ZnO Nanocrystals Research Articles

Convenient and Accurate Detection of Dopamine and Glucose by Modifying Carbon Fiber Electrodes

Fast, sensitive, and low-cost high-performance detectors have gradually become an indispensable tool for people to keep healthy, and sensors are the key devices of detection equipment. In this work, a ZnO nanocrystal modified carbon fiber electrode was prepared using a hydrothermal method, and on this basis, a galvanostatic point deposition method was used to load copper nanoparticles to prepare a sensor electrode. Scanning electron microscopy and X-ray diffraction were used to comprehensively analyze composition, morphology, and environmental adaptability of the prepared electrodes. The DPV test was used to verify the enhanced effect of ZnO nanorods on neurotransmitter detection. The ZnO/CF showed an obvious electrical signal (0.22 V, 4 × 10−5A) in the detection of dopamine (DA) solution, and the Cu-NPs/ZnO/CF also showed excellent detection results in the glucose detection experiment., providing two excellent examples for the development of low-cost electrochemical sensors. The electrodes can specifically detect DA in the presence of ascorbic acid and uric acid, and the detection limit of the electrode for detecting DA is about 0.4 μM. In addition, the Cu-NPs/ZnO/CF electrode successfully realized the enzyme-free detection of glucose, and the detection limit could reach 0.5 μM.

Shelf-Stable Green and Blue Quantum Dot Light-Emitting Diodes with High Efficiencies.

Quantum dot light-emitting diodes (QLEDs) are promising electroluminescent devices for next-generation display and solid-state lighting technologies. Achieving shelf-stable and high-performance QLEDs is crucial for their practical applications. However, the successful demonstration of shelf-stable QLEDs with high efficiencies is limited to red devices. Here, we developed a solution-based amine ligand exchange strategy to passivate the surfaces of optical ZnO (O-ZnO) nanocrystals, leading to suppressed exciton quenching at the green and blue QD/oxide interface. Furthermore, we designed new bilayered oxide electron-transporting layers consisting of amine-modified O-ZnO/conductive ZnO. This design simultaneously offers suppressed interfacial exciton quenching and sufficient electron transport in the green and blue QLEDs, resulting in shelf-stable green and blue devices with high efficiencies. Our devices exhibit neglectable changes in external quantum efficiencies (maximum external quantum efficiencies of 22.4% for green and 14.3% for blue) after storage for 270 days. Our work represents a step forward in the practical applications of QLED technology.

Effect of Solvent Composition on Non-DLVO Forces and Oriented Attachment of Zinc Oxide Nanoparticles.

Oriented attachment (OA) occurs when nanoparticles in solution align their crystallographic axes prior to colliding and subsequently fuse into single crystals. Traditional colloidal theories such as DLVO provide a framework for evaluating OA but fail to capture key particle interactions due to the atomistic details of both the crystal structure and the interfacial solution structure. Using zinc oxide as a model system, we investigated the effect of the solvent on short-ranged and long-ranged particle interactions and the resulting OA mechanism. In situ TEM imaging showed that ZnO nanocrystals in toluene undergo long-range attraction comparable to 1kT at separations of 10 nm and 3kT near particle contact. These observations were rationalized by considering non-DLVO interactions, namely, dipole-dipole forces and torques between the polar ZnO nanocrystals. Langevin dynamics simulations showed stronger interactions in toluene compared to methanol solvents, consistent with the experimental results. Concurrently, we performed atomic force microscopy measurements using ZnO-coated probes for the short-ranged interaction. Our data are relevant to another type of non-DLVO interaction, namely, the repulsive solvation force. Specifically, the solvation force was stronger in water compared to ethanol and methanol, due to the stronger hydrogen bonding and denser packing of water molecules at the interface. Our results highlight the importance of non-DLVO forces in a general framework for understanding and predicting particle aggregation and attachment.

Polymer-Chain Aggregation-induced Electrical Gating at the H- and J-aggregate P3HT

This research explores how aggregation influences the electrical behavior at both the planar - heterojunction poly(3-hexylthiophene) (P3HT)/SiO2 and P3HT/ZnO nanocrystal (NC) interfaces. The formation of H- and J-type aggregates leads to distinct molecular ordering and packing structures, manifesting as changes in threshold voltage shifts (electrical gating) as well as absorption and luminescence properties. Ultrasound irradiation (sonication) significantly alters the molecular arrangement in P3HT, favoring the formation of H-aggregates over the typically formed J-aggregates. In pristine P3HT, J-aggregates facilitate efficient exciton movement and electrical generation, resulting in higher photocurrents compared to sonicated-P3HT, which predominantly forms H-aggregates. Field-effect transistors (FETs) based on sonicated P3HT exhibit a more positive threshold voltage and increased mobility, indicating the presence of more mobile charge carriers, even in the absence of an applied voltage. In interfaces with ZnO NC, pristine P3HT demonstrates a considerable shift in threshold voltage under illumination, attributed to electron trapping. Conversely, sonicated P3HT interfaced with ZnO NC shows less electron trapping and minimal change in threshold voltage. This study underscores how the type of aggregate (H or J) in P3HT significantly dictates light-induced electrical gating. Ultrasound irradiation (sonication), while enhancing mobility by improving crystallinity, leads to a decrease in photocurrent efficiency in H-aggregates compared to the J-aggregates present in pristine-P3HT.

Optical behavior, TL defect center analysis and photocatalytic characterization of Ag2O doped ZnO nano crystals

The objective of the study is to prepare Ag+-dopedZnO nano crystals and to assess their structure, optical behavior, TL analysis, photocatalytic activity. Using sol–gel technique the Ag+-doped ZnO nano crystals prepared. Using the FT-IR, XRD, BET surface area, SEM, EDX characterization techniques, we have examined the structure of the developed samples. The TL analysis of samples was done under a dose of 25 kGy gamma irradiation. Trap depth parameters of the samples evaluated. Which suggested the ZnO nano crystals doped with Ag+ ions are purely TL active. The optical studies such optical absorption, photoluminescence of samples reveal their optical behavior. The optical band gap of the samples also evaluated. Which is increasing with increase in concentration of Ag+ ions in ZnO nano crystals. Using the MV (10 ppm) and CR (10 ppm) dyes, under visible light the photocatalytic activity of the samples reported. At a reaction period of 90 min, the nano powdercontaining 1.0 mol% Ag+-dopedZnO nano crystals and a band gap energy of 2.75 eV demonstrated the best photocatalyticefficiency (∼91 %) in both colors. The evaluationwas done on the impact of radical scavenger research and catalyst dosage on degrading efficiency. The rate of reaction in the presence of 1.0 mol% Ag+-dopedZnO nano crystals was four times higher than the ZnO catalyst's rate constants, and the degradation reaction follows pseudo-first-orderkinetics. The degrading process shows pseudo-first-order kinetics, and the reaction rate was four times higher than the ZnO catalyst in the presence of 1.0 mol% Ag+-dopedZnO nano crystals. It took three cycle runs for the degrading efficiency to drop by 1 %. Thus, 1.0 mol% Ag+-dopedZnO nano crystals was employed as a promising photocatalyst with strong reusability potential for the degradation of textile colors, which will be very beneficial.

Tuning Biocompatibility and Bactericidal Efficacy as a Function of Doping of Gold in ZnO Nanocrystals.

Doping nanoparticles represents a strategy for modulating the energy levels and surface states of nanocrystals (NCs), thereby enhancing their efficiency and mitigating toxicity. Thus, we herein focus on the successful synthesis of pure and gold (Au)-doped zinc oxide (ZnO) nanocrystals (NCs), investigating their physical-chemical properties and evaluating their applicability and toxicity through in vitro and in vivo assessments. The optical, structural, and photocatalytic characteristics of these NCs were scrutinized by using optical absorption (OA), X-ray diffraction (XRD), and methylene blue degradation, respectively. The formation and doping of the NCs were corroborated by the XRD and OA results. While the introduction of Au as a dopant did induce changes in the phase and size of ZnO, a high concentration of Au ions in ZnO led to a reduction in their photocatalytic activity. This demonstrated a restricted antibacterial efficacy against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. Remarkably, Au-doped counterparts exhibited enhanced biocompatibility in comparison to ZnO, as evidenced in both in vitro (murine macrophage cells) and in vivo (Drosophila melanogaster) studies. Furthermore, confocal microscopy images showed a high luminescence of Au-doped ZnO NCs in vivo. Thus, this study underscores the potential of Au doping of ZnO NCs as a promising technique to enhance material properties and increase biocompatibility.

Structural, optical and magnetic properties of Zn0.98Co0.02O dilute magnetic semiconductor nanoparticles

Doped ZnO nanoparticles (NPs) are one of the most promising dilute magnetic semiconductors (DMSs). Zn0.98Co0.02O NPs were synthesized using an aqueous co-precipitation technique. XRD confirmed phase purity and the crystallite size was determined to be 20 nm using the Debye-Scherrer method. For the doped NPs, distinct surface morphology was seen in FE-SEM images. The excitonic absorption peak appeared at 371 nm in pristine ZnO NPs which blue-shifted to 363 nm on 2 % Co-doping. The doped ZnO nanocrystals exhibit considerable ferromagnetic functionality at 7 K and 300 K. The asymmetry in the hysteresis curves confirm the presence of exchange bias and spin canting in the system. The results obtained suggests that the doped NPs could be potentially useful for enhanced optoelectronics and spintronics applications.

Structure and morphology modification of ZnO nanocrystals via substitutional cobalt doping for enhanced electrochemical activity

This study investigated the electrochemical performance of the morphologically and structurally modified Co-doped ZnO nanocrystals synthesized via the chemical co-precipitation method. The structural properties were characterized by XRD, where the lattice parameters and volume got smaller with the increasing amount of Cobalt doping. The compositional analyses showed that 1.5 and 2.5 at% of Cobalt was present in the Co-doped ZnO nanocrystals. The FT-IR analyses showed that Zn–O (tetrahedral) and Zn–O (octahedral) vibrational modes are present for the precipitated ZnO-based nanocrystals. Besides that, the characteristic Raman spectra mode for ZnO displayed redshift, and more modes were activated, which showed a change in the defect chemistry after the cobalt substitution into the ZnO host lattice. A significant change was observed in morphology where the pristine ZnO formed nanoflower composed of nanoflakes and the Co-doped ZnO nanoparticles formed nanospheres. Lastly, cyclic voltammetry was performed at different scan rates where typical Faradaic peaks were observed for all the samples, and the electrochemical performance was increased with the small amount of Co doping into the ZnO lattice. The samples showed improved pseudocapacitive behavior, suggesting that Cobalt doped ZnO nanoparticles synthesized via the chemical co-precipitation method can be a potential electrode material for pseudocapacitor applications.

Highly Efficient and Reproducible Sonochemical Synthesis of ZnO Nanocrystals.

Sonochemical synthesis can be a facile, fast, efficient, versatile and economical way to prepare a large variety of conventional or novel nanostructured materials (metallic, magnetic, semiconducting, polymeric, etc.). In this work, zinc oxide nanocrystals were synthesized by irradiating and heating at 90 °C in a commercial ultrasonic bath a water solution of zinc nitrate hexahydrate and ammonia solution or hexamethylenetetramine as base catalysts. The evolution of the powder morphology and its crystalline structure were investigated at different times of ultrasonic irradiation (0-9 hours) and compared with those of samples obtained by only heating the solutions in a muffle furnace in order to enlighten the growth mechanism. It resulted that: i) the crystal morphology depends on the selected base, ii) for samples obtained by using ultrasounds, the homogeneity of the powders depends on the irradiation time, iii) by comparing all samples obtained at 7 hours of heating, the aspect ratio of the crystals is higher for those that also underwent to ultrasounds.

Synthesis, Structural Characterization and Temperature Effects on Chloroform Vapor Sensing Properties of ZnO Nanocrystals

In this study, nanocrystalline ZnO were synthesized onto glass substrates by using sol-gel method. Structural characterizations were performed by XRD, SEM and AFM techniques. Potential application of nanocrystal ZnO as chloroform sensor was investigated. Response of the fabricated thin films of the ZnO nanocrystals towards chloroform vapor was investigated depending on gas concentration (750-15000 ppm) between the temperatures of 22‒150 ºC in nitrogen ambient. Gas flow rates were controlled by using flow controller and flow meters. All the measurement system was computerized. XRD results revealed that thin film of the ZnO nanocrystals on the glass substrate was in crystal form and can be characterized by 036-1451 JCPDS number. Crystallite sizes of the ZnO nanocrystals were determined both by SEM images and the Scherrer equation. The crystallite sizes were calculated between 27.9 – 50.4 nm using the Scherrer equation. The sensors showed reversible response towards the chloroform vapor in the measured temperature and gas concentration range. Response time and sensitivity values of the sensors towards the chloroform vapor were also calculated. The increase in temperature caused to increase in sensitivity values. The best sensitivity values were obtained at 150 ºC.

Therapeutic Potential of Sol-Gel ZnO Nanocrystals: Anticancer, Antioxidant, and Antimicrobial Tri-Action.

Zinc oxide nanocrystals (ZnO NCs) hold great promise in nanomedicine with fascinating multifunctional properties. We investigated the therapeutic potential of sol-gel synthesized ZnO NCs with crystal sizes of 52.65 and 25.11 nm, focusing on their anticancer effects on HepG2 and HT29 cells, antioxidant properties, and antimicrobial activity. Both samples displayed a hexagonal wurtzite ZnO structure, wherein the crystal sizes diminished with lower calcination temperatures according to X-ray diffraction. The scanning electron microscopy analysis revealed that lowering the calcination temperature resulted in a decrease in the grain size of the ZnO NCs, as expected. This reduction in grain size combined with a decrease in crystal size resulted in a significant 40% reduction in the reflectance of the ZnO NCs in UV-vis-NIR spectroscopy. It was also observed that the ZnO NCs calcined at higher temperatures exhibited larger particle sizes with a reduced surface area mean of 69.30 μm and a stable negative zeta potential of -11.2 mV. In contrast, the ZnO NCs calcined at lower temperatures exhibited a larger surface area mean of 34.56 μm and a positive zeta potential of +10 mV. In both cell lines, the cytotoxic potential was found to be higher in HepG2 cells. Specifically, when ZnO nanocrystals (NCs) with a crystal size of 52.65 nm were used, the lowest cell viability was observed at a concentration of 5.74 μg/mL. Based on oxidative stress index values, a lower crystal size of ZnO NCs displayed greater effectiveness in HT29 cells, while a higher crystal size of ZnO NCs had pronounced effects in HepG2 cells. Moreover, both ZnO NCs exhibited significant antimicrobial activity against Gram-positive bacteria (Enterococcus faecalis and Staphylococcus aureus) and Candida parapsilopsis fungus. These findings emphasize sol-gel ZnO NCs' potential as versatile agents in nanomedicine, spurring research on targeted cancer therapies and antimicrobial innovations.

On the Fate of Lithium Ions in Sol-Gel Derived Zinc Oxide Nanocrystals.

Among diverse chemical synthetic approaches to zinc oxide nanocrystals (ZnO NCs), ubiquitous inorganic sol-gel methodology proved crucial for advancements in ZnO-based nanoscience. Strikingly, unlike the exquisite level of control over morphology and size dispersity achieved in ZnO NC syntheses, the purity of the crystalline phase, as well as the understanding of the surface structure and the character of the inorganic-organic interface, have been limited to vague descriptors until very recently. Herein, ZnO NCs applying the standard sol-gel synthetic protocol are synthesized with zinc acetate and lithium hydroxide and tracked the integration of lithium (Li) cations into the interior and exterior of nanoparticles by combining various techniques, including advanced solid-state NMR methods. In contrast to common views, it is demonstrated that Li+ ions remain kinetically trapped in the inorganic core, enter into a shallow subsurface layer, and generate "swelling" of the surface and interface regions. Thus, this work enabled both the determination of the NCs' structural imperfections and an in-depth understanding of the unappreciated role of the Li+ ions in impacting the doping and the passivation of sol-gel-derived ZnO nanomaterials.

Ethanolamine gas sensors based on NdFeO3 modified hexagonal pyramid shaped ZnO nanocrystals

It is well known that two metal oxides can form depletion layers at the interface by constructing heterojunctions due to the different Fermi energy levels of each metal oxide, which can improve the carrier mobility and provide significant advantages for gas sensing. In this work, NdFeO3 nanoparticles were grown on ZnO with hexagonal cone structure by secondary hydrothermal method to successfully construct n-ZnO/p-NdFeO3 heterojunctions, and the crystal structures, oxygen vacancies, microstructures, optical properties, and gas-sensing properties of the ZnO/NdFeO3 composites were investigated. The ZnO/NdFeO3 sensors showed good ethanolamine (EA) The response characteristics of the ZnO/NdFeO3 sensor to ethanolamine (EA) with a concentration of 100 ppm EA at 240 °C (Rg/Ra) is about 25, which improves the response by a factor of 1.6 and 1.32 compared with that of NdFeO3 and ZnO. Meanwhile, it has excellent selectivity, good cyclic reproducibility, and durable long-term stability with response/recovery times of 19 s/49 s. The improved EA sensing performance of NdFeO3-modified ZnO, in addition to its large specific surface area due to its unique rough inhomogeneous structure, is also related to the higher concentration of oxygen vacancies at the ZnO/NdFeO3 interface after the composite. In addition, the construction of ZnO/NdFeO3 heterostructure brings more efficient carrier migration, which is favorable to the surface reaction and diffusion of EA molecules, and lowers the ZnO operating temperature, thus reducing the energy consumption. The ZnO/NdFeO3 composite sensor based on n-p heterojunction provides a valuable strategy for the detection of volatile organic compounds.

Improving the electrochemical performance of LiNi0.5Mn1.5O4 by ZnO nanocrystals coating

The cathodic material LiNi0.5Mn1.5O4 was produced by the Solution Combustion Synthesis method (SCS). The as-made crystalline nanoparticles were annealed at 900 °C, obtaining micron-sized particles, and then coated with ZnO nanocrystals at a weight relation between 0.5 and 2.5 wt%, also using the SCS method. The nanocrystalline porous coating was confirmed by XRD, SEM and TEM. Electrochemical measurements verified that all materials coated with ZnO nanoparticles improved their electrochemical properties concerning the uncoated material, preventing degradation over the cycles, and stability along cyclic voltammetry cycles. It was observed that a 1 wt% ZnO coating presents the best improvement in discharge capacity and rate capability, and that the charge transfer resistance of the coated material is reduced to 1/3 of the uncoated one after 100 electrochemical cycles. In this work, the simple, time and energy saving SCS method was verified to obtain nanoshell-coated LNMO microparticles with improved electrochemical performance.

Role of Bismuth Doping on Structural and Electrical Properties of ZnO Nanocrystals Prepared by Sol–Gel Method

Role of Bismuth Doping on Structural and Electrical Properties of ZnO Nanocrystals Prepared by Sol–Gel Method

Enhanced photocatalytic activity of copper-doped ZnO nanocrystals synthesized by a hydrothermal route

Zn(1-x)CuxO (x = 0, 1, 3, 5%) nanocrystals were synthesized via a hydrothermal method at 150°C for 24 h. The structural, morphological, optical and photocatalytic properties of the samples were investigated, and found to be dependent on the content of the copper dopant. The UV photocatalytic activities of Zn(1-x)CuxO nanocrystals were evaluated by the photodecomposition of the methyl orange (MO) dye. The nanocrystals with a Cu content of 5% exhibited the highest UV photocatalytic activity with a photodegradation efficiency of 94% during 120 min as compared to that of pure ZnO with 73%. The enhancement of the photocatalytic activity of Zn0.95Cu0.05O originates from the better separation of the photogenerated electron-hole pairs.

Synthesis, characterization of Gd-doped ZnO nanocrystals and their photocatalytic activity in the degradation of C.I. Acid Red 18

In this study, ZnO and Gd doped ZnO with various weight percentages (1, 2, 3, and 4 wt% Gd calcined at 450 °C and 2 wt% Gd doped ZnO calcined at 450, 550, 650, and 750 °C) have been prepared. XRD, TEM, DRS, PL measurements, EDX, and FTIR were used for the characterization of the as-prepared photocatalysts. The photocatalytic activity of the as-synthesized ZnO and Gd-doped ZnO products was assessed by AR18 as a model of textile contaminants degraded in water under UV radiation. The effect of operating parameters such as pH, contact time, the initial dye concentration, and the influence of different contents of gadolinium doping and analysis were estimated. We use some active species such as ethanol, K2Cr2O7, KI, and Oxalate to find the photocatalyst and the formation of the electron-hole mechanism of Gd-doped ZnO. After 40 min, the catalyst calcined at 450°C (at pH = 5.0, [AR18] = 1.0 × 10−5M)showed the highest efficiency (98.28 %). The amount of COD decrease after 40 min of irradiation is 98.6 %.

Toxicity Assessment of New Ag-ZnO/AgO Nanocomposites: An In Vitro and In Vivo Approach.

Zinc oxide nanoparticles (ZnO NPs) are metal oxide nanomaterials, which are important for several applications: antibacterial, anthelmintic, antiprotozoal and antitumoral, among others. These applications are mainly related to the ability to spontaneously produce and induce the production of reactive oxygen species that are important components for the destruction of pathogens and tumor cells. While trying to potentiate ZnO NPs, studies have associated these NPs with silver oxide (AgO) or silver (Ag) NPs. It has already been reported that this combination (Ag-ZnO/AgO NPs) is able to enhance the microbicidal potential. Although possessing much potential for several purposes, it is important to evaluate whether this association also poses the risk of toxicity to cells and experimental models. Therefore, this work aimed to evaluate the toxicity of various Ag-ZnO/AgO NP nanocomposites, in vitro and in vivo. Accordingly, ZnO nanocrystals and nanocomposites with various concentrations of AgO (ZnO:5Ag, ZnO:9Ag or ZnO:11Ag) were used in different cytotoxicity models: Galleria mellonella (G. mellonella), cell lines (VERO and RAW 264.7) and C57BL/6 mice. In the G. mellonella model, four concentrations were used in a single dose, with subsequent evaluation of mortality. In the case of cells, serial concentrations starting at 125 µg/mL were used, with subsequent cytotoxicity assessment. Based on the safe doses obtained in G. mellonella and cell models, the best doses were used in mice, with subsequent evaluations of weight, biochemistry as also renal and liver histopathology. It was observed that the toxicity, although low, of the nanocomposites was dependent upon the concentration of AgO used in association with ZnO NPs, both in vitro and in vivo.

Anti-CD38 targeted nanotrojan horses stimulated by acoustic waves as therapeutic nanotools selectively against Burkitt’s lymphoma cells

The horizon of nanomedicine research is moving toward the design of therapeutic tools able to be completely safe per se, and simultaneously be capable of becoming toxic when externally activated by stimuli of different nature. Among all the stimuli, ultrasounds come to the fore as an innovative approach to produce cytotoxicity on demand in presence of NPs, without invasiveness, with high biosafety and low cost. In this context, zinc oxide nanoparticles (NPs) are among the most promising metal oxide materials for theranostic application due to their optical and semi-conductor properties, high surface reactivity, and their response to ultrasound irradiation. Here, ZnO nanocrystals constitute the stimuli-responsive core with a customized biomimicking lipidic shielding, resembling the composition of natural extracellular vesicles. This core–shell hybrid structure provides high bio- and hemocompatibility towards healthy cells and is here proofed for the treatment of Burkitt’s Lymphoma. This is a very common haematological tumor, typically found in children, for which consolidated therapies are so far the combination of chemo-therapy drugs and targeted immunotherapy. In this work, the proposed safe-by-design antiCD38-targeted hybrid nanosystem exhibits an efficient selectivity toward cancerous cells, and an on-demand activation, leading to a significant killing efficacy due to the synergistic interaction between US and targeted hybrid NPs. Interestingly, this innovative treatment does not significantly affect healthy B lymphocytes nor a negative control cancer cell line, a CD38- acute myeloid leukemia, being thus highly specific and targeted. Different characterization and analyses confirmed indeed the effective formation of targeted hybrid ZnO NPs, their cellular internalization and the damages produced in Burkitt’s Lymphoma cells only with respect to the other cell lines. The presented work holds promises for future clinical applications, as well as translation to other tumor types.Graphical abstract

Synthesis of phytogenically deposed Ag nanospheres on ZnO nanosheets for photocatalytic and catalytic applications

Current study presents the phytogenic deposition of metallic Ag nanospheres on ZnO nanosheets to produce Ag/ZnO nanostructures using Jacobaea Maritima (Silver Ragwort) plant extract and the prepared materials were tested for the photo-mineralization of methylene blue (MB) dye and catalytic reduction of nitroaromatics i.e. 4-nitroaniline (4-NA) and 4-nitrophenol (4-NP) in the presence of NaBH4 solution. The mean grain size and crystallinity of ZnO particles in Ag/ZnO nanostructures were found to be increased while the particle strain and dislocation density decreased with the elevation of Ag level in ZnO, and band gap energy value was reduced that has improved the photodegradation efficiency for MB dye from 45% to 98.60%, however, an excess amount of Ag has suppressed the photo-activity of Ag/ZnO nanostructures due to increase of band gap value and coverage of ZnO nanocrystals by Ag clusters. The catalytic reduction process indicated that the 4-NA and 4-NP were almost decolorized within 8 and 10 min, respectively. The degradation reaction rate of MB dye was enhanced by ∼7 times for Ag/ZnO nanostructures in comparison to pure ZnO nanosheets. The trapping experiments established that the •O2− and •OH radicals were the key active entities engaged in the deprivation of MB dye.