Distribution Of Elements Research Articles

Behaviors of trace elements under varying methane seepage intensity: Insight from tubular seep carbonates in the South China Sea

Seep carbonates are commonly used to study environmental conditions based on trace element patterns. However, the relationship between methane flux and trace element enrichments is not well understood. Tubular seep carbonates, which are interpreted as former fluid conduits, offer an opportunity to investigate how trace element distributions in these structures respond to changes in methane flux. Here, we examined the distribution of trace elements in three tubular seep carbonates collected from Jiulong Methane Reef in the northern South China Sea. The carbonates exhibit low δ13C values (−57.0‰ to −40.4‰ V-PDB). All tubes show a gradual increasing trend in the carbonate contents and a decreasing trend in δ13C values from the outer to the inner portions, indicating an overall increase in methane flux over time. The two tubular carbonates with lower carbon isotopic values likely precipitated in a more reducing environment, as evidenced by relatively higher enrichment factors of Molybdenum (MoEF) and higher Molybdenum/Uranium ratios. The MoEF values show an increasing trend for the outer to the inner portions for the two samples with lower δ13C values, while the UEF values show an increasing trend for the two samples with higher δ13C values. This suggests that the enrichments of Mo and U are influenced by methane flux, which regulates the redox conditions and the rate of elements supplied from seawater. Only Arsenic (As) and antimony (Sb) show identifiable enrichment among the other trace elements, which is unrelated to methane dynamics. This study provides insights into the behavior of redox-sensitive trace elements under changing methane flux, laying a groundwork for using trace element enrichments to reconstruct paleoenvironmental information, particularly in dynamic environments.

Elemental composition and potential health risk of vegetable cultivated in residential area situated close to abandoned gold mine dump: Characteristics of soil quality on the vegetables

The presence of toxic metals in residential areas near abandoned gold mine tailings is a major environmental issue. This study mainly aimed to investigate the elemental distribution of both toxic and essential elements in soils and leafy vegetables (Brassica oleracea) collected from eight different sites around the Davidsonville residential area, located closer to the abandoned Princess gold mine dump, Johannesburg, South Africa. The nutritional value of vegetables in the human diet was determined to assess their value to their health. The vegetables contained metals in the following descending order: Ca > Mg > Ca > Sb > Pb > Fe > Mo > Cr > Se > As > V > Ni > Co > Cd. The bioaccumulation factor (BAF) revealed that vegetables tend to accumulate most metals even (toxic) during the transfer and translocation process. Based on the recommended daily allowance (%RDA) the vegetables showed to contribute 152%, 84% and 75% toward RDA for Se, V and Ca, respectively for most adults and these play a role in human metabolic activities. The vegetables were found to be a good source of essential elements (Ca, Mg, Ni, Na, Fe) but with some traces of toxic metals such as Pb, As and Sb. Based on the health risk assessment, the vegetable posed an adverse health hazard for human consumption due to metals with high HRI >1.

Steering the Selective Production of Glycolic Acid by Electrocatalytic Oxidation of Ethylene Glycol with Nanoengineered PdBi-Based Heterodimers.

Heterodimers of metal nanocrystals (NCs) with tailored elemental distribution have emerged as promising candidates in the field of electrocatalysis, owing to their unique structures featuring heterogeneous interfaces with distinct components. Despite this, the rational synthesis of heterodimer NCs with similar elemental composition remains a formidable challenge, and their impact on electrocatalysis has remained largely elusive. In this study, Pd@Bi-PdBi heterodimer NCs are synthesized through an underpotential deposition (UPD)-directed growth pathway. In this pathway, the UPD of Bi promotes a Volmer-Weber growth mode, allowing for judicious modulation of core-satellite to heterodimer structures through careful control of supersaturation and growth kinetics. Significantly, the heterodimer NCs are employed in the electrocatalytic process of ethylene glycol (EG) with high activity and selectivity. Compared with pristine Pd octahedra and common PdBi alloy NC, the unique heterodimer structure of the Pd@Bi-PdBi heterodimer NCs endows them with the highest electrocatalytic performance of EG and the best selectivity (≈93%) in oxidizing EG to glycolic acid (GA). Taken together, this work not only heralds a new strategy for UPD-directed synthesis of bimetallic NCs, but also provides a new design paradigm for steering the selectivity of electrocatalysts.

Synergistic Strain Suppressing and Interface Engineering in Na4MnV(PO4)3/C for Wide-Temperature and Long-Calendar-Life Sodium-Ion Storage.

A Na4MnV(PO4)3 (NMVP) cathode is regarded as a promising cathode candidate for sodium-ion batteries (SIBs). However, issues such as low electronic conductivity and partial cation dissolution contribute to high polarization and structure distortion. Herein, we engineered the local electron density and reaction kinetic properties of NMVP cathodes with varying oxygen vacancies by introducing varying amounts of Zr doping and carbon coating. The optimized sample exhibited a high-rate capacity of 71.8 mAh g-1 at 30 C (83.1% capacity retention after 1000 cycles) and excellent performance over a wide temperature range (84.1 mAh g-1 at 60 °C and 61.4 mAh g-1 at -30 °C). In situ X-ray diffraction technology confirmed a redox solid solution and a two-phase reaction mechanism, revealing minor changes in cell volume and slight strain variations after Zr doping, effectively suppressing the structural distortion. Theoretical calculations illustrated that Zr doping largely shrinks the band gap of NMVP, enriches local electron density, and slightly alters the local element distribution and bond lengths. Moreover, full-cells have shown high energy density (259.9 Wh kg-1) and outstanding cycling stability (200 cycles). The work provides fresh insights into the synergistic effect of strain suppressing and interface engineering in promoting the development of wide temperature range and long-calendar-life SIBs.

Depositional and post-depositional architectural elements of the Dar es Salaam Platform, central coastal Tanzania: distribution of petroleum system elements and their implications for petroleum prospectivity

Depositional and post-depositional architectural elements of the Dar es Salaam Platform, central coastal Tanzania: distribution of petroleum system elements and their implications for petroleum prospectivity

Microstructure and Mechanical Properties of Similar/Dissimilar Resistance Spot‐Welded Aluminum Alloys for Aerospace Applications

2195 aluminum–lithium (Al–Li) and 2XXX series aluminum alloys are joined using resistance spot welding for the first time. The macrostructure, microstructure, element distribution, microhardness, and tensile‐shear property of spot‐welded joints are investigated. The microstructure of the fusion zone of 2195/2195, 2195/2219, and 2195/2A14 joints  is fine equiaxed spherical grains. It is found that solute segregation of Cu occurs in the grain boundaries in the fusion zone, forming Al2Cu. The microhardness shows that due to the dissolution of strengthening phase T1, the hardness of the fusion zone of the three types of joints is lower than that of the base material. The 2195/2195 joint has the best mechanical performance among the three combinations, with maximum tensile‐shear force and absorbed energy reaching 16893.7 N and 24.9 J, respectively. The fracture surfaces of all three types of joints exhibit mixed ductile‐brittle characteristics.

Distribution and Probabilistic Risk Assessment of Antibiotics, Illegal Drugs, and Toxic Elements in Gastropods from Southeast China

We investigated fourteen antibiotics, three illegal drugs, and two toxic elements in commercially available gastropods from southeast China. The data revealed high detection frequencies (DFs) for florfenicol (61.32%), florfenicol amine (47.33%), and thiamphenicol (39.88%), with maximum concentrations of 1110, 2222, and 136 μg/kg wet weight (ww), respectively. The DFs of illegal drugs were 3.54% for leucomalachite green and 0.3% for chloramphenicol. The average levels of Cd and As were 1.17 and 6.12 mg/kg ww, respectively. All chemicals presented diverse DFs in different sampling months. The highest DFs of florfenicol, florfenicol amine, and thiamphenicol were in July. The health risk assessment showed that targeted hazard quotients (THQs) of antibiotics, Cd, and As for children, teens, and adults were all less than one. Notably, the toxic elements (Cd and As) were identified as the primary health risk in gastropods, contributing to over 90% of the total THQs.

Multicomponent Amorphous Solid Forms of Telmisartan: Insights into Mechanochemical Activation and Physicochemical Attributes.

The present work aims to explore the new solid forms of telmisartan (TEL) with alpha-ketoglutaric acid (KGA) and glutamic acid (GA) as potential coformers using mechanochemical approach and their role in augmentation in physicochemical parameters over pure crystalline TEL. Mechanochemical synthesis was performed using 1:1 stoichiometric ratio of TEL and the selected coformers in the presence of catalytic amount of ethanol for 1h. The ground product was characterized by PXRD, DSC, and FTIR. The new solid forms were evaluated for apparent solubility, intrinsic dissolution, and physical stability. Preliminary characterization revealed the amorphization of the mechanochemical product as an alternate outcome of cocrystallization screening. Mechanistic understanding of the amorphous phase highlights the formation of amorphous-mediated cocrystallization that involves three steps, viz., molecular recognition, intermediate amorphous phase, and product nucleation. The solubility curves of both multicomponent amorphous solid forms (TEL-KGA and TEL-GA) showed the spring-parachute effect and revealed significant augmentation in apparent solubility (8-10-folds), and intrinsic dissolution release (6-9-folds) as compared to the pure drug. Besides, surface anisotropy and differential elemental distributions in intrinsic dissolution compacts of both solid forms were confirmed by FESEM and EDX mapping. Therefore, amorphous phases prepared from mechanochemical synthesis can serve as a potential solid form for the investigation of a cocrystal through amorphous-mediated cocrystallization. This has greater implications in solubility kinetics wherein the rapid precipitation of the amorphous phase can be prevented by the metastable cocrystal phase and contribute to the significant augmentation in the physicochemical parameters.

Photocatalytic oxidation of formaldehyde under visible light using BiVO4-TiO2 synthesized via ultrasonic blending.

Formaldehyde (HCHO) is one of the primary indoor air pollutants, and efficiently eliminating it, especially at low concentrations, remains challenging. In this study, BiVO4-TiO2 catalyst was developed using ultrasonic blending technology for the photocatalytic oxidation of low-level indoor HCHO. The crystal structure, surface morphology, element distribution, and active oxidation species of the catalyst were examined using XRD, SEM, TEM, UV-Vis, EDS, and ESR techniques. Our results demonstrated that the BiVO4-TiO2 catalyst, prepared by ultrasonic blending, exhibited good oxidation performance and stability. The HCHO concentration reduced from 1.050 to 0.030mg/m3 within 48h, achieving a removal rate of 97.1%. The synergy between BiVO4 and TiO2 enhanced the efficiency of separating photogenerated carriers and minimized the likelihood of recombination between photogenerated electrons and holes. Additionally, this synergy significantly enhanced the presence of hydroxyl radicals (·OH) on the catalyst, resulting in an oxidation performance superior to that of either BiVO4 or TiO2. Our research offers valuable insights for the development of new photocatalysts to address HCHO pollution.

High-Entropy Alloy Al0.2Co1.5CrFeNi1.5Ti0.5 Prepared from High-Entropy Oxide (Al0.2Co1.5CrFeNi1.5Ti0.5)3O4 by a Deoxidation Process via a CaH2-Assisted Molten Salt Method

High-entropy alloys (HEAs) have attracted a great deal of research interest these days because of their attractive properties. Low-temperature chemical synthesis methods are being developed to obtain nanoscale HEAs with low energy consumption. In this study, we prepared HEA Al0.2Co1.5CrFeNi1.5Ti0.5 nanoparticles from high-entropy oxide (HEO) (Al0.2Co1.5CrFeNi1.5Ti0.5)3O4 by a deoxidation process via a CaH2-assisted molten salt method at 600 °C. X-ray diffraction measurements demonstrated that the oxide precursor and the reduced product have single-phases of spinel structure and face-centered cubic structures, indicating the formation of HEO and HEA, respectively. The HEA nanoparticles exhibited superior catalytic performance in the liquid-phase hydrogenation of p-nitrophenol at room temperature with little leaching of the component elements. Scanning electron microscopy (SEM) with energy-dispersive X-ray spectrometry (EDX) exhibited a good distribution of constituent elements over the HEA nanoparticles in a micro-sized range. However, transmission electron microscopy (TEM) with EDX revealed a slight deviation of elemental distributions of Al and Ti from those of Co, Cr, Fe, and Ni in a nano-sized range, probably due to the incomplete reduction of aluminum and titanium oxides. The elemental homogeneity in the HEA nanoparticles could be improved by taking advantage of the HEO precursor with homogeneous elemental distributions, but the experimental results suggested the importance of the total reduction of oxide precursors to prepare homogeneous HEAs from HEOs.

“Hidden” mineralogical-geochemical zonality revealed by the laser microanalysis of sulfides at the Kyzyk-Chadr deposit, Republic of Tyva

A comprehensive study of the Kyzyk-Chadr porphyry copper deposit included determination of the composition and spatial distribution of trace elements in ore-forming sulfide minerals over the ore- hosting rock volume. The study was carried out using the mass spectrometric analysis with laser ablation of the analyzed material. Steady qualitative and quantitative elements of a “hidden” mineralogical and geochemical zonality have been identified, that are expressed in variations in the concentration of trace elements and their ratios in pyrites and chalcopyrites over the volume of the ore-bearing porphyry copper stockwork. The identified regularities correlate with the established centrifugal vector and concentric pattern of the mineralogical ore-metasomatic zonality of the ore deposit.

Microstructure Effects on Anodizing High-Silicon Aluminium Alloy AlSi12Cu1(Fe) under Various Surface Conditions and Power Modes

This study investigates the impact of the surface characteristics and the inner close-to-surface characteristics of die-cast Al-Si-Cu alloy on the anodizing process under steady-state voltage and current modes. Samples of industrial-pressure die-cast aluminium–silicon alloy AlSi12Cu1(Fe) underwent anodization in as-die-cast surface conditions and after surface-grinding operations with material removal of 0.1, 0.5, and 1 mm. After surface grinding operations, the anodic layer thickness was significantly greater when subjected to a steady-state voltage of 35 V compared to that formed under a steady-state voltage of 20 V, showing an increase in the range of 2 to 2.5 times more than the thickness at 20 V. Additionally, anodizing under steady-state current mode (1.6 A·dm−2) yielded thicker layers compared to steady-state voltage mode (35 V, 1.6 A·dm−2 max) across all surface states (as-cast, ground). SEM-EDS analysis with element mapping revealed the subsequent effects of element distribution on anodic layer growth and structure. Grinding prior to anodization resulted in larger cavity sizes and lengths, attributed to microstructural variations induced by grinding. Grinding also exposed areas with slower solidification rates, fostering a homogeneous Al phase that facilitated enhanced oxide growth. Moreover, the formation of oxide was directly correlated with the presence of alloying elements, particularly silicon particles, which influenced the presence of the unanodized aluminium regions.

Determination of the Kinetic Parameters of Thermal Degradation and Hydrodemetallization of a Mixture of the Heavy Fraction of Low-Temperature Coal Tar and Coal Shale

The laws of thermal degradation of the mixture of the heavy fraction of low-temperature coal tar and coal shale were investigated using dynamic thermogravimetry. The kinetic characteristics of the process were determined using various methods, including the Ozawa–Flynn-Wall, Friedman, non-parametric kinetics and Šesták–Berggren methods. It is shown that coal shale initiated changes in the kinetic parameters and decomposition rate of the heavy fraction of coal tar. It was found that a 13% content of coal shale in the mixture led to the maximum rate of weight loss of the heavy fraction of coal tar. A hydrodemetallization kinetic model of the mixture of the heavy fraction of low-temperature coal tar and coal shale is proposed. The kinetic parameters of the hydrodemetallization process were determined; in addition, the rate constants at various temperatures were estimated. The study shows that the distribution of trace elements in the hydrogenate from the initial mixture and in the hydrogenate from the solid residue was characterized by relatively low values of reaction rate constants. The maximum microelement distribution rate was achieved in the hydrogenate solid residue. Energy indicators of activation processes indicated that hydrodemetallization at low temperatures is advantageous from an energy point of view.

Achieving strong and ductile Ti-9Cr alloy with deformable TiCr2 nano-particles by direct energy deposition

Due to the strong segregation of Cr, the content of Cr was restricted in the commercial titanium alloy to avoid β-flecks and deterioration of mechanical performance. Here, we prepared a homogeneous Ti-9Cr alloy with uniform distribution of Cr element by additive manufacturing technology. Fine α laths and dispersed TiCr2 nano-particles were acquired in the alloy, generating a high ultimate tensile strength of 1000 MPa with elongation of 16 %. It was demonstrated that the TiCr2 nano-particles showed a face-centered cubic structure. Stacking faults occurred on the {111} plane of the TiCr2 during deformation, which relieved local stress.

Effects of foliar iron oxide nanoparticles (Fe3O4) application on photosynthetic parameters, distribution of mineral elements, magnetic behaviour, and photosynthetic genes in tomato (Solanum lycopersicum var. cerasiforme) plants

This study aims to examine the effect of foliar magnetic iron oxide (Fe3O4) nanoparticles (IONP) application on the physiology, photosynthetic parameters, magnetic character, and mineral element distribution of cherry tomatoes (Solanum lycopersicum var. cerasiforme). The IONP suspension (500 mg L−1) was sprayed once (S1), twice (S2), thrice (S3), and four times (S4) a week on seedlings. Upon 21 days of the treatments, photosynthetic parameters (chlorophyll, carotenoids, photosynthetic yield, electron transport rate) were elucidated. Inductively-coupled plasma-optical emission spectrometer (ICP-OES) and vibrating sample magnetometer (VSM) were used to determine the mineral elements and abundance of magnetic power in the seedlings. In addition, the RT-qPCR method was performed to quantify the expressions of photosystem-related (PsaC, PsbP6, and PsbQ) and ferritin-coding (Fer-1 and Fer-2) genes. Results revealed that the physiological and photosynthetic indices were improved upon S1 treatment. The optimal dosage of IONP spraying enhances chlorophyll, carotenoid, electron transport rate (ETR), and effective photochemical quantum yield of photosystem II (Y(II)) but substantially diminishes non-photochemical quenching (NPQ). However, frequent IONP applications (S2, S3, and S4) caused growth retardation and suppressed the photosynthetic parameters, suggesting a toxic effect of IONP in recurrent treatments. Fer-1 and Fer-2 expressions were strikingly increased by IONP applications, suggesting an attempt to neutralize the excess amount of Fe ions by ferritin. Nevertheless, frequent IONP treatment fluctuated the mineral distribution and caused growth inhibition. Although low-repeat foliar applications of IONP (S1 in this study) may help improve plant growth, consecutive applications (S2, S3, and S4) should be avoided.

Europium in plagioclase-hosted melt inclusions reveals mantle melting modulates oxygen fugacity

To gain insights into the composition and heterogeneity of Earth’s interior, the partial pressure of oxygen (oxygen fugacity, or fO2) in igneous rocks is characterized. A surprising observation is that relative to reference buffers, fO2s of mantle melts (mid-ocean ridge basalts, or MORBs) and their presumed mantle sources (abyssal peridotites) differ. Globally, MORBs have near-uniform fO2s, whereas abyssal peridotites vary by about three orders of magnitude, suggesting these intimately related geologic reservoirs are out of equilibrium. Here, we characterize fO2s of mantle melting increments represented by plagioclase-hosted melt inclusions, which were entrapped as basaltic melts migrated from their sources toward the seafloor. At temperatures and fO2s constrained by rare earth element distributions, a range of fO2s consistent with the abyssal peridotites is recovered. The fO2s are correlated with geochemical proxies for mantle melting, suggesting partial melting of Earth’s mantle decreases its fO2, and that the uniformity of MORB fO2s is a consequence of the melting process and plate tectonic cycling.

Corrosion resistance of powder metallurgy fabricated Cu–10Sn/SiC/mica hybrid composite

Abstract For the first time, bronze/SiC/mica hybrid composite has been manufactured using powder metallurgy method. Mixture – process variable design has been applied to design of experiments and optimization of the composite composition, as well as the production process variables (compaction pressure and sintering temperature) to attain superior corrosion resistance. This involved mixing different compositions of bronze, SiC, and mica powders, which were subsequently subjected to varied pressures and temperatures during the pressing and sintering stages, all in accordance with the experimental design plan. The microstructure, chemical composition, and elemental distribution of the samples were examined using scanning electron microscope equipped by energy dispersive X-ray analyzer, and an optical microscope. In order to study the corrosion resistance, potentiodynamic polarization test and electrochemical impedance spectroscopy were performed in 3.5 wt.% NaCl solution. The results revealed that co-incorporation of SiC and mica particles in Cu–10Sn bronze matrix increases the corrosion resistance, with a synergistic effect between these particles. The result of optimization process showed that the highest corrosion resistance could be achieved for the composite with the composition of Cu–10Sn/9.85SiC/0.67mica. This outcome was subsequently validated through experimental procedures.

Aluminum zirconate nanoparticles in etch and rinse adhesive to caries affected dentine: An in-vitro scanning electron microscopy, elemental distribution, antibacterial, degree of conversion and micro-tensile bond strength assessment.

To incorporate different concentrations of Al2O9Zr3 (1%, 5%, and 10%) nanoparticles (NP) into the ER adhesive and subsequently assess the impact of this addition on the degree of conversion, μTBS, and antimicrobial efficacy. The current research involved a wide-ranging examination that merged various investigative techniques, including the application of scanning electron microscopy (SEM) for surface characterization of NP coupled with energy-dispersive x-ray spectroscopy (EDX), Fourier-transform infrared (FTIR) spectroscopy, μTBS testing, and microbial analysis. Teeth were divided into four groups based on the application of modified and unmodified three-step ER adhesive primer. Group 1 (0% Al2O9Zr3 NPs) Control, Group 2 (1% Al2O9Zr3 NPs), Group 3 (5% Al2O9Zr3 NPs), and Group 4 (10% Al2O9Zr3 NPs). EDX analysis of Al2O9Zr3 NPs was performed showing elemental distribution in synthesized NPs. Zirconium (Zr), Aluminum (Al), and Oxides (O2). After primer application, an assessment of the survival rate of Streptococcus mutans was completed. The FTIR spectra were analyzed to observe the characteristic peaks indicating the conversion of double bonds, both before and after the curing process, for the adhesive Etch and rinse containing 1,5,10 wt% Al2O9Zr3 NPs. μTBS and failure mode assessment were performed using a Universal Testing Machine (UTM) and stereomicroscope respectively. The μTBS and S.mutans survival rates comparison among different groups was performed using one-way ANOVA and Tukey post hoc (p = .05). Group 4 (10 wt% Al2O9Zr3 NPs + ER adhesive) specimens exhibited the minimum survival of S.mutans (0.11 ± 0.02 CFU/mL). Nonetheless, Group 1 (0 wt% Al2O9Zr3 NPs + ER adhesive) displayed the maximum surviving S.mutans (0.52 ± 0.08 CFU/mL). Moreover, Group 2 (1 wt% Al2O9Zr3 NPs + ER adhesive) (21.22 ± 0.73 MPa) samples displayed highest μTBS. However, the bond strength was weakest in Group 1 (0 wt% Al2O9Zr3 NPs + ER adhesive) (14.13 ± 0.32 MPa) study samples. The etch-and-rinse adhesive exhibited enhanced antibacterial activity and micro-tensile bond strength (μTBS) when 1% Al2O9Zr3 NPs was incorporated, as opposed to the control group. Nevertheless, the incorporation of Al2O9Zr3 NPs led to a decrease in DC. RESEARCH HIGHLIGHTS: 10 wt% Al2O9Zr3 NPs + ER adhesive specimens exhibited the minimum survival of S.mutans. 1 wt% Al2O9Zr3 NPs + ER adhesive samples displayed the most strong composite/CAD bond. The highest DC was observed in Group 1: 0 wt% Al2O9Zr3 NPs + ER adhesive.

Investigation on the diffusion mechanism of Ga element and regulation of the V-shaped bandgap in CIGS thin films based on magnetron sputtering with a quaternary target

Gradient bandgap engineering has been acknowledged as an effective approach for improving the efficiency of CIGS solar cells. However, an effective method for achieving gradient bandgap engineering in quaternary sputtered CIGS films has not yet been identified.This is due to the uniform and singular nature of the quaternary target composition, as well as the complex kinetic mechanisms that result in the rearrangement of film elements (particularly Ga) during the annealing process. In this study, a grain boundary migration-driven diffusion mechanism for the Ga element in CIGS thin films was established to address the presented issue. The segregation of Ga element is believed to be caused by the flow velocity field generated from the migration of grain boundaries, and the distribution of Ga element can be precisely calculated using the mass transport equation. By modulating the V-shaped bandgap, a notable enhancement in open-circuit voltage (Voc) was achieved, with an increase from 0.405 V to 0.515 V, leading to an effectively improvement of solar cell's efficiency. By comparing and analyzing the actual performance parameters of the solar cells and the simulated results, we conclude that the increase in Voc is due to the alteration in bandgap structure. This study presents a novel approach to bandgap engineering in quaternary sputtered CIGS films through the quantitative calculation of Ga element distribution.

Synthesis and Thermal Decomposition of High-Entropy Layered Rare Earth Hydroxychlorides.

The synthesis of multicomponent and high-entropy compounds has become a rapidly developing field in advanced inorganic chemistry, making it possible to combine the properties of multiple elements in a single phase. This paper reports on the synthesis of a series of novel high-entropy layered rare earth hydroxychlorides, namely, (Sm,Eu,Gd,Y,Er)2(OH)5Cl, (Eu,Gd,Tb,Y,Er)2(OH)5Cl, (Eu,Gd,Dy,Y,Er)2(OH)5Cl, and (Eu,Gd,Y,Er,Yb)2(OH)5Cl, using a homogeneous hydrolysis technique under hydrothermal conditions. Elemental mapping proved the even distribution of rare earth elements, while luminescence spectroscopy confirmed efficient energy transfer between europium and other rare earth cations, thus providing additional evidence of the homogeneous distribution of rare earth elements within the crystal lattice. The average rare earth cation radii correlated linearly with the unit cell parameters (0.868 < R2 < 0.982) of the high-entropy layered rare earth hydroxychlorides. The thermal stability of the high-entropy layered rare earth hydroxychlorides was similar to that of individual hydroxychlorides and their binary solid solutions.