Thermally induced structural changes and optical properties of tin dioxide nanoparticles synthesized by a conventional precipitation method

2013 ◽  
Vol 16 (6) ◽  
pp. 1784-1790 ◽  
Author(s):  
A. Gaber ◽  
A.Y. Abdel-Latief ◽  
M.A. Abdel-Rahim ◽  
Mahmoud N. Abdel-Salam
2020 ◽  
Vol 110 ◽  
pp. 103470
Author(s):  
Shuyuan Zhao ◽  
Jianglong Dong ◽  
Christian Monte ◽  
Xinyang Sun ◽  
Wenjiao Zhang ◽  
...  

Optik ◽  
2017 ◽  
Vol 136 ◽  
pp. 259-264 ◽  
Author(s):  
Manivannan N. ◽  
Chandar Shekar B. ◽  
Senthil Kumaran C.K. ◽  
Sathyamoorthy R.

2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Panya Khaenamkaew ◽  
Dhonluck Manop ◽  
Chaileok Tanghengjaroen ◽  
Worasit Palakawong Na Ayuthaya

The electrical properties of tin dioxide (SnO2) nanoparticles induced by low calcination temperature were systematically investigated for gas sensing applications. The precipitation method was used to prepare SnO2 powders, while the sol-gel method was adopted to prepare SnO2 thin films at different calcination temperatures. The characterization was done by X-ray diffraction, scanning electron microscopy (SEM), and atomic force microscopy (AFM). The samples were perfectly matched with the rutile tetragonal structure. The average crystallite sizes of SnO2 powders were 45 ± 2, 50 ± 2, 62 ± 2, and 65 ± 2 nm at calcination temperatures of 300, 350, 400, and 450°C, respectively. SEM images and AFM topographies showed an increase in particle size and roughness with the rise in calcination temperature. The dielectric constant decreased with the increase in the frequency of the applied signals but increased on increasing calcination temperature. By using the UV-Vis spectrum, the direct energy bandgaps of SnO2 thin films were found as 4.85, 4.80, 4.75, and 4.10 eV for 300, 350, 400, and 450°C, respectively. Low calcination temperature as 300°C allows smaller crystallite sizes and lower dielectric constants but increases the surface roughness of SnO2, while lattice strain remains independent. Thus, low calcination temperatures of SnO2 are promising for electronic devices like gas sensors.


2019 ◽  
Vol 224 ◽  
pp. 65-72 ◽  
Author(s):  
Hadi Eslami ◽  
Mohammad Hassan Ehrampoush ◽  
Abbas Esmaeili ◽  
Ali Asghar Ebrahimi ◽  
Mohammad Taghi Ghaneian ◽  
...  

2010 ◽  
Vol 75 ◽  
pp. 36-42 ◽  
Author(s):  
Marina Rumyantseva ◽  
Irina Zhurbina ◽  
Elena Varechkina ◽  
Siranuysh Badalyan ◽  
Alexander Gaskov ◽  
...  

Powders of tin dioxide (SnO2) have been prepared by two different modifications of wet chemical synthesis, i.e. (i) by conventional hydrolysis of tin chloride dissolved in aqueous ammonia solution and (ii) by precipitation from tin chloride dissolved in aqueous hydrazine monohydrate (N2H4*H2O) solution. The prepared gels were dried and then annealed at different temperatures varied from 300 to 700 oC in order to form nanocrystals. Structure and optical properties of the samples were investigated by using X-ray diffraction, transmission electron microscopy, thermoprogrammable hydrogen reduction, low temperature nitrogen adsorption method, photoluminescence, infra-red absorption, Raman spectroscopy, and X-ray photoelectron spectroscopy. The samples prepared by hydrazine-based method are characterized by surface area about 127-188 m2/g with high sintering resistance. The optical spectroscopy data revealed pure crystallinity and high defect concentration for the samples prepared by hydrazine-based method. The experimental results are discussed in view of different states of chemisorbed oxygen on SnO2 nanocrystal surfaces, which determine electronic and optical properties of the prepared samples.


2018 ◽  
Author(s):  
Zsuzsanna Vörös ◽  
Gabriella Csík ◽  
Levente Herényi ◽  
Miklós Kellermayer

AbstractViruses are nanoscale infectious agents which may be inactivated by heat treatment. Although heat inactivation is thought to be caused by the release of genetic material from the capsid, the thermally-induced structural changes in viruses are little known. Here we measured the heat-induced changes in the properties of T7 bacteriophage particles exposed to two-stage (65 °C and 80 °C) thermal effect by using AFM-based nanomechanical and topographical measurements. We found that exposure to 65 °C caused the release of genomic DNA due to the loss of the capsid tail which leads to a destabilization of the T7 particles. Further heating to 80 °C surprisingly led to an increase in mechanical stability due to partial denaturation of the capsomeric proteins kept within the global capsid arrangement.


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