Search Results (42)

This study presents the development of Cu-doped NiMo/TiO₂ photoelectrocatalysts for simultaneous green hydrogen production and pharmaceutical pollutant removal under simulated solar irradiation. The catalysts were synthesized via wet impregnation (15 wt.% total metal loading with 0.6 wt.% Cu) and thermally treated at 400 °C and 900 °C to investigate structural transformations and catalytic performance. Comprehensive characterization (XRD, BET, SEM, XPS) revealed phase transitions, enhanced crystallinity, and redistribution of redox states upon Cu incorporation, particularly the formation of NiTiO₃ and an increase in oxygen vacancies. Crystallite sizes for anatase, rutile, and brookite ranged from 21 to 47 nm at NiMoCu400, while NiMoCu900 exhibited only the rutile phase with 55 nm crystallites. BET analysis showed a surface area of 44.4 m²·g⁻¹ for NiMoCu400, and electrochemical measurements confirmed its higher electrochemically active surface area (ECSA, 2.4 cm²), indicating enhanced surface accessibility. In contrast, NiMoCu900 exhibited a much lower BET surface area (1.4 m²·g⁻¹) and ECSA (1.4 cm²), consistent with its inferior photoelectrocatalytic performance. Compared to previously reported binary NiMo/TiO₂ systems, the ternary NiMoCu/TiO₂ catalysts demonstrated significantly improved hydrogen production activity and more efficient photoelectrochemical degradation of paracetamol. Specifically, NiMoCu400 showed an anodic peak current of 0.24 mA·cm⁻² for paracetamol oxidation, representing a 60% increase over NiMo400 and a cathodic current of −0.46 mA·cm⁻² at −0.1 V vs. RHE under illumination, nearly six times higher than the undoped counterpart (–0.08 mA·cm⁻²). Mott–Schottky analysis further revealed that NiMoCu400 retained n-type behavior, while NiMoCu900 exhibited an unusual inversion to p-type, likely due to Cu migration and rutile-phase-induced realignment of donor states. Despite its higher photosensitivity, NiMoCu900 showed negligible photocurrent, confirming that structural preservation and surface redox activity are critical for photoelectrochemical performance. This work provides mechanistic insight into Cu-mediated photoelectrocatalysis and identifies NiMoCu/TiO₂ as a promising bifunctional platform for integrated solar-driven water treatment and sustainable hydrogen production. Full article

Huelva is a city in SW Spain with 150,000 inhabitants, located in the proximity of two heavy chemical industry complexes, the highest naturally occurring radioactive material (NORM) waste (phosphogypsum) stacks of Europe and a highly polluted estuary, with elevated cardiovascular disease and cancer mortality rates. This study analyses the association between cumulated exposure levels to 16 metal(loid)s (Al, As, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Se, Tl, U, V, and Zn) measured in the toenail of a sample (n = 55 participants) of the general control population of Huelva City who were involved in the MCC-Spain study and the spatial proximity patterns to the local polluting sources. Residents of the city of Huelva have higher levels of Fe, Ni, Cr, Se, As, and Co in their toenails compared to the levels found in populations with similar characteristics living in non-polluted areas. Moreover, the highest concentrations of As, Pb, Cd, Mo, and Se were found in toenails of participants living near the NORM waste stack, while the highest Cu, Zn, and Al contents corresponded to people residing near the industrial area. The spatial distribution of most of the metal(loid)s studied appears to be mainly controlled by anthropogenic factors. Full article

The research referred to in this study examines the morphological, structural, and optical characteristics of kesterite (Cu_1−xAg_x)₂ZnSnS₄ (CAZTS) thin films, which are produced using a process known as thermal evaporation (TE). The study’s main goal was to determine how different Ag contents affect the characteristics of CAZTS systems. X-ray diffraction (XRD) and Raman spectroscopy were used to confirm the crystal structure of the CAZTS thin films. Using a mathematical model of spectroscopic ellipsometry, the refractive index (n) represented the real part of the complex thin films, the extinction coefficient (k) portrayed the imaginary part, and the energy bandgap of the fabricated thin films was calculated. The energy bandgap is a crucial parameter for solar cell applications, as it determines the wavelength of light that the material can absorb. The energy bandgap was found to decrease from 1.74 eV to 1.55 eV with the increasing Ag content. The ITO/n-CdS/p-CAZTS/Mo heterojunction was well constructed, and the primary photovoltaic characteristics of the n-CdS/p-CAZTS junctions were examined for use in solar cells. Different Ag contents of the CAZTS layers were used to determine the dark and illumination (current–voltage) characteristics of the heterojunctions. The study’s findings collectively point to CAZTS thin layers as potential absorber materials for solar cell applications. Full article

To improve the gas ionization ratio, the Mo-V-Cu-N coatings were deposited by pulsed dc magnetron sputtering with assistance from an anode layer ion source, and the influence of the V/Mo atomic ratio was explored with regard to the microstructure and mechanical properties of the coatings. The findings of this study indicated that the MoVCuN coatings exhibited a solid solution phase of FCC B1-MoVN with a prominent (220) preferred orientation, and the deposition rate was found to decrease from 4.7 to 1.8 nm/min when the V/Mo atomic ratio increased. The average surface roughness of the MoVCuN coatings gradually decreased, and the lowest surface roughness of 6.9 nm was achieved at a V/Mo atomic ratio of 0.31. Due to the enhanced ion bombardment effect, the coatings changed from a coarse columnar to a dense columnar crystal structure, and promoted grain refinement at higher V/Mo atomic ratios, contributing to a gradual improvement in the compressive residual stress, hardness and adhesion strength of the coatings. Full article

Depending on operating conditions, metals and alloys are exposed to various factors: wear, friction, corrosion, and others. Plasma surface alloying of machine and tool parts is now an effective surface treatment process of commercial and strategic importance. The plasma surface alloying process involves adding the required elements (carbon, chromium, titanium, silicon, nickel, etc.) to the surface layer of the metal during the melting process. A thin layer of the compound is pre-applied to the substrate, then melted and intensively mixed under the influence of a plasma arc, and during the solidification process, a new surface layer with optimal mechanical properties is formed. Copper-based alloys—Cu-X, where X is Fe, Cr, V, Nb, Mo, Ta, and W—belong to an immiscible binary system with high mechanical strength, electrical conductivity, and magnetism (for Fe-Cu) and also high thermal characteristics. At the same time, copper-based alloys have low hardness. In this article, wear tests were carried out on coatings obtained by plasma alloying of CuSn10 and CrxCy under various friction conditions. The following were chosen as a modifying element: chromium carbide to increase hardness and iron to increase surface tension. It is noted that an increase in the chromium carbide content to 20% leads to the formation of a martensitic structure. As a result, the microhardness of the layer increased to 700 HV. The addition of CuSn10 + 20% CrxCy and an additional 5% iron to the composition of the coating improves the formation of the surface layer. Friction tests on fixed abrasive particles were carried out at various loads of 5, 10, and 50 N. According to the test results, the alloy layer of the Fe-Cr-C-Cu-Sn system has the greatest wear resistance under abrasive conditions and dry sliding friction conditions. Full article

One of the major limitations causing deadlock in solar cells with higher sulfur content in the photovoltaic absorber material is the unintended formation of an uncontrollable MoS₂ layer between the absorber material and Mo back contact, which can affect negatively the efficiency of solar cells. Researchers reported that it is very difficult to control the MoS₂ properties such as the conductivity type, thickness, band gap, and carrier concentration in experiments. Considering these challenges, an initial step involved a thorough examination utilizing the one-dimensional solar cell capacitance simulator (SCAPS-1D) to assess the impact of n-MoS₂ interlayer thickness and donor concentration on the performance of CMTS solar cells. Our investigation revealed the formation of a “cliff-like CBO” at the CMTS/n-MoS₂ interface, facilitating the transport of electrons from the p-CMTS absorber to the Mo back contact, resulting in a significantly higher recombination rate. Subsequently, herein a novel approach is proposed, using Cu₂O as a back surface field (BSF) layer due to its low cost, intrinsic p-type properties, and non-toxic nature. Simulation results of a novel heterostructure (Mo/Cu₂O/CMTS/CdS/i-ZnO/AZO/Al) of the CMTS-based solar cell are discussed in terms of recombination rate and conduction band alignment at the absorber/BSF interface. A desired “spike-like CBO” is formed between CMTS/Cu₂O, which hinders the transport of electrons to the back contact. By optimizing the physical parameters such as thickness and the doping density of the Cu₂O layer, an efficiency η of 21.78% is achieved, with an open circuit voltage (Voc) of 1.26 V, short-circuit current density (Jsc) of 24.45 mA/cm², and fill factor (FF) of 70.85%. Our simulation results offer a promising research direction to further develop highly efficient and low-cost CMTS solar cells. Full article

Defective molybdenum disulfide (MoS₂) monolayers (MLs) modified with coinage metal atoms (Cu, Ag and Au) embedded in sulfur vacancies are studied at a dispersion-corrected density functional level. Atmospheric constituents (H₂, O₂ and N₂) and air pollutants (CO and NO), known as secondary greenhouse gases, are adsorbed on up to two atoms embedded into sulfur vacancies in MoS₂ MLs. The adsorption energies suggest that the NO (1.44 eV) and CO (1.24 eV) are chemisorbed more strongly than O₂ (1.07 eV) and N₂ (0.66 eV) on the ML with a cooper atom substituting for a sulfur atom. Therefore, the adsorption of N₂ and O₂ does not compete with NO or CO adsorption. Besides, NO adsorbed on embedded Cu creates a new level in the band gap. In addition, it was found that the CO molecule could directly react with the pre-adsorbed O₂ molecule on a Cu atom, forming the complex OOCO, via the Eley–Rideal reaction mechanism. The adsorption energies of CO, NO and O₂ on Au_2S2, Cu_2S2 and Ag_2S2 embedded into two sulfur vacancies were competitive. Charge transference occurs from the defective MoS₂ ML to the adsorbed molecules, oxidizing the later ones (NO, CO and O₂) since they act as acceptors. The total and projected density of states reveal that a MoS₂ ML modified with copper, gold and silver dimers could be used to design electronic or magnetic devices for sensing applications in the adsorption of NO, CO and O₂ molecules. Moreover, NO and O₂ molecules adsorbed on MoS₂-Au₂s₂ and MoS₂-Cu₂s₂ introduce a transition from metallic to half-metallic behavior for applications in spintronics. These modified monolayers are expected to exhibit chemiresistive behavior, meaning their electrical resistance changes in response to the presence of NO molecules. This property makes them suitable for detecting and measuring NO concentrations. Also, modified materials with half-metal behavior could be beneficial for spintronic devices, particularly those that require spin-polarized currents. Full article

Hydrogen evolution reaction (HER) is a topic of great interest due to its efficient hydrogen production properties, which can address the increasing demand for clean and sustainable energy sources. On the other hand, molybdenum carbide (MoC) has been widely studied due to its noble metal-like surface electronic properties. In the HER process, it is crucial to regulate the Mo−H bonding energy effectively and increase the electron transfer rate on the MoC catalyst surface in a rational manner. In this study, we introduce highly electronegative nitrogen and non-noble transition metal atoms (Cu or Co) into the molybdenum carbide crystal lattice (N−M−MoC, M: Cu, or Co), which leads to a dual—doping effect. This effect results in the rearrangement of the electronic configuration on the catalyst surface and the enrichment of electrons around Mo atom, leading to an optimization in the Mo−H bonding energy. Moreover, the unique two-dimensional nano-sheet structure of the N−M−MoC materials further promotes the electron transfer and exposure of active sites. Benefiting from the above, the HER performance of the N−M−MoC is significantly improved. Among them, N−Cu−MoC exhibits the lowest overpotential (η₁₀ = 158 mV) and highest stability (about 30 h) in alkaline solutions. Full article

The exposure of plants to weak magnetic fields (MFs) of various intensities and for different times is increasingly adopted to sustainably enhance plant growth in plant-based applications such as modern agriculture, phytoremediation and biogas production. However, little is known about the effects of MF exposure on plant chemical composition, and in turn on related ecosystem processes, such as the transfer of potentially toxic elements along food chains and the decomposition of organic matter. To fill this gap, the present research, through the study of the chemical composition of four edible crops (leaves of lettuce, parsley and basil, and fruits of tomato) differently exposed to weak MFs (75 Hz; 1.5 mT), aimed at evaluating the overall effects of the exposure on ecosystem processes. In particular, several essential (B, C, Ca, Cu, K, Fe, Mg, Mn, Mo, N, Ni, P, S, Zn), beneficial (Co, Na, Se, Si) and non-useful (Al, As, Ba, Cd, Cr, Li, Pb, Sr, Ti, V) elements, together with chemical compounds and derived parameters (soluble sugars, starch, chlorophylls, flavonoids, anthocyanins, nitrogen balance index), indicators of plant metabolism and health, and litter decomposability traits (C/N, C/P), were analyzed. Notwithstanding the expected variations in the observed effects among species and MF exposure conditions, the obtained results highlight a general decrease in most of the studied parameters (with the exception of those related to litter decomposability), attributable to a lower absorption/accumulation of the studied chemical elements and to a reduced synthesis of metabolites. The largest average reduction was observed for the non-useful elements, which outweighs the reduction in essential and beneficial elements and provides for an important MFinduced effect, considering their toxic, persistent and biomagnificable characteristics. Similarly, the induced increases in C/N and C/P ratios indicate the production of litter more recalcitrant to the decomposition process, suggesting that weak MF treatments may be useful to enhance soil C storage and reduce CO2 emissions. Full article

Hypereutectic High Chromium Cast Iron (HHCCI) is a new type of corrosion-wear-resistant material developed from ordinary high chromium cast iron by increasing the chromium and carbon content and is often used in abrasive environments where wear and corrosion interact. The corrosion wear resistance of the HHCCI is related to the number, size, shape and distribution of carbides and the microstructure of the matrix. This paper reviews the research progress in improving the corrosion wear resistance of HHCCI from various aspects such as primary carbide refinement, heat treatment, deep cooling treatment and alloying, etc. Among the methods of refining primary carbides are modification, semi-solid treatment and current pulse treatment. In addition, we also analyze the potential of Cr, V, Nb, Mo, Mn, W, Ni, Cu, Si, N and other alloying elements to improve the corrosion wear resistance of HHCCI. The mechanism for improving the corrosion wear resistance of HHCCI is also explored in depth and research contents worthy of attention are proposed to further improve the corrosion wear resistance of HHCCI. In the future, the author believes that modification + alloying + heat treatment is the most potential application method to improve the corrosion wear resistance of HHCCI. The corrosion wear resistance of HHCCI can be further improved by refining the primary carbide (such as adding rare earth, Ti and other modified elements) + heat treatment (with cryogenic treatment) to improve the strength + alloying (such as adding low-cost, high-potential alloy elements such as N and Si) to improve the corrosion wear resistance of the matrix. Full article

In this article, for the transition metal-nitrogen ligand Mn-M@N₆-C (M = Ag, Bi, Cd, Co, Cr, Cu, Fe, Hf, Ir, Mo, Nb, Ni, Os, Pd, Pt, Re, Rh, Ru, Sc, Ta, Tc, V, Y, Zn, Zr, Ti, W), by comparing the amount of change in the length of the N-N triple-bond, and calculating the adsorption energy of N₂ and the change of charge around N₂, it is shown that the activation effect of Sc, Ti, Y, Nb-Mn@N₆-C on the single-atomic layer of graphite substrate is relatively good. The calculation of structural stability shows that the Mn-M@N₆-C (M = Sc, Ti, Y) load is relatively stable when it is on the single-atomic layer of the graphite substrate. Through calculations, a series of data such as the adsorption free energy and reaction path are obtained, and the final results show that the preferred reaction mechanism of NRR is the alternating path on Mn-Ti@N₆-C, and the reaction limit potential is only 0.16 eV, Mn-Ti@N₆-C and has good NRR activity. In addition, the vertical path on Mn-Y@N₆-C has a reaction limit potential of 0.39 eV. Mn-Y@N₆-C also has good NRR catalyzing activity. Full article

This study sought to evaluate the potential of mulched gravel to release nutrients in the field by conducting trials with three variations of wet-and-dry cycling of the soil beneath gravel mulch and bare soil. The results revealed that quartz, muscovite, clinochlore, and albite were the most abundant minerals in the gravels. Throughout the whole wet-and-dry cycle, the total content of 30 elements measured in the gravel-mulched soil was higher than in the bare soil treatment, and the content of the total element rose with increasing wet–dry cycle humidity. The enrichment ratio (B_r) of each element in soil under gravel mulch relative to bare soil was in the sequence Mg > Ca > K > Cr > Na > Mn > V > Zn > Fe > Ti > Si > C > N > B> Co > (B_r = 0) > Pb > Cu > Ga > P > Sn > Sr > Al > Be > Li > Mo > Ni > Se > As > S. Under gravel mulch, the elements impacted by the wet–dry cycle are primarily rock-forming, whereas the elements affected under bare soil are primarily trace elements. The wet-and-dry cycles of gravel affected soil nutrients mainly by increasing soil K, Ca, Na, and Mg contents. The differences in soil K and Ca contents significantly affected the growth of jujube trees and the jujube fruit yield. A dry/wet cycle level of 5 L/d per tree under gravel cover conditions can effectively improve soil nutrients and increase the jujube fruit yield without causing environmental problems. Full article

Geochemical baselines are crucial to explore mineral resources and monitor environmental changes. This study presents the first Laos geochemical baseline values of 69 elements. The National-scale Geochemical Mapping Project of Lao People’s Democratic Republic conducted comprehensive stream sediment sampling across Laos, yielding 2079 samples collected at 1 sample/100 km², and 69 elements were analyzed. Based on the results of LGB value, R-mode factor analysis, and scatter plot analysis, this paper analyzes the relationship between the 69 elements and the geological background, mineralization, hypergene processes and human activities in the study area. The median values of element contents related to the average crustal values were: As, B, Br, Cs, Hf, Li, N, Pb, Sb, Zr, and SiO₂, >1.3 times; Ba, Be, Cl, Co, Cr, Cu, F, Ga, Mn, Mo, Ni, S, Sc, Sr, Ti, Tl, V, Zn, Eu, Al₂O₃, Tot.Fe₂O_3, MgO, CaO, and Na₂O, <0.7 times; and Ag, Au, Bi, Cd, Ge, Hg, I, In, Nb, P, Rb, Se, Sn, Ta, Th, U, W, Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and K₂O, 0.7–1.3 times. R-mode factor analysis based on principal component analysis and varimax rotation showed that they fall into 12 factors related to bedrock, (rare earth, ferrum-group, and major Al₂O₃ and K₂O elements; mineralization–Au, Sb, and As) and farming activities–N, Br, S, and C). This study provides basic geochemical data for many fields, including basic geology, mineral exploration, environmental protection and agricultural production in Laos. Full article

In order to improve the power conversion efficiency (PCE) of Cu(In,Ga)Se₂ (CIGS) solar cells, a BaTiO₃ (BTO) layer was inserted into the Cu(In,Ga)Se₂. The performances of the BTO-coupled CIGS solar cells with structures of Mo/CIGS/CdS/i-ZnO/AZO, Mo/BTO/CIGS/CdS/i-ZnO/AZO, Mo/CIGS/BTO/CdS/i-ZnO/AZO, Mo/CIGS/CdS/BTO/i-ZnO/AZO, Mo/CIGS/BTO/i-ZnO/AZO, Mo/CIGS/CdS/BTO/AZO, and Mo/ CIGS/CdS(5 nm)/BTO(5 nm)/i-ZnO/AZO were systematically studied via the SCAPS-1D software. It was found that the power conversion efficiency (PCE) of a BTO-coupled CIGS solar cell with a device configuration of Mo/CIGS/CdS/BTO/AZO was 24.53%, and its open-circuit voltage was 931.70 mV. The working mechanism for the BTO-coupled CIGS solar cells with different device structures was proposed. Our results provide a novel strategy for improving the PCE of solar cells by combining a ferroelectric material into the p-n junction materials. Full article

Due to the excellent lubricity of V₂O₅ and soft metals, V and Cu have been added to Mo-N based coatings to further improve the tribological properties. In this study, the Mo-V-Cu-N coatings were deposited by high power impulse magnetron sputtering (HIPIMS). The effects of V and Cu on the microstructure and mechanical properties of Mo-N coatings were investigated. With increasing V/Cu content ratio, the deposition rate decreased from 15.4 to 6.5 nm/min, and the microstructure transformed from a featureless structure into a dense columnar structure. At low Cu contents, less than 6.5 at.%, the Mo-V-Cu-N coatings exhibited a single solid solution phase of c-Mo₂(V)N. When the Cu content reached 29.7 at.%, the Mo₄₅V₁Cu₃₀N₂₄ coating showed the lowest surface roughness of 2.0 nm, and the coating changed into a double-phase of c-Mo₂(V)N and c-Cu. The adhesion strength gradually increased from 32.2 to 87.8 N with an increasing V/Cu content ratio. Due to the microstructure densification, a maximum hardness of 27.3 GPa was achieved for the Mo₄₆V₁₅Cu₁N₃₈ coating, which was accompanied by a high compressive residual stress. Full article