Embodiments of the invention will now be described with reference to the drawings.
The method for manufacturing a semiconductor device of this embodiment comprises the steps of depositing a high dielectric film (step S102), low-temperature oxygen annealing (step S104), short-time annealing at 900° C. or less (step S106), thinning the high dielectric film (step S108), and forming an upper layer (step S110).
Before the sequence shown in
After the foregoing preprocess is completed, a high dielectric film is deposited as shown in
Then, low-temperature oxygen annealing is performed (step S104). That is, because oxygen deficiency occurs in forming the amorphous high dielectric film 4, the oxygen deficiency is complemented.
Next, for crystallizing the amorphous high dielectric film 4, short-time annealing at 900° C. or less is performed in an oxygen and nitrogen atmosphere under a pressure of 1 atmosphere or more (step S106). The annealing time is about 30 seconds. Conventionally, a high temperature of 1000° C. or more is required. However, according to this embodiment, crystallization is possible at a temperature of 900° C. or less. By crystallization, a crystallized high dielectric film 5 is formed as shown in
For example, in the case of semiconductor flash memory devices, the required thickness for a high dielectric film is about 2 nm. Therefore the thickly formed and crystallized film is thinned (step S108). Thinning can be performed by dry etching, for example. Specifically, reactive ion etching or other technique is used for etching at a slow rate. As described above, the film is once thickly formed, crystallized, and then thinned. Thus a high dielectric film 6 realized as a crystallized IPD film can be obtained as shown in
Then a control gate electrode 8, for example, is formed as an upper layer to a thickness of 50 to 100 nm. Thus a laminated structure shown in
JP 2006-086525A and JP 10-189921A disclose oxides of aluminum, hafnium, lanthanum, and tantalum used as materials for high dielectric films. However, in JP 2006-086525A and JP 10-189921A, the high dielectric films are only used as they are formed, and different from that obtained in this embodiment.
In this embodiment, first, as shown in
Subsequently, the high dielectric film 5 is thinned by etching to obtain a high dielectric film 6 (step S108). Crystal grains are grown also in the film surface direction. Hence, as shown in
On the other hand, in the comparative example shown in
As described above, according to this embodiment, as shown in
That is, according to this embodiment, crystallization can be performed at lower temperatures than in conventional techniques. Furthermore, the high dielectric film after thinning (step S108) tends to have a relatively large crystal grain size in the film surface direction. Note that in
The method for manufacturing a semiconductor device of this embodiment comprises the steps of depositing a high dielectric film (step S102), low-temperature oxygen annealing (step S104), depositing a silicon nitride film (step S105), short-time annealing at 900° C. or less (step S106), etching the silicon nitride film (step S107), thinning the high dielectric film (step S108), and forming an upper layer (step S110).
The same steps as those in the first embodiment are not described here.
The silicon nitride film 7 serves to apply stress to the amorphous high dielectric film 4. The silicon nitride film 7 is formed by depositing a 2-nm thin film at a low deposition rate in a plurality of (e.g. 10) iterations using low-temperature plasma CVD or other technique. A larger stress can be produced by deposition divided into a plurality of iterations in this manner than by continuous deposition. The stress applied to the amorphous high dielectric film 4 by such a silicon nitride film 7 facilitates initial nucleation for crystallization, which enables the crystallization temperature to be decreased to 900° C. or less. Furthermore, thermal budget can be reduced to a low level by using low-temperature plasma CVD in forming the silicon nitride film 7.
Removal of the silicon nitride film (step S107) can be performed by wet etching using a chemical solution such as high-temperature phosphoric acid. This can prevent the underlying high dielectric film 5 from being etched. As the result of these steps, as shown in
The method similar to that of the first embodiment was applied to an amorphous high dielectric film 4 of aluminum oxide for the following three film thicknesses: 3 nm, 5 nm, and 10 nm. The degree of crystallization was examined by transmission electron microscopy (TEM) and X-ray diffraction (XRD). For a film thickness of 10 nm, by cross-sectional TEM, a clear lattice fringe was observed throughout the film thickness in a film heated at the crystallization temperature of 900° C. for 30 seconds. That is, it was verified that nearly single crystal grains were formed throughout the film thickness and that the size of this crystal grain in the film surface direction was also 10 nm or more.
On the other hand, for a film thickness of 3 nm, by cross-sectional TEM, no lattice fringe was observed for heat treatment at 900° C. for 30 seconds. By planar TEM, a large number of crystallites having an average grain size of less than 1 nm were observed, with a low degree of crystallization.
TABLE 1 summarizes the measurement results by XRD.
For each pair of film thickness and annealing time, the table shows the annealing temperature at which a diffraction peak specific to Al2O3 crystal was observed. In the case of an annealing time of 30 seconds, crystallization occurs at 900° C. for a film thickness of 10 nm. However, for a 3-nm film, only crystallites were obtained even at 1000° C. For a film thickness of 5 nm, crystallization was observed at 900° C. by extending the annealing time to 60 seconds. Furthermore, for a film thickness of 3 nm, it was verified that crystallization occurs at 1000° C. by extending the annealing time to 60 seconds.
From the above results, crystallization of a high dielectric film of aluminum oxide and the like can be performed with reduced thermal budget by forming a film thicker than the finally required film thickness and etching it after crystallization. Specifically, for example, to obtain a crystallized high dielectric film having a film thickness of 2 nm, a high dielectric film of e.g. about 10 nm is formed first. A stress application film may be further introduced on the high dielectric film. The film is crystallized at a low temperature. Then the film is thinned by etching to a predetermined thickness of about 2 nm. Thus, without affecting transistor characteristics, a crystallized high dielectric film can be obtained as an IPD film having a predetermined thickness at a low temperature with reduced thermal budget.
In this example, aluminum oxide is used for the high dielectric film 6. However, as described above, it is also possible to use oxides of hafnium, lanthanum, and tantalum, or oxides in which a plurality of metals are mixed, e.g. HfAxlOy.
The invention is not limited to application to high dielectric films used in flash memories. Furthermore, the material is not limited to metal oxides. The invention is applicable to forming a crystallized ultrathin film, and also to methods for manufacturing various devices in which a crystallized ultrathin film is used.
Number | Date | Country | Kind |
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2006-259313 | Sep 2006 | JP | national |