Citation
Satish N. Vaishnav
Department of Chemistry, Sardar
Vallabhbhai Patel Arts and Science College, Ainpur Tal. Raver, Pin-425507
Corresponding author: drsatishvaishnav @gmail.com
Abstract
In the present study, the
green synthesis of ZnO nanoparticles was carried out by using extraction of
Argemone Mexicana plant. This is one of the low-cost natural way to synthesize
the nanoparticles for sustainable nature. The Argemone Mexicana play a role of
natural reducing and stabilizing agents by eliminating the prerequisite role of
toxic chemical used earlier for the synthesis. The zinc precursor, particularly,
zinc acetate was reacted with the plant extract under controlled conditions
resulting in formation ZnO nanoparticles. The synthesized nanoparticles were characterized
using X-ray diffraction, Field-effect Scanning Microscope and UV-Vis
spectrophotometer to investigate structural, morphological an optical behavior
of the synthesized nanoparticles. It is found that the synthesized ZnO
nanpaticles possesses hexagonal wurtzite ZnO structure with crystalline size
range between 5-10 nm. The optical properties exhibit the optical energy band
gap around 3.03 eV. The green synthesis
approach offers an environmentally sustainable alternative to the conventional
methods which is quite hazardous. The zinc oxide nanoparticles has a
significant potential to use in fabrication of optoelectronic devices and as
well as in antimicrobial activity and photocatalysis applications.
Keywords: Argemone Mexicana, ZnO, XRD,
FE-SEM
1 Introduction
Nanotechnology
has emerged as a rapidly advancing field due to the unique physicochemical
properties of materials at the nanoscale, which differ significantly from their
bulk counterparts [1,2]. Among various metal oxide nanoparticles, zinc oxide
(ZnO) nanoparticles have attracted considerable attention because of their wide
band gap, high exciton binding energy, chemical stability, and biocompatibility
[3]. These properties make ZnO nanoparticles highly suitable for diverse
applications in photocatalysis, optoelectronics, sensors, cosmetics,
antimicrobial agents, environmental remediation, and biomedical fields [3–5].
Conventional
synthesis methods for ZnO nanoparticles, such as chemical precipitation,
sol–gel, and hydrothermal techniques, often require toxic chemicals, high
temperatures, and complex processing steps, leading to environmental and health
concerns [5,6]. To overcome these limitations, green synthesis has emerged as
an eco-friendly, sustainable, and cost-effective alternative that aligns with
the principles of green chemistry [6,7].
Green
synthesis utilizes biological systems including plant extracts, microorganisms,
and biomolecules as reducing, stabilizing, and capping agents, thereby avoiding
hazardous reagents and minimizing energy consumption [7,8]. Among these
approaches, plant-mediated synthesis is particularly advantageous due to its
simplicity, rapid reaction rates, ease of scale-up, and availability of diverse
phytochemicals [9,10]. These phytochemicals—such as flavonoids, alkaloids,
phenolics, terpenoids, and proteins—play a crucial role in metal ion reduction
and nanoparticle stabilization [10,11].
Several
studies have reported the successful green synthesis of ZnO nanoparticles using
various plant extracts, demonstrating excellent antimicrobial, catalytic, and
photocatalytic properties [12–17]. The size, morphology, and functional
properties of ZnO nanoparticles are strongly influenced by the nature of the
plant extract and synthesis parameters [9,13].
Argemone
mexicana is a medicinal plant widely distributed in tropical and subtropical
regions and is known for its rich phytochemical profile and pharmacological
importance [18]. The presence of bioactive compounds in Argemone mexicana makes
it a promising candidate for the green synthesis of metal and metal oxide
nanoparticles [8,18]. However, limited studies are available on the synthesis
of ZnO nanoparticles using Argemone mexicana, highlighting the need for further
investigation.
The present
study focuses on the green synthesis of zinc oxide nanoparticles using Argemone
mexicana plant extract as a natural reducing and capping agent. This
environmentally benign approach provides a sustainable route for ZnO
nanoparticle synthesis while enhancing their potential applicability in
antimicrobial and environmental applications [5,12,15].
Experimental Details
Zinc acetate dihydrate
(Zn(CH₃COO)₂·2H₂O, analytical grade) was used as the zinc precursor. Fresh
leaves of Argemone mexicana were collected locally. All chemicals were of
analytical grade and used without further purification. Double-distilled water
was used throughout the experiment
Fresh leaves of Argemone
mexicana were thoroughly washed with tap water followed by distilled water to
remove dust and impurities. The cleaned leaves were shade-dried and then finely
chopped. About 10 g of chopped leaves were heated in 100 mL of distilled water
at 70 °C for 30 minutes. The resulting mixture was allowed to cool to room
temperature and filtered using Whatman No. 1 filter paper. The clear filtrate
obtained was used as the plant extract for the synthesis of zinc oxide
nanoparticles.
An aqueous solution of
zinc acetate dihydrate (0.1 M) was prepared using distilled water. The prepared
Argemone mexicana leaf extract was added dropwise to the zinc acetate solution
under continuous magnetic stirring at room temperature. The pH of the reaction
mixture was adjusted to alkaline conditions (pH ~10) using sodium hydroxide
solution. The reaction mixture was stirred continuously for 3 hours until the
formation of a pale white precipitate was observed, indicating the formation of
zinc hydroxide precursor.
The obtained precipitate
was centrifuged and washed several times with distilled water followed by
ethanol to remove residual impurities and unreacted biomolecules. The purified
precipitate was then dried in a hot air oven at 100 °C for 12 hours. The dried
powder was subsequently calcined at 500 °C for 1 hours to obtain crystalline
zinc oxide nanoparticles.
The obtained Zinc oxide
nanoparticles were used to study its physical properties, particularly,
structural and optical properties. The study of structural property was carried
by using X-ray diffractometer, the surface morphology was investigated by using
Field-effect Scanning Electron Microscope (FE-SEM) and optical study was done
via UV-Vis spectrophotometer.
Result and Discussion
Figure 1: X-ray
diffraction pattern of green synthesized ZnO nanoparticles.
The FE-SEM image shown in
figure 2 indicate that the growth of ZnO nanoparticles is uniform and possesses
the particle size of 5-10nm. The uniform growth of ZnO nanoparticles promises
that the natural green synthesis is the way forward to adopt the environmentally
sustainable route to industrial-scale the production of ZnO nanoparticles [17].
Figure 2: FE-SEM image of
green synthesized ZnO nanoparticles.
As synthesized ZnO nanoparticles were dissolved in
ethanol solution and sonicated for 15 min. The concentration of solution was
0.5mg/ml. The quartz cuvette having optical path length of 10mm. The baseline
measurement was done with pure ethanol solution followed by the measurement of
ZnO nanoparticles solution. The measuring range was 300 to 800 nm with the scan
speed of 400nm/sec.
Figure 3: UV-Vis spectra of
green synthesized ZnO nanoparticles.
From the Tac’s plot as shown in figure 4, we have calculated the
optical energy band gap of ZnO nanoparticles. It is found that ZnO-Arge-Mxicana
has an optical band-gap of 3.03 eV. So this wideband gap material can be
potentially useful for the optoelectronic devices particularly, organic solar
cell, organic light-emitting diode and transparent transistors.
Figure 4: Tac’s
Plot of (ahnd)2
vs hn
for ZnO nanoparticles
synthesized by Argemone Mexicana plant extraction.
Conclusions
ZnO nanoparticles were
successfully synthesized by using
agremone Mexicana plant extraction. The X-ray diffraction pattern reveals the
hexagonal wurtzite crystal structure of the synthesized nanoparticles without
any impurity. The FE-SEM image confirms the obtained nanoparticles have a
uniform particle size of 5-10 nm. The UV-Vis spectra recorded in the range of
300-800nm exhibit optical band energy
is around 3.03eV.
Acknowledgement
Author is greatly
thankful to Principal Dr. J. B. Anjane of Sardar
Vallabhbhai Patel Arts and Science College, Ainpur Tal. Raver for
his valuable support to carry out the research work. He is also thankful to
Prin. Dr. R. R. Ahire for allowing me to perform optical study at Department of
Physics, Sitaram Govind Patil College, Sakri.
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