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At least 343 records · Page 19

Analytical electron microscopy investigation of elemental composition and bonding structure at the Sb-doped Ni-fully-silicide/SiO{sub 2} interface

It is very important to control the elemental composition and bonding structure at the gate electrode/gate dielectrics interface in metal-oxide-semiconductor transistor devices because this determines the threshold voltage of the gate electrode. In this study, we investigated the structure at the interface between the antimony (Sb)-doped nickel-fully-silicide gate electrode and SiO{sub 2} dielectrics by employing high-spatial resolution techniques such as energy dispersive x-ray spectroscopy and electron energy-loss spectroscopy using a scanning transmission electron microscope. In one region, we found a thin nickel layer at the NiSi/SiO{sub 2} interface originating from the migration of native oxide at the face of the poly-silicon. In another region, a Sb pileup was detected at the NiSi/SiO{sub 2} interface where the Ni L{sub 3}-edge spectrum showed Ni-Sb bonding, then it was suggested that Sb atoms exist at the bottom of NiSi, substituting for Si atoms in NiSi.

36 MATERIALS SCIENCE↗

Structural and optical properties of Sb{sub 2}S{sub 3} nanocrystals in glass

In this work conventional solid state precipitation method is adopted to fabricate Sb{sub 2}S{sub 3} nanocrystals in glass. The glass composition is optimized for proper host glass matrix to grow antimony trisulphide semiconductor quantum dots. The dot size is modified by heat treatment of glass samples in the temperature range from 550°C to 700°C for various time durations. Structural studies are carried out by X-ray diffraction and transmission electron microscopy and nanoparticles with size ranges from 8 nm to 70 nm are obtained. Quantum dots so grown were further characterized by optical absorption spectroscopy and a blue shift is observed for absorption edge energy that conform the quantum confinement effect.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Mode-locked erbium-doped fiber laser based on evanescent field interaction with Sb{sub 2}Te{sub 3} topological insulator

In this Letter, we demonstrate a mode-locked Er-doped fiber laser incorporating antimony telluride (Sb{sub 2}Te{sub 3}) topological insulator (TI) as a saturable absorber (SA). The laser was capable of generating 270 fs-short soliton pulses at 1560 nm wavelength, which are the shortest solitons generated with a TI-based saturable absorber so far. In order to form a saturable absorber, a bulk piece of Sb{sub 2}Te{sub 3} was deposited on a side-polished single-mode fiber with the presence of a low refractive index polymer. Such saturable absorber exhibits modulation depth at the level of 6% with less than 3 dB of non-saturable losses. Our study shows that TI-based saturable absorbers with evanescent field interaction might compete with SAs based on carbon nanomaterials, like graphene or nanotubes. Additionally, thanks to the interaction with the evanescent field, the material is not exposed to high optical power, which allows to avoid optical or thermal damage.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Ambient CdCl{sub 2} treatment on CdS buffer layer for improved performance of Sb{sub 2}Se{sub 3} thin film photovoltaics

Antimony selenide (Sb{sub 2}Se{sub 3}) is appealing as a promising light absorber because of its intrinsically benign grain boundaries, suitable band gap (∼1.1 eV), strong absorption coefficient, and relatively environmentally friendly constituents. Recently, we achieved a certified 5.6% efficiency Sb{sub 2}Se{sub 3} thin film solar cell with the assistance of ambient CdCl{sub 2} treatment on the CdS buffer layer. Here, we focused on investigating the underlying mechanism from a combined materials and device physics perspective applying current density-voltage (J-V) fitting analysis, atomic force microscope, X-ray photoelectron spectroscopy, fluorescence, and UV–Vis transmission spectroscopy. Our results indicated that ambient CdCl{sub 2} treatment on CdS film not only improved CdS grain size and quality, but also incorporated Cl and more O into the film, both of which can significantly improve the heterojunction quality and device performance of CdS/Sb{sub 2}Se{sub 3} solar cells.

36 MATERIALS SCIENCE↗

Synthesis and crystal structure of [(C{sub 7}H{sub 10}N){sub 2}]{sup 2+} [Sb{sub 2}Cl{sub 8}]{sup 2-1}

The reaction of 2,6-dimethylpyridine with SbCl{sub 3} and HCl affords the title compound, the structure of which is ascertained by X-ray diffraction. The unit cell consists of one bridged Sb{sub 2}Cl{sub 8}{sup 2-} anion and two 2,6-dimethylpyridinium cations. The trivalent antimony ion is bonded not only directly to chlorine anions, but also is coordinated with chlorine anions by secondary bonds. In the crystal, there exists infinite coordinated chains of [Sb{sub 2}Cl{sub 8}]{sub n}{sup 2n-} anions running along the a axis, which link 2,6-dimethylpyridinium cations by N-H-Cl hydrogen bonds.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Towards the Stable Chelation of Radioantimony(V) for Targeted Auger Theranostics

Antimony-119 ( 119 Sb) is one of the most attractive Auger-electron emitters identified to date, but it remains practically unexplored for targeted radiotherapy because no chelators have been identified to stably bind this metalloid in vivo. In a departure from current studies focused on chelator development for Sb(III), we explore the chelation chemistry of Sb(V) using the tris-catecholate ligand TREN-CAM. Through a combination of radiolabeling, spectroscopic, solid-state, and computational studies, the radiochemistry and structural chemistry of TREN-CAM with 1XX/nat Sb(V) were established. The resulting [ 1XX Sb]Sb–TREN-CAM complex remained intact for several days in human serum, signifying high stability under biological conditions. Finally, the first in vivo single photon emission computed tomography and positron emission tomography imaging studies were carried out using 117 Sb, the diagnostic analogue of 119 Sb. These studies revealed marked differences in the uptake and distribution of activity in mice administered unchelated [ 117 Sb]Sb(OH) 6 – versus [ 117 Sb]Sb–TREN-CAM, suggesting that 117 Sb is largely retained by TREN-CAM over the time course of the study. Collectively, these findings demonstrate the most physiologically stable complex of no-carrier-added 1XX Sb yet reported, offering new promise for the clinical implementation of radioantimony in nuclear medicine. In conclusion, our results also establish the feasibility of 117 Sb as an elementally matched partner to 119 Sb for theranostic applications.

62 RADIOLOGY AND NUCLEAR MEDICINE↗

Forming Gas Annealing Improves the Performance of Ex Situ Sb-Doped CdSeTe Thin-Film Solar Cells

Group V doping in cadmium-selenide-telluride (CdSeTe) polycrystalline thin-film solar cells has demonstrated improved power conversion efficiencies (PCEs) and long-term stabilities as compared to the traditional Cu doping in the last decade. The dopants can be successfully incorporated by either in situ or ex situ doping. Here, we report that forming gas (FG) annealing enhances the efficiencies of CdSeTe polycrystalline thin-film solar cells utilizing ex situ antimony (Sb) doping via close-space sublimation of SbCl3 at ambient pressure. The FG annealing increases the hole density and carrier lifetime, reduces the back barrier height, and, therefore, leads to improved open-circuit voltages (VOCs) and fill factors (FFs). The champion device achieves a PCE of 19.2% with a VOC of 877 mV, a current density (JSC) of 30.2 mA/cm2, and an FF of 72.4%. Importantly, the Sb-doped devices showed improved stability under stress tests as compared to Cu-doped devices.

14 SOLAR ENERGY↗

Sources and Assessment of Mercury and Other Heavy Metal Contamination in Soils Surrounding the Wuda Underground Coal Fire Area, Inner Mongolia, China

Concentrations of mercury and other heavy metals were measured in soils surrounding the Wuda Coalfield, Inner Mongolia where underground coal fires are regarded as an important contamination source. Soil samples at the downwind direction were nearly all enriched mercury in surface layers, with their concentrations ~ 10 times higher than those from upwind soils. Mercury concentrations generally increased along soil profiles upward, indicative of increasing atmospheric mercury deposition in recent decades. We suggest that underground coal fire emissions were the potential mercury contamination source and the key factor controlling mercury enrichment in soils. Other heavy metals showed no clear spatial and vertical trends, suggesting that underground coal fire emissions may not the main factor for their enrichment in soils. Antimony showed the highest enrichment followed by tin, while chromium, mercury and cadmium only exhibited slight enrichment. Risk evaluation indicated that heavy metals in the studied soils pose no ecological threats.

54 ENVIRONMENTAL SCIENCES↗

Synthesis and structures of zirconium complexes [Et{sub 2}H{sub 2}N]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–}, [Me{sub 3}NCH{sub 2}Ph]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–}•MeCN, [Ph{sub 3}PC{sub 6}H{sub 4}(CHPh{sub 2}-4)]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–}•2 MeCN, and [Ph{sub 4}Sb]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–}

The complexes [Et{sub 2}H{sub 2}N]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–} (1), [Me{sub 3}NCH{sub 2}Ph]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–}•MeCN (2), [Ph{sub 3}PC{sub 6}H{sub 4}(CHPh{sub 2}-4)]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–}•2 MeCN (3), and [Ph{sub 4}Sb]{sup +}{sub 2}[ZrCl{sub 6}]{sup 2–} (4) were synthesized by the reaction of zirconium tetrachloride with tetraorganylammonium, -phosphonium, and -stibonium chlorides in acetonitrile and structurally characterized. The nitrogen, phosphorus, and antimony atoms in the cations have a distorted tetrahedral geometry. The Zr–Cl distances in the centrosymmetric octahedral [ZrCl{sub 6}]{sup 2−} anions of complexes 1–4 have similar values, the longest bonds being observed in the anion of complex 4. Acetonitrile molecules are involved in the structural organization of the crystals of complex 3via weak hydrogen bonding with phenyl hydrogen atoms of the organylphosphonium cations. In the crystal of 2, no hydrogen bonds between the cations and solvent molecules are observed; acetonitrile molecules fill the cavities formed by cations and anions.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Distributions of Ag, Bi, and Sb as Minor Elements between Iron-Silicate Slag and Copper in Equilibrium with Tridymite in the Cu-Fe-O-Si System at T = 1250 °C and 1300 °C (1523 K and 1573 K)

New experimental data on the distributions of silver (Ag), bismuth (Bi), and antimony (Sb) between liquid iron-silicate slag and liquid copper metal in equilibrium with tridymite in the Cu-Fe-O-Si system at T = 1250 °C and 1300 °C (1523 K and 1573 K) have been obtained. The experimental methodology involved high-temperature equilibration, rapid quenching of the equilibrated phases, followed by direct measurement of the equilibrium phases with electron probe X-ray microanalysis (EPMA) for measurement of major element concentrations and laser ablation inductively coupled plasma mass spectrometry (LAICPMS) for the measurement of minor element concentrations. The 4-point test approach was employed to confirm the achievement of chemical equilibrium in the current study. Open-system equilibration on quartz substrates in controlled gas atmospheres (CO/CO{sub 2}/Ar) and closed-system equilibration in sealed quartz ampoules were used. The new experimental data resolve significant discrepancies found in previous studies and can be used as input for the development of thermodynamic databases for copper-making processes.

36 MATERIALS SCIENCE↗

Oxidation Behavior of Copper Concentrate, Gold Concentrate, and Their Mixtures Between 1173 K (900 °C) and 1373 K (1100 °C)

Gold is typically extracted from ores using a cyanidation process. However, environmental regulations and low productivity are the main drawbacks of cyanide usage. Alternative technologies for gold extraction are being studied although development of any new technology necessitates additional investments. In South Korea, recovery of gold and silver is performed by the local copper producer by feeding gold concentrate into a smelter. An integrated copper-making process might be an efficient and feasible alternative for the extraction of precious metals without the use of toxic cyanide. Installed exhaust gas cleaning system of copper smelter would minimize the toxic effects of hazardous elements (arsenic, bismuth, antimony, etc.) contained in gold concentrates. A kinetic and thermodynamic understanding of the effects of gold concentrates on copper metallurgy is necessary for the operation. The effects of various parameters on the oxidation kinetics of sulfides were investigated.

36 MATERIALS SCIENCE↗

Confirmation of Incorporation of Cu and Se Ions in Applied p- and n-Type-Doped Sb2S3 by Photoemission Spectroscopy

The effect of incorporating copper (Cu) and selenium (Se) ions into stibnite (Sb2S3) lattice was investigated using x-ray photoelectron spectroscopy (XPS). The incorporation of Cu and Se ions was verified by comparing the XPS spectra of the undoped (amorphous Sb2S3), doped (p and n-doped) and pure Se and Cu-acetate powders. The main photoelectron Cu 2p(1/2) (951.8 eV) and Cu 2p(3/2) (932.1 eV) lines derived from the Cu-doped and Cu-acetate powder samples were clearly observed, whereas in the undoped sample, none of the characteristic lines of Cu were detected. The Se Auger line (138.6 eV), the only line of Se which does not coincide with the lines of Sb and S, was successfully detected in an Se-doped XPS sample and the spectrum of pure Se, while Se in the undoped sample was not found. Further, the XPS measurements revealed the relative amounts of Cu and Se in antimony sulfide, as well as the oxidation state of copper incorporated into the matrix.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Characterization of basic physical properties of Sb 2 Se 3 and its relevance for photovoltaics

Antimony selenide (Sb 2 Se 3 ) is a promising absorber material for thin film photovoltaics because of its attractive material, optical and electrical properties. In recent years, the power conversion efficiency (PCE) of Sb 2 Se 3 thin film solar cells has gradually enhanced to 5.6%. In this article, we systematically studied the basic physical properties of Sb 2 Se 3 such as dielectric constant, anisotropic mobility, carrier lifetime, diffusion length, defect depth, defect density and optical band tail states. Here, we believe such a comprehensive characterization of the basic physical properties of Sb 2 Se 3 lays a solid foundation for further optimization of solar device performance.

14 SOLAR ENERGY↗

Metal mixtures in urban and rural populations in the US: The Multi-Ethnic Study of Atherosclerosis and the Strong Heart Study

Background: Natural and anthropogenic sources of metal exposure differ for urban and rural residents. We searched to identify patterns of metal mixtures which could suggest common environmental sources and/or metabolic pathways of different urinary metals, and compared metal-mixtures in two population-based studies from urban/sub-urban and rural/town areas in the US: the Multi-Ethnic Study of Atherosclerosis (MESA) and the Strong Heart Study (SHS). Methods: We studied a random sample of 308 White, Black, Chinese-American, and Hispanic participants in MESA (2000–2002) and 277 American Indian participants in SHS (1998–2003). We used principal component analysis (PCA), cluster analysis (CA), and linear discriminant analysis (LDA) to evaluate nine urinary metals (antimony [Sb], arsenic [As], cadmium [Cd], lead [Pb], molybdenum [Mo], selenium [Se], tungsten [W], uranium [U] and zinc [Zn]). For arsenic, we used the sum of inorganic and methylated species (∑As). Results: All nine urinary metals were higher in SHS compared to MESA participants. PCA and CA revealed the same patterns in SHS, suggesting 4 distinct principal components (PC) or clusters (∑As-U-W, Pb-Sb, Cd-Zn, Mo-Se). In MESA, CA showed 2 large clusters (∑As-Mo-Sb-U-W, Cd-Pb-Se-Zn), while PCA showed 4 PCs (Sb-U-W, Pb-Se-Zn, Cd-Mo, ∑As). LDA indicated that ∑As, U, W, and Zn were the most discriminant variables distinguishing MESA and SHS participants. Conclusions: In SHS, the ∑As-U-W cluster and PC might reflect groundwater contamination in rural areas, and the Cd-Zn cluster and PC could reflect common sources from meat products or metabolic interactions. Among the metals assayed, ∑As, U, W and Zn differed the most between MESA and SHS, possibly reflecting disproportionate exposure from drinking water and perhaps food in rural Native communities compared to urban communities around the US. - Highlights: • We identified and compared environmental sources of urinary metals in MESA and SHS. • ∑As-U-W in SHS may reflect groundwater contamination in rural areas. • Cd-Zn in SHS may reflect common sources from meat products or metabolic interaction. • ∑As, U, W, and Zn differed the most between MESA and SHS participants.

54 ENVIRONMENTAL SCIENCES↗

Relationship between domestic smoking and metals and rare earth elements concentration in indoor PM2.5

Highlights: • Tobacco smoke releases heavy metals (HM) and REE in indoor dwellings. • Elemental content in indoor PM{sub 2.5} was measured in smoking and non smoking dwellings. • Extracted and mineralized fractions of elements were evaluated by ICP-MS. • Indoor smoke was associated with increase of specific elemental fractions in PM{sub 2.5}. • Increased levels of HM and REE are associated with respiratory symptoms in children. Cigarette smoke is the main source of indoor chemical and toxic elements. Cadmium (Cd), Thallium (Tl), Lead (Pb) and Antimony (Sb) are important contributors to smoke-related health risks. Data on the association between Rare Earth Elements (REE) Cerium (Ce) and Lanthanum (La) and domestic smoking are scanty. To evaluate the relationship between cigarette smoke, indoor levels of PM{sub 2.5} and heavy metals, 73 children were investigated by parental questionnaire and skin prick tests. The houses of residence of 41 “cases” and 32 “controls” (children with and without respiratory symptoms, respectively) were evaluated by 48-h PM{sub 2.5} indoor/outdoor monitoring. PM{sub 2.5} mass concentration was determined by gravimetry; the extracted and mineralized fractions of elements (As, Cd, Ce, La, Mn, Pb, Sb, Sr, Tl) were evaluated by ICP-MS. PM{sub 2.5} and Ce, La, Cd, and Tl indoor concentrations were higher in smoker dwellings. When corrected for confounding factors, PM{sub 2.5}, Ce, La, Cd, and Tl were associated with more likely presence of respiratory symptoms in adolescents. We found that: i) indoor smoking is associated with increased levels of PM{sub 2.5}, Ce, La, Cd, and Tl and ii) the latter with increased presence of respiratory symptoms in children.

54 ENVIRONMENTAL SCIENCES↗

Body burden of toxic metals and rare earth elements in non-smokers, cigarette smokers and electronic cigarette users

Highlights: • The role of smoking as a source for 42 inorganic element intakes was explored. • The exposure levels of non-smoker, cigarette smokers and e-cigarette users was compared. • Cigarette smokers showed the highest levels of Cu, Mo, Zn, Sb, and Sr. • E-cigarettes users presented the highest concentrations of Se, Ag, and V. • Be, Eu and La were detected more frequently among e-cigarette users. Smoking is considered an important source for inorganic elements, most of them toxic for human health. During the last years, there has been a significant increase in the use of e-cigarettes, although the role of them as source of inorganic elements has not been well established. A cross-sectional study including a total of 150 subjects from Brasov (Romania), divided into three groups (non-smokers, cigarette smokers and electronic cigarettes smokers) were recruited to disclose the role of smoking on the human exposure to inorganic elements. Concentration of 42 elements, including trace elements, elements in the ATSDR's priority pollutant list and rare earth elements (REE) were measured by ICP-MS in the blood serum of participants. Cigarette smokers showed the highest levels of copper, molybdenum, zinc, antimony, and strontium. Electronic cigarette (e-cigarette) users presented the highest concentrations of selenium, silver, and vanadium. Beryllium, europium and lanthanides were detected more frequently among e-cigarette users (20.6%, 23.5%, and 14.7%) than in cigarette smokers (1.7%, 19.0%, and 12.1%, respectively); and the number of detected REE was also higher among e-cigarette users (11.8% of them showed more than 10 different elements). Serum levels of cerium and erbium increased as the duration of the use of e-cigarettes was longer. We have found that smoking is mainly a source of heavy metals while the use of e-cigarettes is a potential source of REE. However, these elements were detected at low concentrations.

54 ENVIRONMENTAL SCIENCES↗

Efficiency and mechanisms of Sb(III/V) removal by Fe-modified biochars using X-ray absorption spectroscopy

Fe-modified biochars (FeBC) are effective antimony (Sb) removal materials; however, the removal mechanisms require further investigation. In this study, aqueous Sb(III) and Sb(V) removal by FeBC (300, 600, and 900 °C) was evaluated, with the adsorption mechanisms investigated using X-ray absorption spectroscopy (XAS). Screening results (based on removal efficiencies) using different types of FeBC indicated the 900 °C FeCl3- modified biochar (FeCl3BC900) achieved the best Sb(III/V) removal performance. The kinetics of the Sb(III/V) removal process were best fitted by a pseudo-second-order model. Additionally, the isothermal results were described by Langmuir and Redlich-Peterson models. Aqueous analysis and X-ray absorption near-edge structure data fitting indicated Sb(III) was oxidized to Sb(V) in the Sb(III)-spiked system, and the oxidation extent increased with increasing pyrolysis temperature. The oxidation process rapidly occurred in both the solution and biochar. No Sb(V) was reduced to Sb(III) in the Sb(V)-spiked system. The XAS results of the isothermal experiment indicated the oxidation capacity of FeCl3BC900 was limited for high initial Sb(III) concentrations. The SbFe1 and Sb-Fe2 bonding distances were 3.05–3.10 and 3.47–3.54 Å, respectively, indicating inner-sphere complexes were formed during the Sb(III/V) removal processes. The Sb(III/V) removal mechanisms included electrostatic adsorption, inner-sphere complexes, and coprecipitation. Oxidation was also involved in Sb(III) removal.

Antimony↗

Solvothermal synthesis of a bimetallic thiometallate containing germanium in two oxidation states

A new layered germanium-antimony sulphide, [Ge(C{sub 2}N{sub 2}H{sub 8}){sub 3}][GeSb{sub 2}S{sub 6}], has been prepared at 463 K under solvothermal conditions in the presence of ethylenediamine. The compound has been characterised by single-crystal X-ray diffraction, thermogravimetry, elemental analysis and reflectance spectroscopy. [Ge(C{sub 2}N{sub 2}H{sub 8}){sub 3}][GeSb{sub 2}S{sub 6}] crystallises in the space group Pbca (a=13.3284(5), b=17.4801(6), c=18.5447(7) A). The structure consists of cyclic [GeSb{sub 2}S{sub 8}]{sup 6-} units that form chains which are cross-linked through Sb{sub 2}S{sub 2} rings to generate layers of stoichiometry [GeSb{sub 2}S{sub 6}]{sup 2-}, between which [Ge(en){sub 3}]{sup 2+} cations are located. [Ge(C{sub 2}N{sub 2}H{sub 8}){sub 3}][GeSb{sub 2}S{sub 6}] contains germanium in both the divalent and tetravalent states. The optical band gap of 2.49(4) eV is in excellent agreement with the value expected on the basis of the correlation with the density of metal centres previously identified for thioantimonates, and is consistent with states at the top of the valence band being predominantly of sulphur 3p character. - Graphical abstract: [Ge(C{sub 2}N{sub 2}H{sub 8}){sub 3}][GeSb{sub 2}S{sub 6}] is a mixed valent germanium compound that contains [GeSb{sub 2}S{sub 8}]{sup 6-} units cross linked through Sb{sub 2}S{sub 2} units to generate layers. Highlights: Black-Right-Pointing-Pointer Preparation and structural characterisation of a new mixed-metal thiometallate. Black-Right-Pointing-Pointer Germanium present in two oxidation states. Black-Right-Pointing-Pointer Optical band gap of 2.49(4) eV. Black-Right-Pointing-Pointer Band gap conforms to a correlation between band gap and density of metal centres.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗