XPS and UV–vis studies of Ga-doped zinc oxide nanoparticles synthesized by gelatin based sol-gel approach

Undoped and gallium-doped ZnO nanoparticles, (ZnO NPs) (Zn_1−xGa_xO, x=0.0, 0.03, 0.06, 0.09, 0.12, 0.15), were synthesized by a gelatin-based, sol–gel method. Structural and morphological studies of the resulting products were carried out via X-ray diffraction analysis (XRD) and transmission electron microscopy (TEM). The XRD results revealed that the sample products were crystalline with a hexagonal wurtzite phase. Furthermore, the TEM images indicated ZnO NPs having approximately spherical shapes, with their particle size distributed over the nanometer range. The XRD and TEM results also showed a decrease in crystallite and particle sizes of NPs from x=0.0 to 0.15. The size-strain plot (SSP) method was employed to study the individual contributions of crystallite sizes and lattice strain to the peak broadening of the undoped and doped ZnO NPs. The effect of doping on the optical band-gap and crystalline quality was also investigated, using ultraviolet-visible (UV–vis), X-ray photoluminescence (XPS), and spectroscopies of the pure and doped ZnO NPs. It was observed that the band-gap and O-vacancies of the doped ZnO NPs were red-shifted in comparison with those of the undoped ZnO NPs in UV–vis and XPS results.     

Optical and electrical properties of p-type Ag-doped ZnO nanostructures

Zn_1−xAg_xO nanoparticles (NPs) (x=0, 0.02, 0.04, and 0.06) were synthesized by a sol–gel method. The synthesized undoped ZnO and Zn_1−xAg_xO-NPs were characterized by X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and UV–visible spectroscopy. The XRD patterns indicated that undoped and Ag-doped ZnO crystallize in a hexagonal wurtzite structure. The TEM images showed ZnO NPs with nearly spherical shapes, with particle size distributed over the nanometer range. Evidence of dopant incorporation is demonstrated in the XPS measurements of the Ag-doped ZnO NPs. The Raman measurements indicated that the undoped and Ag-doped ZnO-NPs had a high crystalline quality. From the result of UV–vis, the band-gap values of prepared undoped and Ag-doped ZnO were found to decrease with an increase in Ag concentration. The obtained undoped and Ag-doped ZnO nanoparticles were used as a source material to grow undoped and Ag-doped ZnO nanowires on n-type Si substrates, using a thermal evaporation set-up. Two probe method results indicated that the Ag-doped ZnO nanowires exhibit p-type properties.     

Optical properties of group-I-doped ZnO nanowires

Undoped and group-I elements doped ZnO nanowires were synthesized using a thermal evaporation method. Field emission scanning electron microscopy (FESEM) results showed that, the undoped ZnO nanowires were ultra-long with uniform diameters. On the other hand, the length of the doped ZnO nanowires was in the range of some hundred of nanometers. X-ray diffraction (XRD) patterns clearly indicated hexagonal structures for all of the products. X-ray photoelectron spectroscopy (XPS) studies confirmed the oxidation states of Li, Na, K, in the ZnO lattice. An asymmetric O 1s peak indicated the presence of oxygen in an oxide layer. The effect of doping on the optical band-gap and crystalline quality was also investigated using photoluminescence (PL), UV–vis, and Raman spectrometers. The Raman spectra of the products indicated a strong E₂ (high) peak. The PL spectra exhibited a strong peak in the ultraviolet (UV) region of the electromagnetic spectrum for all of the ZnO nanowires. The UV peak of the doped ZnO nanowires was red-shifted compared to the undoped ZnO nanowires. In addition, the UV–vis spectra of the samples showed similar results compared to the PL results.     

Effect of crystallite size,Raman surface modes and surface basicity on the gas sensing behavior of terbium-doped SnO2 nanoparticles

In the present work, we report the structural, optical and gas sensing properties of Tb³⁺-doped SnO₂ nanoparticles. XRD results confirmed tetragonal rutile structure of both undoped and Tb³⁺-doped SnO₂ nanoparticles which was further confirmed from Raman results. The increase of dopant concentration resulted in decrease in crystallite size which has been confirmed from XRD and TEM results. Raman spectra exhibited bands positioned at 562 and 487 cm⁻¹ whose contribution has been found to increase with decrease in crystallite size. The shifting and broadening of Raman active bands has been explained by well-known phonon confinement model. EDS analysis inveterate presence of terbium in the doped SnO₂ nanoparticles. It has been observed that 3% doped samples exhibited optimum sensor response towards ethanol vapor. The optimum operable temperature of doped samples has been reduced as compared to undoped samples. The enhanced sensor response of doped nanoparticles is attributed to the small crystallite size, high surface basicity and enhanced contribution of Raman surface vibration modes of nanoparticles.     

Growth and characterization of the Al-doped and Al–Sn co-doped ZnO nanostructures

In the present work, well-dispersed structures of spherical-like pure ZnO, Al doped ZnO (AZO) and Al, Sn co-doped ZnO (ATZO) nanocrystals were successfully synthesized by using zinc acetate dihydrate as the starting material and also the low temperature hydrothermal process without any additional surfactant or catalytic agent. The ZnO structures were characterized by X-ray diffraction (XRD), and transmission electron microscopy (TEM). The XRD results revealed that ZnO powders have a hexagonal crystal structure and the TEM indicated that the nanoparticles self-aggregate. An X-ray photoelectron spectroscopy (XPS) study confirmed the substitution of Zn²⁺ by Sn and Al ions. Optical properties of the ZnO structures were investigated by Raman spectroscopy and room-temperature photoluminescence (PL) spectroscopy. The Raman spectroscopy results demonstrated that the doped ZnO nanoparticles had a higher crystalline quality than that of pure ZnO. Room-temperature PL spectra of these structures showed a strong UV emission peak and a relative weak green emission peak, and the UV peak of the doped ZnO nanoparticles was blue-shifted with respect to that of the undoped ZnO nanoparticles.     

Synthesis and characterization of Gd-doped SnO2 nanostructures and their enhanced gas sensing properties

In the present work, we report the influence of Gd-doping on structural, optical and gas sensing properties of SnO₂ nanoparticles. X-ray diffraction (XRD) and Raman spectroscopy studies confirmed formation of tetragonal rutile type structure of both undoped and Gd-doped SnO₂ nanoparticles. The crystallite size has been found to decrease with increase in dopant concentration which was confirmed from XRD and TEM techniques. It has been observed that Raman surface modes are directly related to the surface area of nanoparticles. Photoluminescence (PL) spectroscopy confirmed large number of oxygen vacancies in 3% Gd-doped SnO₂ nanoparticles. It has been observed that 3% doped sensor displayed exceptionally large sensor response towards ethanol which is about 27 times larger than that of undoped sensor. The optimum operating temperature of doped sensors has reduced as compared to undoped sensor. The enhanced sensor response of Gd-doped nanoparticles has been attributed to small crystallite size, large number of oxygen vacancies, high surface basicity and increased contribution of Raman surface modes. Moreover, it has been observed that 3% Gd doped SnO₂ nanoparticle sensor is highly selective towards ethanol.     

An Amalgam of Mg-Doped TiO2 Nanoparticles Prepared by Sol–Gel Method for Effective Antimicrobial and Photocatalytic Activity

In this study, undoped and Magnesium doped TiO₂ nanoparticles (Mg-TiO₂ NPs) are successfully synthesized via a simple sol–gel method cost-effectively. The prepared Mg- TiO₂ NPs is characterized by UV–Vis, FTIR, PL, XRD, FESEM, TEM, and EDAX. UV–Visible Spectroscopy showed that an increase in the optical bandgap concerning the concentration of dopant Mg increases. The bandgap values were found to be 3.57–3.54 eV. FTIR spectra shows that the presence of the characteristic stretching and bending vibrational band of Ti–O bonding at 468 cm^?1 and shifts in vibrational bands were observed for Mg-TiO₂ NPs. PL spectra of Mg- TiO₂ NPs at different concentrations exhibit a strong UV emission band. X-ray diffraction confirmed the formation of the tetragonal anatase phase. The average crystallite size of synthesized samples was found to be 22–19 nm. The average crystallite size of Mg- TiO₂ NPs decreases with increasing the concentration of dopant Mg. The FESEM and TEM analysis confirmed that the spherical morphology for both TiO₂ and Mg-TiO₂ NPs. SAED pattern confirms the crystalline nature of prepared samples. EDAX spectra confirm the presence of Ti, O, and Mg and confirm that Mg²⁺ ions are present in the TiO₂ lattices. The prepared samples were investigated against gram-positive and gram-negative bacteria. The prepared samples exhibit potent antibacterial activity against gram-negative bacteria than the gram-positive bacteria. The prepared samples exhibit significant photocatalytic degradation for Methylene blue (MB).

     

Green synthesis and biomedical behavior of Mg-doped ZnO nanoparticle using leaf extract of Ficus religiosa

Eco-friendly synthesis of Mg doped ZnO NPs was prepared by Ficus religiosa leaf extract. XRD confirmed the crystalline structure of the prepared Mg-doped ZnO. The functional groups and Zn and O bonding were realized from FTIR and Raman analyses. The surface plasma resonance absorption peak at 363 nm affirmed the formation of Mg–ZnO nanoparticles. The 3.32eV bandgap value of Mg–ZnO NPs was calculated by using Tauc's plot. The photoluminescence spectrum showed the emission behavior and point defect arising from zinc, oxygen vacancies. The hexagonal wurtzite structure of the prepared nanoparticles was observed from FESEM images. From the EDAX study, the elemental compositions have confirmed.The Thermal studies(TG/DTA)study,the Mg doped ZnO Material become thermally stable at 600 °C In XPS spectrum shows good formation of Mg doped ZnO nano materialThe facile synthesized Mg–ZnO NPs using Ficus religiosa leaves showed better antimicrobial properties on gram-positive bacterium, Staphylococcus aureus and fungus, Aspergillus niger. The biomedical behavior of prepared Mg–ZnO NPs was clearly understood from antioxidant(500 μg/mL-87), anti-inflammatory(500 μg/mL-89) and anti-diabetic assays(500μg/mL-82)     

Facile synthesis of different morphologies of Te-doped ZnO nanostructures

Te-doped ZnO nanostructures were synthesized by an annealing (vapor–solid) process under ambient conditions, and characterized in terms of their morphological, structural, compositional and optical properties. The structural and morphological characterizations revealed that the synthesized nanostructures were well-defined multipods, needles and spherical particles, and possessed well-crystalline ZnO wurtzite hexagonal phase. Also, in the X-ray diffraction studies, the presence of a shift in the peak positions towards a lower angle, and a decrease in the intensity, with an increase in the Te concentration, as compared to the undoped ZnO, were observed. The chemical composition confirmed the presence of Te, in the case of multipod and needle morphologies. The effect of doping on the crystalline quality and optical properties was also investigated, by using photoluminescence (PL) and Raman spectrometers. The Raman results demonstrated that the doped ZnO nanostructures had a lower crystalline quality than the undoped ZnO. Moreover, the PL results showed a decrease in the band gap for the doped ZnO nanostructures, in comparison to the undoped ZnO. A possible growth mechanism was also proposed.     

Facile synthesis and X-ray peak broadening studies of Zn1−xMgxO nanoparticles

Magnesium-doped ZnO nanoparticles (NPs) (Zn_1?xMg_xO-NPs, x = 0.0, 0.01, 0.03, and 0.05) were synthesized by a simple sol–gel method. The compounds were synthesized at calcination temperatures of 650 °C for 2 h. The synthesized Zn_1?xMg_xO-NPs were characterized by X-ray diffraction analysis (XRD) and high-magnification transmission electron microscopy (TEM). The XRD results revealed that the sample product was crystalline with a hexagonal wurtzite phase. The TEM showed Zn_1?xMg_xO-NPs with nearly spherical and hexagonal shapes. The size–strain plot (SSP) method was used to study the individual contributions of crystallite sizes and lattice strain on the peak broadening of the Zn_1?xMg_xO-NPs. Physical parameters such as strain, stress, and energy–density values were calculated more precisely for all reflection peaks of XRD corresponding to the wurtzite hexagonal phase of ZnO in the 20°–100° range from the SSP results. The effect of doping on the optical band-gap was also investigated. The results showed that Mg²⁺ is a good dopant to control some of the ZnO properties, with minimum defects to its structure.     

Structural and optical characterization of Zn0.95−xMg0.05AlxO nanoparticles

The structural and optical properties of ZnO nanoparticles doped simultaneously with Mg and Al were investigated. XRD results revealed the hexagonal wurtzite crystalline structure of ZnO. The FE-SEM study confirmed the formation of nano-sized homogeneous grains whose sizes decreased monotonously with increasing doping concentrations of Mg and Al. The absorption spectra showed that band gap increased from 3.20 to 3.31 eV with Mg doping. As the Al concentration changed from x=0.01 to x=0.06 mol% at constant Mg concentration the band gap observed to be decreased. Particle sizes estimated from effective mass approximation using absorption data and these values are in good agreement with the crystallite sizes calculated from XRD data. Raman spectra of ZnO showed a characteristic peak at 436 cm⁻¹ correspond to a non-polar optical phonon E₂ (high). With increase of the Al doping concentrations, E₂ (high) phonon frequency shifted to 439 cm⁻¹ from to 436 cm⁻¹. The origin of E₂ (high) peak shift in ZnO nanoparticles is attributed to optical phonon confinement effects or the presence of intrinsic defects on the nanoparticles. PL spectra indicated that with increase of Al co-doping along with Mg into ZnO, intensity of the peak positioned at 395 nm was initially increased at x=0 and then decreased with increase of the Al concentrations from x=0.01 to x=0.06 mol%.     

Effect of chlorine ion concentration on morphology and optical properties of Cl-doped ZnO nanostructures

Effect of Cl^?1 concentration on morphology and optical properties of Cl-doped ZnO nanostructures was studied. The Cl-doped ZnO nanostructures and undoped ZnO microstructures were grown on Si(1 1 1) substrates using a physical vapor deposition method. The ZnO nanostructures have been doped with different concentrations of chlorine. The Cl-doped ZnO nanostructures with 6% atom Cl, showed a nanodisk morphology with a hexagonal shape, while the Cl-doped ZnO nanostructures with 9% atom Cl, exhibited a stacked nanoplate morphology with smaller thickness in comparison to the Cl-doped ZnO nanodisks. In addition, with increasing Cl content to 13%, morphology of the products changed to more stacked nanoplates with nanoflakes morphology. X-ray diffraction results clearly showed a hexagonal structure for the all samples. Raman spectroscopy results showed a strong crystalline quality for the undoped ZnO microdisks and Cl-doped ZnO nanodisks; while these results indicated a weak crystalline quality for the Cl-doped ZnO nanoplates and nanoflakes. Photoluminescence (PL) studies also confirmed the Raman results and it exhibited a lower optical property for the Cl-doped ZnO nanoplates and nanoflakes in comparison to the undoped ZnO microdisks and Cl-doped ZnO nanodisks. Furthermore, the UV peak of the Cl-doped ZnO nanostructures was blue-shifted with respect to that of the undoped ZnO.     

Tailoring the properties of cerium doped zinc oxide/reduced graphene oxide composite: Characterization,photoluminescence study,antibacterial activity

Ce doped ZnO/rGO composite materials were prepared by a one-pot hydrothermal process without any surfactant. The size, crystallography and morphology of the composite were investigated in detail by X- ray diffraction (XRD) studies, Raman spectroscopy, scanning electron microscopic (SEM), transmission electron microscopic (TEM) studies, UV–Vis spectroscopic analysis and X-ray photoelectron spectroscopic (XPS) analysis. The XRD pattern substantiates the formation of Ce doped ZnO/rGO composite revealing the wurtzite structure of ZnO. The SEM micrograph illustrates flower-like morphology for ZnO/rGO composite which coalesced further after cerium incorporation. Additionally, TEM image illustrated that ZnO hexagons were disoriented from its flower structure in Ce/ZnO/rGO composite. The XPS spectra further reaffirm the formation of cerium doped ZnO/rGO composite. The photoluminescence (PL) spectra confirms that emission occurs in the UV and visible region and several active sub-levels were observed in visible region on deconvolution, due to the incorporation of cerium. Antibacterial activity towards B. subtills and V. harveyi affirmed that the incorporation of Ce in ZnO/rGO composite leads to an improved antibacterial activity.     

Enhancing the magnetic and antibacterial properties of ZnO nanopowders through Mn+Co doping

Undoped and doubly (Mn+Co) doped ZnO nanopowders were synthesized with different doping levels of Co (1, 2, 3, 4 and 5 at%) and constant Mn doping level (10 at%) using a simple soft chemical route. XRD profiles confirmed that the synthesized material is nanocrystalline ZnO with hexagonal wurtzite structure. No peaks other than the characteristic ZnO peaks were observed in the XRD pattern confirming the absence of any secondary phase. Antibacterial activities of synthesized ZnO nanopowders were tested against Staphylococcus aureus bacteria using agar well diffusion method. It was found that the antibacterial efficiency of the doubly doped ZnO nanopowders was remarkably high when the Co doping level was 5 at%. The obtained PL, SEM and TEM results are corroborated well with the antibacterial activity. Magnetic measurements showed that undoped ZnO sample exhibits diamagnetic behavior and as the Co doping level increases, the nanopowder behaves as a ferromagnetic material.     

Novel synthesis of ZnO nanoparticles and their enhanced anticancer activity: Role of ZnO as a drug carrier

In this work, a simple and versatile technique was developed to prepare highly crystalline ZnO nanoparticles (ZnO NPs) by organic precursor method using 5, 6 dimethyl benzimidazole and Zn(CH₃COO)₂·2H₂O followed by calcination. These synthesized ZnO NPs were used as a drug carrier to form 5-Fluorouracil (5 Fu) encapsulated ZnO NPs by varying the molar ratio (100–300:1) of ZnO NPs to 5-Fu. X-ray diffraction (XRD) results indicated that the ZnO NPs had single phase nature with the wurtzite structure. Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) results showed nanometer dimension of the NPs. FTIR analysis further reaffirmed the formation/encapsulation of ZnO NPs. UV–vis spectroscopy determined the encapsulation efficiency (EE) and loading capacity (LC) of 5-Fu drug on ZnO NPs. HPLC analysis of encapsulated NPs indicated release of 5-Fu was higher at tumor cell pH (pH 6.0) than physiological pH. Moreover, the anti-tumor activity of ZnO NPs and 5-Fu-encapsulated ZnO NPs investigated using flow cytometry demonstrated that 5-Fu encapsulated ZnO NPs have more anti-tumor activities than 5-Fu itself toward MCF-7 (Breast cancer) cell line. Also, cytotoxicity of MCF-7 increased with the increase of ZnO NPs: 5-Fu ratio. This research will introduce a new concept to synthesize 5-fluorouracil encapsulated ZnO NPs and its application towards the cancer cell line. Thus, the ZnO NPs could not only apply as the drug carrier to deliver 5-Fluorouracil into the cancer cells, but also enhances anti-tumor activity.     

XPS and optical studies of different morphologies of ZnO nanostructures prepared by microwave methods

Zinc oxide (ZnO) nanostructures of various morphologies were prepared using a microwave-assisted aqueous solution method. Herein, a comparative study between three different morphologies of ZnO nanostructures, namely nanoparticles (NPs), nanoflowers (NFs) and nanorods (NRs) has been reviewed and presented. The morphologies of the prepared powders have been studied using field effect scanning electron microscopy (FESEM). X-ray diffraction (XRD) results prove that ZnO nanorods have biggest crystallite size compared with nanoflowers and nanoparticles. The texture coefficient (T_c) of three morphologies has been calculated. The T_c changed with varying morphology. A comparative study of surfaces of NPs, NFs and NRs were investigated using X-ray photoelectron spectroscopy (XPS). The possible growth mechanisms of ZnO NPs, NFs and NRs have been described. The optical properties of the ZnO nanostructures of various morphologies have been investigated and showed that the biggest crystallite size of ZnO nanostructures has lowest band gap energy. The obtained results are in agreement with experimental and theoretical data of other researchers.     

Effect of indium concentration on morphology and optical properties of In-doped ZnO nanostructures

In-doped ZnO nanostructures with different indium concentrations were grown using a thermal evaporation method. The In-doped ZnO nanostructures with a low concentration of indium exhibited a javelin shape, while the In-doped ZnO nanostructures with a high concentration of indium showed a flake shape. In addition, undoped ZnO nanojavelins were grown under the same conditions, but the sizes of these undoped ZnO nanojavelins were larger than the In-doped ZnO nanojavelins. It was shown that the In³⁺ cations played a crucial role in controlling the size. X-ray diffraction and Raman spectroscopy clearly showed hexagonal structures for all of the products. However, the Raman results demonstrated that the In-doped ZnO nanoflakes had a lower crystalline quality than the In-doped ZnO nanojavelins. Furthermore, photoluminescence (PL) measurements confirmed the Raman results. Moreover, the PL results demonstrated a larger band-gap for the In-doped ZnO nanostructures in comparison to the undoped ZnO.     

Synthesis and Characterization of Rutile TiO2 Nanopowders Doped with Iron Ions

Titanium dioxide nanopowders doped with different amounts of Fe ions were prepared by coprecipitation method. Obtained materials were characterized by structural (XRD), morphological (TEM and SEM), optical (UV/vis reflection and photoluminescence, and Raman), and analytical techniques (XPS and ICP-OES). XRD analysis revealed rutile crystalline phase for doped and undoped titanium dioxide obtained in the same manner. Diameter of the particles was 5–7 nm. The presence of iron ions was confirmed by XPS and ICP-OES. Doping process moved absorption threshold of TiO₂ into visible spectrum range. Photocatalytic activity was also checked. Doped nanopowders showed normal and up-converted photoluminescence.     

Antibacterial and photocatalytic properties of Ag/TiO2/ZnO nano-flowers prepared by facile one-pot hydrothermal process

In this paper, a simple and efficient strategy of one-pot synthesis of Ag doped TiO₂/ZnO photocatalyst was developed using hydrothermal process. Simultaneous crystallization of Ag and ZnO crystals from their precursor solution containing P25 (TiO₂) NPs could form effectively bonded Ag/TiO₂/ZnO composite photocatalyst during hydrothermal treatment. Several analytical techniques, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), FT-IR spectroscopy, and photoluminescence spectroscopy have been used to characterize the resulting Ag/TiO₂/ZnO photocatalyst. Results showed that ZnO nano-flowers doped with TiO₂ and Ag NPs were formed by this simple facile one-step process. The unique properties of Ag NPs on binary semiconductor composite not only provide the decreased rate of electron–hole separation but also prevent from the loss of photocatalyst during recovery due to the fixed attachment of Ag and TiO₂ NPs on the surface of flower shaped large ZnO particles. Therefore, as-synthesized composite is an economically and environmentally friendly photocatalyst.     

Water-dispersible TiO2 nanoparticles via a biphasic solvothermal reaction method

A biphasic solvothermal reaction method has been used for the synthesis of TiO₂ nanoparticles (NPs). In this method, hydrolysis and nucleation occur at the interface of organic phase (titanium (IV) n-propoxide and stearic acid dissolved in toluene) and water phase (tert-butylamine dissolved in water) resulting in the nucleation of the stearic acid-capped TiO₂ NPs. These NPs are hydrophilic due to hydrophobic stearic acid ligands and could be dispersed in toluene, but not in water. These stearic acid-capped TiO₂ NPs were surface-modified with 2,3-dimercaptosuccinic acid (DMSA) in order to make them water soluble. The resultant TiO₂ NPs were easily redispersed in water without any noticeable aggregation. The Rietveld profile fitting of X-ray diffraction (XRD) pattern of the TiO₂ NPs revealed highly crystalline anatase structure. The average crystallite size of TiO₂ NPs was calculated to be 6.89 nm, which agrees with TEM results. These results have important implications for the use of TiO₂ in biomedical, environmental, and industrial applications.