This paper reports that indium tin oxide （ITO） crystalline powders are prepared by coprecipitation method. Fabrication conditions mainly as sintering temperature and Sn doping content are correlated with the phase, ...This paper reports that indium tin oxide （ITO） crystalline powders are prepared by coprecipitation method. Fabrication conditions mainly as sintering temperature and Sn doping content are correlated with the phase, microstructure, infrared emissivity c and powder resistivity of indium tin oxides by means of x-ray diffraction, Fourier transform infrared, and transmission electron microscope. The optimum sintering temperature of 1350℃ and Sn doping content 6～8wt% are determined. The application of ITO in the military camouflage field is proposed.展开更多
hemical co-precipitation method was used to prepare indium tin hydroxide. Indium tin hydroxide has the structure of cubic crystal. The cubic crystal structure transformed to amorphous after heat treatment at 250℃ for...hemical co-precipitation method was used to prepare indium tin hydroxide. Indium tin hydroxide has the structure of cubic crystal. The cubic crystal structure transformed to amorphous after heat treatment at 250℃ for 1 h. When the heat treatment temperature was higher than 280℃, the amorphous transformed to cubic crystal structure. After heat treatment at 600℃ for 1 h, the particle size of indium tin oxide is 8～20 nm. The weight ratio of In∶Sn is near 9∶1. Its granule has spherical shape. The dispersity is good.展开更多
With InCl 3·4H 2O being used as raw materials, the precursor of nano sized In 2O 3 powder was prepared by hydrolysis, peptization and gelation of InCl 3·4H 2O. After calcination, nano sized In 2O 3...With InCl 3·4H 2O being used as raw materials, the precursor of nano sized In 2O 3 powder was prepared by hydrolysis, peptization and gelation of InCl 3·4H 2O. After calcination, nano sized In 2O 3 powder was obtained. The powder was characterized by thermo gravimetric and differential thermal analysis (TG DTA), X ray diffractometry (XRD) and transmission electron microscopy (TEM), respectively. Calculation revealed that the mean crystalline size increased with increasing the calcination temperature, but crystal lattice distortion rate decreased with the increasing in the average crystalline size. This indicated that the smaller the particle size, the bigger the crystal lattice distortion, the worse the crystal growing. The activation energies for growth of nano sized In 2O 3 were calculated to be 4.75 kJ·mol -1 at the calcination temperature up to 500℃ and 66.40 kJ·mol -1 at the calcination temperature over 600℃. TEM photos revealed that the addition of the chemical additive (OP-10) greatly influenced the morphology and size of In 2O 3 particles.展开更多
文摘This paper reports that indium tin oxide （ITO） crystalline powders are prepared by coprecipitation method. Fabrication conditions mainly as sintering temperature and Sn doping content are correlated with the phase, microstructure, infrared emissivity c and powder resistivity of indium tin oxides by means of x-ray diffraction, Fourier transform infrared, and transmission electron microscope. The optimum sintering temperature of 1350℃ and Sn doping content 6～8wt% are determined. The application of ITO in the military camouflage field is proposed.
文摘hemical co-precipitation method was used to prepare indium tin hydroxide. Indium tin hydroxide has the structure of cubic crystal. The cubic crystal structure transformed to amorphous after heat treatment at 250℃ for 1 h. When the heat treatment temperature was higher than 280℃, the amorphous transformed to cubic crystal structure. After heat treatment at 600℃ for 1 h, the particle size of indium tin oxide is 8～20 nm. The weight ratio of In∶Sn is near 9∶1. Its granule has spherical shape. The dispersity is good.
文摘With InCl 3·4H 2O being used as raw materials, the precursor of nano sized In 2O 3 powder was prepared by hydrolysis, peptization and gelation of InCl 3·4H 2O. After calcination, nano sized In 2O 3 powder was obtained. The powder was characterized by thermo gravimetric and differential thermal analysis (TG DTA), X ray diffractometry (XRD) and transmission electron microscopy (TEM), respectively. Calculation revealed that the mean crystalline size increased with increasing the calcination temperature, but crystal lattice distortion rate decreased with the increasing in the average crystalline size. This indicated that the smaller the particle size, the bigger the crystal lattice distortion, the worse the crystal growing. The activation energies for growth of nano sized In 2O 3 were calculated to be 4.75 kJ·mol -1 at the calcination temperature up to 500℃ and 66.40 kJ·mol -1 at the calcination temperature over 600℃. TEM photos revealed that the addition of the chemical additive (OP-10) greatly influenced the morphology and size of In 2O 3 particles.
