Nanostructured amorphous oxide semiconductor film and production method thereof
An amorphous oxide and nanostructure technology, applied in the field of amorphous oxide semiconductor thin film and its preparation, can solve the problems of limiting the application of amorphous oxide semiconductor thin film, small specific surface area, etc., and achieve easy integration and increase in size Specific surface area, easy miniaturization effect
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Embodiment 1
[0029] First prepare the precursor solution: the Sn precursor SnCl 2 2H 2 Precursor C of O and Ti 12 h 28 o 4 Ti and NH respectively 4 NO 3 Mixed with Sn source and Ti source, where NH 4 NO 3 The molar ratio with Sn and Ti is 1:1; then the configured Sn source, Ti source and Zn precursor Zn(NO 3 ) 2 ·6H 2 O, the three were dissolved in dimethoxyethanol solvent respectively, and after the dissolution was completed, acetylacetone and ammonia water were added respectively; the amount of acetylacetone added was 210 μl, 80 μl, and 120 μl respectively; the concentration of ammonia water was 14.5M, and the amount added was 60 μl respectively , 40 μl, and 69 μl; each of them was prepared as a precursor solution of Sn, Ti and Zn with a concentration of 0.2M. Stir at room temperature for 24 hours and then filter; finally, ultrasonically mix uniformly according to the molar ratio of Zn:Sn:Ti=0.36:0.63:0.01, and then age for 24 hours to obtain the sol required for spin coating. ...
Embodiment 2
[0037] First prepare the precursor solution: the Sn precursor SnCl 2 2H 2 Precursor C of O and Ti 12 h 28 o 4 Ti and NH respectively 4 NO 3 Mixed with Sn source and Ti source, where NH 4 NO 3 The molar ratio with Sn and Ti is 1:1; then the configured Sn source, Ti source and Zn precursor Zn(NO 3 ) 2 ·6H 2 O, the three were dissolved in dimethoxyethanol solvent respectively, and after the dissolution was complete, acetylacetone and ammonia water were added respectively, wherein the amount of acetylacetone added was 210 μl, 80 μl, and 120 μl respectively, and the concentration of ammonia water was 14.5M, and the amount added was 60 μl respectively , 40 μl, 69 μl, each made into a precursor solution with a concentration of 0.2M, stirred at 60°C for 12 hours and then filtered; finally, according to the molar ratio of Zn:Sn:Ti=0.34:0.60:0.06, ultrasonically mixed evenly, and then aged for 12 hours Prepare the sol required for spin coating.
[0038] Film formation: The so...
Embodiment 3
[0043] First prepare the precursor solution: the Sn precursor SnCl 2 2H 2 Precursor C of O and Ti 12 h 28 o 4 Ti and NH respectively 4 NO 3 Mixed with Sn source and Ti source, where NH 4 NO 3 The molar ratio of Zn and Ti is 1:1; then the configured Sn source, Ti source and Zn precursor Zn(NO 3 ) 2 ·6H 2 O The three were dissolved in dimethoxyethanol solvent respectively. After the dissolution was complete, acetylacetone and ammonia water were added respectively, wherein the amount of acetylacetone added was 210 μl, 80 μl, and 120 μl respectively, and the concentration of ammonia water was 14.5M, and the amount added was 60 μl respectively. , 40 μl, 69 μl, each made into a precursor solution with a concentration of 0.2M, stirred at 40°C for 18 hours and then filtered; finally, according to the molar ratio of Zn:Sn:Ti=0.4:0.51:0.09, ultrasonically mixed evenly, and then aged for 18 hours Prepare the sol required for spin coating.
[0044] Film formation: The sol prepa...
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