CuO Nanosheets Research Articles

Hierarchical CuO nanosheets encasing nanorods via a singular potential-cycling activation: Innovations in supercapacitor energy density and longevity

Copper oxides (CuO), by virtue of their exceptional electrical conductivity, benign environmental profile, and economic viability, have emerged as indispensable constituents in the design and development of binder-free electrodes for advanced supercapacitor systems. The ongoing quest for the synthesis of CuO nanomaterials through gentle yet economically feasible methodologies held considerable promise for broadening their applicability within the domain of energy storage devices. In this investigation, a novel architectural innovation was achieved through the integration of carbon nanotubes (CNTs) within the framework of an in-situ electrooxidation process, culminating in the formation of a distinctive CuO-CNT nanorod configuration. Subsequent to this fabrication, the electrode material was subjected to an extensive cyclic voltammetry (CV) activation for 2000 cycles, which precipitated a profound morphological evolution. This process resulted in the emergence of 2D hierarchical nanosheet arrays enveloping 1D nanorods, a configuration herein designated as CuO-CNT-2000. This meticulously engineered lamellar structure conferred upon the material an extraordinary specific surface area, quantified at 219.6 m2 g⁻1, and an impressive specific capacitance of 709.1 F g⁻1. Moreover, the asymmetric supercapacitor (ASC) assembled utilizing this advanced material exhibited a remarkable energy density, measured at 38.09 Wh kg⁻1. Notably, even after enduring 60,000 charge-discharge cycles, the device demonstrated a retention of 82.36 % of its initial energy density, coupled with a Coulombic efficiency of 99.43 %, thus attesting to its superior electrochemical stability and longevity. The efficacy of the CV activation technique in facilitating significant morphological refinement, augmenting the specific surface area, and enhancing the electrochemical performance of the material suggests a broad applicability of this method to a diverse array of other electrode materials, potentially revolutionizing the design and fabrication of next-generation energy storage systems.

Experimental and theoretical exploration of bactericidal and photo-catalytical activities of hierarchically porous AuNRs@CuO nanocomposite

In this study, a novel binary nanocomposite consisting of CuO nanosheets functionalized with gold nanorods (AuNRs@CuO), was successfully prepared using a two-step synthetic procedure and further investigated via Density Functional Theory. The physicochemical properties of prepared nanomaterials were analysed using Fourier transform infrared spectroscopy, X-ray diffraction, Field emission scanning electron microscopy, High-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy confirming successful fabrication with improved surface properties. Experimental analyses, including antibacterial assays and morphological studies of bacterial cells demonstrates superior bactericidal properties of AuNRs@CuO nanocomposite compared to pristine CuO nanosheets. Furthermore, molecular docking score provide theoretical insights into the underlying mechanism governing the enhanced antibacterial activity, highlighting the favorable interaction with the bacterial cells. The synergistic effect of CuO nanosheets and AuNRs further improves the photocatalytic efficacy, culminating in a high-yield photocatalyst that achieves 98.7% degradation for Indigo carmine under Xenon lamp irradiation compared to 40.8% and 62.4% for AuNRs and CuO nanosheets alone. Improved charge separation and generation of H+ as major reactive oxygen species from the nanocomposite to Indigo carmine was revealed by radical scavenger activity and photoluminescence studies. After cycles of operation, the morphology and surface state of the photocatalyst remained unchanged, as investigated by FESEM and HRTEM analysis. The novelty of this study lies in the integration of AuNRs and CuO nanosheets as an efficient photocatalytic material for the remediation of toxic organic dyes in wastewater, presenting a promising advancement in sustainable water treatment technologies.

A Click Chemistry Strategy Toward Spin-Polarized Transition-Metal Single Site Catalysts for Dynamic Probing of Sulfur Redox Electrocatalysis.

Catalytic conversion of lithium polysulfides (LiPSs) is a crucial approach to enhance the redox kinetics and suppress the shuttle effect in lithium-sulfur (Li-S) batteries. However, the roles of a typical heterogenous catalyst cannot be easily identified due to its structural complexity. Compared with the distinct sites of single atom catalysts (SACs), each active site of single site catalysts (SSCs) is identical and uniform in their spatial energy, binding mode, and coordination sphere, etc. Benefiting from the well-defined structure, iron phthalocyanine (FePc) is covalently clicked onto CuO nanosheet to prepare low spin-state Fe SSCs as the model catalyst for Li-S electrochemistry. The periodic polarizability evolution of Fe-N bonding is probed during sulfur redox reaction by in situ Raman spectra. Theoretical analysis shows the decreased d-band center gap of Fe (Δd) and delocalization of dxz/dyz after the axial click confinement. Consequently, Li-S batteries with Fe SSCs exhibit a capacity decay rate of 0.029% per cycle at 2 C. The universality of this methodological approach is demonstrated by a series of M SSCs (M = Mn, Co, and Ni) with similar variation of electronic configuration. This work provides guidance for the design of efficient electrocatalysis in Li-S batteries.

Biomimetic heat-localized and solar absorption-enhanced hollow structural nanofibrous membrane for clean water production from saline water and dye wastewater

The rational design of material structures can be an effective approach to enhance the performance of solar-driven clean water production. In this study, a hollow structural nanofibrous membrane was developed by mimicking the hollow structure of polar bear hair using coaxial electrospinning. The shell layer consisted of carbon nanoparticles (C NPs) decorated CuO nanosheets (C@CuO), that exhibited photothermal conversion capacity. Meanwhile, the core layer containing hydrophilic polyvinylpyrrolidone (PVP) was eliminated to generate the hollow structure. The C NPs enhanced the membrane’s light absorption to increase thermal energy harvesting, while the CuO nanosheets improved the membrane’s wettability enhancing the water supply. Furthermore, the hollow structure limited air convection, prevented heat conduction, and minimized heat radiation, enabling heat localization to be achieved inside the membrane to suppress heat loss during evaporation. For 3.5 wt% saline water and actual dye wastewater, the C@CuO nanofibrous membrane achieved high evaporation rates of 1.36 kg·m−2·h−1 and 1.31 kg·m−2·h−1, respectively, under 1 sun illumination. Moreover, even after continuous 6-h evaporation tests, the evaporation rate of the C@CuO membrane remained virtually unchanged, highlighting its long-term stability with regard to salt resistance in real-world applications. Additionally, the remarkable flexibility of the C@CuO membrane offers convenience during operation and guarantees dimensional stability when it is subjected to external stresses. These discoveries should inspire subsequent research on developing delicate architectural materials and exploring their potential applications in various fields, including energy generation, clean water production, and thermal insulation.

Photothermal Effect and Fenton‐Like Oxidation for Synergistic Removal of Fluoroquinolones Antibiotics under Near‐Neutral Conditions

AbstractDefect‐enriched mesoporous CuO nanosheets (NSs) were constructed to investigate the cooperative photo‐Fenton and photothermal‐Fenton catalysis on degradation of fluoroquinolones (FQ) antibiotics. The oxygen vacancies provide abundant active sites to bind the substrates and inhibit charge recombination, by all means to enhance Fenton‐like activity. Two disparate spectral selective functions of photoexcitation and photothermal conversion were achieved on CuO NS, which to promote the Fenton activity synergistically. Visible light induced photoexcitation to facilitate the generation of Cu+ and ⋅OH, while near‐infrared light converted into heat to promote charge separation and accelerate medium transport. Ultimately, as a unitary catalyst system, the CuO NS integrated the Lewis acid catalysis, Fenton‐like catalysis and photothermal catalysis that rapidly and sustainably degraded antibiotics under near‐neutral conditions.

CuO@N/C-ZnO nanoflowers with quantum dots derived from ZIF-8 for efficient CO2 photoreduction

In this pioneering work, an innovative photocatalyst, denoted as the porous erythrocytic-like nanoflower derived from zeolitic imidazolate framework (ZIF-8) (CuO@N/C-ZnONF), has been meticulously crafted. This design integrates a porous nanosheet of nitrogen and carbon co-doped ZnO, strategically refined with CuO nanosheets (CuONS) architecture originating from ZIF-8. This innovative nanomaterial serves as a nanoreactor for converting CO2 into CO and CH4. The distinctive porous nanoflower structure facilitates enhanced mobility of charge carriers throughout the accessible framework, maximizes exposure of active sites, and improves the flow of charge carriers while preventing their recombination. Additionally, the porous characteristics facilitate the diffusion of reactants and products. The synthesized 10CuO/N-C-ZnONF demonstrates superior photocatalytic performance, yielding high CO and CH4 outputs of 286.16 and 39.74 µmol g−1h−1, respectively, and exhibits excellent long-term stability.

CuO-ZIF-8 modified electrode surface as a new electrochemical sensing platform for detection of free chlorine in aqueous solution

This work has applied metal–organic frameworks (MOFs) with high adsorbability and catalytic activity to develop electrochemical sensors to determine free chlorine (free-Cl) concentrations in aqueous media. A zeolitic imidazolate frameworks, Zn(Hmim)2 (ZIF-8) has been synthesized and incorporated with CuO nanosheets to decorate a glassy carbon electrode (GCE) and provide a new sensor for free-Cl determination. The as-prepared ZIF-8 and CuO-ZIF-8 composites have been characterized by FESEM, EDX, XRD, and FT-IR analyses. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) utilized to characterize the CuO-ZIF-8/GC modified electrode electrochemically, demonstrated the ability of the sensor to measure free-Cl concentration. Using differential pulse voltammetry (DPV) and under the optimal conditions, the prepared CuO-ZIF-8/GC modified electrode showed a linear response in the 0.25–60 ppm range with a 12 ppb detection limit (LOD) for free-Cl concentration. Finally, the fabricated sensor was applied to analyze free-Cl from actual swimming pool water samples with promising 97.5 to 103.0% recoveries.

Enhanced synergistic antiviral effects of thermally expanded graphite and copper oxide nanosheets in the form of a novel nanocomposite against herpes simplex virus type 1

Herpes simplex virus type 1 (HSV-1) is responsible for a wide range of human infections, including skin and mucosal ulcers, encephalitis, and keratitis. The gold standard for treating HSV-1 infections is acyclovir. However, the use of this drug is associated with several limitations such as toxic reactions and the development of drug-resistant strains. So, there is an urgent need to discover and develop novel and effective agents against this virus. For the first time, this study aimed to investigate the antiviral effects of the Thermally Expanded Graphite (TEG)-copper oxide (CuO) nanocomposite against HSV-1 and compare results with its constituent components. After microwave (MW)-assisted synthesis of TEG and CuO nanosheets as well as MW-CuO/TEG nanocomposite and characterization of all these nanomaterials, an MTT assay was used to determine their cytotoxicity. The quantitative real-time PCR was then used to investigate the effects of these nanomaterials on viral load. Three-hour incubation of HSV-1 with TEG nanosheets (500 μg/mL), MW-CuO nanosheets (15 μg/mL), and MW-CuO/TEG nanocomposite (35 μg/mL) resulted in a decrease in viral load with an inhibition rate of 31.4 %, 49.2 %, and 74.4 %, respectively. The results from the post-treatment assay also showed that TEG nanosheets (600 μg/mL), MW-CuO nanosheets (15 μg/mL), and MW-CuO/TEG nanocomposite (10 μg/mL) led to a remarkable decrease in viral load with an inhibition rate of 56.9 %, 63 %, and 99.9 %, respectively. The combination of TEG and MW-CuO nanosheets together and the formation of a nanocomposite structure display strong synergy in their ability to inhibit HSV-1 infection. MW-CuO/TEG nanocomposites can be considered a suitable candidate for the treatment of HSV-1 infection.

Enhancement of Flow Boiling Heat Transfer Characteristics on Diamond/Cu Heterogeneous Surface

Surface treatment is an effective method of enhancing the heat transfer performance of flow boiling. Diamond/Cu, as a particle‐reinforced composite, exhibits heterogeneous surface properties and surface microstructures that play distinct roles in heat transfer. To elucidate the synergistic effect of heterogeneous material surfaces and microstructures, pure copper surface (PC), untreated diamond/Cu surface (DC), and surface‐treated diamond/Cu surface (SDC) are prepared for this experiment. These surfaces demonstrate various combinations of diamond, copper, and their corresponding surface microstructures. DC, characterized by heterogeneous wetting properties, demonstrates a heat transfer coefficient (HTC) that is 9%–24% higher than that of PC. The surface treatment of SDC results in the formation of a superhydrophilic CuO nanosheet structure, significantly enhancing both surface roughness and energy. SDC develops microcracks on the surface of diamond. The increased roughness provides numerous nucleation areas for the hydrophobic diamond, enhancing the overall wettability of the surface when combined with the superhydrophilic CuO region. SDC demonstrates the advantage of enhanced flow boiling on the surface of heterogeneous materials. At the identical heat flux, SDC exhibits a reduction of 5–10 °C in wall superheat and an increase of 38%–47% in HTC.

Nanostructured assessment of copper oxide for latent fingerprint recognition

Nanotechnology has revolutionized the different fields of forensic science, particularly in the efficient examination of evidence. In this study, we report scalable synthesis of copper oxide (CuO) nanosheets by using hydrothermal method and its exploration in the forensic examination of latent fingerprints. The identification and structural characterization of CuO nanoparticles were carried out using advanced spectroscopic methods such as powder X-ray diffraction (PXRD), Raman spectroscopy, and Fourier transform infrared spectroscopy (FTIR). The stabilization of CuO nanosheets in monoclinic symmetry (space group C2/c) was confirmed through Le Bail refinements. Morphological studies based on scanning electron microscopy (SEM) revealed that the CuO nanosheets exhibit, a rectangular, thin plate like morphology.The applicability of these nanosheets was tested for examining and developing fresh and aged (7 days old) latent fingerprints on dry, non-absorbent substrates using the powder dusting method. The formulation successfully developed sharp and clear fingerprints on various substrates, allowing the second-level details of the fingerprints to be viewed without any background interference. Additionally, these nanosheets are non-hazardous and cost-effective, making them a suitable fingerprint developing agent for a wide range of dry, non-absorbent surfaces recovered from crime scenes.

PH-Dependent Morphology of Copper (II) Oxide in Hydrothermal Process and Their Photoelectrochemical Application for Non-Enzymatic Glucose Biosensor

In this study, we investigated the influence of pH on the hydrothermal synthesis of copper (II) oxide CuO nanostructures with the aim of tuning their morphology. By varying the pH of the reaction medium, we successfully produced CuO nanostructures with three distinct morphologies including nanoparticles, nanorods, and nanosheets according to the pH levels of 4, 7, and 12, respectively. The observed variations in surface morphology are attributed to fluctuations in growth rates across different crystal facets, which are influenced by the presence of intermediate species within the reaction. This report also compared the structural and optical properties of the synthesized CuO nanostructures and explored their potential for photoelectrochemical glucose sensing. Notably, CuO nanoparticles and nanorods displayed exceptional performance with calculated limits of detection of 0.69 nM and 0.61 nM, respectively. Both of these morphologies exhibited a linear response to glucose within their corresponding concentration ranges (3–20 nM and 20–150 nM). As a result, CuO nanorods appear to be a more favorable photoelectrochemical sensing method because of the large surface area as well as the lowest solution resistance in electroimpedance analysis compared to CuO nanoparticles and nanosheets forms. These findings strongly suggest the promising application of hydrothermal-synthesized CuO nanostructures for ultrasensitive photoelectrochemical glucose biosensors.

A Two-Dimensional Cu-Based Nanosheet Producing Formic Acid Via Glycerol Electro-Oxidation in Alkaline Water.

The sluggishness of the complementary oxygen evolution reaction (OER) is reckoned as one of the major drawbacks in developing an energy-efficient green hydrogen-producing electrolyzer. An array of organic molecule oxidation reactions, operational at a relatively low potential, have been explored as a substitute for the OER. Glycerol oxidation reaction (GOR) has emerged as a leading alternative in this context because glycerol, a waste of biodiesel manufacturing, has become ubiquitous and accessible due to the significant growth in the biodiesel sector in recent decades. Additionally, the GOR generates several value-added organic compounds following oxidation that enhance the cost viability of the overall electrolysis reaction. In this study, a low-cost, room temperature operable, and energy-efficient synthetic methodology has been developed to generate unique two-dimensional CuO nanosheets (CuO NS). This CuO NS material was embedded on a carbon paper electrode, which showcased excellent glycerol electro-oxidation performance operational at a moderately low applied potential. Formic acid is the major product of this CuO NS-driven GOR (Faradaic efficiency ~80 %), as it is formed primarily via the glyceraldehyde oxidation pathway. This CuO NS material was also active for oxidizing other abundant alcohols like ethylene glycol and diethylene glycol, albeit at a relatively poor efficiency. Therefore, this robust CuO NS material has displayed the potential to be used in large-scale electrolyzers functioning with HER/GOR reactions.

Three-Dimensional Porous Cu/Cu2+1O Nanosheet Arrays Promote Electrochemical Nitrate-to-Ammonia Conversion.

The efficiency of electrochemical nitrate (NO3-) reduction to ammonia (NH3) still remains a challenge due to the sluggish kinetics of the complex eight-electron reduction process and competitive hydrogen evolution reaction (HER). Herein, we designed new three-dimensional (3D) porous Cu/Cu2+1O nanosheet arrays (Cu/Cu2+1O NSA) by coupling a template-directed method with in situ electroreduction. Thanks to the 3D porous structure and in-plane heterojunctions, Cu/Cu2+1O NSA can provide abundant active sites and a good interfacial effect, obtaining the maximum Faradaic efficiency (FE) of ammonia (88.09%) and high yield rate of 0.2634 mmol h-1 cm-2, which is higher than that of CuO nanosheets (77.81% and 0.2188 mmol h-1 cm-2) and CuO nanoparticles (34.60% and 0.0692 mmol h-1 cm-2). Experimental results and DFT simulations show that the interface effect of Cu/Cu2+1O can decrease the reaction energy barrier of the key step (*NO to *NOH) and can greatly inhibit the competitive hydrogen evolution reaction, thereby achieving excellent electrocatalytic performance for nitrate-to-ammonia conversion.

Bimetallic-doped three-dimensional carbon skeleton porous material as efficient catalysts for oxygen reduction reaction

The slowness of the oxygen reduction reaction (ORR) kinetics of the fuel cell cathode has terrifically inhibited its development process. Now it is of considerable importance to research low-cost, multi-defect, high-performance non-noble metal ORR catalysts. Specifically, CuO nanosheets are grown in situ on ZIF-8 to form a composite material (zif-8@CuO), and then undergo a high-temperature carbonization process. Finally, the Zn-Cu codoped composite material Zn-xCu-N/C with a porous structure supported by a three-dimensional carbon skeleton can be obtained. The material has a 3D carbon skeleton support and a rich pore structure, which can expose more active sites. The combination of bimetallic Zn and Cu with carbon materials also increases the overall stability and conductivity of the material, which is beneficial to improvement of catalytic performance. The electrochemical performance test results show that the onset potential and half-wave potential of the Zn-0.1Cu-N/C material are 0.889 V and 0.803 V respectively, with a low Tafel slope of 62 mV dec−1 and excellent long-term stability. After 10000 cycles, the ORR curve only changed 18 mV, while the carbon skeleton can still maintain unchanged.

Oxygen Vacancy-Laden Confinement Impact on Degradation of Metal Complexes.

Oxygen vacancies (Vo) have been recognized as the superior active site for PS-mediated environmental remediation; however, the formation and activation of Vo associated with the effects of chemical and spatial environments remain ambiguous. Herein, attributing to the low defect-formation energy of Vo in the presence of sulfonate groups, an in situ nucleating Vo-laden CuO nanosheet was deliberately fabricated inside the phase of a sulfonated mesoporous polystyrene substrate (Vo-CuO@SPM). The as-prepared nanocomposite demonstrated an excellent treatment efficiency toward metal complexes [Cu-EDTA as a case] with ignorable Cu(II) leaching, and it can be repeatedly employed for 25 recycles (not limited). Mechanistically, the electron transfer and the mass transport for PDS nonradical activation were proved to be substantially enhanced by the delocalized electrons and with the assistance of the microchannel environment. This work not only establishes insight into the formation of oxygen vacancies but also reveals the PS activation mechanism in the spatially confined sites.

NIR‐Responsive injectable hydrogel cross-linked by homobifunctional PEG for photo-hyperthermia of melanoma, antibacterial wound healing, and preventing post-operative adhesion

Current therapeutic approaches for skin cancer face significant challenges, including wound infection, delayed skin regeneration, and tumor recurrence. To overcome these challenges, an injectable adhesive near-infrared (NIR)-responsive hydrogel with time-dependent enhancement in viscosity is developed for combined melanoma therapy and antibacterial wound healing acceleration. The multifunctional hydrogel is prepared through the chemical crosslinking between poly(methyl vinyl ether-alt-maleic acid) and gelatin, followed by the incorporation of CuO nanosheets and allantoin. The synergistic inherent antibacterial potential of CuO nanosheets, the regenerative and smoothing effect of allantoin, the extracellular matrix-mimicking effect of gelatin, and the desirable swelling behavior of the hydrogel results in fast wound recovery after photothermal ablation of the tumor. Additionally, the hydrogel can serve as an alternative to sutures owing to its tissue adhesiveness ability, which can further render it the merits for accelerated repair of abdominal lesions while acting as a biocompatible barrier to prevent peritoneal adhesion.

Virtual substrate method: synthesis and growth kinetics of 2D metal oxide nanosheets

We present the experimental decomposition kinetics for the synthesis of metal oxide 2D nanosheets by the virtual substrate method. In this method, acetates of Mg and Cu were used as precursors for the growth of prototype MgO and CuO nanosheets, while the filter paper was utilized as a virtual substrate. The synthesized samples were characterized by X-ray diffraction for the phase analysis of the nanostructures, which confirms the cubic phase of MgO and monoclinic phase of CuO; with a minor Cu2O phase. Field emission scanning electron microscopy was used to determine the surface morphology of the nanosheets. Fourier transform infrared spectroscopy was utilized to identify the vibrational modes of the metal oxides and the functional groups present in the sample. Thermogravimetric analysis revealed the evolution of combustive oxidation of filter paper with the thermal decomposition of acetates situated on its surface.

Kinetics of 4‑nitrophenol reduction with NaBH<sub>4</sub> over Ag/CuO nanomaterial catalyst

In this paper, Ag/CuO nanomaterials were prepared via hydrothermal method combined with chemical reduction and used as catalysts in the reduction of 4-nitrophenol. Kinetic study of 4-nitrophenol (4-NP) reduction into 4-aminophenol (4-AP) by sodium borohydride revealed a first order reaction. The reaction rate constant k increased with amount of silver crystals introduced into CuO nanosheets, with Ag/CuO catalyst concentrations and with temperature. The thermodynamic activation parameters such as activation energy (Ea), enthalpy of activation (∆H#), entropy (∆S#) and Gibbs energy (∆G#) of activation were determined. The value of Ea, ∆H#, ∆S# and ∆G# were 72,33 kJ/mol, –69,86 kJ/mol, –24,28 J/K.mol and –62,50 kJ/mol (303K), respectivement. Ethanol and isopropanol were able to inhibit the 4-NP reduction with NaBH4 in the presence of Ag/CuO catalyst.

Steering the Reconstruction of Oxide-Derived Cu by Secondary Metal for Electrosynthesis of n-Propanol from CO.

As fuel and an important chemical feedstock, n-propanol is highly desired in electrochemical CO2/CO reduction on Cu catalysts. However, the precise regulation of the Cu localized structure is still challenging and poorly understood, thus hindering the selective n-propanol electrosynthesis. Herein, by decorating Au nanoparticles (NPs) on CuO nanosheets (NSs), we present a counterintuitive transformation of CuO into undercoordinated Cu sites locally around Au NPs during CO reduction. In situ spectroscopic techniques reveal the Au-steered formation of abundant undercoordinated Cu sites during the removal of oxygen on CuO. First-principles accuracy molecular dynamic simulation demonstrates that the localized Cu atoms around Au tend to rearrange into disordered layer rather than a Cu (111) close-packed plane observed on bare CuO NSs. These Au-steered undercoordinated Cu sites facilitate CO binding, enabling selective electroreduction of CO into n-propanol with a high Faradaic efficiency of 48% in a flow cell. This work provides new insight into the regulation of the oxide-derived catalysts reconstruction with a secondary metal component.

Room temperature ammonia sensor with high selectivity based on the composite materials assembled by CuO nanosheets and WS2 nanoflakes

In this work, CuO nanosheets are synthesized by one-step hydrothermal method and CuO/WS2 heterostructures are fabricated by introducing CuO doping into WS2, the preparation method was employed to enhance the performance of the gas sensor. The CuO/WS2 heterostructure nanocomposite sensor, doped with 5 % CuO, exhibited a pronounced enhancement in its response to 30 ppm of ammonia gas at ambient temperature, increasing the response value from 3.8 observed in pure WS2-based sensors to 4.7. Specifically, the response time of the CuO/WS2 heterostructure-based gas sensor decreased to 180 s, whereas the WS2-based sensor required 350 s for NH3 detection at room temperature. Furthermore, the CuO/WS2 sensor demonstrated outstanding selectivity for ammonia, maintaining stability over a 90-day test with a response fluctuation of less than 5 %. The heterojunction formed by CuO and WS2 showed superior sensitivity to NH3 compared to pristine WS2, owing to a notable enhancement in the surface catalytic effect. It also displayed sensitivity to humidity, with a response value of 6.25 at a 71 % relative humidity. At last, the gas sensing and enhanced gas sensing performance mechanisms of the composites for NH3 were elucidated. This remarkable multi-functional performance offers valuable insights for the advancement of room temperature gas sensors with diverse sensing functionalities.