Explore the vast range of titles available.

Metal oxide semiconductors have found widespread applications in chemical sensors based on electrical transduction principles, in particular for the detection of a large variety of gaseous analytes, including environmental pollutants and hazardous gases. This review recapitulates the progress in copper oxide nanomaterial-based devices, while discussing decisive factors influencing gas sensing properties and performance. Literature reports on the highly sensitive detection of several target molecules, including volatile organic compounds, hydrogen sulfide, carbon monoxide, carbon dioxide, hydrogen and nitrogen oxide from parts-per-million down to parts-per-billion concentrations are compared. Physico-chemical mechanisms for sensing and transduction are summarized and prospects for future developments are outlined.

In this work, we present an effective process easily adapted in industrial environments for the development of multifunctional nanocomposites for material extrusion (MEX) 3D printing (3DP). The literature is still very limited in this field, although the interest in such materials is constantly increasing. Nanocomposites with binary inclusions were prepared and investigated in this study. Polylactic acid (PLA) was used as the matrix material, and cuprous oxide (Cu2O) and cellulose nanofibers (CNF) were used as nanoadditives introduced in the matrix material to enhance the mechanical properties and induce antibacterial performance. Specimens were built according to international standards with a thermomechanical process. Tensile, flexural, impact, and microhardness tests were conducted. The effect on the thermal properties of the matrix material was investigated through thermogravimetric analysis, and Raman spectroscopic analysis was conducted. The morphological characteristics were evaluated with atomic force microscopy (AFM), scanning electron microscopy (SEM), and energy-dispersive X-ray (EDS) analyses. The antibacterial performance of the prepared nanomaterials was studied against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) bacteria, with a screening agar well diffusion method. All nanocomposites prepared exhibited biocidal properties against the bacteria tested. The tested PLA/1.0 CNF/0.5 Cu2O material had 51.1% higher tensile strength and 35.9% higher flexural strength than the pure PLA material.

Particles of sub-micron size possess significant capacity to adsorb organic molecules from aqueous media. Semiconductor photocatalysts in particle form could potentially be utilized for dye removal through either physical adsorption or photo-induced chemical process. The photocatalytic and adsorption capabilities of Cu2O particles with various exposed crystal facets have been studied through separate adsorption capacity test and photocatalytic degradation test. These crystals display unique cubic, octahedral, rhombic dodecahedral, and truncated polyhedral shapes due to specifically exposed crystal facet(s). For comparison, Cu2O particles with no clear exposed facets were also prepared. The current work confirms that the surface charge critically affects the adsorption performance of the synthesized Cu2O particles. The octahedral shaped Cu2O particles, with exposed 111 facets, possess the best adsorption capability of methyl orange (MO) dye due to the strongest positive surface charge among the different types of particles. In addition, we also found that the adsorption of MO follows the Langmuir monolayer mechanism. The octahedral particles also performed the best in photocatalytic dye degradation of MO under visible light irradiation because of the assistance from dye absorption. On top of the photocatalytic study, the stability of these Cu2O particles during the photocatalytic processes was also investigated. Cu(OH)2 and CuO are the likely corrosion products found on the particle surface after the photocorrosion in MO solution. By adding hole scavengers in the solution, the photocorrosion of Cu2O was greatly reduced. This observation confirms that the photocatalytically generated holes were responsible for the photocorrosion of Cu2O.

Buildings worldwide are becoming more thermally insulated, and air circulation is being reduced to a minimum. As a result, measuring indoor air quality is important to prevent harmful concentrations of various gases that can lead to safety risks and health problems. To measure such gases, it is necessary to produce low-cost and low-power-consuming sensors. Researchers have been focusing on semiconducting metal oxide (SMOx) gas sensors that can be combined with intelligent technologies such as smart homes, smart phones or smart watches to enable gas sensing anywhere and at any time. As a type of SMOx, p-type gas sensors are promising candidates and have attracted more interest in recent years due to their excellent electrical properties and stability. This review paper gives a short overview of the main development of sensors based on copper oxides and their composites, highlighting their potential for detecting CO2 and the factors influencing their performance.

The relentless consumption of fossil fuels and soaring CO2 emissions have plunged the world into an energy and environmental crisis. As society grapples with these challenges, the demand for clean, renewable, and sustainable energy solutions has never been more urgent. However, even though many efforts have been made in this field, there is still room for improvement concerning efficiency, material stability, and catalytic enhancement regarding kinetics and selectivity of photoelectrochemical (PEC) processes. Herein, we provide the experimental proof for the enhancement of the photocurrent efficiency by the critical focus on semiconductor–electrolyte interface (SEI) properties. By tailoring electrolyte composition, researchers can unlock significant improvements in catalytic efficiency and stability, paving the way for advanced PEC technologies. In this study, we investigate the influence of electrolyte composition on SEI properties and its impact on PEC performance. By employing electrolytes enriched with carbonates, borates, sulphates, and alkali cations, we demonstrate their profound role in optimising photoelectrochemical CO2 reduction reaction (CO2RR) efficiency. Central to this work is Cu2O—an affordable, highly promising photocatalyst. While its potential is undeniable, Cu2O’s inherent instability and diverse reduction products, ranging from CH3OH to CO, HCOOH, CH3COOH, and CH3CH2OH, have hindered its widespread adoption in PEC CO2 reduction (CO2RR). Our approach leverages a straightforward yet powerful electrodeposition method, enabling a deeper exploration of SEI dynamics during photocatalysis. Key parameters, such as carbonate concentration, local pH, alkali cation presence, anionic geometry, CO2 solubility, and electrolyte conductivity, are systematically investigated. The findings reveal the formation of a unique “rigid layer” at the photocatalyst surface, driven by specific cation–anion interactions. This rigid layer plays a pivotal role in boosting PEC performance, offering a new perspective on optimising, among other PEC processes, CO2RR catalytic efficiency. This profound study bridges a critical knowledge gap, shedding light on the dual influence of cations and anions on SEI properties and PEC CO2RR. By unravelling these intricate interactions, we provide a roadmap for designing next-generation PEC systems. These insights pave the way for sustainable energy advancements, inspiring innovative strategies to tackle one of the most pressing challenges of our time.

High level of atmospheric carbon dioxide (CO 2 ) concentration is considered one of the main causes of global warming. Electrochemical conversion of CO 2 into valuable chemicals and fuels has promising potential to be implemented into practical and sustainable devices. In order to efficiently realize this strategy, one of the biggest efforts has been focused on the design of catalysts which are inexpensive, active and selective and can be produced through green and up-scalable routes. In this work, copper-based materials are simply synthesized via microwave-assisted process and carefully characterized by physical/chemical/electrochemical techniques. Nanoparticle with a cupric oxide (CuO) surface as well as various cuprous oxide (Cu 2 O) cubes with different sizes is obtained and used for the CO 2 reduction reaction. It is observed that the Cu 2 O-derived electrodes show enhanced activity and carbon monoxide (CO) selectivity compared to the CuO-derived one. Among various Cu 2 O catalysts, the one with the smallest cubes leads to the best CO selectivity of the electrode, attributed to a higher electrochemically active surface area. Under applied potentials, all Cu 2 O cubes undergo structural and morphological modification, even though the cubic shape is retained. The nanoclusters formed during the material evolution offer abundant and active reaction sites, leading to the high performance of the Cu 2 O-derived electrodes. Graphic abstract

With increasingly frequent highly infectious global pandemics, the textile industry has responded by developing commercial fabric products by incorporating antibacterial metal oxide nanoparticles, particularly copper oxide in cleaning products and personal care items including antimicrobial wipes, hospital gowns and masks. Current methods use a surface adsorption method to functionalize nanomaterials to fibers. However, this results in poor durability and decreased antimicrobial activity after consecutive launderings. In this study, cuprous oxide nanoparticles with nanoflower morphology (Cu2O nanoflowers) are synthesized in situ within the cotton fiber under mild conditions and without added chemical reducing agents from a copper (II) precursor with an average maximal Feret diameter of 72.0 ± 51.8 nm and concentration of 17,489 ± 15 mg/kg. Analysis of the Cu2O NF-infused cotton fiber cross-section by transmission electron microscopy (TEM) confirmed the internal formation, and X-ray photoelectron spectroscopy (XPS) confirmed the copper (I) reduced oxidation state. An exponential correlation (R2 = 0.9979) between the UV-vis surface plasmon resonance (SPR) intensity at 320 nm of the Cu2O NFs and the concentration of copper in cotton was determined. The laundering durability of the Cu2O NF-cotton fabric was investigated, and the superior nanoparticle-leach resistance was observed, with the fabrics releasing only 19% of copper after 50 home laundering cycles. The internally immobilized Cu2O NFs within the cotton fiber exhibited continuing antibacterial activity (≥99.995%) against K. pneumoniae, E. coli and S. aureus), complete antifungal activity (100%) against A. niger and antiviral activity (≥90%) against Human coronavirus, strain 229E, even after 50 laundering cycles.

The lithium-ion batteries with high energy density, large power density and long cycle life have attracted much attention. Among various anodes, the CuO anode possesses a high specific capacity of 670 mAh g−1. However, the CuO anode suffers from capacity fading after the first cycle, and the reason is not clear up enough to now. To investigate the nature of CuO anode lithiation–delithiation conversion in lithium-ion batteries, we investigated the phase conversion of CuO anode by in situ X-ray diffraction. We discovered that the specific discharge capacity of CuO during the first discharge cycle is usually more than 670 mAh g−1, but this value decreases to approximately 400–450 mAh g−1 after the second cycle and is stable for the subsequent cycles. The in situ X-ray diffraction observations reveal that in the discharge process of the first cycle, the CuO crystalline phase changes gradually to Cu. However, during the charge process of the first cycle, the delithiation product phase is Cu2O. The same phenomenon occurs again in the second charging–discharging cycle. The obtained scientific understanding reveals that the nature of CuO anode lithiation–delithiation phase conversion in Li-ion battery is between Cu2O and Cu, not CuO and Cu, which is responsible for capacity fading of CuO anode. The present research provides a certain scientific basis for the application of CuO in lithium-ion batteries. The in situ XRD method is helpful to understand the mechanism of electrochemical behaviour of other transition metal oxygen (sulphur, and fluorine) and can make an in-depth study of the searching for commercial anode materials for lithium-ion batteries.

In the present study, Cu2O films were deposited on a glass substrate via RF (radio frequency) magnetron sputtering under substrate temperature conditions that ranged from room temperature (RT, 25 °C) to 400 °C. The structural, compositional, and optical properties of the Cu2O films were analyzed in relation to the experimental variables by applying various measurement methods. The substrate temperature was a crucial factor in shaping the structural, compositional, and optical properties of the Cu2O films that were synthesized via RF-magnetron sputtering. Our findings revealed that the Cu2O films exhibited a cubic structure, which was confirmed by XRD analysis. Specifically, the (111) and (200) planes showed different trends with respect to the substrate temperature. The intensity of the (111) peak increased at 250 °C, and above 300 °C, the preferred orientation of the (111) plane was maintained. The grain size, which was determined via FE-SEM, displayed a positive correlation with the substrate temperature. Additionally, XPS analysis revealed that the binding energy (BE) of the Cu2O film sputtered at 400 °C was similar to that which was previously reported. Notably, the as-grown Cu2O film demonstrated the highest transmittance (15.9%) in the visible region, which decreased with increasing substrate temperature. Furthermore, the energy band gap (Eg) of the Cu2O films remained constant (2.51 eV) at low substrate temperatures (25 °C to 200 °C) but exhibited a slight increase at higher temperatures, reaching 2.57 eV at 400 °C.

Gastrointestinal (GI) tumor is a serious disease with high mortality rates and morbidity rates worldwide. Chemotherapy is a key treatment for GI, however, systematic side effects and inevitable drug resistance complicate the situation. In the process of therapy, P-glycoprotein (P-gp) could remove chemotherapy drugs from cells, thus causing multi-drug resistance. Chemodynamic therapy (CDT) utilizing Fenton chemistry has been used for cancer therapy, along with various combination therapies. The reactive oxygen species produced by CDT could inhibit P-gp's efflux pump function, which reduce chemoagents excretion and reverse drug resistance. In the present study, we developed novel nanocrystals (Cu 2 O@Pt NCs) to overcome drug resistance by reducing mitochondria-derived ATP through chemo/CDT in GI cancer. Furthermore, in vivo results in tumor-bearing mice demonstrated that treatment with Cu 2 O@Pt NCs with CDT and chemotherapy could achieve the most effective antitumor therapeutic effect with the least amounts of adverse effects. As a result, Cu 2 O@Pt NCs could provide a promising strategy for chemo/CDT-synergistic therapy.