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In this work, flexible Cu2−xS films on nylon membranes are prepared by combining a simple hydrothermal synthesis and vacuum filtration followed by hot pressing. The films consist of Cu2S and Cu1.96S two phases with grain sizes from nano to submicron. Doping Se on the S site not only increases the Cu1.96S content in the Cu2−xS to increase carrier concentration but also modifies electronic structure, thereby greatly improves the electrical properties of the Cu2−xS. Specifically, an optimal composite film with a nominal composition of Cu2−xS0.98Se0.02 exhibits a high power factor of ~150.1 μW m−1 K−2 at 300 K, which increases by ~138% compared to that of the pristine Cu2−xS film. Meanwhile, the composite film shows outstanding flexibility (~97.2% of the original electrical conductivity is maintained after 1500 bending cycles with a bending radius of 4 mm). A four-leg flexible thermoelectric (TE) generator assembled with the optimal film generates a maximum power of 329.6 nW (corresponding power density of 1.70 W m−2) at a temperature difference of 31.1 K. This work provides a simple route to the preparation of high TE performance Cu2−xS-based films. [ABSTRACT FROM AUTHOR]

The threat of ozone in indoor spaces and other enclosed environments is receiving increasing attention. Among numerous ozone catalytic decomposition technologies, copper catalytic material has a superior performance and relatively low cost, making it one of the ideal catalyst materials. This review presents the recent Cu catalyst studies on ozone decomposition, particularly morphological design, the construction of heterostructures, and monolithic catalyst design used to improve their performance. Moreover, this review proposes further improvement directions based on Cu materials' inherent limitations and practical needs. On this basis, in the foreseeable future, Cu materials will play a greater role. [ABSTRACT FROM AUTHOR]

Copper-sulfide-based materials have attracted noteworthy attention as thermoelectric materials due to rich elemental reserves, non-toxicity, low thermal conductivity, and adjustable electrical properties. However, research on the flexible thermoelectrics of copper sulfide has not yet been reported. In this work, we developed a facile method to prepare flexible Mn-doped Cu2−xS films on nylon membranes. First, nano to submicron powders with nominal compositions of Cu2−xMnyS (y = 0, 0.01, 0.03, 0.05, 0.07) were synthesized by a hydrothermal method. Then, the powders were vacuum-filtrated on nylon membranes and finally hot-pressed. Phase composition and microstructure analysis revealed that the films contained both Cu2S and Cu1.96S, and the size of the grains was ~20–300 nm. By Mn doping, there was an increase in carrier concentration and mobility, and ultimately, the electrical properties of Cu2−xS were improved. Eventually, the Cu2−xMn0.05S film showed a maximum power factor of 113.3 μW m−1 K−2 and good flexibility at room temperature. Moreover, an assembled four-leg flexible thermoelectric generator produced a maximum power of 249.48 nW (corresponding power density ~1.23 W m−2) at a temperature difference of 30.1 K, and had good potential for powering low-power-consumption wearable electronics. [ABSTRACT FROM AUTHOR]

Electrochemical sensors, due to their excellent and unique features, are of high interest nowadays for the detection and monitoring of several biological compounds. In such a case, serotonin (SRN), an important neurotransmitter, was herein studied for its detection in biological fluids since its presence is more crucial to be monitored and detected in clinical and medical applications. Several study strategies have been used to determine the chemical and physical properties. The crystalline size of the constructed copper sulfide (Cu2S) material was measured to be 25.92 nm. The Cu2S was fabricated over the working surface and further analyzed for several sensor parameters to be optimized. The charge transfer resistance of the copper sulfide-modified glassy carbon electrode (Cu2S/GCE) was determined to be about 277.0 Ω. With the linear range from about 0.029 μM to 607.6 μM for SRN, the limit of detection (LOD) was calculated as 3.2 nM, with a good sensitivity of 13.23 μA μM−1 cm2. The sensor experienced excellent repeatability, reproducibility, and long-term stability. The fabricated electrode was selective with the presence of different interfering compounds. The real sample analysis, as determined with the regular addition method with human serum and urine samples, revealed a good recovery percentage. Thus, the employed fabricated electrode material will be highly effective in sensing other analytes of choice. [ABSTRACT FROM AUTHOR]

The technique of gold collection in matte can effectively improve the trapping efficiency of precious metals such as gold, silver, and platinum. However, the underlying mechanism of gold collection from high-temperature molten matte is complex and not well understood. In this work, the first-principle calculations were utilized to investigate the adsorption behavior of gold atoms on a Cu2S surface. The effects of vacancies and As and Sb doping on the gold-trapping ability of Cu2S were also explored, and the electronic properties of each adsorption system, including the charge density difference, density of states, and charge transfer, were systematically analyzed. The results show that the Cu-terminated Cu2S(111) surface has the lowest surface energy, and the Au atom is chemically adsorbed on the Cu2S(111) with an adsorption energy of −1.99 eV. The large adsorption strength is primarily ascribed to the strong hybridizations between Au-5d and Cu-3d orbitals. Additionally, the Cu vacancy can significantly weaken the adsorption strength of Cu2S(111) towards Au atoms, while the S vacancy can notably enhance it. Moreover, due to the formation of strong covalent As–Au/Sb–Au bonds, doping As and Sb into Cu2S(111) can enhance the gold-trapping capability of Cu2S, and the Sb doping exhibits superior effectiveness. Our studied results can provide theoretical guidance for improving the gold collection efficiency of Cu2S. [ABSTRACT FROM AUTHOR]

Porous C nanosheet/Cu2S composites were prepared using a simple self-template method and vulcanization process. The Cu2S nanoparticles with an average diameter of 140 nm are uniformly distributed on porous carbon nanosheets. When used as the anode of a potassium-ion battery, porous C nanosheet/Cu2S composites exhibit good rate performance and cycle performance (363 mAh g−1 at 0.1 A g−1 after 100 cycles; 120 mAh g−1 at 5 A g−1 after 1000 cycles). The excellent electrochemical performance of porous C nanosheet/Cu2S composites can be ascribed to their unique structure, which can restrain the volume change of Cu2S during the charge/discharge processes, increase the contact area between the electrode and the electrolyte, and improve the electron/ionic conductivity of the electrode material. [ABSTRACT FROM AUTHOR]

Metal sulfide electrocatalyst is developed as a cost-effective and promising candidate for hydrogen evolution reaction (HER). In this work, we report a novel Mo-doped Cu2S self-supported electrocatalyst grown in situ on three-dimensional copper foam via a facile sulfurization treatment method. Interestingly, Mo-Cu2S nanosheet structure increases the electrochemically active area, and the large fleecy multilayer flower structure assembled by small nanosheet facilitates the flow of electrolyte in and out. More broadly, the introduction of Mo can adjust the electronic structure, significantly increase the volmer step rate, and accelerate the reaction kinetics. As compared to the pure Cu2S self-supported electrocatalyst, the Mo-Cu2S/CF show much better alkaline HER performance with lower overpotential (18 mV at 10 mA cm−2, 322 mV at 100 mA cm−2) and long-term durability. Our work constructs a novel copper based in-situ metal sulfide electrocatalysts and provides a new idea to adjust the morphology and electronic structure by doping for promoting HER performance. [ABSTRACT FROM AUTHOR]

In recent years, flexible thermoelectric generators(f-TEG), which can generate electricity by environmental temperature difference and have low cost, have been widely concerned in self-powered energy devices for underground pipe network monitoring. This paper studied the Cu2S films by screen-printing. The effects of different proportions of p-type Cu2S/poly 3,4-ethylene dioxythiophene-polystyrene sulfonate (PEDOT:PSS) mixture on the thermoelectric properties of films were studied. The interfacial effect of the two materials, forming a superconducting layer on the surface of Cu2S, leads to the enhancement of film conductivity with the increase of PEDOT:PSS. In addition, the Seebeck coefficient decreases with the increase of PEDOT:PSS due to the excessive bandgap difference between the two materials. When the content ratio of Cu2S and PEDOT:PSS was 1:1.2, the prepared film had the optimal thermoelectric performance, with a maximum power factor (PF) of 20.60 μW·m−1·K−1. The conductivity reached 75% of the initial value after 1500 bending tests. In addition, a fully printed Te-free f-TEG with a fan-shaped structure by Cu2S and Ag2Se was constructed. When the temperature difference (ΔT) was 35 K, the output voltage of the f-TEG was 33.50 mV, and the maximum power was 163.20 nW. Thus, it is envisaged that large thermoelectric output can be obtained by building a multi-layer stacking f-TEG for continuous self-powered monitoring. [ABSTRACT FROM AUTHOR]

Large-scale Cu2S tetradecahedrons microcrystals and sheet-like Cu2S nanocrystals were synthesized by employing a hydrothermal synthesis (HS) method and wet chemistry method (WCM), respectively. The morphology of β-Cu2S powders prepared by the HS method is a tetradecahedron with the size of 1-7 μm. The morphology of α-Cu2S is a hexagonal sheet-like structure with a thickness of 5-20 nm. The results indicate that the morphologies and phase structures of Cu2S are highly dependent on the reaction temperature and time, even though the precursors are the exact same. The polycrystalline copper sulfides bulk materials were obtained by densifying the as-prepared powders using the spark plasma sintering (SPS) technique. The electrical and thermal transport properties of all bulk samples were measured from 323 K to 773 K. The pure Cu2S bulk samples sintered by using the powders prepared via HS reached the highest thermoelectric figure of merit (ZT) value of 0.38 at 573 K. The main phase of the bulk sample sintered by using the powder prepared via WCM changed from β-Cu2S to Cu1.8S after sintering due to the instability of β-Cu2S during the sintering process. The Cu1.8S bulk sample with a Cu1.96S impurity achieved the highest ZT value of 0.62 at 773 K. [ABSTRACT FROM AUTHOR]

Metal sulfides are considered excellent materials for oxygen evolution reaction because of their excellent conductivity and high electrocatalytic activity. In this report, the NiS-Cu2S composites were prepared on copper foam (NiS-Cu2S-CF) using a facile synthetic strategy. The scanning electron microscopy results confirmed that the NiS nanoneedles were successfully grown on Cu2S nanoflakes, greatly increasing the active sites. Particularly, the optimized 15% NiS-Cu2S-CF composite demonstrated excellent oxygen evolution activity with a small overpotential of 308 mV@20 mA cm−2, which is significantly smaller than that of noble metal-based electrocatalysts and other NiS-Cu2S-CF composites. The enhanced oxygen evolution activity is attributed to the unique morphology that can provide ample active sites, rich ion-transfer pathways, and the synergistic effect between NiS and Cu2S, which can boost the electron transfer rate. [ABSTRACT FROM AUTHOR]

Chalcocite is the most abundant secondary copper sulfide globally, with the highest copper content, and is easily treated by conventional hydrometallurgical processes, making it a very profitable mineral for extraction. Among the various leaching processes to treat chalcocite, chloride media show better results and have a greater industrial boom. Chalcocite dissolution is a two-stage process, the second being much slower than the first. During the second stage, in the first instance, it is possible to oxidize the covellite in a wide range of chloride concentrations or redox potentials (up to 75% extraction of Cu). Subsequently, CuS2 is formed, which is to be oxidized. It is necessary to work at high concentrations of chloride (>2.5 mol/L) and/or increase the temperature to reach a redox potential of over 650 mV, which in turn decreases the thickness of the elemental sulfur layer on the mineral surface, facilitating chloride ions to generate a better porosity of this. Finally, it is concluded that the most optimal way to extract copper from chalcocite is, during the first stage, to work with high concentrations of chloride (50–100 g/L) and low concentrations of sulfuric acid (0.5 mol/L) at a temperature environment, as other variables become irrelevant during this stage if the concentration of chloride ions in the system is high. While in the second stage, it is necessary to increase the temperature of the system (moderate temperatures) or incorporate a high concentration of some oxidizing agent to avoid the passivation of the mineral. [ABSTRACT FROM AUTHOR]

The role of heterogeneous phases in the localized corrosion of materials is an emerging area of research. This work addresses the detrimental role MnS inclusions play in the localized corrosion of carbon steels. We report the results of surface and bulk characterization of MnS inclusions in 1018 carbon steel, using a high-resolution integrated Auger nanoprobe. It is shown that the surface morphology and composition of the inclusions are highly heterogeneous. MnS inclusions are found to be nonstoichiometric and to contain a highly O-enriched surface layer. Some inclusions are covered with a thin (approximately 5 nm) layer of Cu2S. The bulk composition of "MnS" inclusions is found to include 5–7% Fe and O, and these inclusions are believed to occupy Mn and S positions within the "MnS" lattice. Interfaces between "MnS" and host ferric grains are highly disordered. We hypothesize that pitting initiates and develops at these interfaces through a galvanic coupling between the strained and the unstrained ferrite grains. [ABSTRACT FROM AUTHOR]