Hydrothermal Fluid evolution in the Dalli porphyry Cu-Au Deposit: Fluid Inclusion microthermometry studies

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Alireza Zarasvandi

2015-10-01

Full Text Available Introduction A wide variety of world-class porphyry Cu deposits occur in the Urumieh-Dohktar magmatic arc (UDMA of Iran.The arc is composed of calc-alkaline granitoid rocks, and the ore-hosting porphyry intrusions are dominantly granodiorite to quartz-monzonite (Zarasvandi et al., 2015. It is believed that faults played an important role in the emplacement of intrusions and subsequentporphyry-copper type mineralization (Shahabpour, 1999. Three main centers host the porphyry copper mineralization in the UDMA: (1 Ardestan-SarCheshmeh-Kharestan zone, (2 Saveh-Ardestan district; in the central parts of the UDMA, hosting the Dalli porphyry Cu-Au deposit, and (3 Takab-Mianeh-Qharahdagh-Sabalan zone. Mineralized porphyry coppersystems in the UDMA are restricted to Oligocene to Mioceneintrusions and show potassic, sericitic, argillic, propylitic and locally skarn alteration (Zarasvandi et al., 2005; Zarasvandi et al., 2015. In the Dalli porphyry deposit, four hydrothermal alteration zones, includingpotassic, sericitic, propylitic, and argillic types have been described in the two discrete mineralized areas, namely, northern and southern stocks. Hypogenemineralization includes chalcopyrite, pyrite, and magnetite, with minor occurrences of bornite.Supergene activity has produced gossan, oxidized minerals and enrichment zones. The supergene enrichment zone contains chalcocite and covellite with a 10-20 m thickness. Mineralization in the northern stock is mainly composed of pyrite and chalcopyrite. The aim of this study is the investigation and classification of hydrothermal veins and the constraining of physicochemical compositions of ore-forming fluids using systematic investigation of fluid inclusions. Materials and methods Twenty samples were collected from drill holes. Thin and polished sections were prepared from hydrothermal veins of thepotassic, sericitic and propylitic alteration zones. Samples used for fluid inclusion measurements were collected

Iron and chlorine as guides to stratiform Cu-Co-Au deposits, Idaho Cobalt Belt, USA

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Nash, J.T.; Connor, J.J.

1993-01-01

The Cu-Co-Au deposits of the Idaho Cobalt Belt are in lithostratigraphic zones of the Middle Proterozoic Yellowjacket Formation characterized by distinctive chemical and mineralogical compositions including high concentrations of Fe (15- > 30 wt. percent Fe2O3), Cl (0.1-1.10 wt. percent), and magnetite or biotite (> 50 vol. percent). The Cu-Co-Au deposits of the Blackbird mine are stratabound in Fe-silicate facies rocks that are rich in biotite, Fe, and Cl, but stratigraphically equivalent rocks farther than 10 km from ore deposits have similar compositions. A lower lithostratigraphic zone containing magnetite and small Cu-Co-Au deposits extends for more than 40 km. The Fe-rich strata are probably exhalative units related to mafic volcanism and submarine hot springs, but the origin of the high Cl concentrations is less clear. Former chlorine-rich pore fluids are suggested by the presence of supersaline fluid inclusions, by Cl-rich biotite and scapolite (as much as 1.87 percent Cl in Fe-rich biotite), and by high Cl concentrations in rock samples. Chlorine is enriched in specific strata and in zones characterized by soft-sediment deformation, thus probably was introduced during sedimentation or diagenesis. Unlike some metasedimentary rocks containing scapolite and high Cl, the Yellowjacket Formation lacks evidence for evaporitic strata that could have been a source of Cl. More likely, the Cl reflects a submarine brine that carried Fe, K, and base metals. Strata containing anomalous Fe-K-Cl are considered to be a guide to sub-basins favorable for the occurrence of stratiform base-metal deposits. ?? 1993 Springer-Verlag.

Geochronological framework of the early Paleozoic Bainaimiao Cu-Mo-Au deposit, NE China, and its tectonic implications

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Zhou, Zhen-Hua; Mao, Jing-Wen; Ma, Xing-Hua; Che, He-Wei; Ou'yang, He-Gen; Gao, Xu

2017-08-01

The Bainaimiao Cu-Mo-Au deposit of NE China is an important ore deposit in the middle section of the northern margin of the North China Craton. The early Paleozoic Bainaimiao Group is the main ore-hosting rock. The mineralization at the deposit shows features of porphyry alteration and late-stage orogenesis and transformation. Zircon LA-ICP-MS U-Pb age data indicate that the ages of the Third and Fifth formations of the Bainaimiao Group are 492.7 ± 2.9 Ma (MSWD = 0.53) and 488.9 ± 3.1 Ma (MSWD = 0.92), respectively. The age of quartz diorite that intrudes the Bainaimiao Group is 459.3 ± 6.4 Ma (MSWD = 2.20). Molybdenite samples from massive Cu-Mo-bearing ores and quartz veins in the southern ore belt yield a Re-Os isochron age of 438.2 ± 2.7 Ma (MSWD = 0.16), which is consistent with the Re-Os isochron age of molybdenite in the northern ore belt, implying that the two ore belts belong to the same mineralization system. Muscovite from a post-magmatic Cu-Mo-bearing quartz-calcite vein yields an Ar-Ar isochron age of 422.5 ± 3.9 Ma (MSWD = 0.64) with an initial 40Ar/36Ar ratio of 286 ± 21. The well-defined plateau age of the muscovite is 422.4 ± 2.6 Ma (MSWD = 0.05), which represents the time of the post-magmatic orogenic transformation event. Based on our new age data and previous findings, we propose that the Bainaimiao Cu-Mo-Au deposit formed in an active continental margin setting and experienced four stages of ore mineralization: (1) a Late Cambrian-Middle Ordovician volcanic-sedimentary stage; (2) a Late Ordovician porphyry mineralization stage; (3) a Late Silurian regional metamorphism stage; and (4) an orogenic transformation stage. Subhedral and euhedral Paleoproterozoic (2402-1810 Ma) inherited zircons indicate that the Bainaimiao Group has a tectonic affinity with the North China Craton. The Central Asian Orogenic Belt, which is closely related to the complex closure of the Paleo-Asian Ocean, is favorable for prospecting for Paleozoic porphyry Cu

Magma Fertility is the First-Order Factor for the Formation of Porphyry Cu±Au Deposits

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Park, J. W.; Campbell, I. H.; Malaviarachchi, S. P. K.; Cocker, H.; Nakamura, E.; Kay, S. M.

2017-12-01

Magma fertility, the metal abundance in magma, has been considered to be one of the key factors for the formation of porphyry Cu±Au deposits. In this study we provide clear evidence to support the hypothesis that the platinum group element (PGE) can be used to distinguish barren from ore-bearing Cu±Au felsic suites. We determined the PGE contents of three barren volcanic and subvolcanic suites from Argentina and Japan, and compare the results with two porphyry Cu-bearing subvolcanic suites from Chile and two porphyry Cu-Au-bearing suites from Australia. The barren suites are significantly depleted in PGE abundances by the time of fluid exsolution, which is attributed to early sulfide saturation at mid to lower crust depths or assimilation of chalcophile element-poor crustal materials. Barren magma, produced by melting continental crust, may have been initially deficient in chalcophile elements. In contrast, the Cu±Au ore-bearing suites contain at least an order of magnitude higher PGE contents than those of the barren suites by the time of fluid saturation. They are characterized by late sulfide saturation in a shallow magma chamber, which allows the chalcophile elements to concentrate in the fractionating magma from which they are sequestered by ore-forming fluids. We suggest the Pd/MgO and Pd/Pt ratios of igneous rocks can be used as magma fertility indicators, and to distinguish between barren, porphyry Cu and porphyry Cu-Au magmatic systems.

Geochronology and petrogenesis of the Qibaoshan Cu-polymetallic deposit, northeastern Hunan Province: Implications for the metal source and metallogenic evolution of the intracontinental Qinhang Cu-polymetallic belt, South China

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Yuan, Shunda; Mao, Jingwen; Zhao, Panlao; Yuan, Yabin

2018-03-01

The recently recognized Qinhang metallogenic belt (QHMB) is an economically important intracontinental Mesozoic porphyry-skarn Cu-polymetallic metallogenic belt in South China. However, the origin of the ore-bearing magma and the major factors controlling the different metal assemblages in the QHMB are still unclear. The Qibaoshan deposit is a large Cu-Au-Pb-Zn-Ag-Fe deposit located at the juncture between the northern and central parts of the QHMB. In this study, new zircon U-Pb ages, Hf-O isotopic data, molybdenite Re-Os ages, and whole-rock geochemical data are combined to constrain the timing of the mineralization and the origin and petrogenesis of the ore-bearing porphyry in the Qibaoshan deposit. The ages obtained from both zircon U-Pb and molybdenite Re-Os dating fall in the Late Jurassic (between 152.7 and 148.3 Ma), revealing that this deposit is significantly younger than previously estimated (227-184 Ma). The Qibaoshan ore-bearing quartz porphyry shows variable negative zircon εHf(t) values (-14.8 to -5.5), high δ18O values (8.4 to 10.8‰), and high Mg# values (69.1 to 73.0), indicating that it formed via the partial melting of ancient crust triggered by the injection of mantle-derived magma. Zircon Hf-O isotopic modeling of the mixing of two extreme endmembers indicates that the magmatic source comprised 70-80% reworked ancient crustal components and 20-30% depleted mantle components. Based on comparisons with other ore-bearing porphyries in the QHMB, a magmatic source dominated by crust-derived material and relatively low oxygen fugacities (ΔFMQ -1.8 to ΔFMQ +0.8) was responsible for the high (Pb + Zn)/Cu ratio in the Qibaoshan deposit, and the Pb, Zn and Ag were mainly derived from the reworked ancient crust. Although four analyses of inherited Neoproterozoic zircons ( 800 Ma) have variable positive εHf(t) values (0.72 to 11.21), indicating that Neoproterozoic juvenile crust was involved in the formation of the Qibaoshan ore-bearing quartz

Comparative study of post-growth annealing of Cu(hfac)2, Co2(CO)8 and Me2Au(acac) metal precursors deposited by FEBID.

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Puydinger Dos Santos, Marcos Vinicius; Szkudlarek, Aleksandra; Rydosz, Artur; Guerra-Nuñez, Carlos; Béron, Fanny; Pirota, Kleber Roberto; Moshkalev, Stanislav; Diniz, José Alexandre; Utke, Ivo

2018-01-01

Non-noble metals, such as Cu and Co, as well as noble metals, such as Au, can be used in a number modern technological applications, which include advanced scanning-probe systems, magnetic memory and storage, ferroelectric tunnel junction memristors, metal interconnects for high performance integrated circuits in microelectronics and nano-optics applications, especially in the areas of plasmonics and metamaterials. Focused-electron-beam-induced deposition (FEBID) is a maskless direct-write tool capable of defining 3-dimensional metal deposits at nanometre scale for above applications. However, codeposition of organic ligands when using organometallic precursors is a typical problem that limits FEBID of pure metal nanostructures. In this work, we present a comparative study using a post-growth annealing protocol at 100, 200, and 300 °C under high vacuum on deposits obtained from Co 2 (CO) 8 , Cu(II)(hfac) 2 , and Me 2 Au(acac) to study improvements on composition and electrical conductivity. Although the as-deposited material was similar for all precursors, metal grains embedded in a carbonaceous matrix, the post-growth annealing results differed. Cu-containing deposits showed the formation of pure Cu nanocrystals at the outer surface of the initial deposit for temperatures above 100 °C, due to the migration of Cu atoms from the carbonaceous matrix containing carbon, oxygen, and fluorine atoms. The average size of the Cu crystals doubles between 100 and 300 °C of annealing temperature, while the composition remains constant. In contrast, for Co-containing deposits oxygen release was observed upon annealing, while the carbon content remained approximately constant; the cobalt atoms coalesced to form a metallic film. The as-deposited Au-containing material shows subnanometric grains that coalesce at 100 °C, maintaining the same average size at annealing temperatures up to 300 °C. Raman analysis suggests that the amorphous carbonaceous matrix of the as-written Co

Copper isotopic zonation in the Northparkes porphyry Cu-Au deposit, SE Australia

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Li, Weiqiang; Jackson, Simon E.; Pearson, Norman J.; Graham, Stuart

2010-07-01

Significant, systematic Cu isotopic variations have been found in the Northparkes porphyry Cu-Au deposit, NSW, Australia, which is an orthomagmatic porphyry Cu deposit. Copper isotope ratios have been measured in sulfide minerals (chalcopyrite and bornite) by both solution and laser ablation multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). The results from both methods show a variation in δ 65Cu of hypogene sulfide minerals of greater than 1‰ (relative to NIST976). Significantly, the results from four drill holes through two separate ore bodies show strikingly similar patterns of Cu isotope variation. The patterns are characterized by a sharp down-hole decrease from up to 0.8‰ (0.29 ± 0.56‰, 1 σ, n = 20) in the low-grade peripheral alteration zones (phyllic-propylitic alteration zone) to a low of ˜-0.4‰ (-0.25 ± 0.36‰, 1 σ, n = 30) at the margins of the most mineralized zones (Cu grade >1 wt%). In the high-grade cores of the systems, the compositions are more consistent at around 0.2‰ (0.19 ± 0.14‰, 1 σ, n = 40). The Cu isotopic zonation may be explained by isotope fractionation of Cu between vapor, solution and sulfides at high temperature, during boiling and sulfide precipitation processes. Sulfur isotopes also show an isotopically light shell at the margins of the high-grade ore zones, but these are displaced from the low δ 65Cu shells, such that there is no correlation between the Cu and S isotope signatures. Fe isotope data do not show any discernable variation along the drill core. This work demonstrates that Cu isotopes show a large response to high-temperature porphyry mineralizing processes, and that they may act as a vector to buried mineralization.

Geochemical element mobility during the hydrothermal alteration in the Tepeoba porphyry Cu-Mo-Au deposits at Balikesir, NW Turkey

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Abdelnasser, Amr; Kiran Yildirim, Demet; Doner, Zeynep; Kumral, Mustafa

2016-04-01

The Tepeoba porphyry Cu-Mo-Au deposit represents one of the important copper source and mineral deposits in the Anatolian tectonic belt at Balikesir province, NW Turkey. It considered as a vein-type deposit locally associated with intense hydrothermal alteration within the brecciation, quartz stockwork veining, and brittle fracture zones in the main host rock that represented by hornfels, as well as generally related to the shallow intermediate to silicic intrusive Eybek pluton. Based on the field and geologic relationships and types of ore mineral assemblages and the accompanied alteration types, there are two mineralization zones; hypogene (primary) and oxidation/supergene zones are observed associated with three alteration zones; potassic, phyllic, and propylitic zones related to this porphyry deposit. The phyllic and propylitic alterations locally surrounded the potassic alteration. The ore minerals related to the hypogene zone represented by mostly chalcopyrite, Molybdenite, and pyrite with subordinate amount of marcasite, enargite, and gold. On the other hand they include mainly cuprite with chalcopyrite, pyrite and gold as well as hematite and goethite at the oxidation/supergene zone. This study deals with the quantitative calculations of the mass/volume changes (gains and losses) of the major and trace elements during the different episodes of alteration in this porphyry deposit. These mass balance data reveal that the potassic alteration zone that the main Cu- and Mo-enriched zone, has enrichment of K, Si, Fe, and Mg, and depletion of Na referring to replacement of plagioclase and amphibole by K-feldspar, sericite and biotite. While the propylitic alteration that is the main Mo- and Au-enriched zone is accompanied with K and Na depletion with enrichment of Si, Fe, Mg, and Ca forming chlorite, epidote, carbonate and pyrite. On the other hand the phyllic alteration that occurred in the outer part around the potassic alteration, characterized by less amount

High-temperature stability of Au/Pd/Cu and Au/Pd(P)/Cu surface finishes

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Ho, C. E.; Hsieh, W. Z.; Lee, P. T.; Huang, Y. H.; Kuo, T. T.

2018-03-01

Thermal reliability of Au/Pd/Cu and Au/Pd(4-6 wt.% P)/Cu trilayers in the isothermal annealing at 180 °C were investigated by X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectrometry (TOF-SIMS), and transmission electron microscopy (TEM). The pure Pd film possessed a nanocrystalline structure with numerous grain boundaries, thereby facilitating the interdiffusion between Au and Cu. Out-diffusion of Cu through Pd and Au grain boundaries yielded a significant amount of Cu oxides (CuO and Cu2O) over the Au surface and gave rise to void formation in the Cu film. By contrast, the Pd(P) film was amorphous and served as a good diffusion barrier against Cu diffusion. The results of this study indicated that amorphous Pd(P) possessed better oxidation resistance and thermal reliability than crystalline Pd.

Adsorption Behavior of TBPS in the Process of Cu Electrodeposition on an Au Film.

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Chen, Liang-Huei; Liu, Yung-Fang; Krug, Klaus; Lee, Yuh-Lang

2018-05-15

The adsorption behavior of an Cu electroplating additive, 3,3 thiobis-(1-propanesulfonic acid sodium salt) (TBPS) in a process of Cu deposition onto a single crystalline Au(111) surface is studied by an in-situ Surface-Enhanced Infrared Absorption Spectroscopy (SEIRAS). The SEIRAS spectra of the TBPS adlayer on a Cu film is investigated first and compared to that on an Au film. These results are utilized to evaluate the characteristics of TBPS adlayer on the electrode surface during the Cu deposition and stripping processes. The results show that the SEIRAS spectra of TBPS adsorbed on the Cu film resembles closely to that on the Au film, and the most pronounced peaks are symmetric S-O (ss-SO) and asymmetric S-O (as-SO) stretching modes. However, the as-SO band is sharper with a higher intensity on the Cu film. Since the ss-SO and as-SO peaks correspond to the molecular with upright and lie-down orientations, respectively, it implies that the TBPS molecules have higher ratio of lie-down orientation on the Cu film. In the Cu electrodeposition process, the cyclic voltammetry (CV) result shows that the presence of the TBPS in the HClO 4 solution can decrease the inhibition effect of HClO 4 to the Cu deposition. For the spectra measured at various potential during cathodic and anodic sweeping, an obvious change of the spectra occurs at ca. 0.6 V, the initiation of Cu underpotential deposition (Cu-UPD). For potentials higher and lower than 0.6 V, the spectra are similar, respectively, to those measured for the Au and Cu films. This result indicates that the TBPS molecules originally adsorbing on the Au film transfer to the surface of deposited Cu layer. This inference is also confirmed by the variation in wavenumber and peak intensity of ss-SO and as-SO peaks during the potential sweeping.

New insights into the mixing of gold and copper in a nanoparticle from a structural study of Au-Cu nanoalloys synthesized via a wet chemistry method and pulsed laser deposition.

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Prunier, Hélène; Nelayah, Jaysen; Ricolleau, Christian; Wang, Guillaume; Nowak, Sophie; Lamic-Humblot, Anne-Félicie; Alloyeau, Damien

2015-11-14

Gold-copper nanoparticles (Au-Cu NPs) were elaborated by both chemical (polyol reduction method) and physical (laser deposition) routes. The size, composition and crystal structure of these bimetallic nanoalloys were then characterized by aberration corrected transmission electron microscopy (TEM). Using a one-pot polyol method, Au-Cu nanocubes (NCs) with nominal compositions Au3Cu and AuCu3 were synthesized. The size and composition of the NCs were tuned by varying the amount and the ratio of Au(iii) and Cu(ii) ions used as metallic precursors in the reaction. While the particle shape and size were well-controlled, single particle X-ray spectroscopy showed that, irrespective of the targeted compositions, the Cu content in all NCs was about 11-12 at%, i.e. in both samples, the real composition was different from the nominal one. This was ascribed to an incomplete alloying of the two constituent metals of the alloy in the cubes due to different reduction kinetics of the two metallic precursors. To shed light on the alloying of gold and copper at the nanoscale, Au-Cu NPs with targeted compositions Au3Cu and AuCu3 were deposited on amorphous carbon by laser ablation of two monometallic sources, and their structural properties were studied by TEM. These studies show that Au-Cu nanoalloys were synthesized in both samples and that the complete mixing of Au and Cu atoms achieved with this synthesis technique led to the production of Au-Cu NPs with well-controlled compositions. These results constitute a first but major step towards a complete understanding of the details of kinetics and thermodynamics determining the mixing of gold and copper atoms at the nanoscale. Such an understanding is essential for producing Au-Cu bimetallic nanoalloys with well-defined structural properties via wet chemical synthesis.

Mineral Deposit Data for Epigenetic Base- and Precious-metal and Uranium-thorium Deposits in South-central and Southwestern Montana and Southern and Central Idaho

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Klein, T.L.

2004-01-01

Metal deposits spatially associated with the Cretaceous Boulder and Idaho batholiths of southwestern Montana and southern and central Idaho have been exploited since the early 1860s. Au was first discovered in placer deposits; exploitation of vein deposits in bedrock soon followed. In 1865, high-grade Ag vein deposits were discovered and remained economically important until the 1890s. Early high-grade deposits of Au, Ag and Pb were found in the weathered portions of the veins systems. As mining progressed to deeper levels, Ag and Pb grades diminished. Exploration for and development of these vein deposits in this area have continued until the present. A majority of these base- and precious-metal vein deposits are classified as polymetallic veins (PMV) and polymetallic carbonate-replacement (PMR) deposits in this compilation. Porphyry Cu and Mo, epithermal (Au, Ag, Hg and Sb), base- and precious-metal and W skarn, W vein, and U and Th vein deposits are also common in this area. The world-class Butte Cu porphyry and the Butte high-sulfidation Cu vein deposits are in this study area. PMV and PMR deposits are the most numerous in the region and constitute about 85% of the deposit records compiled. Several types of syngenetic/diagenetic sulfide mineral deposits in rocks of the Belt Supergroup or their equivalents are common in the region and they have been the source of a substantial metal production over the last century. These syngenetic deposits and their metamorphosed/structurally remobilized equivalents were not included in this database; therefore, deposits in the Idaho portion of the Coeur d'Alene district and the Idaho Cobalt belt, for example, have not been included because many of them are believed to be of this type.

Genesis of the Bangbule Pb-Zn-Cu polymetallic deposit in Tibet, western China: Evidence from zircon U-Pb geochronology and S-Pb isotopes

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Kan, Tian; Zheng, Youye; Gao, Shunbao

2016-04-01

The Banbule Pb-Zn-Cu skarn deposit is located in the Longger-Gongbujiangda volcanic magma arc in the Gangdese-Nyainqentanglha Plate. It is the only lead-zinc polymetallic deposit discovered in the westernmost Nyainqentanglha metallogenic belt. The measured and indicated resources include 0.9 Mt of Pb+Zn (4.77% Pb and 4.74% Zn, respectively), 6499 t of Cu, and 178 t of Ag (18.75g/t Ag). The orebodies mainly occur as lenses, veins and irregular shapes in the contact zone between the quartz-porphyry and limestone of the Upper Permian Xiala Formation, or in the boundaries between limestone and sandstone. Pb-Zn-Cu mineralization in the Banbule deposit is closely associated with skarns. The ore minerals are dominated by galena, sphalerite, chalcopyrite, bornite, and magnetite, with subordinate pyrite, malachite, and azurite. The gangue minerals are mainly garnet, actinolite, diopside, quartz, and calcite. The ore-related quartz-porphyry displays LA-ICP-MS zircon U-Pb age of 77.31±0.74 Ma. The δ34S values of sulfides define a narrow range of -0.8 to 4.7‰ indicating a magmatic source for the ore-forming materials. Lead isotopic systematics yield 206Pb/204Pb of 18.698 to 18.752, 207Pb/204Pb of 15.696 to 15.760, and 208Pb/204Pb of 39.097 to 39.320. The data points are constrained around the growth curves of upper crust and orogenic belt according to the tectonic discrimination diagrams. The calculated Δβ - Δγ values plot within the magmatic field according to the discrimination diagram of Zhu et al. (1995). The S-Pb isotopic data suggest that Bangbule is a typical skarn deposit, and the Pb-Zn-Cu mineralization is genetically related to the quartz-porphyry in the mining district. The discovery of the Bangbule deposit indicates that there is metallogenic potential in the westernmost Nyainqentanglha belt, which is of great importance for the exploration work in this area.

Magmatic-dominated fluid evolution in the Jurassic Nambija gold skarn deposits (southeastern Ecuador)

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Vallance, Jean; Fontboté, Lluís; Chiaradia, Massimo; Markowski, Agnès; Schmidt, Susanne; Vennemann, Torsten

2009-05-01

and the compositional variability of chlorite, essentially controlled by host rock compositions. Gold was precipitated at this stage as a result of cooling and pH increase related to CO2 effervescence, which both result in destabilization of gold-bearing chloride complexes. Significant ingression of external fluids took place after gold deposition only, as recorded by δ18O values of 0.4‰ to 6.2‰ for fluids depositing quartz (below 350°C) in sulfide-rich barren veins. Low-temperature (bearing skarn deposits, not only the prograde stage but also the gold-precipitating retrograde stage is dominated by fluids of magmatic origin.

Local structure of disordered Au-Cu and Au-Ag alloys

International Nuclear Information System (INIS)

Frenkel, A. I.; Machavariani, V. Sh.; Rubshtein, A.; Rosenberg, Yu.; Voronel, A.; Stern, E. A.

2000-01-01

X-ray-absorption fine structure (XAFS) and x-ray-diffraction (XRD) measurements of disordered alloys Au x Cu 1-x and Au 0.5 Ag 0.5 prepared by melt spinning were performed. In the Au 0.5 Ag 0.5 alloy, no significant local deviations of the atoms from the average fcc lattice were detected while in Au x Cu 1-x alloys, significant deviations of atoms from the average fcc lattice were found. Mean-square vibrations of the Cu-Cu distances revealed by the XAFS in Au x Cu 1-x alloys indicate the weakening of contact between Cu atoms in the dilute limit. Our computer simulation for Au x Cu 1-x clusters of 10 5 atoms reproduces the main features of both the XAFS and XRD data

Geochemical behavior of rare earth elements of the hydrothermal alterations within the Tepeoba porphyry Cu-Mo-Au deposits at Balikesir, NW Turkey

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Doner, Zeynep; Abdelnasser, Amr; Kiran Yildirim, Demet; Kumral, Mustafa

2016-04-01

This work reports the geochemical characteristics and behavior of the rare earth elements (REE) of the hydrothermal alteration of the Tepeoba porphyry Cu-Mo-Au deposit located in the Anatolian tectonic belt at Biga peninsula (Locally Balikesir province), NW Turkey. The Cu-Mo-Au mineralization at this deposit hosted in the hornfels rocks and related to the silicic to intermediate intrusion of Eybek pluton. It locally formed with brecciated zones and quartz vein stockworks, as well as the brittle fracture zones associated with intense hydrothermal alteration. Three main alteration zones with gradual boundaries formed in the mine area in the hornfels rock that represents the host rock, along that contact the Eybek pluton; potassic, propylitic and phyllic alteration zones. The potassic alteration zone that formed at the center having high amount of Cu-sulfide minerals contains biotite, muscovite, and sericite with less amount of K-feldspar and associated with tourmalinization alteration. The propylitic alteration surrounds the potassic alteration having high amount of Mo and Au and contains chlorite, albite, epidote, calcite and pyrite. The phyllic alteration zone also surrounds the potassic alteration containing quartz, sericite and pyrite minerals. Based on the REE characteristics and content and when we correlate the Alteration index (AI) with the light REEs and heavy REEs of each alteration zone, it concluded that the light REEs decrease and heavy REEs increase during the alteration processes. The relationships between K2O index with Eu/Eu* and Sr/Sr* reveals a positive correlation in the potassic and phyllic alteration zones and a negative correlation in the propylitic alteration zone. This refers to the hydrothermal solution which is responsible for the studied porphyry deposits and associated potassic and phyllic alterations has a positive Eu and Sr anomaly as well as these elements were added to the altered rock from the hydrothermal solution. Keywords: Rare

Porphyry Cu-Au mineralization in the Mirkuh Ali Mirza magmatic complex, NW Iran

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Maghsoudi, A.; Yazdi, M.; Mehrpartou, M.; Vosoughi, M.; Younesi, S.

2014-01-01

The Mirkuh Ali Mirza Cu-Au porphyry system in East Azerbaijan Province is located on the western part of the Cenozoic Alborz-Azerbaijan volcanic belt. The belt is also an important Cu-Mo-Au metallogenic province in northwestern Iran. The exposed rocks in the study area consist of a volcaniclastic sequence, subvolcanic rocks and intermediate to mafic lava flows of Neogene age. The volcanic rocks show a typical subduction-related magmatic arc geological and geochemical signature, with low concentration of Nb, Ta, and Ti. Mineralization is hosted by Neogene dacitic tuff and porphyritic dacite situated at the intersections of northeast and northwest faults. Field observations, alteration zonation, geochemical haloes and isotopic data of the Mirkuh Ali Mirza magmatic complex show similarities with typical convergent margin Cu-Au porphyry type deposits. The following features confirm the classic model for Cu-Au porphyry systems: (a) close spatial association with high-K calcalkaline to shoshonitic rock related to post-collision extensional setting (b) low grade Cu (0.57%) (c) stockworks as well as disseminated sulfides (c) zonality of the alteration patterns from intense phyllic at the center to outward weak-phyllic, argillic, and propylitic (d) the presence of a pyritic halo (e) accompanied by sheeted veins and low-sulfidation epithermal gold (f) mineralization spatially associated with intersection of structures, (g) genetically related to diorite porphyry stocks at depth (h) geochemical zonation of (Cu ± Au ± Ag ± Bi) → (Cu + Mo ± Bi ± Au ± Pb ± Zn ± As) → (Au + Mo ± Pb ± Zn) → (As + Ag + Sb + Mn + Ba + Pb + Zn + Hg) → Hg from center to outwards (i) The range of sulfur isotopic values is approximately zero (interpreted to have magmatic source) and similar to other subduction-related porphyry Cu deposits.

Uranium-lead dating of hydrothermal zircon and monazite from the Sin Quyen Fe-Cu-REE-Au-(U) deposit, northwestern Vietnam

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Li, Xiao-Chun; Zhou, Mei-Fu; Chen, Wei Terry; Zhao, Xin-Fu; Tran, MyDung

2018-03-01

The Sin Quyen deposit in northwestern Vietnam contains economic concentrations of Cu, Au and LREE, and sub-economic concentration of U. In this deposit, massive and banded replacement ores are hosted in Neoproterozoic metapelite. The paragenetic sequence includes sodic alteration (stage I), calcic-potassic alteration and associated Fe-REE-(U) mineralization (stage II), Cu-Au mineralization (stage III), and sulfide-(quartz-carbonate) veins (stage IV). The Sin Quyen deposit experienced an extensive post-ore metamorphic overprint, which makes it difficult to precisely determine the mineralization age. In this study, zircon and monazite U-Pb geochronometers and the Rb-Sr isochron method are used to constrain the timing of mineralization. Zircon grains in the ore are closely intergrown or texturally associated with hydrothermal minerals of stage II (e.g., garnet, allanite, and hedenbergite). They may contain primary fluid inclusions and display irregular zoning in cathodoluminescence (CL) images. Zircon grains are rich in U (688 to 2902 ppm) and poor in Th (0.2 to 2.9 ppm). Their δ18OV-SMOW values range from 11.9 to 14.0‰, higher than those of typical magmatic zircon. These textural and compositional features imply that zircon precipitated from 18O- and U-rich hydrothermal fluids, coeval with the minerals of stage II. Monazite occurs in close association with stage II magnetite and allanite and has low contents of Th (<2700 ppm), indicative of a hydrothermal origin. Hydrothermal zircon and monazite have indistinguishable U-Pb ages of 841 ± 12 and 836 ± 18 Ma, respectively, representing the timing of Fe-REE mineralization. There is no direct isotopic constraint on the timing of the Cu-Au mineralization, but geological observations suggest that the Cu-Au and Fe-REE ores most likely formed within a single evolved hydrothermal process. In the plot of 87Rb/86Sr vs. 87Sr/86Sr, the composition of bulk-ore and biotite separates from ore lie along a reference line for 30 Ma

Molecular dynamics simulation of Cu/Au thin films under temperature gradient

International Nuclear Information System (INIS)

Li, Qibin; Peng, Xianghe; Peng, Tiefeng; Tang, Qizhong; Zhang, Xiaomin; Huang, Cheng

2015-01-01

Graphical abstract: Heat transportation in the thin films. - Highlights: • The coherent lattice interface is found at thin films after annealing. • The vacancies are observed clearly in the deposit thin films. • The defect and component will influence the energy transportation in the coatings. • The vacancies and lattice mismatch can enlarge the mobility of atoms. • The phonon transportation in thin films has no apparent rule. - Abstract: Three modulation period thin films, 1.8 nm Cu/3.6 nm Au, 2.7 nm Cu/2.7 nm Au and 3.6 nm Cu/1.8 nm Au, are obtained from deposition method and ideal modeling based on lattice constant, to examine their structures and thermophysical characteristics under temperature gradient. The coherent lattice interface is found both at deposit and ideal thin films after annealing. Also, the vacancies are observed clearly in the deposit thin films. The defect and component of thin films will influence the energy transportation in the coatings. The vacancies and lattice mismatch can enlarge the mobility of atoms and result in the failure of coating under the thermal stress. The power spectrum of atoms’ movement has no apparent rule for phonon transportation in thin films. The results are helpful to reveal the micro-mechanism and provide reasonable basis for the failure of metallic coatings.

Molecular dynamics simulation of Cu/Au thin films under temperature gradient

Energy Technology Data Exchange (ETDEWEB)

Li, Qibin, E-mail: qibinli@cqu.edu.cn [College of Aerospace Engineering, Chongqing University, Chongqing 400030 (China); State Key Laboratory of Coal Mine Disaster Dynamics and Control, Chongqing University, Chongqing 400030 (China); Chongqing Key Laboratory of Heterogeneous Material Mechanics, Chongqing University, Chongqing 400030 (China); Peng, Xianghe [College of Aerospace Engineering, Chongqing University, Chongqing 400030 (China); State Key Laboratory of Coal Mine Disaster Dynamics and Control, Chongqing University, Chongqing 400030 (China); Peng, Tiefeng, E-mail: pengtiefeng@cqu.edu.cn [State Key Laboratory of Coal Mine Disaster Dynamics and Control, Chongqing University, Chongqing 400030 (China); Tang, Qizhong [College of Aerospace Engineering, Chongqing University, Chongqing 400030 (China); Zhang, Xiaomin [College of Aerospace Engineering, Chongqing University, Chongqing 400030 (China); Chongqing Key Laboratory of Heterogeneous Material Mechanics, Chongqing University, Chongqing 400030 (China); Huang, Cheng [College of Aerospace Engineering, Chongqing University, Chongqing 400030 (China)

2015-12-01

Graphical abstract: Heat transportation in the thin films. - Highlights: • The coherent lattice interface is found at thin films after annealing. • The vacancies are observed clearly in the deposit thin films. • The defect and component will influence the energy transportation in the coatings. • The vacancies and lattice mismatch can enlarge the mobility of atoms. • The phonon transportation in thin films has no apparent rule. - Abstract: Three modulation period thin films, 1.8 nm Cu/3.6 nm Au, 2.7 nm Cu/2.7 nm Au and 3.6 nm Cu/1.8 nm Au, are obtained from deposition method and ideal modeling based on lattice constant, to examine their structures and thermophysical characteristics under temperature gradient. The coherent lattice interface is found both at deposit and ideal thin films after annealing. Also, the vacancies are observed clearly in the deposit thin films. The defect and component of thin films will influence the energy transportation in the coatings. The vacancies and lattice mismatch can enlarge the mobility of atoms and result in the failure of coating under the thermal stress. The power spectrum of atoms’ movement has no apparent rule for phonon transportation in thin films. The results are helpful to reveal the micro-mechanism and provide reasonable basis for the failure of metallic coatings.

Multiphase formation of the Obří důl polymetallic skarn deposit, West Sudetes, Bohemian Massif: geochemistry and Re-Os dating of sulfide mineralization

Science.gov (United States)

Veselovský, František; Ackerman, Lukáš; Pašava, Jan; Žák, Karel; Haluzová, Eva; Creaser, Robert A.; Dobeš, Petr; Erban, Vojtěch; Tásler, Radko

2018-06-01

The Obří důl Fe-Cu-As polymetallic sulfide skarn deposit is developed in a metamorphic series in the West Sudetes, Bohemian Massif. It consists of lenses of marble, calc-silicate rocks, and skarns. We studied the Gustav orebody, which is located few hundred meters away from the contact with a large, late-orogenic Variscan Krkonoše-Jizera Plutonic Complex (KJPC) emplaced into shallow crust. Mineralogical and fluid inclusion study evidence indicates that the main sulfide stage, dominated by pyrrhotite, arsenopyrite, and chalcopyrite originated from aqueous hydrothermal fluids with salinity up to 8 wt% NaCl eq. with minimum homogenization temperatures ranging from 324 to 358 °C. These fluids mainly replaced carbonate-rich lithologies. Carbon, oxygen, and strontium isotope data in Ca-rich rocks imply total overprinting by channelized metasomatic fluid flow, which is most probably related to the intrusion of the KJPC, whereas δ34S values of sulfides argue for a magmatic source of sulfur. The Re-Os age of arsenopyrite overlaps published age data for the KJPC and suggests synchronous formation of the main sulfide mineralization and pluton emplacement.

Formation and Schottky barrier height of Au contacts to CuInSe2

International Nuclear Information System (INIS)

Nelson, A.J.; Gebhard, S.; Kazmerski, L.L.; Colavita, E.; Engelhardt, M.; Hoechst, H.

1991-01-01

Synchrotron radiation soft x-ray photoemission spectroscopy was used to investigate the development of the electronic structure at the Au/CuInSe 2 interface. Au overlayers were deposited in steps on single-crystal p and n-type CuInSe 2 at ambient temperature. Reflection high-energy electron diffraction analysis before and during growth of the Au overlayers indicated that the Au overlayer was amorphous. Photoemission measurements were acquired after each growth in order to observe changes in the valence band electronic structure as well as changes in the In 4d and Se 3d core lines. The results were used to correlate the interface chemistry with the electronic structure at these interfaces and to directly determine the Au/CuInSe 2 Schottky barrier height

Native gold from the Inagli Pt-Au placer deposit (the Aldan Shield, Russia): geochemical characteristics and implications for possible bedrock sources

Science.gov (United States)

Svetlitskaya, Tatyana V.; Nevolko, Peter A.; Kolpakov, Vladislav V.; Tolstykh, Nadezhda D.

2018-03-01

The Inagli alluvial Pt-Au placer deposit in the Republic of Sakha (Yakutia), Russia, is linked to the Inagli massif, one of the several Uralian-Alaskan-type alkaline-ultrabasic complexes in the Aldan Shield. Gold from the placer is heterogeneous in composition and is represented by three types. Type 1 gold is the most abundant and is characterized by simple Au-Ag alloys with 4-34 wt% Ag, low Cu (up to 0.08 wt%) and negligible Hg, Pt, and Pd contents, and silver-tellurium sulfosalts (Ag-Cu-Te-S-As compounds) in the inclusion suite. Silicate inclusions are biotite, K-feldspar, Fe-Mg amphibole, chlorite, plagioclase, Fe-Mg pyroxene, zircon, and titanite. Distinctive features of this gold type are most similar to those derived from low-sulfidation systems linked to iron oxide copper-gold or iron skarn types of mineralization. The bedrock source of type 1 gold could be related with monzonite to syenite intrusions surrounding the Inagli massif. Distinctive features of type 2 gold include a wide discontinuous range of Ag content (1-18 wt%), elevated Cu (up to 0.5 wt%), and occasional Pd (up to 0.3 wt%) levels, non-detectable Pt and Hg contents, and rare inclusions of simple sulfides (digenite, pyrrhotite) and Na amphibole. Type 3 gold is distinguished by a narrow range in Ag content (5-8 wt%), elevated Hg (0.5-1 wt%) contents, negligible Cu, Pt and Pd levels, and Au-Pb compounds + K-feldspar inclusions. Microchemical characteristics of type 2 and type 3 gold are interpreted as suggestive of an alkaline-magmatic-related fluid. Based on the grain morphology and microchemical signatures, potential bedrock sources for both gold types could be related to the numerous alkaline veins and potassic alteration zones within the dunite core. A comparison of the Inagli and the Kondyor placer gold allows to generate distinctive generic signatures for gold from Uralian-Alaskan-type alkaline-ultrabasic complexes in the Aldan Shield.

Geochronology and geochemistry constraints of the Early Cretaceous Taibudai porphyry Cu deposit, northeast China, and its tectonic significance

Science.gov (United States)

Zhou, Zhen-Hua; Mao, Jing-Wen; Wu, Xin-Li; Ouyang, Hen-Gen

2015-05-01

The southern Great Xing'an Range (SGXR), located in the southeastern part of Inner Mongolia, China, shows intense Mesozoic tectono-magmatic activity and hosts economically important polymetallic (Cu-Pb-Zn-Sn-Fe-Ag-Au-Mo) mineralization. Here, we present new zircon U-Pb ages, whole-rock geochemical data, Nd-Sr-Hf isotopic data and Re-Os ages for the Taibudai deposit in the SGXR. The Taibudai granitoids show high SiO2 (70.62-72.13 wt.%) and alkali (Na2O + K2O = 7.04-8.60 wt.%) concentrations, low MgO (0.89-1.37 wt.%) and Al2O3 (∼14 wt.%), ASI ratios molybdenite from the deposit yield an ore-forming age of 137.1 ± 1.4 Ma. Re contents range from 4.37 to 41.77 ppm, implying ore material components have a mixed crust-mantle origin. SHRIMP analysis of zircons show that the monzogranitic porphyry and biotite granite in the Taibudai deposit were formed at 137.0 ± 0.9 Ma and 138.3 ± 0.9 Ma, respectively, indicating a temporal link between granitic magmatism and Cu mineralization. This result, combined with the regional geology, tectonic evolution, and age data from the literature, suggests that the Early Cretaceous (∼140 Ma) was the peak metallogenic epoch for the Great Xing'an Range, and the mineralization in this period generally takes the form of porphyry, skarn, or hydrothermal polymetallic ore deposits in an active extensional continental margin environment. The Taibudai porphyry and associated mineralization provides a typical example of magmatism and metallogeny associated with a Paleo-Pacific plate subduction, continental margin, back-arc extensional setting.

In-situ STM study of phosphate adsorption on Cu(111), Au(111) and Cu/Au(111) electrodes

DEFF Research Database (Denmark)

Schlaup, Christian; Horch, Sebastian

2013-01-01

The interaction of Cu(111), Au(111) and Cu-covered Au(111) electrodes with a neutral phosphate buffer solution has been studied by means of cyclic voltammetry (CV) and in situ electrochemical scanning tunneling microscopy (EC-STM). Under low potential conditions, both the Cu(111) and the Au(111......) surface appear apparently adsorbate free, indicated by the presence of a (4×4) structure and the herringbone surface reconstruction, respectively. Upon potential increase, phosphate anions adsorb on both surfaces and for Cu(111) the formation of a (√3×√3)R30° structure is found, whereas on Au(111) a "(√3......×√7)" structure is formed. For a Cu-submonolayer on Au(111), coadsorption of phosphate anions leads to the formation of a (2×2) vacancy structure within an assumed pseudomorphic structure of the Cu-submonolayer with the phosphate anions occupying the vacancies. When desorbing the phosphate anions at low...

Surface chemistry of 2-butanol and furfural on Cu, Au and Cu/Au single crystals

OpenAIRE

Megginson, Rory

2016-01-01

In this study, the adsorption of 2-butanol and furfural was investigated on Au (111), Cu (111) and Cu/Au (111) surfaces. It was hoped that by studying how these species adsorbed on these surfaces , insight would be provided into the roles of Cu and Au in the “hydrogen free” hydrogenation of furfural to furfuryl alcohol. This is a valuable process as currently furfuryl alcohol is derived from crude oil but it is possible to derive furfural from corn husk making it a greener process...

Surface structure and morphology of Cu-free and Cu-covered Au(100) and Au(111) electrodes in alkaline solution

Energy Technology Data Exchange (ETDEWEB)

Schlaup, Christian [Technical University of Denmark, Department of Physics, Fysikvey, DK-2800 Kongens Lyngby (Denmark); Friebel, Daniel [Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sand Hill Rd, Menlo Park, CA 94025 (United States); Wandelt, Klaus [University of Bonn, Institute for Physical und Theoretical Chemistry, Wegelerstr. 12, D-53115 Bonn (Germany)

2011-07-01

For both Cu-free Au-electrodes three different phases were observed as a function of the applied electrode potential. While at low potentials the onset of surface reconstruction points towards an apparently adsorbate free surface and, thus, a weak interaction with species from the electrolyte, a Au-hydroxide and a Au-oxide phase are formed subsequently during potential increase. A similar phase behavior was also found for Cu-covered Au-electrodes, while at low potentials an apparently adsorbate free Cu layer is observed, a Cu-hydroxide coadsorbate phase and a Cu-oxide phase are formed under increased potential conditions. In addition the apparently adsorbate free Cu-film tends to form a Cu-Au alloy phase while keeping the electrode for a sufficient long time at low potential conditions.

Geochemistry and fluid characteristics of the Dalli porphyry Cu-Au deposit, Central Iran

Science.gov (United States)

Zarasvandi, Alireza; Rezaei, Mohsen; Raith, Johann; Lentz, David; Azimzadeh, Amir-Mortaza; Pourkaseb, Hooshang

2015-11-01

The Miocene Dalli porphyry Cu-Au deposit in the central part of Urumieh-Dokhtar magmatic arc is the first reported Au-rich porphyry Cu deposit in the Zagros orogenic belt. The Cu-Au mineralization is mainly hosted in diorite and quartz diorite intrusions, presenting as numerous veinlets in the altered wall rocks, with potassic, phyllic, and propylitic alteration developed. Based on the mineral assemblages and crosscutting relations of veinlets, hydrothermal mineralization-alteration occurred in at least three stages, characterized by veinlets of (1) Qtz + Kfs + Mag ± Ccp, (2) Qtz + Py + Ccp ± Bn ± Cv ± Cc and, (3) Qtz + Chl + Bt. The ore-bearing intrusions exhibit typical geochemical characteristics of subduction zone magmas, including LREE fractionated pattern, strong enrichment in LILE (Cs, Rb, Ba, Pb, and U), and depletion of HFSE, with marked negative Ti and Nb anomalies. The adakite-like ore-hosting porphyry intrusions are characterized by a systematic gradual decreasing and increasing of Y and Eu/Eu∗ with increasing SiO2 content, respectively. Moreover, they exhibit a significant increasing trend of Sr/Y with decreasing of Y, which indicates progressive hornblende fractionation and suppression of plagioclase fractionation during the evolution toward high water content of parental magma. A relatively flat HREE pattern with low Dyn/Ybn and Nb/Ta values may represent that amphibole played a more important role than garnet in the generation of the adakitic melts in the thickened lower crust. Based on the phase assemblages confirmed by detailed laser Raman spectroscopy analyses and proportion of solid, liquid, and gaseous components, five types of fluid inclusions were recognized, which are categorized as; (1) liquid-rich two phase (liquidH2O + vaporH2O) (IIA), (2) vapor-rich two phase (vaporH2O/CO2 + liquidH2O) (IIB), (3) high saline simple fluids (IIIA; liquidH2O + vaporH2O + Hl), (4) high saline opaque mineral-bearing fluids (IIIB; liquidH2O + vaporH2O

An SFG and DFG investigation of polycrystalline Au, Au-Cu and Au-Ag-Cu electrodes in contact with aqueous solutions containing KCN

International Nuclear Information System (INIS)

Bozzini, Benedetto; Busson, Bertrand; De Gaudenzi, Gian Pietro; Mele, Claudio; Tadjeddine, Abderrahmane

2007-01-01

In this paper, the behaviour of polycrystalline Au, Au-Cu (Cu 25%) and Au-Ag-Cu (Ag 10%, Cu 15%) electrodes in contact with neutral aqueous solutions of KCN has been studied as a function of potential by means of in situ sum frequency generation (SFG) and difference frequency generation (DFG) spectroscopies. The potential-dependent spectra have been analysed quantitatively with a model for the second-order non-linear susceptibility accounting for vibrational and electronic effects. The potential-dependence of the CN - stretching band position and of the free-electron contribution to the real part of the non-resonant component of the second-order susceptibility have been accounted for. Spectroelectrochemical results were complemented by cyclic voltammetric measurements. The chief stress in this work has been placed on systematising and quantifying the interaction between the vibrational and electronic structures of the electrodic interfaces studied. The effects of adsorbates on the electronic structure of the adsorbing electrode, as a function of electrode alloy composition and applied potential are particularly critical for the understanding of Au-alloy electrochemistry in the presence of cyanide and cyanocomplexes. The systematic comparison of SFG and DFG spectra measured under the same electrochemical conditions for Au, Au-Cu and Au-Ag-Cu electrodes discloses a rich phenomenology related to the electronic structure of the interface

An SFG and DFG investigation of polycrystalline Au, Au-Cu and Au-Ag-Cu electrodes in contact with aqueous solutions containing KCN

Energy Technology Data Exchange (ETDEWEB)

Bozzini, Benedetto [Dipartimento di Ingegneria dell' Innovazione, Universita di Lecce, v. Monteroni, I-73100 Lecce (Italy)]. E-mail: benedetto.bozzini@unile.it; Busson, Bertrand [CLIO-LCP, Universite Paris-Sud, 91405 Orsay Cedex (France); De Gaudenzi, Gian Pietro [Dipartimento di Ingegneria dell' Innovazione, Universita di Lecce, v. Monteroni, I-73100 Lecce (Italy); Mele, Claudio [Dipartimento di Ingegneria dell' Innovazione, Universita di Lecce, v. Monteroni, I-73100 Lecce (Italy); Tadjeddine, Abderrahmane [UDIL-CNRS, Bat. 201, Centre Universitaire Paris-Sud, BP 34, 91898 Orsay Cedex (France)

2007-01-16

In this paper, the behaviour of polycrystalline Au, Au-Cu (Cu 25%) and Au-Ag-Cu (Ag 10%, Cu 15%) electrodes in contact with neutral aqueous solutions of KCN has been studied as a function of potential by means of in situ sum frequency generation (SFG) and difference frequency generation (DFG) spectroscopies. The potential-dependent spectra have been analysed quantitatively with a model for the second-order non-linear susceptibility accounting for vibrational and electronic effects. The potential-dependence of the CN{sup -} stretching band position and of the free-electron contribution to the real part of the non-resonant component of the second-order susceptibility have been accounted for. Spectroelectrochemical results were complemented by cyclic voltammetric measurements. The chief stress in this work has been placed on systematising and quantifying the interaction between the vibrational and electronic structures of the electrodic interfaces studied. The effects of adsorbates on the electronic structure of the adsorbing electrode, as a function of electrode alloy composition and applied potential are particularly critical for the understanding of Au-alloy electrochemistry in the presence of cyanide and cyanocomplexes. The systematic comparison of SFG and DFG spectra measured under the same electrochemical conditions for Au, Au-Cu and Au-Ag-Cu electrodes discloses a rich phenomenology related to the electronic structure of the interface.

Geology and mineralogy of the Au-As (Ag-Pb-Zn-Cu-Sb polymetallic deposit of Valiña-Azúmara (Lugo, NW Spain

Directory of Open Access Journals (Sweden)

Martínez-Abad, I.

2015-12-01

Full Text Available Valiña-Azúmara is a polymetallic Au-As (Ag-Pb-Zn-Cu-Sb deposit, located in the province of Lugo (NW Spain, that was mined for arsenic at the beginning of the 20th century. The mineralization is hosted in a Variscan thrust fault with a dip direction of N247-261ºE, and N-S and NE-SW Late-Variscan faults. These structures are hosted in black slates, Cambrian in age. To a lesser extent, the mineralization also occurs disseminated within narrow, weakly silicified and sericited selvages. Mineralization is divided into two hypogene stages. The first consists of quartz, calcite, rutile, sericite, arsenopyrite and pyrite. Two types of pyrite (Py-I and Py-II are defined according to their chemical and textural characteristics. Py-II occurs as overgrowth of previous Py-I crystals. Py-II is As-rich (≤1.7 wt.% and often contains traces of Te, Zn, Cu, Bi, Sb and Au. The mineralized drill core sections show a significant correlation between Au and As. This is due to Au occurring as invisible Au within the Py-II grains, with contents of up to 176 ppm. The Au/As ratios of Py-II indicate that Au was deposited as Au1+, as solid solution within the pyrite structure. The second stage of mineralization is enriched in Ag-Pb-Zn-Cu-Sb, replacing the first stage, and consists of quartz, calcite, chlorite, sphalerite, jamesonite, Ag-rich tetrahedrite, freibergite, chalcopyrite, pyrrhotite and galena. Although jamesonite shows traces of Ag, the Cu-Ag sulfosalts are the main carriers of the Ag mineralization in the deposit, with contents that vary from 13.7 to 23.9 wt.% of Ag. In the most superficial levels of the area, secondary Fe oxide and hydroxide, scorodite and anglesite developed due to the oxidation of the ore.Valiña-Azúmara es un yacimiento filoniano de Au-As (Ag-Pb-Zn-Cu-Sb situado en la provincia de Lugo (NO España, que fue explotado por arsénico a principios del siglo XX. La mineralización se encuentra encajada en un cabalgamiento Varisco de direcci

Induced Rashba splitting of electronic states in monolayers of Au, Cu on a W(110) substrate

International Nuclear Information System (INIS)

Shikin, A M; Rybkina, A A; Rybkin, A G; Marchenko, D; Korshunov, A S; Kudasov, Yu B; Frolova, N V; Sánchez-Barriga, J; Varykhalov, A; Rader, O

2013-01-01

The paper sums up a theoretical and experimental investigation of the influence of the spin–orbit coupling in W(110) on the spin structure of electronic states in deposited Au and Cu monolayers. Angle-resolved photoemission spectroscopy reveals that in the case of monolayers of Au and Cu spin–orbit split bands are formed in a surface-projected gap of W(110). Spin resolution shows that these states are spin polarized and that, therefore, the spin–orbit splitting is of Rashba type. The states evolve from hybridization of W 5d, 6p-derived states with the s, p states of the deposited metal. Interaction with Au and Cu shifts the original W 5d-derived states from the edges toward the center of the surface-projected gap. The size of the spin–orbit splitting of the formed states does not correlate with the atomic number of the deposited metal and is even higher for Cu than for Au. These states can be described as W-derived surface resonances modified by hybridization with the p, d states of the adsorbed metal. Our electronic structure calculations performed in the framework of the density functional theory correlate well with the experiment and demonstrate the crucial role of the W top layer for the spin–orbit splitting. It is shown that the contributions of the spin–orbit interaction from W and Au act in opposite directions which leads to a decrease of the resulting spin–orbit splitting in the Au monolayer on W(110). For the Cu monolayer with lower spin–orbit interaction the resulting spin splitting is higher and mainly determined by the W. (paper)

Data integration modeling applied to drill hole planning through semi-supervised learning: A case study from the Dalli Cu-Au porphyry deposit in the central Iran

Science.gov (United States)

Fatehi, Moslem; Asadi, Hooshang H.

2017-04-01

In this study, the application of a transductive support vector machine (TSVM), an innovative semi-supervised learning algorithm, has been proposed for mapping the potential drill targets at a detailed exploration stage. The semi-supervised learning method is a hybrid of supervised and unsupervised learning approach that simultaneously uses both training and non-training data to design a classifier. By using the TSVM algorithm, exploration layers at the Dalli porphyry Cu-Au deposit in the central Iran were integrated to locate the boundary of the Cu-Au mineralization for further drilling. By applying this algorithm on the non-training (unlabeled) and limited training (labeled) Dalli exploration data, the study area was classified in two domains of Cu-Au ore and waste. Then, the results were validated by the earlier block models created, using the available borehole and trench data. In addition to TSVM, the support vector machine (SVM) algorithm was also implemented on the study area for comparison. Thirty percent of the labeled exploration data was used to evaluate the performance of these two algorithms. The results revealed 87 percent correct recognition accuracy for the TSVM algorithm and 82 percent for the SVM algorithm. The deepest inclined borehole, recently drilled in the western part of the Dalli deposit, indicated that the boundary of Cu-Au mineralization, as identified by the TSVM algorithm, was only 15 m off from the actual boundary intersected by this borehole. According to the results of the TSVM algorithm, six new boreholes were suggested for further drilling at the Dalli deposit. This study showed that the TSVM algorithm could be a useful tool for enhancing the mineralization zones and consequently, ensuring a more accurate drill hole planning.

Cu underpotential deposition on Au controlled by in situ spectroscopic ellipsometry

Energy Technology Data Exchange (ETDEWEB)

Prato, Mirko; Cavalleri, Ornella; Mattera, Lorenzo; Canepa, Maurizio [Department of Physics, University of Genova, Genova (Italy); CNISM, Genova (Italy); Gussoni, Antonio [IMEM/CNR, Genova (Italy); Department of Physics, University of Genova, Genova (Italy); Panizza, Marco [Department of Chemical and Process Engineering, University of Genova (Italy)

2008-05-15

We have studied Cu electrodeposition on well defined Au films using real time spectroscopic ellipsometry (SE). SE allows to discriminate the under-potential (UP) and over-potential (OP) regimes. In the UP regime, tiny yet reproducible variations of {psi} and {delta} parameters indicate the formation of two phases with slightly different optical behavior. The phase at the largest coverage is assigned to a Cu monolayer. The SE response in the OP regime shows a marked dependence on the potential scan rate. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

The occurrence of ferropyrosmalite in the mineralized breccias from Igarape Bahia (North region, Brazil) Au-Cu (± ETR-U) deposit, Carajas mineral Province

International Nuclear Information System (INIS)

Tazava, Edison; Gomes, Newton Souza; Oliveira, Claudinei Gouveia de

1999-01-01

In the last years, several works report the presence of pyrosmalite mineral series [(Fe, Mn) 8 Si 6 O 15 (OH, Cl) 10 ] commonly associated with volcanic exhalative massive sulphide or Fe-Mn metamorphosed deposits. In this paper, we present the inedit occurrence of ferropyrosmalite in the Au-Cu (± REE-U) of Igarape Bahia deposit, located in the Au-Cu district of the Carajas Mineral Province. We consider the Igarape Bahia mineralization as being related to the genesis of iron-oxide class deposit, like the Olympic Dam type. Ferropyrosmalite occurs in two different contexts: associated with carbonate veins; associated with heterolithic breccias, composed by BIF and mafic metavolcanic fragments immersed in a magnetic, chalcopyrite, bornite, pyrite, carbonates (calcite to siderite), uranium and REE minerals, and gold, - rich matrix. The growth of ferropyrosmalite is probably due to the substitution of iron rich minerals (chloride, magnetite and siderite), controlled by magmatic fluid influx rich in chlorine. The permeability of breccias and the discontinuity of veins favour fluid percolation. The mode of occurrence of ferropyrosmalite and its relation with amphibole (ferro-hornblende-actinolite) indicate metasomatic growth of the former under temperatures in the transition of greenschist/amphibolite facies. The ferropyrosmalite of the Igarape Bahia deposit represents an uncommon type of occurrence linked to hydrothermal/magmatic conditions. (author)

Covellite CuS as a matrix for "invisible" gold: X-ray spectroscopic study of the chemical state of Cu and Au in synthetic minerals

Science.gov (United States)

Tagirov, Boris R.; Trigub, Alexander L.; Kvashnina, Kristina O.; Shiryaev, Andrey A.; Chareev, Dmitriy A.; Nickolsky, Maximilian S.; Abramova, Vera D.; Kovalchuk, Elena V.

2016-10-01

Geological processes leading to formation of sulfide ores often result in precipitation of gold-bearing sulfides which can contain high concentrations of this metal in ;invisible; (or ;refractory;) state. Covellite (CuS) is ubiquitous mineral in many types of the ore deposits, and numerous studies of the natural ores show that covellite can contain high concentrations of Au. At the same time, Au-bearing covellite withstands cooling in contrast to other minerals of the Cu-Fe-S system (chalcocite, bornite, chalcopyrite), where Au exsolves at low temperatures. This makes covellite a convenient model system for investigation of the chemical state (local environment and valence) of the ;invisible; Au in copper-sulfide ores (copper-porphyry, epithermal, volcanogenic massive sulfide, SEDEX deposits). Therefore, it is necessary to determine the location of Au in the covellite matrix as it will have important implications for the methods employed by mineral processing industry to extract Au from sulfide ores. Here we investigate the chemical state of Cu and Au in synthetic covellite containing up to 0.3 wt.% of Au in the ;invisible; state. The covellite crystals were synthesized by hydrothermal and salt flux methods. Formation of the chemically bound Au is indicated by strong dependence of the concentration of Au in covellite on the sulfur fugacity in the experimental system (d(log C(Au))/d(log f(S2)) ∼ 0.65). The Au concentration of covellite grows with increasing temperature from 400 to 450 °C, whereas further temperature increase to 500 °C has only minor effect. The synthesized minerals were studied using X-ray absorption fine structure spectroscopy (XAFS) in high energy resolution fluorescence detection (HERFD) mode. Ab initio simulations of Cu K edge XANES spectra show that the Cu oxidation state in two structural positions in covellite (tetrahedral and triangular coordination with S atoms) is identical: the total loss of electronic charge for the 3d shell is ∼0

CHARGED PARTICLE MULTIPLICITIES IN ULTRA-RELATIVISTIC AU+AU AND CU+CU COLLISIONS

Science.gov (United States)

Back, B. B.; Alver, B.; Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Busza, W.; Carroll, A.; Chai, Z.; Chetluru, V.; Decowski, M. P.; Garcia, E.; Gburek, T.; George, N.; Gulbrandsen, K.; Halliwell, C.; Hamblen, J.; Harnarine, I.; Hauer, M.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Holynski, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Khan, N.; Kulinich, P.; Kuo, C. M.; Li, W.; Lin, W. T.; Loizides, C.; Manly, S.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Reed, C.; Richardson, E.; Roland, C.; Roland, G.; Sagerer, J.; Seals, H.; Sedykh, I.; Smith, C. E.; Stankiewicz, M. A.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Szostak, A.; Tonjes, M. B.; Trzupek, A.; Vale, C.; Vannieuwenhuizen, G. J.; Vaurynovich, S. S.; Verdier, R.; Veres, G. I.; Walters, P.; Wenger, E.; Willhelm, D.; Wolfs, F. L. H.; Wosiek, B.; Wozniak, K.; Wyngaardt, S.; Wyslouch, B.

The PHOBOS collaboration has carried out a systematic study of charged particle multiplicities in Cu+Cu and Au+Au collisions at the Relativistic Heavy-Ion Collider (RHIC) at Brookhaven National Laboratory. A unique feature of the PHOBOS detector is its ability to measure charged particles over a very wide angular range from 0.5° to 179.5° corresponding to |η| <5.4. The general features of the charged particle multiplicity distributions as a function of pseudo-rapidity, collision energy and centrality, as well as system size, are discussed.

Study of REE behaviors, fluid inclusions, and O, S stable Isotopes in Zafar-abad iron skarn deposit, NW Divandarreh, Kordestan province

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Mehrdad Barati

2014-10-01

Full Text Available Introduction The Zafar-abad iron ore deposit, situated in the NW part of Divandarreh (lat. 36°01'14" and long. 46°58'22". The ore body is located on the northern margin of the Sanandaj-Sirjan igneous metamorphic zone. The Zafar-abad Fe-skarn deposit is one of the important, medium- size mineral deposits in western Iran. REE patterns of skarn magnetite were among others studied in Skarn deposit by (Taylor, 1979 Hydrothermal alteration and fluid-rock interaction significantly affect total contents of REE and their patterns in fluids. Moreover, fractionation of REE by chemical complication, adsorption effects and redox reactions are characteristic processes determining REE behavior during crystallization. Stable isotope data for oxygen and sulfur have been widely used with great success to trace the origin and evolution history of paleo-hydrothermal fluids of meteoric, magmatic, and metamorphic. Materials and methods The present study investigates REE and stable Isotope geochemistry of magnetite and pyrite in Zafar-abad deposit and temperature of trapped fluid inclusions based on geothermometry analysis. In order to study the major, trace and REE compositions of Zafar-abad magnetite, twelve samples were collected from surface of ore exposures. The emphasis during sampling was on ores with primary textures. Discussion The Zafar-abad district is situated in Mesozoic and Cenozoic sedimentary, meta-sedimentary and meta-igneous rocks in Sanandaj-Sirjan igneous metamorphic zone. Sedimentary sequences dominantly composed of calcareous and conglomerate rocks. Various meta-sedimentary rocks are intercalated with the sedimentary rocks, and comprise biotite and muscovite-rich schist, calc-schist, calc-silicate rock. Several distinct ductile tectonic fabrics have been identified around the Zafar-abad deposit. The main ore body at Zafar-abad is in the form of a roughly horizontal, discordant, lens to tabular-shaped body plunging 10° NW, where it appears to

Cu2O-directed in situ growth of Au nanoparticles inside HKUST-1 nanocages.

Science.gov (United States)

Liu, Yongxin; Liu, Ting; Tian, Long; Zhang, Linlin; Yao, Lili; Tan, Taixing; Xu, Jin; Han, Xiaohui; Liu, Dan; Wang, Cheng

2016-12-07

Controllable integration of metal nanoparticles (MNPs) and metal-organic frameworks (MOFs) is attracting considerable attention as the obtained composite materials always show synergistic effects in applications of catalysis, delivery, as well as sensing. Herein, a Cu 2 O-directed in situ growth strategy was developed to integrate Au nanoparticles and HKUST-1. In this strategy, Cu 2 O@HKUST-1 core-shell heterostructures, HKUST-1 nanocages, Cu 2 O@Au@HKUST-1 sandwich core-shell heterostructures and Au@HKUST-1 balls-in-cage heterostructures were successfully synthesized. Cu 2 O@HKUST-1 core-shell heterostructures were synthesized by soaking Cu 2 O nanocrystals in benzene-1,3,5-tricarboxylic acid solution. The well-defined Cu 2 O@HKUST-1 core-shell heterostructures were demonstrated to be dominated by the ratio of Cu 2+ cations to btc 3- ligands in solution during the period of HKUST-1 formation. Cu 2 O@Au@HKUST-1 sandwich core-shell or Au@HKUST-1 balls-in-cage heterostructures were obtained by impregnating HAuCl 4 into Cu 2 O@HKUST-1 core-shell heterostructures. Due to the porosity of HKUST-1 and reducibility of Cu 2 O, HAuCl 4 could pass through the HKUST-1 shell and be reduced by the Cu 2 O core in situ forming Au nanoparticles. Finally, CO oxidation reaction at high temperatures was carried out to assess the catalytic functionality of the obtained composite heterostructures. This strategy can circumvent some drawbacks of the existing approaches for integrating MNPs and MOFs, such as nonselective deposition of MNPs at the outer surface of the MOF matrices, extreme treatment conditions and additional surface modifications.

Influence of Au Nanoparticle Shape on Au@Cu2O Heterostructures

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Jie Zhu

2015-01-01

Full Text Available Synthesis of metal-semiconductor heterostructures may allow the combination of function of the corresponding components and/or the enhanced performance resulting from the interactions between all the components. In this paper, Au@Cu2O core-shell heterostructures are prepared by a seed-growth method, using different-shaped Au nanocrystals as the seeds such as nanorods, octahedra, decahedra, dots, and nanocubes. The results revealed that the final structure of Au@Cu2O was greatly influenced by the shape of the seeds used. Exposure of Cu2O{111} and Cu2O{001} favored when the overgrowth happened on Au{111} and Au{001} surface, respectively. The size of the product can also be tuned by the amount of the seeds. The results reported here provide a thinking clue to modulate the shape and size of core-shell nanocrystals, which is useful in developing new materials with desired performance.

First-principles theory of short-range order in size-mismatched metal alloys: Cu-Au, Cu-Ag, and Ni-Au

International Nuclear Information System (INIS)

Wolverton, C.; Ozolins, V.; Zunger, A.

1998-01-01

We describe a first-principles technique for calculating the short-range order (SRO) in disordered alloys, even in the presence of large anharmonic atomic relaxations. The technique is applied to several alloys possessing large size mismatch: Cu-Au, Cu-Ag, Ni-Au, and Cu-Pd. We find the following: (i) The calculated SRO in Cu-Au alloys peaks at (or near) the left-angle 100 right-angle point for all compositions studied, in agreement with diffuse scattering measurements. (ii) A fourfold splitting of the X-point SRO exists in both Cu 0.75 Au 0.25 and Cu 0.70 Pd 0.30 , although qualitative differences in the calculated energetics for these two alloys demonstrate that the splitting in Cu 0.70 Pd 0.30 may be accounted for by T=0 K energetics while T≠0 K configurational entropy is necessary to account for the splitting in Cu 0.75 Au 0.25 . Cu 0.75 Au 0.25 shows a significant temperature dependence of the splitting, in agreement with recent in situ measurements, while the splitting in Cu 0.70 Pd 0.30 is predicted to have a much smaller temperature dependence. (iii) Although no measurements exist, the SRO of Cu-Ag alloys is predicted to be of clustering type with peaks at the left-angle 000 right-angle point. Streaking of the SRO peaks in the left-angle 100 right-angle and left-angle 1 (1) /(2) 0 right-angle directions for Ag- and Cu-rich compositions, respectively, is correlated with the elastically soft directions for these compositions. (iv) Even though Ni-Au phase separates at low temperatures, the calculated SRO pattern in Ni 0.4 Au 0.6 , like the measured data, shows a peak along the left-angle ζ00 right-angle direction, away from the typical clustering-type left-angle 000 right-angle point. (v) The explicit effect of atomic relaxation on SRO is investigated and it is found that atomic relaxation can produce significant qualitative changes in the SRO pattern, changing the pattern from ordering to clustering type, as in the case of Cu-Ag. copyright 1998 The American

Geology, mineralization, geochemistry and petrology of intrusions in the Kuh Zar Au-Cu deposit, Damghan

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Payam Roohbakhsh

2018-04-01

Full Text Available Introduction Kuh Zar Au-Cu deposit is located in the central part of the Torud-Chah Shirin Volcanic-Plutonic Belt, 100 km southeast of the city of Damghan. Mineralization including quartz-base metal veins are common throughout this Cenozoic volcano-plutonic belt (Liaghat et al., 2008; Mehrabi and Ghasemi Siani, 2010. The major part of the study area is covered with Cenozoic pyroclastic and volcanic rocks that are intruded by subvolcanic rocks. This paper aims to study the geological, geochemical and petrogenesis of the area using exploration keys for new mineral deposits in the Torud-Chah Shirin zone. Materials and methods To better understand the geological units and identify the alteration zones of the area, 200 rock samples were collected from the field and 132 thin sections with 15 polished thin sections were prepared for petrography and mineralization studies. Ten samples of intrusions with the least alteration were analyzed using the XRF at the East Amethyst Laboratory in Mashhad, Iran. These samples were also analyzed for trace and rare earth elements using ICP-MS, following a lithium metaborate/tetraborate fusion in the Acme Analytical Laboratories Ltd, Vancouver, Canada. 137 geochemistry samples were prepared by the chip composite method of alteration and mineralization zones and were analyzed in the Acme laboratory by Aqua Regia AQ250. Results The geology of the area consists of pyroclastic (crystal tuff and volcanic rocks with andesite and latite composition, which were intruded by subvolcanic intrusive rocks with porphyritic texture and monzonitic composition. Monzonite rocks were intruded by younger subvolcanic units with dioritic composition. The intrusion of monzonitic pluton and stocks led to the formation of QSP, propylitic, carbonate and silicification-tourmaline broad alteration zones in the area. Monzonite rocks accompanied with disseminated mineralization of about 1 to 10% of pyrite and these sulfides have been converted to

Contrasting fluids and reservoirs in the contiguous Marcona and Mina Justa iron oxide-Cu (-Ag-Au) deposits, south-central Perú

Science.gov (United States)

Chen, Huayong; Kyser, T. Kurtis; Clark, Alan H.

2011-10-01

The Marcona-Mina Justa deposit cluster, hosted by Lower Paleozoic metaclastic rocks and Middle Jurassic shallow marine andesites, incorporates the most important known magnetite mineralization in the Andes at Marcona (1.9 Gt at 55.4% Fe and 0.12% Cu) and one of the few major iron oxide-copper-gold (IOCG) deposits with economic Cu grades (346.6 Mt at 0.71% Cu, 3.8 g/t Ag and 0.03 g/t Au) at Mina Justa. The Middle Jurassic Marcona deposit is centred in Ica Department, Perú, and the Lower Cretaceous Mina Justa Cu (Ag, Au) prospect is located 3-4 km to the northeast. New fluid inclusion studies, including laser ablation time-of-flight inductively coupled plasma mass spectrometry (LA-TOF-ICPMS) analysis, integrated with sulphur, oxygen, hydrogen and carbon isotope analyses of minerals with well-defined paragenetic relationships, clarify the nature and origin of the hydrothermal fluid responsible for these contiguous but genetically contrasted deposits. At Marcona, early, sulphide-free stage M-III magnetite-biotite-calcic amphibole assemblages are inferred to have crystallized from a 700-800°C Fe oxide melt with a δ18O value from +5.2‰ to +7.7‰. Stage M-IV magnetite-phlogopite-calcic amphibole-sulphide assemblages were subsequently precipitated from 430-600°C aqueous fluids with dominantly magmatic isotopic compositions (δ34S = +0.8‰ to +5.9‰; δ18O = +9.6‰ to +12.2‰; δD = -73‰ to -43‰; and δ13C = -3.3‰). Stages M-III and M-IV account for over 95% of the magnetite mineralization at Marcona. Subsequent non-economic, lower temperature sulphide-calcite-amphibole assemblages (stage M-V) were deposited from fluids with similar δ34S (+1.8‰ to +5.0‰), δ18O (+10.1‰ to +12.5‰) and δ13C (-3.4‰), but higher δD values (average -8‰). Several groups of lower (200°C) fluids can be recognized in the main polymetallic (Cu, Zn, Pb) sulphide stage M-V and may record the involvement of modified seawater. At Mina Justa, early magnetite

Influence of Au Nanoparticle Shape on Au@Cu2O Heterostructures

OpenAIRE

Zhu, Jie; Lu, Na; Chen, Wei; Kong, Lina; Yang, Yun; Ma, Dekun; Huang, Shaoming

2015-01-01

Synthesis of metal-semiconductor heterostructures may allow the combination of function of the corresponding components and/or the enhanced performance resulting from the interactions between all the components. In this paper, Au@Cu2O core-shell heterostructures are prepared by a seed-growth method, using different-shaped Au nanocrystals as the seeds such as nanorods, octahedra, decahedra, dots, and nanocubes. The results revealed that the final structure of Au@Cu2O was greatly influenced by ...

A Au/Cu2O-TiO2 system for photo-catalytic hydrogen production. A pn-junction effect or a simple case of in situ reduction?

KAUST Repository

Sinatra, Lutfan; LaGrow, Alec P.; Peng, Wei; Kirmani, Ahmad R.; Amassian, Aram; Idriss, Hicham; Bakr, Osman

2015-01-01

Photo-catalytic H2 production from water has been studied over Au-Cu2O nanoparticle deposited on TiO2 (anatase) in order to probe into both the plasmon resonance effect (Au nanoparticles) and the pn-junction at the Cu2O-TiO2 interface. The Au-Cu2O

Usability of #betta#-spectrometric method to prospecting for copper-porphyric skarn and gold-quartz-sulfide deposits

International Nuclear Information System (INIS)

Syromyatnikov, N.G.; Ivanova, Eh.I.; Karpukhin, V.G.; Trofimova, L.A.; Tolmachev, I.I.

1982-01-01

Possibility of the prospecting for non-radioactive element deposits by means of radioactive elements as indicators is studied. Radioactive elements (uranium, thorium and potassium) were determined by gamma spectroscopy. Radiometric methods of prospecting are effective and economical. Clark contents of radioelements in rocks were determined in situ by field gamma spectrometers. It is established that copper-porphyric deposits are regularly controlled from the surface by aureoles of increased uranium contents, which sizes reach 400x500 m and can be revealed by gamma spectroscopy during 1:25000 and more large-scale survey. Skarn-ore zones of deposits of different mineral types (copper, polymetallic, iron ore ones) are fixed on the surface by increased radioactivity; this fact can be used as search criterion. Gold-bearing quartz veins differ from barren lodes by a higher level of total radioactivity and high potassium content. Top walls of ore-bearing quartz veins are mainly enriched by radioelements

Fe-U-PGE-Au-Ag-Cu Deposits of the Udokan-Chiney Region (East Siberia, Russia)

Science.gov (United States)

Gongalskiy, B.; Krivolutskaya, N.; Murashov, K.; Nistratov, S.; Gryazev, S.

2012-04-01

Introduction. Cupriferous sandstones-shales and magmatic copper-nickel deposits mark out the western and southern boundaries of the Siberian Craton accordingly. Of special interest are the Paleoproterozoic deposits of the Udokan-Chiney mining district (Gongalskiy, Krivolutskaya, 2008). Copper reserves and resources of this region are estimated at more than 50 Mt. Half of them is concentrated at the unique Udokan Deposit and the second half is distributed among sedimentary (Unkur, Pravoingamakitskoye, Sakinskoye, Krasnoye, Burpala) and magmatic deposits of the Chiney (Rudnoye, Verkhnechineyskoye, Kontaktovoye), Luktur and Maylav massifs. Results. It was established that the ores are characterized by similarity in chemical composition (main, major and rare elements that are Ag, Au, PGE) and mineral assemblages with varying proportions. It is important to emphasize that Fe role in mineralization was previously ignored. Meanwhile the Udokan deposit contains 10 Mt of magnetite metacrystals so as chalcocite ores may contain up to 50% magnetite too. It has been recently found that the Chiney titanomagnetite ores comprise commercially significant uranium and rare-earth metal concentrations (Makaryev et al., 2011). Thus the Udokan-Chiney region comprises Cu, Fe, Ti, V, U, REE, Ag, Au, PGE. These deposits differ from similar objects, the Olympic Dam in particular, by a much smaller content of fluid-bearing minerals. Copper mineralization at the Udokan is represented by chalcocite-bornite ores. They occur as ore beds conformable with sedimentary structures or as cross-cutting veins. The central zones of the former are often brecciated. They are rimmed by fine magnetite, bornite, and chalcocite dissemination. Bornite-chalcopyrite and chalcopyrite-pyrite veins are known at the lower levels of the Udokan ore bed. Such ore compositions are predominant in other ore deposits in sedimentary rocks (Pravoingamakitskoye, Unkur) and have a hydrothermal origin. Silver grades are up to

Dual structural transition in small nanoparticles of Cu-Au alloy

Science.gov (United States)

Gafner, Yuri; Gafner, Svetlana; Redel, Larisa; Zamulin, Ivan

2018-02-01

Cu-Au alloy nanoparticles are known to be widely used in the catalysis of various chemical reactions as it was experimentally defined that in many cases the partial substitution of copper with gold increases catalytic activity. However, providing the reaction capacity of alloy nanoparticles the surface electronic structure strongly depends on their atomic ordering. Therefore, to theoretically determine catalytic properties, one needs to use a most real structural model complying with Cu-Au nanoparticles under various external influences. So, thermal stability limits were studied for the initial L12 phase in Cu3Au nanoalloy clusters up to 8.0 nm and Cu-Au clusters up to 3.0 nm at various degrees of Au atom concentration, with molecular dynamics method using a modified tight-binding TB-SMA potential. Dual structural transition L12 → FCC and further FCC → Ih is shown to be possible under the thermal factor in Cu3Au and Cu-Au clusters with the diameter up to 3.0 nm. The temperature of the structural transition FCC → Ih is established to decrease for small particles of Cu-Au alloy under the increase of Au atom concentration. For clusters with this structural transition, the melting point is found to be a linear increasing function of concentration, and for clusters without FCC → Ih structural transition, the melting point is a linear decreasing function of Au content. Thus, the article shows that doping Cu nanoclusters with Au atoms allows to control the forming structure as well as the melting point.

Nanocrystalline growth and grain-size effects in Au-Cu electrodeposits

International Nuclear Information System (INIS)

Jankowski, Alan F.; Saw, Cheng K.; Harper, Jennifer F.; Vallier, Bobby F.; Ferreira, James L.; Hayes, Jeffrey P.

2006-01-01

The processing-structure-property relationship is investigated for electrodeposited foils of the gold-copper alloy system. A model is presented that relates the deposition process parameters to the nanocrystalline grain size. An activation energy of 1.52 eV atom -1 for growth is determined for a long-pulse (> 10 msec) mode, and is 0.16 eV atom -1 for short pulses ( 6 nm) is observed for Au-Cu samples with 1-12 wt.% Cu as tested in cross-section. The hardness increases three-fold from a rule-of-mixtures value < 1 GPa to a maximum of 2.9 GPa

Geochemistry of rare earth elements in the Baba Ali magnetite skarn deposit, western Iran – a key to determine conditions of mineralisation

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Zamanian Hassan

2016-03-01

Full Text Available The Baba Ali skarn deposit, situated 39 km to the northwest of Hamadan (Iran, is the result of a syenitic pluton that intruded and metamorphosed the diorite host rock. Rare earth element (REE values in the quartz syenite and diorite range between 35.4 and 560 ppm. Although the distribution pattern of REEs is more and less flat and smooth, light REEs (LREEs in general show higher concentrations than heavy REEs (HREEs in different lithounits. The skarn zone reveals the highest REE-enriched pattern, while the ore zone shows the maximum depletion pattern. A comparison of the concentration variations of LREEs (La–Nd, middle REEs (MREEs; Sm–Ho and HREEs (Er–Lu of the ore zone samples to the other zones elucidates two important points for the distribution of REEs: 1 the distribution patterns of LREEs and MREEs show a distinct depletion in the ore zone while representing a great enrichment in the skarn facies neighbouring the ore body border and decreasing towards the altered diorite host rock; 2 HREEs show the same pattern, but in the exoskarn do not reveal any distinct increase as observed for LREEs and MREEs. The ratio of La/Y in the Baba Ali skarn ranges from 0.37 to 2.89. The ore zone has the highest La/Y ratio. In this regard the skarn zones exhibit two distinctive portions: 1 one that has La/Y >1 beingadjacent to the ore body and; 2 another one with La/Y < 1 neighbouring altered diorite. Accordingly, the Baba Ali profile, from the quartz syenite to the middle part of the exoskarn, demonstrates chiefly alkaline conditions of formation, with a gradual change to acidic towards the altered diorite host rocks. Utilising three parameters, Ce/Ce*, Eu/Eu* and (Pr/Ybn, in different minerals implies that the hydrothermal fluids responsible for epidote and garnet were mostly of magmatic origin and for magnetite, actinolite and phlogopite these were of magmatic origin with low REE concentration or meteoric water involved.

Energy and system size dependence of phi meson production in Cu+Cu and Au+Au collisions

Energy Technology Data Exchange (ETDEWEB)

STAR Coll

2008-10-28

We study the beam-energy and system-size dependence of {phi} meson production (using the hadronic decay mode {phi} {yields} K{sup +}K{sup -}) by comparing the new results from Cu + Cu collisions and previously reported Au + Au collisions at {radical}s{sub NN} = 62.4 and 200 GeV measured in the STAR experiment at RHIC. Data presented are from midrapidity (|y| < 0.5) for 0.4 < p{sub T} < 5 GeV/c. At a given beam energy, the transverse momentum distributions for {phi} mesons are observed to be similar in yield and shape for Cu + Cu and Au + Au colliding systems with similar average numbers of participating nucleons. The {phi} meson yields in nucleus-nucleus collisions, normalized by the average number of participating nucleons, are found to be enhanced relative to those from p + p collisions with a different trend compared to strange baryons. The enhancement for {phi} mesons is observed to be higher at {radical}s{sub NN} = 200 GeV compared to 62.4 GeV. These observations for the produced {phi}(s{bar s}) mesons clearly suggest that, at these collision energies, the source of enhancement of strange hadrons is related to the formation of a dense partonic medium in high energy nucleus-nucleus collisions and cannot be alone due to canonical suppression of their production in smaller systems.

Strata-bound Fe-Co-Cu-Au-Bi-Y-REE deposits of the Idaho Cobalt Belt: Multistage hydrothermal mineralization in a magmatic-related iron oxide copper-gold system

Science.gov (United States)

Slack, John F.

2012-01-01

Mineralogical and geochemical studies of strata-bound Fe-Co-Cu-Au-Bi-Y-rare-earth element (REE) deposits of the Idaho cobalt belt in east-central Idaho provide evidence of multistage epigenetic mineralization by magmatic-hydrothermal processes in an iron oxide copper-gold (IOCG) system. Deposits of the Idaho cobalt belt comprise three types: (1) strata-bound sulfide lenses in the Blackbird district, which are cobaltite and, less commonly, chalcopyrite rich with locally abundant gold, native bismuth, bismuthinite, xenotime, allanite, monazite, and the Be-rich silicate gadolinite-(Y), with sparse uraninite, stannite, and Bi tellurides, in a gangue of quartz, chlorite, biotite, muscovite, garnet, tourmaline, chloritoid, and/or siderite, with locally abundant fluorapatite or magnetite; (2) discordant tourmalinized breccias in the Blackbird district that in places have concentrations of cobaltite, chalcopyrite, gold, and xenotime; and (3) strata-bound magnetite-rich lenses in the Iron Creek area, which contain cobaltiferous pyrite and locally sparse chalcopyrite or xenotime. Most sulfide-rich deposits in the Blackbird district are enclosed by strata-bound lenses composed mainly of Cl-rich Fe biotite; some deposits have quartz-rich envelopes.Whole-rock analyses of 48 Co- and/or Cu-rich samples show high concentrations of Au (up to 26.8 ppm), Bi (up to 9.16 wt %), Y (up to 0.83 wt %), ∑REEs (up to 2.56 wt %), Ni (up to 6,780 ppm), and Be (up to 1,180 ppm), with locally elevated U (up to 124 ppm) and Sn (up to 133 ppm); Zn and Pb contents are uniformly low (≤821 and ≤61 ppm, respectively). Varimax factor analysis of bulk compositions of these samples reveals geochemically distinct element groupings that reflect statistical associations of monazite, allanite, and xenotime; biotite and gold; detrital minerals; chalcopyrite and sparse stannite; quartz; and cobaltite with sparse selenides and tellurides. Significantly, Cu is statistically separate from Co and As

Fabrication of a Cu{sub 2}O/Au/TiO{sub 2} composite film for efficient photocatalytic hydrogen production from aqueous solution of methanol and glucose

Energy Technology Data Exchange (ETDEWEB)

Wang, Xi; Dong, Haitai; Hu, Zhe; Qi, Zhong; Li, Laisheng, E-mail: llsh@scnu.edu.cn

2017-05-15

Highlights: • A Cu{sub 2}O/Au/TiO{sub 2} film was synthesized successfully. • Hydrogen production of Cu{sub 2}O/Au/TiO{sub 2} film improved significantly. • The highest hydrogen production rate of the film was 125.3 mmol/h/m{sup 2}. • A Z-scheme charge transfer pathway was proposed. - Abstract: A novel Cu{sub 2}O/Au/TiO{sub 2} photocatalyst composite film was fabricated on a copper substrate for photocatalytic hydrogen production. The composite films, Cu{sub 2}O/Au/TiO{sub 2}, were stepwise synthesized by using electrochemical deposition, photodeposition, and coating methods. First, a Cu{sub 2}O film was synthesized using the electrochemical deposition method, after which Au was deposited onto the Cu{sub 2}O film through in-site photodeposition. Finally, TiO{sub 2} was coated on the surface of the Cu{sub 2}O/Au film. Its morphology and surface chemical composition was characterized by SEM, TEM, XRD and XPS. The optical characteristics (UV–Vis DRS, PL spectrum) of the films were also examined. The photocatalytic hydrogen production rate of the Cu{sub 2}O/Au/TiO{sub 2} composite film from a 20% vol. methanol solution increased to125.3 mmol/h/m{sup 2} under 300 W xenon lamp light irradiation. Compared to the TiO{sub 2} (13.5 mmol/h/m{sup 2}) film and Cu{sub 2}O/TiO{sub 2} film (83.2 mmol/h/m{sup 2}), the Cu{sub 2}O/Au/TiO{sub 2} film showed excellent photocatalytic performance for hydrogen generation. The Cu{sub 2}O/Au/TiO{sub 2} film has highly effective photocatalytic properties, which are attributed to the Z-scheme system and can not only enhance the absorption of solar light but also suppress the recombination of photogenerated electron-hole pairs. It is worth noting that by introducing Au into the interface of Cu{sub 2}O/TiO{sub 2}, the surface plasmon resonance (SPR)-induced local electric field formed at the Au site induces a Z-scheme charge transfer pathway inside the composite film (Cu{sub 2}O/Au/TiO{sub 2}), which promotes both the charge of the

Multiphase formation of the Obří důl polymetallic skarn deposit, West Sudetes, Bohemian Massif: geochemistry and Re–Os dating of sulfide mineralization

Czech Academy of Sciences Publication Activity Database

Veselovský, F.; Ackerman, Lukáš; Pašava, J.; Žák, Karel; Haluzová, Eva; Creaser, R. A.; Dobeš, P.; Erban, V.; Tásler, R.

2018-01-01

Roč. 53, č. 5 (2018), s. 665-682 ISSN 0026-4598 R&D Projects: GA ČR GA13-15390S Institutional support: RVO:67985831 Keywords : Bohemian Massif * polymetallic skarn deposit * West Sudetes * arsenopyrite * Re–Os geochronology Subject RIV: DB - Geology ; Mineralogy OBOR OECD: Geology Impact factor: 3.396, year: 2016

Multiple Mesozoic mineralization events in South China—an introduction to the thematic issue

Science.gov (United States)

Hu, Rui-Zhong; Zhou, Mei-Fu

2012-08-01

Mesozoic mineral deposits in South China include world-class deposits of W, Sn and Sb and those that provide the major sources of Ta, Cu, Hg, As, Tl, Pb, Zn, Au and Ag for the entire country. These deposits can be classified into polymetallic hydrothermal systems closely related to felsic intrusive rocks (Sn-W -Mo granites, Cu porphyries, polymetallic and Fe skarns, and polymetallic vein deposits) and low-temperature hydrothermal systems with no direct connection to igneous activities (MVT deposits, epithermal Au and Sb deposits). Recent studies have shown that they formed in the Triassic (Indosinian), Jurassic-Cretaceous (Early Yanshanian), and Cretaceous (Late Yanshanian) stages. Indosinian deposits include major MVT (Pb-Zn-Ag) deposits and granite-related W-Sn deposits. Early Yanshanian deposits are low-temperature Sb-Au and high-temperature W-Sn and Cu porphyry types. Many Late Yanshanian deposits are low-temperature Au-As-Sb-Hg and U deposits, and also include high-temperature W-Sn polymetallic deposits. The formation of these deposits is linked with a specific tectonothermal evolution and igneous activities. This special issue brings together some of the latest information in eight papers that deal with the origins and tectonic environments of mineral deposits formed in these stages. We anticipate that this issue will stimulate more interests in these ore deposits in South China.

Specific composition of native silver from the Rogovik Au-Ag deposit, Northeastern Russia

Science.gov (United States)

Kravtsova, R. G.; Tauson, V. L.; Palyanova, G. A.; Makshakov, A. S.; Pavlova, L. A.

2017-09-01

The first data on native silver from the Rogovik Au-Ag deposit in northeastern Russia are presented. The deposit is situated in central part of the Okhotsk-Chukchi Volcanic Belt (OCVB) in the territory of the Omsukchan Trough, unique in its silver resources. Native silver in the studied ore makes up finely dispersed inclusions no larger than 50 μm in size, which are hosted in quartz; fills microfractures and interstices in association with küstelite, electrum, acanthite, silver sulfosalts and selenides, argyrodite, and pyrite. It has been shown that the chemical composition of native silver, along with its typomorphic features, is a stable indication of the various stages of deposit formation and types of mineralization: gold-silver (Au-Ag), silver-base metal (Ag-Pb), and gold-silver-base metal (Au-Ag-Pb). The specificity of native silver is expressed in the amount of trace elements and their concentrations. In Au-Ag ore, the following trace elements have been established in native silver (wt %): up to 2.72 S, up to 1.86 Au, up to 1.70 Hg, up to 1.75 Sb, and up to 1.01 Se. Native silver in Ag-Pb ore is characterized by the absence of Au, high Hg concentrations (up to 12.62 wt %), and an increase in Sb, Se, and S contents; the appearance of Te, Cu, Zn, and Fe is notable. All previously established trace elements—Hg, Au, Sb, Se, Te, Cu, Zn, Fe, and S—are contained in native silver of Au-Ag-Pb ore. In addition, Pb appears, and silver and gold amalgams are widespread, as well as up to 24.61 wt % Hg and 11.02 wt % Au. Comparison of trace element concentrations in native silver at the Rogovik deposit with the literature data, based on their solubility in solid silver, shows that the content of chalcogenides (S, Se, Te) exceeds saturated concentrations. Possible mechanisms by which elevated concentrations of these elements are achieved in native silver are discussed. It is suggested that the appearance of silver amalgams, which is unusual for Au-Ag mineralization

Melt recharge, f O2-T conditions, and metal fertility of felsic magmas: zircon trace element chemistry of Cu-Au porphyries in the Sanjiang orogenic belt, southwest China

Science.gov (United States)

Meng, Xuyang; Mao, Jingwen; Zhang, Changqing; Zhang, Dongyang; Liu, Huan

2018-06-01

The magmatic hydrothermal Pulang Cu deposit (Triassic) and the Beiya Au-Cu deposits (Eocene) are located in the Sanjiang copper porphyry belt, southwest China. Zircon chemistry was used to constrain the magmatic evolution and oxidation state of the porphyries. The results show that porphyries of the Beiya district formed from an early oxidized melt and a later relatively reduced and more evolved magma, whereas Pulang experienced a normal Cu porphyry evolutionary trend. The Pulang porphyries crystallized from more oxidized magma (ΔFMQ + 2.9-4.6, average = 4.0 ± 1.0, n = 3) with an average temperature of 709 ± 6 °C compared to the Beiya porphyries (ΔFMQ + 0.6-3.5, average = 1.9 ± 1.3, n = 5) with a mean magmatic temperature of 780 ± 22 °C. These data, combined with data from other Cu- and Au-rich porphyries in the Sanjiang belt (i.e., Machangjing Cu, Yao'an Au), are consistent with previous experimental work showing that elevated Cu and Au solubilities in magma require oxidizing conditions. A compilation of existing geochemical data for magmatic zircons from fertile and barren porphyry systems worldwide establishes an optimal diagnostic interval on CeIV/CeIII-TTi-in-zircon and (Eu/Eu*)N plots for generating magmatic hydrothermal Cu-Au deposits.

Geochemical Peculiarities of Galena and Sphalerite from Polymetallic Deposits of the Dal'negorskii Ore Region (Primorsky Krai, Russia)

Science.gov (United States)

Rogulina, L. I.; Moiseenko, V. G.; Ponomarchuk, V. A.

2018-04-01

New data on the composition of the major minerals from the skarn and vein polymetallic deposits of the Dal'negorskii ore region are reported. Analysis of galena and sphalerite was carried out by the X-ray fluorescent energy-dispersive method of synchrotron radiation for the first time. It is shown that the minor elements in major minerals of different deposits are typomorphic. Among these elements are Fe, Cu, Ni, Cd, Ag, Sn, and Sb, as well as In in sphalerite and Te in galena. The high concentrations of Ag, Cu, Te, Cd, and In in the extracted minerals indicate the complex character of mineralization. The compositional patterns of ore minerals characterize the sequence of mineral formation from the skarn to vein ores, and the sequence of deposits from the mesothermal to epithermal conditions. This provides geochemical evidence for the stage model of the formation of mineralization in the Dal'negorskii ore region.

Magmatic-hydrothermal fluid evolution of the Dalli porphyry Cu-Au deposit; using Amphibole and Plagioclas mineral chemistry

Directory of Open Access Journals (Sweden)

Houshang Pourkaseb

2017-07-01

Full Text Available Introduction The formation of porphyry copper deposits is attributed to the shallow emplacement, and subsequent cooling of the hydrothermal system of porphyritic intrusive rocks (Titley and Bean, 1981. These deposits have usually been developed along the chain of subduction-related volcanic and calc-alkalin batholiths (Sillitoe, 2010. Nevertheless, it is now confirmed that porphyry copper systems can also form in collisional and post collisional settings (Zarasvandi et al., 2015b. Detailed studies on the geochemical features of ore-hosting porphyry Cu-Mo-Au intrusions indicate that they are generally adakitic, water and sulfur- riched, and oxidized (Wang et al., 2014. For example, high oxygen fugacity of magma has decisive role in transmission of copper and gold to the porphyry systems as revealed in (Wang et al., 2014. In this regard, the present work deals with the mineral chemistry of amphibole and plagioclase in the Dalli porphyry Cu-Au deposit. The data is used to achieve the physical and chemical conditions of magma and its impact on mineralization. Moreover, the results of previous studies on the hydrothermal system of the Dalli deposit such as Raman laser spectroscopy and fluid inclusion studies are included for determination of the evolution from magmatic to hydrothermal conditions. Materials and methods In order to correctly characterize the physical and chemical conditions affecting the trend of mineralization, 20 least altered and fractured samples of diorite and quartz-diorite intrusions were chosen from boreholes. Subsequently, 20 thin-polished sections were prepared in the Shahid Chamran University of Ahvaz. Finally, mineral chemistry of amphibole and plagioclase were determined using electron micro probe analyses (EMPA in the central lab of the Leoben University. Results Amphibole that is one of the the main rock-forming minerals can form in a wide variety of igneous and metamorphic rocks. Accordingly, amphibole chemistry can be

Surface diffusion coefficient of Au atoms on single layer graphene grown on Cu

Energy Technology Data Exchange (ETDEWEB)

Ruffino, F., E-mail: francesco.ruffino@ct.infn.it; Cacciato, G.; Grimaldi, M. G. [Dipartimento di Fisica ed Astronomia-Universitá di Catania, via S. Sofia 64, 95123 Catania, Italy and MATIS IMM-CNR, via S. Sofia 64, 95123 Catania (Italy)

2014-02-28

A 5 nm thick Au film was deposited on single layer graphene sheets grown on Cu. By thermal processes, the dewetting phenomenon of the Au film on the graphene was induced so to form Au nanoparticles. The mean radius, surface-to-surface distance, and surface density evolution of the nanoparticles on the graphene sheets as a function of the annealing temperature were quantified by scanning electron microscopy analyses. These quantitative data were analyzed within the classical mean-field nucleation theory so to obtain the temperature-dependent Au atoms surface diffusion coefficient on graphene: D{sub S}(T)=[(8.2±0.6)×10{sup −8}]exp[−(0.31±0.02(eV)/(at) )/kT] cm{sup 2}/s.

Centrality, Rapidity And Transverse-Momentum Dependence of Cold Nuclear Matter Effects on J/Psi Production in D Au, Cu Cu And Au Au Collisions at S(NN)**(1/2)

Energy Technology Data Exchange (ETDEWEB)

Ferreiro, E.G.; /Santiago de Compostela U.; Fleuret, F.; /Ecole Polytechnique; Lansberg, J.P.; /Ecole Polytechnique /SLAC; Rakotozafindrabe, A.; /SPhN, DAPNIA, Saclay

2011-11-11

We have carried out a wide study of Cold Nuclear Matter (CNM) effects on J/{Psi} = production in dAu, CuCu and AuAu collisions at {radical}s{sub NN} = 200 GeV. We have studied the effects of three different gluon-shadowing parameterizations, using the usual simplified kinematics for which the momentum of the gluon recoiling against the J/{Psi} is neglected as well as an exact kinematics for a 2 {yields} 2 process, namely g + g {yields} J/{psi} + g as expected from LO pQCD. We have shown that the rapidity distribution of the nuclear modification factor R{sub dAu}, and particularly its anti-shadowing peak, is systematically shifted toward larger rapidities in the 2 {yields} 2 kinematics, irrespective of which shadowing parameterization is used. In turn, we have noted differences in the effective final-state nuclear absorption needed to fit the PHENIX dAu data. Taking advantage of our implementation of a 2 {yields} 2 kinematics, we have also computed the transverse momentum dependence of the nuclear modification factor, which cannot be predicted with the usual simplified kinematics. All the corresponding observables have been computed for CuCu and AuAu collisions and compared to the PHENIX and STAR data. Finally, we have extracted the effective nuclear absorption from the recent measurements of RCP in dAu collisions by the PHENIX collaboration.

J /ψ production at low pT in Au + Au and Cu + Cu collisions at √sNN =200 GeV with the STAR detector

Science.gov (United States)

Adamczyk, L.; Adkins, J. K.; Agakishiev, G.; Aggarwal, M. M.; Ahammed, Z.; Alekseev, I.; Alford, J.; Anson, C. D.; Aparin, A.; Arkhipkin, D.; Aschenauer, E. C.; Averichev, G. S.; Banerjee, A.; Beavis, D. R.; Bellwied, R.; Bhasin, A.; Bhati, A. K.; Bhattarai, P.; Bichsel, H.; Bielcik, J.; Bielcikova, J.; Bland, L. C.; Bordyuzhin, I. G.; Borowski, W.; Bouchet, J.; Brandin, A. V.; Brovko, S. G.; Bültmann, S.; Bunzarov, I.; Burton, T. P.; Butterworth, J.; Caines, H.; Calderón de la Barca Sánchez, M.; Campbell, J. M.; Cebra, D.; Cendejas, R.; Cervantes, M. C.; Chaloupka, P.; Chang, Z.; Chattopadhyay, S.; Chen, H. F.; Chen, J. H.; Chen, L.; Cheng, J.; Cherney, M.; Chikanian, A.; Christie, W.; Chwastowski, J.; Codrington, M. J. M.; Contin, G.; Cramer, J. G.; Crawford, H. J.; Cui, X.; Das, S.; Davila Leyva, A.; De Silva, L. C.; Debbe, R. R.; Dedovich, T. G.; Deng, J.; Derevschikov, A. A.; Derradi de Souza, R.; di Ruzza, B.; Didenko, L.; Dilks, C.; Ding, F.; Djawotho, P.; Dong, X.; Drachenberg, J. L.; Draper, J. E.; Du, C. M.; Dunkelberger, L. E.; Dunlop, J. C.; Efimov, L. G.; Engelage, J.; Engle, K. S.; Eppley, G.; Eun, L.; Evdokimov, O.; Eyser, O.; Fatemi, R.; Fazio, S.; Fedorisin, J.; Filip, P.; Fisyak, Y.; Flores, C. E.; Gagliardi, C. A.; Gangadharan, D. R.; Garand, D.; Geurts, F.; Gibson, A.; Girard, M.; Gliske, S.; Greiner, L.; Grosnick, D.; Gunarathne, D. S.; Guo, Y.; Gupta, A.; Gupta, S.; Guryn, W.; Haag, B.; Hamed, A.; Han, L.-X.; Haque, R.; Harris, J. W.; Heppelmann, S.; Hirsch, A.; Hoffmann, G. W.; Hofman, D. J.; Horvat, S.; Huang, B.; Huang, H. Z.; Huang, X.; Huck, P.; Humanic, T. J.; Igo, G.; Jacobs, W. W.; Jang, H.; Judd, E. G.; Kabana, S.; Kalinkin, D.; Kang, K.; Kauder, K.; Ke, H. W.; Keane, D.; Kechechyan, A.; Kesich, A.; Khan, Z. H.; Kikola, D. P.; Kisel, I.; Kisiel, A.; Koetke, D. D.; Kollegger, T.; Konzer, J.; Koralt, I.; Kosarzewski, L. K.; Kotchenda, L.; Kraishan, A. F.; Kravtsov, P.; Krueger, K.; Kulakov, I.; Kumar, L.; Kycia, R. A.; Lamont, M. A. C.; Landgraf, J. M.; Landry, K. D.; Lauret, J.; Lebedev, A.; Lednicky, R.; Lee, J. H.; Li, C.; Li, W.; Li, X.; Li, X.; Li, Y.; Li, Z. M.; Lisa, M. A.; Liu, F.; Ljubicic, T.; Llope, W. J.; Lomnitz, M.; Longacre, R. S.; Luo, X.; Ma, G. L.; Ma, Y. G.; Mahapatra, D. P.; Majka, R.; Margetis, S.; Markert, C.; Masui, H.; Matis, H. S.; McDonald, D.; McShane, T. S.; Minaev, N. G.; Mioduszewski, S.; Mohanty, B.; Mondal, M. M.; Morozov, D. A.; Mustafa, M. K.; Nandi, B. K.; Nasim, Md.; Nayak, T. K.; Nelson, J. M.; Nigmatkulov, G.; Nogach, L. V.; Noh, S. Y.; Novak, J.; Nurushev, S. B.; Odyniec, G.; Ogawa, A.; Oh, K.; Ohlson, A.; Okorokov, V.; Oldag, E. W.; Olvitt, D. L.; Page, B. S.; Pan, Y. X.; Pandit, Y.; Panebratsev, Y.; Pawlak, T.; Pawlik, B.; Pei, H.; Perkins, C.; Pile, P.; Planinic, M.; Pluta, J.; Poljak, N.; Poniatowska, K.; Porter, J.; Poskanzer, A. M.; Powell, C. B.; Pruthi, N. K.; Przybycien, M.; Putschke, J.; Qiu, H.; Quintero, A.; Ramachandran, S.; Raniwala, R.; Raniwala, S.; Ray, R. L.; Riley, C. K.; Ritter, H. G.; Roberts, J. B.; Rogachevskiy, O. V.; Romero, J. L.; Ross, J. F.; Roy, A.; Ruan, L.; Rusnak, J.; Rusnakova, O.; Sahoo, N. R.; Sahu, P. K.; Sakrejda, I.; Salur, S.; Sandweiss, J.; Sangaline, E.; Sarkar, A.; Schambach, J.; Scharenberg, R. P.; Schmah, A. M.; Schmidke, W. B.; Schmitz, N.; Seger, J.; Seyboth, P.; Shah, N.; Shahaliev, E.; Shanmuganathan, P. V.; Shao, M.; Sharma, B.; Shen, W. Q.; Shi, S. S.; Shou, Q. Y.; Sichtermann, E. P.; Simko, M.; Skoby, M. J.; Smirnov, D.; Smirnov, N.; Solanki, D.; Sorensen, P.; Spinka, H. M.; Srivastava, B.; Stanislaus, T. D. S.; Stevens, J. R.; Stock, R.; Strikhanov, M.; Stringfellow, B.; Sumbera, M.; Sun, X.; Sun, X. M.; Sun, Y.; Sun, Z.; Surrow, B.; Svirida, D. N.; Symons, T. J. M.; Szelezniak, M. A.; Takahashi, J.; Tang, A. H.; Tang, Z.; Tarnowsky, T.; Thomas, J. H.; Timmins, A. R.; Tlusty, D.; Tokarev, M.; Trentalange, S.; Tribble, R. E.; Tribedy, P.; Trzeciak, B. A.; Tsai, O. D.; Turnau, J.; Ullrich, T.; Underwood, D. G.; Van Buren, G.; van Nieuwenhuizen, G.; Vandenbroucke, M.; Vanfossen, J. A.; Varma, R.; Vasconcelos, G. M. S.; Vasiliev, A. N.; Vertesi, R.; Videbæk, F.; Viyogi, Y. P.; Vokal, S.; Vossen, A.; Wada, M.; Wang, F.; Wang, G.; Wang, H.; Wang, J. S.; Wang, X. L.; Wang, Y.; Wang, Y.; Webb, G.; Webb, J. C.; Westfall, G. D.; Wieman, H.; Wissink, S. W.; Witt, R.; Wu, Y. F.; Xiao, Z.; Xie, W.; Xin, K.; Xu, H.; Xu, J.; Xu, N.; Xu, Q. H.; Xu, Y.; Xu, Z.; Yan, W.; Yang, C.; Yang, Y.; Yang, Y.; Ye, Z.; Yepes, P.; Yi, L.; Yip, K.; Yoo, I.-K.; Yu, N.; Zbroszczyk, H.; Zha, W.; Zhang, J. B.; Zhang, J. L.; Zhang, S.; Zhang, X. P.; Zhang, Y.; Zhang, Z. P.; Zhao, F.; Zhao, J.; Zhong, C.; Zhu, X.; Zhu, Y. H.; Zoulkarneeva, Y.; Zyzak, M.; STAR Collaboration

2014-08-01

The J /ψ pT spectrum and nuclear modification factor (RAA) are reported for pT<5GeV /c and |y|<1 from 0% to 60% central Au +Au and Cu +Cu collisions at √sNN =200GeV at STAR. A significant suppression of pT-integrated J /ψ production is observed in central Au +Au events. The Cu +Cu data are consistent with no suppression, although the precision is limited by the available statistics. RAA in Au +Au collisions exhibits a strong suppression at low transverse momentum and gradually increases with pT. The data are compared to high-pT STAR results and previously published BNL Relativistic Heavy Ion Collider results. Comparing with model calculations, it is found that the invariant yields at low pT are significantly above hydrodynamic flow predictions but are consistent with models that include color screening and regeneration.

Enhanced catalyst activity by decorating of Au on Ag@Cu2O nanoshell

Science.gov (United States)

Chen, Lei; Liu, Maomao; Zhao, Yue; Kou, Qiangwei; Wang, Yaxin; Liu, Yang; Zhang, Yongjun; Yang, Jinghai; Jung, Young Mee

2018-03-01

We successfully synthesized Au-decorated Ag@Cu2O heterostructures via a simple galvanic replacement method. As the Au precursor concentration increased, the density of the Au nanoparticles (NPs) on the Ag@Cu2O surface increased, which changed the catalytic activity of the Ag@Cu2O-Au structure. The combination of Au, Ag, and Cu2O exhibited excellent catalytic properties, which can further effect on the catalyst activity of the Ag@Cu2O-Au structure. In addition, the proposed Ag@Cu2O-Au nanocomposite was used to transform the organic, toxic pollutant, 4-nitrophenol (4-NP), into its nontoxic and medicinally important amino derivative via a catalytic reduction to optimize the material performance. The proposed Au-decorated Ag@Cu2O exhibited excellent catalytic activity, and the catalytic reduction time greatly decreased (5 min). Thus, three novel properties of Ag@Cu2O-Au, i.e., charge redistribution and transfer, adsorption, and catalytic reduction of organic pollutants, were ascertained for water remediation. The proposed catalytic properties have potential applications for photocatalysis and localized surface plasmon resonance (LSPR)- and peroxidase-like catalysis.

Crystal Structural Effect of AuCu Alloy Nanoparticles on Catalytic CO Oxidation

International Nuclear Information System (INIS)

Zhan, Wangcheng; Wang, Jinglin; Wang, Haifeng; Zhang, Jinshui; Liu, Xiaofei

2017-01-01

Controlling the physical and chemical properties of alloy nanoparticles (NPs) is an important approach to optimize NP catalysis. Unlike other tuning knobs, such as size, shape, and composition, crystal structure has received limited attention and not been well understood for its role in catalysis. This deficiency is mainly due to the difficulty in synthesis and fine-tuning of the NPs’ crystal structure. Here, Exemplifying by AuCu alloy NPs with face centered cubic (fcc) and face centered tetragonal (fct) structure, we demonstrate a remarkable difference in phase segregation and catalytic performance depending on the crystal structure. During the thermal treatment in air, the Cu component in fcc-AuCu alloy NPs segregates more easily onto the alloy surface as compared to that in fct-AuCu alloy NPs. As a result, after annealing at 250 °C in air for 1 h, the fcc- and fct-AuCu alloy NPs are phase transferred into Au/CuO and AuCu/CuO core/shell structures, respectively. More importantly, this variation in heterostructures introduces a significant difference in CO adsorption on two catalysts, leading to a largely enhanced catalytic activity of AuCu/CuO NP catalyst for CO oxidation. Furthermore, the same concept can be extended to other alloy NPs, making it possible to fine-tune NP catalysis for many different chemical reactions.

Crystal Structural Effect of AuCu Alloy Nanoparticles on Catalytic CO Oxidation

Energy Technology Data Exchange (ETDEWEB)

Zhan, Wangcheng [East China Univ. of Science and Technology, Shanghai (China); Wang, Jinglin [East China Univ. of Science and Technology, Shanghai (China); Wang, Haifeng [East China Univ. of Science and Technology, Shanghai (China); Zhang, Jinshui [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Liu, Xiaofei [East China Univ. of Science and Technology, Shanghai (China); Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Zhang, Pengfei [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Chi, Miaofang [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Guo, Yanglong [East China Univ. of Science and Technology, Shanghai (China); Guo, Yun [East China Univ. of Science and Technology, Shanghai (China); Lu, Guanzhong [East China Univ. of Science and Technology, Shanghai (China); Sun, Shouheng [Brown Univ., Providence, RI (United States); Dai, Sheng [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Univ. of Tennessee, Knoxville, TN (United States); Zhu, Huiyuan [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2017-06-07

Controlling the physical and chemical properties of alloy nanoparticles (NPs) is an important approach to optimize NP catalysis. Unlike other tuning knobs, such as size, shape, and composition, crystal structure has received limited attention and not been well understood for its role in catalysis. This deficiency is mainly due to the difficulty in synthesis and fine-tuning of the NPs’ crystal structure. Here, Exemplifying by AuCu alloy NPs with face centered cubic (fcc) and face centered tetragonal (fct) structure, we demonstrate a remarkable difference in phase segregation and catalytic performance depending on the crystal structure. During the thermal treatment in air, the Cu component in fcc-AuCu alloy NPs segregates more easily onto the alloy surface as compared to that in fct-AuCu alloy NPs. As a result, after annealing at 250 °C in air for 1 h, the fcc- and fct-AuCu alloy NPs are phase transferred into Au/CuO and AuCu/CuO core/shell structures, respectively. More importantly, this variation in heterostructures introduces a significant difference in CO adsorption on two catalysts, leading to a largely enhanced catalytic activity of AuCu/CuO NP catalyst for CO oxidation. Furthermore, the same concept can be extended to other alloy NPs, making it possible to fine-tune NP catalysis for many different chemical reactions.

Evolution of borate minerals from contact metamorphic to hydrothermal stages: Ludwigite-group minerals and szaibélyite from the Vysoká - Zlatno skarn, Slovakia

Science.gov (United States)

Bilohuščin, Vladimír; Uher, Pavel; Koděra, Peter; Milovská, Stanislava; Mikuš, Tomáš; Bačík, Peter

2017-09-01

Borate minerals of the ludwigite group (LGM) and szaibélyite in association with hydroxylclinohumite, clinochlore, a serpentine mineral, magnesian magnetite, spinel, magnesite, dolomite and sulphide minerals, occur in a magnesian exoskarn in the R-20 borehole located in the Vysoká - Zlatno Cu-Au porphyry-skarn deposit, located within the Štiavnica Neogene stratovolcano, Western Carpathians, central Slovakia. The skarn is developed along the contact of Miocene granodiorite to quartz-diorite porphyry and a Middle-Upper Triassic dolomite-shale-psammite-anhydrite sedimentary sequence. The boron minerals were investigated by electron probe micro-analyser (EPMA) and micro-Raman techniques. The source of boron could have been from the granodiorite/quartz diorite intrusion; however some supply of B from adjacent evaporite-bearing sediments is also possible. Based on textural and compositional data, the minerals originated during two stages. (1) An early high-temperature, contact-metamorphic and metasomatic stage comprises coarse-crystalline aggregate of LGM (types 1 to 3) in association with hydroxylclinohumite, magnetite, and rarely spinel inclusions in LGM. Compositional variations of LGM show a crystallization sequence from early azoproite [≤17 wt% TiO2; 0.40 atoms pre formula unit (apfu) Ti, which correspond to ≤79 mol% of the Mg2(Mg0.5Ti0.5)O2(BO3) end-member], Ti-Al-rich members of LGM, "aluminoludwigite "[≤14 wt% Al2O3; ≤0.53 apfu, ≤53 mol% of Mg2AlO2(BO3) end-member] and Al-rich ludwigite in the central zone of crystals, to Ti-Al-poor ludwigite in outer parts of crystals. (2) Minerals of the late retrograde serpentinization and hydrothermal stage form irregular veinlets and aggregates, including partial alteration of hydroxylclinohumite to the serpentine-group mineral and clinochlore, replacement of LGM by szaibélyite, formation of the latest generation of Fe-rich, Ti-Al poor ludwigite in veinlets (type 4), and precipitation of dolomite, magnesite and

Skarn and ore formation at Seriphos, Greece as a consequence of granodiorite intrusion

NARCIS (Netherlands)

Salemink, J.

1985-01-01

On the island of Seriphos, Greece, the shallow intrusion of a granodiorite pluton into a series of previously regionally metamorphosed gneisses, marbles and marble-bearing schists produced a contact metamorphic aureole and extensive deposits of Ca-Fe-Mg skarns and Fe-ores. Structural and

Synthesis and characterization in AuCu–Si nanostructures

International Nuclear Information System (INIS)

Novelo, T.E.; Amézaga-Madrid, P.; Maldonado, R.D.; Oliva, A.I.; Alonzo-Medina, G.M.

2015-01-01

Au/Cu bilayers with different Au:Cu concentrations (25:75, 50:50 and 75:25 at.%) were deposited on Si(100) substrates by thermal evaporation. The thicknesses of all Au/Cu bilayers were 150 nm. The alloys were prepared by thermal diffusion into a vacuum oven with argon atmosphere at 690 K during 1 h. X-ray diffraction analysis revealed different phases of AuCu and CuSi alloys in the samples after annealing process. CuSi alloys were mainly obtained for 25:75 at.% samples, meanwhile the AuCuII phase dominates for samples prepared with 50:50 at.%. Additionally, the Au:Cu alloys with 75:25 at.%, produce Au 2 Cu 3 and Au 3 Cu phases. The formed alloys were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS) to study the morphology and the elemental concentration of the formed alloys. - Highlights: • AuCu/Si alloy thin films were prepared by thermal diffusion. • Alloys prepared with 50 at.% of Au produce the AuCuII phase. • Alloys prepared with 75 at.% of Au produce Au 3 Cu and Au 2 Cu 3 phases. • All alloys present diffusion of Si and Cu through the CuSi alloy formation

Ultrasonic friction power during thermosonic Au and Cu ball bonding

International Nuclear Information System (INIS)

Shah, A; Mayer, M; Zhou, Y; Qin, I; Huynh, C; Meyer, M

2010-01-01

The ultrasonic friction power during thermosonic ball bonding with Au and Cu wires, both 25 μm in diameter, is derived with an improved method from experimental measurements during the bonding process. Experimental data include the current delivered to the ultrasonic transducer and the tangential force measured using piezoresistive microsensors integrated close to the Al bonding pad. The improvement results from a new, more accurate method to derive the mechanical compliance of the ultrasonic system. The method employs a bond process modification in which the ultrasonic current is ramped up sequentially in three steps. In the first two steps, the ultrasonic current is set to levels that are too low to cause sliding. The bonding takes place during the third step, when the current is ramped up to the optimum value required for making good quality bonds. The ultrasonic compliance values are derived from the first two steps and are 8.2 ± 0.5 μm N -1 and 7.7 ± 0.5 μm N -1 for the Au and Cu processes, respectively. These values are determined within an average error estimate of ±6%, substantially lower than the ±10% estimated with a previously reported method. The ultrasonic compliance in the case of Au is 6% higher due to the lower elastic modulus of Au compared with that of Cu. Typical maximum values of relative sliding amplitude of ultrasonic friction at the interface are 655 nm and 766 nm for the Au and Cu processes. These values are 81% of the free-air vibration amplitude of the bonding capillary tip for the respective ultrasonic current settings. Due to bond growth, which damps relative motion between the ball and the pad, the final relative amplitude at the bond interface is reduced to 4% of the equivalent free-air amplitude. Even though the maximum value of relative amplitude is 17% higher in the Cu process compared with the Au process, the average total interfacial sliding is 519 μm in the Cu process, which is 31% lower than that in the Au process (759 �

New geologic, fluid inclusion and stable isotope studies on the controversial Igarapé Bahia Cu-Au deposit, Carajás Province, Brazil

Science.gov (United States)

Dreher, Ana M.; Xavier, Roberto P.; Taylor, Bruce E.; Martini, Sérgio L.

2008-02-01

The Igarapé Bahia Cu-Au deposit in the Carajás Province, Brazil, is hosted by steeply dipping metavolcano-sedimentary rocks of the Igarapé Bahia Group. This group consists of a low greenschist grade unit of the Archean (˜2,750 Ma) Itacaiúnas Supergroup, in which other important Cu-Au and iron ore deposits of the Carajás region are also hosted. The orebody at Igarapé Bahia is a fragmental rock unit situated between chloritized basalt, with associated hyaloclastite, banded iron formation (BIF), and chert in the footwall and mainly coarse- to fine-grained turbidites in the hanging wall. The fragmental rock unit is a nearly concordant, 2 km long and 30-250 m thick orebody made up of heterolithic, usually matrix-supported rocks composed mainly of coarse basalt, BIF, and chert clasts derived from the footwall unit. Mineralization is confined to the fine-grained matrix and comprises disseminated to massive chalcopyrite accompanied by magnetite, gold, U- and light rare earth element (LREE)-minerals, and minor other sulfides like bornite, molybdenite, cobaltite, digenite, and pyrite. Gangue minerals include siderite, chlorite, amphibole, tourmaline, quartz, stilpnomelane, epidote, and apatite. A less important mineralization style at Igarapé Bahia is represented by late quartz-chalcopyrite-calcite veins that crosscut all rocks in the deposit area. Fluid inclusions trapped in a quartz cavity in the ore unit indicate that saline aqueous fluids (5 to 45 wt% NaCl + CaCl2 equiv), together with carbonic (CO2 ± CH4) and low-salinity aqueous carbonic (6 wt% NaCl equiv) fluids, were involved in the mineralization process. Carbonates from the fragmental layer have δ13C values from -6.7 to -13.4 per mil that indicate their origin from organic and possibly also from magmatic carbon. The δ34S values for chalcopyrite range from -1.1 to 5.6 per mil with an outlier at -10.8 per mil, implying that most sulfur is magmatic or leached from magmatic rocks, whereas a limited

Nature, diversity of deposit types and metallogenic relations of South China

Science.gov (United States)

Zaw, K.; Peters, S.G.; Cromie, P.; Burrett, C.; Hou, Z.

2007-01-01

the 'Northern Golden Triangle' of China. These deposits are mostly epigenetic hydrothermal micron-disseminated gold deposits with associated As, Hg, Sb + Tl mineralisation similar to Carlin-type deposits in USA. The important deposits in the Southern Golden Triangle are Jinfeng (Lannigou), Zimudang, Getang, Yata and Banqi in Guizhou Province, and the Jinya and Gaolong deposits in Guangxi District. The most important deposits in the Northern Golden Triangle are the Dongbeizhai and Qiaoqiaoshang deposits. Many porphyry-related polymetallic copper-lead-zinc and gold skarn deposits occur in South China. These deposits are related to Indosinian (Triassic) and Yanshanian (Jurassic to Cretaceous) magmatism associated with collision of the South China and North China Cratons and westward subduction of the Palaeo-Pacific Plate. Most of these deposits are distributed along the Lower to Middle Yangtze River metallogenic belt. The most significant deposits are Tonglushan, Jilongshan, Fengshandong, Shitouzui and Jiguanzui. Au-(Ag-Mo)-rich porphyry-related Cu-Fe skarn deposits are also present (Chengmenshan and Wushan in Jiangxi Province and Xinqiao, Mashan-Tianmashan, Shizishan and Huangshilaoshan in Anhui Province). The South China fold belt extending from Fujian to Zhejiang Provinces is characterised by well-developed Yanshanian intrusive to subvolcanic rocks associated with porphyry to epithermal type mineralisation and mesothermal vein deposits. The largest porphyry copper deposit in China, Dexing, occurs in Jiangxi Province and is hosted by Yanshanian granodiorite. The high-sulphidation epithermal system occurs at the Zijinshan district in Fujian Province and epithermal to mesothermal vein-type deposits are also found in the Zhejiang Province (e.g., Zhilingtou). Part of Shandong Province is located at the northern margin of the South China Craton and the province has unique world class granite-hosted orogenic gold deposits. Occurrences of Pt-Pd-Ni-Cu-Co are found in Permian

Cu and Cu(Mn) films deposited layer-by-layer via surface-limited redox replacement and underpotential deposition

Energy Technology Data Exchange (ETDEWEB)

Fang, J.S., E-mail: jsfang@nfu.edu.tw [Department of Materials Science and Engineering, National Formosa University, Huwei 63201, Taiwan (China); Sun, S.L. [Department of Materials Science and Engineering, National Formosa University, Huwei 63201, Taiwan (China); Cheng, Y.L. [Department of Electrical Engineering, National Chi-Nan University, Nan-Tou 54561, Taiwan (China); Chen, G.S.; Chin, T.S. [Department of Materials Science and Engineering, Feng Chia University, Taichung 40724, Taiwan (China)

2016-02-28

Graphical abstract: - Abstract: The present paper reports Cu and Cu(Mn) films prepared layer-by-layer using an electrochemical atomic layer deposition (ECALD) method. The structure and properties of the films were investigated to elucidate their suitability as Cu interconnects for microelectronics. Previous studies have used primarily a vacuum-based atomic layer deposition to form a Cu metallized film. Herein, an entirely wet chemical process was used to fabricate a Cu film using the ECALD process by combining underpotential deposition (UPD) and surface-limited redox replacement (SLRR). The experimental results indicated that an inadequate UPD of Pb affected the subsequent SLRR of Cu and lead to the formation of PbSO{sub 4}. A mechanism is proposed to explain the results. Layer-by-layer deposition of Cu(Mn) films was successfully performed by alternating the deposition cycle-ratios of SLRR-Cu and UPD-Mn. The proposed self-limiting growth method offers a layer-by-layer wet chemistry-based deposition capability for fabricating Cu interconnects.

Microstructural evaluation of interfacial intermetallic compounds in Cu wire bonding with Al and Au pads

International Nuclear Information System (INIS)

Kim, Hyung Giun; Kim, Sang Min; Lee, Jae Young; Choi, Mi Ri; Choe, Si Hyun; Kim, Ki Hong; Ryu, Jae Sung; Kim, Sangshik; Han, Seung Zeon; Kim, Won Yong; Lim, Sung Hwan

2014-01-01

A comparative study on the difference in interfacial behavior of thermally aged Cu wire bonding with Al and Au pads was conducted using transmission electron microscopy. During high-temperature lifetime testing of Cu wire bonding with Al and Au pads at 175 °C for up to 2000 h, different growth rates and growth characteristics were investigated in the Cu–Al intermetallic compounds (IMCs), including CuAl 2 , CuAl and Cu 9 Al 4 , and in the Cu–Au IMCs, including (Au,Cu), Cu 3 Au and (Cu,Au). Because of the lower growth rates and greater ductility of Cu–Au IMCs compared to those of Cu–Al IMCs, the Cu wire bonding with the Au pad showed relatively better thermal aging properties of bond pull strength and ball shear strength than those with the Al pad counterpart. In this study, the coherent interfaces were found to retard the growth of IMCs, and a variety of orientation relationships between wire, pad and interfacial IMCs were identified

The discovery and geophysical response of the Atlántida Cu-Au porphyry deposit, Chile

Science.gov (United States)

Hope, Matthew; Andersson, Steve

2016-03-01

The discovery of the Atlántida Cu-Au-Mo porphyry deposit, which is unconformably overlain by 25-80 m of gravels, is a recent example of exploration success under cover in a traditional mining jurisdiction. Early acquisition of geophysics was a key tool in the discovery, and in later guiding further exploration drilling throughout the life of the project. Detailed review of the geophysical response of the deposit, with respect to the distribution of lithologies and alteration, coupled with their petrophysical properties has allowed full characterisation, despite no exposure at the surface of host rock nor porphyry-style mineralisation. Data acquired over the project include induced polarisation, magnetotellurics, ground and airborne magnetics, ground-based gravimetry, and petrophysical sampling. The distribution of the key geological features of the deposit has been inferred via acquisition of petrophysical properties and interpretation of surface geophysical datasets. Magnetic susceptibility is influenced strongly by both alteration and primary lithology, whilst density variations are dominated by primary lithological control. Several studies have shown that electrical properties may map the footprint of the hydrothermal system and associated mineralisation, via a combination of chargeability and resistivity. These properties are observed in geophysical datasets acquired at surface and allow further targeting and sterilisation at the deposit and project scale. By understanding these geophysical characteristics in a geological context, these data can be used to infer distribution of lithological units, depth to exploration targets and the potential for high grade mineralisation. Future exploration will likely be increasingly reliant on the understanding of the surface manifestations of buried deposits in remotely acquired data. This review summarises the application and results of these principles at the Atlántida project of northern Chile. Geophysical data can be

Zircon U-Pb and molybdenite Re-Os geochronology and geological significance of the Baoshan porphyry Cu polymetallic deposit in Jiangxi province

Science.gov (United States)

Jia, Liqiong; Wang, Liang

2017-10-01

Baoshan porphyry Cu polymetallic deposit belongs to Jiujiang-Ruichang Cu-Au ore field, which is a component part of the Middle-Lower Yangtze River Cu-Au metallogenic belt. The U-Pb LA-MC-TCP MS dating of the zircons from Baoshan granodiorite porphyry yields an age of 147.81±0.48Ma (MSWD=1.07). Six molybdenite samples separated from Baoshan deposit are used for Re-Os dating and obtained the weighted average age of 147.42±0.84Ma and an isochron age of 147.7±1.2Ma. These ages suggest that the mineralization in the Baoshan deposit is genetically associated to the granodiorite porphyry, and the process of rock-and ore-forming is continuous. These data indicate that ages of intrusion and ore-body from Baoshan deposit are almost identical to other typical magmatic intrusion and deposits in Jiujiang-Ruichang metallogenic district. Tt is inferred that the Baoshan deposit was formed in the transition from EW-striking Tndosinian tectonic domain to NE-striking Paleo-Pacific tectonic domain.

AuCu@Pt Nanoalloys for Catalytic Application in Reduction of 4-Nitrophenol

Directory of Open Access Journals (Sweden)

Sadia Mehmood

2016-01-01

Full Text Available To enhance and optimize nanocatalyst ability for nitrophenol (4-NP reduction reaction we look beyond Au-metal nanoparticles and describe a new class of Au nanoalloys with controlled composition for core of AuCu-metals and Pt-metal shell. The reduction of 4-NP was investigated in aqueous media spectroscopically on 7.8 nm Au nanospheres (AuNSs, 8.3 nm AuCuNSs, and 9.1 nm AuCu@Pt core-shell NSs in diameter. The rate constants of the catalyzed reaction at room temperature, activation energies, and entropies of activation of reactions catalyzed by the AuCu@Pt core-shell NSs are found to have different values to those of the pure metal NSs. The results strongly support the proposal that catalysis by nanoparticles is taking place efficiently on the surface of NSs. These core-shell nanocatalysts exhibited stability throughout the reduction reaction and proved that heterogonous type mechanisms are most likely to be dominant in nanoalloy based catalysis if the surface of the NSs is not defected upon shell incorporation.

Composition and source of salinity of ore-bearing fluids in Cu-Au systems of the Carajás Mineral Province, Brazil

Science.gov (United States)

Xavier, Roberto; Rusk, Brian; Emsbo, Poul; Monteiro, Lena

2009-01-01

The composition and Cl/Br – NaCl ratios of highly saline aqueous inclusions from large tonnage (> 100 t) IOCG deposits (Sossego, Alvo 118, and Igarapé Bahia) and a Paleoproterozoic intrusion-related Cu-Au-(Mo-W-Bi-Sn) deposit (Breves; Ca-dominated (5 to 10 times more than in porphyry Cu-Au fluids), and contain percent level concentrations of Na and K. IOCG inclusion fluids, however, contain higher Sr, Ba, Pb, and Zn concentrations, but significantly less Bi, than the intrusion-related Breves inclusion fluids. Cu is consistently below detection limits in brine inclusions from the IOCG and intrusion-related systems and Fe was not detected in the latter. Cl/Br and Na/Cl ratios of the IOCG inclusion fluids range from entirely evaporative brines (bittern fluids; e.g. Igarapé Bahia and Alvo 118) to values that indicate mixing with magma-derived brines. Cl/Br and Na/Cl ratios of the Breves inclusion fluids strongly suggest the involvement of magmatic brines, but that possibly also incorporated bittern fluids. Collectively, these data demonstrate that residual evaporative and magmatic brines were important components of the fluid regime involved in the formation of Cu-Au systems in the Carajás Mineral Province.

Laser ablation of Au-CuO core-shell nanocomposite in water for optoelectronic devices

Science.gov (United States)

Ismail, Raid A.; Abdul-Hamed, Ryam S.

2017-12-01

Core-shell gold-copper oxide Au-CuO nanocomposites were synthesized using laser ablation of CuO target in colloidal solution of Au nanoparticles (NPs). The effect of laser fluence on the structural, morphological, electrical, and optical properties of Au-CuO nanocomposites was investigated using x-ray diffraction (XRD), atomic force microscope (AFM), scanning electron microscope (SEM), transmission electron microscope (TEM), photoluminescence (PL), Fourier transformed infrared spectroscopy (FTIR), Hall measurement, and UV-vis spectroscopy. X-ray diffraction results confirm the formation of polycrystalline Au-CuO NPs with monoclinic structure. The optical energy gap for CuO was 4 eV and for the Au-CuO core-shell nanocomposites was found to be in the range of 3.4-3.7 eV. SEM and TEM investigations revealed that the structure and morphology of Au-CuO core-shell nanocomposites were strongly depending on the laser fluence. A formation of Au-CuO nanospheres and platelets structures was observed. The photoluminescence data showed an emission of broad visible peaks between 407 and 420 nm. The effect of laser fluence on the dark and illuminated I-V characteristics of Au-CuO/n-Si heterojunction photodetectors was investigated and analyzed. The experimental data demonstrated that the photodetector prepared at optimum laser fluence exhibited photosensitivity of 0.6 AW-1 at 800 nm.

Dealloying of Cu{sub x}Au studied by hard X-ray photoelectron spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Rajput, Parasmani, E-mail: parasmani.rajput@northwestern.edu [European Synchrotron Radiation Facility, 6 rue Jules Horowitz, F-38043 Grenoble (France); Gupta, Ajay [UGC-DAE Consortium for Scientific Research, University Campus, Khandwa Road, Indore 452 017 (India); Detlefs, Blanka [European Synchrotron Radiation Facility, 6 rue Jules Horowitz, F-38043 Grenoble (France); Kolb, Dieter M. [Institute for Electrochemistry, University of Ulm, D-89069 Ulm (Germany); Potdar, Satish [UGC-DAE Consortium for Scientific Research, University Campus, Khandwa Road, Indore 452 017 (India); Zegenhagen, Jörg [European Synchrotron Radiation Facility, 6 rue Jules Horowitz, F-38043 Grenoble (France)

2013-10-15

Highlights: ► The shift in binding energy of Cu and Au lines in CuAu alloys is opposite to expected from the nobility of the elements. ► The magnitude of the chemical shifts of the metal lines in CuAu alloys is strongly influenced by finite size effects and disorder. ► Cu 3s and/or Au 4f cross-sections are not well described by theory (Scofield). The Cu 3s photoabsorption cross-section seems to be strongly overestimated. ► We find/confirm that (CuAu) dealloying proceeds into depth like a spinodal decomposition. -- Abstract: We studied pristine and leached ultra-thin Cu{sub x}Au (x ≈ 4) films by hard X-ray photoelectron spectroscopy. The Au 4f and Cu 3s core levels show a shift in binding energy which is opposite to expected from the nobility of the elements, which is explained by charge transfer involving differently screening s and d valence levels of the elements [W. Eberhardt, S.C. Wu, R. Garrett, D. Sondericker, F. Jona, Phys. Rev. B 31 (1985) 8285]. The magnitude of the chemical shifts of the metal lines is strongly influenced by the finite size and disorder of the films. Angular dependent photoelectron emission allowed to assess the alloy composition as a function of depth larger than 5 nm. The potential controlled dealloying proceeds into depth like a spinodal decomposition with Cu going into solution and the remaining Au accumulating in the surface region. The compositional gradient did not lead to a significant broadening of the metal photoelectron lines suggesting a non-local screening mechanism.

Single crystal structure analyses of scheelite-powellite CaW1-xMoxO4 solidsolutions and unique occurrence in Jisyakuyama skarn deposits

Science.gov (United States)

Yamashita, K.; Yoshiasa, A.; Miyazaki, H.; Tokuda, M.; Tobase, T.; Isobe, H.; Nishiyama, T.; Sugiyama, K.; Miyawaki, R.

2017-12-01

Jisyakuyama skarn deposit, Fukuchi, Fukuoka, Japan, shows a simple occurrenceformed by penetration of hot water into limestone cracks. A unique occurrence of scheelite-powellite CaW1-xMoxO4 minerals is observed in the skarn deposit. Many syntheticexperiments for scheelite-powellite solid solutions have been reported as research onfluorescent materials. In this system it is known that a complete continuous solid solution isformed even at room temperature. In this study, we have carried out the chemical analyses,crystal structural refinements and detail description of occurrence on scheelite-powelliteminerals. We have also attempted synthesis of single crystal of solid solution in a widecomposition range. The chemical compositions were determined by JEOL scanningelectron microscope and EDS, INCA system. We have performed the crystal structurerefinements of the scheelite-powellite CaW1-xMoxO4 solid solutions (x=0.0-1.0) byRIGAKU single-crystal structure analysis system RAPID. The R and S values are around0.0s and 1.03. As the result of structural refinements of natural products and many solidsolutions, we confirm that most large natural single crystals have compositions at bothendmembers, and large solid solution crystals are rare. The lattice constants, interatomicdistances and other crystallographic parameters for the solid solution change uniquely withcomposition and it was confirmed as a continuous solid solution. Single crystals of scheeliteendmember + powellite endmember + solid solution with various compositions form anaggregate in the deposit (Figure 1). Crystal shapes of powellite and scheelite arehypidiomorphic and allotriomorphic, respectively. Many solid solution crystals areaccompanied by scheelite endmember and a compositional gap is observed betweenpowellite and solid-solution crystals. The presence of several penetration solutions withsignificantly different W and Mo contents may be assumed. This research can be expectedto lead to giving restrictive

Charged hadron multiplicity fluctuations in Au+Au and Cu+Cu collisions from √s.sub.NN./sub. = 22.5 to 200 GeV

Czech Academy of Sciences Publication Activity Database

Adare, A.; Adler, S. S.; Afanasiev, S.; Kubart, J.; Mašek, L.; Mikeš, P.; Tomášek, Lukáš; Vrba, Václav

2008-01-01

Roč. 78, č. 4 (2008), 044902/1-044902/15 ISSN 0556-2813 R&D Projects: GA MŠk LA08015; GA MŠk 1P04LA211; GA ČR GA202/05/0653 Institutional research plan: CEZ:AV0Z10100502 Keywords : charged hadron * multiplicity fluctuations * Au+Au * Cu+Cu Subject RIV: BF - Elementary Particles and High Energy Physics Impact factor: 3.124, year: 2008

Regional setting and geochronology of the Late Cretaceous Banatitic Magmatic and Metallogenetic Belt

Science.gov (United States)

Ciobanu, Cristiana L.; Cook, Nigel J.; Stein, Holly

2002-08-01

The 1,500-km-long Banatitic Magmatic and Metallogenetic Belt (BMMB) of Romania, Serbia and Bulgaria is a complex calc-alkaline magmatic arc of Late Cretaceous age. It hosts a variety of magmatic-hydrothermal Cu, Au, Mo, Zn, Pb and Fe deposits, including Europe's only world-class porphyry-copper deposits. Regional metallogeny can be linked to subduction of the Vardar Ocean during the Late Cretaceous, as part of the closure of the Neotethys Ocean that had separated Europe and Africa in the Mesozoic. Porphyry Cu-(Au)-(Mo) and intimately associated epithermal massive sulphides dominate in the central segments of the belt in southernmost Banat (Romania), Serbia and north-west Bulgaria. These districts are the economically most important today, including major active Cu-Au mines at Moldova Nouă in Romania, Majdanpek, Veliki Krivelj and Bor in Serbia, and Elatsite, Assarel and Chelopech in Bulgaria. More numerous (and mostly mined in the past) are Fe, Cu and Zn-Pb skarns, which occur mainly at the two ends of the belt, in Eastern Bulgaria and in Romania. This paper summarises some of the deposit characteristics within the geodynamic framework of terminal Vardar subduction. Heterogeneous terranes of the belt, including the Apuseni Mountains at the western end, are aligned parallel to the Vardar front following continental collision of the Dacia and Tisza blocks. All available geochronological data (numerous K-Ar and some U-Pb and Re-Os ages) are compiled, and are complemented by a new high-precision Re-Os date for the Dognecea skarn deposit, south-west Romania (76.6±0.3 Ma). These data indicate that magmatism extended over at least 25 million years, from about 90 to 65 Ma in each segment of the belt. Within Apuseni Mountains and Banat, where magma emplacement was related to syn-collisional extension in the orogenic belt of Carpathians, ore formation seems to be restricted in time and maybe constrained by a shared tectonic event.

Au and AuCu Nanoparticles Supported on SBA-15 Ordered Mesoporous Titania-Silica as Catalysts for Methylene Blue Photodegradation

Directory of Open Access Journals (Sweden)

Isabel Barroso-Martín

2018-05-01

Full Text Available The photocatalytic degradation of methylene blue (MB dye has been performed under UV irradiation in aqueous suspension, employing photocatalysts based on Au (1.5 wt % and AuCu (Au/Cu = 1, 2.0 wt %, and supported on SBA-15-ordered mesoporous silica, with and without titania (Si/Ti = 3, in order to evaluate the versatility of this mesoporous support in this type of reaction of great impact from the environmental point of view. Samples were characterized by X-ray diffraction (XRD, transmission electron microscopy (TEM, N2 adsorption-desorption at −196 °C, and X-ray photoelectron spectroscopy (XPS, so as to study their structural, optical, and chemical properties. All the prepared catalysts were found to be active in the test reaction. The bimetallic AuCu-based catalysts attained very high MB degradation values, in particular AuCu/SBA-15 titania-silica sample reached 100% of dye oxidation after the monitored reaction period (120 min.

Mixed Cu(i)/Au(i) coordination polymers as reversible turn-on vapoluminescent sensors for volatile thioethers.

Science.gov (United States)

Varju, Bryton R; Ovens, Jeffrey S; Leznoff, Daniel B

2017-06-13

Vapour-phase thioethers play an important role in a wide number of fields, including plant biology, chemical weapon disposal, and brewing but few sensor materials are known. The emissive coordination polymer Cu 1/2 Au 1/2 CN does not react with vapour phase dimethyl sulphide (DMS) or diethyl sulphide (DES) despite the independent synthesis of emissive [Cu 1/2 Au 1/2 CN] 2 (DMS) and [Cu 1/2 Au 1/2 CN] 2 (DES) from their constituent components in solution. However, the doped Cu 2/3 Au 1/3 CN rapidly reacts in the solid state with both of these vapour phase thioethers reversibly, with a change in emission from 380/560 nm to 460 nm (DMS) or 420 nm (DES), illustrating that doping the inactive parent Cu 1/2 Au 1/2 CN with Cu(i) generates an active sensor material. This response can be thermally cycled with little to no loss in functionality. [Cu 1/2 Au 1/2 CN] 2 (DMS), [Cu 2/3 Au 1/3 CN] 2 (DMS), and [Cu 2/3 Au 1/3 CN] 2 (DES) were structurally characterized as 3-D network structures supported by aurophilic interactions.

Nucleon shadowing effects in Cu + Cu and Au + Au collisions at RHIC within the HIJING code

Science.gov (United States)

Abdel-Waged, Khaled; Felemban, Nuha

2018-02-01

The centrality dependence of pseudorapidity density of charged particles ({{{d}}{N}}{{ch}}/{{d}}η ) in Cu + Cu (Au + Au) collisions at Relativistic Heavy Ion Collider energy of \\sqrt{{s}{{NN}}}=22.4, 62.4 and 200 (19.6, 62.4 and 200) GeV, is investigated within an improved HIJING code. The standard HIJING model is enhanced by a prescription for collective nucleon-nucleon (NN) interactions and more modern parton distribution functions. The collective NN-interactions are used to induce both cascade and nucleon shadowing effects. We find collective cascade broadens the pseudorapidity distributions in the tails (at | η | > {y}{beam}) above 25%-30% collision centrality to be consistent with the {{{d}}{N}}{{ch}}/{{d}}η data at \\sqrt{{s}{{NN}}} =19.6,22.4,62.4 {GeV}. The overall contribution of nucleon shadowing is shown to depress the whole shape of {{{d}}{N}}{{ch}}/{{d}}η in the primary interaction region (at | η | data.

Mass and velocity of fragments from the reaction 17-115 MeV/u 40Ar + Cu, Ag and Au

International Nuclear Information System (INIS)

Colin, E.; Guinet, D.; Stern, M.

1998-01-01

Measurements are reported for fragment masses and velocities from the reactions 17-115 MeV/u 40 Ar + Cu, Ag and Au. High momentum and energy deposition are reported for selected events, even for higher incident energy. Further study is needed to understand their origin. (authors)

Element migration of pyrites during ductile deformation of the Yuleken porphyry Cu deposit (NW-China)

Science.gov (United States)

Hong, Tao; Xu, Xing-Wang; Gao, Jun; Peters, Stephen; Li, Jilei; Cao, Mingjian; Xiang, Peng; Wu, Chu; You, Jun

2017-01-01

The strongly deformed Yuleken porphyry Cu deposit (YPCD) occurs in the Kalaxiangar porphyry Cu belt (KPCB), which occupies the central area of the Central Asian Orogenic Belt (CAOB) between the Sawu’er island arc and the Altay Terrane in northern Xinjiang. The YPCD is one of several typical subduction-related deposits in the KPCB, which has undergone syn-collisional and post-collisional metallogenic overprinting. The YPCD is characterized by three pyrite-forming stages, namely a hydrothermal stage A (Py I), a syn-ductile deformation stage B (Py II) characterized by Cu-Au enrichment, and a fracture-filling stage C (Py III). In this study, we conducted systematic petrographic and geochemical studies of pyrites and coexist biotite, which formed during different stages, in order to constrain the physicochemical conditions of the ore formation. Euhedral, fragmented Py I has low Pb and high Te and Se concentration and Ni contents are low with Co/Ni ratios mostly between 1 and 10 (average 9.00). Py I is further characterized by enrichments of Bi, As, Ni, Cu, Te and Se in the core relative to the rim domains. Anhedral round Py II has moderate Co and Ni contents with high Co/Ni ratios >10 (average 95.2), and average contents of 46.5 ppm Pb and 5.80 ppm Te. Py II is further characterized by decreasing Bi, Cu, Pb, Zn, Ag, Te, Mo, Sb and Au contents from the rim to the core domains. Annealed Py III has the lowest Co content of all pyrite types with Co/Ni ratios mostly <0.1 (average 1.33). Furthermore, Py III has average contents of 3.31 ppm Pb, 1.33 ppm Te and 94.6 ppm Se. In addition, Fe does not correlate with Cu and S in the Py I and Py III, while Py II displays a negative correlation between Fe and Cu as well as a positive correlation between Fe and S. Therefore, pyrites which formed during different tectonic regimes also have different chemical compositions. Biotite geothermometer and oxygen fugacity estimates display increasing temperatures and oxygen

Synthesis of Au and Au/Cu alloy nanoparticles on multiwalled carbon nanotubes by using microwave irradiation

International Nuclear Information System (INIS)

Rangari, Vijaya K.; Dey, Sanchita; Jeelani, Shaik

2010-01-01

Gold nanoparticles and gold-copper alloy nanoparticles were synthesized by reduction of chloroauric acid (HAuCl_4.xH_2O) and co-reduction of chloroauric acid (HAuCl_4.xH_2O) and Copper(II) acetate [(CH_3COO)_2Cu.H_2O] by ethylene glycol through microwave irradiation technique. In this reaction ethylene glycol used as a solvent and also reducing agent. The cetyltrimethyl ammonium bromide (CTAB) used as surfactant. Au nanoparticles and Au-Cu nanoparticles on the surface of multiwalled carbon nanotube also produced by using same procedure. The XRD analysis confirmed the formation of Au and Au-Cu alloy nanoparticles on multiwalled carbon nanotubes(CNTs). The morphology and size of the particles were examined by the transmission electron microscopy. The EDS analysis on individual particles confirmed that the presence of two metals in a particle in case of alloy nanoparticle. The results presented here show that a variety of well defined metal and metal alloy nanoparticles can be produced by using the microwave polyol process with in a short period of time. (author)

Investigation on the age of mineralization in the Sungun porphyry Cu-Mo deposit, NW Iran with a regional metallogenic perspective

Science.gov (United States)

Simmonds, Vartan; Moazzen, Mohssen; Mathur, Ryan

2016-04-01

The Sungun porphyry copper deposit (PCD) is located in NW Iran, neighbouring several other PCDs and prospects in the region and the Lesser Caucasus (south Armenia). It lies on the Urumieh-Dokhtar magmatic arc (UDMA), which formed through the northeast-ward subduction of the Neo-Tethyan oceanic crust beneath the Central Iranian plate during late-Mesozoic and early-Cenozoic [1], and hosts the porphyry copper metallogenic belt of Iran. The Sungun PCD is the second largest deposit in Iran with ore reserves of about 850 Mt at 0.62 wt% Cu and 0.01 wt% Mo and probable reserves over 1Gt. The monzonitic to quartz monzonitic porphyry stock intruded the upper Cretaceous carbonates and Eocene volcano-sedimentary rocks. It produced a skarn-type mineralization at its contact zone with the carbonate rocks, as well as vast hydrothermal alteration zones and porphyry-type Cu and Mo mineralization. The zircon U-Pb age of the host porphyry stock is about 22.5±0.4 to 20.1±0.4 Ma [2]. Re-Os dating of four molybdenite separates from this PCD shows ages ranging between 22.9±0.2 to 21.7±0.2 Ma, with an average of 22.57±0.2 Ma, corresponding to the early Miocene (Aquitanian). These ages indicate that both the porphyry stock and the Cu-Mo mineralization are post-collisional events, similar to many other deposits and prospects in NW and central Iran and south Armenia, and the mineralization occurred shortly after the emplacement of the host stock, corresponding better to the ages obtained from the marginal parts of the stock. Magmatism and mineralization in Sungun coincides with the third metallogenic epoch in the Lesser Caucasus (Eocene to Miocene; [3]), though it is considerably younger than all of the dated PCDs and prospects in the south Armenia. It also postdates Cu-Mo mineralizations in the Saheb Divan (35 Ma), Qaradagh batholith (31.22±0.28 to 25.19±0.19 Ma), as well as Haft Cheshmeh PCD (28.18±0.42 to 27.05±0.37 Ma) in NW Iran, while it seems to be coeval with the Kighal

Au-CuO core-shell nanoparticles design and development for the selective determination of Vitamin B6

International Nuclear Information System (INIS)

Kumar, Deivasigamani Ranjith; Manoj, Devaraj; Santhanalakshmi, Jayadevan; Shim, Jae-Jin

2015-01-01

Highlights: • Seed mediated growth of Au-CuO core-shell nanoparticle. • Au-CuO core-shell nanoparticle provided good peak current for pyridoxine. • Au-CuO/MWCNTs/GC exhibited excellent vitamin B 6 peak separation with other vitamin. - Abstract: This paper reports the synthesis of gold (core)-copper oxide (shell) nanoparticles using a simple seed mediated growth method. Pre-synthesized Au nanoparticles were used as seed materials for copper oxide shell growth, which were shown to be effective for Au-CuO core-shell formation. The novelty of this assembly strategy is that the exploitation of the Cu-ligand, which is thermolyzed on the Au nanoseed surface, results in the formation of CuO. Au-CuO core-shell nanoparticles were characterized by UV-visible spectroscopy, high resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). The as prepared Au-CuO was used to fabricate a Au-CuO/MWCNTs/GC-modified electrode, which was applied to Vitamin B 6 (pyridoxine) determination by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The MWCNTs enhance the pyridoxine oxidation rate by increasing the peak current with Au-CuO, hence pyridoxine oxidized lower operating potentials. The Au-CuO/MWCNTs/GC-modified electrode showed excellent electrochemical performance towards pyridoxine (PY) in the presence of other typical vitamins, such as riboflavin, ascorbic acid and uric acid. The linear calibration graph was obtained over the PY concentration range of 0.79 μM–18.4 μM and the detection limit (S/N = 3) was 0.15 μM. The Au-CuO/MWCNTs/GC-modified electrode showed good stability, repeatability and recovery of real sample analysis

Microstructures and coherent phase diagram for the pseudobinary system (AuCu)1-xPd x with x ≤ 0.10

International Nuclear Information System (INIS)

Luciano, Rhodora H.; Shiraishi, Takanobu; Udoh, Koh-ichi; Tanaka, Yasuhiro; Hisatsune, Kunihiro

2005-01-01

A coherent phase diagram for the pseudobinary system (AuCu) 1-x Pd x with x ≤ 0.10 was constructed based on phase identification and microstructural analysis by transmission electron microscopy. It was confirmed that the addition of palladium exceeding 1.0 at.% to the equiatomic AuCu eliminated the AuCu II long-period superstructure from the phase equilibria and stabilized the AuCu I superstructure. The AuCu-0.5 at.% Pd and AuCu-1.0 at.% Pd alloys isothermally aged for long time at temperatures ranging from 380 to 420 deg. C exhibited seven distinguishable regions; a single-phase region of disordered solid solution (α); a single-phase region of AuCu I ordered phase; a single-phase region of AuCu II ordered phase; a region of the coexisting AuCu I and AuCu II ordered phases; a region of the coexisting AuCu I ordered and α phases; a region of the coexisting AuCu II ordered and α phases; and a region of the coexisting AuCu I and AuCu II ordered and α phases

Petrology and Geochemistry of Shakh Sefid Granitoid and related skarn in the North of Rayen (southeastern of Kerman

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Habib biabangard

2017-11-01

Full Text Available The Shakh Sefid Granitoid pluton and related Skarn are located 80 Km in the southeastern of Kerman and 20 Km north of Rayen. This area   is geologically located in the southeastern of the Lut block in the Central Iran. The Shakh Sefid Granitoid with Eocene-Oligocene age cuts the Cretaceous sedimentary rocks and led to the formation of Skarn. The granitoids are granite and granodiorite in composition composing of quartz, plagioclase, orthoclase, as primary minerals, biotite as minor and chlorite and sericite as secondary minerals. The sedimentary rocks are shale, sandstone, siltstone and limestone. Metamorphic rocks are marble and Skarns. The Skarn is calcic type. Garnet (grossular-andradite, tremolite and magnetite are the main minerals that are often accompanied with hematite, goethite and limonite. Pyrite, chalcopyrite and copper carbonate (malachite and azurite are the other minerals in Skarn. Geochemical studies show that the amount of major and minor elements of granitoid with increasing SiO2 content do not change due to the uniform mass, low dispersion of elements which result from heterogeneous textures and low alteration zone. Spider diagrams from minor elements normalized to Chondrite and primitive mantle show enrichment of all elements except for Ti, positive anomalies of Th, Pb and negative anomalies of Ti, P and Sr for the Sakh Sefid granitoids are probably due to crustal contamination. They are enriched in light rare earth elements (LREE between 10 to 100 times and heavy elements (HREE enrichment between 1 to 10 times compared to the reference (chondrite and regular pattern with approximately the same slope , the parallel trends indicate that the granitoid rocks share  a common source rock . The Shakh Sefid granitoid is I-type, metaluminous to peraluminous belonging to an active continental margin. Mineral and Mineralization in Kuh Shakh Sefid skarn is remarkably similar to iron skarn deposits. Minerals such as garnet and

Preparation and use of Cu nanoclusters as fluorescent probes to determine Au(III) ions

Energy Technology Data Exchange (ETDEWEB)

Liu, Jinshui, E-mail: jsliu@sina.com; Wang, Bin; Xu, Meijiao; Wang, Lizhen; Zhou, Zihan

2017-05-15

Polyethyleneimine-capped Cu nanoclusters (PEI-CuNCs) with a mean diameter of 2.5 nm and that emitted blue light at 485 nm were synthesized. The fluorescence of PEI-CuNCs was strongly quenched when Au(III) ions were present. Because of this specific response, a PEI-CuNC-based fluorescent turn-off sensor was developed. Under optimum conditions, a good linear relationship (R{sup 2}=0.993) was found between the relative fluorescence intensity (F{sub 0}/F) and the Au(III) ion concentration between 0.5 and 15 µM. The detection limit for Au(III) ions was 0.06 µM. The quenching mechanism was assessed by performing X-ray photoelectron spectroscopy spectra studies. The fluorescence quenching was ascribed to photo-induced electron transfer from the PEI-CuNCs to the AuCl{sub 4}{sup −} occur. Using The method described is a new way of quantifying Au(III) ions.

Diffusion-induced grain boundary migration during ion beam mixing of Au/Cu bilayers

International Nuclear Information System (INIS)

Alexander, D.E.; Baldo, P.M.; Rehn, L.E.

1992-09-01

Experiments were performed to evaluate the effect of 1.5 MeV Kr irradiation on diffusion-induced grain boundary migration (DIGM) in Au/Cu bilayers in the temperature range of 300≤T≤050K. The experimental results were consistent with DIGM occurring in bilayers both during irradiation and during annealing treatments. Rutherford backscattering spectrometry showed a nearly uniform distribution of Cu present through the entire thickness of appropriately prepared polycrystalline Au films irradiated or annealed at temperatures ≥400K. No parallel effect was seen in similarly treated single-crystal films. In each polycrystalline sample studied, irradiation resulted in greater amounts of Cu present uniformly in the Au compared to annealing-only. The magnitudes of measured Cu compositions were substantially greater than that expected solely from grain boundary diffusion. A simple analysis of the process indicated that ion irradiation affects DIGM by increasing the composition of Cu present in alloyed zones and/or by increasing the grain boundary velocity in the Au

A Au/Cu2O-TiO2 system for photo-catalytic hydrogen production. A pn-junction effect or a simple case of in situ reduction?

KAUST Repository

Sinatra, Lutfan

2015-02-01

Photo-catalytic H2 production from water has been studied over Au-Cu2O nanoparticle deposited on TiO2 (anatase) in order to probe into both the plasmon resonance effect (Au nanoparticles) and the pn-junction at the Cu2O-TiO2 interface. The Au-Cu2O composite is in the form of ∼10 nm Au nanoparticles grown on ∼475 nm Cu2O octahedral nanocrystals with (111) facets by partial galvanic replacement. X-ray Photoelectron Spectroscopy (XPS) Cu2p and Auger L3M4,5M4,5 lines indicate that the surface of Cu2O is mainly composed of Cu+. The rate for H2 production (from 95 water/5 ethylene glycol; vol.%) over 2 wt.% (Au/Cu2O)-TiO2 is found to be ∼10 times faster than that on 2 wt.% Au-TiO2 alone. Raman spectroscopy before and after reaction showed the disappearance of Cu+ lines (2Eu) at 220 cm-1. These observations coupled with the induction time observed for the reaction rate suggest that in situ reduction from Cu+ to Cu0 occurs upon photo-excitation. The reduction requires the presence of TiO2 (electron transfer). The prolonged activity of the reaction (with no signs of deactivation) despite the reduction to Cu0 indicates that the latter takes part in the reaction by providing additional sites for the reaction, most likely as recombination centers for hydrogen atoms to form molecular hydrogen. This phenomenon provides an additional route for enhancing the efficiency and lifetime of Cu2O-TiO2 photocatalytic systems, beyond the usually ascribed pn-junction effect.

Molybdenite Re/Os dating, zircon U-Pb age and geochemistry of granitoids in the Yangchuling porphyry W-Mo deposit (Jiangnan tungsten ore belt), China: Implications for petrogenesis, mineralization and geodynamic setting

Science.gov (United States)

Mao, Jingwen; Xiong, Bikang; Liu, Jun; Pirajno, Franco; Cheng, Yanbo; Ye, Huishou; Song, Shiwei; Dai, Pan

2017-08-01

The Yangchuling W-Mo deposit, located in the Jiangnan porphyry-skarn (JNB) tungsten ore belt, is the first recognized typical porphyry W-Mo deposit in China in the 1980's. Stockworks and disseminated W-Mo mineralization occur in the roof pendant of a 0.3 km2 monzogranitic porphyry stock that intruded into a granodiorite stock, hosted by Neoproterozoic phyllite and slate. LA-ICPMS zircon U-Pb analyses suggest that of the monzogranitic porphyry and granodiorite were formed at 143.8 ± 0.5 Ma and 149.8 ± 0.6 Ma, respectively. Six molybdenite samples yielded a Re-Os weighted mean age of 146.4 ± 1.0 Ma. Geochemical data show that both granodiorite and monzogranitic porphyry are characterized by enrichment of large ion lithophile elements (LILE) relative to high field strength elements (HFSE), indicating a peraluminous nature (A/CNK = 1.01-1.08). Two granitoids are characterized by a negative slope with significant light REE/heavy REE fractionation [(La/Yb)N = 8.38-23.20] and negative Eu anomalies (Eu/Eu* = 0.69-0.76). The P2O5 contents of the Yangchuling granitoids range from 0.12% to 0.17% and exhibit a negative correlation with SiO2, reflecting that they are highly fractionated I-type. They have high initial 87Sr/86Sr ratios (0.7104-0.7116), low negative εNd(t) (- 5.05 to - 5.67), and homogeneous εHf(t) between - 1.39 and - 2.17, indicating similar sources. Additionally, two-stage Nd model ages (TDM2) of 1.3-1.4 Ga and two-stage Hf model ages (TDM2) of 1.2-1.3 Ga are consistent, indicating that Neoproterozoic crustal rocks of the Shuangqiaoshan Group could have contributed to form the Yangchuling magmas. Considering the two groups of parallel Late Mesozoic ore belts, namely the Jiangnan porphyry-skarn tungsten belt (JNB) in the south and the Middle-Lower Yangtze River porphyry-skarn Cu-Au-Mo-Fe ore belt (YRB) in the north, the Nanling granite-related W-Sn ore belt (NLB) in the south, the neighboring Qin-Hang porphyry-skarn Cu-Mo-hydrothermal Pb-Zn-Ag ore belt (QHB

Charged-particle multiplicity and pseudorapidity distributions measured with the PHOBOS detector in Au+Au, Cu+Cu, d+Au, and p+p collisions at ultrarelativistic energies

Science.gov (United States)

Alver, B.; Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Chai, Z.; Chetluru, V.; Decowski, M. P.; García, E.; Gburek, T.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kotuła, J.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Li, W.; Lin, W. T.; Loizides, C.; Manly, S.; McLeod, D.; Michałowski, J.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Sedykh, I.; Skulski, W.; Smith, C. E.; Steadman, S. G.; Steinberg, P.; Stephans, G. S. F.; Stodulski, M.; Sukhanov, A.; Tonjes, M. B.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Vaurynovich, S. S.; Verdier, R.; Veres, G. I.; Wadsworth, B.; Walters, P.; Wenger, E.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

2011-02-01

Pseudorapidity distributions of charged particles emitted in Au+Au, Cu+Cu, d+Au, and p+p collisions over a wide energy range have been measured using the PHOBOS detector at the BNL Relativistic Heavy-Ion Collider (RHIC). The centrality dependence of both the charged particle distributions and the multiplicity at midrapidity were measured. Pseudorapidity distributions of charged particles emitted with |η|<5.4, which account for between 95% and 99% of the total charged-particle emission associated with collision participants, are presented for different collision centralities. Both the midrapidity density dNch/dη and the total charged-particle multiplicity Nch are found to factorize into a product of independent functions of collision energy, sNN, and centrality given in terms of the number of nucleons participating in the collision, Npart. The total charged particle multiplicity, observed in these experiments and those at lower energies, assumes a linear dependence of (lnsNN)2 over the full range of collision energy of sNN=2.7-200 GeV.

Bifunctional Interface of Au and Cu for Improved CO2 Electroreduction.

Science.gov (United States)

Back, Seoin; Kim, Jun-Hyuk; Kim, Yong-Tae; Jung, Yousung

2016-09-07

Gold is known currently as the most active single-element electrocatalyst for CO2 electroreduction reaction to CO. In this work, we combine Au with a second metal element, Cu, to reduce the amount of precious metal content by increasing the surface-to-mass ratio and to achieve comparable activity to Au-based catalysts. In particular, we demonstrate that the introduction of a Au-Cu bifunctional "interface" is more beneficial than a simple and conventional homogeneous alloying of Au and Cu in stabilizing the key intermediate species, *COOH. The main advantages of the proposed metal-metal bifunctional interfacial catalyst over the bimetallic alloys include that (1) utilization of active materials is improved, and (2) intrinsic properties of metals are less affected in bifunctional catalysts than in alloys, which can then facilitate a rational bifunctional design. These results demonstrate for the first time the importance of metal-metal interfaces and morphology, rather than the simple mixing of the two metals homogeneously, for enhanced catalytic synergies.

Neyshabour turquoise mine: the first Iron Oxide Cu-Au-U-LREE (IOCG mineralized system in Iran

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Mohammad Hasan Karimpour

2011-11-01

Full Text Available Neyshabour turquoise mine is located in northwest of Neyshabour, southern Quchan volcanic belt. Eocene andesite and dacite forming as lava and pyroclastic rocks cover most of the area. Subvolcanic diorite to syenite porphyry (granitoids of magnetite series intruded the volcanic rocks. Both volcanic and subvolcanic rocks are highly altered. Four types of alteration are recognized including: silicification, argillic, calcification and propylitic. Silicification is dominant followed by argillic alteration. Mineralization is present as stockwork, disseminated and hydrothermal breccia. Hypogene minerals are pyrite, magnetite, specularite, chalcopyrite, and bornite. Secondary minerals are turquoise, chalcocite, covellite, and iron oxides. A broad zone of gossan has developed in the area. Oxidized zone has a thickness of about 80 m. Mineralized samples show high anomalies of Cu, Au, Zn, As, Mo, Co, U, LREE, Nb, and Th. Both aeromagnetic and radiometric (U and Th maps show very strong anomalies (10 × 5km within the mineralized area. Based on geology, alteration, mineralization, geochemistry, and geophysics, Neyshabour turquoise mine is a large Iron oxide Cu-Au-U-LREE (IOCG mineralized system. In comparison with other IOCG deposits, it has some similarities with Olympic Dam (Australia and Candelaria (Chile. In comparison with Qaleh Zari and Kuh Zar mines, Neyshabour turquoise mine is the first Iron oxide Cu-Au-U-LREE (IOCG mineralized system discovered in Iran.

Wetting Behavior of Ternary Au-Ge-X (X = Sb, Sn) Alloys on Cu and Ni

Science.gov (United States)

Jin, S.; Valenza, F.; Novakovic, R.; Leinenbach, C.

2013-06-01

Au-Ge-based alloys are potential substitutes for Pb-rich solders currently used for high-temperature applications. In the present work, the wetting behavior of two Au-Ge-X (X = Sb, Sn) ternary alloys, i.e., Au-15Ge-17Sb and Au-13.7 Ge-15.3Sn (at.%), in contact with Cu and Ni substrates has been investigated. Au-13.7Ge-15.3Sn alloy showed complete wetting on both Cu and Ni substrates. Total spreading of Au-15Ge-17Sb alloy on Cu was also observed, while the final contact angle of this alloy on Ni was about 29°. Pronounced dissolution of Cu substrates into the solder alloys investigated was detected, while the formation of Ni-Ge intermetallic compounds at the interface of both solder/Ni systems suppressed the dissolution of Ni into the solder.

Cross-sections of 197Au(n,α)198Au and 63Cu(n,α)64Cu induced by 252Cf neutrons

International Nuclear Information System (INIS)

Mandal, Ranjita; Sengupta, D.; Roy, Malobika; Naik, Mamta; Bhoraskar, V.N.

2014-01-01

Analytical work, employing nuclear techniques, is normally carried out through (n,α) reaction because of the availability of neutrons either from reactors or laboratory sources such as Sb-Be, Am-Be, Ra-Be, Po-Be, 252 Cf, etc. The laboratory neutron sources are though portable and adaptable to a particular experimental arrangement, suffer from the disadvantage of slow neutron yield (except 252 Cf). In this set up since the neutrons available are monoenergetic, it was thought appropriate to initiate a program to measure cross-sections of a few nuclear reactions which have practical applications. Earlier studies on cross-section measurement of the reaction 197 Au(n,α) 198 Au and 63 Cu(n,α) 64 Cu has been carried out using different sources, monitors and techniques

Mineralogical and Geochemical Characterization of the Kimmeria Intrusion-Related Deposit, Xanthi, NE Greece

Science.gov (United States)

Theodoridou, Stella; Melfos, Vasilios; Voudouris, Panagiotis; Miskovic, Aleksandar

2016-04-01

Although intrusion-related systems have not been previously recognized in the European segment of the Tethyan Metallogenic Belt, the Rhodope metallogenic province of SE Balkan peninsula hosts numerous such occurrences. The Kimmeria hydrothermal system incorporates two styles of ore mineralization: i) a massive Au-bearing magnetite-pyrrhotite skarn and ii) a Mo-Cu-Bi-W quartz vein-hosted mineralization, both of which are related to the Oligocene Xanthi pluton (25.5±1.2 to 30±1 My, K-Ar in hornblende and biotite). The Xanthi pluton, consisting of I-type gabbros, monzonites and amphibole-biotite granodiorites, intrudes the basement gneisses, mica schists, amphibolites and marbles of the Southern Rhodope Core Complex; a dome that has gradually exhumed from Paleocene/mid Eocene to Miocene (starting between 65 and >42 to 10 My). The Xanthi pluton emplacement and the magmatically derived hydrothermal fluid circulation were controlled by two major regional structures: the low-angle Kavala-Xanthi-Komotini detachment fault and the Nestos thrust fault. The Kimmeria Au-Cu-Fe skarn mineralization features a well-preserved aureole at the contact between the granodiorite and the surrounding marbles. It consists of two paragenetic stages comprising magnetite and pyrrhotite-rich assemblages. Alteration minerals comprise chlorite and sericite. Bulk chemical analyses of the skarn mineralization revealed relatively high concentration of Cu (1 wt.%), Pb (288 ppm) and Zn (0.74 wt.%). The mineralization is also enriched in As (molybdenite as dominant sulfides. Minor sphalerite, tetrahedrite-tennantite, galena and rutile are also present, while sericite and chlorite as the alteration minerals. The Cu and Mo content of the vein type mineralization exceed 1.0 and 0.2 wt.% respectively, along with < 2.7 ppm Au, 1.3 to 79.5 ppm W and 0.6 to 456 ppm Bi. A first approach fluid study has revealed small variations in δ34S values of sulfides (0 - 2.3 ‰ VCDT) from both types of mineralization

First-principles study of Cu adsorption on vacancy-defected/Au-doped graphene

Science.gov (United States)

Liu, Yang; An, Libao; Gong, Liang

2018-04-01

To enhance the interaction between Cu and graphene in graphene reinforced Cu matrix composites, the first principles calculation was carried out to study the adsorption of Cu atoms on graphene. P-type doping and n-type doping were formed, respectively, on vacancy-defected and Au-doped graphene based on band structure analysis, and this was verified by subsequent investigation on density of states. A computation on charge transfer confirmed that p-type doping could promote the electron transport between Cu and graphene, while n-type doping would prevent it. In addition, adsorption energy and Mulliken population analysis revealed that both vacancy defects and Au doping could improve the stability of the Cu-graphene system. The research conducted in this paper provides useful guidance for the preparation of Cu/graphene composites.

Structure, morphology and optical properties of CuInS2 thin films prepared by modulated flux deposition

International Nuclear Information System (INIS)

Guillen, C.; Herrero, J.; Gutierrez, M.T.; Briones, F.

2005-01-01

The structure, morphology and optical properties of copper indium sulfide thin films prepared by a novel modulated flux deposition procedure have been investigated for layers from 200 to 400 nm thickness. These polycrystalline CuInS 2 films grown onto glass substrates showed CuAu-like structure, similar to epitaxial CuInS 2 films grown onto monocrystalline substrates, and direct band gap values Eg=1.52-1.55 eV, optimum for single-junction photovoltaic applications. The increase in the layer thickness leads to growth of the average crystallite size and increases slightly the surface roughness and the absorption coefficient

Interdiffusion and grain-boundary migration in Au-Cu bilayers during ion-irradiation

International Nuclear Information System (INIS)

Alexander, D.E.; Rehn, L.E.; Baldo, P.M.

1991-11-01

Ion irradiation and annealing experiments have been conducted on Au/Cu bilayer films to evaluate the effect of irradiation on diffusion-induced grain boundary migration (DIGM). The Au films were prepared with a large-grained microstructure with grain boundaries perpendicular to the film surface and extending through the film thickness. Irradiations were conducted with 1.5 MeV Kr at 228 degree C. Rutherford backscattering spectrometry of the samples revealed that interdiffusion was substantially enhanced in the irradiated area relative to the unirradiated area. Both irradiated and annealed-only areas were characterized by a nearly uniform composition of 14 at.% and 7 at.% Cu respectively through the entire thickness of the underlying Au film. Small probe X-ray energy dispersive spectroscopy showed significant lateral compositional homogeneities in both irradiated and annealed areas. These two results are consistent with previous observations of DIGM in the Au/Cu system, suggesting that this previously unexamined mechanism contributes to ion beam mixing

A comparative study of Cu, Ag and Au doped CeO_2 in the total oxidation of volatile organic compounds (VOCs)

International Nuclear Information System (INIS)

Aboukaïs, Antoine; Skaf, Mira; Hany, Sara; Cousin, Renaud; Aouad, Samer; Labaki, Madona; Abi-Aad, Edmond

2016-01-01

Total oxidation of two Volatile Organic Compounds (VOCs), propylene and toluene, was investigated over M/CeO_2 catalysts, where M is a metal from IB group (i.e. Au, Ag, Cu), prepared by two different methods: the conventional wet impregnation and the deposition-precipitation. The catalysts have been characterized by means of total surface area (BET), X-ray diffraction (XRD), electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS), diffuse reflectance ultra-violet-visible spectroscopy (DR-UV/Vis), and temperature-programmed reduction (TPR), in order to explain the differences observed in their catalytic activity towards the studied reactions. By comparing the two different preparation methods, the presence of metal in high oxidation state for gold and silver, and the presence of clusters for copper were the main factors responsible for the high catalytic activity. This latter was also found to be related, when comparing the different IB metals, to the values of the oxidation/reduction potential of the redox couples of the different metals. - Highlights: • IB metals (Au, Ag and Cu) were supported on ceria (CeO_2) by two different methods. • The solids were tested as catalysts for total oxidation of propylene and toluene. • The deposition-precipitation is better for Au whereas for Ag and Cu it is the impregnation. • High oxidation states of gold and silver and clusters of copper enhanced catalytic behavior. • Catalytic activity is linked to the oxidation/reduction potential of the redox IB couples.

Morphological Characteristics of Au Films Deposited on Ti: A Combined SEM-AFM Study

Directory of Open Access Journals (Sweden)

Francesco Ruffino

2018-03-01

Full Text Available Deposited Au films and coatings are, nowadays, routinely used as active or passive elements in several innovative electronic, optoelectronic, sensing, and energy devices. In these devices, the physical properties of the Au films are strongly determined by the films nanoscale structure. In addition, in these devices, often, a layer of Ti is employed to promote adhesion and, so, influencing the nanoscale structure of the deposited Au film. In this work, we present experimental analysis on the nanoscale cross-section and surface morphology of Au films deposited on Ti. In particular, we sputter-deposited thick (>100 nm thickness Au films on Ti foils and we used Scanning Electron Microscopy to analyze the films cross-sectional and surface morphology as a function of the Au film thickness and deposition angle. In addition, we analyzed the Au films surface morphology by Atomic Force Microscopy which allowed quantifying the films surface roughness versus the film thickness and deposition angle. The results establish a relation between the Au films cross-sectional and surface morphologies and surface roughness to the film thickness and deposition angle. These results allow setting a general working framework to obtain Au films on Ti with specific morphological and topographic properties for desired applications in which the Ti adhesion layer is needed for Au.

Origin and evolution of mineralizing fluids and exploration of the Cerro Quema Au-Cu deposit (Azuero Peninsula, Panama) from a fluid inclusion and stable isotope perspective

Science.gov (United States)

Corral, Isaac; Cardellach, Esteve; Corbella, Merce; Canals, Angels; Griera, Albert; Gomez-Gras, David; Johnson, Craig A.

2017-01-01

Cerro Quema is a high sulfidation epithermal Au-Cu deposit with a measured, indicated and inferred resource of 35.98 Mt. @ 0.77 g/t Au containing 893,600 oz. Au (including 183,930 oz. Au equiv. of Cu ore). It is characterized by a large hydrothermal alteration zone which is interpreted to represent the lithocap of a porphyry system. The innermost zone of the lithocap is constituted by vuggy quartz with advanced argillic alteration locally developed on its margin, enclosed by a well-developed zone of argillic alteration, grading to an external halo of propylitic alteration. The mineralization occurs in the form of disseminations and microveinlets of pyrite, chalcopyrite, enargite, tennantite, and trace sphalerite, crosscut by quartz, barite, pyrite, chalcopyrite, sphalerite and galena veins.Microthermometric analyses of two phase (L + V) secondary fluid inclusions in igneous quartz phenocrysts in vuggy quartz and advanced argillically altered samples indicate low temperature (140–216 °C) and low salinity (0.5–4.8 wt% NaCl eq.) fluids, with hotter and more saline fluids identified in the east half of the deposit (Cerro Quema area).Stable isotope analyses (S, O, H) were performed on mineralization and alteration minerals, including pyrite, chalcopyrite, enargite, alunite, barite, kaolinite, dickite and vuggy quartz. The range of δ34S of sulfides is from − 4.8 to − 12.7‰, whereas δ34S of sulfates range from 14.1 to 17.4‰. The estimated δ34SΣS of the hydrothermal fluid is − 0.5‰. Within the advanced argillic altered zone the δ34S values of sulfides and sulfates are interpreted to reflect isotopic equilibrium at temperatures of ~ 240 °C. The δ18O values of vuggy quartz range from 9.0 to 17.5‰, and the δ18O values estimated for the vuggy quartz-forming fluid range from − 2.3 to 3.0‰, indicating that it precipitated from mixing of magmatic fluids with surficial fluids. The δ18O of kaolinite ranges from 12.7 to 18.1‰ and �

Impact of ambient environment on the electronic structure of CuPc/Au sample

Science.gov (United States)

Sinha, Sumona; Mukherjee, M.

2018-02-01

The performances of organic devices are crucially connected with their stability in the ambient environment. The impact of 24 h. Ambient environment exposure to the electronic structures of about 12 nm thick CuPc thin film on clean Au substrate have been studied employing UV photoemission spectroscopy technique. X-ray photoemission spectroscopy (XPS) was used to find out the origin of the change of the electronic structures in the sample with the exposure. The XPS study suggests that the oxidation occurs at the CuPc thin film. Due to the adsorption of oxygen in the CuPc film from the ambient air, charge carriers are formed within the CuPc film. Moreover, the XPS results imply that the CuPc film is sufficiently thinner for diffusing oxygen molecules through it and gets physically absorbed on Au substrate during the ambient exposure. Consequently, the hole injection barrier height of pristine CuPc film, grown on Au substrate, is reduced by about 0.50 eV and work-function of the pristine CuPc sample is enhanced by around 0.25 eV in the exposure. The findings will help to understand the mechanism that governs the degradation of performance of CuPc based devices in ambient environment.

Platinum-group element geochemistry used to determine Cu and Au fertility in the Northparkes igneous suites, New South Wales, Australia

Science.gov (United States)

Hao, Hongda; Campbell, Ian H.; Park, Jung-Woo; Cooke, David R.

2017-11-01

decrease of both Pt and Pd at 1.2 wt.% MgO to sulfide saturation. We suggest that the Goonumbla and Wombin suites are barren because early sulfide saturation locked most of the Cu and Au in a sulfide phase in the cumulus pile of a deep parental magma chamber, well before volatile saturation, so that when the magma reached volatile saturation, it did not have access to the Cu and Au. This contrasts with the relatively late sulfide saturation in the ore-associated suite, which was followed shortly afterwards by volatile saturation. Rayleigh fractionation concentrated incompatible Cu and Au by at least a factor of five before volatile saturation. The short crystallization interval between immiscible sulfide and volatile saturation allowed some Au and Cu to be stripped from the evolving magma. Gold, with its higher partition coefficient into immiscible sulfide melts, was more affected than Cu. The result is a Cu-Au deposit. Our study also suggests that Rayleigh fractionation is as at least as important as the initial concentration of chalcophile elements in the parent magma in determining the fertility of felsic magma suites.

Tracing low-temperature aqueous metal migration in mineralized watersheds with Cu isotope fractionation

International Nuclear Information System (INIS)

Mathur, R.; Munk, L.A.; Townley, B.; Gou, K.Y.; Gómez Miguélez, N.; Titley, S.; Chen, G.G.; Song, S.; Reich, M.; Tornos, F.; Ruiz, J.

2014-01-01

Highlights: • Cu isotope fractionation of ores and waters identifies copper sulfide weathering. • Redox reactions cause isotopic shift measured in areas of sulfide weathering. • Consistent isotope signature in different deposit, climate, or concentration. - Abstract: Copper isotope signatures in waters emanating from mineralized watersheds provide evidence for the source aqueous copper in solution. Low-temperature aqueous oxidation of Cu sulfide minerals produces significant copper isotopic fractionation between solutions and residues. Abiotic experimental data of fractionation (defined as Δ liquid–solid ‰ = δ 65 Cu liquid − δ 65 Cu solid ) are on the order of 1–3‰ and are unique for copper rich-sulfide minerals. Data presented here from ores and waters within defined boundaries of porphyry copper, massive sulfide, skarn, and epithermal ore deposits mimic abiotic experiments. Thus, the oxidation of sulfide minerals appears to cause the signatures in the waters although significant biological, temperature, and pH variations exist in the fluids. Regardless of the deposit type, water type, concentration of Cu in solution, or location, the data provide a means to trace sources of metals in solutions. This relationship allows for tracking sources and degree of metal migration in low temperature aqueous systems and has direct application to exploration geology and environmental geochemistry

A comparative study of Cu, Ag and Au doped CeO{sub 2} in the total oxidation of volatile organic compounds (VOCs)

Energy Technology Data Exchange (ETDEWEB)

Aboukaïs, Antoine, E-mail: aboukais@univ-littoral.fr [Unité de Chimie Environnementale et Interactions sur le Vivant EA 4492, ULCO, Equipe de Catalyse-UCEIV, MREI, 59140, Dunkerque (France); Skaf, Mira, E-mail: miraskaf@hotmail.com [Unité de Chimie Environnementale et Interactions sur le Vivant EA 4492, ULCO, Equipe de Catalyse-UCEIV, MREI, 59140, Dunkerque (France); Department of Chemistry, Faculty of Sciences, University of Balamand, P.O. Box 100, Deir El Balamand, Kelhat-Tripoli (Lebanon); Hany, Sara, E-mail: sarahani@hotmail.com [Unité de Chimie Environnementale et Interactions sur le Vivant EA 4492, ULCO, Equipe de Catalyse-UCEIV, MREI, 59140, Dunkerque (France); Cousin, Renaud, E-mail: Renaud.Cousin@univ-littoral.fr [Unité de Chimie Environnementale et Interactions sur le Vivant EA 4492, ULCO, Equipe de Catalyse-UCEIV, MREI, 59140, Dunkerque (France); Aouad, Samer, E-mail: Samer.Aouad@balamand.edu.lb [Department of Chemistry, Faculty of Sciences, University of Balamand, P.O. Box 100, Deir El Balamand, Kelhat-Tripoli (Lebanon); Labaki, Madona, E-mail: mlabaki@ul.edu.lb [Laboratory of Physical Chemistry of Materials (LCPM)/PR2N, Faculty of Sciences, Lebanese University, Fanar, PO Box 90656, Jdeidet El Metn (Lebanon); Abi-Aad, Edmond, E-mail: abiaad@univ-littoral.fr [Unité de Chimie Environnementale et Interactions sur le Vivant EA 4492, ULCO, Equipe de Catalyse-UCEIV, MREI, 59140, Dunkerque (France)

2016-07-01

Total oxidation of two Volatile Organic Compounds (VOCs), propylene and toluene, was investigated over M/CeO{sub 2} catalysts, where M is a metal from IB group (i.e. Au, Ag, Cu), prepared by two different methods: the conventional wet impregnation and the deposition-precipitation. The catalysts have been characterized by means of total surface area (BET), X-ray diffraction (XRD), electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS), diffuse reflectance ultra-violet-visible spectroscopy (DR-UV/Vis), and temperature-programmed reduction (TPR), in order to explain the differences observed in their catalytic activity towards the studied reactions. By comparing the two different preparation methods, the presence of metal in high oxidation state for gold and silver, and the presence of clusters for copper were the main factors responsible for the high catalytic activity. This latter was also found to be related, when comparing the different IB metals, to the values of the oxidation/reduction potential of the redox couples of the different metals. - Highlights: • IB metals (Au, Ag and Cu) were supported on ceria (CeO{sub 2}) by two different methods. • The solids were tested as catalysts for total oxidation of propylene and toluene. • The deposition-precipitation is better for Au whereas for Ag and Cu it is the impregnation. • High oxidation states of gold and silver and clusters of copper enhanced catalytic behavior. • Catalytic activity is linked to the oxidation/reduction potential of the redox IB couples.

Main characteristics and genesis of the Vale de Pães skarn (Cuba-Vidigueira, Ossa Morena Zone, Portugal

Directory of Open Access Journals (Sweden)

Salgueiro, R.

2010-06-01

Full Text Available The Vale de Pães (Cuba-Vidigueira mineralisation is composed of magnetite ± sulphides and hosted in a Pre-Variscan metamorphic sequence intruded by igneous rocks belonging to the Beja Igneous Complex. Its mineral and chemical features are compatible with a zoned Fe-skarn: Mg-rich (Fo + Di90, oxidised and Ca-rich (Grs + Di81-39, oxidised or relatively reduced. In the Fe-Mg skarn, magnetite deposition occurred along with the anhydrous mineral assemblage at ≈ 600 °C; sulphides precipitated from the retrograde stage onset (≤ 550 °C and during the hydrated and carbonate phases formation period (< 420 °C. In the Fe-Ca skarn, magnetite precipitated during the retrograde stage (< 550 °C together with the hydrated mineral association, and was followed by sulphides at ≈ 400°C. The mineralising process involved moderate-high salinity fluids and was controlled by variations in redox potential and pH.

La mineralización del Vale de Pães (Cuba-Vidigueira, compuesta de magnetita ± sulfuros, se produce dentro de una secuencia metamórfica ante-Varisca intruida por el Complejo Ígneo de Beja (Beja Igneous Complex. Sus características químicas y mineralógicas son consistentes con un skarn de Fe zonificado: rico en Mg (Fo + Di≈90, oxidado y rico en Ca (Grs + Di81-39, oxidado o relativamente reducido. En el skarn de Fe-Mg, la deposición de magnetita acompaña a la paragénesis mineral anhidra (≈ 600 °C; la precipitación de sulfuros se produce desde el comienzo de la etapa retrógrada (≤ 550 °C y continuó durante la formación de fases hidratadas y carbonatadas (< 420 °C. En el skarn de Fe-Ca, la magnetita se genera en la fase de retroceso (< 550 °C, en relación con la asociación de minerales hidratados, seguido de sulfuro (≈ 400 °C. El proceso de mineralización de los fluidos de salinidad moderada-alta era controlado por los cambios en el potencial redox y el pH.

Cu-Al alloy formation by thermal annealing of Cu/Al multilayer films deposited by cyclic metal organic chemical vapor deposition

Science.gov (United States)

Moon, Hock Key; Yoon, Jaehong; Kim, Hyungjun; Lee, Nae-Eung

2013-05-01

One of the most important issues in future Cu-based interconnects is to suppress the resistivity increase in the Cu interconnect line while decreasing the line width below 30 nm. For the purpose of mitigating the resistivity increase in the nanoscale Cu line, alloying Cu with traces of other elements is investigated. The formation of a Cu alloy layer using chemical vapor deposition or electroplating has been rarely studied because of the difficulty in forming Cu alloys with elements such as Al. In this work, Cu-Al alloy films were successfully formed after thermal annealing of Cu/Al multilayers deposited by cyclic metal-organic chemical vapor deposition (C-MOCVD). After the C-MOCVD of Cu/Al multilayers without gas phase reaction between the Cu and Al precursors in the reactor, thermal annealing was used to form Cu-Al alloy films with a small Al content fraction. The resistivity of the alloy films was dependent on the Al precursor delivery time and was lower than that of the aluminum-free Cu film. No presence of intermetallic compounds were detected in the alloy films by X-ray diffraction measurements and transmission electron spectroscopy.

A DFT-based genetic algorithm search for AuCu nanoalloy electrocatalysts for CO2 reduction

DEFF Research Database (Denmark)

Lysgaard, Steen; Mýrdal, Jón Steinar Garðarsson; Hansen, Heine Anton

2015-01-01

Using a DFT-based genetic algorithm (GA) approach, we have determined the most stable structure and stoichiometry of a 309-atom icosahedral AuCu nanoalloy, for potential use as an electrocatalyst for CO2 reduction. The identified core–shell nano-particle consists of a copper core interspersed....... This shows that the mixed Cu135@Au174 core–shell nanoalloy has a similar adsorption energy, for the most favorable site, as a pure gold nano-particle. Cu, however, has the effect of stabilizing the icosahedral structure because Au particles are easily distorted when adding adsorbates....... that it is possible to use the LCAO mode to obtain a realistic estimate of the molecular chemisorption energy for systems where the computation in normal grid mode is not computationally feasible. These corrections are employed when calculating adsorption energies on the Cu, Au and most stable mixed particles...

Order-disorder phase transitions in Au-Cu nanocubes: from nano-thermodynamics to synthesis.

Science.gov (United States)

Mendoza-Cruz, R; Bazán-Diaz, L; Velázquez-Salazar, J J; Samaniego-Benitez, J E; Ascencio-Aguirre, F M; Herrera-Becerra, R; José-Yacamán, M; Guisbiers, G

2017-07-13

Catalysts have been widely used in industries and can be optimized by tuning the composition and chemical ordering of the elements involved in the nano-alloy. Among bi-metallic alloys, the Au-Cu system is of particular interest because it exhibits ordered phases at low temperatures. Nevertheless, the temperature at which these ordered structures are formed is totally unknown at the nanoscale. Consequently, to speed up the development of these catalysts, this paper theoretically predicts the structural phase transitions between ordered and disordered phases for the Au-Cu system by using nano-thermodynamics. Following the predictions, the suggested annealing temperatures have been carefully chosen and consequently, Au-Cu ordered nanocubes have been successfully synthesized through a solventless protocol. The results are fully supported by electron microscopy observations.

Surface structure of AU3Cu(001)

DEFF Research Database (Denmark)

Eckstein, G.A.; Maupai, S.; Dakkouri, A.S.

1999-01-01

The surface morphology, composition, and structure of Au3Cu(001) as determined by scanning tunneling microscopy and surface x-ray diffraction are presented. Atomic resolution STM images reveal distinctive geometric features. The analysis of the surface x-ray diffraction data provides clear evidence...... for the surface structure. [S0163-1829(99)04535-X]....

Au-Cu core-shell nanocube-catalyzed click reactions for efficient synthesis of diverse triazoles.

Science.gov (United States)

Madasu, Mahesh; Hsia, Chi-Fu; Huang, Michael H

2017-06-01

Au-Cu core-shell nanocubes and octahedra synthesized in aqueous solution were employed to catalyze a 1,3-dipolar cycloaddition reaction between phenylacetylene and benzyl azide in water at 50 °C for 3 h. Interestingly, the nanocubes were far more efficient in catalyzing this reaction, giving 91% yield of a regioselective 1,4-triazole product, while octahedra only recorded 46% yield. The Au-Cu nanocubes were subsequently employed to catalyze the click reaction between benzyl azide and a broad range of aromatic and aliphatic alkynes. The product yields ranged from 78 to 99%. Clearly the Au-Cu cubes exposing {100} surfaces are an excellent and green catalyst for click reactions.

A synchrotron radiation study of nonlinear diffusion in Cu-Au

International Nuclear Information System (INIS)

Menon, E.S.K.; Huang, P.; Kraitchman, M.; deFontaine, D.; Hoyt, J.J.; Chow, P.

1992-01-01

This paper reports a study in which alternate layers of pure copper and gold were vapor deposited on a sodium chloride substrate, the average concentration of the films being Cu-16 at% Au and the layering periodicity (modulation wavelength) being 3.31 nm. The composition modulation gives rise to satellite diffraction peaks around the (200) Bragg reelections. Synchrotron radiation at SSRL was able to detect u to third order satellite intensity the evolution of which was measured as a function of annealing time at 515 K. although the first order satellite intensity decayed as expected exponentially with time, intensities of both second and third order satellites decreased very rapidly at first, then increased before decaying exponentially. These results are in conformity with theoretical models of satellite evolution during annealing in a one-dimensional modulated system governed by a nonlinear diffusion equation

SERS study of surface plasmon resonance induced carrier movement in Au@Cu2O core-shell nanoparticles

Science.gov (United States)

Chen, Lei; Zhang, Fan; Deng, Xin-Yu; Xue, Xiangxin; Wang, Li; Sun, Yantao; Feng, Jing-Dong; Zhang, Yongjun; Wang, Yaxin; Jung, Young Mee

2018-01-01

A plasmon induced carrier movement enhanced mechanism of surface-enhanced Raman scattering (SERS) was investigated using a charge-transfer (CT) enhancement mechanism. Here, we designed a strategy to study SERS in Au@Cu2O nanoshell nanoparticles with different shell thicknesses. Among the plasmonically coupled nanostructures, Au spheres with Cu2O shells have been of special interest due to their ultrastrong electromagnetic fields and controllable carrier transfer properties, which are useful for SERS. Au@Cu2O nanoshell nanoparticles (NPs) with shell thicknesses of 48-56 nm are synthesized that exhibit high SERS activity. This high activity originates from plasmonic-induced carrier transfer from Au@Cu2O to 4-mercaptobenzoic acid (MBA). The CT transition from the valence band (VB) of Cu2O to the second excited π-π* transition of MBA, and is of b2 electronic symmetry, which was enhanced significantly. The Herzberg-Teller selection rules were employed to predict the observed enhanced b2 symmetry modes. The system constructed in this study combines the long-range electromagnetic effect of Au NPs, localized surface plasmon resonance (LSPR) of the Au@Cu2O nanoshell, and the CT contribution to assist in understanding the SERS mechanism based on LSPR-induced carrier movement in metal/semiconductor nanocomposites.

Preparation and electric and photoelectric properties of thin deposits of Fe, Co, Ni, Cu, Ag, Au and Pd

International Nuclear Information System (INIS)

Heras, J.M.; Albano, E.V.; Asensio, M.C.; Viscido, L.

1984-01-01

The physics chemical properties of desordered metallic thin films of Fe, Co, Ni, Pd, Ag, Cu and Au are of great interest for its catalitic activity and for its application in radiation absorption of solar cells and micro electronic devices. This work has the purpose of reporting the experimental results obtained by evaporated films of these metals, which present desordered characteristics, small crystal size and high surface-volume rate. (A.C.A.S.) [pt

Atom probe tomography simulations and density functional theory calculations of bonding energies in Cu3Au

KAUST Repository

Boll, Torben; Zhu, Zhiyong; Al-Kassab, Talaat; Schwingenschlö gl, Udo

2012-01-01

In this article the Cu-Au binding energy in Cu3Au is determined by comparing experimental atom probe tomography (APT) results to simulations. The resulting bonding energy is supported by density functional theory calculations. The APT simulations

Deposition of Au/TiO2 film by pulsed laser

International Nuclear Information System (INIS)

Zhao Chongjun; Zhao Quanzhong; Zhao Qitao; Qiu Jianrong; Zhu Congshan

2006-01-01

Au nanoparticles, which were photoreduced by a Nd:YAG laser in HAuCl 4 solution containing TiO 2 colloid and accompanied by the TiO 2 particles, were deposited on the substrate surface. The film consisting of Au/TiO 2 particles was characterized by the absorption spectra, scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The adhesion between the film and substrate was evaluated by using adhesive tape test. It was found that the presence of TiO 2 dramatically enhanced the adhesion strength between the film and the substrate, as well as the deposition rate of film. The mechanism for the deposition of Au/TiO 2 film was also discussed

Crystal and electronic structure study of AgAu and AgCu bimetallic alloy thin films by X-ray techniques

Energy Technology Data Exchange (ETDEWEB)

Ozkendir, O. Murat, E-mail: ozkendir@gmail.com [Mersin University, Faculty of Technology, Energy Systems Engineering, Tarsus (Turkey); Mersin University, Institute of Natural Science, Department of Nanotechnology and Advanced Materials, Mersin (Turkey); Cengiz, E. [Karadeniz Technical University, Faculty of Science, Department of Physics, Trabzon (Turkey); Yalaz, E. [Mersin University, Institute of Natural Science, Department of Nanotechnology and Advanced Materials, Mersin (Turkey); Söğüt, Ö.; Ayas, D.H. [Kahramanmaraş Sütçü İmam Üniversitesi, Faculty of Science and Letters, Department of Physics, Kahramanmaraş (Turkey); Thammajak, B. Nirawat [Synchrotron Light Research Institute (Public Organisation), 111 University Avenue, T. Suranaree, A. Muang, Nakhon Ratchasima 30000 (Thailand)

2016-05-15

Highlights: • Crystal and electronic properties of bimetallic AgCu and AgAu alloy thin films were studied. • Both AgCu and AgAu bimetallic samples were determined to have cubic crystal geometry. • Strong influence of Cu and Au atoms on the electronic structure of the Ag atoms were determined. - Abstract: Crystal and electronic structure properties of bimetallic AgAu and AgCu alloy thin films were investigated by X-ray spectroscopic techniques. The aim of this study is to probe the influence of Au or Cu atoms on the electronic behaviors of Ag ions in bimetallic alloy materials that yields different crystal properties. To identify the mechanisms causing crystal phase transitions, study were supported by the collected EXAFS (Extended X-ray Absorption Fine Structure) data. Crystal structures of both Cu and Au doped bimetallic Ag samples were determined mainly in cubic geometry with “Fm3m” space group. Through the Ag–Au and Ag–Cu molecular interactions during bimetallic alloy formations, highly overlapped electronic levels that supports large molecular band formations were observed with different ionization states. Besides, traces of the d–d interactions in Au rich samples were determined as the main interplay in the broad molecular bond formations. The exact atomic locations and types in the samples were determined by EXAFS studies and supported by the performed calculations with FEFF scientific code.

Microstructure of Co/X (X=Cu,Ag,Au) epitaxial thin films grown on Al2O3(0001) substrates

International Nuclear Information System (INIS)

Ohtake, Mitsuru; Akita, Yuta; Futamoto, Masaaki; Kirino, Fumiyoshi

2007-01-01

Epitaxial thin films of Co/X (X=Cu,Ag,Au) were prepared on Al 2 O 3 (0001) substrates at substrate temperatures of 100 and 300 degree sign C by UHV molecular beam epitaxy. A complicated microstructure was realized for the epitaxial thin films. In-situ reflection high-energy electron diffraction observation has shown that X atoms of the buffer layer segregated to the surface during Co layer deposition, and it yielded a unique epitaxial granular structure. The structure consists of small Co grains buried in the X buffer layer, where both the magnetic small Co grains and the nonmagnetic X layer are epitaxially grown on the single crystal substrate. The structure varied depending on the X element and the substrate temperature. The crystal structure of Co grains is influenced by the buffer layer material and determined to be hcp and fcc structures for the buffer layer materials of Au and Cu, respectively

Late-Hercynian intrusion-related gold deposits: An integrated model on the Tighza polymetallic district, central Morocco

Science.gov (United States)

Éric, Marcoux; Khadija, Nerci; Yannick, Branquet; Claire, Ramboz; Gilles, Ruffet; Jean-Jacques, Peucat; Ross, Stevenson; Michel, Jébrak

2015-07-01

Gold have been recently recognized in the Tighza (formerly Jebel Aouam) district, in the Hercynian belt of central Morocco. This district has long been known for its W mineralization, as well as major Pb-Ag-Zn, and minor Sb-Ba deposits, all geographically associated with late-Hercynian calc-alkaline magmatism. Gold mineralization in the district is mainly hosted by thick W-Au quartz veins located around the "Mine granite" small granitic plug. Within the veins, gold grade is highest (up to 70 g/t) close to the granite but rapidly decreases going outward from the granite, defining a perigranitic zoning. Anomalous gold grades have also been measured in hydrothermal skarn layers close to two other granitic plugs (Kaolin granite and Mispickel granite), associated with disseminated As-Fe sulfides. The paragenetic sequence for the W-Au quartz veins shows three stages: (1) an early oxidized stage with wolframite-scheelite associated with early quartz (Q1), (2) an intermediate Bi-As-Te-Mo-Au sulfide stage with loellingite, bismuth minerals and native gold with a later quartz (Q2), restricted to a narrow distance from the granite, and (3) a late lower temperature As-Cu-Zn-(Pb) stage with abundant massive pyrrhotite, arsenopyrite and sphalerite, locally forming independent veins ("pyrrhotite vein"). Both Q1 hyaline and Q2 saccharoidal gold-bearing quartz display aqua-carbonic fluids with minor H2S and Cu and an homogeneous composition (81 mole% H2O, 18 mole% CO2 and about 1 mole% NaCl). The trapping pressure is estimated to 1.5-2 kbar with temperature ranging from 300 to 350 °C. Q1 inclusions have exploded indicating an uplift of the Tighza block, that lead to saccharoidal Q2 quartz deposition with multiphase NaCl-saturated fluid inclusions. 40Ar/39Ar dating demonstrates that the "Mine granite", tungsten skarnoid, scheelite-molybdenite veins, and very likely gold-bearing veins are coeval, emplaced at 286 ± 1 Ma. Multiple and widespread metal sources are indicated by

Near-side azimuthal and pseudorapidity correlations using neutral strange baryons and mesons in d +Au , Cu + Cu, and Au + Au collisions at √{sN N}=200 GeV

Science.gov (United States)

Abelev, B.; Adamczyk, L.; Adkins, J. K.; Agakishiev, G.; Aggarwal, M. M.; Ahammed, Z.; Alekseev, I.; Aparin, A.; Arkhipkin, D.; Aschenauer, E. C.; Ashraf, M. U.; Attri, A.; Averichev, G. S.; Bai, X.; Bairathi, V.; Barnby, L. S.; Bellwied, R.; Bhasin, A.; Bhati, A. K.; Bhattarai, P.; Bielcik, J.; Bielcikova, J.; Bland, L. C.; Bombara, M.; Bordyuzhin, I. G.; Bouchet, J.; Brandenburg, J. D.; Brandin, A. V.; Bunzarov, I.; Butterworth, J.; Caines, H.; Calderón de la Barca Sánchez, M.; Campbell, J. M.; Cebra, D.; Chakaberia, I.; Chaloupka, P.; Chang, Z.; Chatterjee, A.; Chattopadhyay, S.; Chen, J. H.; Chen, X.; Cheng, J.; Cherney, M.; Christie, W.; Contin, G.; Crawford, H. J.; Das, S.; De Silva, L. C.; Debbe, R. R.; Dedovich, T. G.; Deng, J.; Derevschikov, A. A.; di Ruzza, B.; Didenko, L.; Dilks, C.; Dong, X.; Drachenberg, J. L.; Draper, J. E.; Du, C. M.; Dunkelberger, L. E.; Dunlop, J. C.; Efimov, L. G.; Engelage, J.; Eppley, G.; Esha, R.; Evdokimov, O.; Eyser, O.; Fatemi, R.; Fazio, S.; Federic, P.; Fedorisin, J.; Feng, Z.; Filip, P.; Fisyak, Y.; Flores, C. E.; Fulek, L.; Gagliardi, C. A.; Gaillard, L.; Garand, D.; Geurts, F.; Gibson, A.; Girard, M.; Greiner, L.; Grosnick, D.; Gunarathne, D. S.; Guo, Y.; Gupta, A.; Gupta, S.; Guryn, W.; Hamad, A. I.; Hamed, A.; Haque, R.; Harris, J. W.; He, L.; Heppelmann, S.; Heppelmann, S.; Hirsch, A.; Hoffmann, G. W.; Horvat, S.; Huang, T.; Huang, B.; Huang, X.; Huang, H. Z.; Huck, P.; Humanic, T. J.; Igo, G.; Jacobs, W. W.; Jang, H.; Jentsch, A.; Jia, J.; Jiang, K.; Jones, P. G.; Judd, E. G.; Kabana, S.; Kalinkin, D.; Kang, K.; Kauder, K.; Ke, H. W.; Keane, D.; Kechechyan, A.; Khan, Z. H.; Kikoła, D. P.; Kisel, I.; Kisiel, A.; Kochenda, L.; Koetke, D. D.; Kosarzewski, L. K.; Kraishan, A. F.; Kravtsov, P.; Krueger, K.; Kumar, L.; Lamont, M. A. C.; Landgraf, J. M.; Landry, K. D.; Lauret, J.; Lebedev, A.; Lednicky, R.; Lee, J. H.; Li, C.; Li, Y.; Li, W.; Li, X.; Li, X.; Lin, T.; Lisa, M. A.; Liu, F.; Ljubicic, T.; Llope, W. J.; Lomnitz, M.; Longacre, R. S.; Luo, S.; Luo, X.; Ma, L.; Ma, R.; Ma, G. L.; Ma, Y. G.; Magdy, N.; Majka, R.; Manion, A.; Margetis, S.; Markert, C.; Matis, H. S.; McDonald, D.; McKinzie, S.; Meehan, K.; Mei, J. C.; Miller, Z. W.; Minaev, N. G.; Mioduszewski, S.; Mishra, D.; Mohanty, B.; Mondal, M. M.; Morozov, D. A.; Mustafa, M. K.; Nandi, B. K.; Nattrass, C.; Nasim, Md.; Nayak, T. K.; Nigmatkulov, G.; Niida, T.; Nogach, L. V.; Noh, S. Y.; Novak, J.; Nurushev, S. B.; Odyniec, G.; Ogawa, A.; Oh, K.; Okorokov, V. A.; Olvitt, D.; Page, B. S.; Pak, R.; Pan, Y. X.; Pandit, Y.; Panebratsev, Y.; Pawlik, B.; Pei, H.; Perkins, C.; Pile, P.; Pluta, J.; Poniatowska, K.; Porter, J.; Posik, M.; Poskanzer, A. M.; Pruthi, N. K.; Putschke, J.; Qiu, H.; Quintero, A.; Ramachandran, S.; Ray, R. L.; Ritter, H. G.; Roberts, J. B.; Rogachevskiy, O. V.; Romero, J. L.; Ruan, L.; Rusnak, J.; Rusnakova, O.; Sahoo, N. R.; Sahu, P. K.; Sakrejda, I.; Salur, S.; Sandweiss, J.; Sarkar, A.; Schambach, J.; Scharenberg, R. P.; Schmah, A. M.; Schmidke, W. B.; Schmitz, N.; Seger, J.; Seyboth, P.; Shah, N.; Shahaliev, E.; Shanmuganathan, P. V.; Shao, M.; Sharma, B.; Sharma, A.; Sharma, M. K.; Shen, W. Q.; Shi, Z.; Shi, S. S.; Shou, Q. Y.; Sichtermann, E. P.; Sikora, R.; Simko, M.; Singha, S.; Skoby, M. J.; Smirnov, N.; Smirnov, D.; Solyst, W.; Song, L.; Sorensen, P.; Spinka, H. M.; Srivastava, B.; Stanislaus, T. D. S.; Stepanov, M.; Stock, R.; Strikhanov, M.; Stringfellow, B.; Sumbera, M.; Summa, B.; Sun, Y.; Sun, Z.; Sun, X. M.; Surrow, B.; Svirida, D. N.; Tang, Z.; Tang, A. H.; Tarnowsky, T.; Tawfik, A.; Thäder, J.; Thomas, J. H.; Timmins, A. R.; Tlusty, D.; Todoroki, T.; Tokarev, M.; Trentalange, S.; Tribble, R. E.; Tribedy, P.; Tripathy, S. K.; Tsai, O. D.; Ullrich, T.; Underwood, D. G.; Upsal, I.; Van Buren, G.; van Nieuwenhuizen, G.; Vandenbroucke, M.; Varma, R.; Vasiliev, A. N.; Vertesi, R.; Videbæk, F.; Vokal, S.; Voloshin, S. A.; Vossen, A.; Wang, H.; Wang, Y.; Wang, G.; Wang, Y.; Wang, J. S.; Wang, F.; Webb, G.; Webb, J. C.; Wen, L.; Westfall, G. D.; Wieman, H.; Wissink, S. W.; Witt, R.; Wu, Y.; Xiao, Z. G.; Xie, W.; Xie, G.; Xin, K.; Xu, Y. F.; Xu, Q. H.; Xu, N.; Xu, J.; Xu, H.; Xu, Z.; Yang, Y.; Yang, Q.; Yang, S.; Yang, Y.; Yang, Y.; Yang, C.; Ye, Z.; Ye, Z.; Yi, L.; Yip, K.; Yoo, I.-K.; Yu, N.; Zbroszczyk, H.; Zha, W.; Zhang, S.; Zhang, X. P.; Zhang, Y.; Zhang, S.; Zhang, J. B.; Zhang, J.; Zhang, J.; Zhang, Z.; Zhao, J.; Zhong, C.; Zhou, L.; Zhu, X.; Zoulkarneeva, Y.; Zyzak, M.; STAR Collaboration

2016-07-01

We present measurements of the near side of triggered di-hadron correlations using neutral strange baryons (Λ ,Λ ¯) and mesons (KS0) at intermediate transverse momentum (3 < pT <6 GeV /c ) to look for possible flavor and baryon-meson dependence. This study is performed in d +Au , Cu+Cu, and Au+Au collisions at √{sN N}=200 GeV measured by the STAR experiment at RHIC. The near-side di-hadron correlation contains two structures, a peak which is narrow in azimuth and pseudorapidity consistent with correlations from jet fragmentation, and a correlation in azimuth which is broad in pseudorapidity. The particle composition of the jet-like correlation is determined using identified associated particles. The dependence of the conditional yield of the jet-like correlation on the trigger particle momentum, associated particle momentum, and centrality for correlations with unidentified trigger particles are presented. The neutral strange particle composition in jet-like correlations with unidentified charged particle triggers is not well described by PYTHIA. However, the yield of unidentified particles in jet-like correlations with neutral strange particle triggers is described reasonably well by the same model.

Participant and spectator scaling of spectator fragments in Au + Au and Cu + Cu collisions at √{sN N}=19.6 and 22.4 GeV

Science.gov (United States)

Alver, B.; Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Chai, Z.; Chetluru, V.; Decowski, M. P.; García, E.; Gburek, T.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Harnarine, I.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Li, W.; Lin, W. T.; Loizides, C.; Manly, S.; McLeod, D.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Richardson, E.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Sedykh, I.; Skulski, W.; Smith, C. E.; Stankiewicz, M. A.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Szostak, A.; Tang, J.-L.; Tonjes, M. B.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Vaurynovich, S. S.; Verdier, R.; Veres, G. I.; Walters, P.; Wenger, E.; Willhelm, D.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wyngaardt, S.; Wysłouch, B.; Phobos Collaboration

2016-08-01

Spectator fragments resulting from relativistic heavy ion collisions, consisting of single protons and neutrons along with groups of stable nuclear fragments up to nitrogen (Z =7 ), are measured in PHOBOS. These fragments are observed in Au+Au (√{sNN}=19.6 GeV ) and Cu+Cu (22.4 GeV) collisions at high pseudorapidity (η ). The dominant multiply-charged fragment is the tightly bound helium (α ), with lithium, beryllium, and boron all clearly seen as a function of collision centrality and pseudorapidity. We observe that in Cu+Cu collisions, it becomes much more favorable for the α fragments to be released than lithium. The yields of fragments approximately scale with the number of spectator nucleons, independent of the colliding ion. The shapes of the pseudorapidity distributions of fragments indicate that the average deflection of the fragments away from the beam direction increases for more central collisions. A detailed comparison of the shapes for α and lithium fragments indicates that the centrality dependence of the deflections favors a scaling with the number of participants in the collision.

Magnetic and thermodynamic properties of GdCu4Au

International Nuclear Information System (INIS)

Bashir, Aiman K; Tchokonté, Moise B Tchoula; Britz, Douglas; Sondezi, B M; Strydom, André M

2015-01-01

The results of magnetic susceptibility, χ(T), magnetization, σ(μ 0 H), and specific heat, C P (T), for GdCu 4 Au are presented. The room temperature powder X-ray diffraction studies indicate a cubic MgCu 4 Sn – type crystal structure with space group F4-bar 3m (No.216). The low field dc χ(T) data shows an antiferromagnetic – like (AFM) anomaly associated with a Néel temperature T N = 10.8 K for GdCu 4 Au. In the paramagnetic region above T N , χ(T) data follows the Curies – Weiss law with an effective magnetic moment μ eff = 7.444(1) μ B and paramagnetic Weiss temperature θ P = -15.01(2) K. The experimental value of is close to the calculated value of 7.94 μ B expected for the free Gd 3+ -ion. The field-cooled (FC) and zero-field-cooled (ZFC) χ(T) data provide evidence for the formation of spin-glass state with a freezing temperature T f = 15 K. σ(μ 0 H) measured in the ordering region (below TN) shows that GdCu 4 Au undergoes metamagnetic transition above 0.7 T, characterized by a slight upward curvature above this field. Measurement of σ(μ 0 H) in the paramagnetic regions show a linear behaviour up to 0.7 T and a downward curvature at high fields. C P (T) data shows an AFM – like phase transition at T N = 10.4 K close to the phase transition observed in χ(T) results. The 4f-electron entropy reaches the value of Rln2 close to T N at 9.02 K and reaches the value of Rln(2J + 1) at T = 180 K

Temperature dependence of residual electrical resistivity of Cu-Au in pseudopotential approximation

International Nuclear Information System (INIS)

Khwaja, F.A.; Ahmed, I.; Shaukat, A.

1986-08-01

The problem of temperature dependence of residual electrical resistivity of Cu-Au system is re-examined in the light of static distortion and thermal vibration of the lattice along with the short-range-order of atoms above critical temperature. The extended version of Ziman's formula for resistivity obtained yields a unified version for the calculation of resistivity in pseudopotential approximation. The temperature dependence of the quantity Δρ/ρ in this framework for Cu-Au system is found to be in better agreement with the experimental data as compared to previous calculation. (author)

Cu and Cu2O films with semi-spherical particles grown by electrochemical deposition

International Nuclear Information System (INIS)

Zheng, Jin You; Jadhav, Abhijit P.; Song, Guang; Kim, Chang Woo; Kang, Young Soo

2012-01-01

Cu and Cu 2 O films can be prepared on indium-doped tin oxide glass substrates by simple electrodeposition in a solution containing 0.1 M Cu(NO 3 ) 2 and 3 M lactic acid at different pH values. At low pH (pH = 1.2), the uniform Cu films were obtained; when pH ≥ 7, the pure Cu 2 O films can be deposited. Especially, at pH = 11, the deposited Cu 2 O films exhibited cubic surface morphology exposing mainly {100} plane; in contrast, the films consisting of semi-spherical particles were obtained when the solution was being stirred for 2 weeks prior to use. The possible growth process and mechanism were comparatively discussed. - Highlights: ► Cu and Cu 2 O films were prepared by facile electrodeposition. ► Electrodeposition was preformed in electrolyte at different pH values. ► Dendritic Cu films were obtained at 1.2 pH with relatively high deposition potential. ► Semi-spherical Cu 2 O films were obtained with solution at 11 pH and stirred for 2 weeks. ► The possible growth mechanism of semi-spherical Cu 2 O films was discussed.

Using the concentration-volume (C-V) fractal model in the delineation of gold mineralized zones within the Tepeoba porphyry Cu-Mo-Au, Balikesir, NW Turkey

Science.gov (United States)

Kumral, Mustafa; Abdelnasser, Amr; Karaman, Muhittin; Budakoglu, Murat

2016-04-01

The Tepeoba porphyry Cu-Mo-Au mineralization that located at the Biga peninsula (W Turkey) developed around the Eybek pluton concentrated at its southern contact. This mineralization that hosted in the hornfels rocks of Karakaya Complex is associated with three main alteration zones; potassic, phyllic and propylitic alterations along the fault controlled margins of the Eybek pluton and quartz stockwork veining as well as brecciation zones. As well as two mineralized zones were occurred in the mine area; hypogene and oxidation/supergene zone. The hypogene zone has differentiated alteration types; high potassic and low phyllic alteration, while the oxidation/supergene zone has high phyllic and propylitic alterations. This work deals with the delineation of gold mineralized zone within this porphyry deposit using the concentration-volume (C-V) fractal model. Five zones of gold were calculated using its power-law C-V relationship that revealed that the main phase of gold mineralization stated at 5.3083 ppm Au concentration. In addition, the C-V log-log plot shows that the highly and moderately Au mineralization zone developed in western part of deposit correlated with oxidation zone related to propylitic alteration. On the other hand, its weakly mineralization zone has a widespread in the hypogene zone related to potassic alteration. This refers to the enrichment of gold and depletion of copper at the oxidation/supergene zone is due to the oxidation/supergene alteration processes that enrich the deposits by the meteoric water. Keywords: Concentration-volume (C-V) fractal model; gold mineralized zone; Tepeoba porphyry Cu-Mo-Au; Balikesir; NW Turkey.

Cu-Au alloy nanostructures coated with aptamers: a simple, stable and highly effective platform for in vivo cancer theranostics

Science.gov (United States)

Ye, Xiaosheng; Shi, Hui; He, Xiaoxiao; Yu, Yanru; He, Dinggeng; Tang, Jinlu; Lei, Yanli; Wang, Kemin

2016-01-01

As a star material in cancer theranostics, photoresponsive gold (Au) nanostructures may still have drawbacks, such as low thermal conductivity, irradiation-induced melting effect and high cost. To solve the problem, copper (Cu) with a much higher thermal conductivity and lower cost was introduced to generate a novel Cu-Au alloy nanostructure produced by a simple, gentle and one-pot synthetic method. Having the good qualities of both Cu and Au, the irregularly-shaped Cu-Au alloy nanostructures showed several advantages over traditional Au nanorods, including a broad and intense near-infrared (NIR) absorption band from 400 to 1100 nm, an excellent heating performance under laser irradiation at different wavelengths and even a notable photostability against melting. Then, via a simple conjugation of fluorophore-labeled aptamers on the Cu-Au alloy nanostructures, active targeting and signal output were simultaneously introduced, thus constructing a theranostic platform based on fluorophore-labeled, aptamer-coated Cu-Au alloy nanostructures. By using human leukemia CCRF-CEM cancer and Cy5-labeled aptamer Sgc8c (Cy5-Sgc8c) as the model, a selective fluorescence imaging and NIR photothermal therapy was successfully realized for both in vitro cancer cells and in vivo tumor tissues. It was revealed that Cy5-Sgc8c-coated Cu-Au alloy nanostructures were not only capable of robust target recognition and stable signal output for molecular imaging in complex biological systems, but also killed target cancer cells in mice with only five minutes of 980 nm irradiation. The platform was found to be simple, stable, biocompatible and highly effective, and shows great potential as a versatile tool for cancer theranostics.As a star material in cancer theranostics, photoresponsive gold (Au) nanostructures may still have drawbacks, such as low thermal conductivity, irradiation-induced melting effect and high cost. To solve the problem, copper (Cu) with a much higher thermal conductivity

Developing an aqueous approach for synthesizing Au and M@Au (M = Pd, CuPt) hybrid nanostars with plasmonic properties

OpenAIRE

Du, Jingshan; Yu, Junjie; Xiong, Yalin; Lin, Zhuoqing; Zhang, Hui; Yang, Deren

2014-01-01

Anisotropic Au nanoparticles show unique localized surface plasmon resonance (LSPR) properties, which make it attractive in optical, sensing, and biomedical applications. In this contribution, we report a general and facile strategy towards aqueous synthesis of Au and M@Au (M = Pd, CuPt) hybrid nanostars by reducing HAuCl4 with ethanolamine in the presence of cetyltrimethylammonium bromide (CTAB). According to electron microscopic observation and spectral monitoring, we found that the layered...

Electronic structures of PtCu, PtAg, and PtAu molecules: a Dirac four-component relativistic study

International Nuclear Information System (INIS)

Abe, Minori; Mori, Sayaka; Nakajima, Takahito; Hirao, Kimihiko

2005-01-01

Relativistic four-component calculations at several correlated levels have been performed for diatomic PtCu, PtAg, and PtAu molecules. The ground state spectroscopic constants of PtCu were calculated using the four-component MP2 method, and show good agreement with experiment. We also performed calculations on the experimentally unknown species, PtAg and PtAu, and the mono-cationic systems, PtCu + , PtAg + , and PtAu + . The low-lying excited states of these diatomic molecules were also investigated using the four-component multi-reference CI method

Electrochemical deposition of Cu and Nb from pyrrolidinium based ionic liquid

Energy Technology Data Exchange (ETDEWEB)

Mascia, Michele, E-mail: michele.mascia@unica.it [Dipartimento di Ingegneria Meccanica, Chimica e dei Materiali Università degli Studi di Cagliari, via Marengo 2, 09123 Cagliari (Italy); Vacca, Annalisa; Mais, Laura; Palmas, Simonetta [Dipartimento di Ingegneria Meccanica, Chimica e dei Materiali Università degli Studi di Cagliari, via Marengo 2, 09123 Cagliari (Italy); Musu, Elodia [Laboratorio Telemicroscopia Industriale, Sardegna Ricerche, Polaris, Parco Tecnologico della Sardegna, Edificio 3, Loc. Piscinamanna, 09010 Pula, CA (Italy); Delogu, Francesco [Dipartimento di Ingegneria Meccanica, Chimica e dei Materiali Università degli Studi di Cagliari, via Marengo 2, 09123 Cagliari (Italy)

2014-11-28

A study on the electrochemical deposition of Cu/Nb composites is presented in this work. The electrodeposition tests were performed using 1-butyl-1-methylpyrrolidinium bis (trifluoromethylsulphonyl) imide as solvent. The electrochemical behaviour of copper and niobium ions was investigated by cyclic and linear sweep voltammetries, allowing to obtain information on potentials and mechanisms of deposition. Firstly, the electrodeposition of Nb on Cu substrate and of Cu on Nb substrate was investigated; then, the deposition of Cu and Nb in dual bath mode was considered. All the experimental tests were carried out at 125 °C under inert atmosphere, in order to avoid interference of water and oxygen. According to the electrochemistry of the metals considered and based on the experimental results, the possible reaction path for the oxidation/reduction was proposed. Deposition tests were carried out at different potentials and the related samples were analysed by scanning electron microscopy and energy dispersive X-ray spectroscopy. Structural and chemical analyses indicate that the obtained deposits cover uniformly the electrode surface and exhibit individual layers with a characteristic size ranging between 50 and 100 nm. - Highlights: • Cu/Nb composites were obtained by electro-deposition from ionic liquid. • The electrochemical behaviour was studied by cyclic and linear sweep voltammetries. • Anodic dissolution of Cu and cathodic deposition of Cu, Nb and Cu/Nb were studied. • The Cu, Nb and Cu/Nb deposits were characterised through SEM and EDX analyses. • The characteristic length of the deposits ranges between 50 and 100 nm.

Carboniferous-Permian tectonic transition envisaged in two magmatic episodes at the Kuruer Cu-Au deposit, Western Tianshan (NW China)

Science.gov (United States)

Yu, Jie; Li, Nuo; Qi, Nan; Guo, Jian-Ping; Chen, Yan-Jing

2018-03-01

The Western Tianshan in NW China is one of the most important gold provinces in the Central Asian Orogenic Belt (CAOB). The recently discovered Kuruer Cu-Au deposit has been interpreted to represent a transition from high-sulfidation epithermal to porphyry mineralization system. In this study, we present new LA-ICP-MS zircon U-Pb ages for the many magmatic rock types at Kuruer, including the Dahalajunshan Formation andesitic tuff (333.2 ± 1.6 Ma), diorite porphyry (269.7 ± 2.0 Ma), slightly-altered (264.4 ± 2.6 Ma) and intensively-altered (270.5 ± 2.5 Ma) albite porphyry. These ages reveal two distinct magmatic episodes: The Early Carboniferous Dahalajunshan Formation (wall rocks) andesitic tuff samples contain narrow ranges of SiO2 (60.29-61.28 wt.%), TiO2 (0.96-0.98 wt.%), Al2O3 (16.55-16.57 wt.%) and Fe2O3T (5.36-5.57 wt.%). The tuff is characterized by LREE enrichment and HFSE depletion, as well as LREE/HREE enrichment ((La/Yb)N = 8.31-8.76) and negative Eu anomalies (δEu = 0.64-0.76). Zircon εHf (t) values are 5.4-8.2, and two-stage Hf model ages (TDM2) are 821-1016 Ma, indicating partial melting of a moderately depleted mantle wedge with Precambrian continental crustal input. The ore-forming Middle Permian diorite porphyry and (quartz) albite porphyry have variable major oxide compositions (e.g., SiO2 = 53.09-53.12 wt.% for the diorite porphyry, 70.84-78.03 wt.% for the albite porphyry, and 74.07-75.03 wt.% for the quartz albite porphyry) but similar chondrite-normalized REE and primitive mantle-normalized multi-element patterns. These porphyries display LREE enrichment and HFSE depletion, as well as elevated LREE/HREE enrichment and negative Eu anomalies. The positive zircon εHf(t) values (11.7-15.9 for the diorite porphyry, 8.9-14.9 for the albite porphyry) and young two-stage Hf model ages (TDM2) (282-542 Ma for the diorite porphyry, 337-717 Ma for the albite porphyry) indicate a major juvenile continental crustal involvement. We propose that the

Studies of petrography, metasomatic alteration, and genesis of Kamtal iron-copper skarn, northeast of Kharvana, East-Azarbaijan

Directory of Open Access Journals (Sweden)

Rasool Ferdowsi

2012-04-01

Full Text Available Kamtal skarn is located 15 km northeast of Kharvana, East-Azarbaijan. A quartz-monzonitic stock of Oligocene age intruded the upper Cretaceous sedimentary sequence (claystone, limestone, marl, and siltstone developing noticeable metamorphic (marble, hornfels and metasomatic (skarn alteration zones along the contact. Kamtal skarn is of calcic type and consists of both endoskarn and exoskarn zones. Exoskarn includes two zones of garnet skarn and epidote skarn. Skarnification processes are divided mainly in two major stages (1 prograde and (2 retrograde. During prograde stage, the emplacement of intrusive body caused isochemical metamorphism of the wall rocks and developed marble and hornfels units in enclosing rocks. Crystallization of intrusive body led to evolvement of hydrothermal fluid phase which infiltrated into enclosing rocks. Reaction of these fluids with the early-formed metamorphosed wall rocks brought about extensive progressive metasomatic alteration characterized by the formation of anhydrous calc-silicate minerals such as garnets and pyroxenes at a temperature range of 420-550°C and ¦O2=10-22-10-25. Retrograde stage was accompanied by some physicochemical changes (decrease in temperature to <420°C and increase in ¦S2 which caused the alteration of pre-existing anhydrous calc-silicates to hydrous calc-silicates (epidote, and tremolite-actinolite, silicates (quartz, chlorites, and other clay minerals, oxides (magnetite and hematite, sulfides (pyrite, chalcopyrite, and tetrahedrite, and carbonate (calcite. Comparison of Kamtal skarn with some other ones of corresponding type from Iran and other countries shows that Kamtal skarn well resembles to Anjerd and Pahnavar skarns in East-Azarbaijan.

Hardening mechanism of an Ag-Pd-Cu-Au dental casting alloy

International Nuclear Information System (INIS)

Seol, Hyo-Joung; Kim, Gi-Chul; Son, Kuk-Hyeon; Kwon, Yong Hoon; Kim, Hyung-Il

2005-01-01

Age-hardening behaviour and the related microstructural changes were studied to elucidate the hardening mechanism of an Ag-Pd-Cu-Au dental casting alloy by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). By considering hardness test and XRD results together, it was revealed that the hardness increased during the early stage of phase transformation of α into α 1 . In the SEM photographs, two phases of matrix and particle-like structures were observed, and the precipitation of element from the matrix progressed during isothermal aging. By SEM observations and EPMA analysis, it could be supposed that the increase in hardness was caused by the diffusion and aggregation of Cu atoms from the Ag-rich α matrix containing Au and Cu in the early stage of age-hardening process, and that the decrease in hardness was caused by the progress of coarsening of Cu-rich lamellar precipitates in the later stage of the age-hardening process. The changes in the Ag-rich matrix caused both the increase and decrease in hardness, and the CuPd phase containing small amounts of Zn and Sn did not contribute to the hardness changes

Age-hardening and related phase transformation in an experimental Ag-Cu-Pd-Au alloy

International Nuclear Information System (INIS)

Seol, Hyo-Joung; Lee, Doung-Hun; Lee, Hee-Kyung; Takada, Yukyo; Okuno, Osamu; Kwon, Yong Hoon; Kim, Hyung-Il

2006-01-01

The age-hardening behaviour, phase transformation and related microstructural changes of an experimental Ag-Cu-Pd-Au alloy were examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The specimen alloy showed apparent age-hardenability at the aging temperatures of 350 deg. C and 400 deg. C. By aging the solution-treated specimen at 400 deg. C, two phases of the Ag-rich α 1 phase and the Pd-containing Cu-rich α 2 phase were transformed into four phases of the Ag-rich α 1 ' phase, the Cu-rich α 2 ' phase, the CsCl-type CuPd phase and the AuCu(I) ordered phase. Microstructure of the solution-treated specimen consisted of the Ag-rich α 1 matrix, Cu-rich α 2 particle-like structures of various sizes and the lamellar structure of the α 1 and α 2 phases. When the peak hardness was obtained, the very fine lamellar structure consisting of the Ag-rich α 1 ' and Cu-rich α 2 ' phases was newly formed in the matrix. By further aging, the very fine lamellar structure grew and coarsened apparently, and the matrix was covered with the coarsened lamellar structure. The hardness increase was considered to be caused mainly by the diffusion and precipitation of Cu from the Ag-rich α 1 matrix, and the hardness decrease in the latter stage of age-hardening process was caused by the coarsening of the very fine lamellar structure. The CsCl-type CuPd phase and the AuCu(I) ordered phase did not contribute to the hardness increase

Ammonia synthesis on Au modified Fe(111) and Ag and Cu modified Fe(100) surfaces

DEFF Research Database (Denmark)

Lytken, Ole; Waltenburg, Hanne Neergaard; Chorkendorff, Ib

2003-01-01

In order to investigate any influence of steps and possible positive effects of making surface alloys the ammonia synthesis has been investigated over Au modified Fe(111) and Ag and Cu modified Fe(100) single crystals in the temperature range 603-773 K, using a system combining ultra-high vacuum...... and a high-pressure cell. Ammonia was synthesized from a stoichiometric (N-2:3H(2)) gas mixture at a pressure of 2 bar. By deposition of small amounts of An, the ammonia production activity of the Fe(1 1 1) surface can be enhanced. More important, for the gold modified surface, the reaction order in ammonia...

Geochemical Data for Samples Collected in 2007 Near the Concealed Pebble Porphyry Cu-Au-Mo Deposit, Southwest Alaska

Science.gov (United States)

Fey, David L.; Granitto, Matthew; Giles, Stuart A.; Smith, Steven M.; Eppinger, Robert G.; Kelley, Karen D.

2008-01-01

In the summer of 2007, the U.S. Geological Survey (USGS) began an exploration geochemical research study over the Pebble porphyry copper-gold-molydenum (Cu-Au-Mo) deposit in southwest Alaska. The Pebble deposit is extremely large and is almost entirely concealed by tundra, glacial deposits, and post-Cretaceous volcanic and volcaniclastic rocks. The deposit is presently being explored by Northern Dynasty Minerals, Ltd., and Anglo-American LLC. The USGS undertakes unbiased, broad-scale mineral resource assessments of government lands to provide Congress and citizens with information on national mineral endowment. Research on known deposits is also done to refine and better constrain methods and deposit models for the mineral resource assessments. The Pebble deposit was chosen for this study because it is concealed by surficial cover rocks, it is relatively undisturbed (except for exploration company drill holes), it is a large mineral system, and it is fairly well constrained at depth by the drill hole geology and geochemistry. The goals of the USGS study are (1) to determine whether the concealed deposit can be detected with surface samples, (2) to better understand the processes of metal migration from the deposit to the surface, and (3) to test and develop methods for assessing mineral resources in similar concealed terrains. This report presents analytical results for geochemical samples collected in 2007 from the Pebble deposit and surrounding environs. The analytical data are presented digitally both as an integrated Microsoft 2003 Access? database and as Microsoft 2003 Excel? files. The Pebble deposit is located in southwestern Alaska on state lands about 30 km (18 mi) northwest of the village of Illiamna and 320 km (200 mi) southwest of Anchorage (fig. 1). Elevations in the Pebble area range from 287 m (940 ft) at Frying Pan Lake just south of the deposit to 1146 m (3760 ft) on Kaskanak Mountain about 5 km (5 mi) to the west. The deposit is in an area of

The behaviour of the elements Ni, Co, Cu, Pb, Zn, Au, Ag, Mo, Sn, W and U in the magmatic, hydrothermal, sedimentary and weathering environments

International Nuclear Information System (INIS)

Anderson, J.R.

1978-01-01

In the last two decades much has been published on the behaviour of certain elements in the magmatic, hydrothermal, sedimentary and weathering environments, but the information is scattered throughout the literature. This situation prompted the present study on the elements Ni, Co, Cu, Pb, Zn, Au, Ag, Mo, Sn, W and U. The behaviour of the elements Ni, Cu, Pb, Zn, Au, Sn, W and U has been studied experimentally in some depth. Ag has been moderately studied, but there is very little information about Co and Mo. Studies on the complexes formed by the elements within the hydrothermal and aqueous environment are often inconclusive and controversial, but conclusions are drawn as to the more likely complexes formed. A genetic classification of ore deposits is used as a framework for the discussion. The source of the elements is regarded as being the mantle, and therefore discussion on other possible sources is beyond the scope of this dissertation. The crystal chemistry and geochemistry of the elements are presented and the essay concludes with a discussion on the elements within their depositional environments

On the stability of copper overlayers on Au(1 1 1) and Au(1 0 0) electrodes under low potential conditions and in the presence on CO and CO2

DEFF Research Database (Denmark)

Schlaup, Christian Georg; Horch, Sebastian; Chorkendorff, Ib

2015-01-01

We have studied the stability of Cu overlayers on Au(1 1 1) and Au(1 0 0) electrodes under low potential conditions and in the presence of CO and CO2 by means of electrochemical STM (EC-STM). For preparation we utilized the well known underpotential deposition (UPD) of copper, which, depending...... on the electrolyte (HClO4 and H2SO4), leads to Cu coverages in the submonolayer to monolayer range. For a Cu submonolayer on Au(1 1 1) we found that independent from the actual gas coadsorbate its closed film-like structure collapses at low potentials due to the desorption of coadsorbed anions. In contrast we found...... for a full Cu monolayer on Au(1 1 1) and Au(1 0 0) the formation of an alloy phase under low potential conditions, which also occurs independent from the presence of gas coadsorbates....

Efficient CH3NH3PbI3 perovskite/fullerene planar heterojunction hybrid solar cells with oxidized Ni/Au/Cu transparent electrode

Science.gov (United States)

Lai, Wei-Chih; Lin, Kun-Wei; Guo, Tzung-Fang; Chen, Peter; Liao, Yuan-Yu

2018-02-01

We demonstrated the performance of inverted CH3NH3PbI3 perovskite-based solar cells (SCs) with a thermally oxidized nickel/gold/copper (Ni/Au/Cu) trilayer transparent electrode. Oxidized Ni/Au/Cu is a high transparent layer and has less resistance than the oxidized Ni/Au layer. Like the oxidized Ni/Au layer, oxidized Ni and Cu in oxidized Ni/Au/Cu could perform as a hole transport layer of the perovskite-based SCs. It leads to improved perovskite SC performance on an open circuit voltage of 1.01 V, a short circuit current density of 14.36 mA/cm2, a fill factor of 76.7%, and a power conversion efficiency (η%) of 11.1%. The η% of perovskite SCs with oxidized Ni (10 nm)/Au (6 nm)/Cu (1 nm) improved by approximately 10% compared with that of perovskite SCs with oxidized Ni/Au.

Tin-phthalocyanine adsorption and diffusion on Cu and Au (111) surfaces: A density functional theory study

Science.gov (United States)

Qin, Dan; Ge, Xu-Jin; Lü, Jing-Tao

2018-05-01

Through density functional theory based calculations, we study the adsorption and diffusion of tin phthalocyanine (SnPc) molecule on Au(111) and Cu(111) surfaces. SnPc has two conformers with Sn pointing to the vacuum (Sn-up) and substrate (Sn-down), respectively. The binding energies of the two conformers with different adsorption sites on the two surfaces, including top, bridge, fcc, hcp, are calculated and compared. It is found that the SnPc molecule binds stronger on Cu(111) surface, with binding energy about 1 eV larger than that on Au(111). Only the bridge and top adsorption sites are stable on Cu(111), while all the four adsorption sites are stable on Au(111), with small diffusion barriers between them. Moreover, the flipping barrier from Sn-up to Sn-down conformer is of the same magnitude on the two metal surfaces. These results are consistent with a recent experiment [Zhang, et al., Angew. Chem., 56, 11769 (2017)], which shows that conformation change from Sn-up to Sn-down on Cu(111) surface can be induced by a C60-functionalized STM tip, while similar change is difficult to realize on Au(111), due to smaller diffusion barrier on Au(111).

Molecular oxygen adsorption and dissociation on Au12M clusters with M = Cu, Ag or Ir

Science.gov (United States)

Jiménez-Díaz, Laura M.; Pérez, Luis A.

2018-03-01

In this work, we present a density functional theory study of the structural and electronic properties of isolated neutral clusters of the type Au12M, with M = Cu, Ag, or Ir. On the other hand, there is experimental evidence that gold-silver, gold-copper and gold-iridium nanoparticles have an enhanced catalytic activity for the CO oxidation reaction. In order to address these phenomena, we also performed density functional calculations of the adsorption and dissociation of O2 on these nanoparticles. Moreover, to understand the effects of Cu, Ag, and Ir impurity atoms on the dissociation of O2, we also analyze this reaction in the corresponding pure gold cluster. The results indicate that the substitution of one gold atom in a Au13 cluster by Ag, Cu or Ir diminishes the activation energy barrier for the O2 dissociation by nearly 1 eV. This energy barrier is similar for Au12Ag and Au12Cu, whereas for Au12Ir is even lower. These results suggest that the addition of other transition metal atoms to gold nanoclusters can enhance their catalytic activity towards the CO oxidation reaction, independently of the effect that the substrate could have on supported nanoclusters.

Age-hardening and related phase transformation in an experimental Ag-Cu-Pd-Au alloy

Energy Technology Data Exchange (ETDEWEB)

Seol, Hyo-Joung [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Lee, Doung-Hun [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Lee, Hee-Kyung [Department of Dental Technology, Daegu Health College, San 7 Taejeon-dong, Buk-gu, Daegu 702-722 (Korea, Republic of); Takada, Yukyo [Division of Dental Biomaterials, Graduate School of Dentistry, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575 (Japan); Okuno, Osamu [Division of Dental Biomaterials, Graduate School of Dentistry, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575 (Japan); Kwon, Yong Hoon [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Kim, Hyung-Il [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of)]. E-mail: hilkim@pusan.ac.kr

2006-01-05

The age-hardening behaviour, phase transformation and related microstructural changes of an experimental Ag-Cu-Pd-Au alloy were examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The specimen alloy showed apparent age-hardenability at the aging temperatures of 350 deg. C and 400 deg. C. By aging the solution-treated specimen at 400 deg. C, two phases of the Ag-rich {alpha}{sub 1} phase and the Pd-containing Cu-rich {alpha}{sub 2} phase were transformed into four phases of the Ag-rich {alpha}{sub 1}{sup '} phase, the Cu-rich {alpha}{sub 2}{sup '} phase, the CsCl-type CuPd phase and the AuCu(I) ordered phase. Microstructure of the solution-treated specimen consisted of the Ag-rich {alpha}{sub 1} matrix, Cu-rich {alpha}{sub 2} particle-like structures of various sizes and the lamellar structure of the {alpha}{sub 1} and {alpha}{sub 2} phases. When the peak hardness was obtained, the very fine lamellar structure consisting of the Ag-rich {alpha}{sub 1}{sup '} and Cu-rich {alpha}{sub 2}{sup '} phases was newly formed in the matrix. By further aging, the very fine lamellar structure grew and coarsened apparently, and the matrix was covered with the coarsened lamellar structure. The hardness increase was considered to be caused mainly by the diffusion and precipitation of Cu from the Ag-rich {alpha}{sub 1} matrix, and the hardness decrease in the latter stage of age-hardening process was caused by the coarsening of the very fine lamellar structure. The CsCl-type CuPd phase and the AuCu(I) ordered phase did not contribute to the hardness increase.

Integrating Data of ASTER and Landsat-8 OLI (AO for Hydrothermal Alteration Mineral Mapping in Duolong Porphyry Cu-Au Deposit, Tibetan Plateau, China

Directory of Open Access Journals (Sweden)

Tingbin Zhang

2016-10-01

Full Text Available One of the most important characteristics of porphyry copper deposits (PCDs is the type and distribution pattern of alteration zones which can be used for screening and recognizing these deposits. Hydrothermal alteration minerals with diagnostic spectral absorption properties in the visible and near-infrared (VNIR through the shortwave infrared (SWIR regions can be identified by multispectral and hyperspectral remote sensing data. Six Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER bands in SWIR have been shown to be effective in the mapping of Al-OH, Fe-OH, Mg-OH group minerals. The five VNIR bands of Landsat-8 (L8 Operational Land Imager (OLI are useful for discriminating ferric iron alteration minerals. In the absence of complete hyperspectral coverage area, an opportunity, however, exists to integrate ASTER and L8-OLI (AO to compensate each other’s shortcomings in covering area for mineral mapping. This study examines the potential of AO data in mineral mapping in an arid area of the Duolong porphyry Cu-Au deposit(Tibetan Plateau in China by using spectral analysis techniques. Results show the following conclusions: (1 Combination of ASTER and L8-OLI data (AO has more mineral information content than either alone; (2 The Duolong PCD alteration zones of phyllic, argillic and propylitic zones are mapped using ASTER SWIR bands and the iron-bearing mineral information is best mapped using AO VNIR bands; (3 The multispectral integration data of AO can provide a compensatory data of ASTER VNIR bands for iron-bearing mineral mapping in the arid and semi-arid areas.

Composition of Cu/Al system constructed by means of dynamic atomic deposition

International Nuclear Information System (INIS)

Tashlykov, I.S.; Tul'ev, V.V.

2011-01-01

Rutherford backscattering and RUMP simulation programme have been applied to investigate composition of Cu/Al system prepared using dynamic atomic deposition process when deposition of Cu thin film on Al substrate was assisted with 6 keV Ar + ions irradiation. It is estimated that thin ( ~15 nm) surface layer consists of ~50 at.% Cu, ~10 at.% Ar, ~4 at.% O and the remaining is Al. Dynamic deposition of Cu on Al substrate is accompanied with radiation enhanced diffusion of Cu, O, Ar atoms in substrate and out diffusion of Al atoms in deposited Cu coating. (authors)

A Study of the Influence of Percentage of Copper on the Structural and Optical Properties of Au-Cu Nanoparticle

Directory of Open Access Journals (Sweden)

Parivash Mashayekhi Shams

2016-07-01

Full Text Available Here we present our experimental results in synthesizing Au-Cu nano-particles with tunable localized surface plasmon resonance frequency through wet-chemical at temperature room. The reaction is performed in the presence of ascorbic acid as a reducing agent and polyvinyl pyrrolidone as capping agent via four different procedures: (1 mixture of 90% HAuCl4 and 10% CuSO4.5H2O precursors, (2 mixture of 75% HAuCl4 and 25% CuSO4.5H2O precursors, (3 mixture of 50% HAuCl4 and 50% CuSO4.5H2O precursors (4 mixture of 25% HAuCl4 and 75% CuSO4.5H2O precursors. Effect of different percentages of Cu on Au nanoparticles has been analyzed using X-ray diffraction (XRD, scanning electron microscopy (SEM with EDAX analysis, DRS UV-Vis, and Fourier transform IR spectra (FTIR analysis. X-ray diffraction (XRD analysis revealed that the nanoparticles are of cubic structure without an impure phase. The successful doping of the Cu into the Au host was evident by XRD line shiftings. The increasing percentage of copper leads to the decreasing grain size. With the increase of Cu2+ to Au3+ ratio in the Cu2+/Au3+ mixed solution (> 50% Cu, XRD lines show no shifting. The average crystal sizes of the particles at room temperature were less than 9.9 nm. The surface plasmon resonance peak shifts from 380 to 340 nm, party due to the change in particle size. SEM images show a spherical shape and the size of nanoparticles becomes smaller with increasing the percentage of copper. Moreover, in the molar ratio of Cu2+/Au3+ = 75/25 (>50% Cu, mixture of spherical and trigonal nanoparticles were prepared. Fourier transform infrared spectroscopy (FT-IR showed the coordination and conjugation nanoparticles with N and O atoms of C-N and C=O bonds.

High salinity volatile phases in magmatic Ni-Cu-platinum group element deposits

Science.gov (United States)

Hanley, J. J.; Mungall, J. E.

2004-12-01

The role of "deuteric" fluids (exsolved magmatic volatile phases) in the development of Ni-Cu-PGE (platinum group element) deposits in mafic-ultramafic igneous systems is poorly understood. Although considerable field evidence demonstrates unambiguously that fluids modified most large primary Ni-Cu-PGE concentrations, models which hypothesize that fluids alone were largely responsible for the economic concentration of the base and precious metals are not widely accepted. Determination of the trace element composition of magmatic volatile phases in such ore-forming systems can offer considerable insight into the origin of potentially mineralizing fluids in such igneous environments. Laser ablation ICP-MS microanalysis allows researchers to confirm the original metal budget of magmatic volatile phases and quantify the behavior of trace ore metals in the fluid phase in the absence of well-constrained theoretical or experimental predictions of ore metal solubility. In this study, we present new evidence from major deposits (Sudbury, Ontario, Canada; Stillwater Complex, Montana, U.S.A.) that compositionally distinct magmatic brines and halide melt phases were exsolved from crystallizing residual silicate melt and trapped within high-T fluid conduits now comprised of evolved rock compositions (albite-quartz graphic granite, orthoclase-quartz granophyre). Petrographic evidence demonstrates that brines and halide melts coexisted with immiscible carbonic phases at the time of entrapment (light aliphatic hydrocarbons, CO2). Brine and halide melt inclusions are rich in Na, Fe, Mn, K, Pb, Zn, Ba, Sr, Al and Cl, and homogenize by either halite dissolution at high T ( ˜450-700° C) or by melting of the salt phase (700-800° C). LA-ICPMS analyses of single inclusions demonstrate that high salinity volatile phases contained abundant base metals (Cu, Fe, Sn, Bi) and precious metals (Pt, Pd, Au, Ag) at the time of entrapment. Notably, precious metal concentrations in the inclusions

Deformation of Ag clusters deposited on Au(111) - Experiment and molecular dynamics

Energy Technology Data Exchange (ETDEWEB)

Miroslawski, Natalie; Groenhagen, Niklas; Hoevel, Heinz [TU Dortmund, Experimentelle Physik I (Germany); Issendorff, Bernd von [Universitaet Freiburg, Fakultaet Physik (Germany); Jaervi, Tommi [Fraunhofer Institut fuer Werkstoffmechanik, Freiburg (Germany); Moseler, Michael [Universitaet Freiburg, Fakultaet Physik (Germany); Fraunhofer Institut fuer Werkstoffmechanik, Freiburg (Germany); Freiburger Materialforschungszentrum (Germany)

2011-07-01

Mass selected clusters from Ag{sup +}{sub 55} to Ag{sup +}{sub 147{+-}}{sub 2} were deposited with different deposition energies at 77 K on Au(111) and imaged with STM at 77 K. We observed a deformation of the cluster shape due to the strong metallic interaction between the cluster and the substrate. The clusters became epitaxial and developed a structure composed of several Ag monolayers. The number of these monolayers depends on the number of atoms in the cluster and the deposition energy. The larger the cluster mass the more monolayers the cluster develops on Au(111) and the larger the deposition energy the fewer monolayers occur. These results were verified by molecular dynamic simulations. Additionally the behaviour of Ag{sub N} clusters on Au(111) after different annealing steps was investigated.

Pulsed laser deposition of Tl-Ca-Ba-Cu-O films

International Nuclear Information System (INIS)

Ianno, N.J.; Liou, S.H.; Woollam, J.A.; Thompson, D.; Johs, B.

1990-01-01

Pulsed laser deposition is a technique commonly used to deposit high quality thin films of high temperature superconductors. This paper discusses the results obtained when this technique is applied to the deposition of Tl-Ca-Ba-Cu-O thin films using a frequency doubled Nd:YAG laser operating at 532 nm and an excimer laser operating at 248 nm. Films with onset temperatures of 125 K and zero resistance temperatures of 110 K deposited on (100) oriented MgO from a composite Tl2Ca2Ba2Cu3Ox target were obtained at both wavelengths upon appropriate post deposition annealing. Films deposited at 532 nm exhibit a rough surface, while those deposited at 248 nm are smooth and homogeneous. Upon annealing, films deposited at both wavelengths are single phase Tl2Ca2Ba2Cu3Ox. 12 refs

System size and energy dependence of jet-induced hadron pair correlation shapes in Cu+Cu and Au+Au collisions at square root sNN=200 and 62.4 GeV.

Science.gov (United States)

Adare, A; Adler, S S; Afanasiev, S; Aidala, C; Ajitanand, N N; Akiba, Y; Al-Bataineh, H; Alexander, J; Al-Jamel, A; Aoki, K; Aphecetche, L; Armendariz, R; Aronson, S H; Asai, J; Atomssa, E T; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Baksay, G; Baksay, L; Baldisseri, A; Barish, K N; Barnes, P D; Bassalleck, B; Bathe, S; Batsouli, S; Baublis, V; Bauer, F; Bazilevsky, A; Belikov, S; Bennett, R; Berdnikov, Y; Bickley, A A; Bjorndal, M T; Boissevain, J G; Borel, H; Boyle, K; Brooks, M L; Brown, D S; Bruner, N; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Camard, X; Campbell, S; Chai, J-S; Chand, P; Chang, B S; Chang, W C; Charvet, J-L; Chernichenko, S; Chiba, J; Chi, C Y; Chiu, M; Choi, I J; Choudhury, R K; Chujo, T; Chung, P; Churyn, A; Cianciolo, V; Cleven, C R; Cobigo, Y; Cole, B A; Comets, M P; Constantin, P; Csanád, M; Csörgo, T; Cussonneau, J P; Dahms, T; Das, K; David, G; Deák, F; Deaton, M B; Dehmelt, K; Delagrange, H; Denisov, A; d'Enterria, D; Deshpande, A; Desmond, E J; Devismes, A; Dietzsch, O; Dion, A; Donadelli, M; Drachenberg, J L; Drapier, O; Drees, A; Dubey, A K; Durum, A; Dutta, D; Dzhordzhadze, V; Efremenko, Y V; Egdemir, J; Ellinghaus, F; Emam, W S; Enokizono, A; En'yo, H; Espagnon, B; Esumi, S; Eyser, K O; Fields, D E; Finck, C; Finger, M; Finger, M; Fleuret, F; Fokin, S L; Forestier, B; Fox, B D; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fujiwara, K; Fukao, Y; Fung, S-Y; Fusayasu, T; Gadrat, S; Garishvili, I; Gastineau, F; Germain, M; Glenn, A; Gong, H; Gonin, M; Gosset, J; Goto, Y; Granier de Cassagnac, R; Grau, N; Greene, S V; Grosse Perdekamp, M; Gunji, T; Gustafsson, H-A; Hachiya, T; Hadj Henni, A; Haegemann, C; Haggerty, J S; Hagiwara, M N; Hamagaki, H; Han, R; Hansen, A G; Harada, H; Hartouni, E P; Haruna, K; Harvey, M; Haslum, E; Hasuko, K; Hayano, R; Heffner, M; Hemmick, T K; Hester, T; Heuser, J M; He, X; Hidas, P; Hiejima, H; Hill, J C; Hobbs, R; Hohlmann, M; Holmes, M; Holzmann, W; Homma, K; Hong, B; Hoover, A; Horaguchi, T; Hornback, D; Hur, M G; Ichihara, T; Ikonnikov, V V; Imai, K; Inaba, M; Inoue, Y; Inuzuka, M; Isenhower, D; Isenhower, L; Ishihara, M; Isobe, T; Issah, M; Isupov, A; Jacak, B V; Jia, J; Jin, J; Jinnouchi, O; Johnson, B M; Johnson, S C; Joo, K S; Jouan, D; Kajihara, F; Kametani, S; Kamihara, N; Kamin, J; Kaneta, M; Kang, J H; Kanou, H; Katou, K; Kawabata, T; Kawagishi, T; Kawall, D; Kazantsev, A V; Kelly, S; Khachaturov, B; Khanzadeev, A; Kikuchi, J; Kim, D H; Kim, D J; Kim, E; Kim, G-B; Kim, H J; Kim, Y-S; Kinney, E; Kiss, A; Kistenev, E; Kiyomichi, A; Klay, J; Klein-Boesing, C; Kobayashi, H; Kochenda, L; Kochetkov, V; Kohara, R; Komkov, B; Konno, M; Kotchetkov, D; Kozlov, A; Král, A; Kravitz, A; Kroon, P J; Kubart, J; Kuberg, C H; Kunde, G J; Kurihara, N; Kurita, K; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Lai, Y-S; Lajoie, J G; Lebedev, A; Le Bornec, Y; Leckey, S; Lee, D M; Lee, M K; Lee, T; Leitch, M J; Leite, M A L; Lenzi, B; Lim, H; Liska, T; Litvinenko, A; Liu, M X; Li, X; Li, X H; Love, B; Lynch, D; Maguire, C F; Makdisi, Y I; Malakhov, A; Malik, M D; Manko, V I; Mao, Y; Martinez, G; Masek, L; Masui, H; Matathias, F; Matsumoto, T; McCain, M C; McCumber, M; McGaughey, P L; Miake, Y; Mikes, P; Miki, K; Miller, T E; Milov, A; Mioduszewski, S; Mishra, G C; Mishra, M; Mitchell, J T; Mitrovski, M; Mohanty, A K; Morreale, A; Morrison, D P; Moss, J M; Moukhanova, T V; Mukhopadhyay, D; Muniruzzaman, M; Murata, J; Nagamiya, S; Nagata, Y; Nagle, J L; Naglis, M; Nakagawa, I; Nakamiya, Y; Nakamura, T; Nakano, K; Newby, J; Nguyen, M; Norman, B E; Nyanin, A S; Nystrand, J; O'Brien, E; Oda, S X; Ogilvie, C A; Ohnishi, H; Ojha, I D; Okada, H; Okada, K; Oka, M; Omiwade, O O; Oskarsson, A; Otterlund, I; Ouchida, M; Oyama, K; Ozawa, K; Pak, R; Pal, D; Palounek, A P T; Pantuev, V; Papavassiliou, V; Park, J; Park, W J; Pate, S F; Pei, H; Penev, V; Peng, J-C; Pereira, H; Peresedov, V; Peressounko, D Yu; Pierson, A; Pinkenburg, C; Pisani, R P; Purschke, M L; Purwar, A K; Qualls, J M; Qu, H; Rak, J; Rakotozafindrabe, A; Ravinovich, I; Read, K F; Rembeczki, S; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Roche, G; Romana, A; Rosati, M; Rosendahl, S S E; Rosnet, P; Rukoyatkin, P; Rykov, V L; Ryu, S S; Sahlmueller, B; Saito, N; Sakaguchi, T; Sakai, S; Sakata, H; Samsonov, V; Sanfratello, L; Santo, R; Sato, H D; Sato, S; Sawada, S; Schutz, Y; Seele, J; Seidl, R; Semenov, V; Seto, R; Sharma, D; Shea, T K; Shein, I; Shevel, A; Shibata, T-A; Shigaki, K; Shimomura, M; Shohjoh, T; Shoji, K; Sickles, A; Silva, C L; Silvermyr, D; Silvestre, C; Sim, K S; Singh, C P; Singh, V; Skutnik, S; Slunecka, M; Smith, W C; Soldatov, A; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Staley, F; Stankus, P W; Stenlund, E; Stepanov, M; Ster, A; Stoll, S P; Sugitate, T; Suire, C; Sullivan, J P; Sziklai, J; Tabaru, T; Takagi, S; Takagui, E M; Taketani, A; Tanaka, K H; Tanaka, Y; Tanida, K; Tannenbaum, M J; Taranenko, A; Tarján, P; Thomas, T L; Togawa, M; Toia, A; Tojo, J; Tomásek, L; Torii, H; Towell, R S; Tram, V-N; Tserruya, I; Tsuchimoto, Y; Tuli, S K; Tydesjö, H; Tyurin, N; Uam, T J; Vale, C; Valle, H; vanHecke, H W; Velkovska, J; Velkovsky, M; Vertesi, R; Veszprémi, V; Vinogradov, A A; Virius, M; Volkov, M A; Vrba, V; Vznuzdaev, E; Wagner, M; Walker, D; Wang, X R; Watanabe, Y; Wessels, J; White, S N; Willis, N; Winter, D; Wohn, F K; Woody, C L; Wysocki, M; Xie, W; Yamaguchi, Y L; Yanovich, A; Yasin, Z; Ying, J; Yokkaichi, S; Young, G R; Younus, I; Yushmanov, I E; Zajc, W A; Zaudtke, O; Zhang, C; Zhou, S; Zimányi, J; Zolin, L; Zong, X

2007-06-08

We present azimuthal angle correlations of intermediate transverse momentum (1-4 GeV/c) hadrons from dijets in Cu+Cu and Au+Au collisions at square root sNN=62.4 and 200 GeV. The away-side dijet induced azimuthal correlation is broadened, non-Gaussian, and peaked away from Delta phi=pi in central and semicentral collisions in all the systems. The broadening and peak location are found to depend upon the number of participants in the collision, but not on the collision energy or beam nuclei. These results are consistent with sound or shock wave models, but pose challenges to Cherenkov gluon radiation models.

Diffusion limited Cu and Au nanocrystal formation in thin film SiO2

International Nuclear Information System (INIS)

Johannessen, B.; Kluth, P.; Glover, C.J.; Foran, G.J.; Ridgway, M.C.

2006-01-01

Elemental Cu and Au nanocrystals (NCs) were produced by high-energy ion-implantations into amorphous silica (SiO 2 ) and subsequent thermal annealing. By a combination of X-ray diffraction (XRD) and cross-sectional transmission electron microscopy (XTEM) we confirm both NC species to have the bulk face-centered cubic phase and estimate their average diameter. We concentrate on the investigation of the concentration and size-dependent coordination number (China) of these matrix embedded NCs utilising extended X-ray absorption fine structure (EXAFS) spectroscopy. The CN is found to be suppressed compared to that of a bulk standard. The CN in Au NCs is found to be lower than that of Cu NCs in agreement with smaller average Au NC sizes. We explain this difference by the difference in diffusivity for the two atomic species in SiO 2

Highly selective and sensitive method for Cu2 + detection based on chiroptical activity of L-Cysteine mediated Au nanorod assemblies

Science.gov (United States)

Abbasi, Shahryar; Khani, Hamzeh

2017-11-01

Herein, we demonstrated a simple and efficient method to detect Cu2 + based on amplified optical activity in the chiral nanoassemblies of gold nanorods (Au NRs). L-Cysteine can induce side-by-side or end-to-end assembly of Au NRs with an evident plasmonic circular dichroism (PCD) response due to coupling between surface plasmon resonances (SPR) of Au NRs and the chiral signal of L-Cys. Because of the obvious stronger plasmonic circular dichrosim (CD) response of the side-by-side assembly compared with the end-to-end assemblies, SS assembled Au NRs was selected as a sensitive platform and used for Cu2 + detection. In the presence of Cu2 +, Cu2 + can catalyze O2 oxidation of cysteine to cystine. With an increase in Cu2 + concentration, the L-Cysteine-mediated assembly of Au NRs decreased because of decrease in the free cysteine thiol groups, and the PCD signal decreased. Taking advantage of this method, Cu2 + could be detected in the concentration range of 20 pM-5 nM. Under optimal conditions, the calculated detection limit was found to be 7 pM.

Low-Temperature Cu-Cu Bonding Using Silver Nanoparticles Fabricated by Physical Vapor Deposition

Science.gov (United States)

Wu, Zijian; Cai, Jian; Wang, Junqiang; Geng, Zhiting; Wang, Qian

2018-02-01

Silver nanoparticles (Ag NPs) fabricated by physical vapor deposition (PVD) were introduced in Cu-Cu bonding as surface modification layer. The bonding structure consisted of a Ti adhesive/barrier layer and a Cu substrate layer was fabricated on the silicon wafer. Ag NPs were deposited on the Cu surface by magnetron sputtering in a high-pressure environment and a loose structure with NPs was obtained. Shear tests were performed after bonding, and the influences of PVD pressure, bonding pressure, bonding temperature and annealing time on shear strength were assessed. Cu-Cu bonding with Ag NPs was accomplished at 200°C for 3 min under the pressure of 30 MPa without a post-annealing process, and the average bonding strength of 13.99 MPa was reached. According to cross-sectional observations, a void-free bonding interface with an Ag film thickness of around 20 nm was achieved. These results demonstrated that a reliable low-temperature short-time Cu-Cu bonding was realized by the sintering process of Ag NPs between the bonding pairs, which indicated that this bonding method could be a potential candidate for future ultra-fine pitch 3D integration.

Measurements of directed, elliptic, and triangular flow in Cu + Au collisions at √{sNN}=200 GeV

Science.gov (United States)

Adare, A.; Aidala, C.; Ajitanand, N. N.; Akiba, Y.; Akimoto, R.; Alexander, J.; Alfred, M.; Aoki, K.; Apadula, N.; Asano, H.; Atomssa, E. T.; Awes, T. C.; Azmoun, B.; Babintsev, V.; Bai, M.; Bai, X.; Bandara, N. S.; Bannier, B.; Barish, K. N.; Bathe, S.; Baublis, V.; Baumann, C.; Baumgart, S.; Bazilevsky, A.; Beaumier, M.; Beckman, S.; Belmont, R.; Berdnikov, A.; Berdnikov, Y.; Black, D.; Blau, D. S.; Bok, J. S.; Boyle, K.; Brooks, M. L.; Bryslawskyj, J.; Buesching, H.; Bumazhnov, V.; Butsyk, S.; Campbell, S.; Chen, C.-H.; Chi, C. Y.; Chiu, M.; Choi, I. J.; Choi, J. B.; Choi, S.; Christiansen, P.; Chujo, T.; Cianciolo, V.; Citron, Z.; Cole, B. A.; Cronin, N.; Crossette, N.; Csanád, M.; Csörgő, T.; Danley, T. W.; Datta, A.; Daugherity, M. S.; David, G.; Deblasio, K.; Dehmelt, K.; Denisov, A.; Deshpande, A.; Desmond, E. J.; Ding, L.; Dion, A.; Diss, P. B.; Do, J. H.; D'Orazio, L.; Drapier, O.; Drees, A.; Drees, K. A.; Durham, J. M.; Durum, A.; Engelmore, T.; Enokizono, A.; Esumi, S.; Eyser, K. O.; Fadem, B.; Feege, N.; Fields, D. E.; Finger, M.; Finger, M.; Fleuret, F.; Fokin, S. L.; Frantz, J. E.; Franz, A.; Frawley, A. D.; Fukao, Y.; Fusayasu, T.; Gainey, K.; Gal, C.; Gallus, P.; Garg, P.; Garishvili, A.; Garishvili, I.; Ge, H.; Giordano, F.; Glenn, A.; Gong, X.; Gonin, M.; Goto, Y.; Granier de Cassagnac, R.; Grau, N.; Greene, S. V.; Grosse Perdekamp, M.; Gu, Y.; Gunji, T.; Guragain, H.; Hachiya, T.; Haggerty, J. S.; Hahn, K. I.; Hamagaki, H.; Hamilton, H. F.; Han, S. Y.; Hanks, J.; Hasegawa, S.; Haseler, T. O. S.; Hashimoto, K.; Hayano, R.; He, X.; Hemmick, T. K.; Hester, T.; Hill, J. C.; Hollis, R. S.; Homma, K.; Hong, B.; Hoshino, T.; Hotvedt, N.; Huang, J.; Huang, S.; Ichihara, T.; Ikeda, Y.; Imai, K.; Imazu, Y.; Inaba, M.; Iordanova, A.; Isenhower, D.; Isinhue, A.; Ivanishchev, D.; Jacak, B. V.; Jeon, S. J.; Jezghani, M.; Jia, J.; Jiang, X.; Johnson, B. M.; Joo, K. S.; Jouan, D.; Jumper, D. S.; Kamin, J.; Kanda, S.; Kang, B. H.; Kang, J. H.; Kang, J. S.; Kapustinsky, J.; Kawall, D.; Kazantsev, A. V.; Key, J. A.; Khachatryan, V.; Khandai, P. K.; Khanzadeev, A.; Kijima, K. M.; Kim, C.; Kim, D. J.; Kim, E.-J.; Kim, G. W.; Kim, M.; Kim, Y.-J.; Kim, Y. K.; Kimelman, B.; Kistenev, E.; Kitamura, R.; Klatsky, J.; Kleinjan, D.; Kline, P.; Koblesky, T.; Kofarago, M.; Komkov, B.; Koster, J.; Kotchetkov, D.; Kotov, D.; Krizek, F.; Kurita, K.; Kurosawa, M.; Kwon, Y.; Lacey, R.; Lai, Y. S.; Lajoie, J. G.; Lebedev, A.; Lee, D. M.; Lee, G. H.; Lee, J.; Lee, K. B.; Lee, K. S.; Lee, S.; Lee, S. H.; Leitch, M. J.; Leitgab, M.; Lewis, B.; Li, X.; Lim, S. H.; Liu, M. X.; Lynch, D.; Maguire, C. F.; Makdisi, Y. I.; Makek, M.; Manion, A.; Manko, V. I.; Mannel, E.; Maruyama, T.; McCumber, M.; McGaughey, P. L.; McGlinchey, D.; McKinney, C.; Meles, A.; Mendoza, M.; Meredith, B.; Miake, Y.; Mibe, T.; Mignerey, A. C.; Milov, A.; Mishra, D. K.; Mitchell, J. T.; Miyasaka, S.; Mizuno, S.; Mohanty, A. K.; Mohapatra, S.; Montuenga, P.; Moon, T.; Morrison, D. P.; Moskowitz, M.; Moukhanova, T. V.; Murakami, T.; Murata, J.; Mwai, A.; Nagae, T.; Nagamiya, S.; Nagashima, K.; Nagle, J. L.; Nagy, M. I.; Nakagawa, I.; Nakagomi, H.; Nakamiya, Y.; Nakamura, K. R.; Nakamura, T.; Nakano, K.; Nattrass, C.; Netrakanti, P. K.; Nihashi, M.; Niida, T.; Nishimura, S.; Nouicer, R.; Novák, T.; Novitzky, N.; Nyanin, A. S.; O'Brien, E.; Ogilvie, C. A.; Oide, H.; Okada, K.; Orjuela Koop, J. D.; Osborn, J. D.; Oskarsson, A.; Ozawa, K.; Pak, R.; Pantuev, V.; Papavassiliou, V.; Park, I. H.; Park, J. S.; Park, S.; Park, S. K.; Pate, S. F.; Patel, L.; Patel, M.; Peng, J.-C.; Perepelitsa, D. V.; Perera, G. D. N.; Peressounko, D. Yu.; Perry, J.; Petti, R.; Pinkenburg, C.; Pinson, R.; Pisani, R. P.; Purschke, M. L.; Qu, H.; Rak, J.; Ramson, B. J.; Ravinovich, I.; Read, K. F.; Reynolds, D.; Riabov, V.; Riabov, Y.; Richardson, E.; Rinn, T.; Riveli, N.; Roach, D.; Rolnick, S. D.; Rosati, M.; Rowan, Z.; Rubin, J. G.; Ryu, M. S.; Sahlmueller, B.; Saito, N.; Sakaguchi, T.; Sako, H.; Samsonov, V.; Sarsour, M.; Sato, S.; Sawada, S.; Schaefer, B.; Schmoll, B. K.; Sedgwick, K.; Seele, J.; Seidl, R.; Sekiguchi, Y.; Sen, A.; Seto, R.; Sett, P.; Sexton, A.; Sharma, D.; Shaver, A.; Shein, I.; Shibata, T.-A.; Shigaki, K.; Shimomura, M.; Shoji, K.; Shukla, P.; Sickles, A.; Silva, C. L.; Silvermyr, D.; Singh, B. K.; Singh, C. P.; Singh, V.; Skolnik, M.; Slunečka, M.; Snowball, M.; Solano, S.; Soltz, R. A.; Sondheim, W. E.; Sorensen, S. P.; Sourikova, I. V.; Stankus, P. W.; Steinberg, P.; Stenlund, E.; Stepanov, M.; Ster, A.; Stoll, S. P.; Stone, M. R.; Sugitate, T.; Sukhanov, A.; Sumita, T.; Sun, J.; Sziklai, J.; Takahara, A.; Taketani, A.; Tanaka, Y.; Tanida, K.; Tannenbaum, M. J.; Tarafdar, S.; Taranenko, A.; Tennant, E.; Tieulent, R.; Timilsina, A.; Todoroki, T.; Tomášek, M.; Torii, H.; Towell, C. L.; Towell, R.; Towell, R. S.; Tserruya, I.; van Hecke, H. W.; Vargyas, M.; Vazquez-Zambrano, E.; Veicht, A.; Velkovska, J.; Vértesi, R.; Virius, M.; Vrba, V.; Vznuzdaev, E.; Wang, X. R.; Watanabe, D.; Watanabe, K.; Watanabe, Y.; Watanabe, Y. S.; Wei, F.; Whitaker, S.; White, A. S.; Wolin, S.; Woody, C. L.; Wysocki, M.; Xia, B.; Xue, L.; Yalcin, S.; Yamaguchi, Y. L.; Yanovich, A.; Yokkaichi, S.; Yoo, J. H.; Yoon, I.; You, Z.; Younus, I.; Yu, H.; Yushmanov, I. E.; Zajc, W. A.; Zelenski, A.; Zhou, S.; Zou, L.; Phenix Collaboration

2016-11-01

Measurements of anisotropic flow Fourier coefficients (vn) for inclusive charged particles and identified hadrons π±, K±, p , and p ¯ produced at midrapidity in Cu +Au collisions at √{s NN}=200 GeV are presented. The data were collected in 2012 by the PHENIX experiment at the Relativistic Heavy-Ion Collider (RHIC). The particle azimuthal distributions with respect to different-order symmetry planes Ψn, for n =1 , 2, and 3 are studied as a function of transverse momentum pT over a broad range of collision centralities. Mass ordering, as expected from hydrodynamic flow, is observed for all three harmonics. The charged-particle results are compared with hydrodynamical and transport model calculations. We also compare these Cu +Au results with those in Cu +Cu and Au +Au collisions at the same √{sNN} and find that the v2 and v3, as a function of transverse momentum, follow a common scaling with 1 /(ɛnNpart1 /3) .

Post-deposition treatments of plasma-sprayed YBaCuO coatings deposited on nickel

Energy Technology Data Exchange (ETDEWEB)

Dube, D; Lambert, P; Arsenault, B; Champagne, B [National Research Council of Canada, Boucherville, PQ (Canada)

1990-12-15

As-sprayed YBaCuO coatings do not exhibit superconductivity because of the non-equilibrium solidification conditions of molten particles on the substrate and to the deposit's loss of oxygen. Therefore post-deposition treatments are required to restore the superconductivity. In this study, post-deposition treatments were carried out on thick YBaCuO coatings (200 {mu}m) deposited on cold nickel substrates to modify their microstructure, to restore the oxygen content and to improve their superconducting properties. These treatments consist in heating the coatings at various temperatures above 950deg C followed by controlled solidification cycles. The effect of these treatments on the microstructure of the coatings was assessed and the interaction between the coatings and the nickel substrate was also examined. Solidification cycles including a low cooling rate near the non-congruent melting temperature of YBa{sub 2}Cu{sub 3}O{sub x} and involving a temperature gradient were carried out to create a texture. (orig.).

Effects of supporting electrolyte on galvanic deposition of Cu2O crystals

International Nuclear Information System (INIS)

Wang Lida; Liu Guichang; Xue Dongfeng

2011-01-01

Highlights: → The effects of electrolyte on the galvanic deposition of Cu 2 O crystals have been investigated. → The chemical nature of supporting electrolyte plays important roles in the galvanic deposition of Cu 2 O crystals. → Cubic Cu 2 O crystals are formed in chloride electrolytes. → Truncated octahedral Cu 2 O crystals are produced in nitrate, sulfate and fluoride electrolytes. - Abstract: The effects of introduced supporting electrolyte on the galvanic deposition of Cu 2 O crystals have been investigated using scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray diffraction (XRD). The results show that the chemical nature of supporting electrolytes plays very important roles in the galvanic deposition of Cu 2 O crystals. The chloride stabilizes the (1 0 0) planes of Cu 2 O crystals, resulting in the formation of cubic crystals, while nitrate, sulfate and fluoride stabilize the (1 1 1) planes of Cu 2 O crystals, leading to the deposition of truncated octahedral and octahedral Cu 2 O crystals. It provides a facile way to control the morphology of galvanically obtained Cu 2 O crystals by indirectly adjusting the inorganic adsorption agents.

Band Structure and Optical Properties of Ordered AuCu3

DEFF Research Database (Denmark)

Skriver, Hans Lomholt; Lengkeek, H. P.

1979-01-01

The optical spectra of ordered AuCu3 have been measured at low temperatures by a direct ellipsometric technique. We find several structural elements above the absorption edge as well as in the infrared. The measured spectra are interpreted in terms of the interband absorption calculated from an ab...

Diffusion of single Au, Ag and Cu atoms inside Si(111)-(7 × 7) half unit cells: A comparative study

Energy Technology Data Exchange (ETDEWEB)

Liu, Qin [Department of Physics, Southern University of Science and Technology, Shenzhen, Guangdong 518055 (China); Department of Physics, The Chinese University of Hong Kong, Shatin, New Territory, Hong Kong (China); Science and Technology on Surface Physics and Chemistry Laboratory, Mianyang, Sichuan 621908 (China); Fu, Qiang [Institut für Physik and IRIS Adlershof, Humboldt-Universität zu Berlin, Zum Großen Windkanal 6, 12489 Berlin (Germany); Shao, Xiji; Ma, Xuhang; Wu, Xuefeng [Department of Physics, Southern University of Science and Technology, Shenzhen, Guangdong 518055 (China); Wang, Kedong, E-mail: wangkd@sustc.edu.cn [Department of Physics, Southern University of Science and Technology, Shenzhen, Guangdong 518055 (China); Xiao, Xudong, E-mail: xdxiao@phy.cuhk.edu.hk [Department of Physics, The Chinese University of Hong Kong, Shatin, New Territory, Hong Kong (China)

2017-04-15

Highlights: • Diffusions of Au, Ag and Cu atoms in the half unit cells of Si(111)-(7×7) have been studied by using a STM-based I-t method. • Despite their similar absorption sites, the diffusion dynamics show obvious differences between Ag and the other two. • Theoretical calculations suggest that different potential energy profiles are responsible for the observed differences. - Abstract: The diffusion behaviors of single Au, Ag and Cu atoms on Si(111)-(7 × 7) half unit cells have been investigated via combining scanning tunneling microscopy and first-principles calculations. Despite the similar adsorption sites between both half unit cells among these elements, the diffusion dynamics show obvious differences between Ag and the other two. Although obvious asymmetry has been found in the diffusion behaviors of Au and Cu atoms in two half unit cells of Si(111)-(7 × 7), the asymmetry behaves in a way different from that of Ag atoms and no dual-time character has been observed for the diffusions of Au and Cu in both half unit cells. Theoretical calculations suggest a different potential energy profile caused by the stronger hybridization between d states of Au (Cu) and Si states make the concept of basin useless for the diffusion of Au and Cu atoms inside the half unit cells of Si(111)-(7 × 7).

Carbon monoxide oxidation on a Au(111 surface modified by spontaneously deposited Ru

Directory of Open Access Journals (Sweden)

ROLF-JÜRGEN BEHM

2001-04-01

Full Text Available The spontaneous deposition of Ru on Au(111 was performed in 10-3 M RuCl3 + 0.5 M H2SO4 solution. The obtained surface was characterized by STM under potential control in 0.5 M H2SO4 solution. The coverage of the Au(111 terraces by deposited Ru was estimated by STM to be 0.02 ML. Step decoration could be noticed in the STM images, which indicates that the steps, as lined defects, are active sites for the nucleation of Ru monolayer islands, while the random distribution of Ru nuclei, observed on the terraces indicates point defects as active sites. The electrocatalytic activity of Au(111 surface modified by spontaneously deposited Ru was studied towards CO oxidation. The significant enhancement in the reaction rate compared to CO oxidation on a pure Au(111 surface, indicated that the edges of the deposited Ru islands were the active sites for the reaction.

The influence of cyclic deposition and anneal on growth of isolated and well-dispersed Au nanoisland arrays

Energy Technology Data Exchange (ETDEWEB)

Sun, Xin; Li, Hao, E-mail: liha@missouri.edu

2015-12-01

Highlights: • Isolated and well-dispersed Au nanoislands were prepared by cyclical deposition and anneal. • The morphology of Au nanoislands were shown to be influenced by the number of growth cycles. • SERS sensing application was shown to be viable with as-prepared Au nanoislands. - Abstract: Isolated and well-dispersed Au nanoisland arrays were prepared with sputter deposition and post-deposition anneal in a cyclic fashion. Scanning electron microscopy (SEM) characterization and associated image analysis in aspects of nanoisland size, coverage, circularity, and density were performed to investigate the influence of cyclic deposition and anneal (DAA) on the morphology of as-prepared Au nanoisland arrays. This study revealed that, given a fixed amount of Au deposition per cycle, increasing the number of DAA cycles drove Au nanoislands’ gradual growth that was interpreted with the increase of their size and coverage and decrease of their density and circularity. In addition, given a fixed amount of total Au deposition, dividing the growth process into more cycles was shown to lower the growth rate of Au nanoislands. Moreover, the as-prepared Au nanoisland arrays were demonstrated to be a viable option as surface-enhanced Raman spectroscopy (SERS) sensing platform whose SERS enhancement was found to be highly dependent upon the size of nanoislands.

The influence of cyclic deposition and anneal on growth of isolated and well-dispersed Au nanoisland arrays

International Nuclear Information System (INIS)

Sun, Xin; Li, Hao

2015-01-01

Highlights: • Isolated and well-dispersed Au nanoislands were prepared by cyclical deposition and anneal. • The morphology of Au nanoislands were shown to be influenced by the number of growth cycles. • SERS sensing application was shown to be viable with as-prepared Au nanoislands. - Abstract: Isolated and well-dispersed Au nanoisland arrays were prepared with sputter deposition and post-deposition anneal in a cyclic fashion. Scanning electron microscopy (SEM) characterization and associated image analysis in aspects of nanoisland size, coverage, circularity, and density were performed to investigate the influence of cyclic deposition and anneal (DAA) on the morphology of as-prepared Au nanoisland arrays. This study revealed that, given a fixed amount of Au deposition per cycle, increasing the number of DAA cycles drove Au nanoislands’ gradual growth that was interpreted with the increase of their size and coverage and decrease of their density and circularity. In addition, given a fixed amount of total Au deposition, dividing the growth process into more cycles was shown to lower the growth rate of Au nanoislands. Moreover, the as-prepared Au nanoisland arrays were demonstrated to be a viable option as surface-enhanced Raman spectroscopy (SERS) sensing platform whose SERS enhancement was found to be highly dependent upon the size of nanoislands.

Ion scattering studies of ordered alloy surfaces: CuAu(1 0 0) and NiAl

International Nuclear Information System (INIS)

Beikler, R.; Taglauer, E.

2000-01-01

The composition and structure of alloy surfaces can differ from the corresponding bulk properties due to segregation and relaxation effects. We studied the (1 0 0) surface of the ordered alloy CuAu and amorphous Ni and Al by low-energy Ne + and Na + ion scattering. The interpretation of the experimental results is supported by numerical simulations using the MARLOWE code. In the CuAu system a certain geometry was found to be very sensitive to Au presence in the 2nd layer. Comparison with MARLOWE results also allows to study variations in the ion yields arising from neutralization effects. By trajectory analysis ion survival probabilities are estimated for Ni and Al

Topological description of mechanical behavior of Cu, Ag and Au: A first-principle study

Directory of Open Access Journals (Sweden)

M Saghayezhian

2011-12-01

Full Text Available  Mechanical properties and stress-strain curves of Cu, Ag and Au single crystals are calculated using ab initio methods. Elastic and Plastic regions are scrutinized. Yield stress and slope of these curves can shed light on brittlenesss and ductility of these metals that prove Cu, despite its high ultimate tensile strength, is less ductile than Au and Ag. Analysis of topology of charge density along with stress-strain curves shows that the elastic-plastic transition accompanies topological transition and for these metals, both transitions occur in the same strain. Some charactristics of critical point, especially bond points, are inspected.

Age of the granitic magmatism and the W-Mo mineralization in skarns of the Seridó belt (NE Brazil) based on zircon U-Pb (SHRIMP) and molybdenite Re-Os dating

Science.gov (United States)

Hollanda, Maria Helena B. M. de; Souza Neto, João A.; Archanjo, Carlos J.; Stein, Holly; Maia, Ana C. S.

2017-11-01

Over five hundred W-Mo skarns have been reported in the Neoproterozoic Seridó belt in the northeastern Brazil. The origin of these mineralizations has been attributed to metasomatic reactions occuring after the infiltration of hydrothermal fluids that are mostly derived from the plutonic magmatic activity that ranged between approximately 600 and 525 Ma. Here we date molybdenite using N-TIMS on Re-Os analysis of three major scheelite deposits (Brejuí, Bonfim and Bodó) hosted in the skarn horizons of the metasedimentary sequence. Molybdenite is an integral part of the mineralizations that include scheelite in skarns and, in the Bonfim deposit, gold concentrate in late brittle faults. The Re-Os ages are 554 ± 2 Ma (Brejuí), 524 ± 2 Ma (Bonfim) and 510 ± 2 Ma (Bodó). The age of the Brejuí molybdenite, however, appears to be anomalous based on the local geology of the deposit, which is located next to the contact of a batholith dated ca. 575 Ma. In turn, the Bonfim molybdenite yields similar ages in replicated samples with variable high Re contents. New U-Pb SHRIMP ages of four biotite (leuco)granite plutons vary from 577 ± 5 Ma to 526 ± 8 Ma, which overlap with molybdenite crystallization. These results indicate a close connection between the W-Mo mineralizations and the plutonic activity that intruded the belt after the peak HT/LP metamorphism. The latest pulses of felsic magmatism, which were contemporaneous with the emplacement of Be-Ta-Nb-Li pegmatites, therefore constitute a potential guide in the Seridó belt for prospective W-Mo deposits.

Petrology of skarns in the north and the southwest of Qazan (South Qamsar with emphasis on the mineral chemistry of garnet and pyroxene

Directory of Open Access Journals (Sweden)

Maria Chavideh

2018-03-01

Full Text Available The Oligo-Miocene Qazan granitoid body caused contact metamorphic of surrounding rocks and skarn formation in the wall limestone. The main intrusive rocks are essentially granite to diorite in composition. Two different types of skarn, exo and endoskarn have been developed. On the base of microprobe data, the northern skarn are characterized by zoning and the amounts of andradite and grossular changes oscillatory. While garnets from the southwestern skarn is predominantly andradite in composition. Using Fe/Ti vs. Al/ (Al+Fe+Mn diagram that were calculated based on the mole percent of the used elements, it is estimated that about less than 50 percent hydrothermal waters were involved for the northern skarn whereas it was over this amount for the southwestern skarn. This leds to difference in garnet composition. The composition of clinopyroxene in both skarns is the same (diopside. As a result, hydrothermal fluids have not had much influence on pyroxene genesis. With regards to the occurrence of mineral assemblage and the presence of wollastonite in the skarns under study, these rocks have evolved in temperature above 500 ° C and O2 fugacity in the range of 10-17 to 10-15.

Are Corporate Universities (CU possible in emerging countries? Arcor University (AU.

Directory of Open Access Journals (Sweden)

Leandro A. Viltard

2014-09-01

Full Text Available This article explores CU implementation and whether it is applicable and effective in emerging countries like Argentina (where there are no studies on the subject. Through an in-depth review of Arcor University (AU, Arcor’s Group CU, located in Argentina, the feasibility of the CU is shown, under certain conditions. This analysis is complemented with specialists´ interviews to deepen our insights and investigation’s results. Our conclusion is that the CU complements Corporate Training’s traditional offering, as its programs are directed towards practical contents and performance/organizational improvement. In this way, it is possible to enhance the actual corporate educational paradigm and talent employability. The research design is not experimental and is transversal as it relates to a specific moment in time.

Au nanostructure fabrication by pulsed laser deposition in open air: Influence of the deposition geometry

Directory of Open Access Journals (Sweden)

Rumen G. Nikov

2017-11-01

Full Text Available We present a fast and flexible method for the fabrication of Au nanocolumns. Au nanostructures were produced by pulsed laser deposition in air at atmospheric pressure. No impurities or Au compounds were detected in the resulting samples. The nanoparticles and nanoaggregates produced in the ablated plasma at atmospheric pressure led to the formation of chain-like nanostructures on the substrate. The dependence of the surface morphology of the samples on the deposition geometry used in the experimental set up was studied. Nanocolumns of different size and density were produced by varying the angle between the plasma plume and the substrate. The electrical, optical, and hydrophobic properties of the samples were studied and discussed in relation to their morphology. All of the nanostructures were conductive, with conductivity increasing with the accumulation of ablated material on the substrate. The modification of the electrical properties of the nanostructures was demonstrated by irradiation by infrared light. The Au nanostructures fabricated by the proposed technology are difficult to prepare by other methods, which makes the simple implementation and realization in ambient conditions presented in this work more ideal for industrial applications.

Au nanostructure fabrication by pulsed laser deposition in open air: Influence of the deposition geometry.

Science.gov (United States)

Nikov, Rumen G; Dikovska, Anna Og; Nedyalkov, Nikolay N; Avdeev, Georgi V; Atanasov, Petar A

2017-01-01

We present a fast and flexible method for the fabrication of Au nanocolumns. Au nanostructures were produced by pulsed laser deposition in air at atmospheric pressure. No impurities or Au compounds were detected in the resulting samples. The nanoparticles and nanoaggregates produced in the ablated plasma at atmospheric pressure led to the formation of chain-like nanostructures on the substrate. The dependence of the surface morphology of the samples on the deposition geometry used in the experimental set up was studied. Nanocolumns of different size and density were produced by varying the angle between the plasma plume and the substrate. The electrical, optical, and hydrophobic properties of the samples were studied and discussed in relation to their morphology. All of the nanostructures were conductive, with conductivity increasing with the accumulation of ablated material on the substrate. The modification of the electrical properties of the nanostructures was demonstrated by irradiation by infrared light. The Au nanostructures fabricated by the proposed technology are difficult to prepare by other methods, which makes the simple implementation and realization in ambient conditions presented in this work more ideal for industrial applications.

Kr-Ar and Rb-Sr dating and the genesis of tungsten at the Clea tungsten skarn property, Selwyn Mountains, Yukon Territory

International Nuclear Information System (INIS)

Godwin, C.I.; Armstrong, R.L.; Tompson, K.M.

1980-01-01

Tungsten skarn deposits on the Clea property in the Selwyn Mountains, Y.T., are related genetically to a quartz monzonite stock, about 500 metres in diameter at the surface. Lower Paleozoic sedimentary rocks are metamorphosed for a distance of 3 km from the stock. Tugnsten-bearing skarn mineralization within the altered sedimentary rocks is of two types: sulphide-rich pods and calc-silicate beds. The most significant sheelite concentration is in calc-silicate beds near or adjacent to the quartz monzonite stock. Discordant K-Ar and Rb-Sr isotopic dates indicate that the stock is probably of early Late Cretaceous age, 94 Ma or slightly older, and that it cooled slowly. High initial 87 Sr/ 86 Sr ratios and disequilibrium relationships between K-feldspar phenocrysts and groundmass minerals in the porphyritic phase of the granite rock, and between different granite rock specimens, indicate contamination of crystallizing magma by old sialic continental crust which extends westward under the Selwyn Basin. This study is significant to regional tungsten exploration. Granite rocks associated with tungsten deposits, in this part of the Canadian Cordillera at least, appear to have specific isotope characteristics that indicate they were generated at a specific time and in a particular way. (auth)

Reaction kinetics of metal deposition via surface limited red-ox replacement of underpotentially deposited metal monolayers

International Nuclear Information System (INIS)

Gokcen, Dincer; Bae, Sang-Eun; Brankovic, Stanko R.

2011-01-01

The study of the kinetics of metal deposition via surface limited red-ox replacement of underpotentially deposited metal monolayers is presented. The model system was Pt submonolayer deposition on Au(1 1 1) via red-ox replacement of Pb and Cu UPD monolayers on Au(1 1 1). The kinetics of a single replacement reaction was studied using the formalism of the comprehensive analytical model developed to fit the open circuit potential transients from deposition experiments. The practical reaction kinetics parameters like reaction half life, reaction order and reaction rate constant are determined and discussed with their relevance to design and control of deposition experiments. The effects of transport limitation and the role of the anions/electrolyte on deposition kinetics are investigated and their significance to design of effective deposition process is discussed.

A flexible angle sensor made from MWNT/CuO/Cu{sub 2}O nanocomposite films deposited by an electrophoretic co-deposition process

Energy Technology Data Exchange (ETDEWEB)

Toboonsung, Buppachat, E-mail: buppachattt@yahoo.co.th [Physics and General Science Program, Faculty of Science and Technology, Nakhon Ratchasima Rajabhat University, Nakhon Ratchasima 30000 (Thailand); Singjai, Pisith, E-mail: singjai@hotmail.com [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai, 50200 (Thailand)

2012-08-25

Highlights: Black-Right-Pointing-Pointer MWNT/CuO/Cu{sub 2}Onanocomposite films were coated on a PET sheet. Black-Right-Pointing-Pointer The film resistance and application as angle sensor were investigated. Black-Right-Pointing-Pointer Thesensor showed a linear relation between the film resistance and the bending angle. Black-Right-Pointing-Pointer A minimum loop area and a high stability in sensitivity over a thousand bending cycles were obtained. - Abstract: A flexible angle sensor was prepared using an electrophoretic co-deposition process to form nanocomposite networks of multi-wall carbon nanotube/cupric oxide/cuprous oxide (MWNT/CuO/Cu{sub 2}O) on a polyethylene terephthalate (PET) sheet. The deposition method used copper and stainless steel electrodes, and the effects of varying of electrode separation, MWNT concentration in deionized water, voltage and deposition time were studied. The film resistance of the as-deposited samples decreased with increasing the MWNT concentration up to 0.3 mg/ml. The angle sensor showed a linear relation between the film resistance and the bending angle, a relationship that was illustrated with loop area and sensitivity data. The best angle sensor was successfully made with an electrode separation of 8 mm, a concentration of 0.3 mg/ml, a voltage of 10 V and a deposition time of 3 h, parameters that resulted in a minimum loop area and the most stability in sensitivity over a thousand bending cycles.

Tensile Creep Properties of the 50Au-50Cu Braze Alloy

International Nuclear Information System (INIS)

Stephens, J.J.

1999-01-01

The 50Au-50CU (wt.%) alloy is a solid-solution strengthened braze alloy used extensively in conventional, hermetic metal/ceramic brazing applications where low vapor pressure is a requirement. Typical metal/ceramic base materials would be Kovar TM alloy and metallized and Ni-plated 94% alumina ceramic. The elevated temperature mechanical properties are important for permitting FEA evaluation of residual stresses in metal/ceramic brazes given specific geometries and braze cooldown profiles. For material with an atomic composition of 76.084 at.% CL 23.916 Au (i.e., on the Cu-rich side of Cu 3 Au) that was annealed for 2 hr. at 750 ampersand deg;C and water quenched a Garofalo sinh equation was found to adequately characterize the minimum strain rate data over the temperature mnge 450-850 ampersand deg;C. At lower temperatures (250 arid 350 ampersand deg;C), a conventional power law equation was found to characterize the data. For samples held long periods of time at 375 ampersand deg;C (96 hrs.) and slowly cooled to room temperature, a slight strengthening reaction was observed: with the stress necessary to reach the same strain rate increasing by about 15% above the baseline annealed and quenched data. X-ray diffiction indicates that the 96 hr at 375 ampersand deg;C + slow cool condition does indeed order. The microhardness of the ordered samples indicates a value of 94.5 VHN, compared to 93.7 VHN for the baseline annealed and quenched (disordered FCC) samples. From a brazing perspective, the relative sluggishness of this ordering reaction does not appear to pose a problem for braze joints cooled at reasonable rates following brazing

Developing an aqueous approach for synthesizing Au and M@Au (M = Pd, CuPt) hybrid nanostars with plasmonic properties

Science.gov (United States)

Du, Jingshan; Yu, Junjie; Xiong, Yalin; Lin, Zhuoqing; Zhang, Hui; Yang, Deren

Anisotropic Au nanoparticles show unique localized surface plasmon resonance (LSPR) properties, which make it attractive in optical, sensing, and biomedical applications. In this contribution, we report a general and facile strategy towards aqueous synthesis of Au and M@Au (M = Pd, CuPt) hybrid nanostars by reducing HAuCl4 with ethanolamine in the presence of cetyltrimethylammonium bromide (CTAB). According to electron microscopic observation and spectral monitoring, we found that the layered epitaxial growth mode (i.e., Frank-van der Merwe mechanism) contributes to the enlargement of the core, while, the random attachment of Au nanoclusters onto the cores accounts for the formation of the branches. Both of them are indispensable for the formation of the nanostars. The LSPR properties of the Au nanoparticles have been well investigated with morphology control via precursor amount and growth temperature. The Au nanostars showed improved surface-enhanced Raman spectroscopy (SERS) performance for rhodamine 6G due to their sharp edges and tips, which were therefore confirmed as good SERS substrate to detect trace amount of molecules.

Electrochemical characterization of the underpotential deposition of tellurium on Au electrode

International Nuclear Information System (INIS)

Zhu, W.; Yang, J.Y.; Zhou, D.X.; Bao, S.Q.; Fan, X.A.; Duan, X.K.

2007-01-01

Electrochemical characterization of the underpotential deposition (UPD) of tellurium on Au substrate has been performed in this paper. The mechanism of Te deposition and its voltammetry dependence on the Te ion concentration were studied, and it suggests that variations in the metal ion concentration may affect the UPD process kinetics. The effect of tellurium adsorbates on UPD behavior of Te has also been investigated. The results show that the tellurium adsorbates could be irreversibly adsorbed upon the Au substrate surface under the open-circuit conditions. Subsequent removal of the Te adsorbates was also proved to be very difficult within the Au double-layer region, and a standard electrochemical cleaning procedure is necessary to remove the Te adsorbates completely. When the potential was cycled into the Au oxidation region, a substantial loss of Te adsobates was observed, which occurs simultaneously with the Au oxidation features. Scan rate dependent cyclic voltammetry experiments reveal that the peak current in the Te UPD peak is not a linear function of the scan rate, ν, but of a 2/3 power of the scan rate, ν 2/3 . It is in good consistent with a two-dimension nucleation and growth mechanism

Electrochemical Sensor Coating Based on Electrophoretic Deposition of Au-Doped Self-Assembled Nanoparticles.

Science.gov (United States)

Zhang, Rongli; Zhu, Ye; Huang, Jing; Xu, Sheng; Luo, Jing; Liu, Xiaoya

2018-02-14

The electrophoretic deposition (EPD) of self-assembled nanoparticles (NPs) on the surface of an electrode is a new strategy for preparing sensor coating. By simply changing the deposition conditions, the electrochemical response for an analyte of deposited NPs-based coating can be controlled. This advantage can decrease the difference between different batches of sensor coating and ensure the reproducibility of each sensor. This work investigated the effects of deposition conditions (including deposition voltage, pH value of suspension, and deposition time) on the structure and the electrochemical response for l-tryptophan of sensor coating formed from Au-doped poly(sodium γ-glutamate) with pendant dopamine units nanohybrids (Au/γ-PGA-DA NBs) via the EPD method. The structure and thickness of the deposited sensor coating were measured by atomic force microscopy, which demonstrated that the structure and thickness of coating can be affected by the deposition voltage, the pH value of the suspension, and the deposition time. The responsive current for l-tryptophan of the deposited sensor coating were measured by differential pulse voltammetry, which showed that the responsive current value was affected by the structure and thickness of the deposited coating. These arguments suggested that a rich design-space for tuning the electrochemical response for analyte and a source of variability in the structure of sensor coating can be provided by the deposition conditions. When Au/γ-PGA-DA NBs were deposited on the electrode surface and formed a continuous coating with particle morphology and thinner thickness, the deposited sensor coating exhibited optimal electrochemical response for l-tryptophan.

Electrophoretic deposition on graphene of Au nanoparticles generated by laser ablation of a bulk Au target in water

International Nuclear Information System (INIS)

Semaltianos, N G; Hendry, E; Chang, H; Wears, M L

2015-01-01

The characteristic property of nanoparticles generated by laser ablation of metallic targets in liquids to be surface electrically charged can be exploited for the deposition of the nanoparticles onto electrically conducting substrates directly from the synthesized colloidal solution by using the method of electrophoretic deposition (EPD). The method benefits from the high quality of the interface between the deposited nanoparticles and the substrate due to the ligand-free nanoparticle surfaces and thus providing hybrid materials with advanced and novel properties. In this letter, an Au bulk target was laser ablated in deionized (DI) water for the generation of an Au nanoparticle colloidal solution. Under the present conditions of ablation, nanoparticles with diameters from 4 and up to 67 nm are formed in the solution with 80% of the nanoparticles having diameters below ∼20 nm. Their size distribution follows a log-normal function with a median diameter of 8.6 nm. The nanoparticles were deposited onto graphene on a quartz surface by anodic EPD performed at 30 V for 20 min and a longer time of 1 h. A quite uniform surface distribution of the nanoparticles was achieved with surface densities ranging from ∼15 to ∼40 nanoparticles per μm 2 . The hybrid materials exhibit clearly the plasmon resonance absorption of the Au nanoparticles. Deposition for short times preserves the integrity of graphene while longer time deposition leads to the conversion of graphene to graphene oxide, which is attributed to the electrochemical oxidation of graphene. (letter)

Shape memory effect and microstructures of sputter-deposited Cu-Al-Ni films

International Nuclear Information System (INIS)

Minemura, T.; Andoh, H.; Kita, Y.; Ikuta, I.

1985-01-01

The shape memory effect has been found in many alloy systems which exhibit a thermoelastic martensite transformation. Cu-Al-Ni alloys exhibit an excellent shape memory effect in single crystalline states, but they have not yet been commercially used due to their brittle fracture along the grain boundaries in polycrystalline states. This letter reports the shape memory effect and microstructures of the sputter-deposited Cu-Al-Ni films. Cu-14%Al-4%Ni alloy ingot was prepared. A target for sputter deposition was cut from the ingot. Aluminium foils (20 μm thick) were used for the substrates of sputter deposition. The microstructures and crystal structures of the films were investigated by transmission electron microscopy (TEM) and X-ray diffraction using CuKα radiation, respectively. The effect of the sputtering conditions such as substrate temperature, partial pressure of argon gas, and the sputtering power on the structures of sputter-deposited Cu-14%Al-4%Ni films were investigated by X-ray diffraction. Results are shown and discussed. Photographs demonstrate shape memory behaviour of Cu-14%Al-4%Ni films sputter-deposited on aluminium foils from (a) liquid nitrogen temperature to (d) room temperature. (author)

Zinc-doping enhanced cadmium sulfide electrochemiluminescence behavior based on Au-Cu alloy nanocrystals quenching for insulin detection.

Science.gov (United States)

Zhu, Wenjuan; Wang, Chao; Li, Xiaojian; Khan, Malik Saddam; Sun, Xu; Ma, Hongmin; Fan, Dawei; Wei, Qin

2017-11-15

Novel and sensitive sandwich-type electrochemiluminescence (ECL) immunosensor was fabricated for insulin detection. Au-ZnCd 14 S combined nitrogen doping mesoporous carbons (Au-ZnCd 14 S/NH 2 -NMCs) acted as sensing platform and Au-Cu alloy nanocrystals were employed as labels to quench the ECL of Au-ZnCd 14 S/NH 2 -NMCs. Zinc-doping promoted the ECL behavior of CdS nanocrystals, with the best ECL emission obtained when the molar ratio of Zn/Cd was 1:14. Simultaneously, the modification of gold nanoparticles (Au NPs) and combination with NH 2 -NMC further enhanced the ECL emission of ZnCd 14 S due to its excellent conductivity and large specific surface area, which is desirable for the immunosensor construction. Au-Cu alloy nanocrystals were employed in the ECL system of ZnCd 14 S/K 2 S 2 O 8 triggering ECL quenching effects. The ECL spectra of ZnCd 14 S, acting as the energy donor, exhibited well overlaps with the absorption band of Au-Cu alloy nanocrystals which acted as the energy acceptor, leading to an effective ECL resonance energy transfer (ECL-RET). On the basis of the ECL quenching effects, a sensitive ECL immunosensor for insulin detection was successfully constructed with a linear response range of insulin concentration from 0.1pg/mL to 30ng/mL and the limit of detection was calculated to be 0.03pg/mL (S/N = 3). Copyright © 2017 Elsevier B.V. All rights reserved.

Disruption, segregation, and passivation for Pd and noble-metal overlayers on YBa2Cu3O/sub 6.9/

International Nuclear Information System (INIS)

Wagener, T.J.; Gao, Y.; Vitomirov, I.M.; Aldao, C.M.; Joyce, J.J.; Capasso, C.; Weaver, J.H.; Capone II, D.W.

1988-01-01

We have investigated interfaces formed when Pd and the noble metals Cu, Ag, and Au are deposited onto polycrystalline samples of YBa 2 Cu 3 O/sub 6.9/ fractured in ultrahigh vacuum. Synchrotron-radiation photoemission results show that Cu and Pd overlayers leach oxygen from the underlying YBa 2 Cu 3 O/sub 6.9/ substrate, disrupt the superconductor, and destroy electronic states near the Fermi level. Interface reactions become kinetically limited at room temperature after the deposition of ∼4 A of Cu or Pd, significantly sooner than for the reactive metals Fe, Al, Ti, and In. The presence of Ba near the surface after the deposition of more than 100 A of Cu and Pd reflects substrate disruption and subsequent surface segregation. In contrast, overlayers of Ag and Au do not disrupt the superconductor substrate, no segregation is observed, but the overlayers are nonuniform and the quality of passivation is in question for coverages <100 A

Characterization of sprayed CuInS2 films by XRD and Raman spectroscopy measurements

International Nuclear Information System (INIS)

Lee, Dong-Yeup; Kim, JunHo

2010-01-01

We studied CuInS 2 (CIS) film growth using two deposition methods, which were high electrostatic field assisted ultrasonic spray (HEFAUS) deposition and sulfurization of Cu-In metallic film. The sprayed-films were grown with chalcopyrite ordering and Cu-Au ordering mixed. In order to obtain higher quality CIS films, post-sulfurization was carried out for sprayed-films. The post-sulfurization induced improvement of crystallinity and enhancement of chalcopyrite ordering. However, it was observed that Cu-Au ordering still coexisted in the CIS film after post-sulfurization. With the same sulfurization condition, sulfurization was done to transform Cu-In metallic film into CIS film. The sulfurized metallic film was turned out to be formed as CIS film with higher crystallinity and better chalcopyrite ordering than sulfurized sprayed-films. All fabricated films were characterized by X-ray diffraction, Raman scattering, scanning electron microscope and energy dispersive X-ray analysis measurements.

Reversible and irreversible changes of surface morphology by order-disorder transition in CuAu alloy

International Nuclear Information System (INIS)

Sachl, Jindrich; Sima, Vladimir; Pfeiler, Wolfgang

2004-01-01

The change of symmetry from the disordered fcc structure to tetragonal or orthorhombic structure is accompanied in CuAu alloy by anisotropy of lattice parameters and also by local generation of c-variants of structural antiphase domains. Macroscopic results of these processes can be observed as a dynamic change of the surface morphology. Some surface changes are reversible, on the other hand the internal stresses connected with the order-disorder transformation are also responsible for irreversible surface deformation effects. The domain structure formation can be influenced by external load and a shape memory effect can be observed at special conditions in CuAu. A combination of in-situ microscopic video cinematography and post-mortem 3-D atomic force microscopy (AFM) has been used for the surface study. The AFM images have enabled a detailed analysis of the surface morphology and the cinematography has given an in-situ information dealing with conditions and kinetics of observed surface changes. Measurements on CuAu single- and poly-crystalline samples have been made for a wide variety of experimental conditions (heating/cooling rates, external load, thermal history of the sample)

Reversible and irreversible changes of surface morphology by order-disorder transition in CuAu alloy

Energy Technology Data Exchange (ETDEWEB)

Sachl, Jindrich; Sima, Vladimir; Pfeiler, Wolfgang

2004-09-22

The change of symmetry from the disordered fcc structure to tetragonal or orthorhombic structure is accompanied in CuAu alloy by anisotropy of lattice parameters and also by local generation of c-variants of structural antiphase domains. Macroscopic results of these processes can be observed as a dynamic change of the surface morphology. Some surface changes are reversible, on the other hand the internal stresses connected with the order-disorder transformation are also responsible for irreversible surface deformation effects. The domain structure formation can be influenced by external load and a shape memory effect can be observed at special conditions in CuAu. A combination of in-situ microscopic video cinematography and post-mortem 3-D atomic force microscopy (AFM) has been used for the surface study. The AFM images have enabled a detailed analysis of the surface morphology and the cinematography has given an in-situ information dealing with conditions and kinetics of observed surface changes. Measurements on CuAu single- and poly-crystalline samples have been made for a wide variety of experimental conditions (heating/cooling rates, external load, thermal history of the sample)

B -meson production at forward and backward rapidity in p +p and Cu + Au collisions at √{sN N}=200 GeV

Science.gov (United States)

Aidala, C.; Ajitanand, N. N.; Akiba, Y.; Akimoto, R.; Alexander, J.; Alfred, M.; Andrieux, V.; Aoki, K.; Apadula, N.; Asano, H.; Atomssa, E. T.; Awes, T. C.; Ayuso, C.; Azmoun, B.; Babintsev, V.; Bagoly, A.; Bai, M.; Bai, X.; Bandara, N. S.; Bannier, B.; Barish, K. N.; Bathe, S.; Baublis, V.; Baumann, C.; Baumgart, S.; Bazilevsky, A.; Beaumier, M.; Belmont, R.; Berdnikov, A.; Berdnikov, Y.; Black, D.; Blau, D. S.; Boer, M.; Bok, J. S.; Boyle, K.; Brooks, M. L.; Bryslawskyj, J.; Buesching, H.; Bumazhnov, V.; Butler, C.; Butsyk, S.; Campbell, S.; Canoa Roman, V.; Cervantes, R.; Chen, C.-H.; Chi, C. Y.; Chiu, M.; Choi, I. J.; Choi, J. B.; Choi, S.; Christiansen, P.; Chujo, T.; Cianciolo, V.; Citron, Z.; Cole, B. A.; Connors, M.; Cronin, N.; Crossette, N.; Csanád, M.; Csörgő, T.; Danley, T. W.; Datta, A.; Daugherity, M. S.; David, G.; Deblasio, K.; Dehmelt, K.; Denisov, A.; Deshpande, A.; Desmond, E. J.; Ding, L.; Dion, A.; Dixit, D.; Do, J. H.; D'Orazio, L.; Drapier, O.; Drees, A.; Drees, K. A.; Dumancic, M.; Durham, J. M.; Durum, A.; Elder, T.; Engelmore, T.; Enokizono, A.; En'yo, H.; Esumi, S.; Eyser, K. O.; Fadem, B.; Fan, W.; Feege, N.; Fields, D. E.; Finger, M.; Finger, M.; Fleuret, F.; Fokin, S. L.; Frantz, J. E.; Franz, A.; Frawley, A. D.; Fukao, Y.; Fukuda, Y.; Fusayasu, T.; Gainey, K.; Gal, C.; Gallus, P.; Garg, P.; Garishvili, A.; Garishvili, I.; Ge, H.; Giordano, F.; Glenn, A.; Gong, X.; Gonin, M.; Goto, Y.; Granier de Cassagnac, R.; Grau, N.; Greene, S. V.; Grosse Perdekamp, M.; Gu, Y.; Gunji, T.; Guragain, H.; Hachiya, T.; Haggerty, J. S.; Hahn, K. I.; Hamagaki, H.; Hamilton, H. F.; Han, S. Y.; Hanks, J.; Hasegawa, S.; Haseler, T. O. S.; Hashimoto, K.; Hayano, R.; He, X.; Hemmick, T. K.; Hester, T.; Hill, J. C.; Hill, K.; Hollis, R. S.; Homma, K.; Hong, B.; Hoshino, T.; Hotvedt, N.; Huang, J.; Huang, S.; Ichihara, T.; Ikeda, Y.; Imai, K.; Imazu, Y.; Imrek, J.; Inaba, M.; Iordanova, A.; Isenhower, D.; Isinhue, A.; Ito, Y.; Ivanishchev, D.; Jacak, B. V.; Jeon, S. J.; Jezghani, M.; Ji, Z.; Jia, J.; Jiang, X.; Johnson, B. M.; Joo, K. S.; Jorjadze, V.; Jouan, D.; Jumper, D. S.; Kamin, J.; Kanda, S.; Kang, B. H.; Kang, J. H.; Kang, J. S.; Kapukchyan, D.; Kapustinsky, J.; Karthas, S.; Kawall, D.; Kazantsev, A. V.; Key, J. A.; Khachatryan, V.; Khandai, P. K.; Khanzadeev, A.; Kijima, K. M.; Kim, C.; Kim, D. J.; Kim, E.-J.; Kim, M.; Kim, M. H.; Kim, Y.-J.; Kim, Y. K.; Kincses, D.; Kistenev, E.; Klatsky, J.; Kleinjan, D.; Kline, P.; Koblesky, T.; Kofarago, M.; Komkov, B.; Koster, J.; Kotchetkov, D.; Kotov, D.; Krizek, F.; Kudo, S.; Kurita, K.; Kurosawa, M.; Kwon, Y.; Lacey, R.; Lai, Y. S.; Lajoie, J. G.; Lallow, E. O.; Lebedev, A.; Lee, D. M.; Lee, G. H.; Lee, J.; Lee, K. B.; Lee, K. S.; Lee, S.; Lee, S. H.; Leitch, M. J.; Leitgab, M.; Leung, Y. H.; Lewis, B.; Lewis, N. A.; Li, X.; Li, X.; Lim, S. H.; Liu, L. D.; Liu, M. X.; Loggins, V.-R.; Loggins, V.-R.; Lökös, S.; Lovasz, K.; Lynch, D.; Maguire, C. F.; Majoros, T.; Makdisi, Y. I.; Makek, M.; Malaev, M.; Manion, A.; Manko, V. I.; Mannel, E.; Masuda, H.; McCumber, M.; McGaughey, P. L.; McGlinchey, D.; McKinney, C.; Meles, A.; Mendoza, M.; Meredith, B.; Metzger, W. J.; Miake, Y.; Mibe, T.; Mignerey, A. C.; Mihalik, D. E.; Milov, A.; Mishra, D. K.; Mitchell, J. T.; Mitsuka, G.; Miyasaka, S.; Mizuno, S.; Mohanty, A. K.; Mohapatra, S.; Montuenga, P.; Moon, T.; Morrison, D. P.; Morrow, S. I. M.; Moskowitz, M.; Moukhanova, T. V.; Murakami, T.; Murata, J.; Mwai, A.; Nagae, T.; Nagai, K.; Nagamiya, S.; Nagashima, K.; Nagashima, T.; Nagle, J. L.; Nagy, M. I.; Nakagawa, I.; Nakagomi, H.; Nakamiya, Y.; Nakamura, K. R.; Nakamura, T.; Nakano, K.; Nattrass, C.; Netrakanti, P. K.; Nihashi, M.; Niida, T.; Nouicer, R.; Novák, T.; Novitzky, N.; Novotny, R.; Nyanin, A. S.; O'Brien, E.; Ogilvie, C. A.; Oide, H.; Okada, K.; Orjuela Koop, J. D.; Osborn, J. D.; Oskarsson, A.; Ottino, G. J.; Ozawa, K.; Pak, R.; Pantuev, V.; Papavassiliou, V.; Park, I. H.; Park, J. S.; Park, S.; Park, S. K.; Pate, S. F.; Patel, L.; Patel, M.; Peng, J.-C.; Peng, W.; Perepelitsa, D. V.; Perera, G. D. N.; Peressounko, D. Yu.; Perezlara, C. E.; Perry, J.; Petti, R.; Phipps, M.; Pinkenburg, C.; Pisani, R. P.; Pun, A.; Purschke, M. L.; Qu, H.; Radzevich, P. V.; Rak, J.; Ravinovich, I.; Read, K. F.; Reynolds, D.; Riabov, V.; Riabov, Y.; Richardson, E.; Richford, D.; Rinn, T.; Riveli, N.; Roach, D.; Rolnick, S. D.; Rosati, M.; Rowan, Z.; Runchey, J.; Ryu, M. S.; Safonov, A. S.; Sahlmueller, B.; Saito, N.; Sakaguchi, T.; Sako, H.; Samsonov, V.; Sarsour, M.; Sato, K.; Sato, S.; Sawada, S.; Schaefer, B.; Schmoll, B. K.; Sedgwick, K.; Seele, J.; Seidl, R.; Sekiguchi, Y.; Sen, A.; Seto, R.; Sett, P.; Sexton, A.; Sharma, D.; Shaver, A.; Shein, I.; Shibata, T.-A.; Shigaki, K.; Shimomura, M.; Shioya, T.; Shoji, K.; Shukla, P.; Sickles, A.; Silva, C. L.; Silvermyr, D.; Singh, B. K.; Singh, C. P.; Singh, V.; Skoby, M. J.; Skolnik, M.; Slunečka, M.; Smith, K. L.; Snowball, M.; Solano, S.; Soltz, R. A.; Sondheim, W. E.; Sorensen, S. P.; Sourikova, I. V.; Stankus, P. W.; Steinberg, P.; Stenlund, E.; Stepanov, M.; Ster, A.; Stoll, S. P.; Stone, M. R.; Sugitate, T.; Sukhanov, A.; Sumita, T.; Sun, J.; Syed, S.; Sziklai, J.; Takahara, A.; Takeda, A.; Taketani, A.; Tanaka, Y.; Tanida, K.; Tannenbaum, M. J.; Tarafdar, S.; Taranenko, A.; Tarnai, G.; Tennant, E.; Tieulent, R.; Timilsina, A.; Todoroki, T.; Tomášek, M.; Torii, H.; Towell, C. L.; Towell, R. S.; Tserruya, I.; Ueda, Y.; Ujvari, B.; van Hecke, H. W.; Vargyas, M.; Vazquez-Carson, S.; Vazquez-Zambrano, E.; Veicht, A.; Velkovska, J.; Vértesi, R.; Virius, M.; Vrba, V.; Vukman, N.; Vznuzdaev, E.; Wang, X. R.; Wang, Z.; Watanabe, D.; Watanabe, K.; Watanabe, Y.; Watanabe, Y. S.; Wei, F.; Whitaker, S.; Wolin, S.; Wong, C. P.; Woody, C. L.; Wysocki, M.; Xia, B.; Xu, C.; Xu, Q.; Xue, L.; Yalcin, S.; Yamaguchi, Y. L.; Yamamoto, H.; Yanovich, A.; Yin, P.; Yokkaichi, S.; Yoo, J. H.; Yoon, I.; You, Z.; Younus, I.; Yu, H.; Yushmanov, I. E.; Zajc, W. A.; Zelenski, A.; Zharko, S.; Zhou, S.; Zou, L.; Phenix Collaboration

2017-12-01

The fraction of J /ψ mesons which come from B -meson decay, FB →J /ψ, is measured for J /ψ rapidity 1.2 0 in p +p and Cu+Au collisions at √{sNN} = 200 GeV with the PHENIX detector. The extracted fraction is FB →J /ψ=0.025 ±0.006 (stat) ± 0.010(syst) for p +p collisions. For Cu+Au collisions, FB →J /ψ is 0.094 ± 0.028(stat) ± 0.037(syst) in the Au-going direction (-2.2 Cu-going direction (1.2 Au, of B mesons in Cu+Au collisions is consistent with binary scaling of measured yields in p +p at both forward and backward rapidity.

Nanoscale Study of Clausthalite-Bearing Symplectites in Cu-Au-(U Ores: Implications for Ore Genesis

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Nicholas D. Owen

2018-02-01

Full Text Available Symplectites comprising clausthalite (PbSe and host Cu-(Fe-sulphides (chalcocite, bornite, and chalcopyrite are instructive for constraining the genesis of Cu-Au-(U ores if adequately addressed at the nanoscale. The present study is carried out on samples representative of all three Cu-(Fe-sulphides displaying clausthalite inclusions that vary in size, from a few µm down to the nm-scale (<5 nm, as well as in morphology and inclusion density. A Transmission Electron Microscopy (TEM study was undertaken on foils prepared by Focussed Ion Beam and included atom-scale High-Angle Annular Dark-Field Scanning TEM (HAADF-STEM imaging. Emphasis is placed on phase relationships and their changes in speciation during cooling, as well as on boundaries between inclusions and host sulphide. Three species from the chalcocite group (Cu2–xS are identified as 6a digenite superstructure, monoclinic chalcocite, and djurleite. Bornite is represented by superstructures, of which 2a and 4a are discussed here, placing constraints for ore formation at T > 265 °C. A minimum temperature of 165 °C is considered for clausthalite-bearing symplectites from the relationships with antiphase boundaries in 6a digenite. The results show that alongside rods, blebs, and needle-like grains of clausthalite within the chalcocite that likely formed via exsolution, a second, overprinting set of replacement textures, extending down to the nanoscale, occurs and affects the primary symplectites. In addition, other reactions between pre-existing Se, present in solid solution within the Cu-(Fe-sulphides, and Pb, transported within a fluid phase, account for the formation of composite, commonly pore-attached PbSe and Bi-bearing nanoparticles within the chalcopyrite. The inferred reorganisation of PbSe nanoparticles into larger tetragonal superlattices represents a link between the solid solution and the symplectite formation and represents the first such example in natural materials

Chemical bath deposited and dip coating deposited CuS thin films - Structure, Raman spectroscopy and surface study

Science.gov (United States)

Tailor, Jiten P.; Khimani, Ankurkumar J.; Chaki, Sunil H.

2018-05-01

The crystal structure, Raman spectroscopy and surface microtopography study on as-deposited CuS thin films were carried out. Thin films deposited by two techniques of solution growth were studied. The thin films used in the present study were deposited by chemical bath deposition (CBD) and dip coating deposition techniques. The X-ray diffraction (XRD) analysis of both the as-deposited thin films showed that both the films possess covellite phase of CuS and hexagonal unit cell structure. The determined lattice parameters of both the films are in agreement with the standard JCPDS as well as reported data. The crystallite size determined by Scherrer's equation and Hall-Williamsons relation using XRD data for both the as-deposited thin films showed that the respective values were in agreement with each other. The ambient Raman spectroscopy of both the as-deposited thin films showed major emission peaks at 474 cm-1 and a minor emmision peaks at 265 cm-1. The observed Raman peaks matched with the covellite phase of CuS. The atomic force microscopy of both the as-deposited thin films surfaces showed dip coating thin film to be less rough compared to CBD deposited thin film. All the obtained results are presented and deliberated in details.

Extremely Re-Rich Molybdenite from Porphyry Cu-Mo-Au Prospects in Northeastern Greece: Mode of Occurrence, Causes of Enrichment, and Implications for Gold Exploration

Directory of Open Access Journals (Sweden)

Tamara Kartal

2013-05-01

Full Text Available Extremely Re-rich molybdenite occurs with pyrite in sodic–calcic, sodic–sericitic and sericitic-altered porphyritic stocks of granodioritic–tonalitic and granitic composition in the Sapes–Kirki–Esymi, Melitena and Maronia areas, northeastern Greece. Molybdenite in the Pagoni Rachi and Sapes deposits is spatially associated with rheniite, as well as with intermediate (Mo,ReS2 and (Re,MoS2 phases, with up to 46 wt % Re. Nanodomains and/or microinclusions of rheniite may produce the observed Re enrichment in the intermediate molybdenite–rheniite phases. The extreme Re content in molybdenite and the unique presence of rheniite in porphyry-type mineralization, combined with preliminary geochemical data (Cu/Mo ratio, Au grades may indicate that these deposits have affinities with Cu–Au deposits, and should be considered potential targets for gold mineralization in the porphyry environment. In the post-subduction tectonic regime of northern Greece, the extreme Re and Te enrichments in the magmatic-hydrothermal systems over a large areal extent are attributed to an anomalous source (e.g., chemical inhomogenities in the mantle-wedge triggered magmatism, although local scale processes cannot be underestimated.

Pentacene on Au(1 1 1), Ag(1 1 1) and Cu(1 1 1): From physisorption to chemisorption.

Science.gov (United States)

Lu, Meng-Chao; Wang, Rong-Bin; Yang, Ao; Duhm, Steffen

2016-03-09

We measured the electronic and the molecular surface structure of pentacene deposited on the (1 1 1)-surfaces of coinage metals by means of ultraviolet photoelectron spectroscopy (UPS) and low-energy electron diffraction (LEED). Pentacene is almost flat-lying in monolayers on all three substrates and highly ordered on Au(1 1 1) and on Cu(1 1 1). On Ag(1 1 1), however, weak chemisorption leads to almost disordered monolayers, both, at room temperature and at 78 K. On Cu(1 1 1) pentacene is strongly chemisorbed and the lowest unoccupied molecular orbital becomes observable in UPS by a charge transfer from the substrate. On Ag(1 1 1) and Cu(1 1 1) multilayers adopt a tilted orientation and a high degree of crystallinity. On Au(1 1 1), most likely, also in multilayers the molecular short and long axes are parallel to the substrate, leading to a distinctively different electronic structure than on Ag(1 1 1) and Cu(1 1 1). Overall, it could be demonstrated that the substrate not only determines the geometric and electronic characteristics of molecular monolayer films but also plays a crucial role for multilayer film growth.

Development of bonding techniques between W and Cu-alloys for plasma facing components by HIP method (3). Bonding tests with Au-foil insert

International Nuclear Information System (INIS)

Saito, Shigeru

2002-07-01

In recent years, it has been considered that W (tungsten) is one of candidate materials for armor tiles of plasma a facing components (PFC), like first wall or divertor, of fusion reactor. On the other hand, Cu-alloys, like OFHC-Cu or DS-Cu, are proposed as heat sink materials behind the plasma facing materials because of its high thermal conductivity. It is necessary to develop a reliable bonding techniques in order to fabricate PFC. JAERI has developed the hot isostatic press (HIP) bonding process to bond W with Cu-alloys. In this experiments, bonding tests with Au-foil insert were performed. We could get the best HIP bonding conditions for W and Cu-alloys with Au-foil as 1123K x 2hours x 147MPa. It was shown that the HIP temperature was 150K lower than that of without Au-foil. Furthermore, the tensile strength was similar to that of with without Au-foil. (author)

Electroless deposition and electrical characterization of N- Cu 2 O ...

African Journals Online (AJOL)

This work describes the preparation of n-Cu2O layer by the electroless methods of boiling and immersion of copper plates in 0.001M CuSO4Electron Microscopy (SEM) have been used to characterize the oxide films deposited. XRD studies show, for the first time, that cuprous oxide (Cu2O) and cupric oxide (CuO) were ...

Differences in the neutralization of 2.4--10 keV Ne+ scattered from the Cu and Au atoms of an alloy surface

International Nuclear Information System (INIS)

Buck, T.M.; Wallace, W.E.; Baragiola, R.A.; Wheatley, G.H.; Rothman, J.B.; Gorte, R.J.; Tittensor, J.G.

1993-01-01

The neutralization behavior of low-energy Ne + ions scattered from a compositionally ordered Cu 3 Au(100) surface has been studied over a range of incident energy E 0 from 2.4 to 10 keV. Ion fractions of Ne scattered from Cu atoms in the first, or first two, atom layers exhibited a sharp increase setting in at an E 0 of 4--5 keV, reaching 70% at 10 keV for first-layer scattering. Inelastic energy losses, up to 130 eV, and Auger electron emission from Ne scattered from Cu, were also observed at incident energies above 4 keV. Ne scattered from the Au atoms on the same Cu 3 Au(100) surface showed only the usual velocity-dependent Auger and resonance neutralization. An explanation of the Cu results is given in terms of Ne 2s vacancy creation during the close collision of Ne, which is neutralized on the inward path, followed by autoionization on the outward path after scattering into the vacuum. Conversely, Ne cannot approach Au closely enough to form an appropriate inner-shell vacancy. This is due to the higher Coulombic repulsion created by the greater charge of the Au nucleus

Binary molecular layers of C-60 and copper phthalocyanine on Au(111) : Self-organized nanostructuring

NARCIS (Netherlands)

Stöhr, Meike; Wagner, Thorsten; Gabriel, Markus; Weyers, Bastian; Möller, Rolf

The binary molecular system of C-60 and copper phthalocyanine(CuPc) molecules has been investigated by scanning tunneling microscopy (STM) at room temperature and at 50 K. As substrate Au(111) was chosen. When C-60 and CuPc molecules are sequentially deposited, it is found that well-ordered domains

Optimizing growth conditions for electroless deposition of Au films ...

Indian Academy of Sciences (India)

Unknown

Optimizing growth conditions for electroless deposition of Au films on. Si(111) substrates. BHUVANA and G U KULKARNI*. Chemistry and Physics of Materials Unit and DST Unit on Nanoscience, Jawaharlal Nehru Centre for. Advanced Scientific Research, Jakkur PO, Bangalore 560 064, India. MS received 24 March 2006.

Pulsed laser deposition of Cu-Sn-S for thin film solar cells

DEFF Research Database (Denmark)

Ettlinger, Rebecca Bolt; Crovetto, Andrea; Bosco, Edoardo

Thin films of copper tin sulfide were deposited from a target of the stoichiometry Cu:Sn:S ~1:2:3 using pulsed laser deposition (PLD). Annealing with S powder resulted in films close to the desired Cu2SnS3 stoichiometry although the films remained Sn rich. Xray diffraction showed that the final...... films contained both cubic-phase Cu2SnS3 and orthorhombic-phase SnS...

Neutron scattering near the order-disorder transition in Cu3Au: evidence for a lower spinodal temperature

International Nuclear Information System (INIS)

Rogge, R.B.; Gaulin, B.D.; Svensson, E.C.; Hallman, E.D.; Wei, W.

1995-01-01

The binary alloy Cu 3 Au undergoes a first-order phase transition at 667 ± 3 K Within the context of the Landau theory of phase transitions, there exist, in addition to the order-disorder temperature, T c , upper and lower spinodal temperatures, T su and T si . These mark the first temperatures, upon approaching the phase transition from above and below, respectively, at which metastable droplets of the second phase can fluctuate out of the first phase. Until recently, there has, however, been little physical evidence supporting the existence of the spinodal temperatures. Elastic and inelastic neutron-scattering measurements have been carried out on Cu 3 Au over an extended temperature range with particular emphasis on temperatures near T c . The lattice constant data, order-parameter data, and phonon data provided by these measurements all indicate that there are two temperature regimes just below T c with a crossover between these regimes in the range of (T c - 35) to (T c - 25) K. This crossover temperature is interpreted as the lower spinodal temperature of Cu 3 Au. (author)

Insight into the electronic structure of the supramolecular “rods-in-belt” Au{sup I}-Cu{sup I} and Au{sup I}-Ag{sup I} self-assembled complexes from X-ray photoelectron and absorption spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Makarova, Anna A. [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Institut für Festkörperphysik, Technische Universität Dresden, D-01062 Dresden (Germany); Grachova, Elena V.; Krupenya, Dmitry V. [Department of Chemistry, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Vilkov, Oleg [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Institut für Festkörperphysik, Technische Universität Dresden, D-01062 Dresden (Germany); Fedorov, Alexander [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Leibniz-Institut für Festkörper- und Werkstoffforschung Dresden, Dresden (Germany); Usachov, Dmitry [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Generalov, Alexander [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Institut für Festkörperphysik, Technische Universität Dresden, D-01062 Dresden (Germany); Koshevoy, Igor O. [Department of Chemistry, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Department of Chemistry, University of Eastern Finland, Joensuu 80101 (Finland); Tunik, Sergey P. [Department of Chemistry, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Rühl, Eckart [Physikalische Chemie, Institut für Chemie und Biochemie Freie Universität Berlin (Germany); and others

2014-01-01

Highlights: • Electronic structure of rods-in-belt complexes was described via PES and NEXAFS. • With increasing size the molecule becomes more sensitive to X-ray damage effects. • The HOMO consists of a combination of the d-Cu/Ag and π-C≡C states. • HOMOs are positioned at about 2.2 eV for Au-Cu and 2.5 eV BE for Au-Ag complexes. • LUMOs are located on the C-skeleton including π*-C≡C and π*-C=C{sub aromatic} orbitals. - Abstract: The recently discovered “rods-in-belt” supramolecular complexes with Au-Cu or Au-Ag cluster cores exhibit self-assembly behavior, have a very unusual structural motif, and what is most important, show remarkable light emitting properties. The electronic and photophysical characteristics of these unique objects can be relatively easy tuned by modifying the ligand (alkynyl and phosphine) environment. Because of these properties the “rods-in-belt” supramolecules could serve as building blocks for next generation electronics, and in particular, for light-emitting devices and in bioimaging applications. Herein, we report a comprehensive characterization of the electronic structure of two families of alkynyl-diphosphine supramolecular complexes with the heterometallic Au-Cu and Au-Ag cores. Using X-ray photoemission and absorption spectroscopy we disentangled the structure of their occupied and unoccupied electronic states close to the Fermi level. The results obtained suggest that the major contribution to the highest occupied molecular orbitals is made by the triple bonded carbons hosted in the dialkynyl-gold “rods” and the copper (silver) atoms from the central cluster core of the heterometallic Au-Cu (Au-Ag) molecules. The lowest unoccupied molecular orbitals are located on the carbon skeleton of the complexes and include π*-C≡C and π*-C=C{sub aromatic} orbitals. The onset of the valence band in the Au-Ag systems starts at about 0.3 eV lower than that in the Au-Cu complexes, implying a slightly larger energy

Photoemission studies of zinc-noble metal alloys: Zn--Cu, Zn--Ag, and Zn--Au films on Ru(001)

International Nuclear Information System (INIS)

Rodriguez, J.A.; Hrbek, J.

1993-01-01

Zn and the noble metals alloy when coadsorbed on Ru(001). The properties of Zn--Cu, Zn--Ag, and Zn--Au alloys have been studied using core- and valence-level photoemission and temperature programmed desorption. Alloy formation induces only small shifts (-0.2 to -0.3 eV) in the position of the Zn 2p, 3s, and 3d levels. In contrast, the core and valence levels of the noble metals show large shifts toward higher binding energy. For small amounts of Cu, Ag, and Au dissolved in Zn multilayers, the shifts in the core levels of the nobel metals follow the sequence: Cu(2p 3/2 ), 0.8 eV∼Ag(3d 5/2 ), 0.8 eV 7/2 ), 1.4 eV. The magnitude of the shift increases as the Pauling electronegativity of the noble metal increases. However, the sign of the shifts for the Cu(2p 3/2 ), Ag(3d 5/2 ), or Au(4f 7/2 ) levels is not directly determined by the direction of charge transfer within the corresponding Zn-noble metal bond

Hydrothermal titanite from the Chengchao iron skarn deposit: temporal constraints on iron mineralization, and its potential as a reference material for titanite U-Pb dating

Science.gov (United States)

Hu, Hao; Li, Jian-Wei; McFarlane, Christopher R. M.

2017-09-01

Uranium-lead isotopes and trace elements of titanite from the Chengchao iron skarn deposit (Daye district, Eastern China), located along the contact zones between Triassic marine carbonates and an early Cretaceous intrusive complex consisting of granite and quartz diorite, were analyzed using laser ablation inductively coupled plasma mass spectrometry to provide temporal constraints on iron mineralization and to evaluate its potential as a reference material for titanite U-Pb geochronology. Titanite grains from mineralized endoskarn have simple growth zoning patterns, exhibit intergrowth with magnetite, diopside, K-feldspar, albite and actinolite, and typically contain abundant primary two-phase fluid inclusions. These paragenetic and textural features suggest that these titanite grains are of hydrothermal origin. Hydrothermal titanite is distinct from the magmatic variety from the ore-related granitic intrusion in that it contains unusually high concentrations of U (up to 2995 ppm), low levels of Th (12.5-453 ppm), and virtually no common Pb. The REE concentrations are much lower, as are the Th/U and Lu/Hf ratios. The hydrothermal titanite grains yield reproducible uncorrected U-Pb ages ranging from 129.7 ± 0.7 to 132.1 ± 2.7 Ma (2σ), with a weighted mean of 131.2 ± 0.2 Ma [mean standard weighted deviation (MSWD) = 1.7] that is interpreted as the timing of iron skarn mineralization. This age closely corresponds to the zircon U-Pb age of 130.9 ± 0.7 Ma (MSWD = 0.7) determined for the quartz diorite, and the U-Pb ages for zircon and titanite (130.1 ± 1.0 Ma and 131.3 ± 0.3 Ma) in the granite, confirming a close temporal and likely genetic relationship between granitic magmatism and iron mineralization. Different hydrothermal titanite grains have virtually identical uncorrected U-Pb ratios suggestive of negligible common Pb in the mineral. The homogeneous textures and U-Pb characteristics of Chengchao hydrothermal titanite suggest that the mineral might be a

Phenomenological approach to the spin glass state of (Cu-Mn, Ag-Mn, Au-Mn and Au-Fe) alloys at low temperatures

International Nuclear Information System (INIS)

Al-Jalali, Muhammad A.; Kayali, Fawaz A.

2000-01-01

Full text.The spin glass of: (Cu-Mn, Ag-Mn, Au-Mn, Au-Fe) alloys has been extensively studied. The availability of published and assured experimental data on the susceptibility x(T) of this alloys has enabled the design and application of phenomenological approach to the spin glass state of these interesting alloys. The use of and advanced (S.P.S.S) computer software has resulted revealing some important features of the spin glass in these alloys, the most important of which is that the spin glass state do not represent as phase change

Organic nonvolatile resistive memory devices based on thermally deposited Au nanoparticle

Science.gov (United States)

Jin, Zhiwen; Liu, Guo; Wang, Jizheng

2013-05-01

Uniform Au nanoparticles (NPs) are formed by thermally depositing nominal 2-nm thick Au film on a 10-nm thick polyimide film formed on a Al electrode, and then covered by a thin polymer semiconductor film, which acts as an energy barrier for electrons to be injected from the other Al electrode (on top of polymer film) into the Au NPs, which are energetically electron traps in such a resistive random access memory (RRAM) device. The Au NPs based RRAM device exhibits estimated retention time of 104 s, cycle times of more than 100, and ON-OFF ratio of 102 to 103. The carrier transport properties are also analyzed by fitting the measured I-V curves with several conduction models.

Precipitation hardening of a Cu-free Au-Ag-Pd-In dental alloy

Energy Technology Data Exchange (ETDEWEB)

Seol, Hyo-Joung [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Son, Kuk-Hyeon [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Yu, Chin-Ho [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Kwon, Yong Hoon [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Kim, Hyung-Il [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of)]. E-mail: hilkim@pusan.ac.kr

2005-10-27

The hardening mechanism and related microstructural changes of the Cu-free dental casting alloy composed of Au-Ag-Pd-In was examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The Au-Ag-Pd-In alloy showed apparent age-hardenability. In the SEM photograph, three phases were observed in the solution-treated specimen, that is, the Au-Ag based phase with small amounts of In and Pd as matrix, the InPd phase as particle-like structures, and the Pd-rich phase as lamellar precipitates. By aging the specimen, the very fine Pd-rich inter-granular precipitates grew toward the grain interior as lamellar structure, and finally the coarsened Pd-rich precipitates covered a large part of the Au-Ag based matrix. The hardness increase in the early stage of the age-hardening process was assumed to be caused by the diffusion and aggregation of Pd atoms from the Au-Ag based matrix. The hardness decrease in the later stage of age-hardening process was caused by coarsening of the lamellar precipitates composed of the Pd-rich phase.

Precipitation hardening of a Cu-free Au-Ag-Pd-In dental alloy

International Nuclear Information System (INIS)

Seol, Hyo-Joung; Son, Kuk-Hyeon; Yu, Chin-Ho; Kwon, Yong Hoon; Kim, Hyung-Il

2005-01-01

The hardening mechanism and related microstructural changes of the Cu-free dental casting alloy composed of Au-Ag-Pd-In was examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The Au-Ag-Pd-In alloy showed apparent age-hardenability. In the SEM photograph, three phases were observed in the solution-treated specimen, that is, the Au-Ag based phase with small amounts of In and Pd as matrix, the InPd phase as particle-like structures, and the Pd-rich phase as lamellar precipitates. By aging the specimen, the very fine Pd-rich inter-granular precipitates grew toward the grain interior as lamellar structure, and finally the coarsened Pd-rich precipitates covered a large part of the Au-Ag based matrix. The hardness increase in the early stage of the age-hardening process was assumed to be caused by the diffusion and aggregation of Pd atoms from the Au-Ag based matrix. The hardness decrease in the later stage of age-hardening process was caused by coarsening of the lamellar precipitates composed of the Pd-rich phase

Adsorption and dehydrogenation of tetrahydroxybenzene on Cu(111)

DEFF Research Database (Denmark)

Bebensee, Fabian; Svane, K.; Bombis, Christian

2013-01-01

Adsorption of tetrahydroxybenzene (THB) on Cu(111) and Au(111) surfaces is studied using a combination of STM, XPS, and DFT. THB is deposited intact, but on Cu(111) it undergoes gradual dehydrogenation of the hydroxyl groups as a function of substrate temperature, yielding a pure dihydroxy......-benzoquinone phase at 370 K. Subtle changes to the adsorption structure upon dehydrogenation are explained from differences in molecule–surface bonding....

Tunable thermodynamic stability of Au-CuPt core-shell trimetallic nanoparticles by controlling the alloy composition: insights from atomistic simulations.

Science.gov (United States)

Huang, Rao; Shao, Gui-Fang; Wen, Yu-Hua; Sun, Shi-Gang

2014-11-07

A microscopic understanding of the thermal stability of metallic core-shell nanoparticles is of importance for their synthesis and ultimately application in catalysis. In this article, molecular dynamics simulations have been employed to investigate the thermodynamic evolution of Au-CuPt core-shell trimetallic nanoparticles with various Cu/Pt ratios during heating processes. Our results show that the thermodynamic stability of these nanoparticles is remarkably enhanced upon rising Pt compositions in the CuPt shell. The melting of all the nanoparticles initiates at surface and gradually spreads into the core. Due to the lattice mismatch among Au, Cu and Pt, stacking faults have been observed in the shell and their numbers are associated with the Cu/Pt ratios. With the increasing temperature, they have reduced continuously for the Cu-dominated shell while more stacking faults have been produced for the Pt-dominated shell because of the significantly different thermal expansion coefficients of the three metals. Beyond the overall melting, all nanoparticles transform into a trimetallic mixing alloy coated by an Au-dominated surface. This work provides a fundamental perspective on the thermodynamic behaviors of trimetallic, even multimetallic, nanoparticles at the atomistic level, indicating that controlling the alloy composition is an effective strategy to realize tunable thermal stability of metallic nanocatalysts.

Atomistic modelling of friction of Cu and Au nanoparticles adsorbed on graphene

Directory of Open Access Journals (Sweden)

A.V. Khomenko

2013-01-01

Full Text Available We present classical molecular dynamics calculations of the behavior of copper and gold nanoparticles on a graphene sheet, sheared with a constant applied force Fa. The force Fs acting on the particle from the substrate depends on the material of the nanoparticles (Au or Cu, and exhibits a sawtooth dependency on time, which we attribute to local commensurability between the metal nanoparticle surface atomic positions with the graphene lattice. The time-averaged value of Fs (the friction force acting on Au nanoparticles increases linearly with the contact area, having slopes close to the experimentally observable ones. A qualitative model is proposed to explain the observed results.

Electrochemical Investigation on the Formation of Cu Nanowires by Electroless Deposition

Directory of Open Access Journals (Sweden)

Felizco Jenichi Clairvaux E.

2015-01-01

Full Text Available The growth of copper (Cu nanowires by electroless deposition in aqueous solution at 60-80 °C was studied from an electrochemical perspective using in situ mixed potential measurements and potential-pH diagrams. Scanning Electron Microscopy (SEM showed that thick and short nanowires were obtained at high temperatures, while long and thin nanowires result from low reaction temperatures. In situ mixed potential measurements reveal that Cu(II reduction is more favored at higher reaction temperatures, hastening the reduction reaction. The fast reaction leads to a high concentration of Cu atoms in the solution. As a result, Cu deposition occurs rapidly, such that they attached on both sides and ends of the primary Cu nanowires. This results to the formation of thick and short structures. On the other hand, thin and long nanowires are obtained due to the slow reduction reaction, which gives the Cu atoms more time to orderly attach in a wire-like formation.

Overlayer structure of subphthalocyanine derivative deposited on Au (111) surface by a spray-jet technique

International Nuclear Information System (INIS)

Suzuki, Hitoshi; Yamada, Toshiki; Miki, Hideki; Mashiko, Shinro

2006-01-01

A new spray-jet technique was used to deposit subphthalocyanine derivative (chloro[tri-tert-butyl subphthalocyaninato]boron (TBSubPc)) on Au (111) surface in an ultra-high vacuum (UHV) chamber. The deposited molecular overlayer was observed with UHV scanning tunneling microscopy (STM) at 77 K. The STM images showed that TBSubPc molecules formed a stripe pattern with regular spacing, indicating that they preferentially adsorbed along the herringbone structure of the Au (111) surface. This behavior was very similar to that of TBSubPc molecules deposited by thermal evaporation

Effect of cascade remnants on freely migrating defects in Cu-1% Au alloys

Energy Technology Data Exchange (ETDEWEB)

Iwase, A; Rehn, L E; Baldo, P M; Funk, L [Argonne National Lab., IL (United States). Materials Science Div.

1997-03-01

The effects of cascade remnants on Freely Migrating Defects (FMD) were studied by measuring Radiation-Induced Segregation (RIS) in Cu-1%Au at 400degC during simultaneous irradiation with 1.5-MeV He and (400-800)-keV heavy ions (Ne, Ar or Cu). The large RIS observed during 1.5-MeV He-only irradiation was dramatically suppressed under simultaneous heavy ion irradiation. For Cu simultaneous irradiation, the suppression disappeared immediately after the Cu irradiation ceased, while for simultaneous inert gas (Ne or Ar) irradiation, the suppression persisted after the ion beam was turned off. These results demonstrate that the displacement cascades created by heavy ions introduce additional annihilation sites, which reduce the steady-state FMD concentrations. As the cascade remnants produced by Cu ions are thermally unstable at 400degC, the RIS suppression occurs only during simultaneous irradiation. On the other hand, the inert gas atoms which accumulate in the specimen apparently stabilize the cascade remnants, allowing the suppression to persist. (author)

Magnetism of coherent Co and Ni thin films on Cu(111) and Au(111) substrates: An ab initio study

Energy Technology Data Exchange (ETDEWEB)

Zelený, Martin, E-mail: zeleny@fme.vutbr.cz; Dlouhý, Ivo

2017-02-15

We present an ab initio study of structural and magnetic properties of coherent Co and Ni thin films on Cu(111) and Au(111) substrates with thicknesses of up to 6 monolayers. All studied films on Cu(111) substrates prefer structures close their ground state (hcp for Co and fcc for Ni), whereas only the hcp stacking sequence has been found for both films on Au(111) substrates. All studied films exhibit instability of the first monolayer with respect to decomposition into 2-monolayer- or 3-monolayer-high islands, which is in agreement with experimental findings. All studied films are also ferromagnetic, nevertheless the Ni/Cu(111) films reduce their magnetic moments in the layer adjacent to the substrate due to a stronger Cu–Ni interaction at the interface. The magnetic anisotropy of a Co film does not depend on the film thickness: all the studied Co/Au(111) films exhibit a perpendicular magnetic anisotropy, whereas all the Co/Cu(111) films prefer in-plane magnetization. On the other hand, both Ni films change their preference for in-plane orientation of their easy axis to out-of-plane orientation at a critical thickness of 2 monolayers, however, the magnetic anisotropy energies for films thicker than 1 monolayer are smaller than 1 meV/Ni atom. These behaviors of magnetic anisotropy do not depend on the structure of the studied films. - Highlights: • All films exhibit instability of the first monolayer and prefer grow in islands. • The Cu–Ni interaction is responsible for reduced Ni magnetic moments in Ni/Cu(111) films. • The Co/Au(111) and Co/Cu(111) films show different orientations of magnetic anisotropy. • The Ni films exhibit in-plane magnetization only for single monolayer. • Behaviors of magnetic anisotropy do not depend on the structure of the studied films.

Effect of Magnetic Field on Surface Morphology and Magnetic Properties of FeCu/Cu Nano layers Prepared by Electrodeposition Technique: Investigation of Magneto-hydrodynamic Effect

Directory of Open Access Journals (Sweden)

M. Merikhi

2015-10-01

Full Text Available In this paper, the effect of magnetic field on the morphology, structure and magnetic properties of electrodeposited FeCu/Cu thin films was investigated. The films were deposited on Au2PdAg/glass substrates using electrodeposition technique in potentiostatic control. The magnetic fields of 5000 and 7000 Oe were applied on deposition bath during deposition. Two series of thin films were prepared in the same deposition conditions, one in the presence and the other in absence of magnetic field and the products were compared. The results indicate that applying the magnetic field has a significant effect on the growth process, i.e. morphology, crystal structure and magnetic properties of the films. The morphology and structure of the FeCu/Cu Nano layers were studied using X-ray diffraction (XRD and scanning electron microscopy (SEM. The weight percentages of the elements in the deposited multilayers were determined by energy dispersive X-ray spectroscopy (EDS. Magnetic properties of thin films were studied using the vibrating sample magnetometer (VSM.

CuAlO2 and CuAl2O4 thin films obtained by stacking Cu and Al films using physical vapor deposition

Science.gov (United States)

Castillo-Hernández, G.; Mayén-Hernández, S.; Castaño-Tostado, E.; DeMoure-Flores, F.; Campos-González, E.; Martínez-Alonso, C.; Santos-Cruz, J.

2018-06-01

CuAlO2 and CuAl2O4 thin films were synthesized by the deposition of the precursor metals using the physical vapor deposition technique and subsequent annealing. Annealing was carried out for 4-6 h in open and nitrogen atmospheres respectively at temperatures of 900-1000 °C with control of heating and cooling ramps. The band gap measurements ranged from 3.3 to 4.5 eV. Electrical properties were measured using the van der Pauw technique. The preferred orientations of CuAlO2 and CuAl2O4 were found to be along the (1 1 2) and (3 1 1) planes, respectively. The phase percentages were quantified using a Rietveld refinement simulation and the energy dispersive X-ray spectroscopy indicated that the composition is very close to the stoichiometry of CuAlO2 samples and with excess of aluminum and deficiency of copper for CuAl2O4 respectively. High resolution transmission electron microscopy identified the principal planes in CuAlO2 and in CuAl2O4. Higher purities were achieved in nitrogen atmosphere with the control of the cooling ramps.

Sulfonated poly(ether ether ketone)/poly(vinyl alcohol) sensitizing system for solution photogeneration of small Ag, Au, and Cu crystallites.

Science.gov (United States)

Korchev, A S; Shulyak, T S; Slaten, B L; Gale, W F; Mills, G

2005-04-28

Illumination of air-free aqueous solutions containing sulfonated poly(ether ether ketone) and poly(vinyl alcohol) with 350 nm light results in benzophenone ketyl radicals of the polyketone. The polymer radicals form with a quantum yield 0.02 and decay with a second-order rate constant 6 orders of magnitude lower than that of typical alpha-hydroxy radicals. Evidence is presented that the polymeric benzophenone ketyl radicals reduce Ag+, Cu2+, and AuCl4- to metal particles of nanometer dimensions. Decreases in the reduction rates with increasing Ag(I), Cu(II), and Au(III) concentrations are explained using a kinetic model in which the metal ions quench the excited state of the polymeric benzophenone groups, which forms the macromolecular radicals. Quenching is fastest for Ag+, whereas Cu2+ and AuCl4- exhibit similar rate constants. Particle formation becomes more complex as the number of equivalents needed to reduce the metal ions increases; the Au(III) system is an extreme case where the radical reactions operate in parallel with secondary light-initiated and thermal reduction channels. For each metal ion, the polymer-initiated photoreactions produce crystallites possessing distinct properties, such as a very strong plasmon in the Ag case or the narrow size distribution exhibited by Au particles.

Investigation of Au/Au(100) film growth with energetic deposition by kinetic Monte Carlo simulation

International Nuclear Information System (INIS)

Zhang Qingyu; Ma Tengcai; Pan Zhengying; Tang Jiayong

2000-01-01

The Au/Au(100) epitaxial growth with energetic deposition was simulated by using kinetic Monte Carlo method. The influences of energetic atoms on morphology and atomistic processes in the early stage of film growth were investigated. The reentrant layer-by-layer growth was observed in the temperature range of 450 K to 100 K. The authors found the energetic atoms can promote the nucleation and island growth in the early stages of film growth and enhance the smoothness of film surface at temperatures of film growth in 3-dimensional mode and in quasi-two-dimensional mode. The atomistic mechanism that promotes the nucleation and island growth and enhances the smoothness of film surface is discussed

Moisture barrier properties of single-layer graphene deposited on Cu films for Cu metallization

Science.gov (United States)

Gomasang, Ploybussara; Abe, Takumi; Kawahara, Kenji; Wasai, Yoko; Nabatova-Gabain, Nataliya; Thanh Cuong, Nguyen; Ago, Hiroki; Okada, Susumu; Ueno, Kazuyoshi

2018-04-01

The moisture barrier properties of large-grain single-layer graphene (SLG) deposited on a Cu(111)/sapphire substrate are demonstrated by comparing with the bare Cu(111) surface under an accelerated degradation test (ADT) at 85 °C and 85% relative humidity (RH) for various durations. The change in surface color and the formation of Cu oxide are investigated by optical microscopy (OM) and X-ray photoelectron spectroscopy (XPS), respectively. First-principle simulation is performed to understand the mechanisms underlying the barrier properties of SLG against O diffusion. The correlation between Cu oxide thickness and SLG quality are also analyzed by spectroscopic ellipsometry (SE) measured on a non-uniform SLG film. SLG with large grains shows high performance in preventing the Cu oxidation due to moisture during ADT.

The rational design of a Au(I) precursor for focused electron beam induced deposition

NARCIS (Netherlands)

Marashdeh, Ali; Tiesma, Thiadrik; van Velzen, Niels J. C.; Harder, Sjoerd; Havenith, Remco W. A.; De Hosson, Jeff T. M.; van Dorp, Willem F.

2017-01-01

Au(I) complexes are studied as precursors for focused electron beam induced processing (FEBIP). FEBIP is an advanced direct-write technique for nanometer-scale chemical synthesis. The stability and volatility of the complexes are characterized to design an improved precursor for pure Au deposition.

Reconstructed Jet Results in p + p, d + Au and Cu + Cu collisions at 200 GeV from PHENIX

International Nuclear Information System (INIS)

Perepelitsa, D.V.

2013-01-01

Jet reconstruction in heavy ion collisions at RHIC and the LHC is becoming a popular tool to explore medium effects including the energy loss and modified fragmentation of hard-scattered partons. In p + A and d + A collisions, reconstructed jets are important for evaluating cold nuclear matter effects such as the impact parameter dependence of nuclear parton distribution functions and initial state energy loss. We present current PHENIX results from p + p, d + Au, and Cu + Cu collisions at 200 GeV using the Gaussian filter and anti-k T algorithms. The systematic study of direct jet reconstruction across a variety of collisions systems at PHENIX will help to tell a coherent story of jet physics at RHIC

Atom probe tomography simulations and density functional theory calculations of bonding energies in Cu3Au

KAUST Repository

Boll, Torben

2012-10-01

In this article the Cu-Au binding energy in Cu3Au is determined by comparing experimental atom probe tomography (APT) results to simulations. The resulting bonding energy is supported by density functional theory calculations. The APT simulations are based on the Müller-Schottky equation, which is modified to include different atomic neighborhoods and their characteristic bonds. The local environment is considered up to the fifth next nearest neighbors. To compare the experimental with simulated APT data, the AtomVicinity algorithm, which provides statistical information about the positions of the neighboring atoms, is applied. The quality of this information is influenced by the field evaporation behavior of the different species, which is connected to the bonding energies. © Microscopy Society of America 2012.

Epitaxial growth of unusual 4H hexagonal Ir, Rh, Os, Ru and Cu nanostructures on 4H Au nanoribbons

KAUST Repository

Fan, Zhanxi; Chen, Ye; Zhu, Yihan; Wang, Jie; Li, Bing; Zong, Yun; Han, Yu; Zhang, Hua

2016-01-01

Metal nanomaterials normally adopt the same crystal structure as their bulk counterparts. Herein, for the first time, the unusual 4H hexagonal Ir, Rh, Os, Ru and Cu nanostructures have been synthesized on 4H Au nanoribbons (NRBs) via solution-phase epitaxial growth under ambient conditions. Interestingly, the 4H Au NRBs undergo partial phase transformation from 4H to face-centered cubic (fcc) structures after the metal coating. As a result, a series of polytypic 4H/fcc bimetallic Au@M (M = Ir, Rh, Os, Ru and Cu) core-shell NRBs has been obtained. We believe that the rational crystal structure-controlled synthesis of metal nanomaterials will bring new opportunities for exploring their phase-dependent physicochemical properties and promising applications.

Epitaxial growth of unusual 4H hexagonal Ir, Rh, Os, Ru and Cu nanostructures on 4H Au nanoribbons

KAUST Repository

Fan, Zhanxi

2016-09-12

Metal nanomaterials normally adopt the same crystal structure as their bulk counterparts. Herein, for the first time, the unusual 4H hexagonal Ir, Rh, Os, Ru and Cu nanostructures have been synthesized on 4H Au nanoribbons (NRBs) via solution-phase epitaxial growth under ambient conditions. Interestingly, the 4H Au NRBs undergo partial phase transformation from 4H to face-centered cubic (fcc) structures after the metal coating. As a result, a series of polytypic 4H/fcc bimetallic Au@M (M = Ir, Rh, Os, Ru and Cu) core-shell NRBs has been obtained. We believe that the rational crystal structure-controlled synthesis of metal nanomaterials will bring new opportunities for exploring their phase-dependent physicochemical properties and promising applications.

Critical Factors Controlling Pd and Pt Potential in Porphyry Cu–Au Deposits: Evidence from the Balkan Peninsula

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Demetrios G. Eliopoulos

2014-03-01

Full Text Available Porphyry Cu–Au–Pd±Pt deposits are significant Au resources, but their Pd and Pt potential is still unknown. Elevated Pd, Pt (hundreds of ppb and Au contents are associated with typical stockwork magnetite-bornite-chalcopyrite assemblages, at the central parts of certain porphyry deposits. Unexpected high grade Cu–(Pd+Pt (up to 6 ppm mineralization with high Pd/Pt ratios at the Elatsite porphyry deposit, which is found in a spatial association with the Chelopech epithermal deposit (Bulgaria and the Skouries porphyry deposit, may have formed during late stages of an evolved hydrothermal system. Estimated Pd, Pt and Au potential for porphyry deposits is consistent with literature model calculations demonstrating the capacity of aqueous vapor and brine to scavenge sufficient quantities of Pt and Pd, and could contribute to the global platinum-group element (PGE production. Critical requirements controlling potential of porphyry deposits may be from the metals contained in magma (metasomatized asthenospheric mantle wedge as indicated by significant Cr, Co, Ni and Re contents. The Cr content may be an indicator for the mantle input.

Bioaccumulation, toxicokinetics, and effects of copper from sediment spiked with aqueous Cu, nano-CuO, or micro-CuO in the deposit-feeding snail, Potamopyrgus antipodarum

DEFF Research Database (Denmark)

Pang, Chengfang; Selck, Henriette; Banta, Gary Thomas

2013-01-01

The present study examined the relative importance of copper (aqueous Cu and CuO particles of different sizes) added to sediment to determine the bioaccumulation, toxicokinetics, and effects in the deposit feeder Potamopyrgus antipodarum. In experiment 1, the bioaccumulation of Cu (240 mg Cu/g dr...

Microstructural, electrical and frequency-dependent properties of Au/p-Cu2ZnSnS4/n-GaN heterojunction.

Science.gov (United States)

Rajagopal Reddy, V; Janardhanam, V; Won, Jonghan; Choi, Chel-Jong

2017-08-01

An Au/Cu 2 ZnSnS 4 (CZTS)/n-GaN heterojunction (HJ) is fabricated with a CZTS interlayer and probed its chemical states, structural, electrical and frequency-dependent characteristics by XPS, TEM, I-V and C-V measurements. XPS and TEM results confirmed that the CZTS films are formed on the n-GaN surface. The band gap of deposited CZTS film is found to be 1.55eV. The electrical properties of HJ correlated with the Au/n-GaN Schottky junction (SJ). The Au/CZTS/n-GaN HJ reveals a good rectification nature with high barrier height (0.82eV) compared to the Au/n-GaN SJ (0.69eV), which suggests the barrier height is influenced by the CZTS interlayer. The barrier height values assessed by I-V, Cheung's and Norde functions are closely matched with one other, thus the methods used here are reliable and valid. The extracted interface state density (N SS ) of Au/CZTS/n-GaN HJ is lower compared to the Au/n-GaN SJ that suggests the CZTS interlayer plays an important role in the reduction of N SS . Moreover, the capacitance-frequency (C-f) and conductance-frequency (G-f) characteristics of SJ and HJ are measured in the range of 1kHz-1MHz, and found that the capacitance and conductance strappingly dependent on frequency. It is found that the N SS estimated from C-f and G-f characteristics is lower compared to those estimated from I-V characteristics. Analysis confirmed that Poole-Frenkel emission dominates the reverse leakage current in both SJ and HJ, probably related to the structural defects and trap levels in the CZTS interlayer. Copyright © 2017 Elsevier Inc. All rights reserved.

Synthesis and crystal structure of a new Cu3Au-type ternary phase in the Au-In-Pd system: distribution of atoms over crystallographic positions.

Science.gov (United States)

Ptashkina, Evgeniya A; Kabanova, Elizaveta G; Tursina, Anna I; Yatsenko, Alexandr V; Kuznetsov, Victor N

2018-03-01

A new Cu 3 Au-type ternary phase (τ phase) is found in the AuPd-rich part of the Au-In-Pd system. It has a broad homogeneity range based on extensive (Pd,Au) and (In,Au) replacement, with the composition varying between Au 17.7 In 25.3 Pd 57.0 and Au 50.8 In 16.2 Pd 33.0 . The occupancies of the crystallographic positions were studied by single-crystal X-ray diffraction for three samples of different composition. The sites with m-3m symmetry are occupied by atoms with a smaller scattering power than the atoms located on 4/mmm sites. Two extreme structure models were refined. Within the first, the occupation type changes from (Au,In,Pd) 3 (Pd,In) to (Au,Pd) 3 (In,Pd,Au) with an increase in the Au gross content. For the second model, the occupation type (Au,In,Pd) 3 (Pd,Au) remains essentially unchanged for all Au concentrations. Although the diffraction data do not allow the choice of one of these models, the latter model, where Au substitutes In on 4/mmm sites, seems to be preferable, since it agrees with the fact that the homogeneity range of the τ phase is inclined to the Au corner and provides the same occupation type for all the studied samples of different compositions.

Magmatic Vapor Phase Transport of Copper in Reduced Porphyry Copper-Gold Deposits: Evidence From PIXE Microanalysis of Fluid Inclusions

Science.gov (United States)

Rowins, S. M.; Yeats, C. J.; Ryan, C. G.

2002-05-01

Nondestructive proton-induced X-ray emission (PIXE) studies of magmatic fluid inclusions in granite-related Sn-W deposits [1] reveal that copper transport out of reduced felsic magmas is favored by low-salinity vapor and not co-existing high-salinity liquid (halite-saturated brine). Copper transport by magmatic vapor also has been documented in oxidized porphyry Cu-Au deposits, but the magnitude of Cu partitioning into the vapor compared to the brine generally is less pronounced than in the reduced magmatic Sn-W systems [2]. Consideration of these microanalytical data leads to the hypothesis that Cu and, by inference, Au in the recently established "reduced porphyry copper-gold" (RPCG) subclass should partition preferentially into vapor and not high-salinity liquid exsolving directly from fluid-saturated magmas [3-4]. To test this hypothesis, PIXE microanalysis of primary fluid inclusions in quartz-sulfide (pyrite, pyrrhotite & chalcopyrite) veins from two RPCG deposits was undertaken using the CSIRO-GEMOC nuclear microprobe. PIXE microanalysis for the ~30 Ma San Anton deposit (Mexico) was done on halite-saturated aqueous brine (deposit (W. Australia) was done on halite-saturated "aqueous" inclusions, which contain a small (deposits of the new RPCG subclass demonstrate the greater potential of these systems, compared to the classically oxidized porphyry Cu-Au systems, to transport Cu and probably precious metals in a magmatic aqueous vapor phase. These PIXE data also support the possibility that Cu partitions preferentially into an immiscible CO2-rich magmatic fluid. References: [1] Heinrich, C.A. et al. (1992) Econ. Geol., 87, 1566-1583. [2] Heinrich, C.A. et al. (1999) Geology, 27, 755-758. [3] Rowins, S.M. (2000) Geology, 28, 491-494. [4] Rowins, S.M. (2000) The Gangue, GAC-MDD Newsletter, 67, 1-7 (www.gac.ca). [5] Rowins, S.M. et al. (1993) Geol. Soc. Australia Abs., 34, 68-70.

Geochemical halos of gold and associated elements in Nabijan gold index (SW Kaleibar, NW Iran

Directory of Open Access Journals (Sweden)

Hemayat Jamali

2017-07-01

Full Text Available The Nabijan ore index located 20 km southwest of Kaleibar city, East Azerbaijan province in the Alborz-Azerbaijan structural zone. Geological rock units outcropping in the area consist of volcano-sedimentary rocks (trachyandesite, andesite, shale and limestone of the Cretaceous age which intruded by the Oligo-Miocene monzogranite, monzogranodiorite and diorite. These intrusions and related hydrothermal activities caused the Au mineralization in the Cretaceous host rocks, as well as in the monzogranitic intrusion. The mineralization in the monzogranite occurred as silicic stockwork and sheeted veins with pyrite and minor chalcopyrite, sphalerite and galena. The other type of mineralization is skarn, which present as sparse irregular veinlets with less amount of Au in the Cretaceous carbonates. Preliminary estimation of ore reserve shows 320000t reservoir with average of Au grade about 1.37 gr/ton. According to surface and drilling data, two important anomalies determined. One in the contact zone of intrusive rocks with the Cretaceous volcanics and carbonates (skarn zone. In this anomaly, the correlation coefficient index between Au and Cu, Pb, Zn, Ag, and As is low whereas, in the second one which coincides with stockwork mineralization within monzogranite, it is high.

Paleozoic–Mesozoic Porphyry Cu(Mo and Mo(Cu Deposits within the Southern Margin of the Siberian Craton: Geochemistry, Geochronology, and Petrogenesis (a Review

Directory of Open Access Journals (Sweden)

Anita N. Berzina

2016-11-01

Full Text Available The southern margin of the Siberian craton hosts numerous Cu(Mo and Mo(Cu porphyry deposits. This review provides the first comprehensive set of geological characteristics, geochronological data, petrochemistry, and Sr–Nd isotopic data of representative porphyry Cu(Mo and Mo(Cu deposits within the southern margin of the Siberian craton and discusses the igneous processes that controlled the evolution of these magmatic systems related to mineralization. Geochronological data show that these porphyry deposits have an eastward-younging trend evolving from the Early Paleozoic to Middle Mesozoic. The western part of the area (Altay-Sayan segment hosts porphyry Cu and Mo–Cu deposits that generally formed in the Early Paleozoic time, whereas porphyry Cu–Mo deposits in the central part (Northern Mongolia formed in the Late Paleozoic–Early Mesozoic. The geodynamic setting of the region during these mineralizing events is consistent with Early Paleozoic subduction of Paleo-Asian Ocean plate with the continuous accretion of oceanic components to the Siberian continent and Late Paleozoic–Early Mesozoic subduction of the west gulf of the Mongol–Okhotsk Ocean under the Siberian continent. The eastern part of the study area (Eastern Transbaikalia hosts molybdenum-dominated Mo and Mo–Cu porphyry deposits that formed in the Jurassic. The regional geodynamic setting during this mineralizing process is related to the collision of the Siberian and North China–Mongolia continents during the closure of the central part of the Mongol–Okhotsk Ocean in the Jurassic. Available isotopic data show that the magmas related to porphyritic Cu–Mo and Mo–Cu mineralization during the Early Paleozoic and Late Paleozoic–Early Mesozoic were mainly derived from mantle materials. The generation of fertile melts, related to porphyritic Mo and Mo–Cu mineralization during the Jurassic involved variable amounts of metasomatized mantle source component, the

Structure and properties of (Sr, Ca)CuO2-BaCuO2 superlattices grown by pulsed laser interval deposition

NARCIS (Netherlands)

Koster, Gertjan; Verbist, Karen; Rijnders, Augustinus J.H.M.; Rogalla, Horst; van Tendeloo, Gustaav; Blank, David H.A.

2001-01-01

We report on the preparation of CuBa2(SrxCa1¿x)nCun¿1Oy compounds by fabrication of (Ba,Sr,Ca)CuO2 superlattices with pulsed laser deposition (PLD). A technique called interval deposition is used to suppress multi-level or island growth resulting in high-quality superlattice structures. Both, the

Interdiffusion within model TiN/Cu and TiTaN/Cu systems synthesized by combinatorial thin film deposition

International Nuclear Information System (INIS)

Mühlbacher, M.

2015-01-01

Continued device miniaturization in microelectronics calls for a fundamental understanding of diffusion processes and damage mechanisms in the Cu metallization/TiN barrier layer system. Thus, the starting point of the present study is a combined experimental and theoretical examination of lattice diffusion in ideal single-crystal TiN/Cu stacks grown on MgO(001) by unbalanced DC magnetron sputter deposition. After a 12 h annealing treatment at 1000 °C, a uniform Cu diffusion layer of 7-12 nm is observed by scanning transmission electron microscopy and atom probe tomography (APT). Density-functional theory calculations predict a stoichiometry-dependent atomic diffusion mechanism of Cu in bulk TiN, with Cu diffusing on the N sublattice for the experimental N/Ti ratio of 0.92. These findings are extended to a comparison of grain boundary diffusion of Cu in dense polycrystalline TiN sputter-deposited on Si at 700 °C and underdense polycrystalline TiN grown on Si without external substrate heating. While the Cu diffusion path along dense TiN grain boundaries can be restricted to approximately 30 nm after a 1 h annealing treatment at 900 °C as visualized by 3D APT reconstructions, it already exceeds 500 nm after annealing at 700 °C in the underdense low-temperature TiN barrier. In this case, the formation of the Cu3Si phase, which characteristically grows along the close-packed directions in Si, is identified as the main damage mechanism leading to complete barrier failure. To meet the low-temperature processing needs of semiconductor industry and at the same time exploit the improved performance of dense polycrystalline barrier layers, deposition of TiTaN barriers on Si is demonstrated by a reactive hybrid high-power impulse/DC magnetron sputtering process, where barrier densification is achieved by pulsed irradiation of the growth surface with only a few at.% of energetic Ta ions without external substrate heating. These barrier layers delay the onset of Cu grain

Use of structural geology in exploration for and mining of sedimentary rock-hosted Au deposits

Science.gov (United States)

Peters, Stephen G.

2001-01-01

Structural geology is an important component in regional-, district- and orebody-scale exploration and development of sedimentary rock-hosted Au deposits.Identification of timing of important structural events in an ore district allows analysis and classification of fluid conduits and construction of genetic models for ore formation.The most practical uses of structural geology deal with measurement and definition of various elements that comprise orebodies, which can then be directly applied to ore-reserve estimation,ground control,grade control, safety issues,and mine planning.District- and regional-scale structural studies are directly applicable to long-term strategic planning,economic analysis,and land ownership. Orebodies in sedimentary rock-hosted Au deposits are discrete, hypogene, epigenetic masses usually hosted in a fault zone,breccia mass, or lithologic bed or unit. These attributes allow structural geology to be directly applied to the mining and exploration of sedimentary rock-hosted Au deposits. Internal constituents in orebodies reflect unique episodes relating to ore formation.The main internal constituents in orebodies are ore minerals, gangue, and alteration minerals that usually are mixed with one another in complex patterns, the relations among which may be used to interpret the processes of orebody formation and control.Controls of orebody location and shape usually are due to structural dilatant zones caused by changes in attitude, splays, lithologic contacts,and intersections of the host conduit or unit.In addition,conceptual parameters such as district fabric,predictable distances, and stacking also are used to understand the geometry of orebodies.Controls in ore districts and location and geometry of orebodies in ore districts can be predicted to various degrees by using a number of qualitative concepts such as internal and external orebody plunges,district plunge, district stacking, conduit classification, geochemical, geobarometric and

Origin of dioritic magma and its contribution to porphyry Cu-Au mineralization at Pulang in the Yidun arc, eastern Tibet

Science.gov (United States)

Cao, Kang; Yang, Zhi-Ming; Xu, Ji-Feng; Fu, Bin; Li, Wei-Kai; Sun, Mao-Yu

2018-04-01

The giant Pulang porphyry Cu-Au deposit in the Yidun arc, eastern Tibet, formed due to westward subduction of the Garze-Litang oceanic plate in the Late Triassic. The deposit is hosted in an intrusive complex comprising primarily coarse-grained quartz diorite and cored quartz monzonite. Here, we investigate a suite of simultaneous (216.6 ± 1.9 Ma) diorite porphyries within the complex. The diorite porphyries are geochemically similar to mafic magmatic enclaves (MME) hosted in coarse-grained quartz diorite, and both are characterized by low SiO2 (59.4-63.0 wt%) and high total alkali (Na2O + K2O = 7.0-9.2 wt%), K2O (3.5-6.4 wt%), MgO (3.2-5.5 wt%), and compatible trace element (e.g., Cr = 72-149 ppm) concentrations. They are enriched in large-ion lithophile and light rare earth elements (LILE and LREE, respectively), but depleted in high field-strength and heavy rare earth elements (HFSE and HREE, respectively), and yield variably high (La/Yb)N ratios (17-126, average 65) with weak to negligible Eu anomalies. Furthermore, they yield low (87Sr/86Sr)i ratios (0.7054-0.7067), weakly negative εNd(t) (-2.8 to -0.8) values, and variable zircon εHf(t) (-5.4 to +0.8) and δ18O (6.0‰-6.7‰) values. These geochemical features indicate that the diorite porphyry and MME formed through crustal assimilation of a magma produced during low-degree partial melting of metasomatized phlogopite-rich subcontinental lithospheric mantle. In contrast, the coarse-grained quartz diorite and quartz monzonite have relatively high concentrations of SiO2 (61.1-65.3 wt%), K2O (4.1-5.4 wt%), and total alkali (Na2O + K2O = 7.1-8.1 wt%), and low concentrations of MgO (generally Y ratios (50-63) that indicate an adakitic affinity, and are enriched in LILE, depleted in HFSE, and yield lower (La/Yb)N values (13-20, average 17) than the diorite porphyry and MME. They yield low (87Sr/86Sr)i ratios (0.7046-0.7066), negative εNd(t) (-3.3 to -1.7) values, and zircon εHf(t) and δ18O values of -2.9 to

Comparative Study on The Photocatalytic Hydrogen Production from Methanol over Cu-, Pd-, Co- and Au-Loaded TiO2

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Udani P.P.C.

2015-09-01

Full Text Available Photocatalytic hydrogen production from a methanol-water solution was investigated in a semi-continuous reactor over different metal-loaded TiO2 catalysts under UltraViolet (UV light irradiation. The catalysts were mainly prepared by the incipient wetness impregnation method by varying the metal weight ratio in the range of 1-10 wt%. The effects of metal loading and H2 pre-treatment on the photocatalytic activity were investigated. In addition, the activity of the catalysts was also compared with a reference Au-TiO2 catalyst from the World Gold Council (WGC. The photocatalysts were characterized by using X-Ray Diffraction (XRD and N2 physisorption before and after the activity measurements. The photocatalytic activity decreased in the order of Pd > Au > Cu > Co in the comparative study of Cu-TiO2, Co-TiO2, Au-TiO2 and Pd-TiO2. Optimum hydrogen evolution was achieved with 5 wt% Pd-TiO2 and 5 wt% Cu-TiO2.

Mineralogy, alteration patterns, geochemistry, and fluid properties of the Ag-Au epithermal deposit Nová Baňa, Slovakia

Science.gov (United States)

Majzlan, Juraj; Berkh, Khulan; Kiefer, Stefan; Koděra, Peter; Fallick, Anthony E.; Chovan, Martin; Bakos, František; Biroň, Adrián; Ferenc, Štefan; Lexa, Jaroslav

2018-02-01

In this contribution, we report new data on mineralogy, alteration patterns, geochemistry, fluid properties and source of fluids for the deposit Nová Baňa, one of the smaller epithermal deposits in the Middle Miocene Štiavnica andesite stratovolcano (Western Carpathians, Slovakia). Ore veins and the associated rocks were studied in samples from outcrops and old mines, grab samples, and bore holes from the central part of the deposit (ore structures Althandel, Jozef, Jakub, Vavrinec), northern part (Freischurf), SE part (Gupňa) and SW part (Šibeničný vrch). Pervasive hydrothermal alteration transformed the rock-forming minerals into a mixture of adularia and fine-grained quartz, with lesser amount of pyrite, Ti oxides and Fe oxides. This assemblage was further altered to omnipresent interstratified illite/smectite that was used in this study as a geothermometer, corroborating the results from the fluid inclusion work. Ore minerals comprise predominantly pyrite, sphalerite, galena but all sulfides are relatively sparse in the samples studied. Minerals of precious metals are electrum, Ag-tetrahedrite, acanthite, members of the polybasite-pearceite and pyrargyrite-proustite solid solution, and rare miargyrite, Hg-Ag tetrahedrite, and diaphorite. In the central part, we have found also some stibnite. In the SE part of the deposit, acanthite, uytenbogaardtite, and petrovskaite occur and seem to be related to supergene enrichment of the ores. In bulk ore samples, Zn usually dominates over Pb and Cu. The average Ag:Au ratio for the entire deposit is 64:1. The concentrations of precious metals in the grab samples reach maxima of 50 ppm Au and 570 ppm Ag in the SE part and 116 ppm Au and 1110 ppm Ag in the central part of the deposit. Fluid inclusions show signs of trapping of a heterogeneous fluid. In the central, northern and SE parts of the deposit, homogenization temperatures of 190-260 °C and consistently low salinities of minerals is recalculated to fluid

Sulfur isotope study of the Velardeña skarn (Zn-Pb), Durango, Mexico

Science.gov (United States)

Jimenez, A.

2012-04-01

Sulfur isotope study of the Velardeña skarn (Zn-Pb), Durango, Mexico Abigail Jimenez-Franco1*, Pura Alfonso Abella2, Carles Canet3, Eduardo González-Partida4 1 Posgrado en Ciencias de la Tierra, Universidad Nacional Autónoma de México, Ciudad Universitaria, Delegación Coyoacán, 04510 México D.F., Mexico 2 Departament d'Enginyeria Minera i Recursos Naturals, Universitat Politècnica de Catalunya, Av de Les Bases de Manresa 61-73, 08242 Manresa. 3Instituto de Geofísica, Universidad Nacional Autónoma de México, Ciudad Universitaria, Delegación Coyoacán, 04510 México D.F., Mexico 4Centro de Geociencias, Universidad Nacional Autónoma de México, Campus Juriquilla, Boulevard Juriquilla 3001, 76230 Santiago de Querétaro, Qro., Mexico The Velardeña mining district is located in north-eastern part of the state of Durango, in northern of Mexico. The ore deposit is a lead-zinc, garnet-rich skarn developed at the contact between granite porphyry dikes (Eocene) and well-laminated limestones with interbedded chert (Albian-Cenomanian). A study of sulfur isotopes has been carried out in various sulfide minerals of the ores of Velardeña, in order to: (a) constrain the possible sources of sulfur and, therefore, better understand the sulfide mineralizing processes, and (b) to estimate the temperature of the ore-forming stage of the skarn. Sulfur isotope analyses were performed in 21 pure fractions of sulfide minerals of the ore mineralization (pyrite, chalcopyrite, sphalerite and galena). The mineral separation was performed using a series of sieves, and the purity of the samples was verified under a binocular microscope. Isotopic analyses were done on a Finnigan MAT Delta C flow elemental analyzer coupled to a TC-EA, according with the method of Giesemann et al. (1974). The δ34S values of the analyzed sulfides range mostly between -0.6 and +2.6 ‰ (relative to the CDT standard). These values are indicative of a magmatic source of sulfur. A single analysis falls

Photocatalytically active Au/TiO2 films deposited by two-step spray pyrolysis

International Nuclear Information System (INIS)

Balashev, Konstantin; Georgiev, Petar; Simeonova, Sylvia; Stambolova, Irina; Blaskov, Vladimir; Vassilev, Sasho; Eliyas, Alexander

2016-01-01

Nanocrystalline TiO 2 and surface gold-modified films (Au/TiO 2 ) are obtained by two step spray pyrolysis process. Titanium tetrachloride (TiCl 4 ) was used as inorganic titanium precursor. The Au nanoparticles were deposited on the surface of sprayed TiO 2 films, obtained by the classical Turkevich method. The AFM analyses have revealed that the roughness of Au/TiO 2 is twice lower than that of the reference titania film. Some globular species are visible on the surface, which could be either individual Au nanoparticles or Au nanoparticles’ agglomerates embedded into the TiO 2 film. The photocatalytic activity in the oxidative degradation of Reactive Black 5 dye under visible light of the Au/TiO 2 films was estimated in a semi-batch reactor. Surface gold modified TiO 2 films revealed higher photocatalytic efficiency than the reference sample. Key words: Au nanoparticles, photocatalysis, azo dye, titania, nanosized

The Chahnaly low sulfidation epithermal gold deposit, western Makran volcanic arc, southeastern Iran

Science.gov (United States)

Sholeh, Ali; Rastad, Ebrahim; Huston, David L.; Gemmell, J. Bruce; Taylor, Ryan D.

2016-01-01

The Chahnaly low-sulfidation epithermal Au deposit and nearby Au prospects are located northwest of the intermittently active Bazman stratovolcano on the western end of the Makran volcanic arc, which formed as the result of subduction of the remnant Neo-Tethyan oceanic crust beneath the Lut block. The arc hosts the Siah Jangal epithermal and Kharestan porphyry prospects, near Taftan volcano, as well as the Saindak Cu-Au porphyry deposit and world-class Reko Diq Cu-Au porphyry deposit, near Koh-i-Sultan volcano to the east-northeast in Pakistan. The host rocks for the Chahnaly deposit include early Miocene andesite and andesitic volcaniclastic rocks that are intruded by younger dacitic domes. Unaltered late Miocene dacitic ignimbrites overlie these rocks. Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) U-Pb zircon geochronology data yield ages between 21.8 and 9.9 Ma for the acidic-intermediate regional volcanism. The most recent volcanic activity of the Bazman stratovolcano involved extrusion of an olivine basalt during Pliocene to Quaternary times. Interpretation of geochemical data indicate that the volcanic rocks are synsubduction and calc-alkaline to subalkaline. The lack of a significant negative Eu anomaly, a listric-shaped rare earth element pattern, and moderate La/Yb ratios of host suites indicate a high water content of the source magma.

Non-conventional photocathodes based on Cu thin films deposited on Y substrate by sputtering

Energy Technology Data Exchange (ETDEWEB)

Perrone, A. [Department of Mathematics and Physics “E. De Giorgi”, University of Salento, 73100 Lecce (Italy); National Institute of Nuclear Physics and University of Salento, 73100 Lecce (Italy); D’Elia, M. [Department of Mathematics and Physics “E. De Giorgi”, University of Salento, 73100 Lecce (Italy); Gontad, F., E-mail: francisco.gontad@le.infn.it [Department of Mathematics and Physics “E. De Giorgi”, University of Salento, 73100 Lecce (Italy); National Institute of Nuclear Physics and University of Salento, 73100 Lecce (Italy); Di Giulio, M.; Maruccio, G. [Department of Mathematics and Physics “E. De Giorgi”, University of Salento, 73100 Lecce (Italy); Cola, A. [National Council Research, Institute for Microelectronics and Microsystems, 73100 Lecce (Italy); Stankova, N.E. [Institute of Electronics, Bulgarian Academy of Sciences, 1784 Sofia (Bulgaria); Kovacheva, D.G. [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria); Broitman, E. [Department of Physics, Chemistry and Biology (IFM), Linköping University, SE-581 83 Linköping (Sweden)

2014-07-01

Copper (Cu) thin films were deposited on yttrium (Y) substrate by sputtering. During the deposition, a small central area of the Y substrate was shielded to avoid the film deposition and was successively used to study its photoemissive properties. This configuration has two advantages: the cathode presents (i) the quantum efficiency and the work function of Y and (ii) high electrical compatibility when inserted into the conventional radio-frequency gun built with Cu bulk. The photocathode was investigated by scanning electron microscopy to determine surface morphology. X-ray diffraction and atomic force microscopy studies were performed to compare the structure and surface properties of the deposited film. The measured electrical resistivity value of the Cu film was similar to that of high purity Cu bulk. Film to substrate adhesion was also evaluated using the Daimler–Benz Rockwell-C adhesion test method. Finally, the photoelectron performance in terms of quantum efficiency was obtained in a high vacuum photodiode cell before and after laser cleaning procedures. A comparison with the results obtained with a twin sample prepared by pulsed laser deposition is presented and discussed.

Molecular dynamics simulation of defect formation during energetic Cu deposition

International Nuclear Information System (INIS)

Gilmore, Charles M.; Sprague, James A.

2002-01-01

The deposition of energetic Cu atoms from 5 to 80 eV onto (0 0 1) Cu was simulated with molecular dynamics. The Cu-Cu interaction potential was a spline of the embedded atom potential developed from equilibrium data, and the universal scattering potential. Incident Cu atoms substituted for first layer substrate atoms by an exchange process at energies as low as 5 eV. Incident Cu atoms of 20 eV penetrated to the second substrate layer, and 20 eV was sufficient energy to produce interstitial defects. Incident atoms of 80 eV penetrated to the third atomic layer, produced interstitials 12 atomic layers into the substrate by focused replacement collision sequences, and produced sputtered atoms with a 16% yield. Interstitial clusters of up to 7 atoms were observed. The observed mechanisms of film growth included: the direct deposition of atoms into film equilibrium atom positions, the exchange of substrate atoms to equilibrium film atoms positions, and the migration of interstitials to equilibrium film atom positions. The relative frequency of each process was a function of incident energy. Since all observed growth mechanisms resulted in film atoms in equilibrium atomic positions, these simulations suggest that stresses in homoepitaxial Cu thin films are due to point defects. Vacancies would produce tensile strain and interstitial atoms would produce compressive strain in the films. It is proposed that immobile interstitial clusters could be responsible for retaining interstitial atoms and clusters in growing metal thin films

Composition changes in sputter deposition of Y-Ba-Cu-O films

International Nuclear Information System (INIS)

Hoshi, Y.; Naoe, M.

1989-01-01

The authors discuss the mechanism of the composition change in sputter deposition of Y-BA-Cu-O film from YBa 2 Cu 3 O 7-chi target investigated by means of a rf planar magnetron sputtering apparatus. Film composition changes significantly with not only substrate temperature Ts and sputtering gas pressure, but also substrate position. Lack of Cu and Ba content is significant in the film deposited at the substrate position just above the erosion area of the sputtering target. Suppression of bombardment of the substrate surface by negative ions emitted from the target and substrate is effective in increasing Cu and Ba content in the film. These results indicate not only that the sticking probability of the sputtered particles changes with Ts and incident particle energy, but also that high energy particle bombardment of the substrate surface plays an important role in the change of the film composition

Two-Step Physical Deposition of a Compact CuI Hole-Transport Layer and the Formation of an Interfacial Species in Perovskite Solar Cells.

Science.gov (United States)

Gharibzadeh, Saba; Nejand, Bahram Abdollahi; Moshaii, Ahmad; Mohammadian, Nasim; Alizadeh, Amir Hossein; Mohammadpour, Rahele; Ahmadi, Vahid; Alizadeh, Abdolali

2016-08-09

A simple and practical approach is introduced for the deposition of CuI as an inexpensive inorganic hole-transport material (HTM) for the fabrication of low cost perovskite solar cells (PSCs) by gas-solid phase transformation of Cu to CuI. The method provides a uniform and well-controlled CuI layer with large grains and good compactness that prevents the direct connection between the contact electrodes. Solar cells prepared with CuI as the HTM with Au electrodes displays an exceptionally high short-circuit current density of 32 mA cm(-2) , owing to an interfacial species formed between the perovskite and the Cu resulting in a long wavelength contribution to the incident photon-to-electron conversion efficiency (IPCE), and an overall power conversion efficiency (PCE) of 7.4 %. The growth of crystalline and uniform CuI on a low roughness perovskite layer leads to remarkably high charge extraction in the cells, which originates from the high hole mobility of CuI in addition to a large number of contact points between CuI and the perovskite layer. In addition, the solvent-free method has no damaging side effect on the perovskite layer, which makes it an appropriate method for large scale applications of CuI in perovskite solar cells. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Geochemistry of the Patricia Zn-Pb-Ag Deposit (paguanta, NE Chile)

Science.gov (United States)

Chinchilla Benavides, D.; Merinero Palomares, R.; Piña García, R.; Ortega Menor, L.; Lunar Hernández, R.

2013-12-01

The Patricia Zn-Pb-Ag ore deposit is located within the Paguanta mining project, situated at the northern end of the Andean Oligocene Porphyry Copper Belt of Chile. The sulfide mineralization occurs as W-E oriented veins hosted in volcanic rocks, mainly andesite (pyroclastic, ash and lavas), of Upper Cretaceous to Middle Tertiary age. The ore mineralogy (obtained by EMPA analyses) comprises in order of abundance, pyrite, sphalerite (5.5 - 10.89 wt % Fe, 9.8-19 % molar FeS and 0.52 wt % Cd), galena, arsenopyrite, chalcopyrite and Ag-bearing sulfosalts. The veins show a zoned and banded internal structure with pyrite at the edges and sphalerite in the center. The Ag occurs mostly as Ag-Cu-Sb sulfosalts, in order of abundance: series freibergite - argentotennantite -polybasite and stephanite. Other minor Ag phases such as argentite, pyrargirite and diaphorite were also identified. These Ag phases are typically associated with the base-metal sulfides. Freibergite occurs filling voids within sphalerite, chalcopyrite and at the contact between sphalerite and galena. Polybasite, stephanite, pyrargirite and argentite are mostly in close association with freibergite. In the case of diaphorite, it commonly occurs filling voids between galena crystals or as inclusions within galena. Some minor Ag-bearing sulfosalts are also identified between pyrite crystals. The alteration minerals are dominated by chlorite, illite and kaolinite. The gangue minerals consist of quartz and carbonates identified by XRD as kutnahorite. We obtained linear correlation statistically significant only for Ag, As Au, Cd, Cu, Pb, Sb and Zn and therefore we generated an enhanced scatter plot matrix of these elements. Bulk rock analyses (ICP/MS and XRF) of drill cores show that Ag is strongly and positively correlated with Pb and As, moderately with Cd, Sb, Au and Zn and weakly with Cu, while Au is moderately and positively correlated with Ag, As, Cd, Sb and Zn and weakly with Cu and Pb. These results

Ore-Forming Systems In Volcanogenic-Sedimentary Sequences By The Example Of Base Metal Deposits Of The Caucasus And East Pontic Metallotect

Directory of Open Access Journals (Sweden)

Sergo KEKELIA

2004-06-01

Full Text Available By the example of Alpine volcanogenic base metal deposits of the central part of the AlpineHimalayan fold belt (East Pontic Metallotect and Caucasus, it has been demonstrated that their hydrothermal systems naturally emerge at various stages of active interaction of microplates-continental fragments of Eurasia and Gondwanaland. During the divergence stage, at the microplates-boundary zones within the marginal sea, hydrothermal-sedimentary Cu and polymetallic deposits have been formed; at the early convergence stage, within the paleo-island-arc systems, epigenetic Cu and in lesser extent, barite-polymetallic (Lesser Caucasus, and later both combined (hydrothermal-sedimentary and stockwork and epigenetic (mainly Cu- and Zn-containing deposits have been originated (East Pontic Metallotect. At the beginning of the collisional stage, in connection with antidrome volcanism within the back-arc volcanic structures, polyformational deposits (barite, barite-polymetallic, Cu, Au have been formed. This tendency persists during the whole collisional stage - in the within-plate and transplate Eocene volcanic depressions - mainly polymetallic deposits have been originated in which the increasing contents of Ag take place in comparison to Au. The authors share the opinion that the primarily- anomalous environments for Cu-Zn deposits can have been "specialized" basic and medium-acidic volcanics whereas for baritic and barite polymetallic deposits grey coloured and evaporitic sequences in the volcano-structure pedestals with buried highly mineralized brines seem to be most favorable.

Alloy-dependent deformation behavior of highly ductile nanocrystalline AuCu thin films

International Nuclear Information System (INIS)

Lohmiller, Jochen; Spolenak, Ralph; Gruber, Patric A.

2014-01-01

Nanocrystalline thin films on compliant substrates become increasingly important for the development of flexible electronic devices. In this study, nanocrystalline AuCu thin films on polyimide substrate were tested in tension while using a synchrotron-based in situ testing technique. Analysis of X-ray diffraction profiles allowed identifying the underlying deformation mechanisms. Initially, elastic and microplastic deformation is observed, followed by dislocation-mediated shear band formation, and eventually macroscopic crack formation. Particularly the influence of alloy composition, heat-treatment, and test temperature were investigated. Generally, a highly ductile behavior is observed. However, high Cu concentrations, annealing, and/or large plastic strains lead to localized deformation and hence reduced ductility. On the other hand, enhanced test temperature allows for a delocalized deformation and extended ductility

Alloy-dependent deformation behavior of highly ductile nanocrystalline AuCu thin films

Energy Technology Data Exchange (ETDEWEB)

Lohmiller, Jochen [Karlsruhe Institute of Technology, Institute for Applied Materials, P.O. Box 3640, 76021 Karlsruhe (Germany); Laboratory for Nanometallurgy, Department of Materials, ETH Zurich, Wolfgang-Pauli-Str. 10, 8093 Zurich (Switzerland); Spolenak, Ralph [Laboratory for Nanometallurgy, Department of Materials, ETH Zurich, Wolfgang-Pauli-Str. 10, 8093 Zurich (Switzerland); Gruber, Patric A., E-mail: patric.gruber@kit.edu [Karlsruhe Institute of Technology, Institute for Applied Materials, P.O. Box 3640, 76021 Karlsruhe (Germany)

2014-02-10

Nanocrystalline thin films on compliant substrates become increasingly important for the development of flexible electronic devices. In this study, nanocrystalline AuCu thin films on polyimide substrate were tested in tension while using a synchrotron-based in situ testing technique. Analysis of X-ray diffraction profiles allowed identifying the underlying deformation mechanisms. Initially, elastic and microplastic deformation is observed, followed by dislocation-mediated shear band formation, and eventually macroscopic crack formation. Particularly the influence of alloy composition, heat-treatment, and test temperature were investigated. Generally, a highly ductile behavior is observed. However, high Cu concentrations, annealing, and/or large plastic strains lead to localized deformation and hence reduced ductility. On the other hand, enhanced test temperature allows for a delocalized deformation and extended ductility.

Growth and characterization of NixCu1-x alloy films, NixCu1-x/NiyCu1-y multilayers, and nanowires

International Nuclear Information System (INIS)

Kazeminezhad, I.

2001-12-01

It was found that it is possible to grow Ni x Cu 1-x alloy systems of arbitrary composition by electrodepositing well-defined sub-monolayer quantities of Ni and Cu in alternation using a new method based on that used previously to prepare potentiostatically deposited magnetic multilayers from a single sulphamate-based electrolyte. Following growth, the chemical composition of Ni x Cu 1-x alloy films was obtained by ZAF-corrected energy dispersive X-Ray (EDX) analysis and less than a 4% difference between the nominal and actual composition was observed. The structure of the films was investigated by high-angle X-ray diffractometry (HAXRD) and transmission electron microscopy (TEM). The films grown on polycrystalline Cu substrates had (100) texture, while those grown on Au-coated glass had (111) texture. Some evidence of Ni clustering was obtained by vibrating sample magnetometry (VSM). Self-organisation of the deposited metal was suggested for Ni potentials more positive than ∼-1.4V. The transition from a Ni/Cu multilayer to a Ni x Cu 1-x alloy was also studied and an interesting aspect, namely a plateau region in a plot of magnetisation as a function of Ni layer thickness was observed, suggesting a preferred Ni cluster size in these alloy films. Anisotropic magnetoresistance (AMR) of the films decreased with increasing Cu content at 300K and 77K. SQUID measurements for Ni 0.52 Cu 0.48 and Ni 0.62 CU 0.38 films showed that they become much more strongly ferromagnetic at low temperatures. Evidence for blocked -superparamagnetic behaviour above a blocking temperature (T B ) of the films was obtained from zero-field-cooled (ZFC) and field-cooled (FC) magnetic susceptibility measurements. Ni x Cu 1-x /Ni y Cu 1-y alloy/alloy multilayer films with short repeat distance were successfully fabricated using this method. Up to third order satellite peaks observed in HAXRD showed that the interface is sharp. Room temperature longitudinal magnetoresistance measurements showed

Investigation of Au9+ swift heavy ion irradiation on CdS/CuInSe2 thin films

International Nuclear Information System (INIS)

Joshi, Rajesh A.; Taur, Vidya S.; Singh, Fouran; Sharma, Ramphal

2013-01-01

In the present manuscript we report about the preparation of CdS/CuInSe 2 heterojunction thin films by chemical ion exchange method and investigation of 120 MeV Au 9+ swift heavy ions (SHI) irradiation effect on its physicochemical as well as optoelectronic properties. These pristine (as grown) samples are irradiated with 120 MeV Au 9+ SHI of 5×10 11 and 5×10 12 ions/cm 2 fluencies and later on characterized for structural, compositional, morphological, optical and I–V characteristics. X-ray diffraction (XRD) pattern obtained from pristine and irradiated films shows considerable modifications in peak intensity as well as rising of some new peaks, corresponding to In 2 Se 3 , Cu 3 Se 2 and CuIn 2 Se 3 materials. Transmission electron microscope (TEM) images show decrease in grain size upon increase in irradiation ion fluencies, which is also supported from the observation of random and uneven distribution of nano-grains as confirmed through scanning electron microscope (SEM) images. Presence of Cd, Cu, In, S and Se in energy dispersive X-ray spectrum analysis (EDAX) confirms the expected and observed elemental composition in thin films, the absorbance peaks are related to band to band transitions and spin orbit splitting while energy band gap is observed to increase from 1.36 for pristine to 1.53 eV for SHI irradiated thin films and I–V characteristics under illumination to 100 mW/cm 2 light source shows enhancement in conversion efficiency from 0.26 to 1.59% upon irradiation. - Highlights: • Nanostructured CdS/CuInSe 2 can be grown by chemical ion exchange method. • Physicochemical and optoelectronic properties can be modified by 120 MeV Au 9+ SHI Irradiation. • Solar energy conversion efficiency improved from 0.26 to 1.59% in CdS/CuInSe 2 upon irradiation

Rare Earth Element Fluorocarbonate Minerals from the Olympic Dam Cu-U-Au-Ag Deposit, South Australia

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Danielle S. Schmandt

2017-10-01

Full Text Available Olympic Dam is a world-class breccia-hosted iron-oxide copper-gold-uranium ore deposit located in the Gawler Craton, South Australia. It contains elevated concentrations of rare earth elements (REE which occur as the REE minerals bastnäsite, synchysite, florencite, monazite, and xenotime. This is the first study to focus on the mineralogy and composition of the most abundant REE mineral at Olympic Dam, bastnäsite, and subordinate synchysite. The sample suite extends across the deposit and represents different sulfide mineralization styles (chalcopyrite-bornite and bornite-chalcocite and breccias of various types, ranging from those dominated by clasts of granite, dykes, and hematite. The REE-fluorocarbonates (bastnäsite and synchysite typically occur as fine-grained (<50 μm disseminations in Cu-Fe-sulfides and gangue minerals, and also within breccia matrix. They are also locally concentrated within macroscopic REE-mineral-rich pockets at various locations across the deposit. Such coarse-grained samples formed the primary target of this study. Three general textural groups of bastnäsite are recognized: matrix (further divided into disseminated, fine-grained, and stubby types, irregular (sulfide-associated, and clast replacement. Textures are largely driven by the specific location and prevailing mineral assemblage, with morphology and grain size often controlled by the associated minerals (hematite, sulfides. Major element concentration data reveal limited compositional variation among the REE-fluorocarbonates; all are Ce-dominant. Subtle compositional differences among REE-fluorocarbonates define a spectrum from relatively La-enriched to (Ce + Nd-enriched phases. Granite-derived hydrothermal fluids were the likely source of F in the REE-fluorocarbonates, as well as some of the CO2, which may also have been contributed by associated mafic-ultramafic magmatism. However, transport of REE by Cl-ligands is the most likely scenario. Stubby bastn

Plasmon resonance enhanced photocatalysis under visible light with Au/Cu-TiO2 nanoparticles: Removal Cr (VI) from water as a case of study

KAUST Repository

Gondal, M. A.; Dastageer, Mohamed Abdulkader; Rashid, Shama G.; Zubair, Syed M.; Ali, Mohammada A.; Anjum, Dalaver H.; Lienhard V, John H.; McKinley, Gareth H.; Varanasi, Kripa K.

2013-01-01

Gold modified copper doped titania (Au/Cu:TiO2) nanoparticles were synthesized by a modified sol gel method and characterized using XRD, optical and TEM based techniques. The as-prepared material contained anatase phase particles with quasi-spherical morphology, showing enhanced absorption in the visible region and low photoluminescence emission intensity. Photocatalytic reduction of Cr (VI) in aqueous suspension with the Au/Cu:TiO2catalyst under 532 nm laser radiation and a visible broad band lamp source yielded 96% and 45% removal, respectively, without any additives. The enhanced photocatalytic activity can be attributed to the improved plasmonic effect due to gold modification and the expanded visible absorption due to copper doping. Moreover a comparative study of the material properties and catalytic activity of TiO2, Cu-TiO2and Au/Cu-TiO2 was carried out. © 2013 by American Scientific Publishers.

Plasmon resonance enhanced photocatalysis under visible light with Au/Cu-TiO2 nanoparticles: Removal Cr (VI) from water as a case of study

KAUST Repository

Gondal, M. A.

2013-12-01

Gold modified copper doped titania (Au/Cu:TiO2) nanoparticles were synthesized by a modified sol gel method and characterized using XRD, optical and TEM based techniques. The as-prepared material contained anatase phase particles with quasi-spherical morphology, showing enhanced absorption in the visible region and low photoluminescence emission intensity. Photocatalytic reduction of Cr (VI) in aqueous suspension with the Au/Cu:TiO2catalyst under 532 nm laser radiation and a visible broad band lamp source yielded 96% and 45% removal, respectively, without any additives. The enhanced photocatalytic activity can be attributed to the improved plasmonic effect due to gold modification and the expanded visible absorption due to copper doping. Moreover a comparative study of the material properties and catalytic activity of TiO2, Cu-TiO2and Au/Cu-TiO2 was carried out. © 2013 by American Scientific Publishers.

Centrifugal Deposited Au-Pd Core-Shell Nanoparticle Film for Room-Temperature Optical Detection of Hydrogen Gas.

Science.gov (United States)

Song, Han; Luo, Zhijie; Liu, Mingyao; Zhang, Gang; Peng, Wang; Wang, Boyi; Zhu, Yong

2018-05-06

In the present work, centrifugal deposited Au-Pd core-shell nanoparticle (NP) film was proposed for the room-temperature optical detection of hydrogen gas. The size dimension of 44, 48, 54, and 62 nm Au-Pd core-shell nanocubes with 40 nm Au core were synthesized following a solution-based seed-mediated growth method. Compared to a pure Pd NP, this core-shell structure with an inert Au core could decrease the H diffusion length in the Pd shell. Through a modified centrifugal deposition process, continues film samples with different core-shell NPs were deposited on 10 mm diameter quartz substrates. Under various hydrogen concentration conditions, the optical response properties of these samples were characterized by an intensity-based optical fiber bundle sensor. Experimental results show that the continues film that was composed of 62 nm Au-Pd core-shell NPs has achieved a stable and repeatable reflectance response with low zero drift in the range of 4 to 0.1% hydrogen after a stress relaxation mechanism at first few loading/unloading cycles. Because of the short H diffusion length due to the thinner Pd shell, the film sample composed of 44 nm Au-Pd NPs has achieved a dramatically decreased response/recovery time to 4 s/30 s. The experiments present the promising prospect of this simple method to fabricate optical hydrogen sensors with controllable high sensitivity and response rate at low cost.

Banatitic magmatic and metallogenetic belt: metallogeny of the Romanian Carpathians segment

Directory of Open Access Journals (Sweden)

S̡erban-Nicolae Vlad

2003-04-01

Full Text Available The Romanian Carpathians sector of the Late Cretaceous Banatitic Magmatic and Metallogenetic belt (BMMB contains 1 plutons and volcano-plutonic complexes, i. e. calc-alkaline, I-type granitoids, with related ores; 2 shoshonitic plutons that lack economic interest. Two provinces have been delineated: the Apuseni Mts. Province in the North and the Western South Carpathians in the South. Apuseni Mts. Province is a non-porphyry environment related to more evolved (granodioritic-granitic magmatism. It is subdivided into three zones: Vlădeasa (Pb-Zn ores of restricted metallogenetic potential; Gilău-Bihor (Fe, Bi, Mo, Cu, W, Au, Ni, Co, Pb, Zn, Ag, U, B ores / conspicuous peri-batholitic arrangement and South Apuseni (only one minor Fe-skarn occurrence. Western South Carpathians Province occurs in Romania and extends in Eastern Serbia. It is subdivided into South Banat Mts.–Timok Zone (SBTZ and Poiana Ruscă Mts.– North Banat Mts.– Ridanj-Krepoljin Zone (PR-NB-RKZ. SBTZ is a typical porphyry environment of high metallogenetic potential (Cu, Au, Pb, Zn, while PR-NB-RKZ is a non-porphyry environment with small to medium size Pb, Zn, Fe, Cu deposits/prospects exhibiting commonly a peri-plutonic zoning. The metallogenetic model of the Romanian Carpathians segment of BMMB is conceived based on correlating magma composition/level of emplacement and ore types.

N-Heterocyclic carbenes on close-packed coinage metal surfaces: bis-carbene metal adatom bonding scheme of monolayer films on Au, Ag and Cu.

Science.gov (United States)

Jiang, Li; Zhang, Bodong; Médard, Guillaume; Seitsonen, Ari Paavo; Haag, Felix; Allegretti, Francesco; Reichert, Joachim; Kuster, Bernhard; Barth, Johannes V; Papageorgiou, Anthoula C

2017-12-01

By means of scanning tunnelling microscopy (STM), complementary density functional theory (DFT) and X-ray photoelectron spectroscopy (XPS) we investigate the binding and self-assembly of a saturated molecular layer of model N -heterocyclic carbene (NHC) on Cu(111), Ag(111) and Au(111) surfaces under ultra-high vacuum (UHV) conditions. XPS reveals that at room temperature, coverages up to a monolayer exist, with the molecules engaged in metal carbene bonds. On all three surfaces, we resolve similar arrangements, which can be interpreted only in terms of mononuclear M(NHC) 2 (M = Cu, Ag, Au) complexes, reminiscent of the paired bonding of thiols to surface gold adatoms. Theoretical investigations for the case of Au unravel the charge distribution of a Au(111) surface covered by Au(NHC) 2 and reveal that this is the energetically preferential adsorption configuration.

Optical Property Characterization of Novel Graphene-X (X=Ag, Au and Cu Nanoparticle Hybrids

Directory of Open Access Journals (Sweden)

Sumit Ranjan Sahu

2013-01-01

Full Text Available The present investigation reports new results on optical properties of graphene-metal nanocomposites. These composites were prepared by a solution-based chemical approach. Graphene has been prepared by thermal reduction of graphene oxide (GO at 90°C by hydrazine hydrate in an ammoniacal medium. This ammoniacal solution acts as a solvent as well as a basic medium where agglomeration of graphene can be prevented. This graphene solution has further been used for functionalization with Ag, Au, and Cu nanoparticles (NPs. The samples were characterized by X-ray diffraction (XRD, Raman spectroscopy, UV-Vis spectroscopy, scanning electron microscopy (SEM, and transmission electron microscopy (TEM to reveal the nature and type of interaction of metal nanoparticles with graphene. The results indicate distinct shift of graphene bands both in Raman and UV-Vis spectroscopies due to the presence of the metal nanoparticles. Raman spectroscopic analysis indicates blue shift of D and G bands in Raman spectra of graphene due to the presence of metal nanoparticles except for the G band of Cu-G, which undergoes red shift, reflecting the charge transfer interaction between graphene sheets and metal nanoparticles. UV-Vis spectroscopic analysis also indicates blue shift of graphene absorption peak in the hybrids. The plasmon peak position undergoes blue shift in Ag-G, whereas red shift is observed in Au-G and Cu-G.

The Nokomis Cu-Ni-PGE Deposit, Duluth Complex: A sulfide-bearing, crystal-laden magmatic slurry

Science.gov (United States)

Peterson, D. M.

2009-12-01

Duluth Metals Limited’s Nokomis deposit is the most recently discovered Cu-Ni-PGE deposit in the 1.1 Ga. Duluth Complex, Minnesota. The deposit was discovered utilizing a genetic ore deposit model that identified and back-tracked channelized magma flow within the basal zone of the South Kawishiwi intrusion (SKI). The model led to exploratory drilling in 2006, deposit discovery and initial resource estimation in 2007, and significant resource expansion in 2008, all in a period of 18 months. The deposit’s updated 2008 NI 43-101 compliant Resource Estimate, based on 108 holes drilled by Duluth Metals and 52 historic drill holes on and off the property, contains 449 million tonnes of Indicated Resources grading 0.624% copper, 0.199% nickel, and 0.600 grams per tonne of total precious metals (TPM = Platinum+Palladium+Gold), and an additional 284 million tonnes of Inferred Resources grading 0.627% copper, 0.194% nickel, and 0.718 grams per tonne of TPM. The combined Indicated and Inferred Resources contain approximately 10 billion lbs Cu, 3.1 billion lbs Ni, 165 million lbs Co, 4 million ounces Pt, 9 million ounces Pd, and 2 million ounces of Au. Within these NI 43-101 resources are large tonnages of higher grade material, and the company has commenced an internal research program to identify the geologic controls on the formation nickel-rich and PGE-rich mineralization in the SKI, as well as copper-PGE rich mineralization in the footwall Archean rocks. To date, Duluth Metals has drilled more than 500,000 Ft. (~155,000 m) of core in 155 holes into the deposit, and has only drilled about half of the property. The ore deposit model was developed in cooperation with researchers from the Natural Resources Research Institute of the University of Minnesota, Duluth. As well, research and collaboration with faculty and students at Johns Hopkins University on the Ferrar Dolerites of the Antarctic Dry Valleys has played a key role in developing the magmatic model for the

Femtosecond Laser Fabricated Ag@Au and Cu@Au Alloy Nanoparticles for Surface Enhanced Raman Spectroscopy Based Trace Explosives Detection

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Moram Sree Satya Bharati

2018-03-01

Full Text Available Herein we present results from our detailed studies on the fabrication of Ag@Au and Cu@Au alloy nanoparticles (NPs using the femtosecond laser ablation in liquid technique. The NPs were obtained by ablating the pure Ag, Cu targets (bulk in HAuCl4 (5 mM solution. The absorption properties of the obtained NPs colloids were characterized using UV-Visible absorption spectrometer and their size, shape, and crystallinity were investigated using the XRD, FESEM and TEM techniques. The fabricated NPs were utilized for sensing of explosive molecules such as 2,4,6-trinitrophenol (PA, 2,4-dinitrotoluene (DNT and a common dye methylene blue (MB using the surface enhanced Raman spectroscopy (SERS technique. The detection limit in terms of weight was as low as few nano-grams in the case of nitroaromatic explosive compounds (PA, DNT and few picograms in the case of a common dye molecule (MB. Typical enhancement factors achieved were estimated to be ~104, ~105, and ~107, respectively, for PA, DNT, and MB. The significance of the present work lies in exploring the performance of the prepared NPs being used as SERS substrates for explosives detection using a portable Raman instrument. Such capability enables one to carry the spectrometer to the point of interest in the field and evaluate any hazardous samples within a short period of time.

Timing of porphyry (Cu-Mo) and base metal (Zn-Pb-Ag-Cu) mineralisation in a magmatic-hydrothermal system—Morococha district, Peru

Science.gov (United States)

Catchpole, Honza; Kouzmanov, Kalin; Bendezú, Aldo; Ovtcharova, Maria; Spikings, Richard; Stein, Holly; Fontboté, Lluís

2015-12-01

The Morococha district in central Peru is characterised by economically important Cordilleran polymetallic (Zn-Pb-Ag-Cu) vein and replacement bodies and the large Toromocho porphyry Cu-Mo deposit in its centre. U-Pb, Re-Os, and 40Ar/39Ar geochronology data for various porphyry-related hydrothermal mineralisation styles record a 3.5-Ma multi-stage history of magmatic-hydrothermal activity in the district. In the late Miocene, three individual magmatic-hydrothermal centres were active: the Codiciada, Toromocho, and Ticlio centres, each separated in time and space. The Codiciada centre is the oldest magmatic-hydrothermal system in the district and consists of a composite porphyry stock associated with anhydrous skarn and quartz-molybdenite veins. The hydrothermal events are recorded by a titanite U-Pb age at 9.3 ± 0.2 Ma and a molybdenite Re-Os age at 9.26 ± 0.03 Ma. These ages are indistinguishable from zircon U-Pb ages for porphyry intrusions of the composite stock and indicate a time span of 0.2 Ma for magmatic-hydrothermal activity. The small Ticlio magmatic-hydrothermal centre in the west of the district has a maximum duration of 0.3 Ma, ranging from porphyry emplacement to porphyry mineralisation at 8.04 ± 0.14 Ma (40Ar/39Ar muscovite cooling age). The Toromocho magmatic-hydrothermal centre has a minimum of five recorded porphyry intrusions that span a total of 1.3 Ma and is responsible for the formation of the giant Toromocho Cu-Mo deposit. At least two hydrothermal pulses are identified. Post-dating a first pulse of molybdenite mineralisation, wide-spread hydrous skarn covers an area of over 6 km2 and is recorded by five 40Ar/39Ar cooling ages at 7.2-6.8 Ma. These ages mark the end of the slowly cooling and long-lived Toromocho magmatic-hydrothermal centre soon after last magmatic activity at 7.26 ± 0.02 Ma. District-wide (50 km2) Cordilleran base metal vein and replacement bodies post-date the youngest recorded porphyry mineralisation event at Toromocho

Effects of different needles and substrates on CuInS{sub 2} deposited by electrostatic spray deposition

Energy Technology Data Exchange (ETDEWEB)

Roncallo, S. [Centre for Materials Science and Engineering, Cranfield University, Shrivenham, Swindon, SN6 8LA (United Kingdom); Painter, J.D., E-mail: j.d.painter@cranfield.ac.u [Centre for Materials Science and Engineering, Cranfield University, Shrivenham, Swindon, SN6 8LA (United Kingdom); Healy, M.J.F. [Centre for Materials Science and Engineering, Cranfield University, Shrivenham, Swindon, SN6 8LA (United Kingdom); Ritchie, S.A.; Finnis, M.V. [Department of Engineering Systems and Management, Cranfield University, Shrivenham, Swindon SN6 8LA (United Kingdom); Rogers, K.D. [Cranfield Health, Cranfield University, Cranfield, Bedfordshire, MK43 0AL (United Kingdom); Scragg, J.J. [University of Bath, Claverton Down, Bath, BA2 7AY (United Kingdom); Dale, P.J. [Laboratoire Photovoltaique, University of Luxembourg, 41 Rue du Brill, L-4422, Belvaux (Luxembourg); Zoppi, G. [Northumbria Photovoltaics Applications Centre, Northumbria, University, Newcastle upon Tyne NE1 8ST (United Kingdom)

2011-03-31

Copper indium disulphide (CuInS{sub 2}) thin films were deposited using the electrostatic spray deposition method. The effects of applied voltage and solution flow rate on the aerosol cone shape, film composition, surface morphology and current conversion were investigated. The effect of aluminium substrates and transparent fluorine doped tin oxide (SnO{sub 2}:F) coated glass substrates on the properties of as-deposited CuInS{sub 2} films were analysed. An oxidation process occurs during the deposition onto the metallic substrates which forms an insulating layer between the photoactive film and substrate. The effects of two different spray needles on the properties of the as-deposited films were also studied. The results reveal that the use of a stainless steel needle results in contamination of the film due to the transfer of metal impurities through the spray whilst this is not seen for the glass needle. The films were characterised using a number of different analytical techniques such as X-ray diffraction, scanning electron microscopy, Rutherford back-scattering and secondary ion mass spectroscopy and opto-electronic measurements.

Formation of patterned arrays of Au nanoparticles on SiC surface by template confined dewetting of normal and oblique deposited nanoscale films

Energy Technology Data Exchange (ETDEWEB)

Ruffino, F., E-mail: francesco.ruffino@ct.infn.it; Grimaldi, M.G.

2013-06-01

We report on the formation of patterned arrays of Au nanoparticles (NPs) on 6H SiC surface. To this end, we exploit the thermal-induced dewetting properties of a template confined deposited nanoscale Au film. In this approach, the Au surface pattern order, on the SiC substrate, is established by a template confined deposition using a micrometric template. Then, a dewetting process of the patterned Au film is induced by thermal processes. We compare the results, about the patterns formation, obtained for normal and oblique deposited Au films. We show that the normal and oblique depositions, through the same template, originate different patterns of the Au film. As a consequence of these different starting patterns, after the thermal processes, different patterns for the arrays of NPs originating from the dewetting mechanisms are obtained. For each fixed deposition angle α, the pattern evolution is analyzed, by scanning electron microscopy, as a function of the annealing time at 1173 K (900 °C). From these analyses, quantitative evaluations on the NPs size evolution are drawn. - Highlights: • Micrometric template-confined nanoscale gold films are deposited on silicon carbide. • The dewetting process of template-confined gold films on silicon carbide is studied. • Comparison of dewetting process of normal and oblique deposited gold films is drawn. • Patterned arrays of gold nanoparticles on silicon carbide surface are produced.

Formation of patterned arrays of Au nanoparticles on SiC surface by template confined dewetting of normal and oblique deposited nanoscale films

International Nuclear Information System (INIS)

Ruffino, F.; Grimaldi, M.G.

2013-01-01

We report on the formation of patterned arrays of Au nanoparticles (NPs) on 6H SiC surface. To this end, we exploit the thermal-induced dewetting properties of a template confined deposited nanoscale Au film. In this approach, the Au surface pattern order, on the SiC substrate, is established by a template confined deposition using a micrometric template. Then, a dewetting process of the patterned Au film is induced by thermal processes. We compare the results, about the patterns formation, obtained for normal and oblique deposited Au films. We show that the normal and oblique depositions, through the same template, originate different patterns of the Au film. As a consequence of these different starting patterns, after the thermal processes, different patterns for the arrays of NPs originating from the dewetting mechanisms are obtained. For each fixed deposition angle α, the pattern evolution is analyzed, by scanning electron microscopy, as a function of the annealing time at 1173 K (900 °C). From these analyses, quantitative evaluations on the NPs size evolution are drawn. - Highlights: • Micrometric template-confined nanoscale gold films are deposited on silicon carbide. • The dewetting process of template-confined gold films on silicon carbide is studied. • Comparison of dewetting process of normal and oblique deposited gold films is drawn. • Patterned arrays of gold nanoparticles on silicon carbide surface are produced

Effect of Cu addition on microstructure and corrosion behavior of spray-deposited Zn–30Al alloy

International Nuclear Information System (INIS)

Wang Feng; Xiong Baiqing; Zhang Yongan; Liu Hongwei; Li Zhihui; Li Xiwu; Qu Chu

2012-01-01

Highlights: ► Zn–30Al–xCu alloys were synthesized by the spray atomization and deposition technique. ► Immersion test and electrochemical measurements have been used to estimate the corrosion rate and the behavior. ► The result indicates that the 1 wt.% Cu addition displays superior corrosion resistance. - Abstract: In this study, one binary Zn–30Al and three ternary Zn–30Al–Cu alloys were synthesized by the spray atomization and deposition technique. The microstructures of the spray-deposited alloys were investigated by means of scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD). Immersion test, potentiodynamic polarization and electrochemical impedance measurements have been used to estimate the corrosion rate and the behavior. The results indicate that the 1 wt.% Cu addition to spray-deposited Zn–30Al alloy does not make significant change in microstructure. However, with the 2, 4 wt.% Cu additions to the alloy, some ε-CuZn 4 compounds with particle or irregular shapes were observed on the grain boundaries in the microstructures. Immersion test and electrochemical measurements confirmed that the 1 wt.% Cu addition displays superior corrosion resistance, whereas the 2, 4 wt.% Cu additions have a baneful effect on the corrosion behavior.

Growth mode, magnetic and magneto-optical properties of pulsed-laser-deposited Au/Co/Au(1 1 1) trilayers

International Nuclear Information System (INIS)

Clavero, C.; Cebollada, A.; Armelles, G.; Fruchart, O.

2010-01-01

The growth mode, magnetic and magneto-optical properties of epitaxial Au/Co/Au(1 1 1) ultrathin trilayers grown by pulsed-laser deposition (PLD) under ultra-high vacuum are presented. Sapphire wafers buffered with a single-crystalline Mo(1 1 0) buffer layer were used as substrates. Owing to PLD-induced interfacial intermixing at the lower Co/Au(1 1 1) interface, a close-to layer-by-layer growth mode is promoted. Surprisingly, despite this intermixing, ferromagnetic behavior is found at room temperature for coverings starting at 1 atomic layer (AL). The films display perpendicular magnetization with anisotropy constants reduced by 50% compared to TD-grown or electrodeposited films, and with a coercivity more than one order of magnitude lower (≤5mT). The magneto-optical (MO) response in the low Co thickness range is dominated by Au/Co interface contributions. For thicknesses starting at 3 AL Co, the MO response has a linear dependence with the Co thickness, indicative of a continuous-film-like MO behavior.

Growth of Single- and Bilayer ZnO on Au(111) and Interaction with Copper

Energy Technology Data Exchange (ETDEWEB)

Deng, Xingyi; Yao, Kun; Sun, Keju; Li, Wei-Xue; Lee, Junseok; Matranga, Christopher

2013-05-02

The stoichiometric single- and bi-layer ZnO(0001) have been prepared by reactive deposition of Zn on Au(111) and studied in detail with X-ray photoelectron spectroscopy, scanning tunneling microscopy, and density functional theory calculations. Both single- and bi-layer ZnO(0001) adopt a planar, graphite-like structure similar to freestanding ZnO(0001) due to the weak van der Waals interactions dominating their adhesion with the Au(111) substrate. At higher temperature, the single-layer ZnO(0001) converts gradually to bi-layer ZnO(0001) due to the twice stronger interaction between two ZnO layers than the interfacial adhesion of ZnO with Au substrate. It is found that Cu atoms on the surface of bi-layer ZnO(0001) are mobile with a diffusion barrier of 0.31 eV, and likely to agglomerate and form nanosized particles at low coverages; while Cu atoms tend to penetrate a single layer of ZnO(0001) with a barrier of 0.10 eV, resulting in a Cu free surface.

CuInS2 thin films obtained through the annealing of chemically deposited In2S3-CuS thin films

International Nuclear Information System (INIS)

Pena, Y.; Lugo, S.; Calixto-Rodriguez, M.; Vazquez, A.; Gomez, I.; Elizondo, P.

2011-01-01

In this work, we report the formation of CuInS 2 thin films on glass substrates by heating chemically deposited multilayers of copper sulfide (CuS) and indium sulfide (In 2 S 3 ) at 300 and 350 deg. C in nitrogen atmosphere at 10 Torr. CIS thin films were prepared by varying the CuS layer thickness in the multilayers with indium sulfide. The XRD analysis showed that the crystallographic structure of the CuInS 2 (JCPDS 27-0159) is present on the deposited films. From the optical analysis it was estimated the band gap value for the CIS film (1.49 eV). The electrical conductivity varies from 3 x 10 -8 to 3 Ω -1 cm -1 depending on the thickness of the CuS film. CIS films showed p-type conductivity.

Fabrication and stability investigation of ultra-thin transparent and flexible Cu-Ag-Au tri-layer film on PET

Science.gov (United States)

Prakasarao, Ch Surya; D'souza, Slavia Deeksha; Hazarika, Pratim; Karthiselva N., S.; Ramesh Babu, R.; Kovendhan, M.; Kumar, R. Arockia; Joseph, D. Paul

2018-04-01

The need for transparent conducting electrodes with high transmittance, low sheet resistance and flexibility to replace Indium Tin Oxide is ever growing. We have deposited and studied the performance of ultra-thin Cu-Ag-Au tri-layer films over a flexible poly-ethylene terephthalate substrate. Scotch tape test showed good adhesion of the metallic film. Transmittance of the tri-layer was around 40 % in visible region. Optical profiler measurements were done to study the surface features. The XRD pattern revealed that film was amorphous. Sheet resistance measured by four probe technique was around 7.7 Ohm/Δ and was stable up to 423 K. The transport parameters by Hall effect showed high conductivity and carrier concentration with a mobility of 5.58 cm2/Vs. Tests performed in an indigenously designed bending unit indicated the films to be stable both mechanically and electrically even after 50,000 bending cycles.

Pulsed-laser-deposited, single-crystalline Cu2O films with low resistivity achieved through manipulating the oxygen pressure

Science.gov (United States)

Liu, Xiaohui; Xu, Meng; Zhang, Xijian; Wang, Weiguang; Feng, Xianjin; Song, Aimin

2018-03-01

Low-resistivity, single-crystalline Cu2O films were realized on MgO (110) substrates through manipulating the oxygen pressure (PO2) of pulsed-laser deposition. X-ray diffraction and high resolution transmission electron microscopy measurements revealed that the films deposited at PO2 of 0.06 and 0.09 Pa were single phase Cu2O and the 0.09-Pa-deposited film exhibited the best crystallinity with an epitaxial relationship of Cu2O (110)∥MgO (110) with Cu2O (001)∥MgO (001). The pure phase Cu2O films exhibited higher transmittances and larger band gaps with an optical band gap of 2.56 eV obtained for the 0.09 Pa-deposited film. Hall-effect measurements demonstrated that the Cu2O film deposited at 0.09 Pa had the lowest resistivity of 6.67 Ω cm and highest Hall mobility of 23.75 cm2 v-1 s-1.

Magnetic fluctuations near a quantum phase transition in CeCu5.9Au0.1

DEFF Research Database (Denmark)

Schröder, A.; Aeppli, G.; Bucher, E.

1998-01-01

We present inelastic cold neutron scattering measurements on a single crystal of the heavy-fermion compound CeCu5.9Au0.1, where non-Fermi-liquid behavior near a quantum phase transition was found in the specific heat and resistivity. This compound shows strongly correlated magnetic fluctuations......, most intense at wave vectors Q(1), near(1,0,0), close to the magnetic ordering vector found at higher Au-concentration. The energy dependence can be best described by a modified quasielastic Lorentzian with power alpha = 0.7. Down to the lowest temperature of 0.07 K the relaxation rate Gamma remains...

Electroless deposition of NiCrB diffusion barrier layer film for ULSI-Cu metallization

Energy Technology Data Exchange (ETDEWEB)

Wang, Yuechun [School of Materials Science and Engineering, Yunnan University, Kunming (China); Chen, Xiuhua, E-mail: chenxh@ynu.edu.cn [School of Materials Science and Engineering, Yunnan University, Kunming (China); Ma, Wenhui [National Engineering Laboratory of Vacuum Metallurgy, Kunming University of Science and Technology, Kunming (China); Shang, Yudong; Lei, Zhengtao; Xiang, Fuwei [School of Materials Science and Engineering, Yunnan University, Kunming (China)

2017-02-28

Highlights: • In this paper, the electroless deposited NiCrB thin film was mainly in the form of NiB, CrB{sub 2} compounds and elementary Ni. • The sheet resistance of NiCrB thin film was 3.043 Ω/□, it is smaller than that of the widely used Ta, TaN and TiN diffusion barrier layers. • Annealing experiments showed that the failure temperature of NiCrB thin film regarding Cu diffusion was 900 °C. • NiCrB barrier layer crystallized after 900 °C annealing, Cu grains arrived at Si-substrate through grain boundaries, resulting in the formation of Cu{sub 3}Si. • Eelectroless deposited NiCrB film also had good oxidation resistance, it is expected to become an anti-oxidant layer of copper interconnection. - Abstract: NiCrB films were deposited on Si substrates using electroless deposition as a diffusion barrier layer for Cu interconnections. Samples of the prepared NiCrB/SiO{sub 2}/Si and NiCrB/Cu/NiCrB/SiO{sub 2}/Si were annealed at temperatures ranging from 500 °C to 900 °C. The reaction mechanism of the electroless deposition of the NiCrB film, the failure temperature and the failure mechanism of the NiCrB diffusion barrier layer were investigated. The prepared samples were subjected to XRD, XPS, FPP and AFM to determine the phases, composition, sheet resistance and surface morphology of samples before and after annealing. The results of these analyses indicated that the failure temperature of the NiCrB barrier film was 900 °C and the failure mechanism led to crystallization and grain growth of the NiCrB barrier layer after high temperature annealing. It was found that this process caused Cu grains to reach Si substrate through the grain boundaries, and then the reaction between Cu and Si resulted in the formation of highly resistive Cu{sub 3}Si.

Laser-induced chemical vapor deposition reactions

International Nuclear Information System (INIS)

Teslenko, V.V.

1990-01-01

The results of investigation of chemical reactions of deposition of different substances from the gas phase when using the energy of pulse quasicontinuous and continuous radiation of lasers in the wave length interval from 0.193 to 10.6 μm are generalized. Main attetion is paid to deposition of inorganic substances including nonmetals (C, Si, Ge and others), metals (Cu, Au, Zn, Cd, Al, Cr, Mo, W, Ni) and some simple compounds. Experimental data on the effect of laser radiation parameters and reagent nature (hydrides, halogenides, carbonyls, alkyl organometallic compounds and others) on the deposition rate and deposit composition are described in detail. Specific features of laser-chemical reactions of deposition and prospects of their application are considered

Temperature dependence of spin-orbit torques in Cu-Au alloys

KAUST Repository

Wen, Yan; Wu, Jun; Li, Peng; Zhang, Qiang; Zhao, Yuelei; Manchon, Aurelien; Xiao, John Q.; Zhang, Xixiang

2017-01-01

We investigated current driven spin-orbit torques in Cu40Au60/Ni80Fe20/Ti layered structures with in-plane magnetization. We have demonstrated a reliable and convenient method to separate dampinglike torque and fieldlike torque by using the second harmonic technique. It is found that the dampinglike torque and fieldlike torque depend on temperature very differently. Dampinglike torque increases with temperature, while fieldlike torque decreases with temperature, which are different from results obtained previously in other material systems. We observed a nearly linear dependence between the spin Hall angle and longitudinal resistivity, suggesting that skew scattering may be the dominant mechanism of spin-orbit torques.

Temperature dependence of spin-orbit torques in Cu-Au alloys

KAUST Repository

Wen, Yan

2017-03-07

We investigated current driven spin-orbit torques in Cu40Au60/Ni80Fe20/Ti layered structures with in-plane magnetization. We have demonstrated a reliable and convenient method to separate dampinglike torque and fieldlike torque by using the second harmonic technique. It is found that the dampinglike torque and fieldlike torque depend on temperature very differently. Dampinglike torque increases with temperature, while fieldlike torque decreases with temperature, which are different from results obtained previously in other material systems. We observed a nearly linear dependence between the spin Hall angle and longitudinal resistivity, suggesting that skew scattering may be the dominant mechanism of spin-orbit torques.

Transmission electron microscopy and image simulation study of CuAu domains in CuInS{sub 2} epitaxial layers

Energy Technology Data Exchange (ETDEWEB)

Barcones, B.; Romano-Rodriguez, A.; Arbiol, J.; Alvarez-Garcia, J.; Perez-Rodriguez, A.; Morante, J.R.; Scheer, R

2003-05-01

In this work the occurrence of two polytypic structures, chalcopyrite (CH) and cationic fcc CuAu-ordering (CA), in epitaxial CuInS{sub 2} samples on Si (1 1 1) oriented substrates has been studied. Samples with different Cu-to-In ratios and grown at 500 and 575 deg. C, respectively, have been analysed. Cross-section Transmission electron microscopy (TEM) samples have been prepared and studied in two directions normal to the growth direction [2 2 1]{sub CH}, namely, [1-1 0]{sub CH}, which is parallel to [1 0 0]{sub CA}, and [1 1-1]{sub CH} that is parallel to [0 1-1]{sub CA}. Electron diffraction and high resolution TEM images corroborate the existence of both polytypes and give the orientation relationship between them, namely, [1-1 0]{sub CH} parallel [1 0 0]{sub CA} and (1 1 2){sub CH} parallel (0 1 1){sub CA}. Cu-rich samples have good crystalline quality with large grains and sharp interfaces between both polytypes, the most important being between the (1 1 2){sub CH} and (0 1 1){sub CA} planes. On the contrary, the crystalline quality of Cu-poor samples is minor, no clear interfaces can be observed, and a high density of twins in the (0 1-1){sub CA} planes can be observed. The results on the crystalline quality are in agreement with previous results on polycrystalline CuInS{sub 2} films.

Freely migrating defects in ion-irradiated Cu3Au

International Nuclear Information System (INIS)

Wei, L.C.; Lang, E.; Flynn, C.P.; Averback, R.S.

1999-01-01

The efficiency of producing freely migrating vacancy defects in irradiated Cu 3 Au was examined using electrical resistivity measurements of radiation-induced ordering on highly perfect single-crystal films. Relative efficiencies for He, Ne, and Ar bombardments at different ion energy and specimen temperature were obtained. The ratio of the efficiencies of 0.6 MeV Ne to He increased with temperature from ∼0.25 at 340 K to a saturation value of ∼0.40 at 520 K. For Ar and He, the ratio increased from ∼0.11 at 360 K to ∼0.18 at 540 K. Estimates indicate that about half of all defects created in cascades are freely migrating. copyright 1999 American Institute of Physics

Geochemical, microtextural and petrological studies of the Samba prospect in the Zambian Copperbelt basement: a metamorphosed Palaeoproterozoic porphyry Cu deposit.

Science.gov (United States)

Master, Sharad; Mirrander Ndhlovu, N.

2015-04-01

Ever since Wakefield (1978, IMM Trans., B87, 43-52) described a porphyry-type meta-morphosed Cu prospect, the ca 50 Mt, 0.5% Cu Samba deposit (12.717°S, 27.833°E), hosted by porphyry-associated quartz-sericite-biotite schists in northern Zambia, there has been controversy about its origin and significance. This is because it is situated in the basement to the world's largest stratabound sediment-hosted copper province, the Central African Copperbelt, which is hosted by rocks of the Neoproterozoic Katanga Supergroup. Mineralization in the pre-Katangan basement has long played a prominent role in ore genetic models, with some authors suggesting that basement Cu mineralization may have been recycled into the Katangan basin through erosion and redeposition, while others have suggested that the circulation of fluids through Cu-rich basement may have leached out the metals which are found concentrated in the Katangan orebodies. On the basis of ca 490-460 Ma Ar-Ar ages, Hitzman et al. (2012, Sillitoe Vol., SEG Spec. Publ., 16, 487-514) suggested that Samba represents late-stage impregnation of copper mineralization into the basement, and that it was one of the youngest copper deposits known in the Central African Copperbelt. If the Samba deposit really is that young, then it would have post-dated regional deformation and metamorphism (560-510 Ma), and it ought to be undeformed and unmetamorphosed. The Samba mineralization consists of chalcopyrite and bornite, occurring as disseminations, stringers and veinlets, found in a zone >1 km along strike, in steeply-dipping lenses up to 10m thick and >150m deep. Our new major and trace element XRF geochemical data (14 samples) show that the host rocks are mainly calc-alkaline metadacites. Cu is correlated with Ag (Cu/Ag ~10,000:1) with no Au or Mo. Our study focused on the microtextures and petrology of the Samba ores. We confirm that there is alteration of similar style to that accompanying classical porphyry Cu mineralization

Efficient hole-transporting layer MoO_3:CuI deposited by co-evaporation in organic photovoltaic cells

International Nuclear Information System (INIS)

Barkat, L.; Khelil, A.; Hssein, M.; El Jouad, Z.; Cattin, L.; Louarn, G.; Stephant, N.; Ghamnia, M.; Addou, M.; Morsli, M.; Bernede, J.C.

2017-01-01

In order to improve hole collection at the interface anode/electron donor in organic photovoltaic cells, it is necessary to insert a hole-transporting layer. CuI was shown to be a very efficient hole-transporting layer. However, its tendency to be quite rough tends to induce leakage currents and it is necessary to use a very slow deposition rate for CuI to avoid such negative effect. Herein, we show that the co-deposition of MoO_3 and CuI avoids this difficulty and allows deposition of a homogeneous efficient hole-collecting layer at an acceptable deposition rate. Via an XPS study, we show that blending MoO_3:CuI improves the hole collection efficiency through an increase of the gap state density. This increase is due to the formation of Mo"5"+ following interaction between MoO_3 and CuI. Not only does the co-evaporation process allow for decreasing significantly the deposition time of the hole-transporting layer, but also it increases the efficiency of the device based on the planar heterojunction, CuPc/C_6_0. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

The effects of H sub 2 addition on the enhanced deposition rate and high quality Cu films by MOCVD

CERN Document Server

Lee, J H; Park, S J; Choi, S Y

1998-01-01

High-quality Cu thin films were deposited on the TiN/Si substrate from the hexafluoroacetylacetonate Copper thrmethylvinylsilane [Cu (hfac) (tmvs)] source using a metal organic chemical vapor deposition (MOCVD) technique. The optimum deposition condition is with a substrate temperature of 200 .deg. C and the hydrogen flow rate of 80 sccm. The deposition rate, electrical resistivity, surface morphology, grain size, and optical properties of the deposited Cu films were investigated by the AES, four-point probe, SEM, XRD, and the visible spectrophotometer as a function of hydrogen gas flow rate, The results indicated that additional hydrogen gas affects the CVD hydrogen reduction reaction improving the purity, deposition rate, and electrical resistivity of Cu thin films. A prospective idea will be discussed for the preparation of Cu thin films showing a more enhanced electromigration resistance applicable to the next-generation interconnection.

Cu₂O-Au nanocomposites for enzyme-free glucose sensing with enhanced performances.

Science.gov (United States)

Hu, Qiyan; Wang, Fenyun; Fang, Zhen; Liu, Xiaowang

2012-06-15

A facile method for the synthesis of Cu(2)O-Au nanocomposites has been reported by injecting Cu(2)O nanocubes into Au precursor directly with the assistance of ultrasound radiation at room temperature. The ultrasound radiation is not a necessary requirement but can make the distribution of Au nanoparticles more homogenous. The formation of Cu(2)O-Au nanocomposites is attributed to following two reasons. The first one is the difference in the reduction potential between Cu(2+)/Cu(2)O and AuCl(4)(-)/Au, which can also be considered as the driving force for the redox reaction. The other one is the low lattice mismatch between (200) planes of Cu(2)O and (200) facets of Au, which is favorable for the formation of heterostructure. The electrochemical investigation demonstrates that the performances of Cu(2)O nanocubes in enzyme-free glucose sensing have been improved significantly after the decoration of Au nanoparticles which may be derived from the polarization effect provided by Au nanoparticles. As-prepared Cu(2)O-Au nanocomposites have great potential in enzyme-free glucose sensing. Copyright © 2012 Elsevier B.V. All rights reserved.

Formation of Cu, Ag and Au nanofiims under the influence of hydrogen atoms

Directory of Open Access Journals (Sweden)

Zhavzharov E. L.

2015-12-01

Full Text Available Due to their electrical properties, thin metallic films are widely used in modern micro- and nanoelectronics. These properties allow solving fundamental problems of surface and solid state physics. Up-to-date methods of producing thin films involve high vacuum or multi-stage processes, which calls for complicated equipment. The authors propose an alternative method of producing thin metallic films using atomic hydrogen. Exothermal reaction of atoms recombination in a molecule (about 4.5 eV / recombination act initiated on the solid surface by atomic hydrogen may stimulate local heating, spraying and surface atoms transfer. We investigated the process of atomic hydrogen treatment of Cu, Ag and Au metal films, obtained by thermal vacuum evaporation. There are two methods of obtaining nanofilms using atomic hydrogen treatment: sputtering and vapor-phase epitaxy. In the first method, a film is formed by reducing the thickness of the starting film. This method allows obtaining a film as thick as the monolayer. In the second method, a nanofilm is formed by deposition of metal atoms from the vapor phase. This method allows obtaining a film thickness from monolayer to ~10 nm. These methods allow creating nanofilms with controlled parameters and metal thickness. Such films would be technologically pure and have good adhesion.

Superconducting and structural properties of plasma sprayed YBaCuO layers deposited on metallic substrates

NARCIS (Netherlands)

Hemmes, Herman K.; Jäger, D; Smithers, M.A.; Smithers, M.; van der Veer, J.; van der Veer, J.M.; Stover, D.; Rogalla, Horst

1993-01-01

The properties of plasma sprayed Y-Ba-Cu-O coatings deposited on metallic substrates are studied. Stainless steel, nickel steels and pure nickel are used as substrate. Y-Ba-Cu-O deposited on stainless steel and nickel steel reacts with the substrate. This interaction can be suppressed by using an

Highly porous ZnS microspheres for superior photoactivity after Au and Pt deposition and thermal treatment

Energy Technology Data Exchange (ETDEWEB)

Singla, Shilpa; Pal, Bonamali, E-mail: bpal@thapar.edu

2013-11-15

Graphical abstract: Highly porous ZnS microsphere of size 2–5 μm having large surface area ca. 173.14 m{sup 2} g{sup −1} exhibits superior photocatalytic activity for the oxidation of 4-nitrophenol under UV light irradiation. The rate of photooxidation has been significantly improved by Au and Pt deposition and after sintering, respectively, due to rapid electron acceptance by metal from photoexcited ZnS and growth of crystalline ZnS phase. - Highlights: • Photoactive ZnS microsphere of size 2–5 μm was prepared by hydrothermal route. • Highly porous cubic spherical ZnS crystals possess a large surface area, 173 m{sup 2} g{sup −1}. • 1 wt% Au and Pt photodeposition highly quenched the photoluminescence at 437 nm. • Sintering and metal loading notably improve the photooxidation rate of 4-nitrophenol. • Pt co-catalyst always exhibits superior photoactivity of ZnS microsphere than Au. - Abstract: This work highlights the enhanced photocatalytic activity of porous ZnS microspheres after Au and Pt deposition and heat treatment at 500 °C for 2 h. Microporous ZnS particles of size 2–5 μm with large surface area 173.14 m{sup 2} g{sup −1} and pore volume 0.0212 cm{sup 3} g{sup −1} were prepared by refluxing under an alkaline medium. Photoluminescence of ZnS at 437 nm attributed to sulfur or zinc vacancies were quenched to 30% and 49%, respectively, after 1 wt% Au and Pt loading. SEM images revealed that each ZnS microparticle consist of several smaller ZnS spheres of size 2.13 nm as calculated by Scherrer's equation. The rate of photooxidation of 4-nitrophenol (10 μM) under UV (125 W Hg arc–10.4 mW/cm{sup 2}) irradiation has been significantly improved by Au and Pt deposition followed by sintering due to better electron capturing capacity of deposited metals and growth of crystalline ZnS phase with less surface defects.

Molecular dynamics simulation of temperature effects on deposition of Cu film on Si by magnetron sputtering

Science.gov (United States)

Zhu, Guo; Sun, Jiangping; Zhang, Libin; Gan, Zhiyin

2018-06-01

The temperature effects on the growth of Cu thin film on Si (0 0 1) in the context of magnetron sputtering deposition were systematically studied using molecular dynamics (MD) method. To improve the comparability of simulation results at varying temperatures, the initial status data of incident Cu atoms used in all simulations were read from an identical file via LAMMPS-Python interface. In particular, crystalline microstructure, interface mixing and internal stress of Cu thin film deposited at different temperatures were investigated in detail. With raising the substrate temperature, the interspecies mixed volume and the proportion of face-centered cubic (fcc) structure in the deposited film both increased, while the internal compressive stress decreased. It was found that the fcc structure in the deposited Cu thin films was 〈1 1 1〉 oriented, which was reasonably explained by surface energy minimization and the selectivity of bombardment energy to the crystalline planes. The quantified analysis of interface mixing revealed that the diffusion of Cu atoms dominated the interface mixing, and the injection of incident Cu atoms resulted in the densification of phase near the film-substrate interface. More important, the distribution of atomic stress indicated that the compressive stress was mainly originated from the film-substrate interface, which might be attributed to the densification of interfacial phase at the initial stage of film deposition.

Quantum tunneling in real space: Tautomerization of single porphycene molecules on the (111) surface of Cu, Ag, and Au

Science.gov (United States)

Kumagai, Takashi; Ladenthin, Janina N.; Litman, Yair; Rossi, Mariana; Grill, Leonhard; Gawinkowski, Sylwester; Waluk, Jacek; Persson, Mats

2018-03-01

Tautomerization in single porphycene molecules is investigated on Cu(111), Ag(111), and Au(111) surfaces by a combination of low-temperature scanning tunneling microscopy (STM) experiments and density functional theory (DFT) calculations. It is revealed that the trans configuration is the thermodynamically stable form of porphycene on Cu(111) and Ag(111), whereas the cis configuration occurs as a meta-stable form. The trans → cis or cis → trans conversion on Cu(111) can be induced in an unidirectional fashion by injecting tunneling electrons from the STM tip or heating the surface, respectively. We find that the cis ↔ cis tautomerization on Cu(111) occurs spontaneously via tunneling, verified by the negligible temperature dependence of the tautomerization rate below ˜23 K. Van der Waals corrected DFT calculations are used to characterize the adsorption structures of porphycene and to map the potential energy surface of the tautomerization on Cu(111). The calculated barriers are too high to be thermally overcome at cryogenic temperatures used in the experiment and zero-point energy corrections do not change this picture, leaving tunneling as the most likely mechanism. On Ag(111), the reversible trans ↔ cis conversion occurs spontaneously at 5 K and the cis ↔ cis tautomerization rate is much higher than on Cu(111), indicating a significantly smaller tautomerization barrier on Ag(111) due to the weaker interaction between porphycene and the surface compared to Cu(111). Additionally, the STM experiments and DFT calculations reveal that tautomerization on Cu(111) and Ag(111) occurs with migration of porphycene along the surface; thus, the translational motion couples with the tautomerization coordinate. On the other hand, the trans and cis configurations are not discernible in the STM image and no tautomerization is observed for porphycene on Au(111). The weak interaction of porphycene with Au(111) is closest to the gas-phase limit and therefore the absence

Aerosol deposition of (Cu,Ti) substituted bismuth vanadate films

Energy Technology Data Exchange (ETDEWEB)

Exner, Jörg, E-mail: Functional.Materials@Uni-Bayreuth.de [University of Bayreuth, Department of Functional Materials, Universitätsstraße 30, 95440 Bayreuth (Germany); Fuierer, Paul [Materials and Metallurgical Engineering Department, New Mexico Institute of Mining and Technology, Socorro, NM 87801 (United States); Moos, Ralf [University of Bayreuth, Department of Functional Materials, Universitätsstraße 30, 95440 Bayreuth (Germany)

2014-12-31

Bismuth vanadate, Bi{sub 4}V{sub 2}O{sub 11}, and related compounds with various metal (Me) substitutions, Bi{sub 4}(Me{sub x}V{sub 1−x}){sub 2}O{sub 11−δ}, show some of the highest ionic conductivities among the known solid oxide electrolytes. Films of Cu and Ti substituted bismuth vanadate were prepared by an aerosol deposition method, a spray coating process also described as room temperature impact consolidation. Resultant films, several microns in thickness, were dense with good adhesion to the substrate. Scanning electron microscopy and high temperature X-ray diffraction were used to monitor the effects of temperature on the structure and microstructure of the film. The particle size remained nano-scale while microstrain decreased rapidly up to 500 °C, above which coarsening and texturing increased rapidly. Impedance measurements of films deposited on inter-digital electrodes revealed an annealing effect on the ionic conductivity, with the conductivity exceeding that of a screen printed film, and approaching that of bulk ceramic. - Highlights: • Cu and Ti doped bismuth vanadate films were prepared by aerosol deposition (AD). • Dense 3–5 μm thick films were deposited on alumina, silicon and gold electrodes. • Annealing of the AD-layer increases the conductivity by 1.5 orders of magnitude. • Effect of temperature on structure and microstructure was investigated.

Preliminary study of CdTe and CdTe:Cu thin films nanostructures deposited by using DC magnetron sputtering

Energy Technology Data Exchange (ETDEWEB)

Marwoto, Putut; Made, D. P. Ngurah; Sugianto [Departement of Physics, Faculty of Mathematics and Natural Sciences, Universitas Negeri Semarang, Gunungpati, Semarang 50229 Jawa Tengah (Indonesia); Wibowo, Edy; Astuti, Santi Yuli; Aryani, Nila Prasetya [Materials Research Group, Laboratory of Thin Film, Department of Physics, Universitas Negeri Semarang, Gunungpati, Semarang 50229 Jawa Tengah (Indonesia); Othaman, Zulkafli [Departement of Physics, Universiti Teknologi Malaysia (UTM), Skudai, Johor Bahru (Malaysia)

2013-09-03

Growth and properties of CdTe and CdTe:Cu thin films nanostrucures deposited by using dc magnetron sputtering are reported. Scanning electron microscope (SEM) was used to observe the surface morphologies of the thin films. At growth conditions of 250 °C and 14 W, CdTe films did not yet evenly deposited. However, at growth temperature and plasma power of 325 °C and 43 W, both CdTe and CdTe:Cu(2%) have deposited on the substrates. In this condition, the morphology of the films indicate that the films have a grain-like nanostructures. Grain size diameter of about 200 nm begin to appear on top of the films. Energy Dispersive X-rays spectroscopy (EDX) was used to investigate chemical elements of the Cu doped CdTe film deposited. It was found that the film deposited consist of Cd, Te and Cu elements. XRD was used to investigate the full width at half maximum (FWHM) values of the thin films deposited. The results show that CdTe:Cu(2%) thin film has better crystallographic properties than CdTe thin film. The UV-Vis spectrometer was used to investigate the optical properties of thin films deposited. The transmittance spectra showed that transmittance of CdTe:Cu(2%) film is lower than CdTe film. It was found that the bandgap energy of CdTe and CdTe:Cu(2%) thin films of about 1.48 eV.

Photocatalytic properties of Au-deposited mesoporous SiO_2–TiO_2 photocatalyst under simultaneous irradiation of UV and visible light

International Nuclear Information System (INIS)

Okuno, T.; Kawamura, G.; Muto, H.; Matsuda, A.

2016-01-01

Mesoporous SiO_2 templates deposited TiO_2 nanocrystals are synthesized via a sol–gel route, and Au nanoparticles (NPs) are deposited in the tubular mesopores of the templates by a photodeposition method (Au/SiO_2–TiO_2). The photocatalytic characteristics of Au/SiO_2–TiO_2 are discussed with the action spectra of photoreactions of 2-propanol and methylene blue. Photocatalytic activities of SiO_2–TiO_2 under individual ultraviolet (UV) and visible (Vis) light illumination are enhanced by deposition of Au NPs. Furthermore, Au/SiO_2–TiO_2 shows higher photocatalytic activities under simultaneous irradiation of UV and Vis light compared to the activity under individual UV and Vis light irradiation. Since the photocatalytic activity under simultaneous irradiation is almost the same as the total activities under individual UV and Vis light irradiation, it is concluded that the electrons and the holes generated by lights of different wavelengths are efficiently used for photocatalysis without carrier recombination. - Graphical abstract: This graphic shows the possible charge behavior in Au/SiO_2–TiO_2 under independent light irradiation of ultraviolet and visible light irradiation. Both reactions under independent UV and Vis light irradiation occurred in parallel when Au/SiO_2–TiO_2 photocatalyst was illuminated UV and Vis light simultaneously, and then photocatalytic activity is improved by simultaneous irradiation. - Highlights: • Au nanoparticles were deposited in mesoporous SiO_2–TiO_2 by a photodeposition method. • Photocatalytic activity under UV and Vis light was enhanced by deposition of Au. • Photocatalytic activity of Au/SiO_2–TiO_2 was improved by simultaneous irradiation.

X-ray fluorescence holography studies for a Cu3Au crystal

Science.gov (United States)

Dąbrowski, K. M.; Dul, D. T.; Jaworska-Gołąb, T.; Rysz, J.; Korecki, P.

2015-12-01

In this work we show that performing a numerical correction for beam attenuation and indirect excitation allows one to fully restore element sensitivity in the three-dimensional reconstruction of the atomic structure. This is exemplified by a comparison of atomic images reconstructed from holograms measured for ordered and disordered phases of a Cu3Au crystal that clearly show sensitivity to changes in occupancy of the atomic sites. Moreover, the numerical correction, which is based on quantitative methods of X-ray fluorescence spectroscopy, was extended to take into account the influence of a disturbed overlayer in the sample.

Radiation-induced segregation in Cu-Au alloys

International Nuclear Information System (INIS)

Hashimoto, T.; Rehn, L.E.; Okamoto, P.R.

1987-01-01

Radiation-induced segregation in a Cu-lat.% Au alloy was investigated using in-situ Rutherford backscattering spectrometry. Irradiation with 1.8-MeV helium produced nonequilibrium gold atom depletion in the near surface region. The amount of segregation was measured as a function of dose, dose rate, and temperature. Segregation was observed in the temperature range between about 300 and 500 0 C. For a calculated dose rate of 3.9 x 10/sup -5/ dpa/s, the radiation-induced segregation rate peaked near 400 0 C. Theoretical analysis based on the Johnson-Lam model predicted that the amount of segregation would be directly proportional to dose at the early stage of irradiation, would deviate from linearity with a continuously decreasing slope of intermediate doses, and finally approach a constant value after high doses. The analysis also predicted that the segregation rate would vary as the - 1/4th power of the dose rate at constant dose in the low temperature region. These predictions were all verified experimentally. A procedure for extracting relative defect production efficiencies from similar measurements is discussed

Microstructure processes induced by phase transitions in a CuAu alloy as studied by acoustic emission and optical cinematography

Energy Technology Data Exchange (ETDEWEB)

Masek, P.; Chmelik, F.; Sima, V. [Charles Univ., Prague (Czech Republic). Dept. of Metal Physics; Brinck, A.; Neuhaeuser, H. [Technische Univ. Braunschweig (Germany). Inst. fuer Metallphysik und Nukleare Festkoerperphysik

1999-01-15

Combined acoustic emission measurements and surface cinematography observations have been applied to determine the structure evolution during thermal loading of the CuAu alloy. Thermal history and the fashion of thermal loading have been shown to affect considerably the structure response of the CuAu alloy on temperature changes. On thermal loading, intense plastic deformation occurs in certain temperature intervals due to the relaxation of internal stresses induced by phase transitions and structure anisotropy. The main mechanism is twinning taking place most probably in (110) planes. Dislocation glide and grain-boundary sliding have also been observed as minor mechanisms. A shape-restoration effect associated with the order-disorder transition is revealed. Thermal cycling with upper temperatures over 500 C may also result in structural damage.

Transverse Momentum Spectra of KS0 and K*0 at Midrapidity in d + Au, Cu + Cu, and p+p Collisions at √(sNN)=200 GeV

International Nuclear Information System (INIS)

Zhang, Guo-Xing; Li, Bao-Chun; Guo, Yuan-Yuan

2015-01-01

We analyze transverse momentum spectra of K S 0 and K *0 at midrapidity in d + Au, Cu + Cu, and p+p collisions at √(s NN )=200 GeV in the formworks of Tsallis statistics and Boltzmann statistics, respectively. Both of them can describe the transverse momentum spectra and extract the thermodynamics parameters of matter evolution in the collisions. The parameters are helpful for us to understand the thermodynamics factors of the particle production

Facile fabrication of p-n heterojunctions for Cu2O submicroparticles deposited on anatase TiO2 nanobelts

International Nuclear Information System (INIS)

Li, Li; Lei, Jingguo; Ji, Tianhao

2011-01-01

Graphical abstract: Cu 2 O particle-deposited TiO 2 nanobelts with p-n semiconductor heterojunction structure were successfully prepared via two-step preparation process, and their visible-light photodegradation activities of Rhodamine B were investigated in detail. Highlights: → Cu 2 O particle-deposited TiO 2 nanobelts mainly with diameters in a range of 200-400 nm were successfully prepared. → The amount of Cu 2 O particles deposited on TiO 2 nanobelts can be tuned. → The composite structure with Cu 2 O particles and TiO 2 nanobelts exhibits p-n semiconductor heterojunction performance. → Photocatalytic properties of such composites. -- Abstract: In this paper, Cu 2 O particle-deposited TiO 2 nanobelts with p-n semiconductor heterojunction structure were successfully prepared via a two-step preparation process to investigate electron-transfer performance between p-type Cu 2 O and n-type TiO 2 . Various measurement results confirm that the amount of pure Cu 2 O submicroparticles, with diameters within the range of 200-400 nm and deposited on the surface of TiO 2 nanobelts, can be controlled, and that the purity of Cu 2 O is heavily affected by reaction time. Visible-light photodegradation activities of Rhodamine B show that photocatalysts have little or no photocatalytic activities mainly due to their p-n heterojunction structure, indicating that there hardly appears any electron-transfer from Cu 2 O to TiO 2 .

Effect of deposition time of sputtering Ag-Cu thin film on mechanical and antimicrobial properties

Science.gov (United States)

Purniawan, A.; Hermastuti, R.; Purwaningsih, H.; Atmono, T. M.

2018-04-01

Metallic implants are important components in biomedical treatment. However, post-surgery infection often occurs after installation of implant. The infections are usually treated by antibiotics, but it still causes several secondary problems. As a prevention treatment, the surgical instruments and implants must be in a sterile condition. This action is still not optimal too because the material still can attract the bacteria. From material science point of view, it can be anticipated by developing a type of material which has antibacterial properties or called antimicrobial material. Silver (Ag) and Copper (Cu) have antimicrobial properties to prevent the infection. In this research, the influence of deposition time of Ag-Cu thin film deposition process as antimicrobial material with Physical Vapor Deposition (PVD) RF Sputtering method was analyzed. Deposition time used were for 10, 15 and 20 minutes in Argon gas pressure around 3 x 10-2 mbar in during deposition process. The morphology and surface roughness of Ag-Cu thin film were characterized using SEM and AFM. Based on the results, the deposition time influences the quality morphology that the thin films have good homogeneity and complete structure for longer deposition time. In addition, from roughness measurement results show that increase deposition time decrease the roughness of thin film. Antimicrobial performance was analyzed using Kirby Bauer Test. The results show that all of sample have good antimicrobial inhibition. Adhesion quality was evaluated using Rockwell C Indentation Test. However, the results indicate that the Ag-Cu thin film has low adhesion strength.

A label-free electrochemical immunosensor based on the novel signal amplification system of AuPdCu ternary nanoparticles functionalized polymer nanospheres.

Science.gov (United States)

Yan, Qin; Yang, Yuying; Tan, Zhaoling; Liu, Qing; Liu, Hui; Wang, Ping; Chen, Lei; Zhang, Daopeng; Li, Yueyun; Dong, Yunhui

2018-04-30

A sensitive label-free electrochemical immunosensor was designed using a novel signal amplification system for quantitative detecting hepatitis B surface antigen (HBsAg). Nitrogen-doped graphene quantum dots (N-GQDs) supported surfactant-free AuPdCu ternary nanoparticles (AuPdCu/N-GQDs), which featured with good conductivity and excellent catalytic properties for the reduction of hydrogen peroxide (H 2 O 2 ), was synthesized by a simple and benign hydrothermal procedure. At the same time, the electroactive polymer nanospheres (PS) was synthesized by infinite coordination polymers of ferrocenedicarboxylic acid, which could play as carrier and electronic mediator to load AuPdCu/N-GQDs. The PS not only improved the ability to load antibodies because of the good biocompatibility, but also accelerated electron transport of the electrode interface attribute to plentiful ferrocene unit. Thus, the prepared AuPdCu/N-GQDs@PS has abilities of good biocompatibility, catalytic activity and electrical conductivity to be applied as transducing materials to amplify electrochemical signal in detection of HBsAg. Under optimal conditions, the fabricated immunosensor exhibited high sensitivity and stability in the detection of HBsAg. A linear relationship between current signals and the concentrations of HBsAg was obtained in the range from 10fg/mL to 50ng/mL and the detection limit of HBsAg was 3.3fg/mL (signal-to-noise ratio of 3). Moreover, the designed immunosensor with excellent selectivity, reproducibility and stability shows excellent performance in detection of human serum samples. Furthermore, this label-free electrochemical immunosensor has promising application in clinical diagnosis of HBsAg. Copyright © 2017 Elsevier B.V. All rights reserved.

Electron emission during interactions of multicharged N and Ar ions with Au(110) and Cu(001) surfaces

International Nuclear Information System (INIS)

Meyer, F.W.; Overbury, S.H.; Havener, C.C.; Zeijlmans van Emmichoven, P.A.; Burgdoerfer, J.; Zehner, D.M.

1991-01-01

We report measurements of energy distributions of electrons emitted during interactions 10q-keV N 6+ , and Ar q+ (q=7,8,9) ions with Au(110) and Cu(001) surfaces at grazing angles. The electron energy distributions have been measured as a function of angle of incidence, observation angle, and target-crystal azimuth. For both Au and Cu targets, the projectile KLL Auger peak observed for the case of the N 6+ projectiles is seen to consist of two components whose intensities have strikingly different dependences on incident perpendicular velocity. The main component of the KLL peak is attributed to subsurface electron emission and is modeled using a Monte Carlo simulation of the projectile trajectories in the bulk. The second component, observed only for the smallest incident perpendicular velocities, is attributed to above-surface KLL Auger electron emission and is modeled using computer simulations of the resonance neutralization-autoionization cascade that occurs prior to projectile penetration of the surface. In the case of the Au target, NNV and NVV transitions, attributed to vacancy transfer from the projectile K shell to the N shell of Au, are also observed. The Monte Carlo simulation of the subsurface contribution to the electron emission is able to reproduce the observed angle-of-incidence dependence of both the projectile and the target Auger electron intensities. In addition, it shows reasonable agreement with the observed dependences of the projectile KLL intensity on observation angle and crystal azimuth

Efficient hole-transporting layer MoO{sub 3}:CuI deposited by co-evaporation in organic photovoltaic cells

Energy Technology Data Exchange (ETDEWEB)

Barkat, L.; Khelil, A. [Universite d' Oran 1 - Ahmed Ben Bella, LPCM2E, Oran (Algeria); Hssein, M. [Universite de Nantes, Institut des Materiaux Jean Rouxel (IMN), CNRS, UMR 6502, Nantes (France); Laboratoire Optoelectronique et Physico-chimie des Materiaux, Universite Ibn Tofail, Faculte des Sciences, Kenitra (Morocco); El Jouad, Z. [Laboratoire Optoelectronique et Physico-chimie des Materiaux, Universite Ibn Tofail, Faculte des Sciences, Kenitra (Morocco); Universite de Nantes, MOLTECH-Anjou, CNRS, UMR 6200, Nantes (France); Cattin, L.; Louarn, G.; Stephant, N. [Universite de Nantes, Institut des Materiaux Jean Rouxel (IMN), CNRS, UMR 6502, Nantes (France); Ghamnia, M. [Universite d' Oran 1 - Ahmed Ben Bella, Laboratoire des Sciences de la Matiere Condensee (LSMC), Oran (Algeria); Addou, M. [Laboratoire Optoelectronique et Physico-chimie des Materiaux, Universite Ibn Tofail, Faculte des Sciences, Kenitra (Morocco); Morsli, M. [Universite de Nantes, Faculte des Sciences et des Techniques, Nantes (France); Bernede, J.C. [Universite de Nantes, MOLTECH-Anjou, CNRS, UMR 6200, Nantes (France)

2017-01-15

In order to improve hole collection at the interface anode/electron donor in organic photovoltaic cells, it is necessary to insert a hole-transporting layer. CuI was shown to be a very efficient hole-transporting layer. However, its tendency to be quite rough tends to induce leakage currents and it is necessary to use a very slow deposition rate for CuI to avoid such negative effect. Herein, we show that the co-deposition of MoO{sub 3} and CuI avoids this difficulty and allows deposition of a homogeneous efficient hole-collecting layer at an acceptable deposition rate. Via an XPS study, we show that blending MoO{sub 3}:CuI improves the hole collection efficiency through an increase of the gap state density. This increase is due to the formation of Mo{sup 5+} following interaction between MoO{sub 3} and CuI. Not only does the co-evaporation process allow for decreasing significantly the deposition time of the hole-transporting layer, but also it increases the efficiency of the device based on the planar heterojunction, CuPc/C{sub 60}. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Deposition of Size-Selected Cu Nanoparticles by Inert Gas Condensation

Directory of Open Access Journals (Sweden)

Martínez E

2009-01-01

Full Text Available Abstract Nanometer size-selected Cu clusters in the size range of 1–5 nm have been produced by a plasma-gas-condensation-type cluster deposition apparatus, which combines a grow-discharge sputtering with an inert gas condensation technique. With this method, by controlling the experimental conditions, it was possible to produce nanoparticles with a strict control in size. The structure and size of Cu nanoparticles were determined by mass spectroscopy and confirmed by atomic force microscopy (AFM and scanning electron transmission microscopy (STEM measurements. In order to preserve the structural and morphological properties, the energy of cluster impact was controlled; the energy of acceleration of the nanoparticles was in near values at 0.1 ev/atom for being in soft landing regime. From SEM measurements developed in STEM-HAADF mode, we found that nanoparticles are near sized to those values fixed experimentally also confirmed by AFM observations. The results are relevant, since it demonstrates that proper optimization of operation conditions can lead to desired cluster sizes as well as desired cluster size distributions. It was also demonstrated the efficiency of the method to obtain size-selected Cu clusters films, as a random stacking of nanometer-size crystallites assembly. The deposition of size-selected metal clusters represents a novel method of preparing Cu nanostructures, with high potential in optical and catalytic applications.

Diffraction by one and two direction periodic antiphase of the AuCu{sub 3} type; Diffraction par les antiphases periodiques a une et deux directions du type AuCu{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Perio, P.; Tournarie, M. [Commissariat a l' energie atomique et aux energies alternatives - CEA, Centre d' Etudes nucleaires de Saclay (France)

1960-07-01

A theory is presented describing the diffraction by periodic antiphase structure in ordered AuCu{sub 3} type alloys. The treatment is rigorous and allows for non-integer periods. The general shape of the amplitude distribution in any 00ι reciprocal plane can be determined without any computation and is given for the six possible configurations of two direction antiphase structures. Reprint of a paper published in Acta Crystallographica, Vol. 12, Part 12, 1959, p. 1032-1038.

Chemical solution deposition of CaCu 3 Ti 4 O 12 thin film

Indian Academy of Sciences (India)

CaCu3Ti4O12 (CCTO) thin film was successfully deposited on boron doped silica substrate by chemical solution deposition and rapid thermal processing. The phase and microstructure of the deposited films were studied as a function of sintering temperature, employing X-ray diffractometry and scanning electron ...

Revelation of graphene-Au for direct write deposition and characterization

Directory of Open Access Journals (Sweden)

Deepa Melepurath

2011-01-01

Full Text Available Abstract Graphene nanosheets were prepared using a modified Hummer's method, and Au-graphene nanocomposites were fabricated by in situ reduction of a gold salt. The as-produced graphene was characterized by X-ray photoelectron spectroscopy, ultraviolet-visible spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy (HR-TEM. In particular, the HR-TEM demonstrated the layered crystallites of graphene with fringe spacing of about 0.32 nm in individual sheets and the ultrafine facetted structure of about 20 to 50 nm of Au particles in graphene composite. Scanning helium ion microscopy (HIM technique was employed to demonstrate direct write deposition on graphene by lettering with gaps down to 7 nm within the chamber of the microscope. Bare graphene and graphene-gold nanocomposites were further characterized in terms of their composition and optical and electrical properties.

Chemical bath deposition of CdS thin films doped with Zn and Cu

Indian Academy of Sciences (India)

Abstract. Zn- and Cu-doped CdS thin films were deposited onto glass substrates by the chemical bath technique. ... Cadmium sulfide; chemical bath deposition; doping; optical window. 1. ..... at low temperature (10 K), finding similar trends than.

Fabrication and characterisation of ligand-functionalised ultrapure monodispersed metal nanoparticle nanoassemblies employing advanced gas deposition technique

Science.gov (United States)

Geremariam Welearegay, Tesfalem; Cindemir, Umut; Österlund, Lars; Ionescu, Radu

2018-02-01

Here, we report for the first time the fabrication of ligand-functionalised ultrapure monodispersed metal nanoparticles (Au, Cu, and Pt) from their pure metal precursors using the advanced gas deposition technique. The experimental conditions during nanoparticle formation were adjusted in order to obtain ultrafine isolated nanoparticles on different substrates. The morphology and surface analysis of the as-deposited metal nanoparticles were investigated using scanning electron microscopy, x-ray diffraction and Fourier transform infra-red spectroscopy, which demonstrated the formation of highly ordered pure crystalline nanoparticles with a relatively uniform size distribution of ∼10 nm (Au), ∼4 nm (Cu) and ∼3 nm (Pt), respectively. A broad range of organic ligands containing thiol or amine functional groups were attached to the nanoparticles to form continuous networks of nanoparticle-ligand nanoassemblies, which were characterised by scanning electron microscopy and x-ray photoelectron spectroscopy. The electrical resistance of the functional nanoassemblies deposited in the gap spacing of two microfabricated parallel Au electrodes patterned on silicon substrates ranged between tens of kΩ and tens of MΩ, which is suitable for use in many applications including (bio)chemical sensors, surface-enhanced Raman spectroscopy and molecular electronic rectifiers.

Thermoelectric Properties of Nanograined Si-Ge-Au Thin Films Grown by Molecular Beam Deposition

Science.gov (United States)

Nishino, Shunsuke; Ekino, Satoshi; Inukai, Manabu; Omprakash, Muthusamy; Adachi, Masahiro; Kiyama, Makoto; Yamamoto, Yoshiyuki; Takeuchi, Tsunehiro

2018-06-01

Conditions to achieve extremely large Seebeck coefficient and extremely small thermal conductivity in Si-Ge-Au thin films formed of nanosized grains precipitated in amorphous matrix have been investigated. We employed molecular beam deposition to prepare Si1- x Ge x Au y thin films on sapphire substrate. The deposited films were annealed under nitrogen gas atmosphere at 300°C to 500°C for 15 min to 30 min. Nanocrystals dispersed in amorphous matrix were clearly observed by transmission electron microscopy. We did not observe anomalously large Seebeck coefficient, but very low thermal conductivity of nearly 1.0 W K-1 m-1 was found at around 0.2 Si-Ge bulk material for which dimensionless figure of merit of ZT ≈ 1 was reported at high temperature.

A study of VMS ore deposits by the proton microprobe

International Nuclear Information System (INIS)

Huston, D.L.; Large, R.R.; Bottril, R.S.; Sie, S.H.; Ryan, C.G.

1991-01-01

As part of studies into the mineralogical distribution of gold in volcanogenic massive sulfide (VMS) ore deposits PIXE analysis by the proton microprobe has been used to determine the gold content of pyrite and arsenopyrite from the Rosebery, Mt. Chalmers and Mt. Lyell deposits. In addition, the concentrations of Co, Ni, Cu, Zn, As, Sr, Y, Zr, Mo, Ag, Sb, Te, Au, Tl, Pb and Bi were also determined. 4 refs., 1 tab

Mineralogy, chemistry of magnetite and genesis of Korkora-1 iron deposit, east of Takab, NW Iran

Directory of Open Access Journals (Sweden)

Mohammad Maanijou

2014-10-01

, respectively. Therefore, it fits in the skarn ore deposit domain in Ni/(Cr + Mn versus Ti + V and Ca + Al + Mn versus Ti + V discrimination diagrams of iron ore deposits (Beaudoin et al., 2007. High Mn in the rock samples of Korkora-1 can be resulted from substitution of Fe+2 by Mn+2 in magnetite structure that can be a sign of hydrothermal skarn. Titanium, Mn, V and Zn show a positive correlation and Al, Cu, Mg, P, Si, Ca, Ni and Cr show a negative correlation with Fe. According to the chemistry of magnetite and plotting them on V2O5 versus TiO2 and V2O5 versus Cr2O3 diagrams, it can be recognized that the samples of Korkora-1 deposit resemble exoskarn magnetite of Goto deposit. The analysis of goethite of Korkora-1 show the amount of 2.5 to 4 wt % SiO2, 76 wt % Fe, and Ni (110 ppm without Ti and Cr in its structure. Mineralographical and geochemical evidence from ore, occurrence of iron in contact with carbonates and skarn mineralogy such as garnet, pyroxene, secondary calcite, epidote and chlorite suggest iron skarn genesis for Korkora-1 deposit. Fluids generated from intrusive bodies like diorite and quartz-diorite with variations in physicochemical conditions, produced skarn in contact with carbonates and volcanic rocks. The heat from intrusive bodies caused recrystallization of carbonates and formed marbles in the footwall of the deposit. Meteoric water has also less important contribution in the ore-forming fluids. Fluid inclusion studies show existing of two types of fluids, a low salinity (10 wt % NaCl equiv. and a medium salinity (25 to 30 wt % NaCl equiv. fluid. Mixing magmatic and meteoric waters makes decreasing in the temperatures and deposition of ore fluids. The Korkora-1 deposit formed in four stages: 1 intruding the intrusive bodies, 2 entering Fe and SiO2 into Qom carbonates and forming calc-silicates, 3 mixing magmatic and meteoric fluids, hydrolysis of calc-silicates, consuming H+, instability of Fe complexes and deposition of iron oxides, 4 retrograde

Magnetic susceptibilities of liquid Cr-Au, Mn-Au and Fe-Au alloys

Energy Technology Data Exchange (ETDEWEB)

Ohno, S.; Shimakura, H. [Niigata University of Pharmacy and Applied Life Sciences, Higashijima, Akiha-ku, Niigata 956-8603 (Japan); Tahara, S. [Faculty of Science, University of the Ryukyus, Nishihara-cho, Okinawa 903-0213 (Japan); Okada, T. [Niigata College of Technology, Kamishin’eicho, Nishi-ku, Niigata 950-2076 (Japan)

2015-08-17

The magnetic susceptibility of liquid Cr-Au, Mn-Au, Fe-Au and Cu-Au alloys was investigated as a function of temperature and composition. Liquid Cr{sub 1-c}Au{sub c} with 0.5 ≤ c and Mn{sub 1-c}Au{sub c} with 0.3≤c obeyed the Curie-Weiss law with regard to their dependence of χ on temperature. The magnetic susceptibilities of liquid Fe-Au alloys also exhibited Curie-Weiss behavior with a reasonable value for the effective number of Bohr magneton. On the Au-rich side, the composition dependence of χ for liquid TM-Au (TM=Cr, Mn, Fe) alloys increased rapidly with increasing TM content, respectively. Additionally, the composition dependences of χ for liquid Cr-Au, Mn-Au, and Fe-Au alloys had maxima at compositions of 50 at% Cr, 70 at% Mn, and 85 at% Fe, respectively. We compared the composition dependences of χ{sub 3d} due to 3d electrons for liquid binary TM-M (M=Au, Al, Si, Sb), and investigated the relationship between χ{sub 3d} and E{sub F} in liquid binary TM-M alloys at a composition of 50 at% TM.

Age and geochemistry of host rocks of the Cobre Panama porphyry Cu-Au deposit, central Panama: Implications for the Paleogene evolution of the Panamanian magmatic arc

Science.gov (United States)

Baker, Michael J.; Hollings, Peter; Thompson, Jennifer A.; Thompson, Jay M.; Burge, Colin

2016-04-01

The Cobre Panama porphyry Cu-Au deposit, located in the Petaquilla district of central Panama, is hosted by a sequence of medium- to high-K calc-alkaline volcanic and sub-volcanic rocks. New crystallisation ages obtained from a granodiorite Petaquilla batholith and associated mineralised diorite to granodiorite porphyry stocks and dikes at Cobre Panama indicate that the batholith was emplaced as a multi-phase intrusion, over a period of 4 million years from 32.20 ± 0.76 Ma to 28.26 ± 0.61 Ma, while the porphyritic rocks were emplaced over a 2 million year period from 28.96 ± 0.62 Ma to 27.48 ± 0.68 Ma. Both the volcanic to sub-volcanic host rocks and intrusive rocks of the Cobre Panama deposit evolved via fractional crystallisation processes, as demonstrated by the major elements (e.g. Al2O3, Fe2O3, TiO2 and MgO) displaying negative trends with increasing SiO2. The Petaquilla intrusive rocks, including the diorite-granodiorite porphyries and granodiorite batholith, are geochemically evolved and appear to have formed from more hydrous magmas than the preceding host volcanic rocks, as evidenced by the presence of hornblende phenocrysts, higher degrees of large-ion lithophile element (LILE) and light rare earth element (LREE) enrichment and heavy rare earth element (HREE) depletion, and higher Sr/Y and La/Yb values. However, the degree of LREE enrichment, HREE depletion and La/Yb values are insufficient for the intrusive rocks to be considered as adakites. Collectively, the volcanic and intrusive rocks have LILE, REE and mobile trace element concentrations similar to enriched Miocene-age Cordilleran arc magmatism found throughout central and western Panama. Both the Petaquilla and Cordilleran arc magmatic suites are geochemically more evolved than the late Cretaceous to Eocene Chagres-Bayano arc magmas from northeastern Panama, as they display higher degrees of LILE and LREE enrichment. The geochemical similarities between the Petaquilla and Cordilleran arc magmas

Deposition of superconducting (Cu, C)-Ba-O films by pulsed laser deposition at moderate temperature

International Nuclear Information System (INIS)

Yamamoto, Tetsuro; Kikunaga, Kazuya; Obara, Kozo; Terada, Norio; Kikuchi, Naoto; Tanaka, Yasumoto; Tokiwa, Kazuyasu; Watanabe, Tsuneo; Sundaresan, Athinarayanan; Shipra

2007-01-01

Superconducting (Cu, C)-Ba-O thin films have been epitaxially grown on (100) SrTiO 3 at a low growth temperature of 500-600 deg. C by pulsed laser deposition. The dependences of their crystallinity and transport properties on preparation conditions have been investigated in order to clarify the dominant parameters for carbon incorporation and the emergence of superconductivity. It has been revealed that the CO 3 content in the films increases with increasing both the parameters of partial pressure of CO 2 during film growth and those of growth rate and enhancement of superconducting properties. The present study has also revealed that the structural and superconducting properties of the (Cu, C)-Ba-O films are seriously deteriorated by the irradiation of energetic particles during deposition. Suppression of the radiation damage is another key for a high and uniform superconducting transition. By these optimizations, a superconducting onset temperature above 50 K and a zero-resistance temperature above 40 K have been realized

Genesis of Pb-Zn-Cu-Ag Deposits within Permian Carboniferous-Carbonate Rocks in Madina Regency, North Sumatra

Directory of Open Access Journals (Sweden)

Bhakti Hamonangan Harahap

2015-09-01

Full Text Available DOI:10.17014/ijog.2.3.167-184Strong mineralized carbonate rock-bearing Pb-Zn-Cu-Ag-(Au ores are well exposed on the Latong River area, Madina Regency, North Sumatra Province. The ore deposit is hosted within the carbonate rocks of the Permian to Carboniferous Tapanuli Group. It is mainly accumulated in hollows replacing limestone in the forms of lensoidal, colloform, veins, veinlets, cavity filling, breccia, and dissemination. The ores dominantly consist of galena (126 000 ppm Pb and sphalerite (2347 ppm Zn. The other minerals are silver, azurite, covellite, pyrite, marcasite, and chalcopyrite. This deposit was formed by at least three phases of mineralization, i.e. pyrite and then galena replaced pyrite, sphalerite replaced galena, and pyrite. The last phase is the deposition of chalcopyrite that replaced sphalerite. The Latong sulfide ore deposits posses Pb isotope ratio of 206Pb/204Pb = 19.16 - 20.72, 207Pb/204Pb = 16.16 - 17.29, and 208Pb/204Pb = 42.92 - 40.78. The characteristic feature of the deposit indicates that it is formed by a sedimentary process rather than an igneous activity in origin. This leads to an interpretation that the Latong deposit belongs to the Sedimentary Hosted Massive Sulfide (SHMS of Mississippi Valley-Type (MVT. The presence of SHMS in the island arc such as Sumatra has become controversial. For a long time, ore deposits in the Indonesian Island Arc are always identical with the porphyry and hydrothermal processes related to arc magmatism. This paper is dealing with the geology of Latong and its base metal deposits. This work is also to interpret their genesis as well as general relationship to the regional geology and tectonic setting of Sumatra.

What is the reason for the doubled unit-cell volumes of copper-lead-rich pavonite homologues?

DEFF Research Database (Denmark)

Topa, Dan; Makovicky, Emil; Balic Zunic, Tonci

2008-01-01

The crystal Structure of cupromakovickyite, ideally Cu8Pb4Ag2Bi18S36, from the skarn deposit at Baita Bihor, in Romania, has been solved by direct methods and refined to an RI index of 5.36% for 2680 unique reflections measured with MOKU radiation oil it four-circle diffractometer equipped...... parameter for cupromakovickyite with respect to makovickyite. To be able to compare them, the crystal structure of Cu-bearing makovickyite, Cu2.25Ag1.56 (Pb0.27Cd0.13)(Sigma 0.4)Bi10.46S18, from a scheelite deposit at Felbertal, in Austria, has been refined to in R, index of 4.36% for 1320 unique...

Theoretical study of PTCDA adsorbed on the coinage metal surfaces, Ag(111), Au(111) and Cu(111)

International Nuclear Information System (INIS)

Romaner, L; Nabok, D; Puschnig, P; Ambrosch-Draxl, C; Zojer, E

2009-01-01

A thorough understanding of the adsorption of molecules on metallic surfaces is a crucial prerequisite for the development and improvement of functionalized materials. A prominent representative within the class of π-conjugated molecules is 3,4,9,10-perylene-tetracarboxylic acid dianhydride (PTCDA) which, adsorbed on the Ag(111), Au(111) or Cu(111) surfaces, shows characteristic trends for work-function modification, alignment of molecular levels with the substrate Fermi energy and binding distances. We carried out density functional theory (DFT) calculations to investigate to what extent these trends can be rationalized on a theoretical basis. We used different density functionals (DF) including a fully non-local van der Waals (vdW) DF capable of describing dispersion interactions. We show that, rather independent of the DF, the calculations yield level alignments and work-function modifications consistent with ultra-violet photoelectron spectroscopy when the monolayer is placed onto the surfaces at the experimental distances (as determined from x-ray standing wave experiments). The lowest unoccupied molecular orbital is occupied on the Ag and Cu surfaces, whereas it remains unoccupied on the Au surface. Simultaneously, the work function increases for Ag but decreases for Cu and Au. Adsorption distances and energies, on the other hand, depend very sensitively on the choice of the DF. While calculations in the local density approximation bind the monolayer consistently with the experimental trends, the generalized gradient approximation in several flavors fails to reproduce realistic distances and energies. Calculations employing the vdW-DF reveal that substantial bonding contributions arise from dispersive interactions. They yield reasonable binding energies but larger binding distances than the experiments.

Deposition of CuIn(Se,S)2 thin films by sulfurization of selenized Cu/In alloys

International Nuclear Information System (INIS)

Sheppard, C.J.; Alberts, V.; Bekker, W.J.

2004-01-01

The relatively small band gap values (close to 1eV) of CuInSe 2 thin films limits the conversion efficiencies of completed CuInSe 2 /CdS/ZnO solar cell devices. In the case of traditional two-stage growth techniques, limited success has been achieved to increase the band gap by substituting indium with gallium. In this study, sputtered copper-indium alloys were exposed to a H 2 Se/Ar atmosphere under defined conditions in order to produce partially reacted CuInSe 2 structures. These films were subsequently exposed to a H 2 S/Ar atmosphere to produce monophasic CuIn(Se, S) 2 quaternary alloys. The homogeneous incorporation of S into CuInSe 2 led to a systematic shift in the lattice parameters and band gap of the ab- sorber films. From these studies optimum selenization/sulfurization conditions were determined for the deposition of homogeneous CuIn(Se,S) 2 thin films with an optimum band gap values between 1.15 and 1.2 eV. (copyright 2004 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Particle growth mechanisms in Ag-ZrO2 and Au-ZrO2 granular films obtained by pulsed laser deposition

International Nuclear Information System (INIS)

Konstantinovic, Zorica; Muro, Montserrat Garcia del; Varela, Manuel; Batlle, Xavier; Labarta, AmIlcar

2006-01-01

Thin films consisting of Ag and Au nanoparticles embedded in amorphous ZrO 2 matrix were grown by pulsed laser deposition in a wide range of metal volume concentrations in the dielectric regime (0.08 Ag Au c (Ag)∼0.28 and x c (Au)∼0.52)

Potential dependent adhesion forces on bare and underpotential deposition modified electrode surfaces

Energy Technology Data Exchange (ETDEWEB)

Serafin, J.M.; Hsieh, S.J.; Monahan, J.; Gewirth, A.A. [Univ. of Illinois, Urbana, IL (United States)

1998-12-03

Adhesion force measurements are used to determine the potential dependence of the force of adhesion between a Si{sub 3}N{sub 4} cantilever and a Au(111) surface modified by the underpotential deposition (upd) of Bi or Cu in acid solution or by oxide formation. The measured work of adhesion is near zero for most of the potential region examined in Bi upd but rises after the formation of a full Bi monolayer. The work of adhesion is high at positive potentials for Cu upd but then decreases as the Cu partial and full monolayers are formed. The work of adhesion is low in the oxide region on Au(111) but rises following the sulfate disordering transition at 1.1 V vs NHE. These results are interpreted in terms of the degree of solvent order on the electrode surface.

Seed-mediated co-reduction in a large lattice mismatch system: synthesis of Pd-Cu nanostructures.

Science.gov (United States)

Kunz, Meredith R; McClain, Sophia M; Chen, Dennis P; Koczkur, Kallum M; Weiner, Rebecca G; Skrabalak, Sara E

2017-06-08

Metal nanoparticles (NPs) are of interest for applications in catalysis, electronics, chemical sensing, and more. Their utility is dictated by their composition and physical parameters such as particle size, particle shape, and overall architecture (e.g., hollow vs. solid). Interestingly, the addition of a second metal to create bimetallic NPs adds multifunctionality, with new emergent properties common. However, synthesizing structurally defined bimetallic NPs remains a great challenge. One synthetic pathway to architecturally controlled bimetallic NPs is seed-mediated co-reduction (SMCR) in which two metal precursors are simultaneously co-reduced to deposit metal onto shape-controlled metal seeds, which direct the overgrowth. Previously demonstrated in a Au-Pd system, here SMCR is applied to a system with a larger lattice mismatch between the depositing metals: Pd and Cu (7% mismatch for Pd-Cu vs. 4% for Au-Pd). Through manipulation of precursor reduction kinetics, the morphology and bimetallic distribution of the resultant NPs can be tuned to achieve eight-branched Pd-Cu heterostructures with Cu localized at the tips of the Pd nanocubes as well as branched Pd-Cu alloyed nanostructures and polyhedra. Significantly, the symmetry of the seeds can be transferred to the final nanostructures. This study expands our understanding of SMCR as a route to structurally defined bimetallic nanostructures and the synthesis of multicomponent nanomaterials more generally.

Controlled synthesis of PbS-Au nanostar-nanoparticle heterodimers and cap-like Au nanoparticles

Science.gov (United States)

Zhao, Nana; Li, Lianshan; Huang, Teng; Qi, Limin

2010-11-01

Uniform PbS-Au nanostar-nanoparticle heterodimers consisting of one Au nanoparticle grown on one horn of a well-defined six-horn PbS nanostar were prepared using the PbS nanostars as growth substrates for the selective deposition of Au nanoparticles. The size of the Au nanoparticles on the horns of the PbS nanostars could be readily adjusted by changing the PbS concentration for the deposition of Au nanoparticles. An optimum cetyltrimethylammonium bromide concentration and temperature were essential for the selective deposition of uniform Au nanoparticles on single horns of the PbS nanostars. Unusual PbS-Au nanoframe-nanoparticle heterodimers were obtained by etching the PbS-Au nanostar-nanoparticle heterodimers with oxalic acid while novel cap-like Au nanoparticles were obtained by etching with hydrochloric acid. The obtained heterodimeric nanostructures and cap-like nanoparticles are promising candidates for anisotropic nanoscale building blocks for the controllable assembly of useful, complex architectures.

Building energetic material from novel salix leaf-like CuO and nano-Al through electrophoretic deposition

Energy Technology Data Exchange (ETDEWEB)

Yin, Yan Jun; Li, Xueming [College of Chemistry and Chemical Engineering, Chongqing University, Chongqing (China)

2016-11-15

In this study, an energetic material was prepared by depositing nano-Al on CuO arrays via electrophoretic deposition (EPD), which offers a feasible route for nano-Al integration. The morphology and structure of the CuO arrays and Al/CuO composites were characterized by scanning electron microscopy and X-ray diffraction. The CuO arrays were homogenously salix leaf-like structure with a width of ⁓150 to 200 nm. The energy density of Al/CuO composites was approximate to 1454.5 J/g by integrating the differential scanning calorimetry (DSC) plot and the combustion performance was recorded by a high-speed camera. Moreover, the combustion flames were violent and the whole reaction process only lasted 72.2 ms, indicating that the energy of the Al/CuO nanothermite can be released effectively.

CuInS{sub 2} thin films obtained through the annealing of chemically deposited In{sub 2}S{sub 3}-CuS thin films

Energy Technology Data Exchange (ETDEWEB)

Pena, Y., E-mail: yolapm@gmail.com [Facultad de Ciencias Quimicas, Universidad Autonoma de Nuevo Leon, Pedro de Alba S/N, Ciudad Universitaria, 66451, San Nicolas de los Garza, Nuevo Leon (Mexico); Lugo, S. [Facultad de Ciencias Quimicas, Universidad Autonoma de Nuevo Leon, Pedro de Alba S/N, Ciudad Universitaria, 66451, San Nicolas de los Garza, Nuevo Leon (Mexico); Calixto-Rodriguez, M. [Centro de Investigacion en Energia, Universidad Nacional Autonoma de Mexico, Privada Xochicalco S/N, Col Centro, 62580, Temixco, Morelos (Mexico); Vazquez, A.; Gomez, I.; Elizondo, P. [Facultad de Ciencias Quimicas, Universidad Autonoma de Nuevo Leon, Pedro de Alba S/N, Ciudad Universitaria, 66451, San Nicolas de los Garza, Nuevo Leon (Mexico)

2011-01-01

In this work, we report the formation of CuInS{sub 2} thin films on glass substrates by heating chemically deposited multilayers of copper sulfide (CuS) and indium sulfide (In{sub 2}S{sub 3}) at 300 and 350 deg. C in nitrogen atmosphere at 10 Torr. CIS thin films were prepared by varying the CuS layer thickness in the multilayers with indium sulfide. The XRD analysis showed that the crystallographic structure of the CuInS{sub 2} (JCPDS 27-0159) is present on the deposited films. From the optical analysis it was estimated the band gap value for the CIS film (1.49 eV). The electrical conductivity varies from 3 x 10{sup -8} to 3 {Omega}{sup -1} cm{sup -1} depending on the thickness of the CuS film. CIS films showed p-type conductivity.

X-ray fluorescence holography studies for a Cu{sub 3}Au crystal

Energy Technology Data Exchange (ETDEWEB)

Dąbrowski, K.M., E-mail: karol.dabrowski@uj.edu.pl; Dul, D.T.; Jaworska-Gołąb, T.; Rysz, J.; Korecki, P.

2015-12-01

In this work we show that performing a numerical correction for beam attenuation and indirect excitation allows one to fully restore element sensitivity in the three-dimensional reconstruction of the atomic structure. This is exemplified by a comparison of atomic images reconstructed from holograms measured for ordered and disordered phases of a Cu{sub 3}Au crystal that clearly show sensitivity to changes in occupancy of the atomic sites. Moreover, the numerical correction, which is based on quantitative methods of X-ray fluorescence spectroscopy, was extended to take into account the influence of a disturbed overlayer in the sample.

Effect of Annealing Temperature on Flowerlike Cu3BiS3 Thin Films Grown by Chemical Bath Deposition

Science.gov (United States)

Deshmukh, S. G.; Patel, S. J.; Patel, K. K.; Panchal, A. K.; Kheraj, Vipul

2017-10-01

For widespread application of thin-film photovoltaic solar cells, synthesis of inexpensive absorber material is essential. In this work, deposition of ternary Cu3BiS3 absorber material, which contains abundant and environmentally benign elements, was carried out on glass substrate. Flowerlike Cu3BiS3 thin films with nanoflakes as building block were formed on glass substrate by chemical bath deposition. These films were annealed at 573 K and 673 K in sulfur ambient for structural improvement. Their structure was characterized using Raman spectroscopy, as well as their surface morphological and optical properties. The x-ray diffraction profile of as-deposited Cu3BiS3 thin film revealed amorphous structure, which transformed to orthorhombic phase after annealing. The Raman spectrum exhibited a characteristic peak at 290 cm-1. Scanning electron microscopy of as-deposited Cu3BiS3 film confirmed formation of nanoflowers with diameter of around 1052 nm. Wettability testing of as-deposited Cu3BiS3 thin film demonstrated hydrophobic nature, which became hydrophilic after annealing. The measured ultraviolet-visible (UV-Vis) absorption spectra of the Cu3BiS3 thin films gave an absorption coefficient of 105 cm-1 and direct optical bandgap of about 1.42 eV after annealing treatment. Based on all these results, such Cu3BiS3 material may have potential applications in the photovoltaic field as an absorber layer.

Chemical bath deposition of Cu{sub 3}BiS{sub 3} thin films

Energy Technology Data Exchange (ETDEWEB)

Deshmukh, S.G., E-mail: deshmukhpradyumn@gmail.com; Vipul, Kheraj, E-mail: vipulkheraj@gmail.com [Department of Applied Physics, Sardar Vallabhbhai National Institute of Technology, Ichchhanath, Surat (India); Panchal, A.K. [Department of Electrical Engineering, Sardar Vallabhbhai National Institute of Technology, Ichchhanath, Surat (India)

2016-05-06

First time, copper bismuth sulfide (Cu{sub 3}BiS{sub 3}) thin films were synthesized on the glass substrate using simple, low-cost chemical bath deposition (CBD) technique. The synthesized parameters such as temperature of bath, pH and concentration of precursors were optimized for the deposition of uniform, well adherent Cu{sub 3}BiS{sub 3} thin films. The optical, surface morphology and structural properties of the Cu{sub 3}BiS{sub 3} thin films were studied using UV-VIS-NIR spectra, scanning electron microscopy (SEM) and X-ray diffraction (XRD). The as- synthesized Cu{sub 3}BiS{sub 3} film exhibits a direct band gap 1.56 to 1.58 eV having absorption coefficient of the order of 10{sup 5} cm{sup −1}. The XRD declares the amorphous nature of the films. SEM images shows films were composed of close-packed fine spherical nanoparticles of 70-80 nm in diameter. The chemical composition of the film was almost stoichiometric. The optical study indicates that the Cu{sub 3}BiS{sub 3} films can be applied as an absorber layer for thin film solar cells.

The d-band of disordered Cu3Au as determined by constant initial state photoemission spectroscopy: a search for the origins of the disorder/order phase transition

International Nuclear Information System (INIS)

Stampfl, A.P.J.; Riley, J.D.; Leckey, R.C.G.

1998-01-01

Full text: Binary alloys must either order or phase separate as the temperature is lowered. Substitutionally disordered Cu 3 Au is known to order below a transition temperature of T c =390 deg C. The driving force (of ordering) is believed to be the lowering of free energy as a result of changes to the electronic and compositional structure. Details of the role that particular electronic levels play and the amount of coupling between the electronic and phonon structures, is as yet not fully understood. Gyorffy and Stocks have indeed suggested that instabilities in the electronic structure of the Fermi surface of Cu-Pd alloys may be the driving force for the disorder/order phase transition. It is expected, however, that the Fermi surfaces of ordered and disordered Cu 3 Au to be nearly similar. Our work on the Fermi surface of disordered Cu 3 Au supports this view. Large differences, however, are observed in the d-band region between the ordered and disordered phases and it has been suggested that these states may exhibit a type of electronic instability upon approaching T c . We present our initial study of the d-band region of disordered Cu 3 Au using a constant initial state spectroscopy technique which we previously developed to map the Fermi surface of Cu. Our technique allows the accurate k-space mapping of very flat bands such as d-levels. The k-space shape of the d-bands are compared to calculation and a discussion is given as to their likely role in the phase transition

The conjunction of factors that lead to formation of giant gold provinces and deposits in non-arc settings

Directory of Open Access Journals (Sweden)

David I. Groves

2016-05-01

In contrast to their province scale similarities, the different giant gold deposit styles show contrasting critical controls at the district to deposit scale. For orogenic gold deposits, the giants appear to have formed by conjunction of a greater number of parameters to those that control smaller deposits, with resultant geometrical and lithostratigraphic complexity as a guide to their location. There are few giant IRGS due to their inferior fluid-flux systems relative to orogenic gold deposits, and those few giants are essentially preservational exceptions. Many Carlin-type deposits are giants due to the exceptional conjunction of both structural and lithological parameters that caused reactive and permeable rocks, enriched in syngenetic gold, to be located below an impermeable cap along antiformal “trends”. Hydrocarbons probably played an important role in concentrating metal. The supergiant Post-Betze deposit has additional ore zones in strain heterogeneities surrounding the pre-gold Goldstrike stock. All unequivocal IOCG deposits are giant or near-giant deposits in terms of gold-equivalent resources, partly due to economic factors for this relatively poorly understood, low Cu-Au grade deposit type. The supergiant Olympic Dam deposit, the most shallowly formed deposit among the larger IOCGs, probably owes its origin to eruption of volatile-rich hybrid magma at surface, with formation of a large maar and intense and widespread brecciation, alteration and Cu-Au-U deposition in a huge rock volume.

Patterned electrochemical deposition of copper using an electron beam

Directory of Open Access Journals (Sweden)

Mark den Heijer

2014-02-01

Full Text Available We describe a technique for patterning clusters of metal using electrochemical deposition. By operating an electrochemical cell in the transmission electron microscope, we deposit Cu on Au under potentiostatic conditions. For acidified copper sulphate electrolytes, nucleation occurs uniformly over the electrode. However, when chloride ions are added there is a range of applied potentials over which nucleation occurs only in areas irradiated by the electron beam. By scanning the beam we control nucleation to form patterns of deposited copper. We discuss the mechanism for this effect in terms of electron beam-induced reactions with copper chloride, and consider possible applications.

Pressure-temperature condition and hydrothermal-magmatic fluid evolution of the Cu-Mo Senj deposit, Central Alborz: fluid inclusion evidence

Directory of Open Access Journals (Sweden)

Ebrahim Tale Fazel

2017-02-01

Full Text Available Introduction The Senj deposit has significant potential for different types of mineralization, particularly porphyry-like Cu deposits, associated with subduction-related Eocene–Oligocene calc-alkaline porphyritic volcano-plutonic rocks. The study of fluid inclusions in hydrothermal ore deposits aims to identify and characterize the pressure, temperature, volume and fluid composition, (PTX conditions of fluids under which they were trapped (Heinrich et al., 1999; Ulrich and Heinrich, 2001; Redmond et al., 2004. Different characteristics of the deposit such as porphyrtic nature, alteration assemblage and the quartz-sulfide veins of the stockwork were poorly known. In this approach on the basis of alterations, vein cutting relationship and field distribution of fluid inclusions, the physical and chemical evolution of the hydrothermal system forming the porphyry Cu-Mo (±Au-Ag deposit in Senj is reconstructed. Materials and Methods Over 1000 m of drill core was logged at a scale of 1:1000 by Pichab Kavosh Co. and samples containing various vein and alteration types from different depths were collected for laboratory analyses. A total of 14 samples collected from the altered and least altered igneous rocks in the Senj deposit were analyzed for their major oxide concentrations by X-ray fluorescence in the SGS Mineral Services (Toronto, Canada. The detection limit for major oxide analysis is 0.01%. Trace and rare earth elements (REE were analyzed using inductively coupled plasma-mass spectrometery (ICP-MS, in the commercial laboratory of SGS Mineral Services. The analytical error for most elements is less than 2%. The detection limit for trace elements and REEs analysis is 0.01 to 0.1 ppm. Fluid inclusion microthermometry was conducted using a Linkam THMS600 heating–freezing stage (-190 °C to +600 °C mounted on a ZEISS Axioplan2 microscope in the fluid inclusion laboratory of the Iranian Mineral Processing Research Center (Karaj, Iran. Results

Chemical solution deposition of CaCu3Ti4O12 thin film

Indian Academy of Sciences (India)

Administrator

CaCu3Ti4O12; thin film; chemical solution deposition; dielectric properties. 1. Introduction. The CaCu3Ti4O12. (CCTO) compound has recently attracted considerable ... and Kelvin probe force microscopy (Chung et al 2004). Intrinsic .... SEM images of CCTO thin films as a function of sintering temperature. silicon based ...

Deposition of nanocomposite Cu-TiO2 using heterogeneous colliding plasmas

Science.gov (United States)

Pandey, Pramod K.; Thareja, Raj K.; Singh, Ravi Pratap; Costello, John T.

2018-03-01

The formation of CuTiO2 nanocomposites has been observed in an experiment in which laser plasma plumes of Cu and Ti collide and stagnate in an oxygen atmosphere. The inherent advantage of this technique lies in its simplicity and flexibility where laser, target composition and geometry along with ambient atmosphere are all controllable parameters through which the stoichiometry of the deposited nanocomposites may be selected. The experiment has been performed at three oxygen ambient pressures 10-4, 10-2, 100 mbar and we observe its effect on stoichiometry, and morphology of the deposited nanocomposites. Here, we show how the stoichiometry of deposited nanocomposites can be readily controlled by changing just one parameter, namely the ambient oxygen pressure. The different peaks of photoluminescence spectra λ =390{ nm}( {E=3.18{ eV}} ) corresponding to the anatase phase of TiO2, along with the peaks at λ = 483 nm ( E = 2.56 eV) and 582 nm ( E = 2.13 eV) of deposited nanocomposites, shows the doping/blending effect on the band gaps which may potentially be of value in solar cell technology. The technique can, in principle, be extended to include nanocomposites of other materials making it potentially more widely applicable.

Surface-driven, one-step chemical vapor deposition of γ-Al{sub 4}Cu{sub 9} complex metallic alloy film

Energy Technology Data Exchange (ETDEWEB)

Prud’homme, Nathalie [CIRIMAT, Université de Toulouse - CNRS, 4 allée Emile Monso, BP-44362, 31432 Toulouse Cedex 4 (France); Université Paris-Sud 11, LEMHE/ICMMO, Bat 410, 91405 Orsay Cedex (France); Duguet, Thomas, E-mail: thomas.duguet@ensiacet.fr [CIRIMAT, Université de Toulouse - CNRS, 4 allée Emile Monso, BP-44362, 31432 Toulouse Cedex 4 (France); Samélor, Diane; Senocq, François; Vahlas, Constantin [CIRIMAT, Université de Toulouse - CNRS, 4 allée Emile Monso, BP-44362, 31432 Toulouse Cedex 4 (France)

2013-10-15

The present paper is a paradigm for the one-step formation of complex intermetallic coatings by chemical vapor deposition. It genuinely addresses the challenge of depositing an intermetallic coating with comparable contents of Cu and Al. Depending on processing conditions, a pure γ-Al{sub 4}Cu{sub 9} and multi-phase Al-Cu films are grown with wetting properties of the former being similar to its bulk counterpart. The deposition process and its parametric investigation are detailed. Two metalorganic precursors are used taking into account their transport and chemical properties, and deposition temperature ranges. On line and ex situ characterizations enlighten the competition which occurs at the growing surface between molecular fragments, and which limits growth rates. Notably, introducing a partial pressure of hydrogen gas during deposition reduces Al growth rate from dimethylethylamine alane (DMEAA), by displacing the hydrogen desorption equilibrium. This Al partial growth rate decrease is not sufficient to achieve a Cu/Al atomic ratio that is high enough for the formation of intermetallics with close Al and Cu compositions. A fivefold increase of the flux of the gaseous copper(I) cyclopentadienyl triethylphosphine CpCuPEt{sub 3}, whereas the DMEAA flux remains constant, results in the targeted Al/Cu atomic ratio equal to 44/56. Nevertheless, the global growth rate is rendered extremely low by the deposition inhibition caused by a massive phosphine adsorption (-PEt{sub 3}). Despite these limitations, the results pave the way towards the conformal coating of complex surface geometries by such intermetallic compounds.

Mineralogy and geochemistry of Skarn Fe orebody and syenodioritic intrusive host rock in Zeber Kuh prospect area (SW Bardaskan, South Khorasan province

Directory of Open Access Journals (Sweden)

Hossein Narooie

2017-11-01

Full Text Available The Zeber Kuh prospect area is located southwest of Bardaskan, South Khorasan province, in the northeastern Iran. Lithologically, the area includes Rizu and Soltanieh Formations metamorphosed carbonate rocks, which were intruded by syenogranitic and syenodioritic intrusions. Field observations and laboratory studies such as structural controls of orebody, metasomatic replacement and formation of low temperature H2O-bearing minerals, and the occurrence of magnetite and pyrite associated with chlorite, epidote, calcite, and quartz indicate that  the iron mineralization is low temperature skarn-type. The source of Fe mineralization is probably a younger intrusive rock at depth. Hydrothermal ore fluid was ascended within fault zone and/or contact between the intrusive rock and the  carbonate unit and generated orebody. Iron grade ranges from 54 to 65 wt.% and sulfur value is > 3 wt.%. Magnetite chemistry and Ti, V, Al, Mn, Ni, and Cr contents are similar to skarn deposit. Biotite syenodiorite host rock has hypidiomorphic granular texture and it consists of plagioclase, K-feldspar, biotite, and apatite minerals. Chemically, this intrusive rock is K-series alkaline type, which was generated in within plate zone. This magma is characterized by strong enrichment in LREE, LILE (Rb, Cs, Ba, and K, HFSE (Nb, Zr, and Ti, and P elements. The primary magma is produced by low degree partial melting of garnet lherzolite from asthenospheric to boundary of asthenospheric-lithospheric mantle.

Atmospheric Pressure Spray Chemical Vapor Deposited CuInS2 Thin Films for Photovoltaic Applications

Science.gov (United States)

Harris, J. D.; Raffaelle, R. P.; Banger, K. K.; Smith, M. A.; Scheiman, D. A.; Hepp, A. F.

2002-01-01

Solar cells have been prepared using atmospheric pressure spray chemical vapor deposited CuInS2 absorbers. The CuInS2 films were deposited at 390 C using the single source precursor (PPh3)2CuIn(SEt)4 in an argon atmosphere. The absorber ranges in thickness from 0.75 - 1.0 micrometers, and exhibits a crystallographic gradient, with the leading edge having a (220) preferred orientation and the trailing edge having a (112) orientation. Schottky diodes prepared by thermal evaporation of aluminum contacts on to the CuInS2 yielded diodes for films that were annealed at 600 C. Solar cells were prepared using annealed films and had the (top down) composition of Al/ZnO/CdS/CuInS2/Mo/Glass. The Jsc, Voc, FF and (eta) were 6.46 mA per square centimeter, 307 mV, 24% and 0.35%, respectively for the best small area cells under simulated AM0 illumination.

Characterization of hafnium oxide resistive memory layers deposited on copper by atomic layer deposition

Energy Technology Data Exchange (ETDEWEB)

Briggs, B.D.; Bishop, S.M. [SUNY College of Nanoscale Science and Engineering, 255 Fuller Road, Albany, NY 12203 (United States); Leedy, K.D. [Air Force Research Laboratory, 2241 Avionics Circle, Wright Patterson Air Force Base, Dayton, OH 45433 (United States); Cady, N.C., E-mail: ncady@albany.edu [SUNY College of Nanoscale Science and Engineering, 255 Fuller Road, Albany, NY 12203 (United States)

2014-07-01

Hafnium oxide-based resistive memory devices have been fabricated on copper bottom electrodes. The HfO{sub x} active layers in these devices were deposited by atomic layer deposition (ALD) at 250 °C with tetrakis(dimethylamido)hafnium(IV) as the metal precursor and an O{sub 2} plasma as the reactant. Depth profiles of the HfO{sub x} by X-ray photoelectron spectroscopy and secondary ion mass spectroscopy revealed a copper concentration on the order of five atomic percent throughout the HfO{sub x} film. In addition to the Cu doped HfO{sub x}, a thin layer (20 nm) of Cu{sub x}O is present at the surface. This surface layer is believed to have formed during the ALD process, and greatly complicates the analysis of the switching mechanism. The resistive memory structures fabricated from the ALD HfO{sub x} exhibited non-polar resistive switching, independent of the top metal electrode (Ni, Pt, Al, Au). Resistive switching current voltage (I–V) curves were analyzed using Schottky emission and ionic hopping models to gain insight into the physical mechanisms underpinning the device behavior. During the forming process it was determined that, at voltages in excess of 2.5 V, an ionic hopping model is in good agreement with the I–V data. The extracted ion hopping distance ∼ 4 Å was within the range of interatomic spacing of HfO{sub 2} during the forming process consistent with ionic motion of Cu{sup 2+} ions. Lastly the on state I–V data was dominated at larger voltages by Schottky emission with an estimated barrier height of ∼ 0.5 eV and a refractive index of 2.59. The consequence of the Schottky emission analysis indicates the on state resistance to be a product of a Pt/Cu{sub 2}O/Cu filament(s)/Cu{sub 2}O/Cu structure. - Highlights: • HfO{sub 2} was grown via atomic layer deposition at 250 and 100 °C on Cu substrates. • A Cu{sub 2}O surface layer and Cu doping were observed in post-deposition of HfO{sub 2}. • Resistive memory devices were fabricated and

A Molecular Dynamics Study of the Epitaxial Growth of Metallic Nanoclusters Softly Deposited on Substrates with Very Different Lattice Parameter

International Nuclear Information System (INIS)

Jimenez-Saez, J C; Perez-MartIn, A M C; Jimenez-RodrIguez, J J

2007-01-01

The soft deposition of Cu and Au clusters on Au(001) and Cu(001) surfaces respectively is studied by constant-temperature molecular-dynamics simulations. The initial shape of the nanoclusters is icosahedral or truncated octahedral (Wulff type). Their number of atoms ranges between 12 and 1289 atoms. Bombardment energy is of the order of a few meV/atom. The atomic interactions are mimicked by a many-body potential based on the tightbinding model. The effect of the temperature as activation to get the complete epitaxy is analysed. We have found that Cu clusters manage to align their {002} planes with the substrate by increasing the temperature. However, there is not epitaxial growth in any case since the lattice becomes bcc or important stacking faults are generated. For Au clusters, the alignment of these planes is practically independent of the temperature

Effects of deposition period on the chemical bath deposited Cu4SnS4 thin films

International Nuclear Information System (INIS)

Kassim, Anuar; Wee Tee, Tan; Soon Min, Ho.; Nagalingam, Saravanan

2010-01-01

Cu 4 SnS 4 thin films were prepared by simple chemical bath deposition technique. The influence of deposition period on the structural, morphological and optical properties of films was studied. The films were characterized using X-ray diffraction, atomic force microscopy and UV-Vis Spectrophotometer. X-ray diffraction patterns indicated that the films were polycrystalline with prominent peak attributed to (221) plane of orthorhombic crystal structure. The films prepared at 80 min showed significant increased in the intensity of all diffractions. According to AFM images, these films indicated that the surface of substrate was covered completely. The obtained films also produced higher absorption characteristics when compared to the films prepared at other deposition periods based on optical absorption studies. The band gap values of films deposited at different deposition periods were in the range of 1.6-2.1 eV. Deposition for 80 min was found to be the optimum condition to produce good quality thin films under the current conditions. (author).

Mineralogy, geochemistry and origin of Zafarabad iron deposit based on REE and trace elements of magnetite

Directory of Open Access Journals (Sweden)

Mehrdad Barati

2013-10-01

Full Text Available Zafarabad iron deposit is located northwest of Divandareh, in the northern margin of Sanandaj-Sirjan plutonic-metamorphic zone. The deposit is in lentoid to tubular shape, within a shear zone and occrrued in host rocks of calc-schist and limestone. Magnetite with massive, cataclastic and replacement textures are the main phases, while pyrite and other sulfide minerals are found. Major and trace elements are measured by ICP-MS and ICP-AES methods. Based on some ratios of trace elements in the ore samples and (Ti+V vs. Cal+Al+Mn and Ti+V vs. Ni/(Cr+Mn diagrams which are used for classification of iron deposit types, Zafarabad iron deposit fall in the range of skarn deposits. Spider diagrams show a steady decline from LREE to HREE elements with Eu (mean value of 0.06 ppm and Ce (mean value of 0.94 ppm negative anomalies. Comparing the distribution patterns of REE for the Zafarabad magnetites with those of various types of iron deposits shows that the REE pattern for Zafarabad is similar to these deposits. Analysis of calculated parameters for REE shows that the hydrothermal fluids responsible for mineralization are mainly of magmatic origin through fractionation and crystallization processes of a deep iron rich fluid phase and its emplacement within the carbonate rocks, forming iron skarn.

Study of Cu2O\\ZnO nanowires heterojunction designed by combining electrodeposition and atomic layer deposition

Science.gov (United States)

Makhlouf, Houssin; Weber, Matthieu; Messaoudi, Olfa; Tingry, Sophie; Moret, Matthieu; Briot, Olivier; Chtoutou, Radhouane; Bechelany, Mikhael

2017-12-01

Cu2O/ZnO nanowires (NWs) heterojunctions were successfully prepared by combining Atomic layer Deposition (ALD) and Electrochemical Deposition (ECD) processes. The crystallinity, morphology and photoconductivity properties of the Cu2O/ZnO nanostructures have been investigated. The properties of the Cu2O absorber layer and the nanostructured heterojunction were studied in order to understand the mechanisms lying behind the low photoconductivity measured. It has been found that the interface state defects and the high resistivity of Cu2O film were limiting the photovoltaic properties of the prepared devices. The understanding presented in this work is expected to enable the optimization of solar cell devices based on Cu2O/ZnO nanomaterials and improve their overall performance.

Impact of deposition rate on the structural and magnetic properties of sputtered Ni/Cu multilayer thin films

Energy Technology Data Exchange (ETDEWEB)

Karpuz, Ali [Karamanoglu Mehmetbey Univ., Karaman (Turkey). Dept. of Physics; Colmekci, Salih; Kockar, Hakan; Kuru, Hilal; Uckun, Mehmet [Balikesir Univ. (Turkey). Dept. of Physics

2018-04-01

The structural and corresponding magnetic properties of Ni/Cu films sputtered at low and high deposition rates were investigated as there is a limited number of related studies in this field. 5[Ni(10 nm)/Cu(30 nm)] multilayer thin films were deposited using two DC sputtering sources at low (0.02 nm/s) and high (0.10 nm/s) deposition rates of Ni layers. A face centered cubic phase was detected for both films. The surface of the film sputtered at the low deposition rate has a lot of micro-grains distributed uniformly and with sizes from 0.1 to 0.4 μm. Also, it has a vertical acicular morphology. At high deposition rate, the number of micro-grains considerably decreased, and some of their sizes increased up to 1 μm. The surface of the Ni/Cu multilayer deposited at the low rate has a relatively more grainy and rugged structure, whereas the surface of the film deposited at the high rate has a relatively larger lateral size of surface grains with a relatively fine morphology. Saturation magnetisation, M{sub s}, values were 90 and 138 emu/cm{sup 3} for deposition rates of 0.02 and 0.10 nm/s, respectively. Remanence, M{sub r}, values were also found to be 48 and 71 emu/cm{sup 3} for the low and high deposition rates, respectively. The coercivity, H{sub c}, values were 46 and 65 Oe for the low and high Ni deposition rates, respectively. The changes in the film surfaces provoked the changes in the H{sub c} values. The M{sub s}, M{sub r}, and H{sub c} values of the 5[Ni(10 nm)/Cu(30 nm)] films can be adjusted considering the surface morphologies and film contents caused by the different Ni deposition rates.

Rhodium deposition onto a 4-mercaptopyridine SAM on Au(1 1 1)

Energy Technology Data Exchange (ETDEWEB)

Manolova, M. [Institute of Electrochemistry, University of Ulm, 89069 Ulm (Germany); Kayser, M. [Institute of Electrochemistry, University of Ulm, 89069 Ulm (Germany); Kolb, D.M. [Institute of Electrochemistry, University of Ulm, 89069 Ulm (Germany)]. E-mail: dieter.kolb@uni-ulm.de; Boyen, H.-G. [Institute of Solid State Physics, University of Ulm, 89069 Ulm (Germany); Ziemann, P. [Institute of Solid State Physics, University of Ulm, 89069 Ulm (Germany); Mayer, D. [BASF Electronic Materials GmbH, 67056 Ludwigshafen (Germany); Wirth, A. [BASF Electronic Materials GmbH, 67056 Ludwigshafen (Germany)

2007-02-10

The application of a recently developed method for the deposition of Pd and Pt on top of a SAM, has been successfully extended to Rh, thus proving the versatility of the new concept. Experimental evidence from cyclic voltammetry, in situ STM and ex situ X-ray photoemission spectroscopy is presented for the deposition of monoatomic high rhodium islands onto a 4-mercaptopyridine self-assembled monolayer on a Au(1 1 1) electrode. By repetitive complexation of the Rh ions to the ring-nitrogen and reduction in a Rh-ion free solution, an almost completely covered SAM is obtained. The consequences of making contacts for molecular electronics are briefly discussed.

Stress-Strain Analysis in TiN Nanocoating Deposited on Polymer with respect to Au Nanointerlayer

Directory of Open Access Journals (Sweden)

Magdalena Kopernik

2014-01-01

Full Text Available The multiscale analysis in the authors’ finite element code confirmed possibility of fracture, because of not sufficiently high level of compressive residual stress in the TiN deposited by physical deposition method and varied mechanical properties of the thin film and substrate. The residual stress cannot be identified by X-ray technique for amorphous polymer and layer with domains of crystalline TiN. It is assumed that the buffer biocompatible thin film of Au in the TiN/Bionate II material system will alter the evolution of residual stress and, therefore, will allow to determine the residual stress in profilometry studies, and helps to improve toughness of the connection between TiN and Bionate II. The introduction of Au nanocoating in the material system results in bending of the sample and a compressive residual stress in the TiN coating. Results of finite element simulation show improvement of connection between the polymer and TiN, and an increase of compressive residual stress in the coating by introduction of Au nanointerlayer results in reduction of stress and strain in the substrate (close to the boundary between substrate and coating.

Guided selective deposition of nanoparticles by tuning of the surface potential

Science.gov (United States)

Eklöf, J.; Stolaś, A.; Herzberg, M.; Pekkari, A.; Tebikachew, B.; Gschneidtner, T.; Lara-Avila, S.; Hassenkam, T.; Moth-Poulsen, K.

2017-07-01

Guided deposition of nanoparticles onto different substrates is of great importance for a variety of applications such as biosensing, targeted cancer therapy, anti-bacterial coatings and single molecular electronics. It is therefore important to gain an understanding of what parameters are involved in the deposition of nanoparticles. In this work we have deposited 60 nm, negatively charged, citrate stabilized gold nanoparticles onto microstructures consisting of six different materials, (vanadium (V), silicon dioxide (SiO2), gold (Au), aluminum (Al), copper (Cu) and nickel (Ni)). The samples have then been investigated by scanning electron microscopy to extract the particle density. The surface potential was calculated from the measured surface charge density maps measured by atomic force microscopy while the samples were submerged in a KCl water solution. These values were compared with literature values of the isoelectric points (IEP) of different oxides formed on the metals in an ambient environment. According to measurements, Al had the highest surface potential followed by Ni and Cu. The same trend was observed for the nanoparticle densities. No particles were found on V, SiO2 and Au. The literature values of the IEP showed a different trend compared to the surface potential measurements concluding that IEP is not a reliable parameter for the prediction of NP deposition. Contribution to the Focus Issue Self-assemblies of Inorganic and Organic Nanomaterials edited by Marie-Paule Pileni.

Deposition and characterization of CuInSe2 thin films

International Nuclear Information System (INIS)

Dhere, N.G.; Ferreira, C.L.; Cruz, L.R.O.; Mattoso, I.G.; Alves, R.M.P.

1988-01-01

CuInSe 2 thin films with 1,3 to 1,7 μm of thickness were deposited by the constituent elements (copper, indium and selenium) in glass substrate. The producted films were characterized by scanning microscopy, X-ray diffraction, Auger electron spectroscopy, Hall effect measures and optical absorption. (C.G.C.) [pt

Processing of CuInSe2-Based Solar Cells: Characterization of Deposition Processes in Terms of Chemical Reaction Analyses. Final Report, 6 May 1995 - 31 December 1998

Energy Technology Data Exchange (ETDEWEB)

Anderson, T.J.; Stanbery, B.J.

2001-07-16

This project describes a novel rotating-disc reactor has been designed and built to enable modulated flux deposition of CuInSe2 and its related binary compounds. The reactor incorporates both a thermally activated source and a novel plasma-activated source of selenium vapor, which have been used for the growth of epitaxial and polycrystalline thin-film layers of CuInSe2. A comparison of the different selenium reactant sources has shown evidence of increases in its incorporation when using the plasma source, but no measurable change when the thermally activated source was used. We concluded that the chemical reactivity of selenium vapor from the plasma source is significantly greater than that provided by the other sources studied. Epitaxially grown CuInSe2 layers on GaAs, ZnTe, and SrF2 demonstrate the importance of nucleation effects on the morphology and crystallographic structure of the resulting materials. These studies have resulted in the first reported growth of the CuAu type-I crystallographic polytype of CuInSe2, and the first reported epitaxial growth of CuInSe2 on ZnTe. Polycrystalline binary (Cu,Se) and (In,Se) thin films have been grown, and the molar flux ratio of selenium to metals was varied. It is shown that all of the reported binary compounds in each of the corresponding binary phase fields can be synthesized by the modulated flux deposition technique implemented in the reactor by controlling this ratio and the substrate temperature. These results were employed to deposit bilayer thin films of specific (Cu,Se) and (In,Se) compounds with low melting-point temperature, which were used to verify the feasibility of synthesizing CuInSe2 by subsequent rapid-thermal processing. The studies of the influence of sodium during the initial stages of epitaxy have led to a new model to explain its influences based on the hypothesis that it behaves as a surfactant in the Cu-In-Se material system. This represents the first unified theory on the role of sodium

Study on the preparation of the SiCp/Al-20Si-3Cu functionally graded material using spray deposition

International Nuclear Information System (INIS)

Su, B.; Yan, H.G.; Chen, G.; Shi, J.L.; Chen, J.H.; Zeng, P.L.

2010-01-01

Research highlights: → The SiCp/Al-20Si-3Cu functionally gradient material (FGM) was successfully prepared via the spray deposition technique. → The SiCp/Al-20Si-3Cu functionally gradient material (FGM) was successfully prepared via the spray deposition technique. → In the experimental setup, the novel devices play an important role in adjusting the output of SiCp to prepare the FGM. → The experiment results reveal that the SiCp weight fraction of the as-deposited preform from the top to the bottom ranges almost continuously from 0% to 30%. → The fraction of SiC particles has no obvious influence on the phase constitutions of the SiCp/Al-20Si-3Cu FGM. - Abstract: The SiCp/Al-20Si-3Cu functionally gradient material (FGMs) was successfully prepared via the spray deposition technique accompanied with an automatic control system. The results reveal that the SiCp weight fraction of the as-deposited preform from the top to the bottom ranges almost continuously from 0% to 30%. The part with the higher SiCp weight fraction exhibits a relatively smaller density than that with the lower SiCp weight fraction. However, the microhardness and the porosity increase with the increasing SiCp weight fraction in the as-deposited preform. The X-ray diffraction results exhibit that the secondary phases in the regions with the different amount of SiC particles are the same such as Al 2 Cu and AlCuMg. The spray deposition technology is promising to produce a wide range of other FGMs.

Growth and characterisation of potentiostatically electrodeposited Cu2O and Cu thin films

International Nuclear Information System (INIS)

Wijesundera, R.P.; Hidaka, M.; Koga, K.; Sakai, M.; Siripala, W.

2006-01-01

Cuprous oxide and copper thin films were potentiostatically electrodeposited in an acetate bath. Voltammetric curves were used to investigate the growth parameters; deposition potential, pH and temperature of the bath. Deposition potential dependency on the structural, morphological, optical and electronic properties of the films were investigated by the X-ray diffraction measurements, scanning electron micrographs, absorption measurements and dark and light current-voltage characterisations. It was observed that single phase polycrystalline Cu 2 O can be deposited from 0 to - 300 mV Vs saturated calomel electrode (SCE) and co-deposition of Cu and Cu 2 O starts at - 400 mV Vs SCE. Further increase in deposition potential from - 700 mV Vs SCE produces single phase Cu thin films. Single phase polycrystalline Cu 2 O thin films with cubic grains of 1-2 μm can be possible within the very narrow potential domain around - 200 mV Vs SCE. Enhanced photoresponse in a photoelectrochemical cell is produced by the Cu 2 O thin film prepared at - 400 mV Vs SCE, where Cu is co-deposited with Cu 2 O with random distribution of Cu spheres on the Cu 2 O surface. This study reveals that a single deposition bath can be used to deposit both Cu and Cu 2 O separately and an admixture of Cu-Cu 2 O by controlling the deposition parameters

Atmospheric Deposition of Pb, Zn, Cu, and Cd in Amman, Jordan

International Nuclear Information System (INIS)

Momani, K.A.; Jiries, A.G.; Jaradat, Q.M.

1999-01-01

Atmospheric samples were collected by high-volume air sampler and dust fall containers during the summer of 1995 at different sites in Amman City, Jordan. Heavy metal contents in settle able (dust fall) as well as in air particulates (suspended) were analyzed by graphite furnace atomic absorption spectrophotometry. The atmospheric concentrations of Zn, Cu, Pb, and Cd were 344, 170, 291, and 3.8 ng/m 3 , respectively. On the other hand, the levels of these elements in dust fall deposition were 505, 94, 74, and 3.1 μg/g, respectively. The fluxes and dry deposition velocities of these heavy metals were determined and compared with the findings of other investigators worldwide. Significant enrichment coefficients of heavy metals in dust fall were observed. The enrichment coefficients were 12.1, 6.1, 11.7, and 1.1 for Zn, Cu, Pb, and Cd, respectively

Sputter deposition on gas diffusion electrodes of Pt-Au nanoclusters for methanol oxidation

Energy Technology Data Exchange (ETDEWEB)

Giorgi, L.; Giorgi, R.; Gagliardi, S.; Serra, E. [ENEA Casaccia Research Center, Rome (Italy). Physics Technologies and New Materials; Alvisi, M.; Signore, M.A. [ENEA Brindisi Research Center, Brindisi (Italy). Physics Technologies and New Materials

2008-07-01

Polymer electrolyte fuel cells (PEFCs) are suited for use in commercial electrical vehicle and electric power applications. The gas diffusion electrodes of PEFCs are catalyzed by the deposition of platinum (Pt) nanoparticles on carbon powder. The particles must be localized on the electrode surface in order to achieve high electrocatalyst utilization. This study discussed a method of preparing PEFC electrodes using sputter deposition of a Pt-gold (Au) alloy nanoparticles on carbon powders. The method was designed to improve electrode performance and catalyst utilization. The nano-sized alloy clusters were deposited on a gas diffusion electrode at room temperature. The deposits were then characterized using field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) in order to examine the effect of the deposition technique on the nano-morphology and electrocatalytic performance of the electrode. Results of the study showed that the technique can be used in the large-scale manufacture of fuel cell electrodes. 3 refs., 1 fig.

CuFeO2 formation using fused deposition modeling 3D printing and sintering technique

Science.gov (United States)

Salea, A.; Dasaesamoh, A.; Prathumwan, R.; Kongkaew, T.; Subannajui, K.

2017-09-01

CuFeO2 is a metal oxide mineral material which is called delafossite. It can potentially be used as a chemical catalyst, and gas sensing material. There are methods to fabricate CuFeO2 such as chemical synthesis, sintering, sputtering, and chemical vapor deposition. In our work, CuFeO2 is prepared by Fused Deposition Modeling (FDM) 3D printing. The composite filament which composed of Cu and Fe elements is printed in three dimensions, and then sintered and annealed at high temperature to obtain CuFeO2. Suitable polymer blend and maximum percent volume of metal powder are studied. When percent volume of metal powder is increased, melt flow rate of polymer blend is also increased. The most suitable printing condition is reported and the properties of CuFeO2 are observed by Scanning Electron Microscopy, and Dynamic Scanning Calorimeter, X-ray diffraction. As a new method to produce semiconductor, this technique has a potential to allow any scientist or students to design and print a catalyst or sensing material by the most conventional 3D printing machine which is commonly used around the world.

Synthesis of nanocrystalline Cu1-xTax composites using physical vapor deposition

International Nuclear Information System (INIS)

Savage, H.S.; Wang, H.; Rigsbee, J.M.

1993-01-01

Physical vapor deposition (PVD) processes provide the capability for creating new types of metallic, ceramic, and polymeric composites by allowing atomic-scale engineering of structure and chemistry. Because PVD processes provide the capacity for circumventing thermodynamic factors, such as solubility limits, it is possible to produce nonequilibrium alloys and materials with unique mixtures of phases. The ease by which PVD produces materials with nanocrystalline microstructures is an added benefit of these processes. This paper describes ion plating, a plasma-assisted PVD process, and its application for the development of a new class of nanoscale dispersion-strengthened Cu 1-x Ta x alloys. Copper-tantalum was selected as a model system because the extensive liquid miscibility gap and nearly zero mutual solid solubilities prevent creation of Cu-Ta alloys by conventional or rapid solidification processes. Microchemical analyses of the family of Cu 1-x Ta x alloys indicate that PVD can produce materials with any desired level of Ta. X-ray diffraction and transmission electron microscopy analyses show that the as-deposited microstructures consist generally of a Cu matrix supersaturated with Ta and containing a uniform dispersion of Ta particles with diameters below 10 nm. The Ta particles are face centered cubic (exceptionally large Ta particles, larger than ∼100 nm, are body centered cubic) and are oriented identically with the Cu matrix. Particle coarsening studies, at temperatures up to 900C and for times as long as 100 hours, indicate an extreme degree of microstructural stability. The Ta particles also appear highly effective at maintaining a submicron Cu matrix grain size even after annealing at 900C

Diffusion mechanisms taking place at the early stages of cobalt deposition on Au(111)

International Nuclear Information System (INIS)

Oviedo, O A; Leiva, E P M; Mariscal, M M

2008-01-01

In the present work a detailed atomic-level analysis of some of the main diffusion mechanisms which take place during cobalt adatom deposition are studied within atom dynamics (AD) and the nudged elastic band (NEB) method. Our computer simulations reveal a very fast exchange between Co and Au atoms when the deposit is a single cobalt adatom. However, when the nucleus size increases, a decrease in the exchange probability is observed. Activation energies for different transitions are obtained using AD in combination with the NEB method

Geologic history of the Blackbird Co-Cu district in the Lemhi subbasin of the Belt-Purcell Basin

Science.gov (United States)

Bookstrom, Arthur A.; Box, Stephen E.; Cossette, Pamela M.; Frost, Thomas P.; Gillerman, Virginia; King, George; Zirakparvar, N. Alex

2016-01-01

. Discordant quartz-biotite and quartz-tourmaline breccias, and veins contain cobaltite3 ± xenotime3 (ca. 1058–990 Ma).Mesoproterozoic cobaltite deposition was followed by: (1) within-plate plutonism (530–485 Ma) and emplacement of mafic dikes (which cut cobaltite lodes but are cut by quartz-Fe-Cu-sulfide veins); (2) garnet-grade metamorphism (ca. 151–93 Ma); (3) Fe-Cu-sulfide mineralization (ca. 110–92 Ma); and (4) minor quartz ± Au-Ag ± Bi mineralization (ca. 92–83 Ma).Cretaceous Fe-Cu-sulfide vein, breccia, and replacement-style deposits contain various combinations of chalcopyrite ± pyrrhotite ± pyrite ± cobaltian arsenopyrite (not cobaltite) ± arsenopyrite ± quartz ± siderite ± monazite (ca. 144–88 Ma but mostly 110–92 Ma) ± xenotime (104–93 Ma). Highly radiogenic Pb (in these sulfides) and Sr (in siderite) indicate that these elements resided in Mesoproterozoic source rocks until they were mobilized after ca. 100 Ma. Fe-Cu-sulfide veins, breccias, and replacement deposits appear relatively undeformed and generally lack metamorphic fabrics.Composite Co-Cu-Au ore contains early cobaltite-biotite lodes, cut by Fe-Cu-sulfide veins and breccias, or overprinted by Fe-Cu-sulfide replacement-style deposits, and locally cut by quartz veinlets ± Au-Ag ± Bi minerals.

Enhancement on field emission characteristics of pulsed laser deposited diamondlike carbon films using Au precoatings

International Nuclear Information System (INIS)

Chuang, F.Y.; Sun, C.Y.; Cheng, H.F.; Lin, I.N.

1997-01-01

Using Au precoatings has been observed to significantly enhance the field emission properties of diamondlike carbon (DLC) films deposited on Si substrates. The electron emission can be turned on at a low field as 7 V/μm and a large emission current density as 2000 μA/cm 2 can be obtained at 20 V/μm applied field. However, preannealing the Au-coated Si substrates at 500 degree C for 30 min is necessary to achieve such a performance. Microscopic examination on surface and cross-sectional morphologies of the DLC/Au/Si films using atomic force microscopy and scanning electron microscopy, respectively, in conjunction with the elemental depth profile examination of these films using secondary ion mass spectroscopy, indicated that substantial interdiffusion between DLC, Au, and Si layers has occurred. Such kind of reaction is proposed to lower the resistance for electrons to transport across the interfaces and, thereafter, enhances the field emission properties of the DLC/Au/Si films. copyright 1997 American Institute of Physics

Metallogenic events in the Coastal Cordillera of Copiapo region, northern Chile (26-28o S)

International Nuclear Information System (INIS)

Diaz, A.; Vivallo, W

2001-01-01

The metallogenic province of the Coastal Cordillera in the Copiapo region is characterized by Cu, Cu-Au,Cu-Fe-Au, Fe, Ag and Au deposits. The ore deposits are ranging in ages between Middle to Late Jurassic (1) and Early Cretaceous (2). Results of a geochronology program for ore deposits in this metallogenic province, in addition to existing geochronological control of the ore deposits host rocks (mainly intrusive) allowed to define four different Metallogenic Epochs which could be extended to other zones in the Coastal Cordillera (au)

Operations and Performance of RHIC as a Cu-Cu Collider

CERN Document Server

Pilat, Fulvia Caterina; Bai, Mei; Barton, Donald; Beebe-Wang, Joanne; Blaskiewicz, Michael; Brennan, Joseph M; Bruno, Donald; Cameron, Peter; Connolly, Roger; De Long, Joseph; Drees, Angelika; Fischer, Wolfram; Ganetis, George; Gardner, Chris J; Glenn, Joseph; Harvey, Margaret; Hayes, Thomas; Hseuh Hsiao Chaun; Huang, Haixin; Ingrassia, Peter; Iriso, Ubaldo; Lee, Roger C; Litvinenko, Vladimir N; Luo, Yun; MacKay, William W; Marr, Gregory J; Marusic, Al; Michnoff, Robert; Montag, Christoph; Morris, John; Nicoletti, Tony; Oerter, Brian; Ptitsyn, Vadim; Roser, Thomas; Russo, Thomas; Sandberg, Jon; Satogata, Todd; Schultheiss, Carl; Tepikian, Steven; Tomas, Rogelio; Trbojevic, Dejan; Tsoupas, Nicholaos; Tuozzolo, Joseph; Vetter, Kurt; Zaltsman, Alex; Zeno, Keith; Zhang, S Y; Zhang, Wu

2005-01-01

The 5th year of RHIC operations, started in November 2004 and expected to last till June 2005, consists of a physics run with Cu-Cu collisions at 100 GeV/u followed by one with polarized protons at 100 GeV. We will address here overall performance of the RHIC complex used for the first time as a Cu-Cu collider, and compare it with previous operational experience with Au, PP and asymmetric d-Au collisions. We will also discuss operational improvements, such as a ?* squeeze to 85cm in the high luminosity interaction regions from the design value of 1m, system improvements and machine performance limitations, such as vacuum pressure rise, intra-beam scattering, and beam beam interaction.

Hf and Nd Isotopic and REE Investigations of Magnetite in a Proterozoic IOCG system: Fingerprinting Sources and Timing of Mineralisation

Science.gov (United States)

Schaefer, B. F.

2016-12-01

The Stuart Shelf on the margin of the Gawler Craton, South Australia, contains numerous economic and sub-econmic IOCG mineralised systems, including the giant Olympic Dam Cu-Au-U deposit. Hematite and magnetite have played a critical in the genesis of all of these deposits, and increasingly it appears that magnetite has been in equilibrium with either the final mineralised assemblage or was critical in transporting metals during the ore forming event. 14 magnetites and one hematite from three separate styles of iron oxide mineralisation associated with the Prominent Hill Cu-Au deposit were selected for detailed analysis. The REE and isotopic separations were all conducted by low blank wet chemistry and isotopes determined by TIMS (Nd) and MC-ICPMS (Hf). Magnetites associated with skarn style mineralsiation proximal to the ore body are unformly depleted in REE, whereas hematite within the ore and magmatic magmatites and whole rock gabbros from the nearby 1590Ma White Hill Gabbro intrusion are all relatively LREE enriched and display a comparable range in REE. Significantly however, magnetite separates almost invariably display more evolved Hf isotopic signatures than the host lithologies adjacent the economic mineralisation (dacites and metasediments at Prominent Hill mine) implying that the magnetites were sourcing their REE inventory dominantly from the local crust rather than a mantle derived source. In contrast, the magmatic magnetites from the White Hill Complex display Nd and Hf isotopes which are slightly more primitive, recording a greater relative mantle component, however still requiring a significant crustal input. Significantly, the hematite which contains the Au mineralisation preserves ɛNd (1590) = -4.04 and ɛHf (1590) = -6.05 essentially identical to the magmatic magnetites and their host gabbros in the White Hill complex and the basalts and dacites of the host Gawler Range Volcanics (ɛNd (1590) = -7.10 - -3.72 and ɛHf (1590) = -7.69 - -1

Boosting the performance of Pt electro-catalysts toward formic acid electro-oxidation by depositing sub-monolayer Au clusters

International Nuclear Information System (INIS)

Bi Xuanxuan; Wang Rongyue; Ding Yi

2011-01-01

Highlights: → Au decoration on Pt nanoparticles simultaneously increases the activity and stability. → Sub-monolayer Au decoration changes the reaction path and results in the activity improvement. → Increasing the Au coverage will increase the specific activity. → Proper Au coverage results in a maximum mass specific activity. - Abstract: CO poisoning is the main obstacle to the application of Pt nanoparticles as anode catalysts in direct formic acid fuel cells (DFAFCs). Significant types of Pt alloys have been investigated, which often demonstrate evidently improved catalytic performance governed by difference mechanisms. By using a well-known electrochemical technique of under potential deposition and in situ redox replacement, sub-monolayer Au clusters are deposited onto Pt nanoparticle surfaces in a highly controlled manner, generating a unique surface alloy structure. Under optimum conditions, the modified Pt nanoparticles can exhibit greatly enhanced specific activity (up to 23-fold increase) at potential of -0.2 V vs. MSE toward formic acid electro-oxidation (FAEO). Interestingly, the mass specific activity can also be improved by a factor of 2.3 at potential of -0.35 V vs. MSE although significant amount of surface Pt atoms are covered by the overlayer Au clusters. The much enhanced catalytic activity can be ascribed to a Pt surface ensemble effect, which induces change of the reaction path. Moreover, the sub-monolayer Au coating on the surface also contributes to the enhanced catalyst durability by inhibiting the Pt oxidation. These results show great potential to rationally design more active and stable nanocatalysts by modifying the Pt surface with otherwise inactive materials.

One-step electrodeposition process of CuInSe2: Deposition time effect

Indian Academy of Sciences (India)

Administrator

CuInSe2 thin films were prepared by one-step electrodeposition process using a simplified two- electrodes system. ... homojunctions or heterojunctions (Rincon et al 1983). Efficiency of ... deposition times onto indium thin oxide (ITO)-covered.

Rapid detection of Cu(2+) by a paper-based microfluidic device coated with bovine serum albumin (BSA)-Au nanoclusters.

Science.gov (United States)

Fang, Xueen; Zhao, Qianqian; Cao, Hongmei; Liu, Juan; Guan, Ming; Kong, Jilie

2015-11-21

In this work, bovine serum albumin (BSA)-Au nanoclusters were used to coat a paper-based microfluidic device. This device acted as a Cu(2+) biosensor that showed fluorescence quenching on detection of copper ions. The detection limit of this sensor could be adjusted by altering the water absorbing capacity of the device. Qualitative and semi-quantitative results could be obtained visually without the aid of any advanced instruments. This sensor could test Cu(2+) rapidly with high specificity and sensitivity, which would be useful for point-of-care testing (POCT).

Lead-doped electron-beam-deposited Bi-Sr-Ca-Cu-O superconducting thin films

Energy Technology Data Exchange (ETDEWEB)

Agnihotry, S.A.; Saini, K.K.; Kant, C.; Sharma, C.P.; Ekbote, S.N.; Asthana, P.; Nagpal, K.C.; Chandra, S. (National Physical Lab., New Delhi (India))

1991-03-20

Superconducting thin films of the lead-doped Bi-Sr-Ca-Cu-O system have been prepared on (100) single-crystal SrTiO{sub 3} substrates by an electron beam deposition technique using a single sintered pellet as the evaporation source. As-deposited films are amorphous and non-superconducting; post-deposition annealing at an optimized temperature in air has been found to result in crystalline and superconducting films. The superconducting characteristics of the films have been observed to be sensitive not only to the duration and temperature of post-deposition annealing but also to the lead content and the sintering parameters for the pellet to be used as the evaporation source. A pellet with nominal composition Bi{sub 3}Pb{sub 1}Sr{sub 3}Ca{sub 3}Cu{sub 4}O{sub y} that had been sintered for 200 h zero resistivity Tc{sup 0}=112 K. However, films deposited using such a pellet as the evaporation source had Tc{sup 0} {approx equal} 73-78 K, as had the films deposited from a pellet without any lead. We investigated systematically films deposited from pellets with more lead and sintered for different durations. It is evident from these investigations that pellets with nominal composition Bi{sub 3}Pb{sub 2}Sr{sub 3}Ca{sub 3}Cu{sub 4}O{sub y}, i.e. with an excess of lead, and sintered for about 75 h when used as the evaporation source yield films with Tc{sup 0} {approx equal} 100 K when annealed between 835 and 840deg C for an optimized long duration. The films are characterized by X-ray diffraction and energy-dispersive spectroscopy techniques and have been found to be highly c axis oriented. The effect of lead in promoting a high Tc{sup 0}=110 K phase seems to be similar to that in bulk ceramics. (orig.).

Structural determination of stable MoOx monolayers on O/Cu3Au(1 0 0): DFT calculations

International Nuclear Information System (INIS)

Valadares, George C.S.; Mendes, F.M.T.; Dionízio Moreira, M.; Leitão, A.A.; Niehus, H.

2012-01-01

Highlights: ► Molybdenum oxide is widely used in catalysis in the chemical industry. ► Recently, ultra-thin (monolayer) films of MoO x have been produced on top of O-Cu 3 Au substrates. ► XPS measurements suggest an unusual +5 charge state of the Mo cation. ► Seeking for a low-energy structure with good match to the experimental STM and XPS. ► Bader charges indicate indeed an intermediate charge state as compared to the more common Mo +4 O 2 and Mo +6 O 3 bulk oxides. -- Abstract: Using ab initio calculations based on density functional theory (DFT), we propose a geometrical structure for MoO x monolayers recently grown on O/Cu 3 Au(1 0 0) substrates. The proposed structure reproduces the p(2 × 2) symmetry found by scanning tunneling microscopy (STM) and low-energy electron diffraction (LEED), as well as the intermediate oxidation state between Mo(IV) and Mo(VI) identified by X-ray photoelectron spectroscopy (XPS). Simulated STM images assign the bright spots in the experimental images to oxygen 2p states.

Raman scattering studies of YBa2Cu3O7-x thin films grown by chemical vapor deposition and metal-organic deposition

International Nuclear Information System (INIS)

Lee, E.; Yoon, S.; Um, Y.M.; Jo, W.; Seo, C.W.; Cheong, H.; Kim, B.J.; Lee, H.G.; Hong, G.W.

2007-01-01

We present results of Raman scattering studies of superconducting YBa 2 Cu 3 O 7-x (YBCO) films grown by chemical vapor deposition and metal-organic deposition methods. It is shown by X-ray diffraction that all the as-grown YBCO films have a highly c-axis oriented and in-plane aligned texture. Raman scattering measurements were used to investigate optical phonon modes, oxygen contents, structural properties, and second-phases of the YBCO coated conductors. Raman spectra of YBCO films with lower-transport qualities exhibit additional phonon modes at ∼300 cm -1 , ∼600 cm -1 , and ∼630 cm -1 , which are related to second-phases such as Ba 2 Cu 3 O 5.9 and BaCuO 2 . Our results strongly suggest that Raman scattering be useful for optimizing YBCO film growth conditions

Re-evaluation of microscopic and integral cross-section data for important dosimetry reactions. Re-evaluation of the excitation functions for the 24Mg(n,p)24Na, 32S(n,p)32P, 60Ni(n,p)60m+gCo, 63Cu(n,2n)62Cu, 65Cu(n,2n)64Cu, 64Zn(n,p)64Cu, 115In(n,2n)114mIn, 127I(n,2n)126I, 197Au(n,2n)196Au and 199Hg(n,n')199mHg reactions