Nanoparticle Samples Research Articles

Lanthanum-substituted Cobalt Ferrite Established by the Co-precipitation Process: Annealing Temperature Adjustment of Structural, Magnetic, and Dye Removal Characteristics

Co-precipitation process was used for the synthesis of lanthanum-substituted cobalt ferrite nanoparticles at several annealing temperatures (Ta), i.e., 200 °C, 300 °C, and 400 °C, for 5 h. XRD spectral depicted that the produced nanoparticles sample indicates a single phase of fcc inverse spinel conforming to ICDD No 22-1086. The crystallite size (D) calculation at the strongest peaks shows the increase in enhancing the Ta i.e., 18.99 nm, 19.90 nm, and 23.21 nm for 200 °C, 300 °C, and 400 °C, respectively. The FTIR results showed absorption band at the tetrahedral site, v1 ~575 cm−1 and the octahedral site, v2 ~474 cm−1. The absorption bands indicate that the lanthanum ions have successfully replaced the Fe3+ cations in the original cobalt ferrite structure. According to the hysteresis loop, the coercive field's (HC) magnitude falls from 700 Oe down to 550 Oe as Ta increases. This result is consistent with the anisotropy constant which decreased from 0.77×104 erg/cm3 to 0.56×104 erg/cm3. The obtained nanoparticles also showed superior performance (much larger than 95%) for dye removal of Congo red. Copyright © 2023 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Experimental study of the effect of technological aspects of the two-stage method of nanofluids preparation on their stability

Nanofluids (NFs) can be considered promising working fluids and coolants for power systems. Nanoparticles (NPs) admixtures in liquids significantly affect their thermophysical properties. The NP samples that have been contacted with the ambient air are inhered in the presence of the sorbed surface layer from various air components. For today, the effect of the sorbed layer on the NPs' surface on the colloidal stability of NFs has not been examined. In paper was shown that preliminary removal of the sorbed air components from NPs contributes to obtaining the NFs with enhanced colloidal stability. Experimental studies of the desorption process of the sorbed air components regarding α-Al2O3 NPs that were stored under ambient conditions resulted that the adsorption layer consists mainly of water. A technique for the NFs preparation has been developed. This technique involved preliminary NPs treatment by vacuuming together with heating up to 200 °C, following multiple repeats of the processes of NPs milling in a bead mill with liquid and ultrasonication. The measured hydrodynamic size (DLS) of the NPs' aggregates in the NF obtained by the mentioned technique was smaller than for similar NF prepared without NPs pre-treatment. The obtained results will contribute to improving the technique of preparation of the colloidal stable working fluids and coolants for power systems with high energy efficiency.

Insight into the role of Mg/B and Mg/Cu dual dopant on the properties of ZnO nanoparticles prepared by facile one-step combustion route for photocatalytic and antibacterial application

ZnO semiconductors are widely known to have benefits in photocatalytic and antibacterial applications. In this study, (Mg/B)–ZnO and (Mg/Cu)–ZnO were synthesized using the combustion method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), Raman spectroscopy, Fourier-transform infrared spectroscopy (FTIR), UV–Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The XRD results confirmed a decrease in the crystal size and an increase in the crystallinity of the doped ZnO samples. SEM analysis confirmed the morphological changes in the structure from rod-shaped to spherical, and the particle size decreased in the doped ZnO samples. EDS analysis validated the nanoparticle composition of Zn, O, Mg, B, and Cu without impurities. Raman spectra confirmed the formation of defects due to the substitution of dopants in the ZnO lattice. All samples for FTIR analysis showed functional chemical group vibrations from Zn–O, C–H, and O–H stretching. The existence of dopant bonds with oxygen was also validated from this analysis. The change in band gap energy was observed from 3.13 to 3.10 eV in Mg/Cu–ZnO and 3.12 eV in Mg/B–ZnO sample due to the influence of the addition of dopant ions. The XPS spectra show the chemical composition of the nanoparticle samples and the oxidation numbers that correlate with the results of EDS and XRD analyses. A decrease in the emission intensity in the PL measurement was observed in the green emission region in the Mg/B–ZnO sample, which correlated with the decrease in electron recombination. The Photocatalytic application was performed by measuring its ability to degrade methyl violet dye under visible-light irradiation. The maximum deterioration after 120 min of irradiation was obtained for the Mg/Cu–ZnO, Mg/B–ZnO, and ZnO samples at 92.62 %, 92.20 %, and 80.89 %, respectively. Antibacterial activity increased against S. aureus bacteria in co-doped ZnO samples with inhibition zones of 12.15 mm, 8.15 mm, and 6.45 mm for Mg/B–ZnO, Mg/Cu–ZnO, and ZnO samples, respectively.

Doxorubicin/poly(caprolactone)/polyethylene glycol nanoparticles prepared by electrospray

AbstractThe development of sustainable drug delivery systems is very important in the field of pharmaceutical research and has many advantages over the usual methods of drug administration, including improving effectiveness, reducing side effects, and increasing patient compliance. Among various techniques, electrospraying as a voltage‐driven process has emerged as a promising technology for the fabrication of drug‐loaded nanoparticles. In recent years, the application of electrospray approach for drug release has been widely investigated. However, optimization of electrospray process parameters and development of mathematical models to predict drug release kinetics from microparticles are still challenging. To address these issues, a combination of Central Composite Design (CCD) and Response Surface Methodology (RSM) has been used. This paper focuses on the application of CCD‐RSM for modeling and optimization of doxorubicin (DOX)‐poly(caprolactone) (PCL)‐polyethylene glycol (PEG) microparticles prepared using electrospray method. Doxorubicin, a widely used anticancer drug, exhibits potent cytotoxicity against a wide range of cancers. PCL‐PEG microparticles are promising as drug carriers due to their biocompatibility, controlled release properties, and ability to protect the encapsulated drug from degradation. The CCD‐RSM approach allows systematic investigation and optimization of several formulation and process variables, including polymer concentration, PCL‐PEG weight ratio, and applied voltage on drug release behavior. In addition, the effect of rheology and electrical conductivity of polymer fluid on the size of particles obtained from electrospraying was investigated. The effect of adding folic acid and doxorubicin in the optimized sample of nanoparticles and the effect of different concentrations of doxorubicin were investigated, and SEM, DLS, and FTIR techniques were used to characterize the microparticles, and the MMT test was performed to evaluate their cytotoxicity. The results showed that the optimized formulation is effective for sustained drug release over a long period for drug delivery applications.

Synthesis and characterization of transition metals (Mn, Fe, Co, Ni) doped tin oxide for magnetic and antimicrobial studies

Dilute magnetic semiconductor oxides (DMSOs) are attractive prospects for improved charge and spin degrees of freedom control. The current research presents an overview of the structural analysis and magnetic characteristics of DMSOs based on binary metal oxide nanomaterials with various ferromagnetic or paramagnetic dopants, such as Mn, Fe, Co, and Ni, which display increased ferromagnetic behaviour at ambient temperature. The co-precipitation approach was used to create nanoparticle samples of pure SnO2, Sn0.97Mn0.03O2, Sn0.97Fe0.03O2, Sn0.97Co0.03O2, and Sn0.97Ni0.03O2. The emission spectra for the high, wide emission band are 366 nm and 655 nm. Room temperature magnetic hysteresis loops for Mn, Fe, and Ni-doped SnO2 indicate ferromagnetic behaviour when compared to pure and Co-doped SnO2, with Sn0.97Mn0.03O2, Sn0.97Fe0.07O2, and Sn0.97Ni0.03O2 samples exhibiting increased coercivity and retentivity. The antibacterial activity of pure SnO2, Sn0.97Mn0.03O2, Sn0.97Fe0.03O2, Sn0.97Co0.03O2, and Sn0.97Ni0.03O2 nanoparticles was determined.

Electrical characteristics of different concentration of silica nanoparticles embedded in epoxy resin

In this study, modified epoxy nanocomposite was produced by incorporating SiO2 nanoparticles of 15–30 nm in size, with different concentrations ranging from 1 to 20 wt%. The electrical properties of the epoxy nanocomposite were measured at room temperature in the frequency range of 10−2–107 Hz. To determine the impact of nanoparticles on the epoxy composition, scanning electron microscopy-energy dispersive x-ray spectroscopy (SEM-EDS), Fourier transform infrared spectra (FTIR) spectroscopy, and Raman spectroscopy were conducted. With an increase in filler (SiO2 nanoparticles) content, the electrical characteristics of the epoxy nanocomposite exhibited multiple changes. At low concentrations, all electrical properties experienced a notable increase. The epoxy with 15 wt% of SiO2 nanoparticles samples had a lower permittivity, loss number, conductivity, and capacitance than the unfilled epoxy. At medium concentrations (5 to 15 wt%), the formation of immobilized nanolayers has an impact on permittivity, loss number, conductivity, and capacitance, which have decreased; impedance and modulus increased. The initiation of contact between the nanofillers at a concentration of 20 wt% leads to the formation of continuous interfacial conductive pathways, resulting in a dramatic increase in the permittivity, conductivity, and capacitance of the composites, while concurrently reducing impedance.

Study of structural, morphological and optical properties of Mn+2 doped CdS nanoparticles synthesized at various doping concentration

Manganese-doped cadmium sulphide semiconductor nanoparticles (CdS: Mn) NPs have been created utilizing a microwave-assisted solvothermal technique at different Mn concentrations (0, 1%, 3%, and 5%). The chemicals utilized for the preparation of Mndoped CdS nanoparticles were sodium sulphide (Na2S.xH2O), manganese chloride (MnCl2.4H2O), and cadmium acetate (CH3COO)2Cd., H2O). To determine the structural dimensions of the generated nanoparticles, the Debye-Scherer equation was used to calculate the average crystallite size at the full-width half maximum (FWHM) of the diffraction peaks. FTIR spectra analysis was used to look at the various functional and vibrational groups present in the Mn-doped CdS nanoparticle sample. The structure features of the produced nanoparticles have been examined using X-ray diffraction patterns. Energy dispersive X-rays were employed to ascertain the chemical composition of the synthesized nanoparticles. The optical properties and quantification of the energy band gap of the nanoparticles have been done using UV-V spectroscopy. According to XRD calculations, the cubic zinc-blend structure of the generated NPs had a crystal size of between 4 and 7 nm. By using EDX spectroscopy, the incorporation of Mn at the CdS lattice was confirmed.

Bottom up anatase monodisperse nanoparticles grown on sepiolite showing high thermal stability and optimal optical properties for self-cleaning applications

Powder samples of anatase monodisperse nanoparticles (np's) have been in-situ synthesized from sepiolite microparticles doped with TiIV. The role of this clay is double, by one hand, it acts as a chemical reactor, and on the other hand, it becomes a solid substrate for particles, which pin them up avoiding Ostwald ripening process on heating. In this work we show the high thermal stability of these metastable anatase particles up to 850 °C, around 200 °C above the anatase/rutile transformation for ordinary powder particles. Relevant information about the electron bandstructure has been obtained both, by optical diffuse reflectance and emission spectroscopy, which revealed the nature of photon absorption and recombination around the band-gap which determine the utility of this materials as a self-cleaning agent for solid materials.

Analysis of Brownian motion trajectories of non-spherical nanoparticles using deep learning

As nanoparticles are being put to practical use as useful materials in the medical, pharmaceutical, and industrial fields, the importance of technologies that can evaluate not only nanoparticle populations of homogeneous size and density but also those of rich diversity is increasing. Nano-tracking analysis (NTA) has been commercialized and widely used as a method to measure individual nanoparticles in liquids and evaluate their size distribution by analyzing Brownian motion. We have combined deep learning (DL) for NTA to extract more property information and explored a methodology to achieve an evaluation for individual particles to understand their diversity. Practical NTA always assumes spherical shape when quantifying particle size using the Stokes–Einstein equation, but it is not possible to verify whether the measured particles are truly spherical. We developed a DL model that predicts the shape of nanoparticles using time series trajectory data of BM obtained from NTA measurements to address this problem. As a result, we were able to discriminate with ∼80% accuracy between spherical and rod-shaped gold nanoparticles of different shapes, which are evaluated to have nearly equal particle size without any discrimination by conventional NTA. Furthermore, we demonstrated that the mixing ratio of spherical and rod-shaped nanoparticles can be quantitatively estimated from measured data of mixed samples of nanoparticles. This result suggests that it is possible to evaluate particle shape by applying DL analysis to NTA measurements, which was previously considered impossible, and opens the way to further value-added NTA.

Investigation of sunlight driven SPR assisted photocatalytic activity of Ag doped SnO2 nanoparticles

Photocatalysis triggered by visible light has emerged as a viable method for addressing environmental pollution and the energy crisis in our society. Numerous metal oxide semiconductors are transformed into visible light active photocatalysts by adopting some straightforward methods. One such efficient way of creating a visible light active photocatalyst is doping a pure semiconductor with plasmonic metal nanoparticles. Our work thoroughly investigates the photocatalytic properties of pure SnO2 nanoparticles (NP) and SnO2 doped with 1%, 3%, and 5% ‘Ag’ under sunlight. These samples are prepared using a straightforward sol–gel approach, followed by a hydrothermal procedure. To examine the different properties and morphology of the synthesized samples, several analytical tools, including UV–visible spectrometer, XRD, XPS, TEM, PL spectrometer and FTIR are used. Analysis of UV-visible absorbance spectra shows a noticeable narrowing of the band gap with increased ‘Ag’ doping. XRD analysis confirms the tetragonal structure of all samples. Methyl orange (MO) dye is used as an imitation of an organic pollutant to examine the photocatalytic activity under sunlight. When compared to pure SnO2 NP, every ‘Ag’ doped SnO2 NP sample exhibits a considerable improvement in the photodegradation of methyl orange. Analysis of PL spectra of SnO2 NPs doped with ‘Ag’ suggests that the major causes of this enhancement in photocatalysis are surface defects and the surface plasmon resonance (SPR) effect caused by ‘Ag’ doping. The scavenging test claims that the holes are the primary and the superoxide radicals are the secondary reactive species which are responsible for MO degradation under sunlight.

Synthesis of Metal Nanoparticles Encapsulated with Skewered Porphyrins Assembled by Siloxane Coupling

A protocol for encapsulation of metal nanoparticles with organic shells of porphyrin molecules via silane coupling is described. A strategy with silicon tetrachloride was used to produce a skewered arrangement of porphyrins that are linked through a central silicon atom by siloxane, Si-O-Si bridges. The planar macrocycles align cofacially to surround the periphery of metal nanoparticles (e.g. gold, iron oxide). Skewered ‘shish kebob’ assemblies of porphyrins form an encapsulating shell by attachment to metal cores with silicon-oxygen-metal bridges. Free-base porphyrins were skewered through siloxane coupling using SiCl4, with the silicon atom inserted to the center of the macrocycles. The Si atom binds to the four nitrogens at the center of the macrocycles, and also links to adjacent macrocycles through siloxane bridges. Iron and gold nanoparticles were used as core materials, while the organic shells were prepared with tetraphenyl porphyrin or octaethyl porphyrin. The thickness of the shells can be tuned by synthetic parameters such as concentration and immersion intervals. Structural changes were tracked using UV/Vis spectroscopy to evaluate spectral shifts. Nanoparticle samples were examined with tapping-mode atomic force microscopy to directly view changes in the size and shapes of nanoparticles before and after encapsulation with porphyrins. Phase images enabled sensitive mapping of the nanoparticle composition, revealing a soft organic shell surrounding the hard metal core. The synthetic approach with skewering porphyrins to metal nanoparticles should be generic for preparing metal core-shell nanoparticles encapsulated with shells of macrocyclic porphyrinoid molecules.

Investigating the size-dependent structural, optical, dielectric, and photocatalytic properties of benign-synthesized ZnO nanoparticles

Zinc oxide (ZnO) plays a vital role in numerous technological facets of semiconductors. Due to its captivating characteristics, it has garnered considerable interest in a diverse array of applications. In this study, the egg albumen-facilitated bio-template approach was utilized to fabricate ZnO nanoparticles, aiming to investigate the impact of varying albumen concentration ratios on the crystal structure, dimensions, and shape of the resulting ZnO nanoparticles. This approach provides more precise customization of the dimensions and configuration of the nanocrystals and is compatible with most documented physical techniques. Exploring the morphological impacts of unadulterated or altered zinc oxide nanocrystals on photocatalytic performance is crucial for maximizing solar energy absorption and utilization. However, this aspect has yet to receive much attention in previous studies. The photocatalytic rate was discovered to be independent of the ZnO particle size, but the geometry factor is of paramount significance. ZnO with a nanopencil shape exhibited a minimum of 1.81 times higher efficiency than spherical particles. Furthermore, the dielectric characteristics of ZnO nanoparticles (NPs) were investigated across a frequency range of 75 kHz to 7 MHz, considering the dependence on particle size. As the dimensions of the ZnO NPs diminish, there is a gradual rise in the dielectric permittivity, increasing from 20 to 82 with the escalation in frequency. In the context of ZnO nanoparticles (NPs), the Maxwell- Wagner polarization model can elucidate the phenomenon of robust interfacial polarization, particularly as the ZnO size diminishes. As the frequency increases, the AC conductivity exhibits a gradual augmentation. Likewise, in relation to the dielectric constant and losses, the electrical conductivity characteristics of all ZnO NPs samples exhibit a reliance on the size of the crystals, where a reduction in crystal size corresponds to a decrease in electrical conductivity. The utilization of eco-friendly nanomaterials is anticipated to pave the way for novel possibilities in their exceptional electronic applications as storage materials.

The Optimizing of Prefabricated Solar Cells by Dual Plasmonic Nanoparticles

Background: The quest for improving the efficiency of solar cells has garnered considerable attention in numerous scientific investigations. One promising approach involves utilizing plasmons generated by metal nanoparticles to enhance the performance of photovoltaic solar cells.
 Materials and Methods: High-purity gold nanoparticles (AuNPs), silver nanoparticles (AgNPs), and a combination of both were synthesized using pulsed laser ablation in distilled water. Subsequently, these nanoparticles were deposited onto silicon (Si) substrates and pre-existing Si homo-junction photovoltaic cells.
 Results: The optical analysis of the prepared nanoparticle suspension revealed distinct plasmonic bands located at approximately 400 nm and 523 nm wavelengths for AgNPs and AuNPs, respectively. In the case of the AuNPs:AgNPs mixture, two plasmonic bands were observed, corresponding to the presence of both types of metal nanoparticles. The X-ray diffraction (XRD) analysis of the deposited nanoparticle samples on Si wafers demonstrated a polycrystalline structure for all samples. Scanning electron microscopy (SEM) imaging displayed uniformly distributed spherical Au nanoparticles on the substrate, while AgNPs exhibited some aggregations.
 Conclusion: The photovoltaic (PV) solar cells demonstrated an enhanced performance, attributed to the ability of the plasmonic nanoparticles to facilitate increased light absorption or enhance surface conductivity. The combination of silver and gold particles holds promise for solar surface coating, further optimizing the cells to capture a greater amount of solar radiation within their plasmon peaks. This study highlights the potential of plasmonic nanoparticles to enhance the efficiency of previously prepared PV cells.

Synthesis of silver nanoparticles for use in conductive inks by chemical reduction method

In this study, the chemical reduction method was applied to synthesize silver nanoparticles used to prepare conductive inks. The two variables of polyvinylpyrrolidone (PVP)-stabilized mole in the 0.01–0.03 mol range and hydrazine reducing mole in the 0.1–0.5 mol range, along with constants such as precursor mole (silver nitrate), complexing mole (ethylene diamine) and solvent mole (water), were used. Nine random samples proposed by the Design Expert software were examined and studied. X-ray diffraction (XRD) patterns, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and dynamic light scattering (DLS) were then used to characterize and evaluate the synthesized nanoparticles. According to the results obtained by XRD, FE-SEM and TEM analyses, the sample with 0.025 mol and 0.3 mol PVP had the minimum size of silver nanoparticles, which was around 20 nm, so it was chosen as the optimal sample for further research. The conductive ink was also prepared with the optimal sample of silver nanoparticles in 40% by weight and then characterized and evaluated by applying ultraviolet–visible (UV–Vis), simultaneous thermal analysis (STA), FE-SEM and electrical conductivity analysis. Finally, conductive ink was applied to polyethylene terephthalate (PET) and acrylonitrile butadiene styrene (ABS) substrates. The surface electrical resistance of conductive ink on PET and ABS substrates was then measured at about 6.4 Ω and 2.2 Ω, respectively.

Compact and modular system architecture for a nano-resonator-mass spectrometer.

Mass measurements in the mega-to giga-Dalton range are essential for the characterization of natural and synthetic nanoparticles, but very challenging to perform using conventional mass spectrometers. Nano-electro-mechanical system (NEMS) based MS has demonstrated unique capabilities for the analysis of ultra-high mass analytes. Yet, system designs to date included constraints transferred from conventional MS instruments, such as ion guides and high vacuum requirements. Encouraged by other reports, we investigated the influence of pressure on the performances of the NEMS sensor and the aerodynamic focusing lens that equipped our first-generation instrument. We thus realized that the NEMS spectrometer could operate at significantly higher pressures than anticipated without compromising particle focusing nor mass measurement quality. Based on these observations, we designed and constructed a new NEMS-MS prototype considerably more compact than our original system, and which features an improved aerodynamic lens alignment concept, yielding superior particle focusing. We evaluated this new prototype by performing nanoparticle deposition to characterize aerodynamic focusing, and mass measurements of calibrated gold nanoparticles samples. The particle capture efficiency showed nearly two orders of magnitude improvement compared to our previous prototype, while operating at two orders of magnitude greater pressure, and without compromising mass resolution.

Enhancing the Spectral Characteristics of Rhodamine 610 Laser Dye Doped with Chemically Prepared Gold Nanoparticles

In this study, gold nanoparticle samples were prepared by the chemical reduction method (seed-growth) with 4 ratios (10, 12, 15 and 18) ml of seed, and the growth was stationary at 40 ml. The optical and structural properties of these samples were studied. The 18 ml seed sample showed the highest absorbance. The X- ray diffraction (XRD) patterns of these samples showed clear peaks at (38.25o, 44.5o, 64.4o, and 77.95o). The UV-visible showed that the absorbance of all the samples was in the same range as the standard AuNPs. The field emission-scanning electron microscope (FE-SEM) showed the shape of AuNPs as nanorods and the particle size between 30-50 nm. Rhodamine-610 (RhB) was prepared at 10-5 M concentration, the optical measurements were studied, AuNPs and RhB were mixed at ratios (1:1, 1:2, 1:3), and the fluorescence measurements were done. Full width at half maximum (FHWM) and the intensity of RhB after mixing were changed, and this result showed significant efficacy for many applications. The study shows that this mixing could be used after doping with polymer as a random gain medium or saturation absorber for pulse laser generation.

Synthesis and characterization of borophene for future applications

Distinctive nature, optical and electrical properties of borophene made it an attractive material for research. In this regard, borophene nanoparticles (NPs) have been synthesized in this research in three dispersed media using a sonochemical process from pure boron in three dispersed media such as acetone, methanol and benzyl. The prepared borophene NPs samples were characterized by Raman spectroscopy, FTIR (Fourier Transformed Infrared Spectroscopy), SEM (Scanning Electron Microscopy), Zeta Potential, and UV (Ultraviolet–Visible Spectroscopy). SEM analysis confirmed the formation of borophene NPs on the surface of boron. The synthesized borophene NPs were irregular in shape, and the sizes varied from 400 to 650 nm. Spectra of borophene NPs were visible by Raman spectroscopy from nearly 104 cm−1 to 106 cm−1. The FTIR analysis identified the presence of different functional groups. Less than a 4 eV band gap was identified, which is helpful for semiconductor applications. Peaks identified by the UV–vis analysis confirmed the formation of borophene NPs.The obtained results can be beneficial for electronic applications.

Effect of pH of Ganoderma lucidum aqueous extract on green synthesis of silver nanoparticles

Perspective applications of Ag nanoparticles (NPs) stimulate intense research on their affordable synthesis, including green routes. The use of fungi extracts has advantages over other organisms, because of their relatively easy isolation and higher efficiency in a reduction of metal ions and NP formation. Here we report mycosynthesis of AgNPs based on Ganoderma lucidum fruit body extract with different pH values as the bioreducing and stabilising agent. Stable NPs colloids with distinct plasmonic resonance peaking at 408–418 nm are obtained by using photoreduction in a broad pH range (5 to 11). Synthesis efficiency drops only at very acidic conditions, pH = 2.5. The NP size and morphology are studied by dynamic light scattering and scanning electron microscopy. An analysis of FTIR spectra of pure analyte and NP sample indicates that stabilisation of the AgNPs by the components of Ganoderma lucidum extract may take place via forming chemical bonds with the NP surface. These bio-friendly AgNPs are both optically and chemically active, as inferred from surface-enhanced Raman scattering of a standard dye analytes and charge transfer-induced quenching of the photoluminescence of both dye and inorganic NPs, and can be studied for various applications which require direct access to the AgNP surface.

Modified Hybrid Catalyst of Fe<sub>3</sub>O<sub>4</sub>/Cellulose Nanocomposite-Base and their Potential Application as Dye Waste Adsorbent

The population growth and the industrial revolution caused severe environmental pollution, especially pollution of clean water availability. Several ways have been conducted to overcome the pollution of clean water availability, one of which is by the adsorption of metal and cellulose-based waste materials as a hybrid catalyst. This study aims to fabricate and modify a hybrid catalyst composed of cellulose in the form of nanosized fibrils. Cellulose can be used as a catalyst by incorporating Fe from magnetite (Fe3O4) and can work effectively as an adsorbent for methylene blue (MB) dye waste. The method used in this research is a modified coprecipitation method by combining cellulose and Fe3O4 nanoparticles. Hybrid Catalyst of Fe3O4/Cellulose Nanocomposite-Base has been successfully characterized by using XRD, SEM-EDX, and UV-Vis, respectively to determine the particle structure, morphology, and adsorption capacity of the sample. The results of data analysis showed that Fe3O4/Cellulose could purify MB solution depending on the ratio of Fe3O4 and the mass of cellulose used. The higher the mass ratio of cellulose to Fe3O4, the absorbance value of the Fe3O4/Cellulose nanoparticle sample increases.

Analysis of Crystallographic Structures and Properties of Silver Nanoparticles Synthesized Using PKL Extract and Nanoscale Characterization Techniques.

In this cutting-edge research era, silver nanoparticles impose a substantial impact because of their wide applicability in the field of engineering, science, and industry. Regarding the vast applications of silver nanoparticles, in this study, the crystallographic characteristics and nanostructures of silver nanoparticles extracted from natural resources have been studied. First, biosynthetic silver nanoparticles were synthesized using the Pathor Kuchi leaf (PKL) extract as a mediator, and their crystal structures and characteristics were analyzed by UV-visible absorption spectroscopy, Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), and energy-dispersive X-ray (EDX) analysis. The average crystallite size of the synthesized silver nanoparticle was determined to be 20.26 nm, and also the lattice strain, intrinsic stress, and dislocation density were measured to be 2.19 × 10-3, 0.08235 GPa, and 3.062045 × 10-3/nm2, respectively. Further, the prepared sample of silver nanoparticles shows four peaks in the X-ray diffraction pattern, which correspond to the (111), (200), (220), and (311) face-centered cubic (FCC) crystalline planes. The outstanding finding of this work was that when the lattice parameters of the precursor were increased, the volume of the material did not considerably change, but the particle size decreased. Second, it was clearly demonstrated that this straightforward method is a clean, cost-effective, environmentally sustainable, nontoxic, and efficient route for the synthesis of silver nanoparticles (Ag NPs) using PKL leaf at ambient temperature, which also satisfies the green chemistry requirements. Finally, this study demonstrates the scope for the production of silver nanoparticles using low-cost natural resources.