O.; Endud, Salasiah

    2014-01-01

    Highlights: • FT-IR revealed that the network structures are from borate and phosphate network. • The PL spectrum exhibits a green emission band at 582 nm ( 4 T 1g → 6 A 1g ). • As the concentration of Mn 2+ ions is increased, the emission band had been red shifted. • These glasses are found to have potential applications as luminescent optical materials. - Abstract: Calcium zinc borophosphate glasses (CaZnBP) doped with various concentrations of Mn 2+ ions and borate and phosphate as variable were prepared using conventional melt quenching technique. The structure of obtained glasses were examined by means of use: X-ray diffraction (XRD) and fourier transform infrared (FT-IR). XRD analysis confirmed amorphous nature of glass samples. The FT-IR spectra reveals the presence of both borate and phosphate vibrational modes in the prepared glasses. The doping of Mn 2+ ions (2–10 mol%) shows no significant changes in the main IR vibrational bands. Optical properties were studied by measuring the near infrared photoluminescence (PL) spectra. CaZnBP glasses exhibited intense green emission peak (582 nm) (tetrahedral symmetry), which is assigned to a transition from the upper 4 T 1g → 6 A 1g ground state of Mn 2+ ions. As the concentration of Mn 2+ ions increases, the emission band increases from 582 nm to 650 nm and exhibited a red light emission (octahedral symmetry). The decay curves of 4 T 1g level were examined for all concentrations and the measured lifetimes are found to depend strongly on Mn 2+ concentrations. From the emission characteristic parameters of 6 A 1g (S) level, it shows that the CaZnBP glasses could have potential applications as luminescent optical materials, visible lasers and fluorescent display devices

  10. Optical characterization of luminescent silicon nanocrystals embedded in glass matrices

    Energy Technology Data Exchange (ETDEWEB)

    Debieu, Olivier

    2008-12-16

    Interstellar dust in nebulae and in the Diffuse Interstellar Medium (DISM) of galaxies contains a component which exhibits efficient visible-near infrared luminescence ranging from 500 to 1000 nm, known as Extended Red Emission (ERE). Silicon nanocrystals (nc-Si) are discussed as possible carriers of the ERE. We employed the accelerator facilities of the Institute of Solid State Physics of the University of Jena to implant Si ions into fused silica windows. An excess concentration of silicon atoms is thus produced in the host SiO{sub 2} matrix which, by applying an annealing at 1100 C, condensates to silicon nanoparticles and crystallizes. Although the condensation and crystallization occur after an annealing of one minute,10, 15 the samples were annealed during one hour in order to well-passivate the nc-Si, that means, to reduce effectively the number of Si-dangling bonds at the nc-Si surface that are efficient non-radiative recombination centers. 10, 16 Upon excitation with UV light, most of our nc-Si/SiO{sub 2} samples revealed strong PL. We implanted into our luminescent nc-Si/SiO{sub 2} systems other atomic elements, as for instance magnesium and calcium, which form silicates if their oxide is combined with SiO{sub 2}. The purpose is to simulate the conditions for silicates containing nc-Si. In order to understand the effect of the incorporation of foreign atoms on the PL properties of our nc-Si/SiO{sub 2} systems, we proceeded to similar experiments with Er and Ge. As has been demonstrated by several authors, 17, 18 the presence of nc-Si in a glass matrix enhances considerably the emission of Er{sup 3+} ions at 1.536{mu}m. At the same time, the PL of nc-Si is considerably quenched. Since the solubility of Er in crystalline silicon is about 2 orders of magnitude lower than in SiO{sub 2}, the optically active Er{sup 3+} ions are believed to be localized outside the nc-Si core, demonstrating that ions present in the host SiO{sub 2} matrix influence the PL

  11. Luminescence of YAB:Er single crystal

    Energy Technology Data Exchange (ETDEWEB)

    Foeldvari, I.; Beregi, E.; Watterich, A. [Research Institute for Solid State Physics and Optics, HAS, Konkoly-Thege u. 29-33, 1121 Budapest (Hungary); Solarz, P.; Dominiak-Dzik, G.; Ryba-Romanowski, W. [Institute of Low Temperature and Structure Research, PAS, Okolna 2, 50422 Wroclaw (Poland)

    2007-03-15

    Luminescence spectra of YAB:Er crystals were studied in the ultraviolet-visible region and in the 10-300 K temperature range. The dominant Er{sup 3+}-emission belonged to the {sup 4}S{sub 3/2} {yields} {sup 4}I{sub 15/2} transition (18000-18500 cm{sup -1}). Its Stark components were assigned and found to be consistent with those derived from the absorption spectra. The lifetime of the luminescence was determined as a function of temperature and Er-concentration, and the decay kinetics was analyzed. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  12. Silicon: electrochemistry and luminescence

    NARCIS (Netherlands)

    Kooij, Ernst Stefan

    1997-01-01

    The electrochemistry of crystalline and porous silicon and the luminescence from porous silicon has been studied. One chapter deals with a model for the anodic dissolution of silicon in HF solution. In following chapters both the electrochemistry and various ways of generating visible

  13. Luminescence study of spodumene

    International Nuclear Information System (INIS)

    Isotani, S.; Fujii, A.T.; Antonini, R.; Pontuschka, W.M.; Rabani, S.R.; Furtado, W.W.

    1990-02-01

    A comparative study is made of the luminescence of five kinds of spodumene from Minas Gerais, Brazil, studied previously by optical absorption spectroscopy. Natural gemstones are used which, in the course of the experiments, were irradiated with X-rays. (L.C.) [pt

  14. Luminescent properties of Al2O3: Tb powders

    International Nuclear Information System (INIS)

    Esparza G, A.E.; Garcia, M.; Falcony, C.; Azorin N, J.

    2000-01-01

    In this work the photo luminescent and cathode luminescent characteristics of aluminium oxide (Al 2 O 3 ) powders impurified with terbium (Tb) were studied for their use in dosimetry. The optical, structural, morphological characteristics of the powders as function of variation in the impurity concentration and the annealing temperature will be presented. As regards the optical properties of powders (photoluminescence and cathode luminescence) it was observed a characteristic emission associated with radiative transitions between electron energy levels of terbium, the spectra associated with this emission consists of several peaks associated with such transitions. In the structural and morphological characterization (X-ray diffraction and scanning electron microscopy) it was appreciated that in accordance the annealing temperature of powders is augmented it is evident the apparition of certain crystalline phases. The results show that this is a promissory material for radiation dosimetry. (Author)

  15. Spectroscopic properties of new luminescent system based on vanadate(V) crystal doped with erbium ions

    Energy Technology Data Exchange (ETDEWEB)

    Sobczyk, Marcin, E-mail: marcin@wchuwr.p [Faculty of Chemistry, University of Wroclaw, ul. F. Joliot-Curie 14, 50-383 Wroclaw (Poland); Lisiecki, RadosLaw; Solarz, Piotr; Ryba-Romanowski, Witold [Institute of Low Temperature and Structure Research Polish Academy of Sciences, ul. Okolna 2, 50-422 Wroclaw (Poland)

    2010-04-15

    Er{sup 3+}-doped KCaY(VO{sub 4}){sub 2} microcrystalline samples were synthesized using a high temperature solid-state reaction technique. Spectroscopic properties of Er{sup 3+}: KCaY(VO{sub 4}){sub 2} are studied and the nature of emissions is discussed. A strong green and infrared luminescence were observed under excitation at 314 nm in the O{sup 2-}->V{sup 5+} charge-transfer transitions and direct excitation of Er{sup 3+} ions at 435 nm. A strong emission lines in the blue region are due to the transitions of VO{sub 4}{sup 3-} ions have been observed at 77 K. The Judd-Ofelt parametrization scheme has been applied to the analysis of the room temperature absorption spectra in order to evaluate the intensity parameters, the branching ratios and the radiative lifetimes of the {sup 4}I{sub 13/2}, {sup 4}I{sub 11/2}, {sup 4}F{sub 9/2} and {sup 4}S{sub 3/2} emitting levels. The effective cross-section has been calculated for the {sup 4}I{sub 13/2}->{sup 4}I{sub 15/2} transition, indicating that the title compounds is a promising active medium for application in the three-level laser system. The up-conversion emission in Er{sup 3+}: KCaY(VO{sub 4}){sub 2} was investigated at 300 K. The decay profiles of the Stokes and anti-Stokes emissions were measured and the mechanism of up-conversion luminescence is discussed.

  16. Photo and cathode luminescence emission in oxide silicium films implanted with silicium; Emision de foto y catodoluminiscencia en peliculas de oxido de silicio termico implantadas con silicio

    Energy Technology Data Exchange (ETDEWEB)

    Flores, F; Aceves, M. [Instituto Nacional de Astrofisica Optica y Electronica, Mexico, D.F. (Mexico); Carrillo, J. [Benemrita Universidad Autonoma de Puebla, Puebla (Mexico); Dominguez, C. [Universida Autonoma de Barcelona, Barcelona (Spain); Falcony, C. [Instituto Politecnico Nacional, Mexico, D.F. (Mexico)

    2001-10-01

    We studied the photo and cathodoluminescence of Silicon Rich Oxides (SRO) obtained by ion implant of Si in thermal oxides. Doses of 10{sup 1}6 cm{sup -}2 (low dose) and 10{sup 1}7 cm{sup -}2 (high dose) and implant energy of 150 keV were used. The films were annealed for 30, 60 and 180 minutes in nitrogen at 1100 Celsius degrees. The spectra show photo and cathodoluminescence emission in the visible range, the bands in the spectra change with the conditions of ion implant and annealing. The films without thermal treatment in both dose present photoluminescence bands around 1.9 eV (band B) and 2.4 eV (band C). With the thermal treatments, the band B disappears. In the case of the films with low dose, the band C shows a blue shift and a decrease in intensity. The high dose films have a band centered in 1.7 eV (band A) that increases its intensity with annealings. The cathodoluminescence bands in all the cases are in 2.7 eV (band D) and they present changes with the thermal treatments that it seems they depend on the variation in the implant parameters. [Spanish] Se estudian las propiedades de foto y la catodoluminiscencia de peliculas de oxidos de silicio ricos en Si (Silicon Rich Oxide SRO) obtenidas por implantacion ionica de Si en oxidos termicos. Se usaron dosis de 10{sup 1}6 cm{sup -}2 (dosis baja) y 10{sup 1}7 cm{sup -}2 (dosis alta) y energia de implantacion de 150 keV. Las peliculas se sometieron a tratamientos termicos por 30, 60 y 180 minutos en nitrogeno de 1100 grados centigrados. Se encontro emision foto y catodoluminiscente en el rango visible, las bandas en los espectros cambian con las condiciones de implantacion ionica y con los tratamientos termicos. Las peliculas sin tratamiento termico en ambas dosis presentan bandas de fotoluminiscencia alrededor de 1.9 eV (banda B) y 2.4 eV (banda C). Con los tratamientos termicos, la banda B desaparece. En el caso de las peliculas con dosis baja, la banda C muestra un corrimiento hacia el azul junto con una

  17. New luminescent materials and filters for Luminescent Solar Concentrators

    OpenAIRE

    De Boer, D.K.G.; Ronda, C.R.; Keur, W.C.; Meijerink, A.

    2012-01-01

    In a Luminescent Solar Concentrator (LSC), short-wavelength light isconverted by a luminescent material into long-wavelength light, which is guided towards a photovoltaic cell. In principle, an LSC allows for high concentration, but in practice this is prevented by lossmechanisms like limited sunlight absorption, limited quantum efficiency and high self absorption. To tackle these problems, a suitable luminescent material is needed. Another important loss mechanism is the escape of luminescen...

  18. High enhancement of Eu3+ luminescence in SrAl4O7 phosphor by means of charge compensation with Na+ ions

    Science.gov (United States)

    Puchalska, M.

    2017-10-01

    A comparative study of the luminescent properties of SrAl4O7:Eu3+(x%) and SrAl4O7:Eu3+(x%),Na+(x%) (x = 0.002-0.1) phosphor powders as a function of activator concentration is reported. Upon UV excitation both series of compounds exhibit strong characteristic red Eu3+ photoluminescence with a maximum around 611.5 nm, which intensity increases with an increase of activator content. It was found that the luminescence spectra of singly Eu3+ doped strontium aluminate are much more concentration dependent. As the dopant content increases, the spectra of SrAl4O7:Eu3+ show an increased line broadening and the emergence of new emission components. The observed changes in the studied concentration range are due to an increased disorder of Eu3+ local symmetry induced by the increase in the number of defects in host lattice and by the presence of a new crystalline phase that occurs at the higher dopant content. Charge compensation through Na+ co-doping facilitates an incorporation of Eu3+ into the SrAl4O7 lattice and leads to a smaller symmetry disorder of activator surroundings as well as a significantly enhanced Eu3+ luminescence intensity. The largest increase in emission intensity (∼6.5 times) was observed for 7%-doped sample. Concentration dependences of the luminescence kinetics of both types of materials are clearly different. It was found that for singly Eu3+ doped SrAl4O7 the 5D0 lifetime shortens with the increase of activator content from 1.8 to 1.4 ms while for Na+ co-doped SrAl4O7 this value does not vary over a range of concentrations and is approximately 1.8 ms. SrAl4O7:Eu3+,Na+ powders are potential candidates to be used as luminescent materials.

  19. New cyanopyridone based luminescent liquid crystalline materials: synthesis and characterization.

    Science.gov (United States)

    N, Ahipa T; Adhikari, Airody Vasudeva

    2014-11-01

    A new series of 4-(3,4-bis(akyloxy)phenyl)-6-(4-((1-(4-cyano- or 4-nitro-benzyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-2-oxo-1,2-dihydropyridine-3-carbonitriles carrying terminal di-alkoxy chain lengths (viz. octyloxy, decyloxy, dodecyloxy, tetradecyloxy and hexadodecyloxy) as well as terminal polar groups -CN or -NO2 have been designed and synthesized successfully as luminescent mesogens. Their thermotropic behaviors have been studied by means of differential scanning calorimetry and polarized optical microscopy. The supramolecular organizations in them were explored by the temperature dependent X-ray diffraction method and their photophysical properties were investigated using UV-visible and fluorescence spectral methods. The mesogenic study reveals that the presence of hydrogen bonds, as well as dimerization between the molecules, is mainly responsible for the formation of the ambient temperature hexagonal columnar phase (Colh) in the new molecules. Their photophysical study indicates that the compounds exhibit a strong absorption band at ∼370 nm and a blue emission band at ∼466 nm with good quantum yields of ∼0.62 when compared to quinine sulphate (Φf = 0.54) in chloroform. Also, the compounds show a slightly red shift in the absorption band with increased solvent polarity. In liquid crystalline films, they display a bathochromic shift in the emission band because of the intimate overlap of molecular cores in the hexagonal columnar phase.

  20. Thermal quenching of luminescence of LiSr4 (BO3)3:Eu2+ orange-emitting phosphor.

    Science.gov (United States)

    Zhang, Xinguo; Zhou, Liya; Gong, Menglian

    2014-03-01

    An orange-emitting phosphor, Eu(2+)-activated LiSr4(BO3)3, was synthesized using the conventional solid-state reaction. The photoluminescence excitation and emission spectra, and temperature dependence of the luminescence intensity of the phosphor were investigated. The results showed that LiSr4(BO3)3:Eu(2+) could be efficiently excited by incident light of 250-450 nm, and emits a strong orange light. With increasing temperature, the emission bands of LiSr4(BO3)3:Eu(2+) show an abnormal blue-shift with broadening bandwidth and decreasing emission intensity. Copyright © 2013 John Wiley & Sons, Ltd.

  1. Intrinsic luminescence of YAlO.sub.3./sub. perovskites

    Czech Academy of Sciences Publication Activity Database

    Zorenko, Y.; Voloshinovskii, A.; Gorbenko, V.; Zorenko, T.; Nikl, Martin; Nejezchleb, K.

    2007-01-01

    Roč. 4, č. 3 (2007), s. 963-967 ISSN 1862-6351 R&D Projects: GA ČR GA202/05/2471 Grant - others:INTAS(XE) 04-78-7083 Institutional research plan: CEZ:AV0Z10100521 Keywords : intrinsic emission * perovskites * luminescence * exciton Subject RIV: BM - Solid Matter Physics ; Magnetism

  2. Plasma luminescence feedback control system for precise ultrashort pulse laser tissue ablation

    Science.gov (United States)

    Kim, Beop-Min; Feit, Michael D.; Rubenchik, Alexander M.; Gold, David M.; Darrow, Christopher B.; Marion, John E., II; Da Silva, Luiz B.

    1998-05-01

    Plasma luminescence spectroscopy was used for precise ablation of bone tissue without damaging nearby soft tissue using an ultrashort pulse laser. Strong contrast of the luminescence spectra between bone marrow and spinal cord provided the real time feedback control so bone tissue is selectively ablated while preserving the spinal cord.

  3. Piezoelectrically-induced stress-luminescence phenomenon in CaAl2O4:Eu2+

    International Nuclear Information System (INIS)

    Wei, Yongbin; Wu, Zheng; Jia, Yanmin; Liu, Yongsheng

    2015-01-01

    Piezoelectrically-induced stress-luminescence in the CaAl 2 O 4 :Eu 2+ was investigated. Blue light that was visible to the naked eye could be observed in the dark when a pulse force of ∼7.7 kN was applied to the sample. The intensity of the stress-luminescence strongly depended on the magnitude of the applied force during a pulse cycle. The intensity decreased with repetitive application of pulse stress and was completely recovered after irradiation with ultraviolet light. It is suggested that the stress-luminescence effect in CaAl 2 O 4 :Eu 2+ arises from the piezoelectrically-induced de-trapping of the charge carriers. A CaAl 2 O 4 :Eu 2+ ceramic that exhibits a stress-luminescence effect has potential applications in smart stress optically-sensing devices. - Highlights: • The strong induced stress-luminescence in CaAl 2 O 4 :Eu 2+ was observed. • The stress-luminescent intensity strongly depends on the magnitude of force. • The stress-luminescence could be completely recovered after the UV irradiation. • The strong stress-luminescent effect is potential in stress-light sensors

  4. Comparable luminescence investigation of the La1-xEuxVO4 solid solutions synthesized by two different methods

    OpenAIRE

    Chukova, O. V.; Nedilko, S. G.; Scherbatskii, V.; Nedilko, S. A.; Voytenko, T.

    2012-01-01

    Luminescence properties of the series of the La1-xEuxVO4 solid solutions were investigated. The samples were synthesized by the solid state and co-precipitation methods. Luminescence spectra of the investigated samples consist of weak wide non-structural band of the matrix emission and narrow spectral lines caused by inner f-f electron transitions in the impurity Eu3+ ions. Dependences of the structure, peak positions and intensity of luminescence on the composition, samples tempe...

  5. Dynamics of the Green and Red Upconversion Emissions in Yb3+-Er3+-Codoped Y2O3 Nanorods

    Directory of Open Access Journals (Sweden)

    O. Meza

    2010-01-01

    Full Text Available Efficient green and red upconversion emission in Y2O3:Yb3+, Er3+ nanorods under 978 nm radiation excitation is achieved. Experimental effective lifetimes, luminescent emissions, and nanorod sizes depend strongly on the solvent ratios used during the synthesis. A microscopic nonradiative energy transfer model is used to approach the dynamics of the green, red, and infrared emissions. The excellent agreement between simulated and experimental decay suggests that the energy transfer mechanisms responsible of the visible emission depend on the solvent ratio.

  6. Fabrication and upconversion luminescence properties of YF3:Er3+ hollow nanofibers via monoaxial electrospinning combined with fluorination method.

    Science.gov (United States)

    Li, Dan; Dong, Xiangting; Yu, Wensheng; Wang, Jinxian; Liu, Guixia

    2014-06-01

    YF3:Er3+ hollow nanofibers were successfully fabricated via fluorination of the relevant Y2O3:Er3+ hollow nanofibers which were obtained by calcining the electrospun PVP/[Y(NO3)3 + Er(NO3)3] composite nanofibers. The morphology and properties of the products were investigated in detail by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and fluorescence spectrometer. YF3:Er3+ hollow nanofibers were pure orthorhombic phase with space group Pnma and were hollow-centered structure with the mean diameter of 172 +/- 23 nm, and YF3:Er3+ hollow nanofibers were composed of nanoparticles with the diameter ranging from 30 nm to 50 nm. Upconversion emission spectrum analysis manifested that YF3:Er3+ hollow nanofibers emitted strong green and weak red upconversion emission centering at 524 nm, 543 nm and 653 nm, respectively. The green emissions and the red emission were respectively originated from 2H11/2/4S3/2 --> 4I15/2 and 4F9/2 --> 4I15/2 energy levels transitions of the Er3+ ions. Moreover, the emitting colors of YF3:Er3+ hollow nanofibers were located in the green region in CIE chromaticity coordinates diagram. The luminescent intensity of YF3:Er3+ hollow nanofibers was increased remarkably with the increasing doping concentration of Er3+ ions. The possible formation mechanism of YF3:Er3+ upconversion luminescence hollow nanofibers was also discussed. This preparation technique could be applied to prepare other rare earth fluoride upconversion luminescence hollow nanofibers.

  7. Quantitative luminescence imaging system

    Science.gov (United States)

    Erwin, D.N.; Kiel, J.L.; Batishko, C.R.; Stahl, K.A.

    1990-08-14

    The QLIS images and quantifies low-level chemiluminescent reactions in an electromagnetic field. It is capable of real time nonperturbing measurement and simultaneous recording of many biochemical and chemical reactions such as luminescent immunoassays or enzyme assays. The system comprises image transfer optics, a low-light level digitizing camera with image intensifying microchannel plates, an image process or, and a control computer. The image transfer optics may be a fiber image guide with a bend, or a microscope, to take the light outside of the RF field. Output of the camera is transformed into a localized rate of cumulative digitalized data or enhanced video display or hard-copy images. The system may be used as a luminescent microdosimetry device for radiofrequency or microwave radiation, as a thermal dosimeter, or in the dosimetry of ultra-sound (sonoluminescence) or ionizing radiation. It provides a near-real-time system capable of measuring the extremely low light levels from luminescent reactions in electromagnetic fields in the areas of chemiluminescence assays and thermal microdosimetry, and is capable of near-real-time imaging of the sample to allow spatial distribution analysis of the reaction. It can be used to instrument three distinctly different irradiation configurations, comprising (1) RF waveguide irradiation of a small Petri-dish-shaped sample cell, (2) RF irradiation of samples in a microscope for the microscopic imaging and measurement, and (3) RF irradiation of small to human body-sized samples in an anechoic chamber. 22 figs.

  8. Quantitative luminescence imaging system

    Science.gov (United States)

    Erwin, David N.; Kiel, Johnathan L.; Batishko, Charles R.; Stahl, Kurt A.

    1990-01-01

    The QLIS images and quantifies low-level chemiluminescent reactions in an electromagnetic field. It is capable of real time nonperturbing measurement and simultaneous recording of many biochemical and chemical reactions such as luminescent immunoassays or enzyme assays. The system comprises image transfer optics, a low-light level digitizing camera with image intensifying microchannel plates, an image process or, and a control computer. The image transfer optics may be a fiber image guide with a bend, or a microscope, to take the light outside of the RF field. Output of the camera is transformed into a localized rate of cumulative digitalized data or enhanced video display or hard-copy images. The system may be used as a luminescent microdosimetry device for radiofrequency or microwave radiation, as a thermal dosimeter, or in the dosimetry of ultra-sound (sonoluminescence) or ionizing radiation. It provides a near-real-time system capable of measuring the extremely low light levels from luminescent reactions in electromagnetic fields in the areas of chemiluminescence assays and thermal microdosimetry, and is capable of near-real-time imaging of the sample to allow spatial distribution analysis of the reaction. It can be used to instrument three distinctly different irradiation configurations, comprising (1) RF waveguide irradiation of a small Petri-dish-shaped sample cell, (2) RF irradiation of samples in a microscope for the microscopie imaging and measurement, and (3) RF irradiation of small to human body-sized samples in an anechoic chamber.

  9. Luminescent solar concentrator

    Directory of Open Access Journals (Sweden)

    Tugce Tosun

    2015-07-01

    Full Text Available Luminescent solar concentrator (LSC is a device that has luminescent molecules embedding or topping polymeric or glass waveguide to generate electricity from sunlight with a photovoltaic cell attachment. LSCs can be employed both in small and large scale projects, independent on the direction or angle of the surface with respect to the sun, promising more freedom for integration in urban environments compared to the traditional PV systems. The aim of the SEB&C PDEng project is to investigate the applicability of this innovative technology in the built environment and to bridge the gap of knowledge linking societal, design and technological aspects. The final goal is to exhibit potential application concepts of LSC developed by co-creative methods at SPARK campus which is a hub for open innovation in built environment. Necessity of a paradigm shift towards sustainable and smart cities came into being due to the significant increase in energy demand of the buildings. The challenge is to increase renewable sources in the energy mix while designing aesthetic environments. Thus, building integrated renewable energy technologies represent a great opportunity to help overcome this current challenge. Smart energy, energy efficiency and use of renewable sources are key aspects to be considered nowadays and many innovative technologies need further exploitation to be commercially viable, such as luminescent solar concentrator.

  10. Luminescent Metal Nanoclusters for Potential Chemosensor Applications

    Directory of Open Access Journals (Sweden)

    Muthaiah Shellaiah

    2017-12-01

    Full Text Available Studies of metal nanocluster (M-NCs-based sensors for specific analyte detection have achieved significant progress in recent decades. Ultra-small-size (<2 nm M-NCs consist of several to a few hundred metal atoms and exhibit extraordinary physical and chemical properties. Similar to organic molecules, M-NCs display absorption and emission properties via electronic transitions between energy levels upon interaction with light. As such, researchers tend to apply M-NCs in diverse fields, such as in chemosensors, biological imaging, catalysis, and environmental and electronic devices. Chemo- and bio-sensory uses have been extensively explored with luminescent NCs of Au, Ag, Cu, and Pt as potential sensory materials. Luminescent bi-metallic NCs, such as Au-Ag, Au-Cu, Au-Pd, and Au-Pt have also been used as probes in chemosensory investigations. Both metallic and bi-metallic NCs have been utilized to detect various analytes, such as metal ions, anions, biomolecules, proteins, acidity or alkalinity of a solution (pH, and nucleic acids, at diverse detection ranges and limits. In this review, we have summarized the chemosensory applications of luminescent M-NCs and bi-metallic NCs.

  11. Ion beam induced luminescence of materials

    CERN Document Server

    Brooks, R

    2001-01-01

    luminescence dead zone at the domain walls. Neodymium-yttrium-aluminium garnet (Nd:YAG) was examined and the spectra measured as a function of temperature to show the evolution of intensity of the narrow line emission from the Nd rare earth. Shifts and changes in the intrinsic UV band in the YAG material were also apparent. Thin films of alumina grown on silica on a silicon substrate, along with some that contained copper nanoclusters were also examined. TRIM software was used to model the rate of excitation within the different layers of the material for the various implant energies and to identify the source of the luminescence profile observed in each case. Evidence of thin film interference fringes was apparent in the spectra by fringe patterns modulated onto the luminescence signal as a function of wavelength and film thickness. Analysis of an alkali feldspar material using IBL, and combined with work done using RL and CL experiments, showed a shift towards lower wavelengths of the main red/IR band with ...

  12. Luminescent properties of aluminum hydride

    Energy Technology Data Exchange (ETDEWEB)

    Baraban, A.P.; Gabis, I.E.; Dmitriev, V.A. [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation); Dobrotvorskii, M.A., E-mail: mstislavd@gmail.com [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation); Kuznetsov, V.G. [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation); Matveeva, O.P. [National Mineral Resources University, Saint Petersburg 199106 (Russian Federation); Titov, S.A. [Petersburg State University of Railway Transport, Saint-Petersburg 190031 (Russian Federation); Voyt, A.P.; Elets, D.I. [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation)

    2015-10-15

    We studied cathodoluminescence and photoluminescence of α-AlH{sub 3}– a likely candidate for use as possible hydrogen carrier in hydrogen-fueled vehicles. Luminescence properties of original α-AlH{sub 3} and α-AlH{sub 3} irradiated with ultraviolet were compared. The latter procedure leads to activation of thermal decomposition of α-AlH{sub 3} and thus has a practical implementation. We showed that the original and UV-modified aluminum hydride contain luminescence centers ‐ structural defects of the same type, presumably hydrogen vacancies, characterized by a single set of characteristic bands of radiation. The observed luminescence is the result of radiative intracenter relaxation of the luminescence center (hydrogen vacancy) excited by electrons or photons, and its intensity is defined by the concentration of vacancies, and the area of their possible excitation. UV-activation of the dehydrogenation process of aluminum hydride leads to changes in the spatial distribution of the luminescence centers. For short times of exposure their concentration increases mainly in the surface regions of the crystals. At high exposures, this process extends to the bulk of the aluminum hydride and ends with a decrease in concentration of luminescence centers in the surface region. - Highlights: • Aluminum hydride contains hydrogen vacancies which serve as luminescence centers. • The luminescence is the result of radiative relaxation of excited centers. • Hydride UV-irradiation alters distribution and concentration of luminescence centers.

  13. Strong enhancement of emission efficiency in GaN light-emitting diodes by plasmon-coupled light amplification of graphene

    Science.gov (United States)

    Kim, Jong Min; Kim, Sung; Hwang, Sung Won; Kim, Chang Oh; Shin, Dong Hee; Kim, Ju Hwan; Jang, Chan Wook; Kang, Soo Seok; Hwang, Euyheon; Choi, Suk-Ho; El-Gohary, Sherif H.; Byun, Kyung Min

    2018-02-01

    Recently, we have demonstrated that excitation of plasmon-polaritons in a mechanically-derived graphene sheet on the top of a ZnO semiconductor considerably enhances its light emission efficiency. If this scheme is also applied to device structures, it is then expected that the energy efficiency of light-emitting diodes (LEDs) increases substantially and the commercial potential will be enormous. Here, we report that the plasmon-induced light coupling amplifies emitted light by ∼1.6 times in doped large-area chemical-vapor-deposition-grown graphene, which is useful for practical applications. This coupling behavior also appears in GaN-based LEDs. With AuCl3-doped graphene on Ga-doped ZnO films that is used as transparent conducting electrodes for the LEDs, the average electroluminescence intensity is 1.2–1.7 times enhanced depending on the injection current. The chemical doping of graphene may produce the inhomogeneity in charge densities (i.e., electron/hole puddles) or roughness, which can play a role as grating couplers, resulting in such strong plasmon-enhanced light amplification. Based on theoretical calculations, the plasmon-coupled behavior is rigorously explained and a method of controlling its resonance condition is proposed.

  14. Propagation of a strong x-ray pulse: Pulse compression, stimulated Raman scattering, amplified spontaneous emission, lasing without inversion, and four-wave mixing

    International Nuclear Information System (INIS)

    Sun Yuping; Wang Chuankui; Liu Jicai; Gel'mukhanov, Faris

    2010-01-01

    We study the compression of strong x-ray pulses from x-ray free-electron lasers (XFELs) propagating through the resonant medium of atomic argon. The simulations are based on the three-level model with the frequency of the incident x-ray pulse tuned in the 2p 3/2 -4s resonance. The pulse propagation is accompanied by the self-seeded stimulated resonant Raman scattering (SRRS). The SRRS starts from two channels of amplified spontaneous emission (ASE), 4s-2p 3/2 and 3s-2p 3/2 , which form the extensive ringing pattern and widen the power spectrum. The produced seed field triggers the Stokes ASE channel 3s-2p 3/2 . The population inversion is quenched for longer propagation distances where the ASE is followed by the lasing without inversion (LWI), which amplifies the Stokes component. Both ASE and LWI reshape the input pulse: The compressed front part of the pulse (up to 100 as) is followed by the long tail of the ringing and beating between the pump and Stokes frequencies. The pump pulse also generates weaker Stokes and anti-Stokes fields caused by four-wave mixing. These four spectral bands have fine structures caused by the dynamical Stark effect. A slowdown of the XFEL pulse up to 78% of the speed of light in vacuum is found because of a large nonlinear refractive index.

  15. Luminescence of the octahedral uranate group

    International Nuclear Information System (INIS)

    Hair, J.Th.W. de

    1976-01-01

    The luminescence characteristics of the octahedral uranate group are described. Bands in the excitation spectra are assigned to charge transfer transitions from ligand m.o.'s to the 5f state of the hexavalent uranium ion. The emission is a parity-forbidden electric dipole transition 5f→tsub(1u) which is vibronically allowed by coupling with the ungerade vibrational modes of the UO 6- 6 octahedron. This is confirmed by the dependence of the decay time on temperature. Attention is paid to the difference between the vibrational patterns in the emission of the UO 6- 6 and the UO 2+ 2 groups. From measurements as a function of the uranium concentration it is deduced that energy transfer between uranate groups mutually proceeds over some 25 A. This explains why the vibrational pattern in the emission spectra depends on the uranium concentration. (Auth.)

  16. Thermal luminescence spectroscopy chemical imaging sensor.

    Science.gov (United States)

    Carrieri, Arthur H; Buican, Tudor N; Roese, Erik S; Sutter, James; Samuels, Alan C

    2012-10-01

    The authors present a pseudo-active chemical imaging sensor model embodying irradiative transient heating, temperature nonequilibrium thermal luminescence spectroscopy, differential hyperspectral imaging, and artificial neural network technologies integrated together. We elaborate on various optimizations, simulations, and animations of the integrated sensor design and apply it to the terrestrial chemical contamination problem, where the interstitial contaminant compounds of detection interest (analytes) comprise liquid chemical warfare agents, their various derivative condensed phase compounds, and other material of a life-threatening nature. The sensor must measure and process a dynamic pattern of absorptive-emissive middle infrared molecular signature spectra of subject analytes to perform its chemical imaging and standoff detection functions successfully.

  17. Luminescent properties of praseodymium in some fluorides

    International Nuclear Information System (INIS)

    Potapov, A.S.; Rodnyj, P.A.; Mikhrin, S.B.; Magunov, I.R.

    2005-01-01

    Influence of diverse factors on efficiency of the Pr 3+ cascade emission in BaF 2 : Pr and SrAlF 5 : Pr. The effect of the environment of the luminescence center on the mutual position of the lowest 5d and the 4f level 1 S 0 of Pr 3+ ion is considered. PrF 3 clustering in BaF 2 is observed at a high praseodymium concentration. The promising potential of magnesium as a charge compensator for praseodymium in SrAlF 5 is demonstrated [ru

  18. Growth-morphology-luminescence correlation in ZnO-containing nanostructures synthesized in different media

    International Nuclear Information System (INIS)

    Japic, Dajana; Antonio Paramo, J.; Marinsek, Marjan; Strzhemechny, Yuri M.; Crnjak Orel, Zorica

    2012-01-01

    Zinc hydroxide particles were prepared by a two-step process employing zinc nitrate hexahydrate, urea, ethylene glycol, water and p-toluene-sulfonic acid monohydrate (p-TSA). We used different concentrations of the reactants as well as different volume ratios of the solvents. ZnO particles were obtained by thermal treatment of the reaction products at two different temperatures: 350 °C and 500 °C. The samples were characterized by scanning field emission electron microscopy (SEM), X-ray diffraction (XRD) spectroscopy, BET analysis, thermogravimetry (TG) analysis and photoluminescence (PL) spectroscopy. It was found that after the thermal treatment particles become smaller, with the p-TSA concentration strongly affecting the morphology of the particles. Luminescence properties of the samples probed by PL at 8 K and room temperature exhibited a remarkable correlation with specimens′ nanomorphology. Luminescent features at ∼2.0–2.2 eV, ∼2.4–2.5 eV, ∼2.65 eV, ∼2.9 eV, ∼3.0–3.1 eV and ∼3.3 eV were observed in most specimens, although their relative intensity and temperature dependence were specific to an individual group of samples vis-à-vis their growth history and morphology. - Highlights: ► ZnO-containing nanostructures grown by precipitation were investigated. ► Samples' morphology can be carefully tailored via growth control parameters. ► Strong dependence of optoelectronic properties on specimens' morphology was observed. ► Efficient control of composition, morphology and luminescence via synthesis parameters.

  19. Sol–gel synthesis and luminescence of undoped and Mn-doped zinc orthosilicate phosphor nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    El Ghoul, J., E-mail: ghoultn@yahoo.fr [Laboratoire de Physique des Matériaux et des Nanomatériaux Appliquée à l’Environnement, Faculté des Sciences de Gabès, Cité Erriadh Manara Zrig, 6072 Gabès (Tunisia); El Mir, L. [Laboratoire de Physique des Matériaux et des Nanomatériaux Appliquée à l’Environnement, Faculté des Sciences de Gabès, Cité Erriadh Manara Zrig, 6072 Gabès (Tunisia); Al Imam Mohammad Ibn Saud Islamic University (IMSIU), College of Sciences, Departement of Physics, Riyadh 11623 (Saudi Arabia)

    2014-04-15

    Zn{sub 2}SiO{sub 4} and Zn{sub 2}SiO{sub 4}:Mn particles embedded in SiO{sub 2} host matrix prepared by sol gel method under supercritical conditions of ethyl alcohol in two steps. Were prepared by a simple solid-phase reaction under natural atmosphere at 1200 °C after the incorporation of ZnO and ZnO:Mn nanoparticles, respectively, in silica monolith. In the case of SiO{sub 2}/Zn{sub 2}SiO{sub 4} nanocomposite, the powder with an average particle size of 80 nm shows a strong luminescence band centred at around 760 nm in the visible range. In addition, the PL spectrum for the SiO{sub 2}/Zn{sub 2}SiO{sub 4}:Mn nanocomposite showed that a dominant peak at 525 nm appeared, which originated from the {sup 4}T{sub 1}–{sup 6}A{sub 1} transitions of Mn{sup 2+} ions. The luminescence properties of nanocomposites were characterized by emission and excitation spectra as well their dependencies of upon temperature and power excitation density. -- Highlights: • The Synthesis of Zn{sub 2}SiO{sub 4} nanocomposites. • Structural and optical characterizations of Zn{sub 2}SiO{sub 4} and Zn{sub 2}SiO{sub 4}:Mn nanocomposites. • The willemite α-Zn{sub 2}SiO{sub 4} structure was formed to the heat treatment temperature 1200 °C. • The powder exhibits a nanometric size. • Strong bands of luminescence have appeared.

  20. New luminescent materials and filters for Luminescent Solar Concentrators

    NARCIS (Netherlands)

    De Boer, D.K.G.; Ronda, C.R.; Keur, W.C.; Meijerink, A.

    2012-01-01

    In a Luminescent Solar Concentrator (LSC), short-wavelength light isconverted by a luminescent material into long-wavelength light, which is guided towards a photovoltaic cell. In principle, an LSC allows for high concentration, but in practice this is prevented by lossmechanisms like limited

  1. Luminescent chemical sensing, biosensing, and screening using upconverting nanoparticles.

    Science.gov (United States)

    Achatz, Daniela E; Ali, Reham; Wolfbeis, Otto S

    2011-01-01

    Upconverting nanoparticles (UCNPs) display the unique property of converting near-infrared light (with wavelengths of typically 800-1,000 nm) into visible luminescence. Following a short introduction into the mechanisms leading to the effect, the main classes of materials used are discussed. We then review the state of the art of using UCNPs: (1) to label biomolecules such as antibodies and (synthetic) oligomers for use in affinity assay and flow assays; (2) to act as nanolamps whose emission intensity is modulated by chemical indicators, thus leading to a novel kind of chemical sensors; and (3), to act as donors in luminescence resonance energy transfer in chemical sensors and biosensors.

  2. Development of a battery-operated portable synchronous luminescence spectrofluorometer

    Energy Technology Data Exchange (ETDEWEB)

    Alarie, J.P.; Vo-Dinh, T.; Miller, G.; Ericson, M.N.; Maddox, S.R.; Watts, W. (Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831-6101 (United States)); Eastwood, D.; Lidberg, R.; Dominguez, M. (Lockheed Environmental Systems and Technologies Company, Las Vegas, Nevada 89119 (United States))

    1993-09-01

    A battery-operated portable synchronous luminescence spectrofluorometer was developed for on-site analysis of groundwater or hazardous waste sites. The instrument is capable of either emission, excitation, or synchronous fluorescence measurements. The instrument is suited for trace analysis of important pollutants such as polyaromatic hydrocarbons, creosotes, and polychlorinated biphenyls in complex mixtures. The ability to perform synchronous luminescence measurements on these samples can reduce the complexity of fluorescence spectra and help in rapid field site characterization. A description of the instrumental components is given and an evaluation of the instrument using anthracene and several oil samples is provided to illustrate the usefulness of the instrument.

  3. Hg-Xe exciplex formation in mixed Xe/Ar matrices: molecular dynamics and luminescence study.

    Science.gov (United States)

    Lozada-García, Rolando; Rojas-Lorenzo, Germán; Crépin, Claudine; Ryan, Maryanne; McCaffrey, John G

    2015-03-19

    Luminescence of Hg((3)P1) atoms trapped in mixed Ar/Xe matrices containing a small amount of Xe is reported. Broad emission bands, strongly red-shifted from absorption are recorded which are assigned to strong complexes formed between the excited mercury Hg* and xenon atoms. Molecular dynamics calculations are performed on simulated Xe/Ar samples doped with Hg to follow the behavior of Hg* in the mixed rare gas matrices leading to exciplex formation. The role of Xe atoms in the first solvation shell (SS1) around Hg was investigated in detail, revealing the formation of two kinds of triatomic exciplexes; namely, Xe-Hg*-Xe and Ar-Hg*-Xe. The first species exists only when two xenon atoms are present in SS1 with specific geometries allowing the formation of a linear or quasi-linear exciplex. In the other geometries, or in the presence of only one Xe in SS1, a linear Ar-Hg*-Xe exciplex is formed. The two kinds of exciplexes have different emission bands, the most red-shifted being that involving two Xe atoms, whose emission is very close to that observed in pure Xe matrices. Simulations give a direct access to the analysis of the experimental absorption, emission, and excitation spectra, together with the dynamics of exciplexes formation.

  4. Portable Piezospectroscopy system: non-contact in-situ stress sensing through high resolution photo-luminescent mapping

    International Nuclear Information System (INIS)

    Hanhan, I.; Durnberg, E.; Freihofer, G.; Akin, P.; Raghavan, S.

    2014-01-01

    Through the piezospectroscopic effect, certain photo-luminescent materials, once excited with a laser, produce spectral emissions which are sensitive to the stress or strain that the material experiences. A system that utilizes the piezospectroscopic effect for non-contact stress detection over a material's surface can capture important information on the evolution of mechanical response under various conditions. Therefore, the components necessary for piezospectroscopic mapping and analysis have now been integrated into a versatile and transportable system that can be used with photo-luminescent materials in any load frame or on a variety of structures. This system combines compact hardware components such as a portable laser source, fiber optics, spectrograph, charge-coupled device (CCD), and an X-Y-Z stage (with focusing capabilities) with a series of data analysis algorithms capable of analyzing and outputting high resolution photo-luminescent (PL) maps on-site. Through a proof of concept experiment using a compressed polycrystalline alumina sample with sharp machined corners, this system successfully captured high resolution PL maps with a step size of 28.86μm/pixel and located high stress concentrations in critical areas, which correlated closely with the results of a finite element model. This work represents an important step in advancing the portability of piezospectroscopy for in-situ and non-contact stress detection. The instrumentation developed here has strong implications for the future of non-destructive evaluation and non-invasive structural health monitoring

  5. Microprobe analysis, iono- and photo-luminescence of Mn2+ activated ZnGa2O4 fibres

    International Nuclear Information System (INIS)

    Santos, N.F.; Fernandes, A.J.S.; Alves, L.C.; Sobolev, N.A.; Alves, E.; Lorenz, K.; Costa, F.M.; Monteiro, T.

    2013-01-01

    Cubic ZnGa 2 O 4 fibres have been grown by the laser floating zone technique with different pulling rates. In fibres activated with manganese ions, the room temperature photo- and iono-luminescence is dominated by an intense green emission which is observed by the naked eye. The green band is due to an overlap of the 4 T 1 → 6 A 1 intraionic transitions of the Mn 2+ ions in different sites in the gallate host. The fibres’ photoluminescence spectra have been found to be dependent on the excitation energy. Additionally, the intensity of the green photo- and iono-luminescence is strongly sensitive to the measurement temperature and proton irradiation time. Micro PIXE analysis was used in order to verify the homogeneous distribution of the Mn luminescence activators and determine its concentration as well as for verification of impurity contents that may have been incorporated during the fibres growth. The potential of ionoluminescence measurements for characterization of optical materials is discussed

  6. Controllable synthesis and luminescence properties of TiO2:Eu3+ nanorods, nanoparticles and submicrospheres by hydrothermal method

    Science.gov (United States)

    Qi, Xiaofei; Song, Yanhua; Sheng, Ye; Zhang, Hongguang; Zhao, Huan; Shi, Zhan; Zou, Haifeng

    2014-12-01

    Eu3+-doped TiO2 nanocrystals with three kinds of morphologies (nanorods, nanoparticles, and submicrospheres) have been successfully fabricated in cetyltrimethylammonium bromide (CTAB)/water/cyclohexane/n-pentanol reverse micelle by hydrothermal method for the first time and their photoluminescence (PL) properties have also been studied. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), FT-IR, and PL spectra were used to characterize the samples. The acidic and alkaline conditions of the microemulsion play an important role in determining the geometric morphologies of the final products. TiO2:Eu3+ with three different morphologies all exist only in anatase phase and show high luminescence intensity without further calcinations, which show its advantages of energy saving. The shape of emission spectra was independent of the morphologies of the products but the luminescence intensity of the TiO2:Eu3+ materials is strongly dependent on their morphology. The results show that TiO2:Eu3+ nanorods possess the strongest luminescence intensity among the three nanostructured samples.

  7. Hydrothermal synthesis of highly luminescent blue-emitting ZnSe(S) quantum dots exhibiting low toxicity

    Energy Technology Data Exchange (ETDEWEB)

    Mirnajafizadeh, Fatemeh; Ramsey, Deborah; McAlpine, Shelli [School of Chemistry, University of New South Wales, Sydney, NSW 2052 (Australia); Wang, Fan; Reece, Peter [School of Physics, University of New South Wales, Sydney, NSW 2052 (Australia); Stride, John Arron, E-mail: j.stride@unsw.edu.au [School of Chemistry, University of New South Wales, Sydney, NSW 2052 (Australia); Bragg Institute, Australian Nuclear Science and Technology Organisation, PMB 1, Menai, NSW 2234 (Australia)

    2016-07-01

    Highly luminescent quantum dots (QDs) that emit in the visible spectrum are of interest to a number of imaging technologies, not least that of biological samples. One issue that hinders the application of luminescent markers in biology is the potential toxicity of the fluorophore. Here we show that hydrothermally synthesized ZnSe(S) QDs have low cytotoxicity to both human colorectal carcinoma cells (HCT-116) and human skin fibroblast cells (WS1). The QDs exhibited a high degree of crystallinity, with a strong blue photoluminescence at up to 29% quantum yield relative to 4′,6-diamidino-2-phenylindole (DAPI) without post-synthetic UV-irradiation. Confocal microscopy images obtained of HCT-116 cells after incubation with the QDs highlighted the stability of the particles in cell media. Cytotoxicity studies showed that both HCT-116 and WS1 cells retain 100% viability after treatment with the QDs at concentrations up to 0.5 g/L, which makes them of potential use in biological imaging applications. - Highlights: • Highly luminescent ZnSe(S) QDs were synthesized using a simple, one-step hydrothermal method. • The as-synthesized QDs were found to be nontoxic in the presence of biological cells. • The QDs were stable in biological media with identical emission profile to that in water.

  8. Luminescent Lanthanide Reporters for High-Sensitivity Novel Bioassays

    Energy Technology Data Exchange (ETDEWEB)

    Anstey, Mitchell R. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Fruetel, Julia A. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Foster, Michael E. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Hayden, Carl C. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Buckley, Heather L. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Arnold, John [Sandia National Lab. (SNL-CA), Livermore, CA (United States)

    2013-09-01

    Biological imaging and assay technologies rely on fluorescent organic dyes as reporters for a number of interesting targets and processes. However, limitations of organic dyes such as small Stokes shifts, spectral overlap of emission signals with native biological fluorescence background, and photobleaching have all inhibited the development of highly sensitive assays. To overcome the limitations of organic dyes for bioassays, we propose to develop lanthanide-based luminescent dyes and demonstrate them for molecular reporting applications. This relatively new family of dyes was selected for their attractive spectral and chemical properties. Luminescence is imparted by the lanthanide atom and allows for relatively simple chemical structures that can be tailored to the application. The photophysical properties offer unique features such as narrow and non-overlapping emission bands, long luminescent lifetimes, and long wavelength emission, which enable significant sensitivity improvements over organic dyes through spectral and temporal gating of the luminescent signal.Growth in this field has been hindered due to the necessary advanced synthetic chemistry techniques and access to experts in biological assay development. Our strategy for the development of a new lanthanide-based fluorescent reporter system is based on chelation of the lanthanide metal center using absorbing chromophores. Our first strategy involves "Click" chemistry to develop 3-fold symmetric chelators and the other involves use of a new class of tetrapyrrole ligands called corroles. This two-pronged approach is geared towards the optimization of chromophores to enhance light output.

  9. Luminescence dating of Netherland's sediments

    NARCIS (Netherlands)

    Wallinga, J.; Davids, F.; Dijkmans, J.W.A.

    2007-01-01

    Over the last decades luminescence dating techniques have been developed that allow earth scientists to determine the time of deposition of sediments. In this contribution we revity: 1) the development of the methodology, 2) tests of the reliability of luminescence dating on Netherlands' sediments;

  10. Luminescence dating of Netherlands’ sediments

    NARCIS (Netherlands)

    Wallinga, J.; Davids, F.; Dijkmans, J.W.A.

    2007-01-01

    Over the last decades luminescence dating techniques have been developed that allow earth scientists to determine the time of deposition of sediments. In this contribution we review: 1) the development of the methodology; 2) tests of the reliability of luminescence dating on Netherlands’ sediments;

  11. Luminescence studies of semiconductor electrodes

    NARCIS (Netherlands)

    Kelly, J.J.; Kooij, Ernst S.; Meulenkamp, E.A.

    1999-01-01

    In this paper we review our recent results of in-situ luminescence studies of semiconductor electrodes. Three classes of materials are considered: single crystal compound semiconductors, porous silicon and semiconducting oxides doped with luminescent ions. We show how photoluminescence (PL) and

  12. Emission enhancement within gold spherical nanocavity arrays.

    Science.gov (United States)

    Jose, Bincy; Steffen, Ronald; Neugebauer, Ute; Sheridan, Eoin; Marthi, Reena; Forster, Robert J; Keyes, Tia E

    2009-12-14

    Gold nanocavity arrays were prepared on fluorine-doped tin oxide on glass by electrochemical deposition of gold through monolayers of polystyrene spheres. The impact of the resulting spherical cap architecture on the photophysics of solutions and self-assembled monolayers of luminophore encapsulated within the nanocavities is reported for the first time. From conventional confocal fluorescence microscopy, the emission intensity of solutions of [Ru(bpy)(2)(Qbpy)](2+) (where bpy is 2,2'-bipyridyl and Qbpy is 2,2':4,4'':4,4''-quarterpyridyl) and fullerene (C(60)) encapsulated within the 820 nm diameter nanocavities was demonstrated to increase by approximately an order of magnitude compared with that of the associated bulk solution. Comparison was also made with the emission observed for luminophore solution encapsulated in cobalt nanocavities of comparable dimensions, where plasmonic interactions are not anticipated. Again, approximately an order of magnitude enhancement was observed for the gold arrays. Luminescence lifetime imaging revealed that the enhancement of the emission intensity of this solution within the nanocavity was accompanied by a small but significant decrease in the luminescent lifetime for [Ru(bpy)(2)(Qbpy)](2+). Enhancement was, in addition, strongly influenced by the wavelength of excitation, suggesting that plasmonics may play a role in the enhancement of the excitation process. An important observation from confocal imaging studies was that the dimensions of the luminophore emission field from solution within the cavities were significantly smaller than the dimensions of the cavity aperture and corresponded to a little more than that of the point spread function of the microscope. This indicates that its origin is significantly smaller than the wavelength of the emitted light and suggests that luminescence enhancement is highly localised. When the array was filled with a solution of [Ru(bpy)(2)(Qbpy)](2+) the emission spectrum of this complex

  13. Synthesis and luminescence properties of europium and terbium complexes with pyridine- or bipyridine-linked oligothiophene ligand

    International Nuclear Information System (INIS)

    Liu Ping; Huang Mingsheng; Pan Wanzhang; Zhang Yamin; Hu Jianhua; Deng Wenji

    2006-01-01

    With an aim to develop novel luminescence materials, europium and terbium complexes of 2,5-(2-thiophene)-pyridine (TPY) and 5,5'-bis(5-(2,2'-bithiophene))-2,2'-bipyridine (B2TBPY) were synthesized, and their luminescence properties studied. The complexes exhibit ligand-sensitized emission, which is typical of Eu(III) and Tb(III) ions

  14. Synthesis, Structural Characterization and Up-Conversion Luminescence Properties of NaYF4:Er3+,Yb3+@MOFs Nanocomposites

    Science.gov (United States)

    Giang, Lam Thi Kieu; Marciniak, Lukasz; Huy, Tran Quang; Vu, Nguyen; Le, Ngo Thi Hong; Binh, Nguyen Thanh; Lam, Tran Dai; Minh, Le Quoc

    2017-10-01

    This paper describes a facile synthesis of NaYF4:Er3+,Yb3+ nanoparticles embraced in metal-organic frameworks (MOFs), known as NaYF4:Er3+, Yb3+@MOFs core/shell nanostructures, by using iron(III) carboxylate (MIL-100) and zeolitic imidazolate frameworks (ZIF-8). Morphological, structural and optical characterization of these nanostructures were investigated by field emission-scanning electron microscopy, Fourier transform infrared spectroscopy, x-ray diffraction, and up-conversion luminescence measurements. Results showed that spherical-shaped NaYF4:Er3+,Yb3+@MIL-100 nanocomposites with diameters of 150-250 nm, and rod-shaped NaYF4:Er3+,Yb3+@ZIF-8 nanocomposites with lengths of 300-550 nm, were successfully synthesized. Under a 980-nm laser excitation at room temperature, the NaYF4:Er3+,Yb3+@MOFs nanocomposites exhibited strong up-conversion luminescence with two emission bands in the green part of spectrum at 520 nm and 540 nm corresponding to the 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 transitions of Er3+ ions, respectively, and a red emission band at 655 nm corresponding to the 4F9/2 → 4I15/2 transition of Er3+ ions. The above properties of NaYF4:Er3+,Yb3+@MOFs make them promising candidates for applications in biotechnology.

  15. Preparation and characteristics of Fe3O4-YVO4:Eu3+ bifunctional magnetic-luminescent nanocomposites

    International Nuclear Information System (INIS)

    Peng Hongxia; Liu Guixia; Dong Xiangting; Wang Jinxian; Xu Jia; Yu Wensheng

    2011-01-01

    Graphical abstract: Highlights: → Bifunctional magnetic-luminescent nanocomposites with Fe 3 O 4 nanoparticles as the core and YVO 4 :Eu 3+ as the shell. → A cubic spinel structrue of Fe 3 O 4 core and a tetragonal phase of YVO 4 shell were obtained. → The nanocomposites displayed a strong red emission and superparamagnetic behavior at room temperature. - Abstract: A facile direct precipitation method has been developed for the synthesis of bifunctional magnetic-luminescent nanocomposites with Fe 3 O 4 nanoparticles as the core and YVO 4 :Eu 3+ as the shell. Transmission electron microscopy (TEM) images revealed that the obtained bifunctional nanocomposites had a core-shell structure and a spherical morphology. The average size was ∼150 nm, and the thickness of the shell was ∼15 nm. The X-ray diffraction (XRD) patterns showed that a cubic spinel structure of Fe 3 O 4 core and a tetragonal phase of YVO 4 shell were obtained. Fourier transform infrared (FT-IR) spectra confirmed that the YVO 4 :Eu 3+ had been successfully deposited on the surface of Fe 3 O 4 nanoparticles. Photoluminescence (PL) spectra indicated that the nanocomposites displayed a strong red characteristic emission of Eu 3+ . Magnetic measurements showed that the obtained bifunctional nanocomposites exhibited superparamagnetic behavior at room temperature. Therefore, the bifunctional nanocomposites are expected to develop many potential applications in biomedical fields.

  16. One-step synthesis of solid state luminescent carbon-based silica nanohybrids for imaging of latent fingerprints

    Science.gov (United States)

    Li, Feng; Li, Hongren; Cui, Tianfang

    2017-11-01

    Fluorescent carbon-based nanomaterials(CNs) with tunable visible emission are biocompatible, environment friendly and most suitable for various biomedical applications. Despite the successes in preparing strongly fluorescent CNs, preserving the luminescence in solid materials is still challenging because of the serious emission quenching of CNs in solid state materials. In this work, fluorescent carbon and silica nanohybrids (SiCNHs) were synthesized via a simple one-step hydrothermal approach by carbonizing sodium citrate and (3-aminopropyl)triethoxysilane(APTES), and hydrolysis of tetraethyl orthosilicate(TEOS). The resultant SiCNs were characterized through X-ray diffraction (XRD), transmission electron microscopy (TEM), FT-IR, X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The SiCNs exhibited strong fluorescence in both aqueous and solid states. The luminescent solid state SiCNs power were successfully used as a fluorescent labeling material for enhanced imaging of latent fingerprints(LFPs) on single background colour and multi-coloured surfaces substrates in forensic science for individual identification.

  17. Strong red-emission of Eu{sup 3+}:Li{sub 4}Ti{sub 5}O{sub 12} powders for phosphor applications

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Yan [Kazuo Inamori School of Engineering, New York State College of Ceramics, Alfred University, Alfred, NY 14802 (United States); Jiménez, José A. [Department of Chemistry, University of North Florida, Jacksonville, FL 32224 (United States); Wu, Yiquan, E-mail: wuy@alfred.edu [Kazuo Inamori School of Engineering, New York State College of Ceramics, Alfred University, Alfred, NY 14802 (United States)

    2016-08-15

    The synthesis and photoluminescence properties of trivalent europium doped lithium titanate (Eu{sup 3+}:Li{sub 4}Ti{sub 5}O{sub 12}) with different Eu{sup 3+} concentrations (0.1 mol%, 0.3 mol%, 1.0 mol%, 3.0 mol%) are reported and analyzed as a phosphor. Europium (III) nitrate (Eu(NO{sub 3}){sub 3}) was employed as Eu{sup 3+} source, while lithium acetate dihydrate (CH{sub 3}COOLi·2H{sub 2}O) and titanium n-butoxide (Ti(OC{sub 4}H{sub 9}){sub 4}) were adopted as raw materials to synthesize the host lithium titanate with a Li:Ti stoichiometry of 4.5:1. Phase identification was performed using X-ray diffraction (XRD), and morphology was examined using scanning electron microscopy (SEM). Eu{sup 3+}:Li{sub 4}Ti{sub 5}O{sub 12} powders showed strong red emission at 612 nm, corresponding to the {sup 5}D{sub 0}–{sup 7}F{sub 2} transition, with the strongest excitation peak observed in the blue light region at 464 nm. Decay time analyses revealed relatively short lifetimes accompanying typical exponential decay rates. The effect of Eu{sup 3+} concentration (0.1 mol%, 0.3 mol%, 1.0 mol%, 3.0 mol%) on photoluminescence intensity and decay time was explored, and is reported here. It was determined that the CIE color coordinates (0.66, 0.34) of the doped Li{sub 4}Ti{sub 5}O{sub 12} powders were independent of Eu{sup 3+} concentration, and that the coordinates are very similar to the ideal red chromaticity (0.67, 0.33) designated by the National Television Standard Committee (NTSC) system.

  18. Fiber-coupled Luminescence Dosimetry in Therapeutic and Diagnostic Radiology

    DEFF Research Database (Denmark)

    Andersen, Claus Erik

    2011-01-01

    . Some crystalline phosphors, such as carbon-doped aluminium oxide (Al2O3:C) have the ability to store charge produced in the crystal during irradiation. The stored charge may later be released by fiber-guided laser light under emission of so-called optically stimulated luminescence (OSL). The OSL signal......Fiber-coupled luminescence dosimetry is an emerging technology with several potentially attractive features of relevance for uses in therapeutic and diagnostic radiology: direct water equivalence (i.e. no significant perturbation of the radiation field in a water phantom or a patient), sub......-mm detector size, high dynamic range (below a mGy to several Gy), microsecond time resolution, and absence of electrical wires or other electronics in the dosimeter probe head. Fiber-coupled luminescence dosimetry systems typically consist of one or more small samples of phosphor, e.g. a mg of plastic...

  19. Optical and luminescence properties of zinc oxide (Review)

    Science.gov (United States)

    Rodnyi, P. A.; Khodyuk, I. V.

    2011-11-01

    We generalize and systematize basic experimental data on optical and luminescence properties of ZnO single crystals, thin films, powders, ceramics, and nanocrystals. We consider and study mechanisms by which two main emission bands occur, a short-wavelength band near the fundamental absorption edge and a broad long-wavelength band, the maximum of which usually lies in the green spectral range. We determine a relationship between the two luminescence bands and study in detail the possibility of controlling the characteristics of ZnO by varying the maximum position of the short-wavelength band. We show that the optical and luminescence characteristics of ZnO largely depend on the choice of the corresponding impurity and the parameters of the synthesis and subsequent treatment of the sample. Prospects for using zinc oxide as a scintillator material are discussed. Additionally, we consider experimental results that are of principal interest for practice.

  20. Optically stimulated luminescence dosimetry with gypsum wallboard (drywall).

    Science.gov (United States)

    Thompson, Jeroen W; Burdette, Kevin E; Inrig, Elizabeth L; Dewitt, Regina; Mistry, Rajesh; Rink, W Jack; Boreham, Douglas R

    2010-09-01

    Gypsum wallboard (drywall) represents an attractive target for retrospective dosimetry by optically stimulated luminescence (OSL) in the event of a radiological accident or malicious use of nuclear material. In this study, wallboard is shown to display a radiation-induced luminescence signal (RIS) as well as a natural background signal (NS), which is comparable in intensity to the RIS. Excitation and emission spectra show that maximum luminescence intensity is obtained for stimulation with blue light-emitting diodes (470 nm) and for detection in the ultraviolet region (290-370 nm). It is necessary to decrease the optical stimulation power dramatically in order to adequately separate the RIS from the interfering background signal. The necessary protocols are developed for accurately measuring the absorbed dose as low as 500 mGy and demonstrate that the RIS decays logarithmically with storage time, with complete erasure expected within 1-4 d.

  1. Luminescence and photosensitivity of PbI2 crystals

    International Nuclear Information System (INIS)

    Novosad, S.S.; Novosad, I.S.; Matviishin, I.M.

    2002-01-01

    One studied effect of temperature treatment and storage conditions on spectra features of PbI 2 crystals grown by the Bridgman-Stockbarger method from salt additionally purified by directed crystallization. Spectra of X-ray luminescence, photoluminescence and thermostimulated luminescence were investigated within 85-295 K temperature range under stationary X-ray excitation and emission of N 2 -laser. One studied photoelectret properties of those crystals under 85 K. Luminescence of PbI 2 crystals with maximum within 595 nm region observed following their thermal annealing under 475-495 K temperature and typical for near-the-surface section of specimens may be caused by oxygen-containing centres [ru

  2. Intense Red-Emitting Upconversion Nanophosphors (800 nm-Driven) with a Core/Double-Shell Structure for Dual-Modal Upconversion Luminescence and Magnetic Resonance in Vivo Imaging Applications.

    Science.gov (United States)

    Hong, A-Ra; Kim, Youngsun; Lee, Tae Sup; Kim, Sehoon; Lee, Kwangyeol; Kim, Gayoung; Jang, Ho Seong

    2018-04-18

    In this study, intense single-band red-emitting upconversion nanophosphors (UCNPs) excited with 800 nm near-infrared (NIR) light are reported. When a NaYF 4 :Nd,Yb active-shell is formed on the 12.7 nm sized NaGdF 4 :Yb,Ho,Ce UCNP core, the core/shell (C/S) UCNPs show tunable emission from green to red, depending on the Ce 3+ concentration under excitation with 800 nm NIR light. Ce 3+ -doped C/S UCNPs (30 mol %) exhibit single-band red emission peaking at 644 nm via a 5 F 5 → 5 I 8 transition of Ho 3+ . A high Nd 3+ concentration in the shell results in strong absorption at around 800 nm NIR light, even though the shell thickness is not large, and small-sized C/S UCNPs (16.3 nm) emit bright red light under 800 nm excitation. The formation of a thin NaGdF 4 shell on the C/S UCNPs further enhances the upconversion (UC) luminescence and sub-20 nm sized core/double-shell (C/D-S) UCNPs exhibit 2.8 times stronger UC luminescence compared with C/S UCNPs. Owing to the strong UC luminescence intensity and Gd 3+ ions on the surface of nanocrystals, they can be applied as a UC luminescence imaging agent and a T 1 contrast agent for magnetic resonance (MR) imaging. In vivo UC luminescence and high-contrast MR images are successfully obtained by utilizing the red-emitting C/D-S UCNPs.

  3. A luminescent nisin biosensor

    Science.gov (United States)

    Immonen, Nina; Karp, Matti

    2006-02-01

    Nisin is a lantibiotic, an antibacterial peptide produced by certain Lactococcus lactis strains that kills or inhibits the growth of other bacteria. Nisin is widely used as a food preservative, and its long-time use suggests that it can be generally regarded as safe. We have developed a method for determining the amount of nisin in food samples that is based on luminescent biosensor bacteria. Bacterial luciferase operon luxABCDE was inserted into plasmid pNZ8048, and the construct was transformed by electroporation into Lc. lactis strain NZ9800, whose ability to produce nisin has been erased by deletion of the gene nisA. The operon luxABCDE has been modified to be functional in gram-positive bacteria to confer a bioluminescent phenotype without the requirement of adding an exogenous substrate. In the plasmid pNZ8048, the operon was placed under control of the nisin-inducible nisA promoter. The chromosomal nisRK genes of Lc. lactis NZ9800 allow it to sense nisin in the environment and relay this signal via signal transduction proteins NisK and NisR to initiate transcription from nisA promoter. In the case of our sensor bacteria, this leads to production of luciferase and, thus, luminescence that can be directly measured from living bacteria. Luminescence can be detected as early as within minutes of induction. The nisin assay described here provides a detection limit in the sub-picogram level per ml, and a linear area between 1 - 1000 pg/ml. The sensitivity of this assay exceeds the performance of all previously published methods.

  4. Luminescence of PbCl2 and PbBr2 single crystals II. Luminescence and EPR of uv irradiated crystals

    NARCIS (Netherlands)

    Gruijter, W.C. de; Kerssen, J.

    1972-01-01

    PbCl2 and PbBr2 single crystals show a red luminescence under uv excitation at temperatures below 200°K. Furthermore, PbCl2 shows a yellow emission at temperatures below 40°K. The centers responsible for these emissions have been investigated by EPR measurements. These measurements indicate that due

  5. Luminescence of Eu{sup 3+}/Gd{sup 3+} co-doped silicate sol–gel powders

    Energy Technology Data Exchange (ETDEWEB)

    Szpikowska-Sroka, Barbara, E-mail: barbara.szpikowska-sroka@us.edu.pl [Institute of Chemistry, University of Silesia, Szkolna 9 Street, 40-007 Katowice (Poland); Pawlik, Natalia [Institute of Chemistry, University of Silesia, Szkolna 9 Street, 40-007 Katowice (Poland); Swinarew, Andrzej S. [Institute of Materials Science, University of Silesia, 75 Pułku Piechoty 1A, 41-500 Chorzów (Poland); Pisarski, Wojciech A. [Institute of Chemistry, University of Silesia, Szkolna 9 Street, 40-007 Katowice (Poland)

    2015-10-15

    Eu{sup 3+}/Gd{sup 3+} co-doped silicate sol–gel powders have been successfully obtained. The effect of high concentration of gadolinium ions on visible emission of europium ions in prepared materials has been studied under different excitation wavelengths. Spectroscopic properties of Eu{sup 3+} and Gd{sup 3+} ions in prepared powders were determined based on excitation and emission measurements as well as luminescence decay analysis. In the visible spectral range the observed emission bands correspond to transitions of trivalent Eu{sup 3+} and Gd{sup 3+} ions. The changes of excitation mechanism of optically active dopants significantly affect the increase of luminescence intensities. The luminescence lifetime for the {sup 5}D{sub 0} level of Eu{sup 3+} ions in examined samples upon excitation at λ{sub exc}=273 nm ({sup 8}S{sub 7/2}→{sup 6}I{sub J} transition of Gd{sup 3+}) is about 12 times longer in comparison to excitation at λ{sub exc}=393 nm ({sup 7}F{sub 0}→{sup 5}L{sub 6} transition of Eu{sup 3+}). The luminescence intensity coefficient R (Eu{sup 3+}) was also calculated, and it was found that ratio of the intensity of red to orange emission depends on the excitation wavelength. Based on determined spectroscopic parameters the energy transfer process from Gd{sup 3+} to Eu{sup 3+} ions was confirmed. - Highlights: • Eu{sup 3+}/Gd{sup 3+} co-doped silicate powders have been fabricated. • The emission bands in the visible range correspond to transitions of Eu{sup 3+} and Gd{sup 3+}. • The lifetime for the {sup 5}D{sub 0} state of Eu{sup 3+} upon excitation at 273 nm is strongly prolonged. • Efficient energy transfer from Gd{sup 3+} to Eu{sup 3+} ions was confirmed.

  6. Luminescent macrocyclic lanthanide complexes

    Science.gov (United States)

    Raymond, Kenneth N; Corneillie, Todd M; Xu, Jide

    2014-05-20

    The present invention provides a novel class of macrocyclic compounds as well as complexes formed between a metal (e.g., lanthanide) ion and the compounds of the invention. Preferred complexes exhibit high stability as well as high quantum yields of lanthanide ion luminescence in aqueous media without the need for secondary activating agents. Preferred compounds incorporate hydroxy-isophthalamide moieties within their macrocyclic structure and are characterized by surprisingly low, non-specific binding to a variety of polypeptides such as antibodies and proteins as well as high kinetic stability. These characteristics distinguish them from known, open-structured ligands.

  7. LUMINESCENCE DETERMINATION OF ETODOLAC

    Directory of Open Access Journals (Sweden)

    A. V. Yegorova

    2015-02-01

    Full Text Available A highly sensitive, simple and rapid method for determination of non-steroidal anti- inflammatory drug – etodolac (Et in washings from surfaces of pharmaceutical equipment have been proposed. The intensity of native luminescence of water-n-propanol solutions of etodolac (λex= 274 nm; λlum= 350 nm was used as the analytical signal. The calibration graph is linear in the concentration range 0.014-2.3 μg/ml, the limit of detection is 0.5 ng/ml.

  8. A color-tunable luminescent material with functionalized graphitic carbon nitride as multifunctional supports

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Jiutian; Cao, Yudong; Fan, Hai; Hou, Juying; Ai, Shiyun, E-mail: ashy@sdau.edu.cn

    2015-12-15

    A color-tunable luminescent material was prepared based on the composition of functionalized graphitic carbon nitride (g-C{sub 3}N{sub 4}) and europium (III). The functionalized g-C{sub 3}N{sub 4} layers not only behave as multifunctional supports including ligand coordinated with europium (III) and a support structure for the formation of the luminescent material, but exhibit excitation wavelength-dependent luminescence, thus the energy transfer between the functionalized g-C{sub 3}N{sub 4} and europium (III) can match very well by controlling the emission wavelength of functionalized g-C{sub 3}N{sub 4}. The as-prepared materials was comprehensively characterized via X-ray photoelectron spectroscopy, Fourier Transform Infrared spectroscopy, X-ray scattering techniques, Ultraviolet and Visible spectrophotometer, fluorescence spectrophotometer, thermogravimetric analysis, etc. The luminescent material exhibits multi-color emissions which are consistent with the characteristic emissions of europium (III) and functionalized g-C{sub 3}N{sub 4}, and the photoluminescence quality and density of the europium (III) can be greatly enhanced. The brilliant optical properties of the materials make them suiting for multipurpose applications in practical fields. - Graphical abstract: Schematic illustration of the synthesis and basic composition of the luminescent material. Inset figures were luminescence emission spectra of g-C{sub 3}N{sub 4} (A), europium (III) complex (a) and luminescent material (b) with the same concentration in (B) (K{sub ex}=350 nm) and photographs of (left) H{sub 2}O and (right) the H{sub 2}O dispersion of luminescence emission spectra under 350 nm UV radiation. The energy transfer in the luminescent material matchs very well and it exhibits multi-color emissions simultaneously. The enhanced photoluminescence quality and density of the europium (III) makes them suiting for multipurpose applications in practical fields. - Highlights: • Luminescent

  9. Spatially-resolved luminescence spectroscopy of CdSe quantum dots synthesized in ionic liquid crystal matrices

    International Nuclear Information System (INIS)

    Magaryan, K.A.; Mikhailov, M.A.; Karimullin, K.R.; Knyazev, M.V.; Eremchev, I.Y.; Naumov, A.V.; Vasilieva, I.A.; Klimusheva, G.V.

    2016-01-01

    The paper is devoted to investigation of luminescence properties of new quantum dot (QD)-doped materials. We studied CdSe QDs (1.8 nm and 2.3 nm) grown inside of a liquid crystalline cadmium alcanoate matrix. Temperature dependence of parameters of fluorescence spectra obtained in a wide temperature range using epi-luminescence microscopy technique was analyzed. Spatially-resolved luminescence images were measured for the areas of the samples of 150×150 µm 2 . Strong correlation between fluorescence spectra and sample structure was observed. - Highlights: • Glassy matrix with CdSe quantum dots inside fabricated in liquid crystalline mesophase. • Study of luminescence properties in a wide range of low temperatures. • Strong dependence of the luminescence spectra on spatial inhomogeneities. • Spatially-resolved luminescence imaging of quantum dots in liquid crystalline matrix.

  10. Characterization of dehydration-induced luminescence of kaolinite

    Science.gov (United States)

    Lahav, N.; Coyne, L.; Lawless, J. G.

    1985-01-01

    The dehydration-induced luminescence of a colloidal kaolinite is investigated experimentally, with particular attention given to the effect of various treatments on the luminescence characteristics. It is found that the total photon count of the emitted light is linearly related to the film thickness up to a thickness of 30 microns; mechanical stress in the form of grinding increases the photon output and produces extensive changes in the emission kinetics. A direct check of the emission wavelength dependence (by using color filters) indicates that roughly 75 percent of the emission occurs in the wavelength range below 410 nm. It is also found that incorporation of fluorescent molecules into the kaolinite paste increases the photon output and may indicate the transfer of ultraviolet photons to the fluorescent probe.

  11. Luminescence study of praseodymium complexes with selected phosphonate ligands

    Science.gov (United States)

    Pawlicki, G.; Lis, S.

    2011-08-01

    Spectroscopic properties of Pr(III) complexes with diethyl(phthalimidomethyl)phosphonate (DPIP) and diethyl(2-oxo-2phenylethyl)phosphonate (DEPP) ligands were studied using absorption and luminescence spectroscopy. Absorption spectra of praseodymium nitrate hexahydrate complexes with phosphonate ligands in acetonitrile solutions were measured and used to calculate oscillator strength values. Luminescence (excitation and emission) spectra of the Pr(III) complexes with DPIP and DEPP were measured in CH 3CN, DMSO, methanol and toluene solutions. The sensitized emission of Pr(III), observed from different excited states ( 3P 0 or 1D 2), resulted from the intramolecular energy transfer from the ligands to the emissive levels of Pr(III). The Pr(III) complexes with studied ligands were synthesized and their compositions, as Pr(DEPP) 2(NO 3) 3 and Pr(DPIP) 3(NO 3) 3, were confirmed by elemental analyses. Using IR and 31P NMR spectroscopy coordination mode of the ligands were described.

  12. Mechanoresponsive Luminescent Molecular Assemblies: An Emerging Class of Materials.

    Science.gov (United States)

    Sagara, Yoshimitsu; Yamane, Shogo; Mitani, Masato; Weder, Christoph; Kato, Takashi

    2016-02-10

    The possibility to change the molecular assembled structures of organic and organometallic materials through mechanical stimulation is emerging as a general and powerful concept for the design of functional materials. In particular, the photophysical properties such as photoluminescence color, quantum yield, and emission lifetime of organic and organometallic fluorophores can significantly depend on the molecular packing, enabling the development of molecular materials with mechanoresponsive luminescence characteristics. Indeed, an increasing number of studies have shown in recent years that mechanical force can be utilized to change the molecular arrangement, and thereby the optical response, of luminescent molecular assemblies of π-conjugated organic or organometallic molecules. Here, the development of such mechanoresponsive luminescent (MRL) molecular assemblies consisting of organic or organometallic molecules is reviewed and emerging trends in this research field are summarized. After a brief introduction of mechanoresponsive luminescence observed in molecular assemblies, the concept of "luminescent molecular domino" is introduced, before molecular materials that show turn-on/off of photoluminescence in response to mechanical stimulation are reviewed. Mechanically stimulated multicolor changes and water-soluble MRL materials are also highlighted and approaches that combine the concept of MRL molecular assemblies with other materials types are presented in the last part of this progress report. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Hexagonal hafnium zirconium phosphate luminescent material

    International Nuclear Information System (INIS)

    Chenot, C.F.; Mathers, J.E.; Shaffer, F.N.

    1981-01-01

    A new compound with the chemical formula, (Hfsub(1-x)Zr)sub(3-y) Asub(4y)(POsub(4))sub(4), where x is in the range 0-1, A is at least one alkali metal from the group lithium, sodium, or potassium, and y is in the range 0.4-2.0. The material is luminescent and can be used in X-ray intensifying screens and other intensifying devices with conventional silver halide emulsion X-ray film. It exhibits luminescence both in the self-activated state, in which case it emits in the ultraviolet part of the spectrum, and in the presence of activators, when it emits in the visible region upon excitation by X-rays, ultraviolet, etc. When used with conventional X-ray film, its band emission overlaps, to at least some extent, the absorption edge of the X-ray film base, resulting in good image resolution without substantial crossover. Optimum speed and persistence values are obtained for x of about 0.005-0.5. The compound exhibits about 60 nm bandwidth emission, peaking at about 350 nm, with controlled persistence upon X-ray excitation. The method of preparing the compound is described. (DN)

  14. Enhanced radiation detectors using luminescent materials

    Science.gov (United States)

    Vardeny, Zeev V.; Jeglinski, Stefan A.; Lane, Paul A.

    2001-01-01

    A radiation detecting device comprising a radiation sensing element, and a layer of luminescent material to expand the range of wavelengths over which the sensing element can efficiently detect radiation. The luminescent material being selected to absorb radiation at selected wavelengths, causing the luminescent material to luminesce, and the luminescent radiation being detected by the sensing element. Radiation sensing elements include photodiodes (singly and in arrays), CCD arrays, IR detectors and photomultiplier tubes. Luminescent materials include polymers, oligomers, copolymers and porphyrines, Luminescent layers include thin films, thicker layers, and liquid polymers.

  15. Simple correlation between the main luminescence parameters of the metallocene complex in the liquid phase

    International Nuclear Information System (INIS)

    Lukova, G.V.; Vasil'ev, V.P.; Smirnov, V.A.

    2007-01-01

    The lifetimes (τ) of excited states of the metallocene rac-C 6 H 10 (IndH 4 ) 2 ZrCl 2 (Ind = indenyl) in solutions have been studied. This metallocene features intensive luminescence in the liquid phase at room temperature. The main luminescence characteristics (Φ L and τ) of the complex in solutions are shown to strongly depend on the solvent nature. Long lifetimes and high luminescence yields are observed in solutions with strong solvating ability to metallocene complexes. The solvent defines the rate of radiationless deactivation, that becomes apparent in a linear correlation between Φ L and τ parameters [ru

  16. Luminescence sensitivity changes in quartz as a result of annealing

    DEFF Research Database (Denmark)

    Bøtter-Jensen, L.; Agersnap Larsen, N.; Mejdahl, V.

    1995-01-01

    Retrospective dosimetry using optically stimulated luminescence (OSL) on quartz extracted from (for example) bricks needs to account for strong OSL sensitivity changes that are known to occur depending on the previous thermal treatment of the sample. Non-heated quartz exhibits OSL orders of magni...

  17. Variation of the EuII emission wavelength by substitution of fluoride by hydride in fluorite-type compounds EuHxF2-x (0.20 ≤ x ≤ 0.67)

    NARCIS (Netherlands)

    Kunkel, Nathalie; Meijerink, A; Kohlmann, Holger

    2014-01-01

    Mixed-hydride fluorides EuHxF2-x were prepared by the solid-state reaction of EuF2 and EuH2 under hydrogen gas pressure in an autoclave. EuII luminescence is observed for 0.20 > x > 0.67, while pure EuF2 does not show any emission. The energy of the emission depends strongly on the degree of

  18. Luminescence dating in archaeology

    International Nuclear Information System (INIS)

    Wintle, A.G.

    2001-01-01

    Thermoluminescence (TL) dating is routinely applied to burnt lithic material. Simple fires are capable of enabling stones weighing a few hundred grams to reach 450 o C, thus zeroing the TL signal. TL dates have been obtained for Upper and Lower Paleolithic sites in Europe and the Near East. TL dating continues to be used for dating pottery and for authentification of ceramic works of art. Some recent studies report the use of optically stimulated luminescence (OSL) (also know as photoluminescence) for dating very small samples of quartz, e.g. from small pieces of pottery or frm metallurgical slag The major recent advance has been in the development of a reliable laboratory procedure for using the OSL signal from quartz to obtain the past radiation exposure. The quartz OSL signal is extremely sensitive to light and is reduced to a negligible level on exposure to direct sunlight for radionuclides during burial, signal to date san.sized quartz grains extracted from sediments, The OSL signal is stimulated by 470 nm light from emitting diodes and the detected using flirters centred on 340 nm A similar signal can be obtained from feldspar grain when are exposed to infrared wavelengths around 880 nm. The infrared stimulated luminescence (IRSL) signals is also rapidly depleted by exposure to sunlight, and dating of colluvial deposits from archaeological sites has been reported

  19. The luminescent concentrator illuminated

    Energy Technology Data Exchange (ETDEWEB)

    Slooff, L.H.; Kinderman, R.; Burgers, A.R.; Van Roosmalen, J.A.M. [ECN Solar Energy, Petten (Netherlands); Buechtemann, A.; Danz, R. [Fraunhofer Institute for Applied Polymer Research, Geiselbergstr. 69, D-14476 Golm (Germany); Meyer, T.B. [Solaronix SA, Rue de l' Ouriette 129, CH-1170 Aubonne (Switzerland); Chatten, A.J.; Farell, D.; Barnham, K.W.J. [Physics Department, Imperial College London, SW7 2BW (United Kingdom)

    2006-04-15

    Luminescent concentrator (LC) plates with different dyes were combined with standard multicrystalline silicon solar cells. External quantum efficiency measurements were performed, showing an increase in electrical current of the silicon cell (under AM1.5, 1 sun conditions, at normal incidence) compared to a bare cell. The influence of dye concentration and plate dimensions are addressed. The best results show a 1.7 times increase in the current from the LC/silicon cell compared to the silicon cell alone. This corresponds to an increase in power conversion efficiency of the silicon cell from 15 to 25%. To broaden the absorption spectrum of the LC, a second dye was incorporated in the LC plates. This results in a relative increase of 5-8% with respect to the one dye LC, giving a maximum power conversion efficiency of 26% on cell area. Using an extended ray-tracing model transmission, reflection and external quantum efficiency spectra were simulated and compared with measured spectra. The simulations deliver the luminescent quantum efficiencies of the two dyes as well as the background absorption by the polymer host. It is found that the quantum efficiency of the red emitting dye is 87%, which is one of the major loss factors in the measured LC. Using ray-tracing simulations it can be predicted that increasing the quantum efficiency to 95% would reduce this loss by almost 30%.

  20. Upconversion luminescence properties of Y2O3:Yb3+, Er3+ nanostructures

    International Nuclear Information System (INIS)

    De Gejihu; Qin Weiping; Zhang Jishen; Zhang Jishuang; Wang, Yan; Cao Chunyan; Cui Yang

    2006-01-01

    Cubic Y 2 O 3 nanostructures doped with Yb 3+ and Er 3+ ions were synthesized by a facile hydrothermal method. Three distinct shapes such as nanotubes, nanospheres and nanoflakes formed in the products by adjusting the pH value of reacting solution. Powder X-ray diffraction analyses indicate that all the three nanostructures are pure cubic phase, while electron microscopy measurements confirm the formation of different morphologies. These nanostructures exhibit strong visible upconversion luminescence under the excitation of a 978-nm diode laser. In Yb 3+ - and Er 3+ - codoped Y 2 O 3 nanocrystals, the relative intensity of green emission became stronger as the size and morphology of sample changed from tubes to flakes

  1. Luminescence in Sulfides: A Rich History and a Bright Future

    Directory of Open Access Journals (Sweden)

    Philippe F. Smet

    2010-04-01

    Full Text Available Sulfide-based luminescent materials have attracted a lot of attention for a wide range of photo-, cathodo- and electroluminescent applications. Upon doping with Ce3+ and Eu2+, the luminescence can be varied over the entire visible region by appropriately choosing the composition of the sulfide host. Main application areas are flat panel displays based on thin film electroluminescence, field emission displays and ZnS-based powder electroluminescence for backlights. For these applications, special attention is given to BaAl2S4:Eu, ZnS:Mn and ZnS:Cu. Recently, sulfide materials have regained interest due to their ability (in contrast to oxide materials to provide a broad band, Eu2+-based red emission for use as a color conversion material in white-light emitting diodes (LEDs. The potential application of rare-earth doped binary alkaline-earth sulfides, like CaS and SrS, thiogallates, thioaluminates and thiosilicates as conversion phosphors is discussed. Finally, this review concludes with the size-dependent luminescence in intrinsic colloidal quantum dots like PbS and CdS, and with the luminescence in doped nanoparticles.

  2. Luminescence in Sulfides: A Rich History and a Bright Future

    Science.gov (United States)

    Smet, Philippe F.; Moreels, Iwan; Hens, Zeger; Poelman, Dirk

    2010-01-01

    Sulfide-based luminescent materials have attracted a lot of attention for a wide range of photo-, cathodo- and electroluminescent applications. Upon doping with Ce3+ and Eu2+, the luminescence can be varied over the entire visible region by appropriately choosing the composition of the sulfide host. Main application areas are flat panel displays based on thin film electroluminescence, field emission displays and ZnS-based powder electroluminescence for backlights. For these applications, special attention is given to BaAl2S4:Eu, ZnS:Mn and ZnS:Cu. Recently, sulfide materials have regained interest due to their ability (in contrast to oxide materials) to provide a broad band, Eu2+-based red emission for use as a color conversion material in white-light emitting diodes (LEDs). The potential application of rare-earth doped binary alkaline-earth sulfides, like CaS and SrS, thiogallates, thioaluminates and thiosilicates as conversion phosphors is discussed. Finally, this review concludes with the size-dependent luminescence in intrinsic colloidal quantum dots like PbS and CdS, and with the luminescence in doped nanoparticles.

  3. Luminescence and host lattice structure of crystalline micro and nanoparticles co-doped with lanthanide ions

    International Nuclear Information System (INIS)

    Zurba, Nadia Khaled; Ferreira, Jose Maria da Fonte

    2012-01-01

    This article reports the investigation of crystalline micro and nanoparticles codoped with lanthanide ions, aiming at correlate their host lattice structure and chemical composition to the luminescence features. For this purpose, five phosphors were characterized by X-ray diffraction (XRD), scanning electron microscopy coupled to energy dispersive X-ray (EDX) spectroscopy, and photoluminescence (PL) spectroscopy, namely performed by their chromatic coordinates, radiance, luminance and PL emission spectra. This type of investigation concerning the optical characterization of luminescent crystalline micro and nanoparticles doped with lanthanide ions might be useful for scientific and practical applications, such as in light-emitting devices, luminescent paintings, ceramics, sensors, in nanoscience and nanotechnology. (author)

  4. Effects of Radiation Doses on the Photostimulated Luminescence Response of Certain Herbs and Spices

    Directory of Open Access Journals (Sweden)

    Sandeva Ivana

    2017-03-01

    Full Text Available Ionizing radiation applied on food eliminates harmful microorganisms, prevents sprouting and delays ripening. All methods for detection of irradiated food are based on physical, chemical, biological or microbiological changes caused by the treatment with ionizing radiation. When minerals are exposed to ionizing radiation, they accumulate radiation energy and store it in the crystal lattice, by which some electrons remain trapped in the lattice. When these minerals are exposed to optical stimulation, trapped electrons are released. The phenomenon, called optically stimulated luminescence or photostimulated luminescence, occurs when released electrons recombine with holes from luminescence centers in the lattice, resulting in emission of light with certain wavelengths.

  5. Luminescence properties of Tb3+ doped Sr2SnO4 green phosphor in UV/VUV regions.

    Science.gov (United States)

    Srinivas, M; Rao, B Appa; Vithal, M; Rao, P Raghava

    2013-01-01

    Polycrystalline Sr2SnO4 phosphors doped with Tb(3+) were prepared by conventional solid-state reaction method. Materials were characterized by powder XRD and EDS techniques. The luminescence properties of these materials were investigated under UV and VUV excitation. Upon excitation at 272 nm, phosphors exhibited intense emissions at 492 and 543 nm due to (5)D4 → (7)F6 and (5)D4 → (7)F5 transitions of Tb(3+) ions, respectively. Materials also exhibited strong emissions from these transitions under VUV excitation at 147, 173 and 230 nm. Quantitative analysis of the spectra indicated probable applications of these phosphors for PDP and other display devices as green emitting phosphors. Copyright © 2012 John Wiley & Sons, Ltd.

  6. Effect of AgCl NPs: Physical, thermal, absorption and luminescence properties

    Science.gov (United States)

    Nurhafizah, H.; Rohani, M. S.

    2017-06-01

    Silver nanoparticles (AgCl NPs) are embedded in Er3+/Nd3+ co-doped lithium niobate tellurite glasses of the form (68-x)TeO2-15Li2CO3-15Nb2O5-1Er2O3-1Nd2O3-(x)AgCl with x = 1,2 and 3 mol% via conventional melt-quenching technique. The physical properties such as density, ionic packing density, refractive index and electronic polarizability are computed utilizing the usual method. The existence of AgCl NPs with an average size of 3.7 nm is confirmed using TEM analysis. Moreover, the thermal stability and Hruby criterion of the glass decreases as the AgCl NPs content increases. The direct optical band gap are found decrease as the AgCl NPs content increase, but both indirect optical band gap and Urbach energy are found increases as AgCl NPs content increases. The luminescence spectra shows two strong emission which is the purple emission at 436 nm and red emission at 724 nm which also been observed has strong quenching due to the AgCl NPs, Er3+/Nd3+ dopant and modifier, lithium niobate which possessed magnetic penetration. These glass compositions may be potential for various applications such as solid state devices including laser.

  7. Synthesis of self-assembly plasmonic silver nanoparticles with tunable luminescence color

    Energy Technology Data Exchange (ETDEWEB)

    Al-Ghamdi, Haifa S.; Mahmoud, Waleed E., E-mail: w_e_mahmoud@yahoo.com

    2014-01-15

    Assembly is an elegant and effective bottom-up approach to prepare arrays of nanoparticles from nobel metals. Noble metal nanoparticles are perfect building blocks because they can be prepared with an adequate functionalization to allow their assembly and with controlled sizes. Herein, we report a novel recipe for the synthesis of self-assembled silver nanoparticles with tunable optical properties and sizes. The synthetic route followed here based on the covalent binding among silver nanoparticles by means of poly vinyl alcohol for the first time. The size of silver nanoparticle is governed by varying the amount of sodium borohydride. The as-synthesized nanoparticles were characterized by transmission electron microscopy, x-ray diffraction, energy dispersive x-ray spectroscopy, selected area electron diffraction and UV–vis spectroscopy. Results depicted that self-assembly of mono-dispersed silver nanoparticles with different sizes have been achieved. The silver nanostructure has a single crystalline faced centered cubic structure with growth orientation along (1 1 1) facet. These nanoparticles exhibited localized surface plasmon resonance at 403 nm. The luminescence peaks were red-sifted from violet to green due to the increase of the particle sizes. -- Highlights: • Self-assembled silver nanoparticles based PVA were synthesized. • NaBH{sub 4} amount was found particle size dependent. • Silver nanoparticles strongly affected the surface plasmon resonance. • Highly symmetric luminescence emission band narrow width is obtained. • Dark field image showed a tunable color change from violet to green.

  8. Bridgman growth and luminescence properties of CdMoO4 single crystal

    Science.gov (United States)

    Jiang, Linwen; Chen, Peng; Wang, Zhenhai; Chen, Yaping; Chen, Hongbing; Xue, Mingxuan; Zhang, Yunlong; Xu, Zizong

    2018-04-01

    CdMoO4 single crystal was grown successfully by vertical Bridgman method. The as-grown CdMoO4 crystal presents blue-green color due to the existence of oxygen vacancies, while the color will become light even disappeared by annealing in air atmosphere as a result of oxygen introduction. The transmissivity of unannealed and annealed CdMoO4 crystals reached 60% and 78%, respectively. The photoluminescence peak of annealed CdMoO4 is located at 535 nm, and the emission intensity is obviously higher than that of unannealed sample, indicating that the annealing is favorable to improve the photoluminescence intensity. The X-ray excited luminescence of unannealed CdMoO4 crystal is very weak with low signal-noise ratio due to the strong self-absorption phenomena in crystal. For annealed crystal, the X-ray excited luminescence peak is located around 525 nm. The peak deviates about 10 nm wavelength from the peak of photoluminescence spectra due to the much deeper X-ray penetration.

  9. Synthesis of self-assembly plasmonic silver nanoparticles with tunable luminescence color

    International Nuclear Information System (INIS)

    Al-Ghamdi, Haifa S.; Mahmoud, Waleed E.

    2014-01-01

    Assembly is an elegant and effective bottom-up approach to prepare arrays of nanoparticles from nobel metals. Noble metal nanoparticles are perfect building blocks because they can be prepared with an adequate functionalization to allow their assembly and with controlled sizes. Herein, we report a novel recipe for the synthesis of self-assembled silver nanoparticles with tunable optical properties and sizes. The synthetic route followed here based on the covalent binding among silver nanoparticles by means of poly vinyl alcohol for the first time. The size of silver nanoparticle is governed by varying the amount of sodium borohydride. The as-synthesized nanoparticles were characterized by transmission electron microscopy, x-ray diffraction, energy dispersive x-ray spectroscopy, selected area electron diffraction and UV–vis spectroscopy. Results depicted that self-assembly of mono-dispersed silver nanoparticles with different sizes have been achieved. The silver nanostructure has a single crystalline faced centered cubic structure with growth orientation along (1 1 1) facet. These nanoparticles exhibited localized surface plasmon resonance at 403 nm. The luminescence peaks were red-sifted from violet to green due to the increase of the particle sizes. -- Highlights: • Self-assembled silver nanoparticles based PVA were synthesized. • NaBH 4 amount was found particle size dependent. • Silver nanoparticles strongly affected the surface plasmon resonance. • Highly symmetric luminescence emission band narrow width is obtained. • Dark field image showed a tunable color change from violet to green

  10. Self-assemble nanoparticles based on polypeptides containing C-terminal luminescent Pt-cysteine complex

    Science.gov (United States)

    Vlakh, E. G.; Grachova, E. V.; Zhukovsky, D. D.; Hubina, A. V.; Mikhailova, A. S.; Shakirova, J. R.; Sharoyko, V. V.; Tunik, S. P.; Tennikova, T. B.

    2017-02-01

    The growing attention to the luminescent nanocarriers is strongly stimulated by their potential application as drug delivery systems and by the necessity to monitor their distribution in cells and tissues. In this communication we report on the synthesis of amphiphilic polypeptides bearing C-terminal phosphorescent label together with preparation of nanoparticles using the polypeptides obtained. The approach suggested is based on a unique and highly technological process where the new phosphorescent Pt-cysteine complex serves as initiator of the ring-opening polymerization of α-amino acid N-carboxyanhydrides to obtain the polypeptides bearing intact the platinum chromophore covalently bound to the polymer chain. It was established that the luminescent label retains unchanged its emission characteristics not only in the polypeptides but also in more complicated nanoaggregates such as the polymer derived amphiphilic block-copolymers and self-assembled nanoparticles. The phosphorescent nanoparticles display no cytotoxicity and hemolytic activity in the tested range of concentrations and easily internalize into living cells that makes possible in vivo cell visualization, including prospective application in time resolved imaging and drug delivery monitoring.

  11. Fabrication and luminescent properties of highly transparent Er3Al5O12 ceramics

    Science.gov (United States)

    Hu, Song; Qin, Xianpeng; Liu, Xiaoxia; Zhou, Guohong; Lu, Chunhua; Wang, Shiwei; Xu, Zhongzi

    2017-09-01

    Highly transparent Er3Al5O12 (ErAG) ceramic was fabricated by a solid-state reactive sintering method under vacuum. The optical property, microstructure and up-conversion luminescence of the ErAG ceramic were investigated. For the 3 mm thick sample, the in-line transmittance at the wavelength of 3000 nm and 425 nm were about 84% and 81%, respectively, which was very close to the theoretical transmittance of the Er3Al5O12 single crystal. Micrograph of the ErAG transparent ceramic exhibited a pore-free structure and the density of the ceramic was measured to be 6.38 g/cm3. Average grain size of the ceramic was about 9 μm. When pumped by a 980 nm laser diodes (LD), strong green and red emission in the ErAG ceramic was observed from the photoluminescence (PL) spectrum. The luminescent properties of the ceramic under the excitation of LD with various pumping power were investigated.

  12. Luminescent Rare-earth-based Nanoparticles: A Summarized Overview of their Synthesis, Functionalization, and Applications

    OpenAIRE

    Escudero A.; Carrillo-Carrión C.; Zyuzin M.V.; Parak W.J.

    2016-01-01

    Rare-earth-based nanoparticles are currently attracting wide research interest in material science, physics, chemistry, medicine, and biology due to their optical properties, their stability, and novel applications. We present in this review a summarized overview of the general and recent developments in their synthesis and functionalization. Their luminescent properties are also discussed, including the latest advances in the enhancement of their emission luminescence. Some of their more rel...

  13. HFsub(1-x)2Rsub(x) 3P2O11 luminescent material

    International Nuclear Information System (INIS)

    Chenot, C.F.; Mathers, J.E.; Shaffer, F.N.

    1980-01-01

    A new compound corresponding to an oxide composition of 3:1 (HFsub(1-x)Zrsub(x))O 2 :P 2 O 5 . and having the empircal formula (HFsub(1-x)Zrsub(x)) 3 P 2 O 11 . where x is in the range of about 0 to 0.5. is an effective luminescent material for use in x-ray intensifying screens, and also an effective luminescent material host for Eusup(+2) blue emissions. (auth)

  14. Elevated-temperature luminescence measurements to improve spatial resolution

    Science.gov (United States)

    Pluska, Mariusz; Czerwinski, Andrzej

    2018-01-01

    Various branches of applied physics use luminescence based methods to investigate light-emitting specimens with high spatial resolution. A key problem is that luminescence signals lack all the advantages of high locality (i.e. of high spatial resolution) when structures with strong built-in electric field are measured. Such fields exist intentionally in most photonic structures, and occur unintentionally in many other materials. In this case, as a result of beam-induced current generation and its outflow, information that indicates irregularities, nonuniformities and inhomogeneities, such as defects, is lost. We show that to avoid nonlocality and enable truly local luminescence measurements, an elevated measurement temperature as high as 350 K (or even higher) is, perhaps surprisingly, advantageous. This is in contrast to a widely used approach, where cryogenic temperatures, or at least room temperature, are recommended. The elevated temperature of a specimen, together with the current outflow being limited by focused ion beam (FIB) milling, is shown to improve the spatial resolution of luminescence measurements greatly. All conclusions drawn using the example of cathodoluminescence are useful for other luminescence techniques.

  15. Cu+ luminescence in Na2Sr2Al2PO4Cl9 halophosphate phosphor

    International Nuclear Information System (INIS)

    Yerpude, Vrushali; Dhoble, S.J.; Ghormare, K.B.

    2016-01-01

    This article reports the luminescence of copper doped halophosphate Na 2 Sr 2 Al 2 PO 4 Cl 9 . The phosphor was synthesized by wet chemical method by varying Cu concentrations as 0.02, 0.05, 0.1, 0.2 and 0.5 mole %.The material was further dried in the oven at 80 °C with subsequent quenching at 200°C. Photoluminescence (PL) properties were studied with Shimadzu RF-5301 PC Spectroflurophotometer. PL excitation spectra of monitored at 439 nm emission wavelength, shows a prominent peak around 381 nm from the ground state electronic configuration 3d 10 .The PL emission spectra of the phosphor monitored at 381 nm excitation wavelength in the blue region shows a broadband band around 412 nm with a shoulder peak at 440 nm, corresponding to the 3d 10 ↔ 3d 9 4s transitions of copper, which are strictly forbidden for the free ion but become partially allowed in crystals or glasses by coupling with lattice vibrations of odd parity resulting in broad excitation and emission bands. The luminescence intensity is found to increase progressively with the doping concentrations of activator and the maximum intensity is observed for 0.1 mole %. The PL spectra is found to be the same for all concentrations with difference only in the intensity. The excited states energies and the Stokes shift are reported to be very sensitive to the size and the symmetry of the copper site, leading to strong modulations of the spectral distribution, depending on the nature of the material. (author)

  16. Influence of the ytterbium doping technique on the luminescent properties of ZnSe single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Radevici, Ivan, E-mail: ivarad@utu.fi [Wihuri Physical Laboratory, Department of Physics and Astronomy, University of Turku, FI-20014 Turku (Finland); Faculty of Physics and Engineering, Moldova State University, 60 A. Mateevici str., MD-2009 Chisinau, Republic of Moldova (Moldova, Republic of); Sushkevich, Konstantin [Faculty of Physics and Engineering, Moldova State University, 60 A. Mateevici str., MD-2009 Chisinau, Republic of Moldova (Moldova, Republic of); Huhtinen, Hannu [Wihuri Physical Laboratory, Department of Physics and Astronomy, University of Turku, FI-20014 Turku (Finland); Nedeoglo, Dmitrii [Faculty of Physics and Engineering, Moldova State University, 60 A. Mateevici str., MD-2009 Chisinau, Republic of Moldova (Moldova, Republic of); Paturi, Petriina [Wihuri Physical Laboratory, Department of Physics and Astronomy, University of Turku, FI-20014 Turku (Finland)

    2015-02-15

    Luminescent properties of the ytterbium doped zinc selenide crystals with 0.00–8.00 at % concentrations of the Yb impurity within the temperature interval from 6 K to 300 K were studied. Ytterbium doping was performed within three technological processes: during the growth by chemical vapor transport method and by thermal diffusion from the Bi+Yb or Zn+Yb melt. The influence of ytterbium impurity concentration on spectral position and intensity of the various photoluminescent bands in ZnSe emission spectra in visible and infrared range is analyzed. A tendency of ytterbium ions to form associates with background defects was demonstrated. A strong dependence between ytterbium influence on the zinc selenide emission spectra and concentration of selenium vacancies was shown. - Highlights: • Co-doping of ZnSe crystals with Yb and Bi or I impurities was studied. • Influence of Yb concentration on ZnSe emission spectra in visible and infrared range was analyzed. • Tendency of Yb to form associates with background defects was discussed. • Impact of V{sub Se} on formation of Yb-based emission centers was demonstrated.

  17. The effects of binding type on luminescence LED phosphor based on GGG/Ce3+

    Science.gov (United States)

    Mikhailov, M. M.; Neshchimenko, V. V.; Shavlyuk, V. V.

    2014-12-01

    Luminescence and reflectance spectra of coatings based on gadolinium gallium garnet doped by cerium (GGG/Ce3+) with silicone resin or potassium liquid glass compound were analyzed depending on concentration. It was established that the maximum emissions of the coatings at 75 wt.% compound concentration have luminescence band at 570 nm and absorption band at 470 nm. Both bands were detected by absorption or emission of cerium ions in gadolinium gallium garnet. Ce3+ ion transition into Ce4+ ion was observed upon quantum absorption, and the reverse transition was observed upon quantum emission.

  18. Na-rich feldspar as a luminescence dosimeter in infrared stimulated luminescence (IRSL) dating

    DEFF Research Database (Denmark)

    Sohbati, Reza; Murray, Andrew; Jain, Mayank

    2013-01-01

    for measurement. This latter problem does not apply to Na-rich feldspar because of the absence of internal radioactivity.The potential application of Na-rich feldspar as a luminescence dosimeter for the IRSL dating of rock surfaces is investigated using a variety of sediment samples from different geological......, there is no detectable correlation between fading rates and the measured De values. The residual doses measured from the laboratory-bleached samples and a modern analogue suggest that the IR50 signals in both blue and yellow emissions bleach to the same degree, as do the corresponding pIRIR290 signals...

  19. Reflection measurements for luminescent powders

    Science.gov (United States)

    Kroon, R. E.

    2018-04-01

    Luminescent materials are useful in applications varying from lighting and display technologies to document security features and medical research, amongst many others. Measurement of the excitation range is an important consideration, and absorption bands are often determined from a decrease in the measured diffuse reflectance of the material using a ultraviolet-visible (UV-vis) spectrophotometer with an integrating sphere. Such a system may provide questionable results when used to measure the reflectance of a luminescence material, which is demonstrated for a Tb doped silica phosphor, because the system cannot differentiate between the reflected light and luminescence. It is shown that more reliable results are achieved for this phosphor by measuring the reflectance using a synchronous zero-offset scan in a fluorescence spectrometer equipped with an integrating sphere. This method is therefore recommended instead of traditional reflectance measurements using a UV-vis spectrophotometer for luminescent powders.

  20. Co-Dopant Influence on the Persistent Luminescence of BaAl{sub 2}O{sub 4}:Eu{sup 2+},R{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, Lucas C.V., E-mail: lucascvr@iq.usp.br [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Universidade de São Paulo, Instituto de Química, Av. Prof. Lineu Prestes 748, 05508-000 São Paulo-SP (Brazil); Hölsä, Jorma [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Universidade de São Paulo, Instituto de Química, Av. Prof. Lineu Prestes 748, 05508-000 São Paulo-SP (Brazil); Turku University Centre for Materials and Surfaces (MatSurf), Turku (Finland); Carvalho, José M.; Pedroso, Cássio C.S. [Universidade de São Paulo, Instituto de Química, Av. Prof. Lineu Prestes 748, 05508-000 São Paulo-SP (Brazil); Lastusaari, Mika [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Turku University Centre for Materials and Surfaces (MatSurf), Turku (Finland); Felinto, Maria C.F.C. [Instituto de Pesquisas Energéticas e Nucleares, Centro de Química e Meio Ambiente, Av. Prof. Lineu Prestes 2242, 05508-000 São Paulo-SP (Brazil); Watanabe, Shigeo [Universidade de São Paulo, Instituto de Física, Rua do Matão, Travessa R 187, 05508-090 São Paulo-SP (Brazil); Brito, Hermi F. [Universidade de São Paulo, Instituto de Química, Av. Prof. Lineu Prestes 748, 05508-000 São Paulo-SP (Brazil)

    2014-04-15

    The R{sup 3+} (rare earth) co-dopants may have a surprisingly important role in persistent luminescence – enhancement of up to 1–3 orders of magnitude may be obtained in the performance of these phosphor materials – depending strongly on the R{sup 3+} ion, of course. In this work, the effects of the R{sup 3+} co-dopants in the BaAl{sub 2}O{sub 4}:Eu{sup 2+},R{sup 3+} materials were studied using mainly thermoluminescence (TL) and synchrotron radiation XANES methods. In BaAl{sub 2}O{sub 4}, the conventional and persistent luminescence both arise from the 4f{sup 7}→4f{sup 6}5d{sup 1} transition of Eu{sup 2+}, yielding blue–green emission color. The former, in the presence of humidity, turns to more bluish because of creation of an additional Eu{sup 2+} luminescence centre which is not, however, visible in persistent luminescence. The trap structure in the non-co-doped BaAl{sub 2}O{sub 4}:Eu{sup 2+} is rather complex with 4–5 TL bands above room temperature. With R{sup 3+} co-doping, this basic structure is modified though no drastic change can be observed. This underlines the fact that even very small changes in the trap depths can produce significant modifications in the persistent luminescence efficiency. It should be remembered that basically the persistent luminescence performance is controlled by the Boltzmann population law depending exponentially on both the temperature and trap depth. Some mechanisms for persistent luminescence have suggested the presence of either divalent R{sup 2+} or tetravalent R{sup IV} during the charging of the Eu{sup 2+} doped materials. The present XANES measurements on BaAl{sub 2}O{sub 4}:Eu{sup 2+},R{sup 3+} confirmed the presence of only the trivalent form of the R{sup 3+} co-dopants excluding both of these pathways. It must thus be concluded, that the energy is stored in intrinsic and extrinsic defects created by the synthesis conditions and charge compensation due to R{sup 3+} co-doping. Even though the effect of the

  1. Homeotropic alignment and Förster resonance energy transfer: The way to a brighter luminescent solar concentrator

    Energy Technology Data Exchange (ETDEWEB)

    Tummeltshammer, Clemens; Taylor, Alaric; Kenyon, Anthony J.; Papakonstantinou, Ioannis, E-mail: i.papakonstantinou@ucl.ac.uk [Department of Electronic and Electrical Engineering, University College London, London WC1E 7JE (United Kingdom)

    2014-11-07

    We investigate homeotropically aligned fluorophores and Förster resonance energy transfer (FRET) for luminescent solar concentrators using Monte-Carlo ray tracing. The homeotropic alignment strongly improves the trapping efficiency, while FRET circumvents the low absorption at homeotropic alignment by separating the absorption and emission processes. We predict that this design doped with two organic dye molecules can yield a 82.9% optical efficiency improvement compared to a single, arbitrarily oriented dye molecule. We also show that quantum dots are prime candidates for absorption/donor fluorophores due to their wide absorption band. The potentially strong re-absorption and low quantum yield of quantum dots is not a hindrance for this design.

  2. Modelling the luminescence of iridium cyclometalated complexes encapsulated in cucurbituril.

    Science.gov (United States)

    Alrawashdeh, Lubna R; Cronin, Michael P; Day, Anthony I; Wallace, Lynne; Woodward, Clifford E

    2018-01-15

    Iridium(iii) cyclometalated complexes in aqueous solution often display relatively weak luminescence. It has been shown in previous work that this emission can be significantly enhanced (by up to two orders of magnitude) by encapsulation in cucurbit[10]uril (Q[10]). Luminescence lifetime measurements suggest a dynamic self-quenching mechanism is active, possibly due to displacement of an excited guest complex via collision with an unbound complex. We devise a model for the association of a group of iridium(iii) cyclometalated complexes with Q[10]. The model parameters are then fitted to steady-state emission titration curves. The excellent agreement of experimental data with the model provides valuable mechanistic information relating to the way this class of metal complexes interact and associate with the Q[10] host.

  3. Naturally Efficient Emitters: Luminescent Organometallic Complexes Derived from Natural Products

    Science.gov (United States)

    Zhang, Wen-Hua; Young, David J.

    2013-08-01

    Naturally occurring molecules offer intricate structures and functionality that are the basis of modern medicinal chemistry, but are under-represented in materials science. Herein, we review recent literature describing the use of abundant and relatively inexpensive, natural products for the synthesis of ligands for luminescent organometallic complexes used for organic light emitting diodes (OLEDs) and related technologies. These ligands are prepared from the renewable starting materials caffeine, camphor, pinene and cinchonine and, with the exception of caffeine, impart performance improvements to the emissive metal complexes and resulting OLED devices, with emission wavelengths that span the visible spectrum from blue to red. The advantages of these biologically-derived molecules include improved solution processibility and phase homogeneity, brighter luminescence, higher quantum efficiencies and lower turn-on voltages. While nature has evolved these carbon-skeletons for specific purposes, they also offer some intriguing benefits in materials science and technology.

  4. Strong γ-ray emission from neutron unbound states populated in β-decay: Impact on (n,γ) cross-section estimates

    International Nuclear Information System (INIS)

    Tain, J. L.; Guadilla, V.; Valencia, E.; Algora, A.

    2017-01-01

    Total absorption gamma-ray spectroscopy is used to measure accurately the intensity of γ emission from neutron-unbound states populated in the β-decay of delayed-neutron emitters. From the comparison of this intensity with the intensity of neutron emission one can deduce information on the (n,γ) cross section for unstable neutron-rich nuclei of interest in r process abundance calculations. A surprisingly large γ branching was observed for a number of isotopes. Here, the results are compared with Hauser-Feshbach calculations and discussed.

  5. Development of a Novel Lysosome-Targeted Ruthenium(II) Complex for Phosphorescence/Time-Gated Luminescence Assay of Biothiols.

    Science.gov (United States)

    Gao, Quankun; Zhang, Wenzhu; Song, Bo; Zhang, Run; Guo, Weihua; Yuan, Jingli

    2017-04-18

    Considering the important roles of biothiols in lysosomes of live organisms, and unique photophysical/photochemical properties of ruthenium(II) complexes, a novel ruthenium(II) complex, Ru-2, has been developed as a molecular probe for phosphorescence and time-gated luminescence assay of biothiols in human sera, live cells, and in vivo. Ru-2 is weakly luminescent due to the effective photoinduced electron transfer (PET) from Ru(II) luminophore to electron acceptor, 2,4-dinitrobenzene-sulfonyl (DNBS). In the presence of biothiols, such as glutathione (GSH), cysteine (Cys), and homocysteine (Hcy), the emission of Ru-2 solution was switched ON, as a result of the cleavage of quencher to form the product, Ru-1. Ru-2 showed high selectivity and sensitivity for the detection of biothiols under physiological conditions, with detection limits of 62 nM, 146 nM, and 115 nM for GSH, Cys, and Hcy, respectively. The emission lifetimes of Ru-1 and Ru-2 were measured to be 405 and 474 ns, respectively, which enabled them to be used for the background-free time-gated luminescence detection even in the presence of strongly fluorescent dye, rhodamine B. On the basis of this mode, the quantification of biothiols in human serum samples was achieved without interference of background autofluorescence. A morpholine moiety was introduced into the complex to ensure Ru-2 molecules to be driven into lysosomes of live cells. Ru-2 showed low cytotoxicity and excellent membrane permeability toward live cells. Using Ru-2 as an imaging agent, visualizations of biothiols in lysosomes of live cells and in Daphnia magna were successfully demonstrated. The results suggested the potential of Ru-2 for the biomedical diagnosis of biothiol-related human diseases.

  6. Up- and Downconversion Luminescence Properties of Nd3+ Ions Doped in Bi2O3–BaO–B2O3 Glass System

    Directory of Open Access Journals (Sweden)

    R. Ruamnikhom

    2014-01-01

    Full Text Available Physical, optical, and luminescence properties of Nd3+ ions in bismuth barium borate glass system were studied. The glasses prepared by a melt quenching method were doped at various Nd2O3 concentrations in compositions (40-xB2O3 : 40Bi2O3 : 20BaO : xNd2O3 (where x = 0.00, 0.50, 1.00, 1.50, 2.00, and 2.50 in mol%. Luminescence properties of the glasses were studied under two excitations of 585 and 750 nm for downconversion. From both excitations, the results show emission bands in NIR region corresponding to the transitions between 4F3/2 → 4I9/2 (900 nm, 4F3/2 → 4I11/2 (1,060 nm, and 4F3/2 → 4I13/2 (1,345 nm. The luminescence intensity obtained with 585 nm excitation was stronger than 750 nm, with the strongest NIR emission at 1,060 nm. The upconversion emission spectrum exhibits strong fluorescence bands in the UV region at 394 nm (λex=591 nm. The processes are associated with excited state absorption (ESA from 4F3/2 level to 4D3/2 level and it is the radiative decay from the 4D3/2 to ground levels (4D3/2 → 4I13/2 which are responsible for the emission at 394 nm.

  7. Sexithiophenes as efficient luminescence quenchers of quantum dots

    Directory of Open Access Journals (Sweden)

    Christopher R. Mason

    2011-12-01

    Full Text Available Sexithiophenes 1a and 1b, in which a 4-(dimethylaminophenyl unit is incorporated as an end-capping group, were synthesised and characterised by cyclic voltammetry, absorption spectroscopy and UV–vis spectroelectrochemistry. Additionally, their ability to function as effective luminescence quenchers for quantum dot emission was studied by photoluminescence spectroscopy and compared with the performance of alkyl end-capped sexithiophenes 2a and 2b.

  8. Luminescence properties of piezoelectric single crystals with langasite structure

    International Nuclear Information System (INIS)

    Itoh, Minoru; Takagi, Shinya; Kitaura, Mamoru; Fujita, Masami; Endo, Naoyuki

    2007-01-01

    Luminescence properties of single crystals of langasite (LGS), langataite (LGT), and langanite (LGN) are investigated at 5 K by using synchrotron radiation as an exciting light source. Two emission bands are observed at 420 and 500 nm in LGS, at 410 and 460 nm in LGT, and at 500 and 535 nm in LGN. The origin of these bands is discussed by reference to the electronic structure of LGS

  9. Luminescent nanoparticles and their applications in the life sciences

    Science.gov (United States)

    Sreenivasan, Varun K. A.; Zvyagin, Andrei V.; Goldys, Ewa M.

    2013-05-01

    Nanoparticles have recently emerged as an important group of materials used in numerous disciplines within the life sciences, ranging from basic biophysical research to clinical therapeutics. Luminescent nanoparticles make excellent optical bioprobes significantly extending the capabilities of alternative fluorophores such as organic dyes and genetically engineered fluorescent proteins. Their advantages include excellent photostability, tunable and narrow spectra, controllable size, resilience to environmental conditions such as pH and temperature, combined with a large surface for anchoring targeting biomolecules. Some types of nanoparticles provide enhanced detection contrast due to their long emission lifetime and/or luminescence wavelength blue-shift (anti-Stokes) due to energy upconversion. This topical review focuses on four key types of luminescent nanoparticles whose emission is governed by different photophysics. We discuss the origin and characteristics of optical absorption and emission in these nanoparticles and give a brief account of synthesis and surface modification procedures. We also introduce some of their applications with opportunities for further development, which could be appreciated by the physics-trained readership.

  10. Implementation of a neural network for multispectral luminescence imaging of lake pigment paints.

    Science.gov (United States)

    Chane, Camille Simon; Thoury, Mathieu; Tournié, Aurélie; Echard, Jean-Philippe

    2015-04-01

    Luminescence multispectral imaging is a developing and promising technique in the fields of conservation science and cultural heritage studies. In this article, we present a new methodology for recording the spatially resolved luminescence properties of objects. This methodology relies on the development of a lab-made multispectral camera setup optimized to collect low-yield luminescence images. In addition to a classic data preprocessing procedure to reduce noise on the data, we present an innovative method, based on a neural network algorithm, that allows us to obtain radiometrically calibrated luminescence spectra with increased spectral resolution from the low-spectral resolution acquisitions. After preliminary corrections, a neural network is trained using the 15-band multispectral luminescence acquisitions and corresponding spot spectroscopy luminescence data. This neural network is then used to retrieve a megapixel multispectral cube between 460 and 710 nm with a 5 nm resolution from a low-spectral-resolution multispectral acquisition. The resulting data are independent from the detection chain of the imaging system (filter transmittance, spectral sensitivity of the lens and optics, etc.). As a result, the image cube provides radiometrically calibrated emission spectra with increased spectral resolution. For each pixel, we can thus retrieve a spectrum comparable to those obtained with conventional luminescence spectroscopy. We apply this method to a panel of lake pigment paints and discuss the pertinence and perspectives of this new approach.

  11. Study of Polymeric Luminescent Blend (PC/PMMA) Doped with Europium Complex under Gamma-Iradiation

    International Nuclear Information System (INIS)

    Parra, D. F.

    2006-01-01

    Spectroscopic properties of blends formed by bisphenol-A polycarbonate (PC) and poly(methyl methacrylate) (PMMA) doped with europium in organic complex were studied. Polymeric luminescent blends are potential materials for many applications; however, little information has been reported concerning the stability under thermal and radiation conditions. Luminescent films were synthesized from europium thenoyltrifluoroacetonate at different concentrations doped in PC/PMMA blends. Films produced of the luminescent polymer blend were irradiated in a 60 C o source. Their luminescent properties, in the solid state, as well as, the thermal oxidative resistance after gamma irradiation was investigated. These systems were characterized by elemental analysis, thermogravimetry (TGA), differential scanning calorimetry (DSC) and infrared spectroscopy (FTIR). Based on TGA data, the thermal stability of PC/PMMA:(tta)3 system is higher than the polymer blend. The DSC results indicated that those new systems are chemically stables. The emission spectra of the Eu 3 +-tta complex doped in the PC/PMMA recorded at 298 and 77 K exhibited the characteristic bands arising from the 5 D 0 →7 F J transitions (J = 0-6). The luminescence intensity decreases with increasing of precursor concentration in the doped polymer obtained by chemical reaction. This result is different from that of samples obtained by physical method in melting doping. The blend was irradiated under ionizing radiation of 60 C o source. After irradiation of the luminescent films the physical properties of luminescence, thermal and oxidative stability were evaluated.(Fapesp and Cnpq financial support)

  12. Structural and luminescence properties of Mn{sup 2+} ions doped calcium zinc borophosphate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Wan, Ming Hua, E-mail: wanminghua819@gmail.com [Phosphor Research Group, Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Wong, Poh Sum, E-mail: pohsumwong@gmail.com [Phosphor Research Group, Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Hussin, Rosli, E-mail: roslihussin@utm.my [Phosphor Research Group, Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Lintang, Hendrik O., E-mail: hendrik@ibnusina.utm.my [Catalytic Science and Technology (CST) Research Group, Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Endud, Salasiah, E-mail: salasiah@kimia.fs.utm.my [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia)

    2014-05-15

    Highlights: • FT-IR revealed that the network structures are from borate and phosphate network. • The PL spectrum exhibits a green emission band at 582 nm ({sup 4}T{sub 1g} → {sup 6}A{sub 1g}). • As the concentration of Mn{sup 2+} ions is increased, the emission band had been red shifted. • These glasses are found to have potential applications as luminescent optical materials. - Abstract: Calcium zinc borophosphate glasses (CaZnBP) doped with various concentrations of Mn{sup 2+} ions and borate and phosphate as variable were prepared using conventional melt quenching technique. The structure of obtained glasses were examined by means of use: X-ray diffraction (XRD) and fourier transform infrared (FT-IR). XRD analysis confirmed amorphous nature of glass samples. The FT-IR spectra reveals the presence of both borate and phosphate vibrational modes in the prepared glasses. The doping of Mn{sup 2+} ions (2–10 mol%) shows no significant changes in the main IR vibrational bands. Optical properties were studied by measuring the near infrared photoluminescence (PL) spectra. CaZnBP glasses exhibited intense green emission peak (582 nm) (tetrahedral symmetry), which is assigned to a transition from the upper {sup 4}T{sub 1g} → {sup 6}A{sub 1g} ground state of Mn{sup 2+} ions. As the concentration of Mn{sup 2+} ions increases, the emission band increases from 582 nm to 650 nm and exhibited a red light emission (octahedral symmetry). The decay curves of {sup 4}T{sub 1g} level were examined for all concentrations and the measured lifetimes are found to depend strongly on Mn{sup 2+} concentrations. From the emission characteristic parameters of {sup 6}A{sub 1g} (S) level, it shows that the CaZnBP glasses could have potential applications as luminescent optical materials, visible lasers and fluorescent display devices.

  13. Goldenphilicity: Luminescent gold compounds

    International Nuclear Information System (INIS)

    Sansores, L.E.

    2002-01-01

    In the solids and molecules different types of bonds are presented depending on the involved atoms, covalent bonds are common among elements of open shell, where more bond orbitals are filled than anti bond orbitals. It is expected that ionic bonds among closed shell atoms which have charges of opposite sign. Bonds type Van der Waals are presented among molecules which have a bipolar moment. It would not be expected bonds among zero charge species, or more generally with the same nominal charge and in any case the attractive forces would be very small. In fact it is expected that two metallic cations to be repelled each other. There recently is evidence that in organic or organometallic compounds could exist attractive interactions between two cations of the d 8 -d 10 -s 2 families. These bonds are weak but stronger than those of Van der Waals. They are compared with the hydrogen bonds. In this work it was reviewed some examples in which the goldenphilicity plays an important role in the luminescence that the gold complexes present. Examples of mono, bi and trinuclear and the structures that these organometallic compounds could take are examined. (Author)

  14. Powerful visible (530???770 nm) luminescence in Yb,Ho:GGG with IR diode pumping.

    Science.gov (United States)

    Kir'yanov, Alexander; Aboites, V; Belovolov, A; Timoshechkin, M; Belovolov, M; Damzen, M; Minassian, A

    2002-08-12

    Powerful visible luminescence in a Gadolinium Gallium Garnet (GGG) crystal, co-activated with Yb3+ (~15 at.%) and Ho3+ (~0.1 at.%) ions, is investigated under CW laser diode pumping (lambda = 938 and 976 nm). The main visible emission band is observed in the green with its peak at lambda ~540 nm) and measured to be about 10% with respect to Yb3+ IR luminescence (lambda ~1000 nm). Red (lambda ~650 nm) and near-IR (lambda ~755 nm) emission bands are also observed but are weaker (about 3-5%). Analysis of the crystal absorption and luminescence spectra allows one to conclude that Yb3+ - Ho3+ stepwise up-conversion is the mechanism explaining the phenomenon. Ho3+ ions embedded in the crystal in small concentration are shown to form an effective reservoir for energy transferred from the excited Yb3+ subsystem and to be an efficient source of the visible emission.

  15. Paleodosimetrical properties of sodium alkali feldspars and problems of luminescence dating of sediments

    International Nuclear Information System (INIS)

    Huett, Galina; Jaek, Ivar

    1996-01-01

    Emission spectra of natural alkali feldspars extracted from sediments are studied using a CCD-camera based high sensitivity spectrometer. Applying a semiconductor laser (860± 1 nm), two dominant emission bands, blue (410 nm) and orange (570 nm), are revealed in infrared optically stimulated luminescence (IROSL) spectra for the most of the sediments from Scandinavian sections. Luminescence and dosimetric al properties of the hole traps, the induced orange emission band typical of sodium alkali feldspars are studied. As a result, high light bleach ability but low stability of the dosimetric al information lit sodium alkali feldspars are established. Problems of luminescence dating of sediments based on the mixture of potassium-sodium alkali feldspars are discussed. (author)

  16. Application of Quantum Dot nanocrystal in Luminescent solar concentrators

    Science.gov (United States)

    Bakhoda, Shokoufeh; Khalaji Assadi, Morteza; Ahmadi Kandjani, Sohrab; Kayiem, Hussain H. Al; Hussain Bhat, Aamir

    2018-03-01

    The basic design of luminescent solar concentrator is a transparent plate doped with an appropriate luminescent material (organic dyes, quantum dots), which is able to absorb sunlight (direct and diffuse), and then guides photons produced by photoluminescence to its narrow edges where they are converted by photovoltaic cells. Unfortunately, LSCs have suffered from numerous efficiency losses. Therefore, new luminescent species and novel approaches are needed for its practical application. This paper deals with investigation of nonhazardous, environmental friendly luminescent species include CuInS2/ZnS core/shell QDs. The CuInS2/ZnS QDs possess advantages of Stocks shift as large as more than 130 nm and high photoluminescence quantum yield of 80%. The paper presents the effect of large stock shift CuInS2/ZnS QDs on reducing the reabsorption losses in LSC by using experimental investigation. The LSC sheets were fabricated by dispersing CuInS2/ZnS QDs particles in a polymethylmethacrylate waveguide. A series of LSCs (dimension 4.0 cm × 3.0 cm × 0.3cm) with different CuInS2/ZnS QDs particles concentration (0.015 and 0.03 wt.%) were fabricated and their optical properties (absorptions/emissions) were characterized. The results show that the CuInS2/ZnS QDs-LSC provides a promising way for the reduction of reabsorption losses in LSCs.

  17. Dosimetry based on thermally and optically stimulated luminescence

    International Nuclear Information System (INIS)

    Agersnap Larsen, Niels

    1999-01-01

    Thermally Stimulated Luminescence (TL) and Optically Stimulated Luminescence (OSL) properties of quartz and α-Al 2 O 3 have been investigated. Anneling-induced OSL and TL sensitivity changes in quartz has been investigated by experiments and modelling. This study does not support a pre-dose effect to account for the observed annealing-induced sensitivity change. The experimental data indicates a more simple mechanism that involves alteration of the concentration of the defect centers. Results from modelling of removal or creation of defect centers comparing well with experimentally obtained data. Thermal quenching of luminescence for the main emission center, the F-center, in α-Al 2 O 3 :C has been investigated by analysing TL curves obtained at different heating rates. The thermal quenching dependence of luminescence is found to follow the classical Mott-Seitz expression. Basic investigations of OSL properties of αAl 2 O 3 :C, including: the thermal depth of the OSL traps, the temperature dependence of OSL, and the OSL stimulation spectra. Simultaneous measurements of TL and thermally stimulated conductivity (TSC) are presented for γ-irradiated αAl 2 O 3 :C. Activation energy analysis of the data reveals a superposition of several first-order TL and TSC peaks caused by release of charge carriers from a distribution of trapping states. Furthermore a description of an experimental method developed to determine the sign of the thermally released charge carriers has been presented. (au)

  18. Luminescence properties of novel red-emitting phosphor InNb1-xPxO4:Eu3+ for white light emitting-diodes

    Directory of Open Access Journals (Sweden)

    Tang An

    2015-06-01

    Full Text Available InNb1-xPxO4:Eu3+ red phosphors were synthesized by solid-state reaction and their luminescence properties were also studied through photoluminescence spectra. The excitation and emission spectra make it clear that the as-prepared phosphors can be effectively excited by near-ultraviolet (UV 394 nm light and blue 466 nm light to emit strong red light located at 612 nm, due to the Eu3+ transition of 5D0 → 7F2. The luminescence intensity is dependent on phosphorus content, and it achieves the maximum at x = 0.4. Excessive phosphorus in the phosphors can result in reduction of luminescence intensity owing to concentration quenching.With the increasing content of phosphorus, the phosphors are prone to emit pure red light. This shows that the InNb1.6P0.4O4:0.04Eu3+ phosphor may be a potential candidate as a red component for white light emitting-diodes.

  19. Simultaneous morphology manipulation and upconversion luminescence enhancement of β-NaYF4:Yb3+/Er3+ microcrystals by simply tuning the KF dosage.

    Science.gov (United States)

    Ding, Mingye; Chen, Daqin; Yin, Shilong; Ji, Zhenguo; Zhong, Jiasong; Ni, Yaru; Lu, Chunhua; Xu, Zhongzi

    2015-08-03

    A strategy has been adopted for simultaneous morphology manipulation and upconversion luminescence enhancement of β-NaYF4:Yb(3+)/Er(3+) microcrystals by simply tuning the KF dosage. X-ray power diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and photoluminescence spectra (PL) were used to characterize the samples. The influence of molar ratio of KF to Y(3+) on the crystal phase and morphology has been systematically investigated and discussed. It is found that the molar ratio of KF to Y(3+) can strongly control the morphology of the as-synthesized β-NaYF4 samples because of the different capping effect of F(-) ions on the different crystal faces. The possible formation mechanism has been proposed on the basis of a series of time-dependent experiments. More importantly, the upconversion luminescence of β-NaYF4:Yb(3+)/Er(3+) was greatly enhanced by increasing the molar ratio of KF to RE(3+) (RE = Y, Yb, Er), which is attributed to the distortion of local crystal field symmetry around lanthanide ions through K(+) ions doping. This synthetic methodology is expected to provide a new strategy for simultaneous morphology control and remarkable upconversion luminescence enhancement of yttrium fluorides, which may be applicable for other rare earth fluorides.

  20. Biosensing with Luminescent Semiconductor Quantum Dots

    Directory of Open Access Journals (Sweden)

    Hedi Mattoussi

    2006-08-01

    Full Text Available Luminescent semiconductor nanocrystals or quantum dots (QDs are a recentlydeveloped class of nanomaterial whose unique photophysical properties are helping tocreate a new generation of robust fluorescent biosensors. QD properties of interest forbiosensing include high quantum yields, broad absorption spectra coupled to narrow sizetunablephotoluminescent emissions and exceptional resistance to both photobleaching andchemical degradation. In this review, we examine the progress in adapting QDs for severalpredominantly in vitro biosensing applications including use in immunoassays, asgeneralized probes, in nucleic acid detection and fluorescence resonance energy transfer(FRET - based sensing. We also describe several important considerations when workingwith QDs mainly centered on the choice of material(s and appropriate strategies forattaching biomolecules to the QDs.

  1. Optical luminescence spectroscopy as a probe of the surface mineralogy of Mars

    Science.gov (United States)

    Treiman, A. H.

    1992-01-01

    Optical luminescence (OpL) spectroscopy is an attractive use of a visible-near-IR spectrometer on a Mars lander because mineral products of atmosphere-surface interactions on Mars will probably have characteristic OpL spectra. Optical luminescence spectra would be taken at night, when a spectrometer might otherwise sit idle. Also needed would be a source of exciting radiation, which could be shared with other experiments. Optical luminescence is emission of nonthermal optical photons (near-UV through near-IR) as a response to energy input. On absorption of energy, an atom (or ion) will enter an excited state. The favored decay of many such excited states involving valence-band electrons is emission of an optical photon. Optical luminescence spectra can be useful in determining mineralogy and mineral composition. Optical luminescence in crystals can arise from essential elements (or ions), trace-element substituents (activators), or defects. Common activators in salts of alkali and alkaline earth elements include Mn(2+)(VI), other transition metals, the rare earths, and the actinides. Trace substituents of other species can enhance or quench OpL (e.g., Pb(2+) vs. Fe(3+)). Optical luminescence can also arise from defects in crystal structures, including those caused by radiation and shock.

  2. Superquadratic behavior of upconversion luminescence transients in rare-earth-ion doped laser crystals

    OpenAIRE

    Pollnau, Markus; Laversenne, L.; Limberger, H.G.; Bigotta, S.; Toncelli, A.; Tonelli, M.

    2004-01-01

    Inhomogeneous active-ion distributions in laser materials lead to strong deviations of upconversion versus direct luminescence transients from the quadratic law of energy-transfer upconversion. Measured luminescence decay curves in LaSc3(BO3)4:Nd3+ and GdVO4:Nd3+ confirm experimentally the predicted deviations. Differences in energy migration within the metastable level of Nd3+ are identified.

  3. Near-infrared luminescence of cadmium pigments: in situ identification and mapping in paintings.

    Science.gov (United States)

    Thoury, Mathieu; Delaney, John K; Rie, E René de la; Palmer, Michael; Morales, Kathryn; Krueger, Jay

    2011-08-01

    A comprehensive study of the luminescence properties of cadmium pigments was undertaken to determine whether these properties could be used for in situ identification and mapping of the pigments in paintings. Cadmium pigments are semiconductors that show band edge luminescence in the visible range and deep trap luminescence in the red/infrared range. Emission maxima, quantum yields, and excitation spectra from the band edge and deep trap emissions were studied for sixty commercial cadmium pigments that span the color range from yellow to red (reflectance transition 470 to 660 nm). For paints containing cadmium pigments, luminescence from deep traps was more readily observable than that from the band edge, although the yield varied widely from zero to around 4.5%. Optimal excitation for emission is found to be in the visible for both pigments in powder form and mixed with a medium. The maxima of the deep trap emission shift with the band gap energy, providing a potentially useful way to assign pigment type even when used in pigment mixtures. The usefulness of the results of the study on mockups was demonstrated by the mapping of cadmium pigments of different hues with the aid of calibrated luminescence imaging spectroscopy in a painting by Edward Steichen, entitled Study for 'Le Tournesol' (1920). Analysis of the luminescence image cube reveals at least six unique spectral components, associated with emission from white pigments, paint binder, and cadmium red and yellow pigments. The results were compared with those from X-ray fluorescence spectrometry (XRF) and fiber-optic reflection spectroscopy (FORS) and the results obtained on paint samples containing cadmium pigments. These results show that, when present, the emission from traps can be used as an analytical tool to identify cadmium pigments, to distinguish among cadmium sulfide, cadmium zinc sulfide, and cadmium sulfoselenide, and to map cadmium pigments, even in mixtures.

  4. Origin of the ``Red'' Luminescence Band in Bulk N-doped ZnO

    Science.gov (United States)

    Glaser, E. R.; Garces, N. Y.; Tarun, M. C.; McCluskey, M. D.

    2012-02-01

    Optically detected magnetic resonance (ODMR) at 24 GHz was performed on bulk ZnO crystals doped with nitrogen impurities (of high interest for p-type conductivity) to provide more details on the origin of a recently reported red/near-IR photoluminescence (PL) band.ootnotetextM.C. Tarun et al., AIP Advances 1, 022105 (2011). PL at 7K revealed strong bandedge excitonic recombination at 3.364 eV, a broad ``green'' emission band at 2.45 eV, and a broad ``red'' PL band near 1.7 eV. Two luminescence-increasing ODMR signals were found on this ``red'' emission. The first was a sharp feature with g-value of 1.957 and FWHM of 1 mT and is attributed to shallow donors based on electron spin resonance (ESR) of n-type ZnO. The second feature exhibited a g-value near 2 and a broad, asymmetric lineshape with FWHM of ˜ 10 mT. A simulation of the spectrum showed that the broad resonance could be fit as the sum of three equally spaced lines with magnetic field splitting value and relative intensities in close agreement to those observed for deep nitrogen acceptors as identified from previous ESR studies. Thus, the ODMR results strongly suggest that the ``red'' PL is due to radiative recombination involving residual shallow donors and deep nitrogen acceptor centers.

  5. f-state luminescence of lanthanide and actinide ions in solution

    Energy Technology Data Exchange (ETDEWEB)

    Beitz, J.V.

    1993-09-01

    Detailed studies of the luminescence of aquated Am{sup 3+} are presented in the context of prior lanthanide and actinide ion work. The luminescing state of aquated Am{sup 3+} is confirmed to be {sup 5}D{sub l} based on observed emission and excitation spectra. The luminescence lifetime of Am{sup 3+} in H{sub 2}O solution is (22 {plus_minus} 3) ns and (155 {plus_minus} 4) ns in D{sub 2}O solution at 295 K. Judd-Ofelt transition intensity theory qualitatively describes the observed Am{sup 3+} relative integrated fluorescence intensities. Recent luminescence studies on complexed trivalent f-element ions in solution are reviewed as to the similarities and differences between lanthanide ion 4f state and actinide ion 5f state properties.

  6. Mesoporous material grafted with luminescent molecules for the design of selective metal ion chemosensor

    International Nuclear Information System (INIS)

    Zhang Huidong; Zhang Ping; Ye Kaiqi; Sun Yinghui; Jiang Shimei; Wang Yue; Pang Wenqin

    2006-01-01

    Luminescent Schiff-base groups have been successfully grafted on the surface of mesoporous material MCM-48. The grafted Schiff-base groups were employed to prepare luminescent Schiff-base-Zn complex that was covalently bound to the MCM-48 surface. These luminescent mesoporous materials were characterized with X-ray, UV-VIS and emission spectroscopic methods. Experimental results demonstrated that MCM-48 modified with functional groups exhibited novel luminescent property. The chemosensing property of modified MCM-48 sample was investigated. It was demonstrated that the fluorescence of MCM-48 solid with Schiff-base groups could be completely quenched by Cu 2+ cation and this mesoporous material was suitable for sensing Cu 2+ cation in aqueous media

  7. Circularly Polarized Luminescence of Curium: A New Characterization of the 5f Actinide Complexes

    Science.gov (United States)

    Law, Ga-Lai; Andolina, Christopher M.; Xu, Jide; Luu, Vinh; Rutkowski, Philip X.; Muller, Gilles; Shuh, David K.; Gibson, John K.; Raymond, Kenneth N.

    2012-01-01

    A key distinction between the lanthanide (4f) and actinide (5f) transition elements is the increased role of f-orbital covalent bonding in the latter. Circularly polarized luminescence (CPL) is an uncommon but powerful spectroscopy which probes the electronic structure of chiral, luminescent complexes or molecules. While there are many examples of CPL spectra for the lanthanides, this report is the first for an actinide. Two chiral, octadentate chelating ligands based on orthoamide phenol (IAM) were used to complex curium(III). While the radioactivity kept the amount of material limited to micromole amounts, the spectra of the highly luminescent complexes showed significant emission peak-shifts between the different complexes, consistent with ligand field effects previously observed in luminescence spectra. PMID:22920726

  8. Ion beam induced luminescence from diamond using an MeV ion microprobe

    Energy Technology Data Exchange (ETDEWEB)

    Bettiol, A.A.; Jamieson, D. N.; Prawer, S.; Allen, M.G. [Melbourne Univ., Parkville, VIC (Australia). School of Physics

    1993-12-31

    Analysis of the luminescence induced by a MeV ion beam offers the potential to provide useful information about the chemical properties of atoms in crystals to complement the information provided by more traditional Ion Beam Analysis (IBA) such as Rutherford Backscattering Spectrometry (RBS), ion channeling and Particle Induced X-ray Emission (PIXE). Furthermore, the large penetration depth of the MeV ion beam offers several advantages over the relatively shallow penetration of keV electrons typically employed in cathodoluminescence. An Ion Beam Induced Luminescence (IBIL) detection system was developed for the Melbourne microprobe that allows the spatial mapping of the luminescence signal along with the signals from RBS and PIXE. Homoepitaxial diamond growth has been studied and remarkable shifts in the characteristic blue luminescence of diamond towards the green were observed in the overgrowth. This has been tentatively identified as being due to transition metal inclusions in the epitaxial layers. 8 refs., 2 refs.

  9. Exploring the effect of remote substituents and solution structure on the luminescence of three lanthanide complexes

    Energy Technology Data Exchange (ETDEWEB)

    Tropiano, Manuel; Blackburn, Octavia A.; Tilney, James A.; Hill, Leila R. [Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA (United Kingdom); Just Sørensen, Thomas, E-mail: TJS@chem.ku.dk [Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA (United Kingdom); Nano-Science Center and Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 København Ø (Denmark); Faulkner, Stephen, E-mail: stephen.faulkner@chem.ox.ac.uk [Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA (United Kingdom)

    2015-11-15

    Sensitized luminescence from trivalent lanthanide ions relies on an appropriate energy match between the sensitizer’s excited state (triplet or singlet) and the lanthanide excited state manifold, and also an efficient mechanism of energy transfer between the two. Here, the effect of remote substituents on the luminescence properties of a series of related lanthanide complexes has been investigated. The sensitized lanthanide centered emission is not invariably found to occur following excitation of all chromophores in all systems, and it is shown that only the most structurally congested of the systems investigated exhibited pronounced solvatochromism. - Highlights: • Effect of remote substituents and self-assembly on lanthanide luminescence. • Molecular structure rather than chromophore density defines lanthanide sensitization. • Kimura's and Horrocks' approach to determine lanthanide solvation is revisited. • Solvent alters sensitization pathways in multinuclear lanthanide complexes. • Increasing chromophore density may reduce lanthanide luminescence.

  10. Self absorption in luminescent solar concentrators

    NARCIS (Netherlands)

    Krumer, Z.

    2014-01-01

    Luminescent solar concentrators are photovoltaic devices made of thin transparent material, in which luminescent particles are dispersed. The incident light enters the device through its large facets and is subsequently absorbed by the luminescent particles, which re-emit it whilst changing its

  11. Luminescence study of Eu(3+) doped Li6 Y(BO3 )3 phosphor for solid-state lighting.

    Science.gov (United States)

    Yawalkar, Mrunal M; Zade, G D; Dabre, K V; Dhoble, S J

    2016-06-01

    In this study, Li6 Y1-x Eux (BO3 )3 phosphor was successfully synthesized using a modified solid-state diffusion method. The Eu(3+) ion concentration was varied at 0.05, 0.1, 0.2, 0.5 and 1 mol%. The phosphor was characterized for phase purity, morphology, luminescent properties and molecular transmission at room temperature. The XRD pattern suggests a result closely matching the standard JCPDS file (#80-0843). The emission and excitation spectra were followed to discover the luminescence traits. The excitation spectra indicate that the current phosphor can be efficiently excited at 395 nm and at 466 nm (blue light) to give emission at 595 and 614 nm due to the (5) D0  → (7) Fj transition of Eu(3+) ions. Concentration quenching was observed at 0.5 mol% Eu(3+) in the Li6 Y1-x Eux (BO3 )3 host lattice. Strong red emission with CIE chromaticity coordinates of phosphor is x = 0.63 and y = 0.36 achieved with dominant red emission at 614 nm the (5) D0  → (7)  F2 electric dipole transition of Eu(3+) ions. The novel Li6 Y1-x Eux (BO3 )3 phosphor may be a suitable red-emitting component for solid-state lighting using double-excited wavelengths, i.e. near-UV at 395 nm and blue light at 466 nm. Copyright © 2015 John Wiley & Sons, Ltd. Copyright © 2015 John Wiley & Sons, Ltd.

  12. Geometry flexibility of copper iodide clusters: variability in luminescence thermochromism.

    Science.gov (United States)

    Benito, Quentin; Goff, Xavier F Le; Nocton, Gregory; Fargues, Alexandre; Garcia, Alain; Berhault, Aurélie; Kahlal, Samia; Saillard, Jean-Yves; Martineau, Charlotte; Trébosc, Julien; Gacoin, Thierry; Boilot, Jean-Pierre; Perruchas, Sandrine

    2015-05-04

    An original copper(I) iodide cluster of novel geometry obtained by using a diphosphine ligand is reported and is formulated [Cu6I6(PPh2(CH2)3PPh2)3] (1). Interestingly, this sort of "eared cubane" cluster based on the [Cu6I6] inorganic core can be viewed as a combination of the two known [Cu4I4] units, namely, the cubane and the open-chair isomeric geometries. The synthesis, structural and photophysical characterisations, as well as theoretical study of this copper iodide along with the derived cubane (3) and open-chair (2) [Cu4I4(PPh3)4] forms, were investigated. A new polymorph of the cubane [Cu4I4(PPh3)4] cluster is indeed presented (3). The structural differences of the clusters were analyzed by solid-state nuclear magnetic resonance spectroscopy. Luminescence properties of the three clusters were studied in detail as a function of the temperature showing reversible luminescence thermochromism for 1 with an intense orange emission at room temperature. This behavior presents different feature compared to the cubane cluster and completely contrasts with the open isomer, which is almost nonemissive at room temperature. Indeed, the thermochromism of 1 differs by a concomitant increase of the two emission bands by lowering the temperature, in contrast to an equilibrium phenomenon for 3. The luminescence properties of 2 are very different by exhibiting only one single band when cooled. To rationalize the different optical properties observed, density functional theory calculations were performed for the three clusters giving straightforward explanation for the different luminescence thermochromism observed, which is attributed to different contributions of the ligands to the molecular orbitals. Comparison of 3 with its [Cu4I4(PPh3)4] cubane polymorphs highlights the sensibility of the emission properties to the cuprophilic interactions.

  13. Measurement of Anomalously Strong Emission from the 1s-9p Transition in the Spectrum of H-like Phosphorus Following Charge Exchange with Molecular Hydrogen

    Science.gov (United States)

    Leutenegger, M. A.; Beiersdorfer, P.; Brown, G. V.; Kelley, R. L.; Porter, F. S.

    2010-01-01

    We have measured K-shell x-ray spectra of highly ionized argon and phosphorus following charge exchange with molecular hydrogen at low collision energy in an electron beam ion trap using an x-ray calorimeter array with approx.6 eV resolution. We find that the emission at the high-end of the Lyman series is greater by a factor of two for phosphorus than for argon, even though the measurement was performed concurrently and the atomic numbers are similar. This does not agree with current theoretical models and deviates from the trend observed in previous measurements.

  14. Progress in Direct Dating of Tephra via Thermo- and Optically Stimulated Luminescence

    Science.gov (United States)

    Clark-Balzan, L.; Smith, V.; Preusser, F.

    2016-12-01

    Luminescence dating utilizes natural dosimeters (minerals and mineralloids) to calculate either time elapsed since crystallization or the last exposure to light or intense heat. Direct dating of volcanic materials via luminescence has been attempted for nearly fifty years with varying degrees of success: dim luminescence signals, anomalous signal loss (`fading') from volcanogenic minerals, incomplete mineral separation, and mineralogical and geochemical variability have been problematic (Fattahi and Stokes, 2003). Recent advances in measurement protocols to probe signals less prone to anomalous fading (Tsukamoto et al., 2007; 2010), and the development of equipment that allows direct imaging of luminescence-emitting grains via EMCCD cameras (Clark-Balzan and Schwenninger, 2012) offer new opportunities for tephra dating. The lack of available luminescence data on a wide variety of tephra, however, makes it difficult to predict which measurement techniques will be generally applicable given presumed high inter- and intra-sample variability. Therefore we present first results from a systematic characterization of luminescence emissions from a geochemically and geographically diverse body of tephras. Spectrometric analysis of luminescence emitted from plagioclase, glass, and quartz fractions during thermal and optical stimulation provide key data for optimization and testing of measurement protocols. We also show preliminary results of EMCCD imaging of both mineral separates and bulk tephras, emphasizing identification and characterization of mineral constituents and luminescence properties via the simultaneous measurement of many grains. EMCCD imaging allows luminescence characterization on the single grain level, thereby revealing variability between grains which cannot be measured via standard spectromectric techniques. Clark-Balzan, L., Schwenninger, J.-L., 2012, Radiation Measurements, v. 47, pp. 797-802. Fattahi, M., Stokes, S., 2003, Earth Science Reviews, v. 62

  15. Multidimensional Models of Type Ia Supernova Nebular Spectra: Strong Emission Lines from Stripped Companion Gas Rule Out Classic Single-degenerate Systems

    Science.gov (United States)

    Botyánszki, János; Kasen, Daniel; Plewa, Tomasz

    2018-01-01

    The classic single-degenerate model for the progenitors of Type Ia supernova (SN Ia) predicts that the supernova ejecta should be enriched with solar-like abundance material stripped from the companion star. Spectroscopic observations of normal SNe Ia at late times, however, have not resulted in definite detection of hydrogen. In this Letter, we study line formation in SNe Ia at nebular times using non-LTE spectral modeling. We present, for the first time, multidimensional radiative transfer calculations of SNe Ia with stripped material mixed in the ejecta core, based on hydrodynamical simulations of ejecta–companion interaction. We find that interaction models with main-sequence companions produce significant Hα emission at late times, ruling out these types of binaries being viable progenitors of SNe Ia. We also predict significant He I line emission at optical and near-infrared wavelengths for both hydrogen-rich or helium-rich material, providing an additional observational probe of stripped ejecta. We produce models with reduced stripped masses and find a more stringent mass limit of M st ≲ 1 × 10‑4 M ⊙ of stripped companion material for SN 2011fe.

  16. RE-EVALUATING WASP-12b: STRONG EMISSION AT 2.315 μm, DEEPER OCCULTATIONS, AND AN ISOTHERMAL ATMOSPHERE

    International Nuclear Information System (INIS)

    Crossfield, Ian J. M.; Barman, Travis; Hansen, Brad M. S.; Tanaka, Ichi; Kodama, Tadayuki

    2012-01-01

    We revisit the atmospheric properties of the extremely hot Jupiter WASP-12b in light of several new developments. First, we present new narrowband (2.315 μm) secondary eclipse photometry, which exhibits a planet/star flux ratio of 0.45% ± 0.06%, corresponding to a brightness temperature of 3640 ± 230 K; second, recent Spitzer/Infrared Array Camera and Hubble Space Telescope/Wide Field Camera 3 observations; and third, a recently observed star only 1'' from WASP-12, which has diluted previous observations and which we further characterize here. We correct past WASP-12b eclipse measurements for the presence of this object, and we revisit the interpretation of WASP-12b's dilution-corrected emission spectrum. The resulting planetary emission spectrum is well approximated by a blackbody, and consequently our primary conclusion is that the planet's infrared photosphere is nearly isothermal. Thus, secondary eclipse spectroscopy is relatively ill suited to constrain WASP-12b's atmospheric abundances, and transmission spectroscopy may be necessary to achieve this goal.

  17. The sensitized luminescence of manganese-activated calcite

    Science.gov (United States)

    Schulman, J.H.; Evans, L.W.; Ginther, R.J.; Murata, K.J.

    1947-01-01

    Synthetic manganese-activated calcites are shown to be practically inert to ultraviolet excitation in the range 2000-3500A, while they are luminescent under cathode-ray excitation. The incorporation of small amounts of an auxiliary impurity along with the manganese produces the strong response to ultraviolet radiation hitherto ascribed to CaCO3:Mn itself. Three such impurities have been studied: lead, thallium, and cerium. The first two induce excitation in the neighborhood of the mercury resonance line, while the cerium introduces a response principally to longer wave ultraviolet. The strong response to 2537A excitation shown by some natural calcites is likewise found to be due to the presence of lead along with the manganese, rather than to the manganese alone. The data do not warrant ascribing the longer wave-length ultraviolet-excited luminescence of all natural calcites to the action of an auxiliary impurity. The essential identity of the cathode-ray excited luminescence spectra of CaCO 3:Mn, CaCO3: (Pb+Mn), CaCO3:(Tl+Mn), and CaCO3:(Ce+Mn) with the 2537A-excited spectra of the latter three is evidence that the luminescent center in all cases is the manganese ion or the MnO6 group. It is shown that a "cascade" mechanism for the action of the auxiliary impurities, lead, thallium, and cerium, is incorrect; and that the phenomenon must be considered as a case of sensitized luminescence. Owing to the nature of cathode-ray excitation, the manganese activator can be excited by this agent even in the absence of a second impurity. For optical excitation, however, an absorption band for the ultraviolet must be established by building into the CaCO3:Mn a second impurity or "sensitizer.".

  18. Luminescent materials and their applications

    CERN Document Server

    Virk, Hardev Singh

    2015-01-01

    It is pertinent to note that Luminescence phenomenon has once again occupied a central stage with the announcement of Nobel Prize in October 2014 to three Japanese scientists. The discovery of Galium Nitride proved to be a revolutionary step forward in creation of Blue LEDs. With the advent of LED lamps we now have more long-lasting and more efficient alternatives to older light sources. The Volume under reference consists of 9 Chapters, written by experts in the area of Luminescent Materials. First 5 Chapters are contributed as Review Papers and the last 4 are based on Research Papers.Chapter

  19. Different conjugated system Zn(ii) Schiff base complexes: supramolecular structure, luminescent properties, and applications in the PMMA-doped hybrid materials.

    Science.gov (United States)

    Dong, Yu-Wei; Fan, Rui-Qing; Chen, Wei; Zhang, Hui-Jie; Song, Yang; Du, Xi; Wang, Ping; Wei, Li-Guo; Yang, Yu-Lin

    2017-01-24

    A series of Zn(ii) complexes with different conjugated systems, [ZnL1Cl 2 ] 2 (Zn1), [ZnL2Cl 2 ] (Zn2), [Zn(L3) 2 ]·(ClO 4 ) 2 (Zn3), [Zn 2 L4Cl 4 ] (Zn4), and [ZnL5Cl 2 ] (Zn5), were synthesized and subsequently characterized via single crystal X-ray diffraction, 1 H and 13 C NMR, FT-IR, elemental analyses, melting point, and PXRD. The X-ray diffraction analyses revealed that the supramolecular frameworks of complexes Zn1-Zn5 are constructed by C-HO/Cl hydrogen bonds and ππ interactions. Complexes Zn1-Zn3 feature 3D 6-connected {4 12 ·6 3 } topological structures, whereas complex Zn4 exhibits a 3D 7-connected supramolecular framework with a {4 17 ·6 4 } topological structure. However, complex Zn5 shows one-dimensional "wave-like" chains. Based on these varied structures, the emission maximum wavelengths of complexes Zn1-Zn5 can be tuned in a wide range of 461-592 nm due to the red shift direction of λ em caused by different conjugated systems and their electron donating abilities. Complex Zn3 shows a strong luminescence in the solid state and in the acetonitrile solution. Therefore, a series of Zn3-poly(methylmethacrylate) (Zn3-PMMA) hybrid materials were obtained by controlling the concentration of complex Zn3 in poly(methylmethacrylate) (PMMA). At an optimal concentration of 4%, the doped polymer film of Zn3-PMMA displays strong green luminescence emissions that are 19-fold in the luminescence intensities and 98 °C higher in the thermal stability temperature compared to the Zn3 film.

  20. Nuclear power can reduce emissions and maintain a strong economy: Rating Australia’s optimal future electricity-generation mix by technologies and policies

    International Nuclear Information System (INIS)

    Hong, Sanghyun; Bradshaw, Corey J.A.; Brook, Barry W.

    2014-01-01

    Highlights: • Nuclear power is essential for reducing greenhouse-gas emissions at lower cost. • Physical and economic limits of renewables at high penetrations hamper their growth. • Large-scale fossil fuels are required if nuclear power is not permitted in Australia. • Well-balanced information is a prerequisite for defining an optimal future mix. - Abstract: Legal barriers currently prohibit nuclear power for electricity generation in Australia. For this reason, published future electricity scenarios aimed at policy makers for this country have not seriously considered a full mix of energy options. Here we addressed this deficiency by comparing the life-cycle sustainability of published scenarios using multi-criteria decision-making analysis, and modeling the optimized future electricity mix using a genetic algorithm. The published ‘CSIRO e-future’ scenario under its default condition (excluding nuclear) has the largest aggregate negative environmental and economic outcomes (score = 4.51 out of 8), followed by the Australian Energy Market Operator’s 100% renewable energy scenario (4.16) and the Greenpeace scenario (3.97). The e-future projection with maximum nuclear-power penetration allowed yields the lowest negative impacts (1.46). After modeling possible future electricity mixes including or excluding nuclear power, the weighted criteria recommended an optimized scenario mix where nuclear power generated >40% of total electricity. The life-cycle greenhouse-gas emissions of the optimization scenarios including nuclear power were <27 kg CO 2 -e MW h −1 in 2050, which achieves the IPCC’s target of 50–150 kg CO 2 -e MW h −1 . Our analyses demonstrate clearly that nuclear power is an effective and logical option for the environmental and economic sustainability of a future electricity network in Australia

  1. The effect of Bi3+ and Li+ co-doping on the luminescence characteristics of Eu3+-doped aluminum oxide films

    International Nuclear Information System (INIS)

    Padilla-Rosales, I.; Martinez-Martinez, R.; Cabañas, G.; Falcony, C.

    2015-01-01

    The incorporation of Bi 3+ and Li + as co-dopants in Eu 3+ -doped aluminum oxide films deposited by the ultrasonic spray pyrolysis technique and its effect on the luminescence characteristics of this material are described. Both Bi 3+ and Li + do not introduce new luminescence features but affect the luminescence intensity of the Eu 3+ related emission spectra as well as the excitation spectra. The introduction of Bi 3+ generates localized states in the aluminum oxide host that result in a quenching of the luminescence intensity, while Li + and Bi 3+ co-doping increase the luminescence intensity of these films. - Highlights: • Li and Bi co-doping increase the luminescence. • Bi creates localized states in the Al 2 O 3 host. • Li was incorporated as a co-activator

  2. The effect of Bi{sup 3+} and Li{sup +} co-doping on the luminescence characteristics of Eu{sup 3+}-doped aluminum oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Padilla-Rosales, I., E-mail: ipadilla@cinvestav.mx [Centro de Investigación y de Estudios Avanzados del IPN, Nanociencias y Nanotecnología, Av. IPN 2508, Col. San Pedro Zacatenco, CP 07360 México D.F. (Mexico); Martinez-Martinez, R. [Instituto de Física y Matemáticas, Universidad Tecnológica de la Mixteca, Carretera a Acatlima Km. 2.5, CP 69000 Huajuapan de León, Oax, México (Mexico); Cabañas, G. [Centro de Investigación y de Estudios Avanzados del IPN, Nanociencias y Nanotecnología, Av. IPN 2508, Col. San Pedro Zacatenco, CP 07360 México D.F. (Mexico); Falcony, C. [Centro de Investigación y de Estudios Avanzados del IPN, Departamento de Física, Av. IPN 2508, Col. San Pedro Zacatenco, CP 07360 México D.F. (Mexico)

    2015-09-15

    The incorporation of Bi{sup 3+} and Li{sup +} as co-dopants in Eu{sup 3+}-doped aluminum oxide films deposited by the ultrasonic spray pyrolysis technique and its effect on the luminescence characteristics of this material are described. Both Bi{sup 3+} and Li{sup +} do not introduce new luminescence features but affect the luminescence intensity of the Eu{sup 3+} related emission spectra as well as the excitation spectra. The introduction of Bi{sup 3+} generates localized states in the aluminum oxide host that result in a quenching of the luminescence intensity, while Li{sup +} and Bi{sup 3+} co-doping increase the luminescence intensity of these films. - Highlights: • Li and Bi co-doping increase the luminescence. • Bi creates localized states in the Al{sub 2}O{sub 3} host. • Li was incorporated as a co-activator.

  3. Multifaceted interplay between lipophilicity, protein interaction and luminescence parameters of non-intercalative ruthenium(II) polypyridyl complexes controlling cellular imaging and cytotoxic properties.

    Science.gov (United States)

    Mazuryk, Olga; Magiera, Katarzyna; Rys, Barbara; Suzenet, Franck; Kieda, Claudine; Brindell, Małgorzata

    2014-12-01

    Here, we examine the photophysical properties of five ruthenium(II) complexes comprising two 4,7-diphenyl-1,10-phenanthroline (dip) ligands and functionalized bipyridine (R₁bpy-R₂, where R₁= H or CH3, R₂= H, CH₃, COO⁻,4-[3-(2-nitro-1H-imidazol-1-yl)propyl] or 1,3-dicyclohexyl-1-carbonyl-urea) towards development of luminescence probes for cellular imaging. These complexes have been shown to interact with albumin and the formed adducts exhibited up to eightfold increase in the luminescence quantum yield as well as the average lifetime of emission. It was demonstrated that they cannot bind to DNA through the intercalation mode and its luminescence in the presence of DNA is quenching. Cell viability experiments indicated that all complexes possess significant dose-dependent cytotoxicity (with IC₅₀ 5-19 μM) on 4T1 breast cancer cell line and their anti-proliferative activity correlates very well with their lipophilicity. Cellular uptake was studied by measuring the ruthenium content in cells using ICP-MS technique. As expected, the better uptake is directly related to higher lipophilicity of doubly charged ruthenium complexes while uptake of monocationic one is much lower in spite of the highest lipophilicity. Additionally staining properties were assessed using flow cytometry and fluorescence microscopy. These experiments showed that complex with 1,3-dicyclohexyl-1-carbonyl-urea substituent exhibits the best staining properties in spite of the lowest luminescence quantum yield in buffered solution (pH 7.4). Our results point out that both the imaging and cytotoxic properties of the studied ruthenium complexes are strongly influence by the level of internalization and protein interaction.

  4. Combined Cerenkov luminescence and nuclear imaging of radioiodine in the thyroid gland and thyroid cancer cells expressing sodium iodide symporter: initial feasibility study.

    Science.gov (United States)

    Jeong, Shin Young; Hwang, Mi-Hye; Kim, Jung Eun; Kang, Sungmin; Park, Jeong Chan; Yoo, Jeongsoo; Ha, Jeoung-Hee; Lee, Sang-Woo; Ahn, Byeong-Cheol; Lee, Jaetae

    2011-01-01

    Radioiodine (RI) such as (131)I or (124)I, can generate luminescent emission and be detected with an optical imaging (OI) device. To evaluate the possibility of a novel Cerenkov luminescence imaging (CLI) for application in thyroid research, we performed feasibility studies of CLI by RI in the thyroid gland and human anaplastic thyroid carcinoma cells expressing sodium iodide symporter gene (ARO-NIS). For in vitro study, FRTL-5 and ARO-NIS were incubated with RI, and the luminometric and CLI intensity was measured with luminometer and OI device. Luminescence intensity was compared with the radioactivity measured with γ-counter. In vivo CLI of the thyroid gland was performed in mice after intravenous injection of RI with and without thyroid blocking. Mice were implanted with ARO-NIS subcutaneously, and CLI was performed with injection of (124)I. Small animal PET or γ-camera imaging was also performed. CLI intensities of thyroid gland and ARO-NIS were quantified, and compared with the radioactivities measured from nuclear images (NI). Luminometric assay and OI confirmed RI uptake in the cells in a dose-dependent manner, and luminescence intensity was well correlated with radioactivity of the cells. CLI clearly demonstrated RI uptake in thyroid gland and xenografted ARO-NIS cells in mice, which was further confirmed by NI. A strong positive correlation was observed between CLI intensity and radioactivity assessed by NI. We successfully demonstrated dual molecular imaging of CLI and NI using RI both in vitro and in vivo. CLI can provide a new OI strategy in preclinical thyroid studies. ©The Japan Endocrine Society

  5. Design and optimization of luminescent semiconductor nanocrystals for optoelectronic applications

    OpenAIRE

    Levchuk, Ievgen

    2017-01-01

    Luminescent colloidal semiconductor nanocrystals have attracted prominent attention for the last three decades since their size-dependent optical properties were discovered. Numerous applications in fields of light conversion such as light-emitting diodes (LED), photovoltaics, medicine, lasers and TV displays were developed. Despite the strong and rapid expansion of this field in the scope of material quality reflected by narrow size distribution and photoluminescence quantum yield, simplific...

  6. Amplified Luminescence Quenching of Phosphorescent Metal–Organic Frameworks

    Energy Technology Data Exchange (ETDEWEB)

    Kent, Caleb A. [Department of Chemistry,; Liu, Demin [Department of Chemistry,; Meyer, Thomas J. [Department of Chemistry,; Lin, Wenbin [Department of Chemistry,

    2012-02-22

    Amplified luminescence quenching has been demonstrated in metal–organic frameworks (MOFs) composed of Ru(II)-bpy building blocks with long-lived, largely triplet metal-to-ligand charge-transfer excited states. Strong non-covalent interactions between the MOF surface and cationic quencher molecules coupled with rapid energy transfer through the MOF microcrystal facilitates amplified quenching with a 7000-fold enhancement of the Stern–Völmer quenching constant for methylene blue compared to a model complex.

  7. Size-tunable luminescence in Eu{sup 3+} doped nanocomposite containing In{sub 2}O{sub 3} quantum dots

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Yunlong, E-mail: yunlongyu@yeah.net [College of Electronics and Information Science, Fujian Jiangxia University, Fuzhou, Fujian 350108 (China); Guan, Xiangfeng; Li, Xiaoyan [College of Electronics and Information Science, Fujian Jiangxia University, Fuzhou, Fujian 350108 (China); Li, Wei, E-mail: fjutlw@163.com [School of Materials Science and Engineering, Fujian University of Technology, Fuzhou, Fujian 350108 (China); Jiang, Linqin; Chen, Dagui [College of Electronics and Information Science, Fujian Jiangxia University, Fuzhou, Fujian 350108 (China)

    2016-07-05

    Eu{sup 3+} doped nanocomposite containing In{sub 2}O{sub 3} quantum dots (QDs) was successfully fabricated by a melt quenching technique. The crystallization process of cubic In{sub 2}O{sub 3} phase was revealed by X-ray diffraction and transmissions electron microscopy. The size of In{sub 2}O{sub 3} QDs can be well tuned by adjusting treatment duration and a size-tunable In{sub 2}O{sub 3} emission was obtained. Impressively, In{sub 2}O{sub 3} QDs can act as strong sensitizers for Eu{sup 3+} emission, and the emission intensity enhances up to 26 times with respect to the one without In{sub 2}O{sub 3}. The enhancement factor gradually decreases with increasing In{sub 2}O{sub 3} QDs size. Analyzing the excitation and emission spectra, a possible energy transfer process from In{sub 2}O{sub 3} QDs to Eu{sup 3+} ions was established. These results indicate that In{sub 2}O{sub 3} QDs with suitable size have great potential for use as sensitizers of Eu{sup 3+} ions in high-performance luminescent converter materials. - Highlights: • Eu{sup 3+} doped nanocomposite containing In{sub 2}O{sub 3} QDs was prepared by melt quenching. • The crystallization process of cubic In{sub 2}O{sub 3} phase in glass matrix was revealed. • The QDs size can be tuned and the size-tunable In{sub 2}O{sub 3} luminescence was obtained. • The enhanced Eu{sup 3+} emission induced by energy transfer from In{sub 2}O{sub 3} was confirmed. • Relation between microstructure and enhanced Eu{sup 3+} emission was discussed.

  8. Luminescence spectroscopy and microscopy applied to study gem materials: a case study of C centre containing diamonds

    Science.gov (United States)

    Hainschwang, Thomas; Karampelas, Stefanos; Fritsch, Emmanuel; Notari, Franck

    2013-06-01

    The methods of luminescence spectroscopy and microscopy are widely used for the analysis of gem materials. This paper gives an overview of the most important applications of the analysis of laser and UV excited luminescence by spectroscopy and visually by microscopy with emphasis on diamond, and specifically natural type Ib diamond, little studied so far. Luminescence based techniques are paramount to the gemmological analysis of diamond, in order to determine whether it is natural, treated or synthetic. The great sensitivity of luminescence helps detect some emitting centres that are undetectable by any other analytical method. Hence, especially for diamond, luminescence is an enabling technology, as illustrated by its pioneering use of imagery for the separation of natural and synthetic diamond, and of spectroscopy for the detection of High Pressure-High Temperature treatment. For all other gemstones the applications are at the moment less numerous, but nevertheless they remain highly important. They provide quickly information on the identification of a gem material, and its treatment. Besides the study of broad band emissions caused by various colour centres, the typical PL-causing trace elements (amongst others) are chromium, manganese, uranium and rare earth elements. In pearls the study of broad band luminescence can be useful, and particularly the study of pink to red porphyrin luminescence in pearls from certain species such as Pinctada and Pteria and others can help identify the pearl-producing mollusc, or if a pearl has been dyed or not. Type Ib diamonds are representative of the importance and complexity of the analysis of luminescence by microscopy and spectroscopy. They show a wide range of sometimes very complex emissions that result in luminescence colours from green to yellow to orange or red. These emissions show generally very inhomogeneous distribution. They are caused by a range of defects, however only a few of them are well characterized.

  9. Strong Photoluminescence Enhancement of Silicon Oxycarbide through Defect Engineering

    Directory of Open Access Journals (Sweden)

    Brian Ford

    2017-04-01

    Full Text Available The following study focuses on the photoluminescence (PL enhancement of chemically synthesized silicon oxycarbide (SiCxOy thin films and nanowires through defect engineering via post-deposition passivation treatments. SiCxOy materials were deposited via thermal chemical vapor deposition (TCVD, and exhibit strong white light emission at room-temperature. Post-deposition passivation treatments were carried out using oxygen, nitrogen, and forming gas (FG, 5% H2, 95% N2 ambients, modifying the observed white light emission. The observed white luminescence was found to be inversely related to the carbonyl (C=O bond density present in the films. The peak-to-peak PL was enhanced ~18 and ~17 times for, respectively, the two SiCxOy matrices, oxygen-rich and carbon-rich SiCxOy, via post-deposition passivations. Through a combinational and systematic Fourier transform infrared spectroscopy (FTIR and PL study, it was revealed that proper tailoring of the passivations reduces the carbonyl bond density by a factor of ~2.2, corresponding to a PL enhancement of ~50 times. Furthermore, the temperature-dependent and temperature-dependent time resolved PL (TDPL and TD-TRPL behaviors of the nitrogen and forming gas passivated SiCxOy thin films were investigated to acquire further insight into the ramifications of the passivation on the carbonyl/dangling bond density and PL yield.

  10. Supramolecular luminescence from oligofluorenol-based supramolecular polymer semiconductors.

    Science.gov (United States)

    Zhang, Guang-Wei; Wang, Long; Xie, Ling-Hai; Lin, Jin-Yi; Huang, Wei

    2013-11-13

    Supramolecular luminescence stems from non-covalent exciton behaviors of active π-segments in supramolecular entities or aggregates via intermolecular forces. Herein, a π-conjugated oligofluorenol, containing self-complementary double hydrogen bonds, was synthesized using Suzuki coupling as a supramolecular semiconductor. Terfluorenol-based random supramolecular polymers were confirmed via concentration-dependent nuclear magnetic resonance (NMR) and dynamic light scattering (DLS). The photoluminescent spectra of the TFOH-1 solution exhibit a green emission band (g-band) at approximately ~520 nm with reversible features, as confirmed through titration experiments. Supramolecular luminescence of TFOH-1 thin films serves as robust evidence for the aggregates of g-band. Our results suggest that the presence of polyfluorene ketone defects is a sufficient condition, rather than a sufficient-necessary condition for the g-band. Supramolecular electroluminescence will push organic devices into the fields of supramolecular optoelectronics, spintronics, and mechatronics.

  11. Luminescence response of synthetic opal under femtosecond laser pumping

    International Nuclear Information System (INIS)

    Vasnetsov, M.V.; Bazhenov, V.Yu.; Dmitruk, I.N.; Kudryavtseva, A.D.; Tcherniega, N.V.

    2015-01-01

    Synthetic opal is an artificial photonic metamaterial composed from spherical globules of amorphous silica (SiO 2 ) about 300 nm in diameter. We report, for the first time to our knowledge, the origin of a narrow luminescence spectral peak (4 nm HWHM) and optical second and third harmonic generation in synthetic opal samples under femtosecond laser excitation (800 nm) at liquid-nitrogen temperature. Stimulated-emission effects are discussed related to the possibility of nanocavity lasing at the condition of the first Mie resonance in a dielectric sphere. - Highlights: • Second harmonic generation in a synthetic opal (amorphous material composed from spherical SiO 2 globules) was observed. • Narrow luminescence peak which we assign to a Mie resonance in a globule was detected at liquid-nitrogen temperature

  12. Ion beam induced luminescence characterisation of CVD diamond films

    Energy Technology Data Exchange (ETDEWEB)

    Bettiol, A.A.; Gonon, P.; Jamieson, D.N. [Melbourne Univ., Parkville, VIC (Australia). School of Physics

    1996-12-31

    The characterisation of the band structure properties of materials and devices by ion microprobe techniques has been made possible at the Melbourne MeV ion microprobe facility with the development of Ion Beam Induced Luminescence (IBIL). A number of diamond films grown by Microwave Plasma Chemical Vapour Deposition (MPCVD) on silicon substrates are analysed. A preliminary study of the luminescence properties of these samples has revealed information not previously obtainable via traditional microprobe techniques. The optical effects of incorporating dopants during the deposition process is determined using IBIL. The presence of trace element impurities introduced during growth is examined by Particle Induced X-ray Emission (PIXE), and a measurement of the film thickness is made using Rutherford Backscattering Spectrometry (RBS). 7 refs., 2 figs.

  13. Luminescent Properties of Oxazine 170 Perchlorate Doped PMMA Fiber

    Directory of Open Access Journals (Sweden)

    Piotr Miluski

    2017-04-01

    Full Text Available The article presents fabrication and luminescent properties of poly(methyl methacrylate (PMMA fiber doped by Oxazine 170 perchlorate. The bright fluorescence of polymeric fiber (at molar fluorescent organic dye concentration 4.3 × 10−5 was characterized in terms of spectrum and signal attenuation vs. the fiber length. The significant changes in fluorescence spectrum (λmax red shift average slope 4.6 nm/cm and Full Width at Half Maximum (FWHM increasing slope 6.7 nm/cm have been noticed for the length of the fiber (0.02–0.08 m which corresponds to a high overlapping region of absorption and emission spectra of used dye. The red shift of λmax (c.a. 80 nm was presented in fabricated polymeric fiber at distance 0.85 m. The obtained characteristics can be used for luminescent properties optimization of fluorescent organic-dye-doped PMMA fiber.

  14. Thermally stimulated luminescence and photoluminescence ...

    Indian Academy of Sciences (India)

    2012-01-13

    Jan 13, 2012 ... Peltier cooled photo-multiplier tube as detector (Jain et al. 2008). The acquisition and analysis of the data were carried out by F-900 software supplied by Edinburgh Analytical. Instruments, UK. Thermally stimulated luminescence (TSL) glow curves were recorded using home-built unit between. 300 and ...

  15. Advances in luminescence instrument systems

    DEFF Research Database (Denmark)

    Bøtter-Jensen, L.; Bulur, E.; Duller, G.A.T.

    2000-01-01

    We report on recent advances in the development of luminescence measurement systems and techniques at Riso. These include: (1) optical stimulation units based on new-generation powerful blue light (470 nm) emitting diodes providing up to 28 mW/cm(2) for OSL measurements; (2) an infrared (830 nm...

  16. Hydrothermal synthesis, characterization and luminescent ...

    Indian Academy of Sciences (India)

    Home; Journals; Bulletin of Materials Science; Volume 39; Issue 4. Hydrothermal synthesis, characterization and luminescent properties of lanthanide-doped NaLaF 4 nanoparticles. JIGMET LADOL HEENA KHAJURIA SONIKA KHAJURIA HAQ NAWAZ SHEIKH. Volume 39 Issue 4 August 2016 pp 943-952 ...

  17. Luminescence of uranium in some phosphates

    International Nuclear Information System (INIS)

    Lin Yu; Zhang Rui

    1992-07-01

    The solid fluorescence spectral properties of uranium in phosphates systems have been observed. The NaH 2 PO 4 : U system has been found to be an efficient green phosphor. The luminescence mechanism of the phosphor has been discussed. The crystal structure of NaH 2 PO 4 : U system under different conditions was also studied. Over a wide range of ignition temperatures (200 ∼ 600 C degree), the system with mass ratio of U/NaH 2 PO 4 below 10 -3 transforms into NaPO 3 : U crystal, which emits strong fluorescence. The system is non-crystalline with decreasing fluorescence intensity when the ignition temperature is higher than 650 C degree. The NaPO 3 crystal lattice has distorted as the mass ratio of U/NaH 2 PO 4 of the system greater than 10 -2

  18. Limit of detection of a fiber optics gyroscope using a super luminescent radiation source

    CERN Document Server

    Sandoval, G E

    2003-01-01

    The main objective of this work is to establish the dependence of characteristics of the fiber optics gyroscope (FOG) with respect to the parameters of the super luminescent emission source based on doped optical fiber with rare earth elements (Super luminescent Fiber Source, SFS), argument the pumping rate election of the SFS to obtain characteristics limits of the FOG sensibility. By using this type of emission source in the FOG is recommend to use the rate when the direction of the pumping signal coincide with the super luminescent signal. The most results are the proposition and argumentation of the SFS election as emission source to be use in the FOG of the phase type. Such a decision allow to increase the characteristics of the FOG sensibility in comparison with the use of luminescent source of semiconductors emission which are extensively used in the present time. The use of emission source of the SFS type allow to come closer to the threshold of the obtained sensibility limit (detection limit) which i...

  19. Limit of detection of a fiber optics gyroscope using a super luminescent radiation source

    International Nuclear Information System (INIS)

    Sandoval R, G.E.; Nikolaev, V.A.

    2003-01-01

    The main objective of this work is to establish the dependence of characteristics of the fiber optics gyroscope (FOG) with respect to the parameters of the super luminescent emission source based on doped optical fiber with rare earth elements (Super luminescent Fiber Source, SFS), argument the pumping rate election of the SFS to obtain characteristics limits of the FOG sensibility. By using this type of emission source in the FOG is recommend to use the rate when the direction of the pumping signal coincide with the super luminescent signal. The most results are the proposition and argumentation of the SFS election as emission source to be use in the FOG of the phase type. Such a decision allow to increase the characteristics of the FOG sensibility in comparison with the use of luminescent source of semiconductors emission which are extensively used in the present time. The use of emission source of the SFS type allow to come closer to the threshold of the obtained sensibility limit (detection limit) which is determined with the shot noise. (Author)

  20. Synthesis and luminescent properties of uniform monodisperse LuPO4:Eu3+/Tb3+ hollow microspheres

    Science.gov (United States)

    Gao, Yu; Yu, He; Shi, Cheng; Zhao, Guiyan; Bi, Yanfeng; Xu, Baotong; Ding, Fu; Sun, Yaguang; Xu, Zhenhe

    2017-12-01

    Uniform monodisperse LuPO4:Eu3+/Tb3+ hollow microspheres with diameters of about 2.4 µm have been successfully synthesized by the combination of a facile homogeneous precipitation approach, an ion-exchange process and a calcination process. The possible formation mechanism for the hollow microspheres was presented. Furthermore, the luminescence properties revealed that the LuPO4:Eu3+ and LuPO4:Tb3+ phosphors show strong orange-red and green emissions under ultraviolet excitation, respectively, which endows this material with potential application in many fields, such as light display systems and optoelectronic devices. Since the synthetic process can be carried out at mild conditions, it should be straightforward to scale up the entire process for large-scale production of the LuPO4 hollow microspheres. Furthermore, this general and simple method may be of much significance in the synthesis of many other inorganic materials.

  1. Synthesis and luminescent properties of uniform monodisperse LuPO4:Eu3+/Tb3+hollow microspheres.

    Science.gov (United States)

    Gao, Yu; Yu, He; Shi, Cheng; Zhao, Guiyan; Bi, Yanfeng; Xu, Baotong; Ding, Fu; Sun, Yaguang; Xu, Zhenhe

    2017-12-01

    Uniform monodisperse LuPO 4 :Eu 3+ /Tb 3+ hollow microspheres with diameters of about 2.4 µm have been successfully synthesized by the combination of a facile homogeneous precipitation approach, an ion-exchange process and a calcination process. The possible formation mechanism for the hollow microspheres was presented. Furthermore, the luminescence properties revealed that the LuPO 4 :Eu 3+ and LuPO 4 :Tb 3+ phosphors show strong orange-red and green emissions under ultraviolet excitation, respectively, which endows this material with potential application in many fields, such as light display systems and optoelectronic devices. Since the synthetic process can be carried out at mild conditions, it should be straightforward to scale up the entire process for large-scale production of the LuPO 4 hollow microspheres. Furthermore, this general and simple method may be of much significance in the synthesis of many other inorganic materials.

  2. A Zero-Dimensional Organic Seesaw-Shaped Tin Bromide with Highly Efficient Strongly Stokes-Shifted Deep-Red Emission

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Chenkun [College of Engineering, Tallahassee, FL (United States). Dept. of Chemical and Biomedical Engineering; Lin, Haoran [College of Engineering, Tallahassee, FL (United States). Dept. of Chemical and Biomedical Engineering; Shi, Hongliang [Beihang Univ., Beijing (China). Dept. of Physics; Tian, Yu [Materials Science and Engineering Program, Florida State University, Tallahassee FL 32306 USA; Pak, Chongin [Florida State Univ., Tallahassee, FL (United States). Dept. of Chemistry and Biochemistry; Shatruk, Michael [Florida State Univ., Tallahassee, FL (United States). Dept. of Chemistry and Biochemistry; Zhou, Yan [Florida State Univ., Tallahassee, FL (United States). Dept. of Chemistry and Biochemistry; Djurovich, Peter [Univ. of Southern California, Los Angeles, CA (United States). Dept. of Chemistry; Du, Mao-Hua [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Materials Science and Technology Division, Center for Radiation Detection Materials and Systems; Ma, Biwu [College of Engineering, Tallahassee, FL (United States). Dept. of Chemical and Biomedical Engineering; Beihang Univ., Beijing (China). Dept. of Physics; Florida State Univ., Tallahassee, FL (United States). Dept. of Chemistry and Biochemistry

    2017-12-21

    The synthesis and characterization is reported of (C9NH20)2SnBr4, a novel organic metal halide hybrid with a zero-dimensional (0D) structure, in which individual seesaw-shaped tin (II) bromide anions (SnBr42-) are co-crystallized with 1-butyl-1-methylpyrrolidinium cations (C9NH20+). Upon photoexcitation, the bulk crystals exhibit a highly efficient broadband deep-red emission peaked at 695 nm, with a large Stokes shift of 332 nm and a high quantum efficiency of around 46 %. Furthermore, the unique photophysical properties of this hybrid material are attributed to two major factors: 1) the 0D structure allowing the bulk crystals to exhibit the intrinsic properties of individual SnBr42- species, and 2) the seesaw structure then enables a pronounced excited state structural deformation as confirmed by density functional theory (DFT) calculations.

  3. Luminescent hybrid materials based on (8-hydroxyquinoline)-substituted metal-organic complexes and lead-borate glasses

    Science.gov (United States)

    Petrova, Olga B.; Anurova, Maria O.; Akkuzina, Alina A.; Saifutyarov, Rasim R.; Ermolaeva, Ekaterina V.; Avetisov, Roman I.; Khomyakov, Andrew V.; Taydakov, Ilya V.; Avetissov, Igor Ch.

    2017-07-01

    Novel luminescent organic-inorganic hybrid materials based on 8-hydroxyquinoline metal complexes (Liq, Kq, Naq, Rbq, Mgq2, Srq2, Znq2, Scq3, Alq3, Gaq3, and Inq3) have been synthesized by a high temperature exchange reaction with 80PbF2-20B2O3 inorganic low-melting glass. The mechanical and optical properties, transmission spectra, emission an excitation photoluminescence, and luminescence kinetic of hybrid materials were studied. All hybrid materials showed a wide luminescence band in the range 400-700 nm.

  4. Mechanism of luminescent emission in BaY{sub 2}F{sub 8} scintillators doped with rare earths; Mecanismos de emissao luminescente nos cintiladores de BaY{sub 2}F{sub 8} dopado com terras raras

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Ana Carolina de Mello

    2013-07-01

    In this work samples of Barium Yttrium Fluoride (BaY{sub 2}F{sub 8}-BaYF) doped with different concentrations of Tb{sup 3+}, Er{sup 3+}, Tm{sup 3+} e Nd{sup 3+} ions were characterized, aiming their application in radiation detection devices using their scintillating properties. Two types of samples were produced, polycrystalline samples, obtained via solid state reaction and single crystals, obtained via the floating zone melting method. The radioluminescence measurements (RL) revealed that the samples doped with 2.0 or 3.0 % Tb showed RL intensity at 545 nm two times higher than samples of CsI:Tl, although the total scintillation yield was smaller when compared to this commercial scintillator. Thermoluminescence (TL) results showed that all doped samples exhibited the same peak at 123°C, which is characteristic of the matrix (BaY{sub 2}F{sub 2}). Comparison of the areas under the TL and RL curves for Tb{sup 3+} and Nd{sup 3+} doped BaYF revealed that the trapping centers are competing with the scintillation of the samples. However, this was not true for the Er{sup 3+} and Tm{sup 3+} doped samples and it was found that the scintillation yield is independent of the trap concentration up to a certain concentration limit. From this point on, the scintillation yields started increasing as the trap concentration increased. The radiation damage defects in BaYF:Tb{sup 3+} were studied via optical absorption (OA) and correlated with TL, showing that trapping centers are connected to the color centers. All samples exhibited different luminescence decay processes with time constants ranging from microseconds, for the fast processes, milliseconds, for the intermediate ones, and phosphorescent processes with decay time on the order of seconds. For the Nd{sup 3+} doped samples, very fast decay process was also found with time constants of about 60ns and that is an indication that this material can be used in fast detection systems, although its scintillation efficiency was

  5. Enhanced quantum cutting luminescence by Au nanorods through improving radiative transition rate

    Science.gov (United States)

    Zheng, Biao; Lin, Lin; Feng, Zhuohong; Huang, Lili; Zhuang, Luoqing; Wang, Zhezhe; Zheng, Zhiqiang

    2017-11-01

    Quantum cutting (QC) phosphor β-NaYF4:Tb3+, Yb3+ nanoparticles (NPs) are decorated with Au nanorods (NRs). By tailoring Au NRs longitudinal plasmon resonance to match the emission wavelength of Yb3+ ion, plasmon-enhanced near-infrared (NIR) QC luminescence is achieved through improving Yb3+ ion's radiative transition rate. The decay curves of Yb3+ ion in β-NaYF4:Tb3+, Yb3+ NPs decorated with Au NRs further confirm the improvement of radiative transition rate. The influence of Au NRs concentration on QC luminescence is also investigated, and the results show that the optimal concentration of Au NRs is 0.12% with the maximum enhancement factor about 3. Our study may not only path the way to achieve simultaneous excitation and emission enhancement of QC luminescence, but also provide a potential application as QC layer to silicon-based solar cells.

  6. Synthesis, structural characterization and luminescent properties of a novel europium ternary complex Eu(2-A-4-CBA)3phen

    International Nuclear Information System (INIS)

    Chen, Yongjie; Wu, Shengnan; Xing, Zhenfang; Cao, Shuang; Geng, Xiujuan; Yang, Ying; Xiao, Linjiu

    2015-01-01

    The preparation of a novel europium ternary complex with the formula of Eu(2-A-4-CBA) 3 phen (where, 2-A-4-CBA = 2-amino-4-chlorobenzoic acid, phen = 1,10-phenanthroline) under solvothermal condition is described. The composition and structure of the resulting complex were investigated by elemental analysis, Fourier transform infrared (FT-IR) spectroscopy. The complex is polycrystalline, and the morphology is clean and regular as revealed by scanning electron microscope (SEM). The luminescent and thermal properties of the complex were researched by fluorescence spectroscopy and thermogravimetric analysis, respectively. Of importance here is that, the room-temperature luminescence spectra of the complex show strong characteristic emission of the corresponding Eu 3+ , which is attributed to the energy transfer from ligands to Eu 3+ via an Antenna effect. It is also found that the complex exhibits pure red light and high color purity. In addition, the complex does not decompose until 300 °C, so it exhibits good thermal stability. - Highlights: • A novel Eu(III) complex was synthesized by solvothermal synthesis method. • The structure and properties of complex were studied. • The complex can emits pure red light and has a high color purity. • The complex does not decompose until 300 °C and it has a good thermal stability

  7. Correlation of in vivo tumor response and singlet oxygen luminescence detection in mTHPC-mediated photodynamic therapy

    Directory of Open Access Journals (Sweden)

    Brian C. Wilson

    2015-01-01

    Full Text Available Excited-state singlet oxygen (1O2, generated during photodynamic therapy (PDT, is believed to be the primary cytotoxic agent with a number of clinically approved photosensitizers. Its relative concentration in cells or tissues can be measured directly through its near-infrared (NIR luminescence emission, which has correlated well with in vitro cell and in vivo normal skin treatment responses. Here, its correlation with the response of tumor tissue in vivo is examined, using the photosensitizer meso-tetrahydroxyphenylchlorin (mTHPC in an animal model comprising luciferase- and green fluorescent protein (GFP-transduced gliosarcoma grown in a dorsal window chamber. The change in the bioluminescence signal, imaged pretreatment and at 2, 5 and 9 d post treatment, was used as a quantitative measure of the tumor response, which was classified in individual tumors as "non", "moderate" and "strong" in order to reduce the variance in the data. Plotting the bioluminescence-based response vs the 1O2 counts demonstrated clear correlation, indicating that 1O2 luminescence provides a valid dosimetric technique for PDT in tumor tissue.

  8. Superposition of the luminescence spectra of free and bound excitons in ZnP2-D48

    International Nuclear Information System (INIS)

    Stamov, Ion; Nemerenco, Lucretia; Ivanenco, Iurii; Syrbu, Nicolae

    2011-01-01

    The luminescence spectra of ZnP 2 tetragonal crystals doped Mn, Sn, Cd, Sb at 10 K emission lines of bound excitons is detected. In the spectra non-phonon emission lines of bound and free excitons and their phonon replicas is isolated. The emission lines by the levels of the axial center are described. The composition of the luminescence of free and bound excitons at the axial center is investigated. In the region of phonon replicas of free excitons observed enhancement of lines due to forbidden transitions involving the recombination of excitons. A model of optic recombination transitions of the axial centre is proposed

  9. Luminescence characterization of a sodium rich feldspar

    Energy Technology Data Exchange (ETDEWEB)

    Correcher, V.; Sanchez M, L. [CIEMAT, Av. Complutense 22, 28040 Madrid (Spain); Garcia G, J. [MNCN-CSIC, c/ J. Gutierrez Abascal 2, Madrid 28006 (Spain); Rivera, T. [CICATA-IPN, Av. Legaria 694, 11500 Mexico D.F. (Mexico)

    2006-07-01

    This paper reports on the radioluminescence (RL) and thermoluminescence (TL) properties of a sodium rich feldspar ((Na,K)[AlSi{sub 3}O{sub 8}]) with a mean molecular composition of orthoclase (Or) and albite (Ab) of Or{sub 1}Ab{sub 99}. Despite the complexity of the luminescence signals of the sample, it is possible to determine six different emission bands at about 300, 380, 420, 460, 550 and 680 nm. The 300 nm emission can be associated to structural defects related to the recombination process in which the Na{sup +} ion diffusion-limited is involved. The UV-blue emission band at (i) 380 nm is characteristic of mineral phases containing SiO{sub 4} tetrahedral and could be related to intrinsic defects in the lattice, (ii) the 420 nm band could be associated to the presence of Cu (II) ions placed next to the hole traps or the recombination on a centre formed from a hole-oxygen atom adjacent to two Al atoms (Al-O-Al) and (iii) the 460 nm waveband could be due to the presence of Ti{sup 4+}. The green and red emissions are respectively associated to the presence of Mn{sup 2+} and Fe{sup 3+} ions. The ratio between the relative intensities, peaked at 290 (the more intense waveband) and 550 nm is about 10:1 in both TL and RL; this fact indicates that the efficiency of recombination centres does no changes regardless on the type of the process. (Author)

  10. Single crystalline essentially cubic hafnium, zirconium pyrophosphate luminescent material having improved brightness

    International Nuclear Information System (INIS)

    Chenot, C.F.; Mathrs, J.E.; Shaffer, F.N.

    1980-01-01

    It has been discovered that when (Hf,Zr) P 2 O 5 is prepared by reacting a mixutre of MO 2 , A 2 O and P 2 O 5 . (where M is zirconium, and A is an alkali metal, lithium, sodium or potassium), large single-crystalline cubic particles result, which when separated from an aqueous-soluble alkali metal-containing second phase exhibit improved intensity of ultraviolet emissions upon x-ray excitation. When used in x-ray intensifying screens with conventional silver halide emulsion x-ray film, such improved lumiescent material The invention includes material of the composition (Hfsub(1-x)Zrsub(x)) P 2 O 7 , where range from 0 to 1, having strong emission peaking at about 340 nm with controlled persistence, and also includes a method for producing such luminescent materials, and x-ray intensifying screens incorporating such materials having values of x within the range of about 0.005 to 0.5. (LL)

  11. Luminescence properties of different Eu sites in LiMgPO4:Eu2+, Eu3+

    International Nuclear Information System (INIS)

    Baran, A; Mahlik, S; Grinberg, M; Cai, P; Kim, S I; Seo, H J

    2014-01-01

    The effect of temperature on the luminescence properties of LiMgPO 4 doped with Eu 3+ and Eu 2+ are presented. Depending on the excitation wavelength, luminescence spectra consist of two distinct broad emission bands peaking at 380 nm and 490 nm related to 4f 6 5d 1  → 4f 7 ( 8 S 7/2 ) luminescence of Eu 2+ and to europium-trapped exciton, respectively, and/or several sharp lines between the 580 nm and 710 nm region, ascribed to the 5 D 0  →  7 F J (J = 0, 1, 2, 3 and 4) transitions in Eu 3+ . To explain all the features of the Eu 2+ and Eu 3+ luminescence we discussed the existence of two different Eu sites substituting for Li + , with short and long distance compensation. The evident effect of increasing the intensity of the Eu 2+ luminescence with increasing temperature was observed. It was considered that the charge compensation mechanism for Eu 3+ and Li + as well as Eu 2+ replacing Li + in the LiMgPO 4 is a long distance compensation that allows for the existence of some of the europium ions either as Eu 3+ at low temperature or as Eu 2+ at high temperature. We concluded that Eu 2+ in the Li + site with long distance compensation yields only 4f 6 5d 1  → 4f 7 luminescence, whereas Eu 2+ in the Li + site with short distance compensation yields 4f 6 5d 1  → 4f 7 luminescence and europium-trapped exciton emission. (paper)

  12. Synthesis and luminescence properties of Eu -activated Ca4Mg5 ...

    Indian Academy of Sciences (India)

    Synthesis and luminescence properties of Eu. 2+. -activated Ca4Mg5(PO4)6 for blue-emitting ... Abstract. Ca4Mg5(PO4)6:Eu2+ blue-emitting phosphor was synthesized by the combustion-assisted synthesis method under reductive atmosphere. .... The asymmetric emission spec- trum shows that Eu2+ have more than one ...

  13. Luminescent properties of red-light-emitting phosphors CaWO4: Eu ...

    Indian Academy of Sciences (India)

    The crystal structures of these phosphors were characterized by powder X-ray diffraction, and the luminescent properties of Eu3+-, Li+-codoped CaWO4 were investigated by diffuse reflectance spectra, photoluminescence emission spectra, photoluminescence excitation spectra, and the Commission International de L' ...

  14. Luminescent properties of red-light-emitting phosphors CaWO 4

    Indian Academy of Sciences (India)

    The crystal structures of these phosphors were characterized by powder X-ray diffraction, and the luminescent properties of Eu3+-, Li+-codoped CaWO4 were investigated by diffuse reflectance spectra, photoluminescence emission spectra, photoluminescence excitation spectra, and the Commission International de L' ...

  15. Luminescence performance of Eu 3-doped lead-free zinc phosphate ...

    Indian Academy of Sciences (India)

    Events · Annual Meetings · Mid Year Meetings · Discussion Meetings · Public Lectures · Lecture Workshops · Refresher Courses · Symposia · Live Streaming. Home; Journals; Bulletin of Materials Science; Volume 39; Issue 4. Luminescence performance of Eu$^{3+}-doped lead-free zinc phosphate glasses for red emission.

  16. Formation mechanism and luminescence appearance of Mn-doped zinc silicate particles synthesized in supercritical water

    International Nuclear Information System (INIS)

    Takesue, Masafumi; Suino, Atsuko; Hakuta, Yukiya; Hayashi, Hiromichi; Smith, Richard Lee

    2008-01-01

    Luminescence appearance of Mn-doped zinc silicate (Zn 2 SiO 4 :Mn 2+ , ZSM) formed in supercritical water at 400 deg. C and 29 MPa at reaction times from 1 to 4320 min was studied in the relation to its phase formation mechanism. Appearance of luminescent ZSM from green emission by α-ZSM and yellow emission by β-ZSM occurred over the same time period during the onset of phase formation at a reaction time of 2 min. Luminescence appeared at a much lower temperature and at shorter reaction times than the conventional solid-state reaction. Needle-like-shaped α-ZSM was the most stable particle shape and phase in the supercritical water reaction environment and particles formed via two routes: a homogenous nucleation route and a heterogenous route that involves solid-state diffusion and recrystallization. - Graphical abstract: Luminescence appearance of Mn-doped zinc silicate (Zn 2 SiO 4 :Mn 2+ , ZSM) formed in supercritical water at 400 deg. C and 29 MPa were studied in the relation to its phase formation mechanism. Green emission by α-ZSM and yellow emission by β-ZSM occurred over the same time period during the onset of phase formation

  17. The luminescence of the scheelite NaBi(MoO4)2

    NARCIS (Netherlands)

    Mazurak, Zb.; Blasse, G.; Liebertz, J.

    The luminescent properties of the scheelite NaBi(MoO4)2 are reported. Below 50 K an efficient, red emission occurs. The results agree with those for other bismuth molybdates. The decay measurements indicate an energy level structure of the emitting state which is very similar to that in PbMoO4. The

  18. Nature of sub-band gap luminescent eigenmodes in a ZnO nanowire

    NARCIS (Netherlands)

    Rühle, S.|info:eu-repo/dai/nl/31407659X; van Vugt, L.K.|info:eu-repo/dai/nl/338773800; Li, H.-Y.; Keizer, N.A.; Kuipers, L.; Vanmaekelbergh, D.A.M.|info:eu-repo/dai/nl/304829137

    2008-01-01

    The emission spectrum of individual high-quality ZnO nanowires consists of a series of Fabry-Pérot-like eigenmodes that extend far below the band gap of ZnO. Spatially resolved luminescence spectroscopy shows that light is emitted predominantly at both wire ends, with identical spectra reflecting

  19. Luminescence properties of Ce3+ doped gadolinium-calcium-silicaborate glass scintillator

    International Nuclear Information System (INIS)

    Park, J.M.; Ha, D.H.; Kaewjeang, S.; Maghanemi, U.; Kothan, S.; Kaewkhao, J.; Kim, H.J.

    2016-01-01

    In this work, the Ce 3+ doped gadolinium-calcium-silicaborate glass scintillators of the composition ratio 25Gd 2 O 3 :10CaO:10SiO 2 :(55−x)B 2 O 3 :xCeF 3 , have been fabricated by using the melt-quenching technique. The doping concentration of the Ce 3+ was varied from 0.05 mol% to 2.5 mol%. The 4f-5d transition of the Ce 3+ allowed scintillation with a fast decay time. The absorption spectrum, X-ray induced emission spectrum, photo luminescence spectrum, laser luminescence spectrum and decay time of the scintillators were measured for studying the luminescence properties. From the X-ray induced emission spectrum result, we checked the trend between doping concentration and light yield. The laser induced luminescence spectrum was measured while changing the temperature from 300 K to 10 K. We also measured the decay time by using the laser excitation of the 0.15 mol% Ce 3+ doped glass scintillator. - Highlights: • Ce 3+ doped gadolinium-calcium-silicaborate glass scintillators were developed. • Glass is easily fabricated with large sizes and various doping materials. • The luminescence properties are studied by using various radiation sources. • The light yield and decay time were measured at low temperature. • One decay time component is found.

  20. Luminescent Solar Concentrators – a low cost photovoltaics alternative

    NARCIS (Netherlands)

    Sark, W.G.J.H.M. van

    2013-01-01

    The development and current status of luminescent solar concentrators is reviewed. These solar concentrators generally consist of transparent polymer sheets doped with luminescent species; presently mainly organic dye molecules are used as luminescent species, however semiconductor nanocrystals

  1. Luminescence of LiH(D):Ru monocrystals

    International Nuclear Information System (INIS)

    Sabirzyanov, A.A.; Oparin, D.V.; Pilipenko, G.I.; Gavrilov, F.F.

    1993-01-01

    Luminescence of lithium hydride (deuteride) activated by ruthenium is recorded for the first time. The features connected with the structure and oscillations of the basic lattice are detected in luminescence spectrum. The qualitative model of luminescence spectrum is suggested

  2. Silica-modified luminescent LaPO4 :Eu@LaPO4 @SiO2 core/shell nanorods: Synthesis, structural and luminescent properties.

    Science.gov (United States)

    Ansari, Anees A

    2018-02-01

    Monoclinic-type tetragonal LaPO 4 :Eu (core) and LaPO 4 :Eu@LaPO 4 (core/shell) nanorods (NRs) were successfully prepared using a urea-based co-precipitation process under ambient conditions. An amorphous silica layer was coated around the luminescent core/shell NRs via the sol-gel process to improve their solubility and colloidal stability in aqueous and non-aqueous media. The prepared nano-products were systematically characterized by X-ray diffraction pattern, transmission electron microscopy, energy dispersive X-ray analysis, and FTIR, UV/Vis, and photoluminescence spectroscopy to examine their phase purity, crystal phase, surface chemistry, solubility and luminescence characteristics. The length and diameter of the nano-products were in the range 80-120 nm and 10-15 nm, respectively. High solubility of the silica-modified core/shell/Si NRs was found for the aqueous medium. The luminescent core NRs exhibited characteristic excitation and emission transitions in the visible region that were greatly affected by surface growth of insulating LaPO 4 and silica layers due to the multiphonon relaxation rate. Our luminescence spectral results clearly show a distinct difference in intensities for core, core/shell, and core/shell/Si NRs. Highly luminescent NRs with good solubility could be useful candidates for a variety of photonic-based biomedical applications. Copyright © 2017 John Wiley & Sons, Ltd.

  3. Poly(ethylene glycol)/carbon quantum dot composite solid films exhibiting intense and tunable blue–red emission

    International Nuclear Information System (INIS)

    Hao, Yanling; Gan, Zhixing; Xu, Jiaqing; Wu, Xinglong; Chu, Paul K.

    2014-01-01

    Highlights: • Poly(ethylene glycol)/carbon quantum dots (PEG/CQDs) composite solid films exhibiting strong and tunable blue–red emission were prepared. Successful preparation of tunable emitting CQDs solid films can extend the application of carbon quantum dots in photoelectric devices. • The mechanism of the tunable emission from the PEG/CQDs composite solid films was discussed. • On the basis of the characteristics of the PL from solid films in this work, the complex PL origins of CQDs were further defined. The PL mechanism provides insights into the fluorescence mechanism of CQDs and may promotes their applications. • Poly(ethylene glycol); carbon quantum dots; Strong and tunable blue-red emission; The fluorescent quantum yield of 12.6%. - Abstract: Although carbon quantum dots (CQDs) possess excellent luminescence properties, it is a challenge to apply water-soluble CQDs to tunable luminescent devices. Herein, quaternary CQDs are incorporated into poly(ethylene glycol) to produce poly(ethylene glycol)/CQD composite solid films which exhibit strong and tunable blue–red emission. The fluorescent quantum yield reaches 12.6% which is comparable to that of many liquid CQDs and the photoluminescence characteristics are determined to elucidate the fluorescence mechanism. The CQD solid films with tunable optical properties bode well for photoelectric devices especially displays

  4. Pure zinc sulfide quantum dot as highly selective luminescent probe for determination of hazardous cyanide ion

    Energy Technology Data Exchange (ETDEWEB)

    Shamsipur, Mojtaba, E-mail: mshamsipur@yahoo.com [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Rajabi, Hamid Reza, E-mail: h.rajabi@mail.yu.ac.ir [Chemistry Department, Yasouj University, Yasouj 75918-74831 (Iran, Islamic Republic of)

    2014-03-01

    A rapid and simple fluorescence method is presented for selective and sensitive determination of hazardous cyanide ion in aqueous solution based on functionalized zinc sulfide (ZnS) quantum dot (QD) as luminescent prob. The ultra-small ZnS QDs were synthesized using a chemical co-precipitation method in the presence of 2-mercaptoethanol (ME) as an efficient capping agent. The prepared pure ZnS QDs was applied as an optical sensor for determination of cyanide ions in aqueous solutions. ZnS nanoparticles have exhibited a strong fluorescent emission at about 424 nm. The fluorescence intensity of QDs is linearly proportional to the cyanide ion concentration in the range 2.44 × 10{sup −6} to 2.59 × 10{sup −5} M with a detection limit of 1.70 × 10{sup −7} M at pH 11. The designed fluorescent sensor possesses remarkable selectivity for cyanide ion over other anions such as Cl{sup −}, Br{sup −}, F{sup −}, I{sup −}, IO{sub 3}{sup −}, ClO{sub 4}{sup −}, BrO{sub 3}{sup −}, CO{sub 3}{sup 2−}, NO{sub 2}{sup −}, NO{sub 3}{sup −}, SO{sub 4}{sup 2−}, S{sub 2}O{sub 4}{sup 2−}, C{sub 2}O{sub 4}{sup 2−}, SCN{sup −}, N{sub 3}{sup −}, citrate and tartarate with negligible influences on the cyanide detection by fluorescence spectroscopy. - Highlights: • Preparation of functionalized ZnS quantum dots in aqueous media • Highly selective quantum dot based luminescent probe for determination of cyanide • Fast and sensitive determination of hazardous CN{sup −} by fluorescence quenching.

  5. Identifying irradiated flour by photo-stimulated luminescence technique

    International Nuclear Information System (INIS)

    Ros Anita Ahmad Ramli; Muhammad Samudi Yasir; Zainon Othman; Wan Saffiey Wan Abdullah

    2013-01-01

    Full-text: The photo-stimulated luminescence technique is recommended by European Committee for standardization for the detection food irradiation (EN 13751:2009). This study shows on luminescence technique to identify gamma irradiated five types of flour (corn flour, tapioca flour, wheat flour, glutinos rice flour and rice flour) at three difference dose levels in the range 0.2 - 1 kGy. The signal level is compare with two thresholds (700 and 5000). The majority of irradiated samples produce a strong signal above the upper threshold (5000 counts/ 60 s). All the control samples gave negative screening result while the signals below the lower threshold (700 counts/ 60s) suggest that the sample has not been irradiated. A few samples show the signal levels between the two thresholds (intermediate signals) suggest that further investigation. Reported procedure was also tested over 60 days, confirming the applicability and feasibility of proposed methods. (author)

  6. Material for a luminescent solar concentrator

    Science.gov (United States)

    Andrews, L.J.

    1984-01-01

    A material for use in a luminescent solar concentrator, formed by ceramitizing the luminescent ion Cr/sup 3 +/ with a transparent ceramic glass containing mullite. The resultant material has tiny Cr/sup 3 +/-bearing crystallites dispersed uniformly through an amorphous glass. The invention combines the high luminescent efficiency of Cr/sup 3 +/ in the crystalline phase with the practical and economical advantages of glass technology.

  7. Modern luminescence spectroscopy of minerals and materials

    CERN Document Server

    Gaft, Michael; Panczer, Gerard

    2005-01-01

    Luminescence Spectroscopy of Minerals and Materials presents an overview of the general concepts in luminescence spectroscopy as well as experimental methods and their interpretation. Special emphasis is laid on the fluorescence lifetime and the determination of time-resolved spectra. This method enables the exposure of new luminescence in minerals previously hidden by more intensive centers. Specialists in the fields of solid state physics, chemistry and spectroscopy will find a wealth of new information in this unique book.

  8. A portable luminescence dating instrument

    DEFF Research Database (Denmark)

    Kook, M.H.; Murray, A.S.; Lapp, Torben

    2011-01-01

    in both continuous wave and pulsed mode; photon counting can be gated such that it is active only during the pulse off-period. There are also two bleaching light sources (470nm, 5W and 940nm, 3W), and the luminescence signals can be regenerated using a cold-cathode 30kV X-ray tube, delivering ∼0.06Gy.s−1...

  9. Handbook of luminescent semiconductor materials

    CERN Document Server

    Bergman, Leah

    2011-01-01

    Photoluminescence spectroscopy is an important approach for examining the optical interactions in semiconductors and optical devices with the goal of gaining insight into material properties. With contributions from researchers at the forefront of this field, Handbook of Luminescent Semiconductor Materials explores the use of this technique to study semiconductor materials in a variety of applications, including solid-state lighting, solar energy conversion, optical devices, and biological imaging. After introducing basic semiconductor theory and photoluminescence principles, the book focuses

  10. Luminescence studies on phosphor screens

    International Nuclear Information System (INIS)

    Panayiotakis, G.; Nomikos, C.; Bakas, A.; Proimos, B.

    1994-01-01

    We report our results on x-ray phosphor screens prepared of some new materials focusing attention on their efficiency under fluoroscopy conditions, on optimization conditions and on comparisons among the various materials. All data are presented in absolute values. A theoretical model is presented, that takes into account the granular structure of the screens, permitting the explanation and prediction of the luminescence properties of the screens. (authors)

  11. Cherenkov luminescence measurements with digital silicon photomultipliers: a feasibility study

    Energy Technology Data Exchange (ETDEWEB)

    Ciarrocchi, Esther; Belcari, Nicola; Guerra, Alberto Del [Department of Physics, University of Pisa, Pisa (Italy); INFN, section of Pisa, Pisa (Italy); Cherry, Simon R. [Department of Biomedical Engineering, University of California, Davis, CA (United States); Lehnert, Adrienne; Hunter, William C. J.; McDougald, Wendy; Miyaoka, Robert S.; Kinahan, Paul E. [Department of Radiology, University of Washington, Seattle, WA (United States)

    2015-11-16

    A feasibility study was done to assess the capability of digital silicon photomultipliers to measure the Cherenkov luminescence emitted by a β source. Cherenkov luminescence imaging (CLI) is possible with a charge coupled device (CCD) based technology, but a stand-alone technique for quantitative activity measurements based on Cherenkov luminescence has not yet been developed. Silicon photomultipliers (SiPMs) are photon counting devices with a fast impulse response and can potentially be used to quantify β-emitting radiotracer distributions by CLI. In this study, a Philips digital photon counting (PDPC) silicon photomultiplier detector was evaluated for measuring Cherenkov luminescence. The PDPC detector is a matrix of avalanche photodiodes, which were read one at a time in a dark count map (DCM) measurement mode (much like a CCD). This reduces the device active area but allows the information from a single avalanche photodiode to be preserved, which is not possible with analog SiPMs. An algorithm to reject the noisiest photodiodes and to correct the measured count rate for the dark current was developed. The results show that, in DCM mode and at (10–13) °C, the PDPC has a dynamic response to different levels of Cherenkov luminescence emitted by a β source and transmitted through an opaque medium. This suggests the potential for this approach to provide quantitative activity measurements. Interestingly, the potential use of the PDPC in DCM mode for direct imaging of Cherenkov luminescence, as a opposed to a scalar measurement device, was also apparent. We showed that a PDPC tile in DCM mode is able to detect and image a β source through its Cherenkov radiation emission. The detector’s dynamic response to different levels of radiation suggests its potential quantitative capabilities, and the DCM mode allows imaging with a better spatial resolution than the conventional event-triggered mode. Finally, the same acquisition procedure and data processing could

  12. Luminescent Organic Semiconducting Langmuir Monolayers.

    Science.gov (United States)

    Agina, Elena V; Mannanov, Artur A; Sizov, Alexey S; Vechter, Olga; Borshchev, Oleg V; Bakirov, Artem V; Shcherbina, Maxim A; Chvalun, Sergei N; Konstantinov, Vladislav G; Bruevich, Vladimir V; Kozlov, Oleg V; Pshenichnikov, Maxim S; Paraschuk, Dmitry Yu; Ponomarenko, Sergei A

    2017-05-31

    In recent years, monolayer organic field-effect devices such as transistors and sensors have demonstrated their high potential. In contrast, monolayer electroluminescent organic field-effect devices are still in their infancy. One of the key challenges here is to create an organic material that self-organizes in a monolayer and combines efficient charge transport with luminescence. Herein, we report a novel organosilicon derivative of oligothiophene-phenylene dimer D2-Und-PTTP-TMS (D2, tetramethyldisiloxane; Und, undecylenic spacer; P, 1,4-phenylene; T, 2,5-thiophene; TMS, trimethylsilyl) that meets these requirements. The self-assembled Langmuir monolayers of the dimer were investigated by steady-state and time-resolved photoluminescence spectroscopy, atomic force microscopy, X-ray reflectometry, and grazing-incidence X-ray diffraction, and their semiconducting properties were evaluated in organic field-effect transistors. We found that the best uniform, fully covered, highly ordered monolayers were semiconducting. Thus, the ordered two-dimensional (2D) packing of conjugated organic molecules in the semiconducting Langmuir monolayer is compatible with its high-yield luminescence, so that 2D molecular aggregation per se does not preclude highly luminescent properties. Our findings pave the way to the rational design of functional materials for monolayer organic light-emitting transistors and other optoelectronic devices.

  13. Optical stimulated luminescence (OSL) dating

    International Nuclear Information System (INIS)

    Banerjee, D.

    1999-01-01

    Since the pioneering work by Huntley et al. (1985), optical dating is being increasingly recognised as an important technique for establishing a time frame of deposition of sediments (Aitken, 1998). Optical dating differs from thermoluminescence (TL) dating in that visible/infrared light from lasers or LEDs (light-emitting-diodes) is used as a means of stimulation, in contrast to thermal stimulation. It has several advantages over TL dating: (i) the resetting of the OSL (optically stimulated luminescence) clock is more effective than that of TL clock; for sediments transported under water or in other situations where the sediment grains have undergone inhomogeneous bleaching, this property ensures that ages based on optical dating are generally more reliable than TL ages, (ii) the optical dating technique is non-destructive, and multiple readouts of the optical signal is possible; this feature has resulted in the development of single-aliquot and single-grain protocols (Murray and Wintle, 1999; Banerjee et al. 1999), (iii) the sample is not heated as in TL; thus, spurious luminescence is avoided and there is a significant reduction in blackbody radiation. Dating of materials which change phase on heating is also practical, and finally, (iv) thermal quenching of luminescence is negligible, allowing accurate estimation of kinetic parameters using standard techniques and providing access to deep OSL traps. This characteristic may be helpful in extending the limits of optical dating beyond the last 150 ka from a global point of view

  14. Visible luminescence in polyaniline/(gold nanoparticle) composites

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Renata F. S. [Universidade Federal de Pernambuco, Pos-Graduacao em Ciencia de Materiais (Brazil); Andrade, Cesar A. S. [Universidade Federal de Pernambuco, Departamento de Bioquimica (Brazil); Santos, Clecio G. dos [Instituto de Educacao, Ciencia e Tecnologia de Pernambuco (Brazil); Melo, Celso P. de, E-mail: celso@df.ufpe.br [Universidade Federal de Pernambuco, Pos-Graduacao em Ciencia de Materiais (Brazil)

    2013-01-15

    We describe the use of solution chemistry methods to prepare polyaniline/(gold nanoparticles)-PANI/AuNPs-composites as colloidal particles that exhibit an intense green fluorescence after excitation in the ultraviolet region. Measurements of the relative fluorescence quantum yield indicate that the intensity of the observed luminescence of these nanocomposites is a few orders of magnitude higher than the corresponding fluorescence of either the isolated polymer or the pure AuNPs. Hence, cooperative effects between the conducting polymer chains and the metallic particles must dominate the emission behavior of these materials. Transmission electron microscopy reveals the existence of metal nanoparticle aggregates with sizes in the 2-3 nm range dispersed in the polymer matrix. By implementing an experimental planning, we have been able to change the preparation parameters so as to vary in a controlled manner the intensity and the profile of the luminescence spectrum as well as the size and aggregation characteristics of the colloidal particles. We also show that when the pH of the medium is varied, the dielectric properties (such as the degree of conductivity) of the PANI/AuNPs colloidal solutions and the intensity of their luminescence change in a consistent manner. Due to the polycation nature of the doped PANI chains, we suggest that these composites may find interesting applications as fluorescent markers of biologic molecules.

  15. Discuss on luminescence dose data analysis technology

    International Nuclear Information System (INIS)

    Ma Xinhua; Xiao Wuyun; Ai Xianyun; Shi Zhilan; Liu Ying

    2009-01-01

    This article describes the development of luminescence dose data measurement and processing technology. General design planning of luminescence dose data measurement and processing technology is put forward with the diverse demands. The emphasis is focused on dose data processing method, luminescence curve analysis method, using of network, mechanics of communication among computers, data base management system of individual dose in this paper. The main methods and skills used in this technology as well as their advantages are also discussed. And it offers general design references for development luminescence dose data processing software. (authors)

  16. Monitoring Delamination of Thermal Barrier Coatings During Interrupted High-Heat-Flux Laser Testing using Luminescence Imaging

    Science.gov (United States)

    Eldridge, Jeffrey I.; Zhu, Dongming; Wolfe, Douglas E.

    2011-01-01

    This presentation showed progress made in extending luminescence-base delamination monitoring to TBCs exposed to high heat fluxes, which is an environment that much better simulates actual turbine engine conditions. This was done by performing upconversion luminescence imaging during interruptions in laser testing, where a high-power CO2 laser was employed to create the desired heat flux. Upconverison luminescence refers to luminescence where the emission is at a higher energy (shorter wavelength) than the excitation. Since there will be negligible background emission at higher energies than the excitation, this methods produces superb contrast. Delamination contrast is produced because both the excitation and emission wavelengths are reflected at delamination cracks so that substantially higher luminescence intensity is observed in regions containing delamination cracks. Erbium was selected as the dopant for luminescence specifically because it exhibits upconversion luminescence. The high power CO2 10.6 micron wavelength laser facility at NASA GRC was used to produce the heat flux in combination with forced air backside cooling. Testing was performed at a lower (95 W/sq cm) and higher (125 W/sq cm) heat flux as well as furnace cycling at 1163C for comparison. The lower heat flux showed the same general behavior as furnace cycling, a gradual, "spotty" increase in luminescence associated with debond progression; however, a significant difference was a pronounced incubation period followed by acceleration delamination progression. These results indicate that extrapolating behavior from furnace cycling measurements will grossly overestimate remaining life under high heat flux conditions. The higher heat flux results were not only accelerated, but much different in character. Extreme bond coat rumpling occurred, and delamination propagation extended over much larger areas before precipitating macroscopic TBC failure. This indicates that under the higher heat flux (and

  17. Luminescent hybrid materials functionalized with lanthanide ethylenodiaminotetraacetate complexes containing β-diketonate as antenna ligands

    Energy Technology Data Exchange (ETDEWEB)

    Aguiar, Franklin P.; Costa, Israel F.; Espínola, José Geraldo P.; Faustino, Wagner M.; Moura, Jandeilson L. [Departamento de Química-Universidade Federal da Paraíba, 58051-970 João Pessoa, PB (Brazil); Brito, Hermi F.; Paolini, Tiago B. [Departamento de Química Fundamental-Instituto de Química da Universidade de São Paulo, 05508-900 São Paulo, SP (Brazil); Felinto, Maria Cláudia F.C. [Instituto de Pesquisas energéticas e Nucleares-IPEN, 05508-900 São Paulo, SP (Brazil); Teotonio, Ercules E.S., E-mail: teotonioees@quimica.ufpb.br [Departamento de Química-Universidade Federal da Paraíba, 58051-970 João Pessoa, PB (Brazil)

    2016-02-15

    Three organic–inorganic hybrid materials based on silica gel functionalized with (3-aminopropyl)trimethoxysilane (APTS), [3-(2-aminoetilamino)-propil]-trimetoxissilano (DAPTS) and 3-[2-(2-aminoetilamino)etilamino] propiltrimetoxysilane (TAPTS) and subsequently modified with EDTA derivative were prepared by nonhomogeneous route and were then characterized. The resulting materials named SilXN-EDTA (X=1 for APTS, 2 for DAPTS and 3 for TAPTS) were used to obtain new lanthanide Ln{sup 3+}-β-diketonate (Ln{sup 3+}=Eu{sup 3+}, Gd{sup 3+} and Tb{sup 3+}) complexes covalently linked to the functionalized silica gel surfaces (named SilXN-EDTALn-dik, dik=tta, dbm, bzac and acac). The photophysical properties of the new luminescent materials were investigated and compared with those with similar system presenting water molecules coordinated to the lanthanide ions, SilXN-EDTALn-H{sub 2}O. The SilXN-EDTAEu-dik and SilXN-EDTATb-dik systems displayed characteristic red and green luminescence when excited by UV radiation. Furthermore, the quantitative results showed that the emission quantum efficiency (η), experimental intensity parameters Ω{sub 2} and Ω{sub 4}, and Einstein's emission coefficient (A{sub 0J}) of the SilXN-EDTAEu-dik materials were largely dependent on the ligands. Based on the luminescence data, the most efficient intramolecular energy transfer processes were found to the SilXN-EDTAEu-dik (dik: tta and dbm) and SilXN-EDTATb-acac materials, which exhibited more pure emission colors. These materials are promising red and green phosphors, respectively. - Highlights: • New highly luminescent hybrid materials containing lanthanide-EDTA complexes. • The effect of three silylanting agent on the adsorption and luminescent properties has been studied. • The luminescence sensitizing by different β-diketonate ligands have been investigated.

  18. Highly luminescent Eu{sup 3+}-doped benzenetricarboxylate based materials

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Ivan G.N. [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil); Mustafa, Danilo, E-mail: dmustafa@iq.usp.br [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil); Andreoli, Bruno [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil); Felinto, Maria C.F.C. [Centro de Química do Meio Ambiente, Instituto de Pesquisas Energéticas e Nucleares, Av. Prof. Lineu Prestes 2242, São Paulo 05508-000, SP (Brazil); Malta, Oscar L. [Departamento de Química Fundamental, Universidade Federal de Pernambuco, Av. Prof. Moraes Rego, 1235, Recife 50670-90, PE (Brazil); Brito, Hermi F., E-mail: hefbrito@iq.usp.br [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil)

    2016-02-15

    [RE(TMA)] anhydrous complexes (RE{sup 3+}: Y, Gd and Lu) present high red emission intensity with a quantum efficiency (~45%) for the [Y(TMA):Eu{sup 3+}] complexes, due to the absence of non-radioactive decay pathways mediated by water molecules. The complexes were prepared in mild conditions. All the compounds are crystalline and thermostable up to 460 °C. Phosphorescence data of the complexes with Y, Gd and Lu show that the T{sub 1} state of the TMA{sup 3−} anion has energy higher than the {sup 5}D{sub 0} emitting level of the Eu{sup 3+} ion, indicating that the ligand can act as an intramolecular energy sensitizer. The photoluminescence properties of the doped materials were studied based on the excitation and emission spectra and luminescence decay curves. The experimental intensity parameters (Ω{sub λ}), lifetimes (τ), radiative (A{sub rad}) and non-radiative (A{sub nrad}) decay rates were determined and discussed. - Highlights: • Highly luminescent Europium doped anhydrous complexes. • Efficient monochromatic red light conversion molecular devices (LCMDs). • High emission quantum efficiencies.

  19. Cyto/hemocompatible magnetic hybrid nanoparticles (Ag2S-Fe3O4) with luminescence in the near-infrared region as promising theranostic materials.

    Science.gov (United States)

    Hocaoglu, Ibrahim; Asik, Didar; Ulusoy, Gulen; Grandfils, Christian; Ojea-Jimenez, Isaac; Rossi, François; Kiraz, Alper; Doğan, Nurcan; Acar, Havva Yagci

    2015-09-01

    Small hybrid nanoparticles composed of highly biocompatible Ag2S quantum dots (QD) emitting in the near-infrared region and superparamagnetic iron oxide (SPION) are produced in a simple extraction method utilizing ligand exchange mechanism. Hybrid nanoparticles luminesce at the same wavelength as the parent QD, therefore an array of hybrid nanoparticles with emission between 840 and 912nm were easily produced. Such hybrid structures have (1) strong luminescence in the medical imaging window eliminating the autofluoresence of cells as effective optical probes, (2) strong magnetic response for magnetic targeting and (3) good cyto/hemocompatibility. An interesting size dependent cytotoxicity behavior was observed in HeLa and NIH/3T3 cell lines: smallest particles are internalized significantly more by both of the cell lines, yet showed almost no significant cytotoxicity in HeLa between 10 and 25μg/mL Ag concentration but were most toxic in NIH/3T3 cells. Cell internalization and hence the cytotoxicity enhanced when cells were incubated with the hybrid nanoparticles under magnetic field, especially with the hybrid nanoparticles containing larger amounts of SPION in the hybrid composition. These results prove them as effective optical imaging agents and magnetic delivery vehicles. Combined with the known advantages of SPIONs as a contrast agent in MRI, these particles are a step forward for new theranostics for multimode imaging and magnetic targeting. Copyright © 2015 Elsevier B.V. All rights reserved.

  20. Luminescent and magnetic properties of Fe{sub 3}O{sub 4}@SiO{sub 2}:phen:Eu{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Raphael Lucas de Sousa; Figueiredo, Alberthmeiry Teixeira de; Barrado, Cristiano Morita, E-mail: alberth@ufg.br [Universidade Federal de Goiás (UFG), Catalão, GO (Brazil). Departamento de Química; Sousa, Marcelo Henrique [Universidade de Brasília (UnB), DF (Brazil). Faculdade de Ceilândia

    2017-10-15

    Magnetite was doped with rare earth ions (europium) to produce core-shell materials with both magnetic and luminescent properties, i.e., a magnetic Fe{sub 3}O{sub 4} oxide core and a SiO{sub 2} :phen:Eu{sup 3+} shell. The resulting material was analyzed by X-ray powder diffraction and transmission electron microscopy, and subjected to magnetic and luminescence emission measurements. All the synthesized materials exhibited superparamagnetic behavior and luminescence emission. The magnetic behavior of Fe{sub 3}O{sub 4} and luminescence emission of SiO{sub 2} :phen:Eu{sup 3+} of the materials were compared to precursors. (author)

  1. Size, shape, and composition of luminescent species in oxidized Si nanocrystals and H-passivated porous Si

    Science.gov (United States)

    Schuppler, S.; Friedman, S. L.; Marcus, M. A.; Adler, D. L.; Xie, Y.-H.; Ross, F. M.; Chabal, Y. J.; Harris, T. D.; Brus, L. E.; Brown, W. L.; Chaban, E. E.; Szajowski, P. F.; Christman, S. B.; Citrin, P. H.

    1995-08-01

    Near-edge and extended x-ray-absorption fine-structure measurements from a wide variety of oxidized Si nanocrystals and H-passivated porous Si samples, combined with electron microscopy, ir absorption, forward recoil scattering, and luminescence emission data, provide a consistent structural picture of the species responsible for the luminescence observed in these systems. For porous Si samples whose luminescence wavelengths peak in the visible region, i.e., at <700 nm, their mass-weighted-average structures are determined here to be particles (not wires) whose short-range character is crystalline and whose dimensions-typically <15 Å-are significantly smaller than previously reported or proposed. Results are also presented which demonstrate that the observed visible luminescence is not related to either a photo-oxidized Si species in porous Si or an interfacial suboxide species in the Si nanocrystals. The structural and compositional findings reported here depend only on sample luminescence behavior, not on how the luminescent particles are produced, and thus have general implications in assigning quantum confinement as the mechanism responsible for the visible luminescence observed in both nanocrystalline and porous silicon.

  2. Redox reactions and mechanism of luminescence in BaFCl:Eu

    CERN Document Server

    Upadeo, S V; Gundurao, T K

    1998-01-01

    The phenomenon of stimulable luminescence of phosphors pre-irradiated with high-energy radiation is widely used in the field of imaging. Phosphors such as BaFX:Eu (X = Cl, Br) are extensively used in x-ray screens for digital image processing. There is, however, divided opinion regarding the mechanism responsible for the luminescence process in these materials. In this paper we have discussed the role of Eu sup 3 sup +reversible Eu sup 2 sup + conversion in BaFCl:Eu phosphor using PL, TL, TL emission and ESR techniques. (author)

  3. Radiation-induced luminescence from dry and hydrated DNA and related macromolecules

    International Nuclear Information System (INIS)

    Al-Kazwini, A.T.; O'Neill, P.; Fielden, E.M.; Adams, G.E.

    1988-01-01

    The radiation-induced luminescence from three types of fibrous DNA and a series of polydeoxynucleotides was measured under vacuum or in the presence of oxygen at 77 and 293K. The in-pulse emission spectra, generated by electrons with energies 50% water by wt (1.2:1 w/w, H 2 O/DNA), the in-pulse luminescence spectrum is similar to that of dry DNA. These findings are discussed in terms of energy or charge migration induced in DNA upon irradiation and the possible effects of conformational changes, caused by hydration, on charge migration. (author)

  4. Chiral nematic mesoporous films of ZrO₂:Eu³⁺: new luminescent materials.

    Science.gov (United States)

    Chu, Guang; Feng, Jing; Wang, Yu; Zhang, Xiao; Xu, Yan; Zhang, Hongjie

    2014-11-07

    Integration of luminescent rare earth ions and iridescence into a zirconium oxide photonic material is attractive for the design of new optical devices. The free-standing chiral nematic mesoporous films of ZrO2:Eu(3+) are assembled by a hard-templating approach using nanocrystalline cellulose-templated silica. The ZrO2:Eu(3+) films show tunable optical properties. The chiral nematic structured ZrO2:Eu(3+) exhibits selective suppression of the spontaneous emission of Eu(3+) and the capability to modulate the lifetime of luminescent Eu(3+).

  5. Electrodynamics of a hydrogenlike atom in a strong electromagnetic field

    International Nuclear Information System (INIS)

    Kovarskij, V.A.; Perel'man, N.F.

    1974-01-01

    The quasienergy spectrum of the hydrogen atom in strong electromagnetic radiation is studied, the luminescence of the atom under these conditions is considered. It is shown that in a strong field the atom, being even in the ground state, radiates a spectrum of frequencies corresponding to transitions from the ground state into excited states, the strong field photons being involved. The intensity of such a luminescence is basically a non-linear function of the strong field. The exposure of the atom to two strong electromagnetic fields Ω and ω (Ω>>ω) is considered, the Ω coinciding with one of the natural frquencies of the atom. The effct of modulation of the resonance shift for an atomic level by the ω-field strength is predicted. The dependence of Ω-absorption in the ω-field on the statistic properties of the latter is investigated. (author)

  6. Sol-gel Synthesis and Upconversion Luminescent Properties of Yb3+,Er3+,Eu3+Triply-Doped in YVO4Phosphors.

    Science.gov (United States)

    Cheng, Yuan; Sun, Kangning

    2018-01-01

    Yb 3+ ,Er 3+ ,Eu 3+ triply-doped in YVO 4 with varying molar ratio of Er/Eu were synthesized in a sol-gel method with a subsequent heat treatment for the first time. The optimal molar ratio of Er/Eu for the maximum energy transfer efficiency was 1/39. After molar ratio, the influences of different heat treatment temperatures were also researched and the maximal heat temperature was 1300 °C. Besides, the properties of YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ upconversion phosphors were investigated by X-ray diffraction, scanning electron microscopy and photo luminescent spectra, respectively. In sum, XRD results indicate the crystal structure of as-prepared samples, which is the tetragonal phase of YVO 4 with no other diffraction peaks. SEM images show the morphology of as-prepared samples, which are granular-like nanoparticles. PL spectra demonstrate the upconversion luminescence of as-prepared samples, which emit strong green lights (at 525 nm, 550 nm) and slight red lights (at 590 nm, 615 nm, 695 nm) under the NIR irradiation at 980 nm. Two strong green emissions are attributed to the 2 H 11/2 → 4 I 15/2 and 4 S 3/2 → 4 I 15/2 transitions of Er 3+ ions. Meanwhile, three slight red emissions are attributed to the 5 D 0 → 7 F 1 , 5 D 0 → 7 F 2 and 5 D 0 → 7 F 4 transitions of Eu 3+ ions. All in all, the colorful emissions endow YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ phosphors great potential for some applications, such as display devices, bio-labeling and infrared detection.

  7. The Effect of Magnetic Fields on the Quorum Sensing-Regulated Luminescence of Vibrio fischeri

    Science.gov (United States)

    Barron, Addie; Hagen, Steve; Son, Minjun

    2015-03-01

    Quorum sensing (QS) is a mechanism by which bacteria communicate through the secretion and detection of extracellular signaling molecules known as autoinducers. This research focuses on the quorum sensing regulated bioluminescence of Vibrio fischeri, a marine bacterium that lives in symbiosis with certain fish and squid species. Previous studies of V. harveyi, a close relative of V. fisheri, indicate that a strong magnetic field has a positive effect on V.harveyi bioluminescence. However the effect of magnetic fields on quorum sensing-regulated luminescence is in general poorly understood. We grew V. fischeri in solid and liquid growth media, subject to strong static magnetic fields, and imaged the bioluminescence over a period of forty-eight hours. Luminescence patterns were analyzed in both the spatial and time dimensions. We find no indication that a magnetic field influences Vibrio fischeri luminescence either positively or negatively. This research was funded by the Grant Number NSF DMR-1156737.

  8. Thermoluminescence, luminescence optically stimulated and creation of defects in alkaline halogenides contaminated with Europium

    International Nuclear Information System (INIS)

    Barboza F, M.

    1999-01-01

    The alkaline halogenides have been subject matter of investigations related with the search of sensor materials for X-ray bidimensional images or optical memories. The understanding of the damage formation processes generated by ionizing and non-ionizing radiations is important for the correct design of devices that working as detectors and dosemeters of both type of radiations. In this work we present the investigation results related with the defects produced by the ionizing radiation type X and ultraviolet light in the range of 200-360 nm in crystals of KCl: Eu 2+ and KBr:Eu 2+ . It is examined the thermoluminescence and luminescence spectra with the purpose of identifying the exciton processes, owing to the excitation of the halogenide ions in which the primary defects correspond to the F and H centers. It has been found that the 400-600 nm emission is associated with the luminescence type that in his turn can be associated with autotrapped excitons perturbed by the impurity. On the other hand, it is examined the emission spectra of the luminescence optically stimulated in crystals of KBr: Eu 2+ and KCl: Eu 2+ finding too that such materials would be used as optical memories susceptible of to store information, and through of photostimulation to read this. It was determined that the F centers participate in the luminescence optically stimulated in these crystals, as well as too in the recombination processes responsible by the thermoluminescent emission. (Author)

  9. Analysis of emission of Eu3+ and Dy3+ doped Magnesium Boro-Tellurite (MBT ceramics

    Directory of Open Access Journals (Sweden)

    Bohari Nur Zu Ira

    2015-03-01

    Full Text Available Rare earth (RE ions play an important role in the improvement of the optical properties of ceramics. Rare-earth ceramics are commonly used in display panels, fluorescent lamps and lasers. The luminescence properties of Magnesium Boro-Tellurite (MBT Eu3+ and Dy3+ doped ceramics have not been reported before. Therefore, the aim of this paper is to determine the effect of different compositions on the luminescence properties of the MBT material. A series of xTeO2-(70-xB2O3-30MgO ceramics with 10 ≤ x ≤ 40 mol % doped with 1 mol % of Eu3+ and Dy3+ ions was prepared via the solid-state reaction method. The influence of various compositions on the crystalline phase and photoluminescence properties of the samples were investigated by X-ray diffraction (XRD and luminescence spectroscopy. The crystalline phases obtained in this study are Mg3(BO32, MgB4O7, Mg2B2O5, Mg(Te2O5 and MgTe3O6. It was stated that the crystalline phases have not changed as a result of doping with Eu3+ and Dy3+ ions. The emission spectra of Eu3+: MBT ceramics showed strong red emission at 612 nm due to the transition of 5D0 → 7F2 and meanwhile, the Dy3+: MBT ceramics showed a blue emission at 480 nm due to 4F9/2 → 6H15/2 transition and yellow emission at 576 nm due to 4F9/2→6H13/2 transition. Both the rare-earth doped phosphors showed bright emission.

  10. A novel approach to prepare optically active ion doped luminescent materials via electron beam evaporation into ionic liquids.

    Science.gov (United States)

    Richter, K; Lorbeer, C; Mudring, A-V

    2015-01-04

    A novel approach to prepare luminescent materials via electron-beam evaporation into ionic liquids is presented which even allows doping of host lattices with ions that have a strong size mismatch. To prove this, MgF2 nanoparticles doped with Eu(3+) were fabricated. The obtained nanoparticles featured an unusually high luminescence lifetime and the obtained material showed a high potential for application.

  11. Broadened band C-telecom and intense upconversion emission of Er{sup 3+}/Yb{sup 3+} co-doped CaYAlO{sub 4} luminescent material obtained by an easy route

    Energy Technology Data Exchange (ETDEWEB)

    Perrella, R.V.; Schiavon, M.A. [Grupo de Pesquisa em Química de Materiais – (GPQM), Departamento de Ciências Naturais, Universidade Federal de São João del Rei (UFSJ), Campus Dom Bosco, Praça Dom Helvécio, 74, 36301-160 São João del Rei, MG (Brazil); Pecoraro, E.; Ribeiro, S.J.L. [UNESP, Institute of Chemistry, P.O. Box 355, 14800-970 Araraquara, SP (Brazil); Ferrari, J.L., E-mail: ferrari@ufsj.edu.br [Grupo de Pesquisa em Química de Materiais – (GPQM), Departamento de Ciências Naturais, Universidade Federal de São João del Rei (UFSJ), Campus Dom Bosco, Praça Dom Helvécio, 74, 36301-160 São João del Rei, MG (Brazil)

    2016-10-15

    This work reports on photoluminescence properties of Er{sup 3+}/Yb{sup 3+} co-doped CaYAlO{sub 4} in powder form, synthesized by an easy route using citric acid as ligand to form complex precursor. The 1.2 mol% of Yb{sup 3+} was fixed, while the amount of Er{sup 3+} changed in 0.5, 1.5 and 3 mol% in order to evaluate the photoluminescence properties as a function of the Er{sup 3+} concentration. The structural and thermal properties of the viscous solutions and powder materials obtained after the heat-treatment at 1000, 1100 and 1200 °C for 4 h were evaluated by XRD, FTIR and TG/DTA analysis. The results showed the formation of pure CaYAlO{sub 4} tetragonal crystalline phase after heat-treatment at 1100 °C and 1200 °C. Intense emission in the visible region under excitation at 980 nm was attributed to upconversion process, from Er{sup 3+} intra-configurational f–f transitions. The emissions were assigned to the transitions {sup 2}H{sub 11/2}→{sup 4}I{sub 15/2} and {sup 4}S{sub 3/2}→{sup 4}I{sub 15/2} (green region), and {sup 4}F{sub 9/2}→{sup 4}I{sub 15/2} (red region) energy levels. The ratio between emission band integrated areas assigned to the red and green emissions increased as a function of Er{sup 3+} concentration. Under excitation at 980 nm with 100 mW of power pump, the materials also showed intense and broadening emission with maximum at 1520 nm with FWHM of 84.74 nm for the sample CaYAlO{sub 4}:1.5% Er{sup 3+}/1.2% Yb{sup 3+} heat-treated at 1000 °C for 4 h. The photoluminescence properties showed that these materials are promising for use in C-telecom band as optical amplifier biological marker or/and solid-state laser devices under excitation at 980 nm.

  12. Facile hydrothermal synthesis and luminescent properties of Sm3+/Eu3+ codoped GdPO4 phosphors

    Science.gov (United States)

    Yang, Junfeng; Xiong, Hailong; Dong, Jianchao; Yang, Chunming; Gan, Shucai; Zou, Lianchun

    2017-12-01

    Well-defined GdPO4 nanocrystals were successfully prepared through the facile hydrothermal synthesis route followed by a heat treatment. The microstructure, morphologies and photoluminescence properties of as-prepared samples were investigated via X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), fourier transform infrared spectroscopy (FT-IR), photoluminescence (PL) spectroscopy and luminescence decay, which were significantly affected by the reaction conditions (phosphorus source, acidity of hydrothermal process and surfactants). It is found that Sodium dodecyl sulfate (SDS) as a shape modifier has the dynamic effect by adjusting the growth rate of different facets, resulting in morphology transformation of GdPO4·H2O from the nanowire (without SDS) to the nanorod (with SDS). Strong yellow-orange emissions could be obtained in Sm3+ and Eu3+ ions codoped GdPO4 phosphors under ultraviolet light irradiation. Moreover, the energy transfer mechanism from Sm3+ to Eu3+ has been studied and proved to be a dipole-dipole interaction mechanism. These results show this yellow-orange-emitting phosphors material may have potential applications in field-emission displays.

  13. Luminescence resonance energy transfer-based nucleic acid hybridization assay on cellulose paper with upconverting phosphor as donors.

    Science.gov (United States)

    Zhou, Feng; Noor, M Omair; Krull, Ulrich J

    2014-03-04

    A bioassay based on DNA hybridization on cellulose paper is a promising format for gene fragment detection that may be suited for in-field and rapid diagnostic applications. We demonstrate for the first time that luminescence resonance energy transfer (LRET) associated with upconverting phosphors (UCPs) can be used to develop a paper-based DNA hybridization assay with high sensitivity, selectivity and fast response. UCPs with strong green emission were synthesized and subsequently functionalized with streptavidin (UCP-strep). UCP-strep particles were immobilized on cellulose paper, and then biotinylated single-stranded oligonucleotide probes were conjugated onto the UCPs via streptavidin-biotin linkage. The UCPs served as donors that were LRET-paired with Cy3-labeled target DNA. Selective DNA hybridization enabled the proximity required for LRET-sensitized emission from Cy3, which was used as the detection signal. Hybridization was complete within 2 min, and the limit of detection of the method was 34 fmol, which is a significant improvement in comparison to an analogous fluorescence resonance energy transfer (FRET) assay based on quantum dots. The assay exhibited excellent resistance to nonspecific adsorption of noncomplementary short/long DNA and protein. The selectivity of the assay was further evaluated by one base pair mismatched (1BPM) DNA detection, where a maximum signal ratio of 3.1:1 was achieved between fully complementary and 1BPM samples. This work represents a preliminary but significant step for the development of paper-based UCP-LRET nucleic acid hybridization assays, which offer potential for lowering the limit of detection of luminescent hybridization assays due to the negligible background signal associated with optical excitation by near-infrared (NIR) light.

  14. How do marine bacteria produce light, why are they luminescent, and can we employ bacterial bioluminescence in aquatic biotechnology?

    Directory of Open Access Journals (Sweden)

    Grzegorz Wêgrzyn

    2002-09-01

    Full Text Available Bioluminescence, the phenomenon of light production by living organisms, occurs in forms of life as various as bacteria, fungi and animals. Nevertheless, light-emitting bacteria are the most abundant and widespread of luminescent organisms. Interestingly, most species of such bacteria live in marine environments. In this article, the biochemical mechanism of bacterial luminescence and its genetic regulation are summarized. Although the biochemistry and genetics of light emission by cells have been investigated in detail, the biological role of bacterial luminescence has remained obscure. Here, we discuss recent discoveries that shed new light on this problem. Finally, we provide examples of how bacterial luminescence can be employed in marine biotechnology, especially in the detection of toxic and mutagenic pollution in aquatic environments.

  15. Light-emitting conjugated polymers with microporous network architecture: interweaving scaffold promotes electronic conjugation, facilitates exciton migration, and improves luminescence.

    Science.gov (United States)

    Xu, Yanhong; Chen, Long; Guo, Zhaoqi; Nagai, Atsushi; Jiang, Donglin

    2011-11-09

    Herein we report a strategy for the design of highly luminescent conjugated polymers by restricting rotation of the polymer building blocks through a microporous network architecture. We demonstrate this concept using tetraphenylethene (TPE) as a building block to construct a light-emitting conjugated microporous polymer. The interlocked network successfully restricted the rotation of the phenyl units, which are the major cause of fluorescence deactivation in TPE, thus providing intrinsic luminescence activity for the polymers. We show positive "CMP effects" that the network promotes π-conjugation, facilitates exciton migration, and improves luminescence activity. Although the monomer and linear polymer analogue in solvents are nonemissive, the network polymers are highly luminescent in various solvents and the solid state. Because emission losses due to rotation are ubiquitous among small chromophores, this strategy can be generalized for the de novo design of light-emitting materials by integrating the chromophores into an interlocked network architecture.

  16. Synthesis of zinc oxide microrods and nano-fibers with dominant exciton emission at room temperature

    Energy Technology Data Exchange (ETDEWEB)

    Ramos-Brito, F., E-mail: fro_brito@yahoo.com.m [Laboratorio de Materiales Optoelectronicos del Centro de Ciencias de Sinaloa, Ave. de las Americas 2771 Col. Villa Universidad 80010, Culiacan, Sinaloa (Mexico); Alejo-Armenta, C. [Laboratorio de Materiales Optoelectronicos del Centro de Ciencias de Sinaloa, Ave. de las Americas 2771 Col. Villa Universidad 80010, Culiacan, Sinaloa (Mexico); Garcia-Hipolito, M. [Departamento de Materiales Metalicos y Ceramicos, Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, AP 70-360, Coyoacan 04510, DF (Mexico); Camarillo, E.; Hernandez A, J. [Instituto de Fisica, Universidad Nacional Autonoma de Mexico, AP 20-364, Alvaro Obregon 01000, DF (Mexico); Falcony, C. [Departamento de Fisica, CINVESTAV-IPN, AP 14-740, 07000, DF (Mexico); Murrieta S, H. [Instituto de Fisica, Universidad Nacional Autonoma de Mexico, AP 20-364, Alvaro Obregon 01000, DF (Mexico)

    2011-05-15

    Employing a simple chemical synthesis method, hexagonal-shaped zinc oxide microrods and zinc oxide nano-fibers were deposited on pyrex-glass and aluminum substrates, respectively. Both kinds of deposits showed zincite crystalline phase with lattice parameters: a=3.2498 A and c=5.2066 A. Microrods showed very uniform wide and large sizes of around 1 and 10 {mu}m, respectively. Both deposits were homogeneous over all substrate surfaces. Microrods and nano-fibers resulted with good optical quality and with preferential crystalline growth in [1 0 1 0]and [0 0 0 1]directions. The principal optical characteristics for both microrods and nano-fibers were: a) room-temperature photo and cathodo-luminescent spectra with strong exciton emission centered around 390 nm and with FWHMs around 125 and 160 meV, respectively, b) poor photo and cathode-luminescent emissions in the visible region of the electromagnetic spectrum, c) energy band gap of 3.32 eV, d) good emission efficiency supported by the not-required high energy densities to obtain strong exciton emission and e) good ZnO stoichiometry endorsed by photoluminescent results. These characteristics make of these microrods and nano-fibers good for potential photonic applications. - Research highlights: {yields} Microrods and nano-fibers resulted with good optical quality and with preferential crystalline growth in [1 0 1 0]and [0 0 0 1]directions. {yields} Microrods and nano-fibers resulted with good emission efficiency supported by the not-required high energy densities to obtain strong exciton emission. {yields} The wet chemical method is appropriated for deposition of microrods and nano-fibers with the desired optical properties for its possible application in photonics.

  17. Synthesis of zinc oxide microrods and nano-fibers with dominant exciton emission at room temperature

    International Nuclear Information System (INIS)

    Ramos-Brito, F.; Alejo-Armenta, C.; Garcia-Hipolito, M.; Camarillo, E.; Hernandez A, J.; Falcony, C.; Murrieta S, H.

    2011-01-01

    Employing a simple chemical synthesis method, hexagonal-shaped zinc oxide microrods and zinc oxide nano-fibers were deposited on pyrex-glass and aluminum substrates, respectively. Both kinds of deposits showed zincite crystalline phase with lattice parameters: a=3.2498 A and c=5.2066 A. Microrods showed very uniform wide and large sizes of around 1 and 10 μm, respectively. Both deposits were homogeneous over all substrate surfaces. Microrods and nano-fibers resulted with good optical quality and with preferential crystalline growth in [1 0 1 0] and [0 0 0 1] directions. The principal optical characteristics for both microrods and nano-fibers were: a) room-temperature photo and cathodo-luminescent spectra with strong exciton emission centered around 390 nm and with FWHMs around 125 and 160 meV, respectively, b) poor photo and cathode-luminescent emissions in the visible region of the electromagnetic spectrum, c) energy band gap of 3.32 eV, d) good emission efficiency supported by the not-required high energy densities to obtain strong exciton emission and e) good ZnO stoichiometry endorsed by photoluminescent results. These characteristics make of these microrods and nano-fibers good for potential photonic applications. - Research highlights: → Microrods and nano-fibers resulted with good optical quality and with preferential crystalline growth in [1 0 1 0] and [0 0 0 1] directions. → Microrods and nano-fibers resulted with good emission efficiency supported by the not-required high energy densities to obtain strong exciton emission. → The wet chemical method is appropriated for deposition of microrods and nano-fibers with the desired optical properties for its possible application in photonics.

  18. Violet stimulated luminescence: geo- or thermochronometer?

    DEFF Research Database (Denmark)

    Ankjærgaard, Christina; Guralnik, Benny; Porat, N.

    2015-01-01

    The method of quartz optically stimulated luminescence (OSL) dating is widely used, but generally limited to the past ~0.1 million years (Ma) due to early saturation of the desired signal. Violet stimulated luminescence (VSL) of quartz has previously been shown as a promising alternative...

  19. Receptor-Targeted Luminescent Silver Bionanoparticles

    NARCIS (Netherlands)

    Bunschoten, Anton; Chin, Patrick T.K.; Buckle, Tessa; Linden, van der Marte; Barendregt, Arjan; Verheijen, Marcel A.; Leeuwen, van Fijs W.B.

    2016-01-01

    Luminescent Ag nanoclusters (Ag-NC) provide the next generation in bionanoparticles, wherein the luminescence (650 nm) and large Stokes shift of these inorganic nanoclusters are favorable for biological imaging. By combining these characteristics with those of human serum albumin (HSA; a protein

  20. Luminescence investigation of novel MgPbAl₁₀O₁₇:Tb³⁺ green-emitting phosphor for solid-state lighting.

    Science.gov (United States)

    Panse, V R; Kokode, N S; Dhoble, S J; Yerpude, A N

    2016-05-01

    In this work, we studied the luminescence properties of Tb(3+)-doped MgPbAl10O17 green phosphor. To understand the excitation mechanism and corresponding emission of the prepared phosphor, its structural, morphological and photoluminescence properties were investigated. In general, for green emission, Tb(3) is used as an activator and the obtained excitation and emission spectra indicated that this phosphor can be effectively excited by a wavelength of 380 nm, and exhibits bright green emission centered at 545 nm corresponding to the f → f transition of trivalent terbium ions. The chromaticity coordinates were (C(x) = 0.263, C(y) = 0.723). The impact of Tb(3+) concentration on the relative emission intensity was investigated, and the best doping concentration was found to be 2 mol%. This study suggests that Tb(3+)-doped MgPbAl10O17 phosphor is a strong candidate for a green component in phosphor-converted white light-emitting diodes. Copyright © 2015 John Wiley & Sons, Ltd.

  1. Ultrafast spectral interferometry of resonant secondary emission from quantum wells: From Rayleigh scattering to coherent emission from biexcitons

    DEFF Research Database (Denmark)

    Birkedal, Dan; Shah, Jagdeep; Pfeiffer, L. N.

    1999-01-01

    Recent investigations of secondary emission from quantum well excitons following ultrafast resonant excitation have demonstrated an intricate interplay of coherent Rayleigh scattering and incoherent luminescence. We have very recently demonstrated that it is possible to isolate and time resolve t...

  2. Determination of uranium in sea and ocean waters by a luminescence method with laser excitation

    International Nuclear Information System (INIS)

    Preobrazhenskaya, E.B.; Gvgel, E.S.; Stepanov, A.V.

    1986-01-01

    This paper shows that it is possible to determine uranium insea and ocean waters by a luminescence method with laser excitation. Ocean waters with a low content of luminescent ingredients are analyzed directly by freezing at 77 K to eliminate the quenching effect of the chloride ion. The more polluted waters of inland seas are preferably analyzed at T = 293 K in 1 M H 3 PO 4 after the removal of chloride ions by distillation from a sample containing HNO 3 . The background effect is removed by time selection of the luminescent emission of the uranyl ion. Uranium contents were determined for water from the northwest Atlantic and the North and Baltic Seas

  3. The luminescence properties of the octahedral uranate group in oxides with perovskite structure, ch. 3

    International Nuclear Information System (INIS)

    Hair, J.Th.W. de

    1976-01-01

    This chapter describes how the luminescence properties of the octahedral uranate group are influenced by the chemical constitution of its environment. Especially the quenching temperature of the emission is very sensitive. It is stronger influenced by the nature of the neighbouring B cations in the [100] direction than by the A cations in the [111] direction. This variation of the quenching temperature as a function of the chemical constitution of the host lattice is discussed in terms of a configurational coordinate model. The luminescence properties of uranium-activated oxides A 2+ La 3+ B + B'O 6 are also discussed. Remarkably enough in SrLaNaWO 6 -U the luminescence originates from UO 2 2+ groups. (Auth.)

  4. Optically stimulated luminescence of natural NaCl mineral from Dead Sea exposed to gamma radiation

    Energy Technology Data Exchange (ETDEWEB)

    Roman L, J.; Cruz Z, E. [UNAM, Instituto de Ciencias Nucleares, Ciudad Universitaria, 04510 Ciudad de Mexico (Mexico); Pina L, Y. I. [UNAM, Facultad de Ciencias, Ciudad Universitaria, 04510 Ciudad de Mexico (Mexico); Marcazzo, J., E-mail: jesus.roman@nucleares.unam.mx [Instituto de Fisica Arroyo Seco - UNICEN, Pinto 399, 7000 Tandil (Argentina)

    2016-10-15

    Luminescence properties such as radioluminescence, thermoluminescence and optically stimulated luminescence have been studied on natural sodium chloride (NaCl) for dosimetric purposes in retrospective dosimetry (Timar-Gabor et al., 2013; Druzhyna et al., 2016). In this work, the optically stimulated luminescence (Cw-OSL) emissions of natural salt minerals, collected from Dead Sea in summer of 2015, were studied. The Cw-OSL dose response of natural salt was analyzed in the range between 0.2 and 10 Gy gamma dose of {sup 60}Co. Samples exposed at 3 Gy exhibited good repeatability with a variation coefficient of 4.6%. The thermal stability of the Cw-OSL response was analyzed to different temperatures from 50 up to 250 degrees Celsius using a heating rate of 5 degrees Celsius. The results showed that the natural Dead Sea salt minerals could be applied as natural dosimeter of gamma radiation. (Author)

  5. The first example of intensive luminescence of LMCT state based on metal complexes in solution

    International Nuclear Information System (INIS)

    Lukova, G.V.; Vasil'ev, V.P.; Smirnov, V.A.; Huhn, W.

    2007-01-01

    A bridge complex rac-C 6 H 10 (IndH 4 ) 2 ZrC 2 , featuring a unique long-living luminescence in liquid solutions at 20 deg C, has been prepared for the first time by catalytic hydrogenation of bis-indinyl complex C 6 H 10 (Ind) 2 Zr 2 Cl 2 . It has been identified that quantum yields of luminescence of the complex solutions at room temperature are the greatest ones for the known compounds possessing emission states of charge transfer from ligand to metal. Linear correlations of quantum yield of metal complex luminescence in a solution with steric features of the solvent molecules have been detected for the first time [ru

  6. Electron traps in irradiated alkaline glasses at 77 K studied by stimulated luminescence

    International Nuclear Information System (INIS)

    Truong, T.B.

    1977-01-01

    The results of stimulated luminescence studies at 77 0 K on photoionized tryptophan or tyrosine in alkaline ices or on γ-irradiated alkaline ices reveal that (1) the luminescence emission results from neutralization of bleached electrons with parent cations whose concentration is much more dilute (10 -5 --10 -3 M) than that of the alkaline ions (10M); (2) spatial heterogeneous distribution of OH - exists prior to irradiation in alkaline ices. There are zones where OH - concentration is higher than in others; (3) complementary to the optical absorption and ESR techniques, the stimulated luminescence method can serve to identify negative species other than solvated electrons stabilized in alkaline ices, namely, H - and possibly O/sup

  7. Novel luminescent soft materials of terpyridine-containing ionic liquids and europium(III).

    Science.gov (United States)

    Wang, Dongyue; Wang, Huifang; Li, Huanrong

    2013-07-10

    Herein, we describe novel luminescent soft materials via reaction of Eu(3+)-coordinated carboxyl functionalized ionic liquids with terpyridine-functionalized imidazolium salts that are built from an imidazolium ring substituted on one side with a terpyridine derivative and, on the opposite side, a paraffin chain of various lengths. The obtained materials are either pastelike substances or viscous fluids, depending on the anions of the carboxyl functionalized ionic liquids. The soft luminescent materials were investigated by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetry (TG), and luminescence spectroscopy. The soft materials show bright red emission irradiated with UV light, because of the energy transfer from terpyridine-functionalized imidazolium salts to the Eu(3+) ions. The absolute quantum yields of the materials were determined and the energy transfer efficiency was estimated according to the reported method.

  8. Europium incorporated in silica matrix obtained by sol-gel: luminescent materials

    Directory of Open Access Journals (Sweden)

    Nassar Eduardo José

    2003-01-01

    Full Text Available In this work we report some aspects of the chemistry involved in the preparation of modified silicon oxide by the sol-gel process. Europium III compounds were used as luminescent probe. An organic-inorganic hybrid was obtained by hydrolysis of tetraethylorthosilicate (TEOS and 3-aminopropyltriethoxysilane (APTS. The Eu III compounds were added in different ways. In the first, silica was prepared in the presence of Eu III, and in the second, Eu III was added on the silica surface. These materials were studied by luminescence, infrared spectroscopy and termogravimetric analysis. The results obtained for the hybrid material show different behavior for Eu III emission, which could be excited by the antenna effect and the influence of the surrounding in the luminescence quenching. The thermogravimetric data present different mass loss in samples to range temperature 50 - 150 °C. Thermogravimetric and infrared spectra showed that inorganic polymers incorporated the organic part.

  9. Optically stimulated luminescence of natural NaCl mineral from Dead Sea exposed to gamma radiation

    International Nuclear Information System (INIS)

    Roman L, J.; Cruz Z, E.; Pina L, Y. I.; Marcazzo, J.

    2016-10-01

    Luminescence properties such as radioluminescence, thermoluminescence and optically stimulated luminescence have been studied on natural sodium chloride (NaCl) for dosimetric purposes in retrospective dosimetry (Timar-Gabor et al., 2013; Druzhyna et al., 2016). In this work, the optically stimulated luminescence (Cw-OSL) emissions of natural salt minerals, collected from Dead Sea in summer of 2015, were studied. The Cw-OSL dose response of natural salt was analyzed in the range between 0.2 and 10 Gy gamma dose of 60 Co. Samples exposed at 3 Gy exhibited good repeatability with a variation coefficient of 4.6%. The thermal stability of the Cw-OSL response was analyzed to different temperatures from 50 up to 250 degrees Celsius using a heating rate of 5 degrees Celsius. The results showed that the natural Dead Sea salt minerals could be applied as natural dosimeter of gamma radiation. (Author)

  10. A Eu/Tb-mixed MOF for luminescent high-temperature sensing

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Huizhen; Zhao, Dian; Cui, Yuangjing, E-mail: cuiyj@zju.edu.cn; Yang, Yu; Qian, Guodong, E-mail: gdqian@zju.edu.cn

    2017-02-15

    Temperature measurements and thermal mapping using luminescent MOF operating in the high-temperature range are of great interest in the micro-electronic diagnosis. In this paper, we report a thermostable Eu/Tb-mixed MOF Eu{sub 0.37}Tb{sub 0.63}-BTC-a exhibiting strong luminescence at elevated temperature, which can serve as a ratiometric luminescent thermometer for high-temperature range. The high-temperature operating range (313–473 K), high relative sensitivity and accurate temperature resolution, make such a Eu/Tb-mixed MOF useful for micro-electronic diagnosis. - Graphical abstract: A thermostable Eu/Tb-mixed MOF Eu{sub 0.37}Tb{sub 0.63}-BTC-a was developed as a ratiometric luminescent thermometers in the high-temperature range of 313–473 K. - Highlights: • A thermostable Eu/Tb-codoped MOF exhibiting strong luminescent at elevated temperature is reported. • The high-temperature operating range of Eu{sub 0.37}Tb{sub 0.63}-BTC-a is 313–473 K. • The mechanism of Eu{sub 0.37}Tb{sub 0.63}-BTC-a used as thermometers are also discussed.

  11. An alkaline one-pot reaction to synthesize luminescent Eu-BTC MOF nanorods, highly pure and water-insoluble, under room conditions

    Energy Technology Data Exchange (ETDEWEB)

    Medina-Velazquez, D. Y., E-mail: dyolotzin@correo.azc.uam.mx; Alejandre-Zuniga, B. Y.; Loera-Serna, S.; Ortiz, E. M. [Universidad Autónoma Metropolitana-Azcapotzalco, División de Ciencias Básicas e Ingeniería (Mexico); Morales-Ramirez, A. de J. [CIITEC IPN, Instituto Politécnico Nacional (Mexico); Garfias-Garcia, E. [Universidad Autónoma Metropolitana-Azcapotzalco, División de Ciencias Básicas e Ingeniería (Mexico); Garcia-Murillo, A. [CIITEC IPN, Instituto Politécnico Nacional (Mexico); Falcony, C. [Centro de Investigación y Estudios Avanzados, Departamento de Física (Mexico)

    2016-12-15

    The increasing demand for optoelectronic devices requires the development of luminescent materials with high luminescence efficiency and low energy demands, and the metalorganic frameworks (MOFs) with lanthanides ions offer great potential in this area. The metalorganic materials provide properties of flexibility, low density, low-cost methods of synthesis, and insolubility in water, which gives them an advantage over traditional phosphors. In this study, a benzenetricarboxylate ligand (BTC) with a Eu{sup 3+} MOF was synthesized, and its structural and luminescent properties were measured. The metalorganic compound was generated in a one-pot reaction from europium nitrate and trimesic acid precursors. Through characterization by X-ray diffraction powder, infrared spectroscopy, SEM structural characterization, and luminescent spectroscopy, the formation of Europium benzenetricarboxylate (Eu-BTC) MOF nanorods was tested and the calculated value was in the range of 30–60 nm. A red luminescent emission with high intensity was observed for all the procedures.

  12. Luminescence detection of irradiated foods

    International Nuclear Information System (INIS)

    Sanderson, D.C.W.

    1990-01-01

    The need for forensic tests to identify irradiated foods has been widely recognised at a time of growing international trade in such products and impending changes in UK and EEC legislation to control the process. This paper outlines the requirements for and of such tests, and discusses recent developments in luminescence approaches aimed at meeting the needs of public analysts, retailers and consumers. Detecting whether or not food has been irradiated, and if so to what dose, is one of the challenges which food irradiation poses to the scientist. (author)

  13. Luminescence Properties of ScPO{sub 4} Single Crystals

    Energy Technology Data Exchange (ETDEWEB)

    Boatner, L.A.; Trukhin, A.N.

    1999-08-16

    Flux-grown ScPO{sub 4} single crystals exhibit a number of luminescence bands in their x-ray-excited luminescence spectra - including sharp lines arising from rare-earth elements plus a number of broad bands at 5.6 cV, 4.4 eV, and 3 eV. The band at 5.6 eV was attributed to a self-trapped exciton (STE) [l], and it could be excited at 7 eV and higher energies. This luminescence is strongly polarized (P = 70 %) along the optical axes of the crystal and exhibits a kinetic decay time constant that varies from several ns at room temperature to {approximately}10 {micro}s at 60 K and up to {approximately}1 ms at 10 K. It is assumed that the STE is localized on the SC ions. The band at 3 eV can be excited in the range of the ScPO{sub 4} crystal transparency (decay time = 3 to 4 {micro}s.) This band is attributed to a lead impurity that creates different luminescence centers. At high temperatures, the band at 4.4 eV is dominant in the x-ray-excited TSL and afterglow spectra. Its intensity increases with irradiation time beginning at zero at the initial irradiation time. The 4.4 eV band does not appear in a fast process under a pulsed electron beam, showing that accumulation is necessary for its observation. A sample of ScPO{sub 4} doped with vanadium exhibited a prevalent band at 4.4 eV at T = 480 K.

  14. Near infrared and upconversion luminescence behaviour of Er3+/Yb3+ codoped boro-tellurite glasses

    Science.gov (United States)

    Maheshvaran, K.; Arunkumar, S.; Vijayakumar, R.; Marimuthu, K.

    2014-04-01

    The broadband NIR and upconversion luminescence behavior in a new series of Er3+/Yb3+ codoped TeO2-B2O3-SrO-BaO-Li2O-LiF glasses have been studied exciting at a wavelength of 980 nm using semiconductor laser. A broadband emission is observed from 1450 to 1650 nm with a full width at half maximum (FWHM) around 165 nm in 0.5wt% Yb3+ ion content E0.5YLTB glass. The radiative parameters such as transition probability (A), stimulated emission cross-section (σE), experimental and calculated branching ratios (βR), optical gain width (σp×FWHM) and radiative lifetime (τcal) have been calculated for the 4I13/2→4I15/2 NIR emission. Upconversion luminescence spectra of the prepared glasses have been studied and the ESA & ET processes have also been discussed and reported.

  15. Sensitization effects of supramolecular assemblies on the luminescence of terbium-ion prulifloxacin complexes

    Energy Technology Data Exchange (ETDEWEB)

    Wang Hong; Yi Chongyue; Li Xue; Fang Fang [School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Yang Yajiang, E-mail: yjyang@mail.hust.edu.c [School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2011-04-15

    Luminescence enhancement of terbium-ion prulifloxacin complexes (Tb(III)-PUFX) in supramolecular hydrogels formed by assembly of 1,3:2,4-di-O-benzylidene-D-sorbitol (DBS) was investigated by steady-state fluorescence, varying temperature fluorescence and time-resolved fluorescence. The luminescence images show that Tb(III)-PUFX were dispersed in the DBS gels. The luminescence intensity of Tb(III)-PUFX in the DBS gels was significantly increased in comparison with that in corresponding aqueous solutions. The varying temperature fluorescent spectra show that the luminescence intensity of Tb(III)-PUFX decreased with an increase in the temperature. This implies that the luminescence enhancement of Tb(III)-PUFX is related to the dissociation and the formation of the DBS assemblies. Time-resolved fluorescence measurements show slower rotational motion in DBS gels in comparison with that in the corresponding aqueous solutions. This may be ascribed to a unique microstructure of three-dimensional network formed by DBC aggregates, resulting in deactivation of the nonradiative relaxation. The images of field emission scanning electron microscopy and polarized optical microscopy indicate that the morphology of the DBS assemblies was not influenced upon addition of Tb(III)-PUFX to the DBS gels.

  16. Highly Water-Stable Lanthanide-Oxalate MOFs with Remarkable Proton Conductivity and Tunable Luminescence.

    Science.gov (United States)

    Zhang, Kun; Xie, Xiaoji; Li, Hongyu; Gao, Jiaxin; Nie, Li; Pan, Yue; Xie, Juan; Tian, Dan; Liu, Wenlong; Fan, Quli; Su, Haiquan; Huang, Ling; Huang, Wei

    2017-09-01

    Although proton conductors derived from metal-organic frameworks (MOFs) are highly anticipated for various applications including solid-state electrolytes, H 2 sensors, and ammonia synthesis, they are facing serious challenges such as poor water stability, fastidious working conditions, and low proton conductivity. Herein, we report two lanthanide-oxalate MOFs that are highly water stable, with so far the highest room-temperature proton conductivity (3.42 × 10 -3 S cm -1 ) under 100% relative humidity (RH) among lanthanide-based MOFs and, most importantly, luminescent. Moreover, the simultaneous response of both the proton conductivity and luminescence intensity to RH allows the linkage of proton conductivity with luminescence intensity. This way, the electric signal of proton conductivity variation versus RH will be readily translated to optical signal of luminescence intensity, which can be directly visualized by the naked eye. If proper lanthanide ions or even transition-metal ions are used, the working wavelengths of luminescence emissions can be further extended from visible to near infrared light for even wider-range applications. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Simulation of Eu3+ luminescence spectra of borosilicate glasses by molecular dynamics calculations

    International Nuclear Information System (INIS)

    De Bonfils, J.; Panczer, G.; De Ligny, D.; Champagnon, B.; Peuget, S.; Delaye, J. M.; Chaussedent, S.; Monteil, A.

    2008-01-01

    Simplified inactive rare-earths doped nuclear waste glasses have been obtained by molecular dynamics (MD) simulation in order to investigate the local structure around the rare-earth by luminescence studies. MD calculations were performed with modified Born-Mayer-Huggins potentials and three body angular terms representing Coulomb and covalent interactions. Atomic positions within the glasses are then determined. Simulations of luminescence spectra were then obtained by calculation of the ligand field parameters affecting each luminescent ion. Considering the C 2v symmetry, it is possible to calculate the radiative transition probabilities between the emitter level, 5 D o , and the splitted receptor levels, 7 F J (J=0-3) for each Eu 3+ ion. The simulated emission spectra are obtained by convolution of all the Eu 3+ ions contributions. A comparison with the experimental data issue from fluorescence line narrowing and micro-luminescence spectroscopies allowed us not only to validate the simulation of luminescence spectra from simulated environments, but also to confirm the presence and the identification of two major Eu 3+ sites distribution in the nuclear glasses thanks to spectra-structure correlations. (authors)

  18. Luminescence of the SrCl2:Pr crystals under high-energy excitation

    International Nuclear Information System (INIS)

    Antonyak, O.T.; Voloshinovskii, A.S.; Vistovskyy, V.V.; Stryganyuk, G.B.; Kregel, O.P.

    2014-01-01

    The present research was carried out in order to elucidate the mechanisms of energy transfer from the crystal lattice to Pr 3+ ions in SrCl 2 . The luminescence excitation and emission spectra as well as luminescence kinetics of the SrCl 2 :Pr single crystals containing 0.2 mol% Pr were investigated at 300 and 10 K using the vacuum ultraviolet (VUV) synchrotron radiation. The X-ray excited luminescence spectra of the SrCl 2 :Pr (C Pr =0.2 and 0.5 mol%) and SrCl 2 :Pr, K (C Pr =1.5 mol%; C K =1.5 mol%) crystals were studied at 294 and 80 K. Under optical excitation of the samples in the Pr 3+ absorption bands, there were observed five fast ultraviolet emissions assigned to the 4f 1 5d→4f 2 transitions, and two long-wave bands corresponding to the f–f transitions. Furthermore, the intrinsic emission bands of SrCl 2 were observed at 10 K. The X-ray excited luminescence spectrum of the SrCl 2 :Pr crystal containing 0.2 mol% Pr, besides intrinsic emission band near 400 nm, has got a long-wave band at about 490 nm of the Pr 3+ centers. There were not observed any emission bands of the Pr 3+ centers corresponding to the 4f 1 5d–4f 2 transitions in the X-ray excited luminescence spectrum of the SrCl 2 :Pr crystal. The possible mechanisms of energy transfer from the SrCl 2 matrix to the Pr 3+ centers are discussed. -- Highlights: • Spectral-luminescent properties of SrCl 2 :Pr have been investigated. • The identification of emission 4f–4f and 5d–4f bands of Pr 3+ ions was performed. • Adding of potassium prevents clustering of the Pr 3+ centers in the SrCl 2 :Pr, K crystals. • Under X-ray excitation at 80–300 K only Pr 3+ 4f–4f and intrinsic emission is observed

  19. Spectroscopic investigation on europium doped heavy metal borate glasses for red luminescent application

    Energy Technology Data Exchange (ETDEWEB)

    Hegde, Vinod; Wagh, Akshatha; Kamath, Sudha D. [Manipal University, Department of Physics, Manipal Institute of Technology, Manipal (India); Hegde, Hemanth [Manipal University, Department of Chemistry, Manipal Institute of Technology, Manipal (India); Vishwanath, C.S.D. [Sri Venkateswara University, Department of Physics, Tirupati (India)

    2017-05-15

    The present study explores a new borate family glasses based on 10ZnO-5Na{sub 2}O-10Bi{sub 2}O{sub 3}-(75 - x) B{sub 2}O{sub 3}-xEu{sub 2}O{sub 3} (x = 0, 0.1, 0.5, 1, 1.5, 2, 3 mol%) composition, synthesized by rapid melt quench technique. Prepared glasses were subjected to the density and refractive index measurements and their values were used to calculate other physical properties of the glass matrix as a function of Eu{sup 3+} concentration. XRD confirmed amorphous nature of the glasses. FTIR spectra in the absorption mode were recorded in the 400-4000 cm{sup -1} region to identify different functional groups in the glass matrix. Deconvoluted FTIR spectra showed increase in BO{sub 4} units with rise in europium content which confirmed the 'network strengthener' role of europium ions by creating bridging oxygens (BOs). Optical properties were investigated for their luminescence behavior through various spectroscopic techniques such as UV-Vis-NIR absorption, excitation, emission, decay profiles, and color measurements at room temperature. Lasing properties of the glasses like total radiative life time, branching ratio, emission cross section, and optical gain were obtained from the calculated Judd-Ofelt (Ω{sub 2},Ω{sub 4}) intensity parameters. From the measured values of emission, cross sections, branching ratios, life times, strong photoluminescence features, and CIE chromaticity coordinates, 0.5 mol% of Eu{sup 3+} ions doped ZnNaBiB glasses showed optimum performance and are potential candidate for red light generation at 613 nm. (orig.)

  20. Spectroscopic investigation on europium doped heavy metal borate glasses for red luminescent application

    Science.gov (United States)

    Hegde, Vinod; Wagh, Akshatha; Hegde, Hemanth; Vishwanath, C. S. Dwaraka; Kamath, Sudha D.

    2017-05-01

    The present study explores a new borate family glasses based on 10ZnO-5Na2O-10Bi2O3-(75 - x) B2O3- xEu2O3 ( x = 0, 0.1, 0.5, 1, 1.5, 2, 3 mol%) composition, synthesized by rapid melt quench technique. Prepared glasses were subjected to the density and refractive index measurements and their values were used to calculate other physical properties of the glass matrix as a function of Eu3+ concentration. XRD confirmed amorphous nature of the glasses. FTIR spectra in the absorption mode were recorded in the 400-4000 cm-1 region to identify different functional groups in the glass matrix. Deconvoluted FTIR spectra showed increase in BO4 units with rise in europium content which confirmed the `network strengthener' role of europium ions by creating bridging oxygens (BOs). Optical properties were investigated for their luminescence behavior through various spectroscopic techniques such as UV-Vis-NIR absorption, excitation, emission, decay profiles, and color measurements at room temperature. Lasing properties of the glasses like total radiative life time, branching ratio, emission cross section, and optical gain were obtained from the calculated Judd-Ofelt (Ω2,Ω4) intensity parameters. From the measured values of emission, cross sections, branching ratios, life times, strong photoluminescence features, and CIE chromaticity coordinates, 0.5 mol% of Eu3+ ions doped ZnNaBiB glasses showed optimum performance and are potential candidate for red light generation at 613 nm.

  1. Luminescent lanthanide complexes with 4-acetamidobenzoate: Synthesis, supramolecular assembly via hydrogen bonds, crystal structures and photoluminescence

    International Nuclear Information System (INIS)

    Yin Xia; Fan Jun; Wang Zhihong; Zheng Shengrun; Tan Jingbo; Zhang Weiguang

    2011-01-01

    Four new luminescent complexes, namely, [Eu(aba) 2 (NO 3 )(C 2 H 5 OH) 2 ] (1), [Eu(aba) 3 (H 2 O) 2 ].0.5 (4, 4'-bpy).2H 2 O (2), [Eu 2 (aba) 4 (2, 2'-bpy) 2 (NO 3 ) 2 ].4H 2 O (3) and [Tb 2 (aba) 4 (phen) 2 (NO 3 ) 2 ].2C 2 H 5 OH (4) were obtained by treating Ln(NO 3 ) 3 .6H 2 O and 4-acetamidobenzoic acid (Haba) with different coligands (4, 4'-bpy=4, 4'-bipyridine, 2, 2'-bpy=2, 2'-bipyridine, and phen=1, 10-phenanthroline). They exhibit 1D chains (1-2) and dimeric structures (3-4), respectively. This structural variation is mainly attributed to the change of coligands and various coordination modes of aba molecules. Moreover, the coordination units are further connected via hydrogen bonds to form 2D even 3D supramolecular networks. These complexes show characteristic emissions in the visible region at room temperature. In addition, thermal behaviors of four complexes have been investigated under air atmosphere. The relationship between the structures and physical properties has been discussed. - Graphical abstract: Structure variation of four complexes is attributed to the change of coligands and various coordination modes of aba molecules. Moreover, they show characteristic emissions in the visible region. Highlights: → Auxiliary ligands have played the crucial roles on the structures of the resulting complexes. → Isolated structure units are further assembled via H-bonds to form supramolecular networks. → These solid-state complexes exhibit strong, characteristic emissions in the visible region.

  2. Cerenkov luminescence imaging of medical isotopes.

    Science.gov (United States)

    Ruggiero, Alessandro; Holland, Jason P; Lewis, Jason S; Grimm, Jan

    2010-07-01

    The development of novel multimodality imaging agents and techniques represents the current frontier of research in the field of medical imaging science. However, the combination of nuclear tomography with optical techniques has yet to be established. Here, we report the use of the inherent optical emissions from the decay of radiopharmaceuticals for Cerenkov luminescence imaging (CLI) of tumors in vivo and correlate the results with those obtained from concordant immuno-PET studies. In vitro phantom studies were used to validate the visible light emission observed from a range of radionuclides including the positron emitters (18)F, (64)Cu, (89)Zr, and (124)I; beta-emitter (131)I; and alpha-particle emitter (225)Ac for potential use in CLI. The novel radiolabeled monoclonal antibody (89)Zr-desferrioxamine B [DFO]-J591 for immuno-PET of prostate-specific membrane antigen (PSMA) expression was used to coregister and correlate the CLI signal observed with the immuno-PET images and biodistribution studies. Phantom studies confirmed that Cerenkov radiation can be observed from a range of positron-, beta-, and alpha-emitting radionuclides using standard optical imaging devices. The change in light emission intensity versus time was concordant with radionuclide decay and was also found to correlate linearly with both the activity concentration and the measured PET signal (percentage injected dose per gram). In vivo studies conducted in male severe combined immune deficient mice bearing PSMA-positive, subcutaneous LNCaP tumors demonstrated that tumor-specific uptake of (89)Zr-DFO-J591 could be visualized by both immuno-PET and CLI. Optical and immuno-PET signal intensities were found to increase over time from 24 to 96 h, and biodistribution studies were found to correlate well with both imaging modalities. These studies represent the first, to our knowledge, quantitative assessment of CLI for measuring radiotracer uptake in vivo. Many radionuclides common to both nuclear

  3. Luminescence of vanadium and rare earth ions in alkaline earth sulfates

    NARCIS (Netherlands)

    Blasse, G.; Pietersen, H.G.

    2006-01-01

    The luminescence of samples MeSO4---V, RE (Me = Mg, Ca, Ba) depends strongly on the nature of the Me ions. The amount of association of the V5+ and RE3+ ions can be estimated from the measured quantum efficiencies

  4. Functional silk: colored and luminescent.

    Science.gov (United States)

    Tansil, Natalia C; Koh, Leng Duei; Han, Ming-Yong

    2012-03-15

    Silkworm silk is among the most widely used natural fibers for textile and biomedical applications due to its extraordinary mechanical properties and superior biocompatibility. A number of physical and chemical processes have also been developed to reconstruct silk into various forms or to artificially produce silk-like materials. In addition to the direct use and the delicate replication of silk's natural structure and properties, there is a growing interest to introduce more new functionalities into silk while maintaining its advantageous intrinsic properties. In this review we assess various methods and their merits to produce functional silk, specifically those with color and luminescence, through post-processing steps as well as biological approaches. There is a highlight on intrinsically colored and luminescent silk produced directly from silkworms for a wide range of applications, and a discussion on the suitable molecular properties for being incorporated effectively into silk while it is being produced in the silk gland. With these understanding, a new generation of silk containing various functional materials (e.g., drugs, antibiotics and stimuli-sensitive dyes) would be produced for novel applications such as cancer therapy with controlled release feature, wound dressing with monitoring/sensing feature, tissue engineering scaffolds with antibacterial, anticoagulant or anti-inflammatory feature, and many others. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Skin Friction Measurements Using Luminescent Oil Films

    Science.gov (United States)

    Husen, Nicholas M.

    As aircraft are designed to a greater extent on computers, the need for accurate and fast CFD algorithms has never been greater. The development of CFD algorithms requires experimental data against which CFD output can be validated and from which insight about flow physics can be acquired. Skin friction, in particular, is an important quantity to predict with CFD, and experimental skin friction data sets aid not only with the validation of the CFD predictions, but also in tuning the CFD models to predict specific flow fields. However, a practical experimental technique for collecting spatially and temporally resolved skin friction data on complex models does not yet exist. This dissertation develops and demonstrates a new luminescent oil film skin friction meter which can produce spatially-resolved quantitative steady and unsteady skin friction data on models with complex curvature. The skin friction acting on the surface of a thin film of oil can be approximated by the expression tauw =mu ouh/h, where mu o is the dynamic viscosity of the oil, uh is the velocity of the surface of the oil film, and h is the thickness of the oil film. The new skin friction meter determines skin friction by measuring h and uh. The oil film thickness h is determined by ratioing the intensity of the fluorescent emissions from the oil film with the intensity of the incident light which is scattered from the surface of the model. When properly calibrated, that ratio provides an absolute oil film thickness value. This oil film thickness meter is therefore referred as the Ratioed-Image Film-Thickness (RIFT) Meter. The oil film velocity uh is determined by monitoring the evolution of tagged molecules within the oil film: Photochromic molecules are dissolved into the fluorescent oil and a pattern is written into the oil film using an ultraviolet laser. The evolution of the pattern is recorded, and standard cross-correlation techniques are applied to the resulting sequence of images. This

  6. Ion beam induced luminescence on white inorganic pigments for paintings

    International Nuclear Information System (INIS)

    Quaranta, A.; Dran, J.C.; Salomon, J.; Tonezzer, M.; Scian, C.; Beck, L.; Carturan, S.; Maggioni, G.; Della Mea, G.

    2008-01-01

    Ion beam induced luminescence (IBIL) has been used for studying the emission features and the radiation hardness of white pigments. In particular, ZnO, gypsum and basic lead sulphate pigments have been analyzed with a 3.0 MeV H + beam at the AGLAE Louvre laboratory. The same pigments mixed with different binders have been also analyzed on a canvas, in order to evaluate the contribution of the binders both to the IBIL spectra and to the radiation hardness. It turns out that the binder affects both the IBIL spectra and the radiation hardness of pigments when the emission bands are related to point defects, as occurs for ZnO

  7. Responsive hybrid inorganic-organic system derived from lanthanide luminescence

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Zhan [School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); Zheng, Yuhui, E-mail: yhzheng78@scnu.edu.cn [School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); Jiang, Lasheng; Yang, Jinglian [School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); Wang, Qianming, E-mail: qmwang@scnu.edu.cn [Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); Guangzhou Key Laboratory of Materials for Energy Conversion and Storage, Guangzhou 510006 (China)

    2016-05-15

    Highlights: • A novel covalent hybrid material was used to detect hemoglobin. • All the recognition experiments were performed in buffer solution. • Porous nano-structures was extensively studied for the recognition. - Abstract: Terbium ions were incorporated into new organic-inorganic matrices to achieve intense green emissions. Hemoglobin (HB) interactions lead to dramatic changes in the luminescence emission intensities. Infrared spectra, morphological studies and photoluminescence give information for the speciation and process of hemoglobin additions. The porous material has a large specific surface area of 351 cm{sup 2}/g and the detection limit for HB (0.7 μM) was much lower than its physical doped material (8 μM). This promising hybrid material will lead to the design of versatile optical probes that are efficiently responding to the external targets.

  8. Temperature dependence of fluorescence decay time and emission spectrum of bismuth germanate

    International Nuclear Information System (INIS)

    Melcher, C.L.; Liberman, A.; Schweitzer, J.S.; Simonetti, J.

    1985-01-01

    Bismuth germanate has become an increasingly popular replacement for NaI(Tl) scintillators in recent years, mainly due to its higher detection efficiency. However, its scintillation efficiency and fluorescence decay time are strongly temperature dependent. Optimum performance of detector systems which employ BGO crystals depends on knowledge of the BGO pulse shape and intensity and its emission spectrum at the operating temperature of the detector. Measurements of these quantities are presented over the temperature range -47 0 C to +111 0 C. Although the emission spectrum shifts only slightly over this temperature range, the scintillation efficiency and fluorescence decay time are strongly temperature dependent. In addition to the usefulness of these data for optimizing detector design, the results imply that luminescence quenching in BGO cannot be characterized by a single thermal activation to a radiationless transition but that a more complex model is required to characterize the light output from BGO crystals

  9. Structural and luminescence effects of Ga co-doping on Ce-doped yttrium aluminate based phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Ayvacikli, M. [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Canimoglu, A. [Nigde University, Faculty of Arts and Sciences, Physics Department, Nigde (Turkey); Muresan, L.E., E-mail: laura_muresan2003@yahoo.com [Babes Bolyai University, Raluca Ripan Institute for Research in Chemistry, Fantanele 30, 400294 Cluj-Napoca (Romania); Barbu Tudoran, L. [Babes Bolyai University, Electronic Microscopy Centre, Clinicilor 37, 400006 Cluj Napoca (Romania); Garcia Guinea, J. [Museo Nacional Ciencias Naturales, Jose Gutierrez Abascal 2, Madrid 28006 (Spain); Karabulut, Y. [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Jorge, A. [Museo Nacional Ciencias Naturales, Jose Gutierrez Abascal 2, Madrid 28006 (Spain); Karali, T. [Ege University, Institute of Nuclear Sciences, 35100 Bornova, İzmir (Turkey); Can, N., E-mail: cannurdogan@yahoo.com [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Jazan University, Physics Department, P.O. Box 114, 45142 Jazan (Saudi Arabia)

    2016-05-05

    Herein, we primarily focus on luminescence spectrum measurements of various types of green emitting yttrium aluminate phosphors modified with gallium (Y{sub 3}Al{sub 5-x}Ga{sub x}O{sub 12}) synthesised by solid state reaction. The luminescent emission of samples depends on sample temperature and excitation radiation such as incident X-ray, electron and laser beam. Here, we measured radioluminescence (RL), cathodoluminescence (CL), photoluminescence (PL) along with XRD in order to clarify relationship between lattice defects and the spectral luminescence emissions. The RL and CL spectra of YAG:Ce exhibit an emission band ranging from 300 to 450 nm related to Y{sub Al} antisite defects. The broad emission band of garnet phosphors is shifted from 526 nm to 498 nm with increasing of Ga{sup 3+} content, while full width at half maximum (FWHM) of the band tends to be greater than the width of unmodified YAG:Ce garnet. Deconvolution of the spectrum reveals that three emission bands centred at 139, 234 and 294 °C occur in aluminate host garnets. - Highlights: • We present preparation of YAG:Ce{sup 3+}, Ga{sup 3+} phosphors by a solid state reaction method. • The shape and size of phosphor particles were investigated. • The luminescence properties were studied by different excitation sources.

  10. Luminescence Properties of Self-Aggregating TbIII-DOTA-Functionalized Calix[4]arenes

    Directory of Open Access Journals (Sweden)

    Florian Mayer

    2018-01-01

    Full Text Available Self-aggregating calix[4]arenes carrying four DOTA ligands on the upper rim for stable complexation of paramagnetic GdIII-ions have already been proposed as MRI probes. In this work, we investigate the luminescence properties of TbIII-DOTA-calix[4]arene-4OPr containing four propyl-groups and compare them with those of the analog substituted with a phthalimide chromophore (TbIII-DOTA-calix[4]arene-3OPr-OPhth. We show that, given its four aromatic rings, the calix[4]arene core acts as an effective sensitizer of Tb-centered luminescence. Substituents on the lower rim can modulate the aggregation behavior, which in turn determines the luminescence properties of the compounds. In solid state, the quantum yield of the phthalimide derivative is almost three times as high as that of the propyl-functionalized analog demonstrating a beneficial role of the chromophore on Tb-luminescence. In solution, however, the effect of the phthalimide group vanishes, which we attribute to the large distance between the chromophore and the lanthanide, situated on the opposite rims of the calix[4]arene. Both quantum yields and luminescence lifetimes show clear concentration dependence in solution, related to the strong impact of aggregation on the luminescence behavior. We also evidence the variability in the values of the critical micelle concentration depending on the experimental technique. Such luminescent calix[4]arene platforms accommodating stable lanthanide complexes can be considered valuable building blocks for the design of dual MR/optical imaging probes.

  11. Luminescence Properties of Self-Aggregating TbIII-DOTA-Functionalized Calix[4]arenes

    Science.gov (United States)

    Mayer, Florian; Tiruvadi Krishnan, Sriram; Schühle, Daniel T.; Eliseeva, Svetlana V.; Petoud, Stéphane; Tóth, Éva; Djanashvili, Kristina

    2018-01-01

    Self-aggregating calix[4]arenes carrying four DOTA ligands on the upper rim for stable complexation of paramagnetic GdIII-ions have already been proposed as MRI probes. In this work, we investigate the luminescence properties of TbIII-DOTA-calix[4]arene-4OPr containing four propyl-groups and compare them with those of the analog substituted with a phthalimide chromophore (TbIII-DOTA-calix[4]arene-3OPr-OPhth). We show that, given its four aromatic rings, the calix[4]arene core acts as an effective sensitizer of Tb-centered luminescence. Substituents on the lower rim can modulate the aggregation behavior, which in turn determines the luminescence properties of the compounds. In solid state, the quantum yield of the phthalimide derivative is almost three times as high as that of the propyl-functionalized analog demonstrating a beneficial role of the chromophore on Tb-luminescence. In solution, however, the effect of the phthalimide group vanishes, which we attribute to the large distance between the chromophore and the lanthanide, situated on the opposite rims of the calix[4]arene. Both quantum yields and luminescence lifetimes show clear concentration dependence in solution, related to the strong impact of aggregation on the luminescence behavior. We also evidence the variability in the values of the critical micelle concentration depending on the experimental technique. Such luminescent calix[4]arene platforms accommodating stable lanthanide complexes can be considered valuable building blocks for the design of dual MR/optical imaging probes. PMID:29441345

  12. Synthesis and luminescent properties of a novel green-emitting Tb (Ⅲ) complex based on amino-modified fluorine silicone oil and isophorone diisocyanate

    Science.gov (United States)

    Hao, Haixia; Chu, Yang; Yu, Zhenjiang; Xie, Hongde; Seo, Hyo Jin

    2017-10-01

    The novel luminescent polymer-rare earth complexes, denoted as (PFSi-IPDI)-Tb(Ⅲ)-Phen, have been successfully synthesized and can be made into flexible films. Amino-modified fluorine silicone oil-isophorone diisocyanate (PFSi-IPDI) was used as the host macromolecular ligand, and 1, 10-Phenanthroline (Phen) as the secondary small-molecular co-ligand. The luminescent lanthanide complexes were characterized by fourier transform infrared (FITR), scanning electron microscope (SEM), thermogravimetric analysis (TGA). The luminescent properties were investigated through photoluminescence excitation (PLE) and emission (PL) spectroscopy. FTIR analysis verifies the successful preparation and integration of PFSi-IPDI to Tb3+. The comparatively uniform morphological structure can be observed in the images of SEM. The polymer-rare earth complexes display the typical luminescence emission peaks under the excitation wavelength of 330 nm. From the decay curve, the short lifetime (about 0.89 ms) is observed for (PFSi-IPDI)-Tb(Ⅲ)-Phen (0.6 mol/L). Moreover, these luminescent polymer-rare earth complexes possess superior thermal stability (T5 > 195 °C). All the interesting results suggest the potential application of the luminescent polymer-rare earth complexes in green-emitting luminescent materials under high temperature.

  13. I-V Performance and stability study of dyes for luminescent plate concentrators

    Energy Technology Data Exchange (ETDEWEB)

    Slooff, L.H.; Kinderman, R.; Burgers, A.R.; Van Roosmalen, J.A.M. [ECN Solar Energy, Petten (Netherlands); Buechtemann, A.; Danz, R. [Fraunhofer Institute for Applied Polymer Research, Geiselbergstr. 69, D-14476 Golm (Germany)

    2007-08-15

    In this paper, both the performance and stability of luminescent flat plate concentrator (LFPC) plates in combination with mc-Si photovoltaic cells are studied. It is shown that the electrical current of a silicon solar cell attached to the luminescent plate is improved by a factor 1.5 using a LFPC containing a single dye. It is also shown that most of the dyes are not stable in the polymer plates that are currently used. Screening of the stability of several other dyes indicates that the stability is strongly dependent on the type of dye and the polymer matrix, e.g., additives or the monomer residues.

  14. Luminescence characteristics of caffeine and theophylline1

    Science.gov (United States)

    Andino, M. M.; De Lima, C. G.; Winefordner, J. D.

    The luminescence properties of solutions of caffeine and theophylline in methanol are observed. The effects of the solvent pH, the presence of a heavy atom and the matrix or substrate on the fluorescence and phosphorescence properties of the compounds are evaluated. Caffeine and theophylline fluorescence can be observed at room temperature from dilute methanolic solutions and strong phosphorescence is observed at low temperature when the matrix is in a polycrystalline state. Acidic and basic media cause spectral changes and reduce the intensity of the low temperature phosphorescence. Iodide is a good heavy-atom enhancer of both the low temperature and room temperature phosphorescence of caffeine and theophylline. The intensity of the phosphorescence at room temperature and when spotted on filter paper depends on the type of filter paper and the pH of the spotting solution and/or the pH of the wet surface at the moment of spotting. Theophylline is more sensitive than caffeine to the microenvironment. Under the appropriate experimental conditions, both low temperature and room temperature phosphorescence could be used as analytical tools for the determination of caffeine and theophylline.

  15. Synthesis of cysteine-functionalized water-soluble luminescent copper nanoclusters and their application to the determination of chromium(VI)

    International Nuclear Information System (INIS)

    Cui, Malin; Wang, Chan; Song, Qijun; Song, Ge

    2015-01-01

    A facile, one-pot green method is presented for the preparation of water-soluble luminescent copper nanoclusters (Cu-NCs) from copper dichloride and cysteine as the precursor and stabilizer, respectively. The Cu-NCs are characterized by high resolution transmission electron microscopy, X-ray photoelectron spectroscopy, fluorescence, UV–Vis, and Raman spectroscopy. The Cu-NCs have an average size of 3.5 nm and are stable in aqueous solution at least for 2 weeks. Under photo excitation with 365 nm light, the Cu-NCs display strong green fluorescence with the maximum of emission at 490 nm and a quantum yield of 5.6 %. Fluorescence is quenched by Cr(VI) ion, and this effect was exploited to develop a highly selective method for the determination of Cr(VI). The detection limit of this probe is as low as 43 nM. (author)

  16. Synthesis, Thermal and Luminescence Characteristics of Eu-activated SrZn2Si2O7 as a Nanocrystalline Blue-emitting Phosphor for LEDs Application

    International Nuclear Information System (INIS)

    Sameie, H.; Salimi, R.; Alvani, A.A.S.; Sarabi, A.A.; Farsi, M.A.M.; Roohnikan, M.; Mohammadloo, H.E.; Tahriri, M.

    2011-01-01

    In this research, blue-emitting nanocrystalline phosphor SrZn 2 Si 2 O 7 : Eu 2+ was successfully synthesized with two routes: solid state reaction (SS) and sol-gel method (SG). The effects of preparation processes on the crystallization, morphology and optical properties were investigated by appropriate techniques. From the photoluminescence results, obtained phosphors emit strong blue light due to 4f 6 5d 1 ( 2 D)→4f 7 ( 8 S 7/2 ) transition of Eu 2+ ions which act as luminescence centers. The experimental results reveal that the excitation and emission intensities for SS are better than SG due to higher calcination temperature, whereas the samples synthesized by wet chemical method have relatively regular morphology. (author)

  17. Synthesis, crystal structure, thermal and luminescence properties of CuX(2,3-dimethylpyrazine) (X=Cl, Br, I) coordination polymers.

    Science.gov (United States)

    Jess, Inke; Taborsky, Petr; Pospísil, Jirí; Näther, Christian

    2007-06-14

    Three new coordination polymers based on CuI and 2,3-dimethylpyrazine (2,3-dmpyz) were prepared, structurally characterized and investigated for their thermal and luminescence properties. In the ligand rich 2:3 compound [(CuI)2(2,3-dmpyz)3] (CuI)2 dimers are found, which are connected by the N-donor ligands into chains, whereas in the structure of the 1:1 intermediate [(CuI)(2,3-dmpyz)] (CuI)4 tetramers are found, which are also connected into chains. The crystal structure of the ligand deficient 2:1 compound [(CuI)2(2,3-dmpyz)] is built up of CuI double chains, which are connected by the 2,3-dmpyz ligands into layers. Thermal decomposition of results in its direct transformation into the ligand deficient compound , without the formation of the 1:1 compound as an intermediate. A similar thermal reactivity is found for compound , which transforms into on heating. Stirring of a crystalline suspension of pure or in acetonitrile, always leads to a transformation into the ligand deficient compound indicating that compound is the most stable of all the coordination polymers, whereas compounds and are metastable. The luminescence properties of the CuCl and CuI coordination polymers were investigated at 298 and 77K. It was observed that the emission maxima strongly depends on the nature of the halide atom and the composition and structure of the coordination polymers. In addition, several of these compounds show luminescence thermochromism. These results are compared with those obtained for the previously reported CuCl and CuBr(2,3-dimethylpyrazine) coordination polymers.

  18. Spectrometer for cluster ion beam induced luminescence

    Energy Technology Data Exchange (ETDEWEB)

    Ryuto, H., E-mail: ryuto@kuee.kyoto-u.ac.jp; Sakata, A.; Takeuchi, M.; Takaoka, G. H. [Photonics and Electronics Science and Engineering Center, Kyoto University, Kyoto 615-8510 (Japan); Musumeci, F. [Department of Physics and Astronomy, Catania University, Catania 95123 (Italy); INFN Laboratori Nazionali del Sud, Catania 95123 (Italy)

    2015-02-15

    A spectrometer to detect the ultra-weak luminescence originated by the collision of cluster ions on the surfaces of solid materials was constructed. This spectrometer consists of 11 photomultipliers with band-pass interference filters that can detect the luminescence within the wavelength ranging from 300 to 700 nm and of a photomultiplier without filter. The calibration of the detection system was performed using the photons emitted from a strontium aluminate fluorescent tape and from a high temperature tungsten filament. Preliminary measurements show the ability of this spectrometer to detect the cluster ion beam induced luminescence.

  19. Designing spectrally-selective mirrors for use in luminescent solar concentrators

    Science.gov (United States)

    Connell, Ryan; Pinnell, Christian; Ferry, Vivian E.

    2018-02-01

    Spectrally-selective mirrors improve the performance of luminescent solar concentrators (LSCs) by trapping emitted light within the waveguide. However, this beneficial property comes with a spectral restriction on incident sunlight that enters the concentrator. Especially for luminophores with overlap between the absorption and emission bands, design of the spectrally-selective mirrors requires a tradeoff between transmission of incident sunlight and trapping of luminescent photons. In this paper, we explore how the design of a spectrally-selective top mirror changes for LSCs containing luminophores of varying loading fractions, quantum yield, and overlap between the absorption and emission spectra, as well as LSCs with different back reflectors and lateral sizes. Using CdSe/CdS core/shell nanocrystals as the luminophore, we find that specific conditions favor different mirror designs. Mirrors designed to trap luminescent light have higher predicted performance than mirrors designed for sunlight transmission when the luminophore quantum yield is greater than 0.85, the luminophore optical density is less than 1.4 at 450 nm, the lateral size of the concentrator is greater than 10 cm, or there is low overlap between the luminophore absorption and emission. Mirrors optimized for either transmission or luminescence trapping have comparable performance for quantum yields less than 0.85, and the other conditions favor mirrors optimized for light transmission. For a LSC with unity quantum yield, a lateral size of 1 m × 1 m, and a mirror designed to trap luminescent light, a concentration factor of 37× is possible, as compared to 10× for a LSC with an open top. This research indicates the importance of tailoring the design of the spectrally-selective top mirror to the properties of the luminophore and LSC.

  20. Polymeric Luminescent Compositions Doped with Beta-Diketonates Boron Difluoride as Material for Luminescent Solar Concentrator

    Science.gov (United States)

    Khrebtov, A. A.; Fedorenko, E. V.; Reutov, V. A.

    2017-11-01

    In this paper we investigated polymeric luminescent compositions based on polystyrene doped with beta diketonates boron difluoride. Transparent films with effective absorption in the ultraviolet and blue regions of the spectrum were obtained. Polymeric luminescent compositions based on the mixture of dyes allow expanding the absorption region and increase the radiation shift. A luminescent solar concentrator consisting of a glass plate coated with such film can be used for photovoltaic window application.