Metal organic deposition precursor solution synthesis and terbium-doped SiO2 thin film deposition

Abstract

A method of making a doped silicon oxide thin film using a doped silicon oxide precursor solution includes mixing a silicon source in an organic acid and adding 2-methoxyethyl ether to the silicon source and organic acid to from a preliminary precursor solution. The resultant solution is heated, stirred and filtered. A doping impurity is dissolved in 2-methoxyethanol to from a doped source solution, and the resultant solution mixed with the previously described resultant solution to from a doped silicon oxide precursor solution. A doped silicon oxide thin film if formed on a wafer by spin coating. The thin film and the wafer are baked at progressively increasing temperatures and the thin film and the wafer are annealed.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a block diagram of the method of the invention.

FIG. 2 is a PL spectrum of a terbium-doped SiO₂ thin film.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The method of the invention provides a doped precursor solutions for doped SiO₂ thin film deposition via a spin-coating process. The solution is stable and the synthesis method is reproducible. By adjusting the silicon concentration, a high quality SiO₂ or doped-SiO₂ thin film, in a wide range of thickness, from about 10 nm to 500 nm may be fabricated. The newly developed precursor solutions are low in cost, making commercialization more feasible. Doped SiO₂ thin films have many applications, one example of which is a Tb-doped SiO₂ thin film, which exhibits strong photoluminescence signals, and has application to electroluminescent devices, and is used as an example herein.

The goal of synthesizing a SiO₂ spin coating precursor according to the method of the invention is to fabricate a terbium-doped silicon oxide thin film as the active layer in an electroluminescent device. Thus, the synthesis of the SiO₂ spin coating precursor is the first step, followed by the incorporation of terbium ions into the solution. As previously noted, SiO₂ spin-coating precursors usually incorporate TEOS (Si(OCH₂CH₃)₄) as a source of silicon. Because of the high volatility of TEOS, a single coating of SiO₂ is too thin to be of much use, thus, multiple coating steps are required to build a usable SiO₂ thin film. The incorporation of terbium into a TEOS-based solution results in precipitate formation, which renders the solution unacceptable for spin-on applications. Thus, the SiO₂ spin-coating precursor solution used in the method of the invention uses SiCl₄ as the silicon source.

Because SiCl₄ is highly reactive, large organic molecules may be reacted with SiCl₄ to form a high molecular weight species, which has much less volatility than does a TEOS compound. A high molecular weight acid was initially selected to be reacted with SiCl₄, however, the resultant solution did not provide a sufficiently high quality SiO₂ thin film. Instead of a high molecular weight organic acid, a lower molecular weight ethylene glycol-type organic acid was selected, e.g., diethylene glycol monoethyl ether (DGME). Initially, the molar ratio of SiCl₄ to DGME was 1:4, however, that solution had poor wetting properties on both SiO₂ and silicon. After reducing the molar ratio to 1:2, a precursor solution which resulted in a high quality SiO₂ thin film was synthesized.

The method of the invention, shown generally at 10 in FIG. 1, is as follows: to a 500 mL round bottom flask, having 95 mL of DGME therein, 40 mL of SiCl₄ is slowly added, step 12. Hydrogen gas is generated during the addition, and carried out via nitrogen gas flow. After the addition of SiCl₄, 150 mL of 2-methoxyethyl ether is added, step 14, to from a preliminary precursor solution. The preliminary precursor solution is then heated at 150° C. in an oil bath for 16 hours, with constant stirring, step 16. The solution is filtered through a 0.2 μm filter for purification, step 18.

A doped source solution, containing about 11% terbium, is made by incorporating the impurity into 2-methoxyethanol, which, in the preferred embodiment, includes introducing terbium ions from 12.18 gm of Tb(NO₃)₃ into 14 mL of 2-methoxyethanol, step 20, and mixing, step 22, the doped source solution into the preliminary precursor solution, to form a doped-SiO₂ spin-coating precursor solution. Any resultant solid precipitate may be dissolved by adding a few drops of water to obtain a clear solution. The concentration of silicon in the doped-SiO₂ spin-coating precursor solution may be adjusted by addition of organic solvents. Other doping impurities may be used, e.g., other rare-earth elements.

To produce a Tb-doped SiO₂ thin film, the doped-SiO₂ spin-coating precursor solution is spin-coated on a silicon wafer surface, step 24, and then baked at about 160°, 220° and 300° C. for one minute at each temperature, step 26. Baking may be done in a range of temperatures, e.g., 150° C. to 170° C., 180° C. to 250° C.; and 260° C. to 320° C. The resultant film is further annealed, step 28, at about 700° C. for about 10 minutes in an oxygen atmosphere. To produce a high photoluminescence signal, the film is again annealed, this time at between about 900° to 1100° C. for between about one to forty minutes, an a wet oxygen ambient atmosphere. The typical photoluminescence spectrum for a thin film fabricated according to the method of the invention is depicted in FIG. 2.

Thus, a method of producing a stable, doped SiO₂ spin-coating precursor has been disclosed. It will be appreciated that further variations and modifications thereof may be made within the scope of the invention as defined in the appended claims.

Claims

1. A method of making a doped silicon oxide thin film using a doped silicon oxide precursor solution, comprising: mixing a silicon source in an organic acid;adding 2-methoxyethyl ether to the silicon source and organic acid to from a preliminary precursor solution;heating and stirring the preliminary precursor solution;filtering the preliminary precursor solution;dissolving a doping impurity in 2-methoxyethanol to from a doped source solution;mixing the preliminary precursor solution and the doped source solution to from a doped silicon oxide precursor solution;forming a doped silicon oxide thin film on a wafer by spin coating the doped silicon oxide precursor solution onto the wafer;baking the thin film and the wafer at progressively increasing temperatures; andannealing the thin film and the wafer at least once.

2. The method of claim 1 wherein said mixing a silicon source in an organic acid includes mixing SiCl4 and diethylene glycol monoethyl ether (DGME)

3. The method of claim 2 wherein the ratio of SiCl4 and DGME is no less than 1:2.

4. The method of claim 1 wherein said dissolving a doping impurity in 2-methoxyethanol to from a doped source solution includes dissolving Tb(NO3)3.

5. The method of claim 1 wherein said baking the thin film and the wafer at progressively increasing temperatures includes baking the thin film and the wafer at about 160° C., 220° C. and 300° C. for about one minute at each temperature.

6. The method of claim 1 wherein said annealing includes a first anneal at a temperature of about 700° C. for about ten minutes in an oxygen atmosphere.

7. The method of claim 6 wherein said annealing includes a second anneal at a temperature of between about 900° C. to 1100° C. for between about one minute to about forty minutes in a wet oxygen ambient atmosphere to produce a thin film for generating a high photoluminescence signal.

8. A method of making a doped silicon oxide thin film using a doped silicon oxide precursor solution, comprising: mixing a silicon source in an organic acid;adding 2-methoxyethyl ether to the silicon source and organic acid to from a preliminary precursor solution;heating and stirring the preliminary precursor solution;filtering the preliminary precursor solution;dissolving Tb(NO3)3 in 2-methoxyethanol to from a Tb-doped source solution;mixing the preliminary precursor solution and the Tb-doped source solution to from a Tb-doped silicon oxide precursor solution;forming a Tb-doped silicon oxide thin film on a wafer by spin coating the Tb-doped silicon oxide precursor solution onto the wafer;baking the thin film and the wafer at progressively increasing temperatures; andannealing the thin film and the wafer at least once.

9. The method of claim 8 wherein said mixing a silicon source in an organic acid includes mixing SiCl4 and diethylene glycol monoethyl ether (DGME).

10. The method of claim 9 wherein the ratio of SiCl4 and DGME is no less than 1:2.

11. The method of claim 8 wherein said baking the thin film and the wafer at progressively increasing temperatures includes baking the thin film and the wafer at about 160° C., 220° C. and 300° C. for about one minute at each temperature.

12. The method of claim 8 wherein said annealing includes a first anneal at a temperature of about 700° C. for about ten minutes in an oxygen atmosphere.

13. The method of claim 12 wherein said annealing includes a second anneal at a temperature of between about 900° C. to 1100° C. for between about one minute to about forty minutes in a wet oxygen ambient atmosphere to produce a thin film for generating a high photoluminescence signal.

14. A method of making a doped silicon oxide thin film using a doped silicon oxide precursor solution, comprising: mixing a SiCl4 in an ethylene glycol-type organic acid;adding 2-methoxyethyl ether to the SiCl4 in an ethylene glycol-type organic acid to from a preliminary precursor solution;heating and stirring the preliminary precursor solution;filtering the preliminary precursor solution;dissolving Tb(NO3)3 in 2-methoxyethanol to from a Tb-doped source solution;mixing the preliminary precursor solution and the Tb-doped source solution to from a Tb-doped silicon oxide precursor solution;forming a Tb-doped silicon oxide thin film on a wafer by spin coating the Tb-doped silicon oxide precursor solution onto the wafer;baking the thin film and the wafer at progressively increasing temperatures; andannealing the thin film and the wafer at least once.

15. The method of claim 14 wherein the ethylene glycol-type organic acid is diethylene glycol monoethyl ether (DGME) the ratio of SiCl4 and DGME is no less than 1:2.

16. The method of claim 14 wherein said baking the thin film and the wafer at progressively increasing temperatures includes baking the thin film and the wafer at about 160° C., 220° C. and 300° C. for about one minute at each temperature.

17. The method of claim 14 wherein said annealing includes a first anneal at a temperature of about 700° C. for about ten minutes in an oxygen atmosphere.

18. The method of claim 17 wherein said annealing includes a second anneal at a temperature of between about 900° C. to 1100° C. for between about one minute to about forty minutes in a wet oxygen ambient atmosphere to produce a thin film for generating a high photoluminescence signal.