Effect of content silver and heat treatment temperature on morphological, optical, and electrical properties of ITO films by sol–gel technique

2014 ◽  
Vol 16 (9) ◽  
Author(s):  
Majid Mirzaee ◽  
Abolghasem Dolati
Engineering ◽  
2010 ◽  
Vol 02 (12) ◽  
pp. 969-972
Author(s):  
Hiroyuki Nasu ◽  
Tomoyuki Yamauchi ◽  
Sachio Ninagawa ◽  
Daisuke Hirota ◽  
Tadanori Hashimoto ◽  
...  

2013 ◽  
Vol 712-715 ◽  
pp. 257-261
Author(s):  
Yin Lin Wu ◽  
Qing Hui Wang ◽  
Ling Wang ◽  
Hai Yan Zhao

The La0.75Sr0.25Cr0.5Mn0.5O3-δnanometer powders were prepared by citric acid sol-gel method.The samples were characterized by DTA, FT-IR, XRD, TEM techniques. The preparation process, morphology of synthesized powders, the best heat-treatment temperature and the electrochemical performance had been studied. The results show that the spherical nanometer powders can be obtained and the best heat-treatment temperature is 800°C. The particle size is about 30nm and Ea is 0.071 eV.


2010 ◽  
Vol 105-106 ◽  
pp. 123-125 ◽  
Author(s):  
Yong Li ◽  
Qi Hong Wei ◽  
Ling Li ◽  
Chong Hai Wang ◽  
Xiao Li Zhang ◽  
...  

In this paper, negative thermal expansion coefficient eucryptite powders were prepared by sol-gel method using silica-sol as starting material. The raw blocks were obtained by dry pressing process after the powder was synthesized, and then the raw blocks were heat-treated at 600º, 1150º, 1280º, 1380º, 1420º and 1450°C, respectively. Variations of density, porosity and thermal expansion coefficient at different heat treatment temperatures were investigated. Phase transformation and fracture surface morphology of eucryptite heat-treated at different temperatures, respectively, were observed by XRD and SEM. The results indicate that, with the increasing heat- treatment temperature, the grain size and the bending strength increased, porosity decreased, thermal expansion coefficient decreased continuously. Negative thermal expansion coefficient of -5.3162×10-6~-7.4413×10-6 (0~800°C) was obtained. But when the heat-treatment temperature was more than 1420°C, porosity began to increase, bending strength began to decrease, which were the symbols of over-burning, while the main crystal phase didn’t change.


2012 ◽  
Vol 512-515 ◽  
pp. 1686-1689
Author(s):  
Jie Chen ◽  
Le Fu Mei ◽  
Li Bing Liao

In this paper, porous carbon has been used to carry TiO2 and TiO2-N by a sol-gel process. The effect of soaking time, heat treatment temperature, and heat treatment time on the carrying efficiency have been studied. XRD experiments indicated that TiO2 and TiO2-N crystallized in anatase and rutile with the ratio of 3∶2. SEM images showed that island-like TiO2 and TiO2-N particles with diameters in the range of 1-5um, the biggest size is about 10um, were evenly coated on the surface of the porous carbon.


2014 ◽  
Vol 71 (2) ◽  
pp. 303-312 ◽  
Author(s):  
L. Predoana ◽  
S. Preda ◽  
M. Nicolescu ◽  
M. Anastasescu ◽  
J. M. Calderon-Moreno ◽  
...  

2014 ◽  
Vol 1078 ◽  
pp. 31-35
Author(s):  
Liang Zhao ◽  
Qun Hu Xue ◽  
Dong Hai Ding

MgO-Al2O3-ZrO2composite powders with 3 kinds of mass ratio were synthesized by sol–gel method using MgCl2·6H2O, AlCl3·6H2O and ZrOCl2·8H2O as starting materials, and NH3·H2O as a precipitant. The composite powders which match with zirconium oxide particle size and evenly distribute can are advantageous to the formation of metastable t-ZrO2and restrain the grain growth as the additive of modified sizing nozzle. Chemical composition, mineral phase, particle size distribution and micro-morphology of the composite powders were investigated by X-ray fluorescence instrument, X-ray diffractometer, laser particle size analyzer and scanning electron microscope. Research showed that under the process that the concentration of MgCl2solution 0.2 mol/L, AlCl3and ZrOCl2solution concentration 0.5 mol/L, the pH controlled between 10 ~ 11, PEG as the surfactant, drying at 70°C±5°C, heat treatment temperature at 800°C for 3h, particle size distribution of MgO-Al2O3-ZrO2composite powders were: d10= 1.28 μm, d50= 4.65μm, d90= 11.13μm (MgO 10%); d10= 1.15μm, d50= 5.80μm, d90= 15.13μm (MgO 15%);d10= 1.21μm, d50= 6.59μm, d90= 16.87μm (MgO 20%). With the rising of heat treatment temperature, the crystallization degree of composite powders increased, at 800 °C a small amount of t - ZrO2precipitated, meanwhile MgO and Al2O3are still in the amorphous phase. The MgO-A12O3-ZrO2composite powders under this condition have high reactivity and uniform distribution.


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