Assessment of photocatalytic potentiality and determination of ecotoxicity (using plant model for better environmental applicability) of synthesized copper, copper oxide and copper-doped zinc oxide nanoparticles
Abstract:NPs synthesis, characterization and azo-dye degradationA facile cost effective wet chemical method of synthesis is proposed for Cu-NPs, CuO-NPs and Cu-doped ZnO-NPs. The nanomaterials are opto-physically characterized for nano standard quality. Cu-doped ZnO-NPs based catalytic system is found to possess most efficient photocatalytic activity in degradation of two organic azo-dyes namely methyl red (MR) and malachite green (MG) that are released as industrial effluents in eco-environment intercollegium. Two pos… Show more
“…In this study, we considered ZnO nanoparticles used as antimicrobial agents to fight plant diseases. , The ZnO nanoparticles were observed to be highly dispersed in HRTEM images. High magnification images demonstrate individual particles that are approximately spherical and whose average size is ∼2 nm or less (Figures a,b).…”
Novel technological applications
in catalysis and bactericidal
formulation have emerged for zinc oxide (ZnO) nanoparticles owing
to their ability to generate reactive oxygen species by fostering
H2O dissociation. Rational improvement of those properties
requires a mechanistic understanding of ZnO nanoparticle reactivity,
which is currently lacking. Here, we determine the structural and
electronic properties of nanometer-sized ZnO, determine the binding
energetics of H2O adsorption, and compare to an extended
macroscopic surface. We show that the electronic density of states
of ZnO nanoparticles is size-dependent, exhibiting a decreasing bandgap
with the increase of nanoparticle diameter. The electronic states
near the Fermi energy dominantly arise from O 2p states, which are
spatially localized on “reactive” surface O atoms on
the nanoparticle edges that are doubly coordinated. The frontier electronic
states localized at the low coordinated atoms induce a spontaneous
dissociation of H2O at the nanoparticle edges. The surface
Zn and O atoms have inhomogeneous electronic and geometrical/topological
properties, thus providing nonequivalent sites for dissociative and
molecular H2O adsorption. The free energy of H2O binding is dominated by the electronic DFT interaction energy,
which is site-dependent and correlated with the Bader charge of surface
Zn atom. Entropy is found to stabilize the bound form, because the
increase in the vibrational contribution is greater than the decrease
in the translational and rotational contribution, whereas solvation
stabilizes the unbound state. The absence of rough edges on an extended,
macroscopic ZnO surface prevents spontaneous dissociation of a single
H2O. This study underlies the importance of coupling geometrical
and electronic degrees of freedom in determining the reactivity of
nanoparticles and provides a simple elucidation of the superior catalytic
activity of ZnO nanoparticles compared to ZnO in macroscopic forms.
“…In this study, we considered ZnO nanoparticles used as antimicrobial agents to fight plant diseases. , The ZnO nanoparticles were observed to be highly dispersed in HRTEM images. High magnification images demonstrate individual particles that are approximately spherical and whose average size is ∼2 nm or less (Figures a,b).…”
Novel technological applications
in catalysis and bactericidal
formulation have emerged for zinc oxide (ZnO) nanoparticles owing
to their ability to generate reactive oxygen species by fostering
H2O dissociation. Rational improvement of those properties
requires a mechanistic understanding of ZnO nanoparticle reactivity,
which is currently lacking. Here, we determine the structural and
electronic properties of nanometer-sized ZnO, determine the binding
energetics of H2O adsorption, and compare to an extended
macroscopic surface. We show that the electronic density of states
of ZnO nanoparticles is size-dependent, exhibiting a decreasing bandgap
with the increase of nanoparticle diameter. The electronic states
near the Fermi energy dominantly arise from O 2p states, which are
spatially localized on “reactive” surface O atoms on
the nanoparticle edges that are doubly coordinated. The frontier electronic
states localized at the low coordinated atoms induce a spontaneous
dissociation of H2O at the nanoparticle edges. The surface
Zn and O atoms have inhomogeneous electronic and geometrical/topological
properties, thus providing nonequivalent sites for dissociative and
molecular H2O adsorption. The free energy of H2O binding is dominated by the electronic DFT interaction energy,
which is site-dependent and correlated with the Bader charge of surface
Zn atom. Entropy is found to stabilize the bound form, because the
increase in the vibrational contribution is greater than the decrease
in the translational and rotational contribution, whereas solvation
stabilizes the unbound state. The absence of rough edges on an extended,
macroscopic ZnO surface prevents spontaneous dissociation of a single
H2O. This study underlies the importance of coupling geometrical
and electronic degrees of freedom in determining the reactivity of
nanoparticles and provides a simple elucidation of the superior catalytic
activity of ZnO nanoparticles compared to ZnO in macroscopic forms.
“…Previous studies displayed that the RAPD assay is effective in evaluating the preliminary toxic effects on plants [43]. Recently, a large number of studies on genotoxicity caused by NPs in crop plants have been widely reported [32,[44][45][46]. The appearance of new DNA bands (n = 6) could be described as mutations, whereas the absence of normal DNA bands (n = 2) is possibly characterized as DNA disintegration or rearrangements of genetic materials [7] caused by iron oxide NP oxidative stress-induced genotoxicity.…”
Plants exposed to stress use the variety of gene regulatory mechanisms to achieve cellular homeostasis, including posttranscriptional regulation of gene expression where microRNAs (miRNAs) play a pivotal role. Since various environmental stress factors such as nanoparticles affect crop productivity and quality, the aim of the present study was to evaluate the genotoxicity level and to estimate miRNA expression level and chlorophyll a level in the magnetite (Fe3O4) nanoparticle-stressed rocket (Eruca sativa Mill.) seedlings grown in hydroponics. Rocket seedlings were exposed to 1 mg/L, 2 mg/L, and 4 mg/L Fe3O4 nanoparticles, and after 5 weeks, seed germination rate, root-shoot elongation, genotoxicity, chlorophyll a, and miRNA expression levels were evaluated. The obtained results indicated that 1 mg/L, 2 mg/L, and 4 mg/L concentrations of Fe3O4 nanoparticles induce low genotoxicity and have a positive effect on the growth and development of rocket seedlings and that nanoparticles may improve the ability of plants to stand against environmental stresses.
“…Such effect is the primary indication of toxicity in the cellular system. Engineered NPs are reported to exert both positive (Hojjat and Hojjat 2015) as well as negative (Lee et al 2010;Ma et al 2010;Kumbhakar et al 2016;Das et al 2017) effects on the said physiological attributes in higher plants. Negative effects of NPs on the physiological attributes are the consequences of NP-mediated up-regulating stress-responsive gene expression (Khodakovskaya et al 2009).…”
Section: Seed Germination and Seedling Growthmentioning
The present study highlights the nanoimpact of cadmium sulfide quantum dots on a plant system (Sesamum indicum L.) encompassing uptake of nanoparticles (NPs), subsequent translocation following root to leaf transportation pathway using both water-and food-conducting elements and deposition in nucleus and cytoplasm with no preferential subcellular localization. Nanocrystal agglomeration, mucilaginous sheathing and vesicularization studied are the host toxicity minimization attempt. Cellular stress due to NPs is recorded in the form of elevated production of hydrogen peroxide and malondialdehyde. However, non-synchronous activation of ascorbate peroxidase-monodehydroascorbate reductase-glutathione reductase-glutathione S-transferase enzyme system contributes to failure of anti-oxidative response and persistence of stress environment. Flow cytometric assessment reveals changes in cellular metabolic event along with blockage of cell division at G 1 phase and enhances apoptotic cell death. Nuclear internalization along with oxidative burst results in generation of DNA double-strand break which can be the focal point of genome alteration and subsequent gene mutation.
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