Preparation of Al-doped ZnO Nanoparticulate Film for Optoelectronic Applications

2010 ◽  
Vol 1247 ◽  
Author(s):  
Thu V. Tran ◽  
Shinya Maenosono
Keyword(s):  
Electron Microscopy ◽  
Optical Transmittance ◽  
X Ray Diffraction ◽  
High Concentration ◽  
Polar Solvents ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Doped Zno ◽  
Optoelectronic Applications

AbstractAl-doped ZnO (AZO) nanoparticles (NPs) were synthesized by the solvothermal decomposition. The as-synthesized AZO NPs were characterized by X-ray diffraction and transmission electron microscopy. These NPs were well dispersible in non-polar solvents at high concentration to produce AZO nanoink. The AZO nanoparticulate films were prepared from AZO nanoink by spin coating technique. Thickness, surface morphology, optical transparency and conductivity of the films were characterized by surface profilometer, scanning electron microscopy, UV-Vis spectroscopy and Hall measurements. The AZO nanoparticlulate films had highly optical transmittance and well electrical conductivity, which are potential for optoelectronic applications.

scholarly journals Microwave-assisted preparation of ZnS and ZnSe nanocrystals with different morphologies for photodegradation process of organic dyes

2019 ◽  
Author(s):  
Katarzyna Matras-Postolek ◽  
A. Zaba ◽  
S. Sovinska ◽  
D. Bogdal
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Zinc Sulphide ◽  
Conventional Heating ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy

Zinc sulphide (ZnS) and zinc selenide (ZnSe) and manganese-doped and un-doped with different morphologies from 1D do 3D microflowers were successfully fabricated in only a few minutes by solvothermal reactions under microwave irradiation. In order to compare the effect of microwave heating on the properties of obtained  nanocrystals, additionally the synthesis under conventional heating was conducted additionally in similar conditions. The obtained nanocrystals were systematically characterized in terms of structural and optical properties using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. The photocatalytic activity of ZnSe, ZnS, ZnS:Mn and ZnSe:Mn nanocrystals with different morphologies was evaluated by the degradation of methyl orange (MO) and Rhodamine 6G (R6G), respectively. The results show that Mn doped NCs samples had higher coefficient of degradation of organic dyes under ultraviolet irradiation (UV).

Facile synthesis of water-soluble graphene-based composite: Non-covalently functionalized with chitosan-ionic liquid conjugation

2016 ◽  
Vol 09 (03) ◽  
pp. 1650045 ◽  
Author(s):  
Pei-Ying Li ◽  
Kai-Yu Cheng ◽  
Xiu-Cheng Zheng ◽  
Pu Liu ◽  
Xiu-Juan Xu
Keyword(s):  
Electron Microscopy ◽  
Ionic Liquid ◽  
Chemical Reduction ◽  
Water Soluble ◽  
X Ray Diffraction ◽  
Facile Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Text Interaction

Chitosan-ionic liquid conjugation (CILC), which was prepared through the reaction of 1-(4-bromobutyl)-3-methylimidazolium bromide (BBMIB) with chitosan, was firstly used to prepare functionalized graphene composite via the chemical reduction of graphene oxide (GO). The obtained water soluble graphene-based composite was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), ultraviolet-visible (UV–Vis) spectroscopy and so on. CILC-RGO showed excellent dispersion stability in water at the concentration of 2.0 mg/mL, which was stable for several months without any precipitate. This may be ascribed to the electrostatic attraction and [Formula: see text]–[Formula: see text] interaction between CILC and graphene.

The Preparation and Photocatalytic Activity of Ni-Doped ZnS Nanoparticles

2010 ◽  
Vol 148-149 ◽  
pp. 845-848 ◽  
Author(s):  
Qiao Feng Han ◽  
Guo Zhu Diao ◽  
Xiao Heng Liu ◽  
Xin Wang
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Degradation Efficiency ◽  
X Ray Diffraction ◽  
Zns Nanoparticles ◽  
X Ray ◽  
Ethyl Xanthate ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Zinc Sulfide Nanoparticles

Zinc sulfide nanoparticles as undoped and doped with nickel have been prepared by the reaction of Zn(CH3COO)2 and Ni(CH3COO)2 with potassium O-ethyldithiocarbonate (ethyl xanthate, C2H5OCS2k) at 80 in N, N - dimethylformamide (DMF) solution for 24 h. The structures of the products were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM), and their optical properties were studied by UV-Vis spectroscopy. The photocatalytic experiment by degrading methyl orange in aqueous solution under UV light indicated that the degradation efficiency of Ni (6%)-doped ZnS nanoparticles increased to 75% with comparison to 43% of degradation efficiency for undoped ZnS nanoparticles.

Fabrication of La Doped ZnO Nanorods via a Solvothermal Route

2009 ◽  
Vol 620-622 ◽  
pp. 529-532
Author(s):  
Tie Kun Jia ◽  
Wei Min Wang ◽  
Zheng Yi Fu ◽  
Fei Huang ◽  
Hao Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Zno Nanorods ◽  
Photocatalytic Property ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Doped Zno ◽  
La Doped ◽  
Scanning Electron

La doped ZnO nanorods were synthesized via solvothermal technique using Zn(AC)2 and La(NO3)3 as starting materials. The products were characterized by X-ray diffraction (XRD), field scanning electron microscopy (FESEM) equipped with an energy dispersion X–ray (EDX) spectrometer, photoluminescence spectroscopy and UV-vis spectroscopy. The results of XRD in combination with EDS indicated that La was successful doped in ZnO. The obtained La doped ZnO sample exhibited nanorod like morphology and the diameter was about 30 nm. The photocatalytic property of La doped ZnO was evaluated by the variation of the concentration of RhB.

Synthesis of Fe2+ Ion Doped ZnS Nanoparticles

2014 ◽  
Vol 879 ◽  
pp. 155-163 ◽  
Author(s):  
Rahizana Mohd Ibrahim ◽  
Markom Masturah ◽  
Huda Abdullah
Keyword(s):  
Electron Microscopy ◽  
Optical Properties ◽  
Quantum Confinement Effect ◽  
Band Gap Energy ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Co Precipitation

Nanoparticles of Zn1-xFexS ( x=0.0,0.1,0.2 and 0.3) were prepared by chemical co-precipitation method from homogenous solution of zinc and ferum salt at room temperature with controlled parameter. These nanoparticles were sterically stabilized using Sodium Hexamethaphospate (SHMP). Here, a study of the effect of Fe doping on structure, morphological and optical properties of nanoparticles was undertaken. Elemental analysis, morphological and optical properties have been investigated by Fourier-Transform-Infrared spectroscopy (FT-IR), X-Ray Fluorescence (XRF), Field Emmision Scanning Electron Microscopy (FESEM), X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and UV-Visible Spectroscopy. FTIR measurement confirmed the presence of SHMP in the nanoparticles structure with the FESEM images depicting considerable less agglomeration of particles with the presence of SHMP. While XRF results confirm the presence of Fe2+ ion as prepared in the experiment. The particles sizes of the nanoparticles lay in the range of 2-10 nm obtained from the TEM image were in agreement with the XRD results. The absorption edge shifted to lower wavelengths with an increase in Fe concentration shown in the UV-Vis spectroscopy. The band gap energy value was in the range of 4.95 5.15 eV. The blueshift is attributed to the quantum confinement effect.

scholarly journals Green synthesis of AgNP–ligand complexes and their toxicological effects on Nilaparvata lugens

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Hatem Fouad ◽  
Guiying Yang ◽  
Ahmed A. El-Sayed ◽  
Guofeng Mao ◽  
Diab Khalafallah ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Brown Planthopper ◽  
Nilaparvata Lugens ◽  
Management Program ◽  
X Ray Diffraction ◽  
High Concentration ◽  
Physiochemical Properties ◽  
X Ray ◽  
Toxicological Effects ◽  
Transmission Electron

Abstract Background Despite developments in nanotechnology for use in the pharmaceutical field, there is still a need for implementation of this technology in agrochemistry. In this study, silver nanoparticles (AgNPs) were successfully prepared by a facile and an eco-friendly route using two different ligands, 2ʹ-amino-1,1ʹ:4ʹ,1″-terphenyl-3,3″,5,5″-tetracarboxylic acid (H4L) and 1,3,6,8-tetrakis (p-benzoic acid)-pyrene (TBAPy), as reducing agents. The physiochemical properties of the as-obtained AgNPs were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The toxicity of H4L–AgNP and TBAPy–AgNP against the brown planthopper (BPH, Nilaparvata lugens) was also measured. Results SEM and TEM analyses demonstrated the formation of quasi-spherical AgNP structures in the presence of H4L and TBAPy. Insecticidal assays showed that TBAPy is less effective against N. lugens, with a median lethal concentration (LC50) of 810 mg/L, while the toxicity of H4L increased and their LC50 reached 786 mg/L 168 h posttreatment at a high concentration of 2000 mg/L. H4L–AgNPs were also highly toxic at a low concentration of 20 mg/L, with LC50 =  ~ 3.9 mg/L 168 h posttreatment, while TBAPy–AgNPs exhibited less toxicity at the same concentration, with LC50 =  ~ 4.6 mg/L. Conclusions These results suggest that the synthesized AgNPs using the two ligands may be a safe and cheaper method compared with chemical insecticides for protection of rice plants from pests and has potential as an effective insecticide in the N. lugens pest management program.

scholarly journals Biosynthesis, characterisation and therapeutic applications of plant-mediated silver nanoparticles

2018 ◽  
Vol 83 (5) ◽  
pp. 515-538 ◽  
Author(s):  
Andreia Corciova ◽  
Bianca Ivanescu
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Nanoparticle Synthesis ◽  
Special Importance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Stabilizing Agents ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Nanoparticles Synthesis

Nanotechnology is one of the most studied domains, and nanoparticle synthesis, especially of silver nanoparticles, has gained special importance due to their properties, biocompatibility and applications. Today, the processes of nanoparticles synthesis tend toward the development of inexpensive, simple, non-toxic and environmentally friendly methods. Thus, the use of plants in the synthesis of silver nanoparticles has attracted considerable interest because biomolecules can act as both reducing and stabilizing agents. This survey aims at discussing the conditions for obtaining silver nanoparticles using plants and their characterization by several methods, such as FTIR and UV?Vis spectroscopy, X-ray diffraction, and scanning and transmission electron microscopy. In addition, it examines some of the most common biological uses of silver nanoparticles: antibacterial, antioxidant and cytotoxic.

Facile Enrichment and Photocatalytical Degradation of Low Concentration MB in Aqueous Solution

2011 ◽  
Vol 110-116 ◽  
pp. 2308-2315
Author(s):  
Liu Xue Zhang ◽  
Xiu Lian Wang
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Fine Particles ◽  
X Ray Diffraction ◽  
High Concentration ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Low Concentrations ◽  
Hydrolysis Of

Fine particles of photoactive anatase-type TiO2, prepared by hydrolysis of tetrabutyl orthotitanate and crystallized under microwave (MV) irradiation, were loaded on adsorbent support attapulgite (ATP). The prepared hybrids TiO2-ATP were characterized with transmission electron microscopy (TEM), selected-area electron diffraction (SAED), and X-ray diffraction (XRD) and photoactivity properties were evaluated separately. The substrates of target were adsorbed on the adsorbent support, and then a high concentration environments of the substrate was formed around the loaded TiO2, resulting in an increase in the photodestruction rate. One of the most interesting features of the resulting catalysts with low titania contain (<30%) is their fast decantability in comparison with that of TiO2. This way one of the most important drawbacks of photocatalysis, the catalysts separation from the solution, was overcome by simple sedimentation and decantation. The low concentrations MB may be removed through enrichment and photodegradation using the prepared TiO2-ATP photocatalyst.

scholarly journals Physical Characteristics of Titania Nanofibers Synthesized by Sol-Gel and Electrospinning Techniques

2010 ◽  
Vol 5 (1) ◽  
pp. 155892501000500 ◽  
Author(s):  
Soo-Jin Park ◽  
Yong C. Kang ◽  
Ju Y. Park ◽  
Ed A. Evans ◽  
Rex D. Ramsier ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Average Diameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Ceramic Nanofibers ◽  
Titania Nanofibers

Titania nanofibers were successfully synthesized by sol-gel coating of electrospun polymer nanofibers followed by calcining to form either the pure anatase or rutile phases. Characterization of these materials was carried out using scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-vis spectroscopy techniques. The average diameter of these ceramic nanofibers was observed to be around 200 nm for both the rutile and anatase forms. The valence band structure and optical absorption thresholds differ, however, indicating that nanofibrous mats of titania can be selectively developed for different applications in catalysis and photochemistry.

scholarly journals The Effect of AgInS2, SnS, CuS2, Bi2S3 Quantum Dots on the Surface Properties and Photocatalytic Activity of QDs-Sensitized TiO2 Composite

Catalysts ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 403 ◽  
Author(s):  
Anna Malankowska ◽  
Daria Kulesza ◽  
Jakub Sowik ◽  
Onur Cavdar ◽  
Tomasz Klimczuk ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Photocatalytic Activity ◽  
Surface Properties ◽  
Toluene Degradation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Hot Injection

The effect of type (AgInS2, SnS, CuS2, Bi2S3) and amount (5, 10, 15 wt%) of quantum dots (QDs) on the surface properties and photocatalytic activity of QDs-sensitized TiO2 composite, was investigated. AgInS2, SnS, CuS2, Bi2S3 QDs were obtained by hot-injection, sonochemical, microwave, and hot-injection method, respectively. To characterize of as-prepared samples high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-Vis spectroscopy and photoluminescence (PL) emission spectroscopy were applied. The size of AgInS2, SnS, CuS2, Bi2S3 QDs were 12; 2–6; 2–3, and 1–2 nm, respectively. The QDs and QDs-sensitized TiO2 composites obtained have been tested in toluene degradation under LEDs light irradiation (λmax = 415 nm and λmax = 375 nm). For pristine QDs the efficiency of toluene degradation increased in the order of AgInS2 < Bi2S3 < CuS < SnS under 375 nm and AgInS2 < CuS < Bi2S3 < SnS under 415 nm. In the presence of TiO2/SnS QDs_15% composite, 91% of toluene was degraded after 1 h of irradiation, and this efficiency was about 12 higher than that for pristine QDs under 375 nm. Generally, building the TiO2/AgInS2 and TiO2/SnS exhibited higher photoactivity under 375 nm than the pristine TiO2 and QDs which suggests a synergistic effect between QDs and TiO2 matrix.

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