Morphology Of ZnO Research Articles

Effects of ZnO morphology on tribological behaviors of polyarylene ether nitrile composites

Effects of ZnO morphology on tribological behaviors of polyarylene ether nitrile composites

ZnO/CuO heterojunction prepared by sol-gel: characterization and photocatalytic evaluation

ZnO, CuO and the ZnO/CuO heterojunction were prepared using zin acetate and copper acetate by sol-gel method. The materials were characterized by: TGA, XRD, XPS, SEM, TEM, EDS and UV-Vis. The heterostructure showed a synergistic effect compared to pure materials. The XPS results confirm the existence of a heterostructure. The morphology is a combination of characteristic morphologies of ZnO and CuO. The bandgap of ZnO decreases with the incorporation of CuO. The photocatalytic efficiency of the heterostructure increases; the degradation percentages were better for the heterostructures in both radiations: Ultraviolet and Visible.

Exceptional photocatalytic performance of hexagonal ZnO nanorods for anionic and cationic dyes degradation

This study presents an in-depth investigation of zinc oxide hexagonal nanorods (ZnO NRs) synthesized via a hydrothermal approach at three pH basic values conducted in high-pressure laboratory reactor provided by Parr Instrument Company. The research evaluates the catalytic properties of the ZnO NRs, highlighting their potential for environmental applications. The as-fabricated samples are characterized by various techniques including the X-ray diffraction (XRD), UV–visible spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) analysis, Field emission-scanning electron microscopy (FE-SEM), energy dispersive X-ray analysis (EDAX) and high-resolution transmission electron microscopy (HR-TEM). Rietveld refinement of X-ray diffraction data reveals the formation of high-purity hexagonal Wurtzite-type ZnO phase. Further, it is investigated that by decreasing the pH values, the grain size of ZnO NRs increases from 25.70 nm to 29.91 nm. SEM analyses further confirmed the hexagonal nanorod-shaped morphology of ZnO. The photocatalytic degradation performance of the as-fabricated ZnO NRs for Methylene Blue (MB) and Methyl Orange (MO) dyes increased with the increase in pH value, reaching almost 95 % and 64 %, respectively, after 30 min of UV irradiation. The optimum degradation is achieved at a pH value of 11.

Phyto-mediated synthesis of ZnO/attapulgite nanocomposites using C. limon peel extract for enhancing the resistance against multidrug-resistant bacteria and fungi

ZnO have great potential in combating multidrug-resistant (MDR) bacteria, however, green synthesis and activity regulation still face challenges. In this study, we designed a green bioinspired method mediated by C. limon peel extract to synthesise a series of attapulgite (APT) supported ZnO nanocomposites for enhancing the resistance against MDR pathogenic bacterial and fungal, in which the structure and morphology of ZnO was regulated by APT inducing heterogeneous nucleation of ZnO, thus enhancing the antibacterial activity of the nanocomposites. XRD and TEM analysis demonstrated that ZnO/APT with a unique peg-top-like morphology and well-defined crystal structure was successfully synthesized via the regulation of Zn2+ ions concentration. XPS results confirmed that the oxygen vacancy increased significantly compared with the pure ZnO (has a cubic shape) due to the structural modulation of ZnO induced by APT. The obtained ZnO/APT nanocomposites exhibited excellent biocompatibility and enhanced antibacterial efficacy with a complete inhibition at a concentration of 0.125 mg/mL for MRSA, a high inhibitory rate of 94.68 ± 1.43 % at a concentration of 0.5 mg/mL for ESBLs-E. coli, and the antifungal rate against C. albicans was found to be 95.59 ± 1.08 % at a concentration of 0.25 mg/mL. In addition, the ZnO/APT had a good hemostatic effect and enhanced biocompatibility compared to pure ZnO. The study provides a green way to design efficient ZnO antibacterial nanomaterials with remarkable antimicrobial efficacy and lower cytotoxicity, and the ZnO/APT nanocomposite is potential for clinical applications.

Role of Sulfur in Enhancing UV‐Light Absorption and Photoelectrochemical Performance of ZnO/N,S‐doped CQDs Nanocomposite

AbstractThe modification of ZnO, such as transforming it from 1‐D to 3‐D nanostructures or compositing it with carbon‐based materials, has been extensively explored to enhance light energy harvesting and reduce electron‐hole recombination‐key limitations of ZnO. Herein, the effect of different composite materials, specifically nitrogen‐doped carbon quantum dots (N‐CQDs) and nitrogen, sulfur‐doped carbon quantum dots (N,S‐CQDs), on ZnO's morphology and photocurrent response was studied. Various morphologies were synthesized on conductive glass substrate using a one‐pot hydrothermal method, including flower‐like structure for ZnO/N‐CQDs (∼d = 0.9 µm) and multilayered microspheres for ZnO/N,S‐CQDs (∼d = 1.1 µm). The inclusion of sulfur atoms in the composite resulted in a reduced bandgap value from 3.22 to 3.11 eV, along with enhanced light absorption efficiency and improved separation of photogenerated electron‐hole pairs. Furthermore, the crystallinity of ZnO/N,S‐CQDs was significantly enhanced compared to ZnO without sulfur doping. These improvements were reflected in the photoelectrochemical (PEC) measurements, where ZnO/N,S‐CQDs showed a current density of 21.8 µA/cm2 at 0.5 V (vs. Ag/AgCl), which is 5.5 times higher than that of ZnO/N‐CQDs (4.0 µA/cm2). These findings demonstrate that sulfur doping improves photocatalytic efficiency, making 3D ZnO/N,S‐CQDs a promising candidate for various UV‐driven PEC applications.

Effect of glucose addition on the morphology and activity of ZnO supported on mesoporous zeolite SBA-15 for the removal of hydrogen sulfide

Zinc oxide with its high equilibrium constant for sulfidation, can be utilized to purify H2S-containing gases, but its low kinetics at room temperature limits its sulfur loading capacity. This study use glucose as an organic additive and carbon source to prepare carbon doped ZnO adsorbents with different ZnO loadings (5–20 wt%) through initial wet impregnation. It was observed that the sulfur capacity of 15 wt% Zn/SBA-15-G (10.9 mg/g) was approximately 1.65 times higher than that of 15 wt% Zn/SBA-15 (6.6 mg/g). This improvement was attributed to the use of glucose, which led to better ZnO dispersion, a narrower distribution of ZnO particle size, and the formation of C-O-Zn bonds that increased the number of hydroxyl groups on the ZnO surface. DFT calculations also indicated that carbon doping could lower the activation energy of the reaction between ZnO and H2S and shorten the reaction pathway. Consequently, the prepared ZnO adsorbent demonstrated enhanced desulfurization efficiency at room temperature. Furthermore, regeneration experiments conducted on the desulfurizer after use revealed that achieving complete regeneration is a challenge.

Morphological impact on the supercapacitive performance of nanostructured ZnO electrodes

This study investigated the influence of the ZnO morphology on the energy storage capacity of symmetric supercapacitor devices, focusing on the defect centers present in the materials due to morpho-structural differences. Thus, ZnOs with five different morphologies were synthesized with varying methods in which the nanoparticles have the form of flowers, bullets, pyramids, hexagons, and rods. All materials were thoroughly characterized by scanning/transmission electron microscopy, X-ray diffraction, and spectroscopic techniques like photoluminescence, UV–Vis, Raman, and electron paramagnetic resonance spectroscopy. Subsequently, the ZnO-based materials were assembled in symmetric supercapacitor devices to test their energy storage capabilities. The ZnO with nanorod and hexagonal morphologies showed the best specific capacity (180 and 142 F/g), energy density (25 and 19 Wh/kg), and power density (211 and 252 kW/kg) values. The importance of the defect centers in the materials was highlighted, where the ratio between the Zn and O vacancies, evidenced by EPR spectroscopy, plays a crucial role in the ZnO materials’ energy storage capacity. The Raman results support the proposed model, which underlines the importance of oxygen vacancies. In contrast, BET measurements show that the specific surface area of the morphologically distinct ZnO materials does not change drastically, validating the importance of the defect centers in the materials. A so-called “bottle-neck” effect is proposed to describe the relation between the paramagnetic vacancies and the electric properties of the materials.

Role of Morphology on Zinc Oxide Nanostructures for Efficient Photoelectrochemical Activity and Hydrogen Production.

Energy generation today heavily relies on the field of photocatalysis, with many conventional energy generation strategies now superseded by the conversion of solar energy into chemical or thermal energy for a variety of energy-related applications. Global warming has pointed to the urgent necessity of moving away from non-renewable energy sources, with a resulting emphasis on creating the best photocatalysts for effective solar conversion by investigating a variety of material systems and material combinations. The present study explores the influence of morphological changes on the photoelectrochemical activity of zinc oxide nanostructures by exploiting electrodeposition and capping agents to control the growth rates of different ZnO facets and obtain well-defined nanostructures and orientations. A zinc nitrate (Zn (NO3)2) bath was used to electrodeposit ZnO nanostructures on an indium tin oxide glass (ITO) substrate at 70 °C with an applied potential of -1.0 V. Ethylenediamine (EDA) or ammonium fluoride (NH4F) were added as capping agents to the zinc nitrate bath. Extensive evaluation and characterization of the photoelectrochemical (PEC) capabilities of the resulting morphology-controlled zinc oxide nanostructures confirmed that altering the ZnO morphology can have positive impacts on PEC properties.

Biogenic synthesis and characterization of antimicrobial, antioxidant, and antihemolytic zinc oxide nanoparticles from Desertifilum sp. TN-15 cell extract

Cyanobacteria, being a prominent category of phototrophic organism, exhibit substantial potential as a valuable source of bioactive compounds and phytonutrients, including liposomes, amino derivatives, proteins, and carotenoids. In this investigation, a polyphasic approach was employed to isolate and characterize a newly discovered cyanobacterial strain from a rice field in the Garh Moor district of Jhang. Desertifilum sp. TN-15, a unique and less explored cyanobacterial strain, holds significant promise as a novel candidate for the synthesis of nanoparticles. This noticeable research gap underscores the novelty and untapped potential of Desertifilum sp. TN-15 in the field of nanomedicine. The characterization of the biogenically synthesized ZnO–NPs involved the application of diverse analytical techniques. Ultraviolet–visible spectroscopy revealed a surface plasmon resonance peak at 298 nm. Fourier transform infrared spectral analysis was utilized to confirm the involvement of biomolecules in the biogenic synthesis and stability. Scanning electron microscopy was employed to probe the surface morphology of the biogenic ZnO–NPs unveiling their size of 94.80 nm and star-shaped. Furthermore, X-ray diffraction analysis substantiated the crystalline nature of ZnO–NPs, with a crystalline size measuring 46 nm. To assess the physical stability of ZnO–NPs, zeta potential and dynamic light scattering measurements were conducted, yielding values of + 31.6 mV, and 94.80 nm, respectively, indicative of favorable stability. The antibacterial capabilities of Desertifilum sp. TN-15 are attributed to its abundance of bioactive components, including proteins, liposomes, amino derivatives, and carotenoids. Through the synthesis of zinc oxide nanoparticles (ZnO–NPs) with this strain, we have effectively used these chemicals to generate nanoparticles that exhibit noteworthy antibacterial activity against Staphylococcus aureus (MIC: 30.05 ± 0.003 µg/ml). Additionally, the ZnO–NPs displayed potent antifungal activity and antioxidant properties, as well as significant antihemolytic effects on red blood cells (IC50: 4.8 µg/ml). Cytotoxicity assessment using brine shrimps revealed an IC50 value of 3.1 µg/ml. The multifaceted actions of the biogenically synthesized ZnO–NPs underscore their potential applications in pharmacological and therapeutic fields. This study proposes a novel method for ZnO–NPs production utilizing the recently identified cyanobacterial strain Desertifilum sp. TN-15, highlighting the growing significance of biological systems in the environmentally friendly fabrication of metallic oxide nanomaterials.

Tailoring Sb-F doped ZnO nanoparticles for dual-functionality: Photocatalytic and supercapacitor applications

In the present work, pure zinc oxide nanoparticles (ZnO NPs), antimony doped ZnO nanoparticles (Sb-ZnO NPs), fluorine doped ZnO nanoparticles (F-ZnO NPs), and antimony and fluorine co-doped ZnO nanoparticles (Sb/F-ZnO NPs) with various dopant concentrations are synthesized by co-precipitation method. The optical, structural, morphological, photocatalytic, and electrochemical activities of ZnO nanostructures by the influence of Sb and F doping were investigated. XRD showed crystallite size decreased with increasing Sb/F content, while BET showed 64.25 m2/g surface area for ZnO-5 %Sb-10 %F. SEM and TEM images suggesting Sb/F doping changed the ZnO morphology from spherical to bricks-built and nanorod-built flower structures. XPS verified Sb (+3) and F (−1) oxidation states, while absorption spectroscopy showed increased energy bandgap with 5 % Sb and 10 % F doping in ZnO. The photocatalytic activity for mixture of congo red, rhodamine B, and methylene blue are closer to real polluted water. All the samples exhibited good photocatalytic activity for the methylene blue with degradation efficiency reaching to 99 %. At a constant current density of 1 A/g, symmetric supercapacitors utilizing Sb/F-ZnO electrodes exhibited a specific capacitance of 762 Fg−1, underscoring their superior electrochemical performance and potential for advancing energy storage technologies. Further, physiochemical and electrochemical properties of ZnO can be perfectly tuned by the optimal setting for co-doping in ZnO up to 5 % Sb and 10 % F by the co-precipitation approach.

Zinc oxide morphology-dependent CuOx-ZnO interactions and catalysis in CO oxidation and CO2 hydrogenation

CuO/ZnO catalysts with different ZnO morphologies, i.e. nanoplates (p-ZnO) and nanorods (r-ZnO), have been prepared to test for CO oxidation and CO2 hydrogenation. Strong morphology-dependent CuOx-ZnO interactions were observed, which are tightly associated with the ZnO morphology. p-ZnO predominantly exposing polar {002} facets greatly promote the CuOx-ZnO interactions, contributing to the stabilities of CuOx/ZnO catalysts in both reactions. Experimental evidences reveal that CuO-ZnO interfaces act as the active sites in CO oxidation. CuO/p-ZnO catalyst with stronger CuO-ZnO interactions can facilitate the generations of fine CuO and interfacial Cu(I) species, responsible for the adsorption and reactivity of CO and subsequently the high (intrinsic) activity in CO oxidation. However, CuO/ZnO catalysts undergo in situ restructuring to generate Cu/ZnO in CO2 hydrogenation, whose catalytic performance is determined by the key step of CO2 activation. Consequently, Cu/r-ZnO catalyst possessing more surface basic sites exhibits better catalytic performance. These results greatly deepen the fundamental understanding of Cu-based catalysts in both reactions and broaden the concept of morphology-dependent catalysis of oxide-based nanocrystal catalysts that varies with the reactions catalyzed.

A novel hydrothermal approach to preparing ZnO flower-like using CQDs as growth seeds

This study presents a new synthesis route to prepare ZnO flower-like particles. Firstly, carbon quantum dots (CQDs) were prepared hydrothermally, using the Malva sylvestris flower as the sole carbon source. Subsequently, flower-like particles of ZnO/CQDs were synthesized using CQDs seeds and the same hydrothermal process. The efficiency of the redox process of solar excitation was measured by reducing the dye methylene blue (MB). The SEM and TEM characterization shows ZnO flower-like particles of around 1.5 µm whose petals are formed by crystallites of around 10 nm. ZnO nanocrystals appear embedded in an amorphous carbon matrix. TEM images show carbon quantum dots on the surface of ZnO flowers. Without using Malva sylvestris, ZnO morphologies are not formed; instead, 2D nanolaminates appear. The ZnO/CQDs nanocomposite achieved 98 % MB degradation in 80 min. The small size of CQDs can be a good scenario for the growth of crystalline nanostructures using the nanocarbon seed.

Influence of (Co+Al) co−doping on structural, micro-structural, optical and electrical properties of nanostructured zinc oxide

This study investigates the effect of (Co + Al) co−doping on the physical properties of the ZnO nanoparticles, synthesized via the simple co−precipitation method. X−ray diffraction (XRD) analysis revealed a hexagonal structure for all samples, with a formation of Al2O3 phase in both Zn0.98Co0.01Al0.01O and Zn0.94Co0.01Al0.05O nanoparticles. The crystallite size increased from 26.5 nm for ZnO to 16.6 nm for Zn0.94Co0.01Al0.05O nanoparticles. Scanning electron microscopy (SEM) technique showed a notable alteration in the morphology of ZnO upon the incorporation of Al. A transition from spherical nanoparticles in ZnO and Co doped ZnO to irregular, dendritic-like structures in (Co + Al) co−doped nanoparticles is observed. Transmission electron microscopy (TEM) substantiated the presence of the Al2O3 phase in the co−doped samples. Raman and FTIR spectroscopy confirmed the incorporation of Co and Al into the ZnO lattice through the presence of Co–O–Co and Al–O bonds. Optical characterization indicated a decrease in the band gap energy from 3.18 eV in ZnO to 2.84 eV in Zn0.94Co0.01Al0.05O nanoparticles. Electrical conductivity measurements revealed an increase from 1.2 × 10−4 Ω−1 cm−1 to 1.8 × 10−3 Ω−1 cm−1 as the Al content increased from 0 % to 5 % at the frequency of 103 Hz and the temperature of 423K. Likewise, dielectric constant raised from 775 in ZnO to 5455 in Zn0.94Co0.01Al0.05O nanoparticles at the temperature 423K. These results highlight the potential of (Co + Al) co−doped ZnO nanoparticles for advanced optoelectronic applications.

Silver nanogranules-decorated ZnO hybrid nanostructures with enhanced UV photoresponses

Detecting low-power ultraviolet (UV) light is crucial for practical applications. However, 1D ZnO/Ag based photodetectors (PDs) suffer from high expenses and care due to special operating conditions, posing challenges in capturing weak light signals and response time. To overcome these limitations, we integrate ZnO nanostructures with localized surface plasmon resonance of Ag nanoparticles via a surfactant-free hydrothermal-assisted polyol method, resulting in a notable bandgap reduction. SEM analysis revealed roughly spherical nanostructures for pristine ZnO and a porous structure in ZnO@Ag, around 1.4 µm in size with small agglomerates. XRD patterns showed reduced ZnO diffraction peak intensities in ZnO@Ag, confirming their core-like ZnO morphology. The fabricated ZnO@Ag heterojunction PD on an FTO substrate resulted in notable enhancement of PD performance. The ZnO@Ag heterojunction PD demonstrated a rapid 1.77 s response time, a 0.64 s recovery time and a specific detectivity of 11×107 cmHz1/2W−1, indicating its potential for low-cost and sustainable optoelectronics.

Biogenically Synthesized ZnO and Cu-Doped ZnO Nanoparticles: Effect of Cu-Dopent Concentration and Annealing on Morphology and Optical Properties

In this work, ZnO nanoparticles and Cu-doped ZnO nanoparticles were biogenically synthesized using precipitation method in <i>Cissus quadrangularis</i> plant extract medium. The influence of Cu dopant on the crystalline structure, optical properties, and morphology of ZnO was investigated. The samples were characterized by XRD, FTIR, UV–vis spectroscopy and SEM. XRD patterns confirmed the wurtzite formation of doped and undoped ZnO nanoparticles. The average crystallite size of the neat and Cu-doped samples was ~18 nm irrespective of the amount of dopant. The annealing process enhanced the size of both the neat and Cu-doped samples. However, the influence on the size is less prominent in the Cu-doped sample than in the neat sample. The UV-visible spectral analysis shows that all the synthesized doped and undoped nano zinc oxides absorb at ~400nm. The band gap energy of Cu-doped ZnO particles was greater for unannealed samples whereas it was appreciably lowered on annealing for Cu-doped samples. SEM analysis shows rod-like morphology for the unannealed and annealed undoped zinc oxides. It is changed to flower-like morphology with the addition of 5mM Cu<sup>2+</sup> and then to nano sheet-like structure with the incorporation of higher amount of Cu<sup>2+</sup> ions. Annealing of zinc oxide samples leads to the smoothening of the surfaces with a change in morphology for the ZnO nanoparticles.

UV light-activated Eu/ZnO flower-like microsphere for detecting NO2 gas with high response

In this work, the ZnO microsphere is prepared by hydrothermal method and modified with different concentrations of Eu. The morphology of ZnO:Eu sample shows flower-like microspheres with many nanosheets. The gas performance of ZnO:Eu microsphere is investigated for detecting NO2. Compared with pure ZnO, the response of ZnO:2 % Eu sensor is increased by 8 times, and the optimal operating temperature of that is decreased to 130 °C. Especially, the gas sensing properties of ZnO:2 % Eu sensor is enhanced under UV excitation. The recovery time of ZnO:Eu sensor is reduced by 1200 s, and the response is increased by 3.6 times under UV excitation. The above results show an increase in sensor response due to doping Eu and UV excitation. At last, the possible gas mechanism of ZnO:Eu is discussed with and without UV excitation. This finding provides important guidance for UV-assisted sensors to enhance NO2 response.

Effect of Doping ZnO on Activated Carbon Prepared from Waste Paper for Photocatalytic Applications

Accumulation of untreated and unrecycled paper has a negative impact on the environment. Like liquid waste handling, paper waste handling is also still being developed. It is known that activated carbon (AC) is one of the promising adsorbents that can be used to solve the environmental issue. Activated carbon can be made from organic waste, such as waste paper. The objective of this study is to investigate the operation condition of the pyrolysis process to obtain the activated carbon. The furnace temperature was set at 400°C for 1 hour under N2 stream with a flow rate of 0.5 L/min. To provide a synergistic effect in the adsorption process, ZnO was derived from ZnCl2 as a chemical activator for making active carbon. While Zn (CH3COO)2.2H2O with different concentrations of 0.01, 0.05, and 0.1 M was grown into the pores of activated carbon. The photocatalytic activity of AC/ZnO was identified in the degradation process of methylene blue as a model of organic pollutants. X-ray diffraction (XRD), scanning electron microscope (SEM), and fourier transform infrared (FTIR) were used to characterize the product. The morphology of ZnO was observed in the form of a flower-like and occupying the surface of activated carbon. The photocatalytic activity showed that the methylene blue was completely degraded.

Antifungal Activity of ZnO Nanoparticles Synthesized from Eichhornia crassipes Extract for Construction Applications.

Fungal growth on construction materials in tropical climates can degrade aesthetics and manifestations on modern and historical sick buildings, affecting the health of their inhabitants. This study synthesized ZnO nanoparticles with enhanced antifungal properties using a precipitation method. Different concentrations (25%, 50%, and 100%) of Eichhornia crassipes aqueous extract were used with Zn(NO3)2·6H2O as the precursor to evaluate their spectroscopic, morphological, textural, and antifungal properties. X-ray diffraction confirmed the hexagonal wurtzite phase of ZnO with crystallite sizes up to 20 nm. Fourier-transform infrared spectroscopy identified absorption bands at 426, 503, and 567 cm-1 for ZnO-100, ZnO-50, and ZnO-25, respectively. Nitrogen physisorption indicated a type II isotherm with macropores and a fractal dimension coefficient near 2 across all concentrations. Polydispersity index analysis showed that ZnO-50 had a higher PDI, indicating a broader size distribution, while ZnO-25 and ZnO-100 exhibited lower PDI values, reflecting uniform and monodisperse particle sizes. FESEM observations revealed semi-spherical ZnO morphologies prone to agglomeration, particularly in ZnO-25. Antifungal tests highlighted ZnO-25 as the most effective, especially against Phoma sp. with an MFC/MIC ratio of 78 µg/mL. Poisoned plate assays demonstrated over 50% inhibition at 312 µg/mL for all tested fungi, outperforming commercial antifungals. The results indicate that ZnO NPs synthesized using E. crassipes extract effectively inhibit fungal growth on construction materials. This procedure offers a practical approach to improving the durability of building aesthetics and may contribute to reducing the health risks associated with exposure to fungal compounds.

Flexible NH3 gas sensors based on ZnO nanostructures deposited on kevlar substrates via hydrothermal method

Owing to their flexibility and high thermal resistance, para-aramid based Kevlar™ fabric substrates are an ideal candidate for obtaining flexible gas sensors for new-generation wearable technologies. The morphology of the surface of the substrate where the target gas comes into contact directly affects the important features of the sensor such as detection limit, selectivity, and response. In this context, a feasible technique is introduced to enhance the efficiency of flexible gas sensors utilizing ZnO/Kevlar™, entailing the modification of ZnO morphology. ZnO based gas sensing layers were deposited on Kevlar™ fabric substrates by a two-stage method. Initially, seed layer was produced on Kevlar™ fabric using the ultrasonic bath method, with five different seed layer processing times ranging from 1 min to 20 min. In the nucleation, all nanostructured layers were deposited by hydrothermal method with constant parameters and under the same conditions. As the seeding time was increased, nanorods (1D) formed on the surface became flakes (2D), leading to considerable improvement in NH3 gas sensing properties. The sensor with a 5-min seeding time showed a sensitivity of 49 % at an optimal operating temperature of 190 °C, while the sensor produced in 20 min showed the best response performance with 169 % at 130 °C for 50 ppm NH3 gas. The increase in seeding time not only reduced the operating temperature of the gas sensor through the conversion from 1D nanostructure to 2D, but also significantly increased the sensor response. Under constant hydrothermal conditions and solution concentration, the density per unit area increases. However, after 10 min of seeding, the length of nanorods shortens and turn into a rod-flake hybrid morphology. A superior sensor performance was demonstrated for the samples examined. The obtained results also showed that flexible Kevlar™ fabric could be a feasible and interesting substrate for nanostructured ZnO-based NH3 gas sensors.

The Effect of Different Morphologies of ZnO and Cr Doped ZnO NPs as Heterogeneous Catalyst for Biodiesel Production from Soybean Oil

The Effect of Different Morphologies of ZnO and Cr Doped ZnO NPs as Heterogeneous Catalyst for Biodiesel Production from Soybean Oil