Search

We demonstrate modulation of insulator metal transition (IMT) of VO2 films grown on single crystalline substrates through the effect of in-plane compression with crystallization of capping chalcogenide layer on the targeted VO2 films. Chalcogenide germanium–antimony–telluride (Ge2Sb2Te5: GST), which shows large volume reduction of 6.8% with its phase change from amorphous to crystal, was deposited on VO2 films grown on Al2O3 (001) and TiO2 (001) substrates, where V–V atoms along the cR-axis in the tetragonal VO2 phase align parallel and perpendicular to the substrate surfaces, respectively. As a result, counter shifts in temperature-dependence of resistance characteristics, to lower and higher directions, were observed for VO2 films on Al2O3 (001) and TiO2 (001), consistent with the lattice modulation of VO2 films by the in-plane compression introduced by GST crystallization. The obtained results open a way to realize large resistance change of IMT under constant temperature by controlling GST phases. [ABSTRACT FROM AUTHOR]

Abstract: Structure elucidation plays a critical role across the landscape of medicinal chemistry, including medicinal inorganic chemistry. Herein, we discuss the importance of structure elucidation in drug development and then provide three vignettes that capture key instances of its relevance in the development of biologically active inorganic compounds. In the first, we describe the exploration of the biological activity of the trinuclear Ru compound called ruthenium red and the realization that this activity derived from a dinuclear impurity. We next explore the development of Au‐based antitubercular and antiarthritic drugs, which features a key step whereby ligands were discovered to bind to Au through S atoms. The third exposition traces the development of As‐based antiparasitic drugs, a key step of which was the realization that the reaction of arsenic acid and aniline does not produce an anilide of arsenic acid, as originally thought, but rather an amino arsonic acid. These case studies provide the motivation for an outlook in which the development of Sb‐based antiparasitic drugs is described. Although antileishmanial pentavalent antimonial drugs remain in widespread use to this day, their chemical structures remain unknown.

Copyright of Nonferrous Metals (Extractive Metallurgy) is the property of Beijing Research Institute of Mining & Metallurgy Technology Group and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Metal enrichment in aquatic ecosystems has compromised the potential of fish to enhance food security. The uMgeni River drains urban and industrialized catchment and flows through economically disadvantaged rural communities that opt for fish to supplement their protein needs. However, there are uncertainties on the safety of consuming fish from the uMgeni River. The present study aims to explore metal distribution between the water, sediment, and tissues of the preferred Oreochromis mossambicus, and evaluate whether concentrations in the muscle are safe for human consumption. The water, sediment, and fish samples were collected from Inanda and Nagle dams, and metal concentrations were analysed using inductively coupled plasma mass spectrometry. Alkaline pH was observed at both dams and metals were below detectable level in the water column. Even though metal concentrations in the water column were below detectable levels, significant concentrations were found in the sediment. No consistent trend in metal concentrations was observed across tissues, but higher levels were generally found in the liver, followed by the gill, and then the muscle. Nickel (Ni) and lead (Pb) exhibited concentrations exceeding the permissible limit for human consumption. Similarly, the target hazard quotient exceeded the threshold of 1 for Pb, chromium (Cr), and antimony (Sb) at both dams with Inanda Dam showing higher indices for Sb and Pb. The carcinogenic risk for the three metals was also found to be higher than 10–6. These findings suggest that consumption of O. mossambicus from the uMgeni River should be limited to no more than 150 g per week. [ABSTRACT FROM AUTHOR]

Antimony is one of the world's scarcest metals and is listed as a Critical Raw Material (CRM) for the European Union. To meet the increasing demand for metals in a sustainable way, one of the strategies that could be implemented would be the recovery of metals as by-products. This would decrease the amount of hazardous materials filling mining dumps. The present study investigates the potential for producing antimony as a by-product at the Olympias separation plant in Northern Greece. This plant works a skarn mineralization that shows interesting amounts of Sb. Boulangerite (Pb5Sb4S11) reports on Pb concentrate levels reached 8% in the analyzed product. This pre-enrichment is favorable in terms of boulangerite recovery since it can be separated from galena through froth flotation. Boulangerite distribution in the primary ore is quite heterogeneous in terms of the inclusion relationships and grain size. However, a qualitative assessment shows that the current Pb concentrate grain size is too coarse to successfully liberate a good amount of boulangerite. The use of image analysis and textural assessments is pivotal in determining shape factors and crystal size, which is essential for the targeting of flotation parameters during separation. The extraction of antimony as a by-product is possible through a two-step process; namely, (i) the preliminary concentration of boulangerite, followed by (ii) the hydrometallurgical extraction of the antimony from the boulangerite concentrate. The Olympias enrichment plant could therefore set a positive example by promoting the benefits of targeted Sb extraction as a by-product within similar sulfide deposits within the European territory. [ABSTRACT FROM AUTHOR]

We report on the synthesis, structure and reactivity of [{NCNMe4}Sb(C6H2-tBu2-3,5-O-4)] (3), an organoantimony(III)-oxyaryl species obtained upon Csp2–H bond activation in a phenolate ligand and stabilised by the monoanionic pincer {NCNMe4}−. The mechanism leading to the formation of 3 is highly sensitive to steric considerations. It was probed experimentally and by DFT calculations, and a number of intermediates and related complexes were identified. All data agree with successive heterolytic bond cleaving and bond forming processes involving charged species, rather than a pathway involving free radicals as previously exemplified with congeneric bismuth species. The nucleophilic behaviour of the oxyaryl ligand in 3, a complex that features both zwitterionic and quinoidal attributes, was illustrated in derivatisation reactions. In particular, insertion of CS2 in the Sb–Coxyaryl bond generates [{NCNMe4}Sb(S2C-C6H2-tBu2-3,5-O-4)]. [ABSTRACT FROM AUTHOR]

The gold-antimony ore from Qinghai has a complex mineral composition, with gold primarily encapsulated in sulfides, oxides, and arsenopyrite, and antimony mainly present in stibnite and valentinite. The ore contains a high level of harmful arsenic, making it challenging to process. Mineralogical studies, flotation condition tests, and closed-circuit tests were conducted based on the characteristics of the ore. Under optimal separation conditions, the closed-circuit test yielded an antimony concentrate with a grade of 60. 86 % and a recovery rate of 94. 87 %, and a gold concentrate with a grade of 51. 23 g/t and a recovery rate of 69. 94 %. These promising results provide a reference for the beneficiation process development and utilization of this type of ore. [ABSTRACT FROM AUTHOR]

This study presents the polarization photodetection enhancement in Sb2Se3 nanotube (NT)‐based near‐infrared (NIR) photodetectors through simulation‐based and experimental investigations. High‐quality single‐crystal Sb2Se3 NTs are grown via chemical vapor deposition and characterized by using multiple techniques. The optical simulation reveals a remarkable difference in the light absorption ratio (specifically, absorption along the NT/nanowire (NW) against absorption perpendicular to the NT/NW) between Sb2Se3 NT and NW of the same size in the NIR region. The complementary photodetection experiments present that the fabricated Sb2Se3 NT photodetector demonstrates enhanced polarization photodetection in the NIR range, as indicated by a significantly increased dichroic ratio (3.03 at 850 nm) compared to that of similar‐sized NW counterpart (1.81 at 850 nm). Additionally, the Sb2Se3 NT photodetector exhibits exceptional performance, with a high responsivity of 4.18 A W−1 and specific detectivity of 8.94 × 1010 Jones under 830 nm light illumination. This study provides a comprehensive understanding of the microcavity resonance effect and its role in polarization photodetection enhancement, highlighting the potential of self‐assembled Sb2Se3 NTs in high‐performance near‐infrared polarized photodetection and other relevant applications. [ABSTRACT FROM AUTHOR]

Anode dissolution of lead, silver, antimony and liquid lead-bismuth-antimony alloys has been studied by the polarization method depending on the alloy composition in the molten KCl-PbCl2 eutectic. Lead was found to dissolve and to form Pb2+ ions within the whole range of anode current densities in the Pb-Ag-Sb (49.0–28.0-23.0) and Pb-Ag-Sb (11.0-55.0-34.0) melts. The limiting diffusion current of lead dissolution was observed at the anode current density of 0.34 А cm−2 in the Pb-Ag-Sb (5.0-65.0-30.0) alloy. At the anode current densities exceeding these values the antimony dissolution was observed. To define a mechanism of metals electro dissolution, the number of electrons participating in the electrode reactions was calculated. Based on the polarization curves analysis the regime of electrochemical separation of lead alloys was selected. Metallic lead and the remaining Ag-Sb-Pb alloy with the valuable components concentration exceeding 90 wt% were obtained in the laboratory-scale electrolytic cell. [ABSTRACT FROM AUTHOR]

Antimony (Sb) is currently a widespread element with key roles in telecommunication, sustainable energy, and military industries, among others. Its significant toxicity determines the need to realize sensors for water, air, and soil and the industrial process monitoring of Sb species. Unfortunately, no antimony sensors exist so far, and just laboratory analysis methods are in use. We aimed to contribute to the development of optical sensors for the metalloid by tailoring, for the first time, luminescent Ru(II) and Re(I) polypyridyl complexes to probe and quantify the presence of Sb(III). The molecular design of the complexes includes the multifunctional Sb-binding 2-(2,2′-bithien-5-yl)-1H-imidazo[4,5-f]-1,10-phenanthroline (btip) ligand that ensures the molecular binding of Sb(III) in organic media. The Ru(II)-btip complex is additionally endowed with one 2,2′-bipyrazine (bpz) or two 1,4,5,8-tetraazaphenanthrene (tap) ligands, namely [Ru(bpz)(btip)2]2+ and [Ru(tap)2(btip)]2+, that boost the excited state oxidation potential of the probe, leading to an intramolecular photoinduced electron transfer from btip to the Ru(II) core. The latter is suppressed upon interaction with Sb(III), leading to an 11-fold increase in both the luminescence intensity and lifetime of [Ru(bpz)(btip)2]2+ in the presence of ca. 50 μmol L−1 of SbCl3 in organic medium. The fluorescence intensity of [Re(CO)3(H2O)(btip)]+ also increases upon interaction with Sb(III) but to a much lesser extent due to the intraligand π*→π nature of its emission compared to the Ru(II) ligand-to-metal excited state deactivation. However, the weak π*→d emission band in the red spectral region of the former is quenched by the semimetallic element. The sensing mechanisms of the Ru(II)- and Re(I)-btip probes that allow luminescence intensity (Ru, Re), ratiometric (Ru), and lifetime measurements (Ru) are compared and discussed in this initial solution sensing study. [ABSTRACT FROM AUTHOR]

At present, soil contaminated with arsenic (As) and antimony (Sb) is escalating at an alarming rate, which is harmful to human health. In this study, Fe- and Mn-modified activated carbon (AC) and biochar (BC) were prepared and compared for the remediation of As- and Sb-contaminated soil. The effects on the speciation of As and Sb, soil pH, organic matter (SOM), and enzyme activity with various dosages and remediation times were investigated. The results showed that on the whole, the best stabilization effect of As and Sb was achieved with 3% FeMnBC. Furthermore, with increases in time and dosage, the immobilization effect on As and Sb was more significant. Fe/Mn-modified AC and BC enhanced soil pH, with 3% MnAC being particularly effective; 3% AC and 3% FeMnAC demonstrated the most pronounced enhancement in SOM. The modified carbon materials exhibited a dramatic increase in enzymatic activity. In particular, urease activity showed an increasing trend, and catalase activity first decreased and then increased over 30 days. Among the treatments, 3% MnAC showed the most significant enhancements in catalase and urease activities, whereas 1% FeMnBC had the most pronounced effect on increasing sucrase activity. This study provides theoretical support for the remediation of soil co-contaminated with As and Sb by Fe/Mn-modified AC and BC. [ABSTRACT FROM AUTHOR]

Antimony (Sb) is a metal compound that can cause health problems when it accumulates in the food chain and becomes toxic to the ecosystem. Industrial activities have driven Sb contamination of water, including surface water. At the same time, some drinking water treatment plants (DWTP) use surface water as raw water, which requires adequate treatment. An invention of cheap and accessible technology is needed for developing countries such as Indonesia; hence, this study presents research on modified activated carbon with iron sulfate and manganese sulfate to create a better adsorbent from commercial granular activated carbon (GAC). The independent variables in this study included the type of adsorbent (GAC and GACMF), acidity level, and dosage. Response surface methodology was implemented for the analysis. According to the study, it was found that the optimum state of non-modified GAC for Sb removal appears at pH 3 and a dosage of 0.03 g L-1. In contrast, the presence of modified GAC was more effective for Sb removal with an optimum pH of 6 and a dosage of 0.057 g L-1 for GACMF. This research suggests that GACMF is preferable for DWTP because the optimization shows that GACMF is optimized in a neutral state; therefore, additional chemicals are unnecessary to achieve a neutral acidity state. [ABSTRACT FROM AUTHOR]

Antimony chalcogenide solar cells have captured considerable attention in recent years with an efficiency of over 10%, due to their use of Earth‐abundant materials and superior physical characteristics. Despite these achievements, significant nonradiative recombination processes within these solar cells present a substantial obstacle to further efficiency improvements. Therefore, this review delves into the primary mechanisms responsible for nonradiative recombination losses in antimony chalcogenide solar cells. Additionally, the latest advancements in addressing these losses are summarized. Finally, potential directions for future research efforts aimed at reducing nonrecombination losses and enhancing the overall performance of these devices are outlined. [ABSTRACT FROM AUTHOR]

The Lautenthal sphalerite-galena vein deposit is part of the world-class Upper Harz Pb-Zn-Ag district in the Harz uplift block of the Paleozoic Variscan fold belt in Germany. Its sphalerite-dominated mineral association was studied using bulk-ore chemistry, electron probe microanalysis, and laser ablation-ICP-mass spectrometry. Gallium and locally In are the main high-tech-relevant trace elements hosted by sphalerite, with up to 150 ppm Ga and up to 380 ppm In in hand-picked sphalerite samples (mean In/Zn, 0.70 × 10−3). Ore concentrates (≤ 50 kg) contain up to 65 ppm Ga and up to 109 ppm In (mean In/Zn, 0.36 × 10−3). Accessory Fe-Co-rich gersdorffite-1 occurs in the earlier quartz-sulfide ore stage and Sb-rich gersdorffite-2 in the later carbonate-sulfide stage. Enrichment patterns of In are either defined by overprinting textures in the Fe-richer sphalerite-1 of the earlier stage, or relate to primary growth zoning in Fe-poor sphalerite-2 of the later stage. Using the sphalerite geothermometer GGIMFis, formation temperatures (median) of sphalerite-1 were estimated at ~ 230 °C for the Lautenthal orebody and at ~ 175 °C for the Bromberg orebody, which may indicate lateral T-zonation for the earlier ore stage. Sphalerite-2 data indicate formation temperatures of ~ 185 °C (median). Copper-bearing brines of the carbonate-sulfide stage with assumed temperatures of ~ 250 °C initiated replacement of In-poor sphalerite-1 by chalcopyrite and remobilization of Zn and trace elements. Indium-rich sphalerite-2 occurs associated with calcite and fine-grained galena. A direct spatial or temporal link of ore formation to a magmatic-hydrothermal system is unlikely, which contrasts to In-rich epithermal and tin-polymetallic vein deposits worldwide. [ABSTRACT FROM AUTHOR]

Potassium ion batteries (PIBs) are potentially low-cost and high-voltage alternative energy storage systems to lithium-ion batteries. Anode materials with high density and high specific capacity, such as antimony-based materials, are the most sought-after objects. Herein, microtri-prism Sb4O5Cl2 with a uniform size and high compact density of 3.5 g cm–3 is controllably synthesized by the ball-milling-assisted hydrolysis method. Distilled water and absolute ethanol in an optimized volumetric ratio of 2/1 are introduced as reaction solvents to modify the reaction rate and, in turn, control the products' morphology. The ex situ investigation results indicate that the in situ nanolization conversion from microtri-prisms to nanoparticles of Sb4O5Cl2 during the initial discharge process confers Sb4O5Cl2 an exceptional potassium-ion storage performance. The electrochemical measurement results further manifest that potassium-ion storage performance achieved by the Sb4O5Cl2 microtri-prisms is superior to other reported Sb4O5Cl2. At 0.1, 0.2, 0.5, 1.0, and 2.0 A g–1, K//Sb4O5Cl2 microtri-prisms half PIBs could deliver 501.9, 456.6, 401.1, 325.0, and 249.2 mA h g–1, and retain 193.2 mA h g–1 with a Coulombic efficiency of 99.7% and a capacity retention ratio of 95.1% after 500 cycles at 2.0 mA g–1. [ABSTRACT FROM AUTHOR]

The effective modification of photovoltaic activities in photoelectric devices is significant for enhancing energy conversion efficiency. Here, the pressure‐tunable photovoltaic properties in the SbI3 device with Au/Pt asymmetric electrodes are demonstrated. At initial pressure, the SbI3 device exhibits an anticipated self‐driven photoresponse characteristic at zero external bias, and a significant enhancement in photocurrent response is observed with increasing bias to −0.2 V, nearly two orders of magnitude higher than the initial value. With increasing pressure, the SbI3 device exhibits tunable photocurrent response, reaching a maximum value at ≈1.2 GPa, while the photovoltage response decreases monotonously during compression, which is closely associated with the dynamic evolution of the work function and bandgap of SbI3 upon successive compression. These findings signify that SbI3 is a promising candidate for future photoelectric devices, which opens a new window of opportunity for further exploration, regulation, and understanding of high‐performance photovoltaic devices under extreme conditions. [ABSTRACT FROM AUTHOR]

Heavy metal concentrations, which have increased continuously in the environment this century due to anthropogenic factors, severely threaten human and environmental health. Antimony (Sb) is one of the most toxic and harmful heavy metals in terms of human and environmental health. Therefore, the priority research subjects are monitoring the alteration of Sb pollution in the airborne and reducing pollution. This study was conducted to conclude the proper species to monitor and drop airborne Sb contamination on trees grown in Düzce, the 5th most polluted European city. This study examined samples taken from Pseudotsuga menziesii, Cupressus arizonica, Pinus pinaster, Picea orientalis, and Cedrus atlantica, and the Sb concentration changes based on tree species, route, tissue, and age range in the last 40 years were evaluated. The study hypothesizes that Sb concentration varies depending on (1) tree species, (2) direction, (3) plant tissue, and (4) age range, all confirmed in this study. In conclusion, the maximum concentrations were achieved in the outer bark and east (5.45 µg g−1) and north directions (6.72 µg g−1), with high traffic density. In addition, the mining and industrial places (sources of metal pollution) are not close to the study area. Therefore, it was concluded that traffic pollution was the primary source of Sb pollution in the study area. The study revealed that C. arizonica is the most suitable species for monitoring and reducing the change in Sb pollution because the highest Sb concentration (4.47 µg g−1) in wood (the largest organ) was obtained in C. arizonica. [ABSTRACT FROM AUTHOR]

The evolution of Sb2Se3 heterojunction devices away from CdS electron transport layers (ETL) to wide bandgap metal oxide alternatives is a critical target in the development of this emerging photovoltaic material. Metal oxide ETL/Sb2Se3 device performance has historically been limited by relatively low fill factors, despite offering clear advantages with regards to photocurrent collection. In this study, TiO2 ETLs are fabricated via direct current reactive sputtering and tested in complete Sb2Se3 devices. A strong correlation between TiO2 ETL processing conditions and the Sb2Se3 solar cell device response under forward bias conditions is observed and optimized. Numerical device models support experimental evidence of a spike‐like conduction band offset, which can be mediated, provided a sufficiently high conductivity and low interfacial defect density can be achieved in the TiO2 ETL. Ultimately, a SnO2:F/TiO2/Sb2Se3/P3HT/Au device with the reactively sputtered TiO2 ETL delivers an 8.12% power conversion efficiency (η), the highest TiO2/Sb2Se3 device reported to‐date. This is achieved by a substantial reduction in series resistance, driven by improved crystallinity of the reactively sputtered anatase‐TiO2 ETL, whilst maintaining almost maximum current collection for this device architecture. [ABSTRACT FROM AUTHOR]

Band structure of a semiconducting film critically determines the charge separation and transport efficiency. In antimony selenosulfide (Sb2(S,Se)3) solar cells, the hydrothermal method has achieved control of band gap width of Sb2(S,Se)3 thin film through tuning the atomic ratio of S/Se, resulting in an efficiency breakthrough towards 10 %. However, the obtained band structure exhibits an unfavorable gradient distribution in terms of carrier transport, which seriously impedes the device efficiency improvement. To solve this problem, here we develop a strategy by intentionally regulating hydrothermal temperature to control the chemical reaction kinetics between S and Se sources with Sb source. This approach enables the control over vertical distribution of S/Se atomic ratio in Sb2(S,Se)3 films, forming a favorable band structure which is conducive to carrier transport. Meanwhile, the adjusted element distribution not only ensures the uniformity of grain structure, but also increases the Se content of the films and suppress sulfur vacancy defects. Ultimately, the device delivers a high efficiency of 10.55 %, which is among the highest reported efficiency of Sb2(S,Se)3 solar cells. This study provides an effective strategy towards manipulating the element distribution in mixed‐anion compound films prepared by solution‐based method to optimize their optical and electrical properties. [ABSTRACT FROM AUTHOR]

There is an increasing demand for cost-effective semi-passive water treatment that can withstand challenging climatic conditions and effectively and sustainably manage mine-impacted water in (sub)arctic regions. This study investigated the ability of four pilot-scale bioreactors inoculated with locally sourced bacteria and affected by a freeze–thaw cycle to remove selenium and antimony. The bioreactors were operated at a Canadian (sub)arctic mine for a year. Two duplicate bioreactors were installed in a heated shed that was maintained at 5 °C over the winter, while two other duplicates were installed outdoors and left to freeze. The removal rate of selenium and antimony was monitored weekly, while a genomic characterization of the microbial populations in the bioreactors was performed monthly. The overall percentage of selenium and antimony removal was similar in the outside (10–93% Se, 20–96% Sb) and inside (35–94% Se, 10–95% Sb) bioreactors, apart from the spring thawing period when removal in the outdoor bioreactors was slightly lower for Se. The dominant taxonomic groups of microbial populations in all bioreactors were Bacteroidota, Firmicutes, Desulfobacterota and Proteobacteria. The microbial population composition was consistent and re-established quickly after spring thaw in the outside bioreactors. This demonstrated that the removal capacity of bioreactors inoculated with locally sourced bacteria was mostly unaffected by a freeze–thaw cycle, highlighting the strength of using local resources to design bioreactors in extreme climatic conditions. [ABSTRACT FROM AUTHOR]

Introduction: There are limited data available regarding the connection between heavy metal exposure and mortality among hypertension patients. Aim: We intend to establish an interpretable machine learning (ML) model with high efficiency and robustness that monitors mortality based on heavy metal exposure among hypertension patients. Methods: Our datasets were obtained from the US National Health and Nutrition Examination Survey (NHANES, 2013–2018). We developed 5 ML models for mortality prediction among hypertension patients by heavy metal exposure, and tested them by 10 discrimination characteristics. Further, we chose the optimally performing model after parameter adjustment by genetic algorithm (GA) for prediction. Finally, in order to visualize the model's ability to make decisions, we used SHapley Additive exPlanation (SHAP) and Local Interpretable Model-Agnostic Explanations (LIME) algorithm to illustrate the features. The study included 2347 participants in total. Results: A best-performing eXtreme Gradient Boosting (XGB) with GA for mortality prediction among hypertension patients by 13 heavy metals was selected (AUC 0.959; 95% CI 0.953–0.965; accuracy 96.8%). According to sum of SHAP values, cadmium (0.094), cobalt (2.048), lead (1.12), tungsten (0.129) in urine, and lead (2.026), mercury (1.703) in blood positively influenced the model, while barium (− 0.001), molybdenum (− 2.066), antimony (− 0.398), tin (− 0.498), thallium (− 2.297) in urine, and selenium (− 0.842), manganese (− 1.193) in blood negatively influenced the model. Conclusions: Hypertension patients' mortality associated with heavy metal exposure was predicted by an efficient, robust, and interpretable GA-XGB model with SHAP and LIME. Cadmium, cobalt, lead, tungsten in urine, and mercury in blood are positively correlated with mortality, while barium, molybdenum, antimony, tin, thallium in urine, and lead, selenium, manganese in blood is negatively correlated with mortality. [ABSTRACT FROM AUTHOR]

Antimony (Sb) toxicity is a serious concern across the globe due to its hazardous impacts on plants and living organisms. The co-application of Chinese milk vetch (CMV) and biochar (BC) is a common agricultural practice, however, the effects of combined CMV and BC in mitigating Sb toxicity and bio-availability remain unclear. Therefore, this study investigated the impacts of CMV, rape straw biochar (RBC), and iron-modified biochar (FMB) and their combinations on rice productivity, physiological, and biochemical functioning of rice and Sb availability. Antimony toxicity caused a marked reduction in rice growth and productivity by decreasing chlorophyll, and anthocyanin synthesis, leaf water contents, osmolyte synthesis and antioxidant activities while, increasing hydrogen peroxide (H2O2), electrolyte leakage (EL), and malondialdehyde (MDA) production and Sb accumulation. Co-application of CMV and FMB increased biomass (29.50%) and grain yield (51.07%) of rice by increasing chlorophyll, and anthocyanin synthesis, leaf water contents, osmolyte synthesis, antioxidant activities, and decreasing production of H2O2, EL, and MDA and Sb accumulation in roots (90.41%) and shoots (96.38%). Furthermore, the combined addition of CMV and FMB also reduced the soil available Sb by 75.57% which resulted in less accumulation of Sb in plant parts and improved growth and yield. Given these facts, these findings indicate that co-application of CMV and FMB is a promising approach to remediate Sb-polluted soils and improve sustainable and safer rice productivity. [ABSTRACT FROM AUTHOR]

The title compound was synthesized from perfluoro-1-ethyltetralin and 1,2,3,4-tetrafluorobenzene under the action of antimony pentafluoride as a mixture of cis- and trans-isomers in a 71% isolated yield. The structure and cis-/trans-configuration of the isomers were determined by NMR (19F, 13C), 19F–19F COSY, and 19F–19F NOESY 2D NMR spectroscopy. [ABSTRACT FROM AUTHOR]

Peptide therapeutics play an increasingly important role in modern drug discovery. Improving the pharmacokinetic profile of bioactive peptides has been effectively achieved with chemical modifications, especially macrocyclisation reactions. Consequently, there is a great demand for highly constrained compounds such as bicyclic peptides. In our previous research, we introduced peptide–bismuth bicycles and peptide–arsenic bicycles as new classes of constrained peptides. In this work, we extend our peptide bicyclisation strategy towards antimony. Similar to arsenic and bismuth, antimony(III) selectively binds to three cysteine residues in peptides, enabling the in situ formation of stable bicycles. The bicyclisation reaction occurs instantaneously under biocompatible conditions at physiological pH. Antimony–peptide bicycles remain largely intact in the presence of the common metal chelator ethylenediaminetetraacetic acid (EDTA) and the main endogenous thiol competitor glutathione (GSH). Furthermore, when challenged with bismuth(III) from water-soluble gastrodenol (bismuth tripotassium dicitrate), antimony–peptide bicycles convert into the corresponding bismuth–peptide bicycle, highlighting the superior thiophilicity of bismuth over other pnictogens. Our study further expands the toolbox of peptide multicyclisation with main group elements previously underexplored in chemical biology. Cyclic peptide drugs are important therapeutics. Previously, bismuth and arsenic were introduced to create peptide bicycles by binding three cysteines. Now, antimony complements this set of elements to form stable bicyclic peptides. These remain stable in the presence of a common metal chelator and glutathione. Bismuth outcompetes antimony as the core atom in peptide bicycles. (Image credit: Lani Davies.) This article belongs to the 10th Anniversary Collection of RACI and AAS Award papers. [ABSTRACT FROM AUTHOR]

Antimony (Sb) is one of the most concerning toxic metals globally, making the study of methods for efficiently removing Sb(III) from water increasingly urgent. This study uses graphene oxide and chitosan as the matrix (GOCS), modifying them with FeCl2 and four MnOx to form iron–manganese oxide (FM/GC) at a Fe/Mn molar ratio of 4:1. FM/GC quaternary composite microspheres are prepared, showing that FM/GC obtained from different MnOx exhibits significant differences in the ability to remove Sb(III) from neutral solutions. The order of Sb(III) removal effectiveness is MnSO4 > KMnO4 > MnCl2 > MnO2. The composite microspheres obtained by modifying GOCS with FeCl2 and MnSO4 are selected for further batch experiments and characterization tests to analyze the factors and mechanisms influencing Sb(III) removal. The results show that the adsorption capacity of Sb(III) decreases with increasing pH and solid–liquid ratio, and gradually increases with the initial concentration and reaction time. The Langmuir model fitting indicates that the maximum adsorption capacity of Sb(III) is 178.89 mg/g. The adsorption mechanism involves the oxidation of the Mn-O group, which converts Sb(III) in water into Sb(V). This is followed by ligand exchange and complex formation with O-H in FeO(OH) groups, and further interactions with C-OH, C-O, O-H, and other functional groups in GOCS. [ABSTRACT FROM AUTHOR]

Antimony (Sb) migration in soil and water systems is predominantly governed by its adsorption onto ferrihydrite (FH), a process strongly influenced by natural organic matter. This study investigates the adsorption behavior, stability, and mechanism of FH and FH–humic acid (FH-HA) complexes on Sb(V), along with the fate of adsorbed Sb(V) during FH aging. Batch adsorption experiments reveal that initial pH and concentration significantly influence Sb(V) sorption. Lower pH levels decrease adsorption, while higher concentrations enhance it. Sb(V) adsorption increases with prolonged contact time, with FH exhibiting a higher adsorption capacity than FH-HA complexes. Incorporating HA onto FH surfaces reduces reactive adsorption sites, decreasing Sb(V) adsorption. Adsorbed FH-HA complexes exhibit a higher specific surface area than co-precipitated FH-HA, demonstrating stronger Sb(V) adsorption capacity under various conditions. X-ray photoelectron spectroscopy (XPS) confirms that Sb(V) adsorption primarily occurs through ligand exchange, forming Fe-O-Sb complexes. HA inhibits the migration of Sb(V), thereby enhancing its retention within the FH and FH-HA complexes. During FH transformation, a portion of Sb(V) may replace Fe(III) within converted iron minerals. However, the combination of relatively high adsorption capacity and significantly lower desorption rates makes adsorbed FH-HA complexes promising candidates for sustained Sb adsorption over extended periods. These findings enhance our understanding of Sb(V) behavior and offer insights for effective remediation strategies in complex environmental systems. [ABSTRACT FROM AUTHOR]

In the present study, we show the electrochemical synthesis of Sb, Sn, and Sb-Sn nanowire arrays from the ionic liquid 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonate ([Py1,4]TfO) via templated-assisted approaches. Commercially available track etched polycarbonate template with a nominal pore diameter of 400 nm was utilized as a template. The nanowires were electrochemically deposited inside the pores of the template; then, a supporting copper layer was electrodeposited on the back side of the template. Subsequently, the template was dissolved with dichloromethane, and the structural morphology of the nanowire structures was explored by high-resolution scanning electron microscopy (SEM) and energy dispersive x-ray (EDX). Freestanding, mechanically stable nanowire arrays of Sb, Sn, and Sb-Sn with an average pore diameter of 400 nm were obtained. The charge/discharge characteristics of the electrodeposited nanowire films were investigated to explore the Li storage capacity of the fabricated electrodes. The results revealed that the electrodeposited nanowire films are promising anode candidates for the future generation of Li-ion batteries. [ABSTRACT FROM AUTHOR]

Herein, first-principles calculations predicted the atomic-scale variation of Sb5+ substitution for ZnZrTa 2 O 8 , and combined with the solid-phase reaction method to prepare ZnZr(Ta 1- x Sb x) 2 O 8 (0.0 ≤ x ≤ 0.10) ceramics. ZnZr(Ta 0.94 Sb 0.06) 2 O 8 ceramics demonstrated the optimum microwave dielectric properties after sintering at 1350 °C for 6 h: ε r = 24.92, Q × f = 134053 GHz (@7.18 GHz), and τ f = −46.21 ppm/°C. For the non-intrinsic factors, the relative density increased from 96.54 % to 97.74 % and the average grain size increased from 19.88 μm to 21.85 μm, both of which reduced the dielectric loss. Regarding intrinsic factors, the progressive elevation of the Raman characteristic peak wave number and the heightened ionicity of Ta/Sb–O bonds predominantly account for the observed enhancement in εr. In addition, the attenuation of lattice vibrational damping behavior, the augmentation in electron cloud density, and the escalation of lattice energy collectively contribute to a decrement in dielectric loss. This study refines the examination of ionic substitution in ZnZrTa 2 O 8 ceramics, offering theoretical insights for optimizing their dielectric properties and promoting their application in microwave communications. [ABSTRACT FROM AUTHOR]

The sorption of certain lanthanides from aqueous solutions is the focus of this work using antimony oxide (Sb2O5) sorbent. Sb2O5 sorbent was prepared using the precipitation technique, and it has been described using several analytical methods such as Fourier-transformed infrared (FT-IR), X-ray diffraction pattern (XRD), and scanning electron microscope (SEM). The sorption data were collected on Y(III), Ce(III), and Gd(III) including the effects of pH, shaking time, initial metal concentrations, and temperature. The results revealed that saturation capacity has values of (30.6, 27.5, and 24.1 mg/g) for Y(III), Ce(III), and Gd(III), respectively. The sorption of the studied cations is dependent on pH. The reaction kinetics obeyed the pseudo-2nd-order model, and thermodynamics was endothermic and spontaneous. Sorption isotherms are more relevant to a Langmuir isotherm, whose monolayer capacity values are 27.9, 23.2, and 19.8 mg/g for Y(III), Ce(III), and Gd(III), respectively. The real sample applications illustrate the superiority of antimony oxide sorbent in the removal of Y(III), Ce(III), and Gd(III) from high-grade monazite (HGM). [ABSTRACT FROM AUTHOR]

This work delves into the preparation of ATO thin films and their characterization, fabrication, and calibration of a NO2 gas sensor, as well as the development of the packaged sensor. ATO thin films were prepared by e-beam evaporation using green synthesized ATO nanomaterials on different substrates and annealed at 500 and 600 °C for one hour. The structural and morphological properties of the developed thin films were studied using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD) techniques. An orthorhombic SnO2 crystal structure was recognized through XRD analysis. The granular-shaped nanoparticles were revealed through SEM and TEM images. The films annealed at 600 °C exhibited improved crystallinity. ATO films prepared on normal 5 µm interdigitated electrodes (IDEs) and annealed at 600 °C exhibited a response of 10.31 ± 0.25 with an optimum temperature of 200 °C for a 4.8 ppm NO2 gas concentration. The packaged NO2 gas sensor developed using IDEs with a microheater demonstrated an improved response of 16.20 ± 0.25 for 4.8 ppm of NO2 gas. [ABSTRACT FROM AUTHOR]

The degradation characteristics of aniline and antimony in printing and dyeing wastewater during the micro-oxygenated hydrolytic acidification process and its effect on COD and ammonia nitrogen removal were investigated in this experiment. Firstly, the effects of control factors such as pH, dissolved oxygen (DO), and sludge concentration on COD and ammonia nitrogen removal in the hydrolysis acidification section were optimized. It was recommended that the pH value should be maintained at 6.5; low DO (0–0.5 mg/L) could assist in the conversion of nitrogen for subsequent treatment; the optimum treatment temperature was 25 °C; finally, it was recommended that the sludge concentration should be controlled at 4 mg/L during the operation. Secondly, the effects of aniline and antimony on COD and nitrogen removal were investigated. It was found that when the concentration of aniline was increased from 0.4 mg/L to 5.4 mg/L, the COD concentration in the effluent increased by 96.5%, which indicated that aniline was toxic to anaerobic sludge and obviously inhibited the degradation of COD. When the concentration of antimony was increased from 0.05 mg/L to 2.05 mg/L, the COD removal rate was only 2.9%, which was much lower than that of the water samples with no antimony added. The anaerobic sludge concentration decreased from 5.58 g/L to 3.44 g/L, which indicated that aniline and antimony had a strong inhibitory effect on the activity of anaerobic bacteria and inversely affected COD removal. [ABSTRACT FROM AUTHOR]

Copyright of Rare Metals is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Inorganic Analytical Chemistry / Zhongguo Wuji Fenxi Huaxue is the property of Beijing Research Institute of Mining & Metallurgy Technology Group and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Ahmet Cemal Pazarl&inodot;,1 Hüseyin Alper K&inodot;z&inodot;lo&gbreve;lu,2 Handan Inönü Köseo&gbreve;lu1 1Department of Pulmonary Diseases, Tokat Gaziosmanpasa University Faculty of Medicine, Tokat, Turkey; 2Department of Radiology, Tokat Gaziosmanpasa University Faculty of Medicine, Tokat, TurkeyCorrespondence: Ahmet Cemal Pazarl&inodot;, Department of Pulmonary Diseases, Tokat Gaziosmanpa&scedil;a University Faculty of Medicine, Tokat, Turkey, Tel +90 05053696860, Fax +90 0356 2129500, Email dracp60@gmail.comAim: Pneumoconiosis describes diseases caused by the accumulation of inorganic dust particles in the lungs, leading to tissue damage. The diagnosis relies on a history of exposure and compatible radiological findings.Background: We aimed to investigate the radiological findings in individuals exposed to antimony-inert dust relative to their working periods.Objective: Fifty-six symptomatic male antimony miners were retrospectively evaluated for demographics and chest computed tomography (CT) scans.Methods: The demographic and radiological data of patients with a history of antimony mining, who presented at our pulmonary clinic between June 2017 and June 2023, were analyzed according to the duration of exposure.Results: The study included 56 male patients with a mean age of 58.5± 13.02 years and a mean exposure duration of 13.63 ± 6.82 years. CT scans showed that 73.2% (n=41) had upper and middle lung zone involvement, and 55.4% (n=31) had extensive involvement. Micronodules with centriacinar ground-glass opacities were the most common finding (n=37, 66.1%), followed by nodular opacities with irregular margins (n=22, 39.3%) and solid micronodules (n=20, 35.7%). Patients with over 20 years of exposure had significantly higher rates of respiratory and cardiovascular disease (p< 0.05). Increased exposure time correlated with more extensive parenchymal involvement and higher rates of calcification in mediastinal lymph nodes, solid micronodules, nodular opacities with irregular margins, honeycombing, and conglomerate mass appearance.Conclusion: Radiological findings in pneumoconiosis generally worsen with longer exposure. Given the scarcity of up-to-date information on antimony pneumoconiosis, further studies focusing on radiological findings and chemical analyses of those exposed to antimony mine dust are essential to identify related pathologies.Keywords: rare lung diseases, antimony, pneumoconiosis, computerized thorax tomography, ground-glass opacities, lymph nodes

• The first standardized assessment for soil quality at Sb smelting site is developed. • Soil resilience index (SRI) and soil contamination index (SCI) are both evaluated. • Soil quality in Sb smelting site is mainly limited by low level of soil resilience. • The weak soil resilience is caused by relatively low specific microbial abundances. Antimony smelting activities damage the soil and vegetation surroundings while generating economic value. However, no standardized methods are available to diagnose the extent of soil degradation at antimony smelting sites. This study developed a standardized framework for assessing soil quality by considering microbial-induced resilience and heavy metal contamination at Xikuangshan antimony smelting site. The soil resilience index (SRI) and soil contamination index (SCI) were calculated by Minimum Data Set and geo-accumulation model, respectively. After standardized by a multi-criteria quantitative procedure of modified Nemerow's pollution index (NPI), the integrated assessment of soil quality index (SQI), which is the minimum of SRI NPI and SCI NPI , was achieved. The results showed that Sb and As were the prominent metal(loid) pollutants, and significant correlations between SQI and SRI indicated that the poor soil quality was mainly caused by the low level of soil resilience. The primary limiting factors of SRI were Fungi in high and middle contaminated areas, and Skermanella in low contaminated area, suggesting that the weak soil resilience was caused by low specific microbial abundances. Microbial regulation and phytoremediation are greatly required to improve the soil quality at antimony smelting sites from the perspectives of pollution control and resilience improvement. This study improves our understanding of ecological effects of antimony smelting sites and provides a theoretical basis for ecological restoration and sustainable development of mining areas. [Display omitted] [ABSTRACT FROM AUTHOR]

Heavy metal(loid) (HM) pollution in agricultural soils has become an environmental concern in antimony (Sb) mining areas. However, priority pollution sources identification and deep understanding of environmental risks of HMs face great challenges due to multiple and complex pollution sources coexist. Herein, an integrated approach was conducted to distinguish pollution sources and assess human health risk (HHR) and ecological risk (ER) in a typical Sb mining watershed in Southern China. This approach combines absolute principal component score-multiple linear regression (APCS-MLR) and positive matrix factorization (PMF) models with ER and HHR assessments. Four pollution sources were distinguished for both models, and APCS-MLR model was more accurate and plausible. Predominant HM concentration source was natural source (39.1%), followed by industrial and agricultural activities (23.0%), unknown sources (21.5%) and Sb mining and smelting activities (16.4%). Although natural source contributed the most to HM concentrations, it did not pose a significant ER. Industrial and agricultural activities predominantly contributed to ER, and attention should be paid to Cd and Sb. Sb mining and smelting activities were primary anthropogenic sources of HHR, particularly Sb and As contaminations. Considering ER and HHR assessments, Sb mining and smelting, and industrial and agricultural activities are critical sources, causing serious ecological and health threats. This study showed the advantages of multiple receptor model application in obtaining reliable source identification and providing better source-oriented risk assessments. HM pollution management, such as regulating mining and smelting and implementing soil remediation in polluted agricultural soils, is strongly recommended for protecting ecosystems and humans. [ABSTRACT FROM AUTHOR]

• Oxidative dissolution pathway of stibnite was studied by sulfate oxygen and sulfur isotope compositions. • The relative percentage of water-derived oxygen incorporation into sulfate increase from 5 % to 52 % with longer reaction duration. • A conceptual model of stibnite oxidative dissolution pathway under the aerobic abiotic conditions was proposed. The environmental threat posed by stibnite is an important geoenvironmental issue of current concern. To better understand stibnite oxidation pathways, aerobic abiotic batch experiments were conducted in aqueous solution with varying δ18O H2O value at initial neutral pH for different lengths of time (15-300 days). The sulfate oxygen and sulfur isotope compositions as well as concentrations of sulfur and antimony species were determined. The sulfur isotope fractionation factor (Δ34S SO4-stibnite) values decreased from 0.8‰ to -2.1‰ during the first 90 days, and increased to 2.6‰ at the 180 days, indicating the dominated intermediate sulfur species such as S 2 O 3 2−, S0, and H 2 S (g) involved in Sb 2 S 3 oxidation processes. The incorporation of O into sulfate derived from O 2 (∼100%) indicated that the dissociated O 2 was only directly adsorbed on the stibnite-S sites in the initial stage (0-90 days). The proportion of O incorporation into sulfate from water (27%-52%) increased in the late stage (90-300 days), which suggested the oxidation mechanism changed to hydroxyl attack on stibnite-S sites promoted by nearby adsorbed O 2 on stibnite-Sb sites. The exchange of oxygen between sulfite and water may also contributed to the increase of water derived O into SO 4 2−. The new insight of stibnite oxidation pathway contributes to the understanding of sulfide oxidation mechanism and helps to interpret field data. [ABSTRACT FROM AUTHOR]

Phase-change memory (PCM) is one of the leading candidates for the next generation nonvolatile memory. As a growth-dominated crystalline material, Sb2Te3 is of rapid crystallization speed while its poor thermal stability limits its application. Doping Ti can significantly enhance its amorphous stability but inevitably slows down its crystallization speed. How to balance the contradiction between thermal stability and operation speed remains challenging. In this work, we proposed a gradient Ti-doped Sb2Te3 phase-change material and device. This gradient doping strategy compensates for the negative effect of Ti doping on the crystallization rate of Sb2Te3 via the template effect of the lower doping concentration layer. Very small lattice mismatch between the Sb2Te3 layers with different Ti doping concentrations is verified by x-ray diffraction characterization. The crystallization temperature of a gradient Ti-doped Sb2Te3 thin film is raised up to 172.6 °C and the same 50 ns operation speed as a pure Sb2Te3 device is achieved in the corresponding PCM device. Furthermore, the gradient distribution of Ti elements and the corresponding progressive crystallization phenomenon are verified by transmission electron microscopy revealing the microscopic origin of rapid crystallization speed. Therefore, with our gradient doping strategy, the amorphous stability is improved without sacrificing the crystallization speed in PCM. [ABSTRACT FROM AUTHOR]

Chalcogenide thin films that undergo reversible phase changes show promise for use in next-generation nanophotonics, microelectronics, and other emerging technologies. One of the many studied compounds, Ge2Sb2Te5, has demonstrated several useful properties and performance characteristics. However, the efficacy of benchmark Ge2Sb2Te5 is restricted by amorphous phase thermal stability below ∼150 °C, limiting its potential use in high-temperature applications. In response, previous studies have added a fourth species (e.g., C) to sputter-deposited Ge2Sb2Te5, demonstrating improved thermal stability. Our current research confirms reported thermal stability enhancements and assesses the effects of carbon on crystalline phase radiation response. Through in situ transmission electron microscope irradiation studies, we examine the effect of C addition on the amorphization behavior of initially cubic and trigonal polycrystalline films irradiated using 2.8 MeV Au to various doses up to 1 × 1015 cm−2. It was found that increased C content reduces radiation tolerance of both cubic and trigonal phases. [ABSTRACT FROM AUTHOR]

Supercontinuum (SC) generation from alkali antimony zinc borate glasses was investigated using a femtosecond laser. The optical bandgap values were determined for all the glass samples. An enhancement in the generated SC is seen from sodium-doped glass although it possesses the least bandgap among the glass samples. The physical parameters of the glasses such as density, molar volume, refractive index, oxide ion polarizability, and optical basicity have been analyzed and discussed. The smaller values of the metallization criterion indicate the tendency of the glass samples to exhibit metallic behavior, which, in turn, affects the non-linear optical properties of the glasses. The shift in the binding energies of metal cations and oxygen anions was observed using XPS analysis, which gives an understanding about the extent of overlapping of valence orbitals in the glass system. The observations from the physical and structural investigations provide an insight into the anomaly in the enhanced SC generation from the low bandgap sodium-doped glass. [ABSTRACT FROM AUTHOR]

Arsenic is commonly used in alloy materials and the semiconductor industry, and has promising applications. Arsenic and antimony have similar physicochemical properties, and their binding and separation mechanisms are unknown, thereby limiting the purification and preparation of arsenic. This study, from a microscopic perspective, reveals that arsenic and antimony covalently interact in alloys through a combination of thermodynamic analysis and molecular dynamics simulations. In addition, antimony as arsenic-antimony clusters enters the gas phase, and the diffusion coefficients of the clusters are in the order of As4>As3Sb > As2Sb2>AsSb3. A green and efficient vacuum sublimation-graded condensation process for arsenic purification is proposed based on the different diffusion coefficients to obtain the optimal process parameters. The coalescence of arsenic on a condenser was normally distributed. The removal rate of antimony in the most concentrated area of the condensate was 91.37% under the optimal conditions of 748 K, 60 min, and 10 Pa. Thus, the proposed method effectively solves the challenging problem of separating arsenic and antimony, and the study results provide theoretical support for purifying arsenic via vacuum sublimation.

We describe a web-based tool, MakeSBML (https://sys-bio.github.io/makesbml/), that provides an installation-free application for creating, editing, and searching the Biomodels repository for SBML-based models. MakeSBML is a client-based web application that translates models expressed in human-readable Antimony to the System Biology Markup Language (SBML) and vice-versa. Since MakeSBML is a web-based application it requires no installation on the user’s part. Currently, MakeSBML is hosted on a GitHub page where the client-based design makes it trivial to move to other hosts. This model for software deployment also reduces maintenance costs since an active server is not required. The SBML modeling language is often used in systems biology research to describe complex biochemical networks and makes reproducing models much easier. However, SBML is designed to be computer-readable, not human-readable. We therefore employ the human-readable Antimony language to make it easy to create and edit SBML models.

The pursuit of advanced brain‐inspired electronic devices and memory technologies has led to explore novel materials by processing multimodal and multilevel tailored conductive properties as the next generation of semiconductor platforms, due to von Neumann architecture limits. Among such materials, antimony sulfide (Sb2S3) thin films exhibit outstanding optical and electronic properties, and therefore, they are ideal for applications such as thin‐film solar cells and nonvolatile memory systems. This study investigates the conduction modulation and memory functionalities of Sb2S3 thin films deposited via the vapor transport deposition technique. Experimental results indicate that the Ag/Sb2S3/Pt device possesses properties suitable for memory applications, including low operational voltages, robust endurance, and reliable switching behavior. Further, the reproducibility and stability of these properties across different device batches validate the reliability of these devices for practical implementation. Moreover, Sb2S3‐based memristors exhibit artificial neuroplasticity with prolonged stability, promising considerable advancements in neuromorphic computing. Leveraging the photosensitivity of Sb2S3 enables the Ag/Sb2S3/Pt device to exhibit significant low operating potential and conductivity modulation under optical stimulation for memory applications. This research highlights the potential applications of Sb2S3 in future memory devices and optoelectronics and in shaping electronics with versatility. [ABSTRACT FROM AUTHOR]

Boron subphthalocyanines with chloride and fluoride axial ligands and three antimony complexes chelated by corroles that differ in size and electron‐richness were examined as electrocatalysts for reduction of protons to hydrogen. Experiment‐ and computation‐based investigations revealed that all redox events are ligand‐centered and that the meso‐C of the corroles and the peripheral N atoms of the subphthalocyanines are the largely preferred proton‐binding sites. [ABSTRACT FROM AUTHOR]

Nanosize-controlled antimony oxides (Sb2O3) that can effectively scavenge fluoride species in a cell are incorporated into a PI separator to regulate its porous structure. The incorporation of the Sb2O3 layer onto the PI separator surface prevents the internal short circuit and efficiently removes fluoride species via chemical scavenging reactions, thereby resulting in stable cycling behaviors upon cycling. [ABSTRACT FROM AUTHOR]

The selective formation of antimony‐carbon bonds via organic superbase catalysis under metal‐ and salt‐free conditions is reported. This novel approach utilizes electron‐deficient stibine, Sb(C6F5)3, to give upon base‐catalyzed reactions with weakly acidic aromatic and heteroaromatic hydrocarbons access to a range of new aromatic and heteroaromatic stibines, respectively, with loss of C6HF5. Also, the significantly less electron‐deficient stibines, Ph2SbC6F5 and PhSb(C6F5)2 smoothly underwent base‐catalyzed exchange reactions with a range of terminal alkynes to generate the stibines of formulae PhSb(C≡CPh)2, and Ph2SbC≡CR [R=C6H5, C6H4‐NO2, COOEt, CH2Cl, CH2NEt2, CH2OSiMe3, Sb(C6H5)2], respectively. These formal substitution reactions proceed with high selectivity as only the C6F5 groups serve as a leaving group to be liberated as C6HF5 upon formal proton transfer from the alkyne. Kinetic studies of the base‐catalyzed reaction of Ph2SbC6F5 with phenyl acetylene to form Ph2SbC≡CPh and C6HF5 suggested the empirical rate law to exhibit a first‐order dependence with respect to the base catalyst, alkyne and stibine. DFT calculations support a pathway proceeding via a concerted σ‐bond metathesis transition state, where the base catalyst activates the Sb‐C6F5 bond sequence through secondary bond interactions. [ABSTRACT FROM AUTHOR]

Sb2S3 has been extensively used as light absorber for photoelectrochemical cell. However, its p‐type nature may result in the formation of Schottky junction with substrates, thus hindering the collection of photogenerated holes. Herein, an ultrathin CuxS layer is successfully engineered as the bottom junction for Sb2S3 for the first time. Capitalizing on its impressive electrical properties and superior optical properties, the CuxS layer exhibits a high work function of 4.90 eV, which causes the upward band bending of p‐type Sb2S3, forming a hole‐transparent structure with ohmic contact. The transparency of the ultrathin CuxS layer enables back‐illumination of the Sb2S3/CuxS platform, facilitating the integration of intricate catalyst layers for photoelectrochemical transformation. When modified with Pt nanoparticles, the photocurrent density reaches −5.38 mA cm−2 at 0 V vs. RHE, marking a fourfold increase compared to the photocathode without CuxS layer. When introducing a molecular hybrid TC‐CoPc@carbon black, a remarkable average photocurrent density of −0.44 mA cm−2 at the overpotential of 0 V is obtained for CO2 reduction reaction, while the photocurrent density is less than −0.03 mA cm−2 without CuxS. [ABSTRACT FROM AUTHOR]

Tetrahedrite-(Cu), Cu12Sb4S13, has been approved as a new mineral species (IMA2022–078) from the Bankov magnesite deposit near Košice, Slovak Republic where it occurs as anhedral grains, up to 0.4 mm across, associated with skinnerite, chalcostibite, famatinite, tetrahedrite-(Fe) and zoned aggregates of tennantite-(Cu) to tennantite-(Fe). Tetrahedrite-(Cu) is steel-grey, with a metallic lustre. Mohs hardness is ca. 3½–4 and calculated density is 5.029 g.cm–3. In reflected light, tetrahedrite-(Cu) is isotropic and grey with a bluish shade. Reflectance data for the four COM wavelengths in air are [λ (nm): R (%)]: 470: 31.1; 546: 30.1; 589: 29.9; and 650: 28.1. The empirical formula, based on electron-microprobe data (mean of 17 spot analyses), is Cu11.42Zn0.26Fe0.19(Sb4.06As0.08)Σ4.14S12.99. The ideal formula is Cu6(Cu4Cu2)Sb4S13, which requires (in wt.%) Cu 45.76, Sb 29.23 and S 25.01, total 100.00. Tetrahedrite-(Cu) is cubic, I $\bar{4}$ 3 m , with unit-cell parameters a = 10.3296(15) Å, V = 1102.2(5) Å3 and Z = 2. Its crystal structure was refined by single-crystal X-ray diffraction data to a final R 1 = 0.0347 on the basis of 261 unique reflections with F o > 4σ(F o) and 22 refined parameters. Tetrahedrite-(Cu) is isotypic with other tetrahedrite-group minerals. Previous findings of tetrahedrite-(Cu) are reported and some nomenclature issues, related to the Fe and Cu oxidation states, are discussed. At the Bankov deposit, tetrahedrite-(Cu) is related to hydrothermal, most probably Alpine, solutions strongly enriched in Cu, Sb and S. [ABSTRACT FROM AUTHOR]

Understanding how plant functional traits respond to mining activities and impact metal(loid)s accumulation in dominant species is crucial for exploring the driving mechanisms behind plant community succession and predicting the ecological restoration potential of these plants. In this study, we investigated four dominant herbaceous species (Artemisia argyi, Miscanthus sinensis, Ficus tikoua, and Ageratina adenophora) growing on antimony (Sb) mining sites (MS) with high Sb and arsenic (As) levels, as well as non‐mining sites (NMS). The aim was to analyze the variations in functional traits and their contribution to Sb and As concentrations in plants. Our results indicate that mining activities enhanced soil nitrogen (N) limitation and phosphorus (P) enrichment, while significantly reducing the plant height of three species, except for F. tikoua. The four species absorbed more calcium (Ca) to ensure higher tolerance to Sb and As levels, which is related to the activation of Ca signaling pathways and defense mechanisms. Furthermore, plant Sb and As concentrations were dependent on soil metal(loid) levels and plant element stoichiometry. Overall, these findings highlight the regulatory role of plant element traits in metal(loid) concentrations, warranting widespread attention and further study in the future. [ABSTRACT FROM AUTHOR]