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Microwave-Assisted Synthesis and Photophysical Properties of Poly-Imine Ambipolar Ligands and Their Rhenium(I) Carbonyl Complexes

Description: The phenomenon luminescence rigidochromism has been reported since the 1970s in tricarbonyldiimine complexes with a general formula [R(CO)3LX] using conventional unipolar diimine ligands such as 2,2;-bipyridine or 1,10-phenanthroline as L, and halogens or simple solvents as X. As a major part of this dissertation, microwave-assisted synthesis, purification, characterization and detailed photoluminescence studies of the complex fac-[ReCl(CO)3L], 1, where L = 4-[4,6-bis(3,5-dimethyl-1H-pyrazol-1-yl]-N,N-diethylbenzenamine are reported. The employment of microwaves in the preparation of 1 decreased the reaction time from 48 to 2 hours compared to the conventional reflux method. Stoichiometry variations allows for selective preparation of either a mononuclear, 1, or binuclear, fac-[Re2Cl2(CO)6], 2, complex. The photophysical properties of 1 were analyzed finding that it possesses significant luminescence rigidochromism. The steady state photoluminescence emission spectra of 1 in solution shift from 550 nm in frozen media to 610 nm when the matrix becomes fluid. Moreover, a very sensitive emission spectral analysis of 0.1 K temperatures steps shows a smooth transition through the glass transition temperature of the solvent host. Furthermore, synthetic modifications to L have attained a family of ambipolar compounds that have tunable photophysical, thermophysical and other material properties that render them promising candidates for potential applications in organic electronics and/or sensors - either as is or for their future complexes with various transition metals and lanthanides.
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Date: August 2017
Creator: Salazar Garza, Gustavo Adolfo
Partner: UNT Libraries

Photochemical and Photophysical Properties of Gold(I) Complexes and Phosphorescence Sensitization of Organic Luminophores

Description: Two major topics that involve synthetic strategies to enhance the phosphorescence of organic and inorganic luminophores have been investigated. The first topic involves, the photophysical and photochemical properties of the gold (I) complexes LAuIX (L = CO, RNC where R = alkyl or aryl group; X = halide or pseudohalide), which have been investigated and found to exhibit Au-centered phosphorescence and tunable photochemical reactivity. The investigations have shown a clear relationship between the luminescence energies and association modes. We have also demonstrated for the first time that aurophilic bonding and the ligand p-acceptance can sensitize the photoreactivity of Au(I) complexes. The second topic involves conventional organic fluorophores (arenes), which are made to exhibit room-temperature phosphorescence that originates from spin-orbit coupling owing to either an external or internal heavy atom effect in systematically designed systems that contain d10 metals. Facial complexation of polycyclic arenes to tris[{m-(3,4,5,6-tetrafluorophenylene)}mercury(II)], C18F12Hg3 (1) results in crystalline adducts that exhibit bright RGB (red-green-blue) phosphorescence bands at room temperature. This arene-centered phosphorescence is always accompanied by a reduction of the triplet excited state lifetime due to its sensitization by accelerating the radiative instead of the non-radiative decay. The results of both topics are significant for rational design of efficient metal and arene-centered phosphors for molecular light emitting diodes in addition to the fundamental novelties in inorganic chemistry and molecular spectroscopy.
Date: August 2006
Creator: El-Bjeirami, Oussama
Partner: UNT Libraries

Phosphorescent Emissions of Coinage Metal-Phosphine Complexes: Theory and Photophysics

Description: The major topics discussed are all relevant to the bright phosphorescent emissions of coinage metal complexes (Cu(I), Ag(I) and Au(I)) with an explanation of the theoretical background, computational results and ongoing work on the application in materials and optoelectronic devices. Density functional computations have been performed on the majority of the discussed complexes and determined that the most significant distortion that occurs in Au(I)-phosphine complexes is a near and beyond a T-shape within the P-Au-P angle when the complexes are photoexcited to the lowest phosphorescent excited state. The large distortion is experimentally qualified with the large Stokes' shift that occurs between the excitation and emission spectra and can be as large as 18 000 cm-1 for the neutral Au(I) complexes. The excited state distortion has been thoroughly investigated and it is determined that not only is it pertinent to the efficient luminescence but also for the tunability in the emission. The factors that affect tunability have been determined to be electronics, sterics, rigidity of solution and temperature. The luminescent shifts determined from varying these parameters have been described systematically and have revealed emission colors that span the entire visible spectrum. These astounding features that have been discovered within studies of coinage metal phosphorescent complexes are an asset to applications ranging from materials development to electronics.
Date: December 2009
Creator: Sinha, Pankaj
Partner: UNT Libraries

Detection of hexavalent uranium with inline and field-portable immunosensors

Description: An antibody that recognizes a chelated form of hexavalent uranium was used in the development of two different immunosensors for uranium detection. Specifically, these sensors were utilized for the analysis of groundwater samples collected during a 2007 field study of in situ bioremediation in a aquifer located at Rifle, CO. The antibody-based sensors provided data comparable to that obtained using Kinetic Phosphorescence Analysis (KPA). Thus, these novel instruments and associated reagents should provide field researchers and resource managers with valuable new tools for on-site data acquisition.
Date: October 2, 2008
Creator: Melton, Scott J.; Yu, Haini; Ali, Mehnaaz F.; Williams, Kenneth H; Wilkins, Michael J.; Long, Philip E. et al.
Partner: UNT Libraries Government Documents Department

A Computational Investigation of the Photophysical, Electronic and Bonding Properties of Exciplex-Forming Van der Waals Systems

Description: Calculations were performed on transition-metal complexes to (1) extrapolate the structure and bonding of the ground and phosphorescent states (2) determine the luminescence energies and (3) assist in difficult assignment of luminescent transitions. In the [Pt(SCN)4]2- complex, calculations determined that the major excited-state distortion is derived from a b2g bending mode rather than from the a1g symmetric stretching mode previously reported in the literature. Tuning of excimer formation was explained in the [Au(SCN)2]22- by interactions with the counterion. Weak bonding interactions and luminescent transitions were explained by calculation of Hg dimers, excimers and exciplexes formed with noble gases.
Date: December 2007
Creator: Sinha, Pankaj
Partner: UNT Libraries

Evaluation of kinetic phosphorescence analysis for the determination of uranium

Description: In the past, New Brunswick Laboratory (NBL) has used a fluorometric method for the determination of sub-microgram quantities of uranium. In its continuing effort to upgrade and improve measurement technology, NBL has evaluated the commercially-available KPA-11 kinetic phosphorescence analyzer (Chemchek, Richland, WA). The Chemchek KPA-11 is a bench-top instrument which performs single-measurement, quench-corrected analyses for trace uranium. It incorporates patented kinetic phosphorimetry techniques to measure and analyze sample phosphorescence as a function of time. With laser excitation and time-corrected photon counting, the KPA-11 has a lower detection limit than conventional fluorometric methods. Operated with a personal computer, the state-of-the-art KPA-11 offers extensive time resolution and phosphorescence lifetime capabilities for additional specificity. Interferences are thereby avoided while obtaining precise measurements. Routine analyses can be easily and effectively accomplished, with the accuracy and precision equivalent to the pulsed-laser fluorometric method presently performed at NBL, without the need for internal standards. Applications of kinetic phosphorimetry at NBL include the measurement of trace level uranium in retention tank, waste samples, and low-level samples. It has also been used to support other experimental activities at NBL by the measuring of nanogram amounts of uranium contamination (in blanks) in isotopic sample preparations, and the determining of elution curves of different ion exchange resins used for uranium purification. In many cases, no pretreatment of samples was necessary except to fume them with nitric acid, and then to redissolve and dilute them to an appropriate concentration with 1 M HNO{sub 3} before measurement. Concentrations were determined on a mass basis ({micro}g U/g of solution), but no density corrections were needed since all the samples (including the samples used for calibration) were in the same density matrix (1 M HNO{sub 3}). A statistical evaluation of the determination of uranium using kinetic phosphorimetry is described in this report, along with ...
Date: December 1, 1997
Creator: Croatto, P.V.; Frank, I.W.; Johnson, K.D.; Mason, P.B. & Smith, M.M.
Partner: UNT Libraries Government Documents Department

Computational Studies of Bonding and Phosphorescent Properties of Group 12 Oligomers and Extended Excimers.

Description: Density functional (ca, BLYP, BPW91, B3LYP and B3PW91), MP2 and CCSD(T) methods in combination with LANL2DZ or cc-pVxZ-PP (where x=D(double), T(triple) Q(quadruple), and 5(quintuple)) basis sets have been employed in computing electronic transition energies of zinc and cadmium monomers. CCSD(T)/aug-cc-pV5Z-PP combination finds values that are 150 cm-1 from the experimental value for the zinc monomer and 240 cm-1 remove from the cadmium monomer excitation experimental value. These method/basis set combinations are also used to find spectroscopic values (re, De, we, wexe, Be , and Te) that rival experimental values for dimers and excimers. Examples of this can be seen with the CCSD(T)/aug-cc-pV5Z-PP combination phosphorescent emission results. The values found are within 120 cm-1 of the zinc emission energy and 290 cm-1 of the cadmium emission energy. While this combination rigorously models spectroscopic constants for monomers, dimers, and excimers, it does not efficiently model these constants for larger clusters with available modern computational resources. It is important to show spectroscopic trends (bonding, phosphorescent excitation and emissions) as clusters increase as the monomer and dimer emission energies do not model solid state metallophilic interactions and phosphorescence. The MP2/LANL2DZ combinations show qualitative cooperative bonding trends in group oligomers and extended excimers as size increases and shape change. Changes in excitation and emission energies are also shown as a function of size and shape of the clusters.
Date: August 2008
Creator: Determan, John J.
Partner: UNT Libraries

Sensitization of Lanthanides and Organic-Based Phosphorescence via Energy Transfer and Heavy-Atom Effects

Description: The major topics discussed are the phosphorescence sensitization in the lanthanides via energy transfer and in the organics by heavy atom effects. The f-f transitions in lanthanides are parity forbidden and have weak molar extinction coefficients. Upon complexation with the ligand, ttrpy (4'-p-Tolyl-[2,2':6',2"]-terpyridine) the absorption takes place through the ligand and the excitation is transferred to the lanthanides, which in turn emit. This process is known as "sensitized luminescence." Bright red emission from europium and bright green emission from terbium complexes were observed. There is ongoing work on the making of OLEDs with neutral complexes of lanthanide hexafluoroacetyl acetonate/ttrpy, studied in this dissertation. Attempts to observe analogous energy transfer from the inorganic donor complexes of Au(I) thiocyanates were unsuccessful due to poor overlap of the emissions of these systems with the absorptions of Eu(III) and Tb(III). Photophysics of silver-aromatic complexes deals with the enhancement of phosphorescence in the aromatics. The heavy atom effect of the silver is responsible for this enhancement in phosphorescence. Aromatics such as naphthalene, perylene, anthracene and pyrene were involved in this study. Stern Volmer plots were studied by performing the quenching studies. The quenchers employed were both heavy metals such as silver and thallium and lighter metal like potassium. Dynamic quenching as the predominant phenomenon was noticed.
Date: May 2010
Creator: Arvapally, Ravi K.
Partner: UNT Libraries

Solid-matrix luminescence analysis. Final technical report, June 15, 1986--June 14, 1995

Description: In this report, the major results and conclusions of the research over the last two years and five months will be considered. The report discusses the physicochemical interactions discovered that are important for solid-matrix luminescence (SML), and the development of new interaction models which are very useful for the understanding the phenomena that are relevant for SML. The SML of 4-phenylphenol and 2-phenyl phenol adsorbed on filter paper is described. In addition, some new analytical methodology and applications are discussed.
Date: September 1, 1996
Creator: Hurtubise, R.J.
Partner: UNT Libraries Government Documents Department

Solid-Matrix Luminescence Analysis and Coupling Solid-Matrix Luminescence with Separation Methodology

Description: In this report, the major results and conclusions of the research over the last two years and five months is considered. The report discusses the mechanistic aspects of oxygen quenching of solid-matrix phosphorescence (SMP), mechanistic aspects of moisture quenching of SMP, interactions and methodology to investigate phosphors in glucose glasses, new methods for coating filter paper for solid-phase microextraction with solid-matrix fluorescence (SMF) and SMP detection, mechanistic consideration of the heavy-atom quenching of the SMF and the enhancement of SMP of benzo[a]pyrene-DNA adducts, and new developments in liquid-liquid-liquid microextraction.
Date: June 14, 2004
Creator: Hurtubise, Robert J.
Partner: UNT Libraries Government Documents Department

Solid-matrix luminescence analysis. Progress report, 15 June 1992--31 October 1994

Description: Interaction models were developed for moisture effects on room-temperature fluorescence (RTF) and room-temperature phosphorescence (RTP) of compounds adsorbed on filter paper. The models described both dynamic and matrix quenching and also related the Young modulus of filter paper to quenching of phosphor on moist filter paper. Photophysical parameters for lumiphors in solution and on solid matrices were compared. Results showed that for some compounds, solid-matrix luminescence has greater analytical potential than solution luminescence. Also, the solid-matrix systems into one of two categories depending on how the intersystem crossing rate constants change with temperature. The first study was carried out on effects of heavy atom on solid-matrix luminescence. With some heavy atoms, maximum solid-matrix phosphorescence quantum yield was obtained at room temperature, and there was no need to use low temperature to obtain a strong phosphorescence signal. By studying solid-matrix luminescence properties of phosphors adsorbed on sodium acetate and deuterated sodium acetate, an interaction model was developed for p-aminobenzoic acid anion adsorbed on sodium acetate. It was shown that the energy-gap law was applicable to solid-matrix luminescence. Also, deuterated phenanthrene and undeuterated phenanthrene were used to study nonradiative transition of excited triplet state of adsorbed phosphors. Heat capacities of several solid matrices were obtained vs temperature and related to vibrational coupling of solid matrix with phosphor. Photophysical study was performed on the hydrolysis products of benzo(a)pyrene-DNA adducts. Also, an analytical method was developed for tetrols in human lung fractions. Work was initiated on the formation of room temperature glasses with glucose and trehalose. Also, work has begun for the development of an oxygen sensor by measuring the RTP quenching of triphenylene on filter paper.
Date: December 31, 1994
Creator: Hurtubise, R.J.
Partner: UNT Libraries Government Documents Department

Design, Synthesis, and Characterization of Aqueous Polymeric Hybrid Composites and Nanomaterials of Platinum(II) and Gold(I) Phosphorescent Complexes for Sensing and Biomedical Applications

Description: The two major topics studied in this dissertation are the gold(I) pyrazolate trimer {[Au(3-R,5-R’)Pz]3} complexes in aqueous chitosan polymer and phosphorescent polymeric nanoparticles based on platinum(II) based complex. The first topic is the synthesis, characterization and optical sensing application of gold(I) pyrazolate trimer complexes within aqueous chitosan polymer. A gold(I) pyrazolate trimer complex, {[Au(3-CH3,5-COOH)Pz]3}, shows high sensitivity and selectivity for silver ions in aqueous media, is discussed for optical sensing and solution-processed organic light emitting diodes (OLEDs) applications. Gold(I) pyrazolate trimer complexes are bright red emissive in polymeric solution and their emission color changes with respect to heavy metal ions, pH and dissolved carbon dioxide. These photophysical properties are very useful for designing the optical sensors. The phosphorescent polymeric nanoparticles are prepared with Pt-POP complex and polyacrylonitrile polymer. These particles show excellent photophysical properties and stable up to >3 years at room temperature. Such nanomaterials have potential applications in biomedical and polymeric OLEDs. The phosphorescent hybrid composites are also prepared with Pt-POP and biocompatible polymers, such as chitosan, poly-l-lysine, BSA, pnipam, and pdadmac. Photoluminescent enhancement of Pt-POP with such polymers is also involved in this study. These hybrid composites are promising materials for biomedical applications such as protein labeling and bioimaging.
Date: December 2015
Creator: Upadhyay, Prabhat Kumar
Partner: UNT Libraries

Biological Applications of a Strongly Luminescent Platinum (II) Complex in Reactive Oxygen Species Scavenging and Hypoxia Imaging in Caenorhabditis elegans

Description: Phosphorescent transition metal complexes make up an important group of compounds that continues to attract intense research owing to their intrinsic bioimaging applications that arise from bright emissions, relatively long excited state lifetimes, and large stokes shifts. Now for biomaging assay a model organism is required which must meet certain criteria for practical applications. The organism needs to be small, with a high turn-over of progeny (high fecundity), a short lifecycle, and low maintenance and assay costs. Our model organism C. elegans met all the criteria. The ideal phosphor has low toxicity in the model organism. In this work the strongly phosphorescent platinum (II) pyrophosphito-complex was tested for biological applications as a potential in vivo hypoxia sensor. The suitability of the phosphor was derived from its water solubility, bright phosphorescence at room temperature, and long excited state lifetime (~ 10 µs). The applications branched off to include testing of C. elegans survival when treated with the phosphor, which included lifespan and fecundity assays, toxicity assays including the determination of the LC50, and recovery after paraquat poisoning. Quenching experiments were performed using some well knows oxygen derivatives, and the quenching mechanisms were derived from Stern-Volmer plots. Reaction stoichiometries were derived from Job plots, while percent scavenging (or antioxidant) activities were determined graphically. The high photochemical reactivity of the complex was clearly manifested in these reactions.
Date: December 2015
Creator: Kinyanjui, Sophia Nduta
Partner: UNT Libraries

Optically-Based Array Sensors for Selective In Situ Analysis of Tank Waste

Description: The objective of this research program is to conduct the fundamental research necessary to develop an array of chemically selective sensors, based on highly selective molecular recognition agents and highly sensitive fluorescence and/or phosphorescence techniques, that can be coupled to fiber optics for remote analytical applications. These sensors will be of great value to DOE for the safe and cost-effective in situ characterization of high level waste tanks. Characterization of high level tank waste currently entails obtaining and analyzing core samples at the cost of about $1 million per sample. The ability to detect and measure specific chemicals and radionuclides directly inside a high level waste tank using a remote sensing device could result in considerable benefits with regard to both cost savings and safety issues. This multidisciplinary approach to the design of sensors will be to immobilize agents for selective molecular recognition, chosen from solvent extraction processes, in an organic polymer matrix that mimics the organic medium in an aqueous-nonaqueous extraction. In this manner the matrix will enhance both the separation and the achievement of chemical selectivity.
Date: June 1, 1999
Creator: Brown, Gilbert M.; Walt, David R.; Dabestani, Reza & Bonnesen, Peter V.
Partner: UNT Libraries Government Documents Department

T-1020 NaI crystal test for DM-Ice

Description: This is a memorandum of understanding between the Fermi National Accelerator Laboratory (Fermilab) and the experiments of the NaI Crystal Test for DM-Ice from the University of Wisconsin who have committed to participate in detector tests to be carried out during the 2011-2012 Fermilab Neutrino program. The memorandum is intended primarily for the purpose of recording expectations for budget estimates and work allocations for Fermilab, the funding agencies and the participating institutions. It reflects an arrangement that currently is satisfactory to the parties; however, it is recognized and anticipated that changing circumstances of the evolving research program will necessitate revisions. The parties agree to modify this memorandum to reflect such required adjustments. Actual contractual obligations will be set forth in separate documents. The DM-Ice collaboration is designing a sodium-iodide (NaI) based detector for a direct dark matter search. The detectors should have low readout noise and background levels to carry out a sensitive search. A 17-kg version of the experiment is running at the South Pole, 2500 m deep in the Antarctic ice, and a large scale experiment is currently being designed. One of the keys to the success of the experiment is to have a good understanding of the background levels intrinsic in the NaI detectors. To measure the background level, the detectors have to be shielded against cosmic rays. The lead shielding used for DAMIC in the Minos Underground Areas is a well-suited location for this test since it offers enough overburden to shield against cosmic rays, lead shielding, and experimental infrastructure. The goal of the test is to assess the background levels in the detector and to assess the characteristics of phosphorescence induced by muons and 100 keV-3 MeV gamma rays.
Date: November 3, 2011
Creator: Maruyama, Reina; Heeger, Karsten; Pierpoint, Zachary; Pettus, Walter; Broerman, Benjamin; Hilgenberg, Chris et al.
Partner: UNT Libraries Government Documents Department

From Antenna to Assay: Lessons Learned in Lanthanide Luminescence

Description: Ligand-sensitized luminescent lanthanide(III) complexes are of considerable current interest due to their unique photophysical properties (micro- to millisecond lifetimes, characteristic and narrow emission bands, and large Stokes shifts), which make them well suited to serve as labels in fluorescence-based bioassays. The long-lived Ln(III) emission can be temporally resolved from scattered light and background fluorescence, resulting in vastly enhanced measurement sensitivity. One of the challenges in this field is the design of sensitizing ligands that provide highly emissive Ln(III) complexes that also possess sufficient stability and aqueous solubility required for practical applications. In this account we give an overview of some of the general properties of the trivalent lanthanides and follow with a summary of advances made in our laboratory in the development of highly luminescent Tb(III) and Eu(III) complexes for applications in biotechnology. A focus of our research has been the optimization of these compounds as potential commercial agents for use in Homogeneous Time Resolved Fluorescence (HTRF) technology, the requirements and current use of which will be briefly discussed. Our approach involves developing high-stability octadentate Tb(III) and Eu(III) complexes that rely on all-oxygen donor atoms as well as using multi-chromophore chelates to increase molar absorptivity compared to earlier examples that utilize a single pendant antenna chromophore. We have found that ligands based on 2-hydroxyisophthalamide (IAM) provide exceptionally emissive Tb(III) complexes with quantum yield values up to ca. 60%. Solution thermodynamic studies have indicated that these complexes are stable at the nanomolar concentrations required for commercial assays. Through synthetic modification of the IAM-chromophore, in conjunction with time-dependent density functional theory (TD-DFT) calculations, we have developed a method to predict absorption and emission properties of these chromophores as a tool to guide ligand design. Additionally we have investigated chiral IAM ligands that yield Tb(III) complexes possessing both high quantum yield values and ...
Date: September 25, 2008
Creator: Moore, Evan; Samuel, Amanda & Raymond, Kenneth
Partner: UNT Libraries Government Documents Department

Electronic transitions of some pi-molecular charge transfer complexes. [Anthracene--pyromellitic dianhydride (PMDA) or pyrene--PMDA in naphthalene--PMDA host]

Description: A unique phonon progression in the phosphorescence spectrum of pyrene-PMDA (Py-PMDA) in naphthalene-PMDA (N-PMDA) is reported. Calculations of the electron-phonon coupling strength parameter for the ground and excited states indicate strong coupling for the fractional CT contribution of Py-PMDA to the observed phosphorescent state. Model calculations indicate that the observed low frequency phonon mode corresponds to a low energy rotation of the rigid guest complex and not a symmetric donor-acceptor stretch. The unusual reduction of the phonon mode frequency in the excited ground state is explained in terms of a contracted complex that can more easily rotate in a larger cavity. A brief phonon progression is also observed for the mixed crystal A-PMDA in N-PMDA. For both mixed crystals, Py-PMDA in N-PMDA and A-PMDA in N-PMDA, the energy spacing between the zero-phonon vibrational bands in the mixed CT crystal phosphorescence spectrum are very similar to those obtained from the phosphorescence spectrum of the pure donor in a rigid matrix. There is a large blue shift between the origin band of the mixed CT crystal phosphorescence spectrum and the origin band of the pure donor phosphorescence spectrum for the A-PMDA mixed crystal, but not for the Py-PMDA mixed crystal. The structureless CT absorption spectra of Py-PMDA and A-PMDA mixed crystals indicate strong electron-phonon coupling, as does the structureless CT fluorescence spectrum of A-PMDA in N-PMDA. No CT fluorescence was observed that can be conclusively attributed to Py-PMDA. The CT absorption and emission spectra of the neat N-PMDA host reveal no sharp structure, indicating strong-exciton-phonon coupling. The particularly long absorption tail observed for N-PMDA neat crystals supports the contention that N-PMDA may be disordered.
Date: December 1, 1977
Creator: Beckman, R. L.
Partner: UNT Libraries Government Documents Department

Light output and radiation damage in a YAlO{sub 3}:Ce crystal

Description: The optical absorption, light output and effects of radiation damage have been studied in a 2.1 {times} 2.1 {times} 2.1 cm{sup 3} crystal of YAlO{sub 3}:Ce. The light yield produces approximately 2867 photoelectrons per MeV on a photomultiplier tube with a bialkali photocathode. The scintillation and light transmission properties of the crystal were characterized before and after exposure to 1 Mrad of {sup 60}Co gamma rays. Significant radiation induced optical absorption was observed near the optical band edge of the crystal, along with an extremely intense phosphorescence after irradiation. Partial spontaneous recovery from the damage occurred at room temperature, and it was possible to induce additional recovery by optical bleaching.
Date: August 1, 1994
Creator: Kierstead, J. A.; Stoll, S. P. & Woody, C. L.
Partner: UNT Libraries Government Documents Department

LuAlO{sub 3}: A high density, high speed scintillator for gamma detection

Description: We present measurements of the scintillation properties cerium doped lutetium aluminum perovskite, LuAlO{sub 3}:C, new dense ({rho}=8.34 g/cm{sup 3}) inorganic scintillator. This material has a 511 keV interaction length and photoelectric fraction 1.1 cm and 32% respectively, which are well suited to gamma ray detection. In powdered form with 0.5% cerium concentration, the scintillation light output is estimated to be 9,600 photons/MeV of deposited energy, the emission spectrum is a single peak centered at 390 nm, and the fluorescence lifetime is described by the sum of 3 exponential terms, with 60% of the light being emitted with a 11 ns decay time, 26% with a 28 ns decay time, and 13% with a 835 ns decay time. Single crystals contaminated with =10% lutetium aluminum garnet (Lu{sub 3}Al{sub 5}O{sub l2}) have significantly altered scintillation properties. The light output is 26,000 photons/MeV (3.2 times that of BGO), but the decay time increases significantly (1% of the light is emitted with a 10 ns decay time, 15% with a 245 ns decay time, and 85% with a 2010 ns decay time) and the emission spectrum is dominated by a peak centered at 315 nm with a secondary peak centered at 500 rum. The short decay lifetime, high density, and reasonable light output of LuAlO{sub 3}:C (the perovskite phase) suggest that it is useful for applications where high counting rates, good stopping power, good energy resolution, and fast timing are important. However, it is necessary to grow single crystals that are uncontaminated by the garnet phase to realize these properties.
Date: November 1, 1994
Creator: Moses, W. W.; Derenzo, S. E.; Fyodorov, A.; Korzhik, M.; Gektin, A.; Minkov, B. et al.
Partner: UNT Libraries Government Documents Department

Vacuum uv spectroscopy and photochemistry. V. Spectra, ionization, and molecular interactions. Annual report, September 15, 1966-September 14, 1967

Description: The first part of the report concerns itself with studies on photoionization, ionizing energy transfer and vacuum ultraviolet spectroscopy of olefins. In the second part of the report, semi-empirical methods of calculation have been examined and applied to predict the spectra and ionization potentials of some organo-metallics. The third part of the report contains a basic contribution towards understanding the mechanism of interaction of radiation with matter as well as the interaction between molecules in the condensed phase. The mechanism of the phosphorescence emission is understood and the effects of environmental perturbations is examined. Theoretical and experimental examination of the origin of optical rotation has been carried out and reported.
Date: June 1, 1967
Creator: El-Sayed, M.A.
Partner: UNT Libraries Government Documents Department