Search Results (22)

We present a comprehensive sensitivity study of future CE$\nu$NS detectors, focusing on a cryogenic cesium iodide detector and a tonne-scale liquid argon one, currently being developed by the COHERENT Collaboration. These setups will enable precision measurements of the weak mixing angle at low energies and allow accurate extraction of the neutron nuclear distribution radius. We also demonstrate that next-generation detectors will place constraints on the neutrino charge radius comparable to or better than current global fits. In addition, we explore the sensitivity to non-standard neutrino electromagnetic properties, such as magnetic moments and millicharges, as well as new mediators. These findings reinforce the role of CE$\nu$NS experiments in the upcoming precision era, with future detectors playing a key role in advancing our understanding of neutrino interactions and electroweak physics at low energies. Full article

The behavior of S and Cs during the alternate adsorption of each adsorbate on the Ni(100) surface is studied at room and elevated temperatures by means of low-energy electron diffraction (LEED), Auger electron spectroscopy (AES), thermal desorption spectroscopy (TDS) and work function (WF) measurements. For Cs deposition on the S-covered Ni(100) surface, the presence of sulfur increases the binding energy and the maximum amount of adsorbed cesium, as happens with other alkalis too. The first Cs overlayer is disordered, while the second strongly interacts with S with a tendency toward a Cs_xS_y surface compound formation. This interaction causes the gradual demetallization of the Cs overlayer with the increasing S coverage in the underlayer. When the Cs_xS_y stoicheometry is complete, however, subsequent Cs deposition forms an independent rather metallic overlayer. When the sulfated covers the surface, S(0.5ML)/Ni(100) is preheated to 1100 K, the S-Ni bond strengthens and S-Cs interaction correspondingly weakens to a degree that the S underlayer retains a periodic structure on the Ni substrate. This behavior indicates that the preheated S/Ni(100) surface is passivated to a degree against Cs with reduced mobility of sulfur adatoms. Differently, when S is adsorbed on the Cs-covered Ni(100) surface at room temperature, sulfur adatoms diffuse underneath the Cs overlayer to interact with the nickel substrate and form the same structural phases as on a clean surface. During that process, the sticking coefficient of sulfur remains constant regardless of the amount of pre-deposited cesium. The presence of Cs, however, increases the amount of S that can be deposited on the Ni substrate, probably in favor of the Cs_xS_y compound formation, which demetallizes the surface independent of the sequence of adsorption. Full article

Cesium tungsten bronzes (Cs_xWO₃), as functional materials with excellent near-infrared shielding properties, demonstrate significant potential for applications in smart windows. However, traditional synthesis methods, such as solid-state reactions and solvothermal/hydrothermal approaches, typically require harsh conditions, including high temperatures (above 200 °C), high pressure, inert atmospheres, or prolonged reaction times. In this study, we propose an optimized microwave-assisted solvothermal synthesis strategy that significantly reduces the severity of reaction conditions through precise parameter control. When benzyl alcohol was employed as the solvent, Cs_xWO₃ nanoparticles could be rapidly synthesized within a relatively short duration of 15 min at 180 °C, or alternatively obtained through 2 h at a low temperature of 140 °C. However, when anhydrous ethanol, which is cost-effective and environmentally friendly, was substituted for benzyl alcohol, successful synthesis was also achieved at 140 °C in 2 h. This method overcomes the limitations of traditional high-pressure reaction systems, achieving efficient crystallization under low-temperature and ambient-pressure conditions while eliminating safety hazards and significantly improving energy efficiency. The resulting materials retain excellent near-infrared shielding performance and visible-light transparency, providing an innovative solution for the safe, rapid, and controllable synthesis of functional nanomaterials. Full article

In the recent reports, it is clear that lead-free perovskite materials with low band gaps are desirable candidates for photovoltaic cells. In this regard, it was observed that germanium (Ge) is a less toxic lead-free metal that is significant for the preparation of Ge-based perovskite materials. Ge-based perovskite materials, for example, methyl ammonium germanium iodide (MAGeI₃), cesium germanium iodide (CsGeI₃), and/or formamidinium germanium iodide (FAGeI₃) may be the suitable absorber materials and alternatives towards the fabrication of lead-free photovoltaic cells. In the past few years, few attempts were made to develop FAGeI₃-based perovskite solar cells, but their photovoltaic performance is still under limitations. This is indicating that some significant and effective strategies should be designed and developed for the construction of Ge-based perovskite solar cells. It is believed that optimization of layer thickness, device structure, and selection of a suitable electron transport layer (ETL) may improve the photovoltaic performance of FAGeI₃-based perovskite solar cells. Solar cell capacitance simulation, i.e., SCAPS is one of the promising software programs that can provide significant theoretical findings for the development of FAGeI_3-based perovskite solar cells. The simulation studies via SCAPS may benefit researchers to save their energy and high cost for the optimization process in the laboratories. In this research article, SCAPS was adopted as a simulation tool for the theoretical investigations of FAGeI_3-based perovskite solar cells. The simulation studies exhibited the excellent efficiency of 15.62% via SCAPS. This study proposed the optimized device structure of FTO/TiO₂/FAGeI₃/PTAA/Au with enhanced photovoltaic performance. Full article

Background: Limited evidence links urinary metal exposure to osteoporosis in broad populations, prompting this study to cover this knowledge gap using supervised and unsupervised approaches. Methods: This study included 15,923 participants from the National Health and Nutrition Examination Survey (NHANES) spanning from 1999 to 2020. Urinary concentrations of nine metals—barium (Ba), cadmium (Cd), cobalt (Co), cesium (Cs), molybdenum (Mo), lead (Pb), antimony (Sb), thallium (Tl), and tungsten (Tu)—were measured using inductively coupled plasma mass spectrometry (ICP-MS). Osteoporosis was assessed via dual-energy X-ray absorptiometry. A weighted quantile sum (WQS) regression analysis evaluated each metal’s contribution to osteoporosis risk. Partitioning around medoids (PAM) clustering identified the high- and low-exposure groups, and their association with the risk and prognosis of osteoporosis was evaluated. Results: WQS regression identified Cd as a significant osteoporosis risk factor in the general population (odds ratio (OR) = 1.19, 95% confidence interval (CI): 1.08, 1.31, weight = 0.66). Pb notably affected those individuals aged 30–49 years and classified as Mexican American, while Sb impacted Black individuals. PAM clustering showed that the high-exposure group had a significantly higher risk of osteoporosis (OR = 1.74, 95% CI: 1.43, 2.12) and cumulative mortality risk. Conclusions: Urinary metals are associated with the risk and prognosis of osteoporosis. Full article

Ammonia synthesis is one of the most important chemical reactions. Due to thermodynamic restrictions and the reaction requirements of the current commercial iron catalysts, it is also one of the worst reactions for carbon dioxide emissions and energy usage. Ruthenium-based catalysts can substantially improve the environmental impact as they operate at lower pressures and temperatures. In this work, we provide a screening of more than 40 metals as possible promoter options based on a Ru/Pr₂O₃ catalyst. Cesium was the best alkali promoter and was held constant for the series of double-promoted catalysts. Ten formulations outperformed the Ru-Cs/PrO_x benchmark, with barium being the best second promoter studied and the most cost-effective option. Designs of experiments were utilized to optimize both the pretreatment conditions and the promoter weight loadings of the doubly promoted catalyst. As a result, optimization led to a more than five-fold increase in activity compared to the unpromoted catalyst, therefore creating the possibility for low-ruthenium ammonia synthesis catalysts to be used at scale. Further, we have explored the roles of promoters using kinetic analysis, X-ray Photoelectron Spectroscopy (XPS), and in situ infrared spectroscopy. Here, we have shown that the role of barium is to act as a hydrogen scavenger and donor, which may permit new active sites for the catalyst, and have demonstrated that the associative reaction mechanism is likely used for the unpromoted Ru/PrO_x catalyst with hydrogenation of the triple bond of the dinitrogen occurring before any dinitrogen bond breakage. Full article

Cone-beam computed tomography (CBCT) has emerged in recent years as an adequate alternative to mammography and tomosynthesis due to the several advantages over traditional mammography, including its ability to provide 3D images, its reduced radiation dose, and its ability to image dense breasts more effectively and conduct more effective breast compressions, etc. Furthermore, CBCT is capable of providing images with high sensitivity and specificity, allowing a more accurate evaluation, even of dense breasts, where mammography and tomosynthesis may lead to a false diagnosis. Clinical and experimental CBCT systems rely on cesium iodine (CsI:Tl) scintillators for X-ray energy conversion. This study comprises an investigation among different novel CBCT detector technologies, consisting either of scintillators (BGO, LSO:Ce, LYSO:Ce, LuAG:Ce, CaF₂:Eu, LaBr₃:Ce) or semiconductors (Silicon, CZT) in order to define the optimum detector design for a future experimental setup, dedicated to breast imaging. For this purpose, a micro-CBCT system was adapted, using GATE v9.2.1, consisting of the aforementioned various detection schemes. Two phantom configurations were selected: (a) an aluminum capillary positioned at the center of the field of view in order to calculate the system’s spatial resolution and (b) a breast phantom consisting of spheres of different materials, such that their characteristics are close to the breast composition. Breast phantom contrast-to-noise ratios (CNRs) were extracted from the phantom’s tomographic images. The images were reconstructed with filtered back projection (FBP) and ordered subsets expectation-maximization (OSEM) algorithms. The semiconductors acted satisfactorily in low-density matter, while LYSO:Ce, LaBr₃:Ce, and LuAG:Ce presented adequate CNRs for all the different spheres’ densities. The energy converters that are presented in this study were evaluated for their performance against the standard CsI:Tl crystal. Full article

A superatom is a cluster of atoms that acts like a single atom. Two main groups of superatoms are superalkalis and superhalogens, which mimic the chemistry of alkali and halogen atoms, respectively. The ionization energies of superalkalis are smaller than those of alkalis (<3.89 eV for cesium atom), and the electron affinities of superhalogens are larger than that of halogens (>3.61 eV for chlorine atom). Exploring new superalkali/superhalogen aims to provide reliable data and predictions of the use of such compounds as redox agents in the reduction/oxidation of counterpart systems, as well as the role they can play more generally in materials science. The low ionization energies of superalkalis make them candidates for catalysts for CO₂ conversion into renewable fuels and value-added chemicals. The large electron affinity of superhalogens makes them strong oxidizing agents for bonding and removing toxic molecules from the environment. By using the superatoms as building blocks of cluster-assembled materials, we can achieve the functional features of atom-based materials (like conductivity or catalytic potential) while having more flexibility to achieve higher performance. This feature paper covers the issues of designing such compounds and demonstrates how modifications of the superatoms (superhalogens and superalkalis) allow for the tuning of the electronic structure and might be used to create unique functional materials. The designed superatoms can form stable perovskites for solar cells, electrolytes for Li-ion batteries of electric vehicles, superatomic solids, and semiconducting materials. The designed superatoms and their redox potential evaluation could help experimentalists create new materials for use in fields such as energy storage and climate change. Full article

The study is devoted to one of the important problems of hydrogen energy—the comparative analysis and creation of novel highly conductive and durable medium-temperature proton membranes based on cesium dihydrogen phosphate and fluoropolymers. The proton conductivity, structural characteristics and mechanical properties of (1 − x)CsH₂PO₄-x fluoropolymer electrolytes (x-mass fraction, x = 0–0.3) have been investigated and analyzed. UPTFE and PVDF-based polymers (F2M, F42, and SKF26) with high thermal stability and mechanical properties have been chosen as polymer additives. The used fluoropolymers are shown to be chemical inert matrices for CsH₂PO₄. According to the XRD data, a monoclinic CsH₂PO₄ (P2₁/m) phase was retained in all of the polymer electrolytes studied. Highly conductive and mechanically strong composite membranes with thicknesses of ~50–100 μm were obtained for the soluble fluoropolymers (F2M, F42, and SKF26). The size and shape of CsH₂PO₄ particles and their distribution have been shown to significantly affect proton conductivity and the mechanical properties of the membranes. The thin-film polymer systems with uniform distributions of salt particles (up to ~300 nm) were produced via the use of different methods. The best results were achieved via the pretreatment of the suspension in a bead mill. The ability of the membranes to resist plastic deformation increases with the growth of the polymer content in comparison with the pure CsH₂PO₄, and the values of the mechanical strength characteristics are comparable to the best low-temperature polymer membranes. The proton-conducting membranes (1 − x)CsH₂PO₄-x fluoropolymer with the optimal combination of the conductivity and mechanical and hydrophobic properties are promising for use in solid acid fuel cells and other medium-temperature electrochemical devices. Full article

The interconnection of ionogenic channel structure, cation hydration, water and ionic translational mobility was revealed in Nafion and MSC membranes based on polyethylene and grafted sulfonated polystyrene. A local mobility of Li⁺, Na⁺ and Cs⁺ cations and water molecules was estimated via the ¹H, ⁷Li, ²³Na and ¹³³Cs spin relaxation technique. The calculated cation and water molecule self-diffusion coefficients were compared with experimental values measured using pulsed field gradient NMR. It was shown that macroscopic mass transfer is controlled by molecule and ion motion near sulfonate groups. Lithium and sodium cations whose hydrated energy is higher than water hydrogen bond energy move together with water molecules. Cesium cations in possession of low hydrated energy are directly jumping between neighboring sulfonate groups. Cation Li⁺, Na⁺ and Cs⁺ hydration numbers (h) in membranes were calculated from ¹H chemical shift water molecule temperature dependences. The values calculated from the Nernst–Einstein equation and the experimental conductivity values were close to each other in Nafion membranes. In MSC membranes, calculated conductivities were one order of magnitude more compared to the experimental ones, which is explained by the heterogeneity of the membrane pore and channel system. Full article

Polymer composites were synthesized via melt mixing for radiation shielding in the healthcare sector. A polymethyl-methacrylate (PMMA) matrix was filled with Bi₂O₃ nanoparticles at 10%, 20%, 30%, and 40% weight percentages. The characterization of nanocomposites included their morphological, structural, and thermal properties, achieved using SEM, XRD, and TGA, respectively. The shielding properties for all synthesized samples including pristine PMMA were measured with gamma spectrometry using a NaI (Tl) scintillator detector spanning a wide range of energies and using different radioisotopes, namely Am-241 (59.6 keV), Co-57 (122.2 keV), Ra-226 (242.0), Ba-133 (80.99 and 356.02 keV), Cs-137 (661.6 keV), and Co-60 (1173.2 and 1332.5 keV). A substantial increase in the mass attenuation coefficients was obtained at low and medium energies as the filler weight percentage increased, with minor variations at higher gamma energies (1173 and 1332 keV). The mass attenuation coefficient decreased with increasing energy except under 122 keV gamma rays due to the K-absorption edge of bismuth (90.5 keV). At 40% loading of Bi₂O_3, the mass attenuation coefficient for the cesium ¹³⁷Cs gamma line at 662 keV reached the corresponding value for the toxic heavy element lead. The synthesized PMMA-Bi₂O₃ nanocomposites proved to be highly effective, lead-free, safe, and lightweight shielding materials for X- and gamma rays within a wide energy range (<59 keV to 1332 keV), making them of interest for healthcare applications. Full article

Perovskite-type lead halides exhibit promising performances in optoelectronic applications, for which lasers are one of the most promising applications. Although the bulk structure has some advantages, perovskite has additional advantages at the nanoscale owing to its high crystallinity given by a lower trap density. Although the nanoscale can produce efficient light emission, its comparatively poor chemical and colloidal stability limits further development of devices based on this material. Nevertheless, bulk perovskites are promising as optical amplifiers. There has been some developmental progress in the study of optical response and amplified spontaneous emission (ASE) as a benchmark for perovskite bulk phase laser applications. Therefore, to achieve high photoluminescence quantum yields (PLQYs) and large optical gains, material development is essential. One of the aspects in which these goals can be achieved is the incorporation of a bulk structure of high-quality crystallization films based on inorganic perovskite, such as cesium lead halide (CsPb(Br/Cl)₃), in polymethyl methacrylate (PMMA) polymer and encapsulation with the optimal thickness of the polymer to achieve complete surface coverage, prevent degradation, surface states, and surface defects, and suppress emission at depth. Sequential evaporation of the perovskite precursors using a single-source thermal evaporation technique (TET) effectively deposited two layers. The PL and ASEs of the bare and modified films with a thickness of 400 nm PMMA were demonstrated. The encapsulation layer maintained the quantum yield of the perovskite layer in the air for more than two years while providing added optical gain compared to the bare film. Under a picosecond pulse laser, the PL wavelength of single excitons and ASE wavelength associated with the stimulated decay of bi-excitons were achieved. The two ASE bands were highly correlated and competed with each other; they were classified as exciton and bi-exciton recombination, respectively. According to the ASE results, bi-exciton emission could be observed in an ultrastable CsPb(Br/Cl)₃ film modified by PMMA with a very low excitation energy density of 110 µJ/cm². Compared with the bare film, the ASE threshold was lowered by approximately 5%. A bi-exciton has a binding energy (26.78 meV) smaller than the binding energy of the exciton (70.20 meV). Full article

Fossil additives are a primary energy source and their contribution is around 80% in the world. Therefore, bioadditives that reduce their impact are each very important. This article discusses the chemical transformation of glycerol to carbonate, ethers, esters, ketals, and acetals, compounds with high technological applications, especially in the fuel sector as bioadditives. Mainly, heterogeneous catalysts are important in the production of more than 80% of chemicals in the word. The focus is on demonstrating how the Keggin heteropolyacids (HPAs) are efficient catalysts in the reactions of syntheses of glycerol-derived bioadditives, either in homogeneous or heterogeneous phases. Although solid, HPAs have a low surface area and are soluble in polar solvents, hampering their use as heterogeneous catalysts. Alternatively, they have been successfully used supported on solid matrixes with a high surface area. Another option is converting the Keggin HPAs to insoluble salts simply by exchanging their protons with large cations like potassium, cesium, or ammonium-derivatives. Therefore, solid heteropoly salts have reduced the cost and the environmental impact of bioadditive synthesis processes, being an alternative to traditional mineral acids or solid-supported catalysts. This review describes the most recent advances achieved in the processes of synthesis of glycerol-derived bioadditives over solid-supported HPAs or their solid heteropoly salts. Full article

The metal doping at the Pb²⁺ position provides improved luminescence performance for the cesium lead halide perovskites, and their fabrication methods assisted by microwave have attracted considerable attention due to the advantages of fast heating and low energy consumption. However, the postsynthetic doping strategy of the metal-doped perovskites driven by microwave heating still lacks systematic research. In this study, the assembly of CsPbBr₃/CsPb₂Br₅ with a strong fluorescence peak at 523 nm is used as the CsPbBr₃ precursor, and through the optimization of the postsynthetic conditions such as reaction temperatures, Mn²⁺/Pb²⁺ feeding ratios, and Mn²⁺ sources, the optimum Mn²⁺-doped product (CsPb(Cl/Br)₃:Mn) is achieved. The exciton fluorescence peak of CsPb(Cl/Br)₃:Mn is blueshifted to 437 nm, and an obvious fluorescence peak attributing to the doped Mn²⁺ ions at 597 nm is obtained. Both the CsPbBr₃ precursor and CsPb(Cl/Br)₃:Mn have high PLQY and stability because there are CsPb₂Br₅ microcubic crystals to well disperse and embed the CsPbBr₃ nanocrystals (NCs) in the precursor, and after Mn²⁺-doping, this structure is maintained to form CsPb(Cl/Br)₃:Mn NCs on the surface of their microcrystals. The exploration of preparation parameters in the microwave-assisted method provides insights into the enhanced color-tunable luminescence of the metal-doped perovskite materials. Full article

The technological mineralogical characteristics of cesium-containing minerals in tailings were examined by means of chemical analysis, the energy spectrum analysis method, and MLA (mineral liberation analyzer) to determine the element content, phase analysis, associated mineral components, degree of liberation, particle size, etc. The results showed that the samples mainly contained spodumene, quartz, feldspar, mica, and other minerals. Pollucite was the main cesium-containing mineral in the sample, which had a cesium oxide content that was as high as 34.58%. The mineral content of pollucite in the sample was relatively low—only 1.23%. The pollucite monomer content and the amount of rich intergrowth was 85.25%, and the metal distribution of cesium in the +0.074 mm sample was as high as 87.06%. Spodumene was the main mineral associated with pollucite. The beneficiation evaluation of this tailing sample was conducted using a combined process that integrated desliming, magnetic separation, and froth flotation, and a pollucite concentrate containing 4.45% Cs₂O was obtained with a 63.71 recovery rate. This indicates that little pollucite was removed by means of desliming and magnetic separation before froth flotation recovery, but during the froth flotation stage in spodumene and feldspar, a large pollucite loss was observed. Therefore, to improve pollucite recovery, a pollucite-specific adsorption reagent should be synthesized. Full article