<i>Plectranthus barbatus</i> Leaf Extract-Mediated Synthesis of ZnS and Mg-Doped ZnS NPs: Structural, Optical, Morphological, and Antibacterial Studies

Al-Hammadi, A. H.; Alnehia, Adnan; Al-Sharabi, Annas; Al-Odayni, Abdel-Basit; Abdu, Naaser A. Y.; Saeed, Waseem Sharaf

doi:https://doi.org/10.1155/2023/1399904

Nanomaterials and Nanotechnology

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Abstract Introduction Materials and Methods Results and Discussion Conclusion Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2023 | Article ID 1399904 | https://doi.org/10.1155/2023/1399904

Plectranthus barbatus Leaf Extract-Mediated Synthesis of ZnS and Mg-Doped ZnS NPs: Structural, Optical, Morphological, and Antibacterial Studies

A. H. Al-Hammadi,¹Adnan Alnehia,¹Annas Al-Sharabi,²Abdel-Basit Al-Odayni,³Naaser A. Y. Abdu,⁴and Waseem Sharaf Saeed³

Academic Editor: Dario Zappa

Received03 May 2023

Revised07 Jul 2023

Accepted17 Aug 2023

Published23 Aug 2023

Abstract

In the current study, the researchers have explored the influence of doped Mg ions on the optical, morphological, and structural properties of zinc sulfide (ZnS) nanoparticles (NPs). The green technique was employed to prepare pure and 2% and 5% Mg-doped ZnS NPs using the Plectranthus barbatus leaf extract as a capping agent. XRD, SEM, FTIR, and UV-visible were used in the investigation process. The XRD results showed that all the synthesized materials have a cubic structure with space group F-43m. The D_av was nearly in the range of 2.02–2.20 nm. The SEM images illustrated that NPs were agglomerated. The UV-visible results showed that the optical bandgap increased as Mg²⁺ ions increased, which was in the range of 3.81–4.42 eV. The absorption shoulder of the prepared NPs is blue-shifted with increasing dopant concentration. The FTIR spectrum gives characteristic peaks for Zn-S bonds and asserts NPs’ formation. The antibacterial check against E. coli and S. aureus bacterial strains revealed that pure and Mg-doped ZnS NPs have higher activity for both bacterial strains. The results have shown that the prepared materials can be used for antibacterial activities and optoelectronic applications.

1. Introduction

Among the family of semiconductor compounds, II–VI groups hold tremendous technological importance in many fields of science and technology. For instance, ZnS, CdS, ZnSe, CdTe, etc., are of great importance for solar cells and optoelectronics because they possess exceptional structural, electronic, and optical properties [1, 2]. The unique properties and applications of zinc sulfide (ZnS) nanoparticles (NPs) have recently made them one of the most promising research materials. It is a semiconductor with large band gap energy (3.68 eV at 298 K), wide exciton binding energy, and cubic unit cell with lattice constant a = b = c = 5.406 . Due to their ability to demonstrate new properties when compared to bulk ZnS, NPs have garnered a lot of attention [3–8]. As a result of their excellent optoelectronic properties, low cost, nontoxicity, and natural abundance, ZnS NPs have been utilized for photocatalysts, solar cells, light diodes, and bio-applications [9–14], among others. Generally, chemical approaches for synthesizing nanomaterials are faster and cheaper, and they provide a higher yield than physical approaches. Therefore, such chemical methods are more suitable for industrial scales.

The literature review illustrates that ZnS NPs have been fabricated using different techniques involving sol-gel [15], coprecipitation [16, 17], solvothermal [18], green synthesis [19], microwave [9], and hydrothermal techniques [20]. As it is well known, doping ZnS NPs with different metal atoms, especially alkaline earth metals, is an effective method of modifying the nanocrystals’ optical properties and electrical properties [14, 21–23]. Furthermore, it is well known that NPs have a high surface-to-volume ratio, resulting in unstable properties when oxygen is chemisorbed at their surface in an ambient atmosphere leading to higher resistivity or uncontrolled luminescence emission. To overcome this obstacle, the surface bonds of the NPs can be adequately passivized with appropriate guest atoms, thereby promoting a stable state. Generally, choosing the suitable doping atom depends on the following criteria: (i) the ionic radius values of guest and host atoms should be similar and (ii) the thermal solubility limit should be as high as possible to maintain the high content of guest atoms [4, 24, 25]. Magnesium (Mg) ion is one possible doping atom, being a promising candidate to replace Zn sites in order to tune the optical properties of the host lattice.

In addition, Mg is a naturally abundant and low-toxic element. Moreover, due to its similar ionic radius to Zn, Mg ions are not expected to cause a significant lattice distortion of ZnS [26]. Indeed, doping ZnS NPs by various transition metals has been tried using different approaches [5, 15, 27, 28]. In the middle of these is the green method. It is an efficient approach to preparing ZnS NPs due to its simplicity and scalability. Several valuable reports regarding ZnS’s structural, morphological, and optical properties have been published. For example, a work by Ashokkumar and Boopathyraja [11] has revealed that gets increased with the increase in Mg dopant concentration. The results suggest that these materials can be used in optoelectronic applications [11]. Ayim-Otu et al. [29] have synthesized pure and (3%) Cu-doped ZnS NPs by coprecipitation, showing improved optical bandgap after doping and proving their possible use in photovoltaics [16]. According to the literature [11, 30, 31], doping of ZnS by Mg can be performed using different chemical processes; however, to the best of our knowledge, no research studies on using the Plectranthus barbatus (P. barbatus) leaf extract as a medium for the biosynthesis of Mg-doped ZnS NPs have been reported.

Herein, we focused on synthesizing ZnS pure and doped by Mg using the P. barbatus leaf extract as a capping agent. P. barbatus (also known as Coleus forskohlii) is a medicinal herb that belongs to Lamiaceae family and has proven its value as an antimicrobial, antioxidant, and antiseizure drug [32, 33]. Furthermore, it is used in herbal treatment of many diseases, including hypertension, congestive heart failure, eczema, colic, respiratory disorders, painful urination, insomnia, and convulsions [34]. The P. barbatus leaf extract has exhibited antibacterial, antioxidant, and immunomodulatory activities and were cytotoxic to gastric adenocarcinoma cells. The secondary metabolites of P. barbatus leaves have reported to include eugenol, α-pinene, and β-caryophyllene, which are toxic to larvae of Anopheles subpictus, Stegomyia albopicta, Culex tritaeniorhynchus [35], and A. aegypti fourth-instar larvae, but no insights into the mechanism of action have been reported [36]. A recent report has evaluated the phytochemical components in the P. barbatus leaves from both aqueous and organic extracts. The main findings revealed the presence of flavonoids, cinnamic derivatives, steroids, and ellagic acid, with higher activity for the organic extract [37]. Plants of this species grow in many countries around the world, such as India, Ethiopia, Egypt, tropical East Africa, Yemen, and Brazil [32].

The effect of doping on the morphology, optical, and structural properties of ZnS was investigated, and furthermore, the antibacterial activities against Gram-positive and Gram-negative bacteria were assessed.

2. Materials and Methods

2.1. Materials

Zinc acetate dihydrate (Zn(CH₃OO)₂·2H₂O, 98.5%), sodium sulfide (Na₂S·xH₂O; Himedia Laboratories 60%), magnesium nitrate hexahydrate (Mg(NO₃)₂·6H₂O), and ethanol (EtOH, 99.8%) were purchased from BDH chemical Ltd. (Pool, England, UK). The bacteria strains (Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli)) were kindly obtained as a gift from Al-Jarfi Medical Lab (Dhamar City, Yemen). Mueller–Hinton agar (MHA) was acquired from Sigma–Aldrich (Darmstadt, Germany) and used as recommended. Distilled water (DW) was used wherever.

2.2. Plant Collection

Fresh leaves of the target P. barbatus plant were collected from Dhamar valleys farms, Yemen. They were washed several times with tap water and DW. After that, the leaves were chopped into small pieces and crushed in a mortar with a pestle till they became dough [38].

2.3. Preparation of the Extract

13 g of the dough-like crushed leaves were suspended in 200 mL DW. Then, the mixture was stirred for 90 min at 25°C, during which the color of the solution was changed from colorless to brown. After filtering, the resultant solution was immediately employed for production of the target pure and Mg-doped ZnS NPs [39].

2.4. Green Synthesis of ZnS NPs

To synthesize ZnS NPs, equal moles (3.5 moles) of Zn(CH₃OO)₂·2H₂O and Na₂S were separately prepared in 25 mL each of the P. barbatus leaf extract (termed solutions A and B, respectively). Solution B was then added, in a dropwise manner, to solution A, and the mixture was stirred using a magnetic stirrer for 1 h at 25. After that, the product was filtered, washed with ethanol and DW, and dried at for 48 h. Finally, the obtained powder was further dried at 100°C for 1 h and then quashed into fine powder [39, 40]. The same procedure was repeated for doping ZnS with 2 and 5 mol% Mg. The overall scheme for the biosynthesis of ZnS and Mg-doped ZnS NPs and their bioactivity are summarized in Figure 1.

2.5. Antibacterial Test

The antibacterial effect of the prepared materials was executed for S. aureus (Gram-positive) and E.coli (Gram-negative) bacteria by the disc diffusion route [41, 42]. The concentrations of 70, 140, and 210 mg/mL of the synthesized NPs were taken for the antibacterial check. The inhibition zones were measured after incubation at 36-37 for 24 h.

2.6. Characterization

The X-ray diffraction (XRD) profiles for the pure and doped ZnS were recorded using an XD–2 X-ray diffractometer (Beijing, China) with CuKα radiation of λ = 0.15418 nm. Fourier transform infrared (FTIR) spectra were recorded via the Nicolet iS10 FTIR spectrometer from Thermo Scientific (Madison, WI, USA) on the range of 650–4000 cm⁻¹. The scanning electron micrograph (SEM) was imaged by . Electronic spectra were obtained using a Hitachi UV-vis U3900 spectrophotometer (Tokyo, Japan) coupled with Varian Cary-50 software and acquired in the range of 200–800 nm at room temperature. The NPs were suspended in DW and immediately analyzed using a 1 cm cuvette.

3. Results and Discussion

3.1. XRD Analysis

XRD analysis was employed to define the structural purity and crystallite size of the NPs. The XRD patterns for pure, 2% Mg, and 5% Mg-doped ZnS NPs are offered in Figure 2 and assured agreement PDF card no. 05-0566 [43]. Thus, three prominent peaks coinciding to (111), (220), and (311) planes of ZnS were observed, respectively, at 2θ of 28.75°, 48.01°, and 56.46°. The results revealed well-resolved patterns of ZnS NPs. The broadening in the diffraction peaks might be due to the size effect; therefore, the crystallite size is in the nanoregime. The average crystallite size (D) of the NPs is estimated by Debye Scherrer’s relation [4]. Bragg’s formula was applied to estimated d-spacing [13], while the lattice parameter (a) was calculated using the equation [43], where hkl is Miller’s plans. The peak position (2θ), lattice parameter, d-spacing, and D_ave values for the highest intensity peak are collected in Table 1. From this table, it is found that the D value increases with the increase in the Mg doper concentration, i.e., from 2.021 nm for the undoped ZnS to 2.204 nm for 0.05 Mg-doped ZnS. These results elucidate the role of the plant extract in facilitating the NPs’ production.

Furthermore, it was observed that the position of the diffraction peak of (111) was slightly shifted to higher angles after doping, and it was proven that Mg is well superseded Zn in the ZnS matrix. The lattice (a) parameter and d-spacing values were slightly decreased due to the coalition of smaller ionic radii of Mg into the position of larger ionic radii Zn [11]. The reduction in the parameter of lattice (a) and d-value lead peak position shifts into higher value. The slight increase in D_ave after Mg doping is due to the improvement of crystalline surface growth by the existence of Mg [11]. These results agree with the fact that has been reported by Ashokkumar and Boopathyraja, who prepared pure and Mg-doped zinc sulfide using the coprecipitation method [11].

3.2. SEM Analysis

The SEM analysis was performed to study the surface morphology of the synthesized NPs. Figures 3(a) and 3(c) illustrate the SEM images of pure ZnS and 5% Mg-doped ZnS NPs. It can be seen that the NPs were irregular in shapes and sizes and agglomerated into higher clusters. Furthermore, it could be seen that the pure sample is less lumpy than the doped one, while the extent of particles’ agglomeration was higher after doping. Due to the low magnification of the images, counting of the particles and particle sizes is difficult; however, the insert images (Figures 3(b) and 3(d)) could visualize traced particle sizes.

3.3. UV-Visible Spectroscopic Analysis

The UV-vis absorption spectra of Mg ions doped ZnS NPs are listed in the range 200-900 nm as shown in Figure 4(a). The pure and Mg-doped ZnS NPs revealed an absorbance shoulder at 321, 296, and 270 nm, respectively. In addition, it illustrates that the synthesized samples have excellent absorption at the short wavelength region. Also, it shows that the absorption shoulder of the prepared NPs shifts towards the shorter wavelengths as the concentration of the dopant increases. This can be explained by the strong sp–d exchange interaction between the zinc sulfide band electrons and localized d spins related to the magnesium ions. The energy gap () for the synthesized NPs is computed using the relation [44], where is the cut-off wavelength. The estimated for the synthesized NPs was 3.86, 4.19, and 4.59 eV, respectively.

(a)

(b)

(c)

The Beer–Lambert formula was used to compute the absorption coefficient (α) [4] , where A and t represent the absorbance and the thickness, respectively. Figure 4(b) displays α for all the samples (pure and Mg-doped ZnS) as a function of wavelength (). It illustrates that α decreases as the increases. This made Mg-doped ZnS NPs an excellent nominee material for optoelectronic instruments as a window layer. Figure 4(c) displays the transmission spectra () of ZnS (pure), 2% Mg-doped ZnS, and 5% doped ZnS NPs. By incorporating Mg ions into the Zn-S lattice, distortions and imperfections are created, thereby suppressing transparency. This result was in coincidence with literature [11]. The extinction coefficient (k) as a function of for pure (ZnS) and Mg (0.02 and 0.05) doped ZnS NPs is shown in Figure 4. The k was computed via the equation [45].

Figure 4(c) shows that the extinction coefficient (k) at short wavelengths was increasing, and then as the wavelength increased, the k decreased up to 290 nm, and then a sudden increase was observed. Furthermore, as the wavelength increased, the k increased as well.

For a direct allowed transition, the value was estimated using Tauc’s equation (44). (αhv) = A(hv − )ⁿ, where A is a constant, α is the absorption coefficient, hv is the incident photon energy, and n takes the values 1/2, 3/2, 2, and 3 depending on the material and the type of the optical transition whether it is direct or indirect by using n = 1/2. The estimated is 3.81, 4.19, and 4.42 eV, respectively, as shown in Figure 5. These results are in a close agreement with previous studies reported by Mani et al. [19] and Ashokkumar and Boopathyraja [11].

(a)

(b)

(c)

The values obtained by applying both absorption edge and Tauc’s equation methods were nearly equal. Accordingly, the value of the NPs is larger than that of the bulk material. The increase in the value of a semiconductor is due to the increase in the life-time of holes and electrons. Also, the observed is blue-shifted, which can be attributed to the quantum confinement effects. Indeed, the reproducibility of the particle sizes and optical and other properties of bio-based NPs are challenging. Therefore, the primary concern to using the bio-synthetic route is to optimize the critical protocols. In certain cease, the authors have reported a highly reproducible green method for the production of NPs as assessed by UV-visible spectroscopy [46]. However, this is not always the case, and extensive evaluation is needed.

3.4. FTIR Studies

FTIR spectra of the prepared pure ZnS, 2%, and 5% Mg-doped ZnS are shown in Figure 6. In principle, FTIR analysis helps in identifying the functional groups existing in the synthesized NPs as well as the various adsorbing chemical species. As can be seen, the spectra of pure ZnS and Mg-doped ZnS are nearly the same with a slight difference in some peak positions and intensities assigned to the variation in the crystals’ nanostructures [47]. According to the literature [6, 47, 48], the peaks at 1127, 1109, and 617 cm⁻¹ are due to Zn-S vibrations. After doping ZnS with Mg, a change in its microstructure is expected. The case could be followed through the change in the intensities of peaks at 1127 and 1109 cm⁻¹, thus supporting Mg inclusion into the main ZnS crystal [47]. The broad bands in the range of 3050–3670 cm⁻¹ are due to HO stretching of the adsorbed water molecules on the surface of the nanocrystals [47]. It may also suggest absorption contributed from OH of alcohol and phenol of extract biomolecules. The strong bands at 1557, 1387, 1331, 1022, and 932 cm⁻¹ could be assigned to the stretching bands of C=O, C=C, C-C, asymmetric C-O, and symmetric C-O which associated with the capping biomaterials, driving the production of ZnS and its doped Mg NPs [49].

3.5. Synthetic Mechanism

Based on the phytocompounds reported in the literature [37, 50], the reaction mechanism is depicted in Figure 7. Accordingly, flavonoids, cinnamic derivatives, steroids, terpenoids, saponins, and essential oils were major constituents of the P. barbatus leaf [50]. Notably, diterpenoids, including forskolin [51], plectranthone, and plectrinone [52], are one of the most bioactive compounds in the P. barbatus plant [33]. Hence, to simplify the illustration of the suggested mechanism, the diterpene called forskolin was used to represent the stabilizing agents used to prepare the target NPs (pure and Mg-doped ZnS NPs). As can be seen, forskolin combines several functional groups that could contribute to capping and stabilizing ions for the next production of NPs. Hence, one forskolin molecule could coordinate as one, bi-, or multi-dentate with metal ions (Zn²⁺ and Mg²⁺). On the other hand, essential oils and amino acids can stabilize the sulfide ions. Thus, by further hydrolysis of the coordinated ions, the end NPs can be obtained [53].

3.6. Antibacterial Studies

The antibacterial effect of the as-prepared pure and (0.02, 0.05) Mg-doped ZnS NPs was investigated against S. aureus and E. coli strains to check their utility as potential materials for biological applications. Figures 8(a) and 8(b) show the zone of inhibition (ZOI), and Table 2 displays the measured ZOI for all the prepared compounds. The results indicated higher antibacterial potency of pure ZnS NPs than the Mg-doped one, with lesser activity against Gram-negative than Gram-positive bacteria. The difference can be explicated by the chemical composition and various structures of each cell surfaces, as the cell wall of Gram-positive and Gram-negative bacteria is different [54, 55]. The higher activity is due to the greater ability of prepared NPs to generate reactive oxygen species, which leads to oxidative stress and destruction of bacterial cells [11, 56]. According to previous studies, several mechanisms could be proposed for the antibacterial resistance of NPs. Due to smaller sizes of NPs, they can easily adhere with the cell wall of the bacterium and can cause destruction, which will lead to the death of the cell. The electrostatic interaction of the nanomaterials with the cell wall and photocatalytical light activation are also a common possible reason behind the antibacterial activity of nanomaterials [57, 58].

(a)

(b)

The antibacterial activity of the P. barbatus extract has been reported to be solvent-dependent, with the aqueous extract effect being lower than the organic one [37]. In the present study, the experiment was performed to evaluate the antibacterial activity of the synthesized inorganic NPs; however, the plant extract was not targeted and thus was not compared. It is worth mentioning that even though a trace of the plant phytocompounds can be detected, their effect would not be counted due to the traced concentration. On the other hand, the antibacterial activity of chemically synthesized ZnS NPs is low, as reported elsewhere [59], supporting the advantage of the biosynthesis method in producing NPs with a better performance against microbes.

According to Ashokkumar and Boopathyraja [11], the antibacterial activity of ZnS NPs prepared via a coprecipitation method was dopant-ratio dependent; however, the case was not straightforward, and instead, a peak of efficacy was found at 0.2Mg-doped ZnS among the tested (0.0–0.4)Mg-doped ZnS NPs. A similar trend was seen for ZnS-filled polyvinylpyrrolidone/Chitosan [60] against S. aureus and E. coli, demonstrating a concentration-dependent activity that is higher against S. aureus. The ZOI against S. aureus and E. coli was reported as the greatest among a list of bacterium strains investigated by Segura et al. [61]; however, the study indicated closer susceptibility of both bacteria for ZnS at higher concentrations. It is also reported that other kinds of ZnS nanostructures synthesized by chemical and green methods have shown efficient antibacterial activity against both strains, exhibiting similar ZOI at similar concentrations [59, 62, 63]. Despite the synthesis method, the antibacterial activity of doped ZnS NPs varies depending on the dopant type and concentration. Hence, Ag-doping has enhanced the ZnS activity [64], Mg-doped ZnS has an optimal value [11], and Sn-doping showed the same or slightly lesser activity than pure ZnS [63]. The latter one supports our findings that the activity of pure ZnS is marginally higher activity than that of Mg-doped ones. Such differences are brought about by the various sizes and shapes present in each doped ZnS product, which in turn rely on the synthesis method.

4. Conclusion

In this paper, pure and (2% and 5%) Mg-doped ZnS NPs were successfully prepared via an economical, easy, and environment-friendly route using the P. barbatus leaf extract. The XRD pattern proved the cubic phase with crystallite sizes in the range of 2.02–2.204 nm. The SEM revealed that the obtained NPs are agglomerated. The UV-visible results have shown that the optical band gap was increased as Mg²⁺ ions increased, which were in the range 3.81–4.42 eV. The FTIR study denotes the existence of OH, C-C, and C=O functional groups which are the surface-active molecules that stabilize the ZnS NPs. The antibacterial test demonstrated that the biosynthesized pure ZnS and Mg-doped ZnS NPs had remarkable inhibition of growth of both Gram-negative and Gram-positive bacteria.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

All of the authors mentioned contributed significantly to the development and writing of the paper.

Acknowledgments

The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia, for funding this research (IFKSURC-1-1910).

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Copyright © 2023 A. H. Al-Hammadi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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