Copper Oxide Nanostructures Research Articles

Impact of Light on Coexistence of Memresistance, Meminductance, and Memcapacitance (MEMRIC) in Nanostructured Copper Oxide (CuO) Based Random Access Memory Devices.

We demonstrated the coexistence of memresistance, memcapacitance, and meminductance non-volatile bipolar analog resistive switching in Cu (top electrode)/CuO (active layer)/SS (bottom electrode) memory devices with and without presence of the light. The onset of memcapacitance and meminductance is noticed from the pinched-shaped characteristics in the first and third quadrants. The variation in the scan rate also impacts the coexistence characteristics by shifting the intercept point for low resistance (LRS) and high resistance (HRS) states in positive and negative biasing voltages. The durability and retention are measured over a period of 150 cycles and 1500 s with and without light illumination. The slopes for the Weibull cumulative distribution plot for set/reset state with and without light are 106.80/114.23 and 70.21/102.25, respectively, suggesting that the stability of the device increases with light illumination. Interestingly, the memcapacitance disappears after 600 cycles and after 60 . The double logarithmic I-V characteristics suggest the trap-assisted conduction (higher slope >2) in the higher external electric field, and Ohmic behavior in the lower applied field region. Thus, the present study provides a way for low-power electronics and photoresistors together with memresistance, memcapacitance, and meminductance, simultaneously, i. e., MEMRIC in a single device.

Chirality Engineering of Nanostructured Copper Oxide for Enhancing Oxygen Evolution from Water Electrolysis.

The exploration of a new conceptual strategy for improving the oxygen evolution reaction (OER) of earth-abundant electrocatalysts is critical. In this study, chiral copper oxide nanoflower is explored by a self-assembly method. The characterization suggests the chiral structure originates from the crystal plane-level helical stack of the secondary nanosheets. Of note, the assembly illustrates a record-high degree of spin polarization of 96%, indicating the ideal alignment of electron spin. Moreover, density function theory calculations show the chiral structure reducing the reaction energy barrier (REB) while switching the potential-determining step from *O→*OOH to *OH→*O. Together with the enhanced electrochemical active surface area and accelerated charge transfer, the production of ground-state triplet O2 is improved via a spin-forbidden route that involves the singlet H2O/OH•. Consequently, the chiral nanoflower shows a overpotential of 308mV at 10mA cm-2 and a Tafel slope of 93.5mV dec-1, which is even superior to the commercial RuO2 (310mV, 101mV dec-1). This study presents a new strategy for improving the OER activity by simultaneously enhancing electronic properties and lowering the REB of an non-noble electrocatalyst via chirality engineering.

Development of a 1D-WO3 and CuO nanocomposite modified electrode for enhanced detection of 2,4-dichlorophenol

A common chlorinated phenol known as 2,4-dichlorophenol (2,4-DCP) was investigated electrochemically using cyclic voltammetry (CV) and square wave voltammetry (SWV). The electrochemical investigation was carried out at 1D nanostructured tungsten dioxide (WO3) and copper (II) oxide (CuO) nanocomposite-modified carbon paste electrode (CPE). The electrode's sensitivity was improved by the WO3/CuO nanocomposite, enabling investigators to more precisely measure the 2,4-DCP's electrochemical characteristics. The hydrothermal method was utilized to synthesize the WO3 NPs. The XRD, AFM, SEM, and EDS techniques were used to characterize the nanocomposite and WO3 NPs. Numerous parameters have been studied, including pH, concentration variation, scan rate variation, and accumulation time. Samples of soil, fruits, and vegetables were examined using the fabricated WO3/CuO/CPE. In the concentration range of 7.0 × 10−8 M to 2.6 × 10−7 M, a linear relationship was established along with the lower limit of detection of 0.17 × 10−8 M and the limit of quantification of 0.57 × 10−7 M. The 0.2 M phosphate buffer (PB) of pH 10.4 increased the peak current, which contributed to the WO3/CuO/CPE sensor's sensing performance and was highly sensitive with respect to 2,4-DCP detection. Anodic peak current was observed for the WO3/CuO/CPE is at -7.45 µA whereas for unmodified CPE is at -1.31 µA. According to the findings, the nanostructured WO3 and CuO nanocomposite showed exceptional sensitivity in identifying the electrochemical characteristics and reactions of 2,4-DCP.

Effect of gamma and ultraviolet irradiation on the optical properties of copper oxide nanostructured thin films by chemical spray pyrolysis

Nanostructured copper oxide thin films were grown by the chemical spray pyrolysis (CSP) technique. Utilizing a homemade spray pyrolysis method, thin films are created. This work investigates the role of gamma ray and ultraviolet ray irradiation on the optical properties of copper oxide thin films(CuO) prepared. In this framework, used different substrate temperatures 300 °C, 350 °C, and 400 °C for the layers were grown on glass for the prepared CuO thin films. UV–visible spectrometer, field emission scanning electron microscopy (FE-SEM) and X-ray diffraction patterns(XRD) measurements were all used to characterize the samples. The UV–visible spectroscopy showed a decrease in the absorbance and the optical band gap of CuO thin films with the increase in the higher substrate temperatures before irradiation. Additionally, surface plasmon resonance peaks (λSPR) were observed at 329 nm. FE-SEM images revealed spherical-like shapes with an average diameter range of 48 nm,56 nm and 62 nm for 300 °C, 350 °C, and 400 °C, respectively. An analysis of X-rays revealed that CuO thin films contained the crystallographic planes of a monoclinic and an orthorhombic crystal system. Also, when samples were exposed to gamma and UVC radiation, the absorbance intensity of CuO thin films increased, but the optical band gap decreased.

Carbon fiber fabrics functionalized with monoclinic CuO nanostructures using seed-assisted hydrothermal growth treatment

The woven carbon fibers (WCF) fabrics were functionalized by growing copper-oxide (CuO) nanostructures using Seed-assisted hydrothermal technique. The effective growth of CuO on surface hydrolyzed WCF samples were achieved by seeding followed by growth treatment in the prepared precursor solution. The impact of hydrothermal process parameters such as number of seeding cycles, duration of growth treatment and molar concentration of growth solution were studied by performing 96 set of experiments with three repetitions. In this work detailed analysis of structural, morphological, and elemental attributes of the CuO-coated WCF fabrics samples have been done. The WCF fabrics were uniformly coated with monoclinic CuO nanostructures having nanopellets, nanoflakes, nanowires, and nanoflowers morphologies. Different characterization techniques such as field emission scanning electron microscope, energy dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, FT-IR spectroscopy and thermo-gravimetric analyzer were used to study different attributes of CuO-modified WCF samples. The number of seeding treatments and the length of growth treatment had a significant impact on growth of CuO nanostructures on WCF. The detailed analysis exhibits that the developed CuO-modified WCF samples may enhance interfacial surface area, bonding capacity and reduce void content by allowing nanostructures to cross-link together and with polymer matrix while fabricating composite materials.

Aftermath of Ag embedding on structural, optical, and supercapacitor electrode attributes of USP-grown CuO thin films

Here, ultrasonic spray pyrolysis method (USP) was utilized to produce pure and silver doped copper oxide nanostructures on glass substrates. Thereafter, several characterization techniques were conducted on the grown samples to delve into their morphological, structural, electrochemical, and optical aspects. The mentioned analyses were carried out by performing x-ray photoelectron spectroscopy, scanning electron microscope, X-ray diffraction, electrochemical impedance spectroscopy, galvostatic charge-discharge, cyclic voltammetry, and UV–visible spectroscopy measurements. Thus, the impact of silver impurity doping on the relevant aspects of host material were recorded as well as the features of unspoiled copper oxide films. Accordingly, the samples, as indicated by X-ray diffraction results, possessed (002) preferential plane orientation of copper oxide material along with the crystallite sizes ranging from 52.52 nm to 75.02 nm due to the imperfections caused by the silver doping. The scanning electron microscope images exhibited that the silver doping did not form significant modifications in the host material morphology where nanowire-like structures observed. The presence of the suggested materials in the films was verified by the x-ray photoelectron spectroscopy. Also, the UV–visible spectroscopy measurements detected that optical absorbance edge and bandgap energy values red shifted as a result of the impurity doping. The electrochemical supercapacitors performances of the silver doped copper oxide nanostructured thin films were inspected by using the GCD, EIS, and CV. The silver doped copper oxide films demonstrated a specific capacitance value of 66 F/g at a current density of 1 A/g in 1 M KOH electrolyte. From Nyquist plot, Rs, Rcor, Rpo, Ccor and Cc were obtained as 2.327 × 103 Ω.cm2, 43.63 × 103 Ω.cm2, 4.580 × 103 Ω.cm2, 111.5 × 10-6 S*s^a. cm-2 and 101.1 × 10-6 S*s^a. cm-2, respectively. The results indicated that the electrochemically synthesized the silver doped copper oxide electrodes can be obtained and developed as an alternative electrode material for supercapacitors (SCs).

Chitosan-Integrated Curcumin-Graphene Oxide/Copper Oxide Hybrid Nanocomposites for Antibacterial and Cytotoxicity Applications.

This study deals with the facile synthesis of a single-pot chemical technique for chitosan-curcumin (CUR)-based hybrid nanocomposites with nanostructured graphene oxide (GO) and copper oxide (CuO) as the antibacterial and cytotoxic drugs. The physicochemical properties of synthesized hybrid nanocomposites such as CS-GO, CS-CuO, CS-CUR-GO, and CS-CUR-GO/CuO were confirmed with various advanced tools. Moreover, the in vitro drug release profile of the CS-CUR-GO/CuO nanocomposite exhibited sustained and controlled release during different time intervals. Also, the antibacterial activity of the CS-CUR-GO/CuO hybrid nanocomposite presented the maximum bactericidal effect against Staphylococcus aureus and Escherichia coli pathogens. The hybrid nanocomposites revealed improved cytotoxicity behaviour against cultured mouse fibroblast cells (L929) via cell adhesion, DNA damage, and proliferation. Thus, the chitosan-based hybrid nanocomposites offer rich surface area, biocompatibility, high oxidative stress, and bacterial cell disruption functionalities as a potential candidate for antibacterial and cytotoxicity applications.

Temperature and time dependent morphological evolution of solution phase synthesized copper oxide nanostructures

Temperature and time dependent morphological evolution of solution phase synthesized copper oxide nanostructures

Effect of sandblasting and acid surface pretreatment on the specific capacitance of CuO nanostructures grown by hot water treatment for supercapacitor electrode applications

Crystalline copper oxide (CuO) nanostructures with micro, nano, and micro-nano surface roughness were grown on Cu sheet substrates by a facile, scalable, low-cost, and low-temperature hot water treatment (HWT) method that simply involved immersing Cu sheet in DI water at 75 °C for 24 h without any chemical additives. Various morphological features and sizes of CuO nanostructures were tuned by using different surface pretreatment techniques including acid treatment, sandblasting, or a combination of those two. The surface morphology of the prepared samples was analyzed by scanning electron microscopy. The crystal structure of the CuO nanostructures was investigated by x-ray diffraction XRD and Raman spectroscopy. To study the pseudocapacitive behavior, their potential supercapacitor performance, and equivalent series resistance, electrochemical analysis was done by cyclic voltammetry and electrochemical impedance spectroscopy for all the CuO/Cu samples in 1 M of Na2SO4 electrolyte. Among all, the best supercapacitive performance was achieved for CuO/Cu samples pretreated with Sandblasting followed by Acid treatment resulting in a specific capacitance of about 104 F g−1. The electrode with the sandblasted + acid pretreated sample showed a maximum of ∼69% capacitive retention after 2000 consecutive cycles. Our results indicate that CuO nanostructures on Cu substrates prepared with different surface pretreatment conditions and grown by HWT can be promising electrodes for supercapacitor device applications.

Fabrication of porous copper oxide nanostructure on nickel foam electrode by a co-precipitation method for non-enzymatic glucose detection

A novel porous copper oxide nanostructure on nickel foam (CuO/NF) electrode has been successfully prepared through a co-precipitation way. The porous CuO structure and nickel foam can be integrated into a three-dimensional ordered and hierarchal CuO electrode sensor. The porous CuO structure contains many loosely packed nanoparticles and the nanochannels, which are beneficial for providing more active sites for electrocatalytic oxidation–reduction reactions. The Cu(III)/Cu(II) pair plays an essential role, which completes the charge transfer during the electrochemically catalyzed reaction. Two Cu(III) ions obtain two electrons from one molecule of glucose, which completes two electron transfers to produce one molecule of gluconic acid lactone. The results of the actual detection of Fetal Bovine Serum indicate that the CuO/NF electrode produced could be utilized for the determination of actual samples.

Bifunctional CuO nanostructured materials preparation for ethanol gas and riboflavin sensing applications

Nanomaterial-based sensors are transforming chemical detection, merging nanotechnology's precision with sensor versatility amid growing chemical health concerns. In our study, we synthesized copper oxide (CuO) nanostructures at various pH levels using a low-temperature hydrothermal process and characterized them in detail. We utilized these CuO nanostructures to develop a chemical sensor for detecting ethanol in gas form and riboflavin in liquid solutions. Remarkably, the sensor utilizing CuO nanostructures synthesized at pH 9 exhibited superior sensing performance for ethanol concentrations ranging from 10 to 100 ppm, with an outstanding response of 132% at 100 ppm ethanol and an operating temperature of 250 °C, and a detection limit at 10 ppm with a response of 36%. For riboflavin detection, the CuO nanostructure-based riboflavin sensor demonstrated high sensitivity (183 µA/µM cm²) within a 50–800 nM concentration range. Our study highlights not only the superior performance, reproducibility, stability, selectivity, and application in real samples of these sensors but also their potential for broader applications by integrating enzymes, antibodies, or other modifications.

Synthesis of Copper Oxide Nanostructures by Ar Plasma Jet and Study of Their Structural and Optical Properties

This paper used argon plasma jets to prepare CuO nanostructures. Several techniques, including UV–Vis spectroscopy, X-ray diffraction (XRD), X-ray energy dispersive spectroscopy (EDS), and scanning electron microscopy (SEM), were used for the characterization of the prepared CuO nanoparticles. UV–Vis spectroscopy analysis confirmed that the CuO nanostructures have an energy band gap of 2.7 eV. The XRD analysis showed that the CuO nanostructures have an average crystallite size of 36 nm. Furthermore, the results of the EDX examination demonstrated the creation of CuO nanostructures of high purity. The scanning electron microscope was used to analyze the surface morphology, showing a high agglomeration rate. According to SEM analysis, the average diameter of CuO nanoparticles was 10 nm.

Interference Lithography‐Based Fabrication of 3D Metallic Mesostructures on Reflective Substrates using Electrodeposition‐Compatible Anti‐Reflection Coatings for Power Electronics Cooling

AbstractA nanostructured copper oxide (nCO) coating which can be electrochemically reduced to copper metal is demonstrated as an anti‐reflection coating, enabling interference lithography of three‐dimensionally structured templates on a surface compatible with subsequent electrodeposition steps. The nCO presents a black needle‐like structure which effectively absorbs the incident radiation during interference lithography. Specular and diffused reflectivity measurements confirm nCO has near‐zero reflectivity from at least UV (350 nm) to near IR (700 nm) wavelengths. A particularly important aspect of the nCO is its ability to be reduced to copper metal, enabling electrodeposition inside porous templates fabricated on the nCO. It is demonstrated electrodeposition of copper within 3D templates defined by interference lithography and proximity field nano‐patterning processes, forming mesostructured metals which enhance two‐phase cooling. The resultant 5 µm thick structures exhibited up to 3 times the critical heat flux and 2 times heat transfer coefficient of bare silicon. The structures are optimized via computational tools including Finite Difference Time Domain (FDTD) and COMSOL Multiphysics. The use of the approach demonstrated here can potentially find application in many areas given the broad importance of mesostructured metals for energy, biomedical, and mechanical applications.

Metallo-organic complexes as precursors for nanostructured metal oxides and their studies on protein interactions and drug loading characteristics

In the current study, we have synthesized and characterized Schiff base copper and zinc complexes based on (E)-2,4-dichloro-6-(((2-hydroxy-4-methyl-phenyl)-imino) methyl) phenol ligand obtained from 3,5-dichloro salicylaldehyde and 2-amino,4-methyl phenol. The interactions of these complexes with the protein, Bovine Serum Albumin (BSA) were monitored through the fluorescence spectral technique. The quenching of fluorescence with the incremental addition of the ligand and the complexes provides important information regarding the binding propensity of the tested compounds with the protein. Furthermore, these metal complexes are used as precursors to obtain the pure phases of copper oxide and zinc oxide nanostructures by the thermal decomposition method. The phase formation of the metal oxides was confirmed by powder X-ray diffraction (p-XRD) technique. The metal oxides prepared from their respective metal complexes have unique characteristics in terms of particle size, morphology, and band gap and are compared with the literature reports based on conventional solid-state methods. The studies on the interaction of the prepared metal oxide and curcumin with and without BSA, the drug carrier, have been investigated and the drug loading capacity is assessed.

Fabrication of superhydrophobic (CuO-SiO2) nanocomposite coating for oil/water separation

ABSTRACT The presence of oil-contaminated water due to oil spill disasters or improper industrial waste dumping is now a worldwide danger to both human health and the sustainability of the environment.The use of superhydrophobic materials has attracted considerable attention in the field of oil-water separation, owing to the increasing demand for effective and economical oil-water separation techniques.A new, easy, and inexpensive flame treatment method was used to make a nanocomposite (CuO-SiO2) in order to improve its hierarchical structure (micro-nano).The anodisation process produced copper oxide (CuO) nanostructures (NSs) on a copper mesh. Subsequently, the nanostructures were modified by dip coating with a solution of room-temperature vulcanised silicone rubber (RTV-SR).The coated mesh demonstrated remarkable characteristics of superhydrophobicity and superoleophilicity, with a water contact angle (WCA) of (160 ± 1 ° ) and an oil contact angle (OCA) of (0 ° ), as determined during the measurement of the surface’s wetability. The coated mesh surface was characterised using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and energy dispersive spectroscopy (EDS).The successful separation of kerosene-water and diesel oil-water mixtures is accomplished by using a coated mesh in a simple filtration procedure. Furthermore, it has the capability to separate oils with a high efficiency of (99.8%) for kerosene and (87%) for diesel oil. It also has flux values of (7352.9 L.m -2 .h -1 ) for kerosene and (6112.9 L/m 2 .h) for diesel.

Study and Characterization of Copper and Titanium Oxides Nanostructures for Some Molecular and Biological Applications

In this work, Copper and Titanium nanocomposites (NPs) were prepared by mixture exchange process with ratios (25, 50 and 75 % CuO-TiO2). The biological activity was studied, and it was found that the concentrations of 50 and 100 µg/mL of 50 and 75 % CuO-TiO2 were the best concentrations, Low concentrations of the nanoparticle mixture at 25 µg/mL also stimulated the growth of symbiotic bacteria. The mixture of nanoparticles was easier to prepare and more effective in inhibiting bacterial growth. biochemical test and PCR were performed to confirm the identity of the studied bacteria. While isolating the bacteria, a new type of bacteria was detected and registered in the Global Gen Bank under accession No. OP942239. Surface and structure properties have been studied using FESEM, EDS analysis, XRD and FTIR respectively. It can be seen that the size and diameter of the nanocomposite increase with the weight ratio of CuO-TiO2. The aggregated CuO-TiO2 nanostructures with different ratios were transformed gradually into a uniform spherical shape. The average size of the CuO/TiO2 composite was found to be about 32.122, 29.865 and 27.607 nm at 25, 50 and 75 % CuO-TiO2 respectively. While the mean sizes of CuO and TiO2 were 25.35 and 34.38 nm respectively. The crystalline size decreases after the ion exchange process, which could be due to the diffraction peaks being broad in all the samples of Copper Titanate at the surface. Subsequently, adding Copper particles to the TiO2 film can improve the performance of the material. HIGHLIGHTSThe nanostructure CuO-TiO2 was created through various loading ratios. These NPs’ efficiency was calculated using a number of techniques, including FTIR, X-ray diffraction, EDS spectra, and FESEM. The observations indicate that molecular transition parameters play an essential role in determining the size, shape, and functionality of CuO- TiO2 NPs. The sharp peaks observed in the composites indicated higher crystallinity in CuO. In addition, two types of NPs have shown promising effects in inhibiting NPs aggregation and enhancing biological effects but the potential of these NPs against different bacteria may differ. Thus, further research and testing is needed to assess its efficacy and human health and environmental impact before considering its use. In conclusion, copper and titanium NPs have their distinct advantages in bacterial inhibition, and the choice between them should be based on specific conditions and environmentally friendly factors. GRAPHICAL ABSTRACT

Deposition time effect on copper oxide nano structures, an analysis study using chemical method

Deposition time effect on copper oxide nano structures, an analysis study using chemical method

Eco-Friendly Cost-Effective Formation of Copper Oxide Nanostructures and its Prodigious Potential for Environmental Remediation Applications

<p>The proliferation of environmental pollution, particularly from hazardous industrial dyes, poses a significant threat to ecosystems and aquatic life. This study uses extract from Nerium oleander leaves as a natural capping and reducing agent to produce copper oxide nanoparticles (CuO NPs), an ecologically acceptable way to tackle this problem. The CuO nanoparticles have improved physicochemical characteristics, as shown by their average crystalline size of 15.56 nm and decreased particle size of 31.84 nm. Additional studies such as SEM, EDX, TEM, and zeta potential were accomplished and revealed the spherical structure; an elevated negative zeta potential of -25.6 mV was observed on the surface property. The photodegradation efficacy of these bio-synthesized CuO NPs was assessed against various industrial dyes, including Rhodamine 6G, Malachite Green, Eosin Yellow, and Reactive Black. The results demonstrated exceptional degradation efficiencies, with rates of up to 97.48%, 99.54%, 89.73%, and 89.33% respectively. The decolorization of organic dyes presented a visual cue that the degradation process was progressing. Notably, using Nerium oleander leaves as reducing agents contributed to the nanoparticles' stability, making them suitable for repeated cycles of photocatalysis. This research underscores the potential of green synthesis methods and highlights the vital role of plant-based reducing agents in advancing environmentally friendly nanomaterials for wastewater treatment and environmental remediation. The findings offer a promising pathway toward sustainable and eco-friendly solutions to mitigate the environmental impact of hazardous industrial dyes, fostering responsible industrial practices and preserving aquatic ecosystems.</p>

Chirality Engineering of Colloidal Copper Oxide Nanostructures for Tailored Spin-Polarized Catalysis.

The combination of the chiral concept and inorganic nanostructures holds great potential for significantly impacting catalytic processes and products. However, the synthesis of inorganic nanomaterials with engineered chiroptical activity and identical structure and size presents a substantial challenge, impeding exploration of the relationship between chirality (optical activity) and catalytic efficiency. Here, we present a facile wet-chemical synthesis for achieving intrinsic and tunable chiroptical activity within colloidal copper oxide nanostructures. These nanostructures exhibit strong spin-polarization selectivity compared with their achiral counterparts. More importantly, the ability to engineer chiroptical activity within the same type of chiral nanostructures allows for the manipulation of spin-dependent catalysis, facilitating a study of the connection between the chiroptical magnitude (asymmetric factor) and catalytic performance in inorganic nanostructures. Specifically, using these materials as model catalysts in a proof-of-concept catalytic reaction, we reveal a linear correlation between the asymmetric factor of chiral nanomaterials and the efficiency of the catalytic reaction. This work paves the way for the development of chiral inorganic nanosystems and their application in catalysis through chiroptical engineering.

Cyclic voltammetry and specific capacitance studies of copper oxide nanostructures grown by hot water treatment

Cyclic voltammetry and specific capacitance studies of copper oxide nanostructures grown by hot water treatment