Controlling the Particle Size of Quantum Dots Incorporated in Hybrid Materials

1998 ◽  
Vol 519 ◽  
Author(s):  
Francisco Del Monte ◽  
Yuhuan Xu ◽  
John D. Mackenzie ◽  
B. Claflin ◽  
G. Lucovsky

AbstractSemiconductor PbS quantum dot-doped Ormocers were successfully prepared by the sol-gel technique. Ormocers preparation was based on the use of trifunctional silane precursors at the solution stage. Formation of PbS particles took place in the pores of the Ormocers through lead precursor reaction with H2S gas. It was observed that temperature was an important factor in the reaction leading to the first appearance of PbS particles. The dot size of PbS was controlled through chemical interaction with the non-hydrolyzed groups of the trifunctional silane precursors. These groups prevent uncontrolled nucleation and aggregation processes during the particle formation and growth. The control of particle size was studied at different conditions for nucleation and aggregation. Determination of the average particle size was done by XR-Diffraction. Optical absorption spectra were also measured at the UV-VIS wavelength range. Absorption edge blue shifts show the quantum confinement effect in these materials.

2017 ◽  
Vol 17 (01n02) ◽  
pp. 1760012
Author(s):  
S. Gowreesan ◽  
A. Ruban Kumar

The scope of the present work is in enhancing the particle size, and dielectric properties of Mg-substituted Cobalt ferrites nanoparticles prepared by sol–gel auto combustion method. The different ratios of Mg-substituted Co Ferrites (Co[Formula: see text]MgxFe2O4([Formula: see text], 0.05, 0.10, 0.15, 0.20 and 0.30)) are calcinated at 850[Formula: see text]C. The synthesized nanoparticles were characterized by powder XRD, FTIR, FE-SEM, EDX techniques and dielectric behavior. The structural parameters were confirmed from powder XRD and the average particle size is obtained from 39 to 67 nm due to the substitution of Mg[Formula: see text] which was calculated by Debye Scherrer’s formula. FE-SEM showed the surface morphology of the different ratio of the sample. The dielectric loss has measured the frequency range of 50[Formula: see text]Hz–5[Formula: see text]MHz. From electrical modulus, conductivity relaxation and thermal activation of charge carriers has been discussed.


2006 ◽  
Vol 510-511 ◽  
pp. 786-789 ◽  
Author(s):  
Dong Sik Bae ◽  
Byung Ik Kim ◽  
Kyong Sop Han

ZnO-TiO2 nanoparticles were synthesized by a reverse micelle and sol-gel process. The average particle size of the colloid was below 30 nm and well dispersed in the solution. ZnOTiO2 composite membranes were fabricated by using the dip-coating method on a porous alumina support. ZnO-TiO2 composite membranes showed a crack-free microstructure and narrow particle size distribution even after the heat treatment up to 600°C. The average particle size of the membrane was 30-40nm, and the pore size of ZnO-TiO2 composite membrane was below 10 nm.


2016 ◽  
Vol 709 ◽  
pp. 66-69
Author(s):  
Jeyashelly Andas ◽  
Rahmah Atikah Rosdi ◽  
Nur Izzati Mohd Anuar

A series of Fe-Co nanoparticles were synthesized via sol-gel route at acidic, neutral and basic condition using rice husk as the silica source. The synthesized nanomaterials were designated as Fe-Co3, Fe-Co7 and Fe-Co9 and characterized by Fourier Transform Infrared (FTIR), Transmission Electron Microscope (TEM) and particle size analyzer. The great effect of pH was clearly evidenced from the shifting in the siloxane bond in the FTIR spectrum. TEM investigation confirmed the existence of discrete and almost sphere like nanoparticles. The particle size decreased with an increase in the pH, registering the smallest average particle size at pH 9. In brief, this study promises a fast, rapid and promising method for the conversion of silica rice husk into nanoscale bimetallic materials.


2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Nguyen Lam Uyen Vo ◽  
Thi Thuy Van Nguyen ◽  
Tri Nguyen ◽  
Phung Anh Nguyen ◽  
Van Minh Nguyen ◽  
...  

In this study, CuO-ZnO composite was synthesized via the sol-gel method using oxalic acid to form the medium complex and its applications in antibacterial have been conducted with B. cereus, E. coli, S. aureus, Salmonella, and P. aeruginosa. Then, nanopowder of CuO-ZnO was coated on shoe insoles and their antibacterial effect with S. aureus was tested. The nanocomposite products were characterized by XRD, XPS, SEM, TEM, and UV-Vis. The results showed that the CuO-ZnO composite has the average particle size in a range of 20-50 nm, the point of zero charge of 7.8, and the bandgap of 1.7 eV. XPS result shows the composite structure with Cu2+ in the product. The minimum inhibitory concentration (MIC) of CuO-ZnO nanocomposite was 0.313 mg·mL-1 for S. aureus and Samonella, 0.625 mg·mL-1 for E. coli, and 5 mg·mL-1 for B. cereus and P. aeruginosa. The shoe insoles coated with 0.35 wt.% of CuO-ZnO nanocomposite also had high antibacterial activity against S. aureus, and this antibacterial nanocomposite was implanted durably on the surface of the shoe insoles.


2021 ◽  
Author(s):  
Nelli Maksymovych ◽  
Ludmila Oleksenko ◽  
George Fedorenko

The paper is devoted for a solution of indoors fires prevention at early stage by determination of H2 (fire precursor gas) in air using a semiconductor sensor. A material based on Pt-containing nanosized tin dioxide with an average particle size of 10–11 nm obtained via a sol–gel method was created for a gas sensitive layer of the sensor. The developed sensor has high sensitivity to H2 micro concentration, a wide range of its detectable content in air, selectivity of H2 measuring in the presence of СО and СН4, good dynamic properties. The combination of these properties is very important for prevention of inflammations on their early stages before the open fires appearance. Economic benefit of the proposed sensor is due to a lower cost and higher reliability of the fire situation detection.


2004 ◽  
Vol 847 ◽  
Author(s):  
Christophe Barbé ◽  
Sandrine Calleja ◽  
Linggen Kong ◽  
Elizabeth Drabarek ◽  
Alexandra Bush ◽  
...  

ABSTRACTUsing sol-gel technology combined with water-in-oil (W/O) emulsions, we have developed an innovative method for producing ceramic particles with independent control over the release rate and particle size. The average particle size can be varied from 10 nm to 100 μm and is controlled by the emulsion chemistry. The release rate can be independently varied from mg/hours to mg/month, and is controlled by the internal microstructure of the particles and the initial sol-gel chemistry.


1961 ◽  
Vol 34 (2) ◽  
pp. 433-445 ◽  
Author(s):  
E. Schmidt ◽  
P. H. Biddison

Abstract Knowledge of mass distribution of particle sizes in latex is very important to the latex technologist. Therefore, it is desirable to have available a simple method for the determination of mass distribution of particle sizes. This paper presents a method, based on fractional creaming of latex with sodium alginate, which can be used in any laboratory without special equipment. The method is particularly advantageous for analyzing latexes of very wide particle size distributions. When analyzed with an electron microscope, these latexes require counting a very large number of particles. McGavack found that partial creaming of normal hevea latex with ammonium alginate gives concentrates of larger average particle size than the original latex. He found that the average particle size in the cream approaches that of the original latex as the amount of creaming agent is increased. In a previous paper from this laboratory, Schmidt and Kelsey demonstrated that the phenomenon of fractionation according to particle size with increasing amounts of creaming agent is applicable in a wide variety of anionic latex systems and in colloidal silica. Their results indicated also the existence of a quantitative relationship, independent of the nature of the dispersed particles, between the concentration of creaming agent and size of creamed particles. Maron confirmed fractionation with respect to particle size as a consequence of partial creaming with alginate. He showed that the mass average particle sizes of fractions, determined optically, cumulate to that of the original latex. Although the previous paper by Schmidt and Kelsey implied the basic concept of a method of determining particle size distribution by fractional creaming, it was not exploited at that time. In order to adapt the fractional creaming phenomenon to a quantitative method for particle size determination, we required a more precise knowledge of the relation between creaming agent concentration and size of particles creamed. It was proposed to establish this relationship with the aid of the electron microscope. Various factors influencing the creaming of latex, such as polymer concentration, electrolyte, soap content, and variability of the creaming agent, had to be considered in standardizing the creaming procedure.


2012 ◽  
Vol 600 ◽  
pp. 190-193 ◽  
Author(s):  
Wei Wei ◽  
Jing Yi Zhang ◽  
Li Ping Wu ◽  
Guo Tong Qin

The hydrophobic silica granular aerogels were synthesized via sol-gel synthesis followed by ambient pressure drying. The tetraethyloxylane (TEOS) was used as original precursor. The aerogels were analyzed using nitrogen adsorption, scanning electron microscopy (SEM) and laser particle size analyzer. It was found that the aerogel was mesoporous material with high surface area. The aerogels were prepared in grain form by dipping into disperse solution in order to adsorption application. The average particle size of the aerogel was controlled by pH and disperse solution volume. The pH also affected gel time. The aerogels were used to absorb phenol from water. The saturated adsorption amount could reach up to 145 mg•g-1.


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