Search Results (50)

Numerous mineral microinclusions discovered in the Triassic Ildeus mafic–ultramafic intrusion are dominated by base metal sulfides, gold, silver, and their alloys, as well as rare earth element (REE) minerals. These mineral microinclusions were formed through both the magmatic differentiation of the Ildeus intrusion and the multi-stage interaction of intrusive rocks with late-magmatic, post-magmatic and post-collisional fluids. A comparison of the results of our microinclusions study with ore mineralization discovered within the Ildeus intrusion suggests that microinclusion assemblages in igneous rocks are, in some cases, precursors of potentially economic mineralization. In the case of the Ildeus rocks, sulfide microinclusions correspond to potentially economic disseminated nickel–cobalt sulfide ores, while microinclusions of gold and its alloys correlate with intrusion-hosted, erratic gold mineralization. The occurrence of silver and rare earth element minerals in Ildeus plutonic rocks indicates the possible presence of silver and REE mineralization, which is supported by sub-economic whole-rock silver and REE grades in parts of the Ildeus intrusion. The results of our investigation suggest that studies of mineral microinclusions in magmatic rocks may be useful in the evaluation of their metallogenic specialization and ore-forming potential and could possibly be utilized as an additional prospecting tool in the regional exploration for precious, base, and rare metals. Full article

A highly redox-active ternary nickel sulfide and cobalt-anchored carbon nanocomposite (NiS-Co@C) electrochemical electrode is synthesized by a two-step pyrolysis-hydrothermal method using biomass-derived carbon. The high-crystalline hierarchical porous nanostructure provides abundant voids and cavities, along with a large specific surface area, to improve the interfacial properties. The as-synthesized electrode achieved a specific capacity of 640 C g⁻¹ at 1 A g⁻¹, with a capacity retention of 93% over 5000 cycles, revealing outstanding electrochemical properties. Nickel sulfide nanoparticles embedded in the cobalt-anchored carbon framework improved redox activity, ion transport, and conductivity, resulting in a dominant diffusion-controlled battery-type behavior. Moreover, a hybrid supercapattery, based on battery-type NiS-Co@C as the positrode and capacitive-type activated carbon as the negatrode, achieved a maximum specific energy/power of 33 Wh kg⁻¹/7.1 kW kg⁻¹ with a 91% capacity retention after 5000 cycles. The synergistic effect of the combinatorial battery–capacitor behavior of the hybrid supercapattery has improved the specific energy–power considerably, leading the development of next-generation energy storage technologies. Full article

With the increasing societal demand for sustainable and renewable energy, supercapacitors have become research hotspots. Transition metal oxides, due to their high capacitance and abundant resources, are the preferred electrode materials. However, their poor conductivity and volume changes limit performance enhancement. Therefore, the development of heterogeneous structure electrode materials has become an important research direction. In this study, Zn-CoS@Ni(OH)₂-1 nanosheets were synthesized on a nickel foam substrate via a three-step hydrothermal synthesis method, exhibiting excellent capacitance performance. In terms of capacitance, the material achieved a specific capacitance of 624 F/g at a current density of 1 A/g. When assembled into an asymmetric supercapacitor with Active Carbon materials, the device demonstrated an energy density of 35.4 Wh kg⁻¹. Full article

Critical minerals (CMs) are pivotal in modern industries, such as telecommunications, defense, medicine, and aerospace, contributing significantly to regional and global economic growth. However, the reliance on external sources for 26 out of 50 identified CMs raises concerns about supply chain vulnerabilities. To address this, the research focused on developing a hydrometallurgical process for extracting cobalt, manganese, and nickel from acid mine drainage (AMD) treatment by-products, emphasizing the need to diversify CM supply chains within the United States (US). A solution composed of an REE solvent extraction raffinate loaded with cobalt, manganese, nickel, and various impurity metals was utilized as a feedstock in this study. The developed hydrometallurgical process involved initial sodium hydroxide precipitation to remove impurities like aluminum and iron from an SX raffinate solution generated during the extraction of rare earth elements (REEs). Precipitation stages were performed in a pH region ranging from 2 to 12 to identify the optimum pH values, achieving a tradeoff between recovery and impurity removal. A subsequent precipitation process at pH 5–10 yielded a product rich in CMs, such as manganese, cobalt, and nickel. Further separation steps involved nitric acid washing, resulting in a Mn product with a purity of 47.9% by weight and a solution with extractable concentrations of cobalt and nickel. Stagewise precipitation with sodium sulfide subsequently produced three solid products: cobalt and nickel product at pH 1–5, manganese product at pH 5–10, and magnesium at pH 10–12. The study also explored other separation approaches, including solvent extraction, to enhance the separation of nickel from cobalt. Overall, the developed hydrometallurgical process generated the following products with varying degrees of purities: cobalt (9.92 wt.%), nickel (14 wt.%), manganese (47.9 wt.%), and magnesium (27.49 wt.%). This research aimed to contribute to the sustainable extraction of CMs from secondary sources, reducing the US’ reliance on imports and promoting a more resilient supply chain for these crucial elements. Full article

With the booming of renewable clean energies towards reducing carbon emission, demands for lithium-ion batteries (LIBs) in applications to transportation vehicles and power stations are increasing exponentially. As a consequence, great pressures have been posed on the technological development and production of valuable elements key to LIBs, in addition to concerns about depletion of natural resources, environmental impacts, and management of waste batteries. In this paper, we compile recent information on lithium, nickel, and cobalt, the three most crucial elements utilized in LIBs, in terms of demands, current identified terrestrial resources, extraction technologies from primary natural resources and waste. Most nickel and cobalt are currently produced from high-grade sulfide ores via a pyrometallurgical approach. Increased demands have stimulated production of Ni and Co from low-grade laterites, which is commonly performed through the hydrometallurgical process. Most lithium exists in brines and is extracted via evaporation–precipitation in common industrial practice. It is noteworthy that at present, the pyrometallurgical process is energy-intensive and polluting in terms of gas emissions. Hydrometallurgical processes utilize large amounts of alkaline or acidic media in combination with reducing agents, generating hazardous waste streams. Traditional evaporation–precipitation consumes time, water, and land. Extraction of these elements from deep seas and recycling from waste are emerging as technologies. Advanced energy-saving and environmentally friendly processes are under extensive research and development and are crucial in the process of renewable clean energy implementation. Full article

We herein report successful syntheses of both nickel cobalt sulfide (NCS) and its composite with zeolite (NCS@Z) using a solvothermal method. Techniques such as EDX analysis, SEM, and molar ratio determination were used for product characterization. The incorporation of NCS significantly changed the surface roughness and active sites of the zeolite, improving the efficiency of methylene blue degradation and its reusability, especially under UV irradiation. In comparing the pseudo-first order rates, the highest degradation efficiency of methylene blue was achieved with NCS-2@Z, having a degradation extent of 91.07% under UV irradiation. This environmentally friendly approach offers a promising solution for the remediation of methylene blue contamination in various industries. Full article

Developing highly efficient and stable electrocatalysts for urea electro-oxidation reactions (UORs) will improve wastewater treatment and energy conversion. A low-cost cobalt sulfide-anchored nickel sulfide electrode (CoS/Ni₃S₂@CP) was synthesized by electrodeposition in DMSO solutions and found to be highly effective and long-lasting. The morphology and composition of catalyst surfaces were examined using comprehensive physicochemical and electrochemical characterization. Specifically, CoS/Ni₃S₂@CP electrodes require a potential of 1.52 volts for a 50 mA/cm² current, confirming CoS in the heterointerface CoS/Ni₃S₂@CP catalyst. Further, the optimized CoS/Ni₃S₂@CP catalyst shows a decrease of 100 mV in the onset potential (1.32 V_RHE) for UORs compared to bare Ni₃S₂@CP catalysts (1.42 V_RHE), demonstrating much greater performance of UORs. As compared to Ni₃S₂@CP, CoS/Ni₃S₂@CP exhibits twofold greater UOR efficiency as a result of a larger electroactive surface area. The results obtained indicate that the synthetic CoS/Ni₃S₂@CP catalyst may be a favorable electrode material for managing urea-rich wastewater and generating H₂. Full article

In order to improve the pseudocapacitance performance of metal sulfide electrode materials and obtain supercapacitor energy storage devices with excellent electrochemical reversibility and long-term cycle stability, the synthesis of flower-shaped crystal nickel–cobalt sulfide and its supercapacitor performance were studied. NiCo₂S₄ flower-shaped crystal nickel–cobalt sulfide was prepared by the hydrothermal method with nickel foam as the raw material, and electrode materials were added to prepare supercapacitor electrodes for testing of the supercapacitor performance. The physical properties of flower-shaped crystal nickel–cobalt sulfide were tested by a scanning electron microscope and transmission electron microscope, and the voltammetric cycle and constant current charge and discharge of supercapacitor electrodes prepared from this sulfide were analyzed through experiments. The experimental results showed that the flower crystal microstructure had a positive effect on the electrochemical properties. The capacitance value was always high at different current densities, and the capacity was as high as 3867.8 A/g at pH 12. After 2000 voltage–charge–discharge cycle tests, the petal-like sulfide capacity still had a retention rate of 90.57, the flower crystal nickel–cobalt sulfide still showed an excellent supercapacitor performance and the specific capacity was still high, which demonstrates that this sulfide has excellent cyclic stability and durability in electrochemical applications. Full article

This study presents an experimental approach to address sulfur-induced embrittlement in copper alloys. Building on recent theoretical insights, we identified specific solute elements, such as silicon and silver, known for their strong binding affinity with vacancies. Through experimental validation, we demonstrated the effectiveness of Si and Ag in preventing sulfur-induced embrittlement in copper, even though they are not typical sulfide formers such as zirconium. Additionally, our findings highlight the advantages of these elements over traditional solutes, such as their high solubility and propensity to accumulate along grain boundaries. This approach may have the potential to be applied to other metals prone to sulfur-induced embrittlement, including nickel, iron, and cobalt, offering broader implications for materials engineering strategies and alloy development. Full article

The tetracarbonyl complexes of transition metal chalcogenides M₂X₂(CO)₄, where M = Fe, Co, Ni, Cu and X = S, Se, are examined by density functional theory (DFT). The M₂X₂ core is cyclic with either planar or non-planar geometry. As a sulfide, it is present in natural enzymes and has a selective redox capacity. The reduced forms of the selenide and sulfide complexes are relevant to the hydrogen evolution reaction (HER) and they provide different positions of hydride ligand binding: (i) at a chalcogenide site, (ii) at a particular cation site and (iii) in a midway position forming equal bonds to both cation sites. The full pathway of water decomposition to molecular hydrogen and oxygen is traced by transition state theory. The iron and cobalt complexes, cobalt selenide, in particular, provide lower energy barriers in HER as compared to the nickel and copper complexes. In the oxygen evolution reaction (OER), cobalt and iron selenide tetracarbonyls provide a low energy barrier via OOH* intermediate. All of the intermediate species possess favorable excitation transitions in the visible light spectrum, as evidenced by TD-DFT calculations and they allow photoactivation. In conclusion, cobalt and iron selenide tetracarbonyl complexes emerge as promising photocatalysts in water splitting. Full article

Non-noble metal electrocatalysts for the oxygen evolution reaction (OER) have recently gained particular attention. In the present work, a facile one-step electrodeposition method is applied in situ to synthesize cobalt sulfide nanostructures on nickel foam (NF) electrodes. For the first time, a systematic study is carried out on the impact of the Co/S molar ratio on the structural, morphological, and electrochemical characteristics of Ni-based OER electrodes by employing Co(NO₃)₂·6 H₂O and CH₄N₂S as Co and S precursors, respectively. The optimum performance was obtained for an equimolar Co:S ratio (1:1), whereas sulfur-rich or Co-rich electrodes resulted in an inferior behavior. In particular, the Co_xS_y@NF electrode with Co/S (1:1) exhibited the lowest overpotential value at 10 mA cm⁻² (0.28 V) and a Tafel slope of 95 mV dec⁻¹, offering, in addition, a high double-layer capacitance (C_DL) of 10.7 mF cm⁻². Electrochemical impedance spectroscopy (EIS) measurements confirmed the crucial effect of the Co/S ratio on the charge-transfer reaction rate, which is maximized for a Co:S molar ratio of 1:1. Moreover, field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD) and X-ray fluorescence (XRF) were conducted to gain insights into the impact of the Co/S ratio on the structural and morphological characteristics of the electrodes. Notably, the Co_xS_y@NF electrocatalyst with an equimolar Co:S ratio presented a 3D flower-like nanosheet morphology, offering an increased electrochemically active surface area (ESCA) and improved OER kinetics. Full article

Herein, a novel self-supporting CuO/nickel-cobalt-sulfide (NCS) electrode was designed in a two-step electrodeposition technique followed by a calcination process. Three-dimensional copper foam (CF) was exploited as the current collector and spontaneous source for the in situ preparation of the CuO nanostructures, which ensured sufficient deposition space for the subsequent NCS layer, thus forming abundant electrochemical active sites. Such a hierarchical structure is conducive to providing a smooth path for promoting electronic transmission. Therefore, the optimized CuO/NCS electrode exhibits outstanding energy storage capability with extremely superior specific capacitance (Cs) of 7.08 F cm⁻² at 4 mA cm⁻² and coulombic efficiency of up to 94.83%, as well as excellent cycling stability with capacitance retention of 83.33% after 5000 cycles. The results presented in this work extend our horizons to fabricate novel hierarchical structured electrodes applied to energy storage devices. Full article

Dye-sensitized solar cells (DSSCs) are often viewed as the potential future of photovoltaic systems and have garnered significant attention in solar energy research. In this groundbreaking research, we introduced a novel solvothermal method to fabricate a unique “grass-like” pattern on fluorine-doped tin oxide glass (FTO), specifically designed for use as a counter electrode in dye-sensitized solar cell (DSSC) assemblies. Through rigorous structural and morphological evaluations, we ascertained the successful deposition of nickel cobalt sulfide (NCS) on the FTO surface, exhibiting the desired grass-like morphology. Electrocatalytic performance assessment of the developed NCS-1 showed results that intriguingly rivaled those of the acclaimed platinum catalyst, especially during the conversion of I₃ to I⁻ as observed through cyclic voltammetry. Remarkably, when integrated into a solar cell assembly, both NCS-1 and NCS-2 electrodes exhibited encouraging power conversion efficiencies of 6.60% and 6.29%, respectively. These results become particularly noteworthy when compared to the 7.19% efficiency of a conventional Pt-based electrode under similar testing conditions. Central to the performance of the NCS-1 and NCS-2 electrodes is their unique thin and sharp grass-like morphology. This structure, vividly showcased through scanning electron microscopy, provides a vast surface area and an abundance of catalytic sites, pivotal for the catalytic reactions involving the electrolytes in DSSCs. In summation, given their innovative synthesis approach, affordability, and remarkable electrocatalytic attributes, the newly developed NCS counter electrodes stand out as potent contenders in future dye-sensitized solar cell applications. Full article

Iron-containing nickel sulfides, selenides, and sulfoselenides were synthesized via a simple two-step hydrothermal reaction (temperature ≤ 160 °C) for their application as electrocatalysts in the oxygen evolution reaction (OER) in an alkaline solution (1 mol L⁻¹ KOH). The study demonstrated that iron-containing nickel cobalt sulfides and selenides exhibit superior OER performance with lower overpotentials compared to iron-free nickel cobalt sulfide and selenide, which highlights the significant role of iron in enhancing OER nickel cobalt electrocatalysts: Fe_0.1Ni_1.4Co_2.9(S_0.87O_0.13)₄, η₅₀ = 318 mV; Fe_0.2Ni_1.5Co_2.8(S_0.9O_0.1)₄, η₅₀ = 310 mV; Fe_0.3Ni_1.2Co_2.5(S_0.9O_0.1)₄, η₅₀ = 294 mV; Fe_0.6Ni_1.2Co_2.5(S_0.83O_0.17)₄, η₅₀ = 294 mV; Fe_0.4Ni_0.7Co_1.6(Se_0.81O_0.19)₄, η₅₀ = 306 mV compared to Ni_1.0Co_2.1(S_0.9O_0.1)₄, η₅₀ = 346 mV; and Ni_0.7Co_1.4(Se_0.85O_0.15)₄, η₅₀ = 355 mV (all values at current densities η₅₀ of 50 mA cm⁻²). Furthermore, the iron-containing nickel cobalt sulfoselenide Fe_0.5Ni_1.0Co_2.0(S_0.57Se_0.25O_0.18)₄ displayed exceptional OER performance with η₅₀ = 277 mV, surpassing the benchmark RuO₂ electrode with η₅₀ = 299 mV. The superior performance of the sulfoselenide was attributed to its low charge transfer resistance (Rct) of 0.8 Ω at 1.5 V vs. the reversible hydrogen electrode (RHE). Moreover, the sulfoselenide demonstrated remarkable stability, with only a minimal increase in overpotential (η₅₀) from 277 mV to 279 mV after a 20 h chronopotentiometry test. These findings suggest that trimetallic iron, nickel and cobalt sulfide, selenide, and especially sulfoselenide materials hold promise as high-performance, cost-effective, and durable electrocatalysts for sustainable OER reactions. This study provides a valuable approach for the development of efficient electrocatalytic materials, contributing to the advancement of renewable energy technologies. Full article

This work proposes an environmentally safe and economically feasible method of waste copper-nickel production slag utilization (Kola Mining-Metallurgical Company, Nornickel, Kola Peninsula, Russia). This process involves the decomposition of slag by diluted solutions of sulfuric acid (7–10 wt.% H₂SO₄) with a transfer in a solution of more than 70% silicon, 77% iron and 78% magnesium, and a concentration of non-ferrous metals in the residue (~70%). Copper ions were used in the leaching stage to prevent the release of hydrogen sulfide into the working atmosphere. Dehydration of the solution, followed by washing of water-soluble sulphates from silica, was carried out to separate silica from the leaching solution. The dehydration temperature effect on the silica structural characteristics was determined. The possibility of recovering non-ferrous metals from solutions after silica extraction by precipitation, in the form of copper cementite, and the sum of nickel and cobalt sulfides, was evaluated. Pigment-grade iron dioxide, magnesium sulphate and aluminium hydroxide were obtained by dehydration of the solution after extraction of base metals, calcination and other operations. Sulfuric acid leaching resulted in the disclosure of sulfide grains encapsulated in ferrosilicate, which is a favorable factor for flotation. The depleted residue can be successfully used in the construction industry. Full article