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Pairing transition metals and heavier tetrylenes (Si, Ge, Sn, Pb) holds great potential for cooperative bond activation and catalysis. In this work, we investigate the reactivity of a low-coordinate Pt(0)/Ge(II) system that emerges from the reaction between the monoligated platinum(0) precursor [(PMe2ArDipp2)Pt(olefin)] with germylene dimer [ArDipp2GeCl]2 (where ArDipp2 = C6H3−2,6-(C6H3−2,6-iPr2)2). The resulting complex reveals ability for cooperative bond activation. Stoichiometric reactions with dihydrogen, water, methanol, ammonia and alkynes unveil the formation of Pt(II)-germyl compounds, characterized by distinct isomeric forms, whose flexibility derives from the particularly low-coordination. We explore its catalytic potential in the hydrodehalogenation of aliphatic, aromatic and main-group halides under dihydrogen atmosphere using both thermal and photochemical conditions, demonstrating promising conversions even for more challenging alkyl chlorides. Pairing transition metals and heavier tetrylenes holds potential for cooperative bond activation. Here, the authors investigate the reactivity of a low-coordinate Pt(0)/Ge(II) system that emerges from the reaction between a monoligated platinum(0) precursor with a germylene dimer and explore its application as a hydrodehalogenation catalyst. [ABSTRACT FROM AUTHOR]

This study systematically addresses the challenge of accurately modeling memristors, focusing on four distinct types doped with tungsten, tin, chromium, and carbon, fabricated by Knowm Inc. A comprehensive characterization is performed by subjecting the devices to sinusoidal excitations with varying frequencies and amplitudes, followed by data averaging and high-frequency filtering. The resulting measurements are fitted using three prominent memristor models: VTEAM, MMS, and Yakopcic. Additional bespoke modifications are assessed. These models, typically formulated as coupled algebraic differential equations integrating electrical quantities (voltage and current) with internal state variables governing device dynamics, are optimized using two robust approaches: (1) interior-point optimization with gradient-based search, and (2) Nelder–Mead gradient-free optimization, both with box constraints applied. A thorough comparison and discussion of the optimized model parameters ensue, accompanied by an examination of the sensitivity to diverse frequency and amplitude ranges. The findings inform conclusions and provide a foundation for future refinements, underscoring the importance of multi-model evaluation and advanced optimization strategies in precise memristor modeling. The presented methodology offers a valuable framework for elucidating optimal modeling paradigms tailored to specific memristor architectures and operating regimes, ultimately enhancing their integration in emerging neuromorphic and computational applications. [ABSTRACT FROM AUTHOR]

The corrosion behavior of the TiN monolayer and CrN/TiN multilayer coatings deposited via cathodic arc evaporation physical vapor deposition (CAE‐PVD) on the Ti–6Al–4V substrates were evaluated in Ringer's and Hank's physiological saline electrolytes. XRD (x‐ray diffractometry) and scanning electron microscopy (SEM) analysis were used to characterize the coatings. The corrosion behavior of coatings was assessed by impedance spectroscopy and potentiodynamic polarization techniques. The results showed that the corrosion resistance of coatings was increased in the order of TiN‐Ringer's < TiN‐Hank's < CrN/TiN‐Ringer's < CrN/TiN‐Hank's. Therefore, it can be concluded that the CrN/TiN coating, due to having a large number of interfaces and a smoother surface with fewer macroparticles and pinholes, is more efficient in raising the corrosion resistance properties of titanium than TiN monolayer coating. Moreover, it was observed that Ringer's solution is a more severe environment than Hank's solution. Both coatings, because of the precipitation of a protective corrosion products layer on their surface, showed an enhancement in corrosion resistance with increasing the immersion time from 1 to 14 days in Hank's. The results suggest TiN monolayer and CrN/TiN multilayer coatings as promising candidates for biomedical applications. [ABSTRACT FROM AUTHOR]

With the global ban on tributyltin (TBT), the pollution of triphenyltin (TPhT) is an emerging issue in some aquatic ecosystems. In this study, we investigated the concentrations of typical butyltin and phenyltin compounds in the surface water and sediments in the lower Yangtze River, analyzed their occurrence and sources, and assessed their ecological risks. The findings indicate that butyltin and phenyltin compounds are widespread. The total concentration of organotin compounds in surface water was as high as 42.41 ng Sn/L, with an average of 25.71 ng Sn/L, and the total concentration of organotins in sediments reached up to 111.5 ng Sn/g dw, averaging 61.1 ng Sn/g dw. Since the implementation of the AFS Convention, the concentration of organotins in surface water has been significantly reduced. However, the ecological risk of TBT is still high, and the risk of TPhT is also noteworthy. The findings also suggest that the primary source of butyltins in the lower Yangtze River is historical input residues. In contrast, the main source of PhTs is the recent input of agricultural runoff. Therefore, organotin contamination in the lower Yangtze River has changed, but its governance still presents challenges. [ABSTRACT FROM AUTHOR]

Band structure and gain in a Ge/Ge1-xSnx/Ge quantum well are described theoretically using a 14-band k.p model. It has been shown that the quantum well width and the α-Sn concentration considerably modify the conduction and valence subband structure, and, as a result, the optical gain changes with the insertion of a very small concentration of α-Sn. In particular, we have determined the necessary injection carrier density Nj and the critical α-Sn concentration for elevated high gain lasing. It is found that for Nj = 1.5 × 1018 cm−3, we achieved a maximum peak gain for α-Sn concentration of the order 0.155. We can predict that Ge/Ge1-xSnx/Ge QWs should be manufactured with an α-Sn concentration less than 0.155 in devices for optoelectronics applications such as telecommunication and light emitting laser diodes. [ABSTRACT FROM AUTHOR]

In this study, the tribological characteristics of TiN, AlTiN, and AlTiCrN coatings sliding against a SUS420J1 stainless steel pin were investigated in atmospheric and vacuum environments. The coatings were deposited on SUS440C substrates using the arc-physical vapor deposition technique. The friction and wear behavior of the coatings were evaluated based on the systematic analyses of the friction coefficient data as well as the physical and chemical state of the wear track. The results revealed that the friction coefficients of the SUS440C specimen and AlTiCrN coatings increased, whereas those of the TiN and AlTiN coatings decreased when the environment was changed from atmospheric to vacuum. It was confirmed that the formation of an oxide layer and adsorption of oxides on the surface were dominant factors that influenced the tribological behavior in the atmospheric environment. On the other hand, the compatibility, oxidation inhibition, and droplets of the surface mainly affected the frictional characteristics in the vacuum environment. The results of this work are expected to aid in the selection of proper coating materials for tribological systems operating in a vacuum. [ABSTRACT FROM AUTHOR]

Background: Radiopharmaceutical therapy (RPT) uses radionuclides that decay via one of three therapeutically relevant decay modes (alpha, beta, and internal conversion (IC) / Auger electron (AE) emission) to deliver short range, highly damaging radiation inside of diseased cells, maintaining localized dose distribution and sparing healthy cells. Antimony-119 (119Sb, t1/2 = 38.19 h, EC = 100%) is one such IC/AE emitting radionuclide, previously limited to in silico computational investigation due to barriers in production, chemical separation, and chelation. A theranostic (therapeutic/diagnostic) pair can be formed with 119Sb's radioisotopic imaging analogue 117Sb (t1/2 = 2.80 h, Eγ = 158.6 keV, Iγ = 85.9%, β+ = 262.4 keV, Iβ+ = 1.81%). Results: Within, we report techniques for sustainable and cost-effective production of pre-clinical quality and quantity, radionuclidically pure 119Sb and 117Sb, novel low energy photon measurement techniques for 119Sb activity determination, and physical yields for various tin target isotopic enrichments and thicknesses using (p, n) and (d, n) nuclear reactions. Additionally, we present a two-column separation providing a radioantimony yield of 73.1% ± 6.9% (N = 3) and tin separation factor of (6.8 ± 5.5) x 105 (N = 3). Apparent molar activity measurements for deuteron produced 117Sb using the chelator TREN-CAM were measured at 42.4 ± 25 MBq 117Sb/µmol (1.14 ± 0.68 mCi/µmol), and we recovered enriched 119Sn target material at a recycling efficiency of 80.2% ± 5.5% (N = 6) with losses of 11.6 mg ± 0.8 mg (N = 6) per production. Conclusion: We report significant steps in overcoming barriers in 119Sb production, chemical isolation and purification, enriched target material recycling, and chelation, helping promote accessibility and application of this promising therapeutic radionuclide. We describe a method for 119Sb activity measurement using its low energy gamma (23.87 keV), negating the need for attenuation correction. Finally, we report the largest yet-measured 119Sb production yields using proton and deuteron irradiation of natural and enriched targets and radioisotopic purity > 99.8% at end of purification. [ABSTRACT FROM AUTHOR]

Tin(II) compounds are versatile materials with applications across fields such as catalysis, diagnostic imaging, and therapeutic drugs. However, oxidative stabilization of Sn(II) has remained an unresolved challenge as its reactivity with water and dioxygen results in loss of functionality, limiting technological advancement. Approaches to slow Sn(II) oxidation with chelating ligands or sacrificial electron donors have yielded only moderate improvements. We demonstrate here that the addition of nitrate to pyrophosphate-chelated Sn(II)(aq) suppresses Sn(II) oxidation in water across a broad pH range. Evidence of hydroxyl radical concentration reduction and detection of a radical nitrogen species that only forms in the presence of chelated Sn(II) point to a radical-based reaction mechanism. While this chemistry can be broadly applied, we present that this approach maintains Sn(II)'s antibacterial and anti-inflammatory efficacies as an example of sustained oral chemotherapeutic functionality. [ABSTRACT FROM AUTHOR]

This study aimed to determine the most suitable woody species that can be used to reduce the pollution of Sr, Mo, and Sn, which are heavy metals that are harmful to the ecosystem and human and environmental health. Within the study's scope, samples were taken from the wood parts of 16 woody species growing under similar conditions in Düzce province, which is among the five cities with the most polluted air in Europe. The wood part is the largest organ of higher plants in terms of mass; it traps heavy metals within itself for many years and can remove heavy metals to a great extent. Therefore, plants with a high potential for heavy metal accumulation in the wood part are among the most suitable plants for phytoremediation studies. The study determined Sr, Mo, and Sn concentrations in the wood parts of 16 tree species via inductively coupled plasma optical emission spectroscopy and compared them using statistical methods. Results indicate that Robinia pseudoacacia and Cedrus atlantica species were suitable for reducing pollution by Mo and Sn, while Platanus orientalis and Populus alba species were suitable for reducing Sr pollution. [ABSTRACT FROM AUTHOR]

2D perovskites hold immense promise in optoelectronics due to their strongly bound electron-hole pairs (i.e., excitons). While exciton polaron from interplay between exciton and lattice has been established in 2D lead-based perovskites, the exciton nature and behavior in the emerging 2D tin-based perovskites remains unclear. By combining spin-resolved ultrafast spectroscopy and sophisticated theoretical calculations, we reveal 2D tin-based perovskites as genuine excitonic semiconductors with weak polaronic screening effect and persistent Coulomb interaction, thanks to weak exciton-phonon coupling. We determine an excited state exciton binding energy of ~0.18 eV in n = 2 tin iodide perovskites, nearly twice of that in lead counterpart, despite of same large value of ~0.2 eV from steady state measurement. This finding emphasizes the pivotal role of excited state polaronic effect in these materials. The robust excitons in 2D tin-based perovskites exhibit excitation power-insensitive, high-efficiency and color-purity emission, rendering them superior for light-emitting applications. Combining spin-resolved ultrafast spectroscopy and calculations, Zhou et al. report weak exciton-phonon interactions in 2D tin iodide perovskites, alleviating excited state polaronic screening effect and robust excitons, comparing to their lead counterparts. [ABSTRACT FROM AUTHOR]

The effect of substituting Sn with a fourth element on the functional properties of Heusler NiMnSn alloys has been reported in the literature. In the present work, the influence of the addition of Si to the Heusler NiMnSn system was evaluated, where Ni44Mn44Sn12 (at.%), Ni44Mn44Sn10.5Si1.5 (at.%) and Ni44Mn44Sn9Si3 (at.%) alloys were prepared in an induction furnace without a controlled atmosphere, and were later characterized by optical microscopy, Vickers microhardness, electrical resistivity, and vibrating sample magnetometry. The results revealed that the partial replacement of Sn by 3 at.% Si did not modify the dendritic microstructure and the phases present at room temperature; however, it increased the percentage of the martensite phase from 51% to 76%. This modification in the percentage of this phase is responsible for reducing the average Vickers microhardness values (from 469 HV to 459 HV), increasing the electrical resistivity (from 1.3 mΩ mm to 2.21 mΩ mm), and decreasing the saturation magnetization (from 23.67 emu/g to 19.34 emu/g), coercivity (from 5.56 Oe to 5.14 Oe), and remanent magnetization (from 0.21 emu/g to 0.18 emu/g). With this, our results bring to light a new alternative for doping the NiMnSn alloy as a way of modifying the structural and electrical properties, constituting interesting parameters for technological applications. [ABSTRACT FROM AUTHOR]

This study demonstrates that diffusion doping of ZGP single crystals with impurity atoms (Mg, Se, Sn, Pb) leads to a decrease in the specific conductivity of the samples. Consequently, this results in reduced absorption in the terahertz frequency range (150–1000 μm). It has been shown that doping ZGP samples with selenium (Se) and lead (Pb) atoms reduces absorption in the infrared region from 0.3–0.6 cm−1 to 0.06–0.09 cm−1. Doping with tin (Sn) leads to a decrease in absorption only in the wavelength region near 2.1 μm from 0.2 cm−1 to 0.05 cm−1. The proposed mechanism for the decrease in infrared absorption is a reduction in zinc vacancies due to doping with impurity atoms. This research lays the groundwork for a technology that produces ZGP crystals with minimal absorption within the 2–8 μm wavelength range, eliminating the need for fast electron beam irradiation technology. This advancement will facilitate the fabrication of ZGP crystals with arbitrary apertures. [ABSTRACT FROM AUTHOR]

This correction notice is for an article titled "Synchronized crystallization in tin-lead perovskite solar cells" published in Nature Communications. The correction addresses an error in Figure 1 of the article, specifically the incorrect labels in the Fig. 1b plot. The correct labels should be "Sn 5s" and "Pb 6s" instead of "Sn 5p" and "Pb 6p". The correction has been made in both the PDF and HTML versions of the article. The authors of the article are Yao Zhang, Chunyan Li, Haiyan Zhao, Zhongxun Yu, Xiaoan Tang, Jixiang Zhang, Zhenhua Chen, Jianrong Zeng, Peng Zhang, Liyuan Han, and Han Chen. [Extracted from the article]

[Display omitted] Sodium (Na) metal anodes receive significant attention due to their high theoretical specific energy and cost-effectiveness. However, the high reactivity of Na foil anodes and the irregular surfaces have posed challenges to the operability and reliability of Na metals in battery applications. In the absence of inert environmental protection conditions, constructing a uniform, dense, and sodiophilic Na metal anode surface is crucial for homogenizing Na deposition, but remains less-explored. Herein, we fabricated a Tin (Sn) nanoparticle-assembled film conforming to separator pores, which provided ample space for accommodating volumetric expansion during the Na alloying process. Subsequently, a seamless Na-Sn alloy overlayer was formed and transferred onto the Na foil during Na plating through a separator-assisted technique, thereby overcoming conventional operational limitations of metallic Na. As compared to traditional volumetrically expanded cracked ones, the present autotransferable, highly sodiophilic, ion-conductive, and seamless Na-Sn alloy overlayer serves as uniform nucleation sites, thereby reducing nucleation and diffusion barriers and facilitating the compact deposition of metallic Na. Consequently, the autotransferable alloy layer enables a high average Coulombic efficiency of 99.9 % at 3.0 mA cm−2 and 3.0 mAh cm−2 in the half cells as well as minimal polarization overpotentials in symmetric cells, both during prolonged cycling 1200 h. Furthermore, the assembled Na||Sn-1.0h-PP||Na 3 V 2 (PO 4) 3 @C@CNTs full cell delivers high capacity retention of 97.5 % after 200 cycles at a high cathodic mass loading. [ABSTRACT FROM AUTHOR]

The influence of co-regulating Mo and Sn on the corrosion resistance of low alloy steel in tropical marine atmospheric was investigated. The combined addition of Mo and Sn has been found to significantly improve the corrosion resistance of low alloy steel, augmenting the protective capabilities of the rust layer. This combined addition promotes the formation of protective compounds like α-FeOOH and FeCr2O4 within the alloy rust layer. Furthermore, it facilitates the conversion of Cr, Ni and Cu into corrosion-resistant oxides such as Cr2O3, NiFe2O4 and CuO, thereby enhancing the density of the rust layer. Additionally, as corrosion progresses over time, higher levels of Sn addition lead to increased Sn content within the inner rust layer, consequently bolstering the protective qualities of the rust layer. This comprehensive understanding sheds light on the synergistic effects of Mo and Sn in fortifying the corrosion resistance of low alloy steel, offering insights for the development of advanced corrosion-resistant materials in marine environments. [ABSTRACT FROM AUTHOR]

High density portable energy storage is desirable owing to the energy requirements of portable electronics and electric vehicles. The Li-ion battery's high energy density could be even further improved through the utilization of alternative materials (instead of carbon) for the anode, such as Sn or Si. Nonetheless, the large volume expansion upon lithiation, up to ~300% for Li22Si5, causes pulverization and rapid capacity degradation during cycling. Sn also forms a Li22Sn5 compound with the equivalent stoichiometric Li capacity but with enhanced ductility. Nano-sized Si and Sn have demonstrated distinctive nanoscale properties, facilitating the retention of higher capacities, particularly when coated with carbon, which improves mechanical stability. To date, the methods of synthesizing coated Si, Sn, or Si-Sn alloyed nanoparticles are complicated, costly, and not readily scalable to meet the demands of cost-effective manufacturing. Spark plasma erosion in a hydrocarbon dielectric has been explored as a one-step process to produce Sn-Si alloy nanoparticles coated with a thin carbon film, offering a scalable and cost-effective processing route. The resulting Sn-Si particles exhibited a bi-modal size distribution at ~5 nm and ~500 nm and were carbon-coated, as intended, from the hydrocarbon dielectric breakdown. The spark-eroded nanoparticles were thoroughly characterized using TEM/EDS, XPS, AES, SSNMR, and TGA, and their improved electrochemical performance was assessed through half-cell experiments. [ABSTRACT FROM AUTHOR]

Metal carbenes are widely acknowledged as a category of highly effective intermediates that facilitate otherwise inaccessible transformations. In recent decades, carbene chemistry has made considerable advances and has demonstrated remarkable abilities in the formation of diverse chemical bonds and the synthesis of structurally distinctive molecules. Nevertheless, the majority of research within this field has concentrated on α-carbon-substituted carbenes, with comparatively little investigation of carbenes that have been functionalized with a wider structural variety, particularly those that have been substituted with heteroatoms (e.g., O, N, P, S, Si, Ge, Sn and B). The objective of this review is to elucidate the advancements in enantioselective transfer reactions involving metal carbenes substituted with these elements, thereby highlighting their contribution to the expansion of the structural diversity and synthetic utility of carbenes in contemporary chemistry. [ABSTRACT FROM AUTHOR]

The interface connects the reinforced phase and the matrix of materials, with its microstructure and interfacial configurations directly impacting the overall performance of composites. In this study, utilizing seven atomic layers of Mg(0001) and Ti(0001) surface slab models, four different Mg(0001)/Ti(0001) interfaces with varying atomic stacking configurations were constructed. The calculated interface adhesion energy and electronic bonding information of the Mg(0001)/Ti(0001) interface reveal that the HCP2 interface configuration exhibits the best stability. Moreover, Si, Ca, Sc, V, Cr, Mn, Fe, Cu, Zn, Y, Zr, Nb, Mo, Sn, La, Ce, Nd, and Gd elements are introduced into the Mg/Ti interface layer or interfacial sublayer of the HCP2 configurations, and their interfacial segregation behavior is investigated systematically. The results indicate that Gd atom doping in the Mg(0001)/Ti(0001) interface exhibits the smallest heat of segregation, with a value of −5.83 eV. However, Ca and La atom doping in the Mg(0001)/Ti(0001) interface show larger heat of segregation, with values of 0.84 and 0.63 eV, respectively. This implies that the Gd atom exhibits a higher propensity to segregate at the interface, whereas the Ca and La atoms are less inclined to segregate. Moreover, the electronic density is thoroughly analyzed to elucidate the interfacial segregation behavior. The research findings presented in this paper offer valuable guidance and insights for designing the composition of magnesium-based composites. [ABSTRACT FROM AUTHOR]

In the present research, the impacts of Ce additions at various concentrations (0, 1.0, 3.4, and 4.0 wt.%) on the evolution of the microstructure, mechanical properties, and thermal conductivity of as-cast and as-extruded Mg-3Sn alloys were investigated. The findings demonstrate that adding Ce caused the creation of a new ternary MgSnCe phase in the magnesium matrix. Some new Mg17Ce2 phases are generated in the microstructure when Ce levels reach 4%. The thermal conductivity of the Mg-3Sn alloy is significantly improved due to Ce addition, and the Mg-3Sn-3.4Ce alloy exhibits the highest thermal conductivity, up to 133.8 W/(m·K) at 298 K. After extrusion, both the thermal conductivity and mechanical properties are further improved. The thermal conductivity perpendicular to the extrusion direction of Mg-3Sn-3.4Ce alloy could achieve 136.28 W/(m·K), and the tensile and yield strengths reach 264.3 MPa and 227.2 MPa, with an elongation of 7.9%. Adding Ce decreases the dissolved Sn atoms and breaks the eutectic α-Mg and Mg2Sn network organization, leading to a considerable increase in the thermal conductivity of as-cast Mg-3Sn alloys. Weakening the deformed grain texture contributed to the further enhancement of the thermal conductivity after extrusion. [ABSTRACT FROM AUTHOR]

In the title compound, bis[aqua(2,2′-bipyridine) fluoridotin (II)] hexafluoridotin(IV), [SnF(C10H8N2)(H2O)]2[SnF6], an ionic mixed-valent tin(II)–tin(IV) compound, the bivalent tin atom is the center atom of the cation and the tetravalent tin atom is the center atom of the anion. With respect to the first coordination sphere, the cation is monomeric, with the tin(II) atom having a fourfold seesaw coordination with a fluorine atom in an equatorial position, a water molecule in an axial position and the two nitrogen atoms of the chelating 2,2′-bipyridine ligand in the remaining axial and equatorial positions. The bond lengths and angles of this hypervalent first coordination sphere are described by 2c–2e and 3c–4e bonds, respectively, all of which are based on the orthogonal 5p orbitals of the tin atom. In the second coordination sphere, which is based on an additional, very long tin–fluorine bond that leads to dimerization of the cation, the tin atom is trapezoidal–pyramidally coordinated. The tetravalent tin atom of the centrosymmetric anion has an octahedral coordination. The differences in its tin–fluorine bond lengths are attributed to hydrogen bonding, as the two of the four fluorine atoms are each involved in two hydrogen bonds, linking anions and cations together to form strands. [ABSTRACT FROM AUTHOR]

The susceptibility of either oxidation into Sn(IV) or disproportionation into Sn(IV) and Sn(0) limits the study of metal tin‐(II)‐borate ceramics. We report mullite‐type SnCrBO4 and SnVBO4 synthesized in sealed quartz tubes by conventional solid‐state method. X‐ray powder diffraction data Rietveld refinements confirm that both compounds are isostructural to PbMBO4 phases for M = Al, Ga, Cr, Mn, and Fe. The end‐members show a complete miscibility within the Sn(Cr1−xVx)BO4 solid solution. Both the microstructural (average crystallite size, microstrain, and degree of crystallinity) and crystal structural (metric parameters, bond lengths, polyhedral volume, and polyhedral distortion) parameters are observed with respect to the compositional x‐value. The stereochemical activity of the 5 s2 lone electron pairs of Sn2+ cations has been measured by using the Wang–Liebau eccentricity parameter. The structural features are complemented by 119Sn Mössbauer, Raman, and Fourier‐transformed infrared spectroscopy. The 119Sn Mössbauer isomer shifts and the quadrupole splitting values confirm the SnO4 coordination and an Sn(II) valence state. The electronic band gap has been calculated from the UV/Vis diffuse reflectance spectra, which slightly increases with successive decrease of the cationic radius from V to Cr. Temperature‐dependent inverse DC magnetic susceptibility suggests that SnCrBO4 and SnVBO4 are antiferromagnetic and ferromagnetic (FM) with a Néel temperature of 17.2(1) K and a Curie temperature of 29.8(1) K, respectively. Alike the end‐member SnVBO4, Sn(Cr0.5V0.5)BO4 is also found to be a rare FM insulator. The thermal stability decreases with increasing vanadium content in the solid solution. [ABSTRACT FROM AUTHOR]

To meet the challenge of varied working temperatures of inductance components in new energy vehicle and 5G communication, the high- T C high-permeability MnZn ferrite with excellent temperature stability was developed by the addition of SnO 2. In this series of samples, initial permeability μ i maintains large values in a wide temperature range. With increasing the SnO 2 content, the temperature of the second permeability peak T sp decreases and meanwhile Curie temperature T C maintains as high as 160 °C. For the best sample with 6000 ppm SnO 2 , μ i at 25 °C is 7244 and exhibits the excellent temperature stability with the low specific temperature coefficient of 0.35 × 10−6 °C−1 between 25 and 130 °C. The addition of SnO 2 generates Fe2+ and adjusts the magneto-crystalline anisotropy constant K 1 = 0 point, which is responsible for the wide-temperature high permeability. The effect of SnO 2 addition on magnetization process has also been clarified. [ABSTRACT FROM AUTHOR]

Ternary half-Heusler (HH) alloys are under intense investigations recently towards achieving high thermoelectric (TE) figure-of-merit (ZT). Of particular interest is the ZrNiPb-based HH alloy, where an optimal value of ZT ~ 0.7 at 773 K has been achieved by co-doping Sn and Bi at Pb site. In this work, we identify an excellent ZT of 1.3 in ZrNi1+xPb0.38Sn0.6Bi0.02 (x = 0.03, at 773 K) composite alloy. This is achieved by synergistic modulation of electronic as well as thermal properties via introduction of minor phase of full-Heusler (FH) in the HH matrix through compositional tuning approach. These Ni-rich ZrNi1+xPb0.38Sn0.6Bi0.02 (0 ≤ x ≤ 0.07) alloys were synthesized via energy efficient and time-curbed techniques that involved Arc melting followed by consolidation via spark plasma sintering. These alloys were characterized by XRD and SEM, which show formation of nanocomposites comprising of HH matrix phase and FH secondary minor phases. Enhancement in ZT is mainly attributed to a synchronized increase in power factor (~42%) and ~25% decrease in its thermal conductivity. Here, TE compatibility factor (S) was also calculated for all samples. The value of |S| ~ 2.7 V−1 (at 773 K) is observed for x = 0.03, which is ~17% higher than bare HH composition (x = 0.0). The theoretically calculated TE device efficiency of best-performing sample ZrNi1.03Pb0.38Sn0.6Bi0.02 is estimated to be η ~ 13.6%. Our results imply that deliberately controlled fine tuning in compositions of HH compounds through compositional tuning approach would lead to novel off-stoichiometric HH phases with enhanced ZT value for efficient TE device fabrication. [ABSTRACT FROM AUTHOR]

The infrared optical properties of thick GeSn films (>500 nm) having 10% Sn concentration and of SiGeSn layers, utilized for the growth of strain-relieved, direct-gap GeSn films by molecular beam epitaxy, are investigated. Two growth methods are used: a graded-growth structure and a stepped-growth structure that help us to illustrate the properties of the GeSn and SiGeSn layers. Interestingly, there can be strong absorption in SiGeSn films throughout the infrared. We observe an increase in infrared absorption with increasing Sn concentration up to 21% Sn and in films, where the Sn is held constant at 18%, with increasing Si concentration up to 30%. Cavity effects in the infrared transmission measurement of stepped-growth structures are observed and associated with reflections at growth interfaces. Si–Si bond formation is proposed to occur at high Si concentrations in SiGeSn films, and the bandgap in SiGeSn films appears to decrease with increasing Si and Sn concentrations. [ABSTRACT FROM AUTHOR]

We present a novel method for investigating laser-driven dynamic fragmentation in tin using in situ X-ray diffraction. Our experimental results demonstrate the feasibility of the method for simultaneously identifying the phase and temperature of fragments through analysis of the diffraction pattern. Surprisingly, we observe a deviation from the widely accepted isentropic release assumption, with the temperature of the fragments being found to be more than 100 K higher than expected, owing to the release of plastic work during dynamic fragmentation. Our findings are further verified through extensive large-scale molecular dynamics simulations, in which strain energies are found to be transferred into thermal energies during the nucleation and growth of voids, leading to an increase in temperature. Our findings thus provide crucial insights into the impact-driven dynamic fragmentation phenomenon and reveal the significant influence of plastic work on material response during shock release. [ABSTRACT FROM AUTHOR]

This work describes the fabrication and characterization of a new high surface area nanocomposite electrode containing reduced graphene oxide (rGO) and titanium nitride (TiN) for electrochemical applications. This approach involves electrochemically depositing rGO on a high surface area TiN nanorod array electrode to form a new nanocomposite electrode. The TiN nanorod array was first formed by the glancing angle deposition technique in a DC (Direct Current) sputtering system. GO flakes of ~1.5 μm in diameter, as confirmed by Dynamic Light Scattering (DLS), were electrodeposited on the nanostructured TiN electrode via the application of a fixed potential for one hour. The surface morphology of the as-prepared rGO/TiN electrode was evaluated by scanning electron microscopy (SEM) and the presence of rGO on TiN was confirmed by Raman Microscopy. The CV shows an increase in the capacitive current at rGO/TiN as compared to TiN. The rGO decorated TiN electrode was then used for analyzing the electrocatalytic oxidation of ascorbic acid and dopamine, and the reduction of nitrate by CV and linear sweep voltammetry (LSV), respectively. CV or LSV show that the electrochemical kinetics of these three analytes are significantly faster on rGO/TiN than TiN itself. Overall, the rGO/TiN electrode showed better electrochemical behavior for biomolecules like ascorbic acid and dopamine as well as another target analyte, nitrate ions, compared to TiN by itself. [ABSTRACT FROM AUTHOR]

Industrial activities on the banks of waterways can degrade both the waterbody and the surrounding area and continue to exert pressure on the environment even after the closure of the industries involved. An assessment was undertaken to determine concentration, distribution, mobility and ecological risk of potentially toxic elements (PTE) from legacy contamination in sediments of the Forth and Clyde Canal, UK. Concentrations of PTE, determined by ICP-MS following aqua regia digestion, were 5.54–219 mg kg−1 for As, < 0.025–11.0 mg kg−1 for Cd, 44.8–883 mg kg−1 for Cr, 39.3–618 mg kg−1 for Cu, 35.8–72.1 g kg−1 for Fe, 720–4460 mg kg−1 for Mn, 42.0–154 mg kg−1 for Ni, 93.9–2740 mg kg−1 for Pb, 5.36–122 mg kg−1 for Sn and 288–3640 mg kg−1 for Zn. With the exception of Fe and Mn, higher levels were observed at urban locations than at rural. Enhanced Cr, Pb and Sn content at suburban locations could be attributed to historical industrial activities on the canal bank, while widespread distribution of As and Pb was consistent with atmospheric deposition. In the inner-city area, sediment quality was severely deteriorated, and the potential ecological risk was very high. Fractionation patterns, determined using the modified BCR sequential extraction, indicated a particularly high risk of mobilization for Cd, Mn and Zn, and the highest exchangeable fraction risk from Zn. The research highlights the need to assess and, where necessary, manage legacy contaminated sites in line with the UN 2030 Agenda for Sustainable Development. [ABSTRACT FROM AUTHOR]

Electrosynthesis is a technique that is attracting increased attention and has many appealing features, particularly its potential greenness. At the same time, electrosynthesis requires a solvent and a supporting electrolyte in order for current to pass through the reaction. These are effectively consumable reagents unless a convenient means of recycling can be developed. As part of our interest in unusual solvents and electrochemistry, we explored the application of simple, inexpensive, and recyclable deep eutectic solvents to the allylation of carbonyls. While several sets of conditions were developed, the goal of avoiding stoichiometric amounts of metal has proven elusive. Still, a deep eutectic solvent can be used to plate out and thus recover the metal used, offering an interesting new option for electrochemical allylations.

The wear characteristics of coated H13 tool steel and as-casted H13 tool steel in dry sliding conditions were investigated through a pin-on-disc tribometer, where the H13 steel is used as a pin and EN31 steel is used as disc material. The study was focused on evaluating the tribological behaviour by examining the friction characteristics, surface morphology and wear performance. Initially, to improve the hardness of the untreated (as-casted) H13 steel, the tempering process where carried out on the samples, which helped elevate the hardness from 38 to 55 HRC. The worn surface of the samples was analysed using atomic force microscopy (AFM). Among the four samples (as-casted, heat-treated, AlCrN coated and TiN coated) the as-casted samples were affected by oxidation and adhesive wear. The material loss measured for as-casted, heat-treated, AlCrN and TiN samples was 30.34, 7.85, 0.78 and 0.14 mg, respectively. The measured coefficient of friction was 0.541 for as-casted, 0.492 for the heat-treated, 0.48 for the AlCrN and 0.147 for the TiN sample. From the study, the major conclusion was that the TiN coating offers major wear protection and lower friction.

High density portable energy storage is desirable owing to the energy requirements of portable electronics and electric vehicles. The Li-ion battery’s high energy density could be even further improved through the utilization of alternative materials (instead of carbon) for the anode, such as Sn or Si. Nonetheless, the large volume expansion upon lithiation, up to ~300% for Li22Si5, causes pulverization and rapid capacity degradation during cycling. Sn also forms a Li22Sn5 compound with the equivalent stoichiometric Li capacity but with enhanced ductility. Nano-sized Si and Sn have demonstrated distinctive nanoscale properties, facilitating the retention of higher capacities, particularly when coated with carbon, which improves mechanical stability. To date, the methods of synthesizing coated Si, Sn, or Si-Sn alloyed nanoparticles are complicated, costly, and not readily scalable to meet the demands of cost-effective manufacturing. Spark plasma erosion in a hydrocarbon dielectric has been explored as a one-step process to produce Sn-Si alloy nanoparticles coated with a thin carbon film, offering a scalable and cost-effective processing route. The resulting Sn-Si particles exhibited a bi-modal size distribution at ~5 nm and ~500 nm and were carbon-coated, as intended, from the hydrocarbon dielectric breakdown. The spark-eroded nanoparticles were thoroughly characterized using TEM/EDS, XPS, AES, SSNMR, and TGA, and their improved electrochemical performance was assessed through half-cell experiments.

SnTe, the lead-free and environmentally friendly material, has gained recognition as a low band-gap thermoelectric material. However, it encounters challenges due to the presence of a significant concentration of intrinsic tin vacancies and its extremely small band gap of 0.18 eV. These factors contribute to a low Seebeck coefficient (S) and high electronic thermal conductivity. These challenges can be overcome by tuning the band gap of SnTe which enhance its thermoelectric behaviour. In our study, we investigate the thermoelectric properties of the bulk SnTe by systematically increasing the band gap while keeping the carrier concentration fixed. By varying the band gap from 0.14 to 0.8 eV, we observe significant enhancements in the thermoelectric performance of the material. Specifically, the power factor reaches a value of 420 μ W cm - 1 K - 2 and the electronic thermal conductivity decreases to 2.3 W m - 1 K - 1 when the band gap is 0.8 eV and the carrier concentration is 10 18 cm - 3 . Moreover, the figure of merit (ZT) value of SnTe can be improved up to 15 times. This study can motivate further experimental investigation on interesting compounds. [ABSTRACT FROM AUTHOR]

This study examined the electrophoretic deposition (EPD) of titanium nitride (TiN) on AISI D2 tool steel, analyzing coating properties and TiN nanoparticle stability in the presence of polyethyleneimine as a dispersant in isopropyl alcohol. The parameters investigated were deposition time (5, 10, and 15 minutes), electric field strength (0.2, 0.5, 1, 1.5, and 2 V/m), and suspension concentration (0.2, 0.3, and 0.4 mg/L). Results indicated that a deposition time of 10 minutes with an electric field strength of 0.5 V/m and a suspension concentration of 0.2 mg/L provided optimal results in terms of thickness and micro-hardness. Higher deposition time led to increased thickness but decreased micro-hardness, while increasing electric field intensity for a constant deposition time led to increased deposition mass and thickness but lower quality at higher concentrations. Microstructural examination and micro-hardness testing confirmed these findings. [ABSTRACT FROM AUTHOR]

This study aimed to determine the most suitable woody species that can be used to reduce the pollution of Sr, Mo, and Sn, which are heavy metals that are harmful to the ecosystem and human and environmental health. Within the study’s scope, samples were taken from the wood parts of 16 woody species growing under similar conditions in Düzce province, which is among the five cities with the most polluted air in Europe. The wood part is the largest organ of higher plants in terms of mass; it traps heavy metals within itself for many years and can remove heavy metals to a great extent. Therefore, plants with a high potential for heavy metal accumulation in the wood part are among the most suitable plants for phytoremediation studies. The study determined Sr, Mo, and Sn concentrations in the wood parts of 16 tree species via inductively coupled plasma optical emission spectroscopy and compared them using statistical methods. Results indicate that Robinia pseudoacacia and Cedrus atlantica species were suitable for reducing pollution by Mo and Sn, while Platanus orientalis and Populus alba species were suitable for reducing Sr pollution.

This work describes the fabrication and characterization of a new high surface area nanocomposite electrode containing reduced graphene oxide (rGO) and titanium nitride (TiN) for electrochemical applications. This approach involves electrochemically depositing rGO on a high surface area TiN nanorod array electrode to form a new nanocomposite electrode. The TiN nanorod array was first formed by the glancing angle deposition technique in a DC (Direct Current) sputtering system. GO flakes of ~1.5 μm in diameter, as confirmed by Dynamic Light Scattering (DLS), were electrodeposited on the nanostructured TiN electrode via the application of a fixed potential for one hour. The surface morphology of the as-prepared rGO/TiN electrode was evaluated by scanning electron microscopy (SEM) and the presence of rGO on TiN was confirmed by Raman Microscopy. The CV shows an increase in the capacitive current at rGO/TiN as compared to TiN. The rGO decorated TiN electrode was then used for analyzing the electrocatalytic oxidation of ascorbic acid and dopamine, and the reduction of nitrate by CV and linear sweep voltammetry (LSV), respectively. CV or LSV show that the electrochemical kinetics of these three analytes are significantly faster on rGO/TiN than TiN itself. Overall, the rGO/TiN electrode showed better electrochemical behavior for biomolecules like ascorbic acid and dopamine as well as another target analyte, nitrate ions, compared to TiN by itself.

Abstract Our research focuses on enhancing the broadband absorption capability of organic solar cells (OSCs) by integrating plasmonic nanostructures made of Titanium nitride (TiN). Traditional OSCs face limitations in absorption efficiency due to their thickness, but incorporating plasmonic nanostructures can extend the path length of light within the active material, thereby improving optical efficiency. In our study, we explore the use of refractory plasmonics, a novel type of nanostructure, with TiN as an example of a refractory metal. TiN offers high-quality localized surface plasmon resonance in the visible spectrum and is cost-effective, readily available, and compatible with CMOS technology. We conducted detailed numerical simulations to optimize the design of nanostructured OSCs, considering various shapes and sizes of nanoparticles within the active layer (PM6Y6). Our investigation focused on different TiN plasmonic nanostructures such as nanospheres, nanocubes, and nanocylinders, analyzing their absorption spectra in a polymer environment. We assessed the impact of their incorporation on the absorbed power and short-circuit current (Jsc) of the organic solar cell.

In this work, samples of single-crystalline silicon doped with tin were studied using X-ray diffraction and electron microscopy. It has been established that at a scattering angle of 2θ » 36.6° in the X-ray diffraction patterns of n-Si and Si samples, structural reflections (110) of the corresponding SiO2 nanocrystallites with lattice parameters a = b = 0,4936 нм и c = 0,5212 nm and c = 0.5212 nm, belonging to the hexagonal crystal lattice and space group P321. The formation of tin nanocrystallites with sizes of 9.1 and 8 nm in the near-surface regions of the Si matrix crystal lattice was discovered.

Exploring new applications of negative thermal expansion (NTE) materials is a recent research hotspot. In this work, the IV A element Sn was used to tailor the thermal expansion and dielectric properties of NTE material ZrMgMo 3 O 12 , and the samples Zr 1–x Sn x MgMo 3 O 12 (x = 0.05, 0.10, 0.15, 0.20, 0.25) can be used in the field of high-frequency dielectric ceramics. Both the substitution amount of Sn and sintering temperature have a certain effect on the properties of Zr 1-x Sn x MgMo 3 O 12. The coefficients of thermal expansion (CTE) can be adjusted between near zero thermal expansion (ZTE) (−0.24 × 10−6/K−1) and NTE (−8.16 × 10−6/K−1) and become larger toward negative as the amount of Sn increased under the same sintering temperature. The dielectric constants of Zr 1-x Sn x MgMo 3 O 12 can be adjusted in the range of 130∼155, which are about 25 times than ZrMgMo 3 O 12. The dissipation factors of Zr 1-x Sn x MgMo 3 O 12 were adjustable between 4.37 × 10−4 and 5.54 × 10−4, meeting the application requirements of high-frequency dielectric ceramics. This research shows that Sn can adjust the thermal expansion properties and significantly improves the dielectric properties of ZrMgMo 3 O 12 , so that Zr 1-x Sn x MgMo 3 O 12 materials have high value in the field of high-frequency dielectric ceramics. [ABSTRACT FROM AUTHOR]

Dose optimization in computed tomography (CT) is crucial, especially in CT fluoroscopy (fluoro-CT) used for real-time navigation, affecting both patient and operator safety. This study evaluated the impact of spectral X-ray filtering using a tin filter (Sn filter), and a method called partial-angle computed tomography (PACT), which involves segmentally switching off the X-ray tube current at the ambient dose rate H ˙ * (10) at the interventional radiologist's (IR) position. Measurements were taken at two body regions (upper body: head/neck; lower body: lower legs/feet) using a 120 kV X-ray tube voltage, 3 × 5.0 mm CT collimation, 0.5 s rotation speed, and X-ray tube currents of 43 Eff.mAs (without Sn filter) and 165 Eff.mAs (with Sn filter). The study found significant dose reductions in both body regions when using the Sn filter and PACT together. For instance, in the upper body region, the combination protocol reduced H ˙ * (10) from 11.8 µSv/s to 6.1 µSv/s (p < 0.0001) compared to the protocol without using these features. Around 8% of the reduction (about 0.5 µSv/s) is attributed to the Sn filter (p = 0.0005). This approach demonstrates that using the Sn filter along with PACT effectively minimizes radiation exposure for the IR, particularly protecting areas like the head/neck, which can only be insufficiently covered by (standard) radiation protection material. [ABSTRACT FROM AUTHOR]

A new approach for the thermal reduction of tin dioxide (SnO2) in the carbon/sodium sulfite (Na2SO3) system is demonstrated. The process of tin smelting was experimentally optimized by adjusting the smelting temperature and amounts of the chemical components used for the thermal reduction of SnO2. The numbers obtained are consistent with the thermodynamic characteristics of the system and molar fractions of reactants derived from the proposed mechanism of the SnO2 thermal reduction process. They reveal that the maximum yield of tin is obtained if masses of C, Na2SO3 and SnO2 are approximately in the ratio 1:2:3 and the temperature is set to 1050 °C. The key role in the suggested mechanism is the thermal decomposition of Na2SO3. It was deduced from the available experimental data that the produced sulfur dioxide undergoes carbothermic reduction to carbonyl sulfide—an intermediate product involved in the bulk reduction of SnO2. Replacing sodium sulfite with sodium sulfate, sodium sulfide and even elemental sulfur practically terminated the production of metallic tin. The kinetic analysis was focused on the determination of the reaction orders for the two crucial reactants involved in the smelting process. [ABSTRACT FROM AUTHOR]

Efficiently reconciling the substantial volume strain with maintaining the stabilities of both interfacial protection and three‐dimensional (3D) conductive networks is a scientific and technical challenge in developing tin‐based anodes for sodium ion storage. To address this issue, a proof‐of‐concept self‐adaptive protection for the Sn anode is designed, taking advantage of the arbitrary substrate growth of graphdiyne. This protective layer, employing a flexible chain doping strategy, combines the benefits of 2D graphdiyne and linear chain structures to achieve 2D mechanical stability, electronic and ion conductions, ion selectivity, adequate elongation, and flexibility. It establishes close contact with the Sn particles and can adapt to dynamic size changes while effectively facilitating both electronic and ion transports. It successfully mitigates the detrimental effects of particle pulverization and coarsening induced by large‐volume changes. The as‐obtained Sn electrodes demonstrate exceptional stability, enduring 1800 cycles at a high current density of 2.5 A g−1. This strategy promises to address the general issues associated with large‐strain electrodes in next‐generation of high‐energy‐density batteries. [ABSTRACT FROM AUTHOR]

This study investigates the influence of heat treatments on the corrosion behaviour of CuSn10 tin bronze, additively manufactured using Laser Powder Bed Fusion (LPBF). LPBF enables the creation of finely structured, anisotropic microstructures, whose corrosion behaviour is not yet well understood. After production, specimens were heat-treated at 320 °C, 650 °C, and in a two-stage treatment at 800 °C and 400 °C, followed by hardness and microstructure analysis. Corrosion tests were conducted using linear polarisation, salt spray, and immersion tests. The results show that heat treatments at 320 °C and 650 °C have no significant effect on the corrosion rate, while the two-stage treatment shows a slight improvement in corrosion resistance. Differences in microstructure and hardness were observed, with higher treatment temperatures leading to grain growth and tin precipitates. The formation of a passive protective layer was detected after 30 h of OCP measurement. Results from other studies on corrosion behaviour were partially reproducible. Differences could be attributed to varying chemical compositions and manufacturing parameters. These findings contribute to the understanding of the effects of heat treatments on the corrosion resistance of additively manufactured tin bronze and provide important insights for future applications in corrosive environments. [ABSTRACT FROM AUTHOR]

[Display omitted] • Three zero-dimensional organic metal halides with different emission characteristics were synthesized. • The photophysical properties of the as-synthesized compounds were investigated in detail. • We demonstrated Sb3+-doped compounds in single-component white light illumination latent fingerprint detection. • Based on Sb3+-doped Sn(IV) compounds, a triple-mode reversible PL switch of off-onI-onII-off was achieved under different external stimuli. The host lattice environments of Sb3+ has a great influence on its photophysical properties. Here, we synthesized three zero-dimensional organic metal halides of (TPA) 2 SbCl 5 (1), Sb3+-doped (TPA)SnCl 5 (H 2 O)·2H 2 O (Sb3+-2), and Sb3+-doped (TPA) 2 SnCl 6 (Sb3+-3). Compared with the intense orange emission of 1 , Sb3+-3 has smaller lattice distortion, thus effectively suppressing the exciton transformation from singlet to triplet self-trapped exciton (STE) states, which makes Sb3+-3 has stronger singlet STE emission and further bring a white emission with a photoluminescence quantum efficiency (PLQE) of 93.4%. Conversely, the non-emission can be observed in Sb3+-2 even though it has a similar [SbCl 5 ]2- structure to 1 , which should be due to its indirect bandgap characteristics and the effective non-radiative relaxation caused by H 2 O in the lattice. Interestingly, the non-emission of Sb3+-2 can convert into the bright emission of Sb3+-3 under TPACl DMF solution treatment. Meanwhile, the white emission under 315 nm excitation of Sb3+-3 can change into orange emission upon 365 nm irradiation, and the luminescence can be further quenched by the treatment of HCl. Therefore, a triple-mode reversible luminescence switch of off-onI-onII-off can be achieved. Finally, we demonstrated the applications of Sb3+-doped compounds in single-component white light illumination, latent fingerprint detection, fluorescent anti-counterfeiting, and information encryption. [ABSTRACT FROM AUTHOR]

Piezocatalysis is considered as an evolving technology based on the piezoelectric properties of catalysts, has shown great potential in the field of environmental remediation, water splitting, and biotechnology. In this work, the catalytic performance of (Ba0.95Ca0.05) (Ti1-xSnx)O3 (BCT1-xSx, 0.04 ≤ x ≤ 0.12) piezoelectric ceramics was studied systematically. The relationship between piezoelectric performance and piezo-photocatalytic performance was investigated. As the Sn content increased, the crystalline structure gradually changed from the orthorhombic (O) phase (x = 0.04) to O-pseudocubic (PC) two-phase coexistence (x = 0.08 and x = 0.10), and finally to the PC phase (x = 0.12). The piezoelectric constant d33 exhibited an initial increases followed by a decreases with rising Sn content, reaching peak of 509pC/N at x = 0.10. The enhanced d33 was due to multiphase coexistence and a Curie temperature near room temperature. The piezocatalytic efficacy of BCT1-xSx was linked to d33, with the maximum degradation rate achieved at x = 0.10. However, the optimal piezo-photocatalytic performance was obtained at x = 0.08 instead of x = 0.10 with the highest degradation rate of 69%. The photo-piezocatalytic performance was discovered to be intricately linked not only to the band gap of piezocatalysts but also influenced by their piezoelectric properties. These results will provide guidance for designing new lead-free piezoelectric materials with excellent catalytic properties. [ABSTRACT FROM AUTHOR]

The electroanalytical behavior of SnSx (x = 1, 2) encapsulated into a carbon phase was studied using the galvanostatic intermittent titration technique (GITT) and electrochemical impedance spectroscopy (EIS). These techniques are widely utilized in battery systems to investigate the diffusion of alkali metal cations in anode and cathode materials depending on the concentration of ions in the host material. Here, we report different calculation methods showing how the applied model affects the derived diffusion coefficient. The calculated value of the apparent chemical diffusion coefficient of sodium ions ( D N a + ) is in the range of 1 × 10−10 to 1 × 10−15 cm2/s depending on the technique, mathematical protocol, geometry of the electrode material, and applied potential. [ABSTRACT FROM AUTHOR]

This review details both the conventional and emerging methods of extracting tin from cassiterite. The emerging methods reviewed include sulphuric acid leaching of SnO, cooling crystallization of SnO, sulphide leaching, alkaline leaching, and dry chlorination. From these methods, the conventional approach (direct reduction smelting) stands out as the sole method that is suitable for industrial application, with none of the emerging ones being promising enough to be a contender. The thermodynamics involved in the hydrometallurgical extraction of tin from the mineral are also discussed. Δ G o values calculated at 25 °C for the reduction–dissolution of SnO2 using reducing gases revealed feasibility only when carbon monoxide was used. An indication of the possible species produced during the hydrolysis of the oxide of the metal (SnO2 and SnO) as a function of pH (ranging from −2 to 14 and 0 to 14 for SnO2 and SnO, respectively) was noted and highlighted to link a Pourbaix diagram generated from literature data. This diagram suggests that the solubility of SnO2 in both strongly acidic and alkaline media is possible, but with a small dissolution window in each. The purification and recovery routes of the various processing techniques were then envisaged. [ABSTRACT FROM AUTHOR]

This work explores the effect of a Zn1−xSnxOy (ZTO) layer as a potential replacement for CdS in Sb2(S,Se)3 devices. Through the use of Afors-het software v2.5, it was determined that the ZTO/Sb2(S,Se)3 interface exhibits a lower conduction band offset (CBO) value of 0.34 eV compared to the CdS/Sb2(S,Se)3 interface. Lower photo-generated carrier recombination can be obtained at the interface of the ZTO/Sb2(S,Se)3 heterojunction. In addition, the valence band offset (VBO) value at the ZTO/Sb2(S,Se)3 interface increases to 1.55 eV. The ZTO layer increases the efficiency of the device from 7.56% to 11.45%. To further investigate the beneficial effect of the ZTO layer on the efficiency of the device, this goal has been achieved by five methods: changing the S content of the absorber, changing the thickness of the absorber, changing the carrier concentration of ZTO, using various Sn/(Zn+Sn) ratios in ZTO, and altering the thickness of the ZTO layer. When the S content in Sb2(S,Se)3 is around 60% and the carrier concentration is about 1018 cm−3, the efficiency is optimal. The optimal thickness of the Sb2(S,Se)3 absorber layer is 260 nm. A ZTO/Sb2(S,Se)3 interface with a Sn/(Zn+Sn) ratio of 0.18 exhibits a better CBO value. It is also found that a ZTO thickness of 20 nm is needed for the best efficiency. [ABSTRACT FROM AUTHOR]

Tin(II) perovskite oxides are promising for lead-free ferroelectric applications because Sn(II) is isoelectronic to Pb(II) and is predicted to amplify displacements and polarization. Though typically difficult to synthesize, a metastable perovskite structure of barium zirconate titanate with Sn(II) substituted for Ba was recently reported. In the present work, a detailed structural analysis is performed on 40% Sn(II)-substituted BaZr0.5Ti0.5O3 with high-resolution synchrotron X-ray diffraction. The main diffraction peaks of the cubic perovskite persist with the incorporation of tin into the structure. Additionally, superstructure reflections are observed in the low 2θ region of the diffraction pattern at d-spacings that are multiples of the main perovskite peaks. The origin of these superstructure peaks is attributed to atomic displacements of the Sn and Zr/Ti cations. A Bayesian inference method is applied to conduct a refinement of the atomic displacements in a supercell with no symmetry constraints (i.e., P1 symmetry setting) using the superstructure diffraction reflections. In the absence of a known structure and symmetry, the Bayesian method allows for simultaneous refinement of all atomic positions without convergence to unrealistic local minima, resulting in the most probable configurations of atoms. Through the refined solution, it is found that displacements of the cations result in symmetry-breaking distortions from the parent cubic perovskite structure that can be modeled using a P1 supercell with the potential for ferroelectric polarization. [ABSTRACT FROM AUTHOR]

In this paper, the initiation of interfacial damage in SnPb alloy was investigated at the atomic scale through molecular dynamics simulations. The focus was primarily on the structural stability of the Sn/Pb interface with different orientations, the formation energies of vacancies in different Sn/Pb interfaces, and the short-range interactions between dislocations and the Sn/Pb interface. The results revealed a correlation between the interfacial energies of all four Sn/Pb interfaces and the disorder of Sn and Pb atoms near the interface, where a more regular atomic arrangement resulted in lower interfacial energy. The vacancy formation energies near the Sn/Pb interfaces varied depending on the interface type, although all types contributed to reducing these energies. Furthermore, the Sn/Pb interface acts as a barrier to dislocations in both Pb and β-Sn phases, while leading to the cross-slip of screw dislocations in the Pb phase. Edge dislocations in the β-Sn phase induce significant strain localization at the interface, initiating interfacial damage and crack nucleation. These findings are highly significant for understanding damage mechanisms in SnPb alloy and advancing high-performance solder development. [ABSTRACT FROM AUTHOR]

Background: Cancer-associated fibroblasts have become a new target for therapy. Fibroblasts present within malignancies express the fibroblast activation protein (FAP). Inhibitors to FAP (FAPI) are small molecules recently developed as a theranostic agents for imaging and radiotherapy. All currently used FAPI rely on a linker–chelator complex attached to the 'inhibitor'. We describe a new automated method of the direct attachment of the radioisotope to the inhibitor, resulting in a >50% MW reduction with the hope of an improved tumor-to-background ratio and tumor uptake. Methods: [18F]FluroFAPI was developed from a Sn precursor. This allowed for subsequent automated radioflourination. We obtained the biodistribution of [18F]FluroFAPI in rats, performed estimated human radiation dosimetry, and performed a 100× expected single dose toxicology analysis for eventual first-in-human experiments. Results: The synthesis of the Sn precursor for FluorFAPI and the automated synthesis of [18F]FluroFAPI was demonstrated. [18F]FluroFAPI had favorable estimated human radiation dosimetry, and demonstrated no adverse effects when injected at a dose of 100× that planned for [18F]FluroFAPI. Conclusions: With the successful development of an automated synthesis of [18F]FluroFAPI, first-in-human testing can be planned with the hope of an improved tumor-to-background performance compared to other FAPI agents. [ABSTRACT FROM AUTHOR]