WorldWideScience

Sample records for americium selenides

  1. Chemistry of americium

    Energy Technology Data Exchange (ETDEWEB)

    Schulz, W.W.

    1976-01-01

    Essential features of the descriptive chemistry of americium are reviewed. Chapter titles are: discovery, atomic and nuclear properties, collateral reading, production and uses, chemistry in aqueous solution, metal, alloys, and compounds, and, recovery, separation, purification. Author and subject indexes are included. (JCB)

  2. Formation of copper-indium-selenide and/or copper-indium-gallium-selenide films from indium selenide and copper selenide precursors

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, Calvin J [Lakewood, CO; Miedaner, Alexander [Boulder, CO; Van Hest, Maikel [Lakewood, CO; Ginley, David S [Evergreen, CO; Nekuda, Jennifer A [Lakewood, CO

    2011-11-15

    Liquid-based indium selenide and copper selenide precursors, including copper-organoselenides, particulate copper selenide suspensions, copper selenide ethylene diamine in liquid solvent, nanoparticulate indium selenide suspensions, and indium selenide ethylene diamine coordination compounds in solvent, are used to form crystalline copper-indium-selenide, and/or copper indium gallium selenide films (66) on substrates (52).

  3. The Biokinetic Model of Americium

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    To improve in vivo measurements for detecting internal exposure from transuranium radio nuclides, such as neptunium, plutonium, americium, the bioknetic model was studied. According to ICRP report (1993, 1995, 1997) and other research, the

  4. Precursors for formation of copper selenide, indium selenide, copper indium diselenide, and/or copper indium gallium diselenide films

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, Calvin J; Miedaner, Alexander; Van Hest, Maikel; Ginley, David S

    2014-11-04

    Liquid-based precursors for formation of Copper Selenide, Indium Selenide, Copper Indium Diselenide, and/or copper Indium Galium Diselenide include copper-organoselenides, particulate copper selenide suspensions, copper selenide ethylene diamine in liquid solvent, nanoparticulate indium selenide suspensions, and indium selenide ethylene diamine coordination compounds in solvent. These liquid-based precursors can be deposited in liquid form onto substrates and treated by rapid thermal processing to form crystalline copper selenide and indium selenide films.

  5. Aqueous Chloride Operations Overview: Plutonium and Americium Purification/Recovery

    Energy Technology Data Exchange (ETDEWEB)

    Kimball, David Bryan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Skidmore, Bradley Evan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-06-22

    Acqueous Chloride mission is to recover plutonium and americium from pyrochemical residues (undesirable form for utilization and storage) and generate plutonium oxide and americium oxide. Plutonium oxide is recycled into Pu metal production flowsheet. It is suitable for storage. Americium oxide is a valuable product, sold through the DOE-OS isotope sales program.

  6. 5f-Electron Delocalization in Americium

    DEFF Research Database (Denmark)

    Skriver, Hans Lomholt; Andersen, O. K.; Johansson, B.

    1980-01-01

    The pressure-volume relation for americium has been obtained without adjustable parameters from self-consistent, spin-polarized band calculations. Around 100 kbar we find a first-order transition to a state with low volume and no spin. This is consistent with preliminary high-pressure measurements....

  7. The relative physiological and toxicological properties of americium and plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Carter, R.E.; Busch, E.; Johnson, O. [and others

    1951-11-15

    The relative physiological and toxicological properties of americium and plutonium have been studied following their intravenous administration to rats. The urinary and fecal excretion of americium was similar to that of plutonium administered as Pu(N0{sub 3}){sub 4}. The deposition of americium the tissues and organs of the rat was also similar to that observed for plutonium. The liver and the skeleton were the major sites of deposition. Zirconium citrate administered 15 minutes after injection of americium increased the urinary excretion of americium and decreased the amount found in the liver and the skeleton at 4 and 16 days. LD{sub 30}{sup 50} studies showed americium was slightly less toxic when given in the acute toxic range than was plutonium. The difference was, however, too slight to be important in establishing a larger tolerance does for americium. Survival studies, hematological observations, bone marrow observations, comparison of tumor incidence and the incidence of skeletal abnormalities indicated that americium and plutonium have essentially the same chronic toxicity when given on an equal {mu}c. basis. These studies support the conclusion that the tolerance values for americium should be essentially the same as those for Plutonium.

  8. Thermoelectric Study of Copper Selenide

    Science.gov (United States)

    Yao, Mengliang; Liu, Weishu; Ren, Zhifeng; Opeil, Cyril

    2014-03-01

    Nanostructuring has been shown to be an effective approach in reducing lattice thermal conductivity and improving the figure of merit of thermoelectric materials. Copper selenide is a layered structure material, which has a low thermal conductivity and p-type Seebeck coefficient at low temperatures. We have evaluated several hot-pressed, nanostructured copper selenide samples with different dopants for their thermoelectric properties. The phenomenon of the charge-density wave observed in the nanocomposite, resistivity, Seebeck, thermal conductivity and carrier mobility will be discussed. Funding for this research was provided by the Solid State Solar - Thermal Energy Conversion Center (S3TEC), an Energy Frontier Research Center sponsored by the DOE, Office of Basic Energy Science, Award No. DE-SC0001299/ DE-FG02-09ER46577.

  9. Biological Chemistry of Hydrogen Selenide.

    Science.gov (United States)

    Cupp-Sutton, Kellye A; Ashby, Michael T

    2016-11-22

    There are no two main-group elements that exhibit more similar physical and chemical properties than sulfur and selenium. Nonetheless, Nature has deemed both essential for life and has found a way to exploit the subtle unique properties of selenium to include it in biochemistry despite its congener sulfur being 10,000 times more abundant. Selenium is more easily oxidized and it is kinetically more labile, so all selenium compounds could be considered to be "Reactive Selenium Compounds" relative to their sulfur analogues. What is furthermore remarkable is that one of the most reactive forms of selenium, hydrogen selenide (HSe(-) at physiologic pH), is proposed to be the starting point for the biosynthesis of selenium-containing molecules. This review contrasts the chemical properties of sulfur and selenium and critically assesses the role of hydrogen selenide in biological chemistry.

  10. Biological Chemistry of Hydrogen Selenide

    Directory of Open Access Journals (Sweden)

    Kellye A. Cupp-Sutton

    2016-11-01

    Full Text Available There are no two main-group elements that exhibit more similar physical and chemical properties than sulfur and selenium. Nonetheless, Nature has deemed both essential for life and has found a way to exploit the subtle unique properties of selenium to include it in biochemistry despite its congener sulfur being 10,000 times more abundant. Selenium is more easily oxidized and it is kinetically more labile, so all selenium compounds could be considered to be “Reactive Selenium Compounds” relative to their sulfur analogues. What is furthermore remarkable is that one of the most reactive forms of selenium, hydrogen selenide (HSe− at physiologic pH, is proposed to be the starting point for the biosynthesis of selenium-containing molecules. This review contrasts the chemical properties of sulfur and selenium and critically assesses the role of hydrogen selenide in biological chemistry.

  11. Oxidation Mechanism of Copper Selenide

    Science.gov (United States)

    Taskinen, Pekka; Patana, Sonja; Kobylin, Petri; Latostenmaa, Petri

    2014-09-01

    The oxidation mechanism of copper selenide was investigated at deselenization temperatures of copper refining anode slimes. The isothermal roasting of synthetic, massive copper selenide in flowing oxygen and oxygen - 20% sulfur dioxide mixtures at 450-550 °C indicate that in both atmospheres the mass of Cu2Se increases as a function of time, due to formation of copper selenite as an intermediate product. Copper selenide oxidises to copper oxides without formation of thick copper selenite scales, and a significant fraction of selenium is vaporized as SeO2(g). The oxidation product scales on Cu2Se are porous which allows transport of atmospheric oxygen to the reaction zone and selenium dioxide vapor to the surrounding gas. Predominance area diagrams of the copper-selenium system, constructed for selenium roasting conditions, indicate that the stable phase of copper in a selenium roaster gas with SO2 is the sulfate CuSO4. The cuprous oxide formed in decomposition of Cu2Se is further sulfated to CuSO4.

  12. Surface complexation modeling of americium sorption onto volcanic tuff.

    Science.gov (United States)

    Ding, M; Kelkar, S; Meijer, A

    2014-10-01

    Results of a surface complexation model (SCM) for americium sorption on volcanic rocks (devitrified and zeolitic tuff) are presented. The model was developed using PHREEQC and based on laboratory data for americium sorption on quartz. Available data for sorption of americium on quartz as a function of pH in dilute groundwater can be modeled with two surface reactions involving an americium sulfate and an americium carbonate complex. It was assumed in applying the model to volcanic rocks from Yucca Mountain, that the surface properties of volcanic rocks can be represented by a quartz surface. Using groundwaters compositionally representative of Yucca Mountain, americium sorption distribution coefficient (Kd, L/Kg) values were calculated as function of pH. These Kd values are close to the experimentally determined Kd values for americium sorption on volcanic rocks, decreasing with increasing pH in the pH range from 7 to 9. The surface complexation constants, derived in this study, allow prediction of sorption of americium in a natural complex system, taking into account the inherent uncertainty associated with geochemical conditions that occur along transport pathways.

  13. Self-irradiation and oxidation effects on americium sesquioxide and Raman spectroscopy studies of americium oxides

    Energy Technology Data Exchange (ETDEWEB)

    Horlait, Denis [CEA, DEN, DTEC/SDTC/LEMA, F-30207 Bagnols-sur-Cèze Cedex (France); Caraballo, Richard [CEA, DEN, DTCD/SECM/LMPA, F-30207 Bagnols-sur-Cèze Cedex (France); Lebreton, Florent [CEA, DEN, DTEC/SDTC/LEMA, F-30207 Bagnols-sur-Cèze Cedex (France); Jégou, Christophe [CEA, DEN, DTCD/SECM/LMPA, F-30207 Bagnols-sur-Cèze Cedex (France); Roussel, Pascal [Unité de Catalyse et Chimie du Solide, UMR 8012 CNRS, Ecole Nationale Supérieure de Chimie de Lille BP 90108, 59652 Villeneuve d’Ascq Cedex (France); Delahaye, Thibaud, E-mail: thibaud.delahaye@cea.fr [CEA, DEN, DTEC/SDTC/LEMA, F-30207 Bagnols-sur-Cèze Cedex (France)

    2014-09-15

    Americium oxides samples were characterized by X-ray diffraction (XRD) and Raman spectroscopy, with an emphasis on their structural behavior under oxidation and self-irradiation. Raman spectra of americium dioxide (AmO{sub 2}) and sesquioxide (Am{sub 2}O{sub 3}) were obtained for the first time. With the help of literature data on isostructural oxides, Raman signatures of Ia-3 C-type Am{sub 2}O{sub 3} and P-3m1 A-type Am{sub 2}O{sub 3} are identified. For AmO{sub 2,} a clear band is noted at 390 cm{sup −1}. Its nature is compared to that of the other actinide dioxides. Am{sub 2}O{sub 3} evolution under ambient conditions and against {sup 241}Am α self-irradiation was monitored by powder XRD. The sample, initially composed of A-type Am{sub 2}O{sub 3} as major phase as well as C2/m B-type and C-type structures as minor phases, progressively oxidizes to Fm-3m AmO{sub 2−δ} over a few months. On the basis of diffractogram refinements, evolutions of unit cell volumes caused by self-irradiation are also determined and discussed. - Graphical abstract: The evolution of americium oxide under ambient conditions was monitored using XRD (X-ray diffraction) and Raman spectroscopy. After a thermal treatment under reducing conditions, a polyphasic sample mainly composed of A- and C-type americium sesquioxides is evidenced by XRD and Raman spectroscopy. The sample then evolves through two processes: oxidation and self-irradiation. The first one provokes the progressive appearance of F-type americium dioxide while the initial phases disappear, whereas the main effect of the second is a structural swelling with time. - Highlights: • The first Raman spectroscopy measurements on americium oxides were performed. • Observed Am{sub 2}O{sub 3} Raman bands were identified thanks to data on analogue compounds. • AmO{sub 2} assumed T{sub 2g} band presents a shift compared to the actinide dioxide series. • Am{sub 2}O{sub 3} evolution under self-irradiation and oxidation was also

  14. Plutonium and Americium Geochemistry at Hanford: A Site Wide Review

    Energy Technology Data Exchange (ETDEWEB)

    Cantrell, Kirk J.; Felmy, Andrew R.

    2012-08-23

    This report was produced to provide a systematic review of the state-of-knowledge of plutonium and americium geochemistry at the Hanford Site. The report integrates existing knowledge of the subsurface migration behavior of plutonium and americium at the Hanford Site with available information in the scientific literature regarding the geochemistry of plutonium and americium in systems that are environmentally relevant to the Hanford Site. As a part of the report, key research needs are identified and prioritized, with the ultimate goal of developing a science-based capability to quantitatively assess risk at sites contaminated with plutonium and americium at the Hanford Site and the impact of remediation technologies and closure strategies.

  15. Americium/Curium Disposition Life Cycle Planning Study

    Energy Technology Data Exchange (ETDEWEB)

    Jackson, W.N. [Westinghouse Savannah River Company, AIKEN, SC (United States); Krupa, J.; Stutts, P.; Nester, S.; Raimesch, R.

    1998-04-30

    At the request of the Department of Energy Savannah River Office (DOE- SR), Westinghouse Savannah River Company (WSRC) evaluated concepts to complete disposition of Americium and Curium (Am/Cm) bearing materials currently located at the Savannah River Site (SRS).

  16. Higher Americium Oxidation State Research Roadmap

    Energy Technology Data Exchange (ETDEWEB)

    Mincher, Bruce J. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Law, Jack D. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Goff, George S. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Moyer, Bruce A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Burns, Jon D. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Lumetta, Gregg J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Sinkov, Sergey I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Shehee, Thomas C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hobbs, David T. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2015-12-18

    The partitioning of hexavalent Am from dissolved nuclear fuel requires the ability to efficiently oxidize Am(III) to Am(VI) and to maintain that oxidation state for a length of time sufficient to perform the separation. Several oxidants have been, or are being developed. Chemical oxidants include Ag-catalyzed ozone, Ag-catalyzed peroxydisulfate, Cu(III) periodate, and sodium bismuthate. Hexavalent americium has also now successfully been prepared by electrolysis, using functionalized electrodes. So-called auto-reduction rates of Am(VI) are sufficiently slow to allow for separations. However, for separations based on solvent extraction or ion exchange using organic resins, the high valence state must be maintained under the reducing conditions of the organic phase contact, and a holding oxidant is probably necessary. Until now, only Cu(III) periodate and sodium bismuthate oxidation have been successfully combined with solvent extraction separations. Bismuthate oxidation provided the higher DAm, since it acts as its own holding oxidant, and a successful hot test using centrifugal contactors was performed. For the other oxidants, Ag-catalyzed peroxydisulfate will not oxidize americium in nitric acid concentrations above 0.3 M, and it is not being further investigated. Peroxydisulfate in the absence of Ag catalysis is being used to prepare Am(V) in ion exchange work, discussed below. Preliminary work with Ag-catalyzed ozone has been unsuccessful for extractions of Am(VI) from 6.5 M HNO3, and only one attempt at extraction, also from 6.5 M HNO3, using the electrolytic oxidation has been attempted. However, this high acid concentration was based on the highest Am extraction efficiency using the bismuthate oxidant; which is only sparingly soluble, and thus the oxidation yield is based on bismuthate solubility. Lower acid concentrations may be sufficient with alternative oxidants and work with Ag-ozone, Cu(III) and electrolysis is on-going. Two non

  17. Aqueous Chloride Operations Overview: Plutonium and Americium Purification/Recovery

    Energy Technology Data Exchange (ETDEWEB)

    Gardner, Kyle Shelton [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Kimball, David Bryan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Skidmore, Bradley Evan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-09-28

    These are a set of slides intended for an information session as part of recruiting activities at Brigham Young University. It gives an overview of aqueous chloride operations, specifically on plutonium and americium purification/recovery. This presentation details the steps taken perform these processes, from plutonium size reduction, dissolution, solvent extraction, oxalate precipitation, to calcination. For americium recovery, it details the CLEAR (chloride extraction and actinide recovery) Line, oxalate precipitation and calcination.

  18. Pyrochemical investigations into recovering plutonium from americium extraction salt residues

    Energy Technology Data Exchange (ETDEWEB)

    Fife, K.W.; West, M.H.

    1987-05-01

    Progress into developing a pyrochemical technique for separating and recovering plutonium from spent americium extraction waste salts has concentrated on selective chemical reduction with lanthanum metal and calcium metal and on the solvent extraction of americium with calcium metal. Both techniques are effective for recovering plutonium from the waste salt, although neither appears suitable as a separation technique for recycling a plutonium stream back to mainline purification processes. 17 refs., 13 figs., 2 tabs.

  19. Electrodeposition of americium and physicochemical behaviour of the solution

    Energy Technology Data Exchange (ETDEWEB)

    Becerril-Vilchis, A. (Inst. Nacional de Investigaciones Nucleares, CMRI-LPR, Mexico City (Mexico)); Meas, Y. (CIDETEQ, Queretaro (Mexico)); Rojas-Hernandez, A. (Univ. Autonoma Metropolitana Iztapalapa, Area de Electroquimica, Mexico City (Mexico))

    1994-01-01

    A new method based on concepts of generalized species and equilibria, was applied to represent the thermodynamic distribution of americium species (including condensed phases) in an electrochemical system. Diagrams of the predominance-zone, Existence-predominance and Pourbaix-type for the americium/support electrolyte/water system were constructed. On the basis of these diagrams, the initial distribution of the species in the electrolyte and the deposition conditions were predicted when a current density was applied to a rotating disc electrode in steady-state. These results were related with the Hansen model for actinide electrodeposition. (orig.)

  20. Supercritical Fluid Extraction of Plutonium and Americium from Soil

    Energy Technology Data Exchange (ETDEWEB)

    Fox, R.V.; Mincher, B.J.

    2002-05-23

    Supercritical fluid extraction (SFE) of plutonium and americium from soil was successfully demonstrated using supercritical fluid carbon dioxide solvent augmented with organophosphorus and beta-diketone complexants. Spiked Idaho soils were chemically and radiologically characterized, then extracted with supercritical fluid carbon dioxide at 2,900 psi and 65 C containing varying concentrations of tributyl phosphate (TBP) and thenoyltrifluoroacetone (TTA). A single 45 minute SFE with 2.7 mol% TBP and 3.2 mol% TTA provided as much as 88% {+-} 6.0 extraction of americium and 69% {+-} 5.0 extraction of plutonium. Use of 5.3 mol% TBP with 6.8 mol% of the more acidic beta-diketone hexafluoroacetylacetone (HFA) provided 95% {+-} 3.0 extraction of americium and 83% {+-} 5.0 extraction of plutonium in a single 45 minute SFE at 3,750 psi and 95 C. Sequential chemical extraction techniques were used to chemically characterize soil partitioning of plutonium and americium in pre-SFE soil samples. Sequential chemical extraction techniques demonstrated that spiked plutonium resides primarily (76.6%) in the sesquioxide fraction with minor amounts being absorbed by the oxidizable fraction (10.6%) and residual fractions (12.8%). Post-SFE soils subjected to sequential chemical extraction characterization demonstrated that 97% of the oxidizable, 78% of the sesquioxide and 80% of the residual plutonium could be removed using SFE. These preliminary results show that SFE may be an effective solvent extraction technique for removal of actinide contaminants from soil.

  1. Thermodynamic systematics of oxides of americium, curium, and neighboring elements

    Energy Technology Data Exchange (ETDEWEB)

    Morss, L.R.

    1984-01-01

    Recently-obtained calorimetric data on the sesquioxides and dioxides of americium and curium are summarized. These data are combined with other properties of the actinide elements to elucidate the stability relationships among these oxides and to predict the behavior of neighboring actinide oxides. 45 references, 4 figures, 5 tables.

  2. Reduction Rates for Higher Americium Oxidation States in Nitric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Grimes, Travis Shane [Idaho National Lab. (INL), Idaho Falls, ID (United States); Mincher, Bruce Jay [Idaho National Lab. (INL), Idaho Falls, ID (United States); Schmitt, Nicholas C [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2015-09-30

    The stability of hexavalent americium was measured using multiple americium concentrations and nitric acid concentrations after contact with the strong oxidant sodium bismuthate. Contrary to our hypotheses Am(VI) was not reduced faster at higher americium concentrations, and the reduction was only zero-order at short time scales. Attempts to model the reduction kinetics using zero order kinetic models showed Am(VI) reduction in nitric acid is more complex than the autoreduction processes reported by others in perchloric acid. The classical zero-order reduction of Am(VI) was found here only for short times on the order of a few hours. We did show that the rate of Am(V) production was less than the rate of Am(VI) reduction, indicating that some Am(VI) undergoes two electron-reduction to Am(IV). We also monitored the Am(VI) reduction in contact with the organic diluent dodecane. A direct comparison of these results with those in the absence of the organic diluent showed the reduction rates for Am(VI) were not statistically different for both systems. Additional americium oxidations conducted in the presence of Ce(IV)/Ce(III) ions showed that Am(VI) is reduced without the typical growth of Am(V) observed in the systems sans Ce ion. This was an interesting result which suggests a potential new reduction/oxidation pathway for Am in the presence of Ce; however, these results were very preliminary, and will require additional experiments to understand the mechanism by which this occurs. Overall, these studies have shown that hexavalent americium is fundamentally stable enough in nitric acid to run a separations process. However, the complicated nature of the reduction pathways based on the system components is far from being rigorously understood.

  3. The heat capacity of solid antimony selenide

    Science.gov (United States)

    Pashinkin, A. S.; Malkova, A. S.; Mikhailova, M. S.

    2008-06-01

    The literature data on the heat capacity of solid antimony selenide over the temperature range 53 K- T m were analyzed. The heat capacity of Sb2Se3 was measured from 350 to 600 K on a DSM-2M calorimeter. The experimental data were used to calculate the dependence C p = a + bT + cT -2 and the thermodynamic functions of solid Sb2Se3 over the temperature range 298.15 700 K.

  4. Research program on development of advanced treatment technology for americium-containing aqueous waste in NUCEF

    Energy Technology Data Exchange (ETDEWEB)

    Mineo, Hideaki; Matsumura, Tatsuro; Tsubata, Yasuhiro [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1996-10-01

    A research program was prepared on the development of an advanced treatment process for the americium-containing concentrated aqueous waste in NUCEF, than allows americium recovery for the reuse and the reduction of TRU waste generation. A preliminary analysis was conducted on the separation requirements based on the components estimated for the waste. An R and D strategy was proposed from the view to reduce TRU waste generated in the processing that the highest priority is given on the control of TRU leakage such as americium into the effluent stream after americium recovery and the minimization of salt used in the separation over the decontamination of impurities from americium. The extraction chromatographic method was selected as a candidate technology for americium separation under the principle to use reagents that are functional in acidic conditions such as bidentate extractants of DHEDECMP, CMPO or diamides, considering the larger flexibilities in process modification and possible multi-component separation with compact equipment and the past achievements on the recovery of kg quantities of americium. Major R and D items extracted are screening and evaluation of extractants for americium and plutonium, optimization of separation conditions, selection of denitration method, equipment developments and development of solidification methods of discarded americium after reuse and of various kinds of separation residues. In order to cope these items, four steps of R and D program were proposed, i.e., fundamental experiment in beaker-scale on screening and evaluation of extractants, flowsheet study in bench-scale using simulated and small amount of americium aqueous waste solution to evaluate candidate process, americium recovery test in iron-shielded cell to be installed in NUCEF. It is objected to make recovery of 100g orders of americium used for research on fundamental TRU fuel properties. (J.P.N.)

  5. Supercritical Fluid Extraction of Plutonium and Americium from Soil

    Energy Technology Data Exchange (ETDEWEB)

    Fox, Robert Vincent; Mincher, Bruce Jay

    2002-08-01

    Supercritical fluid extraction (SFE) of plutonium and americium from soil was successfully demonstrated using supercritical fluid carbon dioxide solvent augmented with organophosphorus and beta-diketone complexants. Spiked Idaho soils were chemically and radiologically characterized, then extracted with supercritical fluid carbon dioxide at 2,900 psi and 65°C containing varying concentrations of tributyl phosphate (TBP) and thenoyltrifluoroacetone (TTA). A single 45 minute SFE with 2.7 mol% TBP and 3.2 mol% TTA provided as much as 88% ± 6.0 extraction of americium and 69% ± 5.0 extraction of plutonium. Use of 5.3 mol% TBP with 6.8 mol% of the more acidic beta-diketone hexafluoroacetylacetone (HFA) provided 95% ± 3.0 extraction of americium and 83% ± 5.0 extraction of plutonium in a single 45 minute SFE at 3,750 psi and 95°C. Sequential chemical extraction techniques were used to chemically characterize soil partitioning of plutonium and americium in pre-SFE soil samples. Sequential chemical extraction techniques demonstrated that spiked plutonium resides primarily (76.6%) in the sesquioxide fraction with minor amounts being absorbed by the oxidizable fraction (10.6%) and residual fractions (12.8%). Post-SFE soils subjected to sequential chemical extraction characterization demonstrated that 97% of the oxidizable, 78% of the sesquioxide and 80% of the residual plutonium could be removed using SFE. These preliminary results show that SFE may be an effective solvent extraction technique for removal of actinide contaminants from soil.

  6. Isolation of americium (5) oxalate compounds from solutions

    Energy Technology Data Exchange (ETDEWEB)

    Zubarev, V.G.; Krot, N.N.

    1982-01-01

    Certain conditions of americium (5) isolation with solutions of ammonia and KOH are studied as well as the attitude of hydroxide obtained to heating. Like neptunium (5) hydroxide americium (5) hydroxide probably has the formula AmO/sub 2/OHxxH/sub 2/O, where x is approximately equal to 2.3. It is established that during heating in the air up to 120 deg C hydroxide transforms into AmO/sub 2/. It is shown that in solutions with a high concentration of oxalate-ion americium stability in oxidation state +5 depends greatly on the pH of solution. Complex salts KAmO/sub 2/C/sub 2/O/sub 4/xxH/sub 2/O and CsAmO/sub 2/C/sub 2/O/sub 4/xxH/sub 2/O are synthesized. The identification is made according to the method of preparation and results of analysis of C/sub 2/O/sub 4//sup 2 -/: AmO/sub 2//sup +/ ratio. It is found that the salts are non-isomorphous to similar salts of pentavalent neptunium. CsAmO/sub 2/C/sub 2/O/sub 4/xxH/sub 2/O is identified in cubic crystal system with the lattice constant a=1.25 nm.

  7. Temperature influence study on copper selenide films

    OpenAIRE

    V.RAJENDRAN; PACKIASEELI S. ARULMOZHI; MUTHUMARI S.; Vijayalakshmi, R.

    2016-01-01

    Copper selenide was prepared by film is successfully deposited on a Fluorine-doped Tin Oxide (FTO) substrate by a brush plating technique. The film was uniform, had good adherence to the substrate and was annealed at 300 ◦ C and 500 ◦ C. As the annealing temperature increased, the orientation of the crystallites is more randomized than in the as-prepared film. The structural and optical properties of the film were investigated by XRD, SEM, EDAX, UV-Visible and PL. The XRD pattern indicated th...

  8. Photoluminescence Study of Copper Selenide Thin Films

    Science.gov (United States)

    Urmila, K. S.; Asokan, T. Namitha; Pradeep, B.

    2011-10-01

    Thin films of Copper Selenide of composition of composition Cu7Se4 with thickness 350 nm are deposited on glass substrate at a temperature of 498 K±5 K and pressure of 10-5 mbar using reactive evaporation, a variant of Gunther's three temperature method with high purity Copper (99.999%) and Selenium (99.99%) as the elemental starting material. The deposited film is characterized structurally using X-ray Diffraction. The structural parameters such as lattice constant, particle size, dislocation density; number of crystallites per unit area and strain in the film are evaluated. Photoluminescence of the film is analyzed at room temperature using Fluoro Max-3 Spectrofluorometer.

  9. Separation of americium and curium from complex chemical and radiochemical mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Bochkarev, V.A.; Martynov, N.P.; Slivin, V.G.; Trikanov, A.E.; Fedyaeva, N.V.

    1988-11-01

    This work describes a method for separation and radiochemical purification of nanogram levels of americium and curium from complex chemical and radiochemical mixtures containing tens of milligrams of elements such as aluminum, iron, magnesium, calcium, barium, titanium, potassium, and others, microgram levels of uranium, neptunium, and plutonium, and fission products. Extraction coefficients of americium and curium from these elements are measured. The separation from the macrocomponents was carried out by extraction of americium and curium with butyric acid in the presence of sulfosalicylic acid. Uranium, neptunium, and plutonium were separated from hydrochloric acid solutions, while the rare earth elements were separated from lithium chloride solutions using a column of anion exchange resin AV-17. Alpha measurements were carried out on americium and curium deposited electrolytically on tantalum cathodes. The chemical yield of americium and curium was identical of greater than or equal to 94%, separation time approx. 8 h.

  10. Uncertainty analysis of doses from ingestion of plutonium and americium.

    Science.gov (United States)

    Puncher, M; Harrison, J D

    2012-02-01

    Uncertainty analyses have been performed on the biokinetic model for americium currently used by the International Commission on Radiological Protection (ICRP), and the model for plutonium recently derived by Leggett, considering acute intakes by ingestion by adult members of the public. The analyses calculated distributions of doses per unit intake. Those parameters having the greatest impact on prospective doses were identified by sensitivity analysis; the most important were the fraction absorbed from the alimentary tract, f(1), and rates of uptake from blood to bone surfaces. Probability distributions were selected based on the observed distribution of plutonium and americium in human subjects where possible; the distributions for f(1) reflected uncertainty on the average value of this parameter for non-specified plutonium and americium compounds ingested by adult members of the public. The calculated distributions of effective doses for ingested (239)Pu and (241)Am were well described by log-normal distributions, with doses varying by around a factor of 3 above and below the central values; the distributions contain the current ICRP Publication 67 dose coefficients for ingestion of (239)Pu and (241)Am by adult members of the public. Uncertainty on f(1) values had the greatest impact on doses, particularly effective dose. It is concluded that: (1) more precise data on f(1) values would have a greater effect in reducing uncertainties on doses from ingested (239)Pu and (241)Am, than reducing uncertainty on other model parameter values and (2) the results support the dose coefficients (Sv Bq(-1) intake) derived by ICRP for ingestion of (239)Pu and (241)Am by adult members of the public.

  11. Deposition of copper selenide thin films and nanoparticles

    Science.gov (United States)

    Hu, Yunxiang; Afzaal, Mohammad; Malik, Mohammad A.; O'Brien, Paul

    2006-12-01

    A new method is reported for the growth of copper selenide thin films and nanoparticles using copper acetylacetonate and trioctylphosphine selenide. Aerosol-assisted chemical vapor deposition experiments lead to successful deposition of tetragonal Cu 2Se films. In contrast, hexadecylamine capped nanoparticles are composed of cubic Cu 2-xSe. The deposited materials are optically and structurally characterized. The results of this comprehensive study are described and discussed.

  12. Kilogram-scale purification of americium by ion exchange

    Energy Technology Data Exchange (ETDEWEB)

    Wheelwright, E. J.

    1979-01-01

    Sequential anion and cation exchange processes have been used for the final purification of /sup 241/Am recovered during the reprocessing of aged plutonium metallurgical scrap. Plutonium was removed by absorption of Dowex 1, X-3.5 (30 to 50 mesh) anion exchange resin from 6.5 to 7.5 M HNO/sub 3/ feed solution. Following a water dilution to 0.75 to 1.0 M HNO/sub 3/, americium was absorbed on Dowex 50W, X-8 (50 to 100 mesh) cation exchange resion. Final purification was accomplished by elution of the absorbed band down 3 to 4 successive beds of the same resin, preloaded with Zn/sup 2 +/, with an NH/sub 4/OH buffered chelating agent. The recovery of mixed /sup 241/Am-/sup 243/Am from power reactor reprocessing waste has been demonstrated. Solvent extraction was used to recover a HNO/sub 3/ solution of mixed lanthanides and actinides from waste generated by the reprocessng of 13.5 tons of Shippingport Power Reactor blanket fuel. Sequential cation exchange band-displacement processes were then used to separate americium and curium from the lanthanides and then to separate approx. 60 g of /sup 244/Cm from 1000 g of mixed /sup 241/Am-/sup 243/Am.

  13. Hexavalent Americium Recovery Using Copper(III) Periodate

    Energy Technology Data Exchange (ETDEWEB)

    McCann, Kevin; Brigham, Derek M.; Morrison, Samuel; Braley, Jenifer C.

    2016-11-21

    Separation of americium from the lanthanides is considered one of the most difficult separation steps in closing the nuclear fuel cycle. One approach to this separation could involve oxidizing americium to the hexavalent state to form a linear dioxo cation while the lanthanides remain as trivalent ions. This work considers aqueous soluble Cu3+ periodate as an oxidant under molar nitric acid conditions to separate hexavalent Am with diamyl amylphosphonate (DAAP) in n-dodecane. Initial studies assessed the kinetics of Cu3+ periodate auto-reduction in acidic media to aid in development of the solvent extraction system. Following characterization of the Cu3+ periodate oxidant, solvent extraction studies optimized the recovery of Am from varied nitric acid media and in the presence of other fission product, or fission product surrogate, species. Short aqueous/organic contact times encouraged successful recovery of Am (distribution values as high as 2) from nitric acid media in the absence of redox active fission products. In the presence of a post-PUREX simulant aqueous feed, precipitation of tetravalent species (Ce, Ru, Zr) occurred and the distribution values of 241Am were suppressed, suggesting some oxidizing capacity of the Cu3+ periodate is significantly consumed by other redox active metals in the simulant. The manuscript demonstrates Cu3+ periodate as a potentially viable oxidant for Am oxidation and recovery and notes the consumption of oxidizing capacity observed in the presence of the post-PUREX simulant feed will need to be addressed for any approach seeking to oxidize Am for separations relevant to the nuclear fuel cycle.

  14. Isomorphism and solid solutions among Ag- and Au-selenides

    Energy Technology Data Exchange (ETDEWEB)

    Palyanova, Galina A.; Seryotkin, Yurii V. [Sobolev Institute of Geology and Mineralogy, Novosibirsk (Russian Federation); Novosibirsk State University (Russian Federation); Kokh, Konstantin A., E-mail: k.a.kokh@gmail.com [Sobolev Institute of Geology and Mineralogy, Novosibirsk (Russian Federation); Novosibirsk State University (Russian Federation); Tomsk State University (Russian Federation); Bakakin, Vladimir V. [Nikolaev Institute of Inorganic Chemistry, Novosibirsk (Russian Federation)

    2016-09-15

    Au-Ag selenides were synthesized by heating stoichiometric mixtures of elementary substances of initial compositions Ag{sub 2−x}Au{sub x}Se with a step of x=0.25 (0≤x≤2) to 1050 °C and annealing at 500 °C. Scanning electron microscopy, optical microscopy, electron microprobe analysis and X-ray powder diffraction methods have been applied to study synthesized samples. Results of studies of synthesized products revealed the existence of three solid solutions with limited isomorphism Ag↔Au: naumannite Ag{sub 2}Se – Ag{sub 1.94}Au{sub 0.06}Se, fischesserite Ag{sub 3}AuSe{sub 2} - Ag{sub 3.2}Au{sub 0.8}Se{sub 2} and gold selenide AuSe - Au{sub 0.94}Ag{sub 0.06}Se. Solid solutions and AgAuSe phases were added to the phase diagram of Ag-Au-Se system. Crystal-chemical interpretation of Ag-Au isomorphism in selenides was made on the basis of structural features of fischesserite, naumannite, and AuSe. - Highlights: • Au-Ag selenides were synthesized. • Limited Ag-Au isomorphism in the selenides is affected by structural features. • Some new phases were introduced to the phase diagram Ag-Au-Se.

  15. Oxidative Alkaline leaching of Americium from simulated high-level nuclear waste sludges

    Energy Technology Data Exchange (ETDEWEB)

    Reed, Wendy A.; Garnov, Alexander Yu.; Rao, Linfeng; Nash, Kenneth L.; Bond, Andrew H.

    2004-01-23

    Oxidative alkaline leaching has been proposed to pre-treat the high-level nuclear waste sludges to remove some of the problematic (e.g., Cr) and/or non-radioactive (e.g., Na, Al) constituents before vitrification. It is critical to understand the behavior of actinides, americium and plutonium in particular, in oxidative alkaline leaching. We have studied the leaching behavior of americium from four different sludge simulants (BiPO{sub 4}, BiPO{sub 4 modified}, Redox, PUREX) using potassium permanganate and potassium persulfate in alkaline solutions. Up to 60% of americium sorbed onto the simulants is leached from the sludges by alkaline persulfate and permanganate. The percentage of americium leached increases with [NaOH] (between 1.0 and 5.0 M). The initial rate of americium leaching by potassium persulfate increases in the order BiPO{sub 4} sludge < Redox sludge < PUREX sludge. The data are most consistent with oxidation of Am{sup 3+} in the sludge to either AmO{sub 2}{sup +} or AmO{sub 2}{sup 2+} in solution. Though neither of these species is expected to exhibit long-term stability in solution, the potential for mobilization of americium from sludge samples would have to be accommodated in the design of any oxidative leaching process for real sludge samples.

  16. Ex Situ Formation of Metal Selenide Quantum Dots Using Bacterially Derived Selenide Precursors

    Energy Technology Data Exchange (ETDEWEB)

    Fellowes, Jonathan W.; Pattrick, Richard; Lloyd, Jon; Charnock, John M.; Coker, Victoria S.; Mosselmans, JFW; Weng, Tsu-Chien; Pearce, Carolyn I.

    2013-04-12

    Luminescent quantum dots were synthesized using bacterially derived selenide (SeII-) as the precursor. Biogenic SeII- was produced by the reduction of Se-IV by Veillonella atypica and compared directly against borohydride-reduced Se-IV for the production of glutathione-stabilized CdSe and beta-mercaptoethanol-stabilized ZnSe nanoparticles by aqueous synthesis. Biological SeII- formed smaller, narrower size distributed QDs under the same conditions. The growth kinetics of biologically sourced CdSe phases were slower. The proteins isolated from filter sterilized biogenic SeII- included a methylmalonyl-CoA decarboxylase previously characterized in the closely related Veillonella parvula. XAS analysis of the glutathione-capped CdSe at the S K-edge suggested that sulfur from the glutathione was structurally incorporated within the CdSe. A novel synchrotron based XAS technique was also developed to follow the nucleation of biological and inorganic selenide phases, and showed that biogenic SeII- is more stable and more resistant to beam-induced oxidative damage than its inorganic counterpart. The bacterial production of quantum dot precursors offers an alternative, 'green' synthesis technique that negates the requirement of expensive, toxic chemicals and suggests a possible link to the exploitation of selenium contaminated waste streams.

  17. Amphoteric properties of gold in zinc selenide

    Energy Technology Data Exchange (ETDEWEB)

    Avdonin, A.N. [Department of Physics, State University of Moldova, A. Mateevich Street 60, MD-2009 Kishinev (Moldova, Republic of); Ivanova, G.N. [Department of Physics, State University of Moldova, A. Mateevich Street 60, MD-2009 Kishinev (Moldova, Republic of); Nedeoglo, D.D. [Department of Physics, State University of Moldova, A. Mateevich Street 60, MD-2009 Kishinev (Moldova, Republic of)]. E-mail: nedeoglo@usm.md; Nedeoglo, N.D. [Department of Physics, State University of Moldova, A. Mateevich Street 60, MD-2009 Kishinev (Moldova, Republic of); Sirkeli, V.P. [Department of Physics, State University of Moldova, A. Mateevich Street 60, MD-2009 Kishinev (Moldova, Republic of)

    2005-08-01

    Hall effect, electric conductivity, and charge carriers mobility in n-ZnSe single crystals doped with gold during the process of a long-term high-temperature annealing in Zn+Au melt with various Au contents were investigated in the temperature range from 77 to 300 K. It has been established that, at low gold concentration, Au atoms form mainly donor-type interstitial Au{sub i} defects. The increase of Au concentration in Zn+Au melt leads to the formation of both simple Au{sub Zn} defects and associative acceptors (Au{sub Zn}-Au{sub i}) (Au{sub Zn}-D{sub Zn}), and (Au{sub Zn}-V{sub Se}). These defects determine electrical properties of the crystals and they are responsible for the complex structure of excitonic and impurity radiation spectra. The influence of dopant concentration on both electrical and luminescent properties of n-ZnSe:Zn:Au crystals is investigated. The observed variations of electrical and luminescent properties are due to amphoteric properties of gold impurity in zinc selenide.

  18. The transmutation of americium: the Ecrix experiments in Phenix; Transmutation de l'americium: les experiences ecrix dans Phenix

    Energy Technology Data Exchange (ETDEWEB)

    Garnier, J.C.; Schmidt, N. [CEA Cadarache, Dept. d' Etudes des Combustibles (DEC/SESC), 13 - Saint-Paul-lez-Durance (France); Croixmarie, Y.; Ottaviani, J.P. [CEA Cadarache, Dept. d' Etudes des Combustibles (DEC/SPUA), 13 - Saint-Paul-lez-Durance (France); Varaine, F.; Saint Jean, C. de [CEA Cadarache, Dept. d' Etudes des Reacteurs (DER/SPRC), 13 - Saint-Paul-lez-Durance (France)

    1999-07-01

    The first americium transmutation experiment in a specific target in PHENIX will occur with the ECRIX-B and ECRIX-H experiments. Beside material testing, the objective is also to represent a concept of transmutation whose specificity is to enhance the kinetics of transmutation by using a moderated spectrum. The moderator materials will be {sup 11}B{sub 4}C and CaH{sub 2} for ECRIX-B and ECRIXH respectively, the irradiation conditions have been predicted for both the neutronics and thermal. The targets (MgO-AmO{sub X} pellets) are manufactured in the ATALANTE laboratory and the design is performed according to the PHENIX operating conditions. (authors)

  19. Effect of americium-241 on luminous bacteria. Role of peroxides

    Energy Technology Data Exchange (ETDEWEB)

    Alexandrova, M., E-mail: maka-alexandrova@rambler.r [Siberian Federal University, Svobodny 79, 660041 Krasnoyarsk (Russian Federation); Rozhko, T. [Siberian Federal University, Svobodny 79, 660041 Krasnoyarsk (Russian Federation); Vydryakova, G. [Institute of Biophysics SB RAS, Akademgorodok 50, 660036 Krasnoyarsk (Russian Federation); Kudryasheva, N. [Siberian Federal University, Svobodny 79, 660041 Krasnoyarsk (Russian Federation); Institute of Biophysics SB RAS, Akademgorodok 50, 660036 Krasnoyarsk (Russian Federation)

    2011-04-15

    The effect of americium-241 ({sup 241}Am), an alpha-emitting radionuclide of high specific activity, on luminous bacteria Photobacterium phosphoreum was studied. Traces of {sup 241}Am in nutrient media (0.16-6.67 kBq/L) suppressed the growth of bacteria, but enhanced luminescence intensity and quantum yield at room temperature. Lower temperature (4 {sup o}C) increased the time of bacterial luminescence and revealed a stage of bioluminescence inhibition after 150 h of bioluminescence registration start. The role of conditions of exposure the bacterial cells to the {sup 241}Am is discussed. The effect of {sup 241}Am on luminous bacteria was attributed to peroxide compounds generated in water solutions as secondary products of radioactive decay. Increase of peroxide concentration in {sup 241}Am solutions was demonstrated; and the similarity of {sup 241}Am and hydrogen peroxide effects on bacterial luminescence was revealed. The study provides a scientific basis for elaboration of bioluminescence-based assay to monitor radiotoxicity of alpha-emitting radionuclides in aquatic solutions. - Highlights: {yields} Am-241 in water solutions (A = 0.16-6.7 kBq/L) suppresses bacterial growth.{yields} Am-241 (A = 0.16-6.7 kBq/L) stimulate bacterial luminescence. {yields} Peroxides, secondary radiolysis products, cause increase of bacterial luminescence.

  20. Particulate distribution of plutonium and americium in surface waters from the Spanish Mediterranean coast

    Energy Technology Data Exchange (ETDEWEB)

    Molero, J.; Sanchez-Cabeza, J.A.; Merino, J.; Vidal-Quadras, A. [Universidad Autonoma de Barcelona (Spain); Vives Batlle, J.; Mitchell, P.I. [University Coll., Dublin (Ireland)

    1995-12-31

    Measurements of the particulate distribution of plutonium and americium in Spanish Mediterranean coastal waters have been carried out. Plutonium-239,340 and {sup 241}Am concentrations have been measured in suspended particulate matter by filtering (< 0.22 {mu}m) large volume (200-300 litres) sea water samples. Results indicate that particulate plutonium constitutes on average 11 {+-} 4% of the total concentration in sea water. In the case of americium this percentage rises to 45 {+-} 14%. From the {sup 241}Am/{sup 239,240}Pu activity ratios it is clear that suspended particulate matter is enriched in {sup 241}Am relative to {sup 239,240}Pu by a factor 8 {+-} 4. Plutonium and americium in surface Mediterranean coastal waters appear to be fractionated as they present a different transfer rate to the particles. Our measurements allowed us to estimate sediment-water distribution coefficients (K{sub d}), which are a key parameter to interpret differences between the behaviour of plutonium and americium in sea water. Distribution coefficients K{sub d} have been estimated to be (1.4 {+-} 0.5) x 10{sup 5} litres kg{sup -1} for plutonium and (0.9 {+-} 0.5) x 10{sup 6} litres kg{sup -1} for americium in surface Mediterranean coastal waters. (author).

  1. Electrodeposition of copper selenide films from acidic bath and their properties

    Science.gov (United States)

    Mane, Rajaram S.; Shaikh, Arif V.; Joo, Oh-Shim; Han, Sung-Hwan; Pathan, Habib M.

    2012-06-01

    Copper selenide thin films are successfully deposited using electrodeposition method by combining copper sulfate and sodiumseleno sulfate precursors at room temperature in acidic bath. The chemical composition was a key factor in preparing high-quality uniform and smooth thin films of the copper selenide. We present indium-tin-oxide as a substrate for depositing copper selenide films which usually exists as copper (I) selenide or copper (II) selenide. Obtained brownish films of copper selenide are examined for their structural, morphological, compositional and optical properties by means of X-ray diffraction, scanning electron microscopy, energy dispersive X-ray analysis and optical absorption measurement techniques, respectively for the structural, morphological and optical analysis.

  2. Isotopic and elemental composition of plutonium/americium oxides influence pulmonary and extra-pulmonary distribution after inhalation in rats.

    Science.gov (United States)

    Van der Meeren, A; Grémy, O

    2010-09-01

    The biodistribution of plutonium and americium has been studied in a rat model after inhalation of two PuO(2) powders in lungs and extra-pulmonary organs from 3 d to 3 mo. The main difference between the two powders was the content of americium (approximately 46% and 4.5% of total alpha activity). The PuO(2) with a higher proportion of americium shows an accelerated transfer of activity from lungs to blood as compared to PuO(2) with the lower americium content, illustrated by increased urinary excretion and higher bone and liver actinide retention. The total alpha activity measured reflects mostly the americium biological behavior. The activity contained in epithelial lining fluid, recovered in the acellular phase of broncho-alveolar lavages, mainly contains americium, whereas plutonium remains trapped in macrophages. Epithelial lining fluid could represent a transitional pulmonary compartment prior to translocation of actinides to the blood and subsequent deposition in extra-pulmonary retention organs. In addition, differential behaviors of plutonium and americium are also observed between the PuO(2) powders with a higher dissolution rate for both plutonium and americium being obtained for the PuO(2) with the highest americium content. Our results indicate that the biological behavior of plutonium and americium after translocation into blood differ two-fold: (1) for the two actinides for the same PuO(2) aerosol, and (2) for the same actinide from the two different aerosols. These results highlight the importance of considering the specific behavior of each contaminant after accidental pulmonary intake when assessing extra-pulmonary deposits from the level of activity excreted in urine or for therapeutic strategy decisions.

  3. CuInSe2 thin film solar cells synthesised from electrodeposited binary selenide precursors

    OpenAIRE

    Fischer, Johannes

    2012-01-01

    The box must contain a summary in a maximum of 1,700 characters, spaces included. The fabrication of a CuInSe2 thin film solar cell from an electrodeposited precursor stack consisting of indium selenide and copper selenide layers is demonstrated. A best conversion efficiency of 5.5% was achieved, a higher efficiency than previously reported in literature. The thesis focuses on three main parts: (i) electrochemistry of indium selenide: The incorporation of indium in the deposit require...

  4. Mechanism of copper selenide growth on copper-oxide selenium system

    Science.gov (United States)

    Ishikawa, Y.; Kido, O.; Kimura, Y.; Kurumada, M.; Suzuki, H.; Saito, Y.; Kaito, C.

    2004-01-01

    Transmission electron microscopy was used to study spontaneous copper selenide formation on Cu particles covered with an oxide layer. Even if the copper particle surface was covered with a Cu 2O layer, selenides were formed by diffusion through the metal oxide layer. For a particle size less than 50 nm, selenide was formed in Cu particles by the diffusion of Se atoms passing through the Cu 2O layer. For particles larger than 100 nm in size, selenide was formed in Se film. It was also found that the thickness of the Cu 2O layer on the surface of Cu particle accelerated diffusion of Se atoms to the copper particle.

  5. A one-pot stereoselective synthesis of 1,4-dienyl selenides by hydrostannylation-Stille tandem reaction of acetylenic selenides with Bu3SnH and allylic bromides

    Institute of Scientific and Technical Information of China (English)

    La Mei Yu; Wen Yan Hao; Ming Zhong Cai

    2008-01-01

    1,4-Dienyl selenides can be stereoselectively synthesized in one pot under mild conditions in good yields by the palladium-catalyzed hydrostannylation of acetylenic selenides, followed by Stille coupling with allylic bromides.

  6. Aqueous preparation of surfactant-free copper selenide nanowires.

    Science.gov (United States)

    Chen, Xinqi; Li, Zhen; Yang, Jianping; Sun, Qiao; Dou, Shixue

    2015-03-15

    Uniform surfactant-free copper selenide (Cu2-xSe) nanowires were prepared via an aqueous route. The effects of reaction parameters such as Cu/Se precursor ratio, Se/NaOH ratio, and reaction time on the formation of nanowires were comprehensively investigated. The results show that Cu2-xSe nanowires were formed through the assembling of CuSe nanoplates, accompanied by their self-redox reactions. The resultant Cu2-xSe nanowires were explored as a potential thermoelectric candidate in comparison with commercial copper selenide powder. Both synthetic and commercial samples have a similar performance and their figures of merit are 0.29 and 0.38 at 750K, respectively.

  7. Selenide-Based Electrocatalysts and Scaffolds for Water Oxidation Applications

    KAUST Repository

    Xia, Chuan

    2015-11-05

    Selenide-based electrocatalysts and scaffolds on carbon cloth are successfully fabricated and demonstrated for enhanced water oxidation applications. A max­imum current density of 97.5 mA cm−2 at an overpotential of a mere 300 mV and a small Tafel slope of 77 mV dec−1 are achieved, suggesting the potential of these materials to serve as advanced oxygen evolution reaction catalysts.

  8. The unexpected properties of alkali metal iron selenide superconductors

    Energy Technology Data Exchange (ETDEWEB)

    Dagotto, Elbio R [ORNL

    2013-01-01

    The iron-based superconductors that contain FeAs layers as the fundamental building block in the crystal structures have been rationalized in the past using ideas based on the Fermi surface nesting of hole and electron pockets when in the presence of weak Hubbard U interactions. This approach seemed appropriate considering the small values of the magnetic moments in the parent compounds and the clear evidence based on photoemission experiments of the required electron and hole pockets. However, recent results in the context of alkali metal iron selenides, with generic chemical composition AxFe2ySe2 (A alkali metal element), have challenged those previous ideas since at particular compositions y the low-temperature ground states are insulating and display antiferromagnetic order with large iron magnetic moments. Moreover, angle-resolved photoemission studies have revealed the absence of hole pockets at the Fermi level in these materials. The present status of this exciting area of research, with the potential to alter conceptually our understanding of the ironbased superconductors, is here reviewed, covering both experimental and theoretical investigations. Other recent related developments are also briefly reviewed, such as the study of selenide two-leg ladders and the discovery of superconductivity in a single layer of FeSe. The conceptual issues considered established for the alkali metal iron selenides, as well as several issues that still require further work, are discussed.

  9. National low-level waste management program radionuclide report series, Volume 14: Americium-241

    Energy Technology Data Exchange (ETDEWEB)

    Winberg, M.R.; Garcia, R.S.

    1995-09-01

    This report, Volume 14 of the National Low-Level Waste Management Program Radionuclide Report Series, discusses the radiological and chemical characteristics of americium-241 ({sup 241}Am). This report also includes discussions about waste types and forms in which {sup 241}Am can be found and {sup 241}Am behavior in the environment and in the human body.

  10. Understanding the Chemistry of Uncommon Americium Oxidation States for Application to Actinide/Lanthanide Separations

    Energy Technology Data Exchange (ETDEWEB)

    Leigh Martin; Bruce J. Mincher; Nicholas C. Schmitt

    2007-09-01

    A spectroscopic study of the stability of Am(V) and Am(VI) produced by oxidizing Am(III) with sodium bismuthate is presented, varying the initial americium concentration, temperature and length of the oxidation was seen to have profound effects on the resultant solutions.

  11. Sodium selenide toxicity is mediated by O2-dependent DNA breaks.

    Directory of Open Access Journals (Sweden)

    Gérald Peyroche

    Full Text Available Hydrogen selenide is a recurrent metabolite of selenium compounds. However, few experiments studied the direct link between this toxic agent and cell death. To address this question, we first screened a systematic collection of Saccharomyces cerevisiae haploid knockout strains for sensitivity to sodium selenide, a donor for hydrogen selenide (H(2Se/HSe(-/Se(2-. Among the genes whose deletion caused hypersensitivity, homologous recombination and DNA damage checkpoint genes were over-represented, suggesting that DNA double-strand breaks are a dominant cause of hydrogen selenide toxicity. Consistent with this hypothesis, treatment of S. cerevisiae cells with sodium selenide triggered G2/M checkpoint activation and induced in vivo chromosome fragmentation. In vitro, sodium selenide directly induced DNA phosphodiester-bond breaks via an O(2-dependent reaction. The reaction was inhibited by mannitol, a hydroxyl radical quencher, but not by superoxide dismutase or catalase, strongly suggesting the involvement of hydroxyl radicals and ruling out participations of superoxide anions or hydrogen peroxide. The (•OH signature could indeed be detected by electron spin resonance upon exposure of a solution of sodium selenide to O(2. Finally we showed that, in vivo, toxicity strictly depended on the presence of O(2. Therefore, by combining genome-wide and biochemical approaches, we demonstrated that, in yeast cells, hydrogen selenide induces toxic DNA breaks through an O(2-dependent radical-based mechanism.

  12. SKIN DOSIMETRY IN CONDITIONS OF ITS CONSTANT SURFACE CONTAMINATION WITH SOLUTIONS OF PLUTONIUM-239 AND AMERICIUM-241

    Directory of Open Access Journals (Sweden)

    E. B. Ershov

    2012-01-01

    Full Text Available The article considers, on the basis of experimental data, the issue of assessing dose burdens to the skin basal layer in conditions of its permanent contamination with solutions of plutonium-239 and americium-241 and subsequent decontamination.

  13. Double-Diffusive Convection During Growth of Halides and Selenides

    Science.gov (United States)

    Singh, N. B.; Su, Ching-Hua; Duval, Walter M. B.

    2015-01-01

    Heavy metal halides and selenides have unique properties which make them excellent materials for chemical, biological and radiological sensors. Recently it has been shown that selenohalides are even better materials than halides or selenides for gamma-ray detection. These materials also meet the strong needs of a wide band imaging technology to cover ultra-violet (UV), midwave infrared wavelength (MWIR) to very long wavelength infrared (VLWIR) region for hyperspectral imager components such as etalon filters and acousto-optic tunable filters (AO). In fact AOTF based imagers based on these materials have some superiority than imagers based on liquid crystals, FTIR, Fabry-Perot, grating, etalon, electro-optic modulation, piezoelectric and several other concepts. For example, broadband spectral and imagers have problems of processing large amount of information during real-time observation. Acousto-Optic Tunable Filter (AOTF) imagers are being developed to fill the need of reducing processing time of data, low cost operation and key to achieving the goal of covering long-wave infrared (LWIR). At the present time spectral imaging systems are based on the use of diffraction gratings are typically used in a pushbroom or whiskbroom mode. They are mostly used in systems and acquire large amounts of hyperspectral data that is processed off-line later. In contrast, acousto-optic tunable filter spectral imagers require very little image processing, providing new strategies for object recognition and tracking. They are ideally suited for tactical situations requiring immediate real-time image processing. But the performance of these imagers depends on the quality and homogeneity of acousto-optic materials. In addition for many systems requirements are so demanding that crystals up to sizes of 10 cm length are desired. We have studied several selenides and halide crystals for laser and AO imagers for MWIR and LWIR wavelength regions. We have grown and fabricated crystals of

  14. Photoconductive Properties of Brush Plated Copper Indium Gallium Selenide Films

    OpenAIRE

    Subiramaniyam, N. P.; P. Thirunavukkarasu; Murali, K. R.

    2013-01-01

    Copper indium gallium selenide (CIGS) films were deposited for the first time by the brush electrodeposition technique. X-ray diffraction studies indicated the formation of single phase chalcopyrite CIGS. Lattice parameters, dislocation density, and strain were calculated. Band gap of the films increased from 1.12 eV to 1.63 eV as the gallium concentration increased. Room temperature transport parameters of the films, namely, resistivity increased from 0.10 ohm cm to 12 ohm cm, mobility decre...

  15. Electronic band structure of calcium selenide under pressure

    Energy Technology Data Exchange (ETDEWEB)

    Louail, L. [Faculty of Sciences, Department of Physics, University of Setif, Setif (Algeria)], E-mail: llouail@yahoo.fr; Haddadi, K.; Maouche, D.; Ali Sahraoui, F.; Hachemi, A. [Faculty of Sciences, Department of Physics, University of Setif, Setif (Algeria)

    2008-09-01

    Energy band structures under pressure of calcium selenide (CaSe) were calculated using the plane-wave pseudopotential code CASTEP. The results show a progressive transition from a direct to an indirect gap semiconductor at a pressure of about 2 GPa, in the B1 phase. An insulator-conductor change was also observed at 70 GPa, in the B2 phase. Concerning CaSe, these two results could not be evidenced in previous literature. Hence, our work is a first attempt in this direction.

  16. Strong quantum confinement effects in thin zinc selenide films

    Science.gov (United States)

    Baskoutas, S.; Poulopoulos, P.; Karoutsos, V.; Angelakeris, M.; Flevaris, N. K.

    2006-01-01

    Thin Zinc Selenide films in the thickness range 3-50 nm have been prepared on high quality glass substrates by e-beam evaporation under ultrahigh vacuum conditions. Optical absorption spectroscopy experiments reveal a systematically increasing blue shift of the effective bandgap energy as the film thickness decreases, reaching a maximum value of 0.32 eV for the thinner film. The experimental results, which indicate the presence of strong quantum confinement effects, are fairly well described by theoretical calculations based on the potential morphing method, using as a confining potential the finite square well potential with height of the barriers equal to 5 eV.

  17. Electrochemical synthesis of alkali-intercalated iron selenide superconductors

    Institute of Scientific and Technical Information of China (English)

    申士杰; 应天平; 王刚; 金士锋; 张韩; 林志萍; 陈小龙

    2015-01-01

    Electrochemical method has been used to insert K/Na into FeSe lattice to prepare alkali-intercalated iron selenides at room temperature. Magnetization measurement reveals that KxFe2Se2 and NaxFe2Se2 are superconductive at 31 K and 46 K, respectively. This is the first successful report of obtaining metal-intercalated FeSe-based high-temperature superconductors using electrochemical method. It provides an effective route to synthesize metal-intercalated layered compounds for new superconductor exploration.

  18. Synthesis of Cadmium Selenide Quantum Dots and Their Cytotoxicity

    OpenAIRE

    Liu, Ruoxi

    2013-01-01

    Cadmium selenide (CdSe) nanoparticles (NPs) have applications in biomedical, biochemistry, bioimaging areas through different methods such as cell labelling and drug delivery (Chapter1). This study aims to test the optical and biological properties of CdSe NPs so that its applications can be improved in these areas in the future. Three types of CdSe NPs have been synthesised using a wet chemical method with the molar ratio of Cd:Se 10:1, 4:1 and 1:1. The observed luminescence of the CdSe N...

  19. Influence of biofilms on migration of uranium, americium and europium in the environment; Einfluss von Biofilmen auf das Migrationsverhalten von Uran, Americium und Europium in der Umwelt

    Energy Technology Data Exchange (ETDEWEB)

    Baumann, Nils; Zirnstein, Isabel; Arnold, Thuro

    2015-07-01

    The report on the influence of biofilms on migration of uranium, americium and europium in the environment deals with the contamination problems of uranium mines such as SDAG WISMUT in Saxonia and Thuringia. In mine waters microorganisms form a complex microbiological biocoenosis in spite of low pH values and high heavy metal concentrations including high uranium concentrations. The analyses used microbiological methods like confocal laser scanning microscopy and molecular-biological techniques. The interactions of microorganism with fluorescent radioactive heavy metal ions were performed with TRLFS (time resolved laser-induced fluorescence spectroscopy).

  20. Standard test method for quantitative determination of americium 241 in plutonium by Gamma-Ray spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    1994-01-01

    1.1 This test method covers the quantitative determination of americium 241 by gamma-ray spectrometry in plutonium nitrate solution samples that do not contain significant amounts of radioactive fission products or other high specific activity gamma-ray emitters. 1.2 This test method can be used to determine the americium 241 in samples of plutonium metal, oxide and other solid forms, when the solid is appropriately sampled and dissolved. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  1. Calcium and zinc DTPA administration for internal contamination with plutonium-238 and americium-241.

    Science.gov (United States)

    Kazzi, Ziad N; Heyl, Alexander; Ruprecht, Johann

    2012-08-01

    The accidental or intentional release of plutonium or americium can cause acute and long term adverse health effects if they enter the human body by ingestion, inhalation, or injection. These effects can be prevented by rapid removal of these radionuclides by chelators such as calcium or zinc diethylenetriaminepentaacetate (calcium or zinc DTPA). These compounds have been shown to be efficacious in enhancing the elimination of members of the actinide family particularly plutonium and americium when administered intravenously or by nebulizer. The efficacy and adverse effects profile depend on several factors that include the route of internalization of the actinide, the type, and route time of administration of the chelator, and whether the calcium or zinc salt of DTPA is used. Current and future research efforts should be directed at overcoming limitations associated with the use of these complex drugs by using innovative methods that can enhance their structural and therapeutic properties.

  2. Final Radiological Assessment of External Exposure for CLEAR-Line Americium Recovery Operations

    Energy Technology Data Exchange (ETDEWEB)

    Davis, Adam C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Belooussova, Olga N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Hetrick, Lucas Duane [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2014-11-12

    Los Alamos National Laboratory is currently planning to implement an americium recovery program. The americium, ordinarily isotopically pure 241Am, would be extracted from existing Pu materials, converted to an oxide and shipped to support fabrication of americium oxide-beryllium neutron sources. These operations would occur in the currently proposed Chloride Extraction and Actinide Recovery (CLEAR) line of glove boxes. This glove box line would be collocated with the currently-operational Experimental Chloride Extraction Line (EXCEL). The focus of this document is to provide an in-depth assessment of the currently planned radiation protection measures and to determine whether or not further design work is required to satisfy design-goal and ALARA requirements. Further, this document presents a history of americium recovery operations in the Department of Energy and high-level descriptions of the CLEAR line operations to provide a basis of comparison. Under the working assumptions adopted by this study, it was found that the evaluated design appears to mitigate doses to a level that satisfies the ALARA-in-design requirements of 10 CFR 835 as implemented by the Los Alamos National Laboratory procedure P121. The analyses indicate that extremity doses would also meet design requirements. Dose-rate calculations were performed using the radiation transport code MCNP5 and doses were estimated using a time-motion study developed in consort with the subject matter expert. A copy of this report and all supporting documentation are located on the Radiological Engineering server at Y:\\Rad Engineering\\2013 PROJECTS\\TA-55 Clear Line.

  3. On the Convergence of the Electronic Structure Properties of the FCC Americium (001) Surface

    OpenAIRE

    Gao, Da; Ray, Asok K.

    2006-01-01

    Electronic and magnetic properties of the fcc Americium (001) surface have been investigated via full-potential all-electron density-functional electronic structure calculations at both scalar and fully relativistic levels. Effects of various theoretical approximations on the fcc Am (001) surface properties have been thoroughly examined. The ground state of fcc Am (001) surface is found to be anti-ferromagnetic with spin-orbit coupling included (AFM-SO). At the ground state, the magnetic mome...

  4. Development of the data base for a degradation model of a selenide RTG. [Radioisotope Thermoelectric Generator

    Science.gov (United States)

    Stapfer, G.; Truscello, V. C.

    1977-01-01

    The paper is concerned with the evaluation of the materials used in a selenide radioisotope thermoelectric generator (RTG). These materials are composed of n-type gadolinium selenide and n-type copper selenide. A three-fold evaluation approach is being used: (1) the study of the rate of change of the thermal conductivity of the material, (2) the investigation of the long-term stability of the material's Seebeck voltage and electrical resistivity under current and temperature gradient conditions, and (3) determination of the physical behavior and compatibility of the material with surrounding insulation at elevated temperatures. Programmatically, the third category of characteristic evaluation is being emphasized.

  5. Polystyrene-supported Benzyl Selenide: An Efficient Reagent for Highly Stereocontrolled Synthesis of Substituted Olefins

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Polystyrene-supported benzyl selenide has been prepared. This novel reagent was treated with LDA to produce a selenium stabilized carbanion, which reacted with alkyl halide, followed by selenoxide syn-elimination, to give substituted olefins stereospecificly.

  6. A Model of the Growth of Copper Selenide Thin Films Controlled by Diffusion and Chemical Reaction

    OpenAIRE

    Bottecchia,Otávio Luiz

    1998-01-01

    A model of the growth of thin films of copper selenides is proposed. A mathematical equation that describes the kinetics of the growth is derived. Simulated results and a discussion on the results of the model are presented. A fitting procedure of literature data with the derived equation is carried out. The diffusion coefficient of copper(I) ions in copper selenide is roughly estimated.

  7. Electrochemical synthesis of alkali-intercalated iron selenide superconductors

    Science.gov (United States)

    Shen, Shi-Jie; Ying, Tian-Ping; Wang, Gang; Jin, Shi-Feng; Zhang, Han; Lin, Zhi-Ping; Chen, Xiao-Long

    2015-11-01

    Electrochemical method has been used to insert K/Na into FeSe lattice to prepare alkali-intercalated iron selenides at room temperature. Magnetization measurement reveals that KxFe2Se2 and NaxFe2Se2 are superconductive at 31 K and 46 K, respectively. This is the first successful report of obtaining metal-intercalated FeSe-based high-temperature superconductors using electrochemical method. It provides an effective route to synthesize metal-intercalated layered compounds for new superconductor exploration. Project supported by the National Natural Science Foundation of China (Grant Nos. 51322211and 91422303), the Strategic Priority Research Program (B) of the Chinese Academy of Sciences (Grant No. XDB07020100), Beijing Nova Program of China (Grant No. 2011096), and K. C. Wong Education Foundation, Hong Kong, China.

  8. Thermal lensing in silver gallium selenide parametric oscillator crystals.

    Science.gov (United States)

    Marquardt, C L; Cooper, D G; Budni, P A; Knights, M G; Schepler, K L; Dedomenico, R; Catella, G C

    1994-05-20

    We performed an experimental investigation of thermal lensing in silver gallium selenide (AgGaSe(2)) optical parametric oscillator crystals pumped by a 2-µm laser at ambient temperature. We determined an empirical expression for the effective thermal focusing power in terms of the pump power, beam diameter, crystal length, and absorption coefficient. This relation may be used to estimate average power limitations in designing AgGaSe(2) optical parametric oscillators. We also demonstrated an 18% slope efficiency from a 2-µm pumped AgGaSe(2) optical parametric oscillator operated at 77 K, at which temperature thermal lensing is substantially reduced because of an increase in the thermal conductivity and a decrease in the thermal index gradient dn/dT. Cryogenic cooling may provide an additional option for scaling up the average power capability of a 2-µm pumped AgGaSe(2) optical parametric oscillator.

  9. In Situ Transmission Electron Microscopy of Cadmium Selenide Nanorod Sublimation.

    Science.gov (United States)

    Hellebusch, Daniel J; Manthiram, Karthish; Beberwyck, Brandon J; Alivisatos, A Paul

    2015-02-19

    In situ electron microscopy is used to observe the morphological evolution of cadmium selenide nanorods as they sublime under vacuum at a series of elevated temperatures. Mass loss occurs anisotropically along the nanorod's long axis. At temperatures close to the sublimation threshold, the phase change occurs from both tips of the nanorods and proceeds unevenly with periods of rapid mass loss punctuated by periods of relative stability. At higher temperatures, the nanorods sublime at a faster, more uniform rate, but mass loss occurs from only a single end of the rod. We propose a mechanism that accounts for the observed sublimation behavior based on the terrace-ledge-kink (TLK) model and how the nanorod surface chemical environment influences the kinetic barrier of sublimation.

  10. Selenide isotope generator for the Galileo Mission. Program final report

    Energy Technology Data Exchange (ETDEWEB)

    1979-06-01

    This final report for the Selenide Isotope Generator for the Galileo Mission (SIG/GM) documents the work performed by Teledyne Energy Systems (TES) under US Department of Energy (DOE) Contract No. DE-AC01-78ET33009 (formerly ET-78-C-01-2865) during the period April 10, 1978 to June 30, 1979. Because of technical difficulties with the thermoelectric converter being developed by the 3M Company under separate DOE contract, a Stop Work Order, dated January 29, 1979, was issued by DOE. The TES effort up to the receipt of the Stop Work Order as well as limited technical activities up to the contract conclusion on June 30, 1979 are reported.

  11. Bis(2,4-dimethoxyphenyl(phenylphosphine selenide

    Directory of Open Access Journals (Sweden)

    Alfred Muller

    2011-01-01

    Full Text Available In the title molecule, C22H23O4PSe, the P atom has a distorted tetrahedral environment formed by the selenide atom [P=Se = 2.1219 (5 Å] and three aryl rings. The orientations of the methoxy groups in the two 2,4-dimethoxyphenyl ligands are distinct, as seen from the torsion angles: C—C—O—C = 14.7 (3 and 175.97 (17° in one ligand, and −9.1 (2 and 5.1 (3° in the other. In the crystal, weak intermolecular C—H...Se interactions link the molecules into zigzag chains propagated in [010].

  12. Potentiostatic Electrochemical Preparation and Characterisation of Aluminium Containing Nickel Selenide

    Directory of Open Access Journals (Sweden)

    Sandeep Gohar

    2014-01-01

    Full Text Available The wide range of properties exhibited by Al based alloy makes them suitable for different applications. Aluminium containing nickel Selenide ternary alloy possess considerable corrosion resistance as compared to their pure metal counterparts. The objective of the present work has been focused on the preparation and characterisation of its thin film. Alloying with Aluminium improve the oxidation resistance and increases the heat conductivity of the alloy. There is always a high demand for plating Al and its alloys in automotive and aerospace products, house-hold goods, and artificial jewellery etc,. The morphological and the structural studies of the electrodeposited thin film were determined by Scanning Electron Microscope (SEM images and X-Ray Diffraction Pattern (XRD while elemental composition has been done by Energy Dispersive X-Ray Spectroscopy (EDAX analysis.

  13. Copper selenide thin films by chemical bath deposition

    Science.gov (United States)

    García, V. M.; Nair, P. K.; Nair, M. T. S.

    1999-05-01

    We report the structural, optical, and electrical properties of thin films (0.05 to 0.25 μm) of copper selenide obtained from chemical baths using sodium selenosulfate or N,N-dimethylselenourea as a source of selenide ions. X-ray diffraction (XRD) studies on the films obtained from baths using sodium selenosulfate suggest a cubic structure as in berzelianite, Cu 2- xSe with x=0.15. Annealing the films at 400°C in nitrogen leads to a partial conversion of the film to Cu 2Se. In the case of films obtained from the baths containing dimethylselenourea, the XRD patterns match that of klockmannite, CuSe. Annealing these films in nitrogen at 400°C results in loss of selenium, and consequently a composition rich in copper, similar to Cu 2- xSe, is reached. Optical absorption in the films result from free carrier absorption in the near infrared region with absorption coefficient of ˜10 5 cm -1. Band-to-band transitions which gives rise to the optical absorption in the visible-ultraviolet region may be interpreted in terms of direct allowed transitions with band gap in the 2.1-2.3 eV range and indirect allowed transitions with band gap 1.2-1.4 eV. All the films, as prepared and annealed, show p-type conductivity, in the range of (1-5)×10 3 Ω -1 cm -1. This results in high near infrared reflectance, of 30-80%.

  14. MARIOS: Irradiation of UO{sub 2} containing 15% americium at well defined temperature

    Energy Technology Data Exchange (ETDEWEB)

    D' Agata, E., E-mail: elio.dagata@ec.europa.eu [European Commission, Joint Research Centre, Institute for Energy - P.O. Box 2, 1755 ZG Petten (Netherlands); Hania, P.R. [Nuclear Research and Consultancy Group, P.O. Box 25, 1755 ZG Petten (Netherlands); Bejaoui, S. [Commissariat a l' Energie Atomique, DEC CEA-Cadarache, 13108 St. Paul lez Durance Cedex (France); Sciolla, C.; Wyatt, T.; Hannink, M.H.C. [Nuclear Research and Consultancy Group, P.O. Box 25, 1755 ZG Petten (Netherlands); Herlet, N.; Jankowiak, A. [Commissariat a l' Energie Atomique DTEC CEA Marcoule, 30207 Bagnols sur Ceze Cedex (France); Klaassen, F.C. [Nuclear Research and Consultancy Group, P.O. Box 25, 1755 ZG Petten (Netherlands); Bonnerot, J.-M. [Commissariat a l' Energie Atomique, DEC CEA-Cadarache, 13108 St. Paul lez Durance Cedex (France)

    2012-01-15

    Highlights: Black-Right-Pointing-Pointer MARIOS is designed to check the behaviour of Minor Actinide Blanket Module concept. Black-Right-Pointing-Pointer Main requirement of the experiment is an accurate control of the temperature. Black-Right-Pointing-Pointer The swelling and the helium release will be the main output of the experiment. Black-Right-Pointing-Pointer A complementary experiment (DIAMINO), will be performed in the next future. - Abstract: Americium is a strong contributor to the long term radiotoxicity of high activity nuclear waste. Transmutation by irradiation in nuclear reactors of long-lived nuclides like {sup 241}Am is, therefore, an option for the reduction of radiotoxicity and residual power packages as well as the repository area. The MARIOS irradiation experiment is the latest of a series of experiments on americium transmutation (e.g. EFTTRA-T4, EFTTRA-T4bis, HELIOS). MARIOS experiment is carried out in the framework of the 4-year project FAIRFUELS of the EURATOM 7th Framework Programme (FP7). During the past years of experimental work in the field of transmutation and tests of innovative nuclear fuel containing americium, the release or trapping of helium as well as swelling has shown to be the key issue for the design of such kinds of target. Therefore, the main objective of the MARIOS experiment is to study the in-pile behaviour of UO{sub 2} containing minor actinides (MAs) in order to gain knowledge on the role of the microstructure and of the temperature on the gas release and on fuel swelling. The MARIOS experiment will be conducted in the HFR (high flux reactor) in Petten (The Netherlands) and will start in the beginning of 2011. It has been planned that the experiment will last 11 cycles, corresponding to 11 months. This paper covers the description of the objective of the experiment, as well as a general description of the design of the experiment.

  15. Speciation of americium in seawater and accumulation in the marine sponge Aplysina cavernicola.

    Science.gov (United States)

    Maloubier, Melody; Michel, Hervé; Solari, Pier Lorenzo; Moisy, Philippe; Tribalat, Marie-Aude; Oberhaensli, François R; Dechraoui Bottein, Marie Yasmine; Thomas, Olivier P; Monfort, Marguerite; Moulin, Christophe; Den Auwer, Christophe

    2015-12-21

    The fate of radionuclides in the environment is a cause of great concern for modern society, seen especially in 2011 after the Fukushima accident. Among the environmental compartments, seawater covers most of the earth's surface and may be directly or indirectly impacted. The interaction between radionuclides and the marine compartment is therefore essential for better understanding the transfer mechanisms from the hydrosphere to the biosphere. This information allows for the evaluation of the impact on humans via our interaction with the biotope that has been largely undocumented up to now. In this report, we attempt to make a link between the speciation of heavy elements in natural seawater and their uptake by a model marine organism. More specifically, because the interaction of actinides with marine invertebrates has been poorly studied, the accumulation in a representative member of the Mediterranean coralligenous habitat, the sponge Aplysina cavernicola, was investigated and its uptake curve exposed to a radiotracer (241)Am was estimated using a high-purity Ge gamma spectrometer. But in order to go beyond the phenomenological accumulation rate, the speciation of americium(III) in seawater must be assessed. The speciation of (241)Am (and natural europium as its chemically stable surrogate) in seawater was determined using a combination of different techniques: Time-Resolved Laser-Induced Fluorescence (TRLIF), Extended X-ray Absorption Fine Structure (EXAFS) at the LIII edge, Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy and Scanning Electron Microscopy (SEM) and the resulting data were compared with the speciation modeling. In seawater, the americium(III) complex (as well as the corresponding europium complex, although with conformational differences) was identified as a ternary sodium biscarbonato complex, whose formula can be tentatively written as NaAm(CO3)2·nH2O. It is therefore this chemical form of americium that is

  16. Plutonium and americium in arctic waters, the North Sea and Scottish and Irish coastal zones

    DEFF Research Database (Denmark)

    Hallstadius, L.; Aarkrog, Asker; Dahlgaard, Henning;

    1986-01-01

    collected from the Irish coast in 1983. Fallout is found to dominate as a source of 239+240Pu north of latitude 65°N, while for 238Pu a substantial fraction originates from European nuclear fuel reprocessing facilities. The 238Pu/239+240Pu isotope ratio provides clear evidence of the transport of effluent...... of the Irish Sea) to Spitsbergen. 241Am found in Arctic waters probably originates from the decay of fallout 241Pu and, like Pu, tentatively has a residence time of the order of several years. Americium from Sellafield has an estimated mean residence time of 4–6 months in Scottish waters....

  17. Penetration and decontamination of americium-241 ex vivo using fresh and frozen pig skin.

    Science.gov (United States)

    Tazrart, A; Bolzinger, M A; Moureau, A; Molina, T; Coudert, S; Angulo, J F; Briancon, S; Griffiths, N M

    2017-04-01

    Skin contamination is one of the most probable risks following major nuclear or radiological incidents. However, accidents involving skin contamination with radionuclides may occur in the nuclear industry, in research laboratories and in nuclear medicine departments. This work aims to measure the penetration of the radiological contaminant Americium ((241)Am) in fresh and frozen skin and to evaluate the distribution of the contamination in the skin. Decontamination tests were performed using water, Fuller's earth and diethylene triamine pentaacetic acid (DTPA), which is the recommended treatment in case of skin contamination with actinides such as plutonium or americium. To assess these parameters, we used the Franz cell diffusion system with full-thickness skin obtained from pigs' ears, representative of human skin. Solutions of (241)Am were deposited on the skin samples. The radioactivity content in each compartment and skin layers was measured after 24 h by liquid scintillation counting and alpha spectrophotometry. The Am cutaneous penetration to the receiver compartment is almost negligible in fresh and frozen skin. Multiple washings with water and DTPA recovered about 90% of the initial activity. The rest remains fixed mainly in the stratum corneum. Traces of activity were detected within the epidermis and dermis which is fixed and not accessible to the decontamination.

  18. Using different chemical methods for deposition of copper selenide thin films and comparison of their characterization.

    Science.gov (United States)

    Güzeldir, Betül; Sağlam, Mustafa

    2015-11-05

    Different chemical methods such as Successive Ionic Layer Adsorption and Reaction (SILAR), spin coating and spray pyrolysis methods were used to deposite of copper selenide thin films on the glass substrates. The films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), energy dispersive X-ray analysis (EDX) spectroscopy and UV-vis spectrophotometry. The XRD and SEM studies showed that all the films exhibit polycrystalline nature and crystallinity of copper selenide thin films prepared with spray pyrolysis greater than spin coating and SILAR methods. From SEM and AFM images, it was observed copper selenide films were uniform on the glass substrates without any visible cracks or pores. The EDX spectra showed that the expected elements exist in the thin films. Optical absorption studies showed that the band gaps of copper selenide thin films were in the range 2.84-2.93 eV depending on different chemical methods. The refractive index (n), optical static and high frequency dielectric constants (ε0, ε∞) values were calculated by using the energy bandgap values for each deposition method. The obtained results from different chemical methods revealed that the spray pyrolysis technique is the best chemical deposition method to fabricate copper selenide thin films. This absolute advantage was lead to play key roles on performance and efficiency electrochromic and photovoltaic devices.

  19. Amorphous Indium Selenide Thin Films Prepared by RF Sputtering: Thickness-Induced Characteristics.

    Science.gov (United States)

    Han, Myoung Yoo; Park, Yong Seob; Kim, Nam-Hoon

    2016-05-01

    The influence of indium composition, controlled by changing the film thickness, on the optical and electrical properties of amorphous indium selenide thin films was studied for the application of these materials as Cd-free buffer layers in CI(G)S solar cells. Indium selenide thin films were prepared using RF magnetron sputtering method. The indium composition of the amorphous indium selenide thin films was varied from 94.56 to 49.72 at% by increasing the film thickness from 30 to 70 nm. With a decrease in film thickness, the optical transmittance increased from 87.63% to 96.03% and Eg decreased from 3.048 to 2.875 eV. Carrier concentration and resistivity showed excellent values of ≥1015 cm(-3) and ≤ 10(4) Ω x cm, respectively. The conductivity type of the amorphous indium selenide thin films could be controlled by changing the film-thickness-induced amount of In. These results indicate the possibility of tuning the properties of amorphous indium selenide thin films by changing their composition for use as an alternate buffer layer material in CI(G)S solar cells.

  20. Cu Vacancies Boost Cation Exchange Reactions in Copper Selenide Nanocrystals.

    Science.gov (United States)

    Lesnyak, Vladimir; Brescia, Rosaria; Messina, Gabriele C; Manna, Liberato

    2015-07-29

    We have investigated cation exchange reactions in copper selenide nanocrystals using two different divalent ions as guest cations (Zn(2+) and Cd(2+)) and comparing the reactivity of close to stoichiometric (that is, Cu2Se) nanocrystals with that of nonstoichiometric (Cu(2-x)Se) nanocrystals, to gain insights into the mechanism of cation exchange at the nanoscale. We have found that the presence of a large density of copper vacancies significantly accelerated the exchange process at room temperature and corroborated vacancy diffusion as one of the main drivers in these reactions. Partially exchanged samples exhibited Janus-like heterostructures made of immiscible domains sharing epitaxial interfaces. No alloy or core-shell structures were observed. The role of phosphines, like tri-n-octylphosphine, in these reactions, is multifaceted: besides acting as selective solvating ligands for Cu(+) ions exiting the nanoparticles during exchange, they also enable anion diffusion, by extracting an appreciable amount of selenium to the solution phase, which may further promote the exchange process. In reactions run at a higher temperature (150 °C), copper vacancies were quickly eliminated from the nanocrystals and major differences in Cu stoichiometries, as well as in reactivities, between the initial Cu2Se and Cu(2-x)Se samples were rapidly smoothed out. These experiments indicate that cation exchange, under the specific conditions of this work, is more efficient at room temperature than at higher temperature.

  1. Thermoelectric characterization of individual bismuth selenide topological insulator nanoribbons

    Science.gov (United States)

    Tang, Hao; Wang, Xiaomeng; Xiong, Yucheng; Zhao, Yang; Zhang, Yin; Zhang, Yan; Yang, Juekuan; Xu, Dongyan

    2015-04-01

    Bismuth selenide (Bi2Se3) nanoribbons have attracted tremendous research interest recently to study the properties of topologically protected surface states that enable new opportunities to enhance the thermoelectric performance. However, the thermoelectric characterization of individual Bi2Se3 nanoribbons is rare due to the technological challenges in the measurements. One challenge is to ensure good contacts between the nanoribbon and electrodes in order to determine the thermal and electrical properties accurately. In this work, we report the thermoelectric characterization of individual Bi2Se3 nanoribbons via a suspended microdevice method. Through careful measurements, we have demonstrated that contact thermal resistance is negligible after the electron-beam-induced deposition (EBID) of platinum/carbon (Pt/C) composites at the contacts between the nanoribbon and electrodes. It is shown that the thermal conductivity of the Bi2Se3 nanoribbons is less than 50% of the bulk value over the whole measurement temperature range, which can be attributed to enhanced phonon boundary scattering. Our results indicate that intrinsic Bi2Se3 nanoribbons prepared in this work are highly doped n-type semiconductors, and therefore the Fermi level should be in the conduction band and no topological transport behavior can be observed in the intrinsic system.

  2. Characterization of single phase copper selenide nanoparticles and their growth mechanism

    Science.gov (United States)

    Patidar, D.; Saxena, N. S.

    2012-03-01

    The high quality Cu3Se2 phase of copper selenide nanoparticles was synthesized through the solution-phase chemical reaction between copper and selenium. In this synthesis process, hydrazine hydrate acts as reducing agent whereas ethylene glycol controls the nucleation and growth of particles. An effort has been made to explain the growth mechanism to form copper selenide nanoparticles through the coordination of selenium to the Cu2+ complexes with OH groups of ethylene glycol. Result indicates the formation of Cu3Se2 single phase nanoparticles. The particles with the average particle size 25 nm are spherical in shape having tetragonal structure. The particles are well crystallized having 94% degree of crystallinity. An effort has also been made to determine the energy band gap of copper selenide nanoparticles through the absorption spectra.

  3. Ambient Facile Synthesis of Gram-Scale Copper Selenide Nanostructures from Commercial Copper and Selenium Powder.

    Science.gov (United States)

    Chen, Xin Qi; Li, Zhen; Dou, Shi Xue

    2015-06-24

    Grams of copper selenides (Cu(2-x)Se) were prepared from commercial copper and selenium powders in the presence of thiol ligands by a one-pot reaction at room temperature. The resultant copper selenides are a mixture of nanoparticles and their assembled nanosheets, and the thickness of nanosheets assembled is strongly dependent on the ratio of thiol ligand to selenium powder. The resultant Cu(2-x)Se nanostructures were treated with hydrazine solution to remove the surface ligands and then explored as a potential thermoelectric candidate in comparison with commercial copper selenide powders. The research provides a novel ambient approach for preparation of Cu(2-x)Se nanocrystallines on a large scale for various applications.

  4. High-temperature conductivity in chemical bath deposited copper selenide thin films

    Science.gov (United States)

    Dhanam, M.; Manoj, P. K.; Prabhu, Rajeev. R.

    2005-07-01

    This paper reports high-temperature (305-523 K) electrical studies of chemical bath deposited copper (I) selenide (Cu 2-xSe) and copper (II) selenide (Cu 3Se 2) thin films. Cu 2-xSe and Cu 3Se 2 have been prepared on glass substrates from the same chemical bath at room temperature by controlling the pH. From X-ray diffraction (XRD) profiles, it has been found that Cu 2-xSe and Cu 3Se 2 have cubic and tetragonal structures, respectively. The composition of the chemical constituent in the films has been confirmed from XRD data and energy-dispersive X-ray analysis (EDAX). It has been found that both phases of copper selenide thin films have thermally activated conduction in the high-temperature range. In this paper we also report the variation of electrical parameters with film thickness and the applied voltage.

  5. Characterization of copper selenide thin films deposited by chemical bath deposition technique

    Science.gov (United States)

    Al-Mamun; Islam, A. B. M. O.

    2004-11-01

    A low-cost chemical bath deposition (CBD) technique has been used for the preparation of Cu2-xSe thin films onto glass substrates and deposited films were characterized by X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and UV-vis spectrophotometry. Good quality thin films of smooth surface of copper selenide thin films were deposited using sodium selenosulfate as a source of selenide ions. The structural and optical behaviour of the films are discussed in the light of the observed data.

  6. Spin-Polarized Tunneling Study on Spin-Momentum Locking in the Topological Insulator Bismuth Selenide

    Science.gov (United States)

    Chen, Ching-Tzu; Liu, Luqiao; Richardella, Anthony; Garate, Ion; Zhu, Yu; Samarth, Nitin

    2015-03-01

    In this talk, we will demonstrate that the helical spin texture on topological insulator (TI) surfaces can be electrically detected using four-terminal tunnel junction devices with ferromagnetic top electrodes. Consistent results are obtained in both the Edelstein and spin-galvanic effect configurations, allowing a quantitative determination of the charge-spin conversion efficiency in bismuth selenide. By applying finite DC biases at the junction, we further extract the energy dependence of the effective spin polarization in bismuth selenide. The observed temperature stability up to 200K suggests that TIs can be highly promising for room-temperature spintronics applications

  7. Magnesium ionophore II as an extraction agent for trivalent europium and americium

    Energy Technology Data Exchange (ETDEWEB)

    Makrlik, Emanuel [Czech Univ. of Life Sciences, Prague (Czech Republic). Faculty of Environmental Sciences; Vanura, Petr [Univ. of Chemistry and Technology, Prague (Czech Republic). Dept. of Analytical Chemistry

    2016-11-01

    Solvent extraction of microamounts of trivalent europium and americium into nitrobenzene by using a mixture of hydrogen dicarbollylcobaltate (H{sup +}B{sup -}) and magnesium ionophore II (L) was studied. The equilibrium data were explained assuming that the species HL{sup +}, HL{sup +}{sub 2}, ML{sup 3+}{sub 2}, and ML{sup 3+}{sub 3} (M{sup 3+} = Eu{sup 3+}, Am{sup 3+}; L=magnesium, ionophore II) are extracted into the nitrobenzene phase. Extraction and stability constants of the cationic complex species in nitrobenzene saturated with water were determined and discussed. From the experimental results it is evident that this effective magnesium ionophore II receptor for the Eu{sup 3+} and Am{sup 3+} cations could be considered as a potential extraction agent for nuclear waste treatment.

  8. Imitators of plutonium and americium in a mixed uranium- plutonium nitride fuel

    Science.gov (United States)

    Nikitin, S. N.; Shornikov, D. P.; Tarasov, B. A.; Baranov, V. G.; Burlakova, M. A.

    2016-04-01

    Uranium nitride and mix uranium nitride (U-Pu)N is most popular nuclear fuel for Russian Fast Breeder Reactor. The works in hot cells associated with the radiation exposure of personnel and methodological difficulties. To know the main physical-chemical properties of uranium-plutonium nitride it necessary research to hot cells. In this paper, based on an assessment of physicochemical and thermodynamic properties of selected simulators Pu and Am. Analogues of Pu is are Ce and Y, and analogues Am - Dy. The technique of obtaining a model nitride fuel based on lanthanides nitrides and UN. Hydrogenation-dehydrogenation- nitration method of derived powders nitrides uranium, cerium, yttrium and dysprosium, held their mixing, pressing and sintering, the samples obtained model nitride fuel with plutonium and americium imitation. According to the results of structural studies have shown that all the samples are solid solution nitrides rare earth (REE) elements in UN.

  9. The Role of Colloids in the Transport of Plutonium and Americium: Implications for

    Energy Technology Data Exchange (ETDEWEB)

    Kersting, A B

    2003-09-17

    Colloids are small particulates (ranging in size from 1 to 0.001 micron) composed of inorganic and organic material and found in all natural water. Due to their small size, they have the ability to remain suspended in water and transported. Small amounts of plutonium (Pu) and americium (Am) can adsorb (attach) to colloids, and/or form colloidal-sized polymers and migrate in water. At Rocky Flats Environmental Technology Site (RFETS) sedimentation and resuspension of particulates and colloids in surface waters represent the dominant process for Pu and Am migration. The amount of Pu and Am that can be transported at RFETS has been quantified in the Pathway Analysis Report. The Pathway Analysis Report shows that the two dominant pathways for Pu and Am transport at RFETS are air and surface water. Shallow groundwater and biological pathways are minor.

  10. Standard practice for The separation of americium from plutonium by ion exchange

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2001-01-01

    1.1 This practice describes the use of an ion exchange technique to separate plutonium from solutions containing low concentrations of americium prior to measurement of the 241Am by gamma counting. 1.2 This practice covers the removal of plutonium, but not all the other radioactive isotopes that may interfere in the determination of 241Am. 1.3 This practice can be used when 241Am is to be determined in samples in which the plutonium is in the form of metal, oxide, or other solid provided that the solid is appropriately sampled and dissolved (See Test Methods C758, C759, and C1168). 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  11. The bulk modulus of cubic spinel selenides: an experimental and theoretical study

    DEFF Research Database (Denmark)

    Waskowska, A.; Gerward, Leif; Olsen, J.S.

    2009-01-01

    It is argued that mainly the selenium sublattice determines the overall compressibility of the cubic spinel selenides, AB2Se4, and that the bulk modulus for these compounds is about 100GPa. The hypothesis is supported by experiments using high-pressure X-ray diffraction and synchrotron radiation,...

  12. Polystyrene-supported Selenides and Selenoxide:Versatile Routes to Synthesize Allylic Alcohols

    Institute of Scientific and Technical Information of China (English)

    Wei Ming XU; You Chu ZHANG; Xian HUANG

    2003-01-01

    Several polystyrene-supported selenides and selenoxide have been prepared firstly. These novel reagents were treated with LDA to produce selenium stabilized carbanions, which reacted with aldehydes and alkyl halides, followed by selenoxide syn-elimination and [2,3] sigmatropic rearrangement respectively to give Z-allylic alcohols stereoselectively.

  13. Impact of atmospheric species on copper indium gallium selenide solar cell stability: An overview

    NARCIS (Netherlands)

    Theelen, M.

    2016-01-01

    An overview of the measurement techniques and results of studies on the stability of copper indium gallium selenide (CIGS) solar cells and their individual layers in the presence of atmospheric species is presented: in these studies, Cu(In,Ga)Se2 solar cells, their molybdenum back contact, and their

  14. A simple and effective approach to the synthesis of alkynyl selenides from terminal alkynes

    Institute of Scientific and Technical Information of China (English)

    Barahman Movassagh; Mozhgan Navidi

    2012-01-01

    Alkynyl selenides were prepared under very mild conditions by reacting terminal alkynes with respective diorganic diselenides in the presence of potassium t-butoxide.The advantages of this protocol include the use of readily available substrates and reagent and good yield of the products.

  15. Synthesis and optical properties of cadmium selenide quantum dots for white light-emitting diode application

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Xianmei; Wang, Yilin; Gule, Teri; Luo, Qiang [School of Chemistry and Chemical Engineering, Guangxi University, Nanning 53000 (China); Zhou, Liya, E-mail: zhouliyatf@163.com [School of Chemistry and Chemical Engineering, Guangxi University, Nanning 53000 (China); Gong, Fuzhong [School of Chemistry and Chemical Engineering, Guangxi University, Nanning 53000 (China)

    2013-03-15

    Highlights: ► Stable CdSe QDs were synthesized by the one-step and two-level process respectively. ► The fabricated white LEDs show good white balance. ► CdSe QDs present well green to yellow band luminescence. ► CdSe QDs displayed a broad excitation band. - Abstract: Yellow light-emitting cadmium selenide quantum dots were synthesized using one-step and two-step methods in an aqueous medium. The structural luminescent properties of these quantum dots were investigated. The obtained cadmium selenide quantum dots displayed a broad excitation band suitable for blue or near-ultraviolet light-emitting diode applications. White light-emitting diodes were fabricated by coating the cadmium selenide samples onto a 460 nm-emitting indium gallium nitrite chip. Both samples exhibited good white balance. Under a 20 mA working current, the white light-emitting diode fabricated via the one-step and two-step methods showed Commission Internationale de l’Éclairage coordinates at (0.27, 0.23) and (0.27, 0.33), respectively, and a color rendering index equal to 41 and 37, respectively. The one-step approach was simpler, greener, and more effective than the two-step approach. The one-step approach can be enhanced by combining cadmium selenide quantum dots with proper phosphors.

  16. Surface-initiated atom transfer radical polymerization-induced transformation of selenium nanowires into copper selenide@polystyrene core-shell nanowires.

    Science.gov (United States)

    Wang, Michael C P; Gates, Byron D

    2013-10-09

    This Article reports the first preparation of cuprous and cupric selenide nanowires coated with a ∼5 nm thick sheath of polystyrene (copper selenide@polystyrene). These hybrid nanostructures are prepared by the transformation of selenium nanowires in a one-pot reaction, which is performed under ambient conditions. The composition, purity, and crystallinity of the copper selenide@polystyrene products were assessed by scanning transmission electron microscopy, electron energy-loss spectroscopy, X-ray powder diffraction, and X-ray photoelectron spectroscopy techniques. We determined that the single crystalline selenium nanowires are converted into polycrystalline copper selenide@polystyrene nanowires containing both cuprous selenide and cupric selenide. The product is purified through the selective removal of residual, non-transformed selenium nanowires by performing thermal evaporation below the decomposition temperature of these copper selenides. Powder X-ray diffraction of the purified copper selenide nanowires@polystyrene identified the presence of hexagonal, cubic, and orthorhombic phases of copper selenide. These purified cuprous and cupric selenide@polystyrene nanowires have an indirect bandgap of 1.44 eV, as determined by UV-vis absorption spectroscopy. This new synthesis of polymer-encapsulated nanoscale materials may provide a method for preparing other complex hybrid nanostructures.

  17. Separation of oxidized americium from lanthanides by use of pillared metal(IV) phosphate-phosphonate hybrid materials

    Energy Technology Data Exchange (ETDEWEB)

    Burns, J.D.; Clearfield, A. [Texas A and M Univ., College Station, TX (United States). Dept. of Chemistry; Borkowski, M.; Reed, D.T. [Los Alamos National Laboratory, Carlsbad, NM (United States). Earth and Environmental Sciences Div.

    2012-07-01

    Closing the nuclear fuel cycle in the US poses many challenges, one of which is found in the waste streams, which contain both trivalent lanthanides and actinides. The separation of americium from the raffinate will dramatically reduce the long-term radiotoxicity of the waste. The sorption of americium in both the tri- and pentavalent oxidation states was observed for four M(IV) phosphate-phosphonate ion exchange materials in nitric acid at pH 2. High selectivity was observed for reduced Am(III) with K{sub d} values ca. 6 x 10{sup 5} mL/g, while the K{sub d} values for Am(V) were much lower. A new method of synthesizing and stabilizing AmO{sub 2}{sup +} to yield a lifetime of at least 24 h in acidic media using a combination of sodium persulfate and calcium hypochlorite will be described.

  18. Theoretical investigation of pressure-induced structural transitions in americium using GGA+U and hybrid density functional theory methods

    DEFF Research Database (Denmark)

    Verma, Ashok K.; Modak, P.; Sharma, Surinder M.;

    2013-01-01

    First-principles calculations have been performed for americium (Am) metal using the generalized gradient approximation + orbital-dependent onsite Coulomb repulsion via Hubbard interaction (GGA+U) and hybrid density functional theory (HYB-DFT) methods to investigate various ground state properties...... spectrum at ambient pressure relate, for some parameter choices, well to peak positions in the calculated density of states function of Am-I....

  19. Semiconducting thin films of zinc selenide quantum dots

    Science.gov (United States)

    Pejova, Biljana; Tanuševski, Atanas; Grozdanov, Ivan

    2004-12-01

    A novel chemical route for deposition of zinc selenide quantum dots in thin film form is developed. The deposited films are characterized with very high purity in crystallographic sense, and behave as typical intrinsic semiconductors. Evolution of the average crystal size, lattice constant, lattice strain and the optical properties of the films upon thermal treatment is followed and discussed. The band gap energy of as-deposited ZnSe films is blue-shifted by ≈0.50 eV with respect to the bulk value, while upon annealing treatment it converges to 2.58 eV. Two discrete electronic states which originate from the bulk valence band are observed in the UV-VIS spectra of ZnSe 3D quantum dots deposited in thin film form via allowed electronic transitions to the 1 S electronic state arising from the bulk conduction band—appearing at 3.10 and 3.50 eV. The splitting between these two states is approximately equal to the spin-orbit splitting in the case of bulk ZnSe. The electronic transitions in the case of non-quantized annealed films are discussed in terms of the direct allowed band-to-band transitions with the spin-orbit splitting of the valence band of 0.40 eV. The effective mass approximation model (i.e., the Brus model) with the static relative dielectric constant of bulk ZnSe fails to predict correctly the size dependence of the band gap energy, while only a slight improvement is obtained when the hyperbolic band model is applied. However, when substantially smaller value for ɛr (2.0 instead of 8.1) is used in the Brus model, an excellent agreement with the experimental data is obtained, which supports some earlier indications that the quantum dots ɛr value could be significantly smaller than the bulk material value. The ionization energy of a deep donor impurity level calculated on the basis of the temperature dependence of the film resistivity is 0.82 eV at 0 K.

  20. Vertical and horizontal fluxes of plutonium and americium in the western Mediterranean and the Strait of Gibraltar.

    Science.gov (United States)

    León Vintró, L; Mitchell, P I; Condren, O M; Downes, A B; Papucci, C; Delfanti, R

    1999-09-30

    New data on the vertical distributions of plutonium and americium in the waters of the western Mediterranean and the Strait of Gibraltar are examined in terms of the processes governing their delivery to, transport in and removal from the water column within the basin. Residence times for plutonium and americium in surface waters of approximately 15 and approximately 3 years, respectively, are deduced, and it is shown that by the mid 1990s only approximately 35% of the 239,240Pu and approximately 5% of the 241Am deposited as weapons fallout still resided in the water column. Present 239,240Pu inventories in the water column and the underlying sediments are estimated to be approximately 25 TBq and approximately 40 TBq, respectively, which reconcile well with the time-integrated fallout deposition in this zone, taken to be approximately 69 TBq. The data show that there are significant net outward fluxes of plutonium and americium from the basin through the Strait of Gibraltar at the present time. These appear to be compensated by net inward fluxes of similar magnitude through the Strait of Sicily. Thus, the time-integrated fallout deposition in the western basin can be accounted for satisfactorily in terms of present water column and sediment inventories. Enhanced scavenging on the continental shelves, as evidenced by the appreciably higher transuranic concentrations in shelf sediments, supports this contention.

  1. The behaviour under irradiation of molybdenum matrix for inert matrix fuel containing americium oxide (CerMet concept)

    Science.gov (United States)

    D'Agata, E.; Knol, S.; Fedorov, A. V.; Fernandez, A.; Somers, J.; Klaassen, F.

    2015-10-01

    Americium is a strong contributor to the long term radiotoxicity of high activity nuclear waste. Transmutation by irradiation in nuclear reactors or Accelerator Driven System (ADS, subcritical reactors dedicated to transmutation) of long-lived nuclides like 241Am is therefore an option for the reduction of radiotoxicity of waste packages to be stored in a repository. In order to safely burn americium in a fast reactor or ADS, it must be incorporated in a matrix that could be metallic (CerMet target) or ceramic (CerCer target). One of the most promising matrix to incorporate Am is molybdenum. In order to address the issues (swelling, stability under irradiation, gas retention and release) of using Mo as matrix to transmute Am, two irradiation experiments have been conducted recently at the High Flux Reactor (HFR) in Petten (The Netherland) namely HELIOS and BODEX. The BODEX experiment is a separate effect test, where the molybdenum behaviour is studied without the presence of fission products using 10B to "produce" helium, the HELIOS experiment included a more representative fuel target with the presence of Am and fission product. This paper covers the results of Post Irradiation Examination (PIE) of the two irradiation experiments mentioned above where molybdenum behaviour has been deeply investigated as possible matrix to transmute americium (CerMet fuel target). The behaviour of molybdenum looks satisfying at operating temperature but at high temperature (above 1000 °C) more investigation should be performed.

  2. HELIOS: the new design of the irradiation of U-free fuels for americium transmutation

    Energy Technology Data Exchange (ETDEWEB)

    D' Agata, E. [European Commission, Joint Research Centre, Institute for Energy, P.O. Box 2, 1755 ZG Petten (Netherlands); Klaassen, F.; Sciolla, C. [Nuclear Research and Consultancy Group, Dept. Life Cycle and Innovations, P.O. Box 25 1755 ZG Petten (Netherlands); Fernandez-Carretero, A. [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany); Bonnerot, J.M. [Commissariat a l' Energie Atomique, DEC/SESC/LC2I CEA-Cadarache, 13108 St. Paul lez Durance Cedex (France)

    2009-06-15

    Americium is one of the radioactive elements that mostly contribute to the radiotoxicity of the nuclear spent fuel. Transmutation of long-lived nuclides like Americium is an option for the reduction of the mass, the radiotoxicity and the decay heat of nuclear waste. The HELIOS irradiation experiment is the last evolution in a series of experiments on americium transmutation. The previous experiments, EFTTRA-T4 and T4bis, have shown that the release or trapping of helium is the key issue for the design of such kind of target. In fact, the production of helium, which is characteristic of {sup 241}Am transmutation, is quite significant. The experiment is carried out in the framework of the 4-year project EUROTRANS of the EURATOM 6. Framework Programme (FP6). Therefore, the main objective of the HELIOS experiment is to study the in-pile behaviour of U-free fuels such as CerCer (Pu, Am, Zr)O{sub 2} and Am{sub 2}Zr{sub 2}O{sub 7}+MgO or CerMet (Pu, Am)O{sub 2}+Mo in order to gain knowledge on the role of the fuel microstructure and of the temperature on the gas release and on the fuel swelling. The experiment was planned to be conducted in the HFR (High Flux Reactor) in Petten (The Netherlands) starting the first quarter of 2007. Because of the innovative aspects of the fuel, the fabrication has had some delays as well as the final safety analyses of the original design showed some unexpected deviation. Besides, the HFR reactor has been unavailable since August 2008. Due to the reasons described above, the experiment has been postponed. HELIOS should start in the first quarter of 2009 and will last 300 full power days. The paper will cover the description of the new design of the irradiation experiment HELIOS. The experiment has been split in two parts (HELIOS1 and HELIOS2) which will be irradiated together. Moreover, due to the high temperature achieved in cladding and to the high amount of helium produced during transmutation the experiment previously designed for a

  3. A convenient and stereoselective synthesis of (Z)-allyl selenides via Sm/TMSCI system-promoted coupling of Baylis-Hillman adducts with diselenides

    Institute of Scientific and Technical Information of China (English)

    LIU Yun-kui; XU Dan-qian; XU Zhen-yuan; ZHANG Yong-min

    2006-01-01

    A simple and convenient procedure for stereoselective synthesis of (Z)-allyl selenides has been developed by a one-pot reaction of diselenides with Baylis-Hillman adducts in the presence of samarium metal-trimethylsilyl chloride under mild conditions. Presumably, the diselenides are cleaved by Sm/TMSCl system to form selenide anions, which then undergo SN2' substitution of Baylis-Hillman adducts to produce the (Z)-allyl selenides.

  4. Americium and plutonium in water, biota, and sediment from the central Oregon coast

    Energy Technology Data Exchange (ETDEWEB)

    Nielsen, R. D.

    1982-06-01

    Plutonium-239, 240 and americium-241 were measured in the mussel Mytilus californianus from the region of Coos Bay, OR. The flesh of this species has a plutonium concentration of about 90 fCi/kg, and an Am-241/Pu-239, 240 ratio that is high relative to mixed fallout, ranging between two and three. Transuranic concentrations in sediment, unfiltered water, and filterable particulates were also measured; none of these materials has an Am/Pu ratio as greatly elevated as the mussels, and there is no apparent difference in the Am/Pu ratio of terrestrial runoff and coastal water. Sediment core profiles do not allow accumulation rates or depositional histories to be identified, but it does not appear that material characterized by a high Am/Pu ratio has ever been introduced to this estuary. Other bivalves (Tresus capax and Macoma nasuta) and a polychaete (Abarenicola sp.) do not have an elevated Am/Pu ratio, although the absolute activity of plutonium in the infaunal bivalves is roughly four times that in the mussels.

  5. Development and Testing of an Americium/Lanthanide Separation Flowsheet Using Sodium Bismuthate

    Energy Technology Data Exchange (ETDEWEB)

    Jack Law; Bruce Mincher; Troy Garn; Mitchell Greenhalgh; Nicholas Schmitt; Veronica Rutledge

    2014-04-01

    The separation of Am from the lanthanides and curium is a key step in proposed advanced fuel cycle scenarios. The partitioning and transmutation of Am is desirable to minimize the long-term heat load of material interred in a future high-level waste repository. A separation process amenable to process scale-up remains elusive. Given only subtle chemistry differences within and between the ions of the trivalent actinide and lanthanide series this separation is challenging ; however, higher oxidation states of americium can be prepared using sodium bismuthate and separated via solvent extraction using diamylamylphosphonate (DAAP) extraction. Among the other trivalent metals only Ce is also oxidized and extracted. Due to the long-term instability of Am(VI) , the loaded organic phase is readily selectively stripped to partition the actinide to a new acidic aqueous phase. Batch extraction distribution ratio measurements were used to design a flowsheet to accomplish this separation. Additionally, crossflow filtration was investigated as a method to filter the bismuthate solids from the feed solution prior to extraction. Results of the filtration studies, flowsheet development work and flowsheet performance testing using a centrifugal contactor are detailed.

  6. Americium-based oxides: Dense pellet fabrication from co-converted oxalates

    Energy Technology Data Exchange (ETDEWEB)

    Horlait, Denis; Lebreton, Florent [CEA, DEN, DTEC/SDTC/LEMA, 30207 Bagnols-sur-Cèze (France); Gauthé, Aurélie [CEA, DEN, DRCP/SERA/LCAR, 30207 Bagnols-sur-Cèze (France); Caisso, Marie [CEA, DEN, DTEC/SDTC/LEMA, 30207 Bagnols-sur-Cèze (France); Arab-Chapelet, Bénédicte; Picart, Sébastien [CEA, DEN, DRCP/SERA/LCAR, 30207 Bagnols-sur-Cèze (France); Delahaye, Thibaud, E-mail: thibaud.delahaye@cea.fr [CEA, DEN, DTEC/SDTC/LEMA, 30207 Bagnols-sur-Cèze (France)

    2014-01-15

    Mixed oxides are used as nuclear fuels and are notably envisaged for future fuel cycles including plutonium and minor actinide recycling. In this context, processes are being developed for the fabrication of uranium–americium mixed-oxide compounds for transmutation. The purpose of these processes is not only the compliance with fuel specifications in terms of density and homogeneity, but also the simplification of the process for its industrialization as well as lowering dust generation. In this paper, the use of a U{sub 0.85}Am{sub 0.15}O{sub 2±δ} powder synthesized by oxalate co-conversion as a precursor for dense fuel fabrications is assessed. This study notably focuses on sintering, which yielded pellets up to 96% of the theoretical density, taking advantage of the high reactivity and homogeneity of the powder. As-obtained pellets were further characterized to be compared to those obtained via processes based on the UMACS (Uranium Minor Actinide Conventional Sintering) process. This comparison highlights several advantages of co-converted powder as a precursor for simplified processes that generate little dust.

  7. Experimental studies on the biokinetics of plutonium and americium in the cephalopod Octopus vulgaris

    Energy Technology Data Exchange (ETDEWEB)

    Guary, J.C.; Fowler, S.W.

    1982-03-05

    Radiotracer experiments using the photon-emitters /sup 237/Pu and /sup 241/Am were performed to examine uptake, tissue distribution and retention of plutonium and americium in the cephalopod Octopus vulgaris Cuvier. A 2 wk exposure in contaminated sea water resulted in twice as much /sup 237/Pu being taken up by whole octopus as /sup 241/Am. Immediately following uptake approximately 41% and 73% of the /sup 237/Pu and /sup 241/Am respectively were located in the branchial hearts. Depuration rates for both radionuclides were identical; approximately 46% of both radionuclides initially incorporated were associated with a long-lived compartment which turned over very slowly (Tbsub(1/2) = 1.5 yr). Longer exposures to /sup 241/Am resulted in an increase in the size of the slowly exchanging /sup 241/Am pool in the octopus. After 2 mo depuration, the majority of the residual activity of both radionuclides was in the branchial hearts. On average 33% of the /sup 241/Am ingested with food was assimilated into tissues, primarily the hepatopancreas. Different whole-body /sup 241/Am excretion rates were observed at different times following assimilation and were related to transfer processes taking place within internal tissues, most notably between hepatopancreas and the branchial hearts. Relationships between circulatory and excretory functions of these 2 organs are discussed and a physiological mechanism is proposed to explain the observed patterns of /sup 241/Am excretion in O. vulgaris.

  8. In Vitro Dissolution Tests of Plutonium and Americium Containing Contamination Originating From ZPPR Fuel Plates

    Energy Technology Data Exchange (ETDEWEB)

    William F. Bauer; Brian K. Schuetz; Gary M. Huestis; Thomas B. Lints; Brian K. Harris; R. Duane Ball; Gracy Elias

    2012-09-01

    Assessing the extent of internal dose is of concern whenever workers are exposed to airborne radionuclides or other contaminants. Internal dose determinations depend upon a reasonable estimate of the expected biological half-life of the contaminants in the respiratory tract. One issue with refractory elements is determining the dissolution rate of the element. Actinides such as plutonium (Pu) and Americium (Am) tend to be very refractory and can have biological half-lives of tens of years. In the event of an exposure, the dissolution rates of the radionuclides of interest needs to be assessed in order to assign the proper internal dose estimates. During the November 2011 incident at the Idaho National Laboratory (INL) involving a ZPPR fuel plate, air filters in a constant air monitor (CAM) and a giraffe filter apparatus captured airborne particulate matter. These filters were used in dissolution rate experiments to determine the apparent dissolution half-life of Pu and Am in simulated biological fluids. This report describes these experiments and the results. The dissolution rates were found to follow a three term exponential decay equation. Differences were noted depending upon the nature of the biological fluid simulant. Overall, greater than 95% of the Pu and 93% of the Am were in a very slow dissolving component with dissolution half-lives of over 10 years.

  9. Plutonium and americium monazite materials: Solid state synthesis and X-ray diffraction study

    Energy Technology Data Exchange (ETDEWEB)

    Bregiroux, D. [DEN/DEC/SPUA, Commissariat a l' Energie Atomique, Cadarache, 13108 Saint Paul Lez Durance (France); Laboratoire Science des Procedes Ceramiques et de Traitements de Surface, UMR CNRS-Universite no. 6638, Batiment Chimie, 123 avenue Albert Thomas, 87060 Limoges (France); E-mail: damien.bregiroux@ccr.jussieu.fr; Belin, R. [DEN/DEC/SPUA, Commissariat a l' Energie Atomique, Cadarache, 13108 Saint Paul Lez Durance (France); Valenza, P. [DEN/DEC/SPUA, Commissariat a l' Energie Atomique, Cadarache, 13108 Saint Paul Lez Durance (France); Audubert, F. [DEN/DEC/SPUA, Commissariat a l' Energie Atomique, Cadarache, 13108 Saint Paul Lez Durance (France); Bernache-Assollant, D. [Ecole Nationale Superieure des Mines, 158 Cours Fauriel, 42023 Saint Etienne (France)

    2007-06-30

    High-temperature solid state syntheses of monazite powders containing plutonium (III), plutonium (IV) and americium (III) were performed. Resulting powders were characterized by X-ray diffraction. Pu{sup 3+}PO{sub 4} was readily obtained as a single phase by heating a Pu{sup 4+}O{sub 2}-NH{sub 4}H{sub 2}PO{sub 4} mixture under argon atmosphere. Traces of tetravalent plutonium phosphate Pu{sup 4+}P{sub 2}O{sub 7} were detected when synthesized under air atmosphere. The incorporation of (Pu{sup 4+},Ca{sup 2+}) in the monazite structure was investigated under air and argon atmosphere. We showed that Pu{sup 4+} is fully reduced in Pu{sup 3+} under argon atmosphere whereas, under air, the compound with the formula Pu{sub 0.4}{sup 3+}Pu{sub 0.3}{sup 4+}Ca{sub 0.3}{sup 2+}PO{sub 4} was obtained. Pure Am{sup 3+}PO{sub 4} was also synthesized under argon atmosphere. X-ray patterns revealed a complete amorphisation of the monazite structure at a relatively low cumulative alpha dose for {sup 241}AmPO{sub 4}.

  10. Mutual separation of americium(III) and europium(III) using glycolamic acid and thioglycolamic acid

    Energy Technology Data Exchange (ETDEWEB)

    Suneesh, A.S.; Venkatesan, K.A.; Syamala, K.V.; Antony, M.P.; Vasudeva Rao, P.R. [Indira Gandhi Centre for Atomic Research, Kalpakkam (India). Fuel Chemistry Div.

    2012-07-01

    The extractants, bis(2-ethylhexyl)diglycolamicacid (HDEHDGA) and bis(2-ethylhexy)thiodiglycolamic acid (HDEHSDGA) were synthesized and characterized by {sup 1}H and {sup 13}C NMR, mass and IR spectroscopy. The extraction behaviour of {sup (152+154})Eu(III) and {sup 241}Am(III) from nitric acid medium by a solution of HDEHDGA (or HDEHSDGA) in n-dodecane (n-DD) was studied for the mutual separation of actinides and lanthanides. The effect of various parameters such as the pH, concentrations of HDEHDGA, HDEHSDGA, sodium nitrate, N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) and diethylenetriaminepentaacetic acid (DTPA) on the separation factor (SF) of americium(III) over europium(III) and vice versa was studied, and the conditions needed for the preferential separation were optimised. The results show that HDEHDGA exhibits higher extraction for {sup (152+154)}Eu(III) and HDEHSDGA shows the superior selectivity for {sup 241}Am(III). (orig.)

  11. Solution speciation of plutonium and Americium at an Australian legacy radioactive waste disposal site.

    Science.gov (United States)

    Ikeda-Ohno, Atsushi; Harrison, Jennifer J; Thiruvoth, Sangeeth; Wilsher, Kerry; Wong, Henri K Y; Johansen, Mathew P; Waite, T David; Payne, Timothy E

    2014-09-01

    During the 1960s, radioactive waste containing small amounts of plutonium (Pu) and americium (Am) was disposed in shallow trenches at the Little Forest Burial Ground (LFBG), located near the southern suburbs of Sydney, Australia. Because of periodic saturation and overflowing of the former disposal trenches, Pu and Am have been transferred from the buried wastes into the surrounding surface soils. The presence of readily detected amounts of Pu and Am in the trench waters provides a unique opportunity to study their aqueous speciation under environmentally relevant conditions. This study aims to comprehensively investigate the chemical speciation of Pu and Am in the trench water by combining fluoride coprecipitation, solvent extraction, particle size fractionation, and thermochemical modeling. The predominant oxidation states of dissolved Pu and Am species were found to be Pu(IV) and Am(III), and large proportions of both actinides (Pu, 97.7%; Am, 86.8%) were associated with mobile colloids in the submicron size range. On the basis of this information, possible management options are assessed.

  12. Chemical synthesis of p-type nanocrystalline copper selenide thin films for heterojunction solar cells

    Science.gov (United States)

    Ambade, Swapnil B.; Mane, R. S.; Kale, S. S.; Sonawane, S. H.; Shaikh, Arif V.; Han, Sung-Hwan

    2006-12-01

    Nanocrystalline thin films of copper selenide have been grown on glass and tin doped-indium oxide substrates using chemical method. At ambient temperature, golden films have been synthesized and annealed at 200 °C for 1 h and were examined for their structural, surface morphological and optical properties by means of X-ray diffraction (XRD), scanning electron microscopy and UV-vis spectrophotometry techniques, respectively. Cu 2- xSe phase was confirmed by XRD pattern and spherical grains of 30 ± 4 - 40 ± 4 nm in size aggregated over about 130 ± 10 nm islands were seen by SEM images. Effect of annealing on crystallinity improvement, band edge shift and photoelectrochemical performance (under 80 mW/cm 2 light intensity and in lithium iodide electrolyte) has been studied and reported. Observed p-type electrical conductivity in copper selenide thin films make it a suitable candidate for heterojunction solar cells.

  13. Chemical synthesis of p-type nanocrystalline copper selenide thin films for heterojunction solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Ambade, Swapnil B. [Department of Chemical Engineering, Vishwakarma Institute of Technology, Pune 411037 (India); Mane, R.S. [Inorganic Nanomaterials Laboratory, Department of Chemistry, Hanyang University, Sungdong-Ku, Haengdang-dong 17, Seoul 133-791 (Korea, Republic of); Kale, S.S. [Inorganic Nanomaterials Laboratory, Department of Chemistry, Hanyang University, Sungdong-Ku, Haengdang-dong 17, Seoul 133-791 (Korea, Republic of); Sonawane, S.H. [Department of Chemical Engineering, Vishwakarma Institute of Technology, Pune 411037 (India); Shaikh, Arif V. [Department of Electronic Science, AKI' s Poona College of Arts, Science and Commerce, Camp, Pune 411 001 (India); Han, Sung-Hwan [Inorganic Nanomaterials Laboratory, Department of Chemistry, Hanyang University, Sungdong-Ku, Haengdang-dong 17, Seoul 133-791 (Korea, Republic of)]. E-mail: shhan@hanyang.ac.kr

    2006-12-15

    Nanocrystalline thin films of copper selenide have been grown on glass and tin doped-indium oxide substrates using chemical method. At ambient temperature, golden films have been synthesized and annealed at 200 deg. C for 1 h and were examined for their structural, surface morphological and optical properties by means of X-ray diffraction (XRD), scanning electron microscopy and UV-vis spectrophotometry techniques, respectively. Cu{sub 2-x}Se phase was confirmed by XRD pattern and spherical grains of 30 {+-} 4 - 40 {+-} 4 nm in size aggregated over about 130 {+-} 10 nm islands were seen by SEM images. Effect of annealing on crystallinity improvement, band edge shift and photoelectrochemical performance (under 80 mW/cm{sup 2} light intensity and in lithium iodide electrolyte) has been studied and reported. Observed p-type electrical conductivity in copper selenide thin films make it a suitable candidate for heterojunction solar cells.

  14. Metal ions to control the morphology of semiconductor nanoparticles: copper selenide nanocubes.

    Science.gov (United States)

    Li, Wenhua; Zamani, Reza; Ibáñez, Maria; Cadavid, Doris; Shavel, Alexey; Morante, Joan Ramon; Arbiol, Jordi; Cabot, Andreu

    2013-03-27

    Morphology is a key parameter in the design of novel nanocrystals and nanomaterials with controlled functional properties. Here, we demonstrate the potential of foreign metal ions to tune the morphology of colloidal semiconductor nanoparticles. We illustrate the underlying mechanism by preparing copper selenide nanocubes in the presence of Al ions. We further characterize the plasmonic properties of the obtained nanocrystals and demonstrate their potential as a platform to produce cubic nanoparticles with different composition by cation exchange.

  15. Chemically deposited thin films of sulfides and selenides of antimony and bismuth as solar energy materials

    Science.gov (United States)

    Nair, M. T. S.; Nair, Padmanabhan K.; Garcia, Victor M.; Pena, Y.; Arenas, O. L.; Garcia, J. C.; Gomez-Daza, O.

    1997-10-01

    Chemical bath deposition techniques for bismuth sulfide, bismuth selenide, antimony sulfide, and antimony selenide thin films of about 0.20 - 0.25 micrometer thickness are reported. All these materials may be considered as solar absorber films: strong optical absorption edges, with absorption coefficient, (alpha) , greater than 104 cm-1, are located at 1.31 eV for Bi2Se3, 1.33 eV for Bi2S3, 1.8 eV for Sb2S3, and 1.35 eV for Sb2Se3. As deposited, all the films are nearly amorphous. However, well defined crystalline peaks matching bismuthinite (JCPDS 17- 0320), paraguanajuatite (JCPDS 33-0214), and stibnite (JCPDS 6-0474) and antimony selenide (JCPDS 15-0861) for Bi2S3, Bi2Se3, Sb2S3 and Sb2Se3 respectively, are observed when the films are annealed in nitrogen at 300 degrees Celsius. This is accompanied by a substantial modification of the electrical conductivity in the films: from 10-7 (Omega) -1 cm-1 (in as prepared films) to 10 (Omega) -1 cm-1 in the case of bismuth sulfide and selenide films, and enhancement of photosensitivity in the case of antimony sulfide films. The chemical deposition of a CuS/CuxSe film on these Vx- VIy films and subsequent annealing at 300 degrees Celsius for 1 h at 1 torr of nitrogen leads to the formation of p-type films (conductivity of 1 - 100 (Omega) -1 cm-1) of multinary composition. Among these, the formation of Cu3BiS3 (JCPDS 9-0488) and Cu3SbS4 (JCPDS 35- 0581), CuSbS2 (JCPDS 35-0413) have been clearly detected. Solar energy applications of these films are suggested.

  16. Realization of ultrathin Copper Indium Gallium Di-selenide (CIGSe) solar cells

    OpenAIRE

    Jehl, Zacharie

    2012-01-01

    In this thesis, we investigate on the possibility to realize ultrathin absorber Copper Indium Gallium Di-Selenide (CIGSe) solar cells, by reducing the CIGSe thickness from 2500 nm down to 100 nm, while conserving a high conversion efficiency.Using numerical modeling, we first study the evolution of the photovoltaic parameters when reducing the absorber thickness. A strong decrease of the efficiency of the solar cell is observed, mainly related to a reduced light absorption and carrier collect...

  17. Spectroscopic ellipsometry studies on vacuum-evaporated zinc selenide thin film

    Science.gov (United States)

    Gao, Weidong

    2009-05-01

    Optical constants of vacuum-deposited Zinc selenide (ZnSe) film from far infrared to near ultraviolet spectral region (270nm-30μm) have been determined by variable angle spectroscopic ellipsometry. The surface roughness layer and interface layer between ZnSe film and crystalline silicon have been modeled with Bruggeman effective medium approximation (BEMA). To evaluate the microstructure of ZnSe film, X-ray diffraction (XRD) measurements are also performed.

  18. Study of Linear and Non-Linear Optical Parameters of Zinc Selenide Thin Film

    OpenAIRE

    Desai, H. N.; J. M. Dhimmar

    2015-01-01

    Thin film of Zinc Selenide (ZnSe) was deposited onto transparent glass substrate by thermal evaporation technique. ZnSe thin film was characterized by UV-Visible spectrophotometer within the wavelength range of 310 nm-1080 nm. The Linear optical parameters (linear optical absorption, extinction coefficient, refractive index and complex dielectric constant) of ZnSe thin film were analyzed from absorption spectra. The optical band gap and Urbach energy were obtained by Tauc’s equati...

  19. Cytocompatibility of direct water synthesized cadmium selenide quantum dots in colo-205 cells

    OpenAIRE

    Rodriguez-Torres, Marcos R.; Velez, Christian; Zayas, Beatriz; Rivera, Osvaldo; Arslan, Zikri; Gonzalez-Vega, Maxine N.; Diaz-Diestra, Daysi; Beltran-Huarac, Juan; Morell, Gerardo; Primera-Pedrozo, Oliva M.

    2015-01-01

    Cadmium selenide quantum dots (CdSe QDs), inorganic semiconducting nanocrystals, are alluring increased attraction due to their highly refined chemistry, availability, and super tunable optical properties suitable for many applications in different research areas, such as photovoltaics, light-emitting devices, environmental sciences, and nanomedicine. Specifically, they are being widely used in bio-imaging in contrast to organic dyes due to their high brightness and improved photo-stability, ...

  20. Copper and silver selenide crystal growth rate measurements as a method for determination of ionic conductivity

    Science.gov (United States)

    Vučić, Zlatko; Lovrić, Davorin; Gladić, Jadranko; Etlinger, Božidar

    2004-03-01

    The motivation behind this work is the discrepancy between the measured and calculated growth rates of copper selenide spherical single crystals between 740 and 800 K. The growth of cylindrical polycrystalline samples of copper selenide at high temperatures was monitored in experiments that enabled full control of the geometry of growth. Together with the calculations based on Yokota's transport equation, these measurements eliminated ionic conductivity data as a possible reason behind too high values of the calculated growth rates. The equivalent growth experiments on polycrystalline silver selenide samples were performed as a test of the method, yielding excellent agreement with the results obtained by extrapolation of existing data. On the basis of these measurements and associated analysis, this method is proposed as a method for determination of ionic conductivity of mixed superionic conductors on temperatures up to the temperatures of melting, i.e. in the range in which other methods of ionic conductivity measurements either do not work or are not accurate enough.

  1. Copper selenide nanowires and nanocrystallites in alumina: Carrier relaxation, recombination, and trapping

    Science.gov (United States)

    Statkutė, G.; Tomašiùnas, R.; Jagminas, A.

    2007-06-01

    Nonequilibrium carrier dynamics in copper selenide (Cu2-δSe δ=0.15, Cu3Se2) nanowires (diameter ≈18 nm, height ≈2 μm) and nanocrystallites (diameter≈18 nm) in femto- and picosecond time domains by the means of a transient dynamic grating technique were investigated. Bulk and quantum confinement approaches were used to fit the experimental results using nonequilibrium carrier fast relaxation, recombination, and trapping mechanisms. A nonradiative Auger recombination was concluded to be the main mechanism of nonequilibrium carrier recombination. The Auger coefficient for copper selenide was estimated of the order of 10-30-10-29 cm6 s-1. Hole trapping at shallow impurity centers in nanowires was interpreted. From calculating the experimental results the trapping parameters and high concentration of centers >1020 cm-3 were evaluated. Finally, direct measurement of carrier lifetime in copper selenide nanostructures showed values of the order of ≈10-10 s. Samples were characterized by the means of transmission electron microscopy, scanning electron microscopy, x-ray diffraction, and optical spectroscopy.

  2. Determination of dimethyl selenide and dimethyl sulphide compounds causing off-flavours in bottled mineral waters.

    Science.gov (United States)

    Guadayol, Marta; Cortina, Montserrat; Guadayol, Josep M; Caixach, Josep

    2016-04-01

    Sales of bottled drinking water have shown a large growth during the last two decades due to the general belief that this kind of water is healthier, its flavour is better and its consumption risk is lower than that of tap water. Due to the previous points, consumers are more demanding with bottled mineral water, especially when dealing with its organoleptic properties, like taste and odour. This work studies the compounds that can generate obnoxious smells, and that consumers have described like swampy, rotten eggs, sulphurous, cooked vegetable or cabbage. Closed loop stripping analysis (CLSA) has been used as a pre-concentration method for the analysis of off-flavour compounds in water followed by identification and quantification by means of GC-MS. Several bottled water with the aforementioned smells showed the presence of volatile dimethyl selenides and dimethyl sulphides, whose concentrations ranged, respectively, from 4 to 20 ng/L and from 1 to 63 ng/L. The low odour threshold concentrations (OTCs) of both organic selenide and sulphide derivatives prove that several objectionable odours in bottled waters arise from them. Microbial loads inherent to water sources, along with some critical conditions in water processing, could contribute to the formation of these compounds. There are few studies about volatile organic compounds in bottled drinking water and, at the best of our knowledge, this is the first study reporting the presence of dimethyl selenides and dimethyl sulphides causing odour problems in bottled waters.

  3. Americium/Lanthanide Separations in Alkaline Solutions for Advanced Nuclear Fuel Cycles

    Energy Technology Data Exchange (ETDEWEB)

    Goff, George S. [Los Alamos National Laboratory; Long, Kristy Marie [Los Alamos National Laboratory; Reilly, Sean D. [Los Alamos National Laboratory; Jarvinen, Gordon D. [Los Alamos National Laboratory; Runde, Wolfgang H. [Los Alamos National Laboratory

    2012-06-11

    Project goals: Can used nuclear fuel be partitioned by dissolution in alkaline aqueous solution to give a solution of uranium, neptunium, plutonium, americium and curium and a filterable solid containing nearly all of the lanthanide fission products and certain other fission products? What is the chemistry of Am/Cm/Ln in oxidative carbonate solutions? Can higher oxidation states of Am be stabilized and exploited? Conclusions: Am(VI) is kinetically stable in 0.5-2.0 M carbonate solutions for hours. Aliquat 336 in toluene has been successfully shown to extract U(VI) and Pu(VI) from carbonate solutions. (Stepanov et al 2011). Higher carbonate concentration gives lower D, SF{sub U/Eu} for = 4 in 1 M K{sub 2}CO{sub 3}. Experiments with Am(VI) were unsuccessful due to reduction by the organics. Multiple sources of reducing organics...more optimization. Reduction experiments of Am(VI) in dodecane/octanol/Aliquat 336 show that after 5 minutes of contact, only 30-40% of the Am(VI) has been reduced. Long enough to perform an extraction. Shorter contact times, lower T, and lower Aliquat 336 concentration still did not result in any significant extraction of Am. Anion exchange experiments using a strong base anion exchanger show uptake of U(VI) with minimal uptake of Nd(III). Experiments with Am(VI) indicate Am sorption with a Kd of 9 (10 minute contact) but sorption mechanism is not yet understood. SF{sub U/Nd} for = 7 and SF{sub U/Eu} for = 19 after 24 hours in 1 M K{sub 2}CO{sub 3}.

  4. Concentrations of plutonium and americium in plankton from the western Mediterranean Sea

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez-Cabeza, Joan-Albert; Merino, Juan; Masque, Pere [Insitut de Ciencia i Tecnologia Ambiental-Departament de Fisica, Universitat Autonoma de Barcelona, 08193 Bellaterra, Barcelona (Spain); Mitchell, Peter I.; Vintro, L. Leon [Department of Experimental Physics, University College Dublin, Dublin 4 (Ireland); Schell, William R. [Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261 (United States); Cross, Lluisa; Calbet, Albert [Institut de Ciencies del Mar, Pg. Maritim Barceloneta, 37-49 08003, Barcelona (Spain)

    2003-07-20

    Understanding the transfer of radionuclides through the food chain leading to man and in particular, the uptake of transuranic nuclides by plankton, is basic to assess the potential radiological risk of the consumption of marine products by man. The main sources of transuranic elements in the Mediterranean Sea in the past were global fallout and the Palomares accident, although at present smaller amounts are released from nuclear establishments in the northwestern region. Plankton from the western Mediterranean Sea was collected and analyzed for plutonium and americium in order to study their biological uptake. The microplankton fractions accounted for approximately 50% of the total plutonium contents in particulate form. At Garrucha (Palomares area), microplankton showed much higher {sup 239,240}Pu activity, indicating the contamination with plutonium from the bottom sediments. Concentration factors were within the range of the values recommended by the International Atomic Energy Agency. Continental shelf mesoplankton was observed to efficiently concentrate transuranics. In open seawaters, concentrations were much lower. We speculate that sediments might play a role in the transfer of transuranics to mesoplankton in coastal waters, although we cannot discard that the difference in species composition may also play a role. In Palomares, both {sup 239,240}Pu and {sup 241}Am showed activities five times higher than the mean values observed in continental shelf mesoplankton. As the plutonium isotopic ratios in the contaminated sample were similar to those found in material related to the accident, the contamination was attributed to bomb debris from the Palomares accident. Concentration factors in mesoplankton were also in relatively good agreement with the ranges recommended by IAEA. In the Palomares station the highest concentration factor was observed in the sample that showed predominance of the dynoflagellate Ceratium spp. Mean values of the enrichment factors

  5. Sonochemical synthesis and mechanistic study of copper selenides Cu(2-x)Se, beta-CuSe, and Cu(3)Se(2).

    Science.gov (United States)

    Xie, Yi; Zheng, Xiuwen; Jiang, Xuchuan; Lu, Jun; Zhu, Liying

    2002-01-28

    Nanocrystallites of nonstoichiometric copper selenide (Cu(2-x)Se) and stoichiometric copper selenides (beta-CuSe and Cu(3)Se(2)) were synthesized in different solutions via sonochemical irradiation at room temperature. The influence of solvents, surfactants, and ultrasonic irradiation on the morphology and phase of products has been investigated. The morphological difference of the products was mainly affected by the solvents and surfactants, which can self-aggregate into lamellar structures or microemulsions, and then these unique structures can act as both supramolecular template and microreactor to direct the growth of copper selenides. On the other hand, it was also found that the sonochemical irradiation and solvents played an important role in the formation of different phases of copper selenides. The proposed formation mechanism of copper selenides is discussed.

  6. In situ characterization of uranium and americium oxide solid solution formation for CRMP process: first combination of in situ XRD and XANES measurements.

    Science.gov (United States)

    Caisso, Marie; Picart, Sébastien; Belin, Renaud C; Lebreton, Florent; Martin, Philippe M; Dardenne, Kathy; Rothe, Jörg; Neuville, Daniel R; Delahaye, Thibaud; Ayral, André

    2015-04-14

    Transmutation of americium in heterogeneous mode through the use of U1-xAmxO2±δ ceramic pellets, also known as Americium Bearing Blankets (AmBB), has become a major research axis. Nevertheless, in order to consider future large-scale deployment, the processes involved in AmBB fabrication have to minimize fine particle dissemination, due to the presence of americium, which considerably increases the risk of contamination. New synthesis routes avoiding the use of pulverulent precursors are thus currently under development, such as the Calcined Resin Microsphere Pelletization (CRMP) process. It is based on the use of weak-acid resin (WAR) microspheres as precursors, loaded with actinide cations. After two specific calcinations under controlled atmospheres, resin microspheres are converted into oxide microspheres composed of a monophasic U1-xAmxO2±δ phase. Understanding the different mechanisms during thermal conversion, that lead to the release of organic matter and the formation of a solid solution, appear essential. By combining in situ techniques such as XRD and XAS, it has become possible to identify the key temperatures for oxide formation, and the corresponding oxidation states taken by uranium and americium during mineralization. This paper thus presents the first results on the mineralization of (U,Am) loaded resin microspheres into a solid solution, through in situ XAS analysis correlated with HT-XRD.

  7. Effect of He{sup +} irradiation on the optical properties of vacuum evaporated silver indium selenide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Santhosh Kumar, M.C., E-mail: santhoshmc@yahoo.co [Advanced Materials Laboratory, Department of Physics, National Institute of Technology, Tiruchirappalli, Tamil Nadu 620 015 (India); Pradeep, B. [Solid State Physics Laboratory, Department of Physics, Cochin University of Science and Technology, Cochin, Kerala 682 022 (India)

    2010-04-09

    We prepared polycrystalline silver indium selenide thin films by vacuum evaporation on glass substrate at a high temperature using the stoichiometric powder. The samples were subjected to the irradiation of 1.26 M eV He{sup +} ion. The effect of irradiation on the optical properties has been investigated for different fluencies of He{sup +}. The thin films were characterized by X-ray diffraction and UV-vis-NIR spectroscopy. It is observed that the band gap of silver indium selenide thin films decreases gradually from 1.17 to 0.82 eV with ion fluency.

  8. Influence of the chromium and ytterbium co-doping on the photoluminescence of zinc selenide crystals

    Institute of Scientific and Technical Information of China (English)

    I Radevici

    2014-01-01

    The luminescent properties of ZnSe, ZnSe:Cr (0.05 at.%Cr), ZnSe:Yb (0.03 at.%Yb) and ZnSe:Cr:Yb (0.05 at.%Cr, 0.05 at.%Yb) crystals, doped during the growth process by the chemical vapor transport method, were studied within the temperature in-terval of 6-300 K. At the 6 K temperature in the visible spectral range 2 bands were observed:a band in the excitonic spectral region and a band of self-activated luminescence. It was shown that co-doping of zinc selenide crystals with the chromium and ytterbium led to the combination of the impurities influence on the photoluminescent properties. At the liquid helium temperature in the middle in-frared range of the spectra of the ytterbium and chromium co-doped crystal a band with the maximum localized at 1.7 µm was ob-served, which was overlapped with a complex band in the middle-IR spectral range, characteristic for the chromium doped ZnSe crys-tals. On the basis of obtained data an interaction mechanism of the chromium and ytterbium co-doping impurities was proposed. Guided by the existent model of the ytterbium ion incorporation in the selenide sublattice of the ZnSe crystals, an assumption about stabilization of single charged chromium ions in the zinc sublattice crystal nodes, by means of formation of the local charge compen-sating clusters, was made. It was assumed that the resonant energy transfer from one chromium ion to another, which led to the con-centration quenching of the IR emission in the ZnSe:Cr PL spectra, would lead to the broadening of the IR emission in the spectra of ytterbium and chromium co-doped zinc selenide crystals.

  9. The NIFS protein can function as a selenide delivery protein in the biosynthesis of selenophosphate.

    Science.gov (United States)

    Lacourciere, G M; Stadtman, T C

    1998-11-20

    The NIFS protein from Azobacter vinelandii is a pyridoxal phosphate-containing homodimer that catalyzes the formation of equimolar amounts of elemental sulfur and L-alanine from the substrate L-cysteine (Zheng, L., White, R. H., Cash, V. L., Jack, R. F., and Dean, D. R. (1993) Proc. Natl. Acad. Sci. U. S. A. 90, 2754-2758). A sulfur transfer role of NIFS in which the enzyme donates sulfur for iron sulfur center formation in nitrogenase was suggested. The fact that NIFS also can catalyze the decomposition of L-selenocysteine to elemental selenium and L-alanine suggested the possibility that this enzyme might serve as a selenide delivery protein for the in vitro biosynthesis of selenophosphate. In agreement with this hypothesis, we have shown that replacement of selenide with NIFS and L-selenocysteine in the in vitro selenophosphate synthetase assay results in an increased rate of formation of selenophosphate. These results thus support the view that a selenocysteine-specific enzyme similar to NIFS may be involved as an in vivo selenide delivery protein for selenophosphate biosynthesis. A kinetic characterization of the two NIFS catalyzed reactions carried out in the present study indicates that the enzyme favors L-cysteine as a substrate compared with its selenium analog. A specific activity for L-cysteine of 142 nmol/min/mg compared with 55 nmol/min/mg for L-selenocysteine was determined. This level of enzyme activity on the selenoamino acid substrate is adequate to deliver selenium to selenophosphate synthetase in the in vitro assay system described.

  10. Structural, morphology and electrical properties of layered copper selenide thin film

    Science.gov (United States)

    Ying Chyi Liew, J.; Talib, Zainal; Mahmood, W.; Yunus, M.; Zainal, Zulkarnain; Halim, Shaari; Moksin, Mohd; Yusoff, Wan; Pah Lim, K.

    2009-06-01

    Thin films of copper selenide (CuSe) were physically deposited layer-by-layer up to 5 layers using thermal evaporation technique onto a glass substrate. Various film properties, including the thickness, structure, morphology, surface roughness, average grain size and electrical conductivity are studied and discussed. These properties are characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), ellipsometer and 4 point probe at room temperature. The dependence of electrical conductivity, surface roughness, and average grain size on number of layers deposited is discussed.

  11. Ion beam analysis of copper selenide thin films prepared by chemical bath deposition

    Science.gov (United States)

    Andrade, E.; García, V. M.; Nair, P. K.; Nair, M. T. S.; Zavala, E. P.; Huerta, L.; Rocha, M. F.

    2000-03-01

    Analyses of Rutherford back scattered (RBS) 4He+-particle spectra of copper selenide thin films deposited on glass slides by chemical bath were carried out to determine the changes brought about in the thin film by annealing processes. The atomic density per unit area and composition of the films were obtained from these measurements. This analysis shows that annealing in a nitrogen atmosphere at 400°C leads to the conversion of Cu xSe thin film to Cu 2Se. Results of X-ray diffraction, optical, and electrical characteristics on the films are presented to supplement the RBS results.

  12. Copper Selenide Nanosnakes: Bovine Serum Albumin-Assisted Room Temperature Controllable Synthesis and Characterization

    OpenAIRE

    Huang Peng; Kong Yifei; Li Zhiming; Gao Feng; Cui Daxiang

    2010-01-01

    Abstract Herein we firstly reported a simple, environment-friendly, controllable synthetic method of CuSe nanosnakes at room temperature using copper salts and sodium selenosulfate as the reactants, and bovine serum albumin (BSA) as foaming agent. As the amounts of selenide ions (Se2−) released from Na2SeSO3 in the solution increased, the cubic and snake-like CuSe nanostructures were formed gradually, the cubic nanostructures were captured by the CuSe nanosnakes, the CuSe nanosnakes gre...

  13. Band structure and transport studies of copper selenide: An efficient thermoelectric material

    Science.gov (United States)

    Tyagi, Kriti; Gahtori, Bhasker; Bathula, Sivaiah; Auluck, S.; Dhar, Ajay

    2014-10-01

    We report the band structure calculations for high temperature cubic phase of copper selenide (Cu2Se) employing Hartree-Fock approximation using density functional theory within the generalized gradient approximation. These calculations were further extended to theoretically estimate the electrical transport coefficients of Cu2Se employing Boltzmann transport theory, which show a reasonable agreement with the corresponding experimentally measured values. The calculated transport coefficients are discussed in terms of the thermoelectric (TE) performance of this material, which suggests that Cu2Se can be a potential p-type TE material with an optimum TE performance at a carrier concentration of ˜ 4 - 6 × 10 21 cm - 3 .

  14. Simultaneous phase and morphology controllable synthesis of copper selenide films by microwave-assisted nonaqueous approach

    Science.gov (United States)

    Li, Jing; Fa, Wenjun; Li, Yasi; Zhao, Hongxiao; Gao, Yuanhao; Zheng, Zhi

    2013-02-01

    Copper selenide films with different phase and morphology were synthesized on copper substrate through controlling reaction solvent by microwave-assisted nonaqueous approach. The films were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). The result showed that the pure films could be obtained using cyclohexyl alcohol or benzyl alcohol as solvent. The cubic Cu2-xSe dendrites were synthesized in cyclohexyl alcohol reaction system and hexagonal CuSe flaky crystals were obtained with benzyl alcohol as solvent.

  15. TOPO-capped silver selenide nanoparticles and their incorporation into polymer nanofibers using electrospinning technique

    Energy Technology Data Exchange (ETDEWEB)

    More, D.S. [Department of Chemistry, Faculty of Applied and Computer Sciences, Vaal University of Technology, Private Bag X021, Vanderbijlpark 1900 (South Africa); Moloto, M.J., E-mail: makwenam@vut.ac.za [Department of Chemistry, Faculty of Applied and Computer Sciences, Vaal University of Technology, Private Bag X021, Vanderbijlpark 1900 (South Africa); Moloto, N. [School of Chemistry, Faculty of Science, University of the Witwatersrand, Private Bag 3, Johannesburg 2050 (South Africa); Matabola, K.P. [Nanotechnology Innovation Centre, Advanced Materials Division, Mintek, Private Bag X3015, Randburg 2125 South Africa (South Africa)

    2015-05-15

    Highlights: • Ag{sub 2}Se nanoparticles produced spherical particles with sizes 12 nm (180 °C) and 27 nm (200 °C). • Higher temperature produced increased particle size (∼75 nm) and changed in shape. • Ag{sub 2}Se nanoparticles (0.2–0.6%) added into PVP (35–45%) to yield reduced fiber beading. • Polymer nanofibers electrospun at 11–20 kV produced fiber diameters of 425–461 nm. • Optical properties in the fibers were observed due to the Ag{sub 2}Se nanoparticles loaded. - Abstract: Electrospinning is the most common technique for fabricating polymer fibers as well as nanoparticles embedded polymer fibers. Silver selenide nanoparticles were synthesized using tri-n-octylphosphine (TOP) as solvent and tri-n-octylphosphine oxide (TOPO) as capping environment. Silver selenide was prepared by reacting silver nitrate and selenium with tri-n-octylphosphine (TOP) to form TOP–Ag and TOP–Se solutions. Both absorption and emission spectra signify the formation of nanoparticles as well as the TEM which revealed spherical particles with an average particle size of 22 nm. The polymer, PVP used was prepared at concentrations ranging from (35 to 45 wt%) and the TOPO-capped silver selenide nanoparticles (0.2 and 0.6 wt%) were incorporated into them and electrospun by varying the voltage from 11 to 20 kV. The SEM images of the Ag{sub 2}Se/PVP composite fibers revealed the fibers of diameters with average values of 425 and 461 nm. The X-ray diffraction results show peaks which were identified due to α-Ag{sub 2}Se body centered cubic compound. The sharp peak observed for all the samples at 2θ = 44.5 suggest the presence of Ag in the face centered cubic which can be attributed to higher concentration of silver nitrate used with molar ratio of selenium to silver and the abundance of silver in the silver selenide crystal. Fourier transform infrared spectroscopy, thermogravimetric analysis (TGA) and ultraviolet–visible spectroscopy were used to characterize the

  16. Electrical properties of silver selenide thin films prepared by reactive evaporation

    Indian Academy of Sciences (India)

    M C Santhosh Kumar; B Pradeep

    2002-10-01

    The electrical properties of silver selenide thin films prepared by reactive evaporation have been studied. Samples show a polymorphic phase transition at a temperature of 403 ± 2 K. Hall effect study shows that it has a mobility of 2000 cm2V–1s–1 and carrier concentration of 1018 cm–3 at room temperature. The carriers are of -type. X-ray diffraction study indicates that the as-prepared films are polycrystalline in nature. The lattice parameters were found to be = 4.353 Å, = 6.929 Å and = 7.805 Å.

  17. Ablation and ultrafast dynamics of zinc selenide under femtosecond laser irradiation

    Institute of Scientific and Technical Information of China (English)

    Xiaofeng Wang; Tianqing Jia; Xiaoxi Li; Chengbin Li; Donghai Feng; Haiyi Sun; Shizhen Xu; Zhizhan Xu

    2005-01-01

    The ablation in zinc selenide (ZnSe) crystal is studied by using 150-fs, 800-nm laser system. The images of the ablation pit measured by scanning electronic microscope (SEM) show no thermal stress and melting dynamics. The threshold fluence is measured to be 0.7 J/cm2. The ultrafast ablation dynamics is studied by using pump and probe method. The result suggests that optical breakdown and ultrafast melting take place in ZnSe irradiated under femtosecond laser pulses.

  18. Structural, optical and electrical properties of chemically deposited copper selenide films

    Indian Academy of Sciences (India)

    R H Bari; V Ganesan; S Potadar; L A Patil

    2009-02-01

    Stoichiometric and nonstoichiometric thin films of copper selenide have been prepared by chemical bath deposition technique at temperature below 60°C on glass substrate. The effect of nonstoichiometry on the optical, electrical and structural properties of the film was studied. The bandgap energy was observed to increase with the increase in at % of copper in composition. The grain size was also observed to increase with the decrease of at % of copper in composition. The films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDS), absorption spectroscopy, and AFM. The results are discussed and interpreted.

  19. Dissimilatory Reduction of Elemental Selenium to Selenide in Sediments and Anaerobic Cultures of Selenium Respiring Bacteria

    Science.gov (United States)

    Herbel, M. J.; Switzer-Blum, J.; Oremland, R. S.

    2001-12-01

    Selenium contaminated environments often contain elemental Se (Se0) in their sediments that originates from dissimilatory reduction of Se oxyanions. The forms of Se in sedimentary rocks similarly contain high proportions of Se0, but much of the Se is also in the form of metal selenides, Se-2. It is not clear if the occurrence of these selenides is due to microbial reduction of Se0, or some other biological or chemical process. In this investigation we examined the possibility that bacterial respiratory reduction of Se0 to Se-2 could explain the presence of the latter species in sedimentary rocks. We conducted incubations of anoxic sediment slurries amended with different forms of Se0. High levels of Se0 (mM) were added to San Francisco Bay sediments in order to enhance the detection of soluble HSe-, which was precipitated with Cu2+ then redissolved and quantified by ICP-MS. Concentrations of HSe- were highest in live samples amended with red amorphous Se0 formed by either microbial reduction of Se+4 ("biogenic Se0") or by chemical oxidation of H2Se(g) ("chem. Se0"); very little HSe- was formed in those amended with black crystalline Se0, indicating the general lack of reactivity of this allotrope. Controls poisoned with 10% formalin did not produce HSe- from additions of chem. Se0. Reduction of both forms of red amorphous Se0 to HSe- occurred vigorously in growing cultures of Bacillus selenitireducens, an anaerobic halophile previously isolated from sediments of Mono Lake, CA. Up to 73% and 68% of red amorphous, biogenic Se0 or chem. Se0, respectively, was reduced to HSe- during growth of B. selenitireducens, (incubation time ~ 200 hrs): oxidation of lactate to acetate as well as cell density increases indicated that a dissimilatory reduction pathway was likely. Reduction was most enhanced when cells were previously grown on elemental sulfur or Se+4. In contrast to the growth experiments, washed cell suspensions of B. selenitireducens exhibited no HSe- production

  20. Enhanced performance of hybrid solar cells using longer arms of quantum cadmium selenide tetrapods

    KAUST Repository

    Lee, Kyu-Sung

    2011-12-01

    We demonstrate that enhanced device performance of hybrid solar cells based on tetrapod (TP)-shaped cadmium selenide (CdSe) nanoparticles and conjugated polymer of poly (3-hexylthiophene) (P3HT) can be obtained by using longer armed tetrapods which aids in better spatial connectivity, thus decreasing charge hopping events which lead to better charge transport. Longer tetrapods with 10 nm arm length lead to improved power conversion efficiency of 1.12% compared to 0.80% of device having 5 nm short-armed tetrapods:P3HT photoactive blends.

  1. Structure and physical properties of gallium selenide laser-intercalated with nickel

    Science.gov (United States)

    Pokladok, N. T.; Grygorchak, I. I.; Lukiyanets, B. A.; Popovich, D. I.

    2007-04-01

    Intercalated crystals of indium and gallium selenide are prepared. It is shown that laser intercalation of nickel into GaSe samples leads to a giant magnetoresistive effect whose magnitude and sign depend on the concentration of the guest component. The giant magnetoresistive effect in the InSe intercalation compounds is considerably weaker and does not exceed 5%. The experimental data obtained are explained in terms of magnetic delocalization (localization) of charge carriers with the participation of states of intercalated magnetically active atoms in the vicinity of the Fermi level.

  2. LIBS Spectral Data for a Mixed Actinide Fuel Pellet Containing Uranium, Plutonium, Neptunium and Americium

    Energy Technology Data Exchange (ETDEWEB)

    Judge, Elizabeth J. [Los Alamos National Laboratory; Berg, John M. [Los Alamos National Laboratory; Le, Loan A. [Los Alamos National Laboratory; Lopez, Leon N. [Los Alamos National Laboratory; Barefield, James E. [Los Alamos National Laboratory

    2012-06-18

    Laser-induced breakdown spectroscopy (LIBS) was used to analyze a mixed actinide fuel pellet containing 75% UO{sub 2}/20% PuO{sub 2}/3% AmO{sub 2}/2% NpO{sub 2}. The preliminary data shown here is the first report of LIBS analysis of a mixed actinide fuel pellet, to the authors knowledge. The LIBS spectral data was acquired in a plutonium facility at Los Alamos National Laboratory where the sample was contained within a glove box. The initial installation of the glove box was not intended for complete ultraviolet (UV), visible (VIS) and near infrared (NIR) transmission, therefore the LIBS spectrum is truncated in the UV and NIR regions due to the optical transmission of the window port and filters that were installed. The optical collection of the emission from the LIBS plasma will be optimized in the future. However, the preliminary LIBS data acquired is worth reporting due to the uniqueness of the sample and spectral data. The analysis of several actinides in the presence of each other is an important feature of this analysis since traditional methods must chemically separate uranium, plutonium, neptunium, and americium prior to analysis. Due to the historic nature of the sample fuel pellet analyzed, the provided sample composition of 75% UO{sub 2}/20% PuO{sub 2}/3% AmO{sub 2}/2% NpO{sub 2} cannot be confirm without further analytical processing. Uranium, plutonium, and americium emission lines were abundant and easily assigned while neptunium was more difficult to identify. There may be several reasons for this observation, other than knowing the exact sample composition of the fuel pellet. First, the atomic emission wavelength resources for neptunium are limited and such techniques as hollow cathode discharge lamp have different dynamics than the plasma used in LIBS which results in different emission spectra. Secondly, due to the complex sample of four actinide elements, which all have very dense electronic energy levels, there may be reactions and

  3. Asymmetric supercapacitors with metal-like ternary selenides and porous graphene electrodes

    KAUST Repository

    Xia, Chuan

    2016-04-14

    Asymmetric supercapacitors provide a promising approach to fabricate capacitive energy storage devices with high energy and power densities. In this work, asymmetric supercapacitors with excellent performance have been fabricated using ternary (Ni, Co)0.85Se on carbon fabric as bind-free positive electrode and porous free-standing graphene films as negative electrode. Owing to their metal-like conductivity (~1.67×106 S m−1), significant electrochemical activity, and superhydrophilic nature, our nanostructured ternary nickel cobalt selenides result in a much higher areal capacitance (2.33 F cm−2 at 4 mA cm−2), better rate performance and cycling stability than their binary selenide equivalents, and other ternary oxides and chalcogenides. Those hybrid supercapacitors can afford impressive areal capacitance and stack capacitance of 529.3 mF cm−2 and 6330 mF cm−3 at 1 mA cm−2, respectively. More impressively, our optimized asymmetric device operating at 1.8 V delivers a very high stack energy density of 2.85 mWh cm−3 at a stack power density of 10.76 mW cm−3, as well as 85% capacitance retention after 10,000 continuous charge-discharge cycles. Even at a high stack power density of 1173 mW cm−3, this device still deliveries a stack energy density of 1.19 mWh cm−3, superior to most of the reported supercapacitors.

  4. PROPERTIES AND OPTICAL APPLICATION OF POLYCRYSTALLINE ZINC SELENIDE OBTAINED BY PHYSICAL VAPOR DEPOSITION

    Directory of Open Access Journals (Sweden)

    A. A. Dunaev

    2015-05-01

    Full Text Available Findings on production technology, mechanical and optical properties of polycrystalline zinc selenide are presented. The combination of its physicochemical properties provides wide application of ZnSe in IR optics. Production technology is based on the method of physical vapor deposition on a heated substrate (Physical Vapor Deposition - PVD. The structural features and heterogeneity of elemental composition for the growth surfaces of ZnSe polycrystalline blanks were investigated using CAMEBAX X-ray micro-analyzer. Characteristic pyramid-shaped crystallites were recorded for all growth surfaces. The measurements of the ratio for major elements concentrations show their compliance with the stoichiometry of the ZnSe compounds. Birefringence, optical homogeneity, thermal conductivity, mechanical and optical properties were measured. It is established that regardless of polycrystalline condensate columnar and texturing, the optical material is photomechanically isotropic and homogeneous. The actual performance of parts made of polycrystalline optical zinc selenide in the thermal spectral ranges from 3 to 5 μm and from 8 to 14 μm and in the CO2 laser processing plants with a power density of 500 W/cm2 is shown. The developed technology gives the possibility to produce polycrystalline optical material on an industrial scale.

  5. Thermochemically evolved nanoplatelets of bismuth selenide with enhanced thermoelectric figure of merit

    Energy Technology Data Exchange (ETDEWEB)

    Ali, Zulfiqar; Cao, Chuanbao, E-mail: cbcao@bit.edu.cn; Butt, Faheem K.; Tahir, Muhammad; Tanveer, M.; Aslam, Imran; Rizwan, Muhammad; Idrees, Faryal; Khalid, Syed [Research Centre of Materials Science, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Butt, Sajid [State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2014-11-15

    We firstly present a simple thermochemical method to fabricate high-quality Bi{sub 2}Se{sub 3} nanoplatelets with enhanced figure of merit using elemental bismuth and selenium powders as precursors. The crystal structure of as synthesized products is characterized via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and high resolution transmission electron microscopy (HRTEM) measurements. Morphological and chemical synthetic parameters are investigated through a series of experiments; thickness and composition of the platelets are well controlled in large scale production. Subsequently spark plasma sintering (SPS) is performed to fabricate n-type nanostructured bulk thermoelectric materials. Raman Spectroscopy of the two selected samples with approximately of 50 and 100 nm thicknesses shows three vibrational modes. The lower thickness sample exhibits the maximum red shift of about 2.17 cm{sup -1} and maximum broadening of about 10 cm{sup -1} by in-plane vibrational mode E{sup 2}{sub g}. The enhanced value of figure of merit ∼0.41 is obtained for pure phase bismuth selenide to the best of our knowledge. We observe metallic conduction behavior while semiconducting behavior for nanostructured bismuth selenide is reported elsewhere which could be due to different synthetic techniques adopted. These results clearly suggest that our adopted synthetic technique has profound effect on the electronic and thermoelectric transport properties of this material.

  6. A method for analysis of dimethyl selenide and dimethyl diselenide by LC-ICP-DRC-MS.

    Science.gov (United States)

    Lunøe, Kristoffer; Skov, Søren; Gabel-Jensen, Charlotte; Stürup, Stefan; Gammelgaard, Bente

    2010-12-01

    The aim of this work was to develop a simple and fast high performance liquid chromatography-inductively coupled argon plasma (ICP) mass spectrometry (MS) method capable of separating and detecting the two volatile selenium species dimethyl selenide (DMeSe) and dimethyl diselenide (DMeDSe) in biological samples. Dimethyl selenide and dimethyl diselenide were separated on a short reversed phase column using an eluent containing 40% methanol and detected by dynamic reaction cell ICP-MS monitoring the (80)Se isotope. The limit of detection was 8 nM for both species (corresponding to 0.6 and 1.3 μg Se/L for DMeDSe and DMeSe, respectively). Both compounds exhibited a linear signal-concentration relationship in the investigated concentration range of 0.1-1 μM with a precision on the determinations better than 3%. The method was applied for analysis of samples from cancer cell lines incubated with methylseleninic acid, selenomethionine, Se-methylselenocysteine, and sodium selenite. DMeDSe were detected in some samples. The method offers a simple and fast analysis of DMeDSe and DMeSe using standard liquid chromatography coupled with ICP-MS equipment and interfacing.

  7. Methylselenol formed by spontaneous methylation of selenide is a superior selenium substrate to the thioredoxin and glutaredoxin systems.

    Directory of Open Access Journals (Sweden)

    Aristi P Fernandes

    Full Text Available Naturally occurring selenium compounds like selenite and selenodiglutathione are metabolized to selenide in plants and animals. This highly reactive form of selenium can undergo methylation and form monomethylated and multimethylated species. These redox active selenium metabolites are of particular biological and pharmacological interest since they are potent inducers of apoptosis in cancer cells. The mammalian thioredoxin and glutaredoxin systems efficiently reduce selenite and selenodiglutathione to selenide. The reactions are non-stoichiometric aerobically due to redox cycling of selenide with oxygen and thiols. Using LDI-MS, we identified that the addition of S-adenosylmethionine (SAM to the reactions formed methylselenol. This metabolite was a superior substrate to both the thioredoxin and glutaredoxin systems increasing the velocities of the nonstoichiometric redox cycles three-fold. In vitro cell experiments demonstrated that the presence of SAM increased the cytotoxicity of selenite and selenodiglutathione, which could neither be explained by altered selenium uptake nor impaired extra-cellular redox environment, previously shown to be highly important to selenite uptake and cytotoxicity. Our data suggest that selenide and SAM react spontaneously forming methylselenol, a highly nucleophilic and cytotoxic agent, with important physiological and pharmacological implications for the highly interesting anticancer effects of selenium.

  8. Reduction of Diaryldiselenides by System of Cp2TiCl2/ BuiMgBr/ THF and Its Application in Synthesis of Unsymmetrical Diaryl Selenides

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Reduction of diaryldiselenides by the system of Cp2TiCl2/BuiMgBr/THF gave the nucleophilic arylselenium complex. They reacted with diaryl iodonium salts to afford unsymmetrical diaryl selenides in high yields.

  9. Colloidally stable selenium@copper selenide core@shell nanoparticles as selenium source for manufacturing of copper-indium-selenide solar cells.

    Science.gov (United States)

    Dong, Hailong; Quintilla, Aina; Cemernjak, Marco; Popescu, Radian; Gerthsen, Dagmar; Ahlswede, Erik; Feldmann, Claus

    2014-02-01

    Selenium nanoparticles with diameters of 100-400nm are prepared via hydrazine-driven reduction of selenious acid. The as-prepared amorphous, red selenium (a-Se) particles were neither a stable phase nor were they colloidally stable. Due to phase transition to crystalline (trigonal), grey selenium (t-Se) at or even below room temperature, the particles merged rapidly and recrystallized as micronsized crystal needles. As a consequence, such Se particles were not suited for layer deposition and as a precursor to manufacture thin-film CIS (copper indium selenide/CuInSe2) solar cells. To overcome this restriction, Se@CuSe core@shell particles are presented here. For these Se@CuSe core@shell nanoparticles, the phase transition a-Se→t-Se is shifted to temperatures higher than 100°C. Moreover, a spherical shape of the particles is retained even after phase transition. Composition and structure of the Se@CuSe core@shell nanostructure are evidenced by electron microscopy (SEM/STEM), DLS, XRD, FT-IR and line-scan EDXS. As a conceptual study, the newly formed Se@CuSe core@shell nanostructures with CuSe acting as a protecting layer to increase the phase-transition temperature and to improve the colloidal stability were used as a selenium precursor for manufacturing of thin-film CIS solar cells and already lead to conversion efficiencies up to 3%.

  10. Neutronic Study of Burnup, Radiotoxicity, Decay Heat and Basic Safety Parameters of Mono-Recycling of Americium in French Pressurised Water Reactors

    Directory of Open Access Journals (Sweden)

    Robert Bright Mawuko Sogbadji

    2017-03-01

    Full Text Available The reprocessing of actinides with long half-life has been non-existent except for plutonium (Pu. This work looks at reducing the actinides inventory nuclear fuel waste meant for permanent disposal. The uranium oxide fuel (UOX assembly, as in the open cycle system, was designed to reach a burnup of 46GWd/T and 68GWd/T using the MURE code. The MURE code is based on the coupling of a static Monte Carlo code and the calculation of the evolution of the fuel during irradiation and cooling periods. The MURE code has been used to address two different questions concerning the mono-recycling of americium (Am in present French pressurised water reactors (PWR. These are reduction of americium in the clear fuel cycle and the safe quantity of americium that can be introduced into mixed oxide (MOX as fuel. The spent UOX was reprocessed to fabricate MOX assemblies, by the extraction of plutonium and addition of depleted uranium to reach burnups of 46GWd/T and 68GWd/T, taking into account various cooling times of the spent UOX assembly in the repository. The effect of cooling time on burnup and radiotoxicity was then ascertained. After 30 years of cooling in the repository, the spent UOX fuel required a higher concentration of Pu to be reprocessed into MOX fuel due to the decay of Pu-241. Americium, with a mean half-life of 432 years, has a high radiotoxicity level, high mid-term residual heat and is a precursor for other long-lived isotopes. An innovative strategy would be to reprocess not only the plutonium from the UOX spent fuel but also the americium isotopes, which presently dominate the radiotoxicity of waste. The mono-recycling of Am is not a definitive solution because the once-through MOX cycle transmutation of Am in a PWR is not enough to destroy all americium. The main objective is to propose a ‘waiting strategy’ for both Am and Pu in the spent fuel so that they can be made available for further transmutation strategies. The MOX and

  11. THE FIRST ISOLATION OF AMERICIUM IN THE FORM OF PURE COMPOUNDS - THE SPECIFIC ALPHA-ACTIVITY AND HALF-LIFE OF Am241

    Energy Technology Data Exchange (ETDEWEB)

    Cunningham, B.B.; Asprey, L.B.

    1950-07-20

    The microgram scale isolation and preparation of pure compounds of americium is described. Data are presented to show that the alpha-half-life of the isotope Am{sup 241} is 490 {+-} 14 years. The absorption spectrum of Am(III) in 1M nitric acid in the range 3500-8000 mu is given. The wave lengths of 10 of the most prominent lines in the copper spark emission spectrum of americium are given to the nearest 0.01 {angstrom}. Evidence is presented to show that the potential for the Am(III)-Am(IV) couple in acid solution is more negative than -2v and that the potential for the Am(II)-Am(III) couple is more positive than +0.9v.

  12. Copper Selenide Nanosnakes: Bovine Serum Albumin-Assisted Room Temperature Controllable Synthesis and Characterization

    Science.gov (United States)

    Huang, Peng; Kong, Yifei; Li, Zhiming; Gao, Feng; Cui, Daxiang

    2010-06-01

    Herein we firstly reported a simple, environment-friendly, controllable synthetic method of CuSe nanosnakes at room temperature using copper salts and sodium selenosulfate as the reactants, and bovine serum albumin (BSA) as foaming agent. As the amounts of selenide ions (Se2-) released from Na2SeSO3 in the solution increased, the cubic and snake-like CuSe nanostructures were formed gradually, the cubic nanostructures were captured by the CuSe nanosnakes, the CuSe nanosnakes grew wider and longer as the reaction time increased. Finally, the cubic CuSe nanostructures were completely replaced by BSA-CuSe nanosnakes. The prepared BSA-CuSe nanosnakes exhibited enhanced biocompatibility than the CuSe nanocrystals, which highly suggest that as-prepared BSA-CuSe nanosnakes have great potentials in applications such as biomedical engineering.

  13. Copper Selenide Nanocrystals as a High Performance, Solution Processed Thermoelectric Material

    Science.gov (United States)

    Forster, Jason; Lynch, Jared; Coates, Nelson; Sahu, Ayaskanta; Liu, Jun; Cahill, David; Urban, Jeff

    Nano-structuring a thermoelectric material often results in enhanced performance due to a decrease in the materials' thermal conductivity. Traditional nano-structuring techniques involve ball milling a bulk material followed by spark plasma sintering, a very energy intensive process. In this talk, we will describe the development of a self-assembled, high-performing, nano-structured thin film based on copper selenide nanocrystals. Mild thermal annealing of these films results in concurrent increases in the Seebeck coefficient and electrical conductivity. We are able to achieve power factors at room temperature that are as high as the best spark plasma sintered materials. These solution-processed films have potential applications as conformal, flexible materials for thermoelectric power generation.

  14. Copper Selenide Nanosnakes: Bovine Serum Albumin-Assisted Room Temperature Controllable Synthesis and Characterization

    Directory of Open Access Journals (Sweden)

    Huang Peng

    2010-01-01

    Full Text Available Abstract Herein we firstly reported a simple, environment-friendly, controllable synthetic method of CuSe nanosnakes at room temperature using copper salts and sodium selenosulfate as the reactants, and bovine serum albumin (BSA as foaming agent. As the amounts of selenide ions (Se2− released from Na2SeSO3 in the solution increased, the cubic and snake-like CuSe nanostructures were formed gradually, the cubic nanostructures were captured by the CuSe nanosnakes, the CuSe nanosnakes grew wider and longer as the reaction time increased. Finally, the cubic CuSe nanostructures were completely replaced by BSA–CuSe nanosnakes. The prepared BSA–CuSe nanosnakes exhibited enhanced biocompatibility than the CuSe nanocrystals, which highly suggest that as-prepared BSA–CuSe nanosnakes have great potentials in applications such as biomedical engineering.

  15. Counter electrodes from binary ruthenium selenide alloys for dye-sensitized solar cells

    Science.gov (United States)

    Li, Pinjiang; Cai, Hongyuan; Tang, Qunwei; He, Benlin; Lin, Lin

    2014-12-01

    Dye-sensitized solar cell (DSSC) is a promising solution to global energy and environmental problems because of its merits on clean, cost-effectiveness, relatively high efficiency, and easy fabrication. However, the reduction of fabrication cost without sacrifice of power conversion efficiencies of the DSSCs is a golden rule for their commercialization. Here we design a new binary ruthenium selenide (Ru-Se) alloy counter electrodes (CEs) by a low-temperature hydrothermal reduction method. The electrochemical behaviors are evaluated by cyclic voltammogram, electrochemical impedance, and Tafel measurements, giving an optimized Ru/Se molar ratio of 1:1. The DSSC device with RuSe alloy CE achieves a power conversion efficiency of 7.15%, which is higher than 5.79% from Pt-only CE based DSSC. The new concept, easy process along with promising results provide a new approach for reducing cost but enhancing photovoltaic performances of DSSCs.

  16. Lead Selenide Nanostructures Self-Assembled across Multiple Length Scales and Dimensions

    Directory of Open Access Journals (Sweden)

    Evan K. Wujcik

    2016-01-01

    Full Text Available A self-assembly approach to lead selenide (PbSe structures that have organized across multiple length scales and multiple dimensions has been achieved. These structures consist of angstrom-scale 0D PbSe crystals, synthesized via a hot solution process, which have stacked into 1D nanorods via aligned dipoles. These 1D nanorods have arranged into nanoscale 2D sheets via directional short-ranged attraction. The nanoscale 2D sheets then further aligned into larger 2D microscale planes. In this study, the authors have characterized the PbSe structures via normal and cryo-TEM and EDX showing that this multiscale multidimensional self-assembled alignment is not due to drying effects. These PbSe structures hold promise for applications in advanced materials—particularly electronic technologies, where alignment can aid in device performance.

  17. Searching for new thermoelectric materials: some examples among oxides, sulfides and selenides

    Science.gov (United States)

    Hébert, S.; Berthebaud, D.; Daou, R.; Bréard, Y.; Pelloquin, D.; Guilmeau, E.; Gascoin, F.; Lebedev, O.; Maignan, A.

    2016-01-01

    Different families of thermoelectric materials have been investigated since the discovery of thermoelectric effects in the mid-19th century, materials mostly belonging to the family of degenerate semi-conductors. In the last 20 years, new thermoelectric materials have been investigated following different theoretical proposals, showing that nanostructuration, electronic correlations and complex crystallographic structures (low dimensional structures, large number of atoms per lattice, presence of ‘rattlers’…) could enhance the thermoelectric properties by enhancing the Seebeck coefficient and/or reducing the thermal conductivity. In this review, the different strategies used to optimize the thermoelectric properties of oxides and chalcogenides will be presented, starting with a review on thermoelectric oxides. The thermoelectric properties of sulfides and selenides will then be discussed, focusing on layered materials and low dimensional structures (TiS2 and pseudo-hollandites). Some sulfides with promising ZT values will also be presented (tetrahedrites and chalcopyrites).

  18. Photo-induced cooperative covalent-bond switching in amorphous arsenic selenide

    Energy Technology Data Exchange (ETDEWEB)

    Shpotyuk, O [Lviv Scientific Research Institute of Materials of SRC ' Carat' , 202, Stryjska str., Lviv, UA-290031 (Ukraine); Balitska, V [Lviv Scientific Research Institute of Materials of SRC ' Carat' , 202, Stryjska str., Lviv, UA-290031 (Ukraine); Filipecki, J [Institute of Physics of Jan Dlugosz University, 13/15, Al. Armii Krajowej, Czestochowa, PL-42201 (Poland)

    2005-01-01

    A microstructural mechanism of photoinduced transformations in amorphous arsenic selenide films was studied with IR Fourier-spectroscopy technique in 300-100 cm{sup -1} region. It was shown that stage of irreversible photostructural changes was connected with cooperative process of coordination defect formation accompanied by homopolar chemical bonds switching in heteropolar ones. On the contrary, reversible photoinduced effects were caused by heteropolar chemical bonds switching in homopolar ones, as well as additional channel of bridge heteropolar bonds switching in short-layer ones. The both processes were associated with formation of anomalously coordinated defect pairs and accompanying atomic displacements at the level of medium-range ordering. The developed mathematical simulation procedure testified in a favour of defect-related origin of the reversible photo-thermallyinduced transformations, since their kinetics corresponded to known stretched-exponential dependence, tending to bimolecular behaviour rather then to single-exponential one.

  19. Radiation-induced physical ageing in network arsenic-sulfide/selenide glasses

    Energy Technology Data Exchange (ETDEWEB)

    Shpotyuk, M; Golovchak, R; Kozdras, A; Shpotyuk, O, E-mail: shpotyuk@novas.lviv.ua

    2010-11-15

    Effect of radiation-induced physical ageing is investigated by differential scanning calorimetry method in As{sub x}Se{sub 100-x} (10 {<=} x {<=} 42) and As{sub x}S{sub 100-x} (30 {<=} x {<=} 42) glasses. Obtained results are compared with conventional physical ageing at normal conditions. Significant radiation-induced physical ageing is recorded for glassy As{sub x}S{sub 100-x} within 30 {<=} x < 40 range, while As{sub x}Se{sub 100-x} glasses from the same compositional interval do not show any measurable changes in DSC curves after {gamma}-irradiation. Observed difference in radiation-induced physical ageing in arsenic-sulfide/selenide glasses is explained by a greater lifetime of {gamma}-induced excitations within sulfur-based network in comparison with selenium-based one.

  20. Growth and Low Temperature Transport Measurements of Pure and Doped Bismuth Selenide

    DEFF Research Database (Denmark)

    Mlack, Jerome Thomas

    Se3, which is a strong spin orbit material and a topological insulator. I describe a synthesis technique and low-temperature transport measurements of nanostructures of Bi2Se3, that when annealed with palladium show evidence of superconductivity. The growth method is a catalyst-free atmospheric...... pressure vapor-solid growth. The growth method yields a variety of nanostructures, and materials analysis shows ordered structures of bismuth selenide in all cases. Low-temperature measurements of as-grown nanostructures indicate tunable carrier density in all samples. By doping the nanostructures...... and that the absorption of Pd results in evidence of superconductivity, as shown by transport measurements measurements below 1K....

  1. Searching for new thermoelectric materials: some examples among oxides, sulfides and selenides.

    Science.gov (United States)

    Hébert, S; Berthebaud, D; Daou, R; Bréard, Y; Pelloquin, D; Guilmeau, E; Gascoin, F; Lebedev, O; Maignan, A

    2016-01-13

    Different families of thermoelectric materials have been investigated since the discovery of thermoelectric effects in the mid-19th century, materials mostly belonging to the family of degenerate semi-conductors. In the last 20 years, new thermoelectric materials have been investigated following different theoretical proposals, showing that nanostructuration, electronic correlations and complex crystallographic structures (low dimensional structures, large number of atoms per lattice, presence of 'rattlers'…) could enhance the thermoelectric properties by enhancing the Seebeck coefficient and/or reducing the thermal conductivity. In this review, the different strategies used to optimize the thermoelectric properties of oxides and chalcogenides will be presented, starting with a review on thermoelectric oxides. The thermoelectric properties of sulfides and selenides will then be discussed, focusing on layered materials and low dimensional structures (TiS2 and pseudo-hollandites). Some sulfides with promising ZT values will also be presented (tetrahedrites and chalcopyrites).

  2. Optoelectronic and low temperature thermoelectric studies on nanostructured thin films of silver gallium selenide

    Science.gov (United States)

    Jacob, Rajani; Philip, Rachel Reena; Nazer, Sheeba; Abraham, Anitha; Nair, Sinitha B.; Pradeep, B.; Urmila, K. S.; Okram, G. S.

    2014-01-01

    Polycrystalline thin films of silver gallium selenide were deposited on ultrasonically cleaned soda lime glass substrates by multi-source vacuum co-evaporation technique. The structural analysis done by X-ray diffraction ascertained the formation of nano structured tetragonal chalcopyrite thin films. The compound formation was confirmed by X-ray photo-electron spectroscopy. Atomic force microscopic technique has been used for surface morphological analysis. Direct allowed band gap ˜1.78eV with high absorption coefficient ˜106/m was estimated from absorbance spectra. Low temperature thermoelectric effects has been investigated in the temperature range 80-330K which manifested an unusual increase in Seebeck coefficient with negligible phonon drag toward the very low and room temperature regime. The electrical resistivity of these n-type films was assessed to be ˜2.6Ωm and the films showed good photo response.

  3. Heterogeneous nanocomposites of silver selenide and hollow platinum nanoparticles toward methanol oxidation reaction

    Science.gov (United States)

    Cui, Penglei; He, Hongyan; Liu, Hui; Zhang, Suojiang; Yang, Jun

    2016-09-01

    Making use of the electronic coupling between different domains in composite nanomaterials is an effective way to enhance the activity of electrocatalysts. Herein, we demonstrate the preparation of nanocomposites consisting of silver selenide (Ag2Se) and platinum (Pt) nanoparticles with a hollow interior by combining the inside-out diffusion of Ag in core-shell Ag-Pt nanoparticles with the synthesis of highly active hydrophobic Se species. In specific, the Ag2Se-hPt nanocomposites are found to have superior activity and stability for methanol oxidation reaction in an acidic condition due to the strong electronic coupling effect between semiconductor and metal domains. This strategy may provide a greener and less expensive way to the large-scale synthesis of Pt-based nanocomposites, and might be used to generate other heterogeneous nanomaterials with technological importance.

  4. Novel chemical synthetic route and characterization of zinc selenide thin films

    Science.gov (United States)

    Hankare, P. P.; Chate, P. A.; Delekar, S. D.; Asabe, M. R.; Mulla, I. S.

    2006-11-01

    Zinc selenide (ZnSe) thin film have been deposited using chemical bath method on non-conducting glass substrate in a tartarate bath containing zinc sulfate, ammonia, hydrazine hydrate, sodium selenosulfate in an aqueous alkaline medium at 333 K. The deposition parameter of the ZnSe thin film is interpreted in the present investigation. The films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), optical absorption, electrical measurements, atomic absorption spectroscopy (AAS). The ZnSe thin layers grown with polycrystalline zinc blende system along with some amorphous phase present in ZnSe film. The direct optical band gap ‘Eg’ for the film was found to be 2.81 eV and electrical conductivity in the order of 10-8(Ω cm)-1 with n-type conduction mechanism.

  5. Pulsed laser ablation of zinc selenide in nitrogen ambience: Formation of zinc nitride films

    Science.gov (United States)

    Simi, S.; Navas, I.; Vinodkumar, R.; Chalana, S. R.; Gangrade, Mohan; Ganesan, V.; Pillai, V. P. Mahadevan

    2011-09-01

    Zinc nitride (Zn 3N 2) thin films are prepared using pulsed laser deposition (PLD) from zinc selenide (ZnSe) target at different nitrogen ambient pressures viz. 1, 3, 5, 7 and 10 Pa. The films prepared with nitrogen pressures 1 and 3 Pa are amorphous in nature, whereas the films prepared at 5, 7 and 10 Pa exhibit the presence of cubic bixbyite Zn 3N 2 structure with lattice parameter very close to bulk of Zn 3N 2. The particle size calculated by Debye Scherrer's formula is in the nano regime. Surface morphology of the films is studied by SEM and AFM analysis. Optical parameters such as band gap, refractive index and porosity of the films are calculated. Moreover, the present study confers an outlook about how do various factors such as substrate temperature, reactive supplementing gas and laser-target interaction influence the film developing process during pulsed lased deposition.

  6. Effect of capping agents on optical and antibacterial properties of cadmium selenide quantum dots

    Indian Academy of Sciences (India)

    Deepika; Rakesh Dhar; Suman Singh; Atul Kumar

    2015-09-01

    Cadmium selenide quantum dots (CdSe QDs) were synthesized in aqueous phase by the freezing temperature injection technique using different capping agents (viz. thioglycolic acid, 1-thioglycerol, L-cysteine). Absorption spectra of CdSe QDs exhibited a blue shift as compared to its bulk counterpart, which is an indication of quantum confinement effect. The photoluminescence spectra of CdSe QDs confirmed that the particles are poly-dispersed and possess enhanced luminescent property, depending upon the chemical nature of capping agents. The QDs have been characterized by Fourier-transform infrared spectroscopy, atomic absorption spectroscopy and transmission electron microscopy. Further, antimicrobial activity of as-prepared QDs has also been investigated using the disk diffusion method.

  7. A Rapid and Cost-Effective Laser Based Synthesis of High Purity Cadmium Selenide Quantum Dots.

    Science.gov (United States)

    Gondall, M A; Qahtan, Talal F; Dastageer, M A; Yamani, Z H; Anjum, D H

    2016-01-01

    A rapid and cost effective method is developed to synthesize high purity cadmium Selenide (CdSe) quantum dots in acetone medium using second harmonic of Nd:YAG nanosecond pulsed laser of 532 nm wavelength. The thermal agglomeration due the nanosecond pulse duration of the laser was successfully eliminated by using unfocussed laser beam and thereby providing a favorable conditions for the synthesis of quantum dots having the grain size of 3 nm. The morphological and optical characterizations like XRD, HRTEM, optical absorption of the synthesized CdSe quantum dots, reveal that the material possesses the similar characteristics of the one synthesized through cumbersome wet chemical methods. Relative to the CdSe bulk material, the synthesized CdSe quantum dots showed a blue shift in the measured band gap energy from near infrared spectral region to visible region, making this material very attractive for many solar energy harvesting applications like photo-catalysis and solar cells.

  8. The role of isomorphous substitutions in natural selenides belonging to the pyrite group

    Energy Technology Data Exchange (ETDEWEB)

    Bindi, Luca [Museo di Storia Naturale, sez. di Mineralogia e Litologia, Universita degli Studi di Firenze, via La Pira 4, I-50121 Firenze (Italy)], E-mail: luca.bindi@unifi.it; Cipriani, Curzio [Museo di Storia Naturale, sez. di Mineralogia e Litologia, Universita degli Studi di Firenze, via La Pira 4, I-50121 Firenze (Italy); Pratesi, Giovanni [Museo di Storia Naturale, sez. di Mineralogia e Litologia, Universita degli Studi di Firenze, via La Pira 4, I-50121 Firenze (Italy); Dipartimento di Scienze della Terra, Universita degli Studi di Firenze, via La Pira 4, I-50121 Firenze (Italy); Trosti-Ferroni, Renza [Dipartimento di Scienze della Terra, Universita degli Studi di Firenze, via La Pira 4, I-50121 Firenze (Italy)

    2008-07-14

    The present paper reports chemical and structural data of selenide minerals belonging to the pyrite group. Eighteen samples of minerals in this group with variable chemical composition (7 samples of penroseite, NiSe{sub 2}; 10 samples of krutaite, CuSe{sub 2}; 1 sample of trogtalite, CoSe{sub 2}) were studied by means of X-ray single-crystal diffraction and electron microprobe. On the basis of information gained from the chemical characterization, we can conclude that a complete solid solution between NiSe{sub 2} and CuSe{sub 2} exists in nature with the absence of pure end-members. Although verified only for the Ni-rich members, we also infer a solid solution between NiSe{sub 2} and CoSe{sub 2}. The unit-cell parameters were modeled using a multiple regression method as a function of the Co, Ni, and Cu contents.

  9. Optical and morphological characteristics of zinc selenide-zinc sulfide solid solution crystals

    Science.gov (United States)

    Singh, N. B.; Su, Ching-Hua; Arnold, Bradley; Choa, Fow-Sen

    2016-10-01

    Experiments were performed to study the effect of point defects on the optical and morphological characteristics of zinc selenide-zinc sulfide ZnSe-ZnS (ZnSexS(1-x)) solid solution crystals grown under terrestrial (1-g) condition. We used the composition ZnSe0.91S0.09 and ZnSe0.73S0.27 for the detailed studies. Crystals of 8 mm and 12 mm diameter were grown using physical vapor transport methods. These crystals did not exhibit gross defects such as voids, bubbles or precipitates. The photoluminescence spectra indicated strong red emission for the 610-630-nm wavelength region in both crystals. This emission could be explained on the basis of high energy irradiation of Zn selenide. For the ZnSe0.73S0.27 crystal, absorption starts at a lower wavelength range (300 nm) when compared to the ZnSe0.91S0.09 crystal presumably due to the much higher bandgap of ZnS than that of ZnSe. Sharp peaks at 451 and 455 nm were observed for both samples corresponding to the band edge transitions, followed by a strong peak at 632 nm. These results were consistent with the observations based on Raman spectroscopy studies. Under 532-nm laser illumination both transverse optical (TO) and longitudinal optical (LO) phonon peaks appeared at Raman shifts of 220 and 280 Δcm-1, respectively. These peaks are similar to those observed for pure ZnSe Raman spectra for which TO and LO occur at 200 and 250 Δcm-1 for the x-axis (first order) polarization.

  10. Hydrothermal synthesis of copper selenides with controllable phases and morphologies from an ionic liquid precursor

    Science.gov (United States)

    Liu, Xiaodi; Duan, Xiaochuan; Peng, Peng; Zheng, Wenjun

    2011-12-01

    Cu2-xSe nanocrystals and CuSe nanoflakes are successfully synthesized through a convenient hydrothermal method from an ionic liquid precursor 1-n-butyl-3-ethylimidazolium methylselenite ([BMIm][SeO2(OCH3)]). The phases and morphologies of the copper selenides can be controlled by simply changing the atom ratio of Cu/Se in the reactants and reaction temperature. Furthermore, it is found that the [BMIm][SeO2(OCH3)] not only serves as Se source but also has influence on the shapes of CuSe nanoflakes. The adsorption of alkyl imidazolium rings ([BMIm]+) onto the (0001) facets of covellite CuSe prohibits the growth in the [0001] direction, and CuSe nuclei growth mainly processes along the six symmetric directions (+/-[01&cmb.macr;11], +/-[101&cmb.macr;1&cmb.macr;], and +/-[1&cmb.macr;100]) to form flakelike CuSe. The obtained copper selenides are characterized by XRD, SEM, EDS, XPS, TEM, and HRTEM. The results indicate that the Cu2-xSe nanocrystals are nearly spherical particles with an average diameter of about 20 nm, the hexagonal CuSe nanoflakes are single crystals with an edge length of 100-400 nm and a thickness of 25-50 nm. The potential formation mechanism of the copper selenides is also proposed.Cu2-xSe nanocrystals and CuSe nanoflakes are successfully synthesized through a convenient hydrothermal method from an ionic liquid precursor 1-n-butyl-3-ethylimidazolium methylselenite ([BMIm][SeO2(OCH3)]). The phases and morphologies of the copper selenides can be controlled by simply changing the atom ratio of Cu/Se in the reactants and reaction temperature. Furthermore, it is found that the [BMIm][SeO2(OCH3)] not only serves as Se source but also has influence on the shapes of CuSe nanoflakes. The adsorption of alkyl imidazolium rings ([BMIm]+) onto the (0001) facets of covellite CuSe prohibits the growth in the [0001] direction, and CuSe nuclei growth mainly processes along the six symmetric directions (+/-[01&cmb.macr;11], +/-[101&cmb.macr;1&cmb.macr;], and +/-[1

  11. Tin selenide synthesized by a chemical route: the effect of the annealing conditions in the obtained phase

    Science.gov (United States)

    Bernardes-Silva, Ana Cláudia; Mesquita, A. F.; de Moura Neto, E.; Porto, A. O.; de Lima, G. M.; Ardisson, J. D.; Lameiras, F. S.

    2005-09-01

    The effects of different annealing conditions over the tin selenide obtained from a chemical route are presented in this work. The tin selenide was annealed at 300 and 600 °C under hydrogen, nitrogen and argon atmospheres. The materials were characterized by X-ray diffraction and 119Sn Mössbauer spectroscopy. In the 'as synthetized' material a considerably amount of tin oxide (57%) was detected by Mössbauer spectroscopy. After thermal annealing the amount of these oxides varied according to the temperature and atmosphere used. At 600 °C/hydrogen the smallest amount of tin oxide was obtained (20%). These oxides were formed during the synthetic procedure through the hydrolysis of tin chloride used as reagent.

  12. CONTROL OF LASER RADIATION PARAMETERS: Passive laser Q switches made of glass doped with oxidised nanoparticles of copper selenide

    Science.gov (United States)

    Yumashev, K. V.

    2000-01-01

    Passive Q switching of Nd3+:YAG (λ = 1060 nm) and YAlO3:Nd3+ (1340 nm) lasers, as well as of an Er3+ (1540 nm) glass laser was realised by using glass doped with oxidised nanoparticles of copper selenide. Nonlinear optical properties of the nanoparticles (radius of 25 nm) in a glass matrix were studied by the picosecond absorption spectroscopy technique.

  13. Reduced Species(HSO-2,SO·-2)Promoted One-Pot Efficient Synthesis of Phenyl Alkyl Selenides

    Institute of Scientific and Technical Information of China (English)

    TANG,Ri-Yuan; ZHONG,Ping; LIN,Qiu-Lian

    2007-01-01

    Reduced species(HSO-2,SO·-2)promoted one-pot synthesis of phenyl alkyl selenides has been developed.This synthetic method was achieved by reactions of diphenyl diselenide with alkyl halides at room temperature.It is noteworthy that the reactions were operated under mild reaction conditions,required short time,and got good resuits.A single electron transfer reaction mechanism was proposed for the reaction.

  14. Radioisotope space power generator. Annual report, July 1, 1975--September 30, 1976. [TPM-217 P-type selenides

    Energy Technology Data Exchange (ETDEWEB)

    Elsner, N.B.; Chin, J.; Staley, H.G.; Steeger, E.J.; Gantzel, P.K.

    1977-09-01

    TPM-217 P-type selenide usefulness in thermoelectric converters depends on its dimensional, electrical and thermal stability at high temperature and its compatibility with other converter component materials in a low pressure environment. Experimental efforts have been directed at determining: the vaporization behavior at 900/sup 0/C, the partial pressures of vaporizing species versus temperature, vapor suppression coatings, thermal expansion, dimensional stability, and the high temperature compatibility of TPM-217 with proposed end cap materials.

  15. Fluorescence imaging technology (FI) for high-throughput screening of selenide-modified nano-TiO2 catalysts.

    Science.gov (United States)

    Wang, Liping; Lee, Jianchao; Zhang, Meijuan; Duan, Qiannan; Zhang, Jiarui; Qi, Hailang

    2016-02-18

    A high-throughput screening (HTS) method based on fluorescence imaging (FI) was implemented to evaluate the catalytic performance of selenide-modified nano-TiO2. Chemical ink-jet printing (IJP) technology was reformed to fabricate a catalyst library comprising 1405 (Ni(a)Cu(b)Cd(c)Ce(d)In(e)Y(f))Se(x)/TiO2 (M6Se/Ti) composite photocatalysts. Nineteen M6Se/Tis were screened out from the 1405 candidates efficiently.

  16. Near-IR absorption saturation and mechanism of picosecond recovery dynamics of copper selenide nanostructured via alumina

    Science.gov (United States)

    Statkutė, G.; Mikulskas, I.; Tomašiùnas, R.; Jagminas, A.

    2009-06-01

    Absorption saturation at 1.064 μm wavelength in Cu2-xSe material nanostructured by means of an original method—formation and hosting in an array of electrochemically grown alumina voids—was investigated. Columnlike channels provide growth of copper selenide in a shape of nanowire with a fixed diameter. Experimental results obtained from measuring nanowires of various diameters (∅10, 15, 20, and 70 nm) revealed that the ∅20 nm case is most efficient for absorption saturation, manifesting highest optical modulation depth and lowest interlevel transition rate evaluated. A model to analyze the conditions for absorption saturation and absorption recovery dynamics was developed. Depending on pump intensity the nonmonotonous increase in recovery time for the highest applied values was interpreted as filling up of states at an intermediate energy level. From modeling, important material science parameters, such as concentration of resonant and trapping/recombination states, interlevel transition rate, capture time, characteristic for copper selenide, have been evaluated and compared for different samples. Finally, the consequence of the model to a working copper selenide energy level scheme was considered.

  17. The Short Series of the Oxygen-Poor Lanthanide Oxide Selenides M10OSe14 with M = La–Nd

    Directory of Open Access Journals (Sweden)

    Frank A. Weber

    2012-08-01

    Full Text Available Single crystals and phase pure samples of oxygen-poor ternary lanthanide oxide selenides with the composition M10OSe14 (M = La–Nd; tetragonal, I41/acd; a = 1592.0–1559.8 pm, c = 2106.5–2062.9 pm could be obtained by reacting the corresponding metals, selenium and selenium dioxide as oxygen source. Their crystal structures are isotypic with Pr10OS14 and thus contain isolated [OM4]10+ tetrahedra (d(O2––M3+ = 243–248 pm embedded in a complex anionic {[M6Se14]10–} lanthanide selenide matrix (d(M3+–Se2– = 288–358 pm. All three crystallographically independent M3+ cations exhibit eight contacts to chalcogenide anions (O2– and/or Se2– resulting in the formation of bicapped trigonal prismatic coordination polyhedra. The optical band gaps of the oxide selenides M10OSe14 amount to values between 1.89 and 2.04 eV indicating wide band-gap semiconductors.

  18. Intramolecular sensitization of americium luminescence in solution: shining light on short-lived forbidden 5f transitions.

    Science.gov (United States)

    Sturzbecher-Hoehne, M; Yang, P; D'Aléo, A; Abergel, R J

    2016-06-14

    The photophysical properties and solution thermodynamics of water soluble trivalent americium (Am(III)) complexes formed with multidentate chromophore-bearing ligands, 3,4,3-LI(1,2-HOPO), Enterobactin, and 5-LIO(Me-3,2-HOPO), were investigated. The three chelators were shown to act as antenna chromophores for Am(III), generating sensitized luminescence emission from the metal upon complexation, with very short lifetimes ranging from 33 to 42 ns and low luminescence quantum yields (10(-3) to 10(-2)%), characteristic of Near Infra-Red emitters in similar systems. The specific emission peak of Am(III) assigned to the (5)D1 → (7)F1 f-f transition was exploited to characterize the high proton-independent stability of the complex formed with the most efficient sensitizer 3,4,3-LI(1,2-HOPO), with a log β110 = 20.4 ± 0.2 value. In addition, the optical and solution thermodynamic features of these Am(III) complexes, combined with density functional theory calculations, were used to probe the influence of electronic structure on coordination properties across the f-element series and to gain insight into ligand field effects.

  19. Response of avalanche photo-diodes of the CMS Electromagnetic Calorimeter to neutrons from an Americium-Beryllium source.

    CERN Document Server

    Deiters, Konrad; Renker, Dieter

    2010-01-01

    The response of avalanche photo-diodes (APDs) used in the CMS Electromagnetic Calorimeter to low energy neutrons from an Americium-Beryllium source is reported. Signals due to recoil protons from neutron interactions with the hydrogen nuclei in the protective epoxy layer, mainly close to the silicon surface of the APD, have been identified. These signals increase in size with the applied bias voltage more slowly than the nominal gain of the APDs, and appear to have a substantially lower effective gain at the operating voltage. The signals originating from interactions in the epoxy are mostly equivalent to signals of a few GeV in CMS, but range up to a few tens of GeV equivalent. There are also signals not attributed to reactions in the epoxy extending up to the end of the range of these measurements, a few hundreds of GeV equivalent. Signals from the x-rays from the source can also be in the GeV equivalent scale in CMS. Simulations used to describe events due to particle interactions in the APDs need to take ...

  20. Nano-cerium vanadate: a novel inorganic ion exchanger for removal of americium and uranium from simulated aqueous nuclear waste.

    Science.gov (United States)

    Banerjee, Chayan; Dudwadkar, Nilesh; Tripathi, Subhash Chandra; Gandhi, Pritam Maniklal; Grover, Vinita; Kaushik, Chetan Prakash; Tyagi, Avesh Kumar

    2014-09-15

    Cerium vanadate nanopowders were synthesized by a facile low temperature co-precipitation method. The product was characterized by X-ray diffraction and transmission electron microscopy and found to consist of ∼25 nm spherical nanoparticles. The efficiency of these nanopowders for uptake of alpha-emitting radionuclides (233)U (4.82 MeV α) and (241)Am (5.49 MeV α, 60 keV γ) has been investigated. Thermodynamically and kinetically favorable uptake of these radionuclides resulted in their complete removal within 3h from aqueous acidic feed solutions. The uptake capacity was observed to increase with increase in pH as the zeta potential value decreased with the increase in pH but effect of ionic strength was insignificant. Little influence of the ions like Sr(2+), Ru(3+), Fe(3+), etc., in the uptake process indicated CeVO4 nanopowders to be amenable for practical applications. The isotherms indicated predominant uptake of the radioactive metal ions in the solid phase of the exchanger at lower feed concentrations and linear Kielland plots with positive slopes indicated favorable exchange of the metal ions with the nanopowder. Performance comparison with the other sorbents reported indicated excellent potential of nano-cerium vanadate for removing americium and uranium from large volumes of aqueous acidic solutions.

  1. Determination by gamma-ray spectrometry of the plutonium and americium content of the Pu/Am separation scraps. Application to molten salts; Determination par spectrometrie gamma de la teneur en plutonium et en americium de produits issus de separation Pu/Am. Application aux bains de sels

    Energy Technology Data Exchange (ETDEWEB)

    Godot, A. [CEA Valduc, Dept. de Traitement des Materiaux Nucleaires, 21 - Is-sur-Tille (France); Perot, B. [CEA Cadarache, Dept. de Technologie Nucleaire, Service de Modelisation des Transferts et Mesures Nucleaires, 13 - Saint-Paul-lez-Durance (France)

    2005-07-01

    Within the framework of plutonium recycling operations in CEA Valduc (France), americium is extracted from molten plutonium metal into a molten salt during an electrolysis process. The scraps (spent salt, cathode, and crucible) contain extracted americium and a part of plutonium. Nuclear material management requires a very accurate determination of the plutonium content. Gamma-ray spectroscopy is performed on Molten Salt Extraction (MSE) scraps located inside the glove box, in order to assess the plutonium and americium contents. The measurement accuracy is influenced by the device geometry, nuclear instrumentation, screens located between the sample and the detector, counting statistics and matrix attenuation, self-absorption within the spent salt being very important. The purpose of this study is to validate the 'infinite energy extrapolation' method employed to correct for self-attenuation, and to detect any potential bias. We present a numerical study performed with the MCNP computer code to identify the most influential parameters and some suggestions to improve the measurement accuracy. A final uncertainty of approximately 40% is achieved on the plutonium mass. (authors)

  2. Transfer across the human gut of environmental plutonium, americium, cobalt, caesium and technetium: studies with cockles (Cerastoderma edule) from the Irish Sea.

    Science.gov (United States)

    Hunt, G J

    1998-06-01

    Our previous studies have indicated lower values of the gut transfer factor ('f1 values') for plutonium and americium in winkles (Littorina littorea) than adopted by ICRP. The present study was undertaken primarily to investigate whether this observation extends to other species. Samples of cockles (Carastoderma edule) from Ravenglass, Cumbria were eaten by volunteers who provided 24 h samples of urine and faeces. Urine samples indicated f1 values for cockles which were higher than for winkles; for plutonium these ranged overall up to 7 x 10(-4) with an arithmetic mean in the range (2-3) x 10(-4), and for americium up to 2.6 x 10(-4) with an arithmetic mean of 1.2 x 10(-4). Limited data based on volunteers eating cockles from the Solway suggest that f1 values for americium may be greater at distance from Sellafield. The measured values compare with 5 x 10(-4) used by the ICRP for environmental forms of both elements, which would appear to provide adequate protection when calculating doses from Cumbrian cockles. Data for other nuclides were obtained by analysing faecal samples from the volunteers who ate the Ravenglass cockles. Cobalt-60 showed an f1 value in the region of 0.2, twice the value currently used by ICRP. For 137Cs, variabilities were indicated in the range 0.08 to 0.43, within the ICRP value of f1 = 1.0. Technetium-99 gave f1 values up to about 0.6, in reasonable conformity with the ICRP value of 0.5.

  3. Transfer across the human gut of environmental plutonium, americium, cobalt, caesium and technetium: studies with cockles (Cerastoderma edule) from the Irish Sea

    Energy Technology Data Exchange (ETDEWEB)

    Hunt, G.J. [CEFAS Laboratory, Lowestoft, Suffolk NR33 0HT (United Kingdom)

    1998-06-01

    Our previous studies have indicated lower values of the gut transfer factor ('f{sub L} values') for plutonium and americium in winkles (Littorina littorea) than adopted by ICRP. The present study was undertaken primarily to investigate whether this observation extends to other species. Samples of cockles (Cerastoderma edule) from Ravenglass, Cumbria were eaten by volunteers who provided 24 samples of urine and faeces. Urine samples indicated f{sub L} values for cockles which were higher than for winkles; for plutonium these ranged overall up to 7x10{sup -4} with an arithmetic mean in the range (2-3)x10{sup -4}, and for americium up to 2.6x10{sup -4} with an arithmetic mean of 1.2x10{sup -4}. Limited data based on volunteers eating cockles from the Solway suggest that f{sub L} values for americium may be greater at distance from Sellafield. The measured values compare with 5x10{sup -4} used by the ICRP for environmental forms of both elements, which would appear to provide adequate protection when calculating doses from Cumbrian cockles. Data for other nuclides were obtained by analysing faecal samples from the volunteers who ate the Ravenglass cockles. Cobalt-60 showed an f{sub L} value in the region of 0.2, twice the value currently used by ICRP. For {sup 137}Cs, variabilities were indicated in the range 0.08 to 0.43, within the ICRP value of f{sub L}=1.0. Technetium-99 gave f{sub L} values up to about 0.6, in reasonable conformity with the ICRP value of 0.5. (author)

  4. Effects of residual copper selenide on CuInGaSe 2 solar cells

    Science.gov (United States)

    Hsieh, Tung-Po; Chuang, Chia-Chih; Wu, Chung-Shin; Chang, Jen-Chuan; Guo, Jhe-Wei; Chen, Wei-Chien

    2011-02-01

    Large-grain, copper-poor CuInGaSe2 (CIGS) films are favored in the fabrication of highly efficient solar cells. However, the degradation of cell performance caused by residual copper selenide (Cu2-xSe) remains a problem. This work studies the formation and behavior of excess CuxSe and further compares the cell performance of typical copper-poor with that of copper-rich solar cells. Since excess Cu2-xSe cannot be exhausted during the growth, it fully surrounds the polycrystalline CIGS grains. Excess Cu2-xSe in the CIGS film produces serious shunt paths and causes the pn junction to be of poor quality. A short circuit in copper-rich CIGS solar cells is attributable to the conductive Cu2-xSe. The best way to ensure high-efficiency of the cells is to exhaust Cu2-xSe during growth. Otherwise, a dense, chemically treated CIGS film is required to prevent the negative effects of excess Cu2-xSe.

  5. Electrochemical synthesis and optical characterization of copper selenide nanowire arrays within the alumina pores

    Science.gov (United States)

    Jagminas, A.; Juškėnas, R.; Gailiūtė, I.; Statkutė, G.; Tomašiūnas, R.

    2006-09-01

    By choosing an appropriate aqueous solution containing CuSO 4, H 2SeO 3, MgSO 4, and H 2SO 4 the suitable composition for two- or one-phase copper selenide deposition within the alumina pores under alternating current (AC) electrolysis conditions was created. X-ray diffraction spectra recorded within 15-55° 2 Θ range revealed fabrication of Cu 3Se 2+Cu 2-xSe or almost pure Cu 2-xSe crystalline material. The compositional and morphological studies using XRD, EDX, SEM, and TEM techniques show fabrication of nearly pure Cu 2-xSe with some deficiency of copper, say, Cu 1.75Se, nanowires in length up to several microns when the selenious acid to copper-ion ratio is close to 1:2 and pH of the bath is <1.25. The fundamental absorption spectrum for this nanostructured material was shown to be formed by allowed direct and indirect interband transitions with the evaluated energy band gaps 2.3 and 1.1 eV, respectively.

  6. A transparent nickel selenide counter electrode for high efficient dye-sensitized solar cells

    Science.gov (United States)

    Dong, Jia; Wu, Jihuai; Jia, Jinbiao; Ge, Jinhua; Bao, Quanlin; Wang, Chaotao; Fan, Leqing

    2017-04-01

    Nickel selenide (Ni0.85Se) was synthesized by a facile one-step hydrothermal reaction and Ni0.85Se film was prepared by spin-coating Ni0.85Se ink on FTO and used as counter electrode (CE) in dye-sensitized solar cells (DSSC). The Ni0.85Se CEs not only show high transmittance in visible range, but also possess remarkable electrocatalytic activity toward I-/I3-. The electrocatalytic ability of Ni0.85Se films was verified by cyclic voltammetry, electrochemical impedance spectroscopy and Tafel polarization curves. The DSSC using Ni0.85Se CE exhibits a power conversion efficiency (PCE) of 8.96%, while the DSSC consisting of sputtered Pt CE only exhibits a PCE of 8.15%. When adding a mirror under Ni0.85Se CE, the resultant DSSC exhibits a PCE of 10.76%, which exceeds that of a DSSC based on sputtered Pt CE (8.44%) by 27.49%.

  7. Effect of aluminum and tellurium tetrachloride addition on the loss of arsenic selenide optical fiber

    Science.gov (United States)

    Nguyen, Vinh Q.; Drake, Gryphon; Villalobos, Guillermo; Gibson, Daniel; Bayya, Shyam; Kim, Woohong; Baker, Colin; Chin, Geoff; Kung, Frederic H.; Kotov, Mikhail I.; Busse, Lynda; Sanghera, Jasbinder S.

    2017-02-01

    Arsenic selenide glass optical fibers typically possess extrinsic absorption bands in the infrared wavelength regions associated with residual hydrogen and oxygen related impurities, despite using 6N purified elemental precursors. Consequently, special additives and refined processing steps are utilized in an attempt to reduce these and other impurities. We investigate the formation of particulate impurities during a purification process based on the addition of 0.1 wt% elemental aluminum (Al) and 0.2 wt% tellurium tetrachloride (TeCl4) during glass synthesis. It was found that during purification and melting steps, Al reacts with TeCl4 to form AlCl3, which in turn reacts with oxygen and hydrogen impurities and the fused quartz (SiO2) ampoule to produce HCl and stable submicron Al2SiO5 compounds in the As-Se glass and fibers. The intensity of the H-Se absorption band centered at 4.57 μm has been significantly reduced from 18 dB/m to 0.8 dB/m. Using thermodynamic data, we have identified stable Al2SiO5 submicron inclusions in the glass and fibers. A two-step gettering process is proposed as a solution to eliminating these inclusions.

  8. Liquid-like cationic sub-lattice in copper selenide clusters

    Science.gov (United States)

    White, Sarah L.; Banerjee, Progna; Jain, Prashant K.

    2017-02-01

    Super-ionic solids, which exhibit ion mobilities as high as those in liquids or molten salts, have been employed as solid-state electrolytes in batteries, improved thermoelectrics and fast-ion conductors in super-capacitors and fuel cells. Fast-ion transport in many of these solids is supported by a disordered, `liquid-like' sub-lattice of cations mobile within a rigid anionic sub-lattice, often achieved at high temperatures or pressures via a phase transition. Here we show that ultrasmall clusters of copper selenide exhibit a disordered cationic sub-lattice under ambient conditions unlike larger nanocrystals, where Cu+ ions and vacancies form an ordered super-structure similar to the bulk solid. The clusters exhibit an unusual cationic sub-lattice arrangement wherein octahedral sites, which serve as bridges for cation migration, are stabilized by compressive strain. The room-temperature liquid-like nature of the Cu+ sub-lattice combined with the actively tunable plasmonic properties of the Cu2Se clusters make them suitable as fast electro-optic switches.

  9. Ultrafast charge- and energy-transfer dynamics in conjugated polymer: cadmium selenide nanocrystal blends.

    Science.gov (United States)

    Morgenstern, Frederik S F; Rao, Akshay; Böhm, Marcus L; Kist, René J P; Vaynzof, Yana; Greenham, Neil C

    2014-02-25

    Hybrid nanocrystal-polymer systems are promising candidates for photovoltaic applications, but the processes controlling charge generation are poorly understood. Here, we disentangle the energy- and charge-transfer processes occurring in a model system based on blends of cadmium selenide nanocrystals (CdSe-NC) with poly[2-methoxy-5-(3',7'-dimethyloctyloxy)-1,4-phenylene vinylene] (MDMO-PPV) using a combination of time-resolved absorption and luminescence measurements. The use of different capping ligands (n-butylamine, oleic acid) as well as thermal annealing allows tuning of the polymer-nanocrystal interaction. We demonstrate that energy transfer from MDMO-PPV to CdSe-NCs is the dominant exciton quenching mechanism in nonannealed blends and occurs on ultrafast time scales (<1 ps). Upon thermal annealing electron transfer becomes competitive with energy transfer, with a transfer rate of 800 fs independent of the choice of the ligand. Interestingly, we find hole transfer to be much less efficient than electron transfer and to extend over several nanoseconds. Our results emphasize the importance of tuning the organic-nanocrystal interaction to achieve efficient charge separation and highlight the unfavorable hole-transfer dynamics in these blends.

  10. Synthesis and optoelectrical properties of f-graphene/cadmium selenide hybrid system

    Science.gov (United States)

    Babkair, Saeed Salem; Azam, Ameer; Singh, Kuldeep; Dhawan, Sundeep Kumar; Khan, Mohd Taukeer

    2015-01-01

    The present work demonstrates the synthesis of a hybrid accepter material containing amino-functionalized graphene oxide (GO) and an inorganic semiconducting material, cadmium selenide (CdSe). First, amino-functionalized graphene was synthesized and then nanocrystals (NCs) of CdSe were in situ grown in the functionalized-(GO) matrix named f-GCdSe. Structural studies such as x-ray diffraction, and a scanning electron microscopic were employed to investigate the growth of CdSe NCs in the graphene matrix. To understand the charge generation and transfer process at the donor/acceptor interface, the absorption, photoluminescence (PL), and transient absorption spectroscopic (TAS) studies have been carried out in poly(3-hexylthiophene) (P3HT)/f-GCdSe thin films. PL quenching in P3HT/f-GCdSe thin film suggests that charge transfer takes place at the donor/acceptor interface. TAS shows higher optical density and long lived free carriers for P3HT/f-GCdSe thin film. These results suggest that f-GCdSe is an excellent electron-acceptor material for organic photovoltaic devices.

  11. DFT Study on the Carrier Concentration and Temperature-Dependent Thermoelectric Properties of Antimony Selenide

    Directory of Open Access Journals (Sweden)

    Aditya Jayaraman

    2016-01-01

    Full Text Available We present the thermoelectric properties of Antimony Selenide (Sb2Se3 obtained using first principles calculations. We investigated the electronic band structure using the FP-LAPW method within the sphere of the density functional theory. Thermoelectric properties were calculated using BoltzTrap code using the constant relaxation time (τ approximation at three different temperatures 300 K, 600 K, and 800 K. Seebeck coefficient (S was found to decrease with increasing temperature, electrical conductivity (σ/τ was almost constant in the entire temperature range, and electronic thermal conductivity (κ/τ increased with increasing temperature. With increase in temperature S decreased from 1870 μV/K (at 300 K to 719 μV/K (at 800 K, electronic thermal conductivity increased from 1.56 × 1015 W/m K s (at 300 K to 3.92 × 1015 W/m K s (at 800 K, and electrical conductivity decreased from 22 × 1019/Ω m s (at 300 K to 20 × 1019/Ω m s (at 800 K. The thermoelectric properties were also calculated for different hole concentrations and the optimum concentration for a good thermoelectric performance over a large range of temperatures (from 300 K to 1000 K was found for hole concentration around 1019 cm−3.

  12. Femtosecond Transient Absorption Studies in Cadmium Selenide Nanocrystal Thin Films Prepared by Chemical Bath Deposition Method

    Directory of Open Access Journals (Sweden)

    M. C. Rath

    2007-01-01

    Full Text Available Dynamics of photo-excited carrier relaxation processes in cadmium selenide nanocrystal thin films prepared by chemical bath deposition method have been studied by nondegenerate femtosecond transient pump-probe spectroscopy. The carriers were generated by exciting at 400 nm laser light and monitored by several other wavelengths. The induced absorption followed by a fast bleach recovery observed near and above the bandgap indicates that the photo-excited carriers (electrons are first trapped by the available traps and then the trapped electrons absorb the probe light to show a delayed absorption process. The transient decay kinetics was found to be multiexponential in nature. The short time constant, <1 picosecond, was attributed to the trapping of electrons by the surface and/or deep traps and the long time constant, ≥20 picoseconds, was due to the recombination of the trapped carriers. A very little difference in the relaxation processes was observed in the samples prepared at bath temperatures from 25∘C to 60∘C.

  13. Study of Linear and Non-Linear Optical Parameters of Zinc Selenide Thin Film

    Directory of Open Access Journals (Sweden)

    H. N. Desai

    2015-06-01

    Full Text Available Thin film of Zinc Selenide (ZnSe was deposited onto transparent glass substrate by thermal evaporation technique. ZnSe thin film was characterized by UV-Visible spectrophotometer within the wavelength range of 310 nm-1080 nm. The Linear optical parameters (linear optical absorption, extinction coefficient, refractive index and complex dielectric constant of ZnSe thin film were analyzed from absorption spectra. The optical band gap and Urbach energy were obtained by Tauc’s equation. The volume and surface energy loss function of ZnSe thin film were obtained by complex dielectric constant. The Dispersion parameters (dispersion energy, oscillation energy, moment of optical dispersion spectra, static dielectric constant and static refractive index were calculated using theoretical Wemple-DiDomenico model. The oscillation strength, oscillator wavelength, high frequency dielectric constant and high frequency refractive index were calculated by single Sellmeier oscillator model. Also, Lattice dielectric constant, N/m* and plasma resonance frequency were obtained. The electronic polarizibility of ZnSe thin film was estimated by Clausius-Mossotti local field polarizibility. The nonlinear optical parameters (non-linear susceptibility and non-linear refractive index were estimated.

  14. Band gap engineering of zinc selenide thin films through alloying with cadmium telluride.

    Science.gov (United States)

    Al-Kuhaili, M F; Kayani, A; Durrani, S M A; Bakhtiari, I A; Haider, M B

    2013-06-12

    This work investigates band gap engineering of zinc selenide (ZnSe) thin films. This was achieved by mixing ZnSe with cadmium telluride (CdTe). The mass ratio (x) of CdTe in the starting material was varied in the range x = 0-0.333. The films were prepared using thermal evaporation. The chemical composition of the films was investigated through energy dispersive spectroscopy and Rutherford backscattering spectrometry. Structural analysis was carried out using X-ray diffraction and atomic force microscopy. Normal incidence transmittance and reflectance were measured over the wavelength range 300-1300 nm. The absorption coefficients and band gaps were determined from these spectrophotometric measurements. The band gap monotonically decreased from 2.58 eV (for x = 0) to 1.75 eV (for x = 0.333). Photocurrent measurements indicated that the maximum current density was obtained for films with x = 0.286. A figure of merit, based on crystallinity, band gap, and photocurrent, was defined. The optimum characteristics were obtained for the films with x = 0.231, for which the band gap was 2.14 eV.

  15. Influence of different deposition potential on the structural and optical properties of copper selenide nanowires

    Science.gov (United States)

    Kaur, Harmanmeet; Kaur, Jaskiran; Singh, Lakhwant

    2016-09-01

    In this paper, nanowires were successfully fabricated from the aqueous solution containing 0.2 M/l CuSO4.5H2O, 0.1 M/l SeO2, 1 g/l PVP and a few drops of H2SO4 in Milli-Q water using electrodeposition technique at room temperature. Influence of different deposition potential on structural and optical properties of copper selenide nanowires has been investigated here. Morphological, structural and optical properties were monitored through field emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD) and UV-visible 1800 spectrophotometer. From the XRD analysis, it was found that the stoichiometric (CuSe) nanowires are formed at deposition potential (-0.6 V) and (+0.6 V). Band gap of nanowires were found to be maximum around 3.13 eV for deposition potential (-0.8 V) and minimum of 2.81 eV for deposition potential (-0.6 V).

  16. Highly efficient copper-zinc-tin-selenide (CZTSe) solar cells by electrodeposition.

    Science.gov (United States)

    Jeon, Jong-Ok; Lee, Kee Doo; Seul Oh, Lee; Seo, Se-Won; Lee, Doh-Kwon; Kim, Honggon; Jeong, Jeung-hyun; Ko, Min Jae; Kim, BongSoo; Son, Hae Jung; Kim, Jin Young

    2014-04-01

    Highly efficient copper-zinc-tin-selenide (Cu2ZnSnSe4 ; CZTSe) thin-film solar cells are prepared via the electrodepostion technique. A metallic alloy precursor (CZT) film with a Cu-poor, Zn-rich composition is directly deposited from a single aqueous bath under a constant current, and the precursor film is converted to CZTSe by annealing under a Se atmosphere at temperatures ranging from 400 °C to 600 °C. The crystallization of CZTSe starts at 400 °C and is completed at 500 °C, while crystal growth continues at higher temperatures. Owing to compromises between enhanced crystallinity and poor physical properties, CZTSe thin films annealed at 550 °C exhibit the best and most-stable device performances, reaching up to 8.0 % active efficiency; among the highest efficiencies for CZTSe thin-film solar cells prepared by electrodeposition. Further analysis of the electronic properties and a comparison with another state-of-the-art device prepared from a hydrazine-based solution, suggests that the conversion efficiency can be further improved by optimizing parameters such as film thickness, antireflection coating, MoSe2 formation, and p-n junction properties.

  17. Photoluminescence properties of cadmium-selenide quantum dots embedded in a liquid-crystal polymer matrix

    Energy Technology Data Exchange (ETDEWEB)

    Tselikov, G. I., E-mail: gleb@vega.phys.msu.ru; Timoshenko, V. Yu. [Moscow State University, Faculty of Physics (Russian Federation); Plenge, J.; Ruehl, E. [Free University of Berlin, Institute of Chemistry and Biochemistry (Germany); Shatalova, A. M.; Shandryuk, G. A.; Merekalov, A. S.; Tal' roze, R. V. [Russian Academy of Sciences, Topchiev Institute of Petrochemical Synthesis (Russian Federation)

    2013-05-15

    The photoluminescence properties of cadmium-selenide (CdSe) quantum dots with an average size of {approx}3 nm, embedded in a liquid-crystal polymer matrix are studied. It was found that an increase in the quantum-dot concentration results in modification of the intrinsic (exciton) photoluminescence spectrum in the range 500-600 nm and a nonmonotonic change in its intensity. Time-resolved measurements show the biexponential decay of the photoluminescence intensity with various ratios of fast and slow components depending on the quantum-dot concentration. In this case, the characteristic lifetimes of exciton photoluminescence are 5-10 and 35-50 ns for the fast and slow components, respectively, which is much shorter than the times for colloidal CdSe quantum dots of the same size. The observed features of the photoluminescence spectra and kinetics are explained by the effects of light reabsorption, energy transfer from quantum dots to the liquid-crystal polymer matrix, and the effect of the electronic states at the CdSe/(liquid crystal) interface.

  18. Layered bismuth selenide utilized as hole transporting layer for highly stable organic photovoltaics

    KAUST Repository

    Yuan, Zhongcheng

    2015-11-01

    Abstract Layered bismuth selenide (L-Bi2Se3) nanoplates were implemented as hole transporting layers (HTLs) for inverted organic solar cells. Device based on L-Bi2Se3 showed increasing power conversion efficiency (PCE) during ambient condition storage process. A PCE of 4.37% was finally obtained after 5 days storage, which outperformed the ones with evaporated-MoO3 using poly(3-hexylthiophene) (P3HT) as donor material and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) as acceptor. The improved device efficiency can be attributed to the high conductivity and increasing work function of L-Bi2Se3. The work function of L-Bi2Se3 increased with the storage time in ambient condition due to the oxygen atom doping. Ultraviolet photoelectron spectroscopy and high resolution X-ray photoelectron spectroscopy were conducted to verify the increased work function, which originated from the p-type doping process. The device based on L-Bi2Se3 exhibited excellent stability in ambient condition up to 4 months, which was much improved compared to the device based on traditional HTLs. © 2015 Elsevier B.V.

  19. New route for preparation of luminescent mercaptoethanoate capped cadmium selenide quantum dots

    Indian Academy of Sciences (India)

    Manoj E Wankhede; Shaukatali N Inamdar; Aparna Deshpande; Aniket R Thete; Renu Pasricha; Sulabha K Kulkarni; Santosh K Haram

    2008-06-01

    We report a synthesis of cadmium selenide quantum dots (Q-CdSe) by refluxing a mixture of cadmium acetate, selenium powder, sodium sulfite and 2-mercaptoethanol in N,N′-dimethyl formamide (DMF)/water solution. X-ray and electron diffractions suggest the formation of hexagonal phase of size quantized CdSe. Based on TEM analysis, the formation of nanoparticles with an average diameter of 3.5 ± 0.5 nm is inferred. Their sols in DMF and dimethyl sulphoxide (DMSO) gave characteristic absorption peaks at 300 nm and 327 nm, which is attributed to the formation of high quality, size quantized CdSe particles. Extracted particles from the sol were readily redispersed in DMF and DMSO, which were diluted further with water without losing their optical and colloidal properties. FTIR spectroscopy suggested the formation of 2-mercaptoethanol thiolate on the particle surface, with free –OH groups available for linkage. Sols in DMSO and their solutions in water displayed an intense photoluminescence (PL).

  20. Synthesis of Co-Electrospun Lead Selenide Nanostructures within Anatase Titania Nanotubes for Advanced Photovoltaics

    Directory of Open Access Journals (Sweden)

    Evan K. Wujcik

    2015-06-01

    Full Text Available Inorganic nano-scale heterostructures have many advantages over hybrid organic-inorganic dye-sensitized solar cells (DSSC or Grätzel cells, including their resistance to photo-bleaching, thermal stability, large specific surface areas, and general robustness. This study presents a first-of-its-kind low-cost all-inorganic lead selenide-anatase titania (PbSe/TiO2 nanotube heterostructure material for photovoltaic applications. Herein, PbSe nanostructures have been co-electrospun within a hollow TiO2 nanotube with high connectivity for highly efficient charge carrier flow and electron-hole pair separation. This material has been characterized by transmission electron microscopy (TEM, electron diffraction, energy dispersive X-ray spectroscopy (EDX to show the morphology and material composition of the synthesized nanocomposite. Photovoltaic characterization has shown this newly synthesized proof-of-concept material can easily produce a photocurrent under solar illumination, and, with further refinement, could reveal a new direction in photovoltaic materials.

  1. Photoluminescence properties of lead selenide produced by selenization and a solvothermal method

    Science.gov (United States)

    Kim, Jungdong; Ahn, Hak-Young; Kim, Seung Gi; Oh, Eunsoon; Ju, Byeong-Kwon; Choi, Won Jun; Cho, So-Hye

    2017-01-01

    We studied temperature-dependent photoluminescence (PL) spectra of lead selenide (PbSe) dendrites and cubes grown by a solvothermal method. Their PL peaks were located at ˜8 μm at 10 K with a full width at half maximum (FWHM) of 10 meV. Using the temperature-dependent FWHM values, we obtained carrier-phonon coupling coefficients for PbSe. We also demonstrated mechanochemical synthesis of polycrystalline PbS nanoparticles and their successful conversion into a PbSe layer composed of nanocrystals by a selenization process with thermal treatment. The nanocrystals were found to be formed by the orientation alignment of small grains in the process. The PL peak energies of the PbSe layers as well as the PbSe dendrites and the cubes agreed well with their absorption edges in the transmission spectra, indicating that the photoluminescence originates from the band-edge emission. The band-edge emissions hold promise for the development of potential mid-infrared light sources using PbSe fabricated by these methods.

  2. Nano-cerium vanadate: A novel inorganic ion exchanger for removal of americium and uranium from simulated aqueous nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Banerjee, Chayan; Dudwadkar, Nilesh [Fuel Reprocessing Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Tripathi, Subhash Chandra, E-mail: sctri001@gmail.com [Fuel Reprocessing Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Gandhi, Pritam Maniklal [Fuel Reprocessing Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Grover, Vinita [Waste Management Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Kaushik, Chetan Prakash [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Tyagi, Avesh Kumar, E-mail: aktyagi@barc.gov.in [Waste Management Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

    2014-09-15

    Highlights: • Template free, low temperature synthesis of CeVO{sub 4} nanopowders. • Thermodynamically and kinetically favourable uptake of Am(III) and U(VI) exhibited. • K{sub d} and ΔG° values for Am(III) and U(VI) uptake in pH 1–6 are reported. • Interdiffusion coefficients and zeta potential values in pH 1–6 are reported. • Possible application in low level aqueous nuclear waste remediation. - Abstract: Cerium vanadate nanopowders were synthesized by a facile low temperature co-precipitation method. The product was characterized by X-ray diffraction and transmission electron microscopy and found to consist of ∼25 nm spherical nanoparticles. The efficiency of these nanopowders for uptake of alpha-emitting radionuclides {sup 233}U (4.82 MeV α) and {sup 241}Am (5.49 MeV α, 60 keV γ) has been investigated. Thermodynamically and kinetically favorable uptake of these radionuclides resulted in their complete removal within 3 h from aqueous acidic feed solutions. The uptake capacity was observed to increase with increase in pH as the zeta potential value decreased with the increase in pH but effect of ionic strength was insignificant. Little influence of the ions like Sr{sup 2+}, Ru{sup 3+}, Fe{sup 3+}, etc., in the uptake process indicated CeVO{sub 4} nanopowders to be amenable for practical applications. The isotherms indicated predominant uptake of the radioactive metal ions in the solid phase of the exchanger at lower feed concentrations and linear Kielland plots with positive slopes indicated favorable exchange of the metal ions with the nanopowder. Performance comparison with the other sorbents reported indicated excellent potential of nano-cerium vanadate for removing americium and uranium from large volumes of aqueous acidic solutions.

  3. Plutonium, americium and radiocaesium in the marine environment close to the Vandellos I nuclear power plant before decommissioning

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez-Cabeza, J.A. E-mail: joanalbert.sanchez@uab.es; Molero, J

    2000-11-01

    The Vandellos nuclear power plant (NPP), releasing low-level radioactive liquid waste to the Mediterranean Sea, is the first to be decommissioned in Spain, after an incident which occurred in 1989. The presence, distribution and uptake of various artificial radionuclides (radiocaesium, plutonium and americium) in the environment close to the plant were studied in seawater, bottom sediments and biota, including Posidonia oceanica, fish, crustaceans and molluscs. Seawater, sediments and Posidonia oceanica showed enhanced levels in the close vicinity of the NPP, although the effect was restricted to its near environment. Maximum concentrations in seawater were 11.6{+-}0.5 Bq m{sup -3} and 16.9{+-}1.2 mBq m{sup -3} for {sup 137}Cs and {sup 239,240}Pu, respectively. When sediment concentrations were normalized to excess {sup 210}Pb, they showed both the short-distance transport of artificial radionuclides from the Vandellos plant and the long-distance transport of {sup 137}Cs from the Asco NPP. Posidonia oceanica showed the presence of various gamma-emitters attributed to the impact of the Chernobyl accident, on which the effect of the NPP was superimposed. Seawater, sediment and Posidonia oceanica collected near the plant also showed an enhancement of the plutonium isotopic ratio above the fallout value. The uptake of these radionuclides by marine organisms was detectable but limited. Pelagic fish showed relatively higher {sup 137}Cs concentrations and only in the case of demersal fish was the plutonium isotopic ratio increased. The reported levels constitute a set of baseline values against which the impact of the decommissioning operations of the Vandellos I NPP can be studied.

  4. DFT studies on structural properties and electron density topologies of the iron selenides Fe m Se n (1 ≤ m, n ≤ 4)

    Science.gov (United States)

    Zhang, Jian; Liu, Jianhong

    2016-12-01

    We report the structural properties and electron density topologies of the iron selenides Fe m Se n (1 ≤ m, n ≤ 4) using DFT method. Structural studies reveal the Se atom leads to significant change in the geometries of the iron selenides. We confirm that the bond length between Fe atoms increase owing to the sequential addition of Se atom. Comparable stabilities were investigated based on the variation of averaged binding energies and selenium doping energy. The covalent property of the Fe-Se bond is increased as the coincident bond critical points (BCPs) showed smaller positive nabla _{{ρ _{BCP}}}^2 values than those of original FeSe molecule. Our results demonstrate that the ρFe-Fe values keep in the order of 0.048-0.220 a.u. Almost all of the nabla _{{ρ _{BCP}}}^2 values are positive and consequently mean the closed-shell interactions are conserved in the iron selenides.

  5. Development of high-efficiency solar cells on copper indium selenide single crystals (cadmium sulfide, zinc oxide)

    Energy Technology Data Exchange (ETDEWEB)

    Yip, Lap Sum

    1996-12-31

    Photovoltaic cells with a ZnO/CdS/CuInSe{sub 2} structure were fabricated on bulk CuInSe{sub 2} substrates. Conversion efficiencies of more than or near 10 per cent were obtained on cells with an active area and without the use of antireflection coating. Copper indium selenide single crystals can be used as absorbers in thin film solar cells. In this study, the single crystals were grown by a horizontal Bridgman method. An annealing of the CuInSe{sub 2} substrate before the CdS deposition was found to be essential in obtaining high photovoltaic performance.

  6. NaBH{sub 4}/[bmim]BF{sub 4}: a new reducing system to access vinyl selenides and tellurides

    Energy Technology Data Exchange (ETDEWEB)

    Lenardao, Eder J.; Goncalves, Loren C.C.; Mendes, Samuel R.; Saraiva, Maiara T.; Alves, Diego; Jacob, Raquel G.; Perin, Gelson, E-mail: lenardao@ufpel.edu.b [Universidade Federal de Pelotas (UFPel), RS (Brazil). Inst. de Quimica e Geociencias. Lab. de Sintese Organica Limpa (LASOL)

    2010-07-01

    A general and simple method for the synthesis of vinyl selenides and tellurides starting from terminal alkynes and diorganyl chalcogenides using NaBH{sub 4} and [bmim]BF{sub 4} as a recyclable solvent was developed. This efficient and improved method furnishes the corresponding vinyl chalcogenides preferentially with Z configuration. We also observed that when the same protocol was applied to phenyl acetylene, (E)-bis-phenylchalcogeno styrenes were obtained in good yields and high selectivity. The ionic liquid was reused up three times without lost of efficiency. (author)

  7. The influence of ligand type on self-organization and optical properties of cadmium selenide quantum dots

    Science.gov (United States)

    Ushakova, E. V.; Kormilina, T. K.; Burkova, M. A.; Cherevkov, S. A.; Zakharov, V. V.; Turkov, V. K.; Fedorov, A. V.; Baranov, A. V.

    2017-01-01

    A method for successive replacement of organic shells of colloidal cadmium selenide quantum dots (QDs) of different sizes is proposed. It is found that the spectral parameters of QD samples depend on the type of organic shells. It is shown that the structural morphology is independent of the QD size and is determined by the chemical composition of the organic shell. Spectral analysis of the luminescence of QD-based superstructures shows that the luminescence wavelength and intensity strongly depend on the degree of QD surface passivation.

  8. Parallel molecular dynamics simulations of pressure-induced structural transformations in cadmium selenide nanocrystals

    Science.gov (United States)

    Lee, Nicholas Jabari Ouma

    Parallel molecular dynamics (MD) simulations are performed to investigate pressure-induced solid-to-solid structural phase transformations in cadmium selenide (CdSe) nanorods. The effects of the size and shape of nanorods on different aspects of structural phase transformations are studied. Simulations are based on interatomic potentials validated extensively by experiments. Simulations range from 105 to 106 atoms. These simulations are enabled by highly scalable algorithms executed on massively parallel Beowulf computing architectures. Pressure-induced structural transformations are studied using a hydrostatic pressure medium simulated by atoms interacting via Lennard-Jones potential. Four single-crystal CdSe nanorods, each 44A in diameter but varying in length, in the range between 44A and 600A, are studied independently in two sets of simulations. The first simulation is the downstroke simulation, where each rod is embedded in the pressure medium and subjected to increasing pressure during which it undergoes a forward transformation from a 4-fold coordinated wurtzite (WZ) crystal structure to a 6-fold coordinated rocksalt (RS) crystal structure. In the second so-called upstroke simulation, the pressure on the rods is decreased and a reverse transformation from 6-fold RS to a 4-fold coordinated phase is observed. The transformation pressure in the forward transformation depends on the nanorod size, with longer rods transforming at lower pressures close to the bulk transformation pressure. Spatially-resolved structural analyses, including pair-distributions, atomic-coordinations and bond-angle distributions, indicate nucleation begins at the surface of nanorods and spreads inward. The transformation results in a single RS domain, in agreement with experiments. The microscopic mechanism for transformation is observed to be the same as for bulk CdSe. A nanorod size dependency is also found in reverse structural transformations, with longer nanorods transforming more

  9. Transparent nickel selenide used as counter electrode in high efficient dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Jia, Jinbiao; Wu, Jihuai, E-mail: jhwu@hqu.edu.cn; Tu, Yongguang; Huo, Jinghao; Zheng, Min; Lin, Jianming

    2015-08-15

    Highlights: • A transparent Ni{sub 0.85}Se is prepared by a facile solvothermal reaction. • Ni{sub 0.85}Se electrode has better electrocatalytic activity than Pt electrode. • DSSC with Ni{sub 0.85}Se electrode obtains efficiency of 8.88%, higher than DSSC with Pt. • DSSC with Ni{sub 0.85}Se/mirror electrode achieves an efficiency of 10.19%. - Abstract: A transparent nickel selenide (Ni{sub 0.85}Se) is prepared by a facile solvothermal reaction and used as an efficient Pt-free counter electrode (CE) for dye-sensitized solar cells (DSSCs). Field emission scanning electron microscopy observes that the as-prepared Ni{sub 0.85}Se possesses porous structure. Cyclic voltammogram measurement indicates that Ni{sub 0.85}Se electrode has larger current density than Pt electrode. Electrochemical impedance spectroscopy shows that the Ni{sub 0.85}Se electrode has lower charge-transfer resistance than Pt electrode. Under simulated solar light irradiation with intensity of 100 mW cm{sup −2} (AM 1.5), the DSSC based on the Ni{sub 0.85}Se CE achieves a power conversion efficiency (PCE) of 8.88%, which is higher than the solar cell based on Pt CE (8.13%). Based on the transparency of Ni{sub 0.85}Se, the DSSC with Ni{sub 0.85}Se/mirror achieves a PCE of 10.19%.

  10. Analysis on the Performance of Copper Indium Gallium Selenide (CIGS Based Photovoltaic Thermal

    Directory of Open Access Journals (Sweden)

    Zulkepli Afzam

    2016-01-01

    Full Text Available This paper deals with the efficiency improvement of Copper Indium Gallium Selenide (CIGS Photovoltaic (PV and also solar thermal collector. Photovoltaic thermal (PV/T can improve overall efficiency for PV and also solve the problem of limited roof space at urban area. Objective of this study is to clarify the effect of mass flow rate on the efficiency of the PV/T system. A CIGS solar cell is used with rated output power 65 W and 1.18 m2 of area. 4 set of experiments were carried out, which were: thermal collector with 0.12 kg/s flow rate, PV/T with 0.12 kg/s flow rate, PV/T with 0.09 kg/s flow rate and PV. It was found that PV/T with 0.12 kg/s flow rate had the highest electrical efficiency, 2.92 %. PV/T with 0.09 kg/s flow rate had the lowest electrical efficiency, 2.68 %. It also had 2 % higher overall efficiency. The efficiency gained is low due to several factors. The rated output power of the PV is low for the area of 1.18 m2. The packing factor of the PV also need to be considered as it may not be operated at the optimal packing factor. Furthermore, aluminium sheet of the PV may affect the PV temperature due to high thermal conductivity. Further study on more values of mass flow rate and also other parameters that affect the efficiency of the PV/T is necessary.

  11. Exploring the doping effects of copper on thermoelectric properties of lead selenide

    Science.gov (United States)

    Gayner, Chhatrasal; Sharma, Raghunandan; Mallik, Iram; Das, Malay K.; Kar, Kamal K.

    2016-07-01

    In this work, we have explored the effect of dopant concentration (copper (Cu)) on the thermoelectric performance of Cu doped lead selenide (Pb1-x Cu x Se (0  ⩽  x  ⩽  0.1)). With increasing the dopant concentration, sign inversion of majority charge carriers takes place for x  ⩾  0.04 due to the donor behaviour of Cu in the P-type pristine PbSe. The room temperature Seebeck coefficients of Pb1-x Cu x Se with x  =  0.01, 0.02, 0.04, 0.06 and 0.08 are observed to be 233, 337, -473.7, -392.5 and  -257.6 μV K-1, respectively as compared to that of 186.4 μV K-1 of the pristine PbSe. This increment in Seebeck coefficient is the result of low carrier concentration and is not related to the resonance states created by Cu dopant. At room temperature, the lattice thermal conductivity of pristine PbSe is 0.52 W m-1 K-1 while for Cu doped PbSe, it varies from 0.8 to 1.1 W m-1 K-1. Finally, with ZT of ~0.59 and power factor of ~700 at 500 K, Pb0.98Cu0.02Se exhibits the highest thermoelectric performance among the studied Pb1-x Cu x Se systems. Owing to the high ZT and power factor, a single thermoelement of Pb0.98Cu0.02Se exhibits thermovoltage of  >100 mV at a temperature gradient of 200 °C.

  12. Phase diagram of (Li(1-x)Fe(x))OHFeSe: a bridge between iron selenide and arsenide superconductors.

    Science.gov (United States)

    Dong, Xiaoli; Zhou, Huaxue; Yang, Huaixin; Yuan, Jie; Jin, Kui; Zhou, Fang; Yuan, Dongna; Wei, Linlin; Li, Jianqi; Wang, Xinqiang; Zhang, Guangming; Zhao, Zhongxian

    2015-01-14

    Previous experimental results have shown important differences between iron selenide and arsenide superconductors which seem to suggest that the high-temperature superconductivity in these two subgroups of iron-based families may arise from different electronic ground states. Here we report the complete phase diagram of a newly synthesized superconducting (SC) system, (Li1-xFex)OHFeSe, with a structure similar to that of FeAs-based superconductors. In the non-SC samples, an antiferromagnetic (AFM) spin-density-wave (SDW) transition occurs at ∼127 K. This is the first example to demonstrate such an SDW phase in an FeSe-based superconductor system. Transmission electron microscopy shows that a well-known √5×√5 iron vacancy ordered state, resulting in an AFM order at ∼500 K in AyFe2-xSe2 (A = metal ions) superconductor systems, is absent in both non-SC and SC samples, but a unique superstructure with a modulation wave vector q = (1)/2(1,1,0), identical to that seen in the SC phase of KyFe2-xSe2, is dominant in the optimal SC sample (with an SC transition temperature Tc = 40 K). Hence, we conclude that the high-Tc superconductivity in (Li1-xFex)OHFeSe stems from the similarly weak AFM fluctuations as FeAs-based superconductors, suggesting a universal physical picture for both iron selenide and arsenide superconductors.

  13. [{Cp2(tBuSe)Nb}2E] (E = O and Se) with bridging oxide or selenide ligands.

    Science.gov (United States)

    Hector, Andrew L; Jura, Marek; Levason, William; Reid, Gillian; Reid, Stuart D; Webster, Michael

    2008-10-01

    The title compounds, mu-oxido-bis[(tert-butylselenolato)bis(eta(5)-cyclopentadienyl)niobium(IV)] toluene solvate, [Nb(2)(C(5)H(5))(4)(C(4)H(9)Se)(2)O] x C(7)H(8), and mu-selenido-bis[(tert-butylselenolato)bis(eta(5)-cyclopentadienyl)niobium(IV)], [Nb(2)(C(5)H(5))(4)(C(4)H(9)Se)(2)Se], consist of niobium(IV) centres each bonded to two eta(5)-coordinated cyclopentadienyl groups and one tert-butylselenolate ligand and are the first organometallic niobium selenolates to be structurally characterized. A bridging oxide or selenide completes the niobium coordination spheres of the discrete dinuclear molecules. In the oxide, the O atom lies on an inversion centre, resulting in a linear Nb-O-Nb linkage, whereas the selenide has a bent bridging group [Nb-Se-Nb = 139.76 (2) degrees]. The difference is attributable to strong pi bonding in the oxide case, although the effects on the Nb-C and Nb-Se(t)Bu bond lengths are small.

  14. Methods of making copper selenium precursor compositions with a targeted copper selenide content and precursor compositions and thin films resulting therefrom

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, Calvin J. (Lakewood, CO); Miedaner, Alexander (Boulder, CO); van Hest, Marinus Franciscus Antonius Maria (Lakewood, CO); Ginley, David S. (Evergreen, CO); Leisch, Jennifer (Denver, CO); Taylor, Matthew (West Simsbury, CT); Stanbery, Billy J. (Austin, TX)

    2011-09-20

    Precursor compositions containing copper and selenium suitable for deposition on a substrate to form thin films suitable for semi-conductor applications. Methods of forming the precursor compositions using primary amine solvents and methods of forming the thin films wherein the selection of temperature and duration of heating controls the formation of a targeted species of copper selenide.

  15. Soft chemical control of superconductivity in lithium iron selenide hydroxides Li(1-x)Fe(x)(OH)Fe(1-y)Se.

    Science.gov (United States)

    Sun, Hualei; Woodruff, Daniel N; Cassidy, Simon J; Allcroft, Genevieve M; Sedlmaier, Stefan J; Thompson, Amber L; Bingham, Paul A; Forder, Susan D; Cartenet, Simon; Mary, Nicolas; Ramos, Silvia; Foronda, Francesca R; Williams, Benjamin H; Li, Xiaodong; Blundell, Stephen J; Clarke, Simon J

    2015-02-16

    Hydrothermal synthesis is described of layered lithium iron selenide hydroxides Li(1-x)Fe(x)(OH)Fe(1-y)Se (x ∼ 0.2; 0.02 iron site vacancy concentrations in the iron selenide layers. This iron vacancy concentration is revealed as the only significant compositional variable and as the key parameter controlling the crystal structure and the electronic properties. Single crystal X-ray diffraction, neutron powder diffraction, and X-ray absorption spectroscopy measurements are used to demonstrate that superconductivity at temperatures as high as 40 K is observed in the hydrothermally synthesized samples when the iron vacancy concentration is low (y iron oxidation state is reduced slightly below +2, while samples with a higher vacancy concentration and a correspondingly higher iron oxidation state are not superconducting. The importance of combining a low iron oxidation state with a low vacancy concentration in the iron selenide layers is emphasized by the demonstration that reductive postsynthetic lithiation of the samples turns on superconductivity with critical temperatures exceeding 40 K by displacing iron atoms from the Li(1-x)Fe(x)(OH) reservoir layer to fill vacancies in the selenide layer.

  16. A study on the optics of copper indium gallium (di)selenide (CIGS) solar cells with ultra-thin absorber layers

    NARCIS (Netherlands)

    Xu, M.; Wachters, A.J.H.; Van Deelen, J.; Mourad, M.C.D.; Buskens, P.J.P.

    2014-01-01

    We present a systematic study of the effect of variation of the zinc oxide (ZnO) and copper indium gallium (di)selenide (CIGS) layer thickness on the absorption characteristics of CIGS solar cells using a simulation program based on finite element method (FEM). We show that the absorption in the CIG

  17. The structures of CyMe4-BTBP complexes of americium(iii) and europium(iii) in solvents used in solvent extraction, explaining their separation properties.

    Science.gov (United States)

    Ekberg, Christian; Löfström-Engdahl, Elin; Aneheim, Emma; Foreman, Mark R StJ; Geist, Andreas; Lundberg, Daniel; Denecke, Melissa; Persson, Ingmar

    2015-11-14

    Separation of trivalent actinoid (An(iii)) and lanthanoid (Ln(iii)) ions is extremely challenging due to their similar ionic radii and chemical properties. Poly-aromatic nitrogen compounds acting as tetradentate chelating ligands to the metal ions in the extraction, have the ability to sufficiently separate An(iii) from Ln(iii). One of these compounds, 6,6'-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-benzol[1,2,4]triazin-3-yl)[2,2]bipyridine, CyMe4-BTBP, has proven to be resistant towards acidic environments and strong radiation from radioactive decomposition. EXAFS studies of the dicomplexes of CyMe4-BTBP with americium(iii) and europium(iii) in nitrobenzene, cyclohexanone, 1-hexanol, 1-octanol and malonamide (DMDOHEMA) in 1-octanol have been carried out to get a deeper understanding of the parameters responsible for the separation. The predominating complexes independent of solvent used are [Am(CyMe4-BTBP)2(NO3)](2+) and [Eu(CyMe4-BTBP)2](3+), respectively, which are present as outer-sphere ion-pairs with nitrate ions in the studied solvents with low relative permittivity. The presence of a nitrate ion in the first coordination sphere of the americium(iii) complex compensates the charge density of the complex considerably in comparison when only outer-sphere ion-pairs are formed as for the [Eu(CyMe4-BTBP)2](3+) complex. The stability and solubility of a complex in a solvent with low relative permittivity increase with decreasing charge density. The [Am(CyMe4-BTBP)2(NO3)](2+) complex will therefore be increasingly soluble and stabilized over the [Eu(CyMe4-BTBP)2](3+) complex in solvents with decreasing relative permittivity of the solvent. The separation of americium(iii) from europium(iii) with CyMe4-BTBP as extraction agent will increase with decreasing relative permittivity of the solvent, and thereby also with decreasing solubility of CyMe4-BTBP. The choice of solvent is therefore a balance of a high separation factor and sufficient solubility of the CyMe4-BTBP

  18. Cytocompatibility of direct water synthesized cadmium selenide quantum dots in colo-205 cells

    Science.gov (United States)

    Rodriguez-Torres, Marcos R.; Velez, Christian; Zayas, Beatriz; Rivera, Osvaldo; Arslan, Zikri; Gonzalez-Vega, Maxine N.; Diaz-Diestra, Daysi; Beltran-Huarac, Juan; Morell, Gerardo; Primera-Pedrozo, Oliva M.

    2015-06-01

    Cadmium selenide quantum dots (CdSe QDs), inorganic semiconducting nanocrystals, are alluring increased attraction due to their highly refined chemistry, availability, and super tunable optical properties suitable for many applications in different research areas, such as photovoltaics, light-emitting devices, environmental sciences, and nanomedicine. Specifically, they are being widely used in bio-imaging in contrast to organic dyes due to their high brightness and improved photo-stability, and their ability to tune their absorption and emission spectra upon changing the crystal size. The production of CdSe QDs is mostly assisted by trioctylphosphine oxide compound, which acts as solvent or solubilizing agent and renders the QDs soluble in organic compounds (such as toluene, chloroform, and hexane) that are highly toxic. To circumvent the toxicity-related factor in CdSe QDs, we report the synthesis of CdSe QDs capped with thioglycolic acid (TGA) in an aqueous medium, and their biocompatibility in colo-205 cancer cells. In this study, the [Cd2+]/[TGA] ratio was adjusted to 11:1 and the Se concentration (10 and 15 mM) was monitored in order to evaluate its influence on the optical properties and cytocompatibility. QDs resulted to be quite stable in water (after purification) and RPMI cell medium and no precipitation was observed for long contact times, making them appealing for in vitro experiments. The spectroscopy analysis, advanced electron microscopy, and X-ray diffractometry studies indicate that the final products were successfully formed exhibiting an improved optical response. Colo-205 cells being exposed to different concentrations of TGA-capped CdSe QDs for 12, 24, and 48 h with doses ranging from 0.5 to 2.0 mM show high tolerance reaching cell viabilities as high as 93 %. No evidence of cellular apoptotic pathways was observed as pointed out by our Annexin V assays at higher concentrations. Moreover, confocal microscopy analysis conducted to evaluate the

  19. Cytocompatibility of direct water synthesized cadmium selenide quantum dots in colo-205 cells

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez-Torres, Marcos R. [Universidad Metropolitana, Nanomaterials Science Laboratory, School of Science and Technology (United States); Velez, Christian; Zayas, Beatriz [Universidad Metropolitana, ChemTox Laboratory, School of Environmental Affairs (United States); Rivera, Osvaldo [Universidad Metropolitana, Nanomaterials Science Laboratory, School of Science and Technology (United States); Arslan, Zikri [Jackson State University, Department of Chemistry (United States); Gonzalez-Vega, Maxine N. [Universidad Metropolitana, Nanomaterials Science Laboratory, School of Science and Technology (United States); Diaz-Diestra, Daysi; Beltran-Huarac, Juan; Morell, Gerardo [University of Puerto Rico, Molecular Science Research Center (United States); Primera-Pedrozo, Oliva M., E-mail: oprimera1@suagm.edu [Universidad Metropolitana, Nanomaterials Science Laboratory, School of Science and Technology (United States)

    2015-06-15

    Cadmium selenide quantum dots (CdSe QDs), inorganic semiconducting nanocrystals, are alluring increased attraction due to their highly refined chemistry, availability, and super tunable optical properties suitable for many applications in different research areas, such as photovoltaics, light-emitting devices, environmental sciences, and nanomedicine. Specifically, they are being widely used in bio-imaging in contrast to organic dyes due to their high brightness and improved photo-stability, and their ability to tune their absorption and emission spectra upon changing the crystal size. The production of CdSe QDs is mostly assisted by trioctylphosphine oxide compound, which acts as solvent or solubilizing agent and renders the QDs soluble in organic compounds (such as toluene, chloroform, and hexane) that are highly toxic. To circumvent the toxicity-related factor in CdSe QDs, we report the synthesis of CdSe QDs capped with thioglycolic acid (TGA) in an aqueous medium, and their biocompatibility in colo-205 cancer cells. In this study, the [Cd{sup 2+}]/[TGA] ratio was adjusted to 11:1 and the Se concentration (10 and 15 mM) was monitored in order to evaluate its influence on the optical properties and cytocompatibility. QDs resulted to be quite stable in water (after purification) and RPMI cell medium and no precipitation was observed for long contact times, making them appealing for in vitro experiments. The spectroscopy analysis, advanced electron microscopy, and X-ray diffractometry studies indicate that the final products were successfully formed exhibiting an improved optical response. Colo-205 cells being exposed to different concentrations of TGA-capped CdSe QDs for 12, 24, and 48 h with doses ranging from 0.5 to 2.0 mM show high tolerance reaching cell viabilities as high as 93 %. No evidence of cellular apoptotic pathways was observed as pointed out by our Annexin V assays at higher concentrations. Moreover, confocal microscopy analysis conducted to

  20. Determination of Atto- to Femtogram Levels of Americium and Curium Isotopes in Large-Volume Urine Samples by Compact Accelerator Mass Spectrometry.

    Science.gov (United States)

    Dai, Xiongxin; Christl, Marcus; Kramer-Tremblay, Sheila; Synal, Hans-Arno

    2016-03-01

    Ultralow level analysis of actinides in urine samples may be required for dose assessment in the event of internal exposures to these radionuclides at nuclear facilities and nuclear power plants. A new bioassay method for analysis of sub-femtogram levels of Am and Cm in large-volume urine samples was developed. Americium and curium were co-precipitated with hydrous titanium oxide from the urine matrix and purified by column chromatography separation. After target preparation using mixed titanium/iron oxides, the final sample was measured by compact accelerator mass spectrometry. Urine samples spiked with known quantities of Am and Cm isotopes in the range of attogram to femtogram levels were measured for method evaluation. The results are in good agreement with the expected values, demonstrating the feasibility of compact accelerator mass spectrometry (AMS) for the determination of minor actinides at the levels of attogram/liter in urine samples to meet stringent sensitivity requirements for internal dosimetry assessment.

  1. Artificial radionuclides in the Northern European Marine Environment. Distribution of radiocaesium, plutonium and americium in sea water and sediments in 1995

    Energy Technology Data Exchange (ETDEWEB)

    Groettheim, Siri

    2000-07-01

    This study considers the distribution of radiocaesium, plutonium and americium in the northern marine environment. The highest radiocaesium activity in sea water was observed in Skagerrak, 26 Bq/m{sub 3}, and in surface sediments in the Norwegian Sea, 60 Bq/kg. These enhanced levels were related to Chernobyl. The highest 239,240Pu activity in surface water was measured in the western North Sea, 66 mBq/m{sub 3}. In sea water, sub-surface maxima were observed at several locations with an 239,240Pu activity up to 160 mBq/m{sub 3}, and were related to Sellafield. With the exception to the North Sea, surface sediments reflected Pu from global fallout from weapons tests only. (author)

  2. Development of an automatic method for americium and plutonium separation and preconcentration using an multisyringe flow injection analysis-multipumping flow system.

    Science.gov (United States)

    Fajardo, Yamila; Ferrer, Laura; Gómez, Enrique; Garcias, Francesca; Casas, Monserrat; Cerdà, Víctor

    2008-01-01

    A new procedure for automatic separation and preconcentration of 241Am and 239+240Pu from interfering matrixes using transuranide (TRU)-resin is proposed. Combination of the multisyringe flow injection analysis and multipumping flow system techniques with the TRU-resin allows carrying out the sampling treatment and separation in a short time using large sample volumes. Americium is eluted from the column with 4 mol L(-1) hydrochloric acid, and then plutonium is separated via on-column Pu(IV) reduction to Pu(III) with titanium(III) chloride. The corresponding alpha activities are measured off-line, with a relative standard deviation of 3% and a lower limit of detection of 0.004 Bq mL(-1), by using a multiplanchet low-background proportional counter.

  3. Recovery of Americium-241 from lightning rod by the method of chemical treatment; Recuperacion del Americio-241 provenientes de los pararrayos por el metodo de tratamiento quimico

    Energy Technology Data Exchange (ETDEWEB)

    Cruz, W.H., E-mail: wcruz@ipen.gob.pe [Instituto Peruano de Energia Nuclear (GRRA/IPEN), Lima (Peru). Division de Gestion de Residuos Radiactivos

    2013-07-01

    About 95% of the lightning rods installed in the Peruvian territory have set in their structures, pose small amounts of radioactive sources such as Americium-241 ({sup 241}Am), fewer and Radium 226 ({sup 226}Ra) these are alpha emitters and have a half life of 432 years and 1600 years respectively. In this paper describes the recovery of radioactive sources of {sup 241}Am radioactive lightning rods using the conventional chemical treatment method using agents and acids to break down the slides. The {sup 241}Am recovered was as excitation source and alpha particle generator for analysing samples by X Ray Fluorescence, for fixing the stainless steel {sup 241}Am technique was used electrodeposition. (author)

  4. Americium-241 Decorporation Model

    Science.gov (United States)

    2014-10-01

    sources when combined with beryllium. Radioactive sources are used for a number of industrial applications that range from oil well logging devices...is any exposure resulting in a 50-year whole-body committed effective dose greater than 200 mSv (Rojas- Palma 2009). Therefore, the model can also...Tracheobronchial geometry: Human, dog, rat, hamster (Report LF-53). Lovelace Foundation, Albuquerque, NM Rojas- Palma C, et al. 2009. TMT Handbook

  5. Obtenção de filmes espessos de seleneto de cobre sobre carbono vítreo, ouro, titânio e cobre Obtaining copper selenide thick films on vitreous carbon, gold, titanium and copper

    OpenAIRE

    Adriano César Rabelo; Tatiane Moraes Arantes; Otávio Luiz Bottecchia

    2007-01-01

    Copper selenide (berzelianite) films were prepared on the title substrates using the chemical bath deposition technique (CBD). Film composition was determined by energy dispersion of x-rays. The kinetics of film growth is parabolic and film adherence limits the film thickness. On titanium, copper selenide forms islands that do not completely cover the surface, unless the substrate is prepared with a tin oxide layer; film composition also depends on the titanium oxide layer. On vitreous carbon...

  6. A convenient synthesis of symmetrical selenide with selenides sodium hydrogen via nucleophilic addition%硒氢化钠亲核加成高收率合成对称硒醚

    Institute of Scientific and Technical Information of China (English)

    刘亚娟; 唐渝; 李志豪; 刘坤迪; 杨骏

    2012-01-01

    In this paper,a new preparation method of symmetrical organoselenides was reported. In the presence of nitrogen,selenium was reduced to sodium hydrogen selenide by sodium borohydride at room temperature in water. In this solution, water soluble hydroxyethyl acrylate was added to react with sodium hydrogen selenide via nuchleophilic addition. DMF should be added to this solution for the reactions of water insoluble phenylacetylene or other α,β-unstaturated compounds. Seven symmetrical organoselenides were afforded. Six of the products were new compounds. The products were easy to be purified by thin layer chromatograph. The product of steric hindered methyl methacrylate yielded in 52%. All the other products were obtained in yields higher of 82-94%.%报道了一种制备对称有机硒醚的新方法:在氮气保护下,以水做溶剂,室温下利用硼氢化钠还原硒粉得到硒氢化钠,与水溶的丙烯酸乙酯发生亲核加成反应,对于水不溶的苯乙炔或其他α,β-不饱和化合物需另加入DMF作溶剂进行反应,共合成了7个对称硒醚产物,其中6个化合物尚未见文献报道,位阻较大的甲基丙烯酸甲酯,可以得到52%的分离收率,其他产物分离收率高达82~94%.

  7. Formation of Metal Selenide and Metal-Selenium Nanoparticles using Distinct Reactivity between Selenium and Noble Metals.

    Science.gov (United States)

    Park, Se Ho; Choi, Ji Yong; Lee, Young Hwan; Park, Joon T; Song, Hyunjoon

    2015-07-01

    Small Se nanoparticles with a diameter of ≈20 nm were generated by the reduction of selenium chloride with NaBH4 at -10 °C. The reaction with Ag at 60 °C yielded stable Ag2 Se nanoparticles, which subsequently were transformed into M-Se nanoparticles (M=Cd, Zn, Pb) through cation exchange reactions with corresponding ions. The reaction with Pt formed Pt layers that were evenly coated on the surface of the Se nanoparticles, and the dissolution of the Se cores with hydrazine generated uniform Pt hollow nanoparticles. The reaction with Au generated tiny Au clusters on the Se surface, and eventually formed acorn-shaped Au-Se nanoparticles through heat treatment. These results indicate that small Se nanoparticles with diameters of ≈20 nm can be used as a versatile platform for the synthesis of metal selenide and metal-selenium hybrid nanoparticles with complex structures.

  8. Cuprous Iodide Catalyzed Synthesis of Diaryl Selenide and Telluride from Organoboronic Acids with Diphenyl Diselenide and Ditelluride

    Institute of Scientific and Technical Information of China (English)

    WANG,Lei; WANG,Min; YAN,Jin-Can; LI,Pin-Hua

    2004-01-01

    @@ Organoselenium and tellurium compounds have received much attention not only as synthetic reagents or intermediates in organic synthesis but also as promising donor molecules for conductive materials.[1] A number of synthetic methods have been reported to prepare organoselenium and tellurium derivatives. A convenient and general method to introduce a selenium or tellurium moiety into organic molecules is the reaction of a metal selenolate or tellurolate with appropriate electrophiles such as organic halides, acyl chlorides, epoxides, and α, β-enones.[2] However, it is difficult to synthesize the unsymmetrical diarylselenides and tellurides through the reaction of selenide anion with organic halides because of the less reactivity of aryl halides. To accomplish this purpose, the reaction (iodobenzene with phenylselenol)was generally carried out in the presence of catalysts, ligands and strong bases. But, the reaction needs longer time to accomplish and form the products in moderate yields.

  9. Observation of Low-Temperature Softening of Transverse Elastic Modulus Due to Cobalt Impurities in Mercury Selenide

    Science.gov (United States)

    Zhevstovskikh, Irina V.; Okulov, Vsevolod I.; Gudkov, Vladimir V.; Sarychev, Maksim N.; Medvedev, Kirill A.; Andriichuk, Myroslav D.; Paranchich, Lidiya D.

    2016-12-01

    Influence on elastic moduli of donor electron d-states of cobalt impurities has been investigated in mercury selenide crystals. Experiments have been carried out at the frequency of 53 MHz in the temperature interval of 1.3-100 K. Softening of the (C_{11} - C_{12})/2 modulus below 10 K has been observed in the impurity crystals in contrast with the (C_{11} + C_{12} + 2C_{44})/2 and C_{44} moduli those have exhibited hardening at cooling typical for dielectric and semiconductor crystals. The softening of the elastic modulus has been interpreted as manifestation of hybridization of the impurity d-states in the conduction band of the crystal. Comparison of theoretical calculations with experimental data has been proved to be in good agreement and has made it possible to determine the parameters characterizing the hybridized electron states.

  10. Post-test analysis of components from selenide isotope generator modules M-7, M-15, and M-18

    Energy Technology Data Exchange (ETDEWEB)

    Wei, G.C.; Keiser, J.R.; Crouse, R.S.; Allen, M.D.; Schaffhauser, A.C.

    1979-05-01

    Several critical components removed from SIG (Selenide Isotope Generator) thermoelectric modules M-7, M-15C, M-15D, and M-18 were examined. These modules failed to show the predicted stability and conversion efficiency. Understanding the degradation and identifying means for preventing it necessitated detailed post-test examinations of key parts in the modules. Steel springs, which provided pressure for contacts at the hot and cold ends of P- or N-legs, relaxed more than expected. Beryllium oxide insulators had dark deposits that caused electrical shorts. The GdSe/sub 1/ /sub 49/ N-leg exhibited cracking. The (Cu,Ag)/sub 2/Se P-leg lost weight or sublimed excessively in module M-7 and more than expected in the other modules.

  11. Ecotoxicological assessment of solar cell leachates: Copper indium gallium selenide (CIGS) cells show higher activity than organic photovoltaic (OPV) cells

    Energy Technology Data Exchange (ETDEWEB)

    Brun, Nadja Rebecca [University of Applied Sciences and Arts Northwestern Switzerland, School of Life Sciences, Gründenstrasse 40, CH-4132 Muttenz (Switzerland); Institute of Biogeochemistry and Pollutant Dynamics, ETH Zurich, Universitätsstrasse 16, CH-8092 Zürich (Switzerland); Wehrli, Bernhard [Institute of Biogeochemistry and Pollutant Dynamics, ETH Zurich, Universitätsstrasse 16, CH-8092 Zürich (Switzerland); Fent, Karl, E-mail: karl.fent@fhnw.ch [University of Applied Sciences and Arts Northwestern Switzerland, School of Life Sciences, Gründenstrasse 40, CH-4132 Muttenz (Switzerland); Institute of Biogeochemistry and Pollutant Dynamics, ETH Zurich, Universitätsstrasse 16, CH-8092 Zürich (Switzerland)

    2016-02-01

    Despite the increasing use of photovoltaics their potential environmental risks are poorly understood. Here, we compared ecotoxicological effects of two thin-film photovoltaics: established copper indium gallium selenide (CIGS) and organic photovoltaic (OPV) cells. Leachates were produced by exposing photovoltaics to UV light, physical damage, and exposure to environmentally relevant model waters, representing mesotrophic lake water, acidic rain, and seawater. CIGS cell leachates contained 583 μg L{sup −1} molybdenum at lake water, whereas at acidic rain and seawater conditions, iron, copper, zinc, molybdenum, cadmium, silver, and tin were present up to 7219 μg L{sup −1}. From OPV, copper (14 μg L{sup −1}), zinc (87 μg L{sup −1}) and silver (78 μg L{sup −1}) leached. Zebrafish embryos were exposed until 120 h post-fertilization to these extracts. CIGS leachates produced under acidic rain, as well as CIGS and OPV leachates produced under seawater conditions resulted in a marked hatching delay and increase in heart edema. Depending on model water and solar cell, transcriptional alterations occurred in genes involved in oxidative stress (cat), hormonal activity (vtg1, ar), metallothionein (mt2), ER stress (bip, chop), and apoptosis (casp9). The effects were dependent on the concentrations of cationic metals in leachates. Addition of ethylenediaminetetraacetic acid protected zebrafish embryos from morphological and molecular effects. Our study suggests that metals leaching from damaged CIGS cells, may pose a potential environmental risk. - Highlights: • Photovoltaics may be disposed in the environment after usage. • Copper indium gallium selenide (CIGS) and organic (OPV) cells were compared. • Morphological and molecular effects were assessed in zebrafish embryos. • Environmental condition affected metal leaching and ecotoxicological activity. • Damaged CIGS cells pose higher risk to the environment than OPV cells.

  12. Structure and composition of the superconducting phase in alkali iron selenide KyFe1.6+xSe2

    Science.gov (United States)

    Carr, Scott V.; Louca, Despina; Siewenie, Joan; Huang, Q.; Wang, Aifeng; Chen, Xianhui; Dai, Pengcheng

    2014-04-01

    We use neutron diffraction to study the temperature evolution of the average structure and local lattice distortions in insulating and superconducting potassium iron selenide KyFe1.6+xSe2. In the high temperature paramagnetic state, both materials have a single phase with a crystal structure similar to that of the BaFe2As2 family of iron pnictides. While the insulating KyFe1.6+xSe2 forms a √5 ×√5 iron vacancy ordered block antiferromagnetic (AF) structure at low temperature, the superconducting compounds spontaneously phase separate into an insulating part with √5 ×√5 iron vacancy order and a superconducting phase with chemical composition of KzFe2Se2 and BaFe2As2 structure. Therefore, superconductivity in alkaline iron selenides arises from alkali deficient KzFe2Se2 in the matrix of the insulating block AF phase.

  13. Passively Q-switched Erbium-doped and Ytterbium-doped fibre lasers with topological insulator bismuth selenide (Bi2Se3) as saturable absorber

    Science.gov (United States)

    Haris, H.; Harun, S. W.; Muhammad, A. R.; Anyi, C. L.; Tan, S. J.; Ahmad, F.; Nor, R. M.; Zulkepely, N. R.; Arof, H.

    2017-02-01

    This paper portrays a simple Q-switched Erbium-doped fibre (EDF) and Ytterbium doped fibre (YDF) lasers by using topological insulator (TI) Bismuth Selenide (Bi2Se3) as saturable absorber. The modulation depth of the fabricated Bi2Se3 is about 39.8% while its saturating intensity is about 90.2 MW/cm2. By depositing the TI Bi2Se3 SA onto fibre ferrules and incorporate it inside the proposed cavity, a stable Q-switching operation was achieved at 1 μm and 1.5 μm. The fabricated Bismuth Selenide (Bi2Se3) as saturable absorber (SA) is a broadband SA where it offers a compact and low cost fabrication which is beneficial in various photonic applications.

  14. Actinide Oxidation State and O/M Ratio in Hypostoichiometric Uranium-Plutonium-Americium U0.750Pu0.246Am0.004O2-x Mixed Oxides.

    Science.gov (United States)

    Vauchy, Romain; Belin, Renaud C; Robisson, Anne-Charlotte; Lebreton, Florent; Aufore, Laurence; Scheinost, Andreas C; Martin, Philippe M

    2016-03-07

    Innovative americium-bearing uranium-plutonium mixed oxides U1-yPuyO2-x are envisioned as nuclear fuel for sodium-cooled fast neutron reactors (SFRs). The oxygen-to-metal (O/M) ratio, directly related to the oxidation state of cations, affects many of the fuel properties. Thus, a thorough knowledge of its variation with the sintering conditions is essential. The aim of this work is to follow the oxidation state of uranium, plutonium, and americium, and so the O/M ratio, in U0.750Pu0.246Am0.004O2-x samples sintered for 4 h at 2023 K in various Ar + 5% H2 + z vpm H2O (z = ∼ 15, ∼ 90, and ∼ 200) gas mixtures. The O/M ratios were determined by gravimetry, XAS, and XRD and evidenced a partial oxidation of the samples at room temperature. Finally, by comparing XANES and EXAFS results to that of a previous study, we demonstrate that the presence of uranium does not influence the interactions between americium and plutonium and that the differences in the O/M ratio between the investigated conditions is controlled by the reduction of plutonium. We also discuss the role of the homogeneity of cation distribution, as determined by EPMA, on the mechanisms involved in the reduction process.

  15. Evidence for the involvement of the serotonergic 5-HT2A/C and 5-HT3 receptors in the antidepressant-like effect caused by oral administration of bis selenide in mice.

    Science.gov (United States)

    Jesse, Cristiano R; Wilhelm, Ethel A; Bortolatto, Cristiani F; Nogueira, Cristina W

    2010-03-17

    The present study investigated a possible antidepressant-like activity of bis selenide using two predictive tests for antidepressant effect on rodents: the forced swimming test (FST) and the tail suspension test (TST). Bis selenide (0.5-5 mg/kg, p.o.) decreased the immobility time in the mouse FST and TST. The anti-immobility effect of bis selenide (1 mg/kg, p.o.) in the TST was prevented by the pretreatment of mice with p-chlorophenylalanine methyl ester (PCPA; 100 mg/kg, i.p., an inhibitor of serotonin synthesis), ketanserin (1 mg/kg, i.p., a 5-HT(2A/2C) receptor antagonist), and ondasentron (1 mg/kg, i.p., a 5-HT(3) receptor antagonist). Pretreatment of mice with prazosin (1 mg/kg, i.p., an alpha(1)-adrenoceptor antagonist), yohimbine (1 mg/kg, i.p., an alpha(2)-adrenoceptor antagonist), propranolol (2 mg/kg, i.p., a beta-adrenoceptor antagonist), SCH23390 (0.05 mg/kg, s.c., a dopamine D(1) receptor antagonist), sulpiride (50 mg/kg, i.p., a dopamine D(2) receptor antagonist), or WAY 100635 (0.1 mg/kg, s.c., a selective 5-HT(1A) receptor antagonist) did not block the antidepressant-like effect of bis selenide (1 mg/kg, p.o.) in the TST. Administration of bis selenide (0.1 mg/kg, p.o.) and fluoxetine (1 mg/kg), at subeffective doses, produced an antidepressant-like effect in the TST. Bis selenide did not alter Na(+) K(+) ATPase, MAO-A and MAO-B activities in whole brains of mice. Bis selenide produced an antidepressant-like effect in the mouse TST and FST, which may be related to the serotonergic system (5-HT(2A/2C) and 5-HT(3) receptors).

  16. Study of biosorbents application on the treatment of radioactive liquid wastes with americium-241; Estudo da aplicacao de biossorventes no tratamento de rejeitos radioativos liquidos contendo americio-241

    Energy Technology Data Exchange (ETDEWEB)

    Borba, Tania Regina de

    2010-07-01

    The use of nuclear energy for many different purposes has been intensified and highlighted by the benefits that it provides. Medical diagnosis and therapy, agriculture, industry and electricity generation are examples of its application. However, nuclear energy generates radioactive wastes that require suitable treatment ensuring life and environmental safety. Biosorption and bioaccumulation represent an emergent alternative for the treatment of radioactive liquid wastes, providing volume reduction and physical state change. This work aimed to study biosorbents for the treatment of radioactive liquid wastes contaminated with americium-241 in order to reduce the volume and change the physical state from liquid to solid. The biosorbents evaluated were Saccharomyces cerevisiae immobilized in calcium alginate beads, inactivated and free cells of Saccharomyces cerevisiae, calcium alginate beads, Bacillus subtilis, Cupriavidus metallidurans and Ochrobactrum anthropi. The results were quite satisfactory, achieving 100% in some cases. The technique presented in this work may be useful and viable for implementing at the Waste Management Laboratory of IPEN - CNEN/SP in short term, since it is an easy and low cost method. (author)

  17. Human bones obtained from routine joint replacement surgery as a tool for studies of plutonium, americium and {sup 90}Sr body-burden in general public

    Energy Technology Data Exchange (ETDEWEB)

    Mietelski, Jerzy W., E-mail: jerzy.mietelski@ifj.edu.pl [Henryk Niewodniczanski Institute of Nuclear Physics, Polish Academy of Sciences, Radzikowskiego 152, 31-342 Cracow (Poland); Golec, Edward B. [Traumatology and Orthopaedic Clinic, 5th Military Clinical Hospital and Polyclinic, Independent Public Healthcare Facility, Wroclawska 1-3, 30-901 Cracow (Poland); Orthopaedic Rehabilitation Department, Chair of Clinical Rehabilitation, Faculty of Motor of the Bronislaw Czech' s Academy of Physical Education, Cracow (Poland); Department of Physical Therapy Basics, Faculty of Physical Therapy, Administration College, Bielsko-Biala (Poland); Tomankiewicz, Ewa [Henryk Niewodniczanski Institute of Nuclear Physics, Polish Academy of Sciences, Radzikowskiego 152, 31-342 Cracow (Poland); Golec, Joanna [Orthopaedic Rehabilitation Department, Chair of Clinical Rehabilitation, Faculty of Motor of the Bronislaw Czech' s Academy of Physical Education, Cracow (Poland); Physical Therapy Department, Institute of Physical Therapy, Faculty of Heath Science, Jagiellonian University, Medical College, Cracow (Poland); Nowak, Sebastian [Traumatology and Orthopaedic Clinic, 5th Military Clinical Hospital and Polyclinic, Independent Public Healthcare Facility, Wroclawska 1-3, 30-901 Cracow (Poland); Orthopaedic Rehabilitation Department, Chair of Clinical Rehabilitation, Faculty of Motor of the Bronislaw Czech' s Academy of Physical Education, Cracow (Poland); Szczygiel, Elzbieta [Physical Therapy Department, Institute of Physical Therapy, Faculty of Heath Science, Jagiellonian University, Medical College, Cracow (Poland); Brudecki, Kamil [Henryk Niewodniczanski Institute of Nuclear Physics, Polish Academy of Sciences, Radzikowskiego 152, 31-342 Cracow (Poland)

    2011-06-15

    The paper presents a new sampling method for studying in-body radioactive contamination by bone-seeking radionuclides such as {sup 90}Sr, {sup 239+240}Pu, {sup 238}Pu, {sup 241}Am and selected gamma-emitters, in human bones. The presented results were obtained for samples retrieved from routine surgeries, namely knee or hip joints replacements with implants, performed on individuals from Southern Poland. This allowed to collect representative sets of general public samples. The applied analytical radiochemical procedure for bone matrix is described in details. Due to low concentrations of {sup 238}Pu the ratio of Pu isotopes which might be used for Pu source identification is obtained only as upper limits other then global fallout (for example Chernobyl) origin of Pu. Calculated concentrations of radioisotopes are comparable to the existing data from post-mortem studies on human bones retrieved from autopsy or exhumations. Human bones removed during knee or hip joint surgery provide a simple and ethical way for obtaining samples for plutonium, americium and {sup 90}Sr in-body contamination studies in general public. - Highlights: > Surgery for joint replacement as novel sampling method for studying in-body radioactive contamination. > Proposed way of sampling is not causing ethic doubts. > It is a convenient way of collecting human bone samples from global population. > The applied analytical radiochemical procedure for bone matrix is described in details. > The opposite patient age correlations trends were found for 90Sr (negative) and Pu, Am (positive).

  18. Influence of growth and photocatalytic properties of copper selenide (CuSe) nanoparticles using reflux condensation method

    Science.gov (United States)

    Sonia, S.; Kumar, P. Suresh; Mangalaraj, D.; Ponpandian, N.; Viswanathan, C.

    2013-10-01

    Influence of reaction conditions on the synthesis of copper selenide (CuSe) nanoparticles and their photo degradation activity is studied. Nearly monodispersed uniform size (23-44 nm) nanoparticles are synthesized by varying the reaction conditions using reflux condensation method. The obtained nanoparticles are characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy and UV-visible absorption spectroscopy. The X-ray diffraction analysis of the sample shows the formation of nanoparticles with hexagonal CuSe structure. The result indicates that on increasing the reaction time from 4 to 12 h, the particle size decreases from 44 to 23 nm, but an increase in the reaction temperature increases the particle size. The calculated band gap Eg is ranging from 2.34 to 3.05 eV which is blue shifted from the bulk CuSe (2.2 eV). The photocatalytic degradation efficiency of the CuSe nanoparticles on two organic dyes Methylene blue (MB) and Rhodamine-B (RhB) in aqueous solution under UV region is calculated as 76 and 87% respectively.

  19. Influence of growth and photocatalytic properties of copper selenide (CuSe) nanoparticles using reflux condensation method

    Energy Technology Data Exchange (ETDEWEB)

    Sonia, S. [Department of Nanoscience and Technology, Bharathiar University, Coimbatore 641046 (India); Kumar, P. Suresh [Thin Film and Nanomaterials Laboratory, Department of Physics, Bharathiar University, Coimbatore 641046 (India); Mangalaraj, D., E-mail: dmraj800@yahoo.com [Department of Nanoscience and Technology, Bharathiar University, Coimbatore 641046 (India); Ponpandian, N.; Viswanathan, C. [Department of Nanoscience and Technology, Bharathiar University, Coimbatore 641046 (India)

    2013-10-15

    Influence of reaction conditions on the synthesis of copper selenide (CuSe) nanoparticles and their photo degradation activity is studied. Nearly monodispersed uniform size (23–44 nm) nanoparticles are synthesized by varying the reaction conditions using reflux condensation method. The obtained nanoparticles are characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy and UV–visible absorption spectroscopy. The X-ray diffraction analysis of the sample shows the formation of nanoparticles with hexagonal CuSe structure. The result indicates that on increasing the reaction time from 4 to 12 h, the particle size decreases from 44 to 23 nm, but an increase in the reaction temperature increases the particle size. The calculated band gap E{sub g} is ranging from 2.34 to 3.05 eV which is blue shifted from the bulk CuSe (2.2 eV). The photocatalytic degradation efficiency of the CuSe nanoparticles on two organic dyes Methylene blue (MB) and Rhodamine-B (RhB) in aqueous solution under UV region is calculated as 76 and 87% respectively.

  20. MOF-derived Co-doped nickel selenide/C electrocatalysts supported on Ni foam for overall water splitting

    KAUST Repository

    Ming, Fangwang

    2016-09-01

    It is of prime importance to develop dual-functional electrocatalysts with good activity for overall water splitting, which remains a great challenge. Herein, we report the synthesis of a Co-doped nickel selenide (a mixture of NiSe and NiSe)/C hybrid nanostructure supported on Ni foam using a metal-organic framework as the precursor. The resulting catalyst exhibits excellent catalytic activity toward the oxygen evolution reaction (OER), which only requires an overpotential of 275 mV to drive a current density of 30 mA cm. This overpotential is much lower than those reported for precious metal free OER catalysts. The hybrid is also capable of catalyzing the hydrogen evolution reaction (HER) efficiently. A current density of -10 mA cm can be achieved at 90 mV. In addition, such a hybrid nanostructure can achieve 10 and 30 mA cm at potentials of 1.6 and 1.71 V, respectively, along with good durability when functioning as both the cathode and the anode for overall water splitting in basic media.

  1. Pulsed voltage deposited lead selenide thin film as efficient counter electrode for quantum-dot-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Bin Bin [Key Laboratory of Macromolecular Science of Shaanxi Province & School of Materials Science and Engineering, Shaanxi Normal University, Xi’an 710062 (China); Department of Chemical Engineering, Institute of Chemical Industry, Shaanxi Institute of Technology, Xi’an 710300 (China); Wang, Ye Feng [Key Laboratory of Macromolecular Science of Shaanxi Province & School of Materials Science and Engineering, Shaanxi Normal University, Xi’an 710062 (China); Wang, Xue Qing [Faculty of Chemical, Environmental and Biological Science and Technology, Dalian University of Technology, Dalian 116024 (China); Zeng, Jing Hui, E-mail: jhzeng@ustc.edu [Key Laboratory of Macromolecular Science of Shaanxi Province & School of Materials Science and Engineering, Shaanxi Normal University, Xi’an 710062 (China)

    2016-04-30

    Highlights: • PbSe thin film is deposited on FTO glass by a pulse voltage electrodeposition method. • The thin film is used as counter electrode (CE) in quantum dot-sensitized solar cell. • Superior electrocatalytic activity and stability in the polysulfide electrolyte is received. • The narrow band gap characteristics and p-type conductivity enhances the cell efficiency. • An efficiency of 4.67% is received for the CdS/CdSe co-sensitized solar cells. - Abstract: Lead selenide (PbSe) thin films were deposited on fluorine doped tin oxide (FTO) glass by a facile one-step pulse voltage electrodeposition method, and used as counter electrode (CE) in CdS/CdSe quantum dot-sensitized solar cells (QDSSCs). A power conversion efficiency of 4.67% is received for the CdS/CdSe co-sensitized solar cells, which is much better than that of 2.39% received using Pt CEs. The enhanced performance is attributed to the extended absorption in the near infrared region, superior electrocatalytic activity and p-type conductivity with a reflection of the incident light at the back electrode in addition. The physical and chemical properties were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), energy-dispersive spectroscopy (EDS), reflectance spectra, electrochemical impedance spectroscopy (EIS) and Tafel polarization measurements. The present work provides a facile pathway to an efficient CE in the QDSSCs.

  2. Simultaneous Determination of Adenine and Guanine Using Cadmium Selenide Quantum Dots-Graphene Oxide Nanocomposite Modified Electrode.

    Science.gov (United States)

    Kalaivani, Arumugam; Narayanan, Sangilimuthu Sriman

    2015-06-01

    A novel electrochemical sensor was fabricated by immobilizing Cadmium Selenide Quantum Dots (CdSe QDs)-Graphene Oxide (GO) nanocomposite on a paraffin wax impregnated graphite electrode (PIGE) and was used for the simultaneous determination of adenine and guanine. The CdSe QDs-GO nanocomposite was prepared by ultrasonication and was characterized with spectroscopic and microscopic techniques. The nanocomposite modified electrode was characterized by cyclic voltammetry (CV). The modified electrode showed excellent electrocatalytic activity towards the oxidative determination of adenine and guanine with a good peak separation of 0.31 V. This may be due to the high surface area and fast electron transfer kinetics of the nanocomposite. The modified electrode exhibited wide linear ranges from 0.167 μM to 245 μM for Guanine and 0.083 μM to 291 μM for Adenine with detection limits of 0.055 μM Guanine and 0.028 μM of Adenine (S/N = 3) respectively. Further, the modified electrode was used for the quantitative determination of adenine and guanine in herring sperm DNA with satisfactory results. The modified electrode showed acceptable selectivity, reproducibility and stability under optimal conditions.

  3. Aspects of a Distinct Cytotoxicity of Selenium Salts and Organic Selenides in Living Cells with Possible Implications for Drug Design

    Directory of Open Access Journals (Sweden)

    Ethiene Castellucci Estevam

    2015-07-01

    Full Text Available Selenium is traditionally considered as an antioxidant element and selenium compounds are often discussed in the context of chemoprevention and therapy. Recent studies, however, have revealed a rather more colorful and diverse biological action of selenium-based compounds, including the modulation of the intracellular redox homeostasis and an often selective interference with regulatory cellular pathways. Our basic activity and mode of action studies with simple selenium and tellurium salts in different strains of Staphylococcus aureus (MRSA and Saccharomyces cerevisiae indicate that such compounds are sometimes not particularly toxic on their own, yet enhance the antibacterial potential of known antibiotics, possibly via the bioreductive formation of insoluble elemental deposits. Whilst the selenium and tellurium compounds tested do not necessarily act via the generation of Reactive Oxygen Species (ROS, they seem to interfere with various cellular pathways, including a possible inhibition of the proteasome and hindrance of DNA repair. Here, organic selenides are considerably more active compared to simple salts. The interference of selenium (and tellurium compounds with multiple targets could provide new avenues for the development of effective antibiotic and anticancer agents which may go well beyond the traditional notion of selenium as a simple antioxidant.

  4. Structural and Optical Studies of 100 MeV Ni+7 Irradiated Cadmium Selenide Thin Films

    Directory of Open Access Journals (Sweden)

    Rajesh Singh

    2015-10-01

    Full Text Available The effect of irradiation with Swift (100 MeV Ni+ 7 ions on the structural and optical properties of Cadmium Selenide (CdSe thin films have been investigated at different fluencies in the range of 1  1011-1  1013 ions/cm – 2. The CdSe films on glass substrates were prepared by thermal evaporation. The structural and optical changes with respect to increasing fluence were observed by the means of X-ray diffraction (XRD, UV-VIS and Raman spectroscopy. After irradiating the films with Ni+ 7 ions XRD show the increased in peak intensity and crystallite size with increasing fluence. The UV-VIS-IR spectroscopy revealed that there is decrease in band gap energy of the films after irradiation with increasing fluencies. Raman spectrum for as deposited and irradiated films show two peak, one at 209 cm – 1 and at 410 cm – 1 which is assigned to the longitudinal optical (LO phonon mode.

  5. Ecotoxicological assessment of solar cell leachates: Copper indium gallium selenide (CIGS) cells show higher activity than organic photovoltaic (OPV) cells.

    Science.gov (United States)

    Brun, Nadja Rebecca; Wehrli, Bernhard; Fent, Karl

    2016-02-01

    Despite the increasing use of photovoltaics their potential environmental risks are poorly understood. Here, we compared ecotoxicological effects of two thin-film photovoltaics: established copper indium gallium selenide (CIGS) and organic photovoltaic (OPV) cells. Leachates were produced by exposing photovoltaics to UV light, physical damage, and exposure to environmentally relevant model waters, representing mesotrophic lake water, acidic rain, and seawater. CIGS cell leachates contained 583 μg L(-1) molybdenum at lake water, whereas at acidic rain and seawater conditions, iron, copper, zinc, molybdenum, cadmium, silver, and tin were present up to 7219 μg L(-1). From OPV, copper (14 μg L(-1)), zinc (87 μg L(-1)) and silver (78 μg L(-1)) leached. Zebrafish embryos were exposed until 120 h post-fertilization to these extracts. CIGS leachates produced under acidic rain, as well as CIGS and OPV leachates produced under seawater conditions resulted in a marked hatching delay and increase in heart edema. Depending on model water and solar cell, transcriptional alterations occurred in genes involved in oxidative stress (cat), hormonal activity (vtg1, ar), metallothionein (mt2), ER stress (bip, chop), and apoptosis (casp9). The effects were dependent on the concentrations of cationic metals in leachates. Addition of ethylenediaminetetraacetic acid protected zebrafish embryos from morphological and molecular effects. Our study suggests that metals leaching from damaged CIGS cells, may pose a potential environmental risk.

  6. Production of no-carrier-added radiobromine. new nickel selenide target and optimized separation by dry distillation

    Energy Technology Data Exchange (ETDEWEB)

    Breunig, Katharina; Spahn, Ingo; Spellerberg, Stefan; Coenen, Heinz H. [Forschungszentrum Juelich GmbH (Germany). Inst. fuer Neurowissenschaften und Medizin (INM), Nuklearchemie (INM-5)

    2015-07-01

    Nickel(II) selenide (NiSe) was investigated as a new high-current target material for cyclotron production of radiobromine, as it contains a higher amount of selenium and has a lower melting point than the widely used Cu{sub 2}Se. Using a slanted target system, NiSe was successfully tested up to beam currents of 16 μA so far. With regard to the isolation of no-carrier-added (n.c.a.) radiobromide from the target material, an improved dry distillation device with high yields of 76%-86% was developed. The implementation of a special custom-made quartz funnel decreased the dead volume of the apparatus and a quartz capillary for trapping the radiobromine allowed to concentrate the radioactivity in a small volume of less than 100 μL of 0.1 M NaOH, ready for immediate subsequent radiosyntheses. Thus, the new apparatus improves the handling of the isolation procedure and the radioactive product. The radiochemical purity of the resulting solution of n.c.a. [*Br]bromide was verified by radio-IC where no other species were detected.

  7. The development of 6.7% efficient copper zinc indium selenide devices from copper zinc indium sulfide nanocrystal inks

    Science.gov (United States)

    Graeser, Brian K.

    As solar cell absorber materials, alloys of CuIn(S,Se)2 and Zn(S,Se) provide an opportunity to reduce the usage of indium along with the ability to tune the band gap. Here we report successful synthesis of alloyed (CuInS2)0.5(ZnS)0.5 nanocrystals by a method that solely uses oleylamine as the liquid medium for synthesis. The reactive sintering of a thin film of these nanocrystals via selenization at 500 °C results in a uniform composition alloy (CuIn(S,Se)2)0.5(Zn(S,Se)) 0.5 layer with micron size grains. Due to the large amount of zinc in the film, the sintered grains exhibit the zinc blende structure instead of the usual chalcopyrite structure of CuIn(S,Se)2 films. The use of the selenide films as a p-type absorber layer has yielded solar cells with total area power conversion efficiencies as high as 6.7% (7.4% based on active area). These preliminary results are encouraging and indicate that with further optimization this class of materials has promise as the absorber layer in solar cells.

  8. Investigation of the ablation of zinc oxide thin films on copper-indium-selenide layers by ps laser pulses

    Science.gov (United States)

    Heise, Gerhard; Dickmann, Marcel; Domke, Matthias; Heiss, Andreas; Kuznicki, Thomas; Palm, Jörg; Richter, Isabel; Vogt, Helmut; Huber, Heinz P.

    2011-07-01

    The selective laser structuring of zinc oxide thin films, which serve as the transparent negative electrodes of copper-indium-selenide (CIS) thin film solar cells, is of great common interest as it can replace the mechanical scribing of the so-called pattern 3 (P3) process step for the monolithic serial interconnection of these cells. We present an investigation of the single-pulse ablation behavior of zinc oxide thin films on glass substrates and on CIS layers and of trench scribing with 10-ps laser pulses at 1064 nm and at 532 nm. We show that the ablation behavior strongly depends on the properties of the underling substrate and that the energy required to ablate a specific volume using induced laser processes (often referred to as `lift off') is considerably reduced compared to the direct ablation of zinc oxide. With laser powers below 2 W at a wavelength of 1064 nm process speeds of 6 m/s for the P3 process have been achieved.

  9. Influence of substrate temperature on the structural, optical and electrical properties of zinc selenide (ZnSe) thin films

    Science.gov (United States)

    Venkatachalam, S.; Mangalaraj, D.; Narayandass, Sa K.

    2006-11-01

    Zinc selenide (ZnSe) thin films were deposited onto well cleaned silicon (100) and glass substrates at different substrate temperatures (483-589 K) using vacuum evaporation method under a vacuum of 4 × 10-3 Pa. The compositions of the deposited films were determined by Rutherford backscattering spectrometry and the percentage of iodine concentration is calculated as (ZnSe)I0.001. The x-ray diffractograms reveal the cubic structure of the film oriented along the (111) direction. In optical studies, the transition of the deposited film is found to be a direct allowed transition. The optical energy gaps of the deposited films are found to be in the range from 2.72 to 2.60 eV. ZnSe/silicon Schottky diodes were fabricated. From the current-voltage measurement the ideality factor was found to be in the range 2.01-3.51. From the capacitance-voltage studies, the built in potential was found to be 1.51 V. The values of effective carrier concentration (NA) and the barrier height are calculated as 4.37 × 1011 cm-3 and 1.95 eV, respectively.

  10. Obtenção de filmes espessos de seleneto de cobre sobre carbono vítreo, ouro, titânio e cobre Obtaining copper selenide thick films on vitreous carbon, gold, titanium and copper

    Directory of Open Access Journals (Sweden)

    Adriano César Rabelo

    2007-04-01

    Full Text Available Copper selenide (berzelianite films were prepared on the title substrates using the chemical bath deposition technique (CBD. Film composition was determined by energy dispersion of x-rays. The kinetics of film growth is parabolic and film adherence limits the film thickness. On titanium, copper selenide forms islands that do not completely cover the surface, unless the substrate is prepared with a tin oxide layer; film composition also depends on the titanium oxide layer. On vitreous carbon, CBD and mechanical immobilization techniques lead to films with similar resistances for the electron transfer across the film/substrate interface. On gold, composition studies revealed that film composition is always the same if the pH is in the range from 8 to 12, in contrast to films prepared by an ion-ion combination route. On copper, a new procedure for obtaining copper selenide films as thick as 5 µm has been developed.

  11. Study of the crystallographic phase change on copper (I) selenide thin films prepared through chemical bath deposition by varying the pH of the solution

    Science.gov (United States)

    Sandoval-Paz, M. G.; Rodríguez, C. A.; Porcile-Saavedra, P. F.; Trejo-Cruz, C.

    2016-07-01

    Copper (I) selenide thin films with orthorhombic and cubic structure were deposited on glass substrates by using the chemical bath deposition technique. The effects of the solution pH on the films growth and subsequently the structural, optical and electrical properties of the films were studied. Films with orthorhombic structure were obtained from baths wherein both metal complex and hydroxide coexist; while films with cubic structure were obtained from baths where the metal hydroxide there is no present. The structural modifications are accompanied by changes in bandgap energy, morphology and electrical resistivity of the films.

  12. The construction of TRIGA-TRAP and direct high-precision Penning trap mass measurements on rare-earth elements and americium

    Energy Technology Data Exchange (ETDEWEB)

    Ketelaer, Jens

    2010-06-14

    The construction of TRIGA-TRAP and direct high-precision Penning trap mass measurements on rare-earth elements and americium: Nuclear masses are an important quantity to study nuclear structure since they reflect the sum of all nucleonic interactions. Many experimental possibilities exist to precisely measure masses, out of which the Penning trap is the tool to reach the highest precision. Moreover, absolute mass measurements can be performed using carbon, the atomic-mass standard, as a reference. The new double-Penning trap mass spectrometer TRIGA-TRAP has been installed and commissioned within this thesis work, which is the very first experimental setup of this kind located at a nuclear reactor. New technical developments have been carried out such as a reliable non-resonant laser ablation ion source for the production of carbon cluster ions and are still continued, like a non-destructive ion detection technique for single-ion measurements. Neutron-rich fission products will be available by the reactor that are important for nuclear astrophysics, especially the r-process. Prior to the on-line coupling to the reactor, TRIGA-TRAP already performed off-line mass measurements on stable and long-lived isotopes and will continue this program. The main focus within this thesis was on certain rare-earth nuclides in the well-established region of deformation around N {proportional_to} 90. Another field of interest are mass measurements on actinoids to test mass models and to provide direct links to the mass standard. Within this thesis, the mass of {sup 241}Am could be measured directly for the first time. (orig.)

  13. Physical and biophysical assessment of highly fluorescent, magnetic quantum dots of a wurtzite-phase manganese selenide system

    Science.gov (United States)

    Sarma, Runjun; Das, Queen; Hussain, Anowar; Ramteke, Anand; Choudhury, Amarjyoti; Mohanta, Dambarudhar

    2014-07-01

    Combining fluorescence and magnetic features in a non-iron based, select type of quantum dots (QDs) can have immense value in cellular imaging, tagging and other nano-bio interface applications, including targeted drug delivery. Herein, we report on the colloidal synthesis and physical and biophysical assessment of wurtzite-type manganese selenide (MnSe) QDs in cell culture media. Aiming to provide a suitable colloidal system of biological relevance, different concentrations of reactants and ligands (e.g., thioglycolic acid, TGA) have been considered. The average size of the QDs is ˜7 nm, which exhibited a quantum yield of ˜75% as compared to rhodamine 6 G dye®. As revealed from time-resolved photoluminescence (TR-PL) response, the near band edge emission followed a bi-exponential decay feature with characteristic times of ˜0.64 ns and 3.04 ns. At room temperature, the QDs were found to exhibit paramagnetic features with coercivity and remanence impelled by TGA concentrations. With BSA as a dispersing agent, the QDs showed an improved optical stability in Dulbecco’s Modified Eagle Media® (DMEM) and Minimum Essential Media® (MEM), as compared to the Roswell Park Memorial Institute® (RPMI-1640) media. Finally, the cell viability of lymphocytes was found to be strongly influenced by the concentration of MnSe QDs, and had a safe limit upto 0.5 μM. With BSA inclusion in cell media, the cellular uptake of MnSe QDs was observed to be more prominent, as revealed from fluorescence imaging. The fabrication of water soluble, nontoxic MnSe QDs would open up an alternative strategy in nanobiotechnology, while preserving their luminescent and magnetic properties intact.

  14. Transition from Sign-Reversed to Sign-Preserved Cooper-Pairing Symmetry in Sulfur-Doped Iron Selenide Superconductors.

    Science.gov (United States)

    Wang, Qisi; Park, J T; Feng, Yu; Shen, Yao; Hao, Yiqing; Pan, Bingying; Lynn, J W; Ivanov, A; Chi, Songxue; Matsuda, M; Cao, Huibo; Birgeneau, R J; Efremov, D V; Zhao, Jun

    2016-05-13

    An essential step toward elucidating the mechanism of superconductivity is to determine the sign or phase of the superconducting order parameter, as it is closely related to the pairing interaction. In conventional superconductors, the electron-phonon interaction induces attraction between electrons near the Fermi energy and results in a sign-preserved s-wave pairing. For high-temperature superconductors, including cuprates and iron-based superconductors, prevalent weak coupling theories suggest that the electron pairing is mediated by spin fluctuations which lead to repulsive interactions, and therefore that a sign-reversed pairing with an s_{±} or d-wave symmetry is favored. Here, by using magnetic neutron scattering, a phase sensitive probe of the superconducting gap, we report the observation of a transition from the sign-reversed to sign-preserved Cooper-pairing symmetry with insignificant changes in T_{c} in the S-doped iron selenide superconductors K_{x}Fe_{2-y}(Se_{1-z}S_{z})_{2}. We show that a rather sharp magnetic resonant mode well below the superconducting gap (2Δ) in the undoped sample (z=0) is replaced by a broad hump structure above 2Δ under 50% S doping. These results cannot be readily explained by simple spin fluctuation-exchange pairing theories and, therefore, multiple pairing channels are required to describe superconductivity in this system. Our findings may also yield a simple explanation for the sometimes contradictory data on the sign of the superconducting order parameter in iron-based materials.

  15. Exploring the thermoelectric and magnetic properties of uranium selenides: Tl2Ag2USe4 and Tl3Cu4USe6

    Science.gov (United States)

    Azam, Sikander; Khan, Saleem Ayaz; Din, Haleem Ud; Khenata, Rabah; Goumri-Said, Souraya

    2016-09-01

    The electronic, magnetic and thermoelectric properties of Tl2Ag2USe4 and Tl3Cu4USe6 compounds were investigated using the full potential linear augmented plane wave (FP-LAPW) method based on the density functional theory (DFT). The exchange correlation was treated with the generalized gradient approximation plus optimized effective Hubbard parameter and spin-orbit coupling (GGA+U+SOC). The present uranium selenides show narrow direct energy band gap values of 0.7 and 0.875 eV for Tl2Ag2USe4 and Tl3Cu4USe6 respectively. For both selenides U-d/f states are responsible for electrical transport properties. Uranium atoms were the most contributors in the magnetic moment compared to other atoms and show ferromagnetic nature. The spin density isosurfaces show the polarization of neighboring atoms of Uranium, such as silver/copper and selenium. Thermoelectric calculations reveal that Tl3Cu4USe6 is more suitable for thermoelectric device applications than Tl2Ag2USe4.

  16. Spray pyrolysis of tin selenide thin-film semiconductors: the effect of selenium concentration on the properties of the thin films

    Institute of Scientific and Technical Information of China (English)

    M.R.Fadavieslam; M.M.Bagheri-Mohagheghi

    2013-01-01

    Thin films of tin selenide (SnxSey) with an atomic ratio ofr =[x/y] =0.5,1 and 1.5 were prepared on a glass substrate at T =470 ℃ using a spray pyrolysis technique.The initial materials for the preparation of the thin films were an alcoholic solution consisting of tin chloride (SnCl4· 5H2O) and selenide acide (H2SeO3).The prepared thin films were characterized by X-ray diffraction (XRD),scanning electron microscopy,scanning tunneling microscopy,scanning helium ion microscopy,and UV-vis spectroscopy.The photoconductivity and thermoelectric effects of the Snx Seythin films were then studied.The Snx Sey thin films had a polycrystalline structure with an almost uniform surface and cluster type growth.The increasing atomic ratio ofr in the films,the optical gap,photosensitivity and Seebeck coefficient were changed from 1.6 to 1.37 eV,0.01 to 0.31 and-26.2 to-42.7 mV/K (at T =350 K),respectively.In addition,the XRD patterns indicated intensity peaks in r =1 that corresponded to the increase in the SnSe and SnSe2 phases.

  17. A novel technique for nano-scale lithography of cadmium selenide via a scanning tunneling microscope tip-induced reaction

    Science.gov (United States)

    Olson, Joel Andrew

    In the introductory chapter the physical and interfacial properties of cadmium selenide are presented, as well as a discussion of select surface properties of CdSe. Also, a brief review of scanning probe lithographic techniques currently under investigation is presented. As a portion of the project presented herein, a research-grade scanning tunneling microscope was constructed. The second chapter includes information specific to this instrument. Included are descriptions of the electrical components, descriptions of the mechanical components, and a description of the noise reduction and calibration of the instrument. When cleaved-in-air (112¯0) CdSe is imaged repeatedly under humidified conditions, small (˜20 nm wide and between 6 A and 12 A in height) features are observed to form. The features are similar in shape to one another, suggesting tip imaging. Under an atmosphere of dried nitrogen feature growth is not observed. The growth of the features shows a strong dependence on both the tunneling current and the bias voltage. The initial rate of feature growth increases with tunneling current. Feature growth as a function of bias voltage displays an onset at a sample bias of -1. 2 V to -1. 3 V and is no longer observed at sample biases more negative than -2.5 V. Two possible models are presented for feature growth. The smallest feature observed is ˜6 nm in width. The fourth chapter describes simple and inexpensive classroom demonstrations of nuclear magnetic resonance (NMR) and magnetic resonance imaging (MRI). The demonstrations comprise common orienteering compasses, whose needles represent magnetic dipoles, along with three collinear permanent magnets, and a magnetic stir plate or pulseable electromagnets. The trio of permanent magnets provides a laterally uniform magnetic field, whose strength decreases with distance from the magnets. Resonance can be observed by adjusting the frequency of the magnetic stirrer when it is in close proximity to the compasses

  18. Design and fabrication of anti-reflection coating on Gallium Phosphide, Zinc Selenide and Zinc Sulfide substrates for visible and infrared application

    Directory of Open Access Journals (Sweden)

    Mokrý P.

    2013-05-01

    Full Text Available Results of design and fabrication of a dual-band anti-reflection coating on a gallium phosphide (GaP, zinc selenide (ZnSe and zinc sulfide (ZnS substrates are presented. A multilayer stack structure of antireflection coatings made of zinc sulfide and yttrium fluoride (YF3 was theoretically designed for optical bands between 0.8 and 0.9 μm and between 9.5 and 10.5 μm. This stack was designed as efficient for these materials (GaP, ZnS, ZnSe together. Multilayer stack structure was deposited using thermal evaporation method. Theoretically predicted transmittance spectra were compared with transmitted spectra measured on coated substrates. Efficiency of anti-reflection coating is estimated and discrepancies are analyzed and discussed.

  19. EURADOS action for determination of americium in skull measures in vivo and Monte Carlo simulation; Accion EURADOS para la determinacion de americio en craneo mediante medidas in-vivo y simulacion Monte Carlo

    Energy Technology Data Exchange (ETDEWEB)

    Lopez Ponte, M. A.; Navarro Amaro, J. F.; Perez Lopez, B.; Navarro Bravo, T.; Nogueira, P.; Vrba, T.

    2013-07-01

    From the Group of WG7 internal dosimetry of the EURADOS Organization (European Radiation Dosimetry group, e.V.) which It coordinates CIEMAT, international action for the vivo measurement of americium has been conducted in three mannequins type skull with detectors of Germanium by gamma spectrometry and simulation by Monte Carlo methods. Such action has been raised as two separate exercises, with the participation of institutions in Europe, America and Asia. Other actions similar precede this vivo intercomparison of measurement and modeling Monte Carlo1. The preliminary results and associated findings are presented in this work. The laboratory of the body radioactivity (CRC) of service counter of dosimetry staff internal (DPI) of the CIEMAT, it has been one of the participants in vivo measures exercise. On the other hand part, the Group of numerical dosimetry of CIEMAT is participant of the Monte Carlo2 simulation exercise. (Author)

  20. Americium behaviour in plastic vessels

    Energy Technology Data Exchange (ETDEWEB)

    Legarda, F.; Herranz, M. [Departamento de Ingenieria Nuclear y Mecanica de Fluidos, Escuela Tecnica Superior de Ingenieria de Bilbao, Universidad del Pais Vasco (UPV/EHU), Alameda de Urquijo s/n, 48013 Bilbao (Spain); Idoeta, R., E-mail: raquel.idoeta@ehu.e [Departamento de Ingenieria Nuclear y Mecanica de Fluidos, Escuela Tecnica Superior de Ingenieria de Bilbao, Universidad del Pais Vasco (UPV/EHU), Alameda de Urquijo s/n, 48013 Bilbao (Spain); Abelairas, A. [Departamento de Ingenieria Nuclear y Mecanica de Fluidos, Escuela Tecnica Superior de Ingenieria de Bilbao, Universidad del Pais Vasco (UPV/EHU), Alameda de Urquijo s/n, 48013 Bilbao (Spain)

    2010-07-15

    The adsorption of {sup 241}Am dissolved in water in different plastic storage vessels was determined. Three different plastics were investigated with natural and distilled waters and the retention of {sup 241}Am by these plastics was studied. The same was done by varying vessel agitation time, vessel agitation speed, surface/volume ratio of water in the vessels and water pH. Adsorptions were measured to be between 0% and 70%. The adsorption of {sup 241}Am is minimized with no water agitation, with PET or PVC plastics, and by water acidification.

  1. Tris(4-methoxyphenylphosphine selenide

    Directory of Open Access Journals (Sweden)

    Melina Raymundo

    2016-08-01

    Full Text Available The title compound, C21H21O3PSe, is comprised of a P atom in a distorted tetrahedral environment, attached to the Se atom and three C atoms of the phenyl rings. The P—Se bond length is 2.1214 (12 Å. All three methoxy groups are near coplanar with their respective phenyl rings, with the angles between the phenyl ring and the C—O bond of the methoxy groups being 5.7 (2, 1.5 (4, and 5.7 (3°. The torsion angles of the phenyl rings relative to the P=Se bond are 35.62 (10, 35.07 (13, and 44.50 (11°. No strong intermolecular interactions were observed, but that in addition to van der Waals forces, there are C—H...π and C—H...Se close contacts.

  2. Tris(4-methylphenylphosphine selenide

    Directory of Open Access Journals (Sweden)

    Alfred Muller

    2011-01-01

    Full Text Available In the title molecule, C21H21PSe or PSe(C7H73, the P atom has a distorted PSeC3 tetrahedral environment, formed by the Se atom [P=Se = 2.1119 (5 Å] and three aryl rings. Two short intramolecular C—H...Se contacts occur. In the crystal, weak intermolecular C—H...Se interactions link the molecules into zigzag double chains propagating in [100]. The previous report of this structure [Zhdanov et al. (1953. Dokl. Akad. Nauk SSSR (Russ. (Proc. Nat. Acad. Sci. USSR, 92, 983–985] contained no geometrical data.

  3. Heteroepitaxy of gallium-selenide on silicon(100) and (111): New silicon-compatible semiconductor thin films for nano structure formation

    Science.gov (United States)

    Ohta, Taisuke

    Silicon has been the backbone of modern electronics for decades; however, it is not readily compatible with some new types of electronics, such as optoelectronics or spintronics. We aim at overcoming this limitation by combining gallium-selenide (GaxSey) materials with silicon (Si) through heteroepitaxial growth. GaxSey materials are compatible with Si, and are optically and potentially magnetically active semiconductors. Their unusual crystal structures, layered GaSe and defected zinc-blende Ga2Se 3, may be exploited for unprecedented nanostructure formations. This dissertation demonstrates that GaxSey thin films can be grown epitaxially on Si(100) and (111) substrates into various nanostructure forms, namely 0-dimensional (0-D) "dots", 1-D "wires", 2-D "layers", and 3-D "bulk". We have found that hexagonal layered GaSe is formed on Si(111) with or without arsenic termination (Si(111):As), and defected zinc-blende Ga2Se3 is formed on arsenic terminated Si(100) (Si(100):As). The surfaces of GaSe/Si(111) and Ga 2Se3/Si(100):As are covered by triangle nanodots and oriented nanowire structures, respectively. We propose that different symmetry and bonding of the substrate surfaces induces different configurations of vacancies, resulting in the distinct surface nanostructures. We have achieved a thorough understanding for nanostructure formations of GaxSey by considering vacancies and surfaces as additional "elements" for stabilizing the structures. In contrast to layered GaSe/Si(111), we have found that Ga2Se3-GaAs alloy is formed in a zinc-blende phase at the interface of GaSe/Si(111):As. This signifies the bonding configuration of each element is responsible for determining the local composition; however, the atomic arrangement defined by the substrate symmetry plays a more decisive role in selecting GaxSey crystal structure for Ga xSey/Si heteroepitaxy. Through this study, we propose a generalized concept describing the stable structures of the selenide materials

  4. ([M(NH{sub 3}){sub 6}][Ag{sub 4}M{sub 4}Sn{sub 3}Se{sub 13}]){sub ∞} (M=Zn, Mn): Three-dimensional chalcogenide frameworks constructed from quaternary metal selenide clusters with two different transition metals

    Energy Technology Data Exchange (ETDEWEB)

    Xiong, Wei-Wei [School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798 (Singapore); Miao, Jianwei [School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore 637459 (Singapore); Li, Pei-Zhou; Zhao, Yanli [Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371 (Singapore); Liu, Bin [School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore 637459 (Singapore); Zhang, Qichun, E-mail: qczhang@ntu.edu.sg [School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798 (Singapore)

    2014-10-15

    Herein we report solvothermal syntheses of two new three-dimensional chalcogenide frameworks ([M(NH{sub 3}){sub 6}][Ag{sub 4}M{sub 4}Sn{sub 3}Se{sub 13}]){sub n} (M=Zn (1), Mn (2)), which consist of quaternary metal selenide clusters with two different transition metals. The compounds represent the first Ag–Zn/Mn–Sn–Se based quaternary anionic frameworks. The optical studies show that the band gaps for 1 and 2 are 2.09 eV and 1.71 eV, respectively. Moreover, the photoelectrochemical study indicates that compound 1 displays n-type semiconducting behaviour and is photoactive under visible light illumination (λ>400 nm). - Graphical abstract: Two 3D framework selenides, [M(NH{sub 3}){sub 6}][Ag{sub 4}M{sub 4}Sn{sub 3}Se{sub 13}] (M=Zn (1), Mn (2)), constructed from quaternary metal selenide clusters, have been solvothermally synthesized and are photoactive under visible light illumination. - Highlights: • Two new three-dimensional selenide frameworks. • Quaternary metal selenide clusters with two different transition metals. • Photoelectrochemical study.

  5. Selectivity of bis-triazinyl bipyridine ligands for americium(III) in Am/Eu separation by solvent extraction. Part 1. Quantum mechanical study on the structures of BTBP complexes and on the energy of the separation.

    Science.gov (United States)

    Narbutt, Jerzy; Oziminski, Wojciech P

    2012-12-21

    Theoretical studies were carried out on two pairs of americium and europium complexes formed by tetra-N-dentate lipophilic BTBP ligands, neutral [ML(NO(3))(3)] and cationic [ML(2)](3+) where M = Am(III) or Eu(III), and L = 6,6'-bis-(5,6-diethyl-1,2,4-triazin-3-yl)-2,2'-bipyridine (C2-BTBP). Molecular structures of the complexes have been optimized at the B3LYP/6-31G(d) level and total energies of the complexes in various media were estimated using single point calculations performed at the B3LYP/6-311G(d,p) and MP2/6-311G(d,p) levels of theory. In the calculations americium and europium ions were treated using pseudo-relativistic Stuttgart-Dresden effective core potentials and the accompanying basis sets. Selectivity in solvent extraction separation of two metal ions is a co-operative function of contributions from all extractable metal complexes, which depend on physico-chemical properties of each individual complex and on its relative amount in the system. Semi-quantitative analysis of BTBP selectivity in the Am/Eu separation process, based on the contributions from the two pairs of Am(III) and Eu(III) complexes, has been carried out. To calculate the energy of Am/Eu separation, a model of the extraction process was used, consisting of complex formation in water and transfer of the formed complex to the organic phase. Under the assumptions discussed in the paper, this simple two-step model results in reliable values of the calculated differences in the energy changes for each pair of the Am/Eu complexes in both steps of the process. The greater thermodynamic stability (in water) of the Am-BTBP complexes, as compared with the analogous Eu species, caused by greater covalency of the Am-N than Eu-N bonds, is most likely the main reason for BTBP selectivity in the separation of the two metal ions. The other potential reason, i.e. differences in lipophilic properties of the analogous complexes of Am and Eu, is less important with regard to this selectivity.

  6. Synthesis and structure of an "iron-doped" copper selenide cluster molecule: [Cu30Fe2Se6(SePh)24(dppm)4].

    Science.gov (United States)

    Eichhöfer, Andreas; Olkowska-Oetzel, Jolanta; Fenske, Dieter; Fink, Karin; Mereacre, Valeriu; Powell, Annie K; Buth, Gernot

    2009-09-21

    CuCl and bis(diphenylphosphanyl)methane (dppm) react in the presence of small amounts of FeCl(3) with PhSeSiMe(3) and Se(SiMe(3))(2) to yield [Cu(30)Fe(2)Se(6)(SePh)(24)(dppm)(4)]. The crystal structure of the compound was determined by single-crystal X-ray analysis to give a mixed copper selenide/selenolate cluster molecule of a new structural type incorporating two central iron atoms. The formal oxidation state of the iron atoms was determined by Mössbauer spectroscopy to be +3, in agreement with quantum chemical calculations and modeling of the magnetic data. In addition, Mössbauer studies show no magnetic hyperfine structure in zero field, and the magnetically perturbed spectrum displays a pattern typical for a diamagnetic species in a transverse field, suggesting a singlet ground state. However, the inclusion of the iron atoms has a distinct influence on the optical properties of the compound compared to similar clusters containing only copper and selenium atoms.

  7. Characterizations of chemical bath-deposited zinc oxysulfide films and the effects of their annealing on copper-indium-gallium-selenide solar cell efficiency

    Science.gov (United States)

    Hsieh, Tsung-Min; Lue, Shingjiang Jessie; Ao, Jianping; Sun, Yun; Feng, Wu-Shiung; Chang, Liann-Be

    2014-01-01

    Zinc oxysulfide (Zn(S,O)) thin films are fabricated using a chemical bath deposition method onto glass substrates and the surface of copper-indium-gallium-selenide (CIGS) adsorption layers for solar cell fabrication. The light and electric properties of the Zn(S,O) layers are improved after rapid thermal annealing (RTA). The Zn(S,O) properties of samples annealed under various atmospheres are compared. The resulting annealed Zn(S,O) films are 80-100 nm thick. The band gap decreases from 3.8 eV to 3.3 eV and the light transmittance is improved by more than 95% after annealing under oxygen atmosphere. The oxygen-annealed sample has a S/(S + O) ratio of 0.28 and a S/Zn ratio of 0.72. The CIGS solar cell that consists of the annealed Zn(S,O) buffer layer is more efficient (6.15%) than that of the non-annealed Zn(S,O) (4.56%). The solar cell performance is correlated with the deposited Zn(S,O) characteristics. The significantly higher carrier concentration, increases light transmittance, and improves crystalline structure of the oxygen-annealed Zn(S,O) film contributes to the improved cell performance.

  8. Synthesis, crystal structure, and magnetic properties of quaternary iron selenides: Ba2FePnSe5 (Pn=Sb, Bi)

    Science.gov (United States)

    Wang, Jian; Greenfield, Joshua T.; Kovnir, Kirill

    2016-10-01

    Two new barium iron pnictide-selenides, Ba2FeSbSe5 and Ba2FeBiSe5, were synthesized by a high-temperature solid-state route and their crystal structures were determined using single crystal X-ray diffraction. Both compounds are isomorphic to the high pressure phase Ba3FeS5 and crystallize in the orthorhombic space group Pnma (No. 62) with cell parameters of a=12.603(2)/12.619(2) Å, b=9.106(1)/9.183(1) Å, c=9.145(1)/9.123(1) Å and Z=4 for Ba2FeSbSe5 and Ba2FeBiSe5, respectively. According to differential scanning calorimetry, Ba2FePnSe5 compounds exhibit high thermal stability and melt congruently at 1055(5) K (Pn=Sb) and 1105(5) K (Pn=Bi). Magnetic characterizations reveal strong antiferromagnetic nearest-neighbor interactions in both compounds resulting in an antiferromagnetic ordering at 58(1) K for Ba2FeSbSe5 and 79(2) K for Ba2FeBiSe5. The magnetic interactions between Fe3+ centers, which are at least 6 Å apart from each other, are mediated by superexchange interactions.

  9. Synthesis and magnetic structure of the layered manganese oxide selenide Sr2MnO2Ag1.5Se2

    Science.gov (United States)

    Blandy, Jack N.; Boskovic, Jelena C.; Clarke, Simon J.

    2017-01-01

    The synthesis of a high-purity sample of the layered oxide selenide Sr2MnO2Ag1.5Se2 is reported. At ambient temperature it crystallises in the space group I4/mmm with two formula units in the unit cell and lattice parameters a=4.08771(1) Å, c=19.13087(8) Å. The compound displays mixed-valent manganese in a formal oxidation state close to +2.5 and powder neutron diffraction measurements reveal that below the Néel temperature of 63(1) K this results in an antiferromagnetic structure which may be described as A-type, modelled in the magnetic space group PI4/mnc (128.410 in the Belov, Neronova and Smirnova (BNS) scheme) in which localised Mn moments of 3.99(2) μB are arranged in ferromagnetic layers which are coupled antiferromagnetically. In contrast to the isostructural compound Sr2MnO2Cu1.5S2, Sr2MnO2Ag1.5Se2 does not display long range ordering of coinage metal ions and vacancies, nor may significant amounts of the coinage metal readily be deintercalated using soft chemical methods.

  10. Cadmium telluride (CdTe) and cadmium selenide (CdSe) leaching behavior and surface chemistry in response to pH and O2.

    Science.gov (United States)

    Zeng, Chao; Ramos-Ruiz, Adriana; Field, Jim A; Sierra-Alvarez, Reyes

    2015-05-01

    Cadmium telluride (CdTe) and cadmium selenide (CdSe) are increasingly being applied in photovoltaic solar cells and electronic components. A major concern is the public health and ecological risks associated with the potential release of toxic cadmium, tellurium, and/or selenium species. In this study, different tests were applied to investigate the leaching behavior of CdTe and CdSe in solutions simulating landfill leachate. CdTe showed a comparatively high leaching potential. In the Toxicity Characteristic Leaching Procedure (TCLP) and Waste Extraction Test (WET), the concentrations of cadmium released from CdTe were about 1500 and 260 times higher than the regulatory limit (1 mg/L). In contrast, CdSe was relatively stable and dissolved selenium in both leaching tests was below the regulatory limit (1 mg/L). Nonetheless, the regulatory limit for cadmium was exceeded by 5- to 6- fold in both tests. Experiments performed under different pH and redox conditions confirmed a marked enhancement in CdTe and CdSe dissolution both at acidic pH and under aerobic conditions. These findings are in agreement with thermodynamic predictions. Taken as a whole, the results indicate that recycling of decommissioned CdTe-containing devices is desirable to prevent the potential environmental release of toxic cadmium and tellurium in municipal landfills.

  11. Use of radioanalytical methods for determination of uranium, neptunium, plutonium, americium and curium isotopes in radioactive wastes; Utilizacao de metodos radioanaliticos para a determinacao de isotopos de uranio, plutonio, americio e curio em rejeitos radioativos

    Energy Technology Data Exchange (ETDEWEB)

    Geraldo, Bianca

    2012-07-01

    Activated charcoal is a common type of radioactive waste that contains high concentrations of fission and activation products. The management of this waste includes its characterization aiming the determination and quantification of the specific radionuclides including those known as Difficult-to-Measure Radionuclides (RDM). The analysis of the RDM's generally involves complex radiochemical analysis for purification and separation of the radionuclides, which are expensive and time-consuming. The objective of this work was to define a methodology for sequential analysis of the isotopes of uranium, neptunium, plutonium, americium and curium present in a type of radioactive waste, evaluating chemical yield, analysis of time spent, amount of secondary waste generated and cost. Three methodologies were compared and validated that employ ion exchange (TI + EC), extraction chromatography (EC) and extraction with polymers (ECP). The waste chosen was the activated charcoal from the purification system of primary circuit water cooling the reactor IEA-R1. The charcoal samples were dissolved by acid digestion followed by purification and separation of isotopes with ion exchange resins, extraction and chromatographic extraction polymers. Isotopes were analyzed on an alpha spectrometer, equipped with surface barrier detectors. The chemical yields were satisfactory for the methods TI + EC and EC. ECP method was comparable with those methods only for uranium. Statistical analysis as well the analysis of time spent, amount of secondary waste generated and cost revealed that EC method is the most effective for identifying and quantifying U, Np, Pu, Am and Cm present in charcoal. (author)

  12. Template free-solvothermaly synthesized copper selenide (CuSe, Cu 2- xSe, β-Cu 2Se and Cu 2Se) hexagonal nanoplates from different precursors at low temperature

    Science.gov (United States)

    Kumar, Pushpendra; Singh, Kedar; Srivastava, O. N.

    2010-09-01

    Nonstoichiometric (Cu 2- xSe) and stoichiometric (CuSe, β-Cu 2Se and Cu 2Se) copper selenide hexagonal nanoplates have been synthesized using different general and convenient copper sources, e.g. copper chloride, copper sulphate, copper nitrate, copper acetate, elemental copper with elemental selenium, friendly ethylene glycol and hydrazine hydrate in a defined amount of water at 100 °C within 12 h adopting the solvothermal method. Phase analysis, purity and morphology of the product have been well studied by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray diffraction (EDAX) techniques. The structural and compositional analysis revealed that the products were of pure phase with corresponding atomic ratios. SEM, TEM and HRTEM analyses revealed that the nanoplates were in the range 200-450 nm and the as-prepared products were uniform and highly crystallized. The nanoplates consisted of {0 0 1} facets of top-bottom surfaces and {1 1 0} facets of the other six side surfaces. This new approach encompasses many advantages over the conventional solvothermal method in terms of product quality (better morphology control with high yield) and reaction conditions (lower temperatures). Copper selenide hexagonal nanoplates obtained by the described method could be potential building blocks to construct functional devices and solar cell. This work may open up a new rationale on designing the solution synthesis of nanostructures for materials possessing similar intrinsic crystal symmetry. On the basis of the carefully controlled experiments mentioned herein, a plausible formation mechanism of the hexagonal nanoplates was suggested and discussed. To the best of our knowledge, this is the first report on nonstoichiometric (Cu 2- xSe) as well as stoichiometric (CuSe, β-Cu 2Se and Cu 2Se) copper selenide hexagonal nanoplates with

  13. Determination of the some electronic parameters of nanostructure copper selenide and Cu/Cu{sub 3}Se{sub 2}/n-GaAs/In structure

    Energy Technology Data Exchange (ETDEWEB)

    Güzeldir, B.; Sağlam, M. [Department of Physics, Faculty of Sciences, Atatürk University, 25240 Erzurum (Turkey); Ateş, A. [Department of Material Engineering, Faculty of Engineering and Natural Sciences, Yıldırım Beyazıt University, Ankara (Turkey); Türüt, A. [Department of Physics Engineering, Faculty of Sciences, Istanbul Medeniyet University, 34000 Istanbul (Turkey)

    2015-04-05

    Highlights: • Introducing to a new degree of freedom in the control of effective barrier height by using Cu. • We want to experimentally observe whether or not the diode continues the ideality in the temperature range of 60–400 K. • We have modified the Richardson’s plot using the temperature dependent values of effective area of the patches. - Abstract: The nanostructure copper selenide thin film has been grown on n-type gallium arsenide substrate by Successive Ionic Layer Adsorption and Reaction (SILAR) method. The film has been characterized by X-ray Diffraction (XRD), Scanning Electron Microscope (SEM) and Atomic Force Microscope (AFM) measurements. X-ray diffraction analysis of the film confirms a polycrystalline with preferred orientation. The AFM and SEM micrographs of the film reveal smooth and uniform surface pattern without any dark pits, pinholes and microcracks. The Cu/Cu{sub 3}Se{sub 2}/n-GaAs/In structure has been thermally formed in evaporating system after the SILAR process. The electrical analysis of Cu/Cu{sub 3}Se{sub 2}/n-GaAs/In structure has been investigated by means of current–voltage (I–V) measurements in the temperature range of 60–400 K in dark conditions. The values of barrier height (BH) and ideality factor (n) ranged from 0.21 eV and 4.97 (60 K) to 0.83 eV and 1.14 (400 K), respectively. In the calculations, the electrical parameters of the experimental forward bias I–V characteristics of the Cu/Cu{sub 3}Se{sub 2}/n-GaAs/In with the homogeneity in the 60–400 K range have been explained by means of the thermionic emission (TE), considering Gaussian distribution (GD) of BH with linear bias dependence.

  14. Characterization of copper selenide thin film hole-injection layers deposited at room temperature for use with p-type organic semiconductors

    Science.gov (United States)

    Hiramatsu, Hidenori; Koizumi, Ikue; Kim, Ki-Beom; Yanagi, Hiroshi; Kamiya, Toshio; Hirano, Masahiro; Matsunami, Noriaki; Hosono, Hideo

    2008-12-01

    Copper selenide, CuxSe(x ˜2), was examined as a hole-injection layer for low-temperature organic devices. Crystalline CuxSe films grown at room temperature with atomically flat surfaces exhibited metallic conduction with a high electrical conductivity of 4.5×103 S/cm, a hole concentration of 1.4×1022 cm-3, and a mobility of 2.0 cm2/(V s). Analysis of the free carrier absorption using the Drude model estimated the effective mass of a hole as 1.0me. Photoemission spectroscopy measurements of the interfaces between CuxSe and organic hole transport layers, N ,N'-bis(naphthalen-1-yl)-N ,N'-bis(phenyl) benzidine (NPB) and copper phthalocyanine (CuPc), verified that the hole-injection barriers of these interfaces (0.4 eV for NPB and 0.3 eV for CuPc) are smaller than that of a conventional indium tin oxide (ITO) hole-injection electrode/NPB interface (0.6 eV) but are comparable to that of an ITO electrode/CuPc interface (0.3 eV). Hole-only devices using the CuxSe layer as a hole-injection anode exhibited very low threshold voltages (0.4-0.5 V) and nearly Ohmic characteristics. The NPB layer on the CuxSe layer was found to be highly doped at 1017-1019 cm-3, probably due to copper diffusion, while the CuPc layer is nearly intrinsic with a doping concentration lower than 1015 cm-3. These results indicated that a CuxSe film combined with CuPc is a promising candidate for a low-voltage hole-injection anode or a buffer layer in low-temperature devices such as organic light-emitting diodes and thin film transistors.

  15. Influence of the substrate temperature on the structural, optical, and electrical properties of tin selenide thin films deposited by thermal evaporation method

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, N.; Sharma, V.; Padha, N. [Department of Physics and Electronics, Dr. Ambedkar Road, University of Jammu, Jammu-180 006, Jammu and Kashmir State (India); Shah, N.M.; Desai, M.S.; Panchal, C.J. [Applied Physics Department, Faculty of Technology and Engineering, M. S. University of Baroda, Vadodara-390 001, Gujarat State (India); Protsenko, I.Yu. [Appl. Physics Dept., Faculty of Electronic and Information Technologies, Sumy State University (Ukraine)

    2010-01-15

    Thin films of tin selenide (SnSe) were deposited on sodalime glass substrates, which were held at different temperatures in the range of 350-550 K, from the pulverized compound material using thermal evaporation method. The effect of substrate temperature (T{sub s}) on the structural, morphological, optical, and electrical properties of the films were investigated using x-ray diffraction analysis (XRD), scanning electron microscopy (SEM), transmission measurements, and Hall-effect characterization techniques. The temperature dependence of the resistance of the films was also studied in the temperature range of 80-330 K. The XRD spectra and the SEM image analyses suggest that the polycrystalline thin films having uniform distribution of grains along the (111) diffraction plane was obtained at all T{sub s}. With the increase of T{sub s} the intensity of the diffraction peaks increased and well-resolved peaks at 550 K, substrate temperature, were obtained. The analysis of the data of the optical transmission spectra suggests that the films had energy band gap in the range of 1.38-1.18 eV. Hall-effect measurements revealed the resistivity of films in the range 112-20 {omega} cm for films deposited at different T{sub s}. The activation energy for films deposited at different T{sub s} was in the range of 0.14 eV-0.28 eV as derived from the analysis of the data of low-temperature resistivity measurements. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  16. Functionalization based on the substitutional flexibility: strong middle IR nonlinear optical selenides AX(II)(4)X(III)(5)Se12.

    Science.gov (United States)

    Lin, Hua; Chen, Ling; Zhou, Liu-Jiang; Wu, Li-Ming

    2013-08-28

    Seven nonlinear optical (NLO) active selenides in the middle IR region, AX(II)4X(III)5Se12 (A = K(+)-Cs(+); X(II) = Mn(2+), Cd(2+); X(III) = Ga(3+), In(3+)) adopting the KCd4Ga5S12-type structure, have been synthesized by high-temperature solid-state reaction of an elemental mixture with ACl flux. Their three-dimensional network structures are stacked by M9Se24-layers of vertex sharing MSe4 tetrahedra, of which each center is jointly occupied by X(II) and X(III) atoms. Studies suggest that such tetrahedral building units can be regarded as the "multi-functional sites", on which the Cd(2+)/Ga(3+) pair gives rise to the coexistence of NLO and thermochromic properties, and the Mn(2+)/In(3+) pair leads to the coexistence of NLO and magnetic properties. The density functional theory (DFT) studies and the cutoff-energy-dependent NLO coefficient analyses reveal that such "multi-functional sites" contribute to the origin of the second harmonic generation (SHG) that is ascribed to the electronic transitions from the Se-4p states to the ns, np states of X(II) and X(III) atoms. Remarkably, title compounds show very strong SHG at an incident wavelength of 2.05 μm, roughly 16-40 times that of commercial AgGaS2; among them, ACd4In5Se12 (A = Rb, Cs) represents the strongest SHG among chalcogenides to date.

  17. Cyclopalladation of dimesityl selenide: synthesis, reactivity, structural characterization, isolation of an intermediate complex with C-H···Pd intra-molecular interaction and computational studies.

    Science.gov (United States)

    Kolay, Siddhartha; Wadawale, Amey; Das, Dasarathi; Kisan, Hemanta K; Sunoj, Raghavan B; Jain, Vimal K

    2013-08-14

    The reaction of dimesityl selenide (Mes2Se) with either PdCl2(PhCN)2 in toluene or PdCl2 in toluene-acetonitrile yields a chloro-bridged binuclear palladium complex, [Pd2Cl2(μ-Cl)2(Mes2Se)2] (1), whereas with Na2PdCl4 in refluxing ethanol, a cyclometallated palladium complex, [Pd2(μ-Cl)2{MesSeC6H2(Me2)CH2}2] (2) is afforded. 2 can also be obtained when 1 is refluxed in ethanol. On treatment with Pb(Epy)2 in dichloromethane, 2 afforded the Epy-bridged binuclear complexes, [Pd2(μ-Epy)2{MesSeC6H2(Me2)CH2}2] (3; E = S (3a) or Se (3b)). Treatment of 2 with PPh3 yields a bridge-cleaved monomeric complex, [PdCl{MesSeC6H2(Me2)CH2}(PPh3)]. The molecular structures of 1-3 were established by X-ray diffraction analyses. All the complexes are dimeric, with the palladium atoms acquiring a distorted square planar configuration. There are intra-molecular C-H···Pd interactions (d(M-H): 2.75 Å and

  18. Microbial toxicity of ionic species leached from the II-VI semiconductor materials, cadmium telluride (CdTe) and cadmium selenide (CdSe).

    Science.gov (United States)

    Ramos-Ruiz, Adriana; Zeng, Chao; Sierra-Alvarez, Reyes; Teixeira, Luiz H; Field, Jim A

    2016-11-01

    This work investigated the microbial toxicity of soluble species that can potentially be leached from the II-VI semiconductor materials, cadmium telluride and cadmium selenide. The soluble ions tested included: cadmium, selenite, selenate, tellurite, and tellurate. Their toxicity towards the acetoclastic and hydrogen-consuming trophic groups in a methanogenic consortium as well as towards a bioluminescent marine bacterium, Aliivibrio fischeri (Microtox(®) test), was assessed. The acetoclastic methanogenic activity was the most affected as evidenced by the low 50% inhibiting concentrations (IC50) values obtained of 8.6 mg L(-1) for both cadmium and tellurite, 10.2 mg L(-1) for tellurate, and 24.1 mg L(-1) for selenite. Both tellurium oxyanions caused a strong inhibition of acetoclastic methanogenesis at low concentrations, each additional increment in concentration provided progressively less inhibition increase. In the case of the hydrogenotrophic methanogenesis, cadmium followed by selenite caused the greatest inhibition with IC50 values of 2.9 and 18.0 mg L(-1), respectively. Tellurite caused a moderate effect as evidenced by a 36.8% inhibition of the methanogenic activity at the highest concentration tested, and a very mild effect of tellurate was observed. Microtox(®) analyses showed a noteworthy inhibition of cadmium, selenite, and tellurite with 50% loss in bioluminescence after 30 min of exposure of 5.5, 171.1, and 458.6 mg L(-1), respectively. These results suggest that the leaching of cadmium, tellurium and selenium ions from semiconductor materials can potentially cause microbial toxicity.

  19. Optical phonons in nanostructured thin films composed by zincblende zinc selenide quantum dots in strong size-quantization regime: Competition between phonon confinement and strain-related effects

    Energy Technology Data Exchange (ETDEWEB)

    Pejova, Biljana, E-mail: biljana@pmf.ukim.mk

    2014-05-01

    Raman scattering in combination with optical spectroscopy and structural studies by X-ray diffraction was employed to investigate the phonon confinement and strain-induced effects in 3D assemblies of variable-size zincblende ZnSe quantum dots close packed in thin film form. Nanostructured thin films were synthesized by colloidal chemical approach, while tuning of the nanocrystal size was enabled by post-deposition thermal annealing treatment. In-depth insights into the factors governing the observed trends of the position and half-width of the 1LO band as a function of the average QD size were gained. The overall shifts in the position of 1LO band were found to result from an intricate compromise between the influence of phonon confinement and lattice strain-induced effects. Both contributions were quantitatively and exactly modeled. Accurate assignments of the bands due to surface optical (SO) modes as well as of the theoretically forbidden transverse optical (TO) modes were provided, on the basis of reliable physical models (such as the dielectric continuum model of Ruppin and Englman). The size-dependence of the ratio of intensities of the TO and LO modes was studied and discussed as well. Relaxation time characterizing the phonon decay processes in as-deposited samples was found to be approximately 0.38 ps, while upon post-deposition annealing already at 200 °C it increases to about 0.50 ps. Both of these values are, however, significantly smaller than those characteristic for a macrocrystalline ZnSe sample. - Graphical abstract: Optical phonons in nanostructured thin films composed by zincblende zinc selenide quantum dots in strong size-quantization regime: competition between phonon confinement and strain-related effects. - Highlights: • Phonon confinement vs. strain-induced effects in ZnSe 3D QD assemblies were studied. • Shifts of the 1LO band result from an intricate compromise between the two effects. • SO and theoretically forbidden TO modes were

  20. Optimization of Electrochemically Deposited Highly Doped ZnO Bilayers on Ga-Rich Chalcopyrite Selenide for Cost-Effective Photovoltaic Device Technology

    Directory of Open Access Journals (Sweden)

    Dimitra N. Papadimitriou

    2016-11-01

    Full Text Available High quality polycrystalline bilayers of aluminium doped ZnO (Al:ZnO were successively electrodeposited in the form of columnar structures preferentially oriented along the ( 10 1 ¯ 1 crystallographic direction from aqueous solution of zinc nitrate (Zn(NO32 at negative electrochemical potential of EC = (−0.8–(−1.2 V and moderate temperature of 80 °C on gallium rich (30% Ga chalcopyrite selenide Cu(In,GaSe2 (CIGS with chemically deposited ZnSe buffer (ZnSe/Cu(In,GaSe2/Mo/glass. The aluminium doped ZnO layer properties have initially been probed by deposition of Al:ZnO/i-ZnO bilayers directly on Mo/glass substrates. The band-gap energy of the Al:ZnO/i-ZnO reference layers was found to vary from 3.2 to 3.7 eV by varying the AlCl3 solute dopant concentration from 1 to 20 mM. The electrical resistivity of indium-pellet contacted highly doped Al:ZnO sheet of In/Al:ZnO/i-ZnO/Mo/glass reference samples was of the order ρ ~10−5 Ω·cm; the respective carrier concentration of the order 1022 cm−3 is commensurate with that of sputtered Al:ZnO layers. For crystal quality optimization of the bilayers by maintenance of the volatile selenium content of the chalcopyrite, they were subjected to 2-step annealing under successive temperature raise and N2 flux regulation. The hydrostatic compressive strain due to Al3+ incorporation in the ZnO lattice of bilayers processed successively with 5 and 12 mM AlCl3 dopant was εh = −0.046 and the respective stress σh = −20 GPa. The surface reflectivity of maximum 5% over the scanned region of 180–900 nm and the (optical band gap of Eg = 3.67 eV were indicative of the high optical quality of the electrochemically deposited (ECD Al:ZnO bilayers.

  1. Study on the Synthesis Processing and Content Determination of Corn Silk Polysaccharide Selenide%硒化玉米须多糖的工艺条件及硒含量测定研究

    Institute of Scientific and Technical Information of China (English)

    侯巍; 朱小庆; 楚婧; 高金波

    2012-01-01

    OBJECTIVE Using the polysaccharide from corn silk as the raw material, to study the selenizing process with sodium selenite. METHODS Selenizing conditions were established by single factor and orthogonal design; determining content of polysaccharide selenide by Se( IV )-KSCN-MV extraction spectrophotometry; characterizing the structure of polysaccharide selenide by IR. RESULTS The optimal conditions were: 70 ℃ reaction temperature, 8 hours reaction time, mass ratio of com silk polysaccharide to sodium selenite 1 : 1.2, 0.3% HNO3 of volume fraction. The average content of selenium in corn silk polysaccharide was over 3.17 mg·g‐1 and average yield was 35.72%. IR results showed that corn silk polysaccharide contained Se=O and Se-C. CONCLUSION Corn silk polysaccharide selenide is successfully synthesized and the study provides the foundation for further study and exploiting for corn silk.%目的 以玉米须多糖为原料,用亚硒酸钠进行玉米须多糖的硒化研究.方法 利用单因素和正交试验确立硒化的最佳工艺条件;利用硒-硫氰酸钾-甲基紫萃取光度法测定硒多糖中的硒含量,并通过红外光谱对硒多糖进行了初步表征.结果 最佳工艺条件为反应温度70℃,反应时间8h,玉米须多糖与亚硒酸钠质量比为1∶1.2,硝酸体积分数为0.3%,玉米须硒多糖中硒含量为3.17 mg·g-1,平均收率为35.72%.红外光谱显示:玉米须硒多糖中含有Se=O键和Se-C键.结论 利用该工艺成功合成了玉米须硒多糖,为玉米须的开发和利用奠定基础.

  2. Syntheses, structures, and optical properties of the indium/germanium selenides Cs4In8GeSe16, CsInSe2, and CsInGeSe4

    Science.gov (United States)

    Ward, Matthew D.; Pozzi, Eric A.; Van Duyne, Richard P.; Ibers, James A.

    2014-04-01

    The three solid-state indium/germanium selenides Cs4In8GeSe16, CsInSe2, and CsInGeSe4 have been synthesized at 1173 K. The structure of Cs4In8GeSe16 is a three-dimensional framework whereas those of CsInSe2 and CsInGeSe4 comprise sheets separated by Cs cations. Both Cs4In8GeSe16 and CsInGeSe4 display In/Ge disorder. From optical absorption measurements these compounds have band gaps of 2.20 and 2.32 eV, respectively. All three compounds are charge balanced.

  3. Syntheses, structures, and optical properties of the indium/germanium selenides Cs{sub 4}In{sub 8}GeSe{sub 16}, CsInSe{sub 2}, and CsInGeSe{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Ward, Matthew D.; Pozzi, Eric A.; Van Duyne, Richard P.; Ibers, James A., E-mail: ibers@chem.northwestern.edu

    2014-04-01

    The three solid-state indium/germanium selenides Cs{sub 4}In{sub 8}GeSe{sub 16}, CsInSe{sub 2}, and CsInGeSe{sub 4} have been synthesized at 1173 K. The structure of Cs{sub 4}In{sub 8}GeSe{sub 16} is a three-dimensional framework whereas those of CsInSe{sub 2} and CsInGeSe{sub 4} comprise sheets separated by Cs cations. Both Cs{sub 4}In{sub 8}GeSe{sub 16} and CsInGeSe{sub 4} display In/Ge disorder. From optical absorption measurements these compounds have band gaps of 2.20 and 2.32 eV, respectively. All three compounds are charge balanced. - Graphical abstract: Structure of Cs{sub 4}In{sub 8}GeSe{sub 16}. - Highlights: • The solid-state In/Ge selenides Cs{sub 4}In{sub 8}GeSe{sub 16}, CsInSe{sub 2}, and CsInGeSe{sub 4} have been synthesized. • Both Cs{sub 4}In{sub 8}GeSe{sub 16} and CsInGeSe{sub 4} display In/Ge disorder. • Cs{sub 4}In{sub 8}GeSe{sub 16} and CsInGeSe{sub 4} have band gaps of 2.20 eV and 2.32 eV, respectively.

  4. Quijarroite, Cu6HgPb2Bi4Se12, a New Selenide from the El Dragόn Mine, Bolivia

    Directory of Open Access Journals (Sweden)

    Hans-Jürgen Förster

    2016-11-01

    Full Text Available Quijarroite, ideally Cu6HgPb2Bi4Se12, is a new selenide species from the El Dragόn mine, Department of Potosí, Bolivia. It most frequently occurs as lath-shaped thin plates (up to 150 µm in length and 20 µm in width intimately (subparallel intergrown with hansblockite, forming an angular network-like intersertal texture. Quijarroite is occasionally also present as sub- to anhedral grains up to 200 µm in length and 50 µm in width. It is non-fluorescent, black and opaque with a metallic luster and black streak. It is brittle, with an irregular fracture and no obvious cleavage and parting. In plane-polarized incident light, quijarroite is weakly pleochroic from cream to very slightly more brownish-cream, displaying no internal reflections. Between crossed polars, quijarroite is moderately anisotropic with pale orange-brown to blue rotation tints. Lamellar twinning on {110} is common; parquet twinning occurs rarely. The reflectance values in the air for the COM (Commission on Ore Mineralogy standard wavelengths (R1 and R2 are: 46.7, 46.8 (470 nm, 47.4, 48.2 (546 nm, 47.1, 48.5 (589 nm, and 46.6, 48.7 (650 nm. Electron-microprobe analyses yielded a mean composition of Cu 13.34, Ag 1.02, Hg 7.67, Pb 16.87, Co 0.03, Ni 0.15, Bi 27.65, Se 33.52, total 100.24 wt %. The mean empirical formula, normalized to 25 apfu (atoms per formula unit, is (Cu5.84Ag0.26Σ = 6.10(Hg1.06Ni0.07Co0.01Σ = 1.14Pb2.27Bi3.68Se11.81 (n = 24. The simplified formula is Cu6HgPb2Bi4Se12. Quijarroite is orthorhombic, space group Pmn21, with a = 9.2413(8, b = 9.0206(7, c = 9.6219(8 Å, V = 802.1(1 Å3, Z = 1. The calculated density is 5.771 g·cm−3. The five strongest X-ray powder-diffraction lines (d in Å (I/I0 (hkl are: 5.36 (55 (111, 3.785 (60 (211, 3.291 (90 (022, 3.125 (100 (212, and 2.312 (50 (400. The crystal structure of quijarroite can be considered a galena derivative and could be derived from that of bournonite. It is a primary mineral, deposited from an

  5. Delocalization and new phase in Americium: theory

    Energy Technology Data Exchange (ETDEWEB)

    Soderlind, P

    1999-04-23

    Density-functional electronic structure calculations have been used to investigate the high pressure behavior of Am. At about 80 kbar (8 GPa) calculations reveal a monoclinic phase similar to the ground state structure of plutonium ({alpha}-Pu). The experimentally suggested {alpha}-U structure is found to be substantially higher in energy. The phase transition from fcc to the low symmetry structure is shown to originate from a drastic change in the nature of the electronic structure induced by the elevated pressure. A calculated volume collapse of about 25% is associated with the transition. For the low density phase, an orbital polarization correction to the local spin density (LSD) theory was applied. Gradient terms of the electron density were included in the calculation of the exchange/correlation energy and potential, according to the generalized gradient approximation (GGA). The results are consistent with a Mott transition; the 5f electrons are delocalized and bonding on the high density side of the transition and chemically inert and non-bonding (localized) on the other. Theory compares rather well with recent experimental data which implies that electron correlation effects are reasonably modeled in our orbital polarization scheme.

  6. The proliferation potential of neptunium and americium

    Energy Technology Data Exchange (ETDEWEB)

    An, J. S.; Shin, J. S.; Kim, J. S.; Kwack, E. H.; Kim, B. K

    2000-05-01

    It is recognized that some trans-uranic elements other than plutonium, in particular Np and Am, if will be available in sufficient quantities, could be used for nuclear explosive devices. The spent fuel has been accumulating in number of nuclear power plant and operation of large scale commercial reprocessing plants. However, these materials are not covered by the definition of special fissionable material in the Agency Statute. At the time when the Statute was adopted, the availability of meaningful quantities of separated Np and Am was remote and they were not included in the definition of special fissionable material. Then, IAEA Board decided a measure for control of Np and Am on September 1999. This report contains the control method and the characteristic of Np and Am for using domestic nuclear industries, and it can be useful for understanding how to report and account of Np and Am. (author)

  7. Evaluation of neutron data for americium-241

    Energy Technology Data Exchange (ETDEWEB)

    Maslov, V.M.; Sukhovitskij, E.Sh.; Porodzinskij, Yu.V.; Klepatskij, A.B.; Morogovskij, G.B. [Radiation Physics and Chemistry Problems Inst., Minsk-Sosny (Belarus)

    1997-03-01

    The evaluation of neutron data for {sup 241}Am is made in the energy region from 10{sup -5} eV up to 20 MeV. The results of the evaluation are compiled in the ENDF/B-VI format. This work is performed under the Project Agreement CIS-03-95 with the International Science and Technology Center (Moscow). The Financing Party for the Project is Japan. The evaluation was requested by Y. Kikuchi (JAERI). (author). 60 refs.

  8. Synthesis, structures and DFT calculations of 2-(4,6-dimethyl pyrimidyl)selenolate complexes of Cu(I), Ag(I) and Au(I) and their conversion into metal selenide nanocrystals.

    Science.gov (United States)

    Sharma, Rakesh K; Wadawale, Amey; Kedarnath, G; Manna, Debashree; Ghanty, Tapan K; Vishwanadh, B; Jain, Vimal K

    2014-05-07

    The complexes [M{SeC4H(Me-4,6)2N2}]6 (M = Cu (1), Ag (2)) and [Au{SeC4H(Me-4,6)2N2}(PEt3)] (3) have been prepared and characterized by elemental analyses, UV-vis, NMR ((1)H, (13)C, (77)Se) spectroscopy and single crystal X-ray diffraction. The crystal structures of [Cu{SeC4H(Me-4,6)2N2}]6·H2O (1·H2O), [Ag{SeC4H(Me-4,6)2N2}]6·6MeOH·H2O (2·6MeOH·H2O) and [Au{SeC4H(Me-4,6)2N2}(PEt3)] (3) revealed that their metal centers acquire distorted square-pyramidal, trigonal and linear geometries, respectively. DFT calculations have been carried out to rationalize nuclearity in copper(i) chalcogenolate complexes. The calculations suggest that there is hardly any energy difference between the tetrameric and hexameric forms. Thermal behavior of [Cu{SeC4H(Me-4,6)2N2}]6 was studied by thermogravimetric analysis. Thermolysis of [M{SeC4H(Me-4,6)2N2}]6 (M = Cu, Ag) in 1-dodecanethiol (DDT) at 150 °C gave a cubic phase of Cu7Se4 and an orthorhombic phase of Ag2Se, respectively. Copper selenide (Cu7Se4) thin films were deposited on glass and silicon substrates by using [Cu{SeC4H(Me-4,6)2N2}]6 at 400 °C by AACVD.

  9. Crystal structures of the four new quaternary copper(I)-selenides A0.5CuZrSe3 and ACuYSe3(A=Sr, Ba)

    Science.gov (United States)

    Maier, Stefan; Prakash, Jai; Berthebaud, David; Perez, Olivier; Bobev, Svilen; Gascoin, Franck

    2016-10-01

    The four new quaternary copper(I)-selenides, Sr0.5CuZrSe3 (a=3.8386(7), b=14.197(2), c=10.1577(17) Å), Ba0.5CuZrSe3 (a=3.8386(7), b=14.196(2), c=10.1577(17) Å), SrCuYSe3 (a=10.620(2), b=4.1000(8), c=13.540(3) Å) and BaCuYSe3 (a=4.1800(7), b=13.940(2), c=10.6200(17) Å) were synthesized by high-temperature solid state reactions and their crystal structures were determined using single-crystal X-ray diffraction. A0.5CuZrSe3 (A= Sr, Ba) and BaCuYSe3 crystallize in the KCuZrS3 structure type (Cmcm), while SrCuYSe3 is isostructural to Eu2CuS3 (Pnma). All compounds form layered structures in which the charge of the - ∞ 2[CuZrSe3 and 2 - ∞ 2[CuYSe3 ] layers as well as the site occupancy of the A cations depend on the transition metal. Combining the alkaline earth metals Sr and Ba with tetravalent Zr leads to the formation of cation vacancies between the - ∞ 2[CuZrSe3 ] layers and structure type as well as symmetry are determined by the ratio between the cation and transition metal ionic radii r(A2+)/r(M3+/4+).

  10. Improving the efficiency of copper indium gallium (Di-selenide (CIGS solar cells through integration of a moth-eye textured resist with a refractive index similar to aluminum doped zinc oxide

    Directory of Open Access Journals (Sweden)

    M. Burghoorn

    2014-12-01

    Full Text Available Textured transparent conductors are widely used in thin-film silicon solar cells. They lower the reflectivity at interfaces between different layers in the cell and/or cause an increase in the path length of photons in the Si absorber layer, which both result in an increase in the number of absorbed photons and, consequently, an increase in short-circuit current density (Jsc and cell efficiency. Through optical simulations, we recently obtained strong indications that texturing of the transparent conductor in copper indium gallium (di-selenide (CIGS solar cells is also optically advantageous. Here, we experimentally demonstrate that the Jsc and efficiency of CIGS solar cells with an absorber layer thickness (dCIGS of 0.85 μm, 1.00 μm and 2.00 μm increase through application of a moth-eye textured resist with a refractive index that is sufficiently similar to AZO (nresist = 1.792 vs. nAZO = 1.913 at 633 nm to avoid large optical losses at the resist-AZO interface. On average, Jsc increases by 7.2%, which matches the average reduction in reflection of 7.0%. The average relative increase in efficiency is slightly lower (6.0%. No trend towards a larger relative increase in Jsc with decreasing dCIGS was observed. Ergo, the increase in Jsc can be fully explained by the reduction in reflection, and we did not observe any increase in Jsc based on an increased photon path length.

  11. Improving the efficiency of copper indium gallium (Di-)selenide (CIGS) solar cells through integration of a moth-eye textured resist with a refractive index similar to aluminum doped zinc oxide

    Energy Technology Data Exchange (ETDEWEB)

    Burghoorn, M.; Kniknie, B.; Deelen, J. van; Ee, R. van [The Netherlands Organisation for Applied Scientific Research (TNO), De Rondom 1, 5612 AP, Eindhoven (Netherlands); Xu, M. [The Netherlands Organisation for Applied Scientific Research (TNO), De Rondom 1, 5612 AP, Eindhoven (Netherlands); Delft University of Technology, Optics Group, Van der Waalsweg 8, 2628 CH, Delft (Netherlands); Vroon, Z. [The Netherlands Organisation for Applied Scientific Research (TNO), De Rondom 1, 5612 AP, Eindhoven (Netherlands); Zuyd Hogeschool, Nieuw Eyckholt 300, 6419 DJ, Heerlen (Netherlands); Belt, R. van de [Kriya Materials BV, Urmonderbaan 22, 6167 RD, Geleen (Netherlands); Buskens, P., E-mail: pascal.buskens@tno.nl, E-mail: buskens@dwi.rwth-aachen.de [The Netherlands Organisation for Applied Scientific Research (TNO), De Rondom 1, 5612 AP, Eindhoven (Netherlands); DWI – Leibniz Institute for Interactive Materials, Forckenbeckstrasse 50, 52056, Aachen (Germany)

    2014-12-15

    Textured transparent conductors are widely used in thin-film silicon solar cells. They lower the reflectivity at interfaces between different layers in the cell and/or cause an increase in the path length of photons in the Si absorber layer, which both result in an increase in the number of absorbed photons and, consequently, an increase in short-circuit current density (J{sub sc}) and cell efficiency. Through optical simulations, we recently obtained strong indications that texturing of the transparent conductor in copper indium gallium (di-)selenide (CIGS) solar cells is also optically advantageous. Here, we experimentally demonstrate that the J{sub sc} and efficiency of CIGS solar cells with an absorber layer thickness (d{sub CIGS}) of 0.85 μm, 1.00 μm and 2.00 μm increase through application of a moth-eye textured resist with a refractive index that is sufficiently similar to AZO (n{sub resist} = 1.792 vs. n{sub AZO} = 1.913 at 633 nm) to avoid large optical losses at the resist-AZO interface. On average, J{sub sc} increases by 7.2%, which matches the average reduction in reflection of 7.0%. The average relative increase in efficiency is slightly lower (6.0%). No trend towards a larger relative increase in J{sub sc} with decreasing d{sub CIGS} was observed. Ergo, the increase in J{sub sc} can be fully explained by the reduction in reflection, and we did not observe any increase in J{sub sc} based on an increased photon path length.

  12. Improving the efficiency of copper indium gallium (Di-)selenide (CIGS) solar cells through integration of a moth-eye textured resist with a refractive index similar to aluminum doped zinc oxide

    Science.gov (United States)

    Burghoorn, M.; Kniknie, B.; van Deelen, J.; Xu, M.; Vroon, Z.; van Ee, R.; van de Belt, R.; Buskens, P.

    2014-12-01

    Textured transparent conductors are widely used in thin-film silicon solar cells. They lower the reflectivity at interfaces between different layers in the cell and/or cause an increase in the path length of photons in the Si absorber layer, which both result in an increase in the number of absorbed photons and, consequently, an increase in short-circuit current density (Jsc) and cell efficiency. Through optical simulations, we recently obtained strong indications that texturing of the transparent conductor in copper indium gallium (di-)selenide (CIGS) solar cells is also optically advantageous. Here, we experimentally demonstrate that the Jsc and efficiency of CIGS solar cells with an absorber layer thickness (dCIGS) of 0.85 μm, 1.00 μm and 2.00 μm increase through application of a moth-eye textured resist with a refractive index that is sufficiently similar to AZO (nresist = 1.792 vs. nAZO = 1.913 at 633 nm) to avoid large optical losses at the resist-AZO interface. On average, Jsc increases by 7.2%, which matches the average reduction in reflection of 7.0%. The average relative increase in efficiency is slightly lower (6.0%). No trend towards a larger relative increase in Jsc with decreasing dCIGS was observed. Ergo, the increase in Jsc can be fully explained by the reduction in reflection, and we did not observe any increase in Jsc based on an increased photon path length.

  13. 压力下碱金属铁硒基超导体中的现象与物理∗%Phenomena and findings in pressurized alkaline iron selenide sup erconductors

    Institute of Scientific and Technical Information of China (English)

    郭静; 孙力玲

    2015-01-01

    In the frontiers of condensed matter physics, pressure is widely adopted as an independent control parameter for tuning states of matters and plays an important role in finding new phenomena and corresponding physics, as well as in testing the relevant theories. Remarkably, a great deal of success has been achieved in searching for new superconductors and uncovering the microphysics for known superconductors. In this brief review, we attempt to describe the progress in high pressure studies of alkaline selenide superconductors AxFe2−ySe2 (A=K, Rb, Tl/Rb). The high-pressure studies of Tl0.6Rb0.4Fe1.67Se2, K0.8Fe1.7Se2 and K0.8Fe1.78Se2 superconductors show that after the ambient-pressure superconducting phase is completely suppressed under about 9 GPa, the reemergence of a pressure-induced superconductivity with a maximum Tc of 48.7 K is observed at∼11 GPa, which is the highest Tc in this kind of superconductor. The systematic investigations on transport and structural properties for K0.8FeySe2 (y=1.7 and 1.78) reveal that a pressure-induced quantum phase transition occurs at pressure between 9.2 GPa and 10.3 GPa, where the antiferromagnetic state with Fermi liquid behavior converts into the paramagnetic state with non-Fermi liquid behavior. Therefore, it is proposed that the observed reemergence of superconductivity at high pressure is probably driven by the quantum critical transition. In addition, some intriguing puzzles on these superconductors and corresponding possible answers are also reviewed from the perspective of high-pressure studies, including the roles of the insulating magnetic phase in developing/stabilizing ambient-pressure and high-pressure superconducting phases and the significance of the pressure-induced antiferromag-netic fluctuation state for the emergency of superconductivity in the high-pressure superconducting phase.

  14. Effect of increasing tellurium content on the electronic and optical properties of cadmium selenide telluride alloys CdSe{sub 1-x}Te{sub x}: An ab initio study

    Energy Technology Data Exchange (ETDEWEB)

    Reshak, Ali Hussain, E-mail: maalidph@yahoo.co.uk [Institute of Physical Biology-South Bohemia University, Nove Hrady 37333 (Czech Republic); School of Material Engineering, Malaysia University of Perlis, P.O Box 77, d/a Pejabat Pos Besar, 01007 Kangar, Perlis (Malaysia); Kityk, I.V. [Electrical Engineering Department, Technical University of Czestochowa, Al. Armii Krajowej 17/19, Czestochowa (Poland); Khenata, R. [Laboratoire de Physique Quantique et de Modelisation Mathematique de la Matiere (LPQ3 M), universite de Mascara, Mascara 29000 (Algeria); Department of Physics and Astronomy, King Saud University, P.O. Box 2455, Riyadh 11451 (Saudi Arabia); Auluck, S. [National Physical Laboratory Dr. K S Krishnan Marg, New Delhi 110012 (India)

    2011-06-16

    Highlights: > Theoretical study of effect of vary Te content on band structure, density of states, linear and nonlinear optical susceptibilities of CdSe{sub 1-x}Te{sub x}. > Increasing Te content leads to a decrease in the energy band gap. > Significant enhancement of the electronic properties as a function of tellurium concentration - Abstract: An all electron full potential linearized augmented plane wave method, within a framework of GGA (EV-GGA) approach, has been used for an ab initio theoretical study of the effect of increasing tellurium content on the band structure, density of states, and the spectral features of the linear and nonlinear optical susceptibilities of the cadmium-selenide-telluride ternary alloys CdSe{sub 1-x}Te{sub x} (x = 0.0, 0.25, 0.5, 0.75 and 1.0). Our calculations show that increasing Te content leads to a decrease in the energy band gap. We find that the band gaps are 0.95 (1.76), 0.89 (1.65), 0.83 (1.56), 0.79 (1.44) and 0.76 (1.31) eV for x = 0.0, 0.25, 0.5, 0.75 and 1.0 in the cubic structure. As these alloys are known to have a wurtzite structure for x less than 0.25, the energy gaps are 0.8 (1.6) eV and 0.7 (1.55) eV for the wurtzite structure (x = 0.0, 0.25) for the GGA (EV-GGA) exchange correlation potentials. This reduction in the energy gaps enhances the functionality of the CdSe{sub 1-x}Te{sub x} alloys, at least for these concentrations, leading to an increase in the effective second-order susceptibility coefficients from 16.75 pm/V (CdSe) to 18.85 pm/V (CdSe{sub 0.75}Te{sub 0.25}), 27.23 pm/V (CdSe{sub 0.5}Te{sub 0.5}), 32.25 pm/V (CdSe{sub 0.25}Te{sub 0.75}), and 37.70 pm/V (CdTe) for the cubic structure and from 12.65 pm/V (CdSe) to 21.11 pm/V (CdSe{sub 0.75}Te{sub 0.25}) in the wurtzite structure. We find a nonlinear relationship between the absorption/emission energies and composition, and a significant enhancement of the electronic properties as a function of tellurium concentration. This variation will help in

  15. Antimony selenide thin-film solar cells

    Science.gov (United States)

    Zeng, Kai; Xue, Ding-Jiang; Tang, Jiang

    2016-06-01

    Due to their promising applications in low-cost, flexible and high-efficiency photovoltaics, there has been a booming exploration of thin-film solar cells using new absorber materials such as Sb2Se3, SnS, FeS2, CuSbS2 and CuSbSe2. Among them, Sb2Se3-based solar cells are a viable prospect because of their suitable band gap, high absorption coefficient, excellent electronic properties, non-toxicity, low cost, earth-abundant constituents, and intrinsically benign grain boundaries, if suitably oriented. This review surveys the recent development of Sb2Se3-based solar cells with special emphasis on the material and optoelectronic properties of Sb2Se3, the solution-based and vacuum-based fabrication process and the recent progress of Sb2Se3-sensitized and Sb2Se3 thin-film solar cells. A brief overview further addresses some of the future challenges to achieve low-cost, environmentally-friendly and high-efficiency Sb2Se3 solar cells.

  16. Dislocation Etching Solutions for Mercury Cadmium Selenide

    Science.gov (United States)

    2014-09-01

    be obtained in order to develop better etching solutions. 13 6. References 1. Brill G, Chen Y, Wijewarnasuriya P. J. Elect. Mater. 2011;40...PJ, Jacobs RN, Markunas JK, Jaime-Vasquez M, Almeida LA, Stoltz AJ, Wijewarnasuriya PS, Brill G, Chen Y, Lee U, Vilela MF, Peterson J, Johnson SM...Elect. Mater. 1995;24:505. 5. Doyle K, Swartz CH, Dinan JH, Myers TH, Brill G, Chen Y, VanMil BL, Wijewarnasuriya P. J. Vac. Sci. Technol. B 2013;31

  17. Optimization and photophysics of cadmium selenide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Badr, Y. [National Institute of Laser Enhanced Science, Cairo University, Cairo (Egypt); Mahmoud, M.A. [Chemistry Department, Faculty of Science, Zagazig University, Zagazig (Egypt)]. E-mail: mahmoudchem@yahoo.com

    2005-12-01

    CdSe nanocrystallites of different sizes were prepared in polyvinyl alcohol (PVA) photopolymer films. Particle sizes were optimized by variation in the Cd to Se ions ratio up to 16:1 as well as doping in PVA. X-ray diffraction shows that the degree of crystallinity of PVA was found to decrease due to doping with CdSe NPs and having a cubic unit cell. The UV-vis absorption spectra for the CdSe NPs in both solutions and PVA films showed blue shifts with increasing the ratio of Cd ion leading to the decrease of the particle size. The photoluminescence spectra resulting from 441.5 nm He-Cd excitation of CdSe NPs in PVA show the same behavior of absorption spectra. A blue shift in most of the FT-IR and FT-Raman bands of PVA was observed due to the interaction between PVA and CdSe NPs, which increase by decreasing the particle size. The conductivity of PVA was found to increase by decreasing the particle size of CdSe NPs.

  18. Dicyclohexyl[4-(dimethylaminophenyl]phosphine selenide

    Directory of Open Access Journals (Sweden)

    Zanele H Phasha

    2012-01-01

    Full Text Available In the title molecule, C20H32NPSe, the P atom has a distorted tetrahedral environment resulting in an effective cone angle of 172°. Weak intermolecular C—H...Se interactions are observed.

  19. Tris(4-methylphenyl)phosphine selenide

    OpenAIRE

    Alfred Muller

    2011-01-01

    In the title molecule, C21H21PSe or PSe(C7H7)3, the P atom has a distorted PSeC3 tetrahedral environment, formed by the Se atom [P=Se = 2.1119 (5) Å] and three aryl rings. Two short intramolecular C—H...Se contacts occur. In the crystal, weak intermolecular C—H...Se interactions link the molecules into zigzag double chains propagating in [100]. The previous report of this structure [Zhdanov et al. (1953). Dokl. Akad. Nauk SSSR (Russ.) (Proc. Na...

  20. Mercury Cadmium Selenide for Infrared Detection

    Science.gov (United States)

    2013-06-01

    were grown using elemental mercury (Hg), cadmium (Cd), and selenium (Se) sources. The beam equiva- lent pressure ( BEP ) emanating from all sources was...flux), the BEP measured for the cracker source was found to vary with the cracking zone temperature, tracking with the data found in Ref. 7. This sug...The Se BEP measured for the typical cracking zone temperature of 800 C was found to be close to a factor of two lower than at the typical effusion cell

  1. Fabrication, characterization and applications of iron selenide

    Science.gov (United States)

    Hussain, Raja Azadar; Badshah, Amin; Lal, Bhajan

    2016-11-01

    This review article presents fabrication of FeSe by solid state reactions, solution chemistry routes, chemical vapor deposition, spray pyrolysis and chemical vapor transport. Different properties and applications such as crystal structure and phase transition, band structure, spectroscopy, superconductivity, photocatalytic activity, electrochemical sensing, and fuel cell activity of FeSe have been discussed.

  2. Photoluminescence from semiconductor cadmium selenide nanocrystals

    Science.gov (United States)

    Nazzal, Amjad Yousef

    In this dissertation, the photoluminescence (PL) emission properties from different CdSe nanocrystals (NCs) dispersed in polymer thin films were investigated. The PL spectroscopy was used as a probing tool to study core and surface-related emission properties of the CdSe NCs under investigation. The results found in these studies are promising from the point of view of fundamental understanding as well as the possible employments of the emission properties of CdSe NCs in certain technological applications. The studies presented in this dissertation include the following: (i) PL polarization spectroscopy of single CdSe NCs was performed on a system of colloidal CdSe quantum rods (QRs). Our experimental measurements suggest a strong polarization dependence of both excitation and emission, and confirm the unique linear dipole in the QRs along the long axis of the rod, i.e. the c axis of wurtzite structure, which is in agreement with the previous theoretical predictions. These results are very important because it represents an experimental test to the available theoretical models used in exploring the rich electronic spectra of these NC systems. These results also show the importance of the shape anisotropy on the electronic spectrum of NCs. (ii) Environmental effects on the PL from highly luminescent bare-core CdSe and core/shell CdSe/ZnS NCs were systematically investigated under different atmospheric environments and photo-irradiation conditions. In this study, the PL was used as a probe to detect changes in the electronic spectrum of the NCs due to photo-induced interactions on the surface of the NCs with the local surrounding atmosphere. Such studies are very important to provide a good understanding of the optimum operational conditions for emission applications of NCs in solid-state devices and also give a simple way of studying the surface of the NCs indirectly by investigating the surface interactions with different molecular systems and their effects on the optical emission properties. (iii) The highly luminescent CdSe NCs were employed in a PL-based sensing scheme to detect gases from the amine group. These results are the first experimental demonstration of such sensing capabilities using semiconductor NCs.

  3. Electroluminescent, polycrystalline cadmium selenide nanowire arrays.

    Science.gov (United States)

    Ayvazian, Talin; van der Veer, Wytze E; Xing, Wendong; Yan, Wenbo; Penner, Reginald M

    2013-10-22

    Electroluminescence (EL) from nanocrystalline CdSe (nc-CdSe) nanowire arrays is reported. The n-type, nc-CdSe nanowires, 400-450 nm in width and 60 nm in thickness, were synthesized using lithographically patterned nanowire electrodeposition, and metal-semiconductor-metal (M-S-M) devices were prepared by the evaporation of two gold contacts spaced by either 0.6 or 5 μm. These M-S-M devices showed symmetrical current voltage curves characterized by currents that increased exponentially with applied voltage bias. As the applied biased was increased, an increasing number of nanowires within the array "turned on", culminating in EL emission from 30 to 50% of these nanowires at applied voltages of 25-30 V. The spectrum of the emitted light was broad and centered at 770 nm, close to the 1.74 eV (712 nm) band gap of CdSe. EL light emission occurred with an external quantum efficiency of 4 × 10(-6) for devices with a 0.60 μm gap between the gold contacts and 0.5 × 10(-6) for a 5 μm gap-values similar to those reported for M-S-M devices constructed from single-crystalline CdSe nanowires. Kelvin probe force microscopy of 5 μm nc-CdSe nanowire arrays showed pronounced electric fields at the gold electrical contacts, coinciding with the location of strongest EL light emission in these devices. This electric field is implicated in the Poole-Frenkel minority carrier emission and recombination mechanism proposed to account for EL light emission in most of the devices that were investigated.

  4. Study of the electrochemical oxidation of Am with lacunary heteropolyanions and silver nitrate; Etude de l'oxydation electrochimique de l'americium en presence d'heteropolyanions lacunaires et de nitrate d'argent en milieu aqueux acide

    Energy Technology Data Exchange (ETDEWEB)

    Chartier, D

    1999-07-01

    Electrochemical oxidation of Am(III) with certain lacunary heteropolyanions (LHPA {alpha}{sub 2}-P{sub 2}W{sub 17}O{sub 61}{sup 10-} or {alpha}SiW{sub 11}O{sub 39}{sup 8-}) and silver nitrate is an efficient way to prepare Am(VI). This document presents bibliographic data and an experimental study of the process. Thus, it has been established that Am(IV) is an intermediate species in the reaction and occurs in 1:1 (Amt{sup IV}LHPA) or 1:2 (Am {sup IV}(LHAP){sub 2}) complexes with the relevant LHPA. These 1:1 complexes of Am(IV) have been identified and isolated in this work whereas 1:2 complexes were known from previous studies. The reactivity of these complexes in oxidation shows that 1:1 complexes of Am(IV) are oxidised much more quickly than 1:2 complexes. Apparent stability constants of Am(III) and Am(IV) complexes with the relevant LHPA have been measured for a 1 M nitric acid medium. Thermodynamic data of the reaction are then assessed: redox potentials of Am pairs are computed for a 1 M nitric acid medium containing various amount of LHPA ligands. Those results show that the role of LHPA is to stabilize the intermediate species Am(IV) by lowering the Am(IV)/Am(III) pair potential of about 1 Volt. Nevertheless, if this stabilisation is too strong (i.e. of tungsto-silicate), the oxidation of Am(IV) requires high anodic potential (more than 2 V/ENH). Then, the faradic yield of the oxidation of americium is poor because of water oxidation. This study has also shown that the main role of silver is to catalyze the electrochemical oxidation of Am{sup IV}(LHPA){sub X} complexes. Indeed, these oxidations without silver are extremely slow. An oxygen tracer experiment has been performed during the oxidation of Am(III) in Am(VI). It has been shown that the oxygen atoms of Am(VI) (AMO{sub 2}{sup 2+}) come from water molecules of the solvent and not from the complexing oxygen atoms of the ligands. (author)

  5. Fabrication of targets for transmutation of americium : synthesis of inertial matrix by sol-gel method. Procedure study on the infiltration of a radioactive solutions; Fabricacion de blancos para la transmutacion de americio: sintesis de matrices inertes por el metodo sol-gel. Estudio del procedimiento de infiltracion de disoluciones radiactivas

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez Carretero, A. [Universidad Complutense de Madrid (Spain)

    2002-07-01

    made. In addition a new and unexpected phase formed by the reaction of americium with spinel during the high temperature synthesis process has been identified. This new phase could provide a unique menas to stabilise Am in one particular oxidation state. (Author)

  6. 241镅跟骨骨密度测定在骨质疏松症中的初步应用 ——与腰椎骨密度测定的对比研究%Preliminary application of 241-Americium calcaneus bone mineral density measurement in osteoporosis ——comparison with double X-ray densitometry of the lumber spine

    Institute of Scientific and Technical Information of China (English)

    管梁; 朱承谟; 李培勇; 王辉; 濮鸣芳; 仇季高

    2001-01-01

    Bone mineral density (BMD) of calcaneus in 54 normals, 45 Osteoporosis, 25 suspected osteoporosis and 16 other non-osteoporosis patients, a total of 140 cases were measured by HUAKE (HK-1) 241-Americium BMD absorpmetry, among them 43 were compared with that of lumber spine (L2—L4) measured by Lunar Corporation's Expert-XL absorpmeter. BMD of normal group of calcaneus was (409.8±79.4)mg/cm2. The BMD were decreased slowly with the increased age. The BMD of osteoporosis, suspected osteoporosis and non-osteoporosis group were 230.3±62.3, 395.7±57.4 and 363.3±51.9mg/cm2 respectively. The BMD of osteoporosis group was much lower than that of normal group, and also lower than that of the other two groups, among 26 patients (57.78%) had bone fracture, all was in accordance with the clinical diagnosis of osteoporosis. The BMD of suspected ospteoporosis and non-osteoporosis had no significant difference with normal group. The coefficient variation (CV) of BMD in repeated measurement in calcaneus of 4 pariticipants was less than 1.2%. The correlative coefficient (r) between BMD of calcaneus and lumber spine (L2—L4) group was 0.6824. The correlative coefficient of normal young adult-matched percentage and T value in 2 groups were 0.6863 and 0.6755 respectively, whereas aged-matched percentage, Z value were 0.4614 and 0.5009 respectively. In conclusion 241-Americium calcaneus BMD absorpmetry has the advantage of low price, easy to operate, reliable and valuable in diagnosis osteoporosis. The correlations of calcaneus and lumber spine BMD, normal young adult-matched percentagy and T value were rather good.%为评价跟骨骨密度测定在骨质疏松症中的初步临床应用及与腰椎测定结果的相关性,用国产华科(HK-1型)241镅骨密度仪测定了140例跟骨骨密度(BMD)。其中正常人组54例,骨质疏松确诊组45例,骨质疏松可疑组25例和其他非骨质疏松组16例。其中43例与美国Luner 公司的Expert-XL图像骨密度仪腰

  7. Americium separation from nuclear fuel dissolution using higher oxidation states.

    Energy Technology Data Exchange (ETDEWEB)

    Bruce J. Mincher

    2009-09-01

    Much of the complexity in current AFCI proposals is driven by the need to separate the minor actinides from the lanthanides. Partitioning and recycling Am, but not Cm, would allow for significant simplification because Am has redox chemistry that may be exploited while Cm does not. Here, we have explored methods based on higher oxidation states of Am (AmV and AmVI) to partition Am from the lanthanides. In a separate but related approach we have also initiated an investigation of the utility of TRUEX Am extraction from thiocyanate solution. The stripping of loaded TRUEX by Am oxidation or SCN- has not yet proved successful; however, the partitioning of inextractable AmV by TRUEX shows promise.

  8. Further Studies of Plutonium and Americium at Thule, Greenland

    DEFF Research Database (Denmark)

    Aarkrog, Asker; Dahlgaard, Henning; Nilsson, Karen Kristina;

    1984-01-01

    further away from the impact point and at some locations the vertical distribution indicated a downward displacement of Pu in the sediment column since 1974. Seawater and seaplants showed no evidence of the presence of Pu from sources other than fallout; but Pu in benthos varied nearly proportionally......, but in benthos 241Am/239,240Pu were two times higher than in sediments. Seaplants showed the same value of Am/Pu as seawater. There was no indication of any biomagnification of Pu or Am through the marine food chains at Thule....

  9. Property Data for Simulated Americium/Curium Glasses

    Energy Technology Data Exchange (ETDEWEB)

    Riley, B.J.; Smith, D.E.; Peeler, D.K.; Reamer, I.A.; Vienna, J.D.; Schweiger, M.J.

    1999-10-20

    The authors studied the properties of mixed lanthanide-alumino-borosilicate glasses. Fifty-five glasses were designed to augment a previous, Phase I, study by systematically varying the composition of Ln{sub 2}O{sub 3} and the concentrations of Ln{sub 2}O{sub 3}, SiO{sub 2}, B{sub 2}O{sub 3}, Al{sub 2}O{sub 3}, and SrO in glass. These glasses were designed and fabricated at the Savannah River Technology Center and tested at the Pacific Northwest National Laboratory. The properties measured include the high-temperature viscosity ({eta}) as a function of temperature (T) and the liquidus temperature (T{sub L}) of Phase II test glasses.

  10. Plutonium and americium contamination in Rocky Flats soil, 1973

    Energy Technology Data Exchange (ETDEWEB)

    Krey, P.; Hardy, E.; Volchok, H.; Toonkel, L.; Knuth, R.; Coppes, M.; Tamura, T.

    1976-03-01

    The plutonium mass isotopic analysis and the Am-241 analysis of soil samples from Rocky Flats identify the contamination as Pu which was processed in 1958. The Am-241 activity in the soil will reach its maximum in 2033 and represent 18 percent of the Pu-239-240 activity. Nuclide ratios indicate that current operations at Rocky Flats contribute little to the airborne Pu concentrations which are due to resuspension of the contaminated soil. Root uptake of Pu or Am by vegetation is slight or shows no discrimination among the isotopes and nuclides studied. The relationship between Pu deposition contour and the area enclosed by that contour has been verified for contour values extending over 7 orders of magnitude. This gives confidence to our calculations of the quantities of Pu released on and off the Rocky Flats plant site. (auth)

  11. Biosorption of americium-241 by immobilized Rhizopus arrihizus

    Energy Technology Data Exchange (ETDEWEB)

    Liao Jiali E-mail: liaojiali@163.com; Yang Yuanyou; Luo Shunzhong; Liu Ning; Jin Jiannan; Zhang Taiming; Zhao Pengji

    2004-01-01

    Rhizopus arrihizus (R. arrihizus), a fungus, which in previous experiments had shown encouraging ability to remove {sup 241}Am from solutions, was immobilized by calcium alginate and other reagents. The various factors affecting {sup 241}Am biosorption by the immobilized R. arrihizus were investigated. The results showed that not only can immobilized R. arrihizus adsorb {sup 241}Am as efficiently as free R. arrihizus, but that also can be used repeatedly or continuously. The biosorption equilibrium was achieved within 2 h, and more than 94% of {sup 241}Am was removed from {sup 241}Am solutions of 1.08 MBq/l by immobilized R. arrihizu in the pH range 1-7. Temperature did not affect the adsorption on immobilized R. arrihizus in the range 15-45 deg. C. After repeated adsorption for 8 times, the immobilized R. arrihizus still adsorbed more than 97% of {sup 241}Am. At this time, the total adsorption of {sup 241}Am was more than 88.6 KBq/g, and had not yet reached saturation. Ninety-five percent of the adsorbed {sup 241}Am was desorbed by saturated EDTA solution and 98% by 2 mol/l HNO{sub 3}.

  12. Syntheses and Structures of the New Quaternary Rubidium Selenides Rb Ln2CuSe 4 ( Ln=Sm, Gd, Dy), Rb 1.5Ln2Cu 2.5Se 5 ( Ln=Gd, Dy), and RbSm 2Ag 3Se 5

    Science.gov (United States)

    Huang, Fu Qiang; Ibers, James A.

    2000-05-01

    Six quaternary rubidium selenides RbLn2CuSe4 (Ln=Sm, Gd, Dy), Rb1.5Ln2Cu2.5Se5 (Ln=Gd, Dy), and RbSm2Ag3Se5 have been synthesized at 1073 K with the use of a reactive flux of Rb2Se3. At 153 K all compounds contain four formula units in orthorhombic unit cells. The isostructural compounds RbLn2CuSe4 crystallize in space group Cmcm; the isostructural compounds Rb1.5Ln2Cu2.5Se5 crystallize in space group Pnnm; RbSm2Ag3Se5 crystallizes in space group Cmcm. The cells of RbLn2CuSe4 are (Ln, a, b, c (Å)): Sm, 4.1834(9), 14.308(3), 14.439(3); Gd, 4.1568(8), 14.227(3), 14.409(3); Dy, 4.1237(10), 14.083(4), 14.291(3), and the corresponding R1 indices for the refined structures are 0.023, 0.029, and 0.039. The cells of Rb1.5Ln2Cu2.5Se5 are: Gd, 16.243(3), 16.449(3), 4.0980(7); Dy, 16.120(3), 16.292(3), 4.0610(8), and the R1 indices are 0.036 and 0.043. The cell of RbSm2Ag3Se5 is 4.3223(6), 15.229(2), 17.420(3) Å and the R1 index is 0.025. All six are closely related three-dimensional tunnel structures. Their anionic frameworks are built from LnSe6 octahedra and MSe4 (M=Cu, Ag) tetrahedra. RbLn2CuSe4 contains infinite 1∞[CuSe3] chains of vertex-sharing tetrahedra; Rb1.5Ln2Cu2.5Se5 also contains infinite chains of tetrahedra; and the tunnel in RbSm2Ag3Se5 holds one Rb+ cation in a 10-membered ring consisting of six Ag-Se bonds and four Sm-Se bonds. Rb1.5Dy2Cu2.5Se5, which is paramagnetic, obeys the Curie-Weiss law and has an effective magnetic moment of 10.63(4) μB.

  13. Relaxation of Electronic and Ionic Polarization in Liquid Copper Selenide

    Science.gov (United States)

    Itoh, Keiji; Maruyama, Kenji; Misawa, Masakatsu; Tamaki, Shigeru

    2002-01-01

    The diffusion constants of both cation and anion in liquid Cu2Se have been measured based on the time dependence of decaying residual potential due to the charge polarization after the turning-off of applied current. The experimental decaying curves were fitted by three exponential terms. Two terms correspond to the diffusion process of copper and selenium ions, respectively, and the rest is attributed to a relaxation of electronic polarization. It is found that the temperature dependences of diffusion constants of copper and selenium ions are negligibly small, on the other hand, the relaxation time of electronic polarization increases with increasing temperature.

  14. Photo-induced transmittance in copper selenide nanowires

    Science.gov (United States)

    Statkutė, G.; Mikulskas, I.; Jagminas, A.; Tomašiūnas, R.

    2008-01-01

    Photo-induced transmission was investigated in Cu 1.7Se nanowires electrochemically deposited in alumina matrix pores with a central channel of the diameters of 12, 15 and 60 nm by means of the degenerate picosecond pump-probe technique at 1.064 μm wavelength. Resonant excitation intensity dependencies were interpreted. Absorption saturation was ascertained as a result of the drain of acceptor shallow centers. The estimated absorption cross-section was 10 -12 cm 2, saturation intensity - was 1-10 mJ cm -2.

  15. Pressure-induced phase transitions of indium selenide

    Science.gov (United States)

    Rasmussen, Anya Marie

    In2Se3 has potential as a phase-change material for memory applications. Understanding its phase diagram is important to achieve controlled switching between phases. Pressure-dependent phase transitions of In2Se3 bulk powders and nanowire samples were studied at room temperature and at elevated temperatures using synchrotron x-ray diffraction and diamond-anvil cells (DACs). alpha-In2Se3 transforms into the beta phase at 0.7 GPa, an order of magnitude lower than phase-transition critical pressures in typical semiconductors. The bulk moduli are reported and the c/a ratio for the beta phase is shown to have a highly nonlinear dependence on pressure. gamma-In2Se3, metastable under ambient conditions, transforms into to the high-pressure beta phase between 2.8 GPa and 3.2 GPa in bulk powder samples and at slightly higher pressures, between 3.2 GPa and 3.7 GPa in nanowire samples. While the gamma phase bulk modulus is similar to that of the beta phase, the decrease due to pressure in the unit cell parameter ratio, c/a, is less than half the decrease seen in the beta phase. Using high-temperature DACs, we investigated how elevated temperatures and pressures affect the crystal structure of In 2Se3. From these measurements, the high-pressure beta phase was found to be metastable. The high-pressure beta phase transitions into the high-temperature beta phase at temperatures above 380 °C.

  16. High performance broadband photodetector using fabricated nanowires of bismuth selenide

    Science.gov (United States)

    Sharma, Alka; Bhattacharyya, Biplab; Srivastava, A. K.; Senguttuvan, T. D.; Husale, Sudhir

    2016-01-01

    Recently, very exciting optoelectronic properties of Topological insulators (TIs) such as strong light absorption, photocurrent sensitivity to the polarization of light, layer thickness and size dependent band gap tuning have been demonstrated experimentally. Strong interaction of light with TIs has been shown theoretically along with a proposal for a TIs based broad spectral photodetector having potential to perform at the same level as that of a graphene based photodetector. Here we demonstrate that focused ion beam (FIB) fabricated nanowires of TIs could be used as ultrasensitive visible-NIR nanowire photodetector based on TIs. We have observed efficient electron hole pair generation in the studied Bi2Se3 nanowire under the illumination of visible (532 nm) and IR light (1064 nm). The observed photo-responsivity of ~300 A/W is four orders of magnitude larger than the earlier reported results on this material. Even though the role of 2D surface states responsible for high reponsivity is unclear, the novel and simple micromechanical cleavage (exfoliation) technique for the deposition of Bi2Se3 flakes followed by nanowire fabrication using FIB milling enables the construction and designing of ultrasensitive broad spectral TIs based nanowire photodetector which can be exploited further as a promising material for optoelectronic devices.

  17. Reversibility windows in selenide-based chalcogenide glasses

    Energy Technology Data Exchange (ETDEWEB)

    Shpotyuk, O. [Lviv Scientific Research Institute of Materials of SRC ' Carat' , 202, Stryjska Street, Lviv, UA 79031 (Ukraine); Institute of Physics of Jan Dlugosz University, 13/15, al. Armii Krajowej, Czestochowa, PL 42200 (Poland); Hyla, M. [Institute of Physics of Jan Dlugosz University, 13/15, al. Armii Krajowej, Czestochowa, PL 42200 (Poland); Boyko, V. [Lviv Scientific Research Institute of Materials of SRC ' Carat' , 202, Stryjska Street, Lviv, UA 79031 (Ukraine); Lviv National Polytechnic University, 12, Bandera Street, Lviv, UA 79013 (Ukraine); Golovchak, R. [Lviv Scientific Research Institute of Materials of SRC ' Carat' , 202, Stryjska Street, Lviv, UA 79031 (Ukraine)], E-mail: golovchak@novas.lviv.ua

    2008-10-01

    A simple route for the estimation of the reversibility windows in the sense of non-ageing ability is developed for chalcogenide glasses obeying '8-N' rule at the example of As-Se, Ge-Se and Ge-As-Se glass systems. The low limit of their reversibility windows is determined at the average coordination number Z=2.4 in full agreement with rigidity percolation theory, while the upper limit is shown to be related to the glass preparation conditions and samples prehistory.

  18. Versatile Chromium-Doped Zinc Selenide Infrared Laser Sources

    Science.gov (United States)

    2010-05-01

    Erbium Doped Fiber Amplifiers ( EDFAs ). An EDFA is essentially a normal optical fiber waveguide that has been lightly doped with a rare-earth...element, namely erbium (possibly co-doped with ytterbium to increase the pumping efficiency and gain). In a typical EDFA , 980 nm photons are used to

  19. Iron-Doped Zinc Selenide: Spectroscopy and Laser Development

    Science.gov (United States)

    2014-03-27

    core of the active ion in the presence of the crystal field. Many optical spectroscopy textbooks contain the familiar solution to the Schrödinger...Imbusch, Optical Spectroscopy of Inorganic Solids, ser. Monographs on the Physics And Chemistry of Materials. Clarendon Press, Oxford, 1989. [35] W. G...in Chemistry and Spectroscopy. Academic Press, London, 1994. [37] Y. Tanabe and S. Sugano, “On the Absorption Spectra of Complex Ions II,” Journal of

  20. MEASUREMENT OF NANOMETER SCALE CADMIUM SELENIDE NANOCRYSTALS AND CLUSTER MOLECULES

    Institute of Scientific and Technical Information of China (English)

    Jeffrey Yang

    2003-01-01

    High performance Dynamic Light Scattering (DLS) has been used to determine the hydrodynamic diameters of CdSe nanocrystals as well as CdSe cluster molecules in a size range of 1 to 10 nm (Eichh(o)fer et al., 2001).The method enables the determination of their particle size, including their ligand shells, in solution. The results are consistent with the blue shift of the absorption bands, as well as Transmission Electron Microscope (TEM) experiments.The sizes of the cluster molecules were estimated from space filling models constructed from the results of a single crystal X-ray structure determination. DLS gave comparable results for the size of both types of compound, indicating that it is potentially an important additional measurement technique to TEM, which uses harsh measurement conditions,and to powder X-ray diffraction, which is difficult to interpret below 5 nm.

  1. Optical Properties of Nanoscale Bismuth Selenide and Its Heterocrystals

    Science.gov (United States)

    Vargas, Anthony

    Over the past 12 years since the groundbreaking work on graphene, the field of 2D layered materials has grown by leaps and bounds as more materials are theoretically predicted and experimentically verified. These materials and their unique electronic, optical, and mechanical properties have inspired the scientific community to explore and investigate novel, fundamental physical phenomena as well create and refine technological devices which leverage the host of unique benefits which these materials possess. In the past few years, this burgeoning field has heavily moved towards combining layers of various materials into novel heterostructures. These heterostructures are an exciting area of research because of the plethora of exciting possibilities and results which arise due to the large number of heterostructure combinations and configurations. Particularly, the research into the optical properties of these layered materials and their heterostructures under confinement provides another exciting avenue for developing optoelectric devices. In this dissertation, I present work on the synthesis of Bi2Se 3 nanostructures via chemical vapor deposition (CVD) and the study of the optical properties of these nanostructures and their heterostructures with MoS2. The bulk of the current published work on Bi2Se 3 has focused on the exotic topological properties of its surface states, both interesting fundamental physics purposes as well as for studying avenues for spintronics. In contrast, the work presented here focuses on studying the optical properties of Bi2Se3 nanostructures and how these properties evolve when subjected to confinement. Specifically, the absorbance of singlecrystal Bi2Se3 with sizes tailored down to a few nanometers in diameter and a few quintuple layers (QLs) in thickness. We find a dramatically large bandgap, Eg ≥ 2.5 eV, in the smallest particles which is much higher than that seen in 1QL measurements taken with ARPES. Additionally, utilizing photoluminescence (PL) measurements of CVD-grown Bi 2Se3 nanoplates with few QL thickness and effective diameters in the tens of nanometers, Bi2Se3 nanoplatelets show a strong PL response with photon energies, Eph, in the ˜2.1-2.3 eV region. Annealing of these samples at 200?C for 4 hours increases the PL intensity by a factor of 2.4 to 3 for nanoscale Bi2Se3. Furthermore, this work investigates the synthesis of the novel Bi2Se3-MoS 2 heterocrystal that arises from epitaxial growth of Bi2Se 3 on MoS2 substrates. These heterocrystals consist of n layers of Bi2Se3 perfectly rotationally-aligned epitaxially with the monolayer MoS2 substrate. Investigation into these heterocystals produced results which include 100% PL-suppression of the MoS2 PL response, precisely tunable band-gap ranging from 1.1eV ? 0.75 eV, and a spectacular wide-band enhancement of photo-absorption over nearly the entire solar spectral wavelengths. Finally, a simple laser-treatment appears to dramatically reverse these changes, attributed to breakdown of the rotational congruency between the MoS2 and Bi2Se3 layers. These heterocrystals have immense potentials for novel physics and applications in nanoelectronics, optoelectronics and energy sciences at the atomically-thin scale.

  2. Synthesis and Antibacterial Activities of Selenide Derivatives of Benzisoselenazolone

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A series of Benzisolselenazolone (BISA) derivatives were synthesized and evaluated for their antibacterial activities against E coli. by using LKB-2277 bioactivity monitor. Other bioactivities were tested by the method of High Throughput Screening for pharmaceutical activity compounds (HTP) BISA derivatives 3b,at the concentration of 40 μg/mL, showed 100% antibacterial activity and 62% inhibition rate of aldose reductase(at the concentration of 5μg/mL). These new compound structures have determined by IR, 1H NM Rand MS spectra.

  3. Handbook of Phase Transition Sulfides, Selenides and Tellurides,

    Science.gov (United States)

    1984-07-01

    made (as reported in Ref. 5) in 61899 by Mourlot. More recent studies showed that he actually prepared CrSo.9 7 and that pure CrS should have a density ...1n2S 3 Indium Sulfide or Di-Indium Trisulflde In2S3 exists as cubic a-In 2S3 and tetragonal 0-In 2S3. Until recently, no detailed studies on the...Mn+2 is bonded tetrahedrally through sulfur atoms to its nearest Mn neighbors. The crystal lattice parameters have been studied as a function of 0

  4. Tris(4-methyl­phen­yl)phosphine selenide

    Science.gov (United States)

    Muller, Alfred

    2011-01-01

    In the title mol­ecule, C21H21PSe or PSe(C7H7)3, the P atom has a distorted PSeC3 tetra­hedral environment, formed by the Se atom [P=Se = 2.1119 (5) Å] and three aryl rings. Two short intra­molecular C—H⋯Se contacts occur. In the crystal, weak inter­molecular C—H⋯Se inter­actions link the mol­ecules into zigzag double chains propagating in [100]. The previous report of this structure [Zhdanov et al. (1953 ▶). Dokl. Akad. Nauk SSSR (Russ.) (Proc. Nat. Acad. Sci. USSR), 92, 983–985] contained no geometrical data. PMID:21522754

  5. Tris(4-methyl-phen-yl)phosphine selenide.

    Science.gov (United States)

    Muller, Alfred

    2010-12-08

    In the title mol-ecule, C(21)H(21)PSe or PSe(C(7)H(7))(3), the P atom has a distorted PSeC(3) tetra-hedral environment, formed by the Se atom [P=Se = 2.1119 (5) Å] and three aryl rings. Two short intra-molecular C-H⋯Se contacts occur. In the crystal, weak inter-molecular C-H⋯Se inter-actions link the mol-ecules into zigzag double chains propagating in [100]. The previous report of this structure [Zhdanov et al. (1953 ▶). Dokl. Akad. Nauk SSSR (Russ.) (Proc. Nat. Acad. Sci. USSR), 92, 983-985] contained no geometrical data.

  6. Thermoelectric materials: ternary penta telluride and selenide compounds

    Science.gov (United States)

    Sharp, Jeffrey W.

    2002-06-04

    Ternary tellurium compounds and ternary selenium compounds may be used in fabricating thermoelectric devices with a thermoelectric figure of merit (ZT) of 1.5 or greater. Examples of such compounds include Tl.sub.2 SnTe.sub.5, Tl.sub.2 GeTe.sub.5, K.sub.2 SnTe.sub.5 and Rb.sub.2 SnTe.sub.5. These compounds have similar types of crystal lattice structures which include a first substructure with a (Sn, Ge) Te.sub.5 composition and a second substructure with chains of selected cation atoms. The second substructure includes selected cation atoms which interact with selected anion atoms to maintain a desired separation between the chains of the first substructure. The cation atoms which maintain the desired separation between the chains occupy relatively large electropositive sites in the resulting crystal lattice structure which results in a relatively low value for the lattice component of thermal conductivity (.kappa..sub.g). The first substructure of anion chains indicates significant anisotropy in the thermoelectric characteristics of the resulting semiconductor materials.

  7. Thermoelectric materials ternary penta telluride and selenide compounds

    Science.gov (United States)

    Sharp, Jeffrey W.

    2001-01-01

    Ternary tellurium compounds and ternary selenium compounds may be used in fabricating thermoelectric devices with a thermoelectric figure of merit (ZT) of 1.5 or greater. Examples of such compounds include Tl.sub.2 SnTe.sub.5, Tl.sub.2 GeTe.sub.5, K.sub.2 SnTe.sub.5 and Rb.sub.2 SnTe.sub.5. These compounds have similar types of crystal lattice structures which include a first substructure with a (Sn, Ge) Te.sub.5 composition and a second substructure with chains of selected cation atoms. The second substructure includes selected cation atoms which interact with selected anion atoms to maintain a desired separation between the chains of the first substructure. The cation atoms which maintain the desired separation between the chains occupy relatively large electropositive sites in the resulting crystal lattice structure which results in a relatively low value for the lattice component of thermal conductivity (.kappa..sub.g). The first substructure of anion chains indicates significant anisotropy in the thermoelectric characteristics of the resulting semiconductor materials.

  8. Electrical characterization of nanocrystalline zinc selenide thin films

    Science.gov (United States)

    Sharma, Jeewan; Shikha, Deep; Tripathi, Surya Kant

    2012-08-01

    In the present paper, we have studied the effect of photo-illumination on electrical properties of nanocrystalline ZnSe thin films. The ZnSe thin films with different grain sizes (coherently diffracting domains) have been prepared. The semiconducting material with the composition Zn25Se75 has been prepared using melt-quenching technique. Thermal evaporation technique has been used to prepare nanocrystalline ZnSe thin films on highly cleaned glass substrates at different partial pressures of Ar gas. The grain size has been controlled by the partial pressure of inert gas. The grain size has been calculated using X-ray diffraction plots. Mobility activation has been studied from the photocurrent decay curves. The effective density of states ( N eff), frequency factor ( S), and trap depth ( E) have been calculated for all the films having different grain sizes. Three different types of trap levels have been found in these films. There is a linear distribution of traps having different energies below the conduction band. The increase in photoconductivity is explained in terms of built in potential barriers ( ϕ b) at the grain boundaries.

  9. Thermoelectric transport in indium and aluminum-doped lead selenide

    Science.gov (United States)

    Evola, E. G.; Nielsen, M. D.; Jaworski, C. M.; Jin, H.; Heremans, J. P.

    2014-02-01

    We present galvanomagnetic and thermomagnetic properties of bulk PbSe doped by substituting the donor elements In and Al for Pb. Although prominent resonant level effects are not seen, lightly doped samples display a high thermoelectric figure of merit (zT) in excess of 1.2 at 600 K, a temperature corresponding well to automotive waste heat recovery applications. This material's high zT is achieved without the use of nanostructuring or the relatively rare element Te. Phonon drag contributions to thermopower appear at temperatures below 30 K in Al-doped samples.

  10. Short-range order of germanium selenide glass

    Indian Academy of Sciences (India)

    A H Moharram

    2015-02-01

    Chalcogenide Ge20Se80 glass was prepared using the melt-quench technique. The radial distribution function is obtained from X-ray diffraction data in the scattering vector interval 0.28 ≤ ≤ 6.87 Å-1. ReverseMonte Carlo (RMC) simulations are useful to compute the partial pair distribution functions, $\\text{g}_{ij} (r)$, partial structure factors, $S_{ij} (K)$, and total structure factor. Values of $r_{1}/r_{2}$ ratio and bond angle () indicate that Ge(Se1/2)4 tetrahedra units connected by chains of the chalcogen atoms are present. The partial structure factors have shown that homopolar Ge–Ge and Se–Se bonds are behind the appearance of the first sharp diffraction peak (FSDP) in the total structure factor. Tetrahedral Ge(Se1/2)4 structural units connected by Se–Se chains have been confirmed by the simulated values of the partial coordination numbers and bond angle distributions. Finally, Raman spectra measurements have strongly supported the conclusions obtained either from the calculated Fourier data or from RMC simulations.

  11. Electrolytically deposited Cadmium Selenide Films for Photovoltaic Applications

    Directory of Open Access Journals (Sweden)

    Palaiologopoulou M. D.

    2012-10-01

    Full Text Available CdSe films were electrodeposited on pure nickel substrates. The nickel substrate was polished to a mirror finish by Al2O3 paste, etched in 10% HCl solution for 40 s and rinsed thoroughly by de-ionized water. The deposition bath contained solutions with excessive Cd2+ (0.2M from CdSO4 and small amounts of SeO2 (1x10-3 M. The pH of the bath was adjusted to a value of 2.2 at RT by adding 10% H2SO4. The bath was first thermostated at the required temperature, which varied from 55°C to 65°C. Plating was accomplished at deposition potential 1000 mV (vs. Hg/Hg2SO4. The films formed had a uniform thickness and it was found to be approximately 2.0 μm thick (for 20 min electrodeposition process. The produced CdSe films were characterized by X-Ray diffraction and SEM. The induced semiconductor doping effect by thermal annealing in pure dry nitrogen gas was also investigated. Gold contacts were placed on top of the CdSe films, either by evaporation, or mechanically. Depending on the deposition parameters the electrical characteristics of the Ni/CdSe/Au structures may exhibit rectification properties. The optical excitation of the structure was investigated for various CdSe thicknesses.

  12. Quantitative analysis of cadmium selenide nanocrystal concentration by comparative techniques.

    Science.gov (United States)

    Kuçur, Erol; Boldt, Frank M; Cavaliere-Jaricot, Sara; Ziegler, Jan; Nann, Thomas

    2007-12-01

    In this paper, we compared atomic absorption spectroscopy (AAS), anodic stripping voltammetry (ASV), and UV-vis spectroscopy for the determination of the concentration of CdSe nanocrystal (NC) solutions. The experimental results were combined with crystallographic calculations of the NC size, which led to a very accurate determination of the nanocrystal concentration--a crucial parameter for bioanalytical applications. Furthermore, such a combined approach can be extended to the determination of shell thickness of core/shell materials (e.g., CdSe/ZnS).

  13. Luminescent properties of fluorophosphate glasses with molecular cadmium selenide clusters

    Science.gov (United States)

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

    2015-02-01

    It is experimentally shown that, prior to the formation of CdSe quantum dots in fluorophosphate glasses with cadmium and selenium ions in the process of synthesis, subnanosized molecular clusters (CdSe) n are formed, which exhibit luminescence in the visible spectral region upon UV excitation. Heat treatment of the glasses increases the size of molecular clusters and makes their optical properties closer to the optical properties of CdSe semiconductor quantum dots. An increase in the sample temperature from 20 to 250°C leads to reversible thermal quenching of the luminescence.

  14. The Potentiostatic Electrodeposition of Indium doped Aluminium Selenide Thin Films

    Directory of Open Access Journals (Sweden)

    R.K. Pathak and Sipi Mohan

    2013-12-01

    Full Text Available The In containing AlSe thin films were electrosynthesized by electrochemical co-deposition technique. The morphological properties of thin films were studied through the Scanning Electron Micrograph (SEM while the structural features through X-Ray Diffraction technique (XRD. The deposition current along with the film thickness values, the charge carrier density, flat band potential, corrosion characteristics i.e., corrosion current, corrosion potential and corrosion rate were calculated.

  15. High performance broadband photodetector using fabricated nanowires of bismuth selenide.

    Science.gov (United States)

    Sharma, Alka; Bhattacharyya, Biplab; Srivastava, A K; Senguttuvan, T D; Husale, Sudhir

    2016-01-11

    Recently, very exciting optoelectronic properties of Topological insulators (TIs) such as strong light absorption, photocurrent sensitivity to the polarization of light, layer thickness and size dependent band gap tuning have been demonstrated experimentally. Strong interaction of light with TIs has been shown theoretically along with a proposal for a TIs based broad spectral photodetector having potential to perform at the same level as that of a graphene based photodetector. Here we demonstrate that focused ion beam (FIB) fabricated nanowires of TIs could be used as ultrasensitive visible-NIR nanowire photodetector based on TIs. We have observed efficient electron hole pair generation in the studied Bi2Se3 nanowire under the illumination of visible (532 nm) and IR light (1064 nm). The observed photo-responsivity of ~300 A/W is four orders of magnitude larger than the earlier reported results on this material. Even though the role of 2D surface states responsible for high reponsivity is unclear, the novel and simple micromechanical cleavage (exfoliation) technique for the deposition of Bi2Se3 flakes followed by nanowire fabrication using FIB milling enables the construction and designing of ultrasensitive broad spectral TIs based nanowire photodetector which can be exploited further as a promising material for optoelectronic devices.

  16. Raman scattering in layer indium selenide under pressure

    Science.gov (United States)

    Allahverdi, K.; Babaev, S.; Ellialtioǧlu, Ş.; Ismailov, A.

    1993-08-01

    Experimental results of Raman scattering spectra of ɛ-InSe crystals are presented at 300 K and pressures up to 10.2 kbar. Values of the mode-Grüneisen parameters were calculated using frequency-pressure dependences for five observed phonons. Changes of the shear force constants under pressure were analysed using linear-chain model both for ɛ-InSe and ɛ-GaSe crystals. The decrease of the shear force constants between metallic planes with increasing pressure are explained qualitatively by charge transfer from intralayer to interlayer space.

  17. Properties of sodium-intercalated indium and gallium selenides

    Energy Technology Data Exchange (ETDEWEB)

    Kovalyuk, Z.D.; Luk' yanyuk, V.K.

    1988-03-01

    The authors present the results of an investigation of some physicochemical properties of Na/sub x/InSe and Na/sub x/GaSe (chemical potential, diffusion of the intercalant) and they give an interpretation of the results based on the thermodynamic model of intercalants, constructed for dye chalcogenides of transition metals. Electrochemical and theoretical investigations indicate that first-stage structures form in the concentration ranges x = 0.15-1 for Na/sub x/GaSe. Calculations based on the use of the lattice-gas theory agree well with the experimental data and make it possible to determine the energy of interaction of intercalated ions in the van der Waals gap.

  18. Ab initio transport across bismuth selenide surface barriers

    KAUST Repository

    Narayan, Awadhesh

    2014-11-24

    © 2014 American Physical Society. We investigate the effect of potential barriers in the form of step edges on the scattering properties of Bi2Se3(111) topological surface states by means of large-scale ab initio transport simulations. Our results demonstrate the suppression of perfect backscattering, while all other scattering processes, which do not entail a complete spin and momentum reversal, are allowed. Furthermore, we find that the spin of the surface state develops an out-of-plane component as it traverses the barrier. Our calculations reveal the existence of quasibound states in the vicinity of the surface barriers, which appear in the form of an enhanced density of states in the energy window corresponding to the topological state. For double barriers we demonstrate the formation of quantum well states. To complement our first-principles results we construct a two-dimensional low-energy effective model and illustrate its shortcomings. Our findings are discussed in the context of a number of recent experimental works.

  19. Americium and plutonium separation by extraction chromatography for determination by accelerator mass spectrometry.

    Science.gov (United States)

    Kazi, Zakir H; Cornett, Jack R; Zhao, Xaiolei; Kieser, Liam

    2014-06-04

    A simple method was developed to separate Pu and Am using single column extraction chromatography employing N,N,N',N'-tetra-n-octyldiglycolamide (DGA) resin. Isotope dilution measurements of Am and Pu were performed using accelerator mass spectrometry (AMS) and alpha spectrometry. For maximum adsorption Pu was stabilized in the tetra valent oxidation state in 8M HNO3 with 0.05 M NaNO2 before loading the sample onto the resin. Am(III) was adsorbed also onto the resin from concentrated HNO3, and desorbed with 0.1 M HCl while keeping the Pu adsorbed. The on-column reduction of Pu(IV) to Pu(III) with 0.02 M TiCl3 facilitated the complete desorption of Pu. Interferences (e.g. Ca(2+), Fe(3+)) were washed off from the resin bed with excess HNO3. Using NdF3, micro-precipitates of the separated isotopes were prepared for analysis by both AMS and alpha spectrometry. The recovery was 97.7±5.3% and 95.5±4.6% for (241)Am and (242)Pu respectively in reagents without a matrix. The recoveries of the same isotopes were 99.1±6.0 and 96.8±5.3% respectively in garden soil. The robustness of the method was validated using certified reference materials (IAEA 384 and IAEA 385). The measurements agree with the certified values over a range of about 1-100 Bq kg(-1). The single column separation of Pu and Am saves reagents, separation time, and cost.

  20. Neutron capture and neutron-induced fission experiments on americium isotopes with DANCE

    Science.gov (United States)

    Jandel, M.; Bredeweg, T. A.; Stoyer, M. A.; Wu, C. Y.; Fowler, M. M.; Becker, J. A.; Bond, E. M.; Couture, A.; Haight, R. C.; Haslett, R. J.; Henderson, R. A.; Keksis, A. L.; O'Donnell, J. M.; Rundberg, R. S.; Ullmann, J. L.; Vieira, D. J.; Wilhelmy, J. B.; Wouters, J. M.

    2009-01-01

    Neutron capture cross section data on Am isotopes were measured using the Detector for Advanced Neutron Capture Experiments (DANCE) at Los Alamos National Laboratory. The neutron capture cross section was determined for 241Am for neutron energies between thermal and 320 keV. Preliminary results were also obtained for 243Am for neutron energies between 10 eV and 250 keV. The results on concurrent neutron-induced fission and neutron-capture measurements on 242mAm will be presented where the fission events were actively triggered during the experiments. In these experiments, a Parallel-Plate Avalanche Counter (PPAC) detector that surrounds the target located in the center of the DANCE array was used as a fission-tagging detector to separate (n,γ) events from (n,f) events. The first direct observation of neutron capture on 242mAm in the resonance region in between 2 and 9 eV of the neutron energy was obtained.

  1. Evaluation of the readsorption of plutonium and americium in dynamic fractionations of environmental solid samples

    DEFF Research Database (Denmark)

    Petersen, Roongrat; Hou, Xiaolin; Hansen, Elo Harald

    2008-01-01

    A dynamic extraction system exploiting sequential injection (SI) for sequential extractions incorporating a specially designed extraction column is developed to fractionate radionuclides in environmental solid samples such as soils and sediments. The extraction column can contain a large amount...... of the two radionuclides. However, the dynamic system is fully automated, eliminates manual separations, significantly reduces the operational time required, and offers detailed kinetic information....

  2. Effect of solvent on in vitro dissolution: Summary of results for uranium, americium, and cobalt aerosols

    Energy Technology Data Exchange (ETDEWEB)

    Guilmette, R.A.; Hoover, M.D.

    1995-12-01

    The revised 10 CFR Part 20 has adopted the ICRP Publication 30 method for calculating the committed effective dose equivalent from intakes of radionuclides. This dosimetry scheme requires knowledge or assumptions about the chemical form of the radionuclide, its particle size, and its known or assumed solubility. The solubility is classified as being either D (relatively soluble), W, or Y (relatively insoluble), depending on whether the material dissolves over periods of days, weeks, or years. Although Nuclear Regulatory Commission licensees may wish to take advantage of material-specific knowledge in order to adjust annual limits on intake and derived air concentrations, relatively few radioactive materials to which workers and the general population may be exposed have been adequately characterized either in terms of physicochemical form or solubility. Experimental measurement of solubility using some type of in vitro dissolution measurement system is therefore needed. However, there is currently no clear consensus regarding the appropriate design of in vitro dissolution systems, particularly when considering the range of different radionuclides to be studied, and the complexity of the biological mechanisms involved in the retention and clearance of inhaled deposited radioactive particles. The purpose of this study was to evaluate the effect of the several solvents on the dissolution of four test aerosols ({sup 57}Co{sub 3}O{sub 4}, {sup 241}AmO{sub 2}, ammonium diuranate [ADU], and U{sub 3}O{sub 8}) selected to encompass a variety of chemical and biochemical properties in vivo. The results of this study provide some guidance on the usefulness of in vitro dissolution tests for estimating the solubility of unknown radionuclide particles within the context of a simple model such as the class D, W, and Y formulation of ICRP 30.

  3. Rapid selective separation of americium/curium from simulated nuclear forensic matrices using triazine ligands

    Energy Technology Data Exchange (ETDEWEB)

    Higginson, Matthew A.; Livens, Francis R.; Heath, Sarah L. [Manchester Univ. (United Kingdom). Centre for Radiochemistry Research; Thompson, Paul; Marsden, Olivia J. [AWE, Aldermaston, Reading (United Kingdom); Harwood, Laurence M.; Hudson, Michael J. [Reading Univ. (United Kingdom). Dept. of Chemistry; Lewis, Frank W. [Reading Univ. (United Kingdom). Dept. of Chemistry; Northumbria Univ., Newcastle upon Tyne (United Kingdom). Dept. of Chemical and Forensic Sciences

    2015-07-01

    In analysis of complex nuclear forensic samples containing lanthanides, actinides and matrix elements, rapid selective extraction of Am/Cm for quantification is challenging, in particular due the difficult separation of Am/Cm from lanthanides. Here we present a separation process for Am/Cm(III) which is achieved using a combination of AG1-X8 chromatography followed by Am/Cm extraction with a triazine ligand. The ligands tested in our process were CyMe{sub 4}-BTPhen, CyMe{sub 4}-BTBP, CA-BTP and CA-BTPhen. Our process allows for purification and quantification of Am and Cm (recoveries 80% - 100%) and other major actinides in < 2 d without the use of multiple columns or thiocyanate. The process is unaffected by high level Ca(II)/Fe(III)/Al(III) (10 mg mL{sup -1}) and thus requires little pre-treatment of samples.

  4. Americium-Curium Stabilization - 5'' Cylindrical Induction Melter System Design Basis

    Energy Technology Data Exchange (ETDEWEB)

    Witt, D.C.

    1999-11-08

    Approximately 11,000 liters (3,600) gallons of solution containing isotopes of Am and Cm are currently stored in F-Canyon Tank 17.1. These isotopes were recovered during plutonium-242 production campaigns in the mid- and late-1970s. Experimental work for the project began in 1995 by the Savannah River Technology Center (SRTC). Details of the process are given in the various sections of this document.

  5. Concordant plutonium-241-americium-241 dating of environmental samples: results from forest fire ash

    Energy Technology Data Exchange (ETDEWEB)

    Goldstein, Steven J [Los Alamos National Laboratory; Oldham, Warren J [Los Alamos National Laboratory; Murrell, Michael T [Los Alamos National Laboratory; Katzman, Danny [Los Alamos National Laboratory

    2010-12-07

    We have measured the Pu, {sup 237}Np, {sup 241}Am, and {sup 151}Sm isotopic systematics for a set of forest fire ash samples from various locations in the western U.S. including Montana, Wyoming, Idaho, and New Mexico. The goal of this study is to develop a concordant {sup 241}Pu (t{sub 1/2} = 14.4 y)-{sup 241}Am dating method for environmental collections. Environmental samples often contain mixtures of components including global fallout. There are a number of approaches for subtracting the global fallout component for such samples. One approach is to use {sup 242}/{sup 239}Pu as a normalizing isotope ratio in a three-isotope plot, where this ratio for the nonglobal fallout component can be estimated or assumed to be small. This study investigates a new, complementary method of normalization using the long-lived fission product, {sup 151}Sm (t{sub 1/2} = 90 y). We find that forest fire ash concentrates actinides and fission products with {approx}1E10 atoms {sup 239}Pu/g and {approx}1E8 atoms {sup 151}Sm/g, allowing us to measure these nuclides by mass spectrometric (MIC-TIMS) and radiometric (liquid scintillation counting) methods. The forest fire ash samples are characterized by a western U.S. regional isotopic signature representing varying mixtures of global fallout with a local component from atmospheric testing of nuclear weapons at the Nevada Test Site (NTS). Our results also show that {sup 151}Sm is well correlated with the Pu nuclides in the forest fire ash, suggesting that these nuclides have similar geochemical behavior in the environment. Results of this correlation indicate that the {sup 151}Sm/{sup 239}Pu atom ratio for global fallout is {approx}0.164, in agreement with an independent estimate of 0.165 based on {sup 137}Cs fission yields for atmospheric weapons tests at the NTS. {sup 241}Pu-{sup 241}Am dating of the non-global fallout component in the forest fire ash samples yield ages in the late 1950's-early 1960's, consistent with a peak in NTS weapons testing at that time. The age results for this component are in agreement using both {sup 242}Pu and {sup 151}Sm normalizations, although the errors for the {sup 151}Sm correction are currently larger due to the greater uncertainty of their measurements. Additional efforts to develop a concordant {sup 241}Pu-{sup 241}Am dating method for environmental collections are underway with emphasis on soil cores.

  6. Functional sorbents for selective capture of plutonium, americium, uranium, and thorium in blood.

    Science.gov (United States)

    Yantasee, Wassana; Sangvanich, Thanapon; Creim, Jeffery A; Pattamakomsan, Kanda; Wiacek, Robert J; Fryxell, Glen E; Addleman, R Shane; Timchalk, Charles

    2010-09-01

    Self-assembled monolayer on mesoporous supports (SAMMS) are hybrid materials created from attachment of organic moieties onto very high surface area mesoporous silica. SAMMS with surface chemistries including three isomers of hydroxypyridinone, diphosphonic acid, acetamide phosphonic acid, glycinyl urea, and diethylenetriamine pentaacetate (DTPA) analog were evaluated for chelation of actinides ((239)Pu, (241)Am, uranium, thorium) from blood. Direct blood decorporation using sorbents does not have the toxicity or renal challenges associated with traditional chelation therapy and may have potential applications for critical exposure cases, reduction of nonspecific dose during actinide radiotherapy, and for sorbent hemoperfusion in renal insufficient patients, whose kidneys clear radionuclides at a very slow rate. Sorption affinity (K(d)), sorption rate, selectivity, and stability of SAMMS were measured in batch contact experiments. An isomer of hydroxypyridinone (3,4-HOPO) on SAMMS demonstrated the highest affinity for all four actinides from blood and plasma and greatly outperformed the DTPA analog on SAMMS and commercial resins. In batch contact, a fifty percent reduction of actinides in blood was achieved within minutes, and there was no evidence of protein fouling or material leaching in blood after 24 h. The engineered form of SAMMS (bead format) was further evaluated in a 100-fold scaled-down hemoperfusion device and showed no blood clotting after 2 h. A 0.2 g quantity of SAMMS could reduce 50 wt.% of 100 ppb uranium in 50 mL of plasma in 18 min and that of 500 dpm mL(-1) in 24 min. 3,4-HOPO-SAMMS has a long shelf-life in air and at room temperature for at least 8 y, indicating its feasibility for stockpiling in preparedness for an emergency. The excellent efficacy and stability of SAMMS materials in complex biological matrices suggest that SAMMS can also be used as orally administered drugs and for wound decontamination. By changing the organic groups of SAMMS, they can be used not only for actinides but also for other radionuclides. By using the mixture of these SAMMS materials, broad spectrum decorporation of radionuclides is very feasible.

  7. Subsurface Behavior of Plutonium and Americium at Non-Hanford Sites and Relevance to Hanford

    Energy Technology Data Exchange (ETDEWEB)

    Cantrell, Kirk J.; Riley, Robert G.

    2008-02-01

    Seven sites where Pu release to the environment has raised significant environmental concerns have been reviewed. A summary of the most significant hydrologic and geochemical features, contaminant release events and transport processes relevant to Pu migration at the seven sites is presented.

  8. New Synthetic Methods and Structure-Property Relationships in Neptunium, Plutonium, and Americium Borates. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Albrecht-Schmitt, Thomas Edward

    2013-09-14

    The past three years of support by the Heavy Elements Chemistry Program have been highly productive in terms of advanced degrees awarded, currently supported graduate students, peer-reviewed publications, and presentations made at universities, national laboratories, and at international conferences. Ph.D. degrees were granted to Shuao Wang and Juan Diwu, who both went on to post-doctoral appointments at the Glenn T. Seaborg Center at Lawrence Berkeley National Laboratory with Jeff Long and Ken Raymond, respectively. Pius Adelani completed his Ph.D. with me and is now a post-doc with Peter C. Burns. Andrea Alsobrook finished her Ph.D. and is now a post-doc at Savannah River with Dave Hobbs. Anna Nelson completed her Ph.D. and is now a post-doc with Rod Ewing at the University of Michigan. As can be gleaned from this list, students supported by the Heavy Elements Chemistry grant have remained interested in actinide science after leaving my program. This follows in line with previous graduates in this program such as Richard E. Sykora, who did his post-doctoral work at Oak Ridge National Laboratory with R. G. Haire, and Amanda C. Bean, who is a staff scientist at Los Alamos National Laboratory, and Philip M. Almond and Thomas C. Shehee, who are both staff scientists at Savannah River National Laboratory, Gengbang Jin who is a staff scientist at Argonne National Lab, and Travis Bray who has been a post-doc at both LBNL and ANL. Clearly this program is serving as a pipe-line for students to enter into careers in the national laboratories. About half of my students depart the DOE complex for academia or industry. My undergraduate researchers also remain active in actinide chemistry after leaving my group. Dan Wells was a productive undergraduate of mine, and went on to pursue a Ph.D. on uranium and neptunium chalcogenides with Jim Ibers at Northwestern. After earning his Ph.D., he went directly into the nuclear industry.

  9. Americium-241 and plutonium-237 turnover in mussels ( Mytilus galloprovincialis) living in field enclosures

    Science.gov (United States)

    Guary, J. C.; Fowler, S. W.

    1981-02-01

    Loss of 241Am and 237Pu from contaminated mussels ( Mytilus galloprovincialis) living in situ in the Mediterranean Sea is described as the sum of three exponential functions. In the case of 241Am, two short-lived compartments representing a total of 80% of the incorporated radionuclide turned over rapidly with biological half-lives of 2 and 3 weeks. The remaining fraction of 241Am, associated with a long-lived compartment, was lost at an extremely slow rate ( Tb1/2=1·3 years). Plutonium-237 turnover in the two short-lived compartments (containing 70% of the Pu) was more rapid ( Tb1/2=1-2 days and 2 weeks) than that of 241Am; however, there was some indication that subsequent loss rates of the two radionuclides in long-lived compartments may be similar if determined over comparable periods of time. Loss rates of 241Am differed for the various tissues, with the most rapid rates occurring in gill, viscera and shell. Abrupt changes in loss observed in muscle and mantle suggested a translocation of 241Am to muscle and mantle during depuration. Whole shell contained by far the largest fraction (˜90%) of both 241Am and 237Pu taken up; in addition, these radionuclides are not irreversibly bound to mussel shell but readily leach into the water. These observations suggest that mollusc shell may influence the biogeochemistry of transuranic elements in littoral zones.

  10. Plutonium and americium inventories in atmospheric fallout and sediment cores from Blelham Tarn, Cumbria (UK)

    Energy Technology Data Exchange (ETDEWEB)

    Michel, H. E-mail: herve.michel@unice.fr; Barci-Funel, G.; Dalmasso, J.; Ardisson, G.; Appleby, P.G.; Haworth, E.; El-Daoushy, F

    2002-07-01

    The objective of this paper is to report on the results of a study of {sup 238}Pu, {sup 239+240}Pu and {sup 241}Am inventories onto Blelham Tarn in Cumbria (UK). The atmospheric fallout inventory was obtained by analysing soil cores and the results are in good agreement with the literature: 101 Bq m{sup -2} for {sup 239+240}Pu; 4.5 Bq m{sup -2} for {sup 238}Pu and 37 Bq m{sup -2} for {sup 241}Am. The sediment core inventory for the whole lake is compared to the atmospheric fallout inventory. The sediment activity is 60-80% higher than the estimated fallout activity, showing a catchment area contribution and in particular the stream input.

  11. Plutonium and americium inventories in atmospheric fallout and sediment cores from Blelham Tarn, Cumbria (UK).

    Science.gov (United States)

    Michel, H; Barci-Funel, G; Dalmasso, J; Ardisson, G; Appleby, P G; Haworth, E; El-Daoushy, F

    2002-01-01

    The objective of this paper is to report on the results of a study of 238Pu, 239 + 240Pu and 241Am inventories onto Blelham Tarn in Cumbria (UK). The atmospheric fallout inventory was obtained by analysing soil cores and the results are in good agreement with the literature: 101 Bq m(-2) for 239 + 240Pu; 4.5 Bq m(-2) for 238Pu and 37 Bq m(-2) for 241Am. The sediment core inventory for the whole lake is compared to the atmospheric fallout inventory. The sediment activity is 60-80% higher than the estimated fallout activity, showing a catchment area contribution and in particular the stream input.

  12. Assessment of Neptunium, Americium, and Curium in the Savannah River Site Environment

    Energy Technology Data Exchange (ETDEWEB)

    Carlton, W.H. [Westinghouse Savannah River Company, AIKEN, SC (United States)

    1997-12-17

    A series of documents has been published in which the impact of various radionuclides released to the environment by Savannah River Site (SRS) operations has been assessed. The quantity released, the disposition of the radionuclides in the environment, and the dose to offsite individuals has been presented for activation products, carbon cesium, iodine, plutonium, selected fission products, strontium, technetium, tritium, uranium, and the noble gases. An assessment of the impact of nonradioactive mercury also has been published.This document assesses the impact of radioactive transuranics released from SRS facilities since the first reactor became operational late in 1953. The isotopes reported here are 239Np, 241Am, and 244Cm.

  13. Fundamental chemistry and materials science of americium in selected immobilization glasses

    Energy Technology Data Exchange (ETDEWEB)

    Haire, R.G. [Oak Ridge National Lab., TN (United States); Stump, N.A. [Winston-Salem State Univ., NC (United States). Dept. of Physical Sciences

    1996-12-01

    We have pursued some of the fundamental chemistry and materials science of Am in 3 glass matrices, two being high-temperature (850 and 1400 C mp) silicate-based glasses and the third a sol-gel glass. Optical spectroscopy was the principal tool. One aspect of this work was to determine the oxidation state exhibited by Am in these matrices, as well as factors that control or may alter this state. A correlation was noted between the oxidation state of the f-elements in the two high-temperature glasses with their high-temperature oxide chemistries. One exception was Am: although AmO{sub 2} is the stable oxide encountered in air, when this dioxide was incorporated into the high-temperature glasses, only trivalent Am was found in the products. When Am(III) was used to prepare the sol-gel glasses at ambient temperature, and after these products were heated in air to 800 C, only Am(III) was observed. Potential explanations for the unexpected Am behavior is offered in the context of its basic chemistry. Experimental spectra, spectroscopic assignments, etc. are discussed.

  14. Americium, curium and neodymium analysis in ECRIX-H irradiated pellet. Sample preparation for TIMS measurements

    Energy Technology Data Exchange (ETDEWEB)

    Esbelin, E.; Buravand, E. [Commissariat a l' Energie Atomique, Bagnols-sur-Ceze (France). Centre de Marcoule; Bejaoui, S.; Lamontagne, J.; Bonnerot, J.M. [Commissariat a l' Energie Atomique, St-Paul-Lez-Durance (France). Centre de Cadarache

    2013-08-01

    This paper concerns quantitative isotopic analysis of Am, Cm and Nd contained in an irradiated AmO{sub 1.62}/MgO pellet. The complete analysis protocol is described, from dissolution of the pellets in a shielded line to the laboratory glove separation processes box for TIMS analysis. Emphasis is placed on the separation processes: by ion exchange resin in a hot cell and by HPLC in the laboratory. Intermediate measurements by X-ray fluorescence, alpha spectrometry, and ICP-AES are described. (orig.)

  15. Optimization of TRPO Process Parameters for Americium Extraction from High Level Waste

    Institute of Scientific and Technical Information of China (English)

    CHEN Jing; WANG Jianchen; SONG Chongli

    2001-01-01

    The numerical calculations for Am multistage fractional extraction by trialkyl phosphine oxide (TRPO) were verified by a hot test.1750 L/t-U high level waste (HLW) was used as the feed to the TRPO process.The analysis used the simple objective function to minimize the total waste content in the TRPO process streams.Some process parameters were optimized after other parameters were selected.The optimal process parameters for Am extraction by TRPO are:10 stages for extraction and 2 stages for scrubbing;a flow rate ratio of 0.931 for extraction and 4.42 for scrubbing;nitric acid concentration of 1.35 mol/L for the feed and 0.5 mol/L for the scrubbing solution.Finally,the nitric acid and Am concentration profiles in the optimal TRPO extraction process are given.

  16. Vertical distribution of radiocaesium, plutonium and americium in the Catalan Sea (northwestern Mediterranean)

    Energy Technology Data Exchange (ETDEWEB)

    Molero, J.; Sanchez-Cabeza, J.A.; Merino, J.; Pujol, Ll.; Vidal-Quadras, A. [Universidad Autonoma de Barcelona (Spain). Facultad de Ciencias; Mitchell, P.I. [University Coll., Dublin (Ireland). Lab. of Radiation Physics

    1995-07-01

    Caesium-137, {sup 239,240}Pu and {sup 241}Am concentration profiles (0-1000 m) have been determined in unfiltered large volume water samples collected from the Catalan Sea (northwestern Mediterranean). Results showed that radiocaesium concentration decreases quickly through the water column while the transuranic concentration increases with depth, showing a faster migration to the bottom layers. Comparing our results with those reported by other authors (1975-1980), radiocaesium input from Chernobyl releases has been identified through the profile. In addition, transuranic concentrations have decreased considerably in the different layers of the profile. (Author).

  17. Americium and plutonium separation by extraction chromatography for determination by accelerator mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Kazi, Zakir H. [Department of Earth Science, University of Ottawa, 140 Louis Pasteur Avenue, Ottawa K1N 6N5 (Canada); Cornett, Jack R., E-mail: jack.cornett@uottawa.ca [Department of Earth Science, University of Ottawa, 140 Louis Pasteur Avenue, Ottawa K1N 6N5 (Canada); Zhao, Xaiolei; Kieser, Liam [Department of Physics, University of Ottawa, 140 Louis Pasteur Avenue, Ottawa K1N 6N5 (Canada)

    2014-06-01

    Highlights: • Am and Pu were adsorbed and separated using a single extraction chromatography DGA column. • Pu was eluted from the column completely using on-column reduction of Pu(IV) to Pu(III). • ²⁴¹Am and 239,240Pu measurements by accelerator mass spectrometry (AMS) agree with the certified values in two SRMs. Abstract: A simple method was developed to separate Pu and Am using single column extraction chromatography employing N,N,N',N'-tetra-n-octyldiglycolamide (DGA) resin. Isotope dilution measurements of Am and Pu were performed using accelerator mass spectrometry (AMS) and alpha spectrometry. For maximum adsorption Pu was stabilized in the tetra valent oxidation state in 8 M HNO₃ with 0.05 M NaNO₂ before loading the sample onto the resin. Am(III) was adsorbed also onto the resin from concentrated HNO₃, and desorbed with 0.1 M HCl while keeping the Pu adsorbed. The on-column reduction of Pu(IV) to Pu(III) with 0.02 M TiCl₃ facilitated the complete desorption of Pu. Interferences (e.g. Ca²⁺, Fe³⁺) were washed off from the resin bed with excess HNO₃. Using NdF₃, micro-precipitates of the separated isotopes were prepared for analysis by both AMS and alpha spectrometry. The recovery was 97.7 ± 5.3% and 95.5 ± 4.6% for ²⁴¹Am and ²⁴²Pu respectively in reagents without a matrix. The recoveries of the same isotopes were 99.1 ± 6.0 and 96.8 ± 5.3% respectively in garden soil. The robustness of the method was validated using certified reference materials (IAEA 384 and IAEA 385). The measurements agree with the certified values over a range of about 1–100 Bq kg⁻¹. The single column separation of Pu and Am saves reagents, separation time, and cost.

  18. Criteria Considered in Selecting Feed Items for Americium-241 Oxide Production Operations

    Energy Technology Data Exchange (ETDEWEB)

    Schulte, Louis D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2015-01-30

    The analysis in this document serves the purpose of defining a number of attributes in selection of feed items to be utilized in recovery/recycle of Pu and also production operations of 241AmO2 material intended to meet specification requirements. This document was written in response to a specific request on the part of the 2014 annual program review which took place over the dates of October 28-29, 2014. A number of feed attributes are noted including: (1) Non-interference with existing Pu recovery operations; (2) Content of sufficient 241Am to allow process efficiency in recovery operations; (3) Absence of indications that 243Am might be mixed in with the Pu/241Am material; (4) Absence of indications that Cm might be mixed in with the Pu/241Am material; (5) Absence of indications of other chemical elements that would present difficulty in chemical separation from 241Am; (6) Feed material not expected to present difficulty in dissolution; (7) Dose issues; (8) Process efficiency; (9) Size; (10) Hazard associated with items and package configuration in the vault; (11) Within existing NEPA documentation. The analysis in this document provides a baseline of attributes considered for feed materials, but does not presume to replace the need for technical expertise and judgment on the part of individuals responsible for selecting the material feed to be processed. This document is not comprehensive as regards all attributes that could prove to be important. The value of placing a formal QA hold point on accepting feed items versus more informal management of feed items is discussed in the summation of this analysis. The existing planned QA hold points on 241AmO2 products produced and packaged may be adequate as the entire project is based on QA of the product rather than QA of the process. The probability of introduction of items that would inherently cause the241AmO2 products produced to be outside of specification requirements appears to be rather small.

  19. A Review of Subsurface Behavior of Plutonium and Americium at the 200-PW-1/3/6 Operable Units

    Energy Technology Data Exchange (ETDEWEB)

    Cantrell, Kirk J.; Riley, Robert G.

    2008-01-31

    This report begins with a brief summary of the history and current status of 200-PW-1/3/6 OUs in section 2.0. This is followed by a description of our concentual model of Pu/Am migration at the 200-PW-1/3/6 OUs, during both past artificial recharge conditions and current natural recharge condictions (section 3.0). Section 4.0 discusses data gaps and information needs. The final section (section 5.0) provides recommendations for futher work to address the data gaps and information needs identified in section 4.0.

  20. Input contribution and vertical migration of plutonium, americium and cesium in lake sediments (Belham Tarn, Cumbria, UK)

    Energy Technology Data Exchange (ETDEWEB)

    Michel, H.; Barci-Funel, G.; Barci, V.; Ardisson, G. [Lab. de Radiochimie et de Radioecologie, Univ. de Nice Sophia Antipolis, Nice (France)

    2002-07-01

    The record of the global atmospheric fallout could be found in the lake sediments. A mass balance for fallout radionuclides in Blelham Tarn and its catchment is established. The sediment activity contribution is coming from direct atmospheric fallout and from indirect atmospheric fallout via the catchment. The catchement activity is conveyed to the sediment by the rivers and the direct streaming. A comparison of the fallout and the sediment inventory allows the activity estimation of these different contributions and to understand the mobility of these elements on the catchment and in the sediments. The study of activity profile in sediment core allows to characterise the different radioactive events occurred in the past. For the lake Blelham, the results show two cesium activity peaks and only one peak for transuranic activities. The deepest peaks correspond to the atmospheric nuclear test fallout in the sixties (1963) and the second peak to the Chernobyl accident (1986). The activity ratio {sup 239-240}Pu/{sup 137}Cs allows estimating the ratio between cesium activities in sediments coming from these two events. Plutonium and cesium diffusion coefficients are calculated with a simple analytical model. (orig.)

  1. Analysis of cascade impactor and EPA method 29 data from the americium/curium pilot melter system

    Energy Technology Data Exchange (ETDEWEB)

    Zamecnik, J.R.

    1997-11-01

    The offgas system of the Am/Cm pilot melter at TNX was characterized by measuring the particulate evolution using a cascade impactor and EPA Method 29. This sampling work was performed by John Harden of the Clemson Environmental Technologies Laboratory, under SCUREF Task SC0056. Elemental analyses were performed by the SRTC Mobile Laboratory.Operation of the Am/Cm melter with B2000 frit has resulted in deposition of PbO and boron compounds in the offgas system that has contributed to pluggage of the High Efficiency Mist Eliminator (HEME). Sampling of the offgas system was performed to quantify the amount of particulate in the offgas system under several sets of conditions. Particulate concentration and particle size distribution were measured just downstream of the melter pressure control air addition port and at the HEME inlet. At both locations, the particulate was measured with and without steam to the film cooler while the melter was idled at about 1450 degrees Celsius. Additional determinations were made at the melter location during feeding and during idling at 1150 degrees Celsius rather than 1450 degrees Celsius (both with no steam to the film cooler). Deposition of particulates upstream of the melter sample point may have, and most likely did occur in each run, so the particulate concentrations measured do no necessarily reflect the total particulate emission at the melt surface. However, the data may be used in a relative sense to judge the system performance.

  2. Rapid selective separation of americium/curium\\ud from simulated nuclear forensic matrices using\\ud triazine ligands

    OpenAIRE

    Higginson, Matthew A.; Thompson, Paul; Marsden, Olivia J.; Livens, Francis R.; Harwood, Laurence M.; Lewis, Frank W.; Hudson, Michael J.; Heath, Sarah L.

    2015-01-01

    In analysis of complex nuclear forensic samples\\ud containing lanthanides, actinides and matrix elements,\\ud rapid selective extraction of Am/Cm for quantification\\ud is challenging, in particular due the difficult separation\\ud of Am/Cm from lanthanides. Here we present\\ud a separation process for Am/Cm(III) which is achieved\\ud using a combination of AG1-X8 chromatography followed\\ud by Am/Cm extraction with a triazine ligand. The ligands\\ud tested in our process were CyMe4-BTPhen, CyMe4-\\u...

  3. LITERATURE REVIEW ON THE SORPTION OF PLUTONIUM, URANIUM, NEPTUNIUM, AMERICIUM AND TECHNETIUM TO CORROSION PRODUCTS ON WASTE TANK LINERS

    Energy Technology Data Exchange (ETDEWEB)

    Li, D.; Kaplan, D.

    2012-02-29

    The Savannah River Site (SRS) has conducted performance assessment (PA) calculations to determine the risk associated with closing liquid waste tanks. The PA estimates the risk associated with a number of scenarios, making various assumptions. Throughout all of these scenarios, it is assumed that the carbon-steel tank liners holding the liquid waste do not sorb the radionuclides. Tank liners have been shown to form corrosion products, such as Fe-oxyhydroxides (Wiersma and Subramanian 2002). Many corrosion products, including Fe-oxyhydroxides, at the high pH values of tank effluent, take on a very strong negative charge. Given that many radionuclides may have net positive charges, either as free ions or complexed species, it is expected that many radionuclides will sorb to corrosion products associated with tank liners. The objective of this report was to conduct a literature review to investigate whether Pu, U, Np, Am and Tc would sorb to corrosion products on tank liners after they were filled with reducing grout (cementitious material containing slag to promote reducing conditions). The approach was to evaluate radionuclides sorption literature with iron oxyhydroxide phases, such as hematite ({alpha}-Fe{sub 2}O{sub 3}), magnetite (Fe{sub 3}O{sub 4}), goethite ({alpha}-FeOOH) and ferrihydrite (Fe{sub 2}O{sub 3} {center_dot} 0.5H{sub 2}O). The primary interest was the sorption behavior under tank closure conditions where the tanks will be filled with reducing cementitious materials. Because there were no laboratory studies conducted using site specific experimental conditions, (e.g., high pH and HLW tank aqueous and solid phase chemical conditions), it was necessary to extend the literature review to lower pH studies and noncementitious conditions. Consequently, this report relied on existing lower pH trends, existing geochemical modeling, and experimental spectroscopic evidence conducted at lower pH levels. The scope did not include evaluating the appropriateness of K{sub d} values for the Fe-oxyhydroxides, but instead to evaluate whether it is a conservative assumption to exclude this sorption process of radionuclides onto tank liner corrosion products in the PA model. This may identify another source for PA conservatism since the modeling did not consider any sorption by the tank liner.

  4. Structure-fluctuation-induced abnormal thermoelectric properties in semiconductor copper selenide

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Huili [Chinese Academy of Sciences; Shi, Xun [Chinese Academy of Sciences; Kirkham, Melanie J [ORNL; Wang, Hsin [ORNL; Li, Qiang [Brookhaven National Laboratory (BNL); Uher, Ctirad [University of Michigan; Zhang, Wenqing [Shanghai Institute of Ceramics, Chinese Academy of Sciences (SICCAS); Chen, Lidong [Chinese Academy of Sciences

    2013-01-01

    Thermoelectric effects and related technologies have attracted a great interest due to the world-wide energy harvesting. Thermoelectricity has usually been considered in the context of stable material phases. Here we report that the fluctuation of structures during the second-order phase transition in Cu2Se semiconductor breaks the conventional trends of thermoelectric transports in normal phases, leading to a critically phase-transition-enhanced thermoelectric figure of merit zT above unity at 400K, a three times larger value than for the normal phases. Dynamic structural transformations introduce intensive fluctuations and extreme complexity, which enhance the carrier entropy and thus the thermopower, and strongly scatter carriers and phonons as well to make their transports behave critically.

  5. Formation of Two-Dimensional Copper Selenide on Cu(111) at Very Low Selenium Coverage.

    Science.gov (United States)

    Walen, Holly; Liu, Da-Jiang; Oh, Junepyo; Yang, Hyun Jin; Kim, Yousoo; Thiel, Patricia A

    2016-07-18

    Using scanning tunneling microscopy (STM), we observed that adsorption of Se on Cu(111) produced islands with a (√3×√3)R30° structure at Se coverages far below the structure's ideal coverage of 1/3 monolayer. On the basis of density functional theory (DFT), these islands cannot form due to attractive interactions between chemisorbed Se atoms. DFT showed that incorporating Cu atoms into the √3-Se lattice stabilizes the structure, which provided a plausible explanation for the experimental observations. STM revealed three types of √3 textures. We assigned two of these as two-dimensional layers of strained CuSe, analogous to dense planes of bulk klockmannite (CuSe). Klockmannite has a bulk lattice constant that is 11 % shorter than √3 times the surface lattice constant of Cu(111). This offers a rationale for the differences observed between these textures, for which strain limits the island size or distorts the √3 lattice. STM showed that existing step edges adsorb Se and facet toward ⟨12‾ 1⟩, which is consistent with DFT.

  6. Enhanced thermoelectric performance of spark plasma sintered copper-deficient nanostructured copper selenide

    Science.gov (United States)

    Tyagi, Kriti; Gahtori, Bhasker; Bathula, Sivaiah; Jayasimhadri, M.; Singh, Niraj Kumar; Sharma, Sakshi; Haranath, D.; Srivastava, A. K.; Dhar, Ajay

    2015-06-01

    We report the thermoelectric properties of nanostructured Cu-deficient Cu2Se, which was synthesized by high energy ball milling followed by spark plasma sintering. Our method obtained a significant enhancement in the thermoelectric figure of merit (ZT), i.e., ~1.4 at 973 K, which was ~30% higher than its bulk counterpart. This enhancement in the thermoelectric performance was due mainly to a significant reduction in the lattice thermal conductivity, which was attributed to enhanced phonon scattering at various length scales by nanoscale defects as well as abundant nanograin boundaries. The nanoscale defects were characterized by transmission electron microscopy of the nanostructured Cu2-xSe samples, which formed the basis of the ZT enhancement.

  7. Synthesis and structure determination of potassium copper selenide nanowires and solid-state supercapacitor application

    Science.gov (United States)

    Zhang, Kaiyou; Chen, Hong; Wang, Xue; Guo, Donglin; Hu, Chenguo; Wang, Shuxia; Sun, Junliang; Leng, Qiang

    2014-12-01

    The new ternary alkali metal copper chalcogenide KCu4Se8 nanowires with average length of 30 μm are synthesized using a modified composite-hydroxide mediated (M-CHM) approach. The prepared KCu4Se8 is characterized by XRD, EDS, FESEM and TEM analysis. The structure is determined by the newly developed Rotation Electron Diffraction technique. It is identified to be a body center tetragonal phase. The prepared KCu4Se8 is used to fabricate solid-state supercapacitors in which the thin film of the electrodes are made with pressure of 0 MPa, 5 MPa and 10 MPa, and their electrochemical properties are tested. It is found that 0 MPa supercapacitor displays best electrochemical performance and the specific capacitance of 25.3 F g-1 is obtained at the scan rate of 5 mV s-1. It also shows good long-term cycle property by recording 5000 cycles of galvanostatic charge/discharge operation. The specific capacitance can be enhanced to 93.7 F g-1 at the scan rate of 5 mV s-1 by coating 0.1 mg V2O5 nanowire on 0 MPa KCu4Se8 electrode.

  8. Bath Parameter Dependence of Chemically-Deposited Copper Selenide Thin Film

    Science.gov (United States)

    Al-Mamun; Islam, A. B. M. O.

    In this article, a low cost chemical bath deposition (CBD) technique has been used for the preparation of Cu2-xSe thin films on to glass substrate. Different thin films (0.2-0.6 μm) were prepared by adjusting the bath parameter like concentration of ammonia, deposition time, temperature of the solution, and the ratios of the mixing composition between copper and selenium in the reaction bath. From these studies, it reveals that at low concentration of ammonia or TEA, the terminal thicknesses of the films are less, which gradually increases with the increase of concentrations and then drop down at still higher concentrations. It has been found that complexing the Cu2+ ions with TEA first, and then addition of ammonia yields better results than the reverse process. The film thickness increases with the decrease of value x of Cu2-xSe.

  9. Liquid precursor for deposition of copper selenide and method of preparing the same

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, Calvin J.; Miedaner, Alexander; Franciscus Antonius Maria Van Hest, Marinus; Ginley, David S.; Hersh, Peter A.; Eldada, Louay; Stanbery, Billy J.

    2015-09-08

    Liquid precursors containing copper and selenium suitable for deposition on a substrate to form thin films suitable for semiconductor applications are disclosed. Methods of preparing such liquid precursors and methods of depositing a precursor on a substrate are also disclosed.

  10. Atomically thick bismuth selenide freestanding single layers achieving enhanced thermoelectric energy harvesting.

    Science.gov (United States)

    Sun, Yongfu; Cheng, Hao; Gao, Shan; Liu, Qinghua; Sun, Zhihu; Xiao, Chong; Wu, Changzheng; Wei, Shiqiang; Xie, Yi

    2012-12-19

    Thermoelectric materials can realize significant energy savings by generating electricity from untapped waste heat. However, the coupling of the thermoelectric parameters unfortunately limits their efficiency and practical applications. Here, a single-layer-based (SLB) composite fabricated from atomically thick single layers was proposed to optimize the thermoelectric parameters fully. Freestanding five-atom-thick Bi(2)Se(3) single layers were first synthesized via a scalable interaction/exfoliation strategy. As revealed by X-ray absorption fine structure spectroscopy and first-principles calculations, surface distortion gives them excellent structural stability and a much increased density of states, resulting in a 2-fold higher electrical conductivity relative to the bulk material. Also, the surface disorder and numerous interfaces in the Bi(2)Se(3) SLB composite allow for effective phonon scattering and decreased thermal conductivity, while the 2D electron gas and energy filtering effect increase the Seebeck coefficient, resulting in an 8-fold higher figure of merit (ZT) relative to the bulk material. This work develops a facile strategy for synthesizing atomically thick single layers and demonstrates their superior ability to optimize the thermoelectric energy harvesting.

  11. Tailoring the exciton fine structure of cadmium selenide nanocrystals with shape anisotropy and magnetic field.

    Science.gov (United States)

    Sinito, Chiara; Fernée, Mark J; Goupalov, Serguei V; Mulvaney, Paul; Tamarat, Philippe; Lounis, Brahim

    2014-11-25

    We use nominally spheroidal CdSe nanocrystals with a zinc blende crystal structure to study how shape perturbations lift the energy degeneracies of the band-edge exciton. Nanocrystals with a low degree of symmetry exhibit splitting of both upper and lower bright state degeneracies due to valence band mixing combined with the isotropic exchange interaction, allowing active control of the level splitting with a magnetic field. Asymmetry-induced splitting of the bright states is used to reveal the entire 8-state band-edge fine structure, enabling complete comparison with band-edge exciton models.

  12. Crystal quality of two-dimensional gallium telluride and gallium selenide using Raman fingerprint

    Directory of Open Access Journals (Sweden)

    Jannatul Susoma

    2017-01-01

    Full Text Available We have established Raman fingerprint of GaTe and GaSe to investigate their crystal quality. As unencapsulated, they both oxidise in ambient conditions which can be detected in their Raman analysis. X-ray photoelectron spectroscopy (XPS analysis shows a good agreement with Raman analysis. 50-nm-thick Al2O3 encapsulation layer deposited by atomic layer deposition (ALD inhibits degradation in ambient conditions.

  13. Design and Optimization of Copper Indium Gallium Selenide Thin Film Solar Cells

    Science.gov (United States)

    2015-09-01

    pair to generate power , a photon must displace a valence electron from a bond inside of the crystalline structure of the solar cell. The energy ...7 1. Solar Spectrum and Wavelength Energy ....................................7 2. Photogeneration of Electron Hole Pairs...Expeditionary Energy Office GREENS Ground Renewable Expeditionary Energy System NPS Naval Postgraduate School SPACES Solar Portable Alternative

  14. Theoretical Investigations of the Effects of Lithium Intercalation on the Properties of Indium Selenide

    Science.gov (United States)

    Gomes da Costa, Manuel Pedro Fernandes

    The effect of intercalating lithium into gamma-InSe and beta -InSe has been investigated. The energy bands of pure gamma -InSe and pure beta-InSe were calculated using an overlap-reduced semi-empirical tight-binding method. The parameters for the interactions of Li atoms with In and Se atoms were obtained using the atomic wave-functions of Clementi and Roetti and the Heine-Abarenkov model potential. We established the positions of minimum potential inside the unit cell of the two InSe polytypes where the lithium atoms are most likely to be found. By placing lithium atoms in these sites, we calculated the modifications of the energy bands produced by the introduction of one Li atom per unit cell in gamma-InSe and two lithium atoms per unit cell in beta -InSe. The activation energy for movement of a Li atom between local energy minima was also calculated. The results have been correlated with the optical absorption and photoluminescence data of InSe and Li-intercalated InSe. The lattice dynamics of both the pure gamma- and beta-polytypes of the layer compound InSe have been investigated using a model containing short-range central forces and long -range Coulomb interactions. The normal mode frequencies and eigenvectors were determined by diagonalizing the dynamical matrix. The results have been correlated with the infrared and Raman spectra in InSe. The procedure was then extended to include one lithium ion per unit cell in a site of minimum potential in both the gamma-InSe and the beta-InSe polytypes. The effect of intercalated Li atoms on the vibrational modes and on the infrared and Raman spectra was then investigated.

  15. Photoemission study of CdS heterojunction formation with binary selenide semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, A.J. [National Renewable Energy Laboratory, Golden, Colorado 80401 (United States)

    1995-11-01

    Synchrotron radiation soft x-ray photoemission spectroscopy was used to investigate the development of the electronic structure at the CdS/Cu{sub 2{minus}{ital x}}Se and CdS/In{sub 6}Se{sub 7} heterojunction interfaces. Cu{sub 2{minus}{ital x}}Se and In{sub 6}Se{sub 7} layers were deposited on GaAs (100) by physical vapor deposition from Cu{sub 2}Se and In{sub 2}Se{sub 3} sources. CdS overlayers were then deposited {ital in} {ital situ}, at room temperature, in steps on these layers. Photoemission measurements were acquired after each growth to observe changes in the valence-band electronic structure and changes in the In4{ital d} and Cd4{ital d} core lines. The results were used to correlate the interfacial chemistry with the electronic structure and to directly determine the CdS/Cu{sub 2{minus}{ital x}}Se and CdS/In{sub 6}Se{sub 7} heterojunction valence-band discontinuities and the consequent heterojunction band diagrams. These results are compared to the valence-band offset ({Delta}{ital E}{sub {ital v}}) for the CdS/CuInSe{sub 2} heterojunction interface.

  16. Electrical transport and photoconduction in ambipolar tungsten diselenide and n-type indium selenide

    Science.gov (United States)

    Fralaide, Michael Orcino

    In today's "silicon age" in which we live, field-effect transistors (FET) are the workhorse of virtually all modern-day electronic gadgets. Although silicon currently dominates most of these electronics, layered 2D transition metal dichalcogenides (TMDCs) have great potential in low power optoelectronic applications due to their indirect-to-direct band gap transition from bulk to few-layer and high on/off switching ratios. TMDC WSe2 is studied here, mechanically exfoliated from CVT-grown bulk WSe2 crystals, to create a few-layered ambipolar FET, which transitions from dominant p-type behavior to n-type behavior dominating as temperature decreases. A high electron mobility mu>150 cm2V-1s-1 was found in the low temperature region near 50 K. Temperature-dependent photoconduction measurements were also taken, revealing that both the application of negative gate bias and decreasing the temperature resulted in an increase of the responsivity of the WSe2 sample. Besides TMDCs, Group III-VI van der Waals structures also show promising anisotropic optical, electronic, and mechanical properties. In particular, mechanically exfoliated few-layered InSe is studied here for its indirect band gap of 1.4 eV, which should offer a broad spectral response. It was found that the steady state photoconduction slightly decreased with the application of positive gate bias, likely due to the desorption of adsorbates on the surface of the sample. A room temperature responsivity near 5 AW -1 and external quantum efficiency of 207% was found for the InSe FET. Both TMDC's and group III-VI chalcogenides continue to be studied for their remarkably diverse properties that depend on their thickness and composition for their applications as transistors, sensors, and composite materials in photovoltaics and optoelectronics.

  17. Temperature dependent local atomic displacements in ammonia intercalated iron selenide superconductor.

    Science.gov (United States)

    Paris, E; Simonelli, L; Wakita, T; Marini, C; Lee, J-H; Olszewski, W; Terashima, K; Kakuto, T; Nishimoto, N; Kimura, T; Kudo, K; Kambe, T; Nohara, M; Yokoya, T; Saini, N L

    2016-01-01

    Recently, ammonia-thermal reaction has been used for molecular intercalation in layered FeSe, resulting a new Lix(NH3)yFe2Se2 superconductor with Tc ~ 45 K. Here, we have used temperature dependent extended x-ray absorption fine structure (EXAFS) to investigate local atomic displacements in single crystals of this new superconductor. Using polarized EXAFS at Fe K-edge we have obtained direct information on the local Fe-Se and Fe-Fe bondlengths and corresponding mean square relative displacements (MSRD). We find that the Se-height in the intercalated system is lower than the one in the binary FeSe, suggesting compressed FeSe4 tetrahedron in the title system. Incidentally, there is hardly any effect of the intercalation on the bondlengths characteristics, revealed by the Einstein temperatures, that are similar to those found in the binary FeSe. Therefore, the molecular intercalation induces an effective compression and decouples the FeSe slabs. Furthermore, the results reveal an anomalous change in the atomic correlations across Tc, appearing as a clear decrease in the MSRD, indicating hardening of the local lattice mode. Similar response of the local lattice has been found in other families of superconductors, e.g., A15-type and cuprates superconductors. This observation suggests that local atomic correlations should have some direct correlation with the superconductivity.

  18. Impact of secondary barriers on copper-indium-gallium-selenide solar-cell operation

    Science.gov (United States)

    Pudov, Alexei O.

    Thin-film solar cells based on CuInSe2 (CIS) absorber with a band gap of Eg = 1.0 eV and also based on CuIn1-x GaxSe2 (CIGS) alloy absorbers with a band-gap range of Eg = 1.0--1.67 eV are investigated in this work. Intermediate "buffer" semiconductor layers in p-n junctions of CIGS solar cells often improve photodiode properties of the devices. The primary goal of the thesis is to study secondary barriers in the conduction band at the buffer/absorber interface, which may limit current transport and thus reduce the efficiency of the solar cells. The secondary goal is to explore alternative wide-bandgap buffers in CIGS cell structures. CIGS cells with standard CdS buffer layers, and alternative ZnS(O,OH) and InS(O,OH) buffer layers were studied. CdS/CuIn1-xGaxSe2 solar cells with variable Ga content have a range of conduction-band offsets (DeltaEc) in the junction from moderately positive (spike offsets) in CdS/CuInSe2 to moderately negative (cliff offsets) in CdS/CuGaSe 2. Moderate conduction-band spikes in CdS/CIS and low-Ga CdS/CIGS are expected to cause distortions in diode current-voltage (J-V) curves of such solar cells under "red" illumination (hnu < Eg(buffer)); no J-V distortions are expected for high-Ga CdS/CIGS with cliff offsets. These predictions were confirmed in experiments: the distortions were absent for cells with Eg above 1.2--1.3 eV, at which CdS/CIGS DeltaE c is near zero. Experiments and numerical simulations showed that one approach to reduce secondary barriers and J-V distortions in low-Ga high-spike cells is to thin the buffer layer(s). Blue photons (hnu above Eg(buffer)) in the solar spectrum induce photoconductivity in the otherwise compensated buffers, which also results in lowering of the secondary barriers. It was shown that CIGS cells with CdS, InS(O,OH), and ZnS(O,OH) buffers have a similar response to "blue" photons: J-V distortion, if present under red light, is reduced or entirely disappears with blue-light exposure within minutes. The distortion re-appearance without blue light is the order of a thousand times slower. Using wider-gap buffers, such as InS(O,OH) and ZnS(O,OH), was shown to produce higher photocurrents in solar cells. This photocurrent improvement is a central direction in the effort of further increasing efficiencies of thin-film solar cells.

  19. Effect of tellurium addition on the physical properties of germanium selenide glassy semiconductors

    Science.gov (United States)

    Sharma, Pankaj; Katyal, S. C.

    2008-10-01

    Effect of tellurium (Te) addition on the physical properties, density ( ρ), molar volume ( Vm), compactness ( δ), cohesive energy (CE), coordination number ( m), lone pair electrons ( L) and glass transition temperature ( Tg) of Ge 10Se 90-xTe x ( x=0, 10, 20, 30, 40, 50) bulk glassy alloy has been investigated. The density of the glassy alloys has been found to increase with the increasing Te content. The molar volume and compactness of the structure of the glass, determined from measured density of the glass, have been found to increase with the increase of Te content. The CE of the investigated samples has been calculated using the chemical bond approach (CBA) and is correlated with decrease in optical band gap with the increase of Te content. The glass transition temperature has been estimated using Tichy-Ticha approach and found to increase with the increase of Te content. This has been observed that the estimated glass transition temperature using Tichy-Ticha approach is not consistent with experimental results.

  20. Effect of antimony addition on the optical behaviour of germanium selenide thin films

    Science.gov (United States)

    Sharma, Parikshit; Rangra, V. S.; Sharma, Pankaj; Katyal, S. C.

    2008-11-01

    This paper reports the influence of antimony (Sb) addition on the optical properties (optical energy gap and refractive index) of thin solid films of the chalcogenide glassy Ge0.17Se0.83-xSbx(x = 0, 0.03, 0.09, 0.12, 0.15) system. This has been done by analysing the transmittance (T) and reflectance (R) spectra in the spectral region 400-2000 nm. It was found that the optical energy gap decreases with increasing Sb content from 1.92 to 1.63 eV with an uncertainty of ± 0.01 eV. The results were interpreted in terms of bond energies and on the basis of the concept of electronegativity. The refractive index has been found to increase with increasing Sb content. The increase in the refractive index has been explained on the basis of polarizability. Dispersion of refractive index has been analysed using the Wemple-DiDomenico single oscillator model. The static refractive index increased from 2.45 to 2.91 for the studied compositions. An estimate of the energy gap has also been taken theoretically and it has been found that both the optical energy gap (measured from T and R spectra) and the theoretical energy gap follow similar trends.

  1. Effect of antimony addition on the optical behaviour of germanium selenide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Parikshit; Rangra, V S [Department of Physics, H. P. University, Summer Hill, Shimla (171005) (India); Sharma, Pankaj; Katyal, S C [Department of Physics, Jaypee University of Information Technology, Waknaghat, Solan, H.P. (173215) (India)], E-mail: pankaj.sharma@juit.ac.in, E-mail: sharma_parikshit@yahoo.com

    2008-11-21

    This paper reports the influence of antimony (Sb) addition on the optical properties (optical energy gap and refractive index) of thin solid films of the chalcogenide glassy Ge{sub 0.17}Se{sub 0.83-x}Sb{sub x}(x = 0, 0.03, 0.09, 0.12, 0.15) system. This has been done by analysing the transmittance (T) and reflectance (R) spectra in the spectral region 400-2000 nm. It was found that the optical energy gap decreases with increasing Sb content from 1.92 to 1.63 eV with an uncertainty of {+-} 0.01 eV. The results were interpreted in terms of bond energies and on the basis of the concept of electronegativity. The refractive index has been found to increase with increasing Sb content. The increase in the refractive index has been explained on the basis of polarizability. Dispersion of refractive index has been analysed using the Wemple-DiDomenico single oscillator model. The static refractive index increased from 2.45 to 2.91 for the studied compositions. An estimate of the energy gap has also been taken theoretically and it has been found that both the optical energy gap (measured from T and R spectra) and the theoretical energy gap follow similar trends.

  2. Effect of tellurium addition on the physical properties of germanium selenide glassy semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Pankaj [Department of Physics, Jaypee University of Information Technology, Waknaghat, Solan, H.P. 173215 (India)], E-mail: pankaj.sharma@juit.ac.in; Katyal, S.C. [Department of Physics, Jaypee University of Information Technology, Waknaghat, Solan, H.P. 173215 (India)

    2008-10-01

    Effect of tellurium (Te) addition on the physical properties, density ({rho}), molar volume (V{sub m}), compactness ({delta}), cohesive energy (CE), coordination number (m), lone pair electrons (L) and glass transition temperature (T{sub g}) of Ge{sub 10}Se{sub 90-x}Te{sub x} (x=0, 10, 20, 30, 40, 50) bulk glassy alloy has been investigated. The density of the glassy alloys has been found to increase with the increasing Te content. The molar volume and compactness of the structure of the glass, determined from measured density of the glass, have been found to increase with the increase of Te content. The CE of the investigated samples has been calculated using the chemical bond approach (CBA) and is correlated with decrease in optical band gap with the increase of Te content. The glass transition temperature has been estimated using Tichy-Ticha approach and found to increase with the increase of Te content. This has been observed that the estimated glass transition temperature using Tichy-Ticha approach is not consistent with experimental results.

  3. Facile Formation of Ytterbium Diiodide and Its Use in the Synthesis of Allyl Selenides

    Institute of Scientific and Technical Information of China (English)

    SU,Wei-Ke(苏为科); ZHANG,Yong-Min(张永敏); ZHENG,Yun-Fa(郑云法); LI,Yong-Shu(李永曙)

    2002-01-01

    Ytterbium metal reacts with iodine to generate ytterbium diiodide directly, which can react with diselenides to form ytterbium selenolates (RSeYbI2). These species reacted smoothly with allyl bromide to give allylselenides in moderate to good yields under neutral conditions.

  4. Physical ageing in the above-bandgap photoexposured glassy arsenic selenides

    Energy Technology Data Exchange (ETDEWEB)

    Kozdras, A [Faculty of Physics of Opole University of Technology, 75, Ozimska str., Opole, PL-45370 (Poland); Golovchak, R [Lviv Scientific Research Institute of Materials of SRC ' Carat' , 202, Stryjska str., Lviv, UA-79031 (Ukraine); Shpotyuk, O [Lviv Scientific Research Institute of Materials of SRC ' Carat' , 202, Stryjska str., Lviv, UA-79031 (Ukraine)

    2007-08-15

    Physical ageing induced by above-bandgap light illumination is studied in glassy As-Se using differential scanning calorimetry. It is shown that measurable effect like to known short-term physical ageing is observed only in Se-rich glasses. The kinetics of this effect is compared with that caused by natural storage in a dark.

  5. Study of Ga incorporation in glassy arsenic selenides by high-resolution XPS and EXAFS

    Energy Technology Data Exchange (ETDEWEB)

    Golovchak, R., E-mail: holovchakr@apsu.edu [Department of Physics and Astronomy, Austin Peay State University, Clarksville, Tennessee 37044 (United States); Shpotyuk, Ya. [Equipe Verres et Céramiques UMR-CNRS 6226, Université de Rennes 1, 35042 Rennes Cedex (France); Scientific Research Company “Carat”, 202, Stryjska Str., 79031 Lviv (Ukraine); Nazabal, V.; Boussard-Pledel, C.; Bureau, B. [Equipe Verres et Céramiques UMR-CNRS 6226, Université de Rennes 1, 35042 Rennes Cedex (France); Cebulski, J. [Center for Microelectronics and Nanotechnology, University of Rzeszow, 1, Pigonia Str., 35-310 Rzeszow (Poland); Jain, H. [Department of Materials Science and Engineering, Lehigh University, 5 East Packer Avenue, Bethlehem, Pennsylvania 18015-3195 (United States)

    2015-05-14

    Effect of Ga addition on the structure of vitreous As{sub 2}Se{sub 3} is studied using high-resolution X-ray photoelectron spectroscopy and extended X-ray absorption fine structure techniques. The “8-N” rule is shown to be violated for Ga atoms and, possibly, for certain number of As atoms. On the contrary, Se keeps its 2-fold coordination according to “8-N” rule in the amorphous phase throughout all the compositions. Crystalline inclusions appear in the amorphous structure of the investigated glasses at Ga concentrations greater than 3 at. %. These inclusions are presumably associated with Ga{sub 2}Se{sub 3} crystallites and transition phases/defects formed at the boundaries of these crystallites and host amorphous matrix. The existence of Ga–As and Se–Se bonds in the samples with higher Ga content is supported by present studies.

  6. Study of Ga incorporation in glassy arsenic selenides by high-resolution XPS and EXAFS.

    Science.gov (United States)

    Golovchak, R; Shpotyuk, Ya; Nazabal, V; Boussard-Pledel, C; Bureau, B; Cebulski, J; Jain, H

    2015-05-14

    Effect of Ga addition on the structure of vitreous As2Se3 is studied using high-resolution X-ray photoelectron spectroscopy and extended X-ray absorption fine structure techniques. The "8-N" rule is shown to be violated for Ga atoms and, possibly, for certain number of As atoms. On the contrary, Se keeps its 2-fold coordination according to "8-N" rule in the amorphous phase throughout all the compositions. Crystalline inclusions appear in the amorphous structure of the investigated glasses at Ga concentrations greater than 3 at. %. These inclusions are presumably associated with Ga2Se3 crystallites and transition phases/defects formed at the boundaries of these crystallites and host amorphous matrix. The existence of Ga-As and Se-Se bonds in the samples with higher Ga content is supported by present studies.

  7. Pseudo-self-organized topological phases in glassy selenides for IR photonics

    Energy Technology Data Exchange (ETDEWEB)

    Shpotyuk, O. [Lviv Institute of Materials of Scientific Research Company ' ' Carat' ' 202, Stryjska str., 79031 Lviv (Ukraine); Institute of Physics of Jan Dlugosz University 13/15, al. Armii Krajowej, 42201 Czestochowa (Poland); Golovchak, R. [Lviv Institute of Materials of Scientific Research Company ' ' Carat' ' 202, Stryjska str., 79031 Lviv (Ukraine)

    2011-09-15

    Network-forming cluster approach is applied to As-Se and Ge-Se glasses to justify their tendency to self-organization. It is shown that reversibility windows determined by temperature-modulated differential scanning calorimetry using short-term aged or as-prepared samples do not necessary coincide with self-organized phase in these materials. The obtained results testify also pseudo-self-organization phenomenon in Ge-Se glasses: over-constrained outrigger raft structural units built of two edge- and four corner-shared tetrahedra are interconnected via optimally-constrained {identical_to}Ge-Se-Se-Ge{identical_to} bridges within the range of compositions identified previously as self-organized phase by temperature modulated differential scanning calorimetry technique. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  8. Cluster modeling of quasi-adaptive phases in vitreous germanium selenides

    Energy Technology Data Exchange (ETDEWEB)

    Shpotyuk, Oleh; Golovchak, Roman [Lviv Institute of Materials of SRC, Lviv 79031 (Ukraine); Institute of Physics, Jan Dlugosz University, Czestochowa 42201 (Poland); Boyko, Vitaliy [Lviv Polytechnic National University, Lviv 79013 (Ukraine); Kozyukhin, Sergei [Institute of General and Inorganic Chemistry of RAS, Leninsky Pr. 31, Moscow 199991 (Russian Federation)

    2010-04-15

    The developed cluster modeling approach based on ab-initio calculations with RHF/6-311G{sup *} basis set testifies absence of intermediate optimally-constrained phase in binary Ge{sub x} Se{sub 100-x} system within 20 {<=} x < 26 domain. It is shown, that character ''outrigger raft'' carcass is conserved for all glass compositions within expected reversibility window. Thus, the structure of binary Ge{sub x} Se{sub 100-x} glasses can be described in terms of ''chains crossing'' model in case of x < 12, mixed ''chains crossing'' and ''outrigger raft'' models in case of 12{<=}x< 20 and modified ''outrigger raft'' model in case of x {>=} 20. The expected reversibility window in binary Ge{sub x} Se{sub 100-x} glasses is shown to be only quasi-adaptive phase, based on ''outrigger raft'' structural motive with two edge- and four corner-sharing tetrahedra interconnected by optimally-constrained Ge-Se-Se-Ge bridges with extra Se atoms in ring-like configurations replaced Se-Se dimers. The results of quantum mechanics modeling are confirmed well by high-resolution X-ray photoelectron spectroscopy measurements in this system. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  9. Step-wise kinetics of natural physical ageing in arsenic selenide glasses.

    Science.gov (United States)

    Golovchak, R; Kozdras, A; Balitska, V; Shpotyuk, O

    2012-12-19

    The long-term kinetics of physical ageing at ambient temperature is studied in Se-rich As-Se glasses using the conventional differential scanning calorimetry technique. It is analysed through the changes in the structural relaxation parameters occurring during the glass-to-supercooled liquid transition in the heating mode. Along with the time dependences of the glass transition temperature (T(g)) and partial area (A) under the endothermic relaxation peak, the enthalpy losses (ΔH) and calculated fictive temperature (T(F)) are analysed as key parameters, characterizing the kinetics of physical ageing. The latter is shown to have step-wise character, revealing some kinds of subsequent plateaus and steep regions. A phenomenological description of physical ageing in the investigated glasses is proposed on the basis of an alignment-shrinkage mechanism and first-order kinetic equations.

  10. Zinc selenide photoelectrodes. Efficient radiative recombination in a stable photoelectrochemical cell. Technical report

    Energy Technology Data Exchange (ETDEWEB)

    Smiley, P.M.; Biagioni, R.N.; Ellis, A.B.

    1984-05-25

    Photoluminescence (PL) and electroluminescence (EL) from single-crystal, n-type, A1-doped ZnSe (ZnSe:A1) electrodes have been studied. These samples exhibit both edge emission (lambda(max) approx. 460 nm) and subband gap emission when excited at several ultraband gap wavelengths. The latter PL band is particularly intense, with a measured radiative quantum yield of approx. 0.1 to 0.01; the transition seems at least partially self-activated (SA) in origin, based on previously reported PL data. Excited-state communication involving the two emissive states is inferred from time-resolved PL measurements. Stable photoelectrochemical cells (PEC's) can be constructed from n-ZnSe:A1 electrodes and aqueous diselenide or ditelluride electrolytes. Applied potential quenches both of the photoanodes' PL bands roughly in parallel. The extent of PL quenching is consistent with a dead-layer model previously used to describe quenching in Au-ZnSe Schottky diodes. When used as a dark cathode in aqueous, alkaline peroxydisulfate eletrolyte, EL from ZnSe:A1 electrodes is observed.

  11. Polarization effects in the luminescence of cadmium selenide electrodes. Technical report

    Energy Technology Data Exchange (ETDEWEB)

    Streckert, H.H.; Van Ryswyk, H.; Biagioni, R.N.; Ellis, A.B.

    1983-09-29

    Polarization properties of the emission from single-crystal, n-type CdSe samples have been examined. When excited with several ultrabond gap wavelengths, a-plates of n-CdSe (wurtzite structure) exhibit polarized photo-luminescence (PL) spectra consistent with the reported electronic structure of the solid. The spectra consist of two bands near the band gap energy (approximately 1.7 eV), assignable to transitions between the conduction band and a split valence band having its two highest-energy band edges separated by approximately 0.022 eV; the lower-energy band is preferentially polarized with E is perpendicular toc while the other band displays no polarization preference. Time-resolved PL data, obtained with 620-nm excitation from a N2-pulsed dye laser, were independent of polarization. Intensity-time curves yielded a decay time ( t sub l/e) of approximately 20 ns for both bands, providing evidence that the two emissive excited states are in thermal equilibrium. Emissive properties of n-CdSe, a-plate electrodes were also consistent with thermal equilibration. Polarized electroluminescence (EL) spectra, obtained using the solid as a dark cathode in aqueous peroxydisulfate electrolyte, closely resemble their PL counterparts, demonstrating attainment of similar excited-state populations in the two experiments. And when the semiconductor is used as the photoanode of a photoelectrochemical cell employing diselenide electrolyte, the two PL bands resulting from 514.5- or 632.8-nm excitation are quenched in parallel by the electric field present in the semiconductor.

  12. Zinc selenide photoelectrodes: efficient radiative recombination in a stable photoelectrochemical cell

    Energy Technology Data Exchange (ETDEWEB)

    Smiley, P.M.; Biagioni, R.N.; Ellis, A.B.

    1984-05-01

    A study has been made of photoluminescence (PL) and electroluminescence (EL) from single-crystal n-type ZnSe:Al electrodes. It is shown that emission from the electrodes, with a measured radiative quantum yield of 0.1-0.01, competes favorably with other deactivation paths in stable efficient photoelectrochemical cells. As observed with other semiconductor electrodes, the PL of n-ZnSe:Al electrodes can be perturbed and EL initiated by interfacial charge-transfer processes. It is shown that PL quenching by applied potential is compatible with a dead-layer model used to describe such quenching in other photoelectrochemical cells and in Au-ZnSe Schottky diodes. 24 references.

  13. Syntheses, Structure, Magnetism, and Optical Properties of Lutetium-based Interlanthanide Selenides

    Energy Technology Data Exchange (ETDEWEB)

    Booth, Corwin H; Jin, Geng Bang; Choi, Eun Sang; Guertin, Robert P.; Brooks, James S.; Booth, Corwin H.; Albrecht-Schmitt, Thomas E.

    2007-10-01

    Ln{sub 3}LuSe{sub 6} (Ln = La, Ce), {beta}-LnLuSe{sub 3} (Ln = Pr, Nd), and Ln{sub x}Lu{sub 4-x}Se{sub 6} (Ln = Sm, Gd; x = 1.82, 1.87) have been synthesized using a Sb{sub 2}Se{sub 3} flux at 1000 C. Ln{sub 3}LuSe{sub 6} (Ln = La, Ce) adopt the U{sub 3}ScS{sub 6}-type three-dimensional structure, which is constructed from two-dimensional {infinity}{sup 2} [Ln{sub 3}Se{sub 6}]{sup 3-} slabs with the gaps between these slabs filled by octahedrally coordinated Lu{sup 3+} ions. The series of {beta}-LnLuSe{sub 3} (Ln = Pr, Nd) are isotypic with UFeS{sub 3}. Their structures include layers formed from LuSe6 octahedra that are separated by eight-coordinate larger Ln{sup 3+} ions in bicapped trigonal prismatic environments. Sm{sub 1.82}Lu{sub 2.18}Se{sub 6} and Gd{sub 1.87}Lu{sub 2.13}Se{sub 6} crystallize in the disordered F-Ln{sub 2}S{sub 3} type structure with the eight-coordinate bicapped trigonal prismatic Ln(1) ions residing in the one-dimensional channels formed by three different double chains via edge and corner sharing. These double chains are constructed from Ln(2)Se{sub 7} monocapped trigonal prisms, Ln(3)Se{sub 6} octahedra, and Ln(4)S{sub 6} octahedra, respectively. The magnetic susceptibilities of {beta}-PrLuSe{sub 3} and {beta}-NdLuSe{sub 3} follow the Curie-Weiss law. Sm{sub 1.82}Lu{sub 2.18}Se{sub 6} shows van Vleck paramagnetism. Magnetic measurements show that Gd{sub 1.87}Lu{sub 2.13}Se{sub 6} undergoes an antiferromagnetic transition around 4 K. Ce{sub 3}LuSe{sub 6} exhibits ferromagnetic ordering below 5 K. The optical band gaps for La{sub 3}LuSe{sub 6}, Ce{sub 3}LuSe{sub 6}, {beta}- PrLuSe{sub 3}, {beta}-NdLuSe{sub 3}, Sm{sub 1.82}Lu{sub 2.18}Se{sub 6}, and Gd{sub 1.87}Lu{sub 2.13}Se{sub 6} are 1.26, 1.10, 1.56, 1.61, 1.51, and 1.56 eV, respectively.

  14. 2-Isobutyl-2-phosphabicyclo[3.3.1]nonane 2-selenide

    Directory of Open Access Journals (Sweden)

    2009-03-01

    Full Text Available The title compound, C12H23PSe, represents the first structure of a phosphine containing the bicyclic 2-phosphabicyclo[3.3.1]nonane (VCH unit. It contains two chiral centres per molecule which can be either R,R- or S,S and crystallizes as a centrosymmetric, racemic micture of the enantiomers. The P—Se bond distance of 2.1360 (16 Å is typical for these compounds. The Tolman cone angle (2.28 Å from P was calculated as 163°, and the effective cone angle (using the crystallographically determined P—Se bond distance is 168°.

  15. Preparation and Properties of Zinc Doped Cadmium Selenide Compounds by E-Beam Evaporation

    Directory of Open Access Journals (Sweden)

    N.J. Suthan Kissinger

    2011-01-01

    Full Text Available Cd1 – xZnxSe films with different zinc content were deposited by electron beam evaporation technique onto glass substrates for the application of solid-state photovoltaic devices. The structural, surface morphological and optical properties of Cd1 – xZnxSe films have been studied in the present work. The host material,Cd1 – xZnxSe, have been prepared by the physical vapor deposition method of electron beam evaporation technique (PVD: EBE under a pressure of 1 × 10 – 5 mbar. The X-ray diffractogram indicates that these alloy films are polycrystalline in nature, hexagonal structure with strong preferential orientation of the crystallites along (002 direction. Linear variation of lattice constant with composition (x is observed. The optical properties shows that the band gap (Eg values varies from 2.08 to 2.64 eV as zinc content varies from 0.2 to 0.8. The surface morphological studies show the very small, fine and hardly distinguishable grains smeared all over the surface. It is observed that the grain size is decreasing with increasing zinc content.

  16. Long-term performance analysis of copper indium gallium selenide thin-film photovoltaic modules

    Science.gov (United States)

    Kaul, Ashwani; Pethe, Shirish A.; Dhere, Neelkanth G.

    2012-01-01

    Current accelerated qualification tests of photovoltaic (PV) modules mostly assist in avoiding premature failures but can neither duplicate changes occurring in the field nor predict useful product lifetime. Therefore, outdoor monitoring of field-deployed thin-film PV modules was undertaken at FSEC with the goal of assessing their performance in hot and humid climate under high system-voltage operation. Significant and comparable degradation rate of -5.13±1.53% and -4.5±1.46% per year was found using PVUSA type regression analysis for the positive and negative strings, respectively of 40W glass-to-glass Cu-In-Ga-Se (CIGS) thin-film PV modules in the hot and humid climate of Florida. Using the current-voltage measurements, it was found that the performance degradation within the PV array was mainly due to a few (8% to 12%) modules that had substantially higher degradation. The remaining modules within the array continued to show reasonable performance (>96% of the rated power after ˜ four years).

  17. Liquid precursor for deposition of indium selenide and method of preparing the same

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, Calvin J.; Miedaner, Alexander; van Hest, Marinus Franciscus Antonius Maria; Ginley, David S.; Hersh, Peter A.; Eldada, Louay; Stanbery, Billy J.

    2015-09-22

    Liquid precursors containing indium and selenium suitable for deposition on a substrate to form thin films suitable for semiconductor applications are disclosed. Methods of preparing such liquid precursors and method of depositing a liquid precursor on a substrate are also disclosed.

  18. Synthesis of colloidal nanoscaled copper-indium-gallium-selenide (CIGS) particles for photovoltaic applications.

    Science.gov (United States)

    Mousavi, S H; Müller, T S; de Oliveira, P W

    2012-09-15

    In this work, Cu(In,Ga)Se(2) (CIGS) nanoparticles were synthesized using a wet chemical method. The method is based on a non-vacuum thermal process that does not use selenization. The effects of temperature, source materials, and growth conditions on the phase and particle size were investigated. X-ray diffraction results confirm the formation of a tetragonal CIGS structure as the main phase with the purity more than 99% obtained by energy-dispersive X-ray spectroscopy (EDX). The morphology and size of the samples were investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Using these methods, 20-80nm particles were obtained. Through measurements of the absorption spectra of CIGS nanoparticles, the band gap of the synthesized material was determined to be about 1.44eV, which corresponds to an acceptable wavelength region for absorber layers in solar cells.

  19. Defect States in Copper Indium Gallium Selenide Solar Cells from Two-Wavelength Excitation Photoluminescence Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Jensen, Soren A.; Dippo, Patricia; Mansfield, Lorelle M.; Glynn, Stephen; Kuciauskas, Darius

    2016-11-21

    We use two-wavelength excitation photoluminescence spectroscopy to probe defect states in CIGS thin films. Above-Eg excitation is combined with a tunable IR bias light that modulates the population of the defect states. We find that IR illumination in the range of 1400-2000 nm (0.62-0.89 eV) causes a reduction of the PL intensity, the magnitude of which scales linearly with IR power. Further, KF post deposition treatment has only a modest influence on the effect of the IR excitation. Initial data suggest that we have developed an optical characterization tool for band-gap defect states.

  20. Solid-state reactions to synthesize nanostructured lead selenide semiconductor powders by high-energy milling

    Energy Technology Data Exchange (ETDEWEB)

    Rojas-Chavez, H., E-mail: uu_gg_oo@yahoo.com.mx [Centro de Investigacion e Innovacion Tecnologica - IPN, Cerrada de CECATI s/n, Col. Santa Catarina, Del. Azcapotzalco (Mexico) and Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada - IPN, Legaria 694, Col. Irrigacion, Del. Miguel Hidalgo (Mexico); Reyes-Carmona, F. [Facultad de Quimica - UNAM, Circuito de la Investigacion Cientifica s/n, C.U. Del. Coyoacan (Mexico); Jaramillo-Vigueras, D. [Centro de Investigacion e Innovacion Tecnologica - IPN, Cerrada de CECATI s/n, Col. Santa Catarina, Del. Azcapotzalco (Mexico)

    2011-10-15

    Highlights: {yields} PbSe synthesized from PbO instead of Pb powder do not require an inert atmosphere. {yields} During high-energy milling oxygen has to be chemically reduced from the lead oxide. {yields} Solid-state and solid-gas chemical reactions promote both solid and gaseous products. -- Abstract: Both solid-solid and gas-solid reactions have been traced during high-energy milling of Se and PbO powders under vial (P, T) conditions in order to synthesize the PbSe phase. Chemical and thermodynamic arguments are postulated to discern the high-energy milling mechanism to transform PbO-Se micropowders onto PbSe-nanocrystals. A set of reactions were evaluated at around room temperature. Therefore an experimental campaign was designed to test the nature of reactions in the PbO-Se system during high-energy milling.

  1. Surfactant-thermal syntheses, structures, and magnetic properties of Mn-Ge-sulfides/selenides

    KAUST Repository

    Zhang, Guodong

    2014-10-06

    Although either surfactants or amines have been investigated to direct the crystal growth of metal chalcogenides, the synergic effect of organic amines and surfactants to control the crystal growth has not been explored. In this report, several organic bases (hydrazine monohydrate, ethylenediamine (en), 1,2-propanediamine (1,2-dap), and 1,3-propanediamine (1,3-dap)) have been employed as structure-directing agents (SDAs) to prepare four novel chalcogenides (Mn3Ge2S7(NH3)4 (1), [Mn(en)2(H2O)][Mn(en)2MnGe3Se9] (2), (1,2-dapH)2{[Mn(1,2-dap)2]Ge2Se7} (3), and (1,3-dapH)(puH)MnGeSe4(4) (pu = propyleneurea) under surfactant media (PEG-400). These as-prepared new crystalline materials provide diverse metal coordination geometries, including MnS3N tetrahedra, MnGe2Se7 trimer, and MnGe3Se10 T2 cluster. Compounds 1-3 have been fully characterized by single-crystal X-ray diffraction (XRD), powder XRD, UV-vis spectra, Fourier transform infrared spectroscopy, and thermogravimetric analysis. Moreover, magnetic measurements for compound 1 showed an obvious antiferromagnetic transition at ∼9 K. Our research not only enriches the structural chemistry of the transitional-metal/14/16 chalcogenides but also allows us to better understand the synergic effect of organic amines and surfactants on the crystallization of metal chalcogenides.

  2. Active Edge Sites Engineering in Nickel Cobalt Selenide Solid Solutions for Highly Efficient Hydrogen Evolution

    KAUST Repository

    Xia, Chuan

    2017-01-06

    An effective multifaceted strategy is demonstrated to increase active edge site concentration in NiCoSe solid solutions prepared by in situ selenization process of nickel cobalt precursor. The simultaneous control of surface, phase, and morphology result in as-prepared ternary solid solution with extremely high electrochemically active surface area (C = 197 mF cm), suggesting significant exposure of active sites in this ternary compound. Coupled with metallic-like electrical conductivity and lower free energy for atomic hydrogen adsorption in NiCoSe, identified by temperature-dependent conductivities and density functional theory calculations, the authors have achieved unprecedented fast hydrogen evolution kinetics, approaching that of Pt. Specifically, the NiCoSe solid solutions show a low overpotential of 65 mV at -10 mV cm, with onset potential of mere 18 mV, an impressive small Tafel slope of 35 mV dec, and a large exchange current density of 184 μA cm in acidic electrolyte. Further, it is shown that the as-prepared NiCoSe solid solution not only works very well in acidic electrolyte but also delivers exceptional hydrogen evolution reaction (HER) performance in alkaline media. The outstanding HER performance makes this solid solution a promising candidate for mass hydrogen production.

  3. Effect of deposition pressure on structural, optical and electrical properties of zinc selenide thin films

    Science.gov (United States)

    Sharma, Jeewan; Tripathi, S. K.

    2011-04-01

    ZnSe thin films have been prepared by inert gas condensation method at different gas pressures. The influence of deposition pressure, on structural, optical and electrical properties of polycrystalline ZnSe films have been investigated using X-ray diffraction (XRD), optical transmission and conductivity measurements. The X-ray diffraction study reveals the sphalerite cubic structure of the ZnSe films oriented along the (1 1 1) direction. The structural parameters such as particle size [6.65-22.24 nm], strain [4.01-46.6×10-3 lin-2 m-4] and dislocation density [4.762-18.57×1015 lin m-2] have been evaluated. Optical transmittance measurements indicate the existence of direct allowed optical transition with a corresponding energy gap in the range 2.60-3.00 eV. The dark conductivity (σd) and photoconductivity (σph) measurements, in the temperature range 253-358 K, indicate that the conduction in these materials is through an activated process having two activation energies. σd and σph values decrease with the decrease in the crystallite size. The values of carrier life time have been calculated and are found to decrease with the reduction in the particle size. The conduction mechanism in present samples has been explained, and the density of surface states [9.84-21.4×1013 cm-2] and impurity concentration [4.66-31.80×1019 cm-3] have also been calculated.

  4. Structural and optical properties of zinc selenide thin films deposited by rf magnetron sputtering

    Science.gov (United States)

    Rizzo, Antonella; Caneve, Luisa; Scaglione, Salvatore; Tagliente, M. A.

    1999-09-01

    In this work, ZnSe thin films were deposited by radio frequency magnetron sputtering onto oriented silicon substrates. Three sets of samples were produced by varying the argon working gas pressure, and changing the sputtering power supply. The effect of the different growth conditions on the structural and optical properties of the ZnSe films was investigated by using XRD and FTIR spectroscopy. In particular, x-ray diffraction was used in order to study the residual strains and texture. The ZnSe coatings were grown in the cubic polymorph with the grains preferentially oriented for all the investigated pressures with the exception of 0.5 Pa. An in-plane residual stress reversal, which changed from compressive to tensile by going from the low to the high-pressure sample set, was observed. At the 0.5 Pa pressure, the ZnSe coatings were both in compressive and tensile state, according to the power supply value. These result have been correlated with the momentum of reflected neutral in order to find an exhaustive description of the deposition process. At low momentum values, the ZnSe films show tensile state, low refractive index, grains preferentially oriented, while at high momentum they were in compressive state, refractive index very alike to the bulk and grains randomly oriented.

  5. MBE-VLS grown zinc selenide and zinc sulfide nanowires: Growth mechanisms and photoluminescence properties

    Science.gov (United States)

    Chan, Siu Keung

    A lot of effort was recently devoted in realizing semiconducting nanowires (NWs) that are considered as a channel for electrons and photons no wider than a few thousand atoms. Such a one-dimensional structure will find potential applications in nano-optoelectronics and nano-photonics. The control of the growth orientation of NWs is particularly important because it will eventually affect their optical and transport properties. The ordering of NWs has also been a recent focus due to the fact that some of the above mentioned applications require the NWs fabricated in regular and periodic arrays. In this study, the growth of ZnSe and ZnS nanowires using the molecular beam epitaxy technique via the vapor-liquid-solid reaction with Au alloy droplets as the catalyst is successfully demonstrated. The nanowires resulting from this approach were found to orient along some specific crystallographic directions. Through detailed structural characterization, we have revealed that the preferred growth orientation of NWs depends on the chosen size of the catalyst and growth temperature. A phenomenological model based on the minimization of the total system energy of a nanowire was proposed to explain these observations. Based on these findings, we have successfully grown vertical ZnSe nanowires with a diameter around 10 nm on a GaAs(110) substrate. The interactions between the catalyst and the direct-contact materials (either the GaAs substrate or the ZnSe buffer) were analyzed in details. Through this study, it was found that thermal annealing of Au alloy catalyst droplets on a ZnSe buffer surface could result in nano-trenches along the directions. Based on the results obtained from a number of surface profiling and chemical analysis techniques, a model is proposed to describe the possible formation mechanisms of the observed nanotrenches. An ordered ZnSe NW array fabricated on a GaAs (111) substrate with a novel pre-patterning method associated with plasma etching is also demonstrated in this study. This array shows a high degree of ordering and a good size uniformity of the as-grown NWs. The diameter of the NWs in the array is around 80nm and most of them were found to orient vertically but some tilt to one of the six possible directions of the direction family. ZnS NWs fabricated on a sapphire substrate at growth temperature of 430°C were found to mainly consist of the cubic phase but a little portion is in the hexagonal phase. The analysis of the temperature-dependent band-edge emission of these NWs and that of a ZnS thin film reveals that the energy shift of the interband transition on temperature in ZnS is mainly attributed to the electron-phonon interactions. The observed blue-shift of the band-edge emission of ZnS NWs could be quantitatively explained by the confinement of the excited excitons in the NW geometry.

  6. Co-solvent enhanced zinc oxysulfide buffer layers in Kesterite copper zinc tin selenide solar cells.

    Science.gov (United States)

    Steirer, K Xerxes; Garris, Rebekah L; Li, Jian V; Dzara, Michael J; Ndione, Paul F; Ramanathan, Kannan; Repins, Ingrid; Teeter, Glenn; Perkins, Craig L

    2015-06-21

    A co-solvent, dimethylsulfoxide (DMSO), is added to the aqueous chemical "bath" deposition (CBD) process used to grow ZnOS buffer layers for thin film Cu2ZnSnSe4 (CZTSe) solar cells. Device performance improves markedly as fill factors increase from 0.17 to 0.51 upon the co-solvent addition. X-ray photoelectron spectroscopy (XPS) analyses are presented for quasi-in situ CZTSe/CBD-ZnOS interfaces prepared under an inert atmosphere and yield valence band offsets equal to -1.0 eV for both ZnOS preparations. When combined with optical band gap data, conduction band offsets exceed 1 eV for the water and the water/DMSO solutions. XPS measurements show increased downward band bending in the CZTSe absorber layer when the ZnOS buffer layer is deposited from water only. Admittance spectroscopy data shows that the ZnOS deposited from water increases the built-in potential (Vbi) yet these solar cells perform poorly compared to those made with DMSO added. The band energy offsets imply an alternate form of transport through this junction. Possible mechanisms are discussed, which circumvent the otherwise large conduction band spike between CZTSe and ZnOS, and improve functionality with the low-band gap absorber, CZTSe (Eg = 0.96 eV).

  7. Pulsed laser deposition of chromium-doped zinc selenide thin films for mid-infrared applications

    Science.gov (United States)

    Williams, J. E.; Camata, R. P.; Fedorov, V. V.; Mirov, S. B.

    2008-05-01

    We have grown Cr doped ZnSe thin films by pulsed laser deposition on GaAs, sapphire and Si substrates through KrF excimer laser ablation of hot-pressed targets containing appropriate stoichiometric mixtures of Zn, Se, and Cr species and hot-pressed ceramic targets made of ZnSe and CrSe powders in vacuum and in an He background environment (10-4 Torr). Deposited films were analyzed using X-ray diffraction to determine crystallinity and energy dispersive X-ray fluorescence to confirm Cr incorporation into the films. Photoluminescence measurements on the films show intracenter Cr2+ emission in the technologically important 2 2.6 μm spectral range.

  8. Design and Optimization of Copper Indium Gallium Selenide Solar Cells for Lightweight Battlefield Application

    Science.gov (United States)

    2014-06-01

    those of the author and do not reflect the official policy or position of the Department of Defense or the U.S. Government. IRB Protocol number ____N...Matrix Flatpanel Displays and Devices, Kyoto , Japan, 2012, pp. 67–70. [23] R. Yang, Z. Bai, D. Wang, and D. Wang, “High efficient thin film CdTe solar

  9. Novel Syntheses of Aryl and Benzyl Selenides Promted by Metallic Zinc in Aqueous Media

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    @@ Introduction Recently, organometallic-type of reactions in aqueous media have attracted a considerable interest in organic syntheses[1-4]. The main advantage of making organometallic reactions in strictly anhydrous organic solvents took place in aqueous media is the ease of the reactions so as to obviate the need for inflammable anhydrous organic solvents and troublesome inert atmosphere. For some reactions, e.g., the alkylations of the carbonyl group in carbohydrates didnt need to be altered to take place in organic solvents[5]. The most commonly used metals are zinc, tin and indium[1-4].

  10. Temperature dependent local atomic displacements in ammonia intercalated iron selenide superconductor

    Science.gov (United States)

    Paris, E.; Simonelli, L.; Wakita, T.; Marini, C.; Lee, J.-H.; Olszewski, W.; Terashima, K.; Kakuto, T.; Nishimoto, N.; Kimura, T.; Kudo, K.; Kambe, T.; Nohara, M.; Yokoya, T.; Saini, N. L.

    2016-01-01

    Recently, ammonia-thermal reaction has been used for molecular intercalation in layered FeSe, resulting a new Lix(NH3)yFe2Se2 superconductor with Tc ~ 45 K. Here, we have used temperature dependent extended x-ray absorption fine structure (EXAFS) to investigate local atomic displacements in single crystals of this new superconductor. Using polarized EXAFS at Fe K-edge we have obtained direct information on the local Fe-Se and Fe-Fe bondlengths and corresponding mean square relative displacements (MSRD). We find that the Se-height in the intercalated system is lower than the one in the binary FeSe, suggesting compressed FeSe4 tetrahedron in the title system. Incidentally, there is hardly any effect of the intercalation on the bondlengths characteristics, revealed by the Einstein temperatures, that are similar to those found in the binary FeSe. Therefore, the molecular intercalation induces an effective compression and decouples the FeSe slabs. Furthermore, the results reveal an anomalous change in the atomic correlations across Tc, appearing as a clear decrease in the MSRD, indicating hardening of the local lattice mode. Similar response of the local lattice has been found in other families of superconductors, e.g., A15-type and cuprates superconductors. This observation suggests that local atomic correlations should have some direct correlation with the superconductivity. PMID:27276997

  11. A single-electron transistor made from a cadmium selenide nanocrystal

    OpenAIRE

    Klein, David L.; Roth, Richard; Lim, Andrew K. L.; Alivisatos, A. Paul; McEuen, Paul L.

    1997-01-01

    The techniques of colloidal chemistry permit the routine creation of semiconductor nanocrystals, whose dimensions are much smaller than those that can be realized using lithographic techniques. The sizes of such nanocrystals can be varied systematically to study quantum size effects or to make novel electronic or optical materials with tailored properties. Preliminary studies of both the electrical and optical properties of individual nanocrystals have been performed recently. These studies s...

  12. Quantum Confinement in Cadmium Selenide Multilayer Thin Films Using Physical Vapour Deposition Method

    Directory of Open Access Journals (Sweden)

    M. Melvin David Kumar

    2012-06-01

    Full Text Available Nanocrystals of CdSe have been produced in SiOx matrix layer and in ZnSe heterostructure layer by thermal evaporation method. Structural studies were done by X-ray diffractometer. Quantum confinement effect of CdSe nanocrystals was analyzed from optical studies. Bulk CdSe has band-gap energy of 1.756 eV that can be shifted to larger values by reducing the crystal size to dimensions smaller than the Bohr radius of the exciton. Experimentally measured band-gap shifts with respect to the bulk value for quantum dot thin films are compared with the predictions of the effective mass approximation model (i.e., Brus model and Quantum mechanical model. Sizes of the crystallites calculated from both models were coincident with each other.

  13. Multiple-exciton generation in lead selenide nanorod solar cells with external quantum efficiencies exceeding 120%

    Science.gov (United States)

    Davis, Nathaniel J. L. K.; Böhm, Marcus L.; Tabachnyk, Maxim; Wisnivesky-Rocca-Rivarola, Florencia; Jellicoe, Tom C.; Ducati, Caterina; Ehrler, Bruno; Greenham, Neil C.

    2015-01-01

    Multiple-exciton generation—a process in which multiple charge-carrier pairs are generated from a single optical excitation—is a promising way to improve the photocurrent in photovoltaic devices and offers the potential to break the Shockley–Queisser limit. One-dimensional nanostructures, for example nanorods, have been shown spectroscopically to display increased multiple exciton generation efficiencies compared with their zero-dimensional analogues. Here we present solar cells fabricated from PbSe nanorods of three different bandgaps. All three devices showed external quantum efficiencies exceeding 100% and we report a maximum external quantum efficiency of 122% for cells consisting of the smallest bandgap nanorods. We estimate internal quantum efficiencies to exceed 150% at relatively low energies compared with other multiple exciton generation systems, and this demonstrates the potential for substantial improvements in device performance due to multiple exciton generation. PMID:26411283

  14. The application of the photoacoustic transmittance oscillations for determining elastic constants in gallium and indium selenides

    Science.gov (United States)

    Ferrer, Ch.; Segura, A.; Andrés, M. V.; Muñoz, V.; Pellicer, J.

    1996-03-01

    Transmittance periodic oscillations are observed in GaSe and InSe on excitation with optical pulses. Such oscillations are explained in terms of photoacoustic generation of dilatational waves, which become resonant within the crystal. Spectral analysis of those oscillations in samples of different thickness has led to an accurate determination of the longitudinal acoustic-wave velocity along the crystallographic axis c.

  15. Nanoantenna enhanced terahertz spectroscopy of a monolayer of cadmium selenide quantum dots

    KAUST Repository

    Razzari, Luca

    2014-01-01

    Exploiting the localization and enhancement capabilities of terahertz resonant dipole nanoantennas coupled through nanogaps, we present an effective method to perform terahertz spectroscopy on an extremely small number of nano-objects.

  16. Multiple-exciton generation in lead selenide nanorod solar cells with external quantum efficiencies exceeding 120.

    Science.gov (United States)

    Davis, Nathaniel J L K; Böhm, Marcus L; Tabachnyk, Maxim; Wisnivesky-Rocca-Rivarola, Florencia; Jellicoe, Tom C; Ducati, Caterina; Ehrler, Bruno; Greenham, Neil C

    2015-09-28

    Multiple-exciton generation-a process in which multiple charge-carrier pairs are generated from a single optical excitation-is a promising way to improve the photocurrent in photovoltaic devices and offers the potential to break the Shockley-Queisser limit. One-dimensional nanostructures, for example nanorods, have been shown spectroscopically to display increased multiple exciton generation efficiencies compared with their zero-dimensional analogues. Here we present solar cells fabricated from PbSe nanorods of three different bandgaps. All three devices showed external quantum efficiencies exceeding 100% and we report a maximum external quantum efficiency of 122% for cells consisting of the smallest bandgap nanorods. We estimate internal quantum efficiencies to exceed 150% at relatively low energies compared with other multiple exciton generation systems, and this demonstrates the potential for substantial improvements in device performance due to multiple exciton generation.

  17. A study on the connection and physical properties of Cadmium selenide nanoparticles and zinc sulfide nanoparticles made by ultrasonic method

    Directory of Open Access Journals (Sweden)

    Shabnam Taheriniya

    2016-04-01

    Full Text Available Ultrasonic waves are called to hordes of mechanical waves that their oscillation frequency exceeds from human hearing range (20 Hz- 20 KHz. These waves have various applications due to their properties; ultrasonic frequency acoustic waves (16 KHz to 2 MHz are used for curing and ultrasonic process parameters (amplitude, frequency and power can be controlled properly. Ultrasonic process in fluids is followed by acoustic cavitation phenomenon (cavitation. Indeed, acoustic cavitation refers to the formation of bubbles (pores due to the rapid drop in water caused by passing the sound waves through it. In this research, an action was made to produce CdSe and ZnS nanoparticles using this method. Ultimately, ZnS quantum dots and ZnS nanoparticles were connected to each other using a coupling agent copolymer (PEG-PCA. The optical properties of this nanoparticle were examined by using X-ray diffraction and evaluated using UV-Visblel range of coupling effect.

  18. Phase transition and high temperature thermoelectric properties of copper selenide Cu2-xSe (0 <= x <= 0.25)

    Science.gov (United States)

    Xiao, Xing-Xing; Xie, Wen-Jie; Tang, Xin-Feng; Zhang, Qing-Jie

    2011-08-01

    With good electrical properties and an inherently complex crystal structure, Cu2-xSe is a potential “phonon glass electron crystal" thermoelectric material that has previously not attracted much interest. In this study, Cu2-xSe (0 <= x <= 0.25) compounds were synthesized by a melting-quenching method, and then sintered by spark plasma sintering to obtain bulk material. The effect of Cu content on the phase transition and thermoelectric properties of Cu2-xSe were investigated in the temperature range of 300 K-750 K. The results of X-ray diffraction at room temperature show that Cu2-xSe compounds possess a cubic structure with a space group of Fm3m(#225) when 0.15 <= x <= 0.25, whereas they adopt a composite of monoclinic and cubic phases when 0 <= x <= 0.15. The thermoelectric property measurements show that with increasing Cu content, the electrical conductivity decreases, the Seebeck coefficient increases and the thermal conductivity decreases. Due to the relatively good power factor and low thermal conductivity, the nearly stoichiometric Cu2Se compound achieves the highest ZT of 0.38 at 750 K. It is expected that the thermoelectric performance can be further optimized by doping appropriate elements and/or via a nanostructuring approach.

  19. Effect of a thin intermediate zinc selenide layer on the properties of CuInSe sub 2 solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Yoo, J.B.; Fahrenbruch, A.L.; Bube, R.H. (Stanford Univ., CA (USA). Dept. of Materials Science and Engineering)

    1991-03-01

    We have demonstrated that a thin insulating layer of ZnSe can be a viable alternative to a thin layer of CdS in a CuInSe{sub 2} solar cell, as currently used in the high efficiency ARCO Solar (now Siemens Solar) ZnO/CdS/CuInSe{sub 2} cell. We have investigated the effects of ZnSe thickness and deposition temperature on the properties of CuInSe{sub 2} solar cells, using a CdS window layer for diagnostic purposes. An investigation of the junction transport mechanisms for these cells indicates that in the dark the transport is controlled by recombination in the depletion region at temperatures above room temperature and that multistep tunneling dominates at temperatures below room temperature. The fact that the open-circuit voltage is smaller under illumination that predicted from the dark junction parameters results primarily from a change in the junction transport mechanism upon illumination, associated with an increase in the density of charged acceptors in the CuInSe{sub 2}. (orig.).

  20. Preliminary toxicity studies on bis-[beta-(N,N-dimorpholino) ethyl] selenide (MOSE). A new radioimaging agent.

    Science.gov (United States)

    Kostyniak, P J

    1984-01-01

    The present study describes the acute toxicity of MOSE, a proposed radioimaging agent for brain scintigraphy . Acute intraperitoneal administration of MOSE in mice revealed an LD50 between 1.35 and 6.25 g/kg, with convulsions preceding death. Intravenous administration of MOSE in rats resulted in an LD50 between 400 and 800 mg/kg, with death also preceded by convulsions. The rabbit was more sensitive to the acute effects of MOSE than the rat. The LD50 for MOSE given i.v. in the rabbit was 80 mg/kg. The predominant toxic sign was convulsions, which immediately preceded death at high doses. At intermediate doses convulsions were elicited, followed by a period of lethargy which gave way to hyperactivity on the following day. Normal appearances were restored within a week. Hematology and blood chemistries were similar to controls, except for increased serum LDH in animals receiving MOSE when sampled two weeks after dosing. Repeated administration of MOSE by the intravenous route in rabbits at a dose rate of 1 mg/kg/da, five days per week for two weeks, resulted in no signs of toxicity. Hematology, clinical chemistry, and histology revealed no changes in animals receiving MOSE when compared to control. It was concluded that barring any unusual susceptibility in man, the proposed diagnostic dose to man is unlikely to precipitate any acute toxic effects.

  1. Combinatorial synthesis, in silico, molecular and biochemical studies of tetrazole-derived organic selenides with increased selectivity against hepatocellular carcinoma.

    Science.gov (United States)

    Shaaban, Saad; Negm, Amr; Ashmawy, Abeer M; Ahmed, Dalia M; Wessjohann, Ludger A

    2016-10-21

    Novel tetrazole-based diselenides and selenoquinones were synthesized via azido-Ugi and sequential nucleophilic substitution (SN) strategy. Molecular docking study into mammalian TrxR1 was used to predict the anticancer potential of the newly synthesized compounds. The cytotoxic activity of the compounds was evaluated using hepatocellular carcinoma (HepG2) and breast adenocarcinoma (MCF-7) cancer cells and compared with their cytotoxicity in normal fibroblast (WI-38) cells. The corresponding redox properties of the synthesized compounds were assessed employing 2,2-diphenyl-1-picrylhydrazyl (DPPH), glutathione peroxidase (GPx)-like activity and bleomycin dependent DNA damage. In general, diselenides showed preferential cytotoxicity to HepG2 compared to MCF-7 cells. These compounds exhibited also good GPx catalytic activity compared to ebselen (up to 5 fold). Selenoquinones 18, 21, 22 and 23 were selected to monitor the expression levels of caspase-8, Bcl-2 and Ki-67 molecular biomarkers. Interestingly, these compounds downregulated the Bcl-2 and Ki-67 expression levels and activated the expression of caspase-8 in HepG2 cells compared to untreated cells. These results indicate that some of the newly synthesized compounds possess anti-HepG2 activity.

  2. Structure and Properties of Modified and Charge-Compensated Chalcogenide Glasses in the Na/Ba-Ga-Ge Selenide System

    Science.gov (United States)

    Mao, Alvin W.

    Chalcogenide glasses exhibit unique optical properties such as infrared transparency owing to the low-phonon energies, optical non-linearity, and photo-induced effects that have important consequences for a wide range of technological applications. However, to fully utilize these properties, it is necessary to better understand the atomic-scale structure and structure-property relationships in this important class of materials. Of particular interest in this regard are glasses in the stoichiometric system Na2Se/BaSe--Ga 2Se3--GeSe2 as they are isoelectronic with the well-studied, oxide glasses of the type M2O(M'O)--Al 2O3--SiO2 (M = alkali, M' = alkaline earth). This dissertation investigates the structure of stoichiometric Na 2Se/BaSe--Ga2Se3--GeSe2 and off-stoichiometric BaSe--Ga2Se3--GeSe 2+/-Se glasses using a combination of Fourier-transform Raman and solid state nuclear magnetic resonance (NMR) spectroscopies. The spectroscopic data is then compared to composition-dependent trends in physical properties such as density, optical band gap, glass transition temperature, and melt fragility to develop predictive structural models of the short- and intermediate-range order in the glass network. These models significantly improve our current understanding of the effects of modifier addition on the structure and properties of chalcogenide glasses, and thus enable a more efficient engineering of these highly functional materials for applications as solid electrolytes in batteries or as optical components in infrared photonics. In general, the underlying stoichiometric Ga2Se3--GeSe 2 network consists primarily of corner-sharing (Ga/Ge)Se4 tetrahedra, where the coordination numbers of Ga, Ge, and Se are 4, 4, and 2, respectively. Some edge-sharing exists, but this configuration is relatively unstable and its concentration tends to decrease with any deviation from the GeSe2 composition. Due to the tetrahedral coordination of Ga, the initial addition of Se-deficient Ga2Se3 to GeSe 2 results in the preferential formation of Ge-Ge bonds, which are distributed such that the clustering of ethane-like (Se3)Ge-Ge(Se3) units is avoided to the maximum extent. This behavior is entirely consistent with the continuously-alloyed structural scenario of chalcogenide glasses. However, for contents of Ga2Se3 greater than about 25--30 mol%, the avoidance of Ga-Ga and mixed Ga-Ge bonds results in the appearance of three-coordinated Se as an alternate mechanism to accommodate the Se deficiency. The addition of either Na2Se or BaSe to Ga2Se 3--GeSe2 glasses introduces an ionic bonding character to an otherwise largely covalently bonded network. As a result, the structure responds by adopting characteristics of the charge-compensated structural scenario of oxide glasses. In the stoichiometric Na2Se/BaSe--Ga 2Se3--GeSe2 glasses, the ratio of Na 2Se/BaSe:Ga2Se3 = 1 serves as a chemical threshold, where the network consists predominantly of corner-sharing (Ga/Ge)e4 tetrahedra, and the charge on the Na(Ba) cations is balanced by the GaSe4- tetrahedra. For glasses with Na 2Se/BaSe:Ga2Se3 1, the addition of Na2Se/BaSe results in the formation of non-bridging Se atoms, which break up the connectivity of the glassy network. The major difference between the modifying elements Na and Ba is that the high field strength of the Ba cation induces a higher degree of chemical disorder in the glass network. This conclusion is evidenced by the presence of some Ge-Ge bonds in BaSe--Ga2Se3--GeSe2 glasses even at the chemical threshold composition of BaSe:Ga2Se3 = 1. The structural duality of the Na2Se/BaSe--Ga2Se 3--GeSe2 system is best observed in the off-stoichiometric BaSe--Ga2Se3--GeSe2+/-Se glasses. Here, the removal of Se from a stoichiometric glass with BaSe:Ga2Se 3 > 1 results in Ge-Ge bonds, while its addition in excess of stoichiometry forms Se-Se bonds. Although such behavior is consistent with the continuously-alloyed structural model, it should be contrasted with the response of the network to the removal or addition of BaSe. In the latter case especially

  3. Synthesis and Resonance Energy Transfer in Conjugates of Luminescent Cadmium Selenide Quantum Dots and Chlorin e6 Molecules

    Science.gov (United States)

    Fedosyuk, A. A.; Artemyev, M. V.

    2013-05-01

    We synthesized a new type of conjugates of highly luminescent water soluble CdSe/ZnS colloidal quantum dots covalently bound to Chlorin e6 dye molecules. We observed a resonance energy transfer from quantum dots emitting at 660 nm to Chlorine e6 molecules in our conjugates which can be utilized for phototherapy. Contrary to that quantum dots emitting at 588 nm show non-resonance quenching of excitonic luminescence without the energy transfer to dye molecules.

  4. Computational and experimental investigation for new transition metal selenides and sulfides: The importance of experimental verification for stability

    Science.gov (United States)

    Narayan, Awadhesh; Bhutani, Ankita; Rubeck, Samantha; Eckstein, James N.; Shoemaker, Daniel P.; Wagner, Lucas K.

    2016-07-01

    Expanding the library of known inorganic materials with functional electronic or magnetic behavior is a long-standing goal in condensed matter physics and materials science. Recently, the transition metal chalcogenides including selenium and sulfur have been of interest because of their correlated-electron properties, as seen in the iron-based superconductors and the transition metal dichalcogenides. However, the chalcogenide chemical space is less explored than that of oxides, and there is an open question of whether there may be new materials heretofore undiscovered. We perform a systematic combined theoretical and experimental search over ternary phase diagrams that are empty in the Inorganic Crystal Structure Database containing cations, transition metals, and one of selenium or sulfur. In these 27 ternary systems, we use a probabilistic model to reduce the likelihood of false negative predictions, which results in a list of 24 candidate materials. We then conduct a variety of synthesis experiments to check the candidate materials for stability. While the prediction method did obtain previously unknown compositions that are predicted stable within density functional theory, none of the candidate materials formed in our experiments. We come to the conclusion that these phase diagrams are "empty" in the case of bulk synthesis, but it remains a possibility that alternate synthesis routes may produce some of these phases.

  5. Loading of atorvastatin and linezolid in β-cyclodextrin–conjugated cadmium selenide/silica nanoparticles: A spectroscopic study

    Energy Technology Data Exchange (ETDEWEB)

    Antony, Eva Janet; Shibu, Abhishek [Department of Nanosciences & Technology, Karunya University, Coimbatore 641114, Tamil Nadu (India); Ramasamy, Sivaraj; Paulraj, Mosae Selvakumar [Department of Chemistry, Karunya University, Coimbatore 641114, Tamil Nadu (India); Enoch, Israel V.M.V., E-mail: drisraelenoch@gmail.com [Department of Nanosciences & Technology, Karunya University, Coimbatore 641114, Tamil Nadu (India); Department of Chemistry, Karunya University, Coimbatore 641114, Tamil Nadu (India)

    2016-08-01

    The preparation of β–cyclodextrin–conjugated cadmium selenide–silica nanoparticles, the loading of two drugs viz., Atorvastatin and linezolid in the cyclodextrin cavity, and the fluorescence energy transfer between CdSe/SiO{sub 2} nanoparticles and the drugs encapsulated in the cyclodextrin cavity are reported in this paper. IR spectroscopy, X-ray diffractometry, transmission electron microscopy, and particle size analysis by light–scattering experiment were used as the tools of characterizing the size and the crystal system of the nanoparticles. The nanoparticles fall under hexagonal system. The silica–shell containing CdSe nanoparticles were functionalized by reaction with aminoethylamino–β–cyclodextrin. Fluorescence spectra of the nanoparticles in their free and drug–encapsulated forms were studied. The FÖrster distances between the encapsulated drugs and the CdSe nanoparticles are below 3 nm. The change in the FÖrster resonance energy parameters under physiological conditions may aid in tracking the release of drugs from the cavity of the cyclodextrin. - Highlights: • CdSe/SiO{sub 2} nanoparticles of crystallite size 15 nm are prepared. • β-Cyclodextrin is attached to the surface of the nanoparticles. • Atorvastatin and linezolid get encapsulated in the cyclodextrin cavity. • FRET efficiency between the nanoparticles and the loaded drugs are determined.

  6. Optical, laser spectroscopic, and electrical characterization of transion metal doped zinc selenide and zinc sulfide nano-and-microcrystals

    Science.gov (United States)

    Kim, Changsu

    Middle-infrared lasers operating over a "molecular fingerprint" 2-15 mum spectral range are in great demand for a variety of applications. One of the best choices for lasing in the 2-5 mum spectral range is direct oscillation from divalent transition metal ions (TM2+: Cr 2+, Fe2+, Co2+)-doped wide bandgap II-VI semiconductor crystals. There are three major objectives in this dissertation: (1) Realize and study middle-infrared electroluminescence of n and p-type, Cr doped bulk ZnSe crystals. We have demonstrated a method of ZnSe crystals thermal-diffusion doping with donor (In, Zn, and Al) and acceptor (Cu, Ag, and N through CrN) impurities resulting in n and p-type conductivity of Cr:ZnSe. We are the first to our knowledge to obtain mid-IR electroluminescence in nominally p-type Cr:Ag:ZnSe, which could prove valuable for developing of novel mid-IR laser diodes. (2) En route to low dimensional gain material, develop simple method for making microscopic laser active Cr doped ZnSe, ZnS and CdSe powders, realize and study their laser spectroscopic characteristics. We have demonstrated a simple physical method of Cr2+:ZnSe, ZnS and CdSe powder fabrication with average sizes below ˜ 10mum and ˜1mum (eliminating stage of bulk crystal growth) and demonstrated first ever mid-IR random lasing on these powders under optical excitation. In addition, we have examine suspensions and polymer films impregnated with Cr:II-VI powders for random lasing in the mid-IR. The powder, suspension and polymer samples are fabricated and characterized through the measurement of photoluminescence (PL) spectra, PL kinetics, and lasing threshold energy. (3) En route to low dimensional gain material, develop method for making laser active Cr, Co, and Fe doped ZnSe and ZnS quantum dots (QD), realize and study their laser spectroscopic characteristics. We have demonstrated a novel method of TM doped II-VI QDs fabrication based on laser ablation in liquid and Ar environment. TM doped II-VI QDs demonstrated strong mid-IR luminescence. And we also demonstrated the first mid-IR (2-3 mum) random lasing at room temperature of Cr2+:ZnS QD powders. The results obtained in this work open a new pathway for development of low-cost optically and electrically pumped broadly tunable mid-IR laser sources. Keyword: Middle-Infrared lasers, Electroluminescence, Transition Metal ions, powder random lasers, nanocrystal lasers, Polymer film and Suspension.

  7. Computational studies of reacting flows with applications to zinc selenide nanoparticle synthesis and methane/hydrogen separation

    Science.gov (United States)

    Koutsona, Maria

    This work is a numerical study of the design and operation of two reacting flow systems, each with great potential in their fields. The design of reacting flow systems by computer simulations are successfully used in science and engineering to evaluate design geometries and operation, without resorting to experimental trial and error that is expensive, time consuming and, in some cases, dangerous. The models of the two systems described in this work are based on fundamental conservation equations for momentum and mass transfer coupled with chemical reaction kinetics and particle dynamics. The first part of this work is a study aiming to elucidate the transport phenomena and chemical reactions that control the size of ZnSe nanoparticles formed by a new vapor-phase synthesis route. The nanoparticles are synthesized by reacting vapors of (CH3)2Zn:N(C2H 5)3 adduct with H2Se gas (diluted in hydrogen) fed continuously from opposite sides into a counterflow jet reactor. The nuclei of the nanocrystals are formed by a direct condensation reaction near the stagnation point. The nuclei grow into nanoparticles by coalescence/coagulation and by surface growth reactions. A 2D model of an axially symmetric reactor was developed that includes descriptions of flow, mass transfer by convection and diffusion, chemical kinetics, particle nucleation, coagulation and surface growth. The coupled nonlinear partial differential equations of the model were solved using the Galerkin Finite Element Method. The model was used to study the relative importance of the underlying physical and chemical phenomena in controlling particle size and particle size distribution. Model predictions compared well with the limited experimental data available for this system. The model was also used for model-assisted design of the experimental counterflow jet reactor, where vapor-phase synthesis of ZnSe nanoparticles was demonstrated for the first time. The second part of this work involves the development of a predictive model describing pressure and concentration dynamics during Pressure Swing Adsorption (PSA) of binary (or pseudo-binary) gas mixtures. The separation of metane-hydrogen mixtures over 5A-zeolite was used as an example. The PSA cycle considered in this study includes the following 5 steps: (1) pressurization with product, (2) high-pressure adsorption, (3) cocurrent depressurization, (4) countercurrent blowdown and (5) countercurrent purge with product at low pressure. The PSA mathematical model describes the following processes gas flow in the bed (as axially dispersed plug flow) and the mass balance of the components of the mixture coupled to adsorption/desorption kinetics. The model results in a system of coupled partial differential equations in the axial bed dimension and time. The Galerkin Finite Element Method was used to discretize the equations in the axial direction of the bed. The resulting system of ordinary differential equations (ODE's) in time is solved by using an Euler full-implicit scheme. The model is being used by Chemical Design, Inc., for the initial design of PSA units.

  8. Encapsulation of cadmium selenide quantum dots using a self-assembling nanoemulsion (SANE) reduces their in vitro toxicity.

    Science.gov (United States)

    Edmund, Anton R; Kambalapally, Swetha; Wilson, Thomas A; Nicolosi, Robert J

    2011-02-01

    Although, nanometer-scale semi-conductor quantum dots (QDs) have attracted widespread interest in medical diagnosis and treatment, many can have intrinsic toxicities, especially those composed of CdSe, associated with their elemental composition. Using our self-assembling nanoemulsion (SANE) formulations which we have previously reported to be composed of non-toxic components, i.e., such as vegetable oil, surfactant and water, we hypothesized that their appropriate utilization would reduce the toxicity of QDs by encapsulating the CdSe QDs in our (SANE) system using a modified phase-inversion temperature (PIT) method. SANE encapsulation of the QDs did not alter their emission wavelength of 600nm which remained unchanged during the encapsulation process. In contrast, zeta potential of encapsulated QDs was reduced from -30 to -6.59 mV, which we have previously reported to be associated with beneficial properties (increased bioavailability and efficacy) for SANE-encapsulated bioactives such as pharmaceuticals. Relative to the untreated controls, the viability of HeLa cells exposed for 48 h to un-encapsulated CdSe QDs at a concentration of 115 μg/mL was 22.7±1.7% (p<0.05). In contrast, the percentage of viable HeLa cells following exposure to SANE-encapsulated CdSe QDs at the same concentration was 91.6±3.5% (p<0.05) or a 307% increase in the number of viable cells (p<0.05). When the dose of CdSe QDs was increased to 230 μg/mL, the percentage of viable HeLa cells after exposure to the un-encapsulated CdSe QDs was 16.1±1.3% compared to controls (p<0.05). In contrast, at the same increased concentration (230 μg/mL) of un-encapsulated CdSe QDs, the percentage of viable HeLa cells following exposure to SANE-encapsulated CdSe QDs was 87.9±3.3% relative to controls (p<0.05) or a 448% increase in the number of viable cells (p<0.05). Exposure of HeLa cells to a nanoblank, (nanoemulsion without QDs), showed no significant effect on cell viability (97.2±2.5%) compared to control cell culture. In conclusion, application of our SANE technology for encapsulating QDs increased cell viability of cells exposed to CdSe QDs while maintaining the original emission wavelength and therefore may be applied to reduce QD toxicity.

  9. Harnessing Topological Band Effects in Bismuth Telluride Selenide for Large Enhancements in Thermoelectric Properties through Isovalent Doping.

    Science.gov (United States)

    Devender; Gehring, Pascal; Gaul, Andrew; Hoyer, Alexander; Vaklinova, Kristina; Mehta, Rutvik J; Burghard, Marko; Borca-Tasciuc, Theodorian; Singh, David J; Kern, Klaus; Ramanath, Ganpati

    2016-08-01

    Dilute isovalent sulfur doping simultaneously increases electrical conductivity and Seebeck coefficient in Bi2 Te2 Se nanoplates, and bulk pellets made from them. This unusual trend at high electron concentrations is underpinned by multifold increases in electron effective mass attributable to sulfur-induced band topology effects, providing a new way for accessing a high thermoelectric figure-of-merit in topological-insulator-based nanomaterials through doping.

  10. The antidepressant-like action of a simple selenium-containing molecule, methyl phenyl selenide, in mice.

    Science.gov (United States)

    Sartori Oliveira, Carla Elena; Gai, Bibiana Mozzaquatro; Godoi, Benhur; Zeni, Gilson; Nogueira, Cristina Wayne

    2012-09-05

    Selenium-containing molecules show promising pharmacological properties. The antidepressant-like action of CH(3)SePh in the mouse forced swimming test (FST) and the tail suspension test (TST), models predictive of depressant activity, were investigated in this study. Moreover, the involvement of dopaminergic system in the antidepressant-like action of CH(3)SePh was studied. The behavioral results showed that CH(3)SePh significantly reduced the immobility time in the FST (25 and 50 mg/kg, intragastrically; i.g.) and the TST (50 mg/kg, i.g.), without accompanying changes in ambulation when assessed in the open-field test (OFT). The anti-immobility effect of CH(3)SePh (50 mg/kg, intragastrically; i.g.) in the FST was prevented by pretreatment of mice with haloperidol (0.2 mg/kg, i.p., a dopamine D(2) receptor antagonist), SCH 23390 (R-(+)-8-chloro-2,3,4,5-tetrahydro-3-methyl-5-phenyl-1H-3-benzazepine-7-ol) (0.05 mg/kg, s.c., a dopamine D(1) receptor antagonist) and sulpiride (50 mg/kg, i.p., a dopamine D(2) and D(3) antagonist). These results suggest that CH(3)SePh produced an antidepressant-like action in the mouse FST and TST. The antidepressant-like action of CH(3)SePh, a simple selenium-containing molecule, seems most likely to be mediated through an interaction with the dopaminergic system.

  11. The direct-to-indirect band gap crossover in two-dimensional van der Waals Indium Selenide crystals

    Science.gov (United States)

    Mudd, G. W.; Molas, M. R.; Chen, X.; Zólyomi, V.; Nogajewski, K.; Kudrynskyi, Z. R.; Kovalyuk, Z. D.; Yusa, G.; Makarovsky, O.; Eaves, L.; Potemski, M.; Fal’Ko, V. I.; Patanè, A.

    2016-12-01

    The electronic band structure of van der Waals (vdW) layered crystals has properties that depend on the composition, thickness and stacking of the component layers. Here we use density functional theory and high field magneto-optics to investigate the metal chalcogenide InSe, a recent addition to the family of vdW layered crystals, which transforms from a direct to an indirect band gap semiconductor as the number of layers is reduced. We investigate this direct-to-indirect bandgap crossover, demonstrate a highly tuneable optical response from the near infrared to the visible spectrum with decreasing layer thickness down to 2 layers, and report quantum dot-like optical emissions distributed over a wide range of energy. Our analysis also indicates that electron and exciton effective masses are weakly dependent on the layer thickness and are significantly smaller than in other vdW crystals. These properties are unprecedented within the large family of vdW crystals and demonstrate the potential of InSe for electronic and photonic technologies.

  12. Synthesis and Nanostructures of Metal Selenide Precursors for Cu(In,Ga)Se2 Thin-Film Solar Cells.

    Science.gov (United States)

    Cha, Ji-Hyun; Noh, Se Jin; Jung, Duk-Young

    2015-07-20

    A nanoink solution-based process was developed as a low-costing method for the fabrication of Cu(In,Ga)Se2 (CIGSe) thin-film photovoltaic cells. The sonochemical synthesis of CIGSe nanocrystals of the nanoink through step-by-step mixing of the reactants was investigated. To achieve the ideal stoichiometry of Cu(In0.7 Ga0.3 )Se2 to tune the bandgap and to fabricate high-efficiency photovoltaic cells, the synthetic parameters, the concentration of hydrazine, and the amount used of the gallium precursor were investigated. As the hydrazine concentration increased, gallium loss was observed in the CIGSe product. The gallium content in the reactant mixture strongly affected the metal stoichiometry of the prepared CIGSe nanocrystals. The nanoink solution based fabrication of thin-film photovoltaic cells was also explored, and the resulting device showed a conversion efficiency of 5.17 %.

  13. THE DEVELOPMENT OF 6.7% EFFICIENT COPPER ZINC INDIUM SELENIDE DEVICES FROM COPPER ZINC INDIUM SULFIDE NANOCRYSTAL INKS

    OpenAIRE

    Graeser, Brian Kemp

    2014-01-01

    As solar cell absorber materials, alloys of CuIn(S,Se)2 and Zn(S,Se) provide an opportunity to reduce the usage of indium along with the ability to tune the band gap. Here we report successful synthesis of alloyed (CuInS2 )0.5(ZnS)0.5 nanocrystals by a method that solely uses oleylamine as the liquid medium for synthesis. The reactive sintering of a thin film of these nanocrystals via selenization at 500 °C results in a uniform composition alloy (CuIn(S,Se)2 )0.5 (Zn(S,Se)) 0.5 layer with mic...

  14. Growth mechanism and strain relaxation in zinc selenide and cadmium telluride/zinc telluride semiconductor thin films

    Science.gov (United States)

    Wei, Hsiang-Yi

    The application of II--VI semiconductor devices such as blue-green light emitters (ZnSe-based materials) and HgCdTe infrared detectors are limited by the high density of defects and lack of large size substrates that are lattice matched and chemically compatible with the films. By growing a single thick buffer layer or a composite buffer structure of dissimilar materials can lead to a final top layer that is structurally and chemically compatible with the active layer of the device. Low defect density and flat surface morphology are the basic requirements for an applicable buffer layer. In this work, transmission electron microscopy is used to investigate the crystalline structure and defect generation mechanism in buffer layers for the growth of ZnSe-based and HgCdTe films. We investigate the interface chemistry, defect density, and growth mechanism of ZnSe films grown on GaAs substrates with different surface processing techniques. Undesirable high density of funnel defects (˜1010 cm-2) are always observed when the growth is performed on the epi-ready GaAs. We also observe that Sb can act as a surfactant and promote a truly layer-by-layer growth mode when the ZnSe film is grown on Sb-stabilized GaAs substrates. The defect density can be reduced to values as low as in the low 103 cm-2 range, which is the lowest defect density ever reported for ZnSe films. Moreover, the ZnSe surface exhibits a characteristic brick-like pattern for all of the substrate preparation methods used (except for Sb-stabilized GaAs) and the thickness of the ZnSe epilayers for films grown at ˜280--330°C. At a much higher growth temperature (410°C), a corrugated surface forms with high periodicity along the [110] direction. We propose a kinetics-limited surface roughness mechanism for the ZnSe films based on a competition of nucleation of 2D islands followed by step evolution. In the CdTe/ZnTe/Si epitaxial system, we investigated the influence of different surface precursors on the growth mechanism and defect density in the films. For As---precursor on the Si surface, Te adsorption on the terraces is inhibited and its migration to the step edges is enhanced. Therefore, the growth is expected to proceed in a step-flow growth mode. A strain relaxation mechanism including misfit dislocation generation, twin formation, and crystal tilt is proposed to account for the large lattice mismatch (f = 12.3%) in this system.

  15. Preparation, theory, and biological applications of highly luminescent cadmium selenide/zinc sulfide quantum dots in optical and electron microscopy

    Science.gov (United States)

    Bouwer, James Christopher

    This dissertation describes the preparation, theory, and applications of ZnS overcoated CdSe (core) quantum dots for applications as fluorescent probes in optical microscopy and as electron energy loss spectroscopy (EELS) probes in electron microscopy, with applications to the biological sciences. The dissertation begins with a brief overview of quantum dots and their history. Next, a brief overview of the necessary semiconductor theory is discussed including the origin of the band gap, the origin of holes, the concepts of phonons, and trap states. Then, the role of the confinement potential in the quantum dot fluorescent spectrum is discussed in the context of the 3-dimensional spherical well. Included in this discussion is the role of excitonic electron-hole bound states. To provide a complete document useful to anyone who wishes to continue work along these lines, included is a methods section which describes the complete process of synthesis of the CdSe cores, overcoating the cores with ZnS, size selection of nanocrystals, water solubilization, and protein conjugation. The methods used in live cell labeling are included as well. In the section that follows, a discussion of the mathematical methods of image correlation spectroscopy (ICS) for extracting dynamic constants such as flow rates and diffusion constants from time lapse optical image data is discussed in the context of quantum dot fluorescent probes. Dynamic constants were obtained using live NIH3T3 mouse fibroblast cells labeled with IgG-anti-EGF conjugated quantum dots. These same cells were then fixed, imbedded in resin, sectioned to 100nm thick sections and imaged under the electron microscope. The electron dense cadmium selinide provides the contrast necessary to perform direct imaging of EGF receptor sites. In order to improve the data and move toward multi-channel imaging in the electron microscope, EELS spectroscopy and elemental mapping of quantum dots was performed. The theory along with a discussion of the instruments needed to perform EELS is presented. This data was intended to provide new applications of quantum dots as biological probes in EELS spectroscopy. This dissertation should provide the reader with a thorough understanding of the nature of quantum dots and give a number of biological applications.

  16. Dialkyldiselenophosphinato-metal complexes - a new class of single source precursors for deposition of metal selenide thin films and nanoparticles

    Science.gov (United States)

    Malik, Sajid N.; Akhtar, Masood; Revaprasadu, Neerish; Qadeer Malik, Abdul; Azad Malik, Mohammad

    2014-08-01

    We report here a new synthetic approach for convenient and high yield synthesis of dialkyldiselenophosphinato-metal complexes. A number of diphenyldiselenophosphinato-metal as well as diisopropyldiselenophosphinato-metal complexes have been synthesized and used as precursors for deposition of semiconductor thin films and nanoparticles. Cubic Cu2-xSe and tetragonal CuInSe2 thin films have been deposited by AACVD at 400, 450 and 500 °C whereas cubic PbSe and tetragonal CZTSe thin films have been deposited through doctor blade method followed by annealing. SEM investigations revealed significant differences in morphology of the films deposited at different temperatures. Preparation of Cu2-xSe and In2Se3 nanoparticles using diisopropyldiselenophosphinato-metal precursors has been carried out by colloidal method in HDA/TOP system. Cu2-xSe nanoparticles (grown at 250 °C) and In2Se3 nanoparticles (grown at 270 °C) have a mean diameter of 5.0 ± 1.2 nm and 13 ± 2.5 nm, respectively.

  17. Engineering the Electrical Conductivity of Lamellar Silver-Doped Cobalt(II) Selenide Nanobelts for Enhanced Oxygen Evolution.

    Science.gov (United States)

    Zhao, Xu; Zhang, Hantao; Yan, Yu; Cao, Jinhua; Li, Xingqi; Zhou, Shiming; Peng, Zhenmeng; Zeng, Jie

    2017-01-02

    Precisely engineering the electrical conductivity represents a promising strategy to design efficient catalysts towards oxygen evolution reaction (OER). Here, we demonstrate a versatile partial cation exchange method to fabricate lamellar Ag-CoSe2 nanobelts with controllable conductivity. The electrical conductivity of the materials was significantly enhanced by the addition of Ag(+) cations of less than 1.0 %. Moreover, such a trace amount of Ag induced a negligible loss of active sites which was compensated through the effective generation of active sites as shown by the excellent conductivity. Both the enhanced conductivity and the retained active sites contributed to the remarkable electrocatalytic performance of the Ag-CoSe2 nanobelts. Relative to the CoSe2 nanobelts, the as-prepared Ag-CoSe2 nanobelts exhibited a higher current density and a lower Tafel slope towards OER. This strategy represents a rational design of efficient electrocatalysts through finely tuning their electrical conductivities.

  18. Modified hydrothermal synthesis and characterization of reduced graphene oxide-silver selenide nanocomposites with enhanced reactive oxygen species generation

    Institute of Scientific and Technical Information of China (English)

    Lei Zhu; Shu Ye; Asghar Ali; Kefayat Ulla; Kwang Youn Cho; Won-Chun Oh

    2015-01-01

    A visible‐light photocatalyst containing Ag2Se and reduced graphene oxide (RGO) was synthesized by a facile sonochemical‐assisted hydrothermal method. X‐ray diffraction, scanning electron mi‐croscopy with energy‐dispersive X‐ray analysis, and ultraviolet‐visible diffuse reflectance spectros‐copy results indicated that the RGO‐Ag2Se nanocomposite contained small crystalline Ag2Se nano‐particles dispersed over graphene nanosheets and absorbed visible light. The high crystallinity of the nanoparticles increased photocatalytic activity by facilitating charge transport. N2 adsorp‐tion‐desorption measurements revealed that the RGO‐Ag2Se nanocomposite contained numerous pores with an average diameter of 9 nm, which should allow reactant molecules to readily access the Ag2Se nanoparticles. The RGO‐Ag2Se nanocomposite exhibited higher photocatalytic activity than bulk Ag2Se nanoparticles to degrade organic pollutant rhodamine B and industrial dye Texbrite BA‐L under visible‐light irradiation (λ>420 nm). The generation of reactive oxygen spe‐cies in RGO‐Ag2Se was evaluated through its ability to oxidize 1,5‐diphenylcarbazide to 1,5‐diphenylcarbazone. The small size of the Ag2Se nanoparticles in RGO‐Ag2Se was related to the use of ultrasonication during their formation, revealing that this approach is attractive to form po‐rous RGO‐Ag2Se materials with high photocatalytic activity under visible light.

  19. Investigation of the chemical explosion of an ion exchange resin column and resulting americium contamination of personnel in the 242-Z building, August 30, 1976

    Energy Technology Data Exchange (ETDEWEB)

    1976-10-19

    As a result of an explosion in the Waste Treatment Facility, 242-Z Building, 200 West Area of the Hanford Reservation on August 30, 1976, the Manager of the Richland Operations Office (RL), Energy Research and Development Administration (ERDA), appointed an ERDA Committee to conduct a formal investigation and to prepare a report on their findings of this occurrence. The Committee was instructed to conduct the investigation in accordance with ERDAMC 0502, insofar as circumstances would permit, to cover and explain technical elements of the casual sequence(s) of the occurrence, and to describe management systems which should have or could have prevented the occurrence. This report is the result of the investigation and presents the conclusions of the review.

  20. Aqueous complexation of citrate with neodymium(III) and americium(III): a study by potentiometry, absorption spectrophotometry, microcalorimetry, and XAFS.

    Science.gov (United States)

    Brown, M Alex; Kropf, A Jeremy; Paulenova, Alena; Gelis, Artem V

    2014-05-07

    The aqueous complexation of Nd(III) and Am(III) with anions of citrate was studied by potentiometry, absorption spectrophotometry, microcalorimetry, and X-ray absorption fine structure (XAFS). Using potentiometric titration data fitting the metal-ligand (L) complexes that were identified for Nd(III) were NdHL, NdL, NdHL2, and NdL2; a review of trivalent metal-citrate complexes is also included. Stability constants for these complexes were calculated from potentiometric and spectrophotometric titrations. Microcalorimetric results concluded that the entropy term of complex formation is much more dominant than the enthalpy. XAFS results showed a dependence in the Debye-Waller factor that indicated Nd(iii)-citrate complexation over the pH range of 1.56-6.12.

  1. Americium(III) oxidation by copper(III) periodate in nitric acid solution as compared with the action of Bi(V) compounds of sodium, lithium, and potassium

    Energy Technology Data Exchange (ETDEWEB)

    Sinkov, Sergey I.; Lumetta, Gregg J. [Pacific Northwest National Laboratory, Radiochemical Processing Lab., Richland, WA (United States)

    2015-07-01

    The oxidative action of a Cu(III) periodate compound toward Am(III) in nitric acid was studied. The extent of oxidation of Am(III) to Am(VI) was investigated using a constant initial Cu(III)-to-Am(III) molar ratio of 10:1 and varying nitric acid concentrations from 0.25 to 3.5 mol/L. From 0.25 to 3 mol/L HNO3, more than 98% of the Am(III) was oxidized to Am(VI); however, at 3.5 mol/L HNO{sub 3}, the conversion to Am(VI) was only 80%. Increasing the Cu(III)-to-Am(III) molar ratio to 20:1 in 3.5 mol/L HNO{sub 3} resulted in 98% conversion to Am(VI). For comparison, oxidation of Am(III) with NaBiO{sub 3} was studied at 3.5 mol/L HNO{sub 3} and the same stoichiometric excess of Bi(V) oxidant over Am(III) (stoichiometric ratio of 3.33:1). With NaBiO{sub 3}, the extent of Am(III) conversion to Am(VI) was only 19%, while with the Cu(III) compound this value was found to be about 4 times higher under otherwise identical conditions. Similar results were obtained with other Bi(V) salts. These results show that the Cu(III) periodate compound is a superior oxidant to NaBiO{sub 3}, yielding rapid conversion to Am(VI) in a homogeneous acidic solution, and is, therefore, an excellent candidate for further development of Am separation systems.

  2. Chemical speciation of strontium, americium, and curium in high level waste: Predictive modeling of phase partitioning during tank processing. Annual progress report, October 1996--September 1997

    Energy Technology Data Exchange (ETDEWEB)

    Felmy, A.R. [Pacific Northwest National Lab., Richland, WA (US); Choppin, G. [Florida State Univ., Tallahassee, FL (US)

    1997-12-31

    'The program at Florida State University was funded to collaborate with Dr. A. Felmy (PNNL) on speciation in high level wastes and with Dr. D. Rai (PNNL) on redox of Pu under high level waste conditions. The funding provided support for 3 research associates (postdoctoral researchers) under Professor G. R. Choppin as P.I. Dr. Kath Morris from U. Manchester (Great Britain), Dr. Dean Peterman and Dr. Amy Irwin (both from U. Cincinnati) joined the laboratory in the latter part of 1996. After an initial training period to become familiar with basic actinide chemistry and radiochemical techniques, they began their research. Dr. Peterman was assigned the task of measuring Th-EDTA complexation prior to measuring Pu(IV)-EDTA complexation. These studies are associated with the speciation program with Dr. Felmy. Drs. Morris and Irwin initiated research on redox of plutonium with agents present in the Hanford Tanks as a result of radiolysis or from use in separations. The preliminary results obtained thus far are described in this report. It is expected that the rate of progress will continue to increase significantly as the researchers gain more experience with plutonium chemistry.'

  3. Studies on the feasibility of using completely incinerable reagents for the single-cycle separation of americium(III) from simulated high-level liquid waste

    Energy Technology Data Exchange (ETDEWEB)

    Nayak, P.K.; Kumaresan, R.; Venkatesan, K.A.; Subramanian, G.G.S.; Prathibha, T.; Syamala, K.V.; Selvan, B. Robert; Rajeswari, S.; Antony, M.P.; Rao, P.R. Vasudeva [Indira Gandhi Centre for Atomic Research, Kalpakkam (India). Fuel Chemistry Div.; Chaurasia, Shivkumar; Bhanage, B.M. [Institute of Chemical Technology, Mumbai (India)

    2015-06-01

    The extraction and stripping behavior of various metal ions present in the fast reactor simulated high-level liquid waste (FR-SHLLW) was studied using a solvent phase composed of a neutral extractant, N,N,-didodecyl-N',N'-dioctyl-3-oxapentane-1,5-diamide (D{sup 3}DODGA) and an acidic extractant, di-2-ethylhexyl diglycolamic acid (HDEHDGA) in n-dodecane (n-DD). The third phase formation behavior of the solvent formulation D{sup 3}DODGA + HDEHDGA/n-DD, was studied when it was contacted with FR-SHLLW, and the concentration of neutral and acidic extractant needed to avoid the third phase formation was optimized. The distribution ratio of various metal ions present in FR-SHLLW was measured in a solution of 0.1 M D{sup 3}DODGA + 0.2 M HDEHDGA/n-DD. The extraction of Am(III) was accompanied by the co-extraction of lanthanides and unwanted metal ions such as Zr(IV), Y(III), and Pd(II). A procedure was developed to minimize the extraction of unwanted metal ions by using aqueous soluble complexing agents in FR-SHLLW. Based on those results, the counter-current mixer-settler run was performed in a 20-stage mixer-settler. Quantitative extraction of Am(III), Ln(III), Y(III), and Sr(II) in 0.1 M D{sup 3}DODGA + 0.2 M HDEHDGA/n-DD was observed. The recovery of Am(III) from the loaded organic phase was carried out by the optimized aqueous formulation composed of 0.01 M diethylenetriaminepentaacetic acid (DTPA) + 0.5 M citric acid (CA) at pH 1.5. The stripping of Am(III) was accompanied by co-stripping of some early lanthanides. However the later lanthanides (Eu(III) and beyond) were not back extracted to Am(III) product. Therefore, the studies foresee the possibility of intra-lanthanides as well as lanthanide-actinide separation in a single-processing cycle.

  4. Proceedings of the specialists' meeting on nuclear data of plutonium and americium isotopes for reactor applications. [BNL, Nov. 20-21, 1978

    Energy Technology Data Exchange (ETDEWEB)

    Chrien, R E [ed.

    1979-05-01

    Separate abstracts were prepared for 17 of the papers in these Proceedings. The remaining six have already been cited in ERA, and can be located by referring to the entry CONF-781174-- in the Report Number Index. (RWR)

  5. Determination of Neptunium, Americium and Curium in Spent Nuclear Fuel Samples by Alpha Spectrometry Using {sup 239}Np and {sup 243}Am as a Spike and a Tracer

    Energy Technology Data Exchange (ETDEWEB)

    Jeo, Kih-Soo; Song, Byung-Chul; Kim, Young-Bok; Han, Sun-Ho; Jeon, Young-Shin; Jung, Euo-Chang; Jee, Kwang-Yong [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2007-07-01

    Determination of actinide elements and fission products in spent nuclear fuels is of importance for a burnup determination and source term evaluation. Especially, the amounts of uranium and plutonium isotopes are used for the evaluation of a burnup credit in spent nuclear fuels. Additionally, other actinides such as Np, Am and Cm in spent nuclear fuel samples is also required for the purposes mentioned above. In this study, {sup 237}Np, {sup 241}Am and {sup 244}Cm were determined by an alpha spectrometry for the source term data for high burnup spent nuclear fuels ranging from 37 to 62.9 GWD/MtU as a burnup. Generally, mass spectrometry has been known as the most powerful method for isotope determinations such as high concentrations of uranium and plutonium. However, in the case of minor actinides such as Np, Am and Cm, alpha spectrometry would be recommended instead. Determination of the transuranic elements in spent nuclear fuel samples is different from that for environmental samples because the amount of each nuclide in the spent fuel samples is higher and the relative ratios between each nuclide are also different from those for environmental samples. So, it is important to select an appropriate tracer and an optimum sample size depending on the nuclides and analytical method. In this study {sup 237}Np was determined by an isotope dilution alpha(gamma) spectrometry using {sup 239}Np as a spike, and {sup 241}Am and curium isotopes were determined by alpha spectrometry using {sup 243}Am as a tracer. The content of each nuclide was compared with that by the Origen-2 code.

  6. Recent advances on the copper selenide nanocrystals%硒化铜纳米晶的最近研究进展

    Institute of Scientific and Technical Information of China (English)

    田贵敏; 程永光; 牛金钟

    2013-01-01

    介绍了一种新兴的太阳能电池活性材料——硒化铜纳米晶及其最近的研究进展,对硒化铜纳米晶的合成方法、结构和性质做了详细的介绍,并对硒化铜纳米晶以后的发展进行了探讨与展望.

  7. The effect of silicon and copper-indium-gallium-selenide based solar cell structures and processing on temperature dependent performance losses

    Science.gov (United States)

    Hsieh, Judith

    Temperature dependent current voltage measurements (J-V-T) of solar cells. provide both fundamental and practical information. They give detailed insight into. recombination losses within the device as well as information about module. performance losses at higher outdoor operating temperatures. In this thesis, J-V-T. measurements were applied to two distinctly different types of solar cells: crystalline. silicon heterojunction cells and thin film (AgCu)(InGa)Se2 or ACIGS polycrystalline. cells. Crystalline silicon solar cells with heterojunction structure improve the opencircuit. voltage and efficiency. Interdigitated back contact (IBC) Si solar cells obtain a. higher short-circuit current and fill factor compared to front heterojunction (FHJ) solar. cells. ACIGS solar cells have shown higher efficiencies at wider bandgap compared to. the baseline CIGS solar cells. Two high open-circuit voltage CIGS solar cells are. included and compared with ACIGS solar cells. In this thesis, the impact of different. types of solar cells structure and fabrication on temperature dependent performance. losses will be discussed. Devices with higher bandgap are predicted to have higher. open-circuit voltage and lower temperature coefficient of maximum power output. (Pmax). The correlation between temperature coefficient of Pmax and open-circuit. voltage can be found in Si FHJ cells but not Si IBC or ACIGS cells. However, ACIGS. cells show an inverse correlation between temperature coefficient of Pmax and bandgap. as expected. Analysis of diode quality factor and other parameters are interpreted. Sshape. J-V curve can reduce the device's fill factor with a relative high series resistance. This phenomenon tends to occur in FHJ cells rather than IBC at low temperature. Light-dark crossover and roll over effects are commonly seen in ACIGS cells and the. anomaly is enhanced at lower temperature. Most of FHJ and IBC cells obtain the. ideality factor between 1 and 2 while some of ACIGS cells obtain the ideality factor. less than 1 or larger than 2. The value of the ideality factor may be limited by different. recombination mechanism.

  8. Na3.88Mo15Se19: a novel ternary reduced molybdenum selenide containing Mo6 and Mo9 clusters

    Directory of Open Access Journals (Sweden)

    Diala Salloum

    2013-10-01

    Full Text Available The structure of tetrasodium pentadecamolybdenum nonadecaselenide, Na3.88Mo15Se19, is isotypic with the In3+xMo15Se19 compounds [Grüttner et al. (1979. Acta Cryst. B35, 285–292]. It is characterized by two cluster units, Mo6Sei8Sea6 and Mo9Sei11Sea6 (where i represents inner and a apical atoms, that are present in a 1:1 ratio. The cluster units are centered at Wyckoff positions 2b and 2c and have point-group symmetry -3 and -6, respectively. The clusters are interconnected through additional Mo—Se bonds. In the title compound, the Na+ cations replace the trivalent as well as the monovalent indium atoms present in In3.9Mo15Se19. One Mo, one Se and one Na atom are situated on mirror planes, and two other Se atoms and one Na atom [occupancy 0.628 (14] are situated on threefold rotation axes. The crystal studied was twinned by merohedry with refined components of 0.4216 (12 and 0.5784 (12.

  9. Band gap expansion, shear inversion phase change behaviour and low-voltage induced crystal oscillation in low-dimensional tin selenide crystals.

    Science.gov (United States)

    Carter, Robin; Suyetin, Mikhail; Lister, Samantha; Dyson, M Adam; Trewhitt, Harrison; Goel, Sanam; Liu, Zheng; Suenaga, Kazu; Giusca, Cristina; Kashtiban, Reza J; Hutchison, John L; Dore, John C; Bell, Gavin R; Bichoutskaia, Elena; Sloan, Jeremy

    2014-05-28

    In common with rocksalt-type alkali halide phases and also semiconductors such as GeTe and SnTe, SnSe forms all-surface two atom-thick low dimensional crystals when encapsulated within single walled nanotubes (SWNTs) with diameters below ∼1.4 nm. Whereas previous density functional theory (DFT) studies indicate that optimised low-dimensional trigonal HgTe changes from a semi-metal to a semi-conductor, low-dimensional SnSe crystals typically undergo band-gap expansion. In slightly wider diameter SWNTs (∼1.4-1.6 nm), we observe that three atom thick low dimensional SnSe crystals undergo a previously unobserved form of a shear inversion phase change resulting in two discrete strain states in a section of curved nanotube. Under low-voltage (i.e. 80-100 kV) imaging conditions in a transmission electron microscope, encapsulated SnSe crystals undergo longitudinal and rotational oscillations, possibly as a result of the increase in the inelastic scattering cross-section of the sample at those voltages.

  10. The influence of sodium nanoparticles formation on luminescent properties of fluorophosphate glasses containing molecular clusters and quantum dots of lead selenide

    Science.gov (United States)

    Lipatova, Zh. O.; Kolobkova, E. V.; Sidorov, A. I.; Nikonorov, N. V.

    2016-08-01

    The influence of sodium nanoparticles and secondary heat treatment conditions on the spectralluminescent characteristics of fluorophosphate glasses with PbSe molecular clusters and quantum dots is studied. Experiments with glasses containing no sodium nanoparticles show that their thermal treatment leads to the formation of molecular clusters with subsequent formation of quantum dots having an intense luminescence. The results of numerical simulation for glasses with sodium nanoparticles shows that heat treatment leads to formation of a sodium fluoride shell on the nanoparticles surface. It is shown that quenching of the luminescence of PbSe molecular clusters and quantum dots takes place in these glasses.

  11. An easy shortcut synthesis of size-controlled bismuth nanoparticles and their use in the SLS growth of high-quality colloidal cadmium selenide quantum wires.

    Science.gov (United States)

    Wang, Fudong; Buhro, William E

    2010-02-22

    An easy shortcut synthesis of thermally stable, near-monodisperse Bi nanoparticles from BiCl(3) and Na[N(SiMe(3))(2)] is described. The diameters of the Bi nanoparticles are controlled in the range of 4-29 nm by varying the amounts of BiCl(3) and Na[N(SiMe(3))(2)] employed. Standard deviations in their diameter distributions are 5-15% of the mean diameters, consistent with near monodispersity. These Bi nanoparticles are shown to be the best currently available catalysts for the solution-liquid-solid (SLS) growth of high-quality CdSe quantum wires.

  12. Litochlebite, Ag2PbBi4Se8, a new selenide mineral species from Zalesi, Czech Republic: description and crystal structure

    DEFF Research Database (Denmark)

    Makovicky, Emil; Topa, Dan; Sejkora, Jiri;

    2011-01-01

    , and uranophane. Litochlebite is opaque, dark grey to black, has a dark grey streak and a metallic luster. No cleavage was observed; the mineral is brittle with an irregular fracture. The VHN10g microhardness 230 (227–234) kg/mm2 corresponds to a Mohs hardness of about 3; the calculated density is 7.90 g/cm3...... [Fo > 4s(Fo)] collected on a Bruker AXS diffractometer with a CCD detector and MoKa radiation. The crystal structure contains one lead site, four independent Bi sites, four silver sites and eight independent Se sites. One Ag site is an octahedrally coordinated (2 + 4) site in the pseudotetragonal...

  13. Molten Salt Synthesis, Crystal Structure and Optical Properties of a Novel Quaternary Metal Selenide, K2AgIn3Se6

    Institute of Scientific and Technical Information of China (English)

    Guo, Hong-You(郭洪猷); Wang, Zhi-Xia(王志霞); Shu, Gui-Ming(舒桂明); Wang, Ru-Ji(王如骥); Zhang, Li-Dan(张丽丹); Wang, Ping(王平)

    2004-01-01

    K2AgIn3Se6 was synthesized by a molten-salt (alkali-metal polyselenide flux) reaction at 500 ℃. The orange red granular crystal crystallizes in monoclinic space group C2/c with cell parameters, a=1.16411(7) nm, b=1.16348(8) nm, c=2.14179(12) nm, V=2.8740(9) nm3, and Z=8. The crystal has a new two-dimensional structure containing 2∞[AgIn3Se6]2- anionic layers separated by K+ cations and the 2∞[AgIn3Se6]2- layer is constructed with corner-shared [AgSe4] and [InSe4] tetrahedra. The optical band gap of K2AgIn3Se6 was determined to be ca. 2.9 eV by UV/vis/NIR diffuse reflectance spectra.

  14. Phase transition and high temperature thermoelectric properties of copper selenide Cu2-χSe(0≤χ≤0.25)

    Institute of Scientific and Technical Information of China (English)

    Xiao Xing-Xing; Xie Wen-Jie; Tang Xin-Feng; Zhang Qing-Jie

    2011-01-01

    With good electrical properties and an inherently complex crystal structure,Cu2-xSe is a potential "phonon glass electron crystal" thermoelectric material that has previously not attracted much interest.In this study,Cu2-xSe (0≤x≤0.25)compounds were synthesized by a melting-quenching method,and then sintered by spark plasma sintering to obtain bulk material.The effect of Cu content on the phase transition and thermoelectric properties of Cu2-xSe were investigated in the temperature range of 300 K-750 K.The results of X-ray diffraction at room temperature show that Cu2-xSe compounds possess a cubic structure with a space group of Fm3m(#225)when 0.15 < x≤0.25,whereas they adopt a composite of monoclinic and cubic phases when 0≤x≤0.15.The thermoelectric property measurements show that with increasing Cu content,the electrical conductivity decreases,the Seebeck coefficient increases and the thermal conductivity decreases.Due to the relatively good power factor and low thermal conductivity,the nearly stoichiometric Cu2Se compound achieves the highest ZT of 0.38 at 750 K.It is expected that the thermoelectric performance can be further optimized by doping appropriate elements and/or via a nanostructuring approach.

  15. Advance in Relationship between Gastric Carcinoma and Selenium or Selenide%硒及其化合物与胃癌研究进展

    Institute of Scientific and Technical Information of China (English)

    代明真

    2009-01-01

    Gastric carcinoma is one of the most common malignant tumor in the world,its incidence and mortality are second only to lung cancer, and China owns its highest incidence now. Many studies have shown that selenium and its chemical com-pounds have wide biological action and can stop the existence and deterioration of varied tumors. There may be some considerable relations between selenium and gastric carcinoma,yet not clear and definite. So to have a better understanding to this and make further improvements to clarify relations between the two and their possible function mechanism, this article will summarize rela-tive studies in recent years.%胃癌是全世界发病率和死亡率仅次于肺癌的恶性肿瘤,而我国是世界上胃癌发病率最高的国家之一.大量的研究资料表明,硒及其化合物具有广泛的生物学作用,具有阻止多种肿瘤发生发展的作用,硒与胃癌之间有着较大的关联性,但两者之间的关系尚不明确.为更好地认识硒及其化合物对胃癌发生发展的影响,进一步了解两者之间的关系以及可能的作用机制,本文就近年采相关的研究进行综述.

  16. Optical and electrical characteristics of chromium- and iron-doped zinc selenide thin film and bulk materials for optically and electrically pumped lasers

    Science.gov (United States)

    Gallian, Andrew

    This work is devoted to evaluating new laser systems based upon chromium and iron doped ZnSe structures. These systems are based upon new materials and pumping schemes. These topics can be broken down into three major subgroups: new materials based upon Cr2+:ZnSe, Fe2+:ZnSe lasers and pump sources, and electrically pumped Cr2+:ZnSe systems. Both hot-pressed ceramic and thin film Cr2+:ZnSe samples were evaluated for their potential as laser gain media. This work entailed spectroscopic analysis of both their absorption and emission spectra as well as characterizing their lifetime of luminescence. For hot-pressed ceramic Cr2+:ZnSe the samples were tested in a laser cavity and proven to be the first laser system in the mid-IR to be demonstrated based upon hot-pressed Cr2+:ZnSe. Thin film Cr2+:ZnSe was determined to have different spectroscopic characteristics for luminescence compared to reference bulk samples. This difference is attributed to the location of all of the optical centers within a Fabry-Perot cavity formed by the film surface and the wafer on which it was deposited. Fe2+:ZnSe laser demonstration at room temperature is presented. This laser operates in a spectral region of great interest for spectroscopy. To develop this laser system new pumping systems were required. Such systems as passively Q-switched Er:YSGG and Stokes Stimulated Raman Scattering from a D2 cell are described in great depth. Electrically pumped Transition Metal 2+:II-VI systems are ideal for small portable spectroscopic and scientific tools. The elimination of an optical pump source removes many complications of other systems including, complications due to having a second laser. This work was approached by modeling electrically motivated transitions with sub-band optical excitation. Lasing of Cr 2+:ZnSe was achieved using a 532 nm pump source. This result, in combination with photo-current and photo-Hall measurements, led to the development of some theories explaining possible electroluminescence. Electroluminescence was also achieved in bulk n-type Cr2+:ZnSe using impacts of hot carriers as an excitation source.

  17. Optical phonons in nanostructured thin films composed by zincblende zinc selenide quantum dots in strong size-quantization regime: Competition between phonon confinement and strain-related effects

    Science.gov (United States)

    Pejova, Biljana

    2014-05-01

    Raman scattering in combination with optical spectroscopy and structural studies by X-ray diffraction was employed to investigate the phonon confinement and strain-induced effects in 3D assemblies of variable-size zincblende ZnSe quantum dots close packed in thin film form. Nanostructured thin films were synthesized by colloidal chemical approach, while tuning of the nanocrystal size was enabled by post-deposition thermal annealing treatment. In-depth insights into the factors governing the observed trends of the position and half-width of the 1LO band as a function of the average QD size were gained. The overall shifts in the position of 1LO band were found to result from an intricate compromise between the influence of phonon confinement and lattice strain-induced effects. Both contributions were quantitatively and exactly modeled. Accurate assignments of the bands due to surface optical (SO) modes as well as of the theoretically forbidden transverse optical (TO) modes were provided, on the basis of reliable physical models (such as the dielectric continuum model of Ruppin and Englman). The size-dependence of the ratio of intensities of the TO and LO modes was studied and discussed as well. Relaxation time characterizing the phonon decay processes in as-deposited samples was found to be approximately 0.38 ps, while upon post-deposition annealing already at 200 °C it increases to about 0.50 ps. Both of these values are, however, significantly smaller than those characteristic for a macrocrystalline ZnSe sample.

  18. Photoluminescence spectral study of single cadmium selenide/zinc sulfide colloidal nanocrystals in poly(methyl methacrylate) and quantum dots molecules

    Science.gov (United States)

    Shen, Yaoming

    Quantum dots (QDs)and Nano-crystals (NCs) have been studies for decades. Because of the nanoscale quantum confinement, delta shape like energy density states and narrowband emitters properties, they hold great promise for numerous optoelectronics and photonics applications. They could be used for tunable lasers, white LED, Nano-OLED, non-volatile memory and solar cells. They are also the most promising candidates for the quantum computing. The benefits for NCs over QDs is that NCs can be incorporated into a variety of polymers as well as thin films of bulk semiconductors. These exceptional flexibility and structural control distinguish NCs from the more traditional QD structures fabricated using epitaxial growth techniques. In my research of work, I studied the photoluminescence (PL) and absorption character of ensemble NCs incorporated in Polymethyl methacrylate (PMMA). To understand the behavior of the NCs in PMMA, it is important to measure a singe NC to avoid the inhomogenous broading of many NCs. So I particularly studied the behavior of a single NC in PMMA matrix. A microphotoluminescence setup to optically isolate a single nanocrystal is used. Random spectral shift and blinking behavior (on and off) are found. Addition to that, two color spectral shifting, is a major phenomena found in the system. Other interesting results such as PL intensity changes (decreasing or increasing with time) and quenching effect are observed and explained too. From the correlation function, we can distinguish the phonon replicas. The energy of these phonons can be calculated very accurately from the experiment result. The Huang-Rhys factors can be estimated too. Self-assembled semiconductor quantum dots (QDs), from highly strained-layer heteroepitaxy in the Stranski-Krastanow (S-K) growth mode, have been intensively studied because of the delta-function-like density of states, which is significant for optoelectronic applications. Spontaneous formation of semiconductor quantum-dot molecules (QDMs), which are clusters of a few QDs, has attracted attention as a possible implementation of future quantum devices such as quantum cellular antomata. With the advances in crystal growth techniques, the fabrication methods for nanostructures have been improved continuously. Lateral QDMs have been achieved. As a side topic, lateral QDMs have been studied and the result is presented in the last chapter.

  19. Spatial and RF power dependence of the structural and electrical characteristics of copper zinc tin selenide thin films prepared by single elementary target sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Jo, Yeon Hwa; Jang, Jin Woo; Cho, Yong Soo, E-mail: ycho@yonsei.ac.kr

    2014-11-14

    The spatial variations of the structural, optical and electrical properties of Cu{sub 2}ZnSnSe{sub 4} thin films grown by radio-frequency (RF) magnetron sputtering across a distance of 60 mm were investigated as a function of the discharge power. Noticeable changes in the deposition rate and elemental distribution were observed in the as-deposited films at the central and near-edge regions. After annealing in a Se atmosphere, the dependence of the phase evolution and electrical properties on the spatial position and power was also evident. Deposition at a low power of 30 W seems to be more promising in generating dominant Cu{sub 2}ZnSnSe{sub 4} phase with well-packed crystallites on the surface. On the other hand, deposition at higher power tended to result in a significant portion of a secondary SnSe{sub 2} phase, which is responsible for the higher optical band gap and lower electrical resistivity, depending on the specific region of the film. - Highlights: • Single elementary target sputtering of Cu{sub 2}ZnSnSe{sub 4} thin films for solar cells. • Deposition rate and elemental distribution are different at central and edge regions. • Low RF power is promising in generating single phase with less spatial variation. • High RF power induces a secondary SnSe{sub 2} phase and a higher band gap. • Carrier concentration is smaller at centers than at near-edges of the films.

  20. Simulation of a thin film solar cell based on copper zinc tin sulfo-selenide Cu2ZnSn(S,Se)4

    Science.gov (United States)

    Benmir, Abdelkader; Aida, Mohamed Salah

    2016-03-01

    The aim of this work is to do a simulation of a Cu2ZnSn(S,Se)4 thin film photovoltaic solar cell to link the characteristics of this cell with the materials parameters in order to improve its performances. It is found that, the cell performances are almost invariables while the thickness of the buffer layer is equal to or less than the space charge zone width of its side. But, as soon as it exceeds this width, a slight reduction in these performances is observed. However, the absorber layer thickness must have a value at least equal to the space charge region width of its side and at most equal to the sum of this space charge region width and the electrons diffusion length. An optimum value of the absorber band gap around 1.5 eV is obtained. This value is the compromise between the decreases of the short circuit current density and the increases of the open circuit voltage with the increases of the gap. This leads to a maximum cell efficiency of 12.1%.

  1. Luminescence and bio-imaging response of thio-glycolic acid (TGA) and sodium dodecyl sulfate (SDS)-coated fluorescent cadmium selenide quantum dots

    Energy Technology Data Exchange (ETDEWEB)

    Sarma, Runjun; Mohanta, Dambarudhar, E-mail: best@tezu.ernet.in

    2015-05-15

    We demonstrate the usefulness of surfactant coated CdSe quantum dots in bio-imaging applications after evaluating their steady state and time resolved emission responses. The surfactant coated QDs, with the respective sizes of ~14 nm and 10 nm are synthesized considering two different types of coating agents, namely, thio-glycolic acid (TGA) and sodium dodecyl sulfate (SDS). The steady state luminescence response is characterized by both near band edge (NBE) and defect-related emissions, but with a strong dependency on the nature of surfactant coating. Time resolved photoluminescence (TR-PL) studies have revealed bi-exponential characteristics with CdSe–TGA QDs exhibiting longer life time decay parameters than those of CdSe–SDS QDs. To be specific, the fast (τ{sub 1}) and the slow (τ{sub 2}) components are characterized by ~10 and 30 times larger values in the former than the latter case. In the FT-IR spectra, several stretching and bending vibrations are observed to be adequately influenced by the nature of surfactant coating. The availability of plentiful Na{sup +} counter ions around SDS coated QDs, as evident from the FT-IR spectroscopy studies, can also be responsible for obtaining reduced size of the QDs. In contrast, Raman active modes are apparently distinguishable in TGA coated QDs, with LO and TO mode positions significantly blue-shifted from the bulk values. While attributing to the intense defect mediated emission of TGA coated QDs, the effect of TGA coating presented a stronger fluorescence imaging capability over the SDS coated ones. A detailed assessment of fluorescent counts, as a basis of bio-imaging response, is being discussed on a comparative basis. - Highlights: • Fluorescent CdSe quantum dots are synthesized with two different kinds of surfactant coatings. • Time resolved photoluminescence (TR-PL) studies have revealed bi-exponential decay characteristics. • Both slow and fast decay parameters are found to be longer in CdSe QDs with TGA coating. • Strong bio-imaging capability is realized for TGA-coated QDs over SDS coated ones.

  2. The Magic-Size Nanocluster (CdSe)34 as a Low-Temperature Nucleant for Cadmium Selenide Nanocrystals; Room-Temperature Growth of Crystalline Quantum Platelets

    OpenAIRE

    Wang, Yuanyuan; Zhang, Ying; Wang, Fudong; Giblin, Daryl E.; Hoy, Jessica; Rohrs, Henry W.; Loomis, Richard A.; Buhro, William E.

    2014-01-01

    Reaction of Cd(OAc)2·2H2O and selenourea in primary-amine/secondary-amine cosolvent mixtures affords crystalline CdSe quantum platelets at room temperature. Their crystallinity is established by X-ray diffraction analysis (XRD), high-resolution transmission electron microscopy (TEM), and their sharp extinction and photoluminescence spectra. Reaction monitoring establishes the magic-size nanocluster (CdSe)34 to be a key intermediate in the growth process, which converts to CdSe quantum platele...

  3. Fabrication and characteristics of CH3NH3PbI3 perovskite solar cells with molybdenum-selenide hole-transport layer

    Science.gov (United States)

    Chen, Lung-Chien; Tseng, Zong-Lieng; Chen, Cheng-Chiang; Hsiung Chang, Sheng; Ho, Cheng-Han

    2016-12-01

    We present a solar cell with an FTO/MoSe2/perovskite/C60/bathocuproine (BCP)/silver structure. The hole-transport material (HTM), active photovoltaic layer, electron-transport layer, and electron-buffer layer were made of MoSe2, perovskite, C60, and BCP, respectively. The domain sizes of the CH3NH3PbI3 (MAPbI3) perovskite films that were deposited on the MoSe2 HTM films following annealing at 500, 600, and 700 °C were determined to be 23, 25, and 27 nm, respectively, revealing that the domain size of the MAPbI3 perovskite film increased with the annealing temperature of the MoSe2 HTM film under it. Therefore, the crystallinities of the perovskite layers were improved by increasing the annealing temperatures of the HTM layers. Following optimization, the maximum power-conversion efficiency was 8.23%.

  4. Thin-film semiconductor rectifier has improved properties

    Science.gov (United States)

    1966-01-01

    Cadmium selenide-zinc selenide film is used as a thin film semiconductor rectifier. The film is vapor-deposited in a controlled concentration gradient into a glass substrate to form the required junctions between vapor-deposited gold electrodes.

  5. Interaction and transport of actinides in natural clay rock with consideration of humic substances and clay organics. Characterization and quantification of the influence of clay organics on the interaction and diffusion of uranium and americium in the clay. Joint project

    Energy Technology Data Exchange (ETDEWEB)

    Bernhard, Gert [Helmholtz-Zentrum Dresden-Rossendorf e.V. (Germany). Inst. of Radiochemistry; Schmeide, Katja; Joseph, Claudia; Sachs, Susanne; Steudtner, Robin; Raditzky, Bianca; Guenther, Alix

    2011-07-01

    The objective of this project was the study of basic interaction processes in the systems actinide - clay organics - aquifer and actinide - natural clay - clay organics - aquifer. Thus, complexation, redox, sorption and diffusion studies were performed. To evaluate the influence of nitrogen, phosphorus and sulfur containing functional groups of humic acid (HA) on the complexation of actinides in comparison to carboxylic groups, the Am(III) and U(VI) complexation by model ligands was studied by UV-Vis spectroscopy and TRLFS. The results show that Am(III) is mainly coordinated via carboxylic groups, however, probably stabilized by nitrogen groups. The U(VI) complexation is dominated by carboxylic groups, whereas nitrogen and sulfur containing groups play a minor role. Phosphorus containing groups may contribute to the U(VI) complexation by HA, however, due to their low concentration in HA they play only a subordinate role compared to carboxylic groups. Applying synthetic HA with varying sulfur contents (0 to 6.9 wt.%), the role of sulfur functionalities of HA for the U(VI) complexation and Np(V) reduction was studied. The results have shown that sulfur functionalities can be involved in U(VI) humate complexation and act as redox-active sites in HA for the Np(V) reduction. However, due to the low content of sulfur in natural HA, its influence is less pronounced. In the presence of carbonate, the U(VI) complexation by HA was studied in the alkaline pH range by means of cryo-TRLFS (-120 C) and ATR FT-IR spectroscopy. The formation of the ternary UO{sub 2}(CO{sub 3}){sub 2}HA(II){sup 4-} complex was detected. The complex formation constant was determined with log {beta}{sub 0.1} M = 24.57 {+-} 0.17. For aqueous U(VI) citrate and oxalate species, luminescence emission properties were determined by cryo-TRLFS and used to determine stability constants. The existing data base could be validated. The U(VI) complexation by lactate, studied in the temperature range 7 to 65 C, was found to be endothermic and entropy-driven. In contrast, the complex stability constants determined for U(VI) humate complexation at 20 and 40 C are comparable, however, decrease at 60 C. For aqueous U(IV) citrate, succinate, mandelate and glycolate species stability constants were determined. These ligands, especially citrate, increase solubility and mobility of U(IV) in solution due to complexation. The U(VI) sorption onto crushed Opalinus Clay (OPA, Mont Terri, Switzerland) was studied in the absence and presence of HA or low molecular weight organic acids, in dependence on temperature and CO2 presence using OPA pore water as background electrolyte. Distribution coefficients (K{sub d}) were determined for the sorption of U(VI) and HA onto OPA with (0.0222 {+-} 0.0004) m{sup 3}/kg and (0.129 {+-} 0.006) m{sup 3}/kg, respectively. The U(VI) sorption is not influenced by HA ({<=}50 mg/L), however, decreased by low molecular weight organic acids ({>=} 1 x 10{sup -5} M), especially by citrate and tartrate. With increasing temperature, the U(VI) sorption increases both in the absence and in the presence of clay organics. The U(VI) diffusion in compacted OPA is not influenced by HA at 25 and 60 C. Predictions of the U(VI) diffusion show that an increase of the temperature to 60 C does not accelerate the migration of U(VI). With regard to uranium-containing waste, it is concluded that OPA is suitable as host rock for a future nuclear waste repository since OPA has a good retardation potential for U(VI). (orig.)

  6. Monitored Natural Attenuation of Inorganic Contaminants in Ground Water Volume 3 Assessment for Radionuclides IncludingTritium, Radon, Strontium, Technetium, Uranium, Iodine, Radium, Thorium, Cesium, and Plutonium-Americium

    Science.gov (United States)

    The current document represents the third volume of a set of three volumes that address the technical basis and requirements for assessing the potential applicability of MNA as part of a ground-water remedy for plumes with nonradionuclide and/or radionuclide inorganic contamina...

  7. Study of plutonium and americium contamination in agricultural area, radiological impact caused by consumption of vegetables of this area; Estudio de la contaminacion de plutonio y americio en un area agricola, impacto radiologico ocasionado por consumo de vegetales contaminados

    Energy Technology Data Exchange (ETDEWEB)

    Espinosa, Assuncion; Aragon, Antonio; Cruz, Berta de la; Gutierrez, Jose [Centro de Investigaciones Energeticas Medioambientales y Tecnologicas, Madrid (Spain). Dept. de Impacto Ambiental de la Energia

    2001-07-01

    The transuranide concentration has been studied for 30 years in vegetable production, crops in wide extensions and in private-owned farms, all of them situated within the Pu-contaminated area of Palomares due to an air accident in 1966. Based on these studies, a preliminary estimation of the radiological risk caused by the consumption of these products by the inhabitants was possible. The results show that most of the fruits present a surface contamination, which disappears or is significantly reduced when they are washed. The contamination present in edible parts of the vegetables, as well as the contamination of other products included in the diet, has facilitated the estimation of the effective dose for ingestion and the committed effective dose for 50 years for the inhabitants. The main conclusions are: those plants, whose cultivation period is less than a year, present a low level of contamination; the green parts of the plants have a higher contamination than the fruits; the Pu soil to plant transfer factor is very low. In general, those plants that have remained in the contaminated land for several years present a high contamination level; the ingestion of products from Palomares does not represent an important risk for the population, even in the case that the products were totally consumed by a critical group.( author)

  8. Supported liquid inorganic membranes for nuclear waste separation

    Energy Technology Data Exchange (ETDEWEB)

    Bhave, Ramesh R; DeBusk, Melanie M; DelCul, Guillermo D; Delmau, Laetitia H; Narula, Chaitanya K

    2015-04-07

    A system and method for the extraction of americium from radioactive waste solutions. The method includes the transfer of highly oxidized americium from an acidic aqueous feed solution through an immobilized liquid membrane to an organic receiving solvent, for example tributyl phosphate. The immobilized liquid membrane includes porous support and separating layers loaded with tributyl phosphate. The extracted solution is subsequently stripped of americium and recycled at the immobilized liquid membrane as neat tributyl phosphate for the continuous extraction of americium. The sequestered americium can be used as a nuclear fuel, a nuclear fuel component or a radiation source, and the remaining constituent elements in the aqueous feed solution can be stored in glassified waste forms substantially free of americium.

  9. A nickel iron diselenide-derived efficient oxygen-evolution catalyst

    Science.gov (United States)

    Xu, Xiang; Song, Fang; Hu, Xile

    2016-08-01

    Efficient oxygen-evolution reaction catalysts are required for the cost-effective generation of solar fuels. Metal selenides have been reported as promising oxygen-evolution catalysts; however, their active forms are yet to be elucidated. Here we show that a representative selenide catalyst, nickel selenide, is entirely converted into nickel hydroxide under oxygen-evolution conditions. This result indicates that metal selenides are unstable during oxygen evolution, and the in situ generated metal oxides are responsible for their activity. This knowledge inspired us to synthesize nanostructured nickel iron diselenide, a hitherto unknown metal selenide, and to use it as a templating precursor to a highly active nickel iron oxide catalyst. This selenide-derived oxide catalyses oxygen evolution with an overpotential of only 195 mV for 10 mA cm-2. Our work underscores the importance of identifying the active species of oxygen-evolution catalysts, and demonstrates how such knowledge can be applied to develop better catalysts.

  10. Industrial research for transmutation scenarios

    Science.gov (United States)

    Camarcat, Noel; Garzenne, Claude; Le Mer, Joël; Leroyer, Hadrien; Desroches, Estelle; Delbecq, Jean-Michel

    2011-04-01

    This article presents the results of research scenarios for americium transmutation in a 22nd century French nuclear fleet, using sodium fast breeder reactors. We benchmark the americium transmutation benefits and drawbacks with a reference case consisting of a hypothetical 60 GWe fleet of pure plutonium breeders. The fluxes in the various parts of the cycle (reactors, fabrication plants, reprocessing plants and underground disposals) are calculated using EDF's suite of codes, comparable in capabilities to those of other research facilities. We study underground thermal heat load reduction due to americium partitioning and repository area minimization. We endeavor to estimate the increased technical complexity of surface facilities to handle the americium fluxes in special fuel fabrication plants, americium fast burners, special reprocessing shops, handling equipments and transport casks between those facilities.

  11. Chemistry research and development progress report, May-October, 1978

    Energy Technology Data Exchange (ETDEWEB)

    Miner, F. J.

    1979-08-30

    Work in progress includes: calorimetry and thermodynamics of nuclear materials; americium recovery and purification; optimization of the cation exchange process for recovering americium and plutonium from molten salt extraction residues, photochemical separations of actinides; advanced ion exchange materials and techniques; secondary actinide recovery; removal of plutonium from lathe coolant oil; evaluation of tributyl phosphate-impregnated sorbent for plutonium-uranium separations; plutonium recovery in advance size reduction facility; plutonium peroxide precipitation; decontamination of Rocky Flats soil; soil decontamination at other Department of Energy sites; recovery of actinides from combustible wastes; induction-heated, tilt-pour furnace; vacuum melting; determination of plutonium and americium in salts and alloys by calorimetry; plutonium peroxide precipitation process; silica removal study; a comparative study of annular and Raschig ring-filled tanks; recovery of plutonium and americium from a salt cleanup alloy; and process development for recovery of americium from vacuum melt furnace crucibles.

  12. Thermophysical Properties of Matter - the TPRC Data Series. Volume 14. Master Index - To Materials and Properties

    Science.gov (United States)

    1979-01-01

    2 Cuamg 12 S23 Copper oxides: CuO - 5 s - 8247 - 8 249 - - CU 2 0 2 147 5 76 8 243 8 49C.=O 5 Copper selenide , CuOSe2 1 - - I - Copper ... selenide -copper antimony selenide, mixture 1 1401 Copper allcides: Cu.Si - 13 1211 Cu iSI- - 13 1212 Copper sulfide&: K 6 - - - _- 6 CuaS 2- - - Copper

  13. Thin film solar cells. (Latest citations from the NTIS bibliographic database). Published Search

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-11-01

    The bibliography contains citations concerning research and development of high-efficiency and low-cost thin film solar cells. References discuss the design and fabrication of silicon, gallium arsenide, copper selenide, indium selenide, cadmium telluride, and copper indium selenide solar cells. Applications in space and utilities are examined. Government projects and foreign technology are also reviewed. (Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  14. 硒氢化钠作用下二硫代氨基甲酸酯键的断裂%Bond breaking in dithiocarbamates promoted by sodium hydrogen selenide

    Institute of Scientific and Technical Information of China (English)

    赵华绒; 俞庆森

    2002-01-01

    等摩尔的硒氢化钠与二硫代氨基甲酸酯反应,以较高的产率生成相应的胺以及硫酚(醇).反应条件温和,操作简便,且副反应少.根据实验所得结果,提出了可能的反应机理.

  15. Mesostructured Metal Germanium Sulfide and Selenide Materials Based on the Tetrahedral [Ge 4S 10] 4- and [Ge 4Se 10] 4- Units: Surfactant Templated Three-Dimensional Disordered Frameworks Perforated with Worm Holes

    Science.gov (United States)

    Wachhold, Michael; Kasthuri Rangan, K.; Lei, Ming; Thorpe, M. F.; Billinge, Simon J. L.; Petkov, Valeri; Heising, Joy; Kanatzidis, Mercouri G.

    2000-06-01

    The polymerization of [Ge4S10]4- and [Ge4Se10]4- unit clusters with the divalent metal ions Zn2+, Cd2+, Hg2+, Ni2+, and Co2+ in the presence of various surfactant cations leads to novel mesostructured phases. The surfactants are the quaternary ammonium salts C12H25NMe3Br, C14H29NMe3Br, C16H33NMe3Br, and C18H37NMe3Br, which play the role of templates, helping to assemble a three-dimensional mesostructured metal-germanium chalcogenide framework. These materials are stoichiometric in nature and have the formula of (R-NMe3)2[MGe4Q10] (Q=S, Se). The local atomic structure was probed by X-ray diffuse scattering and pair distribution function analysis methods and indicates that the adamantane clusters stay intact while the linking metal atoms possess a tetrahedral coordination environment. A model can be derived, from the comparison of measured and simulated X-ray powder diffraction patterns, describing the structure as an amorphous three-dimensional framework consisting of adamantane [Ge4Q10]4- units that are bridged by tetrahedral coordinated M2+ cations. The network structures used in the simulations were derived from corresponding disordered structures developed for amorphous silicon. The frameworks in (R-NMe3)2[MGe4Q10] are perforated with worm hole-like tunnels, occupied by the surfactant cations, which show no long-range order. This motif is supported by transmission electron microscopy images of these materials. The pore sizes of these channels were estimated to lie in the range of 20-30 Å, depending on the appointed surfactant cation length. The framework wall thickness of ca. 10 Å is thereby independent from the surfactant molecules used. Up to 80% of the surfactant molecules can be removed by thermal degradation under vacuum without loss of mesostructural integrity. Physical, chemical, and spectroscopic properties of these materials are discussed.

  16. Improving the efficiency of copper indium gallium (Di-)selenide (CIGS) solar cells through integration of a moth-eye textured resist with a refractive index similar to aluminum doped zinc oxide

    NARCIS (Netherlands)

    Burghoorn, M.M.A.; Kniknie, B.J.; Deelen, J. van; Xu, M.; Vroon, Z.A.E.P.; Ee, R.J. van; Belt, R. van de; Buskens, P.J.P.

    2014-01-01

    Textured transparent conductors are widely used in thin-film silicon solar cells. They lower the reflectivity at interfaces between different layers in the cell and/or cause an increase in the path length of photons in the Si absorber layer, which both result in an increase in the number of absorbed

  17. Improving the efficiency of copper indium gallium (Di-)selenide (CIGS) solar cells through integration of a moth-eye textured resist with a refractive index similar to aluminum doped zinc oxide

    OpenAIRE

    M. Burghoorn; B. Kniknie; Deelen, J; Xu., M; Z. Vroon; van Ee, R.; van de Belt, R.; Buskens, P

    2014-01-01

    Textured transparent conductors are widely used in thin-film silicon solar cells. They lower the reflectivity at interfaces between different layers in the cell and/or cause an increase in the path length of photons in the Si absorber layer, which both result in an increase in the number of absorbed photons and, consequently, an increase in short-circuit current density (Jsc) and cell efficiency. Through optical simulations, we recently obtained strong indications that texturing of the transp...

  18. 真空蒸发法制备ZnSe薄膜的X射线光电子能谱研究%Study on XPS of Zinc Selenide Thin Films by Vacuum Evaporation

    Institute of Scientific and Technical Information of China (English)

    余晓艳; 马鸿文

    2007-01-01

    本文用真空蒸发法制备了CIS太阳能电池中做缓冲材料的ZnSe薄膜,利用X射线光电子能谱(XPS)对制备薄膜的表面化学状态及沉积质量进行了研究,并用氩离子溅射进行剥蚀,逐层分析薄膜的化合态随深度的变化关系.XPS分析表明,ZnSe薄膜含有Zn、Se、O、C等元素,其中O、C为样品置于空气中所致,含量随剥蚀深度的加大而逐渐降低.Zn的光电子峰为Zn2p1/2和Zn2p3/2,Zn2p3/2的电子结合能为1021.90eV,对应着Zn2+的化合态,表明薄膜中zn以形式电荷为Zn2+的化合态形式存在;Se的光电子峰为Se3d,其电子结合能为54.30eV,对应着Se2-的化合态,表明薄膜中Se以形式电荷Se2-的化合态形式存在.分别经过1min、3min、7min、11min的剥蚀后,Zn和Se的光电子峰几乎没有改变,表明沉积的ZnSe薄膜表面和内部化学状态稳定一致.

  19. Inhibiting Effects of Eucheuma Polysaccharide Selenide on the Proliferation of Carcinoma Cell Line HEp-2%硒化麒麟菜多糖抑制人喉癌细胞株Hep-2增殖的作用

    Institute of Scientific and Technical Information of China (English)

    白雪; 林晨; 江振友; 袁桂秀; 沈伟哉; 李扬秋; 唐渝

    2007-01-01

    目的 通过比较研究海藻麒麟菜多糖粗提物、无机硒化合物-亚硒酸钠(Na2SeO3)及其共价化合物-硒化麒麟菜多糖对人喉癌细胞株Hep-2的作用,探索新的具有抗肿瘤活性的有机硒化合物.方法 应用不同剂量的样品作用于Hep-2细胞株后,用MTT比色分析法计算肿瘤抑制率.结果 硒化多糖对Hep-2细胞的抑制率高于相同多糖浓度的麒麟菜多糖和相同硒浓度的亚硒酸钠(P<0.05).硒化多糖的抑制率可高达71.53%,其多糖IC50与硒IC50分别为1805μg/ml和7.0μmol/L,分别低于麒麟菜多糖的多糖IC50(3034μg/ml)和亚硒酸钠的硒IC50(9.0μmol/L).结论 硒化麒麟菜多糖具有抗Hep-2细胞增殖的活性,其抑制作用明显优于亚硒酸钠及天然麒麟菜多糖的抗肿瘤活性.

  20. Preparation and Characteristics of Reduced Graphene Oxide-zinc Selenide Nano Optoelectronic Materials%氧化石墨烯/硒化锌纳米光电材料的制备及其蓝光发射特性

    Institute of Scientific and Technical Information of China (English)

    董浩; 赵晓晖; 曲良东; 迟学芬

    2014-01-01

    采用一种简单有效的原位水热合成方法,使用石墨烯氧化物( GO)作为反应物和晶体生长基底成功制备出了还原氧化石墨烯/硒化锌( r-GO/ZnSe)纳米复合材料。采用X射线粉末衍射( XRD)、透射电子显微镜( TEM)、高分辨透射电镜( HRTEM)以及红外-可见光谱( FT-IR)等方法对r-GO/ZnSe纳米复合材料进行了检测。结果表明,平均粒径在30 nm的立方闪锌矿晶体结构的ZnSe粒子均匀分散在氧化石墨烯片层上,构成纳米复合结构。UV-Vis光谱显示,纳米复合材料的光学吸收的起始波长在445 nm附近。 PL光谱显示,纳米复合材料在470 nm附近存在一个很强的发射峰。这种石墨烯基纳米复合材料在白光二极管领域中有重要的应用价值。%Reduced graphene oxide-ZnSe ( r-GO/ZnSe ) nanocomposites were successfully synthe-sized by an easy hydrothermal method. This process used the graphene oxide nanosheets as disper-sant and two-dimensional growth template for ZnSe, resulting in the in situ formation of ZnSe nanop-articles on graphene oxide nanosheets and subsequent reduction of graphene oxide to r-GO. The samples were characterized by XRD, TEM, and FT-IR. The results show that the cubic ZnSe nano-particles with the mean size of 30 nm distribute on r-GO sheets to form compact composites. UV-Vis absorption spectra indicate that the absorption edge of r-GO/ZnSe is at about 445 nm. PL spectra show a strong emission peak at 470 nm excited by 430 nm. The obtained r-GO/ZnSe nanocomposites may play important role in white LED field.

  1. The behaviour of Eu, Pu, Am radionuclide at burning radioactive graphite in an oxygen atmosphere. Computer experiments

    Directory of Open Access Journals (Sweden)

    Kolbin T.S.

    2015-01-01

    Full Text Available Be means of the method of computer thermodynamic simulation we studied the behaviour of the europium, plutonium and americium from the combustion of radioactive graphite in oxygen. Europe is in the form of condensed EuOCl, Eu2O3 and vapour EuO. Pluto is in the form of condensed vapour PuO2 and PuO2. Americium is a condensed AmO2, Am2O3 and vapour Am. The basic reactions occurring compounds with europium, plutonium and americium. Equilibrium constants of the reactions have been determined.

  2. Nanotechnology-Enabled Optical Molecular Imaging of Breast Cancer

    Science.gov (United States)

    2012-07-01

    nanocrystals are copper selenide (Cu2Se) and copper sulfide (CuS). Interestingly, the NIR absorption of these particles is different from gold and other...Rasch, M. Panthani, B. Koo, J. Tunnell, and B. Korgel. Copper selenide nanocrystals for photothermal therapy. Nano Lett. 11(6):2560–2566, 2011. 28Hirsch

  3. Review of selenium thermodynamic data

    Science.gov (United States)

    Cowan, C. E.

    1988-02-01

    This report assesses the accuracy and completeness of available thermodynamic data on selenium. A review of experimental methods from published literature on selenium thermodynamic data focused on chemical reactions responsible for the formation of both aqueous complexes and solid phases of selenate, selenite, and selenide. The reviewer selected best data values, based on the methods used for estimating thermodynamic data. After inclusion of these values into the MINTEQ model, a validation study evaluated model performance for selenite and selenide solid phases. Lack of selenate data precluded model validation for this compound. The review furnished data on 22 aqueous complexes of selenite, 15 of selenide, and 17 of selenate, as well as 21 solid phases of selenite, 20 of selenide and 8 of selenate. These data proved inadequate to represent the formation of species in the solid phase. The validation study gave inconclusive predictions of selenite and selenide solubility and could not be used to assess the accuracy or completeness of the thermodynamic data.

  4. Rubbia proposes a speedier voyage to Mars and back

    CERN Multimedia

    Abbott, A

    1999-01-01

    Carlo Rubbia has designed a propulsion engine that uses fission fragments of americium to directly heat a propulsion gas. He estimates it would allow a manned trip to Mars and back in around a year (8 paragraphs).

  5. Filgrastim (Neupogen)

    Science.gov (United States)

    ... CRC) Simulation Tools Isotopes Americium-241 (Am-241) Cesium-137 (Cs-137) Radioisotope Brief Toxicology FAQs Cobalt- ... a drug that has been used successfully for cancer patients to stimulate the growth of the white ...

  6. Literatuuronderzoek plutoniumanalyses

    NARCIS (Netherlands)

    Glastra P; Kwakman PJM; LSO

    1997-01-01

    Dit rapport beschrijft de laatste ontwikkelingen in de radiochemische bepaling van plutonium in monstermatrices zoals luchtstoffilters, regenwater, gras en bodem. De radiochemische scheiding van plutonium van storende alfastralers, zoals americium en curium, is door de recente ontwikkeling van spec

  7. Study of the properties of the Am-O system in view of the transmutation of Am 241 in fast reactors; Etude des proprietes du systeme Am-O en vue de la transmutation de l`americium 241 en reacteur a neutrons rapides

    Energy Technology Data Exchange (ETDEWEB)

    Casalta, S.

    1996-04-01

    To reduce the long term toxicity of Am 241 it was considered to transmute this isotope in fast reactor. The first part of this thesis is an introduction at this problem. In the second part we give the experimental techniques used for the realisation of an AmO{sub 2}-MgO target (powder metallurgy under inert, oxidizing or reducing atmosphere). The properties of the Am-O system has been analyzed by X diffraction, thermodynamic and ceramography, in the Am{sub 2}O{sub 3}-AmO{sub 2} field. In the third part we study the external exposure risk created by the manufacturing of this target and in the last part the behavior of this target in a fast reactor. 66 refs., 28 figs., 25 tabs., 1 append.

  8. Methodology for the Inventory and Assessment of Americium Contamination Level in 1987 in an Area of Palomares Contaminated with Plutonium Weapon Grade; Estimacion del Contenido de Americio Existente en el Ano 1987 en una Zona de Palomares Contaminada en 1966 por Material de Plutonio Grado Bomba

    Energy Technology Data Exchange (ETDEWEB)

    Espinosa, A.; Aragon, A.; Cruz de la, B.

    2001-07-01

    This paper presents a methodology applied for the assessment of the ''241 Am coming from the decay of ''241 Pu isotope content in a contaminated area of Palomares, where the clean-up work done in 1966, given the negligible agricultural importance of such area at the time and its geographical characteristics, was not of the same magnitude as for the rest of the region. (Author) 4 refs.

  9. AM(VI) partitioning studies. FY14 final report

    Energy Technology Data Exchange (ETDEWEB)

    Mincher, Bruce J. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2014-10-01

    The use of higher oxidation states of americium in partitioning from the lanthanides is under continued investigation by the sigma team. This is based on the hypothesis that Am(VI) can be produced and remain stable in irradiated first cycle raffinate solution long enough to perform solvent extraction for separations. The stability of Am(VI) to autoreduction was measured using millimolar americium concentrations in a 1-cm cell with a Cary 6000 UV/Vis spectrophotometer for data acquisition. At millimolar americium concentrations, Am(VI) is stable enough against its own autoreduction for separations purposes. A second major accomplishment during FY14 was the hot test. Americium oxidation and extraction was performed using a centrifugal contactor-based test bed consisting of an extraction stage and two stripping stages. Sixty-three percent americium extraction was obtained in one extraction stage, in agreement with batch contacts. Promising electrochemical oxidation results have also been obtained, using terpyridine ligand derivatized electrodes for binding of Am(III). Approximately 50 % of the Am(III) was oxidized to Am(V) over the course of 1 hour. It is believed that this is the first demonstration of the electrolytic oxidation of americium in a non-complexing solution. Finally, an initial investigation of Am(VI) extraction using diethylhexylbutyramide (DEHBA) was performed.

  10. NREL preprints for the 23rd IEEE Photovoltaic Specialists Conference

    Energy Technology Data Exchange (ETDEWEB)

    Fitzgerald, M. [ed.

    1993-05-01

    Topics covered include various aspects of solar cell fabrication and performance. Aluminium-gallium arsenides, cadmium telluride, amorphous silicon, and copper-indium-gallium selenides are all characterized in their applicability in solar cells.

  11. Zn/ ZrCl4 System Induced Reductive Cleavage of Se-Se Bond in Diaryl Diselenides: A Novel Method for the Systhesis of Selenoesters

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The Se-Se bond in diaryl diselenides was reduced by Zn/ZrCl4 system to produce selenide anions, which react with acyl chlorides or acid anhydrides to afford selenoesters in THF under mild and neutral conditions.

  12. Langmuir-Blodgett films of alkane chalcogenice (S, Se, Te) stabilized gold nanoparticles

    DEFF Research Database (Denmark)

    Brust, M.; Stuhr-Hansen, N.; Norgaard, K.

    2001-01-01

    Gold nanoparticles stabilized by alkanethiolates, alkaneselenides, and alkanetellurides have been prepared by analogous methods. Chloroform solutions of thiolate and selenide stabilized particles were spread and evaporated on the water/air interface where the particles formed well-defined Langmuir...

  13. Effect of Cu content and temperature on the properties of Cu2ZnSnSe4 solar cells

    Directory of Open Access Journals (Sweden)

    Sahayaraj Sylvester

    2016-01-01

    Full Text Available The complexity involved in obtaining pure Kesterite Cu2ZnSnSe4 (CZTSe thin film primarily arises due to its narrow region of stability, leading to the presence of unavoidable binary selenides of the constituent metals. This study offers an insight on the formation of Cu selenides when the amount of Cu is varied in the precursor from Cu poor to Cu rich. The amount of Cu selenides was found to decrease when the composition of CZTSe absorber approached Cu rich conditions but functional devices were not obtained. Detailed characterizations also showed that the Cu and Sn binary phases were present at the backside interface of CZTSe solar cells. However with an increase in the selenization temperature it was found that the amount of Cu selenides and other secondary phases could be drastically minimized or even eliminated leading to high efficiency devices.

  14. Integration of Solar Cells on Top of CMOS Chips - Part II: CIGS Solar Cells

    NARCIS (Netherlands)

    Lu, Jiwu; Liu, Wei; Kovalgin, Alexey Y.; Sun, Yun; Schmitz, Jurriaan

    2011-01-01

    We present the monolithic integration of deepsubmicrometer complementary metal–oxide–semiconductor (CMOS) microchips with copper indium gallium (di)selenide (CIGS) solar cells. Solar cells are manufactured directly on unpackaged CMOS chips. The microchips maintain comparable electronic performance,

  15. Nucleation, propagation, electronic levels and elimination of misfit dislocations in III-V semiconductor interfaces. Final report, September 1, 1986--August 31, 1993

    Energy Technology Data Exchange (ETDEWEB)

    Ast, D.G.; Watson, G.P.; Matragrano, M.

    1995-03-01

    Misfit dislocations in gallium arsenides, indium arsenides, and zinc selenides are discussed. The growth of strained epitaxial layers, isolation and nucleation, thermal stability, and electronic and structural characteristics of misfit dislocations are described.

  16. Effect of Cu content and temperature on the properties of Cu2ZnSnSe4 solar cells

    Science.gov (United States)

    Sahayaraj, Sylvester; Brammertz, Guy; Buffière, Marie; Meuris, Marc; Vleugels, Jef; Poortmans, Jef

    2016-09-01

    The complexity involved in obtaining pure Kesterite Cu2ZnSnSe4 (CZTSe) thin film primarily arises due to its narrow region of stability, leading to the presence of unavoidable binary selenides of the constituent metals. This study offers an insight on the formation of Cu selenides when the amount of Cu is varied in the precursor from Cu poor to Cu rich. The amount of Cu selenides was found to decrease when the composition of CZTSe absorber approached Cu rich conditions but functional devices were not obtained. Detailed characterizations also showed that the Cu and Sn binary phases were present at the backside interface of CZTSe solar cells. However with an increase in the selenization temperature it was found that the amount of Cu selenides and other secondary phases could be drastically minimized or even eliminated leading to high efficiency devices.

  17. Silica glasses with nanoparticles of copper compounds: spectroscopy properties and laser passive shutter application

    Science.gov (United States)

    Yumashev, Konstantin V.; Prokoshin, Pavel V.; Zolotovskaya, Svetlana A.; Gurin, Valerij S.; Alexeenko, Alexander A.

    2003-11-01

    Sol-gel glasses containing copper selenide nanoparticles and having absorption band at 1.1?2.2 ?m can be used as saturable absorber passive shutter for Q-switching and mode-locking of the solid-state lasers operating in the wavelength range of 1.0?1.5 ?m. The bleaching relaxation time of the glasses was measured to be 0.46?1.4 ns in dependence on copper selenide stoichiometry.

  18. Improved Paintball Design and Alternative Payloads

    Science.gov (United States)

    2006-11-01

    wavelengths depending on the size and composition of the quantum dots (Bruchez et al., 1998). Cadmium selenide and lead selenide nanoparticles of 2-9 nm...markers. A Canon EOS Rebel modified with an X-Nite filter that blocks wavelengths below 750 nm was used to capture photographs in the near IR...Obscurant Payloads Carbon black was dispersed fairly well into vegetable oil. However, the carbon black settles out of solution within a few minutes

  19. Progress in Cleaning and Wet Processing for Kesterite Thin Film Solar Cells

    OpenAIRE

    B. Vermang, A. Mule, N. Gampa, S. Sahayaraj, S. Ranjbar, G. Brammertz, M. Meuris, J. Poortmans

    2016-01-01

    Copper indium gallium selenide/sulfide (CIGS) and copper zinc tin selenide/sulfide (CZTS) are two thin film photovoltaic materials with many similar properties. Therefore, three new processing steps – which are well-known to be beneficial for CIGS solar cell processing – are developed, optimized and implemented in CZTS solar cells. For all these novel processing steps an increase in minority carrier lifetime and cell conversion efficiency is measured, as compared to standard CZTS processing. ...

  20. Growth mechanism of nanowires: binary and ternary chalcogenides

    Science.gov (United States)

    Singh, N. B.; Coriell, S. R.; Su, Ching Hua; Hopkins, R. H.; Arnold, B.; Choa, Fow-Sen; Cullum, Brian

    2016-05-01

    Semiconductor nanowires exhibit very exciting optical and electrical properties including high transparency and a several order of magnitude better photocurrent than thin film and bulk materials. We present here the mechanism of nanowire growth from the melt-liquid-vapor medium. We describe preliminary results of binary and ternary selenide materials in light of recent theories. Experiments were performed with lead selenide and thallium arsenic selenide systems which are multifunctional material and have been used for detectors, acoustooptical, nonlinear and radiation detection applications. We observed that small units of nanocubes and elongated nanoparticles arrange and rearrange at moderate melt undercooling to form the building block of a nanowire. Since we avoided the catalyst, we observed self-nucleation and uncontrolled growth of wires from different places. Growth of lead selenide nanowires was performed by physical vapor transport method and thallium arsenic selenide nanowire by vapor-liquid-solid (VLS) method. In some cases very long wires (>mm) are formed. To achieve this goal experiments were performed to create situation where nanowires grew on the surface of solid thallium arsenic selenide itself.