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Review

State of the Art Synthesis of Ag-ZnO-Based Nanomaterials by Atmospheric Pressure Microplasma Techniques

by
Ayesha Khalid
1,
Muhammad Naeem
1,*,
Omar Atrooz
2,3,
M. R. Mozafari
4,*,
Fatemeh Anari
4,
Elham Taghavi
5,
Umair Rashid
6 and
Bushra Aziz
1
1
Department of Physics, Women University of Azad Jammu and Kashmir Bagh, Bagh 12500, Pakistan
2
Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, Al-Ahliyya Amman University, Amman 19328, Jordan
3
Department of Biological Sciences, Mutah University, Mutah 617102, Jordan
4
Australasian Nanoscience and Nanotechnology Initiative (ANNI), Monash University LPO, Clayton, VIC 3800, Australia
5
Faculty of Fisheries and Food Science, Universiti Malaysia Terengganu, Kuala Nerus 21030, Terengganu, Malaysia
6
Department of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100811, China
*
Authors to whom correspondence should be addressed.
Surfaces 2024, 7(3), 680-697; https://doi.org/10.3390/surfaces7030044
Submission received: 12 July 2024 / Revised: 17 August 2024 / Accepted: 29 August 2024 / Published: 2 September 2024
Browse Figures
Versions Notes

Abstract

:
Atmospheric pressure microplasma is a simple, cost-effective, efficient, and eco-friendly procedure, which is superior to the traditional nanomaterials synthesis techniques. It generates high yields and allows for a controlled growth rate and morphology of nanomaterials. The silver (Ag) nanomaterials, with their unique physical and chemical properties, exhibit outstanding antibacterial and antifungal properties. Similarly, zinc oxide (ZnO) nanomaterials, known for their low toxicity and relatively lower cost, find wide applications in wound repair, bone healing, and antibacterial and anticancer applications. The use of core–shell nanomaterials in certain situations where some nanoparticles can cause serious harm to host tissues or organs is a testament to their potential. A benign material is coated over the core to reduce toxicity in these cases. This review compares the numerous configurations of microplasma systems used for synthesizing nanomaterials and their use in producing Ag, ZnO, and their core–shell (Ag-ZnO) nanomaterials for biomedical applications. The summary also includes the effect of control parameters, including cathode diameter, gas flow rate, precursor concentration, voltage, and current, on the nanomaterial’s characteristics and applications. In addition, it provides a research gap in the synthesis of Ag, ZnO, and core–shell nanomaterials by this technique, as well as the development and limitations of this technique and the use of these nanoparticles for biomedical applications.

Graphical Abstract

1. Introduction

Nanotechnology, one of the most promising technologies of the 21st century, can potentially convert nanoscience theory into beneficial applications. It enables us to observe, compute, handle, collect, monitor, and develop matter at the nanometer scales [1,2,3]. It is an emerging technology in many fields, such as electronics [4], gas sensors [4], photovoltaics [5,6], solar cells [7], photodetectors [7], nanophotonics [8], catalysts [9], and biomedical applications [9]. Nanomaterials, with their widespread applications in biomedical fields such as drug delivery, cancer treatment, immunotherapy, etc., are revolutionizing healthcare [10,11,12]. Nanoparticles are also applied to diagnostic instruments, pharmaceutical products, targeted medicinal products, and imagery and methodologies. Their high surface-area-to-volume ratio allows for maximum absorbance of medicine and quick movement in the bloodstream [13]. Owing to their excellent biocompatibility and biodegradability, nanoparticles can accumulate in defective organs with the most minor side effects. Furthermore, nanoparticles can be slowly released, reducing drug concentration and toxic side effects [14]. Diseases like cancer can be cured if they are detected at an early stage. Still, traditional diagnostic techniques cannot detect these tumors and cancers, and they cannot differentiate between malignant and benign lesions [15]. On the other hand, nanoparticle imaging can yield more appropriate and selective imaging of damaged and diseased tissues [16]. The nanoparticles are extensively applied to deliver chemotherapy drugs to the tumor cells, which reduces the toxicity of healthy tissues.
Zinc oxide (ZnO) nanoparticles are among the most common metal oxide nanoparticles, having distinctive chemical and physical properties that make them suitable for use in many fields as summarized in Figure 1 [17]. They are widely used in self-care products such as skincare, sunscreen, and cosmetics due to their beneficial properties against UV absorption [18]. They are also used in the textile industry; they are added to the fabric and have attractive features of visible light resistance and deodorant [19,20]. ZnO nanoparticles reveal brilliant biomedical applications such as wound healing, drug delivery, diabetes treatment, bio-imaging, antibacterial, anti-inflammation, and anticancer. They are less toxic and relatively cheaper than metal oxide nanoparticles [17,21]. In modern eras, immunotherapy is another approach to combat various diseases by providing immune molecules (antibodies and antigens). ZnO nanoparticles have received the utmost consideration owing to their high biocompatibility with human cells [22,23,24]. ZnO nanoparticles can hinder viral entrance, reproduction, and spreading all over the organ, which causes viral death because of stimulating reactive oxygen species, which results in oxidative stress [22,25].
Over the years, silver (Ag) nanoparticles have earned significant attention because of their exceptional electrical, optical, and antimicrobial properties [26]. It is commonly known that silver nanoparticles have remarkable antibacterial ability and admirable physical properties, which make them useful for applications in water purificants and the disinfection of medical devices [27,28]. Due to their tiny size, they acquire a large surface area, providing a high surface energy and further probable reactive locations. They have low volatility and high thermal stability and are less toxic to human cells [29,30]. They are used in medicine for treating burns, dental tools, and coated stainless steel materials [31,32]. In addition, they are utilized in various applications in textile fabrics, water treatment, and sunscreen lotion [33,34]. More importantly, Ag nanoparticles have the potential to be used for treating diseases that demand the maintained concentration of circulating drugs or the targeting of particular cells or organs [35,36].
Furthermore, the core–shell nanoparticles have also earned much importance because of their great biological stability and good performance [15,37,38,39,40]. Core–shell nanoparticles, including noble metal semiconductors, are the most interesting materials for biomedical applications [40,41,42]. Ag-ZnO core–shell nanoparticles have strong antibacterial and antifungal properties [43]. Core–shell nanoparticles consist of a material core covered in a layer of another material [44]. Compared to simple nanoparticles, core–shells offer significant advantages in biological applications, including improved properties like reduced cytotoxicity, increased dispersibility, biocompatibility, improved conjugation with other bioactive molecules, and enhanced thermal and chemical stability [44]. More specifically, if the desired nanoparticles are toxic, they can cause serious harm to the host tissues and organs. Then, the benign material can be coated over the core to reduce its toxicity. Sometimes, the shell layer enhances the core materials’ properties and is non-toxic. There are two main approaches for nano-synthesis: bottom-up and top-down [45]. Zhang et al. [46] reported a detailed review of the Ag-decorated ZnO-based nanocomposites, focusing on degradation mechanisms, synthesis techniques, and applications in photocatalytic degradation. Usliyanage et al. [47] comprehensively reviewed the biological synthesis approach for Ag/ZnO nanocomposites, physiochemical characteristics, morphological properties, and applications. The microplasma technique is a bottom-up technique with advantages over other techniques, such as its short processing time, environment-friendly nature, and low cost. It also has more benefits like small size, non-toxicity, control of growth, and flexibility, making it suitable for nanosynthesis [48,49].

2. Atmospheric Pressure Microplasma for Nanosynthesis

2.1. Background

In the past few years, research about nano-size particles has earned great attention because nanoparticles have distinct and unique properties compared to bulk materials due to their high surface-to-volume ratio [50]. The main task during nanoparticle synthesis is to control the nanoparticles’ shape, size, and stability because these characteristics greatly influence their properties [51]. This control can be attained by varying the conditions of reactions, such as the concentration of precursors, the stabilizer, and the reducing agents [50]. Various synthesis techniques have been investigated for the synthesis of nanoparticles, such as laser ablation [52], electrochemical [53], microwave-assisted synthesis [54], and chemical reduction [50]. Most of these techniques involve toxic chemicals, long treatment times of several hours or even days, expensive equipment, and high-temperature requirements for synthesis [55]. Plasma discharges with diverse arrangements are among the leading and eco-friendly techniques for nanoparticle synthesis. In particular, atmospheric pressure plasma systems are an essential technique, as they are cheap and simple and require no costly vacuum pumps and systems.

2.2. Synthesis of Nanomaterials

In recent years, various microplasma systems have been used for nanosynthesis, as shown in Figure 2. These systems illustrate the versatility and flexibility of microplasma’s processing conditions. Here, we classify the system into four categories based on electrode geometry, way of injecting precursors, power coupling method, and plasma power source, as described in the following sub-sections [49,50,51].

2.2.1. Plasma Jet System

The atmospheric pressure plasma jet system synthesizes nanoparticles by generating inert gas plasma. Habib et al. [55] demonstrated the synthesis of silver nanoparticles by atmospheric pressure plasma jet using silver nitrate as a precursor and trisodium citrate dihydrate. The microplasma jet system is shown in Figure 3, which consists of a gas flow system and power supply. A high-voltage electrode was coiled around the asymmetric source and was composed of a tube 3.77 mm in width. This system has a large reservoir with a diameter of 38.2 mm, connected to a ground electrode. The support was connected to another ground electrode. The discharge was generated by high voltage. The working gas used in this system was helium, and 8A current and 25 kHz frequency were applied. The surface of the liquid and plasma jet were kept at a distance of 7 mm. The samples were exposed to plasma for 5 min.
In addition, plasma jets have various configurations, such as hollow electrode micro discharge [56], microplasma jets with external electrodes [57], and microplasma jets having consumable electrodes [58].

2.2.2. Dielectric Barrier Discharge

The synthesis of silver nanoparticles by atmospheric pressure dielectric barrier discharge was demonstrated by Janith and co-workers [59], and the schematic diagram of the process is shown in Figure 4. The reactor is a quartz-based cylindrical structure. The sodium citrate solution (34 mM) and aqueous silver nitrate were mixed to prepare a solution of silver precursor. The precursor solution could be injected into the hollow central part of the plasma reactor, which could be sealed by a quartz lid. The central part was linked with the outlet and gas feeding line. The chamber has a total volume of 25 mL; the precursor solution used in this experiment was 4 mL. The bottom and lid of the quartz chamber acted as a dielectric barrier. The dielectric barriers were at a distance of 8 mm from each other. The power supply of 2000 K was used to apply a high voltage to the stainless steel electrodes. The frequency and power supply were 9.1 kHz and 39 kV, respectively [59].

2.2.3. Plasma Torch Method

Another technique for nanomaterials synthesis is the atmospheric plasma torch method. Bjelajac et al. [60] reported the synthesis of Au nanomaterials by the atmospheric pressure plasma torch method. Tetra chloroauric acid trihydrate dissolved in ethanol or water was used as a precursor. The atmospheric pressure plasma torch consists of two hollow quartz tubes. The plasma was generated between the outer plasma tube (7 mm inner diameter and 9 mm outer diameter) and the inner tube (4 mm inner diameter and 6 mm outer diameter). The inner tube was grounded, and its outer surface was coated with a thick Pt film of 300 nm. Physical vapor deposition was used to deposit Pt film. The aluminum foil 5 cm long covered the external quartz tube, and the aluminum foil was connected to the high-voltage (HV) generator. The plasma was produced in the space between the two tubes by applying a sinusoidal high voltage to the external electrodes. The internal hollow electrode carried the nebulized gold precursor solution close to the discharge. The schematic diagram of the plasma torch setup is given in Figure 5.

2.2.4. Plasma–Liquid System

A plasma–liquid system is extensively used for nanomaterial synthesis and is also called an atmospheric pressure microplasma or microplasma electrochemical synthesis, as shown in Figure 6. Ming and colleagues [61] reported the synthesis of cuprous oxide nanoparticles by microplasma electrochemical synthesis. It consisted of a stainless steel tube (0.7 mm inside diameter, 8 cm length) placed 3 cm away from the copper electrode. A 2 mm space was maintained between the liquid surface and the capillary tube end. The argon gas flow was connected to the tube, and the glass rotameter was used to control the flow rate at 60 mL/min. The discharge was ignited by applying a high voltage, keeping the current constant. The precursors used in this synthesis were NaOH, NaCl, and NaNO3 with H2O ethylene glycol or DI water as solvents. The plasma was generated at the interface of the gas solution. A ballast resistor stabilized the current and voltage. A magnetic stirrer was used to stir the solution gently to avoid agglomeration. The sediments collected were washed and centrifuged many times. The advantages and disadvantages of plasma-based nanosynthesis techniques are summarized in Table 1.

3. State-of-the-Art of the Microplasma Technique Applications

Thong and colleagues [65] synthesized silver nanoparticles using a D.C. helium microplasma jet and examined the stabilizing effect of sucrose at various molar concentrations added to the AgNO3 solution. In this setup, the gap between the surface of the solution and the capillary was kept small to lower the voltage required to cause the microplasma to ignite. Bisht et al. [66] reported the synthesis of silver nanoparticles using atmospheric pressure microplasma. Silver nitrate solution in DI water was used as a precursor. In order to avoid agglomeration, sucrose was used as a stabilizing agent. They synthesized silver nanoparticles with uniform radii ranging from 7–13 nm. The microplasma caused the reduction and nucleation of aqueous metal ions into nanoparticles without using any chemical reducing agents. The obtained nanoparticles were analyzed using dynamic light scattering (DLS), SEM, and UV–visible absorption. Kondeti et al. [67] described the surfactant-free synthesis of silver nanoparticles using Argon and Ar + 0.64% H2 plasma. A sinusoidal voltage wave modulated at 20 kHz with a 20% duty cycle and 13.4 MHz radio frequency to generate the plasma. It was observed that Ar + 0.64%H2 synthesized nanoparticles of small size with a maximum 2–3 nm diameter, whereas Ar gas plasma synthesized nanoparticles of broad size distribution. Shepida et al. [68] demonstrated the formation of silver nanoparticles in a solution of AgNO3 and sodium polyacrylate, a non-toxic surfactant. This setup used tungsten wire as a cathode, and the voltage was kept constant at 250 V. The silver nanoparticles in the range 2–20 nm were formed at a concentration of 0.05–0.2 mMol L−1 of AgNO3 with 0.5 gL−1 of NaPA. The synthesized silver nanoparticles had established antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Candida albicans. Huang et al. [69] declared the synthesis of silver nanoparticles by plasma-assisted electrochemical technique. They demonstrated that the interparticle spacing and the size of nanoparticles in the solution could be adjusted by altering the synthesis parameters so that the plasmonic response could be tuned. It was evident that larger-sized, highly dispersive silver nanoparticles were produced at higher solution concentrations and higher temperatures. Additionally, they revealed that silver nanoparticle synthesis can be accomplished without using a stabilizer, allowing control of nanoparticles dispersion. Shuaib et al. [70] synthesized AgNPs using the microplasma technique. They investigated the role of variation in the molar concentration of fructose on the size of nanoparticles. They concluded that AgNPs with better efficiency against fungi and bacteria can be obtained by using 2 mM fructose sample, due to the production of A g + ions. Lin et al. [71] demonstrated the combination of Gemini surfactant with AgNPs to attain a stable nano-surfactant system with strong antibacterial activities. Plasma-aided technique prepared high-quality crystalline nanostructures, where electrons acted as reductants, replacing conventional chemical reducing agents. The XRD results (as presented in Figure 7) showed that five diffraction peaks corresponding to fcc AgNPs at 38.20°, 44.37°, 64.50°, 77.48° and 81.64° were observed, and no impurity peaks appeared. It suggests that pure AgNPs can be formed using Gemini surfactant in a plasma-assisted technique. The TEM images of synthesized nanoparticles (presented in Figure 8a,b) reveal the formation of partially aggregated nanoparticles with a spherical geometry. The high-resolution TEM image (Figure 8c) and selected area diffraction (SAED) (Figure 8d) show the formation of nanoparticle lattice fringes, which indicates the crystalline nature of nanoparticles. The size and size distribution of nanoparticles were assessed using the histogram, as shown in Figure 8d, which shows the formation of nanoparticles with a size of 9.64 nm. It shows that nanoparticles assisted with the microplasma technique had a narrower size distribution than the conventional technique. The surfactants stabilized the silver nanoparticles by preventing AgNPs from aggregating. Antibacterial studies were conducted against S. aureus and E. coli, demonstrating the synergetic effects of the compounding systems [72].
Habib et al. [55] reported the silver nanoparticle synthesis in a quick and environment-friendly way using an atmospheric pressure plasma jet. They examined the role of variations in AgNo3 (precursor) and citrate concentration and determined the optimal conditions for synthesizing silver nanoparticles. They found their effective applications in the bio-medical field (antibacterial activities), photonic, and catalytic activities. Saleem et al. [73] demonstrated that by changing the type or concentration of capping agents in optimized microplasma parameters, the size of AgNPs could be modified. Therefore, it influenced the stability of AgNPs. The results from DLS indicated that Polyvinyl Alcohol (PVA) capped AgNPs were the most stable over 15 days compared to Polyvinyl Pyrrolidone PVP capping agents and sucrose. The AgNP’s size variations were within the range of less than 5 nm limit. They suggested that these stability results had practical applications in cancer therapy. Skiba et al. [74] examined the catalytic effect of silver nanoparticles synthesized by a non-equilibrium low-temperature plasma technique. The characteristics and formation of nanoparticles were analyzed by DLS, ultraviolet–visible spectroscopy, and scanning electron microscopy. Then, silver nanoparticles were effectively used in the catalytic reduction of 4-NP, and they demonstrated outstanding catalytic performance with a quick reaction time. Iqbal et al. [75] reported that the atmospheric microplasma approach was successfully employed to generate two-dimensional stumbled silver nanosheets. SEM analysis was used to verify the surface morphology of the synthesized nanosheets, and it showed that their lateral dimensions increased as the precursor concentration increased. The antibacterial activity of silver nanosheets was found to be highly effective against various types of bacteria and to be correlated with the size of nanosheets.
Iqbal and co-workers [76] reported the synthesis of ZnO nanostructure using different ionic surfactants and non-ionic fructose using the microplasma technique. The changes in the properties of nanoparticles were observed by changing the surfactant, including sodium dodecyl sulfate (SDS), fructose, and cetrimonium bromide (CTAB). The XRD pattern presented in Figure 9 shows the presence of characteristics peaks of ZnO at 31.73°, 34.3792°, 36.21°, 47.48°, 56.54°, 62.77°, 66.31°, 67.87° and 69.01°, which correspond to (1 0 0), (0 0 2), (1 0 1), (1 0 2), (1 1 0), (1 0 3), (2 0 0), (1 1 2) and (2 0 1) planes. The obtained peaks followed the standard peaks of JCPDS#76-0704. No impurity peaks were observed, and thus they suggested ZnO nanomaterials with high purity and hexagonal phase (Wurtzite structure) can be obtained using the atmospheric pressure microplasma technique. The SEM analysis was used to analyze the surface morphology of nanomaterials, as presented in Figure 10, and they found that morphology strongly depends on the type of surfactant used. Hexagonal ZnO nanosheets were observed (Figure 10a) while using the anion surfactant of SDS. On the other hand, when non-ionic fructose surfactant was used, hexagonal plates, termed ZnO nanodrum, were obtained (Figure 10b). In addition, a ZnO needle-like structure with orientation along the c-axis was obtained while using the CTAB surfactant. Thus, it shows that ZnO nanomaterials with high purity and numerous morphologies, including nanosheets, nano drums, and needle-like structures, can be obtained by changing the type of surfactant in atmospheric pressure microplasma.
Schwan et al. [77] successfully synthesized morphology-controlled ZnO nanoparticles using zinc powder and oxygen with an atmospheric pressure plasma jet. It was discovered that the rate of oxygen in carrier gas and plasma, the energy within the reactor, and the discharge current all affected the particle’s morphology. Jain et al. [78] described the synthesis and deposition of ZnO nanocrystalline materials by atmospheric pressure plasma synthesis. Radiofrequency power generated plasma, and the precursor was metallic zinc wire. The aggregation of synthesized nanostructures formed a porous film at the substrate. The synthesized nanostructures were thoroughly studied and characterized by UV–visible absorption, transmission electron microscopy, and X-ray diffraction. Abdullah et al. [79] demonstrated the capability of atmospheric pressure plasma jets to prepare high-purity, nanometer-sized ZnO in the gas or liquid phase. The obtained ZnO nanocrystals were characterized by transmission electron microscopy, Fourier transformation infrared (FTIR), and X-ray powder diffraction. The findings revealed that electrolytic media, current density, and reaction temperature influenced the morphology of ZnO nanocrystals.
Rawi and co-workers [80] reported the synthesis of core–shell nanoparticles of Ag-ZnO by an atmospheric pressure plasma jet technique and described their antibacterial and antifungal properties. The characterization of these Ag-ZnO core–shell nanoparticles was done using different techniques such as ultraviolet–visible spectroscopy (UV–vis), transmission electron microscopy (TEM), XRD, energy-dispersive X-ray spectroscopy (EDX), and field-emission scanning electron microscopy (FE-SEM). The pureness of synthesized Ag-ZnO core–shell NPs was proved by XRD and EDX analysis. The antibacterial activity of these core–shell nanoparticles was evaluated on two different types of Gram-positive (Staphylococcus aureus and Staphylococcus epidermidis) and Gram-negative bacteria (pneumonia and Escherichia coli). The TEM image is presented in Figure 11, which shows the appearance of two distinguishable areas. The contrast in the images specifies the formation of the dark and bright regions that correspond to the core and shell of nanoparticles, respectively. Furthermore, the antifungal activity of these core–shell N.P.s was evaluated against two distinct types of yeast. Khalid et al. [81] observed the formation of gold–silver core–shell nanoparticles using cold atmospheric pressure microplasma. They revealed that the precursor concentration affected the average size of particles; the average size of particles increased with the increase in concentration. Skiba et al. [78] recently reported synthesizing gold, bimetallic gold–silver core–shell, and alloy nanoparticles using the liquid-phase anode plasma technique. They examined the role of control parameters, including solution plasma discharge time and molar contents (0.25, 0.72, and 1.2-mM solution of silver nitrate), on the properties of nanoparticles. They observed that core–shell nanoparticles exhibit better antibacterial efficiency against C. albicans fungus and Gram-negative bacteria over other nanoparticles. Using a TEM image (shown in Figure 12), they observed that the core and shell of nanoparticles could be distinguished, and it was observed that the shell thickness of 1–2 nm, 10–12 nm, and 14–15 nm increased while using the silver nitrate solution of 0.25, 0.72, and 1.2-mM. The total diameter of core–shell nanoparticles was 18–20 nm. Thus, it showed that the core–shell nanoparticles could be obtained effectively using the liquid-phase anode plasma technique with a controlled diameter and shell thickness by tuning the control parameters. The review of plasma configuration and their use for the synthesis of silver, zinc oxide, and core–shell nanoparticles are also summarized in Table 2.

4. Summary of Review

Some important factors influencing nanoparticle size, morphology, and properties are discussed here and are summarized in Table 3. In nanoparticle synthesis, solution/precursor concentration affects the nanoparticles’ size and anti-microbial properties. Early studies revealed that increasing precursor concentration enhanced the nanoparticles’ size and anti-microbial properties. Another factor that is significantly important in nanoparticle size and morphology is processing time. The increase in processing time (5–45 min) causes an increase in the size of nanoparticles and improves the crystallinity of nanoparticles. The concentration of the stabilizing agent or surfactants added to the precursor to avoid agglomeration is important. (Usually, fructose and sucrose are used as stabilizers in the synthesis of nanoparticles). The increase in concentration or molar ratio of surfactants or stabilizing agents increases the average size of nanoparticles. The gas flow rate also affects nanoparticle size; when the flow rate rises, the nanoparticle size decreases. All these factors are of great importance in nanoparticle synthesis of silver and zinc oxide, as they affect the structural properties and their biomedical applications. By altering these factors, the properties of nanoparticles can be varied.

5. Conclusions and Final Remarks

The atmospheric pressure plasma is an advanced and novel technique that can produce nanoparticles at ambient conditions. It has low thermal temperatures, faster processes, simplified equipment, and a cheap, eco-friendly system with various dimensions and configurations. Recent studies are presented here for nanomaterial synthesis by different configurations of atmospheric pressure microplasma depending on the slight difference in their setups. This brief review revealed that silver and zinc oxide and their core–shell nanomaterials have great biological properties such as antibacterial, anticancer, and antifungal. The contribution of numerous control parameters like electrode dimension, flow of gas, type of gas, precursors concentration, operating voltage and current, distance between electrodes, and configuration of plasma system on nanoparticle characteristics (size, shape, and applications) is summarized. Nowadays, wide research is being conducted on atmospheric pressure microplasma nano synthesis. Still, there is a broad scope for the development of research, and a research gap is provided in this article. This review highlights plasma-based Ag-ZnO-based nanoparticle synthesis techniques, which offer an eco-friendly, cost-effective approach with noteworthy biological applications. Although silver and zinc oxide nanoparticles by this technique are widely reported, the literature on their core–shell nanoparticles is very limited and needs to be investigated in the future, specifically the pros and cons of such core–shell nanoparticles for biomedical applications.

Author Contributions

Conceptualization, M.N., A.K. and M.R.M.; validation, B.A., U.R., M.N. and A.K.; resources, M.N.; writing—original draft preparation, A.K. and M.N.; writing—review and editing, U.R., B.A., O.A., F.A. and E.T.; supervision, M.N. and M.R.M.; project administration, M.N. All authors have read and agreed to the published version of the manuscript.

Funding

M. Naeem thanks the Higher Education Commission of Pakistan for granting PhD studentship to Ayesha Khalid under NRPU-14417.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Applications of Zinc Oxide nanoparticles in diverse fields and conventional synthesis techniques.
Figure 1. Applications of Zinc Oxide nanoparticles in diverse fields and conventional synthesis techniques.
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Figure 2. Atmospheric pressure plasma-based approaches for nanosynthesis.
Figure 2. Atmospheric pressure plasma-based approaches for nanosynthesis.
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Figure 3. Schematic diagram of atmospheric pressure plasma jet system for nanomaterials synthesis (redrawn from Reference [55]).
Figure 3. Schematic diagram of atmospheric pressure plasma jet system for nanomaterials synthesis (redrawn from Reference [55]).
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Figure 4. Schematic diagram of atmospheric dielectric barrier discharge for nanomaterials synthesis (redrawn from Reference [59]).
Figure 4. Schematic diagram of atmospheric dielectric barrier discharge for nanomaterials synthesis (redrawn from Reference [59]).
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Figure 5. Schematic diagram of atmospheric pressure plasma torch method for nanomaterials synthesis: 1: quartz tube, 2: Pt coated injection tube, 3: aluminum foil, 4: generator (redrawn from Reference [60]).
Figure 5. Schematic diagram of atmospheric pressure plasma torch method for nanomaterials synthesis: 1: quartz tube, 2: Pt coated injection tube, 3: aluminum foil, 4: generator (redrawn from Reference [60]).
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Figure 6. Schematic diagram of atmospheric pressure plasma method for nanomaterials synthesis (redrawn from Reference [61]).
Figure 6. Schematic diagram of atmospheric pressure plasma method for nanomaterials synthesis (redrawn from Reference [61]).
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Figure 7. XRD pattern of silver nanoparticles prepared using the microplasma-assisted technique. (Reprinted with permission from Ref. [71].)
Figure 7. XRD pattern of silver nanoparticles prepared using the microplasma-assisted technique. (Reprinted with permission from Ref. [71].)
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Figure 8. (a,b) TEM images of nanoparticles, (c) high-resolution TEM image of nanoparticles, (d) SAED image, and (e) size distribution histogram of nanoparticles. (Reprinted with permission from Ref. [71].)
Figure 8. (a,b) TEM images of nanoparticles, (c) high-resolution TEM image of nanoparticles, (d) SAED image, and (e) size distribution histogram of nanoparticles. (Reprinted with permission from Ref. [71].)
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Figure 9. XRD pattern of ZnO nanomaterials prepared by numerous surfactants, (a) SDS, (b) fructose, and (c) CTAB. (Reprinted with permission from Ref. [76].)
Figure 9. XRD pattern of ZnO nanomaterials prepared by numerous surfactants, (a) SDS, (b) fructose, and (c) CTAB. (Reprinted with permission from Ref. [76].)
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Figure 10. SEM images of ZnO nanomaterials prepared by numerous surfactants, (a) SDS, (b) fructose and (c) CTAB. (Reprinted with permission from Ref. [76].)
Figure 10. SEM images of ZnO nanomaterials prepared by numerous surfactants, (a) SDS, (b) fructose and (c) CTAB. (Reprinted with permission from Ref. [76].)
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Figure 11. TEM images of Ag-ZnO core–shell nanoparticles synthesized using the micro-jet plasma technique. (Reprinted with permission from Ref. [80], Copyright @2023, World Scientific Publishing Co Pte Ltd.)
Figure 11. TEM images of Ag-ZnO core–shell nanoparticles synthesized using the micro-jet plasma technique. (Reprinted with permission from Ref. [80], Copyright @2023, World Scientific Publishing Co Pte Ltd.)
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Figure 12. TEM images of gold–silver core–shell nanoparticles using a silver nitrate solution of (a) 0.25 and (b) 1.2-mM. (Reprinted with permission from Ref. [82].)
Figure 12. TEM images of gold–silver core–shell nanoparticles using a silver nitrate solution of (a) 0.25 and (b) 1.2-mM. (Reprinted with permission from Ref. [82].)
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Table 1. Summary of advantages and disadvantages of various plasma-based nano synthesis techniques.
Table 1. Summary of advantages and disadvantages of various plasma-based nano synthesis techniques.
TechniqueAdvantagesDisadvantagesRef.
Plasma jet systemEfficient, high-purity products, flexibleCostly and complex power supply, broad size distribution, large particle size[62]
Dielectric barrier discharge systemLonger lifetime, better stability, simple geometric configurationLower energy efficiency, deposition of surplus carbon[63]
Plasma torch methodContinuous process, no expensive vacuum systemThe wide distribution of particle size, low surface area[64]
Plasma liquid systemSimple, efficient, highly confined high radical density, ultra-fine particle size, flexible precursors, narrow size distributionUnclear mechanism, post-treatment required [62]
Table 2. A literature review of atmospheric plasma configurations for synthesizing silver, zinc oxide, and silver–zinc oxide core–shell nanomaterial.
Table 2. A literature review of atmospheric plasma configurations for synthesizing silver, zinc oxide, and silver–zinc oxide core–shell nanomaterial.
No.Plasma
Configuration		NanomaterialsApplicationsCapillary
Diameter		PrecursorGas Flow RateVoltage &
Current		Ref.
01Atmospheric Pressure Microplasma jetSilverOptoelectronics, sensing, biomedical applicationsInternal diameter 0.26 mmAgNO3 + sucrose26 sccm2 mA[65]
02Atmospheric Pressure MicroplasmaSilverNanosensorsInternal diameter 0.7 mmAgNO3 + sucrose25 sccm0–15 kV[66]
03R.F. atmospheric pressure Microplasma jetSilverPhotovoltaicInternal diameter 5.25 mmAgNO31.5 slm [67]
04Microplasma SynthesisSilverAntibacterial activityInternal diameter 0.1 mmAgNO3 + NaPA 250 V[68]
05Atmospheric Microplasma electrochemistrySilverPlasmonic applications as sensingInternal diameter 0.175 mmAgNO3 + fructose25 sccm3 mA and 2 kV[69]
06Plasma liquid synthesisSilverAntibacterial and antifungal activitiesInternal diameter 0.34 mmAgNO3 + fructose100 sccm15 mA and 600 V[70]
07Plasma-aided green and controllable synthesisSilverAntibacterial activityInternal diameter 0.5 mmAgNO3 + Acetone30 sccm [71]
08Atmospheric pressure Plasma jetSilverBioactivity, catalysisInternal diameter 3.7 mmAgNO3 + trisodium citrate3 L/min8 A[55]
09Microplasma assisted synthesisSilverCancer therapyInternal diameter < 1 mmAgNO3 + PVA, PVP & sucrose600 sccm3–5 kV[73]
10Atmospheric discharge plasmaSilverCatalytic propertiesInternal diameter 2.4 mmAgNO3 + AlgNa 500–1000 V[74]
11Atmospheric pressure MicroplasmaSilverAntibacterial activityInternal diameter 0.2 mmAgNO3 + fructose150 sccm1000 V[75]
12Atmospheric pressure Microplasma electrochemical processZinc oxideAntibacterial applicationsInternal diameter 0.2 mmZn (NO3)2 + surfactant150 sccm1000 V[76]
13Atmospheric pressure plasma jet techniqueZinc oxidePiezoelectric sensors Zinc powder10 L/min200–400 A[77]
14Atmospheric pressure plasma (R.F. Power)Zinc oxideLight-emitting diodesInternal diameter 0.7 mmZinc wire150 sccm [78]
15Atmospheric pressure plasma jetZinc oxideSolar cells, Gas sensorsInternal diameter
0.6 mm		Zinc anode + NaOH + HNO3 + sucrose60 mL/min3 kV
5–10 mA		[79]
16Atmospheric pressure Microplasma JetAg-ZnO core shellsAntimicrobial activity AgNO3 + Zn (NO3)2 13 kV[80]
17Atmospheric pressure MicroplasmaAu-Ag core shellsOptical and biological propertiesInternal diameter 1 mmAgNO3 + HAuCl4. 3H2O2 l/min10 kV[81]
18Liquid-phase anode-type plasma dischargeAu-Ag core–shellAntibacterial and antifungal properties2.4 mm diameterHAuCl4⋅3H2O+ AgNO3 + sodium citrate-0.5–1 kV[82]
Table 3. Summary of influence of control parameters on the properties of silver, zinc oxide, and core–shell nanoparticles.
Table 3. Summary of influence of control parameters on the properties of silver, zinc oxide, and core–shell nanoparticles.
MaterialControl ParametersEffect of ParametersRef.
SilverSolution concentration
  • The size of nanosheets increases with increase in solution concentration;
  • Antibacterial activity of silver nanosheets enhanced with an increase in solution concentration.
[75]
  • The average size of nanoparticles increases with an increase in precursor concentration;
  • An increase in precursor concentration causes a significant increase in the inhibition zone against bacteria and fungi.
[83]
  • The large size and highly dispersive nanoparticles formed by increasing solution concentration.
[69]
ZnOProcessing time
  • An increase in processing time improves the crystallinity.
[79]
  • The average diameter and size of nanoparticles increase with the increase in processing time.
[84]
Silver
  • Increasing the exposure time to plasma increases the average size of nanoparticles.
[66]
SilverStabilizing agent concentration
  • The greater the concentration of fructose as a stabilizing agent, the more dispersed and relatively smaller nanoparticles are formed, and it reduces agglomeration. At greater fructose concentrations, the smaller nanoparticles have enhanced properties against bacteria.
[70]
SilverStabilizing agent concentration
  • The average size of nanoparticles decreases by increasing the molar ratio of sucrose in the precursor.
[65]
Molybdenum oxideGas flow rate
  • The size of nanoparticles reduces as the flow rate of gases rises.
[85]
Silver–gold core–shell Silver nitrate solution 0.25, 0.72, and 1.2-mM
  • The size of nanoparticles and shell thickness increases as the solution concentration increases.
[82]
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Khalid, A.; Naeem, M.; Atrooz, O.; Mozafari, M.R.; Anari, F.; Taghavi, E.; Rashid, U.; Aziz, B. State of the Art Synthesis of Ag-ZnO-Based Nanomaterials by Atmospheric Pressure Microplasma Techniques. Surfaces 2024, 7, 680-697. https://doi.org/10.3390/surfaces7030044

AMA Style

Khalid A, Naeem M, Atrooz O, Mozafari MR, Anari F, Taghavi E, Rashid U, Aziz B. State of the Art Synthesis of Ag-ZnO-Based Nanomaterials by Atmospheric Pressure Microplasma Techniques. Surfaces. 2024; 7(3):680-697. https://doi.org/10.3390/surfaces7030044

Chicago/Turabian Style

Khalid, Ayesha, Muhammad Naeem, Omar Atrooz, M. R. Mozafari, Fatemeh Anari, Elham Taghavi, Umair Rashid, and Bushra Aziz. 2024. "State of the Art Synthesis of Ag-ZnO-Based Nanomaterials by Atmospheric Pressure Microplasma Techniques" Surfaces 7, no. 3: 680-697. https://doi.org/10.3390/surfaces7030044

APA Style

Khalid, A., Naeem, M., Atrooz, O., Mozafari, M. R., Anari, F., Taghavi, E., Rashid, U., & Aziz, B. (2024). State of the Art Synthesis of Ag-ZnO-Based Nanomaterials by Atmospheric Pressure Microplasma Techniques. Surfaces, 7(3), 680-697. https://doi.org/10.3390/surfaces7030044

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