BIS(ALKYLTETRAMETHYLCYCLOPENTADIENYL)ZINC, PRECURSOR FOR CHEMICAL VAPOR DEPOSITION, AND PRODUCTION METHOD FOR ZINC-CONTAINING THIN FILM

Abstract

Provided is a precursor for chemical vapor deposition for depositing a zinc-containing thin film. Bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (1) which is liquid at room temperature and is therefore easy to handle (in the formula (1), R.sup.1 and R.sup.2 are alkyl group having 3 carbon atoms); a precursor for chemical vapor deposition comprising bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (2) (in the formula (2), R.sup.3 and R.sup.4 are alkyl group having 2-5 carbon atoms); and a production method for a zinc-containing thin film through chemical vapor deposition.

Claims

1. Bis(alkyltetramethylcyclopentadienyl)zinc represented by the following formula (1): ##STR00006## in the formula (1), R.sup.1 and R.sup.2 are alkyl group having 3 carbon atoms.

2. A precursor for chemical vapor deposition comprising bis(alkyltetramethylcyclopentadienyl)zinc represented by the following formula (2) as a main component: ##STR00007## in the formula (2), R.sup.3 and R.sup.4 are alkyl group having 2 to 5 carbon atoms.

3. The precursor for chemical vapor deposition according to claim 2, being liquid at 23° C.

4. A production method for zinc-containing thin film by chemical vapor deposition using a precursor which is liquid at 23° C. for chemical vapor deposition comprising bis(alkyltetramethylcyclopentadienyl)zinc represented by the following formula (2) as a main component: ##STR00008## in the formula (2), R.sup.3 and R.sup.4 are alkyl group having 2 to 5 carbon atoms.

5. The production method for zinc-containing thin film according to claim 4, wherein the chemical vapor deposition is atomic layer deposition.

Description

DESCRIPTION OF EMBODIMENTS

[0017] Hereinafter, bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (1) of the present invention will be described.

##STR00004##

[0018] In the formula (1), R.sup.1 and R.sup.2 are alkyl group having 3 carbon atoms. R.sup.1 and R.sup.2 may be the same or different, but it is desirable that they are the same because of ease of synthesis.

[0019] The alkyl group having 3 carbon atoms includes n-propyl group and isopropyl group, and preferably n-propyl group.

[0020] Bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (1) is liquid at 23° C., atmospheric pressure, and has high vapor pressure. Therefore, it is suitable for a precursor for chemical vapor deposition.

[0021] The precursor for chemical vapor deposition of the present invention comprise bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (2) as a main component.

##STR00005##

[0022] In the formula (2), R.sup.3 and R.sup.4 are alkyl group having 2 to 5 carbon atoms. R.sup.3 and R.sup.4 may be the same or different, but it is desirable that they are the same because of ease of synthesis.

[0023] The alkyl group having 2 to 5 carbon atoms includes ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, neopentyl group, 3-methylbutyl group, 1-methylbutyl group, 1-ethylpropyl group, and 1,1-dimethylpropyl group.

[0024] Among these, R.sup.3 and R.sup.4 are preferably alkyl groups each having 3 to 5 carbon atoms. To be specific, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, and tert-butyl group are preferable; n-propyl group and isopropyl group are more preferable; and n-propyl group is particularly preferable.

[0025] It is desirable that bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (1) or (2) be liquid at room temperature. Therefore its melting point is preferably below room temperature, specifically below 35° C., more preferably below 23° C., further preferably below 20° C., and particularly preferably below 10° C.

[0026] The content of bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (2) in the precursor for chemical vapor deposition is desirably almost 100%, but a very small amount of impurities are allowed to be contained as long as they neither react on bis(alkyltetramethylcyclopentadienyl)zinc nor vaporize at a temperature when bis(alkyltetramethylcyclopentadienyl)zinc is used as the precursor for vapor deposition.

[0027] By the chemical vapor deposition (CVD), a thin film is deposited using bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (1), or the precursor for chemical vapor deposition comprising bis(alkyltetramethylcyclopentadienyl)zinc represented by the formula (2) as a main component, according to the present invention. In the chemical vapor deposition, the container of the precursor filled with bis(alkyltetramethylcyclopentadienyl)zinc is heated up to vaporization, and the vapor is supplied to the reaction chamber. In order to supply the precursor, namely, bis(alkyltetramethylcyclopentadienyl)zinc to the substrate in the reaction chamber, the temperature of a supply pipe that connects the precursor container with a reaction chamber and the reaction chamber needs to be set at a temperature where the precursor does not thermally decompose but maintains a gaseous state; in other words, a temperature that is higher than the temperature of the precursor container (i.e., the vaporization temperature of the precursor) and lower than the thermal decomposition temperature of the precursor. To enlarge the range of temperature for film deposition, i.e., the substrate temperature, it is desirable that the temperature of the precursor container be as low as possible and that the precursor used have sufficiently high vapor pressure even at low temperature.

[0028] The chemical vapor deposition includes thermal CVD in which deposition is formed by the continuous thermal decomposition on the substrate, and atomic layer deposition (ALD) in which individual atomic layers are deposited one layer at a time; and among them, atomic layer deposition (ALD) is preferable. For example, in an ALD, alternatively supplying bis(alkyltetramethylcyclopentadienyl)zinc as the precursor and an oxidant, and allowing them to react on the surface of the substrate, the zinc oxide-based thin film defined by an atomic layer scale can be deposited. The oxidant includes water vapor, ozone, and plasma-activated oxygen.

[0029] Bis(alkyltetramethylcyclopentadienyl)zinc of the present invention is liquid at room temperature, which enables the rate of precursor gas supply to be precisely controlled with a flow rate controller.

[0030] In case the precursor for vapor deposition is solid at room temperature, it becomes harder to adjust the rate of precursor supply with a flow rate controller. As a result, the rate of supplying the precursor to the reaction chamber fails to be controlled easily and precisely.

EXAMPLES

[0031] Hereinafter, the present invention will be described in detail with reference to examples, but the present invention is not restricted to the examples.

Example 1

[0032] To a 1 L four-necked flask, 400 ml of THF, 14.4 g (0.37 mol) of potassium metal, and 142.2 g (0.87 mol) of C.sub.5(CH.sub.3).sub.4(n-C.sub.3H.sub.7)H were added, and the mixture was allowed to react for 52 hours. THF was distilled off at 100° c. under reduced pressure to obtain C.sub.5(CH.sub.3).sub.4(n-C.sub.3H.sub.7)K.

[0033] To the C.sub.5(CH.sub.3).sub.4(n-C.sub.3H.sub.7)K, 600 ml of THF and 24.7 g (0.18 mol) of ZnCl.sub.2 were added, and the mixture was stirred at 50° C. for 5.5 hours. By distilling off THF at 50° c. under reduced pressure, solid content was obtained.

[0034] Distilling the solid content twice using a simple distillation apparatus at 100-150° C. and at 0.4-0.5 torr gave 37.6 g (0.096 mol) of yellow liquid in 53.3% yield (based on ZnCl.sub.2).

[0035] Analysis through the following (1) to (3) proved the obtained sample to be Zn[C.sub.5(CH.sub.3).sub.4(n-C.sub.3H.sub.7)].sub.2.

(1) Composition Analysis

[0036] ICP atomic emission spectrophotometry of the liquid obtained by wet decomposition of the sample showed that the Zn content was 15.9% (theoretical value: 16.7%).

(2) .SUP.1.H-NMR

[0037] Measurement condition: 400 MHz Varian UNITY INOVA-400S spectrometer; THF-d8 solvent; and 1D method

[0038] 1.87 (12H, singlet) ppm: C.sub.5(CH.sub.3).sub.4, 1.84 (12H, singlet) ppm: C.sub.5(CH.sub.3).sub.4, 2.23-2.19 (4H, multiplet) ppm: CH.sub.2CH.sub.2CH.sub.3, 1.24-1.19 (4H, sextet) ppm, CH.sub.2CH.sub.2CH.sub.3, 0.98-0.84 (6H, triplet) ppm: CH.sub.2CH.sub.2CH.sub.3

(3) .SUP.13.C-NMR

[0039] Measurement condition: 100 MHz Varian UNITY INOVA-400S spectrometer; THF-d8 solvent; and 1D method

[0040] 114.01, 113.28, 109.79 ppm: C5,

[0041] 29.13, 25.89, 14.37, 10.99, 10.84 ppm: C(CH.sub.3).sub.4(n-C.sub.3H.sub.7)

[0042] Next, sealed cell differential scanning calorimetry (SC-DSC) at a heating rate of 10° C./min showed that the compound has a melting point of approximately 5° C. and does not thermally decompose until the temperature reaches approximately 250° C. The vaporization rate calculated from weight change at 150° C. in 1 atm argon atmosphere was approximately 50 μg/min.

[0043] Accordingly, Zn[C.sub.5(CH.sub.3).sub.4(n-C.sub.3H.sub.7)].sub.2 being liquid at room temperature certainly has thermal stability and vaporizability indispensable for chemical vapor deposition.

Comparative Example 1

[0044] To a 1 L four-necked flask, 400 ml of THF, 11.6 g (0.30 mol) of potassium metal and 42.1 g (0.45 mol) of C.sub.5H.sub.4(C.sub.2H.sub.5)H were added, and the mixture was allowed to react for 21 hours. THF was distilled off at 40° c. under reduced pressure to obtain C.sub.5H.sub.4(C.sub.2H.sub.5)K.

[0045] To the C.sub.5H.sub.4(C.sub.2H.sub.5)K, 600 ml of THF and 19.4 g (0.14 mol) of ZnCl.sub.2 were added at −78° c., and the mixture was stirred at 50° C. for 6 hours. By distilling off THF at 50° c. under reduced pressure, solid content was obtained.

[0046] Distilling the solid content twice using a simple distillation apparatus at 120-190° C. and at 0.4-0.5 torr gave 8.1 g (0.032 mol) of pale yellow solid in 22.9% yield (based on ZnCl.sub.2).

[0047] Analysis through the following (1) to (3) proved the obtained sample to be Zn[C.sub.5H.sub.4(C.sub.2H.sub.5)].sub.2.

(1) Composition Analysis

[0048] ICP atomic emission spectrophotometry of the liquid obtained by wet decomposition of the sample showed that the Zn content was 25.7% (theoretical value: 26.0%).

(2) .SUP.1.H-NMR

[0049] Measurement condition: 400 MHz Varian UNITY INOVA-400S spectrometer; THF-d8 solvent; and 1D method 5.72-5.71 (4H, doublet) ppm: C.sub.5H.sub.4, 5.35-5.34 (4H, doublet) ppm: C.sub.5H.sub.4, 2.57-2.51 (4H, quartet) ppm: CH.sub.2CH.sub.3, 1.23-1.19 (6H, triplet) ppm: CH.sub.2CH.sub.3

(3) .SUP.13.C-NMR

[0050] Measurement condition: 100 MHz Varian UNITY INOVA-400S spectrometer; THF-d8 solvent; and 1D method

[0051] 138.50, 138.18, 109.51, 109.49, 99.28, 99.27 ppm: C5,

[0052] 23.67, 15.81 ppm: CH.sub.2CH.sub.3

[0053] Next, sealed cell differential scanning calorimetry (SC-DSC) at a heating rate of 10° C./min showed that the compound has a melting point of approximately 90° C. and thermal decomposition starts at approximately 184° C. The vaporization rate calculated from weight change at 150° C. in 1 atm argon atmosphere was approximately 0.7 μg/min.

[0054] Accordingly, Zn[C.sub.5H.sub.4(C.sub.2H.sub.5)].sub.2 being solid at room temperature is inferior to the compound of the present invention in both thermal stability and vaporizability.