Cuprous Oxide Research Articles

Color design for cotton fabric by rapid in-situ synthesis of metal oxides on the fiber surface using organic solvent-assisted method

The coloration of cotton fabric with wild application has attracted extensive attention to cotton fiber, due to the efficient utilization of renewable industrial crops. However, the utilization of rapid in-situ synthesis of metal oxides with color is inadequate. Herein, a rapid strategy for constructing multi-color cotton fabric is designed to propose a rapid in-situ synthesis of metal oxides on the surface of cotton fiber in a high-temperature organic solvent system within 40 s. The colored metal oxide of cuprous oxide (Cu2O), tungsten trioxide (WO3), and cobalt molybdate (CoMoO4) are in-situ synthesis on the surface of cotton fibers by different precursor solutions. The bright-colored cotton fabrics are developed within 40 s as well as satisfactory K/S values of 7.53, 2.67, and 0.98, for Cu2O (Cu2O-Cotton), WO3 (WO3-Cotton), and CoMoO4 (CoMoO4-Cotton), respectively. The stable structure of the various colored cotton fabrics is demonstrated by level 3 of rubbing fastness and washing fastness, and acceptable air permeability. Moreover, assigned to the nature of particles, the colored cotton fabrics are fabricated with thermal stability and better ultraviolet protection factors. The rapid in-situ metal oxides with precursor solutions provide a time- and water-saving method to prepare colored cotton fabrics, which exhibits an ideal efficiency, and practical potential application for coloring and functionalization.

Effects of Postdeposition Annealing on the Electrical Properties of Cu2O/4H–SiC PiN Diodes

Copper oxide (Cu2O) is a promising p‐type material owing to its high absorption coefficient, suitable bandgap width, chemical stability, nontoxicity, and abundance. In this study, the effect of postdeposition annealing (PDA) on the electrical properties of Cu2O thin films deposited on silicon carbide (SiC) substrates is investigated. The films are subjected to PDA using radio‐frequency sputtering at various temperatures in air. During PDA, the Cu2O films are maintained at <300 °C and transitioned to cupric oxide (CuO) at 400 °C. The as‐deposited Cu2O film exhibits a low oxidation peak (Cu2+), whereas the phase‐transformed CuO films exhibit a higher binding energy with the emergence of satellite peaks. The rectification ratios of the Cu2O device annealed at 300 °C and CuO device annealed at 400 °C are determined as 2.02 × 107 and 1.01 × 105, respectively, denoting the substantial enhancement of approximately 55.04 for the Cu2O/SiC device and degradation of approximately 0.28 for the CuO/SiC device relative to their non‐annealed counterparts. Therefore, in this study, the significant improvement in the performance of Cu2O thin films with the meticulous deposition control of potential p‐type materials, such as Cu2O and CuO, for high‐throughput and low‐cost electronic applications is demonstrated.

Dual-Function Hybrid Coatings Based on Polytetrafluoroethylene and Cu2O for Anti-Biocorrosion and Anti-Wear Applications

Corrosion and wear issues of motion components exposed to water-based corrosion mediums, e.g., naval vessels and oil extraction equipment, pose challenges for the lifespan and reliability of the motion systems. In this work, epoxy-based coatings modified with polytetrafluoroethylene (PTFE) and cuprous oxide (Cu2O) nanoparticles were prepared. The anti-corrosion performance of the coatings was comparatively investigated by electrical impedance spectroscopy and Tafel tests in sterile and sulphate-reducing bacteria (SRB) mediums. Moreover, the tribological behaviors of the coatings were examined under water lubrication conditions. Our results demonstrate that the epoxy coatings lower significantly the corrosion current density icorr and the charge transfer resistance of the electrical double layer Rct of the carbon steel substrate. Interestingly, the hybrid coatings filled with both PTFE and Cu2O exhibit excellent anti-corrosion and anti-wear performance. After being immersed in the SRB medium for 18 days, the icorr of the pure EP coating and hybrid coatings are 1.10 × 10−7 Amp/cm2 and 0.3 × 10−7 Amp/cm2, and the Rct values are 1.04 × 103 Ω·cm2 and 3.87 × 103 Ω·cm2, respectively. A solid tribofilm forms on the stainless steel counterface sliding against the hybrid coating, which is surmised to be essential for the low friction coefficients and wear. The present work paves a route for formulating the dual-function coatings of anti-biocorrosion and anti-wear.

Double-Layered Hollow Mesoporous Cuprous Oxide Nanoparticles for Double Drug Sequential Therapy of Tumors.

Cancer stem cells (CSCs) are one of the determinants of tumor heterogeneity and are characterized by self-renewal, high tumorigenicity, invasiveness, and resistance to various therapies. To overcome the resistance of traditional tumor therapies resulting from CSCs, a strategy of double drug sequential therapy (DDST) for CSC-enriched tumors is proposed in this study and is realized utilizing the developed double-layered hollow mesoporous cuprous oxide nanoparticles (DL-HMCONs). The high drug-loading contents of camptothecin (CPT) and all-trans retinoic acid (ATRA) demonstrate that the DL-HMCON can be used as a generic drug delivery system. ATRA and CPT can be sequentially loaded in and released from CPT3@ATRA3@DL-HMCON@HA. The DDST mechanisms of CPT3@ATRA3@DL-HMCON@HA for CSC-containing tumors are demonstrated as follows: 1) the first release of ATRA from the outer layer induces differentiation from CSCs with high drug resistance to non-CSCs with low drug resistance; 2) the second release of CPT from the inner layer causes apoptosis of non-CSCs; and 3) the third release of Cu+ from DL-HMCON itself triggers the Fenton-like reaction and glutathione depletion, resulting in ferroptosis of non-CSCs. This CPT3@ATRA3@DL-HMCON@HA is verified to possess high DDST efficacy for CSC-enriched tumors with high biosafety.

Lanthanide coordination polymers@CuO nanoparticles: Enhanced self-cascade nanoenzyme activity and ratiometric fluorescence assay of glutathione

Tandem enzyme can catalyze some cascade reactions with high efficiency, and some few tandem enzyme-like mimics have been discovered recently. Further improving the catalytic efficiency of tandem nanoenzymes with facile method may undoubtedly promote and broaden their applications in various fields. In this work, cupric oxide nanoparticles (CuO NPs) with dual-functional enzyme mimics were synthesized using the rapid deposition method in advance, which simultaneously combined with lanthanide infinite coordination polymers (Ln ICPs) during the self-assemble of Tb3+, guanine-5′-triphosphate (GTP) and auxiliary ligand terephthalic acid (TA). Excitingly, the obtained Tb-GTP/TA@CuO ICPs, not only displayed obviously enhanced tandem catalytic activity compared with pure CuO NPs, but also provided a versatile ratiometric platform for ultrahigh selective and sensitive detection of glutathione (GSH) under single-wavelength excitation. A good linear relationship between the ratio signal and the GSH concentration was spanning from 0.001 to 20 μM with an impressive detection limit of 0.50 nM. This study opens a new and universal avenue for preparing integrated multifunctional probes by coupling of nanoenzyme catalytic activity with superior luminescent Ln ICPs through facile method.

Argyreia nervosa-driven biosynthesis of Cu-Ag bimetallic nanoparticles from plant leaves extract unveils enhanced antibacterial properties.

Our study specifically explores the biosynthesis of copper-silver bimetallic nanoparticles (Cu-Ag BMNPs) using Argyreia nervosa (AN) plant leaf green extract as a versatile agent for capping, reducing, and stabilizing. This biosynthesis method is characterized by its simplicity and cost-effectiveness, utilizing silver nitrate (AgNO3) and cupric oxide (CuO) as precursor materials. Our comprehensive characterization of the Cu-Ag BMNPs, employing techniques such as X-ray diffraction (XRD), UV-Vis spectrometry, scanning electron microscopy (SEM), Zetasizer, and Fourier transformed infrared spectrometry (FTIR). FTIR analysis reveals biofunctional groups and chemical bands, while SEM and XRD analyses provide morphological and structural details. To evaluate the antimicrobial properties of the Cu-Ag BMNPs, we conducted disc diffusion and minimum inhibitory concentration (MIC) assays against Escherichia coli (E. coli), with results compared to the standard gentamicin antibiotic. It is observed that the 2% and 5% CuO concentrations of AN Cu-Ag BMNPs exhibit substantial antibacterial activity in comparison to AN extract when tested on EPEC. Among these, the Cu-Ag BMNPs at a 2% concentration demonstrate higher antibacterial activity, potentially attributed to the enhanced dispersion of BMNPs facilitated by the lower CuO doping concentration. These two assays showcased the improved antimicrobial activity of Cu-Ag BMNPs, highlighting their synergistic effect, characterized by high MIC values and a broad zone of inhibition in the disc diffusion tests against E. coli. These results emphasize the significant antibacterial potential of the synthesized BMNPs, with a medicinal plant AN leaf extract playing a pivotal role in enhancing antibacterial activity.

Experimental Study of Thermal Contacts for the Enhancement of Interfacial Heat Transfer

Abstract The thermal management in high-performance electronic devices demands the enhanced rate of heat dissipation for controlling operational temperatures and achieving optimal functioning. There are many interfaces in the heat dissipation circuit where thermal interface materials are applied to enhance heat transfer rate. An experimental investigation is presented on metallic contacts to study the interfacial heat transfer with and without a thermal interface material. Thermal contact conductance is known to be an important parameter estimated for the analysis of interfacial heat transfer across the thermal contacts. Therefore, the thermal contact conductance has been evaluated to identify an effective thermal interface material suitable for the present range of contact pressure and heat flux conditions. Silicone grease is a widely used thermal interface material in electronic industry. Thus, commercially available Silicone grease is evaluated in different boundary line thicknesses for a range of contact pressure and mean interface temperatures. Further, a novel composite thermal paste has been prepared by mixing cupric oxide nanopowder and Silicone grease in three different mass concentrations. Eventually, the results for the new thermal paste showed improved thermal contact conductance and lower interfacial temperature drops as compared to Silicone grease for similar test conditions with few limitations.

Effect of electrolytes on supercapacitive behavior of cubic shaped pristine cuprous oxide synthesized via sol-gel approach

The present study uses the sol-gel approach to employ cuprous oxide (Cu2O) as an electrode material for the electrochemical energy storage application. Scanning electron microscopy (SEM) examines the structural and surface morphological characteristics of the synthesized material, and pure phase development is verified by the X-ray Diffraction (XRD) patterns. The synthesized material has a high value of specific capacitance, notable porosity, and a well-defined cubic shape. In the three-electrode set-up, the electrochemical analysis uses different aqueous electrolytes, i.e., KOH and NaOH. The electrochemical outcomes indicate that the synthesized material has a maximum specific capacitance (Cs) of 362.77 Fg-1 with excellent stability (104 %) in 6 M NaOH than KOH electrolyte (225 Fg-1). EIS data for Cu2O-based electrodes have been modeled using various equivalent circuits. The ESR value of Cu2O in NaOH electrolyte is much smaller (0.503 Ω) than in KOH electrolyte, indicating the creation of more active sites and enhanced accessibility of ions. Capacitive and diffusion current contributions are shown by using the Trassati and Dunn techniques. Thus, all our findings suggest that sol-gel synthesized pristine cuprous oxide is a potential option for energy storage gadgets.

Electrodeposition of Phase–Pure n–Type Cu2O: Role of Electrode Reactions and Local pH

Cuprous oxide (Cu2O) thin films, antithetically exhibiting n-type conductivity, were electro–deposited on Fluorine-doped Tin Oxide (FTO) coated glass substrates. Linear sweep voltammetry, chronoamperometry, and chronopotentiometry studies coupled with structural characterization of the deposit identify the occurrence of multiple reduction reactions, including “corrosion” of Cu2O to Cu. Interestingly, an underpotential conversion (negative of +0.039 V vs Ag/AgCl) of the Cu2O film to Cu islands is observed during potentiostatic deposition. The same process is also shown as a potential spike in chronopotentiometry curves, during galvanostatic deposition, at current densities that are cathodic of −0.2 mAcm−1. The reason for the formation of Cu is attributed to the decrease in local pH in the vicinity of the working electrode, whence thermodynamic conditions favor the formation of Cu. The proroguation of Cu formation is achieved by continuously stirring the solution, thereby stabilizing the pH at the electrode. Deferment of film corrosion to increasingly longer times is observed with increasing stirring rates. Mott-Schottky analysis of phase-pure films reveals the formation of degenerately doped n-type Cu2O films (n ∼1020 cm−3). The phase pure Cu2O films could be used as an electron transport layer in several photo-conversion devices and ultimately pave the way for an oxide homojunction device.

Photo-induced in-situ synthesis of Cu2O@C nanocomposite for efficient photocatalytic evolution of hydrogen

Cuprous oxide (Cu2O) is an ideal visible light catalyst owing to its narrow band gap, environmental benignity and abundant storage; however, the fast recombination of photogenerated charge carriers and poor stability of Cu2O has impeded its application in photocatalysis. Herein, we demonstrate that Cu2O@C nanocomposite can spontaneously evolve from a methanol aqueous solution containing cupric ions under the induction of irradiation. Compared with the traditional carbon coating method, the Cu2O@C nanocomposite obtained by the photo-induced in-situ synthesis can reserve superior original characteristics of the semiconductor under mild reaction conditions, promote the charge transfer and enhance the separation efficiency of charge carriers; in addition, the carbon shells can also effectively prevent Cu2O from photo-corrosion. As a result, the Cu2O@C nanocomposite exhibits excellent photocatalytic activity in the hydrogen evolution in comparison with the Cu2O particles; the H2 evolution rate over the Cu2O@C nanocomposite reaches 1.28 mmol/(g·h) under visible light, compared with the value of 0.065 mmol/(g·h) over Cu2O. Moreover, the Cu2O@C nanocomposite displays good cycle stability, viz., without any deactivation in the catalytic activity after five cycles.

Electrical, optical and nonlinear optical process in spray pyrolyzed Zn:CuO nanostructures for optoelectronic device applications

Nanostructured pure and Zn doped CuO thin films were deposited on a glass substrate at 400 °C using the chemical spray pyrolysis method. The fabricated thin films were characterized to study the compositional, structural, morphological, optical and electrical properties. X-ray diffraction spectra show the polycrystalline nature of the sample and confirm the monoclinic phase of copper oxide. Raman analysis further confirms the absence of cuprous oxide phases and impurities. High absorbance in the visible region was observed for the films with bandgap values ranging from 1.7–2.0 eV. A near-band edge emission peak in the red region is recorded in the photoluminescence spectra. Uniformly distributed nanoparticles are observed in SEM images. Hall effect measurements indicate p-type conductivity and 5% Zn doped copper oxide showed the highest conductivity and carrier concentration. The non-linear absorption coefficient (β eff) of the samples was obtained with the help of z-scan method with a Helium-Neon laser under the CW regime. Zn doping results in an increase in nonlinear absorption, supporting the use of Zn:CuO for optoelectronic devices.

Evaluation of the antimicrobial efficacy of copper oxide nanoparticles synthesized by green methods using Justicia adhatoda

This work describes the eco-friendly production of copper oxide (CuO) nanoparticles using Justicia adhatoda plant extract as a reducing and capping agent. FTIR, dynamic light scattering, XRD, and scanning electron microscopy were used to analyse the generated cupric oxide nanoparticles. The data showed that CuO nanoparticles were cubic with an average particle size of less than 19.27 nm. The CuO nanoparticles were examined for their capacity to inhibit Gram-positive, Gram-negative, and fungus using the agar well diffusion technique. According to the findings, CuO nanoparticles display a substantial level of bactericidal activity against all examined microorganisms. As a result, this investigation offers a strategy that is favourable to the environment and economical for the production of CuO nanoparticles. It also emphasises these particles’ significant antibacterial properties for biological applications.

Metal oxide-dispersed PDMS nanocomposite films with enhanced heat-shielding ability and optical transparency

Coatings that transmit visible light and shield near-infrared (NIR) rays of sunlight have potential applications in smart windows, thermal camouflage, and heat shielding encapsulations. Here, we report metal oxide-dispersed polymer nanocomposites as potential coating materials that possess a combination of NIR reflection and visible light transmission. Film coatings (∼600 μm) comprising nanocrystalline zinc oxide (ZnO), titanium dioxide (TiO2), and cupric oxide (CuO) in the range of 0–2 wt% in polydimethylsiloxane (PDMS) matrix are fabricated. At optimal compositions, these coatings provided up to 52 % reduction in the interior air temperature, measured at distances ∼3 cm beneath the surface, while, at the same time, retaining up to 70 % of visible light transparency. The NIR reflection may be attributed to a combination of the band gap of the pigment material and the difference between the refractive indices of the pigments and the polymer matrix. We present a design map that highlights different regimes of heat-shielding and light transmission space for PDMS nanocomposite films. The performance, when compared with existing reports, suggests that films fabricated in this work outperform previously reported polymeric coatings in providing a combination of heat shielding and optical transparency.

Multispectral Holographic Intensity and Phase Imaging of Semitransparent Ultrathin Films.

In this paper, we demonstrate a novel optical characterization method for ultrathin semitransparent and absorbing materials through multispectral intensity and phase imaging. The method is based on a lateral-shearing interferometric microscopy (LIM) technique, where phase-shifting allows extraction of both the intensity and the phase of transmitted optical fields. To demonstrate the performance in characterizing semitransparent thin films, we fabricated and measured cupric oxide (CuO) seeded gold ultrathin metal films (UTMFs) with mass-equivalent thicknesses from 2 to 27 nm on fused silica substrates. The optical properties were modeled using multilayer thin film interference and a parametric model of their complex refractive indices. The UTMF samples were imaged in the spectral range from 475 to 750 nm using the proposed LIM technique, and the model parameters were fitted to the measured data in order to determine the respective complex refractive indices for varying thicknesses. Overall, by using the combined intensity and phase not only for imaging and quality control but also for determining the material properties, such as complex refractive indices, this technique demonstrates a high potential for the characterization of the optical properties, of (semi-) transparent thin films.

Optimization of Cu2O Thickness to Enhance Photocatalytic Properties of Electrodeposited Cu2O/FTO Photoanode

Currently, n-type cuprous oxide (Cu2O) is a promising material as photocatalyst because of its energy gap of 2 eV that absorbs visible light up to a wavelength of 600 nm. As a photoelectrode, the thickness of Cu2O is crucial, where the improper thickness may worsen the photocatalytic properties. This work aimed to enhance the photocatalytic properties of Cu2O electrodeposited on fluorine-doped tin oxide (FTO), called Cu2O/FTO, by optimizing the Cu2O thickness. The thickness of Cu2O was controlled by adjusting the deposition time in the electrochemical deposition of Cu2O/FTO. By changing the deposition time from 5 to 45 min, the morphology of Cu2O changed from a leaf-like shape to an irregular facet shape with highly dense coverage, and the average thickness increased from 370 to 1100 nm. The increasing Cu2O thickness resulted in the increasing light absorption. The Cu2O/FTO demonstrated anodic photocurrent, which increased with the Cu2O thickness up to a threshold value of 1000 nm (35 min deposition time). At a thickness of 1000 nm, Cu2O/FTO achieved the highest photocurrent (150 and 58 µA under irradiation of 365 and 470 nm, respectively) due to the highly dense morphology and high absorption. In addition, with a thickness of 1000 nm, the charge diffusion was still good. Further, the increase of Cu2O film thickness higher than 1000 nm caused low photocatalytic properties even though the morphology was highly dense, and the absorption was the highest. This condition could be due to the relatively too-high resistance of Cu2O that caused poor charge diffusion. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Simultaneous Detection of Epicatechin and Theophylline in Black Tea with Nano Cupric Oxide Infused Graphite Electrode

Simultaneous Detection of Epicatechin and Theophylline in Black Tea with Nano Cupric Oxide Infused Graphite Electrode

Detoxification of toxic nerve agent sarin utilizing cupric oxide functionalized activated carbon fabric composite for advanced NBC Protective Clothing

ABSTRACT This investigation delves into the development of cupric oxide functionalized activated carbon fabrics (ACF@CuO) as a filter material for self-decontaminating protective clothing designed to counter chemical warfare agents (CWAs). Three variants of samples were developed by controlling functionalization levels (7.5%, 13.0%, 16.0% w/w) through optimized precursor concentrations, integrating CuO particles onto ACF surfaces. Comprehensive analysis using techniques like FTIR, BET surface area, SEM, EDX, STEM, XRD, TGA, and XPS explored the material’s properties. The studies concentrated on evaluating the performance through kinetic studies of self-detoxification of CWA Sarin (GB) using developed ACF@CuO materials analyzed by Gas Chromatography-Mass Spectrometry (GC-MS). ACF@CuO with 16% w/w functionalization exhibited superior self-decontamination against GB, achieving 92.87% efficiency within 18 hours, in contrast to 26.55% for ACF alone. Additionally, materials were tested for tensile strength, air-permeability, and Sulfur Mustard breakthrough time (HDBTT) as per IS 17377:2020 standard. The material with 13% w/w functionalization emerged as the recommended filter layer for CWA protective clothing designed for defense and civilian safety applications. The significant improvements in the self-decontamination efficiency of the material were attributed to the synergistic effects of ACF’s adsorption capabilities combined with the decontamination properties of CuO rod-shaped crystals embedded in the surface of ACF.

Structural, Optical and Dielectric Properties of Some Nanocomposites Derived from Copper Oxide Nanoparticles Embedded in Poly(vinylpyrrolidone) Matrix.

Polymer nanocomposite films based on poly(vinyl pyrrolidone) incorporated with different amounts of copper oxide (CuO) nanoparticles were prepared by the solution casting technique. The PVP/CuO nanocomposites were analyzed by X-ray diffractometry (XRD), scanning electron microscopy, UV-Visible absorption spectroscopy and dielectric spectroscopy. The XRD analysis showed that the monoclinic structure of cupric oxide was maintained in the PVP host matrix. The key optical parameters, such as optical energy gap Eg, Urbach energy EU, absorption coefficient and refractive index, were estimated based on the UV-Vis data. The optical characteristics of the nanocomposite films revealed that their transmittance and absorption were influenced by the addition of CuO nanoparticles in the PVP matrix. Incorporation of CuO nanoparticles into the PVP matrix led to a significant decrease in band gap energy and an increase in the refractive index. The dielectric and electrical behaviors of the PVP/CuO nanocomposites were analyzed over a frequency range between 10 Hz and 1 MHz. The effect of CuO loading on the dielectric parameters (dielectric constant and dielectric loss) of the metal oxide nanocomposites was also discussed.

Transition metal (Fe, Co, Ni)-doped cuprous oxide nanowire arrays as self-supporting catalysts for electrocatalytic CO2 reduction reaction to ethylene

The transition metal (Fe, Co, Ni)-doped cuprous oxide (Cu2O) nanowire arrays on Cu mesh (CM) (M-Cu2O@CM, M = Fe, Co, Ni) are successfully synthesized for the electrocatalytic CO2 reduction reaction (CO2RR) to ethylene (C2H4) through the simple calcination and impregnation-exchange methods. Systematic characterizations have demonstrated that the Ni/Co doping in Cu2O@CM is conducive to stabilizing the Cu+ sites due to the electron transfer from Cu2O to Ni/Co, while the Fe doping has the opposite effect. Consequently, they show the different electrocatalytic performances of Ni-Cu2O@CM > Co-Cu2O@CM > Cu2O@CM > Fe-Cu2O@CM for CO2RR to C2H4 in an H-cell. Among them, Ni-Cu2O@CM exhibits the ∼2.0-fold faradaic efficiency for C2H4 (58.2 % vs. 28.7 %) and the ∼2.5-fold current density (−37.6 vs. −15.0 mA·cm−2) at −1.1 V vs. RHE, as compared with Cu2O@CM. Further experiments reveal that during the electrocatalytic CO2RR, the Ni-Cu2O@CM can generate more *CO, which promotes the C–C coupling reaction. The activity of Co-Cu2O@CM is lower than Ni-Cu2O@CM because of the strong adsorption of *COOH, while the Fe-Cu2O@CM even exhibits a lower activity than Cu2O@CM. This work provides an insight into the effect of transition metal-doped Cu2O array on the electrocatalytic CO2RR to C2H4 products.

Photo-electric properties of ultra-thin cuprous oxide films prepared by electrodeposition

Photo-electric properties of ultra-thin cuprous oxide films prepared by electrodeposition