Luminescence of Er3+ doped double lead halide crystals under X-ray, UV, VIS and IR excitation

Science.gov (United States)

Serazetdinov, A. R.; Smirnov, A. A.; Pustovarov, V. A.; Isaenko, L. I.

2017-09-01

Er3+ doped double lead halide crystals incorporate a number of properties making them interesting for practical use in light conducting materials. X-ray excited luminescence (XRL) spectra, photoluminescence (PL) spectra in region of 1.5-3.5 eV, photoluminescence excitation (PLE) spectra (2.75-5 eV) and anti-stokes luminescence (ASL) spectra were measured at room temperature in KPb2Cl5 (KPC) and RbPb2Br5 (RPB) matrices doped with Er3+ (1%) ions and in KPC doped with Er3++ Yb3+ ions(1:3 ratio concentration). Intraconfigurational f→f transitions are observed in Er3+ ions in most of the cases. The concrete spectrum form is strongly dependent on the excitation energy. Under 980 nm excitation upper Er3+ levels are excited, showing upconversional processes. In case of 313 nm (UV) and 365 nm (VIS) excitation self trapped exciton luminescence was detected in RPB crystal. Additional Yb3+ doping ions strongly increase quantum yield under 980 nm excitation and this doping cause insignificant influence on quantum yield under VIS or UV excitation.

Soft X-ray excited optical luminescence from functional organic materials

Energy Technology Data Exchange (ETDEWEB)

Sham, T.K., E-mail: tsham@uwo.ca

2015-10-01

Highlights: • Many functional organic materials convert X-ray energy into visible light. • The X-ray induced luminescence (XEOL) across an absorption edge can be site and excitation channel specific. • XEOL is composition, morphology, size and crystallinity dependent. • XEOL using the time structure of a synchrotron can reveal the decay and energy transfer dynamics of the sample. • The combined use of XEOL and XAS in the analysis of functional organic materials is illustrated. - Abstract: This brief report reviews some of the recent findings in the study of synchrotron based X-ray excited optical luminescence (XEOL) from representative organic light emitting device (OLED) and related functional organic materials. The systems of interest include Alq{sub 3}, aluminium tris(8-hydroxylquinoline); Ru(bipy){sub 3}{sup 2+}, tris-(2,2-bipyridine) ruthenium(II); Ir(bpy){sub 3}, tris(2-phenyl-bipyridine)iridium; PVK (poly(N-vinylcarbazole)) and [Au{sub 2}(dppe)(bipy)]{sup 2+}, a Au(I) polymer containing 1,2-bis(diphenylphosphino)ethane and the 4,40-bipyridyl ligands, as well as TBPe (2,5,8,11-tetra-tert-butylperylene) polyhedral crystals and fluorescein isothiocyanate (FITC) and FITC-labelled proteins. It is shown that tunable and pulsed X-rays from synchrotron light sources enable the detailed tracking of the optical properties of organic functional materials by monitoring the luminescence in both the energy and time domain as the excitation energy is scanned across an element-specific absorption edge. The use of XEOL and X-ray absorption spectroscopy (XAS) in materials analysis is illustrated.

X-Ray Absorption Near-Edge Structure (XANES) of Calcium L3,2 Edges of Various Calcium Compounds and X-Ray Excited Optical Luminescence (XEOL) Studies of Luminescent Calcium Compounds

International Nuclear Information System (INIS)

Ko, J. Y. Peter; Zhou Xingtai; Sham, T.-K.; Heigl, Franziskus; Regier, Tom; Blyth, Robert

2007-01-01

X-ray absorption at calcium L3,2 edges of various calcium compounds were measured using a high resolution Spherical Grating Monochromator (SGM) at the Canadian Light Source (CLS). We observe that each compound has its unique fine structure of L3,2 edges. This uniqueness is due to differences in local structure of compounds. We also performed (X-ray Excited Optical Luminescence) XEOL of selected luminescent calcium compounds to investigate their optical properties. XEOL is a photon-in-photon-out technique in which the optical luminescence that is excited by tunable x-rays from a synchrotron light source is monitored. Depending on excitation energy of the x-ray, relative intensities of luminescence peaks vary. Recent findings of the results will be presented here

X-ray excited optical luminescence, photoluminescence, photostimulated luminescence and x-ray photoemission spectroscopy studies on BaFBr:Eu

CERN Document Server

Subramanian, N; Govinda-Rajan, K; Mohammad-Yousuf; Santanu-Bera; Narasimhan, S V

1997-01-01

The results of x-ray excited optical luminescence (XEOL), photoluminescence (PL), photostimulated luminescence (PSL) and x-ray photoemission spectroscopy (XPS) studies on the x-ray storage phosphor BaFBr:Eu are presented in this paper. Analyses of XEOL, PL and PSL spectra reveal features corresponding to the transitions from 4f sup 6 td sup 1 to 4f sup 7 configurations in different site symmetries of Eu sup 2 sup +. Increasing x-ray dose is seen to lead to a red shift in the maximum of the PL excitation spectrum for the 391 nm emission. The XEOL and XPS spectra do not show any signature of Eu sup 3 sup + in the samples studied by us, directly raising doubts about the model of Takahashi et al in which Eu sup 2 sup + is expected to ionize to Eu sup 3 sup + upon x-ray irradiation and remain stable until photostimulation. XEOL and PSL experiments with simultaneous x-ray irradiation and He - Ne laser excitation as well as those with sequential x-ray irradiation and laser stimulation bring out the competition betwe...

Electric field dependence of the total excimer luminescence of xenon excited below the atomic ionization limit

International Nuclear Information System (INIS)

Anon.

1987-01-01

In the spectral region of interest (i.e., 11.1 eV ≤ h nu ≤ 11.9 eV), the photoionization yield of electrons from excited-state dimers of xenon, increases monotonically to relatively high values (e.g., Y(11.7 eV) = 0.43 electrons/absorbed photon). It is also known however, that the luminescence intensity excited by photons in this region is quite high, even at low pressures. These two observations can be reconciled only by assuming that one of the processes leading to excimer luminescence involves dimer-ion + electron recombination. If this assumption is correct, application of an electric field, with concomitant collection of the free charges generated by the incident photons, should lead to a decrease in luminescence intensity; moreover, this decrease should follow the energy dependence of the photoionization yield function. The present report demonstrates experimentally that this is indeed the case. Such experiments combining luminescence and electric fields were made, until now, only by high-energy excitation. In this case the deconvolution of the various decay channels is hardly possible

Luminescence decay in condensed argon under high energy excitation

International Nuclear Information System (INIS)

Carvalho, M.J.; Klein, G.

1978-01-01

α and β particles were used to study the luminescence of condensed argon. The scintillation decay has always two components independently of the phase and the kind of the exciting particles. Decay time constants are given for solid, liquid and also gaseous argon. Changes in the relative intensity values of the two components are discussed in terms of track effects

A novel low cost pulse excitation source to study trap spectroscopy of persistent luminescent materials

Science.gov (United States)

Chandrasekhar, Ngangbam; Singh, Nungleppam Monorajan; Gartia, R. K.

2018-04-01

Luminescent techniques require one or the other source of excitations which may vary from high cost X-rays, γ-rays, β-rays etc. to low cost LED. Persistent luminescent materials or Glow-in-the-Dark phosphors are the optical harvesters which store the optical energy from day light illuminating a whole night. They are so sensitive that they can be excited even with the low light of firefly. Therefore, instead of using a high cost excitation source authors have developed a low cost functioning of excitation source controlling short pulses of LED to excite persistent phosphors with the aid of ExpEYES Junior (Hardware/software framework developed by IUAC, New Delhi). Using this, the authors have excited the sample under investigation upto 10 ms. Trap spectroscopy of the pre-excited sample with LED is studied using Thermoluminescence (TL) technique. In this communication, development of the excitation source is discussed and demonstrate the its usefulness in the study of trap spectroscopy of commercially available CaS:Eu2+, Sm3+. Trapping parameters are also evaluated using Computerized Glow Curve Deconvolution (CGCD) technique.

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

STM-excited luminescence of porous and spark-processed silicon

International Nuclear Information System (INIS)

Andrienko, I.; Kuznetsov, V.; Yuan, J.; Haneman, D.

1998-01-01

Full text: Scanning tunneling microscopy (STM) permits highly local electronic excitation of light emission (LE) from the surface of silicon. Measuring STM LE, one can study simultaneously both the topography and the luminescence properties of areas down to nm dimensions and thus make conclusions about the luminescence mechanism of the material. We have built an STM spectroscopy system which allows measurement of spectra of visible light emitted from areas as small as 13 x 13 nm 2 (porous silicon) and 10 x 10 nm 2 (spark-processed silicon). Porous silicon shows a broad emission band centered at 630 nm, and spark-processed silicon, one at 690 nm. The STM LE spectra of spark-processed silicon obtained for the first time. We have found that visible light is emitted only from areas containing nanometer-scale structures down to around 2 nm in diameter. STM LE occurs under negative bias voltage applied to the tip, i.e. when electrons are injected into the sample. Other workers used p-type silicon for the sample preparations, but it has been found that STM LE can be induced also from n-type silicon. Furthermore, we have shown that STM LE spectra can be resolved using much lover voltages and tunneling currents: -(7-9) V and 25 - 50 nA vs -(25-50) V and 100 nA. To consider different excitation mechanisms, the STM LE measurements are compared with photoluminescence and electroluminescence spectra of similar samples. We suggest that excitation of individual quantum confinement structures has been observed

Table-top instrumentation for time-resolved luminescence spectroscopy of solids excited by nanosecond pulse of soft X-ray source and/or UV laser

International Nuclear Information System (INIS)

Bruza, Petr; Fidler, Vlastimil; Nikl, Martin

2011-01-01

The practical applicability of the rare-earth doped scintillators in high-speed detectors is limited by the slow decay components in the temporal response of a scintillator. The study of origin and properties of material defects that induce the slow decay components is of major importance for the development of new scintillation materials. We present a table-top, time-domain UV-VIS luminescence spectrometer, featuring extended time and input sensitivity ranges and two excitation sources. The combination of both soft X-ray/XUV and UV excitation source allows the comparative measurements of luminescence spectra and decay kinetics of scintillators to be performed under the same experimental conditions. The luminescence of emission centers of a doped scintillator can be induced by conventional N 2 laser pulse, while the complete scintillation process can be initiated by a soft X-ray/XUV pulse excitation from the laser-produced plasma in gas puff target of 4 ns duration. In order to demonstrate the spectrometer, the UV-VIS luminescence spectra and decay kinetics of cerium doped Lu 3 Al 5 O 12 single crystal (LuAG:Ce) scintillator excited by XUV and UV radiation were acquired. Luminescence of the doped Ce 3+ ions was studied under 2.88 nm (430 eV) XUV excitation from the laser-produced nitrogen plasma, and compared with the luminescence under 337 nm (3.68 eV) UV excitation from nitrogen laser. In the former case the excitation energy is deposited in the LuAG host, while in the latter the 4f-5d 2 transition of Ce 3+ is directly excited. Furthermore, YAG:Ce and LuAG:Ce single crystals luminescence decay profiles are compared and discussed.

Luminescence of yttrium niobium-tantalate doubly activated by europium and/or terbium under X-ray and electron beam excitation

Energy Technology Data Exchange (ETDEWEB)

Arellano, I.D., E-mail: arellano@utp.edu.co [Department of Physics, Technological University of Pereira, Vereda La Julita, Pereira (Colombia); Nazarov, M.V. [Institute of Applied Physics, Academy of Sciences of Moldova, Republic of Moldova (Moldova, Republic of); School of Materials and Mineral Resources Engineering Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Cortes, J.A. [Department of Physics, Technological University of Pereira, Vereda La Julita, Pereira (Colombia); Ahmad Fauzi, M.N [School of Materials and Mineral Resources Engineering Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia)

2012-09-15

This paper reports the luminescence emission spectra of Y(Ta,Nb)O{sub 4} activated by rare earth ions such as Eu{sup 3+} and Tb{sup 3+}. The influence of these rare earth ions on the luminescence of yttrium niobium-tantalate phosphors was investigated. The luminescent properties were studied under X-ray and electron beam excitations. Under these excitations, the emission centers of the rare earth activators (Eu{sup 3+},Tb{sup 3+}) were found to contribute efficiently to the overall luminescence. Changing the mol concentration of the incorporated activators resulted in a broad variation of visible photoluminescence. Color cathodoluminescence images showed clearly the dependence of chromaticity on the different activators. With their various luminescence chromaticities, these rare earth activated phosphors are promising materials for solid-state lighting applications as well as for X-ray intensifying screens in medical diagnosis, providing a broad variation of visible photoluminescence from blue to red. - Highlights: Black-Right-Pointing-Pointer The Y(Ta,Nb)O{sub 4} phosphors were activated by rare earth ions such as Eu{sup 3+} and Tb{sup 3+}. Black-Right-Pointing-Pointer The phosphors were studied under X-ray and electron beam excitations. Black-Right-Pointing-Pointer The emission centers contribute efficiently to the overall luminescence. Black-Right-Pointing-Pointer Changing the concentration of the activators resulted in a broad luminescence.

Fabrication of bright and thin Zn₂SiO₄ luminescent film for electron beam excitation-assisted optical microscope.

Science.gov (United States)

Furukawa, Taichi; Kanamori, Satoshi; Fukuta, Masahiro; Nawa, Yasunori; Kominami, Hiroko; Nakanishi, Yoichiro; Sugita, Atsushi; Inami, Wataru; Kawata, Yoshimasa

2015-07-13

We fabricated a bright and thin Zn₂SiO₄ luminescent film to serve as a nanometric light source for high-spatial-resolution optical microscopy based on electron beam excitation. The Zn₂SiO₄ luminescent thin film was fabricated by annealing a ZnO film on a Si₃N₄ substrate at 1000 °C in N₂. The annealed film emitted bright cathodoluminescence compared with the as-deposited film. The film is promising for nano-imaging with electron beam excitation-assisted optical microscopy. We evaluated the spatial resolution of a microscope developed using this Zn₂SiO₄ luminescent thin film. This is the first report of the investigation and application of ZnO/Si₃N₄ annealed at a high temperature (1000 °C). The fabricated Zn₂SiO₄ film is expected to enable high-frame-rate dynamic observation with ultra-high resolution using our electron beam excitation-assisted optical microscopy.

Luminescence Properties of Surface Radiation-Induced Defects in Lithium Fluoride

Science.gov (United States)

Voitovich, A. P.; Kalinov, V. S.; Martynovich, E. F.; Novikov, A. N.; Runets, L. P.; Stupak, A. P.

2013-11-01

Luminescence and luminescence excitation spectra are recorded for surface radiation-induced defects in lithium fluoride at temperatures of 77 and 293 K. The presence of three bands with relatively small intensity differences is a distinctive feature of the excitation spectrum. These bands are found to belong to the same type of defects. The positions of the peaks and the widths of the absorption and luminescence bands for these defects are determined. The luminescence decay time is measured. All the measured characteristics of these surface defects differ from those of previously known defects induced by radiation in the bulk of the crystals. It is found that the luminescence of surface defects in an ensemble of nanocrystals with different orientations is not polarized. The number of anion vacancies in the surface defects is estimated using the polarization measurements. It is shown that radiative scattering distorts the intensity ratios of the luminescence excitation bands located in different spectral regions.

X-ray excited optical luminescence studies on the system BaXY (X ...

Indian Academy of Sciences (India)

Home; Journals; Pramana – Journal of Physics; Volume 65; Issue 2. X-ray excited optical luminescence studies on the system Ba (, =F, Cl, Br, I) ... India; Department of Chemical Engineering, National Taiwan University, Republic of China ... Proceedings of the International Workshop/Conference on Computational ...

Luminescence and excited state dynamics in Bi3+-doped LiLaP4O12 phosphates

International Nuclear Information System (INIS)

Babin, V.; Chernenko, K.; Demchenko, P.; Mihokova, E.; Nikl, M.; Pashuk, I.; Shalapska, T.; Voloshinovskii, A.; Zazubovich, S.

2016-01-01

Photo- and X-ray-excited luminescence characteristics of Bi-doped LiLaP 4 O 12 phosphates with different bismuth contents (from 1 to 25 at% in the melt) are investigated in the 4.2–300 K temperature range and compared with the characteristics of the undoped LiLaP 4 O 12 phosphate. The broad 2.95 eV emission band of LiLaP 4 O 12 :Bi excited around 5.4 eV is found to arise from the bismuth dopant. Relatively large FWHM and Stokes shift of the emission band and especially the data on the low-temperature decay kinetics of the 2.95 eV emission and its temperature dependence, indicating a very small spin-orbit splitting energy of the corresponding excited state, allow the conclusion that this emission arises from the radiative decay of the triplet state of an exciton localized around a Bi 3+ ion. No spectral bands are observed, arising from the electron transitions between the energy levels of Bi 3+ ions. Phenomenological model is proposed for the description of the excited state dynamics of the Bi 3+ -related localized exciton in LiLaP 4 O 12 :Bi and the parameters of the triplet localized exciton state are determined. Keywords: Photoluminescence; Time-resolved spectroscopy; Excited states; Bi 3+ centers; LiLaP 4 O 12 :Bi powders

Preparation and determination of the luminescent characteristics of ZrO2 in powder

International Nuclear Information System (INIS)

Rivera M, T.; Olvera T, L.; Azorin N, J.; Soto E, A.M.; Velazquez O, C.; Campero C, A.

2004-01-01

In this work the luminescent characteristics of the ZrO 2 are presented using the method of Thermally Stimulated Luminescence (TSL), also called thermoluminescence (Tl). The powders of ZrO 2 were obtained by two preparation methods: for precipitation and for evaporation of Sol-gel. The luminescent characteristics of the ZrO 2 are determined using a lamp of radiation of UV light and a radiation source of beta particles of 90 Sr/ 90 Y. Using the method of thermal stimulation the curve representative thermoluminescent of the previously irradiated material was obtained. The curve Tl of the ZrO 2 irradiated with UV light presents a maximum in 180 C. Likewise, the spectrum of the curve Tl of the ZrO 2 irradiated with particles beta presents a maximum centered in 181 C. While using gamma radiation like excitement source one has a spectrum with a peak centered in 184 C. When subjecting the materials obtained by sol-gel to a process of calcination at 1000 C for 24 hours a curved Tl it presents with two maxim in 185 and in 290 C respectively. The intensity of the response induced in the material it is a decisive factor to continue studying the dosimetric characteristics of the ZrO 2 what allows to consider it as a potential material to use it in the beta particle dosimetry and of the UV light using the thermoluminescence method (Tl). (Author)

Luminescence excitation characteristics of Ca-, Na- and K-aluminosilicates (feldspars), in the stimulation range 20-500 eV: optical detection of XAS

CERN Document Server

Poolton, N R J; Quinn, F M; Pantos, E; Andersen, C E; Bøtter-Jensen, L; Johnsen, O; Murray, A S

2003-01-01

We demonstrate that the visible/UV luminescence from common feldspar crystals (NaAlSi sub 3 O sub 8 , KAlSi sub 3 O sub 8 and CaAl sub 2 Si sub 2 O sub 8) can be used to detect detailed L-edge and associated near-edge absorption structure of the main constituent atoms (Ca, K, Na, Al, Si), when exciting in the energy range 20-500 eV. Comparisons of the spectral features are drawn with similar measurements made on the associated materials SiO sub 2 , Al sub 2 O sub 3 and CaCO sub 3. The potential for using optically detected x-ray absorption spectroscopy as a method for identifying the luminescent components of mixed mineral samples is considered.

Studies of nanostructures using time-resolved x-ray excited optical luminescence*

International Nuclear Information System (INIS)

Rosenberg, R.A.; Shenoy, G.K.; Smita, S.; Burda, C.; Sham, T.K.

2004-01-01

Full text:The scientific community is currently investing a great deal of effort into understanding the physics and chemistry of nanoscale structures. Synchrotron radiation techniques are being used to study the physical, electronic, and magnetic structure of nanosystems, albeit at a relatively large size (greater than 30 nm). A major challenge facing researchers is finding methods that can probe structures of the smallest scale (less than 10 nm). Optical luminescence has been shown to be directly sensitive to structures in this size range due to quantum confinement phenomena. X-ray-excited optical luminescence (XEOL) provides the capability to chemically map the sites responsible for producing low-energy (1-6 eV) fluorescence. By taking advantage of the time structure of the x-ray pulses at the Advanced Photon Source (70 ps wide, 153 ns separation), it also possible to determine the dynamic behavior of the states involved in the luminescence. In this paper we will present results of time-resolved XEOL experiments on various nanostructures including porous silicon, silicon nanowires, and CdSe nanodots

Excitation-resolved cone-beam x-ray luminescence tomography.

Science.gov (United States)

Liu, Xin; Liao, Qimei; Wang, Hongkai; Yan, Zhuangzhi

2015-07-01

Cone-beam x-ray luminescence computed tomography (CB-XLCT), as an emerging imaging technique, plays an important role in in vivo small animal imaging studies. However, CB-XLCT suffers from low-spatial resolution due to the ill-posed nature of reconstruction. We improve the imaging performance of CB-XLCT by using a multiband excitation-resolved imaging scheme combined with principal component analysis. To evaluate the performance of the proposed method, the physical phantom experiment is performed with a custom-made XLCT/XCT imaging system. The experimental results validate the feasibility of the method, where two adjacent nanophosphors (with an edge-to-edge distance of 2.4 mm) can be located.

The origin of luminescence from di[4-(4-diphenylaminophenyl)phenyl]sulfone (DAPSF), a blue light emitter: an X-ray excited optical luminescence (XEOL) and X-ray absorption near edge structure (XANES) study.

Science.gov (United States)

Zhang, Duo; Zhang, Hui; Zhang, Xiaohong; Sham, Tsun-Kong; Hu, Yongfeng; Sun, Xuhui

2016-03-07

The electronic structure and optical properties of di[4-(4-diphenylaminophenyl)phenyl]sulfone (denoted as DAPSF), a highly efficient fluorophor, have been investigated using X-ray excited optical luminescence (XEOL) and X-ray absorption near edge structure (XANES) spectroscopy at excitation energies across the C, N, O K-edges and the sulfur K-edge. The results indicate that the blue luminescence is mainly related to the sulfur functional group.

P 8: Table-top instrumentation for time-resolved luminescence spectroscopy of solids excited by soft X-ray from a laser induced plasma source and/or UV-VIS laser

International Nuclear Information System (INIS)

Bruza, P.; Fidler, V.; Nikl, M.

2010-01-01

The design and use of a novel, table-top UV-VIS luminescence spectrometer with two excitation sources is described: a soft X-ray/XUV pulse excitation from the laser-produced plasma in gas puff target of about 4 ns duration, and a conventional N 2 pulse laser excitation at 337 nm (or any other UV-VIS pulse laser excitation). The XUV plasma source generates photons of either quasi-monochromatic (N target, E = 430 eV) or wide (Ar target, E = 200 ∼ 600 eV) spectral range. A combination of both X-ray/XUV and UV-VIS excitation in one experimental apparatus allows to perform comparative luminescence spectra and kinetics measurements under the same experimental conditions. In order to demonstrate the spectrometer, the UV-VIS luminescence spectra and decay kinetics of cerium doped Lu 3 Al 5 O 12 single crystal (LuAG:Ce) scintillator excited by XUV and UV radiation were acquired. Luminescence of doped Ce 3+ ions was studied under XUV 430 eV excitation from the laser-produced nitrogen plasma, and compared with the luminescence under 337 nm (3,68 eV) UV excitation from nitrogen laser. In the former case the excitation energy is deposited in the LuAG host, while in the latter the 4f-5d transition of Ce 3+ is directly excited. Furthermore, LuAG:Ce single crystals and single crystalline films luminescence decay profiles are compared and discussed. (authors)

Comparison of the luminescent properties of Lu3Al5O12:Pr crystals and films under synchrotron radiation excitation

International Nuclear Information System (INIS)

Zorenko, Yu.; Gorbenko, V.; Zorenko, T.; Voznyak, T.; Nizankovskiy, S.

2016-01-01

The work is dedicated to comparative investigation of the luminescent properties of Lu 3 Al 5 O 12 :Pr(LuAG:Pr) single crystals and single crystalline films using excitation by synchrotron radiation with an energy of 3.7–25 eV in the exciton range of LuAG host. We have found that the differences in the excitation spectra and luminescence decay kinetics of LuAG:Pr crystals and films are caused by involving the LuAl antisite defects and oxygen vacancies in the crystals and Pb 2+ flux related dopants in the films in the excitation processes of the Pr 3+ luminescence. Taking into account these differences, we have determined the energy structure of the Pr 3+ ions in LuAG host and estimated the differences in the energies of creation of excitons bound with the isolated Pr 3+ ions in LuAG:Pr films and the dipole Pr–LuAl antisite defect centers in the crystal counterpart. - Highlights: • Comparison of the luminescent properties of LuAG:Pr single crystals and films. • Superposition of the Pr 3+ and defect centers luminescence of LuAG:Pr crystal. • Different creation energies of an excitons bound with the Pr 3+ in LuAG:Pr crystals and films. • More faster decay kinetics of the Pr 3+ luminescence in LuAG:Pr films. • Low content of slow emission component in LuAG:Pr films.

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

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

Luminescence of Ce3+ doped LaPO4 nanophosphors upon Ce3+ 4f-5d and band-to-band excitation

International Nuclear Information System (INIS)

Stryganyuk, G.; Trots, D.M.; Voloshinovskii, A.; Shalapska, T.; Zakordonskiy, V.; Vistovskyy, V.; Pidzyrailo, M.; Zimmerer, G.

2008-01-01

Luminescence spectral-kinetic studies have been performed for pure and Ce-doped LaPO 4 micro- and nanosized phosphates using synchrotron radiation for the excitation within 5-20 eV energy range at T=8-300 K. Mechanisms for the excitation of Ce 3+ 5d-4f emission as well as the quenching processes are discussed. The influence of surface defects has been considered to modify considerably the luminescent properties of nanosized phosphors upon the excitation in the energy range of Ce 3+ 4f-5d transitions and LaPO 4 host absorption

A visible-light-excited europium(III) complex-based luminescent probe for visualizing copper ions and hydrogen sulfide in living cells

Science.gov (United States)

Wang, Yiren; Wang, Huan; Yang, Mei; Yuan, Jingli; Wu, Jing

2018-01-01

Development of visible-light-excited lanthanide (III) complex-based luminescent probes is highly appealing due to their superiority of less damage to the living biosystems over the conventional UV-light-excited ones. In this work, a visible-light-excited europium (III) complex-based luminescent probe, BPED-BHHCT-Eu3+-BPT, has been designed and synthesized by conjugating the Cu2+-binding N,N-bis(2-pyridylmethyl)ethanediamine (BPED) to a tetradentate β-diketone ligand 4,4‧-bis(1″,1″,1″,2″,2″,3″,3″-heptafluoro-4″,6″-hexanedione-6″-yl)chlorosulfo-o-terphenyl (BHHCT) and coordinating with a coligand 2-(N,N-diethylanilin-4-yl)-4,6-bis(pyrazol-1-yl)-1,3,5-triazine) (BPT) for the time-gated luminescence detection of Cu2+ ions and hydrogen sulfide (H2S) in living cells. BPED-BHHCT-Eu3+-BPT exhibited a sharp excitation peak at 407 nm and a wide excitation window extending to beyond 460 nm. Upon its reaction with Cu2+ ions, the luminescence of BPED-BHHCT-Eu3+-BPT was efficiently quenched, which could be reversibly restored by the addition of H2S due to the strong affinity between Cu2+ ions and H2S. The "on-off-on" type luminescence behavior of BPED-BHHCT-Eu3+-BPT towards Cu2+ ions and H2S enabled the sensing of the two species with high sensitivity and selectivity. The performances of BPED-BHHCT-Eu3+-BPT for visualizing intracellular Cu2+ ions and H2S were investigated, and the results have demonstrated the practical applicability of the probe for molecular imaging of cells.

Anomalous enhancement of nanodiamond luminescence upon heating

Science.gov (United States)

Khomich, A. A.; Kudryavtsev, O. S.; Dolenko, T. A.; Shiryaev, A. A.; Fisenko, A. V.; Konov, V. I.; Vlasov, I. I.

2017-02-01

Characteristic photoluminescence (PL) of nanodiamonds (ND) of different origin (detonation, HPHT, extracted from meteorite) was studied in situ at high temperatures in the range 20-450 °C. Luminescence was excited using 473 nm laser and recorded in the range 500-800 nm. In contrast to decrease of point defect PL in bulk diamond with temperature, we found that the ND luminescence related to ND surface defects increases almost an order of magnitude upon heating to 200-250 °C. The observed effect reveals that water adsorbed on ND surfaces efficiently quenches PL; water desorption on heating leads to dramatic increase of the radiative de-excitation.

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

Energy Technology Data Exchange (ETDEWEB)

Pustovarov, V.A., E-mail: vpustovarov@bk.ru [Ural Federal University, 19 Mira Street, 620002 Yekaterinburg (Russian Federation); Smirnova, T.P.; Lebedev, M.S. [Nikolaev Institute of Inorganic Chemistry, Siberian Branch of Russian Academy of Science, Novosibirsk 630090 (Russian Federation); Gritsenko, V.A. [Institute of Semiconductor Physics, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090 (Russian Federation); Novosibirsk National Research University, 2 Pirogova Street, 630090 Novosibirsk (Russian Federation); Kirm, M. [Institute of Physics, University of Tartu, 14c Ravila, 50411 Tartu (Estonia)

2016-02-15

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{sub x}Hf{sub y}O{sub 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{sub 2} and Al{sub 2}O{sub 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.

Laser-excited luminescence of trace Nd3+ impurity in LaBr3 revealed by Raman spectroscopy

Science.gov (United States)

Yu, Jinqiu; Cui, Lei; He, Huaqiang; Hu, Yunsheng; Wu, Hao; Zeng, Jia; Liu, Yuzhu

2012-10-01

Unexpected additional bands with obvious non-vibrational features were observed in Raman spectra of LaBr3. Extensive study was carried out to reveal the origin of these bands. Results indicate that the additional bands correspond to laser-excited luminescence of trace Nd3+ impurity unintentionally introduced from the La2O3 raw material, which was further confirmed by Raman spectra of specially prepared Nd3+-doped LaBr3 and LaOBr samples. The luminescence properties of Nd3+ in different matrix were compared and discussed. The ultrasensitivity of Raman spectroscopy in detecting trace luminescent lanthanide ions shows good potential for analytical applications.

Upconversion luminescent logic gates and turn-on sensing of glutathione based on two-photon excited quantum dots conjugated with dopamine.

Science.gov (United States)

Gui, Rijun; Jin, Hui; Liu, Xifeng; Wang, Zonghua; Zhang, Feifei; Xia, Jianfei; Yang, Min; Bi, Sai

2014-12-07

Under the two-photon excitation, upconversion luminescent "INHIBIT" and "OR" logic gates of water-dispersed CdTe quantum dots (QDs) were constituted by conjugating the QDs with dopamine. This facilitated the development of a novel QDs-based upconversion luminescent probe for efficient turn-on sensing of glutathione.

8 nm nanodiamonds as markers for 2 photon excited luminescent microscopy

International Nuclear Information System (INIS)

Kharin, A; Rogov, A; Bonacina, L; Geloen, A; Lysenko, V

2016-01-01

Structural and luminescent properties of stable suspensions of fluorescent nanodiamonds were investigated. Measurement of the effective hydrodynamic radius yields particles less than 30 nm diameter, while the TEM measurements made on the same particles shows average diameter about 8 nm. It was found that NDs have relatively low toxicity. Upon incubation, 3T3-L1 cells spontaneously take up nanodiamonds that uniformly distribute in cells cytoplasm. The possibility of fluorescent imaging using both single ore two-photon excitation was shown. (paper)

Luminescence of highly excited nonpolar a-plane GaN and AlGaN/GaN multiple quantum wells

International Nuclear Information System (INIS)

Jursenas, S.; Kuokstis, E.; Miasojedovas, S.; Kurilcik, G.; Zukauskas, A.; Chen, C.Q.; Yang, J.W.; Adivarahan, V.; Asif Khan, M.

2004-01-01

Carrier recombination dynamics in polar and nonpolar GaN epilayers and GaN/AlGaN multiple quantum wells grown over sapphire substrates with a various crystallographic orientation were studied under high photoexcitation by 20 ps laser pulses. The transient luminescence featured a significant enhancement on nonradiative recombination of free carriers for nonpolar a-plane GaN epilayers compared to conventional c-plane samples. The epitaxial layer overgrowth technique was demonstrated to significantly improve the quality of nonpolar a-plane films. This was proved by more than 40-fold increase in luminescence decay time (430 ps compared to ≤ 10 ps in the ordinary a-plane epilayer). Under high-excitation regime, a complete screening of built-in electric field by free carriers in multiple quantum wells grown on c-plane and r-plane sapphire substrates was achieved. Under such high excitation, luminescence efficiency and carrier lifetime of multiple quantum wells were shown to be determined by the substrate quality. (author)

Luminescence decay of S Zn::Ag and O Zn:Ga scintillation detectors excited by a pulsed laser

International Nuclear Information System (INIS)

Romero, L.; Campos, J.

1981-01-01

In the present work a high sensitivity experimental set up for luminescence decay measurements in the 1 0 - 1 sec range has been developed. As an application, luminescence light decay In S Zn:Ag and 0Zn:Ga after excitation by a pulsed N 2 laser has been measured. In SZnrAg, measurements of total light decay was compared with donor acceptor pairs theory. In both substances, spectral evolution in the first 15 sec was investigated. (Author) 4 refs

Investigation on luminescence enhancement and decay characteristics of long afterglow nanophosphors for dark-vision display applications

Energy Technology Data Exchange (ETDEWEB)

Swati, G.; Chawla, S.; Mishra, S.; Rajesh, B.; Vijayan, N.; Sivaiah, B.; Dhar, A.; Haranath, D., E-mail: haranath@nplindia.org

2015-04-01

Graphical abstract: - Highlights: • Synthesis and structural characterization has been performed on long afterglow SrAl{sub 2}O{sub 4}:Eu{sup 2+}, Dy{sup 3+} nanophosphor having afterglow time of ∼12 h. • Studied the effect of various fuels used for synthesis of nanophosphors on the decay and luminescence characteristics. Interestingly, afterglow times varied significantly with different fuels used for the synthesis of the nanophosphor. • Excitation by different illuminants has profound influence on the luminescence intensity and afterglow times of the synthesized nanophosphor. • Such studies could be guidelines for appropriate usage of nanophosphor under different lighting environment. - Abstract: Long afterglow SrAl{sub 2}O{sub 4}:Eu{sup 2+},Dy{sup 3+} nanophosphors were synthesized via a facile but effectual auto-combustion technique followed by post-annealing treatment at elevated temperatures. The influence of various fuels during synthesis and thereafter improvement in the luminescence decay characteristics under various illuminant irradiations of long afterglow nanophosphors have been reported. Extensive studies on structural, morphological and luminescent properties of the as-synthesized afterglow nanophosphors have been presented. Powder X-ray diffraction studies confirm the presence of high-purity, single-phase monoclinic nanophosphors. HRTEM investigations confirm the formation of nanophosphors of particle size less than 50 nm. Photoluminescence emission is attributed to the characteristic d–f transition (4f{sup 6}5d{sup 1}→4f{sup 7}) of Eu{sup 2+} ions and was positioned at 512 nm. As-synthesized nanophosphors exhibit considerable confinement effects resulting into blue shift in emission maxima as compared to their bulk counterparts. The mechanism underlined for long afterglow has been discussed using trapping–detrapping model. The nanophosphor being multifunctional finds many interesting applications including dark-vision display

Selective excitation of the yellow and blue luminescence in n- and p-doped Gallium Nitride

International Nuclear Information System (INIS)

Colton, John S.

2000-01-01

GaN is an interesting material: technologically very useful, but still having many unexplained features. Two such features are the broad defect-related luminescence bands: the YL of n-type GaN and the BL of Mg-doped p-type GaN. We have employed selective excitation to investigate these bands. In the case of the YL, most of the previous evidence has supported a recombination model between distant donors and acceptors, most likely a transition involving a shallow donor to a deep acceptor. Our selective excitation experiments have resolved finer structures within the YL. Our results indicate that the YL in bulk samples is related to the YL in film samples. We suggest that selectively excited YL involves recombination at DAP complexes, rather than between spatially distant DAPs (however other recombination channels, including that of distant DAPs may become significant under other excitation conditions). Characteristics of the DAP complexes within our YL model include (a) an electron localization energy of around 60-70 meV, (b) a localized phonon energy of around 40 meV, and (c) excited states of the complex at 200 and 370 meV above the ground state. In the case of the BL, the deep defect responsible for the BL is unknown, and there may not even be a deep defect involved. Also in dispute is the role of potential fluctuations in the properties of the BL. Our results have been explain in a model whereby emission is from DAPs, and significant effects are produced by doping-related potential fluctuations and disorder. Characteristics of the our model for the BL include (a) an Urbach tail, having width E 0 = 33 meV, (b) a strong electron-LO phonon coupling occurring with a Frank-Condon shift of ∼ 180 meV between excitation and emission, (c) a mobility gap at 2.8 eV, separating highly mobile states and highly localized states, and (d) PL-like behavior for excitation energies larger than 2.8 eV, having a blue-shift with increasing excitation energy caused by the increased

X-ray excited optical luminescence of polynuclear aromatic hydrocarbons

Energy Technology Data Exchange (ETDEWEB)

Oestreich, G.J.

1979-05-01

X-ray excited optical luminescence (XEOL) coupled with time resolved spectroscopy was employed to analyze polynuclear aromatic hydrocarbons (PAH) in n-alkane solvents at 10 K. A pulsed XEOL system which was designed around minicomputer control of a medical x-ray unit was developed. Computer software which generated variable width x-ray pulses, monitored timing reference pulses, controlled data acquisition, and analyzed data was written. Phosphorescence decay constants of several PAHs were determined. Synthetic mixtures of zone refined PAHs were prepared and time resolved with the pulsed XEOL technique. Analytical results obtained from the five component mixtures of PAHs at the part per million level were tabulated. Systematic improvements and further development of the pulsed XEOL method were considered.

Luminescence and excited state dynamics in Bi{sup 3+}-doped LiLaP{sub 4}O{sub 12} phosphates

Energy Technology Data Exchange (ETDEWEB)

Babin, V. [Institute of Physics AS CR, Cukrovarnicka 10, 16200 Prague (Czech Republic); Chernenko, K., E-mail: nuclearphys@yandex.ru [Institute of Physics, University of Tartu, Ravila 14c, 50411 Tartu (Estonia); Peter the Great Saint-Petersburg Polytechnic University, Polytekhnicheskaya 29, 195251 St.Petersburg (Russian Federation); Demchenko, P. [Ivan Franko National University of Lviv, Kyryla i Mefodiya 8a, 79005 Lviv (Ukraine); Mihokova, E.; Nikl, M. [Institute of Physics AS CR, Cukrovarnicka 10, 16200 Prague (Czech Republic); Pashuk, I. [Ivan Franko National University of Lviv, Kyryla i Mefodiya 8a, 79005 Lviv (Ukraine); Shalapska, T. [Institute of Physics, University of Tartu, Ravila 14c, 50411 Tartu (Estonia); Voloshinovskii, A. [Ivan Franko National University of Lviv, Kyryla i Mefodiya 8a, 79005 Lviv (Ukraine); Zazubovich, S. [Institute of Physics, University of Tartu, Ravila 14c, 50411 Tartu (Estonia)

2016-08-15

Photo- and X-ray-excited luminescence characteristics of Bi-doped LiLaP{sub 4}O{sub 12} phosphates with different bismuth contents (from 1 to 25 at% in the melt) are investigated in the 4.2–300 K temperature range and compared with the characteristics of the undoped LiLaP{sub 4}O{sub 12} phosphate. The broad 2.95 eV emission band of LiLaP{sub 4}O{sub 12}:Bi excited around 5.4 eV is found to arise from the bismuth dopant. Relatively large FWHM and Stokes shift of the emission band and especially the data on the low-temperature decay kinetics of the 2.95 eV emission and its temperature dependence, indicating a very small spin-orbit splitting energy of the corresponding excited state, allow the conclusion that this emission arises from the radiative decay of the triplet state of an exciton localized around a Bi{sup 3+} ion. No spectral bands are observed, arising from the electron transitions between the energy levels of Bi{sup 3+} ions. Phenomenological model is proposed for the description of the excited state dynamics of the Bi{sup 3+}-related localized exciton in LiLaP{sub 4}O{sub 12}:Bi and the parameters of the triplet localized exciton state are determined. Keywords: Photoluminescence; Time-resolved spectroscopy; Excited states; Bi{sup 3+} centers; LiLaP{sub 4}O{sub 12}:Bi powders.

Three-photon-excited luminescence from unsymmetrical cyanostilbene aggregates: morphology tuning and targeted bioimaging.

Science.gov (United States)

Mandal, Amal Kumar; Sreejith, Sivaramapanicker; He, Tingchao; Maji, Swarup Kumar; Wang, Xiao-Jun; Ong, Shi Li; Joseph, James; Sun, Handong; Zhao, Yanli

2015-05-26

We report an experimental observation of aggregation-induced enhanced luminescence upon three-photon excitation in aggregates formed from a class of unsymmetrical cyanostilbene derivatives. Changing side chains (-CH3, -C6H13, -C7H15O3, and folic acid) attached to the cyanostilbene core leads to instantaneous formation of aggregates with sizes ranging from micrometer to nanometer scale in aqueous conditions. The crystal structure of a derivative with a methyl side chain reveals the planarization in the unsymmetrical cyanostilbene core, causing luminescence from corresponding aggregates upon three-photon excitation. Furthermore, folic acid attached cyanostilbene forms well-dispersed spherical nanoaggregates that show a high three-photon cross-section of 6.0 × 10(-80) cm(6) s(2) photon(-2) and high luminescence quantum yield in water. In order to demonstrate the targeted bioimaging capability of the nanoaggregates, three cell lines (HEK293 healthy cell line, MCF7 cancerous cell line, and HeLa cancerous cell line) were employed for the investigations on the basis of their different folate receptor expression level. Two kinds of nanoaggregates with and without the folic acid targeting ligand were chosen for three-photon bioimaging studies. The cell viability of three types of cells incubated with high concentration of nanoaggregates still remained above 70% after 24 h. It was observed that the nanoaggregates without the folic acid unit could not undergo the endocytosis by both healthy and cancerous cell lines. No obvious endocytosis of folic acid attached nanoaggregates was observed from the HEK293 and MCF7 cell lines having a low expression of the folate receptor. Interestingly, a significant amount of endocytosis and internalization of folic acid attached nanoaggregates was observed from HeLa cells with a high expression of the folate receptor under three-photon excitation, indicating targeted bioimaging of folic acid attached nanoaggregates to the cancer cell line

SrAl2O4:Eu2+ (1%) luminescence under UV, VUV and electron beam excitation

Science.gov (United States)

Nazarov, M.; Mammadova, S.; Spassky, D.; Vielhauer, S.; Abdullayeva, S.; Huseynov, A.; Jabbarov, R.

2018-01-01

This paper reports the luminescence properties of nanosized SrAl2O4:Eu2+ (1%) phosphors. The samples were prepared by combustion method at 600 °C, followed by annealing of the resultant combustion ash at 1000 °C in a reductive (Ar + H2) atmosphere. X-ray diffraction (XRD), photo luminescence (PL) and cathodoluminescence (CL) analysis and thermal stimulated luminescence (TSL) method were applied to characterize the phosphor. For the first time a peak at 375 nm was observed in CL spectra of SrAl2O4:Eu2+ (1%) nanophosphors. Luminescence excitation spectra analysis have shown that this peak is related to crystal defects. Also in TSL curve one strong peak was observed in the region above room temperature (T = 325 K), which is attributed to lattice defects, namely oxygen vacancies. A green LED was fabricated by the combination of the SrAl2O4:Eu2+ (1%) nanosized phosphor and a 365 nm UV InGaN chip.

Development of X-ray excitable luminescent probes for scanning X-ray microscopy

International Nuclear Information System (INIS)

Moronne, M.M.

1999-01-01

Transmission soft X-ray microscopy is now capable of achieving resolutions that are typically 5 times better than the best-visible light microscopes. With expected improvements in zone plate optics, an additional factor of two may be realized within the next few years. Despite the high resolution now available with X-ray microscopes and the high X-ray contrast provided by biological molecules in the soft X-ray region (λ=2-5 nm), molecular probes for localizing specific biological targets have been lacking. To circumvent this problem, X-ray excitable molecular probes are needed that can target unique biological features. In this paper we report our initial results on the development of lanthanide-based fluorescent probes for biological labeling. Using scanning luminescence X-ray microscopy (SLXM, Jacobsen et al., J. Microscopy 172 (1993) 121-129), we show that lanthanide organo-polychelate complexes are sufficiently bright and radiation resistant to be the basis of a new class of X-ray excitable molecular probes capable of providing at least a fivefold improvement in resolution over visible light microscopy. Lanthanide probes, able to bind 80-100 metal ions per molecule, were found to give strong luminescent signals with X-ray doses exceeding 10 8 Gy, and were used to label actin stress fibers and in vitro preparations of polymerized tubulin. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

Luminescence of BaCl2:Eu2+ particles dispersed in the NaCl host excited by synchrotron radiation

International Nuclear Information System (INIS)

Pushak, A.S.; Savchyn, P.V.; Vistovskyy, V.V.; Demkiv, T.M.; Dacyuk, J.R.; Myagkota, S.V.; Voloshinovskii, A.S.

2013-01-01

BaCl 2 :Eu 2+ microcrystals embedded in the NaCl host have been obtained in the NaCl–BaCl 2 (1 mol%)–EuCl 3 (0.02 mol%) crystalline system. The influence of the annealing conditions on the formation of such particles has been studied. In particular, long-term annealing (at 200 °S during 100 h) promotes the microcrystals formation in the NaCl–BaCl 2 –Eu crystalline system. The subsequent heat treatment (annealed at 600 °S during 72 h and quenched to room temperature) is shown to lead to the destruction of the majority of these particles. The luminescent-kinetic properties of BaCl 2 :Eu 2+ microcrystals have been studied upon the ultra-violet excitation by the synchrotron radiation. The X-ray excited luminescence has been measured in order to estimate the distribution of europium ions between microcrystals and the NaCl host. The excitation mechanisms of Eu 2+ ions in the NaCl–BaCl 2 –Eu crystalline system are discussed. - Highlights: ► The formation of BaCl 2 :Eu 2+ microcrystals of 1–100 μm size embedded in the NaCl host is revealed. ► Annealing at 600 °C leads to the destruction of significant number of embedded microcrystals. ► The luminescent parameters of microcrystals is similar to ones of single crystal analogs.

Highly sensitive time resolved singlet oxygen luminescence detection using LEDs as the excitation source

International Nuclear Information System (INIS)

Hackbarth, S; Schlothauer, J; Preuss, A; Röder, B

2013-01-01

For the first time singlet oxygen luminescence kinetics in living cells were detected at high precision using LED light for excitation. As LED technology evolves, the light intensity emitted by standard LEDs allows photosensitized singlet oxygen luminescence detection in solution and cell suspensions. We present measurements superior to those of most actual laser powered setups regarding precision of singlet oxygen kinetics in solutions and cell suspensions. Data presented here show that LED based setups allow the determination of the photosensitizer triplet and singlet oxygen decay times in vitro with an accuracy of 0.1 μs. This enables monitoring of the photosensitizer efficiency and interaction with the cellular components using illumination doses small enough not to cause cell death. (letter)

Application of pulse spectro- zonal luminescent method for the rapid method of material analysis

International Nuclear Information System (INIS)

Lisitsin, V.M.; Oleshko, V.I.; Yakovlev, A.N.

2004-01-01

Full text: The scope of luminescent methods of the analysis covers enough a big around of substances as the luminescence can be excited in overwhelming majority of nonmetals. Analytical opportunities of luminescent methods can be essentially expanded by use of pulse excitation and registration of spectra of a luminescence with the time resolved methods. The most perspective method is to use pulses of high-current electron beams with the nanosecond duration for excitation from the following reasons: excitation is carried out ionizing, deeply enough by a penetrating radiation; the pulse of radiation has high capacity, up to 10 8 W, but energy no more than 1 J; the pulse of radiation has the nanosecond duration. Electrons with energy in 300-400 keV will penetrate on depth into some tenth shares of mm, i.e. they create volumetric excitation of a sample. Therefore the luminescence raised by an electronic beam has the information about volumetric properties of substance. High density of excitation allow to find out and study the centers (defects) having a small yield of a luminescence, to analyze the weakly luminescent objects. Occurrence of the new effects is possible useful to analyze of materials. There is an opportunity of reception of the information from change of spectral structure of a luminescence during the time after the ending of a pulse of excitation and kinetic characteristics of attenuation of luminescence. The matter is the energy of radiation is absorbed mainly by a matrix, then electronic excitations one is transferred the centers of a luminescence (defects) of a lattice. Therefore during the time after creation electronic excitations the spectrum of a luminescence can repeatedly change, transferring the information on the centers (defects) which are the most effective radiators at present time. Hence, the study of change of spectra of radiation during the time allows providing an additional way of discrimination of the information on the centers of a

Spectral-luminescent investigation of polymers doped with europium trisphenoyltrifluoroacetonate compound with 1,10-phenanthroline

International Nuclear Information System (INIS)

Karasev, V.E.; Mirochnik, A.G.; Shchelokov, R.N.

1983-01-01

Spectral-luminescent characteristics of europium tristhenoyltrifluoroacetonate with 1.10-phenanthpoline in polystyrepe and polyvinyl chloride are investigated. E 4 (TTA) 3 phen during introduction into polymers preserves its composition and structure. Weak temperature dependence of half-Width of luminescent lines qualitatively different from the case of crystal chelate is characteristic for polymers doped with E 4 (TTA) 3 xphen. Investigation into temperature dependence of E 4 3+ luminescent intensity in chelate doped polymers proves the conclusion on weakening processes of excitation energy relaxation by vibration constituents of close and far environment during chelate introduction into polymers

Synthesis and luminescent properties of Y(As, Nb, P, V)O4:Eu3+ red phosphors by combinatorial chemistry method

International Nuclear Information System (INIS)

Zeon, Il Woon; Park, Hee Dong; Sohn, Kee Sun; Ryu, Seung Kon

2001-01-01

Eu doped YRO 4 (R=As, Nb, P, V)red phosphors were prepared by the combinatorial chemistry method. The quaternary material library of tetrahedron-type composition array was designed to investigate the luminescence of the host material under UV and VUV excitations (254, 147 nm). The photoluminescent characteristics of the samples were comparable to the commercially available red phosphors such as (Y, Gd)BO 3 :Eu 3+ and Y 2 O 3 :Eu 3+ . In view of the luminescence yield, V rich region was found to be optimum under UV excitation. But the results under VUV excitation were different from those of UV excitation, the samples of the composition containing a large amount of P shows the highest luminescence. Especially, higher luminescence was obtained in Y 0.9 (As 0.06 Nb 0.06 P 0.83 V 0.06 )O 4 :Eu 0.1 phosphors than commercial (Y, Gd)BO 3 red phosphors under 147 nm excitation

Enhancement of Cerenkov luminescence imaging by dual excitation of Er(3+,Yb(3+-doped rare-earth microparticles.

Directory of Open Access Journals (Sweden)

Xiaowei Ma

Full Text Available Cerenkov luminescence imaging (CLI has been successfully utilized in various fields of preclinical studies; however, CLI is challenging due to its weak luminescent intensity and insufficient penetration capability. Here, we report the design and synthesis of a type of rare-earth microparticles (REMPs, which can be dually excited by Cerenkov luminescence (CL resulting from the decay of radionuclides to enhance CLI in terms of intensity and penetration.Yb(3+- and Er(3+- codoped hexagonal NaYF4 hollow microtubes were synthesized via a hydrothermal route. The phase, morphology, and emission spectrum were confirmed for these REMPs by power X-ray diffraction (XRD, scanning electron microscopy (SEM, and spectrophotometry, respectively. A commercial CCD camera equipped with a series of optical filters was employed to quantify the intensity and spectrum of CLI from radionuclides. The enhancement of penetration was investigated by imaging studies of nylon phantoms and nude mouse pseudotumor models.the REMPs could be dually excited by CL at the wavelengths of 520 and 980 nm, and the emission peaks overlaid at 660 nm. This strategy approximately doubled the overall detectable intensity of CLI and extended its maximum penetration in nylon phantoms from 5 to 15 mm. The penetration study in living animals yielded similar results.this study demonstrated that CL can dually excite REMPs and that the overlaid emissions in the range of 660 nm could significantly enhance the penetration and intensity of CL. The proposed enhanced CLI strategy may have promising applications in the future.

Long term in vivo imaging with Cr{sup 3+} doped spinel nanoparticles exhibiting persistent luminescence

Energy Technology Data Exchange (ETDEWEB)

Viana, B., E-mail: bruno.viana@chimie-paristech.fr [PSL Research University, Chimie ParisTech−CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France); Chimie-ParisTech, Paris cedex F-75231 (France); Sharma, S.K.; Gourier, D. [PSL Research University, Chimie ParisTech−CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France); Chimie-ParisTech, Paris cedex F-75231 (France); Maldiney, T.; Teston, E.; Scherman, D. [Unité de Technologies Chimiques et Biologiques pour la Santé (UTCBS), CNRS UMR 8258, INSERM U 1022, Paris cedex F-75270 (France); Université Paris Descartes, Sorbonne Paris Cité, Faculté des Sciences Pharmaceutiques et Biologiques, Paris cedex F-75270 (France); Chimie-ParisTech, Paris cedex F-75231 (France); Richard, C., E-mail: cyrille.richard@parisdescartes.fr [Unité de Technologies Chimiques et Biologiques pour la Santé (UTCBS), CNRS UMR 8258, INSERM U 1022, Paris cedex F-75270 (France); Université Paris Descartes, Sorbonne Paris Cité, Faculté des Sciences Pharmaceutiques et Biologiques, Paris cedex F-75270 (France); Chimie-ParisTech, Paris cedex F-75231 (France)

2016-02-15

Persistent luminescence is a singular property of some materials which are able to store the excitation or light irradiation energy at intrinsic traps or defects before slowly emitting lower energy photons within several hours. When such compounds are prepared as nanoparticles (NPs), when functionalization is realized to get colloidal materials well dispersed in aqueous medium, such nanoprobes open the use of the persistent luminescence for bioimaging applications. Recently, the numbers of in vivo applications increased with new modalities and new expectations. In this review, we focused our attention on the ZnGa{sub 2}O{sub 4}:Cr (ZGO:Cr) nanoparticles. When ZnGa{sub 2}O{sub 4} (ZGO), a normal spinel is doped with Cr{sup 3+} ions, a high brightness persistent luminescence material with an emission spectrum perfectly matching the transparency window of living tissues is obtained. It allows in vivo mouse imaging with an excellent target-to-background ratio. One interesting characteristic of ZGO:Cr lies in the fact that its persistent luminescence can be excited with orange/red light, well below its band gap energy and in the transparency window of living tissues. This important property allows multiple re-excitations to perform long term bioimaging. Antisite defects of the direct spinel structure are assumed to provide shallow traps which store the excitation light. Charge release by room temperature thermal excitation and recombination center, here trivalent chromium, are responsible for the persistent luminescence. Following a primary excitation (UV or visible), one also observed that trapped charges can be released under 977 nm light stimulation for several spinel gallate materials, therefore increasing the modalities and the materials envisioned for in vivo excitation of these NPs. - Highlights: • Review of the persistent luminescence for bio-imaging. • Long term bioimaging by in vivo excitation and photostimulation. • Challenges and main advances in the

Long-lived visible luminescence of UV LEDs and impact on LED excited time-resolved fluorescence applications

International Nuclear Information System (INIS)

Jin, D; Connally, R; Piper, J

2006-01-01

We report the results of a detailed study of the spectral and temporal properties of visible emission from three different GaN-based ultraviolet (UV) light emitting diodes (UV LEDs). The primary UV emission in the 360-380 nm band decays rapidly (less than 1 μs) following switch-off; however, visible luminescence (470-750 nm) with a decay lifetime of tens of microseconds was observed at approximately 10 -4 of the UV intensity. For applications of UV LEDs in time-resolved fluorescence (TRF) employing lanthanide chelates, the visible luminescence from the LEDs competes with the target Eu 3+ or Tb 3+ fluorescence in both spectral and temporal domains. A UV band-pass filter (Schott UG11 glass) was therefore used to reduce the visible luminescence of the UV LEDs by three orders of magnitude relative to UV output to yield a practical excitation source for TRF

Luminescence characteristics of dental ceramics for retrospective dosimetry: a preliminary study

International Nuclear Information System (INIS)

Bailiff, I.K.; Correcher, V.; Delgado, A.; Goksu, Y.; Huebner, S.

2002-01-01

Ceramic materials that are widely employed in dental prosthetics and repairs exhibit luminescent properties. Because of their use in the body, these materials are potentially of interest in situations where retrospective dosimetry for individuals is required but where monitoring was not planned. The luminescent properties of dental ceramics obtained in Germany, Spain and the UK were examined. Linear dose-response characteristics were obtained in the range <100 mGy to 10 Gy using thermoluminescence (TL), optically stimulated luminescence and infrared-stimulated luminescence measurement techniques. Measurements of time-resolved luminescence were also performed to examine the nature of the luminescence recombination under visible (470 nm) and IR (855 nm) stimulation. The results obtained by TL and optically stimulated techniques suggest that there may be deeper traps than previously observed in certain types of dental ceramic. Such traps may be less susceptible to optical and athermal fading than was reported in earlier studies. (author)

Thermostimulated luminescence in KBr-In crystals after optical creation of electronic excitation

International Nuclear Information System (INIS)

Popov, A.I.

1990-01-01

Thermal stability of the radiation defects produced in KBr-In by optical creation of the electronic excitation (optical creation of the excitons or optical ionization of In + -ions under C-band illumination) is investigated by the method of thermostimulated luminescence (TSL). A method of detection of prehistory defects, when the optical ionization of In + -ions and TSL are performed, is proposed. Quadratic dependence of V 2 -center creation upon dose is shown. This dependence confirms assocative mechanism of the creation of V 2 -centers from two interstitial centers

Optical methods for the evaluation of lanthanide excited state thermal ionization barrier in luminescent materials

Czech Academy of Sciences Publication Activity Database

Fasoli, M.; Vedda, A.; Mihóková, Eva; Nikl, Martin

2012-01-01

Roč. 85, č. 8 (2012), "085127-1"-"085127-8" ISSN 1098-0121 R&D Projects: GA AV ČR KAN300100802; GA MŠk(CZ) ME10084 Institutional research plan: CEZ:AV0Z10100521 Keywords : Lu 2 Si 2 O 7 * Pr-doped * luminescence * scintillator * excited state ionization Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 3.767, year: 2012

Crystal structure and luminescence of complexes of Eu(III) and Tb(III) with furan-2,5-dicarboxylate

NARCIS (Netherlands)

Akerboom, S.; Fu, W.T.; Lutz, M.; Bouwman, E.

2012-01-01

Four new Ln(III) complexes (Ln = Eu, Tb) with furan-2,5-dicarboxylic acid (H2FDA) as a ligand have been synthesized and characterized in the solid state. Luminescence studies indicate that the compounds exhibit line-like luminescence characteristic of the lanthanide centre upon excitation in the

Luminescence of Ce3+ at two different sites in ?-Sr2P2O7 under vacuum ultraviolet-UV and x-ray excitation

NARCIS (Netherlands)

Hou, D.; Han, B.; Chen, W.; Liang, H.; Su, Q.; Dorenbos, P.; Huang, Y.; Gao, Z.; Tao, Y.

2010-01-01

A series of Ce3+ doped ?-Sr2?2xCexNaxP2O7 phosphor compounds has been prepared using a high-temperature solid-state reaction technique. The luminescence properties under vacuum ultraviolet-UV and x-ray excitation were studied. Luminescence spectra reveal three UV-emitting peaks at about 310, 330,

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)

Size-dependent abnormal thermo-enhanced luminescence of ytterbium-doped nanoparticles.

Science.gov (United States)

Cui, Xiangshui; Cheng, Yao; Lin, Hang; Huang, Feng; Wu, Qingping; Wang, Yuansheng

2017-09-21

Thermal quenching above 300 K is widely expected in photoluminescence. Luminescence quenching is usually ascribed to the non-radiative relaxation of excited electrons to the ground state of the activators, during which a high temperature always plays a role in pushing the excited electrons towards the quenching channels, leading to thermal quenching. For the lanthanide-doped nanoparticles, however, there is a special luminescence quenching channel that does not exist in their bulk counterparts, i.e., energy migration-induced surface quenching. Herein, a size-dependent abnormal thermal enhancement of luminescence in the temperature range of 300 K to 423 K in the ytterbium-doped fluoride nanoparticles is presented for the first time. Importantly, in this work, we originally demonstrate that the energy migration-induced surface quenching can be suppressed by increasing temperature, which results in the abnormal thermal enhancement of luminescence. According to the temperature-dependent X-ray diffraction and lifetime analyses, an underlying mechanism based on the effect of thermal lattice expansion on ytterbium-mediated energy migration is proposed. This new finding adds new insights to the size effect on the luminescent characteristics of nanoparticles, which could be utilized to construct some unique nanostructures, especially for many important temperature-related purposes, such as thermal sensing technology.

Electron-Impact Excitation of Uracil Luminescence on a Ceramic Surface

Science.gov (United States)

Shafranyosh, I. I.; Mitropolskiy, I. E.; Kuzma, V. V.; Svyda, Yu. Yu.; Sukhoviya, M. I.

2018-03-01

Photoelectron spectroscopy was applied to pyrimidine nitrogenous bases, an important class of six-membered heterocyclic compounds incorporated into nucleic acids. The emission spectrum of uracil adsorbed on a ceramic surface that was obtained by bombardment with 600-eV electrons in a high vacuum was analyzed. Broad bands with maxima at 335, 435, and 495 nm were observed in the UV and visible regions. The strongest band (λ = 335 nm) was attributed to fluorescence and corresponded to a singlet-singlet transition from the first excited electronic state into the molecular ground state. Electronic transitions from a triplet T1 into the ground state formed a weaker phosphorescence band (λ = 435 nm). The nature of the band maximum at 495 nm is discussed. The obtained luminescence spectrum was compared with photoluminescence spectra in various phases.

Crystal structure, intensity luminescence characteristics and stimulated radiation of disordered gallate LaSr2Ga11O20-Nd3+

International Nuclear Information System (INIS)

Kaminskij, A.A.; Mill', B.V.; Belokoneva, E.L.; Butashin, A.V.; Sarkisov, S.Eh.; Kurbanov, K.; Khodzhabagyan, G.G.

1986-01-01

LnA 2 2+ Ga 11 O 20 and A 3 2+ M 0.5 5+ Ga 10.5 O 20 compounds are synthesized, LaSr 2 Ga 11 O 20 and LaSr 2 Ga 11 O 20 -Nd 3+ monocrystals are grown by Czochralski method. Their X-ray diffraction analysis is conducted, absorption - luminescence characteristics are obtained, stimulated Nd 3+ ion radiation is excited and investigated in two generating channel waves 4 F 3/2 → 4 I 11/2,13/2 at 300 K

Suppression of concentration quenching of Er-related luminescence in Er-doped GaN

International Nuclear Information System (INIS)

Chen Shaoqiang; Tomita, Shigeo; Kudo, Hiroshi; Akimoto, Katsuhiro; Dierre, Benjamin; Lee, Woong; Sekiguchi, Takashi

2010-01-01

Erbium-doped GaN with different doping concentrations were grown by ammonia-source molecular beam epitaxy. The intra-4f-shell transitions related green luminescence were observed by both photoluminescence (PL) and cathodoluminescence (CL) measurements. It was found that concentration quenching of Er-related luminescence was observed in PL measurements while not in CL measurements. The different excitation and relaxation processes are suggested as the cause of the concentration quenching characteristics between PL and CL. The strong Er-related CL intensity in highly doped GaN demonstrates that high energy excitation is a promising approach to suppress the concentration quenching in Er-doped GaN.

Luminescence spectroscopy with synchrotron radiation: History, highlights, future

International Nuclear Information System (INIS)

Zimmerer, Georg

2006-01-01

Luminescence spectroscopy and the investigation of dynamical processes with synchrotron radiation (SR) started about 35 years ago in nearly all SR laboratories existing at that time. In the present paper, the pioneering experiments are particularly emphasized. The exciting development is illustrated presenting highlights for the whole period from the beginning to the present day. The highlights are taken from fields like exciton self-trapping, inelastic electron-electron scattering, optically stimulated desorption, cross luminescence, or probing of cluster properties with luminescence spectroscopic methods. More technological aspects play a role in present day's experiments, like quantum cutting in rare-earth-doped insulators. Promising two-photon excitation and light amplification experiments with SR will be included, as well as the first results obtained in a luminescence experiment with selective Vaccum ultraviolet-free electron laser excitation. Finally, a few ideas concerning the future development of luminescence spectroscopy with SR will be sketched

Application of multi-step excitation schemes for detection of actinides and lanthanides in solutions by luminescence/chemiluminescence laser spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Izosimov, I. [Joint Institute for Nuclear Research, Joliot Curie 6, Dubna 141980 (Russian Federation)

2016-07-01

The use of laser radiation with tunable wavelength allows the selective excitation of actinide/lanthanide species with subsequent registration of luminescence/chemiluminescence for their detection. This work is devoted to applications of the time-resolved laser-induced luminescence spectroscopy and time-resolved laser-induced chemiluminescence spectroscopy for the detection of lanthanides and actinides. Results of the experiments on U, Eu, and Sm detection by TRLIF (Time Resolved Laser Induced Fluorescence) method in blood plasma and urine are presented. Data on luminol chemiluminescence in solutions containing Sm(III), U(IV), and Pu(IV) are analyzed. It is shown that appropriate selectivity of lanthanide/actinide detection can be reached when chemiluminescence is initiated by transitions within 4f- or 5f-electron shell of lanthanide/actinide ions corresponding to the visible spectral range. In this case chemiluminescence of chemiluminogen (luminol) arises when the ion of f element is excited by multi-quantum absorption of visible light. The multi-photon scheme of chemiluminescence excitation makes chemiluminescence not only a highly sensitive but also a highly selective tool for the detection of lanthanide/actinide species in solutions. (author)

Luminescence from ZnSe excited by picosecond mid-infrared FEL pulses

International Nuclear Information System (INIS)

Mitsuyu, T.; Suzuki, T.; Tomimasu, T.

1998-01-01

We have observed blue band-edge emission from a ZnSe crystal under irradiation of mid-infrared picosecond free electron laser (FEL) pulses. The emission characteristics including spectrum, excitation power dependence, excitation wavelength dependence, and decay time have been investigated. The experimental results have indicated that it is difficult to understand the excitation process by multiphoton excitation, thermal excitation, or excitation through mid-gap levels. (Copyright (c) 1998 Elsevier Science B.V., Amsterdam. All rights reserved.)

Doped luminescent materials and particle discrimination using same

Science.gov (United States)

Doty, F. Patrick; Allendorf, Mark D; Feng, Patrick L

2014-10-07

Doped luminescent materials are provided for converting excited triplet states to radiative hybrid states. The doped materials may be used to conduct pulse shape discrimination (PSD) using luminescence generated by harvested excited triplet states. The doped materials may also be used to detect particles using spectral shape discrimination (SSD).

Ionic liquid-assisted hydrothermal synthesis and excitation wavelength-dependent luminescence of YBO3:Eu3+ nano-/micro-crystals

International Nuclear Information System (INIS)

Tian, Yue; Tian, Bining; Chen, Baojiu; Cui, Cai’e; Huang, Ping; Wang, Lei; Hua, Ruinian

2014-01-01

Graphical abstract: Three dimensional (3D) architectures YBO 3 :Eu 3+ phosphors were prepared via ionic liquid assisted hydrothermal process. The pH values and ionic liquid play an important role on the morphology of products. Excitation wavelength-dependent luminescent behavior was found in the as-prepared tyre-like YBO 3 :Eu 3+ microspheres. Highlights: • YBO 3 :Eu 3+ phosphors were prepared via ionic liquid assisted hydrothermal process. • pH values and ionic liquid play an important role on the morphology of products. • Excitation wavelength-dependent luminescent behavior was found. -- Abstract: Three dimensional (3D) architectures YBO 3 :Eu 3+ phosphors were prepared via ionic liquid-assisted hydrothermal process and characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM) and photoluminescence (PL). The pH value and ionic liquid play an important role in the control of morphology of products. By comparing with the corresponding bulk, the tyre-like YBO 3 :5 mol%Eu 3+ microspheres demonstrate a red shift of the charge transfer band (CTB), appearance of a long excitation tail at the long wavelength side of the CTB and high improved chromaticity. Two Eu 3+ environments in the tyre-like sample, namely interior and outside Eu 3+ , were found by selective excitation under the different wavelength light. Finally, fluorescent decays and Judd–Ofelt (J–O) theory were utilized to analyze the local crystal environments around Eu 3+ ions in the tyre-like and bulk phosphors

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.

Near-surface layer radiation color centers in lithium fluoride nanocrystals: Luminescence and composition

Energy Technology Data Exchange (ETDEWEB)

Voitovich, A.P., E-mail: voitovich@imaph.bas-net.by; Kalinov, V.S.; Stupak, A.P.; Novikov, A.N.; Runets, L.P.

2015-01-15

Lithium fluoride nanocrystals are irradiated by gamma quanta at 77 K. The radiation color centers formed in a near-surface layer of nanocrystals are studied. Absorption, luminescence and luminescence excitation spectra of the surface defects have been measured. It has been found that the luminescence excitation spectra for aggregated surface centers consist of two or three bands with not very much different intensities. Reactions of the surface centers separately with electrons and with anion vacancies have been investigated. Numbers of anion vacancies and electrons entering into the centers composition have been established and it has been found that F{sub S1}, F{sub S1}{sup −}, F{sub S2}, F{sub S2}{sup −}, F{sub S3}{sup +} and F{sub S3} types of the surface centers are formed. The degree of luminescence polarization has been defined and it has been determined that the polarization degree for F{sub S2}{sup +} centers changes sign under transition from one excitation band to another. It has been shown that during irradiation at 77 K radiation-induced defects are formed more efficiently on the surface than in the bulk. - Highlights: • Radiative color centers were fabricated in lithium fluoride nanocrystals. • The unique absorption and luminescence characteristics are inherent in the centers. • The reactions of these centers with electrons and anion vacancies were studied. • The degree of luminescence polarization was defined. • Numbers of anion vacancies and electrons forming the centers were established.

Optical luminescence from alkyl-passivated Si nanocrystals under vacuum ultraviolet excitation: Origin and temperature dependence of the blue and orange emissions

OpenAIRE

Chao, Y; Houlton, A; Horrocks, BR; Hunt, MRC; Poolton, NRJ; Yang, J; Šiller, L

2006-01-01

The origin and stability of luminescence are critical issues for Si nanocrystals which are intended for use as biological probes. The optical luminescence of alkyl-monolayer-passivated silicon nanocrystals was studied under excitation with vacuum ultraviolet photons (5.1–23 eV). Blue and orange emission bands were observed simultaneously, but the blue band only appeared at low temperatures (8.7 eV). At 8 K, the peak wavelengths of the emission bands were 430±2 nm (blue) and 600±2 nm (orange)....

Luminescent characteristics of UV excited Sr_0_._5Ca_0_._5TiO_3: Pr"3"+ reddish-orange phosphor

International Nuclear Information System (INIS)

Vidyadharan, Viji; Mohan P, Remya; Joseph, Cyriac; Unnikrishnan, N.V.; Biju, P.R.

2016-01-01

Pr"3"+ doped Sr_0_._5Ca_0_._5TiO_3 phosphors were synthesised by solid state reaction process. The structure, surface morphology and photoluminescence of the prepared phosphors were analysed using XRD, SEM and photoluminescence spectroscopy respectively. The XRD pattern confirmed orthorhombic perovskite structure of the Sr_0_._5Ca_0_._5TiO_3: x Pr"3"+ phosphor. Agglomeration of particles with irregular shapes is observed from the SEM images. The emission spectra of Sr_0_._5Ca_0_._5TiO_3: x Pr"3"+ phosphor shows the samples can be effectively excited with UV light at 336 nm and exhibit a strong reddish-orange emission at 611 nm. Concentration dependence of emission intensity shows concentration quenching effect on increasing Pr"3"+ concentration after x = 0.1 because of dipole–dipole interaction. Using Blasse's formula, critical distance for energy transfer was calculated. The CIE co-ordinates, CCT, colour purity and luminescence decay of the prepared phosphors were also calculated. These results offer the prepared phosphor as a suitable candidate for various photonic applications. - Highlights: • Sr_0_._5Ca_0_._5TiO_3: x Pr"3"+ perovskite structured phosphors were synthesized. • Under UV excitation, the PL spectra show strong reddish-orange emission. • The emission from "3P_J levels of Pr"3"+ were absent due to the presence of IVCT band. • Concentration quenching due to dipole–dipole interaction was observed. • For x = 0.1, sample shows a maximum emission intensity with 91.7% colour purity.

Luminescence and circularly polarized luminescence of macrocyclic Eu(III) and Tb(III) complexes embedded in xerogel and sol-gel SiO2 glasses

International Nuclear Information System (INIS)

Morita, M.; Rau, D.; Kai, T.

2002-01-01

Luminescence, time-resolved luminescence, circularly polarized luminescence (CPL) and decay profiles of Ln(III)(15-crownether-5) (Ln=Ce, Sm, Eu, Tb) and Tb(III)-(R),(S)-cyclen derivative complexes doped in xerogel and sol-gel silica glasses are measured at temperatures down to 10 K to characterize luminescence properties and the electronic structure in the excited states. Luminescence spectral profiles and calculation of crystal field parameters (B 0 (2) ,B 2 (2) ) in the 5 D 0 → 7 F J (J=1,2) transition give evidence of the fact that the pentagonal and planar structure of Eu(III) (15-crownether-5) does hold in xerogel and sol-gel glasses prepared at temperatures below 100 deg. C. As annealing temperatures are increased from 80 deg. C to 750 deg. C, Eu(III) complexes in sol-gel glasses are found to decompose gradually to SiO 2 :Eu 3+ . Tb(III)-(R) and (S)-cyclen derivative complexes in xerogel reveal at room temperature and 10 K sharp CPL spectra with luminescence dissymmetry factors g lum =-0.1 and 0.1, respectively. These complexes doped in sol-gel glasses represent luminescence characteristics of rare earth ions encapsulated in the nano-porous host

The extended Beer-Lambert theory for ray tracing modeling of LED chip-scaled packaging application with multiple luminescence materials

Science.gov (United States)

Yuan, Cadmus C. A.

2015-12-01

Optical ray tracing modeling applied Beer-Lambert method in the single luminescence material system to model the white light pattern from blue LED light source. This paper extends such algorithm to a mixed multiple luminescence material system by introducing the equivalent excitation and emission spectrum of individual luminescence materials. The quantum efficiency numbers of individual material and self-absorption of the multiple luminescence material system are considered as well. By this combination, researchers are able to model the luminescence characteristics of LED chip-scaled packaging (CSP), which provides simple process steps and the freedom of the luminescence material geometrical dimension. The method will be first validated by the experimental results. Afterward, a further parametric investigation has been then conducted.

Hydrothermal synthesis and luminescent properties of LnPO4:Tb,Bi (Ln=La,Gd) phosphors under UV/VUV excitation

International Nuclear Information System (INIS)

Wang Yuhua; Wu Chunfang; Wei Jie

2007-01-01

Monoclinic LnPO 4 :Tb,Bi (Ln=La,Gd) phosphors were prepared by hydrothermal reaction and their luminescent properties under ultraviolet (UV) and vacuum ultraviolet (VUV) excitation were investigated. LaPO 4 :Tb,Bi phosphor and GdPO 4 :Tb phosphor showed the strongest emission intensity under 254 and 147 nm excitation, respectively, because of the different energy transfer models. In UV region, Bi 3+ absorbed most energy then transferred to Tb 3+ , but in VUV region it was the host which absorbed most energy and transferred to Tb 3+

Luminescence and energy transfer

Energy Technology Data Exchange (ETDEWEB)

Blasse, G; Bleijenberg, K C; Powell, R C

1980-01-01

This paper deals with the luminescence of uranate centres in solids. The luminescence properties are influenced by the coordination number of the hexavalent uranium ion and by the crystallographic surroundings of the uranate centre. Transitions playing a role in the luminescence processes within the octahedral UO/sub 6//sup 6 -/ group are discussed using the results from both theoretical and experimental studies on another octahedral uranium complex: UF/sub 6/. The luminescence of the octahedral uranate group in oxidic compounds is discussed. Attention is paid to the vibrational structure, which is observed in the luminescence spectra at low temperatures and to the temperature quenching of the luminescence. The temperature quenching of the uranate luminescence in uranium-doped tungstates with ordered perovskite structure can be described in terms of a three state single configurational coordinate diagram. The complicated luminescence spectra of uranium-activated sodium fluoride (NaF-U) crystals have been unraveled using chemical variation of the crystal compositions and using site selective laser excitation techniques. Four different luminescent uranate centres have been observed in NaF-U. A model for the configurations of the luminescent centres has been deduced using the results from ionic conductivity experiments.

Review of present trends in luminescence research

International Nuclear Information System (INIS)

Williams, F.; Delaware Univ., Newark

1981-01-01

The difficulties of a comprehensive review of the broad and diverse branches of molecular and solid-state luminescence research are noted. This review is thus limited to selective topics. Some general concepts and trends are then introduced, including: luminescence excitation as a collective excitation of a many-body problem, encompassing in some cases the source and probe in its formulation; continuing trends towards extremal conditions of experiments and towards inhomogeneous and structured materials, from man-made superlattices to biological materials; and increased attention to applications of luminescence research to lamps, displays, solar devices and biological research. Representative recent and new specific research areas include: site selection spectroscopy and 'hole burning'; picosecond delayed coherent anti-Stokes Raman scattering; computer simulation of dynamical processes in luminescence; electron-hole expansion from the Fermi pressure of e-h plasmas; and hot electron phenomena and hot luminescence. Finally some pending problems in luminescence research, such as reconciling the configuration coordinate model and the electronic band theory and clarifying multi-phonon non-radiative processes, are discussed. (orig.)

Synthesis, characteristics and luminescent properties of a new Tb(III) ternary complex applied in near UV-based LED

Science.gov (United States)

Sun, Naiqun; Li, Liping; Yang, Yamin; Zhang, Aiqin; Jia, Husheng; Liu, Xuguang; Xu, Bingshe

2015-11-01

A novel Tb(III) ternary complex, Tb(p-BBA)3UA, was synthesized with 4-benzoylbenzoic acid (p-BBA) as primary ligand and undecylenic acid (UA) as reactive ligand. Tb(III) complex exhibits high thermal stability and wide and strong excitation bands from 310 nm to 400 nm when monitored at 543 nm, which matches well with the 365 nm UV chip. The complex displays Tb(III) characteristic peaks at 488, 543, 584 and 619 nm under the excitation of 365 nm UV-light. The intramolecular energy transfer process was also discussed. Meanwhile, the complex has longer fluorescence lifetime (1.317 ms) and higher quantum yield (44.8%). When used in LED with 365 nm UV chip (power efficiency is 17.3 lm/W), the complex still maintained its qualified luminescent performance. All the results indicate that Tb(p-BBA)3UA can be applied as a green component for fabrication of near UV-based white LED.

Mechanism of band-edge luminescence in cuprous iodide single crystals

International Nuclear Information System (INIS)

Gao, Pan; Gu, Mu; Liu, Xi; Liu, Bo; Zheng, Yan-Qing; Shi, Er-Wei; Shi, Jun-Yan; Zhang, Guo-bin

2014-01-01

Highlights: • The luminescence properties of CuI crystals are influenced by the quality of the as-grown crystals. • The emission peaks of free-exciton and bound-exciton are observed in the CuI single crystals. • The ultrafast component luminescence is warranted to the donor-acceptor pair recombination. • The exciton absorption and electron excitation multiplication processes were observed in CuI. - Abstract: The photoluminescence spectra of CuI crystals using synchrotron radiation as an excitation light source were obtained at 60 K. The emission peaks at 405, 415, 420 and 443 nm were observed. The possible origins of these peaks were discussed by the temperature dependence of luminescence spectra for CuI material. Meanwhile, the photoluminescence spectra of CuI powder with different excitation intensity were measured and the ultrafast luminescence component of CuI crystals was warranted to be attributed to the recombination of donor acceptor pair. Furthermore, the excitation process was studied by measuring the photoluminescence excitation spectra of CuI crystals and powder

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

Luminescent properties of LuPO4-Pr and LuPO4-Eu nanoparticles

International Nuclear Information System (INIS)

Vistovskyy, V.; Malyi, T.; Vas’kiv, A.; Chylii, M.; Mitina, N.; Zaichenko, A.; Gektin, A.; Voloshinovskii, A.

2016-01-01

Spectral-luminescence parameters of LuPO 4 -Eu and LuPO 4 -Pr nanoparticles of different sizes are studied upon excitation by the synchrotron radiation with photon energies 4–40 eV. Influence of the nanoparticle size on Eu 3+ and Pr 3+ impurity luminescence is analyzed for intracenter and recombination excitation. It is shown that the luminescence intensity of impurities in the case of recombination excitation significantly stronger decreases with decreasing of nanoparticle size compared to intracenter excitation. This feature is explained by the influence of thermalization length to nanoparticle size ratio on the recombination luminescence. Electron recombination luminescence inherent for LuPO 4 -Eu nanoparticles shows a weaker dependence on the nanoparticle size than the hole one in LuPO 4 -Pr nanoparticles. The difference between energy states of praseodymium impurity ions in nanoparticles of different sizes is revealed.

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)

Dependence on liquid temperature and purity of light emission characteristics in single cavitation bubble luminescence

Energy Technology Data Exchange (ETDEWEB)

Barbaglia, Mario O; Bonetto, Fabian J [Consejo Nacional de Investigaciones Cientificas y Tecnicas and Instituto Balseiro, Centro Atomico Bariloche, Av. Bustillo 9500, CP8400, Rio Negro (Argentina); Consejo Nacional de Investigaciones Cientificas y Tecnicas, Instituto Balseiro, and Comision Nacional de Energia Atomica, Laboratorio de Cavitacion y Biotecnologia, Centro Atomico Bariloche, Av. Bustillo 9500, CP8400, Rio Negro (Argentina)

2004-02-15

We produced single bubbles in water using a visible pulsed laser and studied the characteristics of the light emitted during the bubble collapse time as a function of the water temperature for different water purity values. The water temperature ranged from freezing point (0 deg. C) to near boiling. We measured the luminescence pulse for the mentioned temperature range at various purity values. We also obtained the average bubble lifetime and the average luminescence pulse emitted as a function of water temperature. The main conclusion was that the luminescence can be modified by the water quality and by the water temperature. Maximum luminescence was obtained near the water freezing point.

Dependence on liquid temperature and purity of light emission characteristics in single cavitation bubble luminescence

International Nuclear Information System (INIS)

Barbaglia, Mario O.; Bonetto, Fabian J.

2004-01-01

We produced single bubbles in water using a visible pulsed laser and studied the characteristics of the light emitted during the bubble collapse time as a function of the water temperature for different water purity values. The water temperature ranged from freezing point (0 deg. C) to near boiling. We measured the luminescence pulse for the mentioned temperature range at various purity values. We also obtained the average bubble lifetime and the average luminescence pulse emitted as a function of water temperature. The main conclusion was that the luminescence can be modified by the water quality and by the water temperature. Maximum luminescence was obtained near the water freezing point

Fluorescence enhancement and quenching of Eu(TTFA)3 by Ag nanoparticles at different excitations

International Nuclear Information System (INIS)

Wang, Qingru; Shi, Qiang; Li, Shuhong; Wang, Wenjun; Zheng, Shiling

2015-01-01

The luminescence properties of Eu(TTFA) 3 complex in presence of silver nanoparticles were investigated at three excitation wavelengths of 350 nm, 383 nm and 463 nm, respectively. Luminescence quenching and enhancement were both observed at three different excitation and emission wavelengths. Luminescence at 612 nm, 578 nm, 590 nm and 650 nm were enhanced at excitation wavelength of 350 nm, and quenched at excitation wavelength of 383 nm. The enhancement factor reached to 1.6 and the quench factor was about 0.65. For 463 nm excitation, the luminescence at 612 nm was quenched, and the quench factor reached to 0.85. Luminescence at other three emission wavelengths (578 nm, 590 nm, and 650 nm) was enhanced, with the greatest enhancement factor of ∼5. - Highlights: • The luminescence enhancement and quenching were both obtained by using the Ag nanoparticles. • The luminescence enhancement and quenching highly depends on the excitation and emission wavelengths. • The enhancement factor of luminescence also has a great relationship with the intrinsic quantum yield

Anti-Stokes Luminescence in High Quality Quantum Wells

Science.gov (United States)

Vinattieri, A.; Bogani, F.; Miotto, A.; Ceccherini, S.

1997-11-01

We present a detailed investigation of the anti-Stokes (AS) luminescence which originates from exciton recombination when below gap excitation is used, in a set of high quality quantum well structures. We observe strong excitonic resonances in the AS signal as measured from photoluminescence and photoluminescence excitation spectra. We demonstrate that neither the electromagnetic coupling between the wells nor the morphological disorder can explain this up-conversion effect. Time-resolved luminescence data after ps excitation and fs correlation spectroscopy results provide clear evidence of the occurrence of a two-step absorption which is assisted by the exciton population resonantly excited by the first photon.

Signal intensity analysis and optimization for in vivo imaging of Cherenkov and excited luminescence

Science.gov (United States)

LaRochelle, Ethan P. M.; Shell, Jennifer R.; Gunn, Jason R.; Davis, Scott C.; Pogue, Brian W.

2018-04-01

During external beam radiotherapy (EBRT), in vivo Cherenkov optical emissions can be used as a dosimetry tool or to excite luminescence, termed Cherenkov-excited luminescence (CEL) with microsecond-level time-gated cameras. The goal of this work was to develop a complete theoretical foundation for the detectable signal strength, in order to provide guidance on optimization of the limits of detection and how to optimize near real time imaging. The key parameters affecting photon production, propagation and detection were considered and experimental validation with both tissue phantoms and a murine model are shown. Both the theoretical analysis and experimental data indicate that the detection level is near a single photon-per-pixel for the detection geometry and frame rates commonly used, with the strongest factor being the signal decrease with the square of distance from tissue to camera. Experimental data demonstrates how the SNR improves with increasing integration time, but only up to the point where the dominance of camera read noise is overcome by stray photon noise that cannot be suppressed. For the current camera in a fixed geometry, the signal to background ratio limits the detection of light signals, and the observed in vivo Cherenkov emission is on the order of 100×  stronger than CEL signals. As a result, imaging signals from depths  <15 mm is reasonable for Cherenkov light, and depths  <3 mm is reasonable for CEL imaging. The current investigation modeled Cherenkov and CEL imaging of two oxygen sensing phosphorescent compounds, but the modularity of the code allows for easy comparison of different agents or alternative cameras, geometries or tissues.

An optical authentication system based on imaging of excitation-selected lanthanide luminescence.

Science.gov (United States)

Carro-Temboury, Miguel R; Arppe, Riikka; Vosch, Tom; Sørensen, Thomas Just

2018-01-01

Secure data encryption relies heavily on one-way functions, and copy protection relies on features that are difficult to reproduce. We present an optical authentication system based on lanthanide luminescence from physical one-way functions or physical unclonable functions (PUFs). They cannot be reproduced and thus enable unbreakable encryption. Further, PUFs will prevent counterfeiting if tags with unique PUFs are grafted onto products. We have developed an authentication system that comprises a hardware reader, image analysis, and authentication software and physical keys that we demonstrate as an anticounterfeiting system. The physical keys are PUFs made from random patterns of taggants in polymer films on glass that can be imaged following selected excitation of particular lanthanide(III) ions doped into the individual taggants. This form of excitation-selected imaging ensures that by using at least two lanthanide(III) ion dopants, the random patterns cannot be copied, because the excitation selection will fail when using any other emitter. With the developed reader and software, the random patterns are read and digitized, which allows a digital pattern to be stored. This digital pattern or digital key can be used to authenticate the physical key in anticounterfeiting or to encrypt any message. The PUF key was produced with a staggering nominal encoding capacity of 7 3600 . Although the encoding capacity of the realized authentication system reduces to 6 × 10 104 , it is more than sufficient to completely preclude counterfeiting of products.

Luminescence of Quantum Dots by Coupling with Nonradiative Surface Plasmon Modes in a Scanning Tunneling Microscope

International Nuclear Information System (INIS)

Romero, M.J.; van de Lagemaat, J.

2009-01-01

The electronic coupling between quantum dots (QDs) and surface plasmons (SPs) is investigated by a luminescence spectroscopy based on scanning tunneling microscopy (STM). We show that tunneling luminescence from the dot is excited by coupling with the nonradiative plasmon mode oscillating at the metallic tunneling gap formed during the STM operation. This approach to the SP excitation reveals aspects of the SP-QD coupling not accessible to the more conventional optical excitation of SPs. In the STM, luminescence from the dot is observed when and only when the SP is in resonance with the fundamental transition of the dot. The tunneling luminescence spectrum also suggests that excited SP-QD hybrid states can participate in the excitation of QD luminescence. Not only the SP excitation regulates the QD luminescence but the presence of the dot at the tunneling gap imposes restrictions to the SP that can be excited in the STM, in which the SP cannot exceed the energy of the fundamental transition of the dot. The superior SP-QD coupling observed in the STM is due to the tunneling gap acting as a tunable plasmonic resonator in which the dot is fully immersed.

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....

Luminescent properties of fluorophosphate glasses with lead chalcogenides molecular clusters

International Nuclear Information System (INIS)

Kolobkova, E.V.; Kukushkin, D.S.; Nikonorov, N.V.; Shakhverdov, T.A.; Sidorov, A.I.; Vasiliev, V.N.

2015-01-01

Fluorophosphate glasses containing lead, selenium, and sulfur exhibit an intense luminescence in the 400–620 nm spectral region when excited by the 240–420 nm radiation. This luminescence is due to the presence of (PbSe) n and/or (PbS) n molecular clusters in the glasses, which appear in the as-prepared glasses before quantum dots formation. The thermal treatment at temperatures less than the glass transition temperature results in the red-shift of the luminescence bands and in an increase in the luminescence intensity. Heating the thermally treated glass samples leads to the reversible thermal quenching of the luminescence. - Highlights: • Fluorophosphate glasses with Pb, Se, and S ions contain (PbSe) n or (PbS) n molecular clusters. • (PbSe) n and (PbS) n molecular clusters possess luminescence in the visible with UV excitation. • Heating the glass leads to the reversible thermal quenching of the luminescence

Controlled agglomeration of Tb-doped Y2O3 nanocrystals studied by x-ray absorption fine structure, x-ray excited luminescence, and photoluminescence

International Nuclear Information System (INIS)

Soo, Y.L.; Huang, S.W.; Kao, Y.H.; Chhabra, V.; Kulkarni, B.; Veliadis, J.V.; Bhargava, R.N.

1999-01-01

Local environment surrounding Y atoms in Y 2 O 3 :Tb nanocrystals under various heat treatment conditions has been investigated by using the extended x-ray absorption fine structure (EXAFS) technique. X-ray excited luminescence (XEL) with the incident x-ray energy near Y K edge and Tb L edges has also been measured to investigate the mechanisms of x-ray-to-visible down conversion in these doped nanoparticles. The observed changes in EXAFS, XEL, and photoluminescent data can be explained on the basis of increased average size of the nanoparticles as confirmed by transmission electron microscopy studies. Our results thus demonstrate that the doped nanoparticles can agglomerate to a controllable degree by varying the heat treatment temperature. At higher temperatures, the local environment surrounding Y atoms in the nanoparticles is found to become similar to that in bulk Y 2 O 3 while the XEL output still shows the characteristics of nanocrystals. These results indicate that appropriate heat treatment can afford an effective means to control the intensity and signal-to-background ratio of green luminescence output of these doped nanocrystal phosphors, potentially useful for some device applications. copyright 1999 American Institute of Physics

Single fiber temperature probe configuration using anti-Stokes luminescence from Cr:GdAlO3

Science.gov (United States)

Eldridge, Jeffrey I.

2018-06-01

Single-photon excitation of anti-Stokes-shifted emission from a thermographic phosphor allows operation of a luminescence decay-based single fiber temperature probe with negligible interference from background fiber-generated Raman scattering. While single fiber probe configurations for luminescence-based fiber optic thermometers offer advantages of simple design, compactness, and superior emission light collection efficiency, their effective use has been limited by interference from Raman scattering in the fiber probe and excitation delivery fiber that produces distortion of the luminescence decay that follows the excitation pulse. The near elimination of interference by background fiber-generated Raman scattering was demonstrated by incorporating a Cr-doped GdAlO3 (Cr:GdAlO3) thermographic phosphor as the sensing element at the end of a single fiber luminescence decay-based thermometer and detecting anti-Stokes-shifted luminescence centered at 542 or 593 nm produced by 695 nm excitation. Measurements were performed using both silica (up to 1150 °C) and single-crystal YAG (up to 1200 °C) fiber-based thermometers. Selection of emission detection centered at 542 nm greatly benefited the YAG fiber probe measurements by practically eliminating detection of otherwise significant luminescence from Cr3+ impurities in the YAG fiber. For both the silica and YAG fiber probes, the relative benefit of adopting single-photon excitation of anti-Stokes-shifted luminescence was evaluated by comparison with results obtained by conventional 532 nm excitation of Stokes-shifted luminescence.

Luminescence and scintillation properties of LuPO4-Ce nanoparticles

International Nuclear Information System (INIS)

Vistovskyy, V.; Malyy, T.; Pushak, A.; Vas’kiv, A.; Shapoval, A.; Mitina, N.; Gektin, A.; Zaichenko, A.; Voloshinovskii, A.

2014-01-01

Study of the spectral-luminescence parameters of LuPO 4 -Ce nanoparticles upon the excitation by X-ray quanta and synchrotron radiation with photon energies of 4–25 eV was performed. Nanoparticles with mean size about a=35 nm and nanoparticles with size less than 12 nm reveal the different structures of cerium centers. Luminescence efficiency of LuPO 4 -Ce nanoparticles of a 4 -Ce nanoparticles studied using synchrotron and X-ray excitation. • Different structure of Ce 3+ -centers has been revealed for LuPO 4 -Ce nanoparticles. • Luminescence of LuPO 4 -Ce with size less than 12 nm is strongly quenched upon the X-ray excitation

Positron-Induced Luminescence

Science.gov (United States)

Stenson, E. V.; Hergenhahn, U.; Stoneking, M. R.; Pedersen, T. Sunn

2018-04-01

We report on the observation that low-energy positrons incident on a phosphor screen produce significantly more luminescence than electrons do. For two different wide-band-gap semiconductor phosphors (ZnS:Ag and ZnO:Zn), we compare the luminescent response to a positron beam with the response to an electron beam. For both phosphors, the positron response is significantly brighter than the electron response, by a factor that depends strongly on incident energy (0-5 keV). Positrons with just a few tens of electron-volts of energy (for ZnS:Ag) or less (for ZnO:Zn) produce as much luminescence as is produced by electrons with several kilo-electron-volts. We attribute this effect to valence band holes and excited electrons produced by positron annihilation and subsequent Auger processes. These results demonstrate a valuable approach for addressing long-standing questions about luminescent materials.

Luminescence properties of Tm3+ ions single-doped YF3 materials in an unconventional excitation region.

Science.gov (United States)

Chen, Yuan; Liu, Qing; Lin, Han; Yan, Xiaohong

2018-05-01

According to the spectral distribution of solar radiation at the earth's surface, under the excitation region of 1150 to 1350 nm, the up-conversion luminescence of Tm 3+ ions was investigated. The emission bands were matched well with the spectral response region of silicon solar cells, achieved by Tm 3+ ions single-doped yttrium fluoride (YF 3 ) phosphor, which was different from the conventional Tm 3+ /Yb 3+ ion couple co-doped materials. Additionally, the similar emission bands of Tm 3+ ions were achieved under excitation in the ultraviolet region. It is expected that via up-conversion and down-conversion routes, Tm 3+ -sensitized materials could convert photons to the desired wavelengths in order to reduce the energy loss of silicon solar cells, thereby enhancing the photovoltaic efficiency. Copyright © 2018 John Wiley & Sons, Ltd.

Determination of molecular structures of aromatic hydrocarbons of crystal fractions of Noriysk crude by a series of luminescent-spectral methods

Energy Technology Data Exchange (ETDEWEB)

Ogloblina, A.I.; Alekseyeva, T.A.; Barabadze, Sh.Sh.; Melikadze, L.D.; Teplitskaya, T.A.

1979-01-01

The structure of crystalline aromatic hydrocarbons isolated from the high boiling fraction (540-560 degrees) of Noriysk crude was studied using methods of luminescent-spectral analysis. The individual composition of the crystalline aromatic hydrocarbons was analyzed by a combination of fine structure luminescent spectroscopy and spectrofluorimetric methods in frozen matrices using spectra of fluorescence, phosphorescence and excitation of luminescence. The composite method used at 77 K is very effective and allows detailed characteristics of the molar-group composition of complex mixtures of petroleum aromatic hydrocarbons to the point of identification of individual components.

Luminescent and structural properties of Zn_xMg_1_-_xWO_4 mixed crystals

International Nuclear Information System (INIS)

Krutyak, N.; Nagirnyi, V.; Spassky, D.; Tupitsyna, I.; Dubovik, A.; Belsky, A.

2016-01-01

The structural and luminescent properties of perspective scintillating Zn_xMg_1_-_xWO_4 mixed crystals were studied. The following characteristics were found to depend linearly on x value: the energy of several vibrational modes detected by Raman spectroscopy, the bandgap width deduced from the shift of the excitation spectrum onset of a self-trapped exciton (STE) emission, the position of thermally stimulated luminescence peaks. It is also shown that the thermal stability of the STE luminescence decreases gradually when x decreases. These data indicate that each Zn_xMg_1_-_xWO_4 mixed crystal is not a mixture of two constituents, but possesses its original crystalline structure, as well as optical and luminescent properties. - Highlights: • The structural and luminescent properties of Zn_xMg_1_-_xWO_4 were studied. • The energy of Raman modes, the bandgap width, TSL peak position linearly depend on x. • Each Zn_xMg_1_-_xWO_4 possesses its original crystalline structure.

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.

Luminescence and luminescence quenching of Eu{sub 2}Mo{sub 4}O{sub 15}

Energy Technology Data Exchange (ETDEWEB)

Janulevicius, Matas; Grigorjevaite, Julija; Merkininkaite, Greta [Department of Analytical and Environmental Chemistry, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Sakirzanovas, Simas [Department of Applied Chemistry, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Katelnikovas, Arturas, E-mail: arturas.katelnikovas@chf.vu.lt [Department of Analytical and Environmental Chemistry, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania)

2016-11-15

A polycrystalline Eu{sub 2}Mo{sub 4}O{sub 15} phosphor sample was prepared by high temperature solid state reaction. Phase purity and morphological features of the phosphor were investigated by X-ray diffraction and scanning electron microscopy, respectively. Reflectance spectra showed that the optical band gap of Eu{sub 2}Mo{sub 4}O{sub 15} is 2.95 eV. Phosphor emits intensive red light when excited with 394 and 465 nm radiation. Temperature dependent emission and luminescence lifetime measurements revealed that external and internal quantum yields decrease at the same rate and that luminescence quenches due to photoionization. The calculated external quantum yields for 394 and 465 nm excitation were 7.8% and 53.5%, respectively.

Efficient green luminescence of terbium oxalate crystals: A case study with Judd-Ofelt theory and single crystal structure analysis and the effect of dehydration on luminescence

Science.gov (United States)

Alexander, Dinu; Joy, Monu; Thomas, Kukku; Sisira, S.; Biju, P. R.; Unnikrishnan, N. V.; Sudarsanakumar, C.; Ittyachen, M. A.; Joseph, Cyriac

2018-06-01

Design and synthesis of Lanthanide based metal organic framework is a frontier area of research owing to their structural diversity enabling specific applications. The luminescence properties of rare earths, tuned by the structural features of Ln-MOFs are investigated extensively. Rare earth oxalates which can be synthesized in a facile method, ensuring the structural features of MOFs with excellent photoluminescence characteristics deserves much attention. This work is the first time report on the single crystal structure and Judd-Ofelt (JO) theoretical analysis - their correlation with the intense and sharp green luminescence of Terbium oxalate crystals. The intense green luminescence observed for Terbium oxalate crystals for a wide range of excitation from DUV to visible region despite the luminescence limiting factors are discussed. The absence of concentration quenching and lifting up of forbidden nature of f-f transitions, allowing direct excitation of Terbium ions is analysed with the help of JO theory and single crystal structure analysis. The JO analysis predicted the asymmetry of Terbium sites, allowing the electric dipole transitions and from the JO intensity parameters, promising spectroscopic parameters - emission cross section, branching ratio, gain band width and gain coefficient of the material were calculated. The single crystal structure analysis revealed the asymmetry of Tb sites and structure of Terbium oxalate is formed by the hydrogen bonded stacking of overlapped six Terbium membered rings connected by the oxalate ligands. The molecularly thick layers thus formed on the crystal surface are imaged by the atomic force microscopy. The presence of water channels in the structure and the effect of lattice water molecules on the luminescence intensity are also investigated.

Visible luminescence peculiar to sintered silica nanoparticles: Spectral and decay properties

Energy Technology Data Exchange (ETDEWEB)

Vaccaro, L. [Dipartimento di Fisica e Chimica, Università di Palermo, Via Archirafi 36, I-90123 Palermo (Italy); Cannas, M., E-mail: marco.cannas@unipa.it [Dipartimento di Fisica e Chimica, Università di Palermo, Via Archirafi 36, I-90123 Palermo (Italy); Cangialosi, C. [Dipartimento di Fisica e Chimica, Università di Palermo, Via Archirafi 36, I-90123 Palermo (Italy); Laboratoire H. Curien, UMR CNRS 5516, Université St-Etienne, St-Etienne F-42000 (France); Spallino, L.; Gelardi, F.M. [Dipartimento di Fisica e Chimica, Università di Palermo, Via Archirafi 36, I-90123 Palermo (Italy)

2015-10-15

We report that the sintering at 1000 °C of silica nanoparticles (an average diameter of 14 nm) produces a transparent sample that exhibits a bright visible emission under UV excitation. The use of time resolved luminescence spectroscopy and a tunable laser source allows us to single out three contributions centered at 1.96 eV, 2.41 eV and 3.43 eV. The excitation spectra of these emissions evidence bell shaped bands consistent with transitions between localized defects’ states. For each emission we study the intensity and the lifetime in the temperature range from 300 K down to 10 K, thus evidencing the competition between radiative and non-radiative processes in the optical cycle of luminescent centers. The comparison with the luminescence properties of silica, both nanoparticles and bulk, points out that the observed emissions are peculiar to the sintered silica network. - Highlights: • Solid-phase sintering at 1000 °C of silica nanoparticles produces a transparent sample. • Sintered silica nanoparticles emit a bright luminescence under UV excitation. • Three emissions, centered around 2.0 V, 2.4 eV and 3.4 eV, are distinguished on the basis of the excitation and decay properties. • The observed excitation/emission bands originate from localized defect states peculiar to the sintered silica network. • The luminescence efficiency decreases with temperature due to the activation of non-radiative channels.

LUMINESCENT PROPERTIES OF SILICATE GLASSES WITH CERIUM IONS AND ANTIMONY

Directory of Open Access Journals (Sweden)

A. M. Klykova

2014-05-01

Full Text Available The paper deals with the results of an experimental study of luminescence excitation spectra and luminescence of silicate glasses containing cerium ions and antimony. The aim of this work was to study the features of the luminescence and the effect of UV irradiation and heat treatment on luminescence and the state of cerium ions and antimony in glass. We investigated glass system Na2O-ZnO-Al2O3-SiO2-NaF-NaBr with additives CeO2 and Sb2O3. Synthesis was carried out in platinum crucibles in the air at 14500C. The samples were polished glass plates with a thickness of 0.5-1 mm. UV irradiation was carried out with a mercury lamp having a wide range of radiation in the spectral range 240-390 nm. It was conducted in a Nabertherm muffle furnaces. Luminescence spectra and excitation spectra were measured using a spectrofluorimeter MPF-44A (PerkinElmer at the room temperature. Measured luminescence spectra were corrected in view of the spectral sensitivity of the photodetector for spectrofluorimeter. Adjustment of the excitation spectra for the spectral dependence of the intensity of the excitation source was not carried out. During the experiments it was found that in silicate glasses Sb3+ ions can exist in two energy states, which corresponds to a different environment with oxygen ions. Heat treatment of these glasses in an oxidizing atmosphere leads to an increase in ion concentration of Sb3+ ions with a greater amount of oxygen in the environment. In glasses containing antimony and cerium ions, ultraviolet irradiation causes a change in the valence of cerium ions and antimony, which is accompanied by luminescence quenching. Subsequent heat treatment of glass leads to the inverse processes and restore luminescence excitation spectra. The study of fluorescent properties of silicate glasses with cerium and antimony ions led to the conclusion of the practical significance of this work. Promising multifunctional materials can be created on the basis of

Quantitative analysis of time-resolved infrared stimulated luminescence in feldspars

Energy Technology Data Exchange (ETDEWEB)

Pagonis, Vasilis, E-mail: vpagonis@mcdaniel.edu [McDaniel College, Physics Department, Westminster, MD 21157 (United States); Ankjærgaard, Christina [Soil Geography and Landscape Group & Netherlands Centre for Luminescence dating, Wageningen University, PO Box 47, 6700 AA Wageningen (Netherlands); Jain, Mayank [Center for Nuclear Technologies, Technical University of Denmark, DTU Risø Campus, Roskilde (Denmark); Chithambo, Makaiko L. [Department of Physics and Electronics, Rhodes University, PO BOX 94, Grahamstown 6140 (South Africa)

2016-09-15

Time-resolved infrared-stimulated luminescence (TR-IRSL) from feldspar samples is of importance in the field of luminescence dating, since it provides information on the luminescence mechanism in these materials. In this paper we present new analytical equations which can be used to analyze TR-IRSL signals, both during and after short infrared stimulation pulses. The equations are developed using a recently proposed kinetic model, which describes localized electronic recombination via tunneling between trapped electrons and recombination centers in luminescent materials. Recombination is assumed to take place from the excited state of the trapped electron to the nearest-neighbor center within a random distribution of luminescence recombination centers. Different possibilities are examined within the model, depending on the relative importance of electron de-excitation and recombination. The equations are applied to experimental TR-IRSL data of natural feldspars, and good agreement is found between experimental and modeling results.

Electroluminescence from graphene excited by electron tunneling

International Nuclear Information System (INIS)

Beams, Ryan; Bharadwaj, Palash; Novotny, Lukas

2014-01-01

We use low-energy electron tunneling to excite electroluminescence in single layer graphene. Electrons are injected locally using a scanning tunneling microscope and the luminescence is analyzed using a wide-angle optical imaging system. The luminescence can be switched on and off by inverting the tip–sample bias voltage. The observed luminescence is explained in terms of a hot luminescence mechanism. (paper)

Characteristic of selected frequency luminescence for samples collected in deserts north to Beijing

International Nuclear Information System (INIS)

Li Dongxu; Wei Mingjian; Wang Junping; Pan Baolin; Zhao Shiyuan; Liu Zhaowen

2009-01-01

Surface sand samples were collected in eight sites of the Horqin and Otindag deserts located in north to Beijing. BG2003 luminescence spectrograph was used to analyze the emitted photons and characteristic spectra of the selected frequency luminescence were obtained. It was found that high intensities of emitted photons stimulated by heat from 85 degree C-135 degree C and 350 degree C-400 degree C. It belong to the traps of 4.13 eV (300 nm), 4.00 eV (310 nm), 3.88 eV (320 nm) and 2.70 eV (460 nm), and the emitted photons belong to traps of 4.00 eV (310 nm), 3.88 eV (320 nm) and 2.70 eV (460 nm) were stimulated by green laser. And sand samples of the eight sites can respond to the increase of definite radiological dose at each wavelength, which is the characteristic spectrum to provide radiation dosimetry basis for dating. There are definite district characteristic in their characteristic spectra. (authors)

The effect of thermal oxidation on the luminescence properties of nanostructured silicon.

Science.gov (United States)

Liu, Lijia; Sham, Tsun-Kong

2012-08-06

Herein is reported a detailed study of the luminescence properties of nanostructured Si using X-ray excited optical luminescence (XEOL) in combination with X-ray absorption near-edge structures (XANES). P-type Si nanowires synthesized via electroless chemical etching from Si wafers of different doping levels and porous Si synthesized using electrochemical method are examined under X-ray excitation across the Si K-, L(3,2) -, and O K-edges. It is found that while as-prepared Si nanostructures are weak light emitters, intense visible luminescence is observed from thermally oxidized Si nanowires and porous Si. The luminescence mechanism of Si upon oxidation is investigated by oxidizing nanostructured Si at different temperatures. Interestingly, the two luminescence bands observed show different response with the variation of absorption coefficient upon Si and O core-electron excitation in elemental silicon and silicon oxide. A correlation between luminescence properties and electronic structures is thus established. The implications of the finding are discussed in terms of the behavior of the oxygen deficient center (OCD) and non-bridging oxygen hole center (NBOHC). Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Luminescence due to peptide linkage observed in L-cysteine molecules irradiated by infrared laser light

Energy Technology Data Exchange (ETDEWEB)

Tsujibayashi, Toru, E-mail: toru-t@cc.osaka-dent.ac.jp [Department of Physics, Osaka Dental University, 8-1 Kuzuha-hanazono, Hirakata, Osaka 573-1121 (Japan); Matsubara, Eiichi; Ichimiya, Masayoshi [Department of Physics, Osaka Dental University, 8-1 Kuzuha-hanazono, Hirakata, Osaka 573-1121 (Japan); Ohno, Nobuhito [Fundamental Electronics Research Institute, Osaka Electro-Communication University, 18-8 Hatsu-Cho, Neyagawa, Osaka 572-8530 (Japan)

2016-01-15

The sequence of amino acids in peptide chains consisting of proteins is the most fundamental information of living things. A direct and nondestructive method of reading is highly required as an alternative to the method based on the gene analysis. Luminescence detection is a very sensitive tool for investigating various materials. In order to find characteristic luminescence of each amino acid we study L-cysteine and L-tyrosine using UV laser of 3.36 eV with pulse duration of 1.5 ps. In addition to a common 2.66 eV band of the luminescence we have found 2.89 eV band for L-cysteine and 2.92 eV band for L-tyrosine. It can be interpreted that the side chain makes difference on the luminescence by affecting the peptide linkage or carbonyl group. - Highlights: • Luminescence from L-cysteine and L-tyrosine are studied. • Analyzing the luminescence enables to distinguish those two amino acids. • The lifetimes and the peak photon energies under UV laser excitation are presented.

Persistent luminescent nanoparticles for super-long time in vivo and in situ imaging with repeatable excitation

International Nuclear Information System (INIS)

Sun, Meng; Li, Zhan-Jun; Liu, Chun-Lin; Fu, Hai-Xia; Shen, Jiang-Shan; Zhang, Hong-Wu

2014-01-01

In order to realize super-long time (more than 3 days) in vivo imaging, SrAl 2 O 4 :Eu 2+ ,Dy 3+ (SAO) nanoparticles were employed as probes with in situ repeatable excitation capability. In our experiments, strontium aluminate nanoparticles were prepared. After surface modified with pyrophosphoric acid (PPA), grafted by PEG-5000-OCH 3 and irradiated with 365 nm UV light for 10 min, the afterglow signal can be observed in real time for more than 30 min in live mouse after intravenous injection. In order to monitor for a super-long time, the mouse was re-illuminated for 10 min by a white-light LED lamp and then the imaging signals were recovered and also persisted for 30 min again. The super-long time in vivo imaging was achieved by employing these repeatedly excited luminescent nanoprobes. -- Highlights: • The water-resistance and dispersity abilities of strontium aluminate nanoparticles were achieved by surface modification with pyrophosphoric acid and polyethylene glycol (PEG). • The synthesized nanoparticles were successfully employed in in vivo imaging. • A super-long time in vivo imaging was realized by the in situ re-excitation via a LED lamp

Preparation and determination of the luminescent characteristics of ZrO{sub 2} in powder; Preparacion y determinacion de las caracteristicas luminiscentes del ZrO{sub 2} en polvo

Energy Technology Data Exchange (ETDEWEB)

Rivera M, T. [ESIME-IPN Unidad Culhuacan Mexico D.F. (Mexico); Olvera T, L.; Azorin N, J.; Soto E, A.M.; Velazquez O, C.; Campero C, A. [UAM-I, 09340 Mexico D.F. (Mexico)

2004-07-01

In this work the luminescent characteristics of the ZrO{sub 2} are presented using the method of Thermally Stimulated Luminescence (TSL), also called thermoluminescence (Tl). The powders of ZrO{sub 2} were obtained by two preparation methods: for precipitation and for evaporation of Sol-gel. The luminescent characteristics of the ZrO{sub 2} are determined using a lamp of radiation of UV light and a radiation source of beta particles of {sup 90}Sr/{sup 90}Y. Using the method of thermal stimulation the curve representative thermoluminescent of the previously irradiated material was obtained. The curve Tl of the ZrO{sub 2} irradiated with UV light presents a maximum in 180 C. Likewise, the spectrum of the curve Tl of the ZrO{sub 2} irradiated with particles beta presents a maximum centered in 181 C. While using gamma radiation like excitement source one has a spectrum with a peak centered in 184 C. When subjecting the materials obtained by sol-gel to a process of calcination at 1000 C for 24 hours a curved Tl it presents with two maxim in 185 and in 290 C respectively. The intensity of the response induced in the material it is a decisive factor to continue studying the dosimetric characteristics of the ZrO{sub 2} what allows to consider it as a potential material to use it in the beta particle dosimetry and of the UV light using the thermoluminescence method (Tl). (Author)

Relaxation electron excitations in Al2O3, Y3Al5O12 and YAlO3

International Nuclear Information System (INIS)

Kuznetsov, A.I.; Namozov, B.R.; Myurk, V.V.

1985-01-01

Excitation spectra of short-wave Al 2 O 3 , YAlO 3 and Y 3 Al 5 O 12 crystal luminescence, cathodoluminescence (including time resolution) and lay-temperature thermoluminescence are investigated. Analysis of experimental data permits to distingnish among these objects pairs of bands of supposedly characteristic luminescences: 7.5 and 3.8 eV (Al 2 O 3 ), 5.9 and 4.2 eV (YAlO 3 ), and 4.9 and 4.2 eV (Y 3 Al 5 O 12 ), where recombination luminescence is characteristic for long-wave ones, at that time exciton-like luminescence - for short-wave ones. A hypothesis about strong difference between states of an autolocalized exciton and ''autolocalized hole + electron'' (responsible for short-wave and long-wave bands of characteristic luminescence) is expressed; the difference is based on their genetic origin from different regions of a valent zone (in particular, long-wave bands - from the subzone of heavy holes of a valent zone ceiling, originating from nonbinding 2p-orbitals of oxygen)

Luminescence properties of some food dye-stuffs

International Nuclear Information System (INIS)

Astanov, S.Kh.; Muminova, Z.A.; Urunov, R.G.

2004-01-01

The luminescence properties of the natural food dye-stuffs and vitamins in temperature range of 300-5.2 K are studied. On the basis of experimental data on quantum yields of the fluorescence, trans-cis-isomerization and luminescence of the molecular oxygen the main ways of the inactivation of electronic excitations in researching compounds have been defined. (author)

Luminescence spectroscopy of Rb2KTiOF5 oxyfluoride single crystals

Science.gov (United States)

Kozlov, A. V.; Pustovarov, V. A.; Sarychev, M. N.; Isaenko, L. I.

2017-09-01

Spectra of photoluminescence (PL) and X-ray excited luminescence (XRL) in region of 1.5-5.5 eV, PL excitation spectra using synchrotron radiation (3.7-22 eV), time-resolved impulse cathode-luminescence (ICL) spectra, the temperature depending of the XRL, decay kinetics as well as thermoluminescence curves were measured for single crystals Rb2KTiOF5, a promising nonlinear optical material. Single crystals are transparent in microwave, visible and near UV range, inter-band transition energy is Eg = 4.2 eV. Crystalline structure has two disordered mixed position O/F, phase transition in the region of 215 K. All the obtained results indicate that in luminescence spectra nonelementary band 2.2 eV is connected to the emission of self-trapped excitons. Nonelementary band 2.2 eV associated with the presence local distortion in the octahedron TiOF5. It is observed that at interband excitation in VUV region at energies more than 3.5 Eg the effect of multiplication of electronic excitations appears. That determines the high output of XRL and ICL. Luminescence methods of quality control of grown crystals are proposed.

Electron excitations in BeAl2O4, Be2SiO4 and Be3Al2Si6O18 crystals

International Nuclear Information System (INIS)

Ivanov, V.Yu.; Pustovarov, V.A.; Shlygin, E.S.; Korotaev, A.V.; Kruzhalov, A.V.

2005-01-01

Low-temperature (T = 7 K) time-resolved selectively photoexcited luminescence spectra (2-6 eV) and luminescence excitation spectra (8-35 eV) of wide-bandgap chrysoberyl BeAl 2 O 4 , phenacite Be 2 SiO 4 , and beryl Be 3 Al 2 Si 6 O 18 crystals have been studied using time-resolved VUV spectroscopy. Both the intrinsic luminescence of the crystals and the luminescence associated with structural defects were assigned. Energy transfer to impurity luminescence centers in alexandrite and emerald was investigated. Luminescence characteristics of stable crystal lattice defects were probed by 3.6-MeV accelerated helium ion beams [ru

Luminescence of Ce3+ ions in Y3Al5O12 - Y3Ga5O12 solid solution

International Nuclear Information System (INIS)

Zorenko, Yu.V.; Nazar, I.V.; Limarenko, L.N.; Pashkovskij, M.V.

1996-01-01

Regularities of changes in spectral and energetic characteristics of the Ce 3+ ions radiation in the Y 3 Al 5-x Ga x O 12 solid solutions, related to change in the matrix crystal field force and dissipation of the luminescence excitation energy because of transfers between the valency zone ceiling and the Ce 3+ excited ion basis state are obtained. 9 refs., 3 figs., 1 tab

Further investigations into pulsed optically stimulated luminescence from feldspars using blue and green light

DEFF Research Database (Denmark)

Ankjærgaard, Christina; Jain, Mayank; Kalchgruber, R.

2009-01-01

The purpose of this paper is to investigate characteristics of luminescence signals resulting from pulsed optical stimulation of feldspars and thereby to understand the underlying processes giving rise to the signal. Fourteen different feldspar specimens were investigated using time-resolved opti......The purpose of this paper is to investigate characteristics of luminescence signals resulting from pulsed optical stimulation of feldspars and thereby to understand the underlying processes giving rise to the signal. Fourteen different feldspar specimens were investigated using time...... suggests that the TR-OSL signal decay is governed by the recombination process and not by the excited state lifetime. Furthermore data from the TR-OSL signal dependence on stimulation time and preheat temperature suggest that the recombination process may not be a sum of exponentials, although the model...... cannot be rejected definitively....

Luminescence from Ce in sol-gel SiO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Kroon, R.E., E-mail: KroonRE@ufs.ac.za [Department of Physics, University of the Free State, IB51, Box 339, Bloemfontein 9300 (South Africa); Seed Ahmed, H.A.A.; Ntwaeaborwa, O.M. [Department of Physics, University of the Free State, IB51, Box 339, Bloemfontein 9300 (South Africa); Koao, L.F. [Department of Physics, University of the Free State (Qwaqwa Campus), Private Bag X13, Phuthaditjhaba 9866 (South Africa); Nagpure, I.M.; Gusowski, M.A. [Department of Physics, University of the Free State, IB51, Box 339, Bloemfontein 9300 (South Africa); Botha, J.R. [Department of Physics, Nelson Mandela Metropolitan University, Box 77000, Port Elizabeth 6031 (South Africa); Swart, H.C. [Department of Physics, University of the Free State, IB51, Box 339, Bloemfontein 9300 (South Africa)

2012-05-15

The sol-gel process provides an attractive low temperature alternative to the melt process for producing Ce-doped silica, but reports of the emission wavelength have not been consistent. In this paper, luminescence measurements using a variety of excitation methods, including cathodoluminescence not yet reported by other researchers, are compared and evaluated in the light of previously published data. Several papers report luminescence around 350 nm but emission near this wavelength was not found from our samples. This luminescence originates from Ce that has not yet been incorporated in the silica and is found in samples that have not undergone high temperature annealing. Our photoluminescence results from samples annealed in a reducing atmosphere suggest that emission from Ce incorporated in the silica lattice occurs near 455 nm, and some indication of the emission from Ce in amorphous clusters at 400 nm is also found. However, our results also confirm earlier indications that intrinsic defects in silica can create photoluminescence near both these wavelengths, which can make identification of the luminescence due to Ce difficult. Finally, it has been found that samples which have been annealed in air, and therefore display poor photoluminescence because most of the Ce occurs in the tetravalent form, are luminescent under electron beam excitation. It is suggested that during cathodoluminescence measurements Ce{sup 4+} ions capture electrons to form excited Ce{sup 3+} ions from which the luminescence originates.

Sample and plume luminescence in fast heavy ion induced desorption

International Nuclear Information System (INIS)

Tuszynski, W.; Koch, K.; Hilf, E.R.

1996-01-01

The luminescence arising in 252 Cf-fission fragment induced desorption events has been measured using the time-correlated single photon counting technique. Photons emitted from the sample have been guided from a plasma desorption ion source to a photodetector by an optical fibre. Spectra and decay functions have been obtained using thin layers of Coronene or POPOP as samples. The results are strongly dependent on the acceleration field applied for ion extraction. Approximately 10 photons per fission fragment have been produced when applying no accelerating voltage. The results clearly show that these photons come from radiative electronic relaxations of molecules in the solid sample. Considerably more photons per fission fragment have been produced when applying a positive acceleration voltage. The intensity increases almost linearly for acceleration fields below 10 kV/cm and saturates at a nearly 10-fold higher value when compared to no acceleration. The intensity is also affected by the homogeneity of the accelerating field. These additional photons are attributed to radiative electronic relaxations of desorbed neutral molecules in the plume excited by inelastic collisions with accelerated positive ions. No additional photons have been observed when extracting negative ions. The negative ions produced do obviously not hit and/or excite desorbed neutral molecules, presumably due to their specific desorption characteristics. The experimental data have been analyzed by comparing with the cw and time-resolved sample luminescence obtained by optical excitation. The findings demonstrate that valuable information on ion-solid interactions, on specific desorption quantities and on processes in the plume can be obtained by measuring and analyzing the luminescence induced by the impact of high energy primary ions. (orig.)

Luminescence and origin of lead-related centers in single crystalline films of Y2SiO5 and Lu2SiO5

International Nuclear Information System (INIS)

Babin, V.; Gorbenko, V.; Krasnikov, A.; Mihokova, E.; Nikl, M.; Zazubovich, S.; Zorenko, Yu.

2013-01-01

In the temperature range 4.2–350 K, the steady-state and time-resolved emission and excitation spectra and luminescence decay kinetics are studied for the undoped Y 2 SiO 5 and Lu 2 SiO 5 single crystalline films grown by liquid phase epitaxy method from the PbO-based flux and, owing to that, containing lead ions substituting for Y 3+ or Lu 3+ ions. Luminescence characteristics of Pb-related centers of different types are identified. On the basis of the results obtained, we suggest that the ultraviolet emission of Pb-related centers arises from the Pb 2+ ions substituting for Y 3+ or Lu 3+ ions in the Y1 and Lu1 lattice sites of the X 2 structure. Possible hypotheses on the origin of the intense complex lead-related blue emission are discussed. We propose phenomenological models describing the excited-state dynamics of the studied luminescence centers. We also determine characteristic parameters of the corresponding relaxed excited states, in particular, the energy separations between the excited states and the rates of the radiative and non-radiative transitions from these states. -- Highlights: •Emission of lead centers in Y 2 SiO 5 and Lu 2 SiO 5 single crystalline films is studied. •The ultraviolet emission arises from Pb 2+ ions located in Y1 or Lu1 lattice sites. •Possible hypotheses on the origin of the blue emission are proposed and discussed. •The relaxed excited states parameters of various Pb-related centers are determined

Two types of fundamental luminescence of ionization-passive electrons and holes in optical dielectrics—Intraband-electron and interband-hole luminescence (theoretical calculation and comparison with experiment)

Science.gov (United States)

Vaisburd, D. I.; Kharitonova, S. V.

1997-11-01

A short high-power pulse of ionizing radiation creates a high concentration of nonequilibrium electrons and holes in a dielectric. They quickly lose their energy, generating a multiplicity of secondary quasiparticles: electron—hole pairs, excitons, plasmons, phonons of all types, and others. When the kinetic energy of an electron becomes less that some value EΔ≈(1.3-2)Eg it loses the ability to perform collisional ionization and electron excitations of the dielectric medium. Such an electron is said to be ionization-passive. It relaxes to the bottom of the lower conduction band by emitting phonons. Similarly a hole becomes ionization-passive when it “floats up” above some level EH and loses the ability for Auger ionization of the dielectric medium. It continues to float upward to the ceiling of the upper valance band only by emitting phonons. The concentrations of ionization-passive electrons and holes are larger by several orders of magnitude than those of the active electrons and holes and consequently make of a far larger contribution to many kinetic processes such as luminescence. Intraband and interband quantum transitions make the greatest contribution to the fundamental (independent of impurities and intrinsic defects) electromagnetic radiation of ionization-passive electrons and holes. Consequently the brightest types of purely fundamental luminescence of strongly nonequilibrium electrons and holes are intraband and interband luminescence. These forms of luminescence, discovered relatively recently, carry valuable information on the high-energy states of the electrons in the conduction band and of the holes in the valence band of a dielectric. Experimental investigations of these types of luminescence were made, mainly on alkali halide crystals which were excited by nanoseconal pulses of high-current-density electrons and by two-photon absorption of the ultraviolet harmonics of pulsed laser radiation beams of nanosecond and picosecond duration. The

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

Developing luminescent lamps with a narrowband emission spectrum and a methodology for testing them

Energy Technology Data Exchange (ETDEWEB)

Deviatykh, E.V.; Prokudova, M.A.; Solov' eva, A.B.

1981-01-01

During the building of luninescent lamps with tripolar luminophors, several types of narrowband rare-earth luminophors were examined that emit in the blue (lambda maximum=450-455 nanometers), the green (lambda maximum=542-544 namometers) and the red (lambda maximum is approximately equal to 610 nanometers) portions of the spectrum. The basic characteristics of these luminophors are given: the granular composition, emission spectrum and excitation, quantum output, relative brightness, photo and thermal stability, etc. The LBTsT 40 white luminescent lamp with a luminophor composition containing L-47 and L-48 aluminates, and with yttrium oxide (L-49), generated 75-79 lumens per watt after 100 hours of operation. R /sub a/ =83. Efforts are made to develop a luminescent lamp with a perfected luminophor in a 26 millimeter bulb with luminescence of 93 to 100 lumens per watt.

Luminescence properties of In(Zn)P alloy core/ZnS shell quantum dots

Science.gov (United States)

Thuy, Ung Thi Dieu; Reiss, Peter; Liem, Nguyen Quang

2010-11-01

Chemically synthesized InP/ZnS core/shell quantum dots (QDs) are studied using time-resolved photoluminescence spectroscopy and x-ray diffraction. Zinc stearate, which is added during the synthesis of the InP core, significantly improves the optical characteristics of the QDs. The luminescence quantum yield (QY) reaches 60%-70% and the emission is tunable from 485 to 586 nm by varying the Zn2+:In3+ molar ratio and growth temperature. The observed increased Stokes shift, luminescence decay time, and QY in the presence of Zn are rationalized by the formation of an In(Zn)P alloy structure that causes band-edge fluctuation to enhance the confinement of the excited carriers.

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.

Luminescence properties of LiPrxCe1-xP4O12

International Nuclear Information System (INIS)

Shalapska, T.; Stryganyuka, G.; Trotsc, D.; Demkiv, T.; Gektin, A.; Voloshinovskii, A.; Dorenbos, P.

2010-01-01

LiPr 1-x Ce x P 4 O 12 (x=0, 0.002, 0.02; 0.1) powder samples were prepared using the melt solution technique. Luminescent parameters of LiPr 1-x Ce x P 4 O 12 phosphors have been investigated under ultraviolet-vacuum ultraviolet (3-12 eV) synchrotron radiation and X-rays excitation at room and near liquid He temperatures. Excitation luminescence spectra of Ce 3+ emission, luminescent spectra and decay curves from the lower excited state levels of the 4f 1 5d 1 and 5d 1 electronic configuration of the Pr 3+ and Ce 3+ , respectively, clearly indicate energy transfer from Pr 3+ to Ce 3+ . Energy migration proceeds via the Pr-sublattice followed by nonradiation transfer from Pr 3+ to Ce 3+ ions.

Luminescence characteristics of quartz from Hsuehshan Range (Central Taiwan) and implications for thermochronometry

International Nuclear Information System (INIS)

Wu, Tzu-Shuan; Jain, Mayank; Guralnik, Benny; Murray, Andrew S.; Chen, Yue-Gau

2015-01-01

The mountain building processes in Taiwan are currently among the most rapid in the world. However, the spatial and temporal dynamics of this orogen are still poorly resolved within the <0.5 Ma timescale, reflecting methodological gaps in addressing young and rapid bedrock cooling by erosion. Optically Stimulated Luminescence (OSL) from quartz is an emerging thermochronometer that could potentially provide valuable low-temperature markers on a ∼0.1 Ma timescale. Here we study four meta-sandstone samples from the Hsuehshan Range in central Taiwan. We characterize the OSL from these samples in terms of feldspar contamination, saturation dose, signal components, and thermal stability. We conclude that the OSL is dominated by the fast component, and is therefore amenable to dose measurement using the SAR protocol. Based on the luminescence characteristics and ambient dose rate, we suggest that these samples may be valuable for evaluating recent cooling rates exceeding 360 ± 100 °C/Ma, in places where the alternative thermal scenarios (instantaneous cooling or prolonged isothermal storage) may be ruled out by external geological constraints. - Highlights: • Bedrock quartz with well-behaved luminescence characteristics are found in Taiwan. • Kinetic parameters for samples in this study are confirmed as typical quartz. • Quartz OSL-thermochronometer may work for cooling rate exceeding 360 ± 100 °C/Ma.

Down- and up-conversion luminescent carbon dot fluid: inkjet printing and gel glass fabrication

Science.gov (United States)

Wang, Fu; Xie, Zheng; Zhang, Bing; Liu, Yun; Yang, Wendong; Liu, Chun-Yan

2014-03-01

Room temperature liquid-like nanoparticles have emerged as an exciting new research and development area, because their properties could be tailored over a broad range by manipulating geometric and chemical characteristics of the inorganic core and organic canopy. However, related applications are rarely reported due to the multi-step synthesis process and potential toxicity of cadmium based nanomaterials. In this study, we prepared inexpensive and eco-friendly carbon dot fluid by the direct thermal decomposition method. The carbon dot fluid can be excited from UV to near infrared light, and can be prepared as highly concentrated luminescent ink or incorporated into sol-gel derived organically modified silicate glass, suggesting that it has great application potential in the field of printable electronics, solid state lighting and so on.Room temperature liquid-like nanoparticles have emerged as an exciting new research and development area, because their properties could be tailored over a broad range by manipulating geometric and chemical characteristics of the inorganic core and organic canopy. However, related applications are rarely reported due to the multi-step synthesis process and potential toxicity of cadmium based nanomaterials. In this study, we prepared inexpensive and eco-friendly carbon dot fluid by the direct thermal decomposition method. The carbon dot fluid can be excited from UV to near infrared light, and can be prepared as highly concentrated luminescent ink or incorporated into sol-gel derived organically modified silicate glass, suggesting that it has great application potential in the field of printable electronics, solid state lighting and so on. Electronic supplementary information (ESI) available: Details of FTIR, XRD and DLS of CDF, optical properties of CDF, TEM images of other obtained products, luminescent spectra of CDF at different temperatures, and the optical photographs of CDF inks and silica glasses with different concentrations

Luminescence dating on Mars: OSL characteristics of Martian analogue materials and GCR dosimetry

DEFF Research Database (Denmark)

Jain, M.; Andersen, C.E.; Bøtter-Jensen, L.

2006-01-01

, and sedimentary precipitates such as sulphates and chlorides. We present here a preliminary investigation of the luminescence characteristics (sensitivity, dose response, fading) of some Martian analogue mineral and rock samples. These materials are likely to be zeroed by the solar UV light (200-300nm) under sub...

Optically stimulated luminescence (OSL) and some other luminescence images from granite slices exposed with radiations

International Nuclear Information System (INIS)

Hashimoto, T.; Notoya, S.; Ojima, T.; Hoteida, M.

1995-01-01

Optically stimulated luminescence (OSL) images of some X- and γ-irradiated granite slices were obtained using photon detection through a 570 nm bandpass filter with diode-laser excitation of 910 nm. Alternative photo-induced phosphorescence (PIP) images, which were colour photographed immediately after the sunlight exposure of slice samples, were also found to be helpful in the observation of the luminescence properties and to filter selection for OSL measurements. These OSL and PIP images were compared with some other colour luminescence images, including thermoluminescence images (TLCI) and after-glow images (AGCI). It was obvious that there exists a variety of coloured emissions derived mainly from feldspar constituents and these were found to be dependent on the geological history or metamorphism of the granites. (Author)

Solid-state surface luminescence of polycyclic aromatic hydrocarbons adsorbed on cellulose diacetate matrices

Science.gov (United States)

Rogacheva, Svetlana M.; Shipovskaya, Anna B.; Volkova, Elena V.; Khurshudyan, Grachia N.; Suska-Malawska, Malgorzata; Gubina, Tamara I.

2018-04-01

The spectral-kinetic characteristics of luminescence of 17 polycyclic aromatic hydrocarbons (PAH) sorbed from a "water-organic solvent" medium on cellulose diacetate (CDA) matrices were studied. A significant increase in the fluorescence signal on the CDA matrix was observed for 13 PAHs in comparison with aqueous solutions. The highest detection sensitivity was found for pyrene, benzo(a)pyrene, and benzo(k)fluoranthene. The fluorescence spectra of two PAH indicator pairs (anthracene-phenanthrene and pyrene-fluoranthene) used to control toxicant emission sources were studied with the simultaneous presence of isomers in the analyte, depending on the excitation wavelength. For both isomer pairs, it has been found that the spectra of their solid-state luminescence overlap insignificantly, the characteristic peaks do not coincide and do not overlap, the sensitivities of detection are close to each other, which makes it possible to consider this technique as promising to control PAH contamination sources.

Quenching methods for background reduction in luminescence-based probe-target binding assays

Energy Technology Data Exchange (ETDEWEB)

Cai, Hong [Los Alamos, NM; Goodwin, Peter M [Los Alamos, NM; Keller, Richard A [Los Alamos, NM; Nolan, Rhiannon L [Santa Fe, NM

2007-04-10

Background luminescence is reduced from a solution containing unbound luminescent probes, each having a first molecule that attaches to a target molecule and having an attached luminescent moiety, and luminescent probe/target adducts. Quenching capture reagent molecules are formed that are capable of forming an adduct with the unbound luminescent probes and having an attached quencher material effective to quench luminescence of the luminescent moiety. The quencher material of the capture reagent molecules is added to a solution of the luminescent probe/target adducts and binds in a proximity to the luminescent moiety of the unbound luminescent probes to quench luminescence from the luminescent moiety when the luminescent moiety is exposed to exciting illumination. The quencher capture reagent does not bind to probe molecules that are bound to target molecules and the probe/target adduct emission is not quenched.

Low-Energy Electron-Stimulated Luminescence of Thin H20 and D20 Layers on Pt(111)

International Nuclear Information System (INIS)

Petrik, Nikolay G.; Kimmel, Greg A.

2005-01-01

The electron-stimulated luminescence (ESL) from amorphous solid water and crystalline ice films deposited on Pt(111) at 100 K is investigated as a function of the film thickness, incident electron energy (5 ? 1000 eV), isotopic composition, and film structure. The ESL emission spectrum has a characteristic double-peaked shape that has been attributed to a transition between a superexcited state ( ) and the dissociative, first excited state ( ) in water: Comparing the electron-stimulated luminescence and O2 electron-stimulated desorption (ESD) yields versus incident electron energy, we find the ESL threshold blue-shifted from the O2 ESD threshold by ∼3 eV, which is close to the center of the emission spectrum near 400 nm and supports the assignment for the ESL. For thin films, radiative and non-radiative interactions with the substrate tend to quench the luminescence. The luminescence yield increases with coverage since the interactions with the substrate become less important. The ESL yield from D2O is ∼ 4 times higher than from H2O. Using layered films of H2O and D2O, this sizable isotopic effect on the ESL is exploited to spatially profile the luminescence emission within the ASW films. These experiments show that most of the luminescence is emitted from within the penetration depth of the incident electron. However, the results depend on the order of the isotopes in the film, and this asymmetry can be modeled by assuming some migration of the excited states within the film. The ESL is very sensitive to defects and structural changes in solid water, and the emission yield is significantly higher from amorphous films than from crystalline ice

Evaluation of a reconfigurable portable instrument for copper determination based on luminescent carbon dots.

Science.gov (United States)

Salinas-Castillo, Alfonso; Morales, Diego P; Lapresta-Fernández, Alejandro; Ariza-Avidad, María; Castillo, Encarnación; Martínez-Olmos, Antonio; Palma, Alberto J; Capitan-Vallvey, Luis Fermin

2016-04-01

A portable reconfigurable platform for copper (Cu(II)) determination based on luminescent carbon dot (Cdots) quenching is described. The electronic setup consists of a light-emitting diode (LED) as the carbon dot optical exciter and a photodiode as a light-to-current converter integrated in the same instrument. Moreover, the overall analog conditioning is simply performed with one integrated solution, a field-programmable analog array (FPAA), which makes it possible to reconfigure the filter and gain stages in real time. This feature provides adaptability to use the platform as an analytical probe for carbon dots coming from different batches with some variations in luminescence characteristics. The calibration functions obtained that fit a modified Stern-Volmer equation were obtained using luminescence signals from Cdots quenching by Cu(II). The analytical applicability of the reconfigurable portable instrument for Cu(II) using Cdots has been successfully demonstrated in tap water analysis.

Organic scintillators with long luminescent lifetimes for radiotherapy dosimetry

DEFF Research Database (Denmark)

Beierholm, Anders Ravnsborg; Lindvold, Lars René; Andersen, Claus Erik

2011-01-01

of experiments performed using two organic scintillators, one commercially available and one custom made. The luminescent lifetimes of the scintillators have been measured using i) optical excitation by pulsed UV light, and ii) irradiative excitation using high-energy X-rays from a linac. A luminescent lifetime...... component on the order of 20 μs was estimated for the custom-made organic scintillator, while the commercial scintillator exhibited a fast component of approximately 5 ns lifetime (7 ns as stated by the manufacturer) and an approximate 10 μs lifetime slow component. Although these lifetimes are not long...

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.

From plasmon-induced luminescence enhancement in gold nanorods to plasmon-induced luminescence turn-off: a way to control reshaping.

Science.gov (United States)

Molinaro, Céline; Marguet, Sylvie; Douillard, Ludovic; Charra, Fabrice; Fiorini-Debuisschert, Céline

2018-04-24

Two-photon luminescence (TPL) turn-off in small single gold nanorods (GNRs) exposed to increased resonant femtosecond laser excitation (800 nm wavelength, pulse energy density varying from 125 μJ cm-2 to 2.5 mJ cm-2) is investigated. The origin is shown to be a photo-induced decrease of the rod aspect ratio. This aspect ratio reduction could reasonably be assigned to gold atom diffusion away from the rod tips, where hot spots are localized. The two-photon luminescence signal can be recovered after a blue-shift of the incident excitation wavelength. No change in the excitation wavelength results in an out of resonance excitation of the rods and thus a reduced absorption, acting as feedback to stabilize the GNR shape and size. A theoretical analysis is presented evidencing limited thermal effects in the femtosecond regime for small nanoparticles, in good agreement with complementary topographic characterizations using scanning electron microscopy (SEM) and atomic force microscopy (AFM). We show finally that TPL reveals itself as a highly sensitive tool to follow tiny changes resulting from the photo-induced reshaping of GNRs.

Luminescence basic concepts, applications and instrumentation

CERN Document Server

Virk, Hardev Singh

2014-01-01

The word luminescence was first used by a German physicist, Eilhardt Wiedemann, in 1888. He also classified luminescence into six kinds according to the method of excitation. No better basis of classification is available today. He recognized photoluminescence, thermoluminescence, electroluminescence, crystalloluminescence, triboluminescence, and chemiluminescence. The designations are obvious, characterized by the prefix. This Volume consists of 9 Chapters, including 8 Review Papers and one Case Study. The first two papers are based on OLEDs. Organic light emitting diodes (OLEDs) have been th

Synthesis, characterization and luminescent properties of lanthanide complexes with an unsymmetrical tripodal ligand

Energy Technology Data Exchange (ETDEWEB)

Yan Zhenzhong [State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China); Tang Yu [State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China)], E-mail: tangyu@lzu.edu.cn; Liu Weisheng; Tan Minyu [State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China)

2008-09-15

Solid complexes of lanthanide nitrates with a new unsymmetrical tripodal ligand, bis[(2'-benzylaminoformyl)phenoxyl)ethyl](ethyl)amine (L) have been synthesized and characterized by elemental analysis, infrared spectra and molar conductivity measurements. At the same time, the luminescent properties of the Sm(III), Eu(III), Tb(III) and Dy(III) nitrate complexes in solid state were also investigated. Under the excitation of UV light, these complexes exhibited characteristic emission of central metal ions.

A study of vibrational relaxation of electronically-excited molecules

International Nuclear Information System (INIS)

Datsyuk, V.V.; Izmailov, I.A.; Kochelap, V.A.

1992-09-01

The time kinetics of the vibrational relaxation of excimers is studied in the diffusional approximation. Simple formulae for functions of nonstationary vibrational distribution are found for the electronically excited molecules. Some spectral-kinetic dependencies of the excimer luminescence are explained in a new way. The possibilities of the determination of excimer parameters are discussed. The dependence of energetical characteristics of excimer lasers on these parameters is particularly emphasized. (author). 22 refs, 5 figs

Analysis of thermal treatment effects upon optico-luminescent and scintillation characteristics of oxide and chalcogenide crystals

International Nuclear Information System (INIS)

Ryzhikov, Vladimir D.; Grinyov, Boris V.; Pirogov, Evgeniy N.; Galkin, Sergey N.; Nagornaya, Lyudmila L.; Bondar, Vladimir G.; Babiychuk, Inna P.; Krivoshein, Vadim I.; Silin, Vitaliy I.; Lalayants, Alexandr I.; Voronkin, Evgeniy F.; Katrunov, Konstantin A.; Onishchenko, Gennadiy M.; Vostretsov, Yuriy Ya.; Malyi, Pavel Yu.; Lisetskaya, Elena K.; Lisetskii, Longin N.

2005-01-01

This work has been aimed at analyzing the effects of various thermal treatment factors upon optical-luminescent, scintillation and other functional characteristics of complex oxide and chalcogenide crystals. The crystals considered in this work are scintillators with intrinsic (PWO, CWO, BGO), activator (GSO:Ce) or complex-defect ZnSe(Te) type of luminescence. Important factors of thermal treatment are not only the temperature and its variation with time, but also the chemical composition of the annealing medium, its oxidation-reduction properties

Investigation into scanning tunnelling luminescence microscopy

International Nuclear Information System (INIS)

Manson-Smith, S.K.

2001-01-01

This work reports on the development of a scanning tunnelling luminescence (STL) microscope and its application to the study of Ill-nitride semiconductor materials used in the production of light emitting devices. STL microscopy is a technique which uses the high resolution topographic imaging capabilities of the scanning tunnelling microscope (STM) to generate high resolution luminescence images. The STM tunnelling current acts as a highly localised source of electrons (or holes) which generates luminescence in certain materials. Light generated at the STM tunnelling junction is collected concurrently with the height variation of the tunnelling probe as it is scanned across a sample surface, producing simultaneous topographic and luminescence images. Due to the very localised excitation source, high resolution luminescence images can be obtained. Spectroscopic resolution can be obtained by using filters. Additionally, the variation of luminescence intensity with tunnel current and with bias voltage can provide information on recombination processes and material properties. The design and construction of a scanning tunnelling luminescence microscope is described in detail. Operating under ambient conditions, the microscope has several novel features, including a new type of miniature inertial slider-based approach motor, large solid-angle light collection optical arrangement and a tip-height regulation system which requires the minimum of operator input. (author)

Characterization and Luminescence Properties of Color-Tunable Dy3+-Doped BaY2ZnO5 Nanophosphors

Science.gov (United States)

Sonika; Khatkar, S. P.; Khatkar, Avni; Kumar, Rajesh; Taxak, V. B.

2015-01-01

Dy3+-doped BaY2ZnO5 nanophosphors were successfully synthesized by use of a solution combustion process. The effects of sintering temperature and dysprosium concentration on the structural and luminescence characteristics of the phosphors were investigated. X-ray diffraction (XRD) analysis confirmed the formation of pure orthorhombic BaY2ZnO5 with the space group Pbnm at 1100°C. Morphological investigation revealed spherical nanoparticles with smooth surfaces. The luminescence features of the nanophosphor were studied by use of photoluminescence excitation (PLE) and photoluminescence emission (PL), with luminescence decay curves and color ( x, y) coordinates. On excitation at 355 nm, BaY2ZnO5 nanophosphor doped with trivalent dysprosium ion emits white light as a mixture of blue (4F9/2 → 6H15/2) and yellow (4F9/2 → 6H13/2) emission. Concentration quenching is explained on the basis of cross-relaxation between intermediate Dy3+ states. Thus, BaY2ZnO5:Dy3+ nanophosphor may be suitable for producing efficient white light for ultraviolet-light-emitting diodes (UV-LEDs), fluorescent lamps, and a variety of optical display panels.

Electronic structure and optical properties of CdS{sub x}Se{sub 1−x} solid solution nanostructures from X-ray absorption near edge structure, X-ray excited optical luminescence, and density functional theory investigations

Energy Technology Data Exchange (ETDEWEB)

Murphy, M. W. [DESY (Deutsches Elektronen-Synchrotron), FS-PEX, Notkestrasse 85, 22607 Hamburg (Germany); Yiu, Y. M., E-mail: yyiu@uwo.ca; Sham, T. K. [Department of Chemistry, University of Western Ontario, London, ON N6A5B7 (Canada); Ward, M. J. [Cornell High Energy Synchrotron Source (CHESS), Cornell University, Ithaca, NY 14853 (United States); Liu, L. [Institute of Functional Nano and Soft Materials (FUNSOM) and Soochow University-Western University Center for Synchrotron Radiation Research, Soochow University, Suzhou, Jiangsu, 215123 (China); Hu, Y. [Canadian Light Source, University of Saskatchewan, Saskatoon, SK S7N2V3 (Canada); Zapien, J. A. [Center Of Super-Diamond and Advanced Films (COSDAF) and Department of Physics and Materials Science, City University of Hong Kong, Hong Kong SAR (China); Liu, Yingkai [Institute of Physics and Electronic Information, Yunnan Normal University, Kunming, Yunnan, 650500 (China)

2014-11-21

The electronic structure and optical properties of a series of iso-electronic and iso-structural CdS{sub x}Se{sub 1−x} solid solution nanostructures have been investigated using X-ray absorption near edge structure, extended X-ray absorption fine structure, and X-ray excited optical luminescence at various absorption edges of Cd, S, and Se. It is found that the system exhibits compositions, with variable local structure in-between that of CdS and CdSe accompanied by tunable optical band gap between that of CdS and CdSe. Theoretical calculation using density functional theory has been carried out to elucidate the observations. It is also found that luminescence induced by X-ray excitation shows new optical channels not observed previously with laser excitation. The implications of these observations are discussed.

Excited states

CERN Document Server

Lim, Edward C

1974-01-01

Excited States, Volume I reviews radiationless transitions, phosphorescence microwave double resonance through optical spectra in molecular solids, dipole moments in excited states, luminescence of polar molecules, and the problem of interstate interaction in aromatic carbonyl compounds. The book discusses the molecular electronic radiationless transitions; the double resonance techniques and the relaxation mechanisms involving the lowest triplet state of aromatic compounds; as well as the optical spectra and relaxation in molecular solids. The text also describes dipole moments and polarizab

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.

The luminescence of CaWO4: Bi single crystals

International Nuclear Information System (INIS)

Zorenko, Yu.; Pashkovsky, M.; Voloshinovskii, A.; Kuklinski, B.; Grinberg, M.

2006-01-01

Influence of doping with Bi 3+ ions and Bi 3+ -Na + or Bi 3+ -Li + ions pairs on luminescence, emission kinetics and light yield of CaWO 4 crystals has been investigated. It has been shown that under excitation in the A-band at 272 and 287nm, related to the Bi 3+ ions absorption, the luminescence peaked at 468nm decaying with time τ=0.41μs is observed. For bismuth concentration 50-500ppm and the equimolar concentrations of the Bi 3+ ions accompanied by Na + or Li + ions compensators the significant suppression of the phosphorescence peaked at 520nm, related to the defect WO 3 -V O complex, and an improvement of scintillation characteristics of the CaWO 4 are noticed. Energy transfer from the defect WO 3 -V O and regular WO 4 2- oxy-anions to Bi 3+ ions have been observed at room temperatures and discussed

Highly visible-light luminescence properties of the carboxyl-functionalized short and ultrashort MWNTs

International Nuclear Information System (INIS)

Luo Yongsong; Xia Xiaohong; Liang Ying; Zhang Yonggang; Ren Qinfeng; Li Jialin; Jia Zhijie; Tang Yiwen

2007-01-01

Luminescence of the short multiwalled carbon nanotubes (MWNTs) conjugated with carboxylic acid groups has been studied. The results show that the carboxyl-functionalized short MWNTs could emit luminescence and the emission peak appears at 500 nm with a corresponding optimal excitation wavelength centering at 310 nm. When the short MWNTs are filtered through 0.15 μm polytetrafluoroethylene (PTFE) membrane, the ultrashort MWNTs are obtained from the filtrate. An interesting feature for the ultrashort MWNTs is that the emission intensity is strengthened and the peak is slightly blue shifted to 460 nm. This result indicates that the luminescence properties of MWNTs are strongly affected by the tube length. After chemical oxidization cutting, defects and carboxylic acid groups at the tube end and/or sidewall can be produced; the more shorten of MWNTs, the better dispersion and carboxylic passivation of the nanotubes, and the more intense luminescence emissions. The broad emissions are logically attributed to the trapping of excitation energy by defect sites in the carboxyl-functionalized nanotube structure. - Graphical abstract: Luminescence of the short and ultrashort multiwalled carbon nanotubes (MWNTs) conjugated with carboxylic acid groups, which is logically attributed to the trapping of excitation energy by defect sites, has been studied

Effect of particle size and morphology on the properties of luminescence in ZnWO4

International Nuclear Information System (INIS)

Lisitsyn, V.M.; Valiev, D.T.; Tupitsyna, I.A.; Polisadova, E.F.; Oleshko, V.I.; Lisitsyna, L.A.; Andryuschenko, L.A.; Yakubovskaya, A.G.; Vovk, O.M.

2014-01-01

We investigated pulsed photoluminescence and pulsed cathodoluminescence in ZnWO 4 crystals and composite materials based on dispersed powders of zinc tungstate in the polymer matrix. It is shown that the size of crystal particles affects the luminescence decay time in excitation by electron and laser radiation. The decay time obtained for the composite material with nanoparticles 25 nm and 100 nm in size is equal to 5 µs and 7 µs, respectively. Relative values of the light yield of composite containing zinc tungstate crystals in the form of rods are found to be larger in comparison with crystallites in the form of grains. The mechanisms of luminescence recombination in laser and electron excitation are discussed. - Highlights: • Pulsed photoluminescence and pulsed cathodoluminescence spectra and decay kinetics of nano- and microcrystals of zinc tungstate in the organosilicic matrix compared to a single crystal were studied. • The luminescence decay kinetics and life-time of the excited state depend on the size of particles in the composite materials and on the type of excitation. • The probability of excitation of luminescence centers responsible for the band at 490 nm is higher which is apparently due to the larger capture cross-section and quantum yield

X-ray spectroscopy studies of nonradiative energy transfer processes in luminescent lanthanide materials

Science.gov (United States)

Pacold, Joseph I.

Luminescent materials play important roles in energy sciences, through solid state lighting and possible applications in solar energy utilization, and in biomedical research and applications, such as in immunoassays and fluorescence microscopy. The initial excitation of a luminescent material leads to a sequence of transitions between excited states, ideally ending with the emission of one or more optical-wavelength photons. It is essential to understand the microscopic physics of this excited state cascade in order to rationally design materials with high quantum efficiencies or with other fine-tuning of materials response. While optical-wavelength spectroscopies have unraveled many details of the energy transfer pathways in luminescent materials, significant questions remain open for many lanthanide-based luminescent materials. For organometallic dyes in particular, quantum yields remain limited in comparison with inorganic phosphors. This dissertation reports on a research program of synchrotron x-ray studies of the excited state electronic structure and energy-relaxation cascade in trivalent lanthanide phosphors and dyes. To this end, one of the primary results presented here is the first time-resolved x-ray absorption near edge spectroscopy studies of the transient 4f excited states in lanthanide-activated luminescent dyes and phosphors. This is a new application of time-resolved x-ray absorption spectroscopy that makes it possible to directly observe and, to some extent, quantify intramolecular nonradiative energy transfer processes. We find a transient increase in 4f spectral weight associated with an excited state confined to the 4f shell of trivalent Eu. This result implies that it is necessary to revise the current theoretical understanding of 4f excitation in trivalent lanthanide activators: either transient 4f-5d mixing effects are much stronger than previously considered, or else the lanthanide 4f excited state has an unexpectedly large contribution

The synthesis and luminescence quenching of the water-soluble polymer-supported tris(2,2'-bipyridine)ruthenium(II) analogue

International Nuclear Information System (INIS)

Kurimura, Yoshimi; Shinozaki, Norio; Ito, Fumio; Uratani, Yasuyo; Shigehara, Kiyotaka; Tsuchida, Eishun; Kaneko, Masao; Yamada, Akira.

1982-01-01

The p-aminostyrene-N-vinylpyrrolidone copolymer-supported tris(2,2'-bipyridine)ruthenium (II) analogue, [Ru(bpy) 2 (pbyCOOH)] 2 + (bpy = 2,2'-bipyridine and pbyCOOH = polymeric bipyridine ligand), has been prepared, and the luminescence behavior of the polymer complex has been investigated in an aqueous solution. The efficiency of the quenching of the excited state of the polymer complex with [Fe(CN) 6 ] 4 - , [Co(phen) 3 ] 2 + , and Cu 2 + is compared with that of [Ru(bpy) 3 ] 2 + . The quenching of the excited state of the polymer complex by Cu 2 + is strongly enhanced by the effect of the polymer chains. In the polymer complex/Cu 2 + system, the quenching by Cu 2 + in the presence of poly(p-styrenesulfonate) is much more effective than in the absence of the polyion. The characteristics of the polymer complex in terms of the luminescence behavior are discussed. (author)

Search for the dose-sensitive optically stimulated luminescence response in natural carbonates

International Nuclear Information System (INIS)

Jaek, Ivar; Huett, Galina; Rammo, Ilmar; Vasilchenko, Valeri

2001-01-01

Carbonates of different origin, such as Iceland spar, calcites, and mollusc shells, used as electron spin resonance and thermoluminescence paleodosimeters, were studied in order to determine their suitability for optically stimulated luminescence dating. The stimulation/excitation spectra of the afterglow of the samples were recorded in the wavelength range of 250-1100 nm. The results of the study show that these spectra present either excitation spectra of Mn 2+ ion fluorescence (samples of calcites and Iceland spar, red emission recorded) or the excitation spectra of primary phosphorescence (samples of carbonates, including molluscs shells; short-wave emission bands recorded). The recorded stimulation spectra revealed no spectral bands sensitive to stimulation by ionizing radiation, which would disappear as a result of heating and could thus be related to deep traps in carbonates, needed dating. The cause of this situation which is unusual in luminescent crystals, including luminescence (paleo)dosimeters, and the ways of overcoming the difficulties in optical dating of natural carbonates are discussed. (author)

Fluorescence study of some xanthine dyes under stepped laser excitation

International Nuclear Information System (INIS)

Chirkova, L.V.; Ketsle, G.A.; Ermagambetov, K.T.

1996-01-01

Paper is devoted to definition of triplet state in molecules of xanthine dyes and study of intramolecular energy circulation. Stepped two-quanta excitation of dyes has been carried out with help of experimental unit. Intensive luminescence activated by excitation of triplet molecules of dyes within triplet-triplet band with wave length of 1060 nm was registered for eosin. Given luminescence spectrally coincides with fast fluorescence. 5 refs., 6 figs

Bistable luminescence of trivalent rare-earth ions in crystals

International Nuclear Information System (INIS)

Sole, Jose Garcia; Ramirez O, Maria de la; Rodenas, Airan; Jaque, Daniel; Bausa, Luisa; Bettinelli, Marco; Speghini, Adolfo; Cavalli, Enrico; Ivleva, Lioudmila

2006-01-01

In this work, we have examined three new bistable systems based on the luminescence of three different crystals activated with trivalent rare earth ions. We have focussed our attention on Yb 3+ ions activators, for which the most relevant results are obtained. The first crystal, Sr 0.6 Ba 0.4 Nb 2 O 6 , is a ferroelectric material with a relatively low phase transition temperature (∼370 K), which provides bistability in the luminescence of Yb 3+ ions due to the thermal hysteresis associated with phase transition. The second crystal, LiNbO 3 , provides an intrinsic bistability in the luminescence of Yb 3+ ions, which is driven by changes in the excitation intensity. In the third crystal, NdPO 4 , a new mechanism of excitation intensity driven bistability is obtained when activated with Yb 3+ ions, due to a interplay between the Nd 3+ ↔Yb 3+ energy transfer and back transfer processes

Luminescent characteristics of UV excited Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: Pr{sup 3+} reddish-orange phosphor

Energy Technology Data Exchange (ETDEWEB)

Vidyadharan, Viji; Mohan P, Remya; Joseph, Cyriac; Unnikrishnan, N.V.; Biju, P.R., E-mail: prb.mgu@gmail.com

2016-02-15

Pr{sup 3+} doped Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3} phosphors were synthesised by solid state reaction process. The structure, surface morphology and photoluminescence of the prepared phosphors were analysed using XRD, SEM and photoluminescence spectroscopy respectively. The XRD pattern confirmed orthorhombic perovskite structure of the Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: x Pr{sup 3+} phosphor. Agglomeration of particles with irregular shapes is observed from the SEM images. The emission spectra of Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: x Pr{sup 3+} phosphor shows the samples can be effectively excited with UV light at 336 nm and exhibit a strong reddish-orange emission at 611 nm. Concentration dependence of emission intensity shows concentration quenching effect on increasing Pr{sup 3+} concentration after x = 0.1 because of dipole–dipole interaction. Using Blasse's formula, critical distance for energy transfer was calculated. The CIE co-ordinates, CCT, colour purity and luminescence decay of the prepared phosphors were also calculated. These results offer the prepared phosphor as a suitable candidate for various photonic applications. - Highlights: • Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}: x Pr{sup 3+} perovskite structured phosphors were synthesized. • Under UV excitation, the PL spectra show strong reddish-orange emission. • The emission from {sup 3}P{sub J} levels of Pr{sup 3+} were absent due to the presence of IVCT band. • Concentration quenching due to dipole–dipole interaction was observed. • For x = 0.1, sample shows a maximum emission intensity with 91.7% colour purity.

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

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

Low temperature luminescence and charge carrier trapping in a cryogenic scintillator Li{sub 2}MoO{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Spassky, D.A., E-mail: deris2002@mail.ru [Institute of Physics, University of Tartu, Ravila 14c, 50411 Tartu (Estonia); Skobeltsyn Institute of Nuclear Physics, Moscow State University, 119991 Moscow (Russian Federation); Nagirnyi, V. [Institute of Physics, University of Tartu, Ravila 14c, 50411 Tartu (Estonia); Savon, A.E. [Skobeltsyn Institute of Nuclear Physics, Moscow State University, 119991 Moscow (Russian Federation); Kamenskikh, I.A. [Physics Faculty, Moscow State University, 119991 Moscow (Russian Federation); Barinova, O.P.; Kirsanova, S.V. [D. Mendeleyev University of Chemical Technology of Russia, 125047 Moscow (Russian Federation); Grigorieva, V.D.; Ivannikova, N.V.; Shlegel, V.N. [Nikolaev Institute of Inorganic Chemistry, SB RAS, 630090 Novosibirsk (Russian Federation); Aleksanyan, E. [Institute of Physics, University of Tartu, Ravila 14c, 50411 Tartu (Estonia); A.Alikhanyan National Science Laboratory, 2 Br. Alikhanyan Str., 0036 Yerevan (Armenia); Yelisseyev, A.P. [Sobolev Institute of Geology and Mineralogy, SB RAS, 630090 Novosibirsk (Russian Federation); Belsky, A. [Institute of Light and Matter, CNRS, University Lyon1, 69622 Villeurbanne (France)

2015-10-15

The luminescence and optical properties of promising cryogenic scintillator Li{sub 2}MoO{sub 4} were studied in the temperature region of 2–300 K. The data on luminescence spectra and decay characteristics, excitation spectra, thermostimulated luminescence curves and spectra as well as transmission and reflectivity spectra are presented for the single crystals grown by two different procedures, the conventional Czochralski method and the low-temperature gradient Czochralski technique. The bandgap of Li{sub 2}MoO{sub 4} is estimated from the analysis of transmission, luminescence excitation and reflectivity spectra. Up to three luminescence bands with the maxima at 1.98, 2.08 and 2.25 eV are detected in the emission spectra of crystals and their origin is discussed. In the thermoluminescence curves of both studied crystals, two high-intensity peaks were observed at 22 and 42 K, which are ascribed to the thermal release of self-trapped charge carriers. The coexistence of self-trapped electrons and holes allows one to explain the poor scintillation light yield of Li{sub 2}MoO{sub 4} at low temperatures. - Highlights: • Single crystals of Li{sub 2}MoO{sub 4} were grown by two methods. • The transparency cutoff (~4.3 eV) and bandgap values (<4.9 eV) are estimated. • The emission 2.08 eV is ascribed to self-trapped excitons and quenches at T>7 K. • Shallow traps considerably influence the energy transfer to emission centres. • Co-existence of self-trapped holes and electrons results in a low light yield.

Luminescence centers in bismuth orthogermanate

International Nuclear Information System (INIS)

Bordun, O.M.

2001-01-01

The luminescence and photoexcitation spectra of single crystals,ceramics,and thin films of Bi 4 Ce 3 O 1 2 are studied.The decomposition of the luminescence spectra into elementary components by the Alentsev-Fock method showed that they consist of three bands with maxima at 2.7,2.4,and 2.05 eV.The bands with maxima at 2.7 and 2.4 eV are assigned to the emission of self-trapped Frenkel excitons describing the excited state of a (BiO 6 ) 9- molecular ion. Emission bands with maxima at 2.0 5 eV are assigned to recombination on traps caused by structural defects

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

, which display very different behaviour. The first involves the internal transitions of common transition metal ions. The second is typical of centres not displaying excited states within the band gap that are likely to arise from direct recombination between the conduction band and the ground state......The technique of optically stimulated luminescence has important uses in the dose evaluation of irradiated feldspars. The luminescence process involves the eviction of electrons from donor traps, charge transfer through the conduction band, and recombination at acceptor sites; each...

Upconversion luminescence and blackbody radiation in tetragonal YSZ co-doped with Tm(3+) and Yb(3+).

Science.gov (United States)

Soares, M R N; Ferro, M; Costa, F M; Monteiro, T

2015-12-21

Lanthanide doped inorganic nanoparticles with upconversion luminescence are of utmost importance for biomedical applications, solid state lighting and photovoltaics. In this work we studied the downshifted luminescence, upconversion luminescence (UCL) and blackbody radiation of tetragonal yttrium stabilized zirconia co-doped with Tm(3+) and Yb(3+) single crystals and nanoparticles produced by laser floating zone and laser ablation in liquids, respectively. The photoluminescence (PL) and PL excitation (PLE) were investigated at room temperature (RT). PL spectra exhibit the characteristic lines in UV, blue/green, red and NIR regions of the Tm(3+) (4f(12)) under resonant excitation into the high energy (2S+1)LJ multiplets. Under NIR excitation (980 nm), the samples placed in air display an intense NIR at ∼800 nm due to the (1)G4→(3)H5/(3)H4→(3)H6 transitions. Additionally, red, blue/green and ultraviolet UCL is observed arising from higher excited (1)G4 and (1)D2 multiplets. The power excitation dependence of the UCL intensity indicated that 2-3 low energy absorbed photons are involved in the UCL for low power levels, while for high powers, the identified saturation is dependent on the material size with a enhanced effect on the NPs. The temperature dependence of the UCL was investigated for single crystals and targets used in the ablation. An overall increase of the integrated intensity was found to occur between 12 K and the RT. The thermally activated process is described by activation energies of 10 meV and 30 meV for single crystals and targets, respectively. For the NPs, the UCL was found to be strongly sensitive to pressure conditions. Under vacuum conditions, instead of the narrow lines of the Tm(3+), a wide blackbody radiation was detected, responsible for the change in the emission colour from blue to orange. This phenomenon is totally reversible when the NPs are placed at ambient pressure. The UCL/blackbody radiation in the nanosized material exhibits

K2SO4 and LiKSO4 crystals luminescence

International Nuclear Information System (INIS)

Charapiev, B.; Nurakhmetov, T.N.

2002-01-01

In the paper a nature of X-ray and tunnel luminescence in LiKSO 4 and Li 2 SO 4 ·H 2 O crystals are discussed. It is shown, that X-ray luminescence and Li 2 SO 4 ·H 2 O and LiKSO 4 appeals in the result of electrons recombination with auto-localized holes (SO 4 - ), and tunnel luminescence appeals at electrons transfer from ground state of electron center into hole center capture ground state. Under heating of irradiated crystal de-localized holes at recombination moment with electron capture centers are forming auto-localized excitons, which are disintegrating with photon emitting, and so X-ray luminescence spectrum and thermally induces luminescence peaks are coinciding. Nature of radiation appealing in LiKSO 4 at ultraviolet excitation is discussing

On the half-life of luminescence signals in dosimetric applications: A unified presentation

Science.gov (United States)

Pagonis, V.; Kitis, G.; Polymeris, G. S.

2018-06-01

Luminescence signals from natural and man-made materials are widely used in dosimetric and dating applications. In general, there are two types of half-lives of luminescence signals which are of importance to experimental and modeling work in this research area. The first type of half-life is the time required for the population of the trapped charge in a single trap to decay to half its initial value. The second type of half-life is the time required for the luminescence intensity to drop to half of its initial value. While there a handful of analytical expressions available in the literature for the first type of half-life, there are no corresponding analytical expressions for the second type. In this work new analytical expressions are derived for the half-life of luminescence signals during continuous wave optical stimulation luminescence (CW-OSL) or isothermal luminescence (ITL) experiments. The analytical expressions are derived for several commonly used luminescence models which are based on delocalized transitions involving the conduction band: first and second order kinetics, empirical general order kinetics (GOK), mixed order kinetics (MOK) and the one-trap one-recombination center (OTOR) model. In addition, half-life expressions are derived for a different type of luminescence model, which is based on localized transitions in a random distribution of charges. The new half-life expressions contain two parts. The first part is inversely proportional to the thermal or optical excitation rate, and depends on the experimental conditions and on the cross section of the relevant luminescence process. The second part is characteristic of the optical and/or thermal properties of the material, as expressed by the parameters in the model. A new simple and quick method for analyzing luminescence signals is developed, and examples are given of applying the new method to a variety of dosimetric materials. The new test allows quick determination of whether a set of

Luminescent properties of Eu{sup 3+}-doped glass ceramics containing BaCl{sub 2} nanocrystals under NUV excitation for White LED

Energy Technology Data Exchange (ETDEWEB)

Jin, Han; Mo, Zhaojun, E-mail: mzjmzj163@163.com; Zhang, Xiaosong; Yuan, Linlin; Yan, Ming; Li, Lan, E-mail: lilan@tjut.edu.cn

2016-07-15

Eu{sup 3+} doped fluorozirconate glass ceramics containing BaCl{sub 2} nanocrystals were successfully fabricated by melt quenching method, and their structural and luminous properties were investigated. The existence of BaCl{sub 2} nanocrystals in the glass ceramics plays an important role on the improvement of luminescent properties. The emission intensity in glass ceramics was remarkably enhanced, which attributes to the phonon energy decrease by Eu{sup 3+} ions into BaCl{sub 2} nanocrystals. Meanwhile, the extended average fluorescence decay lifetime from 4.60 ms to 5.42 ms and the decreased Red/Orange ratio and spark splitting of {sup 7}F{sub 1} energy level also confirmed this view. Additionally, the excitation spectra showed that glass ceramics could be effectively excited by NUV light. The CIE chromaticity coordinates of glass ceramics (GC320) were calculated as (0.611, 0.371), which was close to the NTSC standard values for red (0.67, 0.33). The results suggested that the glass ceramics may be used as potential red phosphors under UV light excitation for white light-emitting diodes.

Luminescence and color center distributions in K3YB6O12:Ce3+ phosphor

International Nuclear Information System (INIS)

Yang, Li; Wan, Yingpeng; Weng, Honggen; Huang, Yanlin; Chen, Cuili; Seo, Hyo Jin

2016-01-01

Polycrystalline Ce 3+ -doped K 3 YB 6 O 12 (1–14 mol%) phosphors were prepared by facile chemical sol–gel synthesis. The phase formation of the phosphors was confirmed by x-ray powder diffraction (XRD) analysis. The photoluminescence excitation spectra (PLE), emission spectra (PL) and the luminescence decay curves were tested. Under the near-UV light, the phosphors present the emission from blue color to yellowish green due to the allowed 4 f  –5 d transitions of Ce 3+ ions. The absolute quantum efficiency (QE) of K 3 YB 6 O 12 :Ce 3+ can reach 53% under the excitation of near-UV light. The luminescence thermal quenching of the phosphor was investigated by the temperature-dependent spectra. The crystallographic site of Ce 3+ ions in the lattice was identified and discussed on the basis of luminescence characteristics and structural data. There is only one isolated Ce 3+ center occupying the Y(II) sites in the lightly doped samples presenting a typical doublet emission profile. While the Ce 3+ multi-centers could be created with the enhancement of the doping levels, which could induce the distinct red-shift of the spectra due to the dipole–dipole interactions. The result in this work could be useful for the further investigation of other rare earth ions in this host. (paper)

f-state luminescence of lanthanide and actinide ions in solution

International Nuclear Information System (INIS)

Beitz, J.V.

1993-01-01

Detailed studies of the luminescence of aquated Am 3+ are presented in the context of prior lanthanide and actinide ion work. The luminescing state of aquated Am 3+ is confirmed to be 5 D l based on observed emission and excitation spectra. The luminescence lifetime of Am 3+ in H 2 O solution is (22 ± 3) ns and (155 ± 4) ns in D 2 O solution at 295 K. Judd-Ofelt transition intensity theory qualitatively describes the observed Am 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

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)

Visible luminescence studies in the infrared multiphoton dissociation of 1,2-dichloro-1,1-difluoroethane

Science.gov (United States)

Pushpa, K. K.; Kumar, Awadesh; Naik, P. D.; Annaji Rao, K.; Parthasarathy, V.; Sarkar, S. K.; Mittal, J. P.

1997-11-01

A strong visible luminescence was observed in the CO 2 laser induced infrared multiphoton dissociation of 1,2-dichloro-1,1-difluoroethane. The emission observed between 350-750 nm is attributed to electronically excited carbene CF 2ClCH. The temporal profile of this luminescence was studied as a function of laser pulse duration, pulse energy, excitation frequency and substrate pressure. A suitable dissociation mechanism is presented considering various channels of IRMPD of this molecule.

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.

Modelling the thermal quenching mechanism in quartz based on time-resolved optically stimulated luminescence

International Nuclear Information System (INIS)

Pagonis, V.; Ankjaergaard, C.; Murray, A.S.; Jain, M.; Chen, R.; Lawless, J.; Greilich, S.

2010-01-01

This paper presents a new numerical model for thermal quenching in quartz, based on the previously suggested Mott-Seitz mechanism. In the model electrons from a dosimetric trap are raised by optical or thermal stimulation into the conduction band, followed by an electronic transition from the conduction band into an excited state of the recombination center. Subsequently electrons in this excited state undergo either a direct radiative transition into a recombination center, or a competing thermally assisted non-radiative process into the ground state of the recombination center. As the temperature of the sample is increased, more electrons are removed from the excited state via the non-radiative pathway. This reduction in the number of available electrons leads to both a decrease of the intensity of the luminescence signal and to a simultaneous decrease of the luminescence lifetime. Several simulations are carried out of time-resolved optically stimulated luminescence (TR-OSL) experiments, in which the temperature dependence of luminescence lifetimes in quartz is studied as a function of the stimulation temperature. Good quantitative agreement is found between the simulation results and new experimental data obtained using a single-aliquot procedure on a sedimentary quartz sample.

Nonlinear Characteristics of Randomly Excited Transonic Flutter

DEFF Research Database (Denmark)

Christiansen, Lasse Engbo; Lehn-Schiøler, Tue; Mosekilde, Erik

2002-01-01

. When this model is extended by the introduction of nonlinear terms, it can reproduce the subcritical Hopf bifurcation. We hereafter consider the effects of subjecting simplified versions of the model to random external excitations representing the fluctuations present in the airflow. These models can......The paper describes the effects of random external excitations on the onset and dynamical characteristics of transonic flutter (i.e. large-amplitude, self-sustained oscillations) for a high aspect ratio wing. Wind tunnel experiments performed at the National Aerospace Laboratory (NAL) in Japan have...

Probing luminescence centers in Na rich feldspar

DEFF Research Database (Denmark)

Prasad, Amit Kumar; Lapp, Torben; Kook, Myung Ho

2016-01-01

our understanding of the luminescence mechanisms and recombination sites, in a sample of Na rich plagioclase feldspar (oligoclase). Both the UV and violet–blue emissions show resonant excitations arising from a distribution of energy levels. We propose, contrary to the general understanding...

Defect-Induced Luminescence of a Self-Activated Borophosphate Phosphor

Science.gov (United States)

Han, Bing; Liu, Beibei; Dai, Yazhou; Zhang, Jie

2018-05-01

A self-activated borophosphate phosphor Ba3BPO7 was prepared via typical solid-state reaction in thermal-carbon reduction atmosphere. The structural and luminescence properties were investigated using x-ray powder diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, and photoluminescence spectroscopy. Upon excitation with ultraviolet (UV) light, the as-prepared phosphor shows bright greenish-yellow emission with a microsecond-level fluorescence lifetime, which could result from the oxygen vacancies produced in the process of solid-state synthesis. The possible luminescence mechanism is proposed. Through the introduction of defects in the host, this work realizes visible luminescence in a pure borophosphate compound that does not contain any rare earth or transition metal activators, so it is helpful to develop defect-related luminescent materials in view of energy conservation and environmental protection for sustainable development.

Direct determination of graphene quantum dots based on terbium-sensitized luminescence

Science.gov (United States)

Llorent-Martínez, Eulogio J.; Molina-García, Lucía; Durán, Gema M.; Ruiz-Medina, Antonio; Ríos, Ángel

2018-06-01

Graphene quantum dots (GQD) were determined in water samples using terbium-sensitized luminescence (TSL). Terbium ions complex with GQD due to the carboxylic groups that are usually present in these nanomaterials, increasing the luminescence signal of terbium. In Tb(III)-GQD complexes, GQD absorb energy at their characteristic excitation wavelength and transfer it to terbium ion, which emits at its particular emission wavelength. The analytical signal, measured at λexc = 257 nm and λem = 545 nm, increases proportionally to GQD concentration between 50 and 500 μg L-1. Under optimum conditions, the proposed method presents a detection limit of 15 μg L-1 and is selective to GQD in the presence of other nanomaterials of similar size. As GQD are highly water-soluble, they are potential contaminants in environmental or drinking waters water samples, and hence the method was applied to the analysis of different drinking waters which were the target samples for the application of the developed method.

Luminescence induced by electrons outside zinc oxide nanoparticles driven by intense terahertz pulse trains

International Nuclear Information System (INIS)

Nagai, Masaya; Aono, Shingo; Ashida, Masaaki; Kawase, Keigo; Irizawa, Akinori; Isoyama, Goro

2017-01-01

We investigated the behaviours of electrons from ZnO nanoparticles via a strong terahertz field. Luminescence from ZnO nanoparticles and surrounding nitrogen molecules was observed when the nanoparticles were irradiated with a terahertz free-electron laser (FEL). These excitations arose from the collision of electrons released via field electron emission with the ZnO nanoparticles and neighbouring nitrogen molecules. The strong excitation frequency dependence of the luminescence reflected the kinetic energy and trajectory of electrons outside the nanoparticles. We also observed spectral changes in the luminescence during macropulses of the FEL, even though the carrier lifetime of the nanoparticles was shorter than the interval between the micropulses. These changes were caused by the nanoparticles becoming charged due to electron emission, resulting in the electrons being re-emitted outside the nanoparticles. The electrons outside the nanoparticles were accelerated more efficiently by the terahertz field than the electrons inside the nanoparticles, and thus the motion of these exterior electrons provided a new excitation path. (paper)

Preparation, characterization and luminescence of nanocrystalline Y2O3:Ho

International Nuclear Information System (INIS)

Biljan, Tomislav; Gajovic, Andreja; Meic, Zlatko; Mestrovic, Ernest

2007-01-01

Nanocrystalline Y 2 O 3 :Ho was synthesized by solution combustion method with ethylene glycol as fuel. Material was characterized using powder X-ray diffraction and transmission electron microscopy (TEM). X-ray diffraction and TEM showed that the material is nanostructured. Luminescence properties were studied using Raman spectrometers with excitation in near infrared (NIR) and visible regions. The visible and NIR luminescence spectra of nanocrystalline Y 2 O 3 :Ho show some important differences from those of bulk material. The convenience of using Raman instruments for studying luminescence of lanthanide ions is demonstrated

Further investigations into pulsed optically stimulated luminescence from feldspars using blue and green light

International Nuclear Information System (INIS)

Ankjaergaard, C.; Jain, M.; Kalchgruber, R.; Lapp, T.; Klein, D.; McKeever, S.W.S.; Murray, A.S.; Morthekai, P.

2009-01-01

The purpose of this paper is to investigate characteristics of luminescence signals resulting from pulsed optical stimulation of feldspars and thereby to understand the underlying processes giving rise to the signal. Fourteen different feldspar specimens were investigated using time-resolved optically stimulated luminescence (TR-OSL), and these signals can be mathematically described as a sum of 4 exponential components (a, b, c, d). The slowest component, d, increases with the duration of the light pulse as expected from the exponential model. The stimulation temperature dependence experiment suggests that the TR-OSL signal decay is governed by the recombination process and not by the excited state lifetime. Furthermore data from the TR-OSL signal dependence on stimulation time and preheat temperature suggest that the recombination process may not be a sum of exponentials, although the model cannot be rejected definitively.

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

The research of characteristic difference of selected frequency luminescence for desert sand

International Nuclear Information System (INIS)

Liu Chao; Wei Mingjian; Li Huhou

2011-01-01

The characters of selected frequency luminescence of four groups of samples from Badain Jaran desert are measured by BG2003 luminescence spectrograph. The measurement subjects include selected frequency optical stimulate luminescence spectrum, selected frequency thermoluminescence spectrum and the dose response curve. A double-peak map is obtained by the result from all groups of data and spectrum. The difference is emerged between each group. The optical stimulate luminescence and thermoluminescence is applied in the measurement process. The dispersion of photon count on every response wavelength is analyzed. Based on the analysis, a better result can be gained by selected frequency thermoluminescence. (authors)

Influence of excitonic effects on luminescence quantum yield in silicon

Energy Technology Data Exchange (ETDEWEB)

Sachenko, A.V.; Kostylyov, V.P.; Vlasiuk, V.M. [V. Lashkaryov Institute of Semiconductor Physics, NAS of Ukraine, 41 prospect Nauky, 03028 Kyiv (Ukraine); Sokolovskyi, I.O., E-mail: isokolovskyi@mun.ca [V. Lashkaryov Institute of Semiconductor Physics, NAS of Ukraine, 41 prospect Nauky, 03028 Kyiv (Ukraine); Department of Physics and Physical Oceanography, Memorial University of Newfoundland, St. John' s, NL, A1B 3X7 Canada (Canada); Evstigneev, M. [Department of Physics and Physical Oceanography, Memorial University of Newfoundland, St. John' s, NL, A1B 3X7 Canada (Canada)

2017-03-15

Nonradiative exciton lifetime in silicon is determined by comparison of the experimental and theoretical curves of bulk minority charge carriers lifetime on doping and excitation levels. This value is used to analyze the influence of excitonic effects on internal luminescence quantum yield at room temperature, taking into account both nonradiative and radiative exciton lifetimes. A range of Shockley-Hall-Reed lifetimes is found, where excitonic effects lead to an increase of internal luminescence quantum yield.

Optical and luminescent properties of the lead and barium molybdates

Energy Technology Data Exchange (ETDEWEB)

Spassky, D.A. E-mail: dima@opts.phys.msu.ru; Ivanov, S.N.; Kolobanov, V.N.; Mikhailin, V.V.; Zemskov, V.N.; Zadneprovski, B.I.; Potkin, L.I

2004-12-01

Time-resolved luminescence as well as excitation and reflectivity spectra of the oriented lead and barium molybdate single crystals were studied using synchrotron radiation. Features in reflectivity spectra in the fundamental absorption region were analyzed. The contribution of electronic states of lead cation to the formation of the bandgap in PbMoO{sub 4} is supposed. The role of lead states in the intrinsic luminescence of PbMoO{sub 4} is discussed.

Nanoshells for in vivo imaging using two-photon excitation microscopy

Energy Technology Data Exchange (ETDEWEB)

Gao Liang; Nammalvar, Vengadesan [Department of Bioengineering, Rice University, Houston, TX 77005 (United States); Vadakkan, Tegy J, E-mail: lg3@rice.edu, E-mail: venkyn@rice.edu [Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030 (United States)

2011-09-07

Gold nanoshells have been intensively investigated and applied to various biomedical fields because of their flexible optical tunability and biological compatibility. They hold great potential to serve as luminescent contrast agents excitable with near-infrared (NIR) lasers. In this paper, we describe the development of nanoshells with a peak of plasmon resonance at 800 nm and their subsequent use for in vivo blood vessel imaging using two-photon excitation microscopy at an excitation wavelength of 750 nm. We were able to image single nanoshell particles in blood vessels and generate optical contrast for blood vessel structure using luminescent signals. These results confirm the feasibility of engineering nanoshells with controlled optical properties for single-particle-based in vivo imaging.

Optimising the separation of quartz and feldspar optically stimulated luminescence using pulsed excitation

International Nuclear Information System (INIS)

Ankjaergaard, C.; Jain, M.; Thomsen, K.J.; Murray, A.S.

2010-01-01

In luminescence dating, the two most commonly used natural minerals, quartz and feldspar, are exposed to different dose rates in the natural environment, and so record different doses. The luminescence signals also have different stabilities. For accurate dosimetry, the signals from these two minerals must be separated, either by physical separation of the mineral grains, or by instrumental separation of the luminescence signals. The luminescence signals from quartz and feldspar have different luminescence lifetimes under pulsed optical stimulation. This difference in lifetime can be used to discriminate between the two signals from a mixed quartz-feldspar sample. The purpose of this study is to identify optimum measurement conditions for the best separation of quartz OSL from that of feldspar in a mixed sample using pulsed stimulation and time-resolved OSL. We integrate the signal from 5 μs after the LEDs are switched off until just before the LEDs are switched on again, with the pulse on-time equal to the pulse off-time of 50 μs. By using only the initial interval of the pulsed OSL decay curve (equivalent to 0.2 s of CW-OSL using blue light at 50 mW cm -2 ) we find that the quartz to feldspar pulsed OSL intensity ratio is at a maximum. By using these parameters with an additional infrared (IR) stimulation at 175 o C before measurement (to further reduce the feldspar signal intensity), we obtain a factor of 25 enhancement in signal separation compared to that from a conventional prior-IR CW measurement. This ratio can be further improved if the counting window in the pulse off-time is restricted to detect between 20 and 50 μs instead of the entire off-period.

Uranyl(VI) luminescence spectroscopy at elevated temperatures

Energy Technology Data Exchange (ETDEWEB)

Steudtner, Robin; Franzen, Carola; Brendler, Vinzenz [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Div. Surface Processes; Haubitz, Toni [Brandenburg Univ. of Technology, Cottbus-Senftenberg (Germany)

2016-07-01

We studied the influence of temperature and ionic strength on the luminescence characteristics (band position, decay time and intensity) of the free uranyl ion (UO{sub 2}{sup 2+}) in acidic aqueous solution. Under the chosen conditions an increasing temperature reduced both intensity and luminescence decay time of the UO{sub 2}{sup 2+} luminescence, but the individual U(VI) emission bands did not change.

Synthesis and luminescence characteristics of Dy{sup 3+} doped KLa(PO{sub 3}){sub 4}

Energy Technology Data Exchange (ETDEWEB)

Chemingui, S.; Ferhi, M., E-mail: ferhi.mounir@gmail.com; Horchani-Naifer, K.; Férid, M.

2015-10-15

Polycrystalline powders of KLa{sub (1−x)}Dy{sub x}(PO{sub 3}){sub 4} (x=0.5%, 1%, 5% and 10%) with linear chain have been grown by solid state reaction. The obtained powders are characterized by X-ray powder diffraction, FTIR and Raman spectroscopies. Emission, excitation spectra and decay curves analysis have been used to study the spectroscopic properties of Dy{sup 3+} in KLa(PO{sub 3}){sub 4}. The photoluminescence spectra show two characteristic blue and yellow bands of Dy{sup 3+}. The yellow-to-blue emission intensity ratios and CIE chromaticity coordinates have been determined from emission spectra to evaluate the emitted light as function of Dy{sup 3+} concentration. The measured decay rates for {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} deviated from exponential to non-exponential shape with increase of Dy{sup 3+} concentration. The observed non-exponential behavior of the decay curve has been fitted to Inokuti–Hirayama model, which indicates that the energy transfer between the donor and the acceptor is of dipole–dipole nature. The energy transfer, between the donor (excited Dy{sup 3+}) and the acceptor (unexcited Dy{sup 3+}), increases with Dy{sup 3+} ions concentration. - Highlights: • Polycrystalline powders of KLa{sub (1−x)}Dy{sub x}(PO{sub 3}){sub 4} were grown by solid state reaction. • The obtained samples are characterized by XRD, FTIR and Raman spectroscopies. • The luminescent properties of Dy{sup 3+} in KLa(PO{sub 3}){sub 4} are investigated. • Lifetime and chromatic coordinates depend strongly on Dy{sup 3+} concentration. • White and blue emissions are obtained at high and low concentration, respectively.

SPORT: A new sub-nanosecond time-resolved instrument to study swift heavy ion-beam induced luminescence - Application to luminescence degradation of a fast plastic scintillator

Science.gov (United States)

Gardés, E.; Balanzat, E.; Ban-d'Etat, B.; Cassimi, A.; Durantel, F.; Grygiel, C.; Madi, T.; Monnet, I.; Ramillon, J.-M.; Ropars, F.; Lebius, H.

2013-02-01

We developed a new sub-nanosecond time-resolved instrument to study the dynamics of UV-visible luminescence under high stopping power heavy ion irradiation. We applied our instrument, called SPORT, on a fast plastic scintillator (BC-400) irradiated with 27-MeV Ar ions having high mean electronic stopping power of 2.6 MeV/μm. As a consequence of increasing permanent radiation damages with increasing ion fluence, our investigations reveal a degradation of scintillation intensity together with, thanks to the time-resolved measurement, a decrease in the decay constant of the scintillator. This combination indicates that luminescence degradation processes by both dynamic and static quenching, the latter mechanism being predominant. Under such high density excitation, the scintillation deterioration of BC-400 is significantly enhanced compared to that observed in previous investigations, mainly performed using light ions. The observed non-linear behaviour implies that the dose at which luminescence starts deteriorating is not independent on particles' stopping power, thus illustrating that the radiation hardness of plastic scintillators can be strongly weakened under high excitation density in heavy ion environments.

Dipole-Dipole Electron Excitation Energy Transfer in the System CdSe/ZnS Quantum Dot - Eosin in Butyral Resin Matrix

Science.gov (United States)

Myslitskaya, N. A.; Samusev, I. G.; Bryukhanov, V. V.

2014-11-01

The electron excitation energy transfer from CdSe/ZnS quantum dots to eosin molecules in the polymer matrix of butyral resin is investigated. The main characteristics of energy transfer are determined. By means of luminescence microscopy and correlation spectroscopy methods we found that quantum dots in the polymer are in an aggregate state.

Luminescence and structural study of porous silicon films

Science.gov (United States)

Xie, Y. H.; Wilson, W. L.; Ross, F. M.; Mucha, J. A.; Fitzgerald, E. A.; Macaulay, J. M.; Harris, T. D.

1992-03-01

A combination of photoluminescence, TEM, and Fourier transform IR spectroscopy is used to investigate the luminescence properties of 3-micron thick, strongly emitting, and highly porous silicon films. TEMs indicate that these samples have structures of predominantly 6-7-nm size clusters. In the as-prepared films, there is a significant concentration of Si-H bonds which is gradually replaced by Si-O bonds during prolonged aging in air. Upon optical excitation these films exhibit strong visible emission, peaking at about 690 nm. The excitation edge is shown to be emission-wavelength dependent, revealing the inhomogeneous nature of both the initially photoexcited and luminescing species. The correlation of the spectral and structural information suggest that the source of the large blue shift of the visible emission compared to the bulk Si bandgap energy is due to quantum confinement in the nanometer-size Si clusters.

Thermostimulated luminescence in KBr-In crystals after optical creation of electronic excitation. Termostimulirovannaya lyuminestsentsiya v kristallakh KBr-In pri opticheskom sozdanii ehlektronnykh vozbuzhdenij

Energy Technology Data Exchange (ETDEWEB)

Popov, A I [AN Latvijskoj SSR, Riga (USSR). Inst. Fiziki

1990-01-01

Thermal stability of the radiation defects produced in KBr-In by optical creation of the electronic excitation (optical creation of the excitons or optical ionization of In{sup +}-ions under C-band illumination) is investigated by the method of thermostimulated luminescence (TSL). A method of detection of prehistory defects, when the optical ionization of In{sup +}-ions and TSL are performed, is proposed. Quadratic dependence of V{sub 2}-center creation upon dose is shown. This dependence confirms assocative mechanism of the creation of V{sub 2}-centers from two interstitial centers.

Core shell structured nanoparticles of Eu3+ doped SnO2 with SiO2 shell: luminescence studies

International Nuclear Information System (INIS)

Ningthoujam, R.S.; Sudarsan, V.; Kulshreshtha, S.K.

2005-01-01

Re dispersible SnO 2 nanoparticles with and without Eu 3+ doping nanoparticles were prepared at 185 deg C by the urea hydrolysis of Sn 4+ in ethylene glycol medium. X-ray diffraction and 119 Sn MAS NMR studies of these particles revealed that these nanoparticles are crystalline with Cassiterite structure having an average crystallite size of 7 nm. Undoped SnO 2 gave a emission peak centered around 470 nm characteristic of the traps present in the nanoparticles. For Eu 3+ doped samples, emission around 590 and 615 nm was observed on both direct excitation as well as indirect excitation through traps, indicating that there is an energy transfer between the traps present in the nanoparticles and Eu 3+ ions. The asymmetric ratio of luminescence (relative intensity ratio of 590 to 615 nm transitions) has been found to be 1.2. For SnO 2 :Eu(5%)-SiO 2 nanoparticles, the asymmetric ratio of luminescence change significantly indicating the formation of nanoparticles with SnO 2 :Eu(5%) core covered with SiO 2 shell. (author)

Modeling the influence of silver nanoparticles on the f–f luminescence of the EuEDTA complex in the polyvinylpirrolidone polymer

Energy Technology Data Exchange (ETDEWEB)

Couto dos Santos, M.A., E-mail: marcoscouto@ufs.br [Departamento de Física, Universidade Federal de Sergipe/CCET, São Cristóvão, SE 49100-000 (Brazil); Malta, O.L. [Departamento de Química Fundamental, Universidade Federalde Pernambuco/CCEN, Cidade Universitária, Recife, PE 50670-901 (Brazil); Reisfeld, R. [The Hebrew University of Jerusalem, Chemistry Institute, E. Safra Campus, 91904 Jerusalem (Israel)

2016-02-15

A theoretical analysis on experimental results previously obtained on the influence of silver nanoparticles in a polyvinylpirrolidone (PVP) polymer film containing a trivalent europium complex with EDTA ligand is made. Depending on the excitation source (at 393 nm with a xenon lamp or at 532 nm with a focused diode laser) the characteristic Eu{sup 3+} luminescence is observed to be enhanced by factors between 5 and 50. The theoretical analysis presumes a migration process of the EuEDTA complex units towards the silver nanoparticles, during the synthesis of the composite samples, and subsequently the treatment of the competition between local high field gradient effects and Eu{sup 3+} ion to the silver nanoparticles energy transfer successfully accounts for the observed luminescence enhancement factors. - Highlights: • Unusual luminescence enhancement of EuEDTA–silver nanoparticles–polyvinylpyrrolidone is treated theoretically. • A migration process of the EuEDTA complex units towards the silver nanoparticles is assumed. • The local high field gradient effects successfully accounts for the observed unusual luminescence enhancement factor of 50.

Luminescence of YbP3O9 upon excitation in the UV-VUV range

International Nuclear Information System (INIS)

Stryganyuk, G; Trots, D; Berezovskaya, I; Shalapska, T; Voloshinovskii, A; Dotsenko, V; Zimmerer, G

2007-01-01

X-ray powder diffraction and luminescence spectral-kinetic studies have been performed for ytterbium metaphosphate (YbP 3 O 9 ) in the 12-290 K temperature range. The diffraction investigation has shown YbP 3 O 9 to be of monoclinic P 2 1 /c structure at T = 12-290 K. Charge transfer luminescence originating from Yb 3+ ion has been revealed. The carrier confinement within the Yb 3+ charge transfer state is pronounced at T = 12 K. A tendency has been revealed for charge carriers in YbP 3 O 9 to be localized in a trapped exciton state at room temperature. The quenching mechanisms for Yb 3+ charge transfer luminescence and processes competing with the formation of the Yb 3+ charge transfer state are discussed

Persistent luminescence of Eu, Mn, Dy doped calcium phosphates for in-vivo optical imaging

Energy Technology Data Exchange (ETDEWEB)

Rosticher, Céline [UPMC Univ Paris 06, CNRS, UMR 7574, Chimie de la Matière Condensée de Paris, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05 (France); Viana, Bruno, E-mail: bruno.viana@chimie-paristech.fr [PSL Research University, Chimie ParisTech-CNRS, Institut de Recherche de Chimie Paris, 11 rue Pierre et Marie Curie, 75005 Paris (France); Maldiney, Thomas; Richard, Cyrille [Unité de Technologies Chimiques et Biologiques pour la Santé, CNRS, UMR 8258, Paris Cedex F-75270 (France); Inserm U1022, Paris Cedex F-75270 (France); Faculté des Sciences Pharmaceutiques et Biologiques, Université Paris Descartes, Sorbonne Paris Cité, Paris Cedex F-75270 (France); Chanéac, Corinne, E-mail: corinne.chaneac@upmc.fr [UPMC Univ Paris 06, CNRS, UMR 7574, Chimie de la Matière Condensée de Paris, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05 (France)

2016-02-15

Biocompatible nanoparticles possessing persistent luminescence properties offer attractive possibilities for in vivo imaging applications as it allows an excitation of the sensors outside the animal before injection and a long-lasting emission of light. Here we report the development of highly biocompatible calcium phosphate nanoparticles doped with europium, Mn{sup 2+} and Ln{sup 3+} (Ln{sup 3+}=Dy{sup 3+}, Pr{sup 3+}) ions synthesized by hydrothermal route and tailored to present red-near infrared persistent luminescence after UV excitation. Nanosize biphasic HAp/β-TCP compounds with sphere and rod-shaped were obtained. Two emission bands in the red-near infrared range were observed and attributed to {sup 4}T{sub 1}→{sup 6}A{sub 1} transitions of Mn{sup 2+} ions in HAp/β-TCP. An annealing treatment in reductive atmosphere post-synthesis was essential to reveal persistent luminescence properties. Indeed, such thermal treatment allows reducing Eu{sup 3+} ions in Eu{sup 2+} ions and generating required defaults as oxygen vacancies in the crystal necessary for red emission in accordance with persistent luminescence mechanism. These nanoparticles have been tested for the first time for in vivo imaging on small animal as proof of concept of prospective highly biocompatible nanoprobes. - Highlights: • Biocompatible HAp/b-TCP nanoparticles with persistent luminescence are investigated. • Reducing step induced persistent luminescence. • Nanoparticles have been tested for the first time for in vivo imaging. • Persistent luminescence is observed after 10 min in vivo.

Excitonic surface polaritons in luminescence from ZnTe crystals

International Nuclear Information System (INIS)

Brodin, M.S.; Bandura, V.M.; Matsko, M.G.

1984-01-01

The form and structure of reflection and exciton-polariton luminescence spectra of ZnTe crystals are studied in the region of the ground (n = 1) exciton state. The longitudinal-transverse splitting magnitude ΔE/sub LT/ is determined from the shape of the reflection spectra. A detected doublet structure of an emission band from the lower polariton branch is associated with the k-linear term. The evolution of bulk and surface polariton luminescence spectra versus temperature and wavelength of the exciting light is investigated. (author)

Excitonic surface polaritons in luminescence from ZnTe crystals

Energy Technology Data Exchange (ETDEWEB)

Brodin, M.S.; Bandura, V.M.; Matsko, M.G. (AN Ukrainskoj SSR, Kiev. Inst. Fiziki)

1984-10-01

The form and structure of reflection and exciton-polariton luminescence spectra of ZnTe crystals are studied in the region of the ground (n = 1) exciton state. The longitudinal-transverse splitting magnitude ..delta..E/sub LT/ is determined from the shape of the reflection spectra. A detected doublet structure of an emission band from the lower polariton branch is associated with the k-linear term. The evolution of bulk and surface polariton luminescence spectra versus temperature and wavelength of the exciting light is investigated.

Nanostructured Ag-zeolite Composites as Luminescence-based Humidity Sensors

Science.gov (United States)

Dieu, Bjorn; Roeffaers, Maarten B.J.; Hofkens, Johan

2016-01-01

Small silver clusters confined inside zeolite matrices have recently emerged as a novel type of highly luminescent materials. Their emission has high external quantum efficiencies (EQE) and spans the whole visible spectrum. It has been recently reported that the UV excited luminescence of partially Li-exchanged sodium Linde type A zeolites [LTA(Na)] containing luminescent silver clusters can be controlled by adjusting the water content of the zeolite. These samples showed a dynamic change in their emission color from blue to green and yellow upon an increase of the hydration level of the zeolite, showing the great potential that these materials can have as luminescence-based humidity sensors at the macro and micro scale. Here, we describe the detailed procedure to fabricate a humidity sensor prototype using silver-exchanged zeolite composites. The sensor is produced by suspending the luminescent Ag-zeolites in an aqueous solution of polyethylenimine (PEI) to subsequently deposit a film of the material onto a quartz plate. The coated plate is subjected to several hydration/dehydration cycles to show the functionality of the sensing film. PMID:27911397

Effect of ultrasound treatment on the morpho-structural and luminescent characteristics of cerium doped yttrium silicate phosphors

Energy Technology Data Exchange (ETDEWEB)

Muresan, L.E., E-mail: laura_muresan2003@yahoo.com [“Raluca Ripan” Institute for Research in Chemistry, Babeş Bolyai University, Fântânele 30, 400294 Cluj-Napoca (Romania); Cadis, A.I.; Perhaita, I. [“Raluca Ripan” Institute for Research in Chemistry, Babeş Bolyai University, Fântânele 30, 400294 Cluj-Napoca (Romania); Silipas, D.T. [National Institute for R& D of Isotopic and Molecular Technologies, Donath 67-103, 400293 Cluj-Napoca (Romania); Tudoran, L. Barbu [Electronic Microscopy Centre, Babeş Bolyai University, Clinicilor 37, 400006 Cluj-Napoca (Romania)

2015-08-15

Highlights: • Y{sub 2}SiO{sub 5}:Ce is prepared by gel combustion in ultrasound conditions (US). • Morpho-structural characteristics are revealed based on FTIR, SEM, XRD, BET. • Incorporation of Ce{sup 3+} in X1/X2 type centers depends on preparative conditions. • US treatment increases the luminescent performances up to 151%. - Abstract: Cerium activated yttrium silicate (Y{sub 2}SiO{sub 5}:Ce) phosphors were prepared by gel-combustion, using yttrium–cerium nitrate as oxidizer, aspartic acid as fuel and TEOS as source of silicon. Two modalities for samples preparation were approached namely: the classical gel-combustion and sonication gel-combustion. The ultrasound treatment during the gelling stage has a positive effect on the structural and luminescent characteristics of the final product. Therefore, a well crystallized single X2–Y{sub 2}SiO{sub 5} phase phosphor was obtained at 1200 °C. Based on FT-IR and XRD investigations, conversion of X1 to X2–Y{sub 2}SiO{sub 5} phases is observed as the firing temperature is varied (1100 °C, 1200 °C, 1300 °C 1400 °C). The ultrasound treatment leads to smaller particle size and enhances the luminescent performances up to 151% in comparison with samples prepared by classical way.

submitter Preparation and luminescence properties of ZnO:Ga – polystyrene composite scintillator

CERN Document Server

Burešová, Hana; Turtos, Rosana Martinez; Jarý, Vítězslav; Mihóková, Eva; Beitlerová, Alena; Pjatkan, Radek; Gundacker, Stefan; Auffray, Etiennette; Lecoq, Paul; Nikl, Martin; Čuba, Václav

2016-01-01

Highly luminescent ZnO:Ga-polystyrene composite (ZnO:Ga-PS) with ultrafast subnanosecond decay was prepared by homogeneous embedding the ZnO:Ga scintillating powder into the scintillating organic matrix. The powder was prepared by photo-induced precipitation with subsequent calcination in air and Ar/H2 atmospheres. The composite was subsequently prepared by mixing the ZnO:Ga powder into the polystyrene (10 wt% fraction of ZnO:Ga) and press compacted to the 1 mm thick pellet. Luminescent spectral and kinetic characteristics of ZnO:Ga were preserved. Radioluminescence spectra corresponded purely to the ZnO:Ga scintillating phase and emission of polystyrene at 300-350 nm was absent. These features suggest the presence of non-radiative energy transfer from polystyrene host towards the ZnO:Ga scintillating phase which is confirmed by the measurement of X-ray excited scintillation decay with picosecond time resolution. It shows an ultrafast rise time below the time resolution of the experiment (18 ps) and a single-...

Luminescence decay of S Zn::Ag and O Zn:Ga scintillation detectors excited by a pulsed laser; Evolucion temporal de la luminiscencia producida por un laser pulsado de los detectores de centello SZn:Ag y OZn:Ga

Energy Technology Data Exchange (ETDEWEB)

Romero, L.; Campos, J.

1981-07-01

In the present work a high sensitivity experimental set up for luminescence decay measurements in the 1 0 {sup -}1 sec range has been developed. As an application, luminescence light decay In S Zn:Ag and 0Zn:Ga after excitation by a pulsed N{sub 2} laser has been measured. In SZnrAg, measurements of total light decay was compared with donor acceptor pairs theory. In both substances, spectral evolution in the first 15 sec was investigated. (Author) 4 refs.

Luminescence characteristics of Pb2+ centres in undoped and Ce3+-doped Lu3Al5O12 single-crystalline films and Pb2+→Ce3+ energy transfer processes

International Nuclear Information System (INIS)

Babin, V.; Gorbenko, V.; Makhov, A.; Mares, J.A.; Nikl, M.; Zazubovich, S.; Zorenko, Yu.

2007-01-01

At 4.2-350 K, the steady-state and time-resolved emission and excitation spectra and luminescence decay kinetics were studied under excitation in the 2.5-15 eV energy range for the undoped and Ce 3+ -doped Lu 3 Al 5 O 12 (LuAG) single-crystalline films grown by liquid phase epitaxy method from the PbO-based flux. The spectral bands arising from the single Pb 2+ -based centres were identified. The processes of energy transfer from the host lattice to Pb 2+ and Ce 3+ ions and from Pb 2+ to Ce 3+ ions were investigated. Competition between Pb 2+ and Ce 3+ ions in the processes of energy transfer from the LuAG crystal lattice was evidenced especially in the exciton absorption region. Due to overlap of the 3.61 eV emission band of Pb 2+ centres with the 3.6 eV absorption band of Ce 3+ centres, an effective nonradiative energy transfer from Pb 2+ ions to Ce 3+ ions takes place, resulting in the appearance of slower component in the luminescence decay kinetics of Ce 3+ centres and decrease of the Ce 3+ -related luminescence intensity

Luminescent properties of UV excitable blue emitting phosphors MSr4(BO3)3:Ce3+ (M = Li and Na)

International Nuclear Information System (INIS)

Guo Chongfeng; Ding Xu; Seo, Hyo Jin; Ren Zhaoyu; Bai Jintao

2011-01-01

Research highlights: → Novel blue emitting phosphors borate MSr 4 (BO 3 ) 3 (M = Li or Na) were prepared first. → Luminescent properties of phosphors borate MSr 4 (BO 3 ) 3 (M = Li or Na) were investigated extensively as candidates of blue emitting phosphor used for UV excited LED. → The optimal concentrations of dopant Ce 3+ ions in compound MSr 4 (BO 3 ) 3 (M = Li or Na) were determined as 0.05 for Li and x = 0.09 for Na excited by UV light respectively. - Abstract: A series of Ce 3+ doped novel borate phosphors MSr 4 (BO 3 ) 3 (M = Li or Na) were successfully synthesized by traditional solid-state reaction. The crystal structures and the phase purities of samples were characterized by powder X-ray diffraction. The optimal concentrations of dopant Ce 3+ ions in compound MSr 4 (BO 3 ) 3 (M = Li or Na) were determined through the measurements of photoluminescence spectra of phosphors. Ce 3+ doped phosphors MSr 4 (BO 3 ) 3 (M = Li or Na) show strong broad band absorption in UV spectral region and bright blue emission under the excitation of 345 nm light. In addition, the temperature dependences of emission spectra of M 1+x Sr 4-2x Ce x (BO 3 ) 3 (M = Li or Na) phosphors with optimal composition x = 0.05 for Li and x = 0.09 for Na excited under 355 nm pulse laser were also investigated. The experimental results indicate that the M 1+x Sr 4-2x Ce x (BO 3 ) 3 (M = Li or Na) phosphors are promising blue emitting phosphors pumped by UV light.

On the correlation between annealing and variabilities in pulsed-luminescence from quartz

International Nuclear Information System (INIS)

Chithambo, M.L.

2006-01-01

Properties of luminescence lifetimes in quartz related to annealing between 500 and 900 deg. C have been investigated. The luminescence was pulse-stimulated at 470nm from sets of granular quartz annealed at 500, 600, 700, 800, and 900 deg. C. The lifetimes decrease with annealing temperature from about 42 to 33μs when the annealing temperature is increased from 500 to 900 deg. C. Luminescence lifetimes are most sensitive to duration of annealing at 600 deg. C, decreasing from 40.2+/-0.7μs by as much as 7μs when the duration of annealing is changed from 10 to 60min. However, at 800-900 deg. C lifetimes are essentially independent of annealing temperature at about 33μs. Increasing the exciting beta dose causes an increase in the lifetimes of the stimulated luminescence in the sample annealed at 800 deg. C but not in those annealed at either 500 or 600 deg. C. The temperature-resolved distribution of luminescence lifetimes is affected by thermal quenching of luminescence. These features may be accounted for with reference to two principal luminescence centres involved in the luminescence emission process

Luminescent rare earth vanadate nanoparticles doped with Eu3+ and Bi3 for sensing and imaging applications

Science.gov (United States)

Escudero, Alberto; Carrillo-Carrión, Carolina; Zyuzin, Mikhail; Hartmann, Raimo; Ashraf, Sumaira; Parak, Wolfgang J.

2016-03-01

Nanoparticles (NPs) are attracting interest in nanomedicine due to their potential medical applications, ranging from optical biolabels and contrast agents for magnetic resonance imaging to carriers for drug and gene delivery for disease therapy.[1] Rare earth (RE) based nanophosphors exhibit important advantages compared with other available luminescent materials, such as quantum dots and nanostructures functionalized with organic dyes, due to their lower toxicities, photostabilities, high thermal and chemical stabilities, high luminescence quantum yields, and sharp emission bands.[2] Yttrium orthovanadate NPs doped with Eu3+ and Bi3+, functionalized with poly acryl acid (PAA), and excitable by near-ultraviolet light have been synthesized by homogeneous precipitation at 120 °C from solutions of rare earth precursors (yttrium acetylacetonate and europium nitrate), bismuth nitrate, sodium orthovanadate, and PAA, in an ethylene glycol/water mixture. Quasispheres with sizes from 93 to 51 nm were obtained. The as synthesized NPs were already functionalized with PAA. The NPs showed the typical red luminescence of Eu3+, which can be excited with near-UV light through an energy transfer from the vanadate anion. The presence of Bi3+ shifts the maximum of the broad excitation band from 280 nm to 342 nm. This excitation path is much more efficient than the direct excitation of the Eu3+ electronic levels, and results in a much higher luminescence. The NPs can be uptaken by HeLa cells, and are eventually located in the lysosomes after being internalized. Finally, the functionalization with PAA provides -COOH anchors for adding functional ligands of biomedical interest that can be used for sensing applications.

Luminescent properties of Pr3+-sensitized LaPO4:Gd3+ ultraviolet-B phosphor under vacuum-ultraviolet light excitation

International Nuclear Information System (INIS)

Okamoto, Shinji; Uchino, Rika; Kobayashi, Keisuke; Yamamoto, Hajime

2009-01-01

Luminescent properties of Pr 3+ -sensitized LaPO 4 :Gd 3+ under vacuum-ultraviolet (vuv) light excitation have been investigated. The energy transfer probably occurs from the 5d levels in Pr 3+ ions to Gd 3+ ions under 172 nm light excitation. LaPO 4 :Gd 3+ ,Pr 3+ shows efficient ultraviolet-B (uv-B) emission at 312 nm, whose peak intensity reaches its maximum at Gd=35 mol % and Pr=5 mol %. (La 0.65 Gd 0.35 ) 0.95 Pr 0.05 PO 4 is about 1.6 times higher than a typical uv-B phosphor for vuv lamp, Y 0.75 Gd 0.25 Al 3 (BO 3 ) 4 , in Gd 3+ -emission intensity under 172 nm light excitation. This result implies that the Pr 3+ -sensitized LaPO 4 :Gd 3+ is a candidate of uv-B phosphors for xenon-excimer discharge vuv lamps. In order to evaluate the effect of the narrow-band uv-B emission by LaPO 4 :Gd 3+ ,Pr 3+ phosphor, irradiation test on DNA was performed. The irradiation damage of pUC 18 DNA by the narrow-band uv-B light from the LaPO 4 :Gd 3+ ,Pr 3+ phosphor is in the same magnitude as that by uv-A light from a filtered Hg lamp, even though the uv-B lamp is higher than the uv-A lamp in power density and photon energy.

Persistent luminescence and thermoluminescence of UV/VIS -irradiated SrAl2O4: Eu2+, Dy3+ phosphor

International Nuclear Information System (INIS)

Pereyda-Pierre, C.; Meléndrez, R.; García, R.; Pedroza-Montero, M.; Barboza-Flores, M.

2011-01-01

The persistent luminescence and thermoluminescence properties of SrAl 2 O 4 : Eu 2+ , Dy 3+ phosphors excited with UV–VIS light in the 200–500 nm region were investigated. The thermoluminescence glow curve was found to be composed of peaks around 70, 125 and 245 °C. The persistent luminescence and thermoluminescence excitation spectra exhibited a broad band around 300–500 nm centered at 400 and 420 nm respectively. A linear behavior of the integrated thermoluminescence intensity and persistent luminescence versus irradiation time was found for the first 60 s. The charge detrapping from the 70 °C trapping levels was the major contributor to the observed persistent luminescence at room temperature. The SrAl 2 O 4 : Eu 2+ , Dy 3+ phosphors have suitable properties to be applied as storage and persistent luminescence UV–VIS irradiation dose phosphor. -- Highlights: ► SrAl 2 O 4 :Eu 2+ , Dy 3+ persistent luminescence and thermoluminescence was measured. ► The phosphor was irradiated with UV–VIS photons in the 200–500 nm wavelength range. ► SrAl 2 O 4 :Eu 2+ , Dy 3+ behaves adequately as persistent and storage UV–VIS dosimeter. ► The persistent luminescence dosimetry does not require heat or light stimulation.

X-ray micro-modulated luminescence tomography (XMLT)

Science.gov (United States)

Cong, Wenxiang; Liu, Fenglin; Wang, Chao; Wang, Ge

2014-01-01

Imaging depth of optical microscopy has been fundamentally limited to millimeter or sub-millimeter due to strong scattering of light in a biological sample. X-ray microscopy can resolve spatial details of few microns deep inside a sample but contrast resolution is inadequate to depict heterogeneous features at cellular or sub-cellular levels. To enhance and enrich biological contrast at large imaging depth, various nanoparticles are introduced and become essential to basic research and molecular medicine. Nanoparticles can be functionalized as imaging probes, similar to fluorescent and bioluminescent proteins. LiGa5O8:Cr3+ nanoparticles were recently synthesized to facilitate luminescence energy storage with x-ray pre-excitation and subsequently stimulated luminescence emission by visible/near-infrared (NIR) light. In this paper, we propose an x-ray micro-modulated luminescence tomography (XMLT, or MLT to be more general) approach to quantify a nanophosphor distribution in a thick biological sample with high resolution. Our numerical simulation studies demonstrate the feasibility of the proposed approach. PMID:24663898

Luminescence sensitivity changes in quartz

CERN Document Server

Wintle, A G

1999-01-01

In the luminescence dating of sedimentary or heated quartz, some heat treatment is usually applied to the sample immediately prior to the measurement of the optically stimulated luminescence. In this paper we report experiments on a 30,000-year-old sedimentary quartz, in which we use the luminescence response to a test dose to monitor the changes in sensitivity that are caused by holding the quartz at temperatures from 160 to 280 deg. C for times from 10 s to 22 h. For an optically bleached sample, the monitoring is by both optically stimulated luminescence and the 110 deg. C TL peak; both luminescence signals are shown to have the same sensitisation (i.e. activation energy) characteristics. For natural or laboratory irradiated samples only the 110 deg. C TL peak can be used; sensitivity increases of up to a factor of 1.3 and 3 are observed for the natural and laboratory irradiated aliquots, respectively. Up to four exponential components are used to deconvolve the sensitivity change data; the dominant compon...

Excitation mechanism of Er{sup 3+} in a-Si:H; Anregungsmechanismus von Er{sup 3+} in a-Si:H

Energy Technology Data Exchange (ETDEWEB)

Kuehne, H.

2004-07-01

The aim of this work is the examination of the optoelectronical material a-Si:H (Er). It is characterised in the good electronic properties of the a-Si:H and the emission wavelength of 1.5 micrometer of erbium which coincides with the absorbtion minimum of glasfibres. Photoluminescence measurements confirm the assumption that oxigen is necessary for the optical activation of Er{sup 3+} in addition to the symmetrical breaking of the crystal field. The flexible lattice of a-Si:H enables a high concentration of Erbium up to 5.10{sup 21}/cm{sup 3} with a quantum efficiency of the luminescence of 0.5-1.5.10{sup -4} at room temperature. Photoluminescence excitation and absorption measurements of a-Si:H (Er) show, that there is no direct excitation of the erbium ions because the absorption of the Er{sup 3+} ions is two orders of magnitude below the absorption of silicon. The excitation or the Er{sup 3+} ions takes place through the absorption in silicon with additional energy transfer to Erbium. Photoluminescence measurements are done in order to differentiate between the possible excitation channels, the intrinsic bond-bond channel and the excitation through defects. The different temperature dependence of the intensity of the intrinsic luminescence (77 K - 300 K >3 orders of magnitude) in comparison with the defect luminescence and the Erbium luminescence (both 1-1.5 orders of magnitude) shows that the energy transfer takes place over defects. Luminescence and absorption measurements with boron doped a-Si:H (Er) show no dependence of the Erbium luminescence in dependence of defect density or the electrical charge of the defects. The luminescence spectra show a break in the defect luminescence at 0.84 eV. This agrees with the first excited state of the Er{sup 3+} ion combined with a clearly smaller line width of the defect luminescence (0.18 eV in comparision with >0.3 eV in erbium free a-Si:H). This result shows the resonance of the energy transfer. The resonance is

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.)

Study of the absorption and energy transfer processes in inorganic luminescent materials in the UV and VUV region; Etude des processus d`absorption et de transfert d`energie au sein de materiaux inorganiques luminescents dans le domaine UV et VUV

Energy Technology Data Exchange (ETDEWEB)

Mayolet, A

1995-11-29

In order to find a green emitting phosphor showing high quantum efficiency and a short decay time which can be used in the color Plasma Display Panels developed by Thomson-TTE-TIV company, a VUV spectrophotometer built at IPN Orsay, using the synchrotron radiation from the SUPER-ACO storage ring as an excitation source, allow us the simultaneous recording of the luminescence excitation and diffuse reflectivity spectra of the inorganic compounds in the UV-VUV range. In addition, this experimental set-up enable us to determine the luminescence quantum efficiency of phosphors in the whole energy range of investigation. The chemical synthesis of rare-earth ortho-- and metaborate and rare-earth ortho- and metaphosphate doped with trivalent lanthanide ions cerium, praseodymium, europium and terbium have been made. The energy variation of the thresholds of the luminescence excitation mechanisms in function of the nature and the structure of the host matrix is discussed. We have determined the influence of the nephelauxetic effect and the crystal field intensity on the energy of the f-d inter-configuration transitions. The variation of the luminescence quantum efficiency of the dopant ion is interpreted through the `impurity bound exciton` model. The systematic comparison of the cerium and terbium trivalent ions spectroscopic properties in the Y(AG)G host lattice series stands to reason that the self-ionized state of the luminescent center plays an important role in the rate of the non radiative relaxation. It is the redox power of the host matrix which imposes to the luminescent center, the energy of this state. (author) 134 refs.

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.

Oxygen influence on luminescence properties of rare-earth doped NaLaF{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Tuomela, A., E-mail: anu.tuomela@oulu.fi [Research Center of Molecular Materials, University of Oulu, P.O. Box 3000, FIN-90014 (Finland); Pankratov, V., E-mail: vladimirs.pankratovs@oulu.fi [Research Center of Molecular Materials, University of Oulu, P.O. Box 3000, FIN-90014 (Finland); Sarakovskis, A.; Doke, G.; Grinberga, L. [Institute of Solid State Physics, University of Latvia, 8 Kengaraga, LV-1063 Riga (Latvia); Vielhauer, S. [Institute of Physics, University of Tartu, Riia 142, Tartu 51014 (Estonia); Huttula, M. [Research Center of Molecular Materials, University of Oulu, P.O. Box 3000, FIN-90014 (Finland)

2016-11-15

Luminescence properties of erbium and europium doped NaLaF{sub 4} with different oxygen content have been studied. Vacuum ultraviolet (VUV) excitation luminescence spectroscopy technique has been applied by using synchrotron radiation excitation. It was found that oxygen impurity leads to significant degradation of Er{sup 3+} or Eu{sup 3+} emission under VUV excitation. The intensive O{sup 2−}–Er{sup 3+} charge transfer excitation band has been detected from oxygen abundant NaLaF{sub 4} in the 150–165 nm spectral range. This band reveals a competing absorption mechanism in oxygen containing NaLaF{sub 4}. It is clearly demonstrated that one reason for the Er{sup 3+} emission degradation in oxygen abundant NaLaF{sub 4} is strong suppression of 4f–5d transitions in Er{sup 3+} ion. The degradation of the Eu{sup 3+} emission under VUV excitation was explained by diminishing of F{sup −}–Eu{sup 3+} charge transfer absorption band as well as by competing relaxation centers in the oxygen abundant NaLaF{sub 4}.

Time-resolved luminescence of Eu2+-aggregate centers in CsBr crystals

International Nuclear Information System (INIS)

Zorenko, Yu.V.; Turchak, R.M.; Voznjak, T.I.; Stryganjuk, G.B.

2005-01-01

The luminescence of Eu 2+ -V Cs dipole centers and CsEuBr 3 aggregate centers, as well as the features of the energy transfer to these centers by excitons have been studied in CsBr:Eu crystals by means of investigation of the time-resolved emission spectra and luminescence decay kinetics under excitation by synchrotron radiation at RT. (copyright 2005 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Luminescence characteristics of quartz and feldspar from tectonically uplifted terraces in Kashmir Basin, Jammu and Kashmir, India

International Nuclear Information System (INIS)

Jaiswal, Manoj K.; Bhat, M.I.; Bali, B.S.; Ahmad, Shabir; Chen, Y.G.

2009-01-01

The Kashmir Valley or the Jhelum basin is an intermontane-basin in NW Himalaya bounded by the Pir Panjal Range in the south and southwest and the Great Himalayan Range in the north and northeast. The valley is marked by active major thrust boundaries in its south and southwestern parts. Remote sensing studies and morphometric analysis suggest neo-tectonic activities and the formation of tectonic terraces due to uplift on the major thrust boundaries in NW Himalayas. The quartz from freshly eroded mountain belts is usually found to show very poor luminescence sensitivity and thus not suitable for optical dating. Similar problems occurred with the quartz from the Srinagar Basin. Due to this, feldspar was selected as a natural dose meter for dating tectonically uplifted terraces in an active and dynamic belt of the NW Himalayas. We report here for the first time the luminescence characteristics of quartz and feldspar minerals from the study area. However, feldspar also shows poor luminescence sensitivity, although enough to perform optical dating. Athermal fading was observed in all the feldspar samples, which was corrected using 'g' values; a large scatter was found in the g values, probably due to intermixing of feldspar grains from varying source rock types and also due to poor luminescence sensitivity. An average g value correction to the mean paleodose was found to agree if compared with the thermo-luminescence date of loess deposit dated earlier. The ages show that the terrace formation started taking place at ∼100 ka in the southwestern part of the Jhelum basin and continued with pulses at 50 ka and 11 ka towards the northwestern part.

Efficient and thermally stable red luminescence from nano-sized phosphor of Gd6MoO12:Eu3+

International Nuclear Information System (INIS)

Qin, Lin; Wei, Donglei; Huang, Yanlin; Kim, Sun Il; Yu, Young Moon; Seo, Hyo Jin

2013-01-01

A novel red-emitting nano-phosphor of Eu 3+ -doped Gd 6 MoO 12 was successfully synthesized by the Pechini method. The crystalline phase was confirmed by X-ray powder diffraction analysis. The morphology of the nano-phosphor was analyzed by scanning electron microscopy, indicating a good crystallization with particles smaller than 500 nm. The luminescence properties such as photoluminescence spectra and decay curves were investigated. The phosphors can be efficiently excited by near-ultraviolet (near-UV) light and exhibit a bright red luminescence around 613 nm ascribed to the forced electric dipole transition 5 D 0 → 7 F 2 of Eu 3+ ions. The thermal stabilities were investigated from the temperature-dependent luminescence decay curves (lifetimes) and spectra intensities. The luminescence properties in relation to applications in white light-emitting diodes (W-LEDs) such as the absolute luminescence quantum efficiency, excitation wavelength, and color coordinates were discussed. The Gd 6 MoO 12 :Eu 3+ nano-phosphor is a promising red-emitting candidate for the fabrication of W-LEDs with near-UV chips

Dual-excitation upconverting nanoparticle and quantum dot aptasensor for multiplexed food pathogen detection.

Science.gov (United States)

Kurt, Hasan; Yüce, Meral; Hussain, Babar; Budak, Hikmet

2016-07-15

In this report, a dual-excitation sensing method was developed using aptamer-functionalized quantum dots and upconverting nanoparticles, exhibiting Stokes and anti-Stokes type excitation profiles, respectively. Conjugation of the aptamer-functionalized luminescent nanoparticles with the magnetic beads, comprising short DNA sequences that were partially complementary to the aptamer sequences, enabled facile separation of the analyte-free conjugates for fluorescent measurement. UV-Visible spectroscopy, Circular Dichroism spectroscopy, Dynamic Light Scattering and Polyacrylamide Gel Electrophoresis techniques were used to characterize the aptamer probes developed. The target-specific luminescent conjugates were applied for multiplex detection of model food pathogens, Salmonella typhimurium, and Staphylococcus aureus, in which the fluorescent emission spectra were obtained under UV excitation at 325nm for quantum dots and NIR excitation at 980nm for upconverting nanoparticles, respectively. The dual-excitation strategy was aimed to minimize cross-talk between the luminescent signals for multiplexed detection, and yielded limit of detection values of 16 and 28cfumL(-1) for Staphylococcus aureus, and Salmonella typhimurium, respectively. By employing a greater number of quantum dots and upconverting nanoparticles with non-overlapping fluorescent emissions, the proposed methodology might be exploited further to detect several analytes, simultaneously. Copyright © 2016 Elsevier B.V. All rights reserved.

Study of the absorption and energy transfer processes in inorganic luminescent materials in the UV and VUV region

International Nuclear Information System (INIS)

Mayolet, A.

1995-01-01

In order to find a green emitting phosphor showing high quantum efficiency and a short decay time which can be used in the color Plasma Display Panels developed by Thomson-TTE-TIV company, a VUV spectrophotometer built at IPN Orsay, using the synchrotron radiation from the SUPER-ACO storage ring as an excitation source, allow us the simultaneous recording of the luminescence excitation and diffuse reflectivity spectra of the inorganic compounds in the UV-VUV range. In addition, this experimental set-up enable us to determine the luminescence quantum efficiency of phosphors in the whole energy range of investigation. The chemical synthesis of rare-earth ortho-- and metaborate and rare-earth ortho- and metaphosphate doped with trivalent lanthanide ions cerium, praseodymium, europium and terbium have been made. The energy variation of the thresholds of the luminescence excitation mechanisms in function of the nature and the structure of the host matrix is discussed. We have determined the influence of the nephelauxetic effect and the crystal field intensity on the energy of the f-d inter-configuration transitions. The variation of the luminescence quantum efficiency of the dopant ion is interpreted through the 'impurity bound exciton' model. The systematic comparison of the cerium and terbium trivalent ions spectroscopic properties in the Y(AG)G host lattice series stands to reason that the self-ionized state of the luminescent center plays an important role in the rate of the non radiative relaxation. It is the redox power of the host matrix which imposes to the luminescent center, the energy of this state. (author)

Optically stimulated luminescence dosimetry with gypsum wallboard (drywall)

International Nuclear Information System (INIS)

Thompson, J. W.; Burdette, K. E.; Inrig, E. L.; Dewitt, R.; Mistry, R.; Rink, W. J.; Boreham, D. R.

2010-01-01

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. (authors)

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.

Electrons in feldspar II: A consideration of the influence of conduction band-tail states on luminescence processes

DEFF Research Database (Denmark)

Poolton, H.R.J.; Ozanyan, K.B.; Wallinga, J.

2002-01-01

consider what influence the band tails have on the luminescence properties of feldspar, where electrons travel through the sample prior to recombination. The work highlights the dominant role that 0.04-0.05-eV phonons play in both the luminescence excitation and emission processes of these materials...

In situ variations of the scintillation characteristics in GaN and CdS layers under irradiation by 1.6 MeV protons

Energy Technology Data Exchange (ETDEWEB)

Gaubas, E., E-mail: eugenijus.gaubas@ff.vu.lt; Ceponis, T.; Pavlov, J.; Tekorius, A.

2015-12-15

Evolution of the non-radiative and radiative recombination in GaN and CdS 2.5–20 μm thick layers has been examined by the in situ measurements of the 1.6 MeV proton induced luminescence and laser excited photoconductivity characteristics. The introduction rate of radiation defects has been evaluated by the comparative analysis of the laser and proton beam induced luminescence for the examined GaN and CdS layers.

Hard X-ray-induced optical luminescence via biomolecule-directed metal clusters†

Science.gov (United States)

Pratx, Guillem; Sun, Conroy; Sakamoto, Masanori; Ahmad, Moiz; Volotskova, Olga; Ong, Qunxiang; Teranishi, Toshiharu; Harada, Yoshie

2014-01-01

Here, we demonstrate that biomolecule-directed metal clusters are applicable in the study of hard X-ray excited optical luminescence, promising a new direction in the development of novel X-ray-activated imaging probes. PMID:24463467

Towards Luminescence Dating Of Mosaic Glass

Science.gov (United States)

Galli, A.; Martini, M.; Sibila, E.; Villa, I.

The possibility of dating archaeological glass by means of luminescent techniques has been investigated in recent years, despite the difficulties of this application, mainly linked to the amorphous structure of the material. We focused in particular on mosaic glass, after the encouraging results obtained on byzantine and medieval samples. Further studies were devoted to the comprehension of the luminescent mechanisms in silica glasses, and to the investigation of the relationships between luminescence, colouring or opacifier ions and crystalline phase of the vitreous matrix. The results of a study on the dosimetric characteristics of thermoluminescence (TL) and Optically Stimulated Luminescence (OSL) of a few medieval blue-green mosaic glasses from the San Lorenzo church (Milan) are presented, and the experimental protocols established to identify their suitability for dating are discussed.

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.

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)

Spectral tuning via multi-phonon-assisted stokes and anti-stokes excitations in LaF{sub 3}: Tm{sup 3+} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Gao, Dangli, E-mail: gaodangli@163.com [School of Materials & Mineral Resources, Xi' an University of Architecture and Technology, Xi' an, Shaanxi 710055 (China); College of Science, Xi' an University of Architecture and Technology, Xi' an, Shaanxi 710055 (China); Shaanxi Key Laboratory of Nano Materials and Technology, Xi' an, Shaanxi 710055 (China); Tian, Dongping, E-mail: dptian@xauat.edu.cn [School of Materials & Mineral Resources, Xi' an University of Architecture and Technology, Xi' an, Shaanxi 710055 (China); College of Science, Xi' an University of Architecture and Technology, Xi' an, Shaanxi 710055 (China); Chong, Bo; Li, Long [College of Science, Xi' an University of Architecture and Technology, Xi' an, Shaanxi 710055 (China); Zhang, Xiangyu [College of Science, Chang' an University, Xi' an, Shaanxi 710064 (China)

2016-09-05

We present a facile and highly effective method to tailor upconversion (UC) emission from LaF{sub 3}: Tm{sup 3+} nanoparticles (NPs) by adjusting ambient temperature from 20 K to 400 K accompanied with the pulse laser excitation. Spectral tuning mechanism controlled by ambient temperature at pulse laser excitation is revealed, and a mechanism based on the modification on multi-phonon relaxation rates for the rapid population of intermediate level {sup 3}H{sub 4} and multi-phonon-assisted excited state absorption is proposed. Based on multi-phonon relaxation theory and time-resolved photoluminescence studies, it is reasonable that UC luminescence under short-pulse laser excitation mainly originates from the ions at/near the surface of NPs. These exciting findings in ambient temperature accompanied with the short-pulse excitation dependent UC selectivity offer a general approach to tailoring lanthanide related UC emissions, which will benefit multicolor displays and imaging. - Graphical abstract: An effective method to tailor upconversion from LaF{sub 3}: Tm{sup 3+} nanoparticles by adjusting ambient temperature accompanied with the short-pulse laser excitation is presented and the spectral tuning mechanism based the modification on multi-phonon relaxation rate and multi-phonon-assisted excited state absorption is also revealed. - Highlights: • The luminescence switching is controlled by temperature and pulse duration. • The mechanism based on the multi-phonon-assisted excitations is proposed. • Blue luminescence under short-pulse excitation originates from the surface ions. • Temperature has a big effect on luminescence color output.

Soft X-ray excited colour-centre luminescence and XANES studies of calcium oxide

International Nuclear Information System (INIS)

Ko, J.Y.P.; Heigl, F.; Yiu, Y.M.; Zhou, X.-T.; Regier, T.; Blyth, R.I.R.; Sham, T.-K.

2007-01-01

In this study, we show that colour centres can be produced by irradiating calcium oxide with soft X-rays from a synchrotron radiation source. Using the X-ray excited optical Iuminescence (XEOL) technique, two colour centres, F-centre, and F + -centre can be identified. These colour centres emit photons at characteristic wavelengths. In addition, by performing time-resolved XEOL (TRXEOL), we are able to reveal timing and decay characteristics of the colour centres. We also present X-ray absorption near-edge structure (XANES) spectra collected across oxygen K-edge, calcium L 3,2 -edge, and calcium K-edge. Experimental results are compared with density functional theory (DFT) calculations. (author)

Two- and three-photon excitation of Gd3+ in CaAl12O19

International Nuclear Information System (INIS)

Heerdt, M.L.H. ter; Basun, S.A.; Imbusch, G.F.; Yen, W.M.

2002-01-01

We have employed two-photon excitation to study the higher energy levels of Gd 3+ ions in CaAl 12 O 19 and we compare the results with those obtained using conventional UV excitation techniques. Under two-photon excitation, the luminescence intensity exhibits an unusual temporal behavior, a very long build-up followed by a decrease by orders of magnitude, ascribed to a recombination-assisted luminescence excitation mechanism assuming photo-ionization of Gd 3+ ions and trapping of free electrons on deep traps. We also find that the two-photon excitation spectra contain an additional broadening contribution which can be attributed to homogeneous broadening of excitation levels caused by excited state absorption into the conduction band. We believe that this may be a general phenomenon whenever participating photons produce ionization of impurity ions from metastable excited states. The phenomenon can manifest itself also in two-photon ionization spectral hole burning and in up-conversion processes (in the latter case, the homogeneous broadening can be caused by an intra-ion excited-state absorption)

Luminescence properties of Y3Al5O12:Ce nanoceramics

International Nuclear Information System (INIS)

Zorenko, Yu.; Voznyak, T.; Gorbenko, V.; Zych, E.; Nizankovski, S.; Dan'ko, A.; Puzikov, V.

2011-01-01

Comparative analysis of the luminescent properties of Y 3 Al 5 O 12 :Ce (YAG:Ce) transparent optical ceramics (OS) with those of single crystal (SC) and single crystalline film (SCF) analogues has been performed under excitation by pulsed synchrotron radiation in the fundamental absorption range of YAG host. It has been shown that the properties of YAG:Ce OC are closer to the properties of the SCF counterpart, where Y Al antisite defects are completely absent, rather than to the properties of SC of this garnet with large concentration of Y Al antisite defects. At the same time, the luminescence spectra of YAG:Ce OC show weak emission bands in the 200-470 nm range related to Y Al antisite defects and charged oxygen vacancies (F + and F centers). YAG:Ce OS also possesses significantly larger contribution of slow components in the Ce 3+ luminescence decay under high-energy excitation in comparison with SC and SCF of this garnet due to the involvement of antisite defects, charged oxygen vacancies as well as boundaries of grains in the energy transfer processes from the host to the Ce 3+ ions.

Improved scintillation luminescence and thermal stability of In{sub 2}Si{sub 2}O{sub 7} ceramic phosphor

Energy Technology Data Exchange (ETDEWEB)

Xu, Jian; Cao, Lei; Feng, Yongyi [State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Huang, Yanlin, E-mail: hang@suda.edu.cn [State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Wang, Yaorong [State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Qin, Lin [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of)

2017-03-15

In{sub 2}Si{sub 2}O{sub 7} is a known indium-based scintillator with fast ultraviolet photoluminescence. Unfortunately the emission only can be detected below 200 K. the poor thermal stability limits its application at room temperature. In this work, the luminescence improvement of In{sub 2}Si{sub 2}O{sub 7} was realized by F{sup −}-ions doping in the lattices. The ceramic phosphors were via typical solid-state reaction method. The pure crystalline phase with thortveirite-type structure was confirmed by X-ray diffraction (XRD) Rietveld refinements. The photoluminescence (PL) emission and excitation spectra together with the luminescence thermal stability were tested. The fluorescence decay curves CIE emission Stokes shifts were measured. The ceramic samples could present blue luminescence with maximum wavelength at about 340 nm under the excitation of UV light or high energy X-ray irradiation. The pure sample only presents luminescence below 200 K, however, the F-doping can be greatly enhance the luminescence thermal stability. The F-doped In{sub 2}Si{sub 2}O{sub 7} could present emission signals with fast decay lifetime of 850 ns at room temperature. The luminescence transitions from the In{sup 3+}-O{sup 2−} charge transfer (CT) were discussed on the structure properties.

Concentration characteristics and cell arrangement in luminescent concentrator PV modules; Keiko shukogata taiyo denchi module no cell haichi to shuko tokusei

Energy Technology Data Exchange (ETDEWEB)

Inamura, A [Science University of Tokyo, Tokyo (Japan); Sakuta, K [Electrotechnical Laboratory, Tsukuba (Japan)

1997-11-25

A luminescent concentrator PV module requires no tracking equipment and can use scattered light. A mini PV module was prepared from a luminescent plate of 100times100times3mm, and a single-crystalline PV cell of 100times20mm. Characteristics of various prototype modules with different PV cell areas and cell arrangements were also measured. Four kinds of edge reflecting materials with different reflectances by various white coating were applied to Al sashes for module frames, and each sash was fixed on one edge of the luminescent plate. In experiment, 3 other edges were covered with black tapes to reduce each reflectance to 0%. Although PV module output was affected by reflectance of edges, the output was satisfactory at 90% or more in reflectance showing no difference in output. A concentrating efficiency decreased with an increase in luminescent plate (concentrator) area, while it was improved by cell arrangement with short optical pass length, and cell arrangement hardly affected by edge reflection. 4 refs., 7 figs.

Luminescence in Eu2+ and Ce3+ doped SrCaP2O7 phosphors

Directory of Open Access Journals (Sweden)

K.N. Shinde

Full Text Available Eu2+ and Ce3+ doped SrCaP2O7 has been achieved by modified solid state diffusion in reducing atmosphere. The prepared phosphor powders have been identified by their characteristic X-ray diffraction patterns. The mixed phases of α-Sr2P2O7 type with orthorhombic and α-Ca2P2O7 type with monoclinic form were investigated. Its excitation wavelength ranging from 250 to 430 nm fits well with the characteristic emission of UV light-emitting diode (LED. The excitation and emission spectra indicate that these phosphors can be effectively excited by the near-UV light, and emits blue (visible range due to 4f7 → 4f65d1 transition of Eu2+ particularly, SrCaP2O7: Eu2+ whereas, photoluminescence excitation spectrum measurements of Ce3+ activated SrCaP2O7 shows that the phosphor can be efficiently excited by UV–Vis light from 280 to 310 nm to realize emission in the near visible range due to the 5d–4f transition of Ce3+ ions which is applicable for scintillation purpose. The impacts of doping of divalent europium and trivalent cerium on photoluminescence properties on SrCaP2O7 pyrophosphate phosphors were investigated and I propose a feasible interpretation. Keywords: Phosphor, Luminescence, XRD, LED, FTIR

Infrared to visible upconversion luminescence in Er3+/Yb3+ co-doped CeO2 inverse opal

International Nuclear Information System (INIS)

Yang, Zhengwen; Wu, Hangjun; Liao, Jiayan; Li, Wucai; Song, Zhiguo; Yang, Yong; Zhou, Dacheng; Wang, Rongfei; Qiu, Jianbei

2013-01-01

Highlights: • UC emission of Er 3+ was modified by introducing the structure of inverse opal. • Color tuning of CeO 2 :Yb, Er inverse opal was realized by inhibition of UC emission. • Two-photon excitation processes were observed in CeO 2 :Yb, Er inverse opal. -- Abstract: Infrared to visible upconversion luminescence has been investigated in Er 3+ /Yb 3+ co-doped CeO 2 inverse opal. Under the excitation of 980 nm diode lasers, visible emissions centered at 525, 547, 561, 660 and 680 nm are observed, which are assigned to the Er 3+ transitions of 2 H 11/2 → 4 I 15/2 (525 nm), 4 S 3/2 → 4 I 15/2 (547, 561 nm), 4 F 9/2 → 4 I 15/2 (660 and 680 nm), respectively. The effect of photonic band gap on the upconversion luminescence intensity was also obtained. Additionally, the upconversion luminescence mechanism was studied. The dependence of Er 3+ upconversion emission intensity on pump power reveals that it is a two-photon excitation process

Sol-gel synthesis and luminescent properties of red-emitting Y(P,V)O4:Eu(3+) phosphors.

Science.gov (United States)

Zhang, Xinguo; Zhou, Fangxiang; He, Pei; Zhang, Min; Gong, Menglian

2016-02-01

Eu(3+)-activated Y(P,V)O4 phosphors were prepared by the EDTA sol-gel method, and the corresponding morphologies and luminescent properties were investigated. The sample particles were relatively spheroid with size of 2-3 µm and had a smooth surface. The excitation spectra for Y(P,V)O4:Eu(3+) consisted of three strong excitation bands in the 200-350 nm range, which were attributed to a Eu(3+)- O(2-) charge-transfer band and (1)A1-(1) T1/(1) T2 transitions in VO4(3-). The as-synthesized phosphors exhibited a highly efficient red luminescence at 613 nm due to the Eu(3+5) D0-(7) F2 electric dipole transition. With the increase in the V(5+)/P(5+) ratio, the luminescence intensity of the red phosphor under UV excitation was greatly improved due to enhanced VO4(3-) → Eu(3+) energy transfer. Copyright © 2015 John Wiley & Sons, Ltd.

Optically stimulated luminescence from quartz measured using the linear modulation technique

DEFF Research Database (Denmark)

Bulur, E.; Bøtter-Jensen, L.; Murray, A.S.

2000-01-01

The optically stimulated luminescence (OSL) from heated natural quartz has been investigated using the linear modulation technique (LMT), in which the excitation light intensity is increased linearly during stimulation. In contrast to conventional stimulation, which usually produces a monotonical...

Recent Advance of Biological Molecular Imaging Based on Lanthanide-Doped Upconversion-Luminescent Nanomaterials

Directory of Open Access Journals (Sweden)

Yuanzeng Min

2014-02-01

Full Text Available Lanthanide-doped upconversion-luminescent nanoparticles (UCNPs, which can be excited by near-infrared (NIR laser irradiation to emit multiplex light, have been proven to be very useful for in vitro and in vivo molecular imaging studies. In comparison with the conventionally used down-conversion fluorescence imaging strategies, the NIR light excited luminescence of UCNPs displays high photostability, low cytotoxicity, little background auto-fluorescence, which allows for deep tissue penetration, making them attractive as contrast agents for biomedical imaging applications. In this review, we will mainly focus on the latest development of a new type of lanthanide-doped UCNP material and its main applications for in vitro and in vivo molecular imaging and we will also discuss the challenges and future perspectives.

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.

Structure and luminescence properties of Dy2O3 doped bismuth-borate glasses

International Nuclear Information System (INIS)

Mugoni, Consuelo; Gatto, C.; Pla-Dalmau, A.; Siligardi, C.

2017-01-01

In this study heavy bismuth-borate glasses were studied as host matrices of Dy 2 O 3 rare earth, for potential application as scintillator materials in high energy physics experiments and in general radiation detection systems. Glass matrices were prepared from 20BaO-xBi 2 O 3 -(80-x)B 2 O 3 (x = 20, 30, 40 mol%) ternary systems and synthesized by the melt-quenching method at different temperatures in order to obtain high density and high transparency in the UV/Vis range. Particularly, the glass manifesting the higher transparency and with sufficiently high density was doped with Dy 2 O 3 (2.5 and 5 mol%) in order to induce the luminescence characteristics. The effects of Bi 2 O 3 and Dy 2 O 3 on density, thermal behaviour, transmission as well as luminescence properties under UV excitation, were investigated. The experimental results show that the synthesized glasses can be considered promising candidate materials as dense scintillators, due to the Dy 3+ centres emission.

Measuring modulated luminescence using non-modulated stimulation: Ramping the sample period

DEFF Research Database (Denmark)

Poolton, N.R.J.; Bøtter-Jensen, L.; Andersen, C.E.

2003-01-01

. Directly analogous results to LM-OSL can, however, be achieved with non-modulated excitation sources, by ramping the sample period (RSP) of luminescence detection. RSP-OSL has the distinct advantage over LM-OSL in that, since the excitation remains at full power, data accumulation times (that can...... be considerable) can be reduced by typically 50%. RSP methods are universally applicable and can be employed, for example, where the excitation source is constant heat, rather than light: here, iso-thermal decay of phosphorescence becomes recorded as a sequence of peaks, corresponding to de-trapping of charge...

Luminescence of Tb.sup.3+./sup.-doped high silica glass under UV and X-ray excitation

Czech Academy of Sciences Publication Activity Database

Chewpraditkul, W.; Shen, Y.; Chen, D.; Beitlerová, Alena; Nikl, Martin

2013-01-01

Roč. 35, č. 3 (2013), s. 426-430 ISSN 0925-3467 R&D Projects: GA MŠk LH12185 Institutional support: RVO:68378271 Keywords : Tb 3+ * luminescence * luminescence decays * porous silica glass * scintillation Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.075, year: 2013 http://dx.doi.org/10.1016/j.optmat.2012.09.012

Microwave assisted synthesis of luminescent carbonaceous nanoparticles from silk fibroin for bioimaging.

Science.gov (United States)

Gao, Hongzhi; Teng, Choon Peng; Huang, Donghong; Xu, Wanqing; Zheng, Chaohui; Chen, Yisong; Liu, Minghuan; Yang, Da-Peng; Lin, Ming; Li, Zibiao; Ye, Enyi

2017-11-01

Bombyx mori silk as a natural protein based biopolymer with high nitrogen content, is abundant and sustainable because of its mass product all over the world per year. In this study, we developed a facile and fast microwave-assisted synthesis of luminescent carbonaceous nanoparticles using Bombyx mori silk fibroin and silk solution as the precursors. As a result, the obtained carbonaceous nanoparticles exhibit a photoluminescence quantum yield of ~20%, high stability, low cytotoxicity, high biocompatibility. Most importantly, we successfully demonstrated bioimaging using these luminescent carbonaceous nanoparticles with excitation dependent luminescence. In addition, the microwave-assisted hydrothermal method can be extended to convert other biomass into functional nanomaterials. Copyright © 2017 Elsevier B.V. All rights reserved.

Features of the mechanoluminescence of thin metal films, excited by short and long laser pulses

International Nuclear Information System (INIS)

Banishev, A.F.; Panchenko, V.Ya.; Shishkov, A.V.

2004-01-01

The results of the study on the deformation-induced luminescence of the fine grain metal films, originating by the impact of the short (submicrosecond) and long (millisecond) laser pulses, are presented. The supposition os made relative to the luminescence excitation mechanism [ru

IR and visible luminescence studies in the infrared multiphoton dissociation of 1,2-dibromo-1,1-difluoroethane

Science.gov (United States)

Pushpa, K. K.; Kumar, Awadhesh; Vatsa, R. K.; Naik, P. D.; Annaji Rao, K.; Mittal, J. P.; Parthasarathy, V.; Sarkar, S. K.

1995-07-01

The infrared multiphoton dissociation of 1,2-dibromo-1,1-difluoroethane gives rise to IR and visible luminescence. Vibrationally excited parent molecules dissociate via two primary channels yielding bromine and vibrationally excited HBr. The strong visible emission observed between 350 to 750 nm has been assigned to electronically excited carbene CF 2Br CH.

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

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)

The effects of Tb 3+ doping concentration on luminescence ...

Indian Academy of Sciences (India)

BaF2 phosphor; crystal structure; luminescence properties; X-ray diffraction; concentration quenching. 1. Introduction ... reported that the particle size, shape, crystallinity, etc., sig- nificantly ... Figure 3 shows the excitation and emission spectra of sam- ple with 4 ... gies obtained earlier.9,10 The ground term of the Tb3+ ion is.

Luminescence enhancement of uranyl ion by benzoic acid in acetonitrile

International Nuclear Information System (INIS)

Satendra Kumar; Maji, S.; Joseph, M.; Sankaran, K.

2014-01-01

Uranyl ion is known for its characteristic green luminescence and therefore luminescence spectroscopy is a suitable technique for characterizing different uranyl species. In aqueous medium, luminescence of uranyl ion is generally weak due to its quenching by water molecules and therefore in order to enhance the luminescence of uranyl ion in aqueous medium, luminescence enhancing reagents such as H 3 PO 4 , H 2 SO 4 , HCIO 4 have been widely used. The other method to enhance the uranyl luminescence is by ligand sensitized luminescence, a method well established for lanthanides. In this work, luminescence of uranyl ion is found to be enhanced by benzoic acid in acetonitrile medium. In aqueous medium benzoic acid does not enhance the uranyl luminescence although it forms 1:1 and 1:2 complexes with uranyl ion. Luminescence spectra of uranyl benzoate revealed that enhancement is due to sensitization of uranyl luminescence by benzoate ions. UV-Vis spectroscopy has been utilized to characterize the specie formed in the in acetonitrile medium. UV-Vis spectroscopy along with luminescence spectra revealed that the specie to be tribenzoate complex of uranyl (UO 2 (C 6 H 5 COO) 3 ) - having D 3 h symmetry. (author)

X-ray-excited optical luminescence of protein crystals: a new tool for studying radiation damage during diffraction data collection.

Science.gov (United States)

Owen, Robin L; Yorke, Briony A; Pearson, Arwen R

2012-05-01

During X-ray irradiation protein crystals radiate energy in the form of small amounts of visible light. This is known as X-ray-excited optical luminescence (XEOL). The XEOL of several proteins and their constituent amino acids has been characterized using the microspectrophotometers at the Swiss Light Source and Diamond Light Source. XEOL arises primarily from aromatic amino acids, but the effects of local environment and quenching within a crystal mean that the XEOL spectrum of a crystal is not the simple sum of the spectra of its constituent parts. Upon repeated exposure to X-rays XEOL spectra decay non-uniformly, suggesting that XEOL is sensitive to site-specific radiation damage. However, rates of XEOL decay were found not to correlate to decays in diffracting power, making XEOL of limited use as a metric for radiation damage to protein crystals. © 2012 International Union of Crystallography

The spatially resolved characterisation of Egyptian blue, Han blue and Han purple by photo-induced luminescence digital imaging.

Science.gov (United States)

Verri, G

2009-06-01

The photo-induced luminescence properties of Egyptian blue, Han blue and Han purple were investigated by means of near-infrared digital imaging. These pigments emit infrared radiation when excited in the visible range. The emission can be recorded by means of a modified commercial digital camera equipped with suitable glass filters. A variety of visible light sources were investigated to test their ability to excite luminescence in the pigments. Light-emitting diodes, which do not emit stray infrared radiation, proved an excellent source for the excitation of luminescence in all three compounds. In general, the use of visible radiation emitters with low emission in the infrared range allowed the presence of the pigments to be determined and their distribution to be spatially resolved. This qualitative imaging technique can be easily applied in situ for a rapid characterisation of materials. The results were compared to those for Egyptian green and for historical and modern blue pigments. Examples of the application of the technique on polychrome works of art are presented.

Luminescence investigation of Yb3+/Er3+ codoped single LiYF4 microparticle

International Nuclear Information System (INIS)

Gao, Wei; Zheng, Hairong; He, Enjie; Lu, Ying; Gao, Fangqi

2014-01-01

Tetragonal phase LiYF 4 :Yb 3+ /Er 3+ microparticles are synthesized via facile hydrothermal method. Single LiYF 4 microparticle is excited with IR laser at 980 nm in a confocal setup, and strong green and weak red emissions are observed. It is found that single LiYF 4 :Yb 3+ /Er 3+ microparticle with sub-structure presents stronger upconversion luminescence emission and smaller intensity ratio of red to green emission than that from LiYF 4 :Yb 3+ /Er 3+ microparticle with no sub-structure. The possible mechanism, the influence of particle size and the existence of EDTA on the upconversion luminescence emission are investigated. The current study suggests that the luminescence observation with single micropaticle can effectively avoid the influence of environment and neighbor particles, which is important for investigating the luminescence properties of micro- or nano-crystals and for extending their application. - Highlights: • Single LiYF 4 microparticle is excited with IR laser at 980 nm in a confocal setup, and strong green and weak red emissions are observed. • Single LiYF 4 microparticle with different morphology exhibits different fluorescence emission intensity and intensity ratio of red to green emission. • The possible mechanism, the influence of particle size and the existence of EDTA on the upconversion emission are investigated

High pressure luminescence studies of localized excitations in ZnS doped with Pb2+ and Mn2+

International Nuclear Information System (INIS)

House, G.L.; Drickamer, H.G.

1977-01-01

High pressure luminescence measurements have been made on ZnS doped with Pb +2 and Mn +2 . The data include changes in peak energy and shape, integrated intensities, and lifetimes. These localized emissions are treated in terms of a single configuration coordinate model. For Pb +2 the emission peak shifted to lower energy by a moderate amount and narrowed. For excitation in the Pb +2 absorption the intensity was independent of pressure, which is consistent with the fact that the energy barrier for radiationless return to the ground state was high at all pressures. For excitation in the ZnS absorption edge the intensity decreased significantly with pressure above about 80 kbar. Data on shifts of the conduction band with pressure would indicate that one is approaching a transition from a direct to indirect transition at high pressure so that decrease in emission intensity may be associated with decreased absorption efficiency. The Mn+ 2 emission peak shifted strongly to lower energy with increasing pressure. The direction and magnitude of the shift were consistent with the predictions of ligand field theory. The intensity doubled in 100 kbar, while the lifetime decreased by roughly a factor of 2. These results could be described in terms of a model for a phonon assisted transition. In addition, peak location, intensity, and lifetime measurements were made on ZnS:Pb:Mn. There is clear evidence of energy transfer by exchange, but in addition there is a nonradiative process in the doubly doped crystal which affects both intensities and lifetimes

Time-resolved luminescence studies in hydrogen uranyl phosphate intercalated with amines

Energy Technology Data Exchange (ETDEWEB)

Novo, Joao Batista Marques [Departamento de Quimica, Universidade Federal do Parana, CP 19081, 81531-990 Curitiba-PR (Brazil)]. E-mail: jbmnovo@quimica.ufpr.br; Batista, Fabio Roberto [Departamento de Quimica, Universidade Federal do Parana, CP 19081, 81531-990 Curitiba-PR (Brazil); Cunha, Carlos Jorge da [Departamento de Quimica, Universidade Federal do Parana, CP 19081, 81531-990 Curitiba-PR (Brazil); Dias, Lauro Camargo Jr. [Departamento de Quimica, Universidade Federal do Parana, CP 19081, 81531-990 Curitiba-PR (Brazil); Teixeira Pessine, Francisco Benedito [Instituto de Quimica, Universidade Estadual de Campinas, CP 6154, 13084-971 Campinas-SP (Brazil)

2007-05-15

Time-resolved luminescence decays of intercalated compounds of hydrogen uranyl phosphate (HUP) with p-toluidinium (HUPPT), benzylaminium (HUPBZ), {alpha}-methylbenzylaminium (HUPMBZ) and hydroxylaminium (HUPHAM) were studied. The prepared compounds belong to the tetragonal P4/ncc space group and showed 00 l reflections shifted to lower angles relative to HUP, indicating that the intercalation increases the c parameter of the unit cell. The luminescence decays of the compounds with 100% of intercalation ratio (HUPHAM and HUPBZ) were analyzed by Global Analysis, assuming Lianos' stretched exponential as the model function, which can be applied to compounds with restricted geometry and mobile donor and quencher molecules. It was remarkable that the luminescence decays showed that the quenching of the emission of the uranyl ions by the intercalated protonated amines is not restricted by low dimensionality of the host uranyl phosphate, and that a diffusion mechanism occurs. Benzylaminium cation efficiently quenches the excited energy of the uranyl ions at close distance, but the long-range and long-lifetime quenching is hindered. A different situation is found in the case of the small hydroxylaminium cation, where the long distance diffusion of the species is fast, playing an important role in the quenching of the excited uranyl ions at longer times.

Time-resolved luminescence studies in hydrogen uranyl phosphate intercalated with amines

International Nuclear Information System (INIS)

Novo, Joao Batista Marques; Batista, Fabio Roberto; Cunha, Carlos Jorge da; Dias, Lauro Camargo Jr.; Teixeira Pessine, Francisco Benedito

2007-01-01

Time-resolved luminescence decays of intercalated compounds of hydrogen uranyl phosphate (HUP) with p-toluidinium (HUPPT), benzylaminium (HUPBZ), α-methylbenzylaminium (HUPMBZ) and hydroxylaminium (HUPHAM) were studied. The prepared compounds belong to the tetragonal P4/ncc space group and showed 00 l reflections shifted to lower angles relative to HUP, indicating that the intercalation increases the c parameter of the unit cell. The luminescence decays of the compounds with 100% of intercalation ratio (HUPHAM and HUPBZ) were analyzed by Global Analysis, assuming Lianos' stretched exponential as the model function, which can be applied to compounds with restricted geometry and mobile donor and quencher molecules. It was remarkable that the luminescence decays showed that the quenching of the emission of the uranyl ions by the intercalated protonated amines is not restricted by low dimensionality of the host uranyl phosphate, and that a diffusion mechanism occurs. Benzylaminium cation efficiently quenches the excited energy of the uranyl ions at close distance, but the long-range and long-lifetime quenching is hindered. A different situation is found in the case of the small hydroxylaminium cation, where the long distance diffusion of the species is fast, playing an important role in the quenching of the excited uranyl ions at longer times

Novel Luminescent Probe Based on a Terbium(III) Complex for Hemoglobin Determination

Science.gov (United States)

Yegorova, A. V.; Leonenko, I. I.; Aleksandrova, D. I.; Scrypynets, Yu. V.; Antonovich, V. P.; Ukrainets, I. V.

2014-09-01

We have studied the spectral luminescent properties of Tb(III) and Eu(III) complexes with a number of novel derivatives of oxoquinoline-3-carboxylic acid amides (L1-L5 ). We have observed quenching of the luminescence of 1:1 Tb(III)-L1-5 complexes by hemoglobin (Hb), which is explained by resonance energy transfer of electronic excitation from the donor (Tb(III)-L1-5 ) to the acceptor (Hb). Using the novel luminescent probe Tb(III)-L1, we have developed a method for determining Hb in human blood. The calibration Stern-Volmer plot is linear in the Hb concentration range 0.6-36.0 μg/mL, detection limit 0.2 μg/mL (3·10-9 mol/L).

Time-resolved luminescent spectroscopy of YAG:Ce single crystal and single crystalline films

International Nuclear Information System (INIS)

Zorenko, Yu.; Gorbenko, V.; Savchyn, V.; Vozniak, T.; Puzikov, V.; Danko, A.; Nizhankovski, S.

2010-01-01

The peculiarities of the luminescence and energy transfer from YAG host to the emission centers formed by the Y Al antisite defects and Ce 3+ ions have been studied in YAG:Ce single crystals, grown from the melt by modified Bridgman method in Ar and CO 2 + H 2 atmospheres, and YAG:Ce single crystalline film, grown by liquid phase epitaxy method, using the comparative time-resolved luminescent spectroscopy under excitation by synchrotron radiation in the range of fundamental adsorption of this garnet.

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.

Construction of order mesoporous (Eu–La)/ZnO composite material and its luminescent characters

Energy Technology Data Exchange (ETDEWEB)

Bao, Na; Liu, Yu; Li, Zi-Wei [School of Chemistry & Environmental Engineering, Changchun University of Science and Technology, Changchun 130022 (China); Yu, Hui, E-mail: yh2001101@163.com [School of Chemistry & Environmental Engineering, Changchun University of Science and Technology, Changchun 130022 (China); Bai, Hao-tian [School of Chemistry & Environmental Engineering, Changchun University of Science and Technology, Changchun 130022 (China); Xia, Long, E-mail: xialong_aron@163.com [School of Materials Science and Engineering, Harbin Institute of Technology at Weihai, Weihai 264209 (China); Feng, Da-wei [Changchun University of Science and Technology Science Park, Changchun 130022 (China); Guangdong College of Business and Technology, Zhaoqing 526020 (China); Zhang, Hong-bo; Dong, Xiang-ting; Wang, Tian-yang; Han, Ji; Wu, Rong-yi; Zhang, Qi [School of Chemistry & Environmental Engineering, Changchun University of Science and Technology, Changchun 130022 (China)

2016-09-15

For the first time, the order mesoporous zinc oxide was synthesized by a soft template synthesis method. The Eu and La phosphate were introduced into the prepared mesoporous zinc oxide by the high temperature solid phase method, and got the mesoporous rare earth/zinc oxide composite materials. The luminescence characters of the materials were studied. The influences of La to Eu luminescent properties had been studied, and the optimum proportion of Eu and La was discussed. The influences of La and Eu to ZnO luminescence properties were also been studied. La phosphate had the large influence to Eu luminescent. ZnO had a strong emission peak at 469 nm, which overlapped with the {sup 7}F{sub 0}–{sup 5}D{sub 2} transition excitation peak of Eu at 465 nm. It indicated that the effective energy transfer happened between ZnO and Eu, which strongly enhanced the luminescence intensity of Eu. At the same time, the Eu and La phosphates could regulate the defect density of ZnO, which could regulate the luminescent intensity of ZnO, and realized the adjustment of luminescent color between green and red light.

ZnO Luminescence and scintillation studied via photoexcitation, X-ray excitation, and gamma-induced positron spectroscopy

Science.gov (United States)

Ji, J.; Colosimo, A. M.; Anwand, W.; Boatner, L. A.; Wagner, A.; Stepanov, P. S.; Trinh, T. T.; Liedke, M. O.; Krause-Rehberg, R.; Cowan, T. E.; Selim, F. A.

2016-08-01

The luminescence and scintillation properties of ZnO single crystals were studied by photoluminescence and X-ray-induced luminescence (XRIL) techniques. XRIL allowed a direct comparison to be made between the near-band emission (NBE) and trap emissions providing insight into the carrier recombination efficiency in the ZnO crystals. It also provided bulk luminescence measurements that were not affected by surface states. The origin of a green emission, the dominant trap emission in ZnO, was then investigated by gamma-induced positron spectroscopy (GIPS) - a unique defect spectroscopy method that enables positron lifetime measurements to be made for a sample without contributions from positron annihilation in the source materials. The measurements showed a single positron decay curve with a 175 ps lifetime component that was attributed to Zn vacancies passivated by hydrogen. Both oxygen vacancies and hydrogen-decorated Zn vacancies were suggested to contribute to the green emission. By combining scintillation measurements with XRIL, the fast scintillation in ZnO crystals was found to be strongly correlated with the ratio between the defect luminescence and NBE. This study reports the first application of GIPS to semiconductors, and it reveals the great benefits of the XRIL technique for the study of emission and scintillation properties of materials.

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.

Supramolecular assembly of borate with quaternary ammonium: Crystal structure and tunable luminescent properties

Energy Technology Data Exchange (ETDEWEB)

Liang, Jie; Wang, Yong-gang [Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Wang, Ying-xia, E-mail: wangyx@pku.edu.cn [Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Liao, Fu-hui [Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Lin, Jian-hua, E-mail: jhlin@pku.edu.cn [Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)

2013-04-15

A new borate [C{sub 6}H{sub 16}N][B{sub 5}O{sub 6}(OH){sub 4}] (1) is synthesized hydrothermally by the reaction of isopropyltrimethylammonium hydroxide with boric acid. It crystallizes in the triclinic space group P-1 with the parameters a=9.1578(10) Å, b=9.372(9) Å, c=9.9812(10) Å, α=66.508(2)°, β=74.751(2)°, γ=81.893(2)°. The [B{sub 5}O{sub 6}(OH){sub 4}]{sup −} anions are interlinked via hydrogen bonding forming a 3D supramolecular network containing large cavities, where reside the (CH{sub 3}){sub 3}(i-C{sub 3}H{sub 7}) N{sup +} cations. This borate shows tunable luminescent properties with temperature, heating-treatment, exciting-light, and solvents. The fluorescent intensity of 1 enhances 6-fold with decreasing the temperature from 25 K to 78 K. By treatment under different temperatures, the luminescence of 1 shifted from blue to white and the sample treated at 230 °C emits bright white light to naked eyes. The hybrid borate can disperse in different solvents, and shows a red-shifted and intense emission in polar solvents. - Graphical abstract: The new quaternary ammonium borate [C{sub 6}H{sub 17}N][B{sub 5}O{sub 6}(OH){sub 4}] contains a 3D supramolecular network formed by hydrogen bond linked [B{sub 5}O{sub 6}(OH){sub 4}]{sup −} anions and shows tunable luminescent properties with temperature, excitation light, and solvents. Highlights: ► A novel quaternary ammonium borate was synthesized. ► It possesses a supramolecular network fomed by H-bonded [B{sub 5}O{sub 6}(OH){sub 4}]{sup −} anions. ► This borate shows tunable luminescent properties with temperature, heating treatment, excitation light, and solvents.

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

Excitation power dependence of photoluminescence spectra of GaSb type-II quantum dots in GaAs grown by droplet epitaxy

Energy Technology Data Exchange (ETDEWEB)

Kawazu, T., E-mail: KAWAZU.Takuya@nims.go.jp; Noda, T.; Sakuma, Y. [National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan); Sakaki, H. [National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan); Toyota Technological Institute, 2-12-1 Hisakata, Tempaku-ku, Nagoya 468-8511 (Japan)

2016-04-15

We investigated the excitation power P dependence of photoluminescence (PL) spectra of GaSb type-II quantum dots (QDs) in GaAs grown by droplet epitaxy. We prepared two QD samples annealed at slightly different temperatures (380 {sup o}C and 400 {sup o}C) and carried out PL measurements. The 20 {sup o}C increase of the annealing temperature leads to (1) about 140 and 60 times stronger wetting layer (WL) luminescence at low and high P, (2) about 45% large energy shift of QD luminescence with P, and (3) the different P dependence of the PL intensity ratio between the QD and the WL. These differences of the PL characteristics are explained by the effects of the WL.

Water dispersible LiNdP{sub 4}O{sub 12} nanocrystals: New multifunctional NIR–NIR luminescent materials for bio-applications

Energy Technology Data Exchange (ETDEWEB)

Marciniak, L., E-mail: l.marciniak@int.pan.wroc.pl [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, Okólna 2, 50-422 Wroclaw (Poland); Prorok, K.; Bednarkiewicz, A. [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, Okólna 2, 50-422 Wroclaw (Poland); Department of Nanotechnology, Wroclaw Research Centre EIT+, Stabłowicka 147, 54-066 Wrocław (Poland); Kowalczyk, A. [Department of Nanotechnology, Wroclaw Research Centre EIT+, Stabłowicka 147, 54-066 Wrocław (Poland); Hreniak, D.; Strek, W. [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, Okólna 2, 50-422 Wroclaw (Poland)

2016-08-15

The synthesis and luminescent properties of water colloidal solution of LiNdP{sub 4}O{sub 12} nanocrystals were presented together with demonstrations of their suitability for bio-imaging, remote nano-thermometry and hyperthermal therapy bio-applications. Due to efficient and photostable luminescence at 860 nm under ~808 nm excitation, NPs luminescence was measured in chicken breast at down to 30 mm depths. Moreover temperature dependent spectroscopic features were used in order to remotely measure the temperature of the local environment. Simultaneously, the most heavily Nd{sup 3+} doped NCs demonstrated intentional heating – under 1.5 W of excitation power at 800 nm, local 60 K photo-induced temperature rise was observed. The experimental confirmation of bioimaging of LiNdP{sub 4}O{sub 12} nanoparticles in HEK was presented.

Hydrothermal synthesis and upconversion luminescent properties of YVO4:Yb3+,Er3+ nanoparticles

International Nuclear Information System (INIS)

Liang, Yanjie; Chui, Pengfei; Sun, Xiaoning; Zhao, Yan; Cheng, Fuming; Sun, Kangning

2013-01-01

Graphical abstract: YVO 4 :Yb 3+ ,Er 3+ nanoparticles have been successfully prepared via a facile hydrothermal technique in the presence of citric acid as a complexing agent followed by a subsequent heat treatment process. The PL intensity of the sample increases with the increase of annealing temperature and excitation power. Under the excitation of a 980 nm diode laser, the samples show bright green luminescence. Highlights: ► YVO 4 :Yb 3+ ,Er 3+ nanoparticles were prepared by a hydrothermal approach. ► Bright green luminescence is observed under the excitation of a 980 nm laser diode. ► The PL intensity increases with the increase of annealing temperature. ► Energy transfer properties between Yb 3+ ion and Er 3+ ion were analyzed. -- Abstract: In this paper, YVO 4 :Yb 3+ ,Er 3+ nanoparticles have been successfully prepared via a facile hydrothermal technique in the presence of citric acid as a complexing agent followed by a subsequent heat treatment process. The nanostructures, morphologies and upconversion luminescent properties of the as-prepared YVO 4 :Yb 3+ ,Er 3+ upconverting nanoparticles were investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescent (PL) spectra. XRD results indicate that all the diffraction peaks of samples can be well indexed to the tetragonal phase of YVO 4 . TEM images demonstrate that the samples synthesized hydrothermally consist of granular-like nanoparticles ranging in size from about 30 to 50 nm. After being calcined at 500–800 °C for 2 h, the grain sizes of nanoparticles increase slightly. Additionally, the as-prepared nanoparticles show bright green luminescence corresponding to the 2 H 11/2 → 4 I 15/2 and 4 S 3/2 → 4 I 15/2 transitions of Er 3+ ions under the excitation of a 980 nm diode laser, which might find potential applications in fields such as phosphor powders, infrared detection and display devices

Luminescence characteristics of quartz from the Southern Kenyan Rift Valley: Dose estimation using LM-OSL SAR

International Nuclear Information System (INIS)

Choi, J.H.; Duller, G.A.T.; Wintle, A.G.; Cheong, C.-S.

2006-01-01

Linearly modulated (LM) optically stimulated luminescence (OSL) measurements have revealed that some sedimentary quartz samples from the Kenyan Rift Valley do not have a fast OSL component, but contain a medium component and several slow components. It was impossible to recover a known dose for these samples using the conventional single-aliquot regenerative-dose (SAR) procedure. The dose-response curves and continuous wave (CW) OSL decay curves for these samples showed several undesirable properties for dating. We have compared various luminescence characteristics of these samples with other quartz samples from elsewhere in the world for which the SAR procedure has been shown to be appropriate; the latter were dominated by a fast OSL component. The characteristics include photoionisation cross-sections for each component and the relative proportions of the different components in the initial and total OSL signals. It was found that those samples that had greater than 90% of the initial 0.8 s of their OSL signal from the fast component were suitable for dating using the conventional SAR protocol. A novel method of displaying the relative contributions of the different OSL components in a ternary diagram is proposed. The thermal stability of each component was investigated using pulse-annealing experiments. We then examined the possibility of applying an LM-OSL SAR protocol to samples that have a substantial medium component

A luminescence-optical spectroscopy study of Rb2KTiOF5 single crystals

Science.gov (United States)

Pustovarov, V. A.; Ogorodnikov, I. N.; Kozlov, A. V.; Isaenko, L. I.

2018-06-01

Large single crystals of Rb2KTiOF5 (RKTF), grown by slow solidification method, were studied (7-400 K) for various types of optical and radiation effects. The optical absorption spectra, the parameters of the Urbach rule at 293 K (σ = 0.24 and EU = 105 meV), the low-temperature reflection spectra (T = 7 K, E = 3.7-22 eV) were determined. The luminescence spectra (1.2-6.2 eV) and luminescence decay kinetics are studied upon excitation by a nanosecond electron beam (PCL), ultraviolet and vacuum ultraviolet light (PL), or X-rays radiation (XRL). PL excitation spectra under selective photoexcitation by synchrotron radiation (E = 3.7-22 eV, T = 7 K), temperature dependences of the intensity of steady-state XRL in different emission bands, as well as thermoluminescence (7-400 K) are studied. In the visible spectral region, we detected three luminescence bands that were attributed to radiative annihilation of intrinsic excitons (2.25 eV), recombination-type luminescence (2.1 eV) and luminescence of higher TiOF5 complexes (1.9 eV). The exponential component with lifetime of about 19 μs was revealed in the PCL decay kinetics at 2.25 eV. The low-energy onset of the intrinsic host absorption Ec = 3.55 eV was determined on the basis of the experimental data obtained. Spectra of optical constants were calculated by the Kramers-Krönig method, the energy of the onset of the interband transitions Eg = 4.2 eV was determined, and the main peaks of the optical spectra were identified.

Filament-induced luminescence and supercontinuum generation in undoped, Yb-doped, and Nd-doped YAG crystals

Science.gov (United States)

Kudarauskas, D.; Tamošauskas, G.; Vengris, M.; Dubietis, A.

2018-01-01

We present a comparative spectral study of filament-induced luminescence and supercontinuum generation in undoped, Yb-doped, and Nd-doped YAG crystals. We show that supercontinuum spectra generated by femtosecond filamentation in undoped and doped YAG crystals are essentially identical in terms of spectral extent. On the other hand, undoped and doped YAG crystals exhibit remarkably different filament-induced luminescence spectra whose qualitative features are independent of the excitation wavelength and provide information on the energy deposition to embedded dopants, impurities, and the crystal lattice itself. Our findings suggest that filament-induced luminescence may serve as a simple and non-destructive tool for spectroscopic studies in various transparent dielectric media.

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.

Photoluminescence and excited state structure in Bi3+-doped Y2SiO5 single crystalline films

International Nuclear Information System (INIS)

Babin, V.; Gorbenko, V.; Krasnikov, A.; Mihokova, E.; Nikl, M.; Zazubovich, S.; Zorenko, Yu.

2013-01-01

Single crystalline films of Bi-doped Y 2 SiO 5 are studied at 4.2–350 K by the time-resolved luminescence methods under excitation in the 3.8–6.2 eV energy range. Ultraviolet luminescence of Y 2 SiO 5 :Bi (≈3.6 eV) is shown to arise from the radiative decay of the metastable and radiative minima of the triplet relaxed excited state (RES) of Bi 3+ centers which are related to the 3 P 0 and 3 P 1 levels of a free Bi 3+ ion, respectively. The lowest-energy excitation band of this emission, located at ≈4.5 eV, is assigned to the 1 S 0 → 3 P 1 transitions of a free Bi 3+ ion. The phenomenological model is proposed to describe the excited-state dynamics of Bi 3+ centers in Y 2 SiO 5 :Bi, and parameters of the triplet RES are determined. -- Highlights: •Luminescence of Y 2 SiO 5 :Bi is investigated for the first time. •Ultraviolet emission arises from Bi 3+ ions located in Y lattice sites. •The triplet relaxed excited states parameters of Bi 3+ centers are determined

Time-resolved luminescence spectroscopy of trace uranyl in wet sand

International Nuclear Information System (INIS)

Freed, D.

1993-01-01

The objective of the project was to develop a technique to observe and characterize the behaviour of uranium in unsaturated groundwater flow systems, particularly with regard to unstable ''fingered'' flow, which could drastically reduce time of travel. The actual experimental work described was a study of the feasibility of detecting uranyl at the parts-per-billion level in aqueous solution by means of its luminescence spectrum. A high-power UV laser was used to excite aqueous uranyl in a wet sand mixture; the characteristic green phosphorescence emitted in the decay transition was detected by a photomultiplier tube; and the amplified signal was sent to an oscilloscope in communication with Macintosh data acquisition software. At the time of the conference, a more sophisticated sample configuration for imaging the flow of uranyl was already under development. 5 refs., 3 figs

Time-resolved luminescence spectroscopy of trace uranyl in wet sand

Energy Technology Data Exchange (ETDEWEB)

Freed, D [Massachusetts Inst. of Tech., Cambridge, MA (United States)

1994-12-31

The objective of the project was to develop a technique to observe and characterize the behaviour of uranium in unsaturated groundwater flow systems, particularly with regard to unstable ``fingered`` flow, which could drastically reduce time of travel. The actual experimental work described was a study of the feasibility of detecting uranyl at the parts-per-billion level in aqueous solution by means of its luminescence spectrum. A high-power UV laser was used to excite aqueous uranyl in a wet sand mixture; the characteristic green phosphorescence emitted in the decay transition was detected by a photomultiplier tube; and the amplified signal was sent to an oscilloscope in communication with Macintosh data acquisition software. At the time of the conference, a more sophisticated sample configuration for imaging the flow of uranyl was already under development. 5 refs., 3 figs.

Luminescence optically stimulated: theory and applications

International Nuclear Information System (INIS)

Rivera M, T.; Azorin N, J.

2002-01-01

The thermally stimulated luminescence (Tl) has occupied an important place in the Solid state physics (FES) by the flexibility of the phenomena, mainly for its applications in the fields of Radiation Physics (FR) and Medical Physics (MF). The reason of this phenomena lies in the fact of the electrons release by the action of heat. Under that same reason, it can be used the action of another stimulant agent for releasing the trapped electrons in the metastable states (EM), this agent is the light which has the same effect that the heat, giving as result the production of light photons at using light in the visible spectra, of different wavelength that the excitation light. This phenomena is called Luminescence optically stimulated (LOE). The LOE has a great impact in the Solid State Physics (FES), dating and now in the use of the phenomena as a dosimetric method, alternate to the Tl, for its use in the ionizing and non-ionizing radiations fields. (Author)

Charge transfer luminescence of Yb3+ ions in LiY1-xYbxP4O12 phosphates

International Nuclear Information System (INIS)

Stryganyuk, G; Zazubovich, S; Voloshinovskii, A; Pidzyrailo, M; Zimmerer, G; Peters, R; Petermann, K

2007-01-01

Spectral-kinetic studies have been performed for LiY 1-x Yb x P 4 O 12 (x = 0; 0.1; 0.9) phosphates at T = 8-320 K using synchrotron radiation for excitation within the 5-17 eV energy range. Mechanisms for the excitation of Yb 3+ charge transfer and f-f luminescence are discussed. The quasimolecular character of Yb 3+ charge transfer luminescence (CTL) is pointed out. The central Yb 2+ ion and hole delocalized over the surrounding ligands are proposed for consideration as a 'charge transfer cluster' (Yb 2+ CT cluster). Possible mechanisms of Yb 3+ CTL quenching are presumed

Afterglow luminescence in sol-gel/Pechini grown oxide materials: persistence or phosphorescence process? (Conference Presentation)

Science.gov (United States)

Sontakke, Atul; Ferrier, Alban; Viana, Bruno

2017-03-01

Persistent luminescence and phosphorescence, both yields afterglow luminescence, but are completely different mechanisms. Persistent luminescence involves a slow thermal release of trapped electrons stored in defect states, whereas the phosphorescence is caused due to triplet to singlet transition [1,2]. Many persistent luminescence phosphors are based on oxide inorganic hosts, and exhibit long afterglow luminescence after ceasing the excitation. We observed intense and long afterglow luminescence in sol-gel/pechini grown inorganic oxides, and as a first interpretation thought to be due to persistence mechanism. However, some of these materials do not exhibit defect trap centers, and a detailed investigation suggested it is due to phosphorescence, but not the persistence. Phosphorescence is not common in inorganic solids, and that too at room temperature, and therefore usually misinterpreted as persistence luminescence [3]. Here we present a detailed methodology to distinguish phosphorescence from persistence luminescence in inorganic solids, and the process to harvest highly efficient long phosphorescence afterglow at room temperature. 1. Jian Xu, Setsuhisa Tanabe, Atul D. Sontakke, Jumpei Ueda, Appl. Phys. Lett. 107, 081903 (2015) 2. Sebastian Reineke, Marc A. Baldo, Scientific Reports, 4, 3797 (2014) 3. Pengchong Xue, Panpan Wang, Peng Chen, Boqi Yao, Peng Gong, Jiabao Sun, Zhenqi Zhang, Ran Lu, Chem. Sci. (2016) DOI: 10.1039/C5SC03739E

Efficient and thermally stable red luminescence from nano-sized phosphor of Gd{sub 6}MoO{sub 12}:Eu{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Qin, Lin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Wei, Donglei [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Huang, Yanlin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Kim, Sun Il [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Yu, Young Moon [Pukyong National University, LED-Marin Convergence Technology R and BD Center (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of)

2013-09-15

A novel red-emitting nano-phosphor of Eu{sup 3+}-doped Gd{sub 6}MoO{sub 12} was successfully synthesized by the Pechini method. The crystalline phase was confirmed by X-ray powder diffraction analysis. The morphology of the nano-phosphor was analyzed by scanning electron microscopy, indicating a good crystallization with particles smaller than 500 nm. The luminescence properties such as photoluminescence spectra and decay curves were investigated. The phosphors can be efficiently excited by near-ultraviolet (near-UV) light and exhibit a bright red luminescence around 613 nm ascribed to the forced electric dipole transition {sup 5}D{sub 0}{yields}{sup 7}F{sub 2} of Eu{sup 3+} ions. The thermal stabilities were investigated from the temperature-dependent luminescence decay curves (lifetimes) and spectra intensities. The luminescence properties in relation to applications in white light-emitting diodes (W-LEDs) such as the absolute luminescence quantum efficiency, excitation wavelength, and color coordinates were discussed. The Gd{sub 6}MoO{sub 12}:Eu{sup 3+} nano-phosphor is a promising red-emitting candidate for the fabrication of W-LEDs with near-UV chips.

Photoluminescence, reddish orange long persistent luminescence and photostimulated luminescence properties of praseodymium doped CdGeO3 phosphor

International Nuclear Information System (INIS)

Jin, Yahong; Hu, Yihua; Chen, Li; Fu, Yinrong; Mu, Zhongfei; Wang, Tao; Lin, Jun

2014-01-01

Highlights: • A novel phosphor CdGeO 3 :Pr 3+ was synthesized successfully. • The persistent luminescence properties of CdGeO 3 :Pr 3+ were studied. • The photostimulated luminescence properties of CdGeO 3 :Pr 3+ were investigated. • The persistent and photostimulated luminescence mechanisms were discussed in detail. - Abstract: Praseodymium doped CdGeO 3 phosphors were prepared successfully by a conventional high temperature solid-state reaction method. It showed reddish orange long persistent luminescence (LPL) after the short UV-irradiation. The reddish orange photostimulated luminescence (PSL) was also observed upon near infrared stimulation at 980 nm after per-exposure into UV light. The origin of LPL and PSL was identified with the emission from Pr 3+ ions with the aid of traps in host lattice. The optimal concentration of Pr 3+ ions for the brightest photoluminescence (PL) emission and the best LPL characteristic were experimentally to be about 3% and 0.5 mol%, respectively. The trapping and de-trapping processes of charge carriers between shallower and deep traps were illustrated. A model was proposed on the basis of experimental results to study the mechanisms of LPL and PSL

Luminescent features of sol–gel derived rare-earth multi-doped oxyfluoride nano-structured phosphors for white LED application

International Nuclear Information System (INIS)

Gouveia-Neto, A.S.; Silva, A.F. da; Bueno, L.A.; Costa, E.B. da

2012-01-01

Rare-earth doped oxyfluoride 75SiO 2 :25PbF 2 nano-structured phosphors for white-light-emitting diodes were synthesized by thermal treatment of precursor sol–gel derived glasses. Room temperature luminescence features of Eu 3+ , Sm 3+ , Tb 3+ , Eu 3+ /Tb 3+ , and Sm 3+ /Tb 3+ ions incorporated into low-phonon-energy PbF 2 nanocrystals dispersed in the aluminosilicate glass matrix and excited with UV light emitting diode were investigated. The luminescence spectra exhibited strong emission signals in the red (600, 610, 625, and 646 nm), green (548 and 560 nm), and blue (485 nm) wavelength regions. White-light emission was observed in Sm/Tb and Eu/Tb double-doped activated phosphors employing UV-LED excitation at 395 nm. The dependence of the luminescence emission intensities upon annealing temperature and rare-earth concentration was also examined. The results indicated that there exist optimum annealing temperature and activator ion concentration in order to obtain intense visible emission light with high color rendering index. The study suggests that the nanocomposite phosphor based upon 75SiO 2 :25PbF 2 host herein reported is a promising contender for white-light LED applications. - Highlights: ► White-light emission in double-doped activated phosphors employing UV-LED excitation. ► Luminescent features of europium, samarium, and terbium in nanocrystals dispersed in aluminosilicate glass. ► New nanocomposite phosphor host for white-light LED applications.

Luminescence as a new detection method for non-relativistic highly ionizing particles in water/ice neutrino telescopes

Energy Technology Data Exchange (ETDEWEB)

Pollmann, Anna [Bergische Universitaet Wuppertal (Germany); Collaboration: IceCube-Collaboration

2016-07-01

Cosmic ray detectors use air as a radiator for luminescence. In water and ice detectors Cherenkov light is the dominant light producing mechanism when the particle velocity exceeds the Cherenkov threshold, approximately three quarters of the speed of light. Luminescence is produced by highly ionizing particles passing through matter due to the excitation of the surrounding atoms. The observables of luminescence, such as the wavelength spectrum and decay times, are highly dependent on the properties of the medium. Therefore, the results of measurements, in which luminescence was produced by particles passing through water or ice, vary by two orders of magnitude in intensity. It is shown that, even for the most conservative intensity value, luminescence can be used as a detection method for highly ionizing particles with velocities below the Cherenkov threshold. These could be magnetic monopoles or other massive and highly penetrating exotic particles. In the most optimistic case, luminescence contributes even to the light output of standard model particles.

Electron paramagnetic resonance and luminescence of chromium in calcium germanate crystals

CERN Document Server

Gorshkov, O N; Tyurin, S A; Chigineva, A B; Chigirinskij, Y I

2002-01-01

One observed luminescence of Cr sup 4 sup + :Ca sub 2 GeO sub 4 single crystals near 1.3 mu m wave length at excitation by a semiconducting laser up to 573 K. At T < 110 K one detected the EPR spectrum identified as one belonging to Cr sup 4 sup + ions substituting for germanium. One determined the components of g-tensor and its basic axes. In calcium germanate this impurity centre slightly violates crystal symmetry. Detected deviation from the Curie law in EPR temperature dependence is explained by transition into the excited state with activation low energy. The giant efficient multiplicity of degeneration of the excited state is explained by induction of soft phonon modes of crystal at excitation of a defect

Optical excitation processes in the near band-edge region of KAlSi₃O₈ and NaAlSi₃O₈ feldspar

DEFF Research Database (Denmark)

Poolton, N.R.J.; Mauz, B.; Lang, A.

2006-01-01

-stimulated phosphorescence and energy-dependent photo-transferred optically stimulated luminescence. The photo-transferred OSL confirms the bandgap energy of alkali feldspars to be 7.7eV at 10K, and highlights the role played by a dominant optically active defect 4.4 eV below the conduction band, associated with blue......)) yielding a characteristically narrow feature at 4.61 eV: significantly, excitation to this level allows photo-transferred OSL to take place, a process that is not obviously identifiable with the other transitions of the set. The conclusion of the work is that synchrotron-based luminescence methods can...

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

Fingermark detection on non-porous and semi-porous surfaces using YVO4:Er,Yb luminescent upconverting particles.

Science.gov (United States)

Ma, Rongliang; Shimmon, Ronald; McDonagh, Andrew; Maynard, Philip; Lennard, Chris; Roux, Claude

2012-04-10

This article describes the use of an anti-Stokes luminescent material (upconverter), yttrium vanadate doped with ytterbium and erbium (YVO(4):Er,Yb), for the development of latent fingermarks on a range of non-porous surfaces. Anti-Stokes luminescent materials emit light at shorter wavelengths than the excitation wavelength. This property is unusual in both natural and artificial materials commonly found as exhibits in forensic science casework. As a result, fingermark detection techniques based on anti-Stokes luminescence are potentially extremely sensitive and selective. Latent fingermarks on non-luminescent and inherently luminescent substrates, including Australian polymer banknotes (a well-known 'difficult' surface), were developed with YVO(4):Er,Yb by dry powder and wet powder techniques. The effectiveness of YVO(4):Er,Yb for fingermark detection was compared with that of cyanoacrylate fuming and of sodium yttrium tetrafluoride doped with ytterbium and erbium (NaYF(4):Er,Yb). The results illustrate some benefit of luminescent up-converting phosphors over traditional luminescence techniques for the detection of latent fingermarks. Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

Radiation induced luminescence from a dipole immersed in a thin film

International Nuclear Information System (INIS)

Nkoma, J.S.

1990-08-01

Luminescence is modelled as electromagnetic radiation from a dipole immersed in a thin film. Maxwell's equations are solved for the cases when the dipole in the thin film is oriented normal and parallel to the interfaces. Expressions for emitted electric fields outside the thin film are derived and are found to have a resonant denominator that vanishes at the surface polariton excitation frequencies for a thin film. Luminescent spectra are plotted and peaks are found that are identified to be associated with both surface response and bulk response. Numerical results are presented to illustrate the model by considering a vacuum-GaP-sapphire system. (author). 9 refs, 5 figs

Optical spectroscopy and luminescence quenching of LuI3:Ce3+

International Nuclear Information System (INIS)

Birowosuto, M.D.; Dorenbos, P.; Haas, J.T.M. de; Eijk, C.W.E. van; Kraemer, K.W.; Guedel, H.U.

2006-01-01

Optical spectroscopy of LuI 3 doped with Ce 3+ using ultraviolet and visible light excitation is reported. LuI 3 host excitation and emission and 4f-5d excitation and emission of Ce 3+ are observed. An empirical model based on crystal field splitting was used to estimate the energy of the highest 4f-5d excitation band. The crystal field splitting and centroid shift were compared to those of LuCl 3 :Ce 3+ and LuBr 3 :Ce 3+ . Temperature dependence of X-ray excited luminescence spectra shows thermal quenching, whereas that of the decay curve of Ce 3+ emission excited at the lowest 5d band of Ce 3+ does not indicate the presence of quenching of Ce 3+ emission for temperature below 625K. The quenching in LuI 3 :Ce 3+ therefore occurs before the 5d Ce 3+ emission takes place

Assessment of terbium (III) as a luminescent probe for the detection of tuberculosis biomarkers

International Nuclear Information System (INIS)

Bamogo, W.; Mugherli, L.; Banyasz, A.; Novelli-Rousseau, A.; Mallard, F.; Tran-Thi, T.-H.

2015-01-01

A detection method for nicotinic acid, a specific metabolite marker of Mycobacterium tuberculosis present in cultures and patients' breath, is studied in complex solutions containing other metabolites and in biological media such as urine, saliva and breath condensate. The method is based on the analysis of the luminescence increase of Tb 3+ complexes in the presence of nicotinic acid due to the energy transfer from the excited ligand to the lanthanide ion. It is shown that other potential markers found in M. tuberculosis culture supernatant, such as methyl phenylacetate, p-methyl anisate, methyl nicotinate and 2-methoxy biphenyl, can interfere with nicotinic acid via a competitive absorption of the excitation photons. A new strategy to circumvent these interferences is proposed with an upstream trapping of volatile markers preceding the detection of nicotinic acid in the liquid phase via the luminescence of Tb 3+ complexes. The cost of the method is evaluated and compared with the Xpert MTB/RIF test endorsed by the World Health Organization. - Highlights: • Nicotinic acid, a specific marker of M. tuberculosis, can be detected via luminescence. • The detection limit with a commercial phosphorimeter is 0.4 µmol·L -1 . • Other metabolites of M. tuberculosis can interfere via absorbed excitation light. • The interference can be removed via trapping of the most volatile metabolites. • A breath analysis procedure's cost is compared with the Xpert TBM/RIF test.

Assessment of terbium (III) as a luminescent probe for the detection of tuberculosis biomarkers

Energy Technology Data Exchange (ETDEWEB)

Bamogo, W. [CNRS, IRAMIS, UMR 3685 NIMBE/LEDNA, F-91191 Gif-sur-Yvette (France); Mugherli, L. [CEA, IRAMIS, UMR 3685 NIMBE/LEDNA, F-91191 Gif-sur-Yvette (France); Banyasz, A. [CNRS, IRAMIS, LIDyL/Laboratoire Francis Perrin, URA 2453, F-91191 Gif-sur-Yvette (France); Novelli-Rousseau, A.; Mallard, F. [BioMérieux SA, F-38000 Grenoble (France); Tran-Thi, T.-H., E-mail: thu-hoa.tran-thi@cea.fr [CNRS, IRAMIS, UMR 3685 NIMBE/LEDNA, F-91191 Gif-sur-Yvette (France)

2015-10-08

A detection method for nicotinic acid, a specific metabolite marker of Mycobacterium tuberculosis present in cultures and patients' breath, is studied in complex solutions containing other metabolites and in biological media such as urine, saliva and breath condensate. The method is based on the analysis of the luminescence increase of Tb{sup 3+} complexes in the presence of nicotinic acid due to the energy transfer from the excited ligand to the lanthanide ion. It is shown that other potential markers found in M. tuberculosis culture supernatant, such as methyl phenylacetate, p-methyl anisate, methyl nicotinate and 2-methoxy biphenyl, can interfere with nicotinic acid via a competitive absorption of the excitation photons. A new strategy to circumvent these interferences is proposed with an upstream trapping of volatile markers preceding the detection of nicotinic acid in the liquid phase via the luminescence of Tb{sup 3+} complexes. The cost of the method is evaluated and compared with the Xpert MTB/RIF test endorsed by the World Health Organization. - Highlights: • Nicotinic acid, a specific marker of M. tuberculosis, can be detected via luminescence. • The detection limit with a commercial phosphorimeter is 0.4 µmol·L{sup -1}. • Other metabolites of M. tuberculosis can interfere via absorbed excitation light. • The interference can be removed via trapping of the most volatile metabolites. • A breath analysis procedure's cost is compared with the Xpert TBM/RIF test.

Rupture luminescence from natural fibers

Science.gov (United States)

Li, W.; Haneman, D.

1999-12-01

Fibers of cotton and wool, and samples of paper, have been ruptured in tension in vacuum and in air, and give detectable luminescence in the visible range. All have a common emission peak at around 2.0 eV, which is ascribed to the deexcitation of states excited by the rupture of organic chain molecule bonds. Rubber bands give stronger emission in air, but no emission in vacuum, suggesting the material breaks only at weak interchain bonds. Mohair, cat, and horse hair also give emission in air. The phenomena reveal effects that would occur widely in nature.

Plasmon-enhanced luminescence of Sm complex using silver nanoparticles in Polyvinyl Alcohol

Energy Technology Data Exchange (ETDEWEB)

Kaur, Gagandeep; Verma, R.K.; Rai, D.K. [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, India 221005 (India); Rai, S.B., E-mail: sbrai49@yahoo.co.in [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, India 221005 (India)

2012-07-15

Silver (Ag) nanoparticles (NPs) were prepared by laser ablation in water with an aim to enhance the luminescence of rare earth coordinated complex in polymer host. A fixed concentration of the complex containing Samarium (Sm), Salicylic acid (Sal) and 1, 10-phenanthroline (Phen) were combined with different concentrations of silver NPs in PolyVinyl Alcohol at room temperature. Absorption spectrum and XRD patterns of the sample show that the Sm(Sal){sub 3}Phen complex is accompanied by Ag NPs. The luminescence from the complex was recorded in the presence and absence of Ag NPs using two different excitation wavelengths viz. 400 and 355 nm. Of these, 400 nm radiation falls in the surface plasmon resonance of Ag NPs. It was found that the Ag NPs led to a significant enhancement in luminescence of the complex. Surprisingly, a high concentration of Ag NPs tends to quench the luminescence. - Highlights: Black-Right-Pointing-Pointer Sm complex with Ag nanoparticles in PVA was prepared at room temperature. Black-Right-Pointing-Pointer UV-vis absorption and XRD confirms the presence of Sm complex and Ag NPs. Black-Right-Pointing-Pointer Enhancement in luminescence of complex was observed with Ag NPs. Black-Right-Pointing-Pointer Coupling between radiative transitions of Sm and SPR of NPs enhances the emission. Black-Right-Pointing-Pointer The higher concentration of Ag NPs quenches the luminescence of the complex.

Joint excitation synchronization characteristics of fatigue test for offshore wind turbine blade

Science.gov (United States)

Zhang, Lei-an; Yu, Xiang-yong; Wei, Xiu-ting; Liu, Wei-sheng

2018-02-01

In the case of the stiffness of offshore wind turbine blade is relatively large, the joint excitation device solves the problem of low accuracy of bending moment distribution, insufficient driving ability and long fatigue test period in single-point loading. In order to study the synchronous characteristics of joint excitation system, avoid blade vibration disturbance. First, on the base of a Lagrange equation, a mathematical model of combined excitation is formulated, and a numerical analysis of vibration synchronization is performed. Then, the model is constructed via MATLAB/Simulink, and the effect of the phase difference on the vibration synchronization characteristics is obtained visually. Finally, a set of joint excitation platform for the fatigue test of offshore wind turbine blades are built. The parameter measurement scheme is given and the correctness of the joint excitation synchronization in the simulation model is verified. The results show that when the rotational speed difference is 2 r/min, 30 r/min, the phase difference is 0, π/20, π/8 and π/4, as the rotational speed difference and the phase difference increase, the time required for the blade to reach a steady state is longer. When the phase difference is too large, the electromechanical coupling can no longer make the joint excitation device appear self-synchronizing phenomenon, so that the value of the phase difference develops toward a fixed value (not equal to 0), and the blade vibration disorder is serious, at this time, the effect of electromechanical coupling must be eliminated. The research results provide theoretical basis for the subsequent decoupling control algorithm and synchronization control strategy, and have good application value.

Joint excitation synchronization characteristics of fatigue test for offshore wind turbine blade

Directory of Open Access Journals (Sweden)

Lei-an Zhang

2018-02-01

Full Text Available In the case of the stiffness of offshore wind turbine blade is relatively large, the joint excitation device solves the problem of low accuracy of bending moment distribution, insufficient driving ability and long fatigue test period in single-point loading. In order to study the synchronous characteristics of joint excitation system, avoid blade vibration disturbance. First, on the base of a Lagrange equation, a mathematical model of combined excitation is formulated, and a numerical analysis of vibration synchronization is performed. Then, the model is constructed via MATLAB/Simulink, and the effect of the phase difference on the vibration synchronization characteristics is obtained visually. Finally, a set of joint excitation platform for the fatigue test of offshore wind turbine blades are built. The parameter measurement scheme is given and the correctness of the joint excitation synchronization in the simulation model is verified. The results show that when the rotational speed difference is 2 r/min, 30 r/min, the phase difference is 0, π/20, π/8 and π/4, as the rotational speed difference and the phase difference increase, the time required for the blade to reach a steady state is longer. When the phase difference is too large, the electromechanical coupling can no longer make the joint excitation device appear self-synchronizing phenomenon, so that the value of the phase difference develops toward a fixed value (not equal to 0, and the blade vibration disorder is serious, at this time, the effect of electromechanical coupling must be eliminated. The research results provide theoretical basis for the subsequent decoupling control algorithm and synchronization control strategy, and have good application value.

Recombination luminescence from H centers and conversion of H centers into I centers in alkali iodides

International Nuclear Information System (INIS)

Berzina, B.J.

1981-01-01

The study is aimed at the search for H-plus-electron centers of luminescence and the investigation of the conversion of H- into I centers by the luminescence of H-plus-electron centers in alkali iodide crystals. KI, RbI and NaI crystals were studied at 12 K. H and F centers were created by irradiation with ultraviolet light corresponding to the absorption band of anion excitons. Then the excitation of electron centers by red light irradiation was followed. The spectra of stimulated recombination luminescence were studied. The luminescence of H-plus- electron centers had been observed and the conclusion was made that this center was formed on immobile H centers. In case of stable H centers the optically stimulated conversion of H centers into I centers occurs. The assumption is advanced on the spontaneous annihilation of near placed unstable F, H centers which leads to the creation of H-plus-electron luminescence centers and to the spontaneous H-I-centers conversion [ru

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

Two-Photon Luminescence and Second Harmonic Generation from Gold Micro-Plates

Directory of Open Access Journals (Sweden)

Xu Wang

2014-09-01

Full Text Available Micron-sized gold plates were prepared by reducing chloroauric acid with lemongrass extract. Their two-photon luminescence (TPL and second harmonic generation (SHG were investigated. The results show that the TPL and SHG intensity of gold plates is dependent on the wavelength and polarization of excitation laser. The TPL intensity of gold plates decreases with the increase of the excitation wavelength except for a small peak around 820–840 nm, while SHG intensity increases with the excitation wavelength redshift. In addition, it is found that the TPL intensity of the gold plate’s edge is related with the angle between the edge orientation and the polarization direction of the excitation light. The TPL intensity increases with the angle increase from 0° to 90°.

Luminescence of CsPbBr3 films under high-power excitation

OpenAIRE

高橋, 一彰; 斎藤, 忠昭; 近藤, 新一; 浅田, 拡志

2004-01-01

Highly excited photoluminescence of CsPbBr3 has been measured for thin films prepared by crystallization from the amorphous phase into microcrystalline/ polycrystalline states. With the increase of excitation intensity, there occurs jumping of the dominant emission band from a free-exciton band to a new band originating from exciton-exciton inelastic collision. Stimulated emission is observed for the new band at very low threshold excitation intensities of the order of 10kW/cm2.

Thermal quenching of the yellow luminescence in GaN

Science.gov (United States)

Reshchikov, M. A.; Albarakati, N. M.; Monavarian, M.; Avrutin, V.; Morkoç, H.

2018-04-01

We observed varying thermal quenching behavior of the yellow luminescence band near 2.2 eV in different GaN samples. In spite of the different behavior, the yellow band in all the samples is caused by the same defect—the YL1 center. In conductive n-type GaN, the YL1 band quenches with exponential law, and the Arrhenius plot reveals an ionization energy of ˜0.9 eV for the YL1 center. In semi-insulating GaN, an abrupt and tunable quenching of the YL1 band is observed, where the apparent activation energy in the Arrhenius plot is not related to the ionization energy of the defect. In this case, the ionization energy can be found by analyzing the shift of the characteristic temperature of PL quenching with excitation intensity. We conclude that only one defect, namely, the YL1 center, is responsible for the yellow band in undoped and doped GaN samples grown by different techniques.

Preparation and luminescence of silica aerogel composites containing an europium (III) phenanthroline nitrate complex

Energy Technology Data Exchange (ETDEWEB)

Gutzov, Stoyan, E-mail: sgutzov@chem.uni-sofia.bg [University of Sofia “St. Kliment Ohridski”, Department of Physical Chemistry, J. Bourchier Blvd. 1, 1164 Sofia (Bulgaria); Danchova, Nina; Kirilova, Rada; Petrov, Vesselin [University of Sofia “St. Kliment Ohridski”, Department of Physical Chemistry, J. Bourchier Blvd. 1, 1164 Sofia (Bulgaria); Yordanova, Stanislava [University of Sofia “St. Kliment Ohridski”, Department of Organic Chemistry, J. Bourchier Blvd. 1, 1164 Sofia (Bulgaria)

2017-03-15

A simple two step procedure for the functionalization of hydrophobic silica aerogel microgranules with europium ions and/or 1,10 - phenanthroline is demonstrated. The activation procedure is based on soaking aerogels in a europium nitrate solution, followed by functionalization with 1,10 – phenanthroline. The functionalized materials display strong red or blue emission at UV-excitation, coming from the formation of [Eu(phen){sub 2}](NO{sub 3}){sub 3} or Si(IV)– 1,10-phenathroline complexes in the porous system of the aerogels. The most probable site symmetry of the europium cation is C{sub 2v} confirmed by luminescence spectra analysis. Room temperature diffuse reflectance spectra and excitation/luminescence spectra are used to describe the optical properties of the hybrid composites. Excitation spectra prove an efficient energy transfer between 1,10 – phenanthroline and the Eu{sup 3+} ion. - Graphical abstract: An effective activation procedure for functionalization of silica aerogel granules with [Eu(phen){sub 2}](NO{sub 3}){sub 3} and/or 1,10 – phenanthroline /phen/ has been demonstrated in order to obtain red or blue emitting materials. Luminescence spectra (excitation at 355 nm) of functionalized aerogel granules: 1 – SiO{sub 2}:0.18phen; 2 – [Eu(phen){sub 2}](NO{sub 3}){sub 3}; 3– SiO{sub 2}:0.007Eu(phen){sub 2}(NO{sub 3}){sub 3}. The Eu{sup 3+} f-f {sup 5}D{sub 0} →{sup 7}F {sub 0,1,2,3,4} emission transitions are denoted as 0-0, 0-1, 0-2, 0-3, 0-4. The most probable site symmetry of Eu3{sup +} ion is C{sub 2v}.

Luminescence investigation of Yb{sup 3+}/Er{sup 3+} codoped single LiYF{sub 4} microparticle

Energy Technology Data Exchange (ETDEWEB)

Gao, Wei; Zheng, Hairong, E-mail: hrzheng@snnu.edu.cn; He, Enjie; Lu, Ying; Gao, Fangqi

2014-08-01

Tetragonal phase LiYF{sub 4}:Yb{sup 3+}/Er{sup 3+} microparticles are synthesized via facile hydrothermal method. Single LiYF{sub 4} microparticle is excited with IR laser at 980 nm in a confocal setup, and strong green and weak red emissions are observed. It is found that single LiYF{sub 4}:Yb{sup 3+}/Er{sup 3+} microparticle with sub-structure presents stronger upconversion luminescence emission and smaller intensity ratio of red to green emission than that from LiYF{sub 4}:Yb{sup 3+}/Er{sup 3+} microparticle with no sub-structure. The possible mechanism, the influence of particle size and the existence of EDTA on the upconversion luminescence emission are investigated. The current study suggests that the luminescence observation with single micropaticle can effectively avoid the influence of environment and neighbor particles, which is important for investigating the luminescence properties of micro- or nano-crystals and for extending their application. - Highlights: • Single LiYF{sub 4} microparticle is excited with IR laser at 980 nm in a confocal setup, and strong green and weak red emissions are observed. • Single LiYF{sub 4} microparticle with different morphology exhibits different fluorescence emission intensity and intensity ratio of red to green emission. • The possible mechanism, the influence of particle size and the existence of EDTA on the upconversion emission are investigated.

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.

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.

Laser-excited photoluminescence of three-layer GaAs double-heterostructure laser material

International Nuclear Information System (INIS)

Nash, F.R.; Dixon, R.W.; Barnes, P.A.; Schumaker, N.E.

1975-01-01

The successful fabrication of high-quality DH GaAs lasers from a simplified three-layer structure is reported. A major asset of this structure is the transparency of its final layer to recombination radiation occurring in the active layer, thus permitting the use of nondestructive photoluminescent techniques for material evaluation prior to device fabrication. In the course of photoluminescence investigations on this material the additional important observation has been made that indirect excitation (in which photocarriers are generated in the top ternary layer) has significant advantages over direct excitation (in which photocarriers are generated directly in the active layer). These include (i) the direct measurement of Al concentrations in both upper layers, (ii) the measurements of the minority-carrier diffusion length in the upper layer, (iii) an easily obtained indication of taper in the thickness of the upper layer, and (iv) surprisingly effective excitation of the active layer. By combining direct and indirect excitation it is shown that a clearer understanding of the location and detrimental influences of defects in the GaAs laser structure may be obtained. For example, the width of the region of reduced luminescence associated with many defects is found to be very excitation dependent and is confirmed to arise fr []m reduced active region luminescence. The photoluminescent excitation techniques described should be useful in the study of other heterostructure devices and material systems

Analysis of art objects by means of ion beam induced luminescence

International Nuclear Information System (INIS)

Quaranta, A; Dran, J C; Salomon, J; Pivin, J C; Vomiero, A; Tonezzer, M; Maggioni, G; Carturan, S; Mea, G Della

2006-01-01

The impact of energetic ions on solid samples gives rise to the emission of visible light owing to the electronic excitation of intrinsic defects or extrinsic impurities. The intensity and position of the emission features provide information on the nature of the luminescence centers and on their chemical environments. This makes ion beam induced luminescence (IBIL) a useful complement to other ion beam analyses, like PIXE, in the cultural heritage field in characterizing the composition and the provenience of art objects. In the present paper, IBIL measurements have been performed on inorganic pigments for underlying the complementary role played by IBIL in the analysis of artistic works. Some blue and red pigment has been presented as case study

Quantitative cone beam X-ray luminescence tomography/X-ray computed tomography imaging

International Nuclear Information System (INIS)

Chen, Dongmei; Zhu, Shouping; Chen, Xueli; Chao, Tiantian; Cao, Xu; Zhao, Fengjun; Huang, Liyu; Liang, Jimin

2014-01-01

X-ray luminescence tomography (XLT) is an imaging technology based on X-ray-excitable materials. The main purpose of this paper is to obtain quantitative luminescence concentration using the structural information of the X-ray computed tomography (XCT) in the hybrid cone beam XLT/XCT system. A multi-wavelength luminescence cone beam XLT method with the structural a priori information is presented to relieve the severe ill-posedness problem in the cone beam XLT. The nanophosphors and phantom experiments were undertaken to access the linear relationship of the system response. Then, an in vivo mouse experiment was conducted. The in vivo experimental results show that the recovered concentration error as low as 6.67% with the location error of 0.85 mm can be achieved. The results demonstrate that the proposed method can accurately recover the nanophosphor inclusion and realize the quantitative imaging

Data reading with the aid of one-photon and two-photon luminescence in three-dimensional optical memory devices based on photochromic materials

International Nuclear Information System (INIS)

Akimov, Denis A; Zheltikov, Aleksei M; Koroteev, Nikolai I; Naumov, A N; Fedotov, Andrei B; Magnitskiy, Sergey A; Sidorov-Biryukov, D A; Sokolyuk, N T

1998-01-01

The problem of nondestructive reading of the data stored in the interior of a photochromic sample was analysed. A comparison was made of the feasibility of reading based on one-photon and two-photon luminescence. A model was proposed for the processes of reading the data stored in photochromic molecules with the aid of one-photon and two-photon luminescence. In addition to photochromic transitions, account was taken of the transfer of populations between optically coupled transitions in molecules under the action of the exciting radiation. This model provided a satisfactory description of the kinetics of decay of the coloured form of bulk samples of spiropyran and made it possible to determine experimentally the quantum yield of the reverse photoreaction as well as the two-photon absorption cross section of the coloured form. Measurements were made of the characteristic erasure times of the data stored in a photochromic medium under one-photon and two-photon luminescence reading conditions. It was found that the use of two-photon luminescence made it possible to enhance considerably the contrast and localisation of the optical data reading scheme in three-dimensional optical memory devices. The experimental results were used to estimate the two-photon absorption cross section of the coloured form of a sample of indoline spiropyran in a polymethyl methacrylate matrix. (laser applications and other topics in quantum electronics)

Investigations of gamma irradiation on the properties of luminescent films of polycarbonate(PC) matrix doped with europium complex [Eu(tta)3(H2O)2

International Nuclear Information System (INIS)

Forster, Pedro L.; Lugao, Ademar B.; Martins, Natalia A.; Egute, Nayara S.; Parra, Duclerc F.; Brito, Hermi F.

2009-01-01

Luminescent lanthanide complexes have attracted much recent interest for their application as luminescent materials. The combination of unique spectroscopic properties from rare earth complexes associated to physical and chemical intrinsic properties of polymers became more attractive in the last years. A number of advantages of these substances have been reported or realized over the much studied conjugated polymers and nonlanthanide. Luminescent films composed by diaquatris(thenoyltrifluoroacetonate)europium(III) complex [Eu(tta) 3 (H 2 O) 2 ] doped into a polycarbonate (PC) matrix were prepared and irradiated at gamma radiation with 5, 10, and 20 kGy. The PC polymer was doped with 1% (w/w) of the Eu 3+ complex. The thermal properties was investigated by utilization of differential scanning calorimeter (DSC) changes in thermal stability was observed due to the addition of doping agent into the polycarbonate matrix. Changes in photophysical properties due of gamma radiation was observed by emission, excitation spectra and fourier transformed infrared spectra (FTIR). Based on the emission spectra of PC:1% Eu(tta)3 film were observed the characteristic bands arising from the 5 D 0 7 F J transitions of Eu 3+ ion (J=0-4), indicating the ability to obtain the luminescence films. (author)

Luminescence and energy transfer mechanism in Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} nanocrystal rods

Energy Technology Data Exchange (ETDEWEB)

Ahemen, I., E-mail: ahemior@gmail.com; Dejene, F. B. [University of the Free State-QwaQwa Campus, Department of Physics (South Africa)

2017-01-15

Nanocrystal rods of Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} were synthesized using a simple chemical precipitation technique. Both ions were successfully doped into the Zr{sup 4+} ion site in a mixed structure containing both monoclinic and tetragonal phases. The Eu{sup 3+} or Tb{sup 3+} singly doped zirconia produced red and green luminescence which are characteristics of Eu{sup 3+} and Tb{sup 3+} ions, respectively. The co-doped zirconia samples produced blue emission from defect states transitions in the host ZrO{sub 2}, red and green luminescence from dopant ions giving cool to warm white light emissions. The phosphors were efficiently excited by ultraviolet and near-ultraviolet/blue radiations giving white and red light, respectively. The decay lifetime was found to increase with increasing donor ion concentration contrary to conventional observations reported by previous researchers. Weak quadrupole–quatdrupole multipolar process was responsible for energy transfer from Tb{sup 3+} (donor) ion to Eu{sup 3+} ion. No energy back-transfer from Eu{sup 3+} to Tb{sup 3+} ion was observed from the excitation spectra. Temperature-dependent photoluminescence shows the presence of defects at low temperature, but these defects vanished at room temperature and beyond. The Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} nanocrystal rod is a potential phosphor for white light application using UV as an excitation source. Thermoluminescence measurements show that the inclusion of Tb{sup 3+} ion increases trap depths in the host zirconia.

Influence of surface functionalization on structural and photo-luminescence properties of CeF{sub 3}:Tb nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Ansari, Anees A., E-mail: aneesaansari@gmail.com

2017-07-01

Graphical abstract: We designed highly aqueous dispersible CeF{sub 3}:Tb@LaF{sub 3}@SiO{sub 2} nanoparticles. The epitaxial growth of inert LaF{sub 3} shell and further amorphous silica, respectively, enhanced their optical and luminescence properties, which is highly usable for luminescent biolabeling, and optical bio-probe etc. - Abstract: Highly luminescent and aqueous soluble CeF{sub 3}:Tb (core),CeF{sub 3}:Tb@LaF{sub 3}(core/shell) and CeF{sub 3}:Tb@LaF{sub 3}@ SiO{sub 2} (core/shell/Si) nanoparticles(NPs) with mean particle size 12 nm were prepared by co-precipitation method at low temperature. X-ray diffraction pattern verified the phase purity, high crystallinity of hexagonal structure. The TEM image and SAED pattern revealed the single phase polycrystalline nature, well-dispersed irregular shaped hexagonal structure. FTIR spectra show the characteristic infrared peaks of silica, it suggests the successful silica surface coating around the core/shell NPs. The excitation and emission intensity of core/shell NPs were remarkably increased then their counterpart core NPs. It implies that a significant amount of nonradiative transition centers existing on the surface of core NPs has been eliminated due to the formation of passivated LaF{sub 3} layer. The silica surface modification over the core/shell NPs strikingly enhanced the solubility character in an aqueous environment.

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.

Effect of structural packing on the luminescence properties in tungsten bronze compounds M{sub 2}KNb{sub 5}O{sub 15} (M=Ca, Sr, Ba)

Energy Technology Data Exchange (ETDEWEB)

Yin Xin; Shi Liu [State Key Laboratory of High Performance Ceramics and Superfine Microstructures and CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Wei Ang, E-mail: iamawei@njupt.edu.cn [Key Laboratory for Organic Electronics and Information Displays, 9 Wenyuan Road, Nanjing 210046 (China); Wan Dongyun; Wang Yaoming [State Key Laboratory of High Performance Ceramics and Superfine Microstructures and CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Huang Fuqiang, E-mail: huangfq@mail.sic.ac.cn [State Key Laboratory of High Performance Ceramics and Superfine Microstructures and CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)

2012-08-15

Tungsten bronze compounds M{sub 2}KNb{sub 5}O{sub 15} (M=Ca, Sr, Ba) were successfully synthesized, and the luminescence properties were investigated. Among the three compounds, Ca{sub 2}KNb{sub 5}O{sub 15} showed an obviously broad band of host luminescence at 460 nm with exciting at 269 nm. By doping Eu{sup 3+} into the M sites, Ca{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} displayed strong red emission from Eu{sup 3+} ions characteristic transitions, nearly four times higher than Sr{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} and seven times higher than Ba{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+}. Crystal packing factor (PF) was introduced to account for this luminescence difference, lower PF being correlated to higher luminescence intensity for perovskite-related structure. Both the as-prepared compounds and the literature examples were proved to fit this correlation. This can be explained through the influence of the structural packing on the environment distortion and crystal field splitting of the doping site. - Graphical abstract: Tungsten bronze compounds M{sub 2}KNb{sub 5}O{sub 15} (M=Ca, Sr, Ba) show the dependence of luminescence properties on structural packing, among which Ca{sub 2}KNb{sub 5}O{sub 15} has the superior luminescence. Highlights: Black-Right-Pointing-Pointer Tungsten bronze compounds were synthesized by solid state reaction. Black-Right-Pointing-Pointer Ca{sub 2}KNb{sub 5}O{sub 15} displayed remarkably blue host luminescence. Black-Right-Pointing-Pointer Ca{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} showed more intense red emission than M{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} (M=Sr, Ba). Black-Right-Pointing-Pointer The relationship between crystal packing factor and luminescence was obtained.

Effects of Er3+ concentration on UV/blue upconverted luminescence and a three-photon process in the cubic nanocrystalline Y2O3:Er3+

International Nuclear Information System (INIS)

Wang Xin; Shan Guiye; Chao Kefu; Zhang Youlin; Liu Ruilin; Feng Liyun; Zeng Qinghui; Sun Yajuan; Liu Yichun; Kong Xianggui

2006-01-01

Ultraviolet (UV)/blue upconverted luminescent properties of the cubic Y 2 O 3 :Er 3+ nanocrystals as a function of the erbium concentration were investigated upon 488 nm Ar + laser excitation. The remarkable decrease of upconverted emission intensity and the quenching of the 2 P 3/2 → 4 I 11/2 / 4 I 13/2 transitions were observed in the Y 2 O 3 nanocrystals with high erbium concentration. The emission spectra and the exciting power dependence of upconverted luminescent intensities reveal that the possible upconversion mechanisms are excited-state absorption (ESA) and energy transfer (ET). Moreover, a UV/violet upconverted emission spectrum of nanocrystalline Y 2 O 3 :Er 3+ upon 980 nm light excitation was also observed and a three-photon process made a contribution to this upconverted emission

Infrared stimulated luminescence dating of an Eemian (MIS 5e) site in Denmark using K-feldspar

DEFF Research Database (Denmark)

Buylaert, Jan-Pieter; Huot, Sebastian; Murray, Andrew S.

2011-01-01

Infrared stimulated luminescence (IRSL) dating of K-feldspars may be an alternative to quartz optically stimulated luminescence (OSL) dating when the quartz OSL signal is too close to saturation or when the quartz luminescence characteristics are unsuitable. In this paper, Eemian (MIS 5e) coastal...

Site symmetry and crystal field of Ce{sup 3+} luminescent centres in KMgF{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Yamaga, M. [Department of Electrical and Electronic Engineering, Faculty of Engineering, Gifu University, Gifu (Japan); Honda, M.; Kawamata, N. [Faculty of Science, Naruto University of Education, Naruto (Japan); Fujita, T.; Shimamura, K.; Fukuda, T. [Institute for Materials Research, Tohoku University, Sendai (Japan)

2001-04-09

The electron-spin resonance (ESR) spectra of Ce{sup 3+} in KMgF{sub 3} observed at low temperatures (<20 K) show that two tetragonal and two orthorhombic Ce{sup 3+} centres exist in the absence of a cubic centre. These Ce{sup 3+} centres are strongly associated with substitution of Ce{sup 3+} ions for K{sup +} ions with K{sup +}-ion vacancies at three different sites and for a Mg{sup 2+} ion with a vacancy of the nearest neighbour Mg{sup 2+} ion along the [101] direction as charge compensators. The optical absorption spectrum of Ce{sup 3+} in KMgF{sub 3} measured at room temperature consists of two intense broadbands with peaks at 229 and 237 nm, and two weak bands with peaks at 203 and 211 nm corresponding to the transition from the ground state {sup 2}F{sub 5/2} to the 5d{sup 1} excited states of Ce{sup 3+}. The Ce{sup 3+} luminescence spectrum excited at 229 or 237 nm at room temperature is composed of broadbands with double peaks at 265 and 282 nm, which are due to the ground-state splitting between {sup 2}F{sub 5/2} and {sup 2}F{sub 7/2}. The peak of the weak luminescence band excited at a tail (250-280 nm) of the intense absorption bands is shifted to lower energy. The intense and weak Ce{sup 3+} luminescence bands are assigned to Ce{sup 3+} ions substituting for K{sup +} ions away from and near to K{sup +}-ion vacancies, respectively. The luminescence from Ce{sup 3+} ions substituting for Mg{sup 2+} ions could not be observed at room temperature. (author)

VUV and UV–vis optical study on KGd2F7 luminescent host doped with terbium and co-doped with europium

International Nuclear Information System (INIS)

Lisiecki, Radosław

2013-01-01

The KGd 2 F 7 :Tb and KGd 2 F 7 :Tb,Eu samples were obtained using a solid state reaction. Excitation spectra and emission spectra are reported and analyzed within the VUV–UV–vis spectral range. The intense green luminescence is observed in the KGd 2 F 7 :Tb while the combined emission of terbium and europium in the KGd 2 F 7 :Tb,Eu covers substantially the region of white light. The materials under study can be effectively excited making use of intense f–d transitions of Tb 3+ in the VUV–UV region. Experimental lifetimes of luminescent levels have been measured and discussed. It was found that the considerable energy transfer from Tb 3+ to Eu 3+ occurs. -- Highlights: • The prospective green and white emitting phosphors. • The effective VUV and UV–vis excitation process. • The considerable energy transfer among optically active ions. • The influence of (Tb, Eu) co-doping on relaxation dynamic of excited states

Luminescence of La3+ and Sc3+ impurity centers in YAlO3 single-crystalline films

International Nuclear Information System (INIS)

Zorenko, Yu.; Gorbenko, V.; Voznyak, T.; Zorenko, T.; Nikl, M.; Nejezchleb, K.

2008-01-01

The luminescence of La Y 3+ and Sc Y 3+ and Sc Al 3+ centers created by lanthanum and scandium ions at Y 3+ and Al 3+ cation sites of YAlO 3 perovskite lattice was investigated. The features of emission of excitons localized at the mentioned centers in YAlO 3 :La and YAlO 3 :Sc single-crystalline films were analyzed by means of time-resolved emission spectroscopy and luminescence decay kinetics measurements under excitation by synchrotron radiation at 9 and 300 K

Exciplex formation accompanied with excitation quenching.

Science.gov (United States)

Fedorenko, Stanislav G; Burshtein, Anatoly I

2010-04-08

The competence of the reversible exciplex formation and parallel quenching of excitation (by electron or energy transfer) was considered using a non-Markovian pi-forms approach, identical to integral encounter theory (IET). General equations accounting for the reversible quenching and exciplex formation are derived in the contact approximation. Their general solution was obtained and adopted to the most common case when the ground state particles are in great excess. Particular cases of only photoionization or just exciplex formation separately studied earlier by means of IET are reproduced. In the case of the irreversible excitation quenching, the theory allows specifying the yields of the fluorescence and exciplex luminescence, as well as the long time kinetics of excitation and exciplex decays, in the absence of quenching. The theory distinguishes between the alternative regimes of (a) fast equilibration between excitations and exciplexes followed by their decay with a common average rate and (b) the fastest and deep excitation decay followed by the weaker and slower delayed fluorescence, backed by exciplex dissociation.

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.

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.

Luminescence dating

International Nuclear Information System (INIS)

Rieser, U.

2008-01-01

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

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.

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

Comparative studies of upconversion luminescence characteristics and cell bioimaging based on one-step synthesized upconversion nanoparticles capped with different functional groups

Energy Technology Data Exchange (ETDEWEB)

Tsang, Ming-Kiu [Department of Applied Physics, The Hong Kong Polytechnic University, Hong Kong (China); Chan, Chi-Fai; Wong, Ka-Leung [Department of Chemistry, Hong Kong Baptist University (Hong Kong); Hao, Jianhua, E-mail: jh.hao@polyu.edu.hk [Department of Applied Physics, The Hong Kong Polytechnic University, Hong Kong (China)

2015-01-15

Herein, three types of upconverting NaGdF{sub 4}:Yb/Er nanoparticles (UCNPs) have been synthesized via one-step hydrothermal synthesis with polyethylene glycol (PEG), polyethylenimine (PEI) and 6-aminocapronic acid (6AA) functionalization. To evident the presence of these groups, FTIR spectra and ζ-potentials were measured to support the successful capping of PEG, PEI and 6AA on the UCNPs. The regular morphology and cubic phase of these functionalized UCNPs were attributed to the capping effect of the surfactants. Tunable upconversion luminescence (UCL) from red to green were observed under 980 nm laser excitation and the UCL tuning was attributed to the presence of various surface ligands. Moreover, surface group dependent UCL bioimaging was performed in HeLa cells. The enhanced UCL bioimaging demonstrated by PEI functionalized UCNPs evident high cell uptake. The significant cell uptake is explained by the electrostatic attraction between the amino groups (–NH{sub 2}) and the cell membrane. Moreover, the functionalized UCNPs demonstrated low cytotoxicity in MTT assay. Additional, paramagnetic property was presented by these UCNPs under magnetic field. - Highlights: • Tunable upconversion emission by capped functional groups under fixed composition. • Surface dependent upconversion luminescence bioimaging in HeLa cells. • Low cytotoxicity. • Additional paramagnetic property due to Gd{sup 3+} ions.

Luminescent Enhancement of Na+ and Sm3+ Co-doping Reddish Orange SrCa3Si2O8 Phosphors

Science.gov (United States)

Chun, Fengjun; Zhang, Binbin; Li, Wen; Liu, Honggang; Deng, Wen; Chu, Xiang; Osman, Hanan; Zhang, Haitao; Yang, Weiqing

2018-04-01

Reddish orange SrCa3Si2O8 phosphors, prepared by the facile solid state reaction method, are a luminescent enhancement of Na+ and Sm3+ co-doping luminescent material. Na+ was designed to compensate the charge imbalance of Sm3+ ion substituting for the Sr2+ ion of orthorhombic SrCa3Si2O8 crystals. The results suggest that Na+ can effectively enhance the luminescent intensity of the reddish orange light peaked at about 562 nm (4 G 5/2 → 6 H 5/2), 600 nm (4 G 5/2 → 6 H 7/2) and 645 nm (4 G 5/2 → 6 H 9/2) excited by the near ultraviolet excited light 404 nm (4 L 13/2 → 6 H 5/2). The energy transfer has been further verified by the florescence lifetime. Additionally, the luminescent lifetime τ of as-grown phosphors was separated into two parts, a rapid lifetime and a slow lifetime. The average lifetime results ranged from 2.098 to 1.329 ms which were influenced by the concentration of Sm3+ doping. The systematic researches of as-grown phosphors have clearly suggested a potential application for white-light-emitting diodes ( w-LEDs).

Synthesis and functionalization of persistent luminescence nanoparticles with small molecules and evaluation of their targeting ability.

Science.gov (United States)

Maldiney, Thomas; Byk, Gerardo; Wattier, Nicolas; Seguin, Johanne; Khandadash, Raz; Bessodes, Michel; Richard, Cyrille; Scherman, Daniel

2012-02-14

We have recently reported the design and use of inorganic nanoparticles with persistent luminescence properties. Such nanoparticles can be excited with a UV lamp for 2min and emit light in the near-infrared area for dozen of minutes without any further excitation. This property is of particular interest for small animal optical imaging, since it avoids the autofluorescence of endogenous fluorophores which is one major problem encountered when using fluorescent probes. We report herein the synthesis of persistent luminescence nanoparticles (PLNPs) and their functionalization with two small targeting molecules: biotin and Rak-2. We provide characterization of each PLNP as well as preliminary evidence of the ability of PLNP-PEG-Biotin to target streptavidin and PLNP-PEG-Rak-2 to bind prostate cancer cells in vitro. Copyright © 2011 Elsevier B.V. All rights reserved.

Luminescence properties of undoped CsCaCl3 and CsSrCl3 crystalline scintillators

International Nuclear Information System (INIS)

Fujimoto, Yutaka; Saeki, Keiichiro; Koshimizu, Masanori; Asai, Keisuke; Yanagida, Takayuki

2015-01-01

Intrinsic luminescence properties of undoped CsCaCl 3 and CsSrCl 3 crystalline scintillators were studied. The crystal samples were grown by a vertical Bridgman method. Photoluminescence spectra of the crystals showed Auger-free luminescence (AFL) at 310 nm and self-trapped emission (STE) at 400 nm for CsCaCl 3 and 465 nm for CsSrCl 3 , when vacuum ultraviolet (VUV) light at 84 nm and 160 nm excited the crystals. X-ray excited radioluminescence spectra of the crystals showed some emission bands in the 280-600 nm wavelength range, which are owing to AFL, STE, and other origins such as lattice defects and impurities. Scintillation light yield was 400-300 ph/MeV, and the principal scintillation decay time about 2.5 ns and 12 ns for CsCaCl 3 and 1.8 ns and 13 ns for CsSrCl 3 . (author)

Study of the cathodic region of a hydrogen luminescent discharge: spectroscopic diagnoses

International Nuclear Information System (INIS)

Barbeau, Claude

1991-01-01

This research thesis addresses the study of the cathodic region of a hydrogen luminescent discharge in direct current, and belongs to the field of studies on plasma-surface interactions, notably in order to understand and optimise electric discharges in H_2CH_4 mixtures used for steel cementation and hard carbon deposition. The author first presents the main characteristics of the abnormal discharge, and details operation conditions as well as the characteristics of the different experimental assemblies. The experimental study of the cathodic region has been mainly performed by high resolution emission spectroscopy, and multi-photon laser spectroscopy (laser-induced fluorescence, optogalvanic effect). In the second part, the author reports an analysis of the Doppler broadening of emission profiles of atomic lines (notably the Balmer series). Experimental results are compared with those of Monte Carlo simulation which addresses mechanisms of creation of excited atoms as well as their energetic distribution. The next parts report the development of methods and techniques for the measurement of the electric field of the cathodic drop and of gas temperature, experimental results and their interpretation [fr

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.

Electronic band structure in porous silicon studied by photoluminescence and photoluminescence excitation spectroscopy

International Nuclear Information System (INIS)

Lee, Ki-Won; Kim, Young-You

2004-01-01

In this research, we used photoluminescence (PL) and photoluminescence excitation (PLE) to visualize the electronic band structure in porous silicon (PS). From the combined results of the PLE measurements at various PL emission energies and the PL measurements under excitation at various PLE absorption energies, we infer that three different electronic band structures, originating from different luminescent origins, give rise to the PL spectrum. Through either thermal activation or diffusive transfer, excited carriers are moved to each of the electronic band structures.

Characteristics Analysis of an Excitation Assistance Switched Reluctance Wind Power Generator

DEFF Research Database (Denmark)

Liu, Xiao; Wang, Chao; Chen, Zhe

2015-01-01

In order to fully analyze the characteristics of an excitation assistance switched reluctance generator (EASRG) applied in wind power generation, a static model and a dynamic model are proposed. The static model is based on the 3-D finite-element method (FEM), which can be used to obtain the stat...

Synthesis and characterization of the europium (III) complex as an organic luminescent material

International Nuclear Information System (INIS)

Zhuo Zuliang; Zhang Fujun; Xu Zheng; Lu Lifang; Li Junming; Wang Yongsheng; Lv Yuguang

2010-01-01

The red emission organic material Eu(coumarin) 3 ·2H 2 O complex was synthesized and its morphology, energy level alignment and luminescence characteristics were studied by using scanning electron microscopy, Fourier transform infrared spectra, cyclic voltammetry and ultraviolet-visible absorption spectra and fluorescence spectra. Eu(coumarin) 3 ·2H 2 O shows bright red emission originating from Eu 3+ ions under 345 nm light excitation. The luminescence lifetime of Eu 3+ in this complex is about 580 μs. To improve the quality of Eu(coumarin) 3 ·2H 2 O thin films, Eu(coumarin) 3 ·2H 2 O was doped with a poly(N-vinylcarbazole) (PVK) solution. The organic materials 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and aluminum quinoline (Alq 3 ) were used as hole-blocking and electron-transporting layers in our fabricated electroluminescence (EL) devices on indium tin oxide (ITO) substrates, respectively. The EL devices ITO/poly-(3,4-ethylenedioxythiophene):poly-(styrenesulphonic acid) (PEDOT:PSS)/emitting layer (PVK:Eu)/BCP/Alq 3 /Al were fabricated, and EL spectra were measured under different driving voltages. There is one emission peaking at 490 nm in addition to the characteristic emission peaks of Eu 3+ , which should be attributed to the spectral overlap between the PVK emission and electroplex emission originating from PVK and BCP interfaces. This explanation can be positively supported by the dependence of the EL spectral variation of ITO/ PVK/BCP/Alq 3 /Al devices on the driving voltage.

Synthesis and characterization of the europium (III) complex as an organic luminescent material

Science.gov (United States)

Zhuo, Zuliang; Zhang, Fujun; Lv, Yuguang; Xu, Zheng; Lu, Lifang; Li, Junming; Wang, Yongsheng

2010-11-01

The red emission organic material Eu(coumarin)3·2H2O complex was synthesized and its morphology, energy level alignment and luminescence characteristics were studied by using scanning electron microscopy, Fourier transform infrared spectra, cyclic voltammetry and ultraviolet-visible absorption spectra and fluorescence spectra. Eu(coumarin)3·2H2O shows bright red emission originating from Eu3+ ions under 345 nm light excitation. The luminescence lifetime of Eu3+ in this complex is about 580 μs. To improve the quality of Eu(coumarin)3·2H2O thin films, Eu(coumarin)3·2H2O was doped with a poly(N-vinylcarbazole) (PVK) solution. The organic materials 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and aluminum quinoline (Alq3) were used as hole-blocking and electron-transporting layers in our fabricated electroluminescence (EL) devices on indium tin oxide (ITO) substrates, respectively. The EL devices ITO/poly-(3,4-ethylenedioxythiophene):poly-(styrenesulphonic acid) (PEDOT:PSS)/emitting layer (PVK:Eu)/BCP/Alq3/Al were fabricated, and EL spectra were measured under different driving voltages. There is one emission peaking at 490 nm in addition to the characteristic emission peaks of Eu3+, which should be attributed to the spectral overlap between the PVK emission and electroplex emission originating from PVK and BCP interfaces. This explanation can be positively supported by the dependence of the EL spectral variation of ITO/ PVK/BCP/Alq3/Al devices on the driving voltage.

The temperature-sensitive luminescence of (Y,Gd)VO4:Bi3+,Eu3+ and its application for stealth anti-counterfeiting

International Nuclear Information System (INIS)

Chen, Lei; Zhang, Yao; Luo, Anqi; Liu, Fayong; Jiang, Yang; Hu, Qingzhuo; Chen, Shifu; Liu, Ru-Shi

2012-01-01

Anti-counterfeiting technologies are desired to protect products far away from the violation of dummy, fake and shoddy goods. The phosphor of (Y,Gd)VO 4 :Bi 3+ ,Eu 3+ was synthesized for the application of this purpose. Its photoluminescence was investigated by exciting with different wavelengths at variant temperatures. Wide emission color ranged from green through yellow to orange was tuned up by tailor-ing Bi 3+ and Eu 3+ concentrations. The temperature dependent luminescence and wavelength selective excitation of (Y,Gd)VO 4 :Bi 3+ ,Eu 3+ were observed, which provide different encryptions in anti-counterfeiting. To verify the feasibility in application, two anti-counterfeiting patterns were fabricated practically and excellent performance was obtained. Moreover, the physical mechanisms for the different phenomena of luminescence were elucidated from excitation spectra combining with the configuration coordinate model. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Investigation of electro-optical properties for electrochemical luminescence device with a new electrode structure

Science.gov (United States)

Ok, Jung-Woo; Pooyodying, Pattarapon; Anuntahirunrat, Jirapat; Sung, Youl-Moon

2018-04-01

In this paper, we investigate electrochemical luminescent (ECL) device with a new structure and the ECL cell device with proposed electrode configuration works reliably at AC voltage. In particular, the conventional ECL cell has counter electrodes in which a cathode and an anode are opposed to each other, whereas the proposed structure has parallel electrodes in which a cathode and an anode are arranged on a single substrate. The proposed electrode configuration has a structural feature that electric short-circuiting is less likely to occur during bending than the conventional electrode configuration. The electro-optical characteristics of the new electrode configuration such as the current density, the light emission intensity, and the time evolution of the emission are investigated. The proposed ECL device exhibited higher light emitting efficiency than the conventional structure. Especially, at AC operation mode, the new structure showed the distinctive luminescence characteristic which is combined the first luminescence near the surface of electrode with the delayed second luminescence near the center of between electrodes. It was closely related to the behavior of luminescent particles. The proposed the ECL cell structure is expected to be utilized as a flexible display device by taking advantage of its characteristics and practicality.

Controllable synthesis and tunable luminescence of glass ceramic containing Mn2+:ZnAl2O4 and Pr3+:YF3 nano-crystals

International Nuclear Information System (INIS)

Yu, Yunlong; Li, Xiaoyan

2016-01-01

Highlights: • Glass ceramic containing ZnAl 2 O 4 and YF 3 nano-crystals is fabricated. • Mn 2+ and Pr 3+ are selectively incorporated into ZnAl 2 O 4 and YF 3 , respectively. • The luminescence color can be tuned by adjusting the excitation wavelength. - Abstract: Glass ceramic containing spinel ZnAl 2 O 4 :Mn 2+ and orthorhombic YF 3 :Pr 3+ nano-crystals has been successfully prepared by a melt-quenching technique. X-ray diffraction and transmission electron microscopy demonstrated that two nano-phases, i.e. ZnAl 2 O 4 and YF 3 , were homogeneously distributed among the glass matrix. Importantly, the selective incorporation of Pr 3+ ions into the Y 3+ nine-fold coordinated sites of YF 3 and the segregation of Mn 2+ dopants in the Zn 2+ tetrahedral sites of ZnAl 2 O 4 were confirmed based on the excitation/emission spectra and the crystal field calculation. Under blue light excitation, both Pr 3+ and Mn 2+ in the glass ceramic can be simultaneously excited, and emit red and green luminescence, respectively, owing to the suppression of energy transfer between them. The luminescence color of the obtained glass ceramic can be easily tuned by adjusting the excitation wavelength. These results indicate the potential application of the glass ceramic as converting phosphor to generate white-light after coupling with the blue LED chip.

Dual mode NIR long persistent phosphorescence and NIR-to-NIR Stokes luminescence in La{sub 3}Ga{sub 5}GeO{sub 14}: Cr{sup 3+}, Nd{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Wu, Yiling; Li, Yang, E-mail: msliyang@scut.edu.cn; Qin, Xixi; Chen, Ruchun; Wu, Dakun; Liu, Shijian; Qiu, Jianrong, E-mail: qjr@scut.edu.cn

2015-11-15

Recently, long persistent phosphors (LPPs) have been considered to be the most prominent candidates for biomedical applications. However, the LPPs suffer from a dramatic decrease in luminescence intensity after incorporation into the tissue. Therefore, it is very necessary to develop the more competitive LPPs and acquire the reproducible tissue imaging. Here, we propose and experimentally demonstrate an effective bifunctional La{sub 3}Ga{sub 5}GeO{sub 14}: Cr{sup 3+}, Nd{sup 3+} phosphor with the interesting characteristic of near-infrared long persistent phosphorescence and NIR-to-NIR Stokes luminescence. Cr{sup 3+} and Nd{sup 3+} ions are simultaneously selected as the emission centers in order to take advantage of the remarkable phosphorescence properties of Cr{sup 3+}, and the appropriate energy level characteristic of NIR-excitation band (808 nm) and NIR-emission (1064 nm), and the ability as the brilliant auxiliary to create more efficient defects of Nd{sup 3+}. The efficient dual-modal emission is, accordingly utilized to realize the convenient, high-resolution global detection and local imaging. - Highlights: • Dual mode phosphor with NIR long afterglow and NIR-to-NIR Stokes luminescence. • Increasing the persistent duration due to the codoping of Nd. • Avoiding the noteworthy overheating effect due to the strong absorption at 980 nm.

Spectral characteristics of europium-doped lead iodide

International Nuclear Information System (INIS)

Novosad, I.S.; Novosad, S.S.

2013-01-01

Optical absorption and x-ray luminescence spectra and thermally stimulated luminescence curves of a PbI 2 :EuCl 3 crystal grown by the Stockbarger method were investigated in the temperature range 85-295 K. It was presumed based on results of EPR spectral studies that the europium ions in this material existed in the divalent state and replaced matrix cations. An intense broad non-elementary band at 780 nm in addition to a weak band with a maximum in the range 512-520 nm were observed in the PbI 2 :Eu 2+ x-ray luminescence spectrum at 85 K. The intensity of the long-wavelength emission increased slightly upon increasing the crystal temperature from 85 to 130 K and was quenched in several stages upon increasing the temperature further to 220 K. The maximum shifted to 740 nm. It was proposed based on an analysis of the obtained data and results of a study of the luminescence properties of PbI 2 and PbI 2 :Mn 2+ crystals that the non-elementary emission band of the PbI 2 :Eu 2+ crystal at 780 nm could be represented as a superposition of three individual Gaussian bands with maxima near 715, 740, and 800 nm that were due to centers characteristic of the matrix and additional centers that were formed by Eu ions through association with intrinsic and dopant oxygen-containing defects, respectively. Doping PbI 2 with Eu 2+ ions did not affect the spectrum of matrix trapping levels. The nature of emission and trapping centers and luminescence excitation mechanisms of PbI 2 :Eu 2+ were discussed. (authors)

Biosynthesis of luminescent quantum dots in an earthworm

Science.gov (United States)

Stürzenbaum, S. R.; Höckner, M.; Panneerselvam, A.; Levitt, J.; Bouillard, J.-S.; Taniguchi, S.; Dailey, L.-A.; Khanbeigi, R. Ahmad; Rosca, E. V.; Thanou, M.; Suhling, K.; Zayats, A. V.; Green, M.

2013-01-01

The synthesis of designer solid-state materials by living organisms is an emerging field in bio-nanotechnology. Key examples include the use of engineered viruses as templates for cobalt oxide (Co3O4) particles, superparamagnetic cobalt-platinum alloy nanowires and gold-cobalt oxide nanowires for photovoltaic and battery-related applications. Here, we show that the earthworm's metal detoxification pathway can be exploited to produce luminescent, water-soluble semiconductor cadmium telluride (CdTe) quantum dots that emit in the green region of the visible spectrum when excited in the ultraviolet region. Standard wild-type Lumbricus rubellus earthworms were exposed to soil spiked with CdCl2 and Na2TeO3 salts for 11 days. Luminescent quantum dots were isolated from chloragogenous tissues surrounding the gut of the worm, and were successfully used in live-cell imaging. The addition of polyethylene glycol on the surface of the quantum dots allowed for non-targeted, fluid-phase uptake by macrophage cells.

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)

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...

Dual-excitation upconverting nanoparticle and quantum dot aptasensor for multiplexed food pathogen detection

OpenAIRE

Kurt, Hasan; Yüce, Meral; Yuce, Meral; Hussain, Babar; Budak, Hikmet

2016-01-01

In this report, a dual-excitation sensing method was developed using aptamer-functionalized quantum dots and upconverting nanoparticles, exhibiting Stokes and anti-Stokes type excitation profiles, respectively. Conjugation of the aptamer-functionalized luminescent nanoparticles with the magnetic beads, comprising short DNA sequences that were partially complementary to the aptamer sequences, enabled facile separation of the analyte-free conjugates for fluorescent measurement. UV–Visible spect...

Comparison of exciplex generation under optical and X-ray excitation

Science.gov (United States)

Kipriyanov, A. A.; Melnikov, A. R.; Stass, D. V.; Doktorov, A. B.

2017-09-01

Exciplex generation under optical and X-ray excitation in identical conditions is experimentally compared using a specially chosen model donor-acceptor system, anthracene (electron acceptor) and N,N-dimethylaniline (electron donor) in non-polar solution, and the results are analyzed and interpreted based on analytically calculated luminescence quantum yields. Calculations are performed on the basis of kinetic equations for multistage schemes of bulk exciplex production reaction under optical excitation and combination of bulk and geminate reactions of radical ion pairs under X-ray excitation. These results explain the earlier experimentally found difference in the ratio of the quantum yields of exciplexes and excited electron acceptors (exciplex generation efficiency) and the corresponding change in the exciplex generation efficiency under X-irradiation as compared to the reaction under optical excitation.

Luminescence studies of molecular materials

International Nuclear Information System (INIS)

Miller, P.F.

2000-01-01

Molecular materials have been widely studied for their potential uses in novel semiconductor devices. They occupy the intellectually interesting area between molecular and bulk descriptions of matter, and as such often have unique and useful characteristics. The design and engineering of these structures is inter-disciplinary in its nature, embracing the fields of physics, electrical engineering and both synthetic and physical chemistry. In this thesis luminescence studies of molecular materials will be presented that probe the nature of the excited states in two promising semiconductor systems. Luminescence techniques provide a powerful and sensitive tool in the investigation of kinetic pathways of radiative and non-radiative emission from these samples. This is particularly appropriate here, as the materials being studied are of potential use in electroluminescent devices. The suitability of photoluminescence techniques comes from both the electroluminescence and photoluminescence sharing the same emitting state. The first class of material studied here is an organic semiconducting polymer, cyano-substituted polyphenylenevinylene (CN-PPV). Conjugated polymers combine semiconducting electronic properties with favourable processing properties and offer the possibility of tuning their optical and electronic properties chemically. The cyanosubstitution increases the electron affinity of the polymer backbone, facilitating electron injection in light-emitting diodes. The polymers are soluble in solvents such as toluene and chloroform due the presence of alkoxy sidegroups. CdSe semiconductor nanocrystals are the other class of material characterised in this work. Semiconductor nanocrystals exhibit interesting size-tunable optical properties due to the confinement of the electronic wave functions. Characterisation of samples produced by different synthetic routes has been carried out to demonstrate the advantages of a novel synthetic method in terms of physical and

Increase of (CdSe/ZnS)Cys quantum dot luminescence intensity in the presence of TPPS4 porphyrin

International Nuclear Information System (INIS)

Parra, Gustavo G.; Borissevitch, Iouri E.; Oleinikov, Vladimir A.

2012-01-01

Full text: Nanocrystal semiconductor particles or Quantum Dots (QD) possess extraordinary photophysical characteristics, such as extreme high fluorescence quantum yield and optical absorption and very narrow fluorescence band, which can be easily shifted by changing of QD particle size. Due to these characteristics, QD is promising for fluorescence cancer diagnostics and photodynamic treatment. The efficiency of these processes can be in- creased by energy transfer between QD and classic fluorescence probes and photosensitizers (PS). In this work we present on the study of the increase of (CdSe/ZnS)Cys quantum dot luminescence intensity, stimulated by interaction with TPPS 4 porphyrin. The optical absorption and steady-state and time-resolved fluorescence techniques were employed. Water soluble QD (CdSe/ZnS) with emission at 580 nm, functionalized with cysteine (Cys), were studied. TPPS 4 porphyrin was used as a stimulator of QD luminescence. All experiments were realized in PBS buffer (pH 7.3; 7.5 mM) in Milli-Q quality water. The TPPS 4 adding into the QD solutions until the 5μM concentration produced an increase in QD luminescence intensity and lifetime, while for TPPS 4 concentrations higher than 20μM the reduction of the fluorescence intensity was observed, the emission spectra and fluorescence decays profile being unchanged. This effect can not be due to the electrostatic interaction between (CdSe/ZnS)Cys and TPPS 4 because both, (CdSe/ZnS)Cys and TPPS 4 , are negatively charged. We suppose that TPPS 4 porphyrin interacts directly with QD (ZnS) shell, reducing the dangling bound number. This reduction decreases, in turn, the probability of nonradiative ways of the excitation energy dissipation. When the majority of dangling bound is occupied by the TPPS 4 molecules, the effect of QD luminescence reduction (quenching) by porphyrin predominates, probably, via the energy transfer from QD to TPPS 4 . However, because of complexity in the systems involving

Structural, vibrational and luminescence properties of the (1−x)CaWO{sub 4}−xCdWO{sub 4} system

Energy Technology Data Exchange (ETDEWEB)

Taoufyq, A. [Institut Matériaux Microélectronique et Nanosciences de Provence, Aix Marseille Université, CNRS, Université de Toulon, IM2NP UMR 7334, 83957, La Garde (France); Laboratoire Matériaux et Environnement LME, Faculté des Sciences, Université Ibn Zohr, BP 8106, Cité Dakhla, Agadir, Maroc (Morocco); CEA/DEN, Département d’Études des Réacteurs, Laboratoire Dosimétrie Capteurs Instrumentation, CEA Cadarache, 13108, Saint-Paul-lez-Durance (France); Société CESIGMA, Signals and Systems, 1576 Chemin de La Planquette, 83130 La Garde (France); Guinneton, F.; Valmalette, J-C.; Arab, M. [Institut Matériaux Microélectronique et Nanosciences de Provence, Aix Marseille Université, CNRS, Université de Toulon, IM2NP UMR 7334, 83957, La Garde (France); Benlhachemi, A.; Bakiz, B. [Laboratoire Matériaux et Environnement LME, Faculté des Sciences, Université Ibn Zohr, BP 8106, Cité Dakhla, Agadir, Maroc (Morocco); Villain, S. [Institut Matériaux Microélectronique et Nanosciences de Provence, Aix Marseille Université, CNRS, Université de Toulon, IM2NP UMR 7334, 83957, La Garde (France); and others

2014-11-15

In the present work, we investigate the structural, microstructural, vibrational and luminescence properties of the system (1−x)CaWO{sub 4}−xCdWO{sub 4} with x ranging between 0 and 1. Polycrystalline samples were elaborated using a coprecipitation technique followed by thermal treatment at 1000 °C. The samples were then characterized using X-ray diffraction, scanning electron microscopy, Raman spectroscopy and luminescence analyses. X-ray diffraction profile analyses using Rietveld method showed that two kinds of solid solutions Ca{sub 1−x}Cd{sub x}WO{sub 4} having scheelite and wolframite structures, with respectively tetragonal and monoclinic crystal cells, were observed, with a biphasic system for compositions x=0.6 and 0.7. The scanning electron microscopy experiments showed a complex evolution of morphologies and crystallite sizes as x increased. The vibration modes of Raman spectra were characteristic of composition-dependent disordered solid solutions with decreasing wavenumbers as x increased. Luminescence experiments were performed under UV-laser light irradiation. The energies of emission bands increased linearly with cadmium composition x. The integrated intensity of luminescence reached a maximum value for the substituted wolframite phase with composition x=0.8. - Graphical abstract: Luminescence on UV excitation (364.5 nm) of (1−x)CaWO{sub 4−x}CdWO{sub 4} system, elaborated from coprecipitation technique at 1000 °C, with 0luminescence intensity for the composition x=0.8. - Highlights: • Solid solutions Ca{sub 1−x}Cd{sub x}WO{sub 4} are elaborated from coprecipitation technique. • The structures of two types of solid solutions are refined using Rietveld method. • A maximum of luminescence is obtained for an intermediate composition x=0.8.

Luminescent lanthanide coordination polymers synthesized via in-situ hydrolysis of dimethyl-3,4-furandicarboxylate

International Nuclear Information System (INIS)

Greig, Natalie E.; Einkauf, Jeffrey D.; Clark, Jessica M.; Corcoran, Eric J.; Karram, Joseph P.; Kent, Charles A.; Eugene, Vadine E.; Chan, Benny C.; Lill, Daniel T. de

2015-01-01

Dimethyl-3,4-furandicarboxylate undergoes hydrolysis under hydrothermal conditions with lanthanide (Ln) ions to form two-dimensional coordination polymers, [Ln(C 6 H 2 O 5 )(C 6 H 3 O 5 )(H 2 O)] n (Ln=Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu). The resulting materials exhibit luminescent properties with quantum yields and lifetimes for the Eu(III) and Tb(III) compounds of 1.1±0.3% and 0.387±0.0001 ms, and 3.3±0.8% and 0.769±0.006 ms, respectively. Energy values for the singlet and triplet states were determined for dimethyl-3,4-furandicarboxylate and 3,4-furandicarboxylic acid. Excited state dynamics and structural features are examined to explicate the reported quantum yields. A series of other FDC structures is briefly presented. - Graphical abstract: A new two-dimensional coordination polymer derived from the in-situ hydrolysis of a furan dimethyl ester with lanthanide(III) ions was obtained in order to study its photophysical behavior when constructed from trivalent Eu and Tb. Quantum yields, lifetime measurements, and singlet/triplet state energies values were obtained. The nature of the material's excited state dynamics is examined and correlated to its structure in order to explain the overall luminescent efficiency of the system. - Highlights: • A new lanthanide–furandicarboxylate coordination polymer is presented. • Eu and Tb compounds display luminescent properties, albeit with low quantum yields. • Photophysical behavior explained through the compound's triplet state and structure. • Nonradiative deactivation of luminescence through high-energy oscillators was noted. • Molecular modeling of the organic moiety was conducted

Luminescent lanthanide coordination polymers synthesized via in-situ hydrolysis of dimethyl-3,4-furandicarboxylate

Energy Technology Data Exchange (ETDEWEB)

Greig, Natalie E.; Einkauf, Jeffrey D.; Clark, Jessica M.; Corcoran, Eric J.; Karram, Joseph P.; Kent, Charles A.; Eugene, Vadine E. [Department of Chemistry & Biochemistry, Florida Atlantic University, 777 Glades Road, Boca Raton, FL 33431 (United States); Chan, Benny C. [Department of Chemistry, The College of New Jersey, 2000 Pennington Road, Ewing, NJ 08628 (United States); Lill, Daniel T. de, E-mail: ddelill@fau.edu [Department of Chemistry & Biochemistry, Florida Atlantic University, 777 Glades Road, Boca Raton, FL 33431 (United States)

2015-05-15

Dimethyl-3,4-furandicarboxylate undergoes hydrolysis under hydrothermal conditions with lanthanide (Ln) ions to form two-dimensional coordination polymers, [Ln(C{sub 6}H{sub 2}O{sub 5})(C{sub 6}H{sub 3}O{sub 5})(H{sub 2}O)]{sub n} (Ln=Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu). The resulting materials exhibit luminescent properties with quantum yields and lifetimes for the Eu(III) and Tb(III) compounds of 1.1±0.3% and 0.387±0.0001 ms, and 3.3±0.8% and 0.769±0.006 ms, respectively. Energy values for the singlet and triplet states were determined for dimethyl-3,4-furandicarboxylate and 3,4-furandicarboxylic acid. Excited state dynamics and structural features are examined to explicate the reported quantum yields. A series of other FDC structures is briefly presented. - Graphical abstract: A new two-dimensional coordination polymer derived from the in-situ hydrolysis of a furan dimethyl ester with lanthanide(III) ions was obtained in order to study its photophysical behavior when constructed from trivalent Eu and Tb. Quantum yields, lifetime measurements, and singlet/triplet state energies values were obtained. The nature of the material's excited state dynamics is examined and correlated to its structure in order to explain the overall luminescent efficiency of the system. - Highlights: • A new lanthanide–furandicarboxylate coordination polymer is presented. • Eu and Tb compounds display luminescent properties, albeit with low quantum yields. • Photophysical behavior explained through the compound's triplet state and structure. • Nonradiative deactivation of luminescence through high-energy oscillators was noted. • Molecular modeling of the organic moiety was conducted.

Luminescence properties of pure and Eu-doped SrI{sub 2} crystals purified by a “Liquinert” process and grown by vertical Bridgman method

Energy Technology Data Exchange (ETDEWEB)

Kawai, Taketoshi, E-mail: buri@p.s.osakafu-u.ac.jp [Osaka Prefecture University, Gakuen-cho 1-1, Naka-ku, Sakai, Osaka 599-8531 (Japan); Sakuragi, Shiro; Hashimoto, Satoshi [Union Materials Inc. 1640 Oshido, Tone-machi, Ibaraki 300-1602 (Japan)

2016-08-15

We have prepared high quality crystals of pure SrI{sub 2} and Eu-doped SrI{sub 2} by our original “Liquinert” process and investigated their luminescence properties. Under the excitation with the 193 nm light of an ArF excimer laser, which corresponds to the wavelength above the bandgap of SrI{sub 2} bulk crystals, the pure and Eu doped SrI{sub 2} crystals exhibit no luminescence band related to defects or impurities around 560 nm. This fact indicates that the crystals prepared by the “Liquinert” process contain lower defects and/or impurities. When the Eu-doped SrI{sub 2} crystals are excited with the 325 nm light of a He–Cd laser, only the luminescence band due to the 5d→4f transition in the Eu{sup 2+} ions is observed around 425 nm. The 425 nm band observed at a forward configuration exhibits the shift to the longer wavelength side and the decrease of the luminescence intensity with increasing Eu concentration. The Eu concentration dependences of the peak wavelength and luminescence intensity are simulated on the basis of a simple self-absorption model. - Highlights: • Our original “Liquinert” process allows us to prepare high quality crystals of SrI{sub 2}. • No luminescence band related with impurities and/or defects is observed. • The 425 nm luminescence bands due to Eu{sup 2+} ions are affected by a self-absorption. • A simple self-absorption model reproduces the changes of the 425 nm bands.

High-efficient, bicolor-emitting GdVO_4:Dy"3"+ phosphor under near ultraviolet excitation

International Nuclear Information System (INIS)

Lu, Jinjin; Zhou, Jia; Jia, Huayu; Tian, Yue

2015-01-01

Bicolor emitting GdVO_4:Dy"3"+ phosphor with short columniation-shape was prepared via a simple co-precipitation process. The optimal doping concentration for obtaining maximal luminescent intensity was confirmed to be 0.3 mol% and the electric dipole–dipole interaction is responsible for concentration quenching of Dy"3"+ emission in GdVO_4 phosphor. In order to evaluate the luminescent performance of as-prepared phosphor, the luminescent efficiency and color coordinates were studied. The results show that luminescent efficiency of this phosphor is very high under near UV excitation and twice times higher than commercial Y_2O_2S:Eu"3"+ phosphor. In addition, the color coordinates for optimal Dy"3"+ concentration are (0.339, 0.379), which are close to equal energy point. Therefore, the GdVO_4:Dy"3"+ phosphor may have potential application for solid state lighting.

Synthesis and characterization of lanthanide-based luminescent nanoparticles: toward new bio-labels

International Nuclear Information System (INIS)

Lechevallier, Severine

2010-01-01

This work deals with the development of luminescent nanoparticles (NPs) suitable as bio-labels. Inorganic NPs have been synthesized, in which luminescent ion (Eu 3+ in most of cases) is substituting ions of the oxide host matrix. NPs of Ln(OH)CO 3 :Eu 3+ (Ln = Y or Gd), Ln 2 O 3 :Eu 3+ , Ln 2 O 2 S:Eu 3+ and SiO 2 :Eu 3+ have been characterized by the way of TGA, WAXS-XRD, TEM, IR and photoluminescence (PL) techniques. The controlled precipitation using urea as precipitating agent is the way chosen and optimized to obtain spherical and monodispersed in size (150±15 nm) NPs. These particles of amorphous lanthanide hydroxycarbonate can directly be used as luminescent bio-labels or after their conversion in oxide or oxi-sulfide. For the silica particles, the synthesis by aerosol pyrolysis has been used. The obtained particles are spherical with a main diameter of 350 nm. In a second step, the surface of the inorganic NPs has been modified, in order to graft amino-reactive functions. Several modification ways have been explored: with APTES (aminopropyltriethoxysilane), with TEOS (tetra-ethoxysilane) and then APTES, or with a TEOS/APTES mixture. The same characterizations techniques have been applied to the modified particles, and chemical analysis, solid state NMR and XPS. DLS and ζ-potential of the NPs dispersed in water have also been measured. These analyses have been completed by the evaluation of the number of accessible amine functions by coupling with FITC (fluorescein isothiocyanate). The direct modification of oxides (Y 2 O 3 or Gd 2 O 3 ) with APTES is the best way, and an homogenous layer of 1 nm with a high number of accessible amine can be graft. Finally, to move toward luminescent bio-labelling in biological medium, the luminescence of the NPs has been observed and analyzed using: - A spectro-fluorimeter, after their dispersion in water; - A fluorescence microscope, on glass slides, under broad band excitation; - A confocal microscope, under laser

Synthesis of porous silicon nano-wires and the emission of red luminescence

International Nuclear Information System (INIS)

Congli, Sun; Hao, Hu; Huanhuan, Feng; Jingjing, Xu; Yu, Chen; Yong, Jin; Zhifeng, Jiao; Xiaosong, Sun

2013-01-01

This very paper is focusing on the characterization of porous silicon nano-wires prepared via a two-step route, the electroless chemical etching and the following post-treatment of HF/HNO 3 solution. Hence, scanning electron microscopy, transmission electron microscopy and confocal fluorescence microscopy are employed for this purpose. From the results of experiments, one can find that the as-prepared silicon nano-wire is of smooth surface and that no visible photo-luminescence emission could be seen. However, the porous structure can be found in the silicon nano-wire treated with HF/HNO 3 solution, and the clear photo-luminescence emission of 630 nm can be recorded with a confocal fluorescence microscope. The transmission electron microscopy test tells that the porous silicon nano-wire is made up of a porous crystalline silicon nano-core and a rough coating of silicon oxide. Besides, based on the post-HF- and -H 2 O 2 - treatments, the emission mechanism of the red luminescence has been discussed and could be attributed to the quantum confinement/luminescence center model which could be simply concluded as that the electron–hole pairs are mainly excited inside the porous silicon nano-core and then tunneling out and recombining at the silicon oxide coating.

Synthesis of porous silicon nano-wires and the emission of red luminescence

Energy Technology Data Exchange (ETDEWEB)

Congli, Sun [School of Materials Science and Engineering, Sichuan University (China); Hao, Hu [National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, Sichuan (China); Huanhuan, Feng; Jingjing, Xu; Yu, Chen; Yong, Jin; Zhifeng, Jiao [School of Materials Science and Engineering, Sichuan University (China); Xiaosong, Sun, E-mail: sunxs@scu.edu.cn [School of Materials Science and Engineering, Sichuan University (China)

2013-10-01

This very paper is focusing on the characterization of porous silicon nano-wires prepared via a two-step route, the electroless chemical etching and the following post-treatment of HF/HNO{sub 3} solution. Hence, scanning electron microscopy, transmission electron microscopy and confocal fluorescence microscopy are employed for this purpose. From the results of experiments, one can find that the as-prepared silicon nano-wire is of smooth surface and that no visible photo-luminescence emission could be seen. However, the porous structure can be found in the silicon nano-wire treated with HF/HNO{sub 3} solution, and the clear photo-luminescence emission of 630 nm can be recorded with a confocal fluorescence microscope. The transmission electron microscopy test tells that the porous silicon nano-wire is made up of a porous crystalline silicon nano-core and a rough coating of silicon oxide. Besides, based on the post-HF- and -H{sub 2}O{sub 2}- treatments, the emission mechanism of the red luminescence has been discussed and could be attributed to the quantum confinement/luminescence center model which could be simply concluded as that the electron–hole pairs are mainly excited inside the porous silicon nano-core and then tunneling out and recombining at the silicon oxide coating.

Luminescence detection of phase transitions in crystals and nanoparticle inclusions

International Nuclear Information System (INIS)

Townsend, P. D.; Yang, B.; Wang, Y.

2008-01-01

Luminescence measurements are extremely sensitive to variations in structural environment and thus have the potential to probe distortions of fluorescence sites. Changes can be monitored via luminescence efficiency, emission spectra or excited state lifetimes and these factors are influenced by the local neighbourhood around the emission site, and therefore by structure, composition, pressure and temperature. A rarely exploited approach for condensed matter has been to use the changes in luminescence responses during heating or cooling of a material to provide a rapid survey to detect the presence of phase transitions. One can often differentiate between bulk and surface effects by contrasting results from radioluminescence for bulk responses, and cathodoluminescence or photoluminescence for surface effects. One expects that discontinuous changes in optical parameters occur during temperature changes through phase transitions of insulating materials. In practice, optical signals also exist from surface states of fullerenes and high temperature superconductors etc which identify the presence of structural or superconducting transitions. Numerous examples are cited which match standard documented transitions. Interestingly many examples show the host signals are strongly sensitive to impurity phase transitions from inclusions such as nanoparticles of water, N 2 , O 2 or CO 2 . Recent luminescence data reveal many examples of new transitions, hysteresis and irreversible changes. The signals equally respond to relaxations of a structure and surprisingly indicate that in some materials, such as SrTiO 3 or ZnO, ion implantation of the surface triggers relaxations and phase changes throughout the bulk of the material. Luminescence routes to detect phase transitions are powerful tools but have a tiny literature and so the subject is ideal for rapid exploitation and development. (Author)

Luminescent ultra-small gold nanoparticles obtained by ion implantation in silica

Energy Technology Data Exchange (ETDEWEB)

Cesca, T., E-mail: tiziana.cesca@unipd.it [Department of Physics and Astronomy and CNISM, University of Padova, via Marzolo 8, I-35131 Padova (Italy); Maurizio, C.; Kalinic, B.; Scian, C. [Department of Physics and Astronomy and CNISM, University of Padova, via Marzolo 8, I-35131 Padova (Italy); Trave, E.; Battaglin, G. [Department of Molecular Sciences and Nanosystems, Ca’ Foscari University of Venice, Dorsoduro 2137, I-30123 Venice (Italy); Mazzoldi, P.; Mattei, G. [Department of Physics and Astronomy and CNISM, University of Padova, via Marzolo 8, I-35131 Padova (Italy)

2014-05-01

The room temperature photoluminescence properties of ultra-small Au nanoclusters (made by 5–10 atoms) obtained by ion implantation in silica are presented. The results show a broad and intense luminescent emission in three different spectral regions around 750 nm, 980 nm and 1150 nm. The luminescence properties of the molecule-like Au clusters have been also correlated to the energy-transfer process to Er{sup 3+} ions in Au–Er co-implanted silica samples. A partial quenching of the 980 nm component is observed due to the Er{sup 3+} absorption level at 980 nm that acts as a de-excitation channel through which the photon energy is transferred from the Au nanoclusters to the Er ions, eventually producing the Er-related emission at 1.5 microns.

Optical and magnetic properties of new luminescent inorganic materials

International Nuclear Information System (INIS)

Acevedo, R; Hurtado, O.F; Poblete, V; Navarro, G

1999-01-01

The theoretical and experimental study of radiative and non radiative processes in luminescent inorganic materials is a permanent topic of interest in lineal and non lineal physics. This article aims to present a review and update of the mechanistic aspects associated with spectral intensities in stoichiometric cubic crystals type elpasolite (Cs-2NaLnZ-6), where Ln 3+ is a positive trivalent lanthanide and Z represents a halogen, essentially fluorine, chlorine and bromine, which belong to the spatial Fm3m group. From a theoretical point of view we will be interested in focusing our attention on cutting edge topics such as: the preparation of new models and calculus formalisms for the case of electronic excitations prohibited by parity and electronic spin. We wish to show the set of different complementary and competitive processes that define the relative force values of the electric oscillator and the magnetic one for cubic crystals. We will illustrate our work with a novel system, Cs-2NaEuCI-6, which has theoretical and experimental complexities with unsuspected characteristics

Luminescence and energy transfer of Ce{sup 3+} and Pr{sup 3+} in LaBSiO{sub 5}

Energy Technology Data Exchange (ETDEWEB)

Zhou, Lei; Zhou, Weijie; Shi, Rui; Liu, Chunmeng [MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, KLGHEI of Environment and Energy Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China); Huang, Yan; Tao, Ye [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100039 (China); Liang, Hongbin, E-mail: cesbin@mail.sysu.edu.cn [MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, KLGHEI of Environment and Energy Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China)

2016-09-15

Ce{sup 3+}, Pr{sup 3+} singly doped and Ce{sup 3+}–Pr{sup 3+} doubly doped LaBSiO{sub 5} phosphors were prepared by a high-temperature solid state reaction route. The synchrotron radiation VUV–UV excitation spectra of Ce{sup 3+} and Pr{sup 3+} were measured and the luminescence properties were discussed. The band gap of host compound LaBSiO{sub 5} was estimated from the VUV excitation spectrum of sample activated with Gd{sup 3+}. Furthermore, the influence of temperature on luminescence of Ce{sup 3+} was discussed and the activation energy for thermal quenching was evaluated. The occurrence of energy transfer from excited 5d states of Pr{sup 3+} to Ce{sup 3+} was confirmed by the emission spectra of co-doped samples La{sub 0.99−x}Pr{sub x}Ce{sub 0.01}BSiO{sub 5} and La{sub 0.995−x}Pr{sub 0.005}Ce{sub x}BSiO{sub 5} with different x values.

Charge-transfer state excitation as the main mechanism of the photodarkening process in ytterbium-doped aluminosilicate fibres

Energy Technology Data Exchange (ETDEWEB)

Bobkov, K K; Rybaltovsky, A A; Vel' miskin, V V; Likhachev, M E; Bubnov, M M; Dianov, E M [Fiber Optics Research Center, Russian Academy of Sciences, Moscow (Russian Federation); Umnikov, A A; Gur' yanov, A N; Vechkanov, N N [G.G.Devyatykh Institute of Chemistry of High-Purity Substances, Russian Academy of Sciences, Nizhnii Novgorod (Russian Federation); Shestakova, I A [Open Joint-Stock Company M.F. Stel' makh Polyus Research Institute, Moscow (Russian Federation)

2014-12-31

We have studied photodarkening in ytterbium-doped fibre preforms with an aluminosilicate glass core. Analysis of their absorption and luminescence spectra indicates the formation of stable Yb{sup 2+} ions in the glass network under IR laser pumping at a wavelength λ = 915 nm and under UV irradiation with an excimer laser (λ = 193 nm). We have performed comparative studies of the luminescence spectra of the preforms and crystals under excitation at a wavelength of 193 nm. The mechanism behind the formation of Yb{sup 2+} ions and aluminium – oxygen hole centres (Al-OHCs), common to ytterbium-doped YAG crystals and aluminosilicate glass, has been identified: photoinduced Yb{sup 3+} charge-transfer state excitation. (optical fibres)

Luminescent properties of LuAG:Yb and YAG:Yb single crystalline films grown by Liquid Phase Epitaxy method

International Nuclear Information System (INIS)

Zorenko, Yu; Zorenko, T.; Gorbenko, V.; Voznyak, T.; Popielarski, P.; Batentschuk, M.; Osvet, A.; Brabec, Ch; Kolobanov, V.; Spasky, D.; Fedorov, A.

2016-01-01

In this work, investigation of the spectroscopic parameters of the luminescence of Yb"3"+ ions in single crystalline films of Lu_3Al_5O_1_2 and Y_3Al_5O_1_2 garnets was performed using the synchrotron radiation excitation with the energy in the range of Yb"3"+ charge transitions (CT), exciton range and the onset of interband transitions of these garnets. The basic spectroscopic parameters of the Yb"3"+ CT luminescence in LuAG and YAG hosts were determined and summarized with taking into account the differences in the band gap structure of these garnets. - Highlights: • Single crystalline films of Yb doped LuAG and YAG garnets were grown by LPE method. • Yb"3"+ luminescence of LuAG:Yb and YAG:Yb film were studied using synchrotron radiation. • Basic parameters of Yb"3"+ charge transfer luminescence in LuAG and YAG were determined.

Kinetics of non-equilibrium processes in non-linear crystals of lithium borates excited with synchrotron radiation

CERN Document Server

Ogorodnikov, I N; Isaenko, L I; Zinin, E I; Kruzhalov, A V

2000-01-01

The paper presents the results of a study of the LiB sub 3 O sub 5 and Li sub 2 B sub 4 O sub 7 crystals by the use of the luminescent spectroscopy with the sub-nanosecond time resolution under excitation of the high-power synchrotron radiation. The commonness in the origin of the non-equilibrium processes in these crystals as well as the observed differences in the luminescence manifestations is discussed.

Kinetics of non-equilibrium processes in non-linear crystals of lithium borates excited with synchrotron radiation

Energy Technology Data Exchange (ETDEWEB)

Ogorodnikov, I.N. E-mail: ogo@dpt.ustu.ru; Pustovarov, V.A.; Isaenko, L.I.; Zinin, E.I.; Kruzhalov, A.V

2000-06-21

The paper presents the results of a study of the LiB{sub 3}O{sub 5} and Li{sub 2}B{sub 4}O{sub 7} crystals by the use of the luminescent spectroscopy with the sub-nanosecond time resolution under excitation of the high-power synchrotron radiation. The commonness in the origin of the non-equilibrium processes in these crystals as well as the observed differences in the luminescence manifestations is discussed.

Eu/Tb ions co-doped white light luminescence Y2O3 phosphors

International Nuclear Information System (INIS)

Tu Dong; Liang Yujun; Liu Rong; Li Daoyi

2011-01-01

Y 2 O 3 :Eu 3+ , Tb 3+ phosphors with white emission are prepared with different doping concentration of Eu 3+ and Tb 3+ ions and synthesizing temperatures from 750 to 950 deg. C by the co-precipitation method. The resulted phosphors were characterized by X-ray diffraction (XRD) and photoluminescence (PL) spectroscopy. The results of XRD indicate that the crystallinity of the synthesized samples increases with enhancing the firing temperature. The photoluminescence spectra indicate the Eu 3+ and Tb 3+ co-doped Y 2 O 3 phosphors show five main emission peaks: three at 590, 611 and 629 nm originate from Eu 3+ and two at 481 and 541 nm originate from Tb 3+ , under excitation of 250-320 nm irradition. The white light luminescence color could be changed by varying the excitation wavelength. Different concentrations of Eu 3+ and Tb 3+ ions were induced into the Y 2 O 3 lattice and the energy transfer from Tb 3+ →Eu 3+ ions in these phosphors was found. The Commission International de l'Eclairage (CIE) chromaticity shows that the Y 2 O 3 :Eu 3+ , Tb 3+ phosphors can obtain an intense white emission. - Highlights: → Novel phosphors Y 2 O 3 :Eu 3+ , Tb 3+ have been synthesized by co-precipitation method. → Samples emit white light with excellent color coordinates under UV excitation. → Luminescence color could be changed by varying the excitation wavelength. → Energy transfer from Tb 3+ →Eu 3+ ions in these phosphors was found.

Multichannel Luminescence Properties of Mixed-Valent Eu2+/Eu3+ Coactivated SrAl3BO7 Nanocrystalline Phosphors for Near-UV LEDs.

Science.gov (United States)

Liu, Xiaoming; Xie, Weijie; Lü, Ying; Feng, Jingchun; Tang, Xinghua; Lin, Jun; Dai, Yuhua; Xie, Yu; Yan, Liushui

2017-11-20

Up to now, orchestrating the coexistence of Eu 2+ and Eu 3+ activators in a single host lattice has been an extremely difficult task, especially for the appearance of the characteristic emission of Eu 2+ and Eu 3+ in order to generate white light. Nevertheless, here we demonstrate a new Eu 2+ /Eu 3+ coactivated SrAl 3 BO 7 nanocrystalline phosphor with abundant and excellent multichannel luminescence properties. A series of Eu 2+ /Eu 3+ coactivated SrAl 3 BO 7 nanocrystalline phosphors were prepared through a Pechini-type sol-gel method followed by a reduction process. With excitation of UV/NUV light, the prepared SrAl 3 BO 7 :Eu 2+ ,Eu 3+ phosphors show not only the characteristic f-f transitions of Eu 3+ ion ( 5 D J → 7 F J,J' , J, J' = 0-3), but also the 5d → 4f transitions of Eu 2+ ion with comparable intensity from 400 to 700 nm in the whole visible spectral region. The luminescence color of the SrAl 3 BO 7 :Eu 2+ ,Eu 3+ phosphor can be tuned from blue, blue-green, white, and orange to orange-red by changing the excitation wavelength, the overall doping concentration of europium ions (Eu 2+ , Eu 3+ ), and the relative ratio of Eu 2+ to Eu 3+ ions to some extent. A single-phase white-light emission has been realized in SrAl 3 BO 7 :Eu 2+ ,Eu 3+ phosphor. The obtained SrAl 3 BO 7 :Eu 2+ ,Eu 3+ phosphor has potential application in the area of NUV white-light-emitting diodes.

Output pressure and harmonic characteristics of a CMUT as function of bias and excitation voltage

DEFF Research Database (Denmark)

Lei, Anders; Diederichsen, Søren Elmin; Hansen, Sebastian Molbech

2015-01-01

of the transmitted signal. The generation of intrinsic harmonics by the CMUT can be minimized by decreasing the excitation signal. This, however, leads to lower fundamental pressure which limits the desired generation of harmonics in the medium. This work examines the output pressure and harmonic characteristics...... of a CMUT as function of bias and excitation voltage. The harmonic to fundamental ratio of the surface pressures declines for decreasing excitation voltage and increasing bias voltage. The ratio, however, becomes unchanged for bias levels close to the pull-in voltage. The harmonic limitations of the CMUT...

Cathodoluminescence imaging and spectroscopy of excited states in InAs self-assembled quantum dots

International Nuclear Information System (INIS)

Khatsevich, S.; Rich, D.H.; Kim, Eui-Tae; Madhukar, A.

2005-01-01

We have examined state filling and thermal activation of carriers in buried InAs self-assembled quantum dots (SAQDs) with excitation-dependent cathodoluminescence (CL) imaging and spectroscopy. The InAs SAQDs were formed during molecular-beam epitaxial growth of InAs on undoped planar GaAs (001). The intensities of the ground- and excited-state transitions were analyzed as a function of temperature and excitation density to study the thermal activation and reemission of carriers. The thermal activation energies associated with the thermal quenching of the luminescence were measured for ground- and excited-state transitions of the SAQDs, as a function of excitation density. By comparing these activation energies with the ground- and excited-state transition energies, we have considered various processes that describe the reemission of carriers. Thermal quenching of the intensity of the QD ground- and first excited-state transitions at low excitations in the ∼230-300-K temperature range is attributed to dissociation of excitons from the QD states into the InAs wetting layer. At high excitations, much lower activation energies of the ground and excited states are obtained, suggesting that thermal reemission of single holes from QD states into the GaAs matrix is responsible for the observed temperature dependence of the QD luminescence in the ∼230-300-K temperature range. The dependence of the CL intensity of the ground-and first excited-state transition on excitation density was shown to be linear at all temperatures at low-excitation density. This result can be understood by considering that carriers escape and are recaptured as excitons or correlated electron-hole pairs. At sufficiently high excitations, state-filling and spatial smearing effects are observed together with a sublinear dependence of the CL intensity on excitation. Successive filling of the ground and excited states in adjacent groups of QDs that possess different size distributions is assumed to

Synthesis and characterization of the europium (III) complex as an organic luminescent material

Energy Technology Data Exchange (ETDEWEB)

Zhuo Zuliang; Zhang Fujun; Xu Zheng; Lu Lifang; Li Junming; Wang Yongsheng [Key Laboratory of Luminescence and Optical Information (Beijing Jiaotong University), Ministry of Education, Beijing 100044 (China); Lv Yuguang, E-mail: fjzhang@bjtu.edu.c [The Provincial Key Laboratory of Biomaterials, College of Chemistry and Pharmacy, Jiamusi University, Jiamusi 154007 (China)

2010-11-15

The red emission organic material Eu(coumarin){sub 3{center_dot}}2H{sub 2}O complex was synthesized and its morphology, energy level alignment and luminescence characteristics were studied by using scanning electron microscopy, Fourier transform infrared spectra, cyclic voltammetry and ultraviolet-visible absorption spectra and fluorescence spectra. Eu(coumarin){sub 3{center_dot}}2H{sub 2}O shows bright red emission originating from Eu{sup 3+} ions under 345 nm light excitation. The luminescence lifetime of Eu{sup 3+} in this complex is about 580 {mu}s. To improve the quality of Eu(coumarin){sub 3{center_dot}}2H{sub 2}O thin films, Eu(coumarin){sub 3{center_dot}}2H{sub 2}O was doped with a poly(N-vinylcarbazole) (PVK) solution. The organic materials 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and aluminum quinoline (Alq{sub 3}) were used as hole-blocking and electron-transporting layers in our fabricated electroluminescence (EL) devices on indium tin oxide (ITO) substrates, respectively. The EL devices ITO/poly-(3,4-ethylenedioxythiophene):poly-(styrenesulphonic acid) (PEDOT:PSS)/emitting layer (PVK:Eu)/BCP/Alq{sub 3}/Al were fabricated, and EL spectra were measured under different driving voltages. There is one emission peaking at 490 nm in addition to the characteristic emission peaks of Eu{sup 3+}, which should be attributed to the spectral overlap between the PVK emission and electroplex emission originating from PVK and BCP interfaces. This explanation can be positively supported by the dependence of the EL spectral variation of ITO/ PVK/BCP/Alq{sub 3}/Al devices on the driving voltage.

Synthesis of novel Dy3+ activated phosphate phosphors for NUV excited LED

International Nuclear Information System (INIS)

Shinde, K.N.; Dhoble, S.J.; Kumar, Animesh

2011-01-01

The new trivalent dysprosium activated X 6 AlP 5 O 20 (where X=Sr, Ba, Ca and Mg) phosphors were prepared by the combustion method. The prepared phosphors are characterized by XRD, photoluminescence and SEM techniques. Excited by 350 nm near-ultraviolet (NUV) light, the phosphors show an efficient blue and yellow band emissions, which originates from the 4 F 9/2 → 6 H 15/2 and 4 F 9/2 → 6 H 13/2 transitions of Dy 3+ ion, respectively. The excitation spectra of the phosphors are broadband extending from 340 to 400 nm, which are characteristics of NUV excited LED. The effect of the Dy 3+ concentration on the luminescence properties of X 6 AlP 5 O 20 :Dy 3+ (where X=Sr, Ba, Ca and Mg) phosphors is studied. Ca 6 AlP 5 O 20 phosphors show strong PL emission intensity around 25 times more as compared to Ba 6 AlP 5 O 20 , Sr 6 AlP 5 O 20 and Mg 6 AlP 5 O 20 phosphors. The investigated prepared phosphors are suitable for a NUV excited LED. - Research highlights: → Novel Dy 3+ activated X 6 AlP 5 O 20 (where X=Sr,Ba,Ca and Mg) phosphors were prepared by combustion method which is very low cost and time saving synthesis method. → The excitation spectra of the phosphors are broad band extending from 340 nm to 400 nm, which is characteristics of NUV excited LED. → PL emission spectra show two emissions (485 and 573 nm) and X 6 AlP 5 O 20 :Dy 3+ 0.5 mol% (where X=Sr,Ba,Ca and Mg) phosphors shows strongest PL emission intensity. → SEM analysis indicates that phosphor particles have irregular shape, porous morphology and less than 3-4 μm in size, which is suitable for the solid state lighting (coating purpose).

Morphology and luminescence characteristics of combustion synthesized Y{sub 2}O{sub 3}: (Eu, Dy, Tb) nanoparticles with various amino-acid fuels

Energy Technology Data Exchange (ETDEWEB)

Mukherjee, S.; Sudarsan, V. [Chemistry Division Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Sastry, P.U.; Patra, A.K. [Solid State Physics Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Tyagi, A.K., E-mail: aktyagi@barc.gov.in [Chemistry Division Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India)

2014-01-15

Y{sub 2}O{sub 3} nanoparticles doped with Dy{sup 3+}, Eu{sup 3+} and Tb{sup 3+} together were prepared by the gel combustion method using a variety of amino acids namely, glycine, phenyl alanine, arginine, glutamic and aspartic acids. Number of carboxylate groups present in the amino acids used for combustion reaction was found to have strong influence on powder characteristics as well as luminescence from the samples. Based on small angle X-ray scattering studies, it is inferred that the nanoparticles prepared by using glycine and arginine as the fuels have smooth surface compared to those prepared using other amino acids. For the nanoparticles prepared using glutamic and aspartic acids, there exist a diffused pore-grain interface due to the lesser extent of heat generated in the reaction which leads to smaller particle size, poor crystallinity and improper burning of the organic materials. Lower surface area and smooth surface of the nanoparticles prepared using glycine leads to their improved luminescence properties. -- Highlights: • Surface smoothness of Y{sub 2}O{sub 3} (Dy, Eu, Tb) nanoparticles vary with amino acids. • Optimum luminescence intensity is observed when glycine is used as the fuel. • Diffused pore grain interface when glutamic and aspartic acids are used as fuels.

Luminescence from cavitation bubbles deformed in uniform pressure gradients

Science.gov (United States)

Supponen, Outi; Obreschkow, Danail; Kobel, Philippe; Farhat, Mohamed

2017-09-01

Presented here are observations that demonstrate how the deformation of millimetric cavitation bubbles by a uniform pressure gradient quenches single-collapse luminescence. Our innovative measurement system captures a broad luminescence spectrum (wavelength range, 300-900 nm) from the individual collapses of laser-induced bubbles in water. By varying the bubble size, driving pressure, and perceived gravity level aboard parabolic flights, we probed the limit from aspherical to highly spherical bubble collapses. Luminescence was detected for bubbles of maximum radii within the previously uncovered range, R0=1.5 -6 mm, for laser-induced bubbles. The relative luminescence energy was found to rapidly decrease as a function of the bubble asymmetry quantified by the anisotropy parameter ζ , which is the dimensionless equivalent of the Kelvin impulse. As established previously, ζ also dictates the characteristic parameters of bubble-driven microjets. The threshold of ζ beyond which no luminescence is observed in our experiment closely coincides with the threshold where the microjets visibly pierce the bubble and drive a vapor jet during the rebound. The individual fitted blackbody temperatures range between Tlum=7000 and Tlum=11 500 K but do not show any clear trend as a function of ζ . Time-resolved measurements using a high-speed photodetector disclose multiple luminescence events at each bubble collapse. The averaged full width at half-maximum of the pulse is found to scale with R0 and to range between 10 and 20 ns.

Thermally and optically stimulated luminescence of early medieval blue-green glass mosaics

Energy Technology Data Exchange (ETDEWEB)

Galli, A. E-mail: anna.galli@mater.unimib.it; Martini, M.; Montanari, C.; Sibilia, E

2004-12-01

The preliminary results of a study related to luminescent mechanisms in glass mosaic tesserae are presented. The samples came from a medieval glass deposit found during archaeological excavations in the S. Lorenzo Church in Milan. Energy Dispersive X-rays Fluorescence (EDXRF) measurements were performed to obtain information on the elemental composition of the materials. Thermally Stimulated Luminescence (TSL, both conventional and wavelength resolved) and Optically Stimulated Luminescence (OSL) analyses allowed to get information about traps and luminescence centres. The observed luminescence characteristics were close to that of quartz, showing the presence of an easy to bleach trap (300 deg. C, 1.95 eV) and of a hard to bleach trap (350 deg. C, 2.20 eV); charge transfer phenomena, involving the low-temperature peaks have been observed. There is a strong indication that the easy to bleach traps are responsible for both OSL and TSL emission at 300 deg. C.

Thermally and optically stimulated luminescence of early medieval blue-green glass mosaics

International Nuclear Information System (INIS)

Galli, A.; Martini, M.; Montanari, C.; Sibilia, E.

2004-01-01

The preliminary results of a study related to luminescent mechanisms in glass mosaic tesserae are presented. The samples came from a medieval glass deposit found during archaeological excavations in the S. Lorenzo Church in Milan. Energy Dispersive X-rays Fluorescence (EDXRF) measurements were performed to obtain information on the elemental composition of the materials. Thermally Stimulated Luminescence (TSL, both conventional and wavelength resolved) and Optically Stimulated Luminescence (OSL) analyses allowed to get information about traps and luminescence centres. The observed luminescence characteristics were close to that of quartz, showing the presence of an easy to bleach trap (300 deg. C, 1.95 eV) and of a hard to bleach trap (350 deg. C, 2.20 eV); charge transfer phenomena, involving the low-temperature peaks have been observed. There is a strong indication that the easy to bleach traps are responsible for both OSL and TSL emission at 300 deg. C

Yb3+,Er3+,Eu3+-codoped YVO4 material for bioimaging with dual mode excitation

International Nuclear Information System (INIS)

Thao, Chu Thi Bich; Huy, Bui The; Sharipov, Mirkomil; Kim, Jin-Ik.; Dao, Van-Duong; Moon, Ja-Young; Lee, Yong-Ill

2017-01-01

We propose an efficient bioimaging strategy using Yb 3+ ,Er 3+ ,Eu 3+ -triplet doped YVO 4 nanoparticles which were synthesized with polymer as a template. The obtained particles possess nanoscale, uniform, and flexible excitation. The effect of Eu 3+ ions on the luminescence properties of YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ was investigated. The upconversion mechanism of the prepared material was also discussed. The structure and optical properties of the prepared material were characterized by using X-ray diffraction (XRD), Fourier-transform IR spectroscopy (FTIR), scanning electron microscopy (SEM), Transmission electron microscopy (TEM) upconversion and photoluminescence spectra. The Commission International de I′Eclairage (CIE) chromaticity coordinates was investigated to confirm the performance of color luminescent emission. The prepared YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ nanoparticles could be easily dispersed in water by surface modification with cysteine (Cys) and glutathione (GSH). The aqueous dispersion of the modified YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ exhibits bright upconversion and downconversion luminescence and has been applied for bioimaging of HeLa cells. Our developed material with dual excitation offers a promising advance in bioimaging. - Highlights: • Prepared particles possess nanoscale size, uniform, and larger scale. • The material exhibits strong emission under dual mode excitations. • The surface material has been applied for bioimaging of HeLa cell. • Low cytotoxicity, no auto-fluorescence

Exciton luminescence in CdxMn1-xTe compounds

International Nuclear Information System (INIS)

Caraman, M.; Gashin, P.; Metelitsa, Snejana; Nicorici, Valentina; Nicorici, A.

2002-01-01

The Cd x Mn 1-x Te (0.5 7 W/cm 2 . The luminescence spectra were observed at 78 K. The results of the study had shown that the presence of relatively narrow luminescence peaks localized in the region of the fundamental absorption edge is characteristic for these spectra and for the majority of the crystals a wide maximum in the long wavelength region is observed. The luminescence maxima with an accuracy of ∼ 5 meV correspond to the resonance energy of the excitons of the state with n=1 determined from the absorption spectra. Hence, these maxima can be considered as exciton luminescence stimulated either by the excitons of the state n=1 or bounded to the exciton ionization centers. From the analysis of the absorption and exciton luminescence spectra one can make a conclusion about the fact that the homogeneity extent of the crystals decreases from CdTe to the compounds with x= 0.8 - 0.7 and slightly increases at the x decrease to 0.5. The exciton luminescence lines in CdTe and Cd 0.99 Mn 0.01 Te crystals is shifting by 7 - 10 meV relatively to the lines of free excitons absorption. This fact is explained by the fact that in these crystals, probably, excitons bounding to the lattice inherited defects with the binding energy of 7 - 10 meV participate in the luminescence. In the long wavelength region a wide peak is observed on which the impurity lines are not displayed. In the luminescence spectra of CdTe with 0.1%. As crystals three maxima at 1.51 eV, 1.46 eV and 1.42 eV are revealed. For pure CdTe the maximum at 1.4 eV is also revealed. These maxima are explained by the luminescence through the recombination levels localized at 0.46 eV. (authors)

Luminescence thermometry with Eu{sup 3+} doped GdAlO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Lojpur, Vesna, E-mail: vesna.lojpur@yahoo.com; Ćulubrk, Sanja; Medić, Mina; Dramicanin, Miroslav

2016-02-15

Eu{sup 3+} doped GdAlO{sub 3} powder synthesized by solid state reaction was investigated for application in luminescence thermometry. Phase composition of material was confirmed by X-ray powder diffraction analysis. The photoluminescence emission spectra were collected under excitation of 399 nm, while elevating the temperature of the sample from the room temperature to 793 K. Emissions from {sup 5}D{sub 1}→{sup 7}F{sub 1} and {sup 5}D{sub 0}→{sup 7}F{sub 2} characteristic transitions of Eu{sup 3+} ions are selected for the temperature-dependence study using the fluorescence intensity ratio method. Emission decay curves measured at the strongest emission peak centered at 614 nm were recorded in a same temperature range. Data analysis showed that thermometry by fluorescence intensity ratio method can be used over the temperature region 293–793 K with the maximal relative sensitivity of 2.96% K{sup −1} (at 293 K). Temporal dependence of emission (lifetime) provides temperature sensing from 620 to 793 K with the maximal relative sensitivity of 2.28% K{sup −1}. - Highlights: • GdAlO{sub 3}: 4 at% of Eu{sup 3+} can be used for luminescence thermometry in the 293–793 K range. • Combined FIR and lifetime thermometry provide >0.5% K{sup −1} relative sensitivity. • Temperature dependence of lifetime is well described energy gap law model.

Upconversion luminescence resonance energy transfer-based aptasensor for the sensitive detection of oxytetracycline.

Science.gov (United States)

Zhang, Hui; Fang, Congcong; Wu, Shijia; Duan, Nuo; Wang, Zhouping

2015-11-15

In this work, a biosensor based on luminescence resonance energy transfer (LRET) from NaYF4:Yb,Tm upconversion nanoparticles (UCNPs) to SYBR Green I has been developed. The aptamers are covalently linked to UCNPs and hybridized with their complementary strands. The subsequent addition of SYBR Green allows SYBR Green I to insert into the formed double-stranded DNA (dsDNA) duplex and brings the energy donor and acceptor into close proximity, leading to the fluorescence of UCNPs transferred to SYBR Green I. When excited at 980 nm, the UCNPs emit luminescence at 477 nm, and this energy is transferred to SYBR Green I, which emits luminescence at 530 nm. In the presence of oxytetracycline (OTC), the aptamers prefer to bind to its corresponding analyte and dehybridize with the complementary DNA. This dehybridization leads to the liberation of SYBR Green I, which distances SYBR Green I from the UCNPs and recovers the UCNPs' luminescence. Under optimal conditions, a linear calibration is obtained between the ratio of I530 to I477 nm (I530/I477) and the OTC concentration, which ranges from 0.1 to 10 ng/ml with a limit of detection (LOD) of 0.054 ng/ml. Copyright © 2015 Elsevier Inc. All rights reserved.

Simple and rapid measurement of α-rays on smear samples using air luminescence

International Nuclear Information System (INIS)

Takiue, M.

1980-01-01

The α-activity collected on smear samples has been measured indirectly using an air luminescence counting method and a liquid scintillation spectrometer. In this method, air luminescence, attributed to the fluorescence emitted by nitrogen molecules excited by α-rays in air, serves to detect α-rays. Thus, sample preparation and α-ray measurement are simple and rapid, and moreover, no radioactive waste solution is produced. Taking into account a low background and a counting efficiency between 10 and 20%, it is estimated that the detectable limit for α-ray measurement is about 1 x 10 -7 μCi/cm 2 for loose contamination. This method is convenient to use in the routine analysis of α-ray-emitting nuclides on smear paper. (author)

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.

Changes in optically stimulated luminescent dosimeter (OSLD) dosimetric characteristics with accumulated dose

International Nuclear Information System (INIS)

Jursinic, Paul A.

2010-01-01

Purpose: A new type of in vivo dosimeter, an optically stimulated luminescent dosimeter (OSLD), has now become commercially available for clinical use. The OSLD is a plastic disk infused with aluminum oxide doped with carbon (Al 2 O 3 :C). Crystals of Al 2 O 3 :C, when exposed to ionizing radiation, store energy that is released as luminescence (420 nm) when the OSLD is illuminated with stimulation light (540 nm). The intensity of the luminescence depends on the dose absorbed by the OSLD and the intensity of the stimulation light. The effects of accumulated dose on OSLD response were investigated. Methods: The OSLDs used in this work were nanodot dosimeters, which were read with a MicroStar reader (Landauer, Inc., Glenwood, IL). Dose to the OSLDs was delivered by 6 MV x rays and gamma rays from Co-60 and Ir-192. The signal on the OSLDs after irradiation is removed by optical annealing with a 150 W tungsten-halogen lamp or a 14 W compact fluorescent lamp was investigated. Results: It was found that OSLD response to dose was supralinear and this response was altered with the amount of accumulated dose to the OSLD. The OSLD response can be modeled by a quadratic and an exponential equation. For accumulated doses up to 60 Gy, the OSLD sensitivity (counts/dose) decreases and the extent of supralinear increases. Above 60 Gy of accumulated dose the sensitivity increases and the extent of supralinearity decreases or reaches a plateau, depending on how the OSLDs were optically annealed. With preirradiation of OSLDs with greater than 1 kGy, it is found that the sensitivity reaches a plateau 2.5 folds greater than that of an OSLD with no accumulated dose and the supralinearity disappears. A regeneration of the luminescence signal in the dark after full optical annealing occurs with a half time of about two days. The extent of this regeneration signal depends on the amount of accumulated dose. Conclusions: For in vivo dosimetric measurements, a precision of ±0.5% can be

UV luminescence of dendrimer-encapsulated gold nanoclusters

Energy Technology Data Exchange (ETDEWEB)

Shim, Hyeong Seop; Kim, Jun Myung; Sohn, So Hyeong; Han, Noh Soo; Park, Seung Min [Dept. of Chemistry, Kyung Hee University, Seoul (Korea, Republic of)

2016-10-15

Size-dependent luminescence color is one of the interesting properties of metal nanocrystals, whose sizes are in the dimension of the Fermi wavelength of an electron. Despite the short Fermi wavelength of electrons in gold (-0.7 nm), luminescence of gold nanoclusters has been reported to range from the near-infrared to near-ultraviolet, depending on the number of atoms in the nanoclusters. The photoluminescence of G4-OH (Au) obtained by the excitation of 266 nm showed UV emission in addition to the well-known blue emission. The higher intensity and red-shifted emission of the gold nanoclusters was distinguished from the emission of dendrimers. The UV emission at 352 nm matched the emission energy of Au{sub 4} in the spherical jellium model, rather than the planar Au{sub 8}, which supported the emission of Au{sub 4} formed in G4-OH. Despite the change of [HAuCl{sub 4} ]/[G4-OH], the relative population between Au{sub 4} and Au{sub 8} was similar in G4-OH(Au), which indicated that the closed electronic and geometric structures stabilized the magic number of Au{sub 4}.

Luminescence properties of the Sm-doped borate glasses

International Nuclear Information System (INIS)

Kindrat, I.I.; Padlyak, B.V.; Drzewiecki, A.

2015-01-01

The optical absorption and photoluminescence (emission and excitation) spectra as well as decay kinetics of a series of the Sm-doped glasses with Li 2 B 4 O 7 , LiKB 4 O 7 , CaB 4 O 7 , and LiCaBO 3 compositions were investigated and analysed. The Li 2 B 4 O 7 :Sm, LiKB 4 O 7 :Sm, CaB 4 O 7 :Sm, and LiCaBO 3 :Sm glasses of high optical quality have been obtained from the corresponding polycrystalline compounds in the air atmosphere, using a standard glass technology. On the basis of electron paramagnetic resonance (EPR) and optical spectra analysis it was shown that the samarium impurity is incorporated into the glass network as Sm 3+ (4f 5 , 6 H 5/2 ) ions, exclusively. All observed 4f – 4f transitions of the Sm 3+ centres in the optical absorption and luminescence spectra of the investigated glasses are identified. Most intense emission band of the Sm 3+ ions peaked about 598 nm ( 4 G 5/2 → 6 H 7/2 transition) is characterised by a single exponential decay with typical lifetime values, which depend on the basic glass composition as well as concentration and local structure of the Sm 3+ luminescence centres. The quantum efficiency has been evaluated for observed transitions of the Sm 3+ centres using obtained experimental lifetimes and radiative lifetimes calculated by Judd–Ofelt theory. The calculated high quantum efficiencies and measured quantum yields of luminescence show that the investigated borate glasses are perspective luminescence materials. Energy transfer from the Ce 3+ non-controlled impurity and intrinsic luminescence centres to the Sm 3+ centres has been observed. Peculiarities of the Sm 3+ local structure in the network of investigated glasses have been discussed based on the obtained spectroscopic results and structural data. - Highlights: • The Sm-doped Li 2 B 4 O 7 , LiKB 4 O 7 , CaB 4 O 7 , and LiCaBO 3 glasses of high quality were obtained. • EPR, optical absorption and luminescence spectra of Sm 3+ ions in obtained glasses were

Characterization and luminescent properties of Eu3+ doped Gd2Zr2O7 nanopowders

International Nuclear Information System (INIS)

Rabasovic, M.S.; Sevic, D.; Krizan, J.; Terzic, M.; Mozina, J.; Marinkovic, B.P.; Savic-Sevic, S.; Mitric, M.; Rabasovic, M.D.; Romcevic, N.

2015-01-01

Highlights: • Nanopowders Gd 2 Zr 2 O 7 doped by europium ions (Eu 3+ ) have been synthesized. • Their luminescence properties have been measured at room temperature. • The temporal evolution of laser induced phenomena are presented using time-resolved technique. • Lifetime analysis for luminescence bands in emission spectra has been done. - Abstract: Nanopowders based on gadolinium zirconium oxide (Gd 2 Zr 2 O 7 ) doped by europium ions (Eu 3+ ) were successfully prepared using a flame combustion method. This material is suitable for various optical devices. The structure of prepared materials has been confirmed and characterized using X-ray powder diffraction (XRD), scanning electron microscope (SEM) and photoluminescence (PL) techniques. The luminescence properties of synthesized nanopowders were characterized by emission spectra and luminescence lifetimes by using the streak camera system. PL spectra were obtained at three different excitation wavelengths (Optical Parametric Oscilator (OPO) at 360 nm, laser diode at 365 nm and Ar laser line at 514.5 nm). The strong emission lines at 611 nm and 630 nm corresponding to the 5 D 0 → 7 F 2 long lived transition could be used as a new red light source in optical devices

Photon cascade luminescence from Pr3+ ions in LiPrP4O12 polyphosphate

International Nuclear Information System (INIS)

Shalapska, T; Stryganyuk, G; Romanyshyn, Yu; Demchenko, P; Voloshinovskii, A; Trots, D; Gektin, A; Dorenbos, P

2010-01-01

The spectral-kinetic properties of luminescence from LiY 1-x Pr x P 4 O 12 (x = 1, 0.1) phosphors are studied in the 10-300 K temperature range upon excitation within the UV-VUV spectral range. The luminescence observed for LiPrP 4 O 12 at low temperatures is attributed to both intra-configurational 4f 2 → 4f 2 and inter-configurational 4f5d → 4f 2 radiative transitions of Pr 3+ . The temperature dependence of emission and the decay kinetics of Pr 3+ luminescence from LiY 1-x Pr x P 4 O 12 (x = 1, 0.1) phosphors are explained by temperature stimulated transitions from the 1 S 0 to the Pr 3+ 4f5d state. At low temperatures, the energy potential barrier between the 1 S 0 and 4f5d states is 0.014 eV for LiPrP 4 O 12 . The spectral overlap of the 1 S 0 and 4f5d states of Pr 3+ in LiY 0.9 Pr 0.1 P 4 O 12 determines the luminescence properties in the entire temperature range studied.

Influence of silver and copper doping on luminescent properties of zinc-phosphate glasses after x-ray irradiation

Science.gov (United States)

Murashov, Alexander A.; Sidorov, Alexander I.; Shakhverdov, Teimur A.; Stolyarchuk, Maxim V.

2017-11-01

It is shown, experimentally, that in silver- and copper-containing zinc-phosphate glasses, metal molecular clusters are formed during the glass synthesis. X-ray irradiation of these glasses led to the considerable increase of its luminescence in visible spectral range. This effect is caused by the transformation of the charged metal molecular clusters into the neutral state. Luminescence and excitation spectra of the glass, doped with silver and copper simultaneously, change significantly in comparison with the spectra of glasses doped with one metal. The reason for this can be the formation of hybrid AgnCum molecular clusters. The computer simulation of the structure and optical properties of such clusters by the time-dependent density functional theory method is presented. It is shown that the optimal luminescent material for photonics application, in comparison with other studied materials, is glass, containing hybrid molecular clusters.

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)

Luminescence quenching by reversible ionization or exciplex formation/dissociation.

Science.gov (United States)

Ivanov, Anatoly I; Burshtein, Anatoly I

2008-11-20

The kinetics of fluorescence quenching by both charge transfer and exciplex formation is investigated, with an emphasis on the reversibility and nonstationarity of the reactions. The Weller elementary kinetic scheme of bimolecular geminate ionization and the Markovian rate theory are shown to lead to identical results, provided the rates of the forward and backward reactions account for the numerous recontacts during the reaction encounter. For excitation quenching by the reversible exciplex formation, the Stern-Volmer constant is specified in the framework of the integral encounter theory. The bulk recombination affecting the Stern-Volmer quenching constant makes it different for pulse excited and stationary luminescence. The theory approves that the free energy gap laws for ionization and exciplex formation are different and only the latter fits properly the available data (for lumiflavin quenching by aliphatic amines and aromatic donors) in the endergonic region.

Luminescence and energy transfer mechanisms in CaWO{sub 4} single crystals

Energy Technology Data Exchange (ETDEWEB)

Spassky, D., E-mail: deris2002@mail.ru [Skobeltsyn Institute of Nuclear Physics, M.V. Lomonosov Moscow State University, Vorob' evy Gory, 119991 Moscow (Russian Federation); Mikhailin, V. [Skobeltsyn Institute of Nuclear Physics, M.V. Lomonosov Moscow State University, Vorob' evy Gory, 119991 Moscow (Russian Federation); Nazarov, M. [School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Institute of Applied Physics, Academiei Street 5, Chisinau MD-2028 (Moldova, Republic of); Ahmad-Fauzi, M.N. [School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Zhbanov, A. [Department of Medical System Engineering, Gwangju Institute of Science and Technology, 1 Oryong-dong, Buk-gu, Gwangju 500-712 (Korea, Republic of)

2012-10-15

The processes of the excitation energy transfer to the emission centers have been investigated for calcium tungstate crystals taking into account features of the electronic structure of valence band and conduction band. The calculations of the electronic structure of host lattice CaWO{sub 4} were performed in the framework of density functional theory. The underestimation of the bandgap value in the calculations has been corrected according to the experimental data. Luminescence of two samples grown using Czochralski (cz) and hydrothermal (ht) techniques were studied. Intrinsic emission band related to excitons, self-trapped on WO{sub 4} complexes has been observed for the both samples while the additional low-energy emission band related to the defects of crystal structure has been observed only for (ht) sample indicating the enhanced concentration of the defects in the sample. It was shown that the features of the conduction band electronic structure are reproduced in the excitation spectrum of intrinsic luminescence only for the (ht) sample while for (cz) sample the correlation is absent. The enhanced role of the competitive channels in the process of excitation energy transfer to intrinsic emission centers in (ht) sample is responsible for the observed difference. - Highlights: Black-Right-Pointing-Pointer The band structure of CaWO{sub 4} was calculated in the framework of DFT LAPW method. Black-Right-Pointing-Pointer Calculation results were validated via joint analysis with experimental data. Black-Right-Pointing-Pointer The bandgap E{sub g} of CaWO{sub 4} was determined as 4.90{+-}0.15 eV. Black-Right-Pointing-Pointer The correlation between the band structure and excitation spectrum is demonstrated. Black-Right-Pointing-Pointer Influence of competitive relaxation channel on energy transfer to STE is shown.

Combustion synthesis and preliminary luminescence studies of ...

Indian Academy of Sciences (India)

The polycrystalline sample of LiBaPO4 : Tb3+ (LBPT) was successfully synthesized by solution combustion synthesis and studied for its luminescence characteristics. The thermoluminescence (TL) glow curve of LBPT material consists of two peaks at 204.54 and 251.21°C. The optimum concentration was 0.005 mol to ...

The temperature-sensitive luminescence of (Y,Gd)VO{sub 4}:Bi{sup 3+},Eu{sup 3+} and its application for stealth anti-counterfeiting

Energy Technology Data Exchange (ETDEWEB)

Chen, Lei; Zhang, Yao; Luo, Anqi; Liu, Fayong; Jiang, Yang; Hu, Qingzhuo [School of Materials Science and Engineering, Hefei University of Technology (China); Chen, Shifu [Department of Chemistry, Huaibei Normal University (China); Liu, Ru-Shi [Department of Chemistry, National Taiwan University, Taipei (China)

2012-07-15

Anti-counterfeiting technologies are desired to protect products far away from the violation of dummy, fake and shoddy goods. The phosphor of (Y,Gd)VO{sub 4}:Bi{sup 3+},Eu{sup 3+} was synthesized for the application of this purpose. Its photoluminescence was investigated by exciting with different wavelengths at variant temperatures. Wide emission color ranged from green through yellow to orange was tuned up by tailor-ing Bi{sup 3+} and Eu{sup 3+} concentrations. The temperature dependent luminescence and wavelength selective excitation of (Y,Gd)VO{sub 4}:Bi{sup 3+},Eu{sup 3+} were observed, which provide different encryptions in anti-counterfeiting. To verify the feasibility in application, two anti-counterfeiting patterns were fabricated practically and excellent performance was obtained. Moreover, the physical mechanisms for the different phenomena of luminescence were elucidated from excitation spectra combining with the configuration coordinate model. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Development and measurement of luminescence properties of Ce-doped Cs2LiGdBr6 crystals irradiated with X-ray, γ-ray and proton beam

Science.gov (United States)

Jang, Jonghun; Kim, H. J.; Rooh, Gul; Kim, Sunghwan

2017-12-01

The effect of higher Ce-concentration on the luminescence and scintillation properties of Cs2LiGdBr6 single crystals are studied. We used the Bridgman method for the growth of Ce-doped Cs2LiGdBr6 single crystals. Luminescence properties of the grown crystals are measured by X-ray and proton excitations. We measured the pulse height and fluorescence decay time spectra of Cs2LiGdBr6:Ce3+ with a bi-alkali photo multiplier tube (PMT) under γ-ray excitation from 137Cs source. Improvements in the scintillation properties are observed with the increase of Ce-concentration in the lattice. Detailed procedure of the crystal growth is also discussed.

Polysiloxane-based luminescent elastomers prepared by thiol-ene "click" chemistry.

Science.gov (United States)

Zuo, Yujing; Lu, Haifeng; Xue, Lei; Wang, Xianming; Wu, Lianfeng; Feng, Shengyu

2014-09-26

Side-chain vinyl poly(dimethylsiloxane) has been modified with mercaptopropionic acid, methyl 3-mercaptopropionate, and mercaptosuccinic acid. Coordinative bonding of Eu(III) to the functionalized polysiloxanes was then carried out and crosslinked silicone elastomers were prepared by thiol-ene curing reactions of these composites. All these europium complexes could be cast to form transparent, uniform, thin elastomers with good flexibility and thermal stability. The networks were characterized by FTIR, NMR, UV/Vis, and luminescence spectroscopy as well as by scanning electron microscopy, thermogravimetric analysis, and X-ray photoelectron spectroscopy. The europium elastomer luminophores exhibited intense red light at 617 nm under UV excitation at room temperature due to the (5)D0 →(7)F2 transition in Eu(III) ions. The newly synthesized luminescent materials offer many advantages, including the desired mechanical flexibility. They cannot be dissolved or fused, and so they have potential for use in optical and electronic applications. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Preparation and tunable luminescence of CaCO{sub 3}: Eu{sup 3+}, Tb{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Cheng, Qijun; Dong, Yanwei; Kang, Ming, E-mail: dyw510@126.com; Zhang, Ping

2014-12-15

Luminescent tunable phosphors CaCO{sub 3}: Eu{sup 3+}, Tb{sup 3+} were synthesized by a microwave co-precipitation method. The structure and micro-morphology of samples were characterized and analyzed by an X-ray powder diffraction (XRD) and a scanning electronic microscope (SEM), results showed that Tb{sup 3+} and Eu{sup 3+} ions were uniformly introduced into the host lattice of CaCO{sub 3} entering substitutionally in Ca{sup 2+} sites. The photoluminescence (PL) properties were characterized by PL, PL excitation spectroscopy and chromaticity coordinates. Under the excitation at 235 nm and 267 nm, the transitions of {sup 5}D{sub 4}→{sup 7}F{sub J} (J=3–6) for Tb{sup 3+} and {sup 5}D{sub 0}→{sup 7}F{sub J} (J=0–3) for Eu{sup 3+} were observed, and the luminescent intensities and emitting colors of Eu{sup 3+}–Tb{sup 3+} co-doped CaCO{sub 3} phosphors could be gradually changed between red and green by changing the Eu/Tb atomic ratio and the excitation wavelength. - highlights: • A new phosphor CaCO{sub 3}: Eu{sup 3+}, Tb{sup 3+} was prepared by the microwave co-precipitation method. • The phosphors exhibited green and red color under UV excitation. • The emission color could be gradually tuned between green and red. • The phosphors had the potential as materials for anti-counterfeiting technologies.

Photoluminescence characteristics of Pb-doped, molecular-beam-epitaxy grown ZnSe crystal layers

International Nuclear Information System (INIS)

Mita, Yoh; Kuronuma, Ryoichi; Inoue, Masanori; Sasaki, Shoichiro; Miyamoto, Yoshinobu

2004-01-01

The characteristic green photoluminescence emission and related phenomena in Pb-doped, molecular-beam-epitaxy (MBE)-grown ZnSe crystal layers were investigated to explore the nature of the center responsible for the green emission. The intensity of the green emission showed a distinct nonlinear dependence on excitation intensity. Pb-diffused polycrystalline ZnSe was similarly examined for comparison. The characteristic green emission has been observed only in MBE-grown ZnSe crystal layers with moderate Pb doping. The results of the investigations on the growth conditions, luminescence, and related properties of the ZnSe crystal layers suggest that the green emission is due to isolated Pb replacing Zn and surrounded with regular ZnSe lattice with a high perfection

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.

Luminescence enhancement in Eu3+, Sm3+ co-doped liy(MoO4)2 nano-phosphors by sol-gel process.

Science.gov (United States)

Zhou, Xianju; Wang, Guangchuan; Zhou, Tonghui; Zhou, Kaining; Li, Qingxu; Wang, Zhongqing

2014-05-01

A series of LiY(0.95-x)Eu(0.05)Sm(x)(MoO4)2 red light emitting phosphors were synthesized by sol-gel technique. The phase impurity and spectroscopic properties were characterized by X-ray Diffraction (XRD), Photo-Luminescence (PL) and Photo-Luminescence Excitation (PLE) spectra, respectively. It is found that the PLE spectra of the Eu3+, Sm3+ co-doped nanoparticles are enhanced and broadened as compared with the solely doped samples, which will make the co-doped phosphors match better with blue and/or UV GaN based LED chips. The red emission intensity of Eu3+ is largely enhanced by the energy transfer from Sm3+. The mechanism of the enhancement is clearly proven to be the increase in the quantum efficiency of 5D0 state of Eu3+ rather than the increase in the absorption of Eu3+. Meanwhile, the characteristic f-f transitions of Sm3+ are greatly reduced, resulting in little influence in the color purity of the co-doped phosphors. The present material is an amendatory promising red light emitting phosphor for white LEDs.

Synthesis of KMgCl{sub 3} nanomaterial and luminescence of Ce{sup 3+}/Dy{sup 3+}/Eu{sup 3+} by different routes

Energy Technology Data Exchange (ETDEWEB)

Poddar, Anuradha [Department of Physics, Sindhu Mahavidyalaya, Nagpur 440017 (India); Gedam, S.C., E-mail: gedam_sc@rediffmail.com [Department of Physics, K.Z.S. Science College, Kalmeshwar, Nagpur 441501 (India); Dhoble, S.J. [Department of Physics, RTM Nagpur University, Nagpur 440033 (India)

2015-02-15

The present KMgCl{sub 3} phosphor has been synthesized through wet chemical synthesis (WCS), solid state diffusion (SSD) and Hispersed centrifuge (HC) routes in the same atmospheric conditions and characterized for luminescence properties. XRDs of the sample prepared by all three methods have been placed at the same position, phase and matched well with standard data. The particle size of 20 nm of KMgCl{sub 3} by a Hispersed centrifuged method was detected using a transmission electron microscope (TEM). The PL emission spectra have been observed for Ce{sup 3+} at 353 nm and 375 nm due to 5d→4f transition, whereas luminescence of Dy{sup 3+} efficiently observed at 484 nm and 579 nm for an excitation of 384 nm due to {sup 4}F{sub 9/2}→ {sup 6}H{sub 15/2} and {sup 6}H{sub 13/2} (blue–yellow region) transition and Eu{sup 3+} is peaking at 596 nm and 616 nm (λ{sub ex}=394 nm) due to level {sup 5}D{sub 0} to {sup 7}F{sub j} (j=0, 1, 2, and 3) radiative transitions. The presented phosphors are excited in the range of 300–400 nm which is mercury free excited range. Synthesis and photoluminescence spectra of trivalent Ce, Dy or Eu rare-earths in KMgCl{sub 3} are described for all three routes, for the first time in the present work. The CIE chromaticity coordinates were also calculated for KMgCl{sub 3}:X (Ce{sup 3+}, Dy{sup 3+} and Eu{sup 3+}) phosphors, which are close to the NTSC standard values. KMgCl{sub 3} matrix is not only suitable for different and easy synthesis but efficient luminescence also. The paper discuses the XRD, crystallinity (morphology) and luminescence of Ce, Dy or Eu rare-earths in KMgCl{sub 3} synthesized by three (WCS, SSD and HC) different routes. - Highlights: • The particle size 20 nm of KMgCl{sub 3} was detected by Hispersed centrifuged method using TEM. • The phosphors are prepared by very simple WCM, SSD and HS technique. • An efficient luminescence is observed in KMgCl{sub 3}:X (X=Ce{sup 3+}, Dy{sup 3+} and Eu{sup 3

Photoluminescence and thermally stimulated luminescence characteristics of rice flour

International Nuclear Information System (INIS)

Murthy, K.V.R.; Rey, L.; Belon, P.

2007-01-01

The present paper reports the photoluminescence (PL) and the thermoluminescence (TL) characteristics of rice flour. This study is undertaken to consider storage of rice at low temperature and irradiation for disinfection. From the Indian market a few varieties of rice was bought. All the samples of rice was ground using an agate motor and pestle. Thereafter, the powder was sieved to the size of 140 μm using appropriate sieves. When comparing the PL characteristics of the different rice powders studied, it is interesting to note that the PL emission wavelength (around 445 nm) is nearly same for all the rice varieties studied even though the excitation wave length is different. TL characteristics are studied in the temperature range 77-230 K as well as 300-700 K. TL is recorded for the virgin samples and also on irradiation of the same by exposing it to X-ray at 77 K, beta at 300 K and gamma at 77 K. The two varieties are given an X-ray dose of 1 kGy. The TL is recorded for 200 mg rice powder. The TL displayed for the as-received 1 kGy X- ray dose peak is around 160 K with a broad shoulder around 120 K. Basmati variety is given a gamma dose of 12.5 kGy and the TL and TL emission is recorded. It is seen that a well-defined low-temperature TL peak around 119 K and a hump around 145 K are observed in the sample. The TL emission is around 430 nm.The TL peak observed in most of the rice samples above room temperature is around 558 K

Green and red luminescence in co-precipitation synthesized Pr:LuAG nanophosphor

Energy Technology Data Exchange (ETDEWEB)

Kumar, S. Arun; Kumar, K. Ashok; Gunaseelan, M.; Senthilselvan, J., E-mail: jsselvan@hotmail.com [Department of Nuclear Physics, University of Madras, Guindy Campus, Chennai–600 025, Tamil Nadu (India); Asokan, K. [Materials Science Group, Inter University Accelerator Centre, New Delhi-110067 (India)

2016-05-06

Pr:LuAG nanophosphor is an effective candidate in magnetic resonance imaging coupled positron emission tomography (MRI-PET) for medical imaging and scintillator applications. LuAG:Pr (0.05, 0.15 mol%) nanoscale ceramic powders were synthesized by co-precipitation method using urea as precipitant. Effect of antisite defect on structure and luminescence behavior was investigated. Pr:LuAG nanoceramic powders are found crystallized in cubic structure by high temperature calcination at 1400 °C and it shows antisite defect. HR-SEM analysis revealed spherically shaped Pr:LuAG nanoceramic particulate powders with ∼100 nm size. By the excitation at 450 nm, Pr:LuAG nanophosphor exhibit green to red luminescence in the wavelength range of 520 to 680 nm, which is originated from multiplet transition of Pr{sup 3+} ions.

Characterization of luminescent praseodymium-doped ZrO{sub 2} coatings deposited by ultrasonic spray pyrolysis technique

Energy Technology Data Exchange (ETDEWEB)

Ramos-Brito, F [Laboratorio de Materiales Optoelectronicos, DiDe, Centro de Ciencias de Sinaloa, Av. De las Americas No. 2771 Nte. Col. Villa Universidad, C.P. 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); Alejo-Armenta, C [Laboratorio de Materiales Optoelectronicos, DiDe, Centro de Ciencias de Sinaloa, Av. De las Americas No. 2771 Nte. Col. Villa Universidad, C.P. 80010 Culiacan, Sinaloa (Mexico); Alvarez-Fragoso, O [Departamento de Materiales Metalicos y Ceramicos, Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, AP 70-360 Coyoacan 04510 DF (Mexico); Falcony, C [Departamento de Fisica, CINVESTAV-IPN, Apdo. Postal 14-740, 07000 DF (Mexico)

2007-11-07

ZrO{sub 2} : Pr films were synthesized by the ultrasonic spray pyrolysis process. X-ray diffraction studies, as a function of the deposition temperature, indicate a tetragonal crystal structure of zirconia as the substrate temperature was increased. Luminescence (photo- and cathodoluminescence) properties of the films were studied as a function of growth parameters such as the substrate temperature and the praseodymium concentration. For an excitation wavelength of 290 nm, all the photoluminescent emission spectra show peaks located at 490, 510, 566, 615, 642, 695, 718, 740 and 833 nm, associated with the electronic transitions {sup 3} P{sub 0} {yields} {sup 3}H{sub 4}, {sup 3}P{sub 0} {yields} {sup 3} H{sub 4}, {sup 3}P{sub 1} + {sup 1}I{sub 6} {yields} {sup 3}H{sub 5}, {sup 1}D{sub 2} {yields} {sup 3}H{sub 4}, {sup 3} P{sub 0} {yields} {sup 3}H{sub 6}, {sup 1}D{sub 2} {yields} {sup 3} H{sub 5}, {sup 1}D{sub 2} {yields} {sup 3}H{sub 5}, {sup 3} P{sub 0} {yields} {sup 3}F{sub 3,4} and {sup 1}D{sub 2} {yields} {sup 3} F{sub 2} of the Pr{sup 3+} ion. As the deposition temperature is increased, an increasing intensity of the luminescence emission is observed. Also, quenching of the luminescence, with increasing doping concentration, is observed. The chemical composition of the films as determined by energy dispersive spectroscopy is reported as well. In addition, the surface morphology characteristics of the films, as a function of the deposition temperature, are presented.

Near Infrared-Emitting Cr3+/Eu3+ Co-doped Zinc Gallogermanate Persistence Luminescent Nanoparticles for Cell Imaging

Science.gov (United States)

Wang, Qiaoqiao; Zhang, Shuyun; Li, Zhiwei; Zhu, Qi

2018-02-01

Near infrared (NIR)-emitting persistent luminescent nanoparticles have been developed as potential agents for bioimaging. However, synthesizing uniform nanoparticles with long afterglow for long-term imaging is lacking. Here, we demonstrated the synthesis of spinel structured Zn3Ga2Ge2O10:Cr3+ (ZGGO:Cr3+) and Zn3Ga2Ge2O10:Cr3+,Eu3+ (ZGGO:Cr3+,Eu3+) nanoparticles by a sol-gel method in combination with a subsequent reducing atmosphere-free calcination. The samples were investigated via detailed characterizations by combined techniques of XRD, TEM, STEM, selected area electron diffraction, photoluminescence excitation (PLE)/photoluminescence (PL) spectroscopy, and temperature-dependent PL analysis. The single-crystalline nanoparticles are homogeneous solid solution, possessing uniform cubic shape and lateral size of 80-100 nm. Upon UV excitation at 273 nm, ZGGO:Cr3+,Eu3+ exhibited a NIR emission band at 697 nm (2E → 4A2 transition of distorted Cr3+ ions in gallogermanate), in the absence of Eu3+ emission. NIR persistent luminescence of the sample can last longer than 7200 s and still hold intense intensity. Eu3+ incorporation increased the persistent luminescence intensity and the afterglow time of ZGGO:Cr3+, but it did not significantly affect the thermal stability. The obtained ZGGO:Cr3+,Eu3+-NH2 nanoparticles possessed an excellent imaging capacity for cells in vitro.

Preparation and luminescence properties of Ca3(VO4)2: Eu3+, Sm3+ phosphor for light-emitting diodes

International Nuclear Information System (INIS)

Huang Jiaping; Li Qiuxia; Chen Donghua

2010-01-01

Rare-earth ions co-activated red phosphors Ca 3 (VO 4 ) 2 : Eu 3+ , Sm 3+ were synthesized by modified solid-state reactions. The samples were characterized by X-ray powder diffractometer (XRD), energy-dispersive X-ray spectrometer (EDS), transmission electron microscopy (TEM) and luminescence spectrometer (LS). The results showed that the Eu-Sm system exhibits higher emission intensity than those of the Eu single-doped system and Sm separate-doped system under blue light. Samarium (III) ions are effective in broadening and strengthening absorptions around 467 nm. Furthermore, they exhibit enhanced luminescence emission. Luminescent measurements showed that the phosphors can be efficiently excited by ultraviolet (UV) to visible region, emitting a red light with a peak wavelength of 616 nm. The material has potential application as a phosphor for light-emitting diodes (LEDs).

Sub-diffraction positioning of a two-photon excited and optically trapped quantum dot

DEFF Research Database (Denmark)

Pedersen, Liselotte Jauffred; Kyrsting, Anders Højbo; Christensen, Eva Arnspang

2014-01-01

Colloidal quantum dots are luminescent long-lived probes that can be two-photon excited and manipulated by a single laser beam. Therefore, quantum dots can be used for simultaneous single molecule visualization and force manipulation using an infra-red laser. Here, we show that even a single opti...

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.

Cone Beam X-ray Luminescence Computed Tomography Based on Bayesian Method.

Science.gov (United States)

Zhang, Guanglei; Liu, Fei; Liu, Jie; Luo, Jianwen; Xie, Yaoqin; Bai, Jing; Xing, Lei

2017-01-01

X-ray luminescence computed tomography (XLCT), which aims to achieve molecular and functional imaging by X-rays, has recently been proposed as a new imaging modality. Combining the principles of X-ray excitation of luminescence-based probes and optical signal detection, XLCT naturally fuses functional and anatomical images and provides complementary information for a wide range of applications in biomedical research. In order to improve the data acquisition efficiency of previously developed narrow-beam XLCT, a cone beam XLCT (CB-XLCT) mode is adopted here to take advantage of the useful geometric features of cone beam excitation. Practically, a major hurdle in using cone beam X-ray for XLCT is that the inverse problem here is seriously ill-conditioned, hindering us to achieve good image quality. In this paper, we propose a novel Bayesian method to tackle the bottleneck in CB-XLCT reconstruction. The method utilizes a local regularization strategy based on Gaussian Markov random field to mitigate the ill-conditioness of CB-XLCT. An alternating optimization scheme is then used to automatically calculate all the unknown hyperparameters while an iterative coordinate descent algorithm is adopted to reconstruct the image with a voxel-based closed-form solution. Results of numerical simulations and mouse experiments show that the self-adaptive Bayesian method significantly improves the CB-XLCT image quality as compared with conventional methods.

Cu"+ luminescence in Na_2Sr_2Al_2PO_4Cl_9 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_2Sr_2Al_2PO_4Cl_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"1"0.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"1"0 ↔ 3d"94s 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)

Luminescence detection of shellfish

International Nuclear Information System (INIS)

Sanderson, D.C.W.; Carmichael, L.A.; Spencer, J.Q.; Naylor, J.D.

1996-01-01

The Scottish Universities Research and Reactor Centre (SURRC) has been active in the development and application of luminescence techniques in the detection of irradiated foods, in support of UK legislation. Thermoluminescence (TL), photostimulated luminescence (PSL) and photo-transfer luminescence (PTTL) are radiation-specific phenomena which arise due to energy stored by trapped charge carriers following irradiation. The energy released following stimulation is accompanied by detectable luminescence. The TL method involves preparation of pure silicate extracts from the sample and subsequent TL analysis, whereas PSL uses stimulation by electromagnetic radiation (visible, or near visible wavelengths) thus avoiding heating the sample. (author)

Luminescence of Bi3+ ions in Y3Al5O12:Bi single crystalline films

International Nuclear Information System (INIS)

Zorenko, Yu.; Gorbenko, V.; Voznyak, T.; Vistovsky, V.; Nedilko, S.; Nikl, M.

2007-01-01

The absorption and cathodoluminescence spectra of single crystalline films (SCF) of Y 3 Al 5 O 12 :Bi garnet depending on Bi concentration were analyzed. For consideration of the nature of the UV and visible Bi-related emission bands the time-resolved luminescence of Bi 3+ (ns 2 ) ions in YAG:Bi SCF was studied at 10 K under excitation by synchrotron radiation. The difference in the excitation spectra and emission decay of the UV and visible bands has been explained via radiative relaxation from the 3 P 1,0 excited states to the 1 S 0 ground state of the isolated and pair/clustered Bi 3+ emission centers in the garnet lattice, respectively

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.

Recombination luminescence in irradiated silicon - Effects of thermal annealing and lithium impurity.

Science.gov (United States)

Johnson, E. S.; Compton, W. D.

1971-01-01

Use of luminescence in irradiated silicon to determine the thermal stability of the defects responsible for the recombination. It is found that the defect responsible for the zero-phonon line at 0.97 eV has an annealing behavior similar to that of the divacancy and that the zero-phonon line at 0.79 eV anneals in a manner similar to the G-15 or K-center. Annealing at temperatures up to 500 C generates other defects whose luminescence is distinct from that seen previously. Addition of lithium to the material produces defects with new characteristic luminescence. Of particular importance is a defect with a level at E sub g -1.045 eV.

Increase of (CdSe/ZnS)Cys quantum dot luminescence intensity in the presence of TPPS{sub 4} porphyrin

Energy Technology Data Exchange (ETDEWEB)

Parra, Gustavo G.; Borissevitch, Iouri E. [Universidade de Sao Paulo (FFCLRP/USP), Ribeirao Preto, SP (Brazil). Fac. de Filosofia, Ciencias e Letras de Ribeirao Preto. Dept. de Fisica; Kuzmin, Vladimir A. [Emanuel Institute of Biophysical Chemistry, RAS-RU, Moscow (Russian Federation); Oleinikov, Vladimir A. [Shemyakin and Ovchinnikov Institute of Biooganic Cemistry, RAS-RU, Moscow (Russian Federation)

2012-07-01

Full text: Nanocrystal semiconductor particles or Quantum Dots (QD) possess extraordinary photophysical characteristics, such as extreme high fluorescence quantum yield and optical absorption and very narrow fluorescence band, which can be easily shifted by changing of QD particle size. Due to these characteristics, QD is promising for fluorescence cancer diagnostics and photodynamic treatment. The efficiency of these processes can be in- creased by energy transfer between QD and classic fluorescence probes and photosensitizers (PS). In this work we present on the study of the increase of (CdSe/ZnS)Cys quantum dot luminescence intensity, stimulated by interaction with TPPS{sub 4} porphyrin. The optical absorption and steady-state and time-resolved fluorescence techniques were employed. Water soluble QD (CdSe/ZnS) with emission at 580 nm, functionalized with cysteine (Cys), were studied. TPPS{sub 4} porphyrin was used as a stimulator of QD luminescence. All experiments were realized in PBS buffer (pH 7.3; 7.5 mM) in Milli-Q quality water. The TPPS{sub 4} adding into the QD solutions until the 5{mu}M concentration produced an increase in QD luminescence intensity and lifetime, while for TPPS{sub 4} concentrations higher than 20{mu}M the reduction of the fluorescence intensity was observed, the emission spectra and fluorescence decays profile being unchanged. This effect can not be due to the electrostatic interaction between (CdSe/ZnS)Cys and TPPS{sub 4} because both, (CdSe/ZnS)Cys and TPPS{sub 4}, are negatively charged. We suppose that TPPS{sub 4} porphyrin interacts directly with QD (ZnS) shell, reducing the dangling bound number. This reduction decreases, in turn, the probability of nonradiative ways of the excitation energy dissipation. When the majority of dangling bound is occupied by the TPPS{sub 4} molecules, the effect of QD luminescence reduction (quenching) by porphyrin predominates, probably, via the energy transfer from QD to TPPS{sub 4}. However

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

Efficient UV-emitting X-ray phosphors: octahedral Zr(PO4)6 luminescence centers in potassium hafnium-zirconium phosphates K2Hf1-xZrx(PO4)2 and KHf2(1-x)Zr2x(PO4)3

International Nuclear Information System (INIS)

Torardi, C.C.; Miao, C.R.; Li, J.

2003-01-01

Potassium hafnium-zirconium phosphates, K 2 Hf 1-x Zr x (PO 4 ) 2 and KHf 2(1-x) Zr 2x (PO 4 ) 3 , are broad-band UV-emitting phosphors. At room temperature, they have emission peak maxima at approximately 322 and 305 nm, respectively, under 30 kV peak molybdenum X-ray excitation. Both phosphors demonstrate luminescence efficiencies that make them up to ∼60% as bright as commercially available CaWO 4 Hi-Plus. The solid-state and flux synthesis conditions, and X-ray excited UV luminescence of these two phosphors are discussed. Even though the two compounds have different atomic structures, they contain zirconium in the same active luminescence environment as that found in highly efficient UV-emitting BaHf 1-x Zr x (PO 4 ) 2 . All the three materials have hafnium and zirconium in octahedral coordination via oxygen-atom corner sharing with six separate PO 4 tetrahedra. This octahedral Zr(PO 4 ) 6 moiety appears to be an important structural element for efficient X-ray excited luminescence, as are the edge-sharing octahedral TaO 6 chains for tantalate emission

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)

Dose effects on the long persistent luminescence properties of beta irradiated SrAl2O4:Eu2+, Dy3+ phosphor

International Nuclear Information System (INIS)

Pedroza-Montero, M.; Castaneda, B.; Gil-Tolano, M.I.; Arellano-Tanori, O.; Melendrez, R.; Barboza-Flores, M.

2010-01-01

The SrAl 2 O 4 :Eu 2+ , Dy 3+ is a phosphor characterized by a long persistent luminescence (PLUM) when it is excited with UV-VIS light and ionizing radiation. In this paper, we study the PLUM behavior as a function of beta irradiation dose in the 0-650 Gy range with a fixed dose rate of 5 Gy/min. The PLUM intensity showed a complex decay behavior, exhibiting a near linear response in the 0-1.7 Gy low dose range and gradually increasing up to 160 Gy. The PLUM reached the saturation for higher doses (>275 Gy) with a slight decrease in the range of 300-650 Gy. In addition, a systematic PLUM enhancement was produced after a thermal cleaning procedure and irradiation at RT in a series of 10 cycles. The observed phenomenon may be related to a radiation-induced process of charge trapping accumulation, which is triggered by thermal stimulation during the irradiation stage. It improves the luminescent characteristics of SrAl 2 O 4 :Eu 2+ , Dy 3+ phosphors rendering them suitable for permanent display and illumination devices.

Luminescence properties of the Sm-doped borate glasses

Energy Technology Data Exchange (ETDEWEB)

Kindrat, I.I. [University of Zielona Góra, Institute of Physics, Division of Spectroscopy of Functional Materials, 4a Szafrana Street, 65-516 Zielona Góra (Poland); Padlyak, B.V., E-mail: B.Padlyak@if.uz.zgora.pl [University of Zielona Góra, Institute of Physics, Division of Spectroscopy of Functional Materials, 4a Szafrana Street, 65-516 Zielona Góra (Poland); Vlokh Institute of Physical Optics, 23 Dragomanov Street, 79-005 Lviv (Ukraine); Drzewiecki, A. [University of Zielona Góra, Institute of Physics, Division of Spectroscopy of Functional Materials, 4a Szafrana Street, 65-516 Zielona Góra (Poland)

2015-10-15

The optical absorption and photoluminescence (emission and excitation) spectra as well as decay kinetics of a series of the Sm-doped glasses with Li{sub 2}B{sub 4}O{sub 7}, LiKB{sub 4}O{sub 7}, CaB{sub 4}O{sub 7}, and LiCaBO{sub 3} compositions were investigated and analysed. The Li{sub 2}B{sub 4}O{sub 7}:Sm, LiKB{sub 4}O{sub 7}:Sm, CaB{sub 4}O{sub 7}:Sm, and LiCaBO{sub 3}:Sm glasses of high optical quality have been obtained from the corresponding polycrystalline compounds in the air atmosphere, using a standard glass technology. On the basis of electron paramagnetic resonance (EPR) and optical spectra analysis it was shown that the samarium impurity is incorporated into the glass network as Sm{sup 3+} (4f{sup 5}, {sup 6}H{sub 5/2}) ions, exclusively. All observed 4f – 4f transitions of the Sm{sup 3+} centres in the optical absorption and luminescence spectra of the investigated glasses are identified. Most intense emission band of the Sm{sup 3+} ions peaked about 598 nm ({sup 4}G{sub 5/2} → {sup 6}H{sub 7/2} transition) is characterised by a single exponential decay with typical lifetime values, which depend on the basic glass composition as well as concentration and local structure of the Sm{sup 3+} luminescence centres. The quantum efficiency has been evaluated for observed transitions of the Sm{sup 3+} centres using obtained experimental lifetimes and radiative lifetimes calculated by Judd–Ofelt theory. The calculated high quantum efficiencies and measured quantum yields of luminescence show that the investigated borate glasses are perspective luminescence materials. Energy transfer from the Ce{sup 3+} non-controlled impurity and intrinsic luminescence centres to the Sm{sup 3+} centres has been observed. Peculiarities of the Sm{sup 3+} local structure in the network of investigated glasses have been discussed based on the obtained spectroscopic results and structural data. - Highlights: • The Sm-doped Li{sub 2}B{sub 4}O{sub 7}, LiKB{sub 4}O{sub 7}, Ca

Luminescent nanocrystals in the rare-earth niobate–zirconia system formed via hydrothermal method

International Nuclear Information System (INIS)

Hirano, Masanori; Dozono, Hayato

2013-01-01

Luminescent nanocrystals based on the rare-earth niobates (Ln 3 NbO 7 , Ln=Y, Eu) and zirconia (ZrO 2 ) that were composed of 50 mol% Ln 3 NbO 7 and 50 mol% ZrO 2 , were hydrothermally formed as cubic phase under weakly basic conditions at 240 °C. The lattice parameter of the as-prepared nanoparticles corresponding to the composition of Y 3−x Eu x NbO 7 –4ZrO 2 that was estimated as a single phase of cubic gradually increased as the content of europium x increased. The existence of small absorbance peaks at 395 and 466 nm corresponding to the Eu 3+7 F 0 → 5 L 6 , and 7 F 0 → 5 D 2 excitation transition, respectively, was clearly observed in the diffuse reflectance spectra of the as-prepared samples containing europium. The optical band gap of the as-prepared samples was in the range from 3.5 to 3.7 eV. The photoluminescence spectra of the as-prepared nanocrystals containing europium showed orange and red luminescences with main peaks at 590 and 610 nm, corresponding to 5 D 0 → 7 F 1 and 5 D 0 → 7 F 2 transitions of Eu 3+ , respectively, under excitation at 395 nm Xe lamp. The emission intensity corresponding to 5 D 0 → 7 F 2 transition increased as heat-treatment temperature rose from 800 to 1200 °C. - Graphical abstract: This graphical abstract shows the excitation and emission spectra and a transmission electron microscopy image of nanocrystals (with composition based on the rare-earth niobates (Ln 3 NbO 7 , Ln=Y, Eu) and zirconia (ZrO 2 ) that were composed of 50 mol% Ln 3 NbO 7 and 50 mol% ZrO 2 ) formed via hydrothermal route. Display Omitted - Highlights: • Nanocrystals composed of 50 mol% Y 3−x Eu x NbO 7 and 50 mol% ZrO 2 was directly formed. • The nanocrystals were hydrothermally formed under weakly basic conditions at 240 °C. • The Y 3 NbO 7 showed an UV-blue and broad-band emission under excitation at 240 nm. • The emission is originated from the niobate octahedral group [NbO 6 ] 7− . • The nanocrystals showed orange and

High temperature luminescence of ZnSe:Yb crystals

Directory of Open Access Journals (Sweden)

Makhniy V. P.

2016-05-01

Full Text Available The problem of obtaining of effective edge luminescence with high temperature stability in the zinc selenide crystals is discussed. This task is solved by using as the dopant rare-earth element yttrium, which is introduced into the undoped ZnSe crystal by diffusion method. Doping was carried out in an evacuated to 10 -4 Torr. and a sealed quartz ampoule, in the opposite ends of which is a sample and a mixture of the crushed Yb and Se. It has been found that the diffusion coefficient of yttrium at a temperature of 1400 K is about 5⋅10 -7 cm 2/sec. It is shown that in the luminescence spectra of ZnSe:Yb samples in the temperature range 295-470 K only blue band is observed. Dependencies of parameters of this band from the excitation level are typical for the annihilation of excitons at their inelastic scattering by free carriers. The efficacy of blue radiation at 300 K is about 30% and does not fall more than twice with increasing temperature up to 470 K, indicating its high thermal stability.

Electron beam excitation assisted optical microscope with ultra-high resolution.

Science.gov (United States)

Inami, Wataru; Nakajima, Kentaro; Miyakawa, Atsuo; Kawata, Yoshimasa

2010-06-07

We propose electron beam excitation assisted optical microscope, and demonstrated its resolution higher than 50 nm. In the microscope, a light source in a few nanometers size is excited by focused electron beam in a luminescent film. The microscope makes it possible to observe dynamic behavior of living biological specimens in various surroundings, such as air or liquids. Scan speed of the nanometric light source is faster than that in conventional near-field scanning optical microscopes. The microscope enables to observe optical constants such as absorption, refractive index, polarization, and their dynamic behavior on a nanometric scale. The microscope opens new microscopy applications in nano-technology and nano-science.

Investigations of the luminescence of phosphate glasses with respect to their application as solid dosemeters

International Nuclear Information System (INIS)

Regulla, D.F.

1977-03-01

A comprehensive presentation of the luminescent properties of phosphate glass is worked out. The extensive investigations show an essential enlargement of the knowledge on the luminescence of phosphate glass existing hitherto. These results form the basis for a detailed discussion of the luminescence mechanism. By applying additional results of measurements concerning optical and paramagnetic absorption, enabling the access to the atomic effect, propositions were developed for models of absorption, excitation and luminous centers relevant for dosimetry for which Ag ++ was found to be the constituent determining the centers. The interpretation of the luminescence phenomena within the frame of these models leads to considerable corrections on the existing concepts. At the same time the comparability of Ag-doped phosphate glasses and alkali halogenides is shown with respect to their luminescence behaviour, and with it an argument for the existence of crystal-like short-order regions in the amorphous glass is provided. This result serves as a basis for a discussion of the centers in the band model. Further investigations dealt with the quantities of influence for the practical application of the dosemeter. By interpretation of these results explanations are given for the effect of irradiation and evaluation temperatures, of LET, the dose, and UV light on the measuring signal. The phenomenon of 'pre-dose', for which especially surface effects have been detected as cause, is discussed under the aspect of a boundary layer theory. (orig./HP) [de

Luminescence investigations of rare earth doped lead-free borate glasses modified by MO (M = Ca, Sr, Ba)

Energy Technology Data Exchange (ETDEWEB)

Janek, Joanna, E-mail: janek.joanna@gmail.com; Sołtys, Marta; Żur, Lidia; Pietrasik, Ewa; Pisarska, Joanna; Pisarski, Wojciech A.

2016-09-01

Series of lead-free borate glasses with different oxide modifiers and lanthanide ions were prepared. The effect of oxide modifiers MO (M = Ca, Sr, Ba) on spectroscopic properties of trivalent Ln{sup 3+} (Ln = Eu, Er, Pr) were systematically investigated. Especially, the luminescence spectra of Ln{sup 3+}-doped lead-free borate glasses are presented and discussed in relation to the impact of selective components (CaO, SrO and BaO). Several spectroscopic parameters, such as the fluorescence intensity ratio R/O (Eu{sup 3+}) and measured luminescence lifetimes for the {sup 5}D{sub 0} (Eu{sup 3+}), {sup 4}I{sub 13/2} (Er{sup 3+}) and {sup 1}D{sub 2} (Pr{sup 3+}) excited states of lanthanide ions were analyzed in details. The research proved that spectroscopic properties of trivalent Ln{sup 3+} depend significantly on kind of presence oxide modifiers MO (M = Ca, Sr, Ba) in glass host matrices. - Highlights: • Luminescence of Ln{sup 3+}-doped borate glasses was presented and discussed. • Effect of glass modifiers on spectroscopic properties of rare earths was studied. • Measured luminescence lifetimes of Ln{sup 3+} (Ln = Eu, Er, Pr) were analyzed. • Luminescence intensity ratios R/O (Eu{sup 3+}) were determined.

Luminescence behavior of the dibenzoyl methane europium(III) complexes in sol-gel derived host materials

International Nuclear Information System (INIS)

Wang Feng; Fan Xianping; Wang Minquan; Zhang Xianghua

2005-01-01

The luminescence behavior of the dibenzoyl methane europium(III) complexes (Eu(DBM) 3 ) in sol-gel derived host materials have been investigated. The steady-state excitation and emission spectra and the time-resolved spectra of the 1% EuCl 3 and 3% DBM co-doped gel indicated an efficient ligand-to-metal energy transfer. The Eu(DBM) 3 complexes in the gel showed longer 5 D 0 lifetimes in comparison with Eu(DBM) 3 .3H 2 O complexes. The luminescence intensity of the 1% EuCl 3 and 3% DBM co-doped gel decreased continuously with increasing temperature and time of heat treatment, which indicated the gradual decomposition of the Eu(DBM) 3 complexes in the gel during heat treatment

Europium concentration effect on characteristics and luminescent properties of hydroxyapatite nanocrystalline powders

Science.gov (United States)

Nikolaev, Anton; Kolesnikov, Ilya; Frank-Kamenetskaya, Olga; Kuz'mina, Maria

2017-12-01

Series of Eu-apatites were synthesized by precipitation from aqueous solutions with the Eu/Ca atomic ratio from 0.5% to 5% at T = 90 °C. Resulting precipitates were studied using different experimental techniques including X-ray powder diffraction, infrared and raman spectroscopy, scanning elecrton microscopy, EDX and photoluminescent spectroscopy. Eu-doped Ca-deficit nanosized non-stoichiometric hydroxyapatite with high water content has been obtained throughout the experiment. Europium content in the synthesized apatites reaches 0.24 apfu (Eu/Ca = 2.5%). Relations between Eu content is the solution and precipitate have been established. It was shown that Eu-monacite starts to precipitate as secondary phase at Eu/Ca ratio in starting solution 1% or higher. Maximum luminescence is observed in apatite with ∼2% Eu/Ca ratio (which equals to ∼0.2 apfu and corresponds to 3% Eu/Ca ratio in the starting solution). As an important and brand-new result, apatite with 2% Eu/Ca ratio can be considered as the most appropriate material for the producing biolabels for luminescent research in medicine and biology.

Long-time Luminescence Kinetics of Localized excitons and conduction Band Edges Smearing in ZnSe(1-c)Tec Solid Solutions

DEFF Research Database (Denmark)

Klochikhin, O.; Ogloblin, S. G.; Permogorov, S.

2000-01-01

It is shown that the integrated luminescence intensity of localized excitons in solid solutions ZnSe(1 - c)Tec has a component slowly decaying with time. After the excitation above the mobility threshold, the long-time intensity decreases exponentially, with a fractional exponent changing from...

Luminescence quantum efficiency determination in LiYF4:Nd3+ using photoacoustic spectroscopy

International Nuclear Information System (INIS)

Franca, E.J.

1989-01-01

Optical properties of LiYF 4 :Nd 3+ were studied using absorption, emission, excitation and photo acoustic spectroscopies. The Nd 3+ transitions were identified and the Stark sublevels were determined for the 4 I 9/2 , 4 I 11/2 and 4 F 3/2 levels. It is also presented and analysed three methods for the luminescence quantum efficiency determination, based on parameters from the spectra mentioned above. These methods were applied to four groups centered on 517, 577, 743 and 792nm. The first method provided values too high due to its assumption that the material has only one luminescent channel. The values obtained from the second one are still somewhat high but closer to the expected ones. The superestimation can be atributed to the imprecision in the existing branching ratios values, needed in this method. The third one, developed from the other two, provided values closer to the expected ones, but also affected by experimental conditions limitations, mainly related to the spectral resolution of the photoacustic spectra. The obtained results show that this method, once improved and associated to better experimental conditions, will lead to more accurate luminescence quantum efficiency values. (author) [pt

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.

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

1994-12-31

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.

Preparation and luminescence properties of terbium-doped lanthanum oxide nanofibers by electrospinning

Energy Technology Data Exchange (ETDEWEB)

Song Lixin; Du Pingfan [Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Zhejiang Sci-Tech University), Ministry of Education, Hangzhou 310018 (China); Xiong Jie, E-mail: jxiong@zstu.edu.cn [Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Zhejiang Sci-Tech University), Ministry of Education, Hangzhou 310018 (China); Fan Xiaona; Jiao Yuxue [Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Zhejiang Sci-Tech University), Ministry of Education, Hangzhou 310018 (China)

2012-01-15

Terbium-doped lanthanum oxide (La{sub 2}O{sub 3}:Tb{sup 3+}) nanofibers were prepared by electrospinning followed by calcination at high temperature. Thermogravimetric analyzer (TGA), field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and photoluminescence (PL) were used to characterize the obtained fibers. The results reveal that the nanofibers have an average diameter of ca. 95{+-}25 nm and are composed of pure La{sub 2}O{sub 3} phase. Under the excitation of 274 nm light, the La{sub 2}O{sub 3}:Tb{sup 3+} nanofibers exhibit the characteristic emission resulting from the {sup 5}D{sub 4}{yields}{sup 7}F{sub J} (J=3, 4, 5, 6) transitions of Tb{sup 3+} ions. And the PL emission intensity is stronger than that of their nanoparticle counterparts. - Highlights: > Tb{sup 3+}-doped La{sub 2}O{sub 3} (La{sub 2}O{sub 3}:Tb{sup 3+}) fluorescent nanofibers were prepared via a simple electrospinning technique. > Luminescent properties and other characteristics of the nanofibers were investigated in details. > Potential applications of La{sub 2}O{sub 3}:Tb{sup 3+} nanofibers and electrospinning technique described in this paper are suggested.

Impact of firing temperature on multi-wavelength selective Stokes and anti-Stokes luminescent behavior by Gd2O2S:Er,Yb phosphor and its application in solar energy harvesting

Science.gov (United States)

Kataria, V.; Mehta, D. S.

2018-04-01

Erbium (Er3+)-ytterbium (Yb3+) doped gadolinium oxysulphide (Gd2O2S) phosphor has been developed via a facile method of solid-state flux fusion, and offers two-fold spectrum modification with highly intense Stokes and anti-Stokes shift. The effect of the firing cycle on the photoluminescent response and morphology of Gd2O2S:Er,Yb is scrutinized, wherein the firing temperature was varied (1000 °C-1250 °C), keeping firing time and all other parameters constant. Interestingly, the nanostructures fired below 1150 °C showed nanorods of diameter ~200 nm and length ~1-2 µm, whereas firing at 1150 °C and above rendered nanospheres with small diameter, ~350 nm. Highly bright upconversion (UC) emission was achieved even under an extremely low excitation power density of 800 µW cm-2 from a 980 nm laser, and was comfortably visible to the naked eye. The incident power dependent studies disclosed increase in UC-emission intensity with increasing excitation power and a quasi-linear dependence on excitation power density. Intense characteristic UC-emission of Er3+ excited states at 525 nm, 556 nm and 668 nm were observed, and the green emission band was found to be dominant over the red band in intensity. Concurrently, downconversion (DC) emission at 556 nm and 669 nm was also exhibited under ultraviolet excitation (285 nm and 380 nm), with the red band being more powerful than the green, unlike UC-emission. Firing temperature dependent studies divulged the dependence of luminescence intensity on the firing cycle of the luminophore and formation of the respective luminescent phase. The UC-emission intensity was found to be maximum for samples fired at 1150 °C, whereas samples fired at 1000 °C showed the highest DC-emission intensity. The excitation and emission profile of single Gd2O2S:Er,Yb phosphor lying in the desired spectral region and as a dual spectral converter marks its possible application for enhanced harvesting of sunlight.

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

NIR Ratiometric Luminescence Detection of pH Fluctuation in Living Cells with Hemicyanine Derivative-Assembled Upconversion Nanophosphors.

Science.gov (United States)

Li, Haixia; Dong, Hao; Yu, Mingming; Liu, Chunxia; Li, Zhanxian; Wei, Liuhe; Sun, Ling-Dong; Zhang, Hongyan

2017-09-05

It is crucial for cell physiology to keep the homeostasis of pH, and it is highly demanded yet challenging to develop luminescence resonance energy transfer (LRET)-based near-infrared (NIR) ratiometric luminescent sensor for the detection of pH fluctuation with NIR excitation. As promising energy donors for LRET, upconversion nanoparticles (UCNPs) have been widely used to fabricate nanosensors, but the relatively low LRET efficiency limits their application in bioassay. To improve the LRET efficiency, core/shell/shell structured β-NaGdF 4 @NaYF 4 :Yb,Tm@NaYF 4 UCNPs were prepared and decorated with hemicyanine dyes as an LRET-based NIR ratiometric luminescent pH fluctuation-nanosensor for the first time. The as-developed nanosensor not only exhibits good antidisturbance ability, but it also can reversibly sense pH and linearly sense pH in a range of 6.0-9.0 and 6.8-9.0 from absorption and upconversion emission spectra, respectively. In addition, the nanosensor displays low dark toxicity under physiological temperature, indicating good biocompatibility. Furthermore, live cell imaging results revealed that the sensor can selectively monitor pH fluctuation via ratiometric upconversion luminescence behavior.

Luminescent properties of BaCl2-Eu microcrystals embedded in a CsI matrix

International Nuclear Information System (INIS)

Pushak, A.; Vistovskyy, V.; Voloshinovskii, A.; Savchyn, P.; Antonyak, O.; Demkiv, T.; Dacyuk, Yu.; Myagkota, S.; Gektin, A.

2013-01-01

The spectral-luminescent properties of CsI-BaCl 2 (1 mol%)-Eu(0.02 mol%) crystalline system are studied. Europium ion doped BaCl 2 microcrystals embedded in a CsI matrix are revealed on CsI-BaCl 2 (1 mol%)-Eu(0.02 mol%) freshly cleaved surface by the scanning electron microscopy. The size of microcrystals is shown to be within 0.5–5 microns. The luminescent parameters of the BaCl 2 -Eu 2+ microcrystals are shown to be similar to ones of a single crystal analogue. The 4f → 5d absorption transitions in europium ions and the reabsorption of the intrinsic emission of the CsI host are the main excitation mechanisms of europium luminescence in the BaCl 2 microcrystals. -- Highlights: ► The formation of chloride BaCl 2 :Eu microcrystals in the case of BaCl 2 doped CsI crystal has been revealed. ► The observed size of microcrystals at BaCl 2 concentration of 1% is about 0.5–5 μm. ► Majority of Eu 2+ ions in CsI-BaCl 2 -EuCl 3 crystalline system enters into BaCl 2 microcrystals. ► The luminescent parameters of the BaCl 2 :Eu 2+ microcrystals and its bulk analogue are similar

Applications of a table-top time-resolved luminescence spectrometer with nanosecond soft X-ray pulse excitation

Czech Academy of Sciences Publication Activity Database

Brůža, P.; Pánek, D.; Fidler, V.; Benedikt, P.; Čuba, V.; Gbur, T.; Boháček, Pavel; Nikl, Martin

2014-01-01

Roč. 61, č. 1 (2014), s. 448-451 ISSN 0018-9499 R&D Projects: GA ČR GA13-09876S Institutional support: RVO:68378271 Keywords : LiCaAlF 6 * luminescence * scintillators * soft x-ray * SrHfO 3 * time-resolved spectroscopy * ZnO :Ga Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.283, year: 2014

Temperature dependent luminescence Cr3+doped GdAl3(BO3)4 and YAl3(BO3)4

NARCIS (Netherlands)

Malysa, B.; Meijerink, A; Jüstel, Thomas

Chromium activated YAl3(BO3)4 (YAB) and GdAl3(BO3)4 (GAB) were synthesized and show efficient broad band near infrared emission under excitation in the UV, blue and orange spectral regions. Temperature dependent luminescence measurements for GAB:1%Cr3+ and YAB:1%Cr3+ reveal high quenching

Tunneling-recombination luminescence between Ag0 and Ag2+ in KCl:AgCl

International Nuclear Information System (INIS)

Delbecq, C.J.; Dexter, D.L.; Yuster, P.H.

1978-01-01

Appropriate treatment of a KCl:AgCl crystal results in the trapping of electrons as silver atoms, Ag 0 , and positive holes as AgCl 4 2- , Ag 2+ , centers. Optical excitation of Ag 0 in such a crystal at T 0 and Ag 2+ pairs, similar to the Ag 0 -Cl 2 - tunneling-recombination studies we previously reported. We have shown that Ag 2+ centers are involved in the emission process by preferentially orienting the anisotropic Ag 2+ at 6 K by excitation with polarized light and observing that the afterglow is polarized. Upon warming to 50 K, where the preferentially oriented Ag 2+ can change orientation, a strong reversal in the degree of polarization occurs which finally decays to zero. The characteristics of this luminescence can be understood if we assume: (i) a tunneling-recombination mechanism in which the orientation of the electric vector of the emitted radiation depends on the position of the Ag 0 relative to the Ag 2+ and (ii) the tunneling is anisotropic and depends on the location of the Ag 0 relative to the anisotropic Ag 2+ . The latter assumption is based on the tetragonal (d-like) symmetry of the Ag 2+ complex. Good quantitative agreement between theory and experiment has been obtained on the decay kinetics, the degree of polarization, and the polarization reversal