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At least 793 records · Page 44

Effect of thermal history on Mossbauer signature and hyperfine interaction parameters of copper ferrite

Two specimens of copper ferrite, CuFe{sub 2}O{sub 4}, have been synthesized by double sintering ceramic technique with different thermal history i.e. slow cooled and quenched. X-ray diffractometry has confirmed single phase fcc spinel structure for slow cooled sample while tetragonal distortion is present in quenched sample. Mossbauer spectral analysis for slow-cooled copper ferrite reveals super position of two Zeeman split sextets along with paramagnetic singlet in the centre position corresponds to delafossite (CuFeO{sub 2}) phase that is completely absent in quenched sample. The hyperfine interaction parameters are highly influenced by heat treatment employed.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Low-cost copper complexes as p-dopants in solution processable hole transport layers

We demonstrate the usage of the Lewis-acidic copper(II)hexafluoroacetylacetonate (Cu(hfac){sub 2}) and copper(II)trifluoroacetylacetonate (Cu(tfac){sub 2}) as low-cost p-dopants for conductivity enhancement of solution processable hole transport layers based on small molecules in organic light emitting diodes (OLEDs). The materials were clearly soluble in mixtures of environmentally friendly anisole and xylene and spin-coated under ambient atmosphere. Enhancements of two and four orders of magnitude, reaching 4.0 × 10{sup −11} S/cm with a dopant concentration of only 2 mol% Cu(hfac){sub 2} and 1.5 × 10{sup −9} S/cm with 5 mol% Cu(tfac){sub 2} in 2,2′,7,7′-tetra(N,N-ditolyl)amino-9,9-spiro-bifluorene (spiro-TTB), respectively, were achieved. Red light emitting diodes were fabricated with reduced driving voltages and enhanced current and power efficiencies (8.6 lm/W with Cu(hfac){sub 2} and 5.6 lm/W with Cu(tfac){sub 2}) compared to the OLED with undoped spiro-TTB (3.9 lm/W). The OLED with Cu(hfac){sub 2} doped spiro-TTB showed an over 8 times improved LT{sub 50} lifetime of 70 h at a starting luminance of 5000 cd/m{sup 2}. The LT{sub 50} lifetime of the reference OLED with PEDOT:PSS was only 8 h. Both non-optimized OLEDs were operated at similar driving voltage and power efficiency.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Growth and characterization of single phase Cu{sub 2}O by thermal oxidation of thin copper films

We report a simple and efficient technique to form high quality single phase cuprous oxide films on glass substrate using thermal evaporation of thin copper films followed by controlled thermal oxidation in air ambient. Crystallographic analysis and oxide phase determination, as well as grain size distribution have been studied using X-ray diffraction (XRD) method, while scanning electron microscopy (SEM) has been utilized to investigate the surface morphology of the as grown oxide films. The formation of various copper oxide phases is found to be highly sensitive to the oxidation temperature and a crystalline, single phase cuprous oxide film can be achieved for oxidation temperatures between 250°C to 320°C. Cu{sub 2}O film surface appeared in a faceted morphology in SEM imaging and a direct band gap of about 2.1 eV has been observed in UV-visible spectroscopy. X-ray photoelectron spectroscopy (XPS) confirmed a single oxide phase formation. Finally, a growth mechanism of the oxide film has also been discussed.

36 MATERIALS SCIENCE↗

Sensing response of copper phthalocyanine salt dispersed glass with organic vapours

Copper Phthalocyanine and other Metal Phthalocyanines are very flexible and tuned easily to modify their structural, spectroscopic, optical and electrical properties by either functionalizing them with various substituent groups or by replacing or adding a ligand to the central metal atom in the phthalocyanine ring and accordingly can be made sensitive and selective to various organic species or gaseous vapours. In the present work, we have dispersed Copper Phthalocyanine Salt (CuPcS) in sol-gel glass form using chemical route sol-gel method and studied its sensing mechanism with organic vapours like methanol and benzene and found that current increases onto their exposure with vapours. A variation in the activation energies was also observed with exposure of vapours.

36 MATERIALS SCIENCE↗

Non-enzymatic glucose sensor based on electrodeposited copper on carbon paste electrode (Cu/CPE)

The development of non-enzymatic glucose sensor has much attention due to their applications in glucose monitoring. In this research, copper oxide is used as a non-enzymatic glucose sensor by oxidizing glucose to gluconolactone. Copper was electrodeposited on Carbon paste electrode (CPE) at constant potential. The experimental condition was varied in electrodeposition of Cu with the following parameters: Electrodeposition time 60 s, 120 s and 180 s and potential reduction -0.166 V, -0.266 V and -0.366 V. The effective performance of these working electrodes in sensing glucose was investigated. The Cu/CPE which used -0.366 V potential reduction and 120 s electrodeposition time shows the best performance. The amperometric response current in concentration range 1.6-62.5 mM of glucose gives the good linearity R{sup 2} = 0.9988, low detection limit 0.6728 mM and high sensitivity 1183.59 µA mM{sup −1}cm{sup −2}. Furthermore this sensor exhibited a good repeatability with %RSD = 1.31% (n=10) and high stability with %RSD = 1.51% (n=5 days). The homogeneity of Cu particles on CPE was investigated by Scanning Electron Microscope (SEM).

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Copper bromide vapour laser with a pulse repetition rate up to 700 kHz

The results of the experimental study of a copper bromide vapour laser at high repetition rates of regular pump pulses are presented. A record-high pulse repetition rate of 700 kHz is attained for lasing at self-terminating transitions in copper atoms. To analyse the obtained results, use is made of the data of numerical modelling of the plasma kinetics in the phase of pumping and discharge afterglow. (lasers)

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗

Optical Properties of Copper-Doped Lithium Niobate Crystals

We have studied the optical properties of copper-doped lithium niobate crystals using semiconductor light-emitting diodes and lasers emitting in the visible and ultraviolet spectral regions as excitation sources. The results demonstrate that, at an excitation frequency approaching the frequency of electronic absorption in copper ions, there is discrete resonance Raman scattering in the form of a frequency comb. The observed Raman satellites of discrete light scattering are due to polar longitudinal A{sub 1} optical modes of the lithium niobate single crystal. Under excitation by a light-emitting diode with a wavelength of 520 nm, we observe a sharp increase in discrete light scattering intensity in comparison with the photoluminescence excited by shorter wavelength excitation sources.

36 MATERIALS SCIENCE↗

Studies of concentration and temperature dependences of precipitation kinetics in iron-copper alloys using kinetic Monte Carlo and stochastic statistical simulations

The previously developed ab initio model and the kinetic Monte Carlo method (KMCM) are used to simulate precipitation in a number of iron-copper alloys with different copper concentrations x and temperatures T. The same simulations are also made using an improved version of the previously suggested stochastic statistical method (SSM). The results obtained enable us to make a number of general conclusions about the dependences of the decomposition kinetics in Fe-Cu alloys on x and T. We also show that the SSM usually describes the precipitation kinetics in good agreement with the KMCM, and using the SSM in conjunction with the KMCM allows extending the KMC simulations to the longer evolution times. The results of simulations seem to agree with available experimental data for Fe-Cu alloys within statistical errors of simulations and the scatter of experimental results. Comparison of simulation results with experiments for some multicomponent Fe-Cu-based alloys allows making certain conclusions about the influence of alloying elements in these alloys on the precipitation kinetics at different stages of evolution.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Modification of Graphene on a Copper Grid during Femtosecond Laser Irradiation: Electron Diffraction and Raman Spectroscopy Studies

The modification of a graphene sheet, which was fabricated by chemical vapor deposition on a close-meshed copper grid, during powerful femtosecond laser irradiation is studied. The process of long-term irradiation of a sample in vacuum is found to be accompanied by (1) breaking carbon bonds, which is indicated by a decrease in the intensities of the reflections corresponding to electron-beam diffraction by graphene and (2) the formation of new products, which is indicated by the appearance of new diffraction rings and a change in the Raman spectrum of the sample. The compositions of the forming chemical compounds are analyzed. Copper oxides Cu{sub 2}O and CuO are shown to form predominantly on the sample surface as a result of the chemical reactions induced by powerful femtosecond laser pulses.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Optical Properties of CdS Nanocrystals Doped with Zinc and Copper

Cadmium-sulfide nanocrystals are produced by the colloidal method. Doping with zinc and copper is conducted during nanocrystal growth. The optical absorption and photoluminescence spectra are studied. The maximum concentration of the optically active copper impurity is determined from a shift of the fundamental absorption edge to lower energies. It is shown that the long-wavelength luminescence of CdS and CdS:Zn nanocrystals is defined by optical transitions at donor–acceptor pairs. In CdS:Cu nanocrystals, optical absorption and photoluminescence in the visible spectral region are defined by recombination transitions involving the ground state of Cu{sub Zn}{sup 2+} ions. The infrared absorption and photoluminescence of CdS:Cu quantum dots are defined by intracenter transitions within Cu{sub Zn}{sup 2+} ions.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Copper Complexes with Diazoolefin Ligands and their Photochemical Conversion into Alkenylidene Complexes

Homometallic copper complexes with alkenylidene ligands are discussed as intermediates in catalysis but the isolation of such complexes has remained elusive. Herein, we report the structural characterization of copper complexes with bridging and terminal alkenylidene ligands. The compounds were obtained by irradiation of CuI complexes with N-heterocyclic diazoolefin ligands. Furthermore, the complex with a terminal alkenylidene ligand required isolation in a crystalline matrix, and its structural characterization was enabled by in crystallo photolysis at low temperature.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Structural, Electronic, and Photophysical Insights into a Few Atom Copper-Sulfur Cluster in the Solid and Solution States

Coinage-metal chalcogenide clusters are widely studied for their attractive photoluminescence properties. Copper chalcogenides are especially promising, but are often confined to solid-state investigations due to their limited solution stability and the difficulty of synthesizing stable, well-defined clusters. Here, we investigate copper–sulfur clusters incorporating a small number of Cu atoms to elucidate fundamental atomic interactions, ground- and excited-state characteristics, and photophysical behavior in both solid and solution. We have synthesized the Cu6(4,6-dimethyl-2-mercaptopyrimidine)6 cluster in both neutral and charged states, Cu6 and Cu6-2H2+, respectively, by selective ligand protonation. The molecular structures are determined using single-crystal X-ray diffraction, while Cu K-edge X-ray absorption spectroscopy is used to probe Cu electronic structure differences arising from the ligand modification. Steady-state and pump-probe optical spectroscopy is used to investigate photophysical properties, interpreted using density functional theory methods. Both clusters exhibit good stability in the solid state and in solution and show characteristic near-infrared emission with microsecond lifetimes. Overall, the Cu6S6 clusters display favorable charge–transfer characteristics and show potential for further use in driving photochemical transformations.

Copper-sulfur clusters↗

Copper Tantalate by a Sodium-Driven Flux-Mediated Synthesis for Photoelectrochemical CO 2 Reduction

Copper-tantalate, Cu 2 Ta 4 O 11 (CTO), shows significant promise as an efficient photocathode for multi-carbon compounds (C 2+ ) production through photoelectrochemical (PEC) CO 2 reduction, owing to its suitable energy bands and catalytic surface. However, synthesizing CTO poses a significant challenge due to its metastable nature and thermal instability. In this study, this challenge is addressed by employing a flux-mediated synthesis technique using a sodium-based flux to create sodium-doped CTO (Na-CTO) thin films, providing enhanced nucleation and stabilization for the CTO phase. To evaluate the PEC performance and catalytic properties of the films, copper(II) oxide (CuO) at the Na-CTO surface is selectively etched. The etched Na-CTO shows a lower dark current, with decreased contribution from photocorrosion, unlike the non-etched Na-CTO which has remaining CuO on the surface. Furthermore, Na-CTO exhibits 7.3-fold ethylene selectivity over hydrogen, thus highlighting its promising potential as a photocathode for C 2+ production through PEC CO 2 reduction.

copper tantalate↗

Catalytic Aquathermolysis of High-Viscosity Oil Using Iron, Cobalt, and Copper Tallates

The results of a study of the composition of active forms of the catalyst formed upon degradation of the precursor, based on the results of physical modeling of a sample of high-viscosity oil having high asphaltene and resin contents, are presented. Oil-soluble iron, cobalt, and copper tallates were used as the objects of the study. The composition of the separated powder of the active form of the catalyst was determined by X-ray diffraction analysis, and the catalyst particle size was determined by scanning electron microscopy. The SARA (saturate, aromatic, resin and asphaltene) analysis data revealed a marked decrease in high-molecular-weight oil components due to thermocatalytic cracking. The basic transformation mechanism is breakdown of the high-molecular-weight compounds along the sulfur-bearing bonds, as indicated by elemental CHNS (carbon, hydrogen, nitrogen and sulfur) analysis data. It is shown that the cobalt- and copper-based oil-soluble complexes turn are converted to sulfide forms and the iron-based complex is converted to the oxide form. According to the results of scanning electron microscopic analysis of the catalyst, the particle size is about 60 nm.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Structural and Optical Study of Copper-Doped Zinc Sulfide Nanoparticles

Copper-doped zinc sulfide nanoparticles have been synthesized using a wet chemical method. The synthesized nanoparticles exhibit a zinc blende structure with the crystallite size of 3.8 nm. The morphological and optical studies of the synthesized nanoparticles have been performed. It is found that the band gap varies from 3.6 to 4.4 eV depending upon the concentration of copper. The room temperature photoluminescence of the synthesized nanoparticles has been also investigated.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Ferrocene-containing tri- and tetranuclear cyclic copper(I) and silver(I) pyrazolates

New tri- and tetranuclear macrocyclic silver(I) and copper(I) 3-ferrocenyl-5-(trifluoromethyl)pyrazolates were prepared: [{(3-((η"5-C_5H_4)Fe(η"5-C_5H_5))-5-(CF_3)-Pz}M]{sub 3} (M = Cu (1), Ag (2)) and [{(3-(( η"5-C_5H_4)Fe(η"5-C_5H_5))-5-(CF_3)-Pz}Cu]{sub 4} (3). The structures of compounds were established by X-ray diffraction analysis. In the crystalline state, a planar trinuclear silver-containing macrocycliс pyrazolate and a saddle-shaped tetranuclear copper-containing macrocycle are formed. The introduction of a bulky substituent, ferrocene, into the pyrazole ligand results in complete shielding of the acidic metal sites, which precludes the coordination of base molecules.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Three-dimensional copper(II) carboxylates based on 4,4′,4″-benzene-1,3,5-triyltris(benzoic acid)

The homochiral coordination polymers [Cu{sub 4}(CH{sub 3}OH)(H{sub 2}O){sub 4}(Hbtb)(S-mal){sub 2}]•4H{sub 2}O and [Cu{sub 4}(CH{sub 3}OH)(H{sub 2}O){sub 4}(Hbtb)(R-mal){sub 2}]•4H{sub 2}O were synthesized by heating S- or R-malic acid (H{sub 3}mal), 4,4′,4″-benzene-1,3,5-triyltris(benzoic acid) (H{sub 3}btb), and copper(II) acetate in an aqueous methanolic solution. The reaction with copper(II) nitrate in aqueous dioxane afforded the coordination framework [Cu{sub 6}(C{sub 4}H{sub 8}O{sub 2}){sub 3}(H{sub 2}O){sub 3}(btb){sub 4}]•4C{sub 4}H{sub 8}O{sub 2}•10H{sub 2}O, which does not contain chiral ligands. The compositions and crystal structures of the new compounds were determined by single-crystal X-ray diffraction and confirmed by X-ray powder diffraction, IR spectroscopy, thermogravimetric and elemental analysis.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

The Effect of Deposit Temperature on the Catalytic SO{sub 2}-to-SO{sub 3} Conversion in a Copper Flash Smelting Heat Recovery Boiler

The aim of the work was to study the catalytic role of copper flash smelter deposit in the SO{sub 2}-to-SO{sub 3} conversion. In addition, the effect of process gas temperature at 548 K to 1173 K (275 °C to 900 °C) on the amount of SO{sub 3} formed was addressed both in the absence and presence of genuine copper flash smelter deposit. The SO{sub 3} conversion rate changed as a function of process gas temperature, peaking at 1023 K (750 °C). A dramatic increase in the SO{sub 2}-to-SO{sub 3} conversion was observed when process dust was present, clearly indicating that process dust catalyzes the SO{sub 2}-to-SO{sub 3} conversion. Based on these results, the catalytic ability of the deposit may lead to sulfuric acid dew point corrosion.

36 MATERIALS SCIENCE↗