This invention relates to the processing of high-purity tantalum to produce a physical vapor deposition (PVD) component with a microstructure that is desirable for uniform deposition. In particular, the invention relates to the manufacture of high-purity tantalum with a mean grain size of less than 100 μm and a uniform, predominately (111)<uvw> crystallographic texture throughout the component thickness.
Tantalum is currently used extensively in the electronics industry, which employs tantalum in the manufacture of highly effective electronic capacitors. Its use is mainly attributed to the strong and stable dielectric properties of the oxide film on the anodized metal. Both wrought thin foils and powders are used to manufacture bulk capacitors. In addition, thin film capacitors for microcircuit applications are formed by anodization of tantalum films, which are normally produced by sputtering. Tantalum is also sputtered in an Ar—N2 ambient to form an ultra thin TaN layer which is used as a diffusion barrier between a Cu layer and a silicon substrate in new generation chips to ensure that the cross section of the interconnects can make use of the high conductivity properties of Cu. It is reported that the microstructure and stoichiometry of the TaN film are, unlike TiN, relatively insensitive to the deposition conditions. Therefore, TaN is considered a much better diffusion barrier than TiN for chip manufacture using copper as metallization material. For these thin film applications in the microelectronics industry, high-purity tantalum sputtering targets are needed.
The typical tantalum target manufacture process includes electron-beam (EB) melting ingot, forging/rolling ingot into billet, surface machining billet, cutting billet into pieces, forging and rolling the pieces into blanks, annealing blanks, final finishing, and bonding to backing plates. The texture in tantalum plate is very dependent on processing mechanisms and temperatures. According to Clark et al. in the publication entitled “Effect of Processing Variables on Texture and Texture Gradients in Tantalum” (Metallurgical Transactions A, September 1991), the texture expected to develop in cold-rolled and annealed body-centered cubic (bcc) metals and alloys consists of orientations centered about the ideal orientations, {001}<110>, {112}<110>, {111}<110>, and {111}<112>. Generally, conventionally processed tantalum is forged or rolled from ingot to final thickness, with only one (1) or no intermediate annealing stages. A final anneal is usually applied to the plate simply to recrystallize the material. The direction of the deformation influences the strengths of resulting annealed textures but generally little attention is given to the resulting distribution of textures. In conventionally processed tantalum, significant texture variation exists in the cross-section of the plate, as described by Clark et al., “Influence of Transverse Rolling on the Microstructural and Texture Development in Pure Tantalum,” Metallurgical Transactions, Vol. 23A, August 1992, p. 2183-2191m; Raabe et al., “Texture and Microstructure of Rolled and Annealed Tantalum,” Materials Science and Technology, Vol. 10, April 1994, p. 299-305; and Michaluk et al., “Methodologies for Determining the Global Texture of Tantalum Plate Using X-ray Diffraction,” Tantalum, The Minerals, Metal & Materials Society, 1996, p. 123-131.
Typically the above mentioned textures exist in stratified bands through the thickness of the rolled plate, or form a gradient of one texture on the surface usually {100}<uvw>, with a gradual transition to a different texture at the centerline of the plate, usually {111}<uvw>. Wright et al., “Effect of Annealing Temperature on the Texture of Rolled Tantalum and Tantalum-10 wt. % Tungsten” (Proceedings of the 2nd International Conference on Tungsten and Refractory Metals, pg 501-508, 1994). Another cause of texture variation through the target thickness is the non-uniformity of the deformation processes used to form the plate. Texture non-uniformity results in variable sputter deposition rates and sputter surface irregularities, which in turn is believed to be a source of micro-arcing.
Micro-arcing is believed to believed to be the principle cause of particle generation and is thus undesirable in the semiconductor industry.
In
In one aspect of the invention, a method for producing a tantalum PVD component includes a minimum of three stages, each of which include a deformation step followed by a high-temperature anneal. The deformation occurs in air and at a component temperature less than or equal to 750° F. in at least one of the minimum of three stages. The anneal occurs at a component temperature of at least 2200° F. in at least the first two of the minimum of three stages. By way of example, the annealing may occur in an inert atmosphere. The tantalum component exhibits a uniform texture that is predominately {111}<uvw> throughout a thickness of the component.
In another aspect of the invention, a method for producing a tantalum PVD component comprising a minimum of three stages, each of which include a deformation step followed by a high-temperature anneal. The deformation occurs in air and at a component temperature of from 200° F. to 750° F. in at least the last stage or the third stage of the minimum of three stages. The anneal occurs at a component temperature of from 1500° F. to 2800° F. in at least three of the minimum of three stages. By way of example, the annealing may occur in an inert atmosphere. The tantalum component exhibits a uniform texture that is predominately {111}<uvw> throughout a thickness of the component.
Preferred embodiments of the invention are described below with reference to the following accompanying drawings.
In accordance with the present invention there is provided a processing route for producing high purity tantalum PVD components with a mean fine grain size of less than 100 microns and uniform crystallographic texture throughout the component thickness. As known to those of ordinary skill, PVD includes, but is not limited to sputtering.
The method includes forging, rolling and annealing high-purity, vacuum-melted tantalum ingots in such a way as to eliminate remnant as-cast grain structure, and produce a homogeneous fine-grain size (mean<100 μm) microstructure with a uniform, predominately {111}<uvw> texture throughout the thickness of the target. Significant sputtering problems have been reported when the texture of the target is not uniform throughout the target thickness. Sputtering rates and film deposition rates can change as a function of target crystallographic texture. This variable sputter rate across a target surface causes film thickness uniformity problems and also produces unwanted surface topography in the form of “ridging,” which in turn is believed to cause micro-arcing.
In one aspect, the invention uses a series of deformation techniques, with a minimum of three (3) intermediate, high-temperature inert-atmosphere anneals, preferably under vacuum conditions, to produce a fine-grain size (mean<100 μm) tantalum targets with a uniform, predominately {111}<uvw> texture throughout the target thickness that, until now, was unseen in the industry. “Uniform texture throughout the target thickness” refers to a homogeneous distribution of textural components with no visible banding at a resolution of 20× from the target surface to at least mid-thickness. “Inert” refers to an atmosphere that is non-reactive with the tantalum-containing mass.
Experiments associated with this invention also revealed that, by controlling the annealing temperature, the most desirable texture for collimated sputtering, the (111) texture, can be generated. The (111) texture is the only texture that has one of the close-packed directions aligned normal to the target surface. This direction is a dominant emission direction and is, therefore, the texture required for collimated sputtering.
The high-purity tantalum material of the present invention is preferably 3N5 (99.95%) pure and contains less than 500 ppm total metallic impurities, excluding gases. The methods of chemical analysis used to derive the chemical descriptions set forth herein are the methods known as glow discharge mass spectroscopy (GDMS) for metallic elements and LECO gas analyzer for non-metallic elements.
In the context of the present document, the term “PVD components” includes, but is not limited to, PVD targets. Deposition may occur from other components in a deposition chamber such as coils, pins, etc. and, thus, a desire may exist for PVD components other than targets to contain the materials and/or be formed by the methods described herein.
Electron beam (EB), Vacuum Arc Melted (VAR), or other vacuum melted tantalum ingots are deformed perpendicular to the ingot centerline to break up the as-cast grain microstructure. This deformation can be forging, rolling, or extrusion whereby significant cross-sectional area or thickness reduction takes place. The reduction in cross-sectional area may be greater than a reduction ratio of 3:1 (cross-sectional area of ingot to cross-sectional area of the forged billet), or equivalent to no less than about 40% strain reduction from starting thickness to final thickness. The forged billet may then be annealed in an inert atmosphere, preferably vacuum, at a high temperature greater than about 1500° F. or, advantageously, greater than 2200° F. to achieve a recrystallized microstructure. As a practical matter, anneal temperature may be from about 1500° F. to about 2800° F. or, advantageously, from 2000° F. to 2500° F. to avoid processing too hot. A particularly advantageous anneal temperature that achieves excellent results is from 2200° F. to 2400° F.
The resulting billet/plate is then deformed no less than an additional 35%, preferably 45-65%, of its thickness and subjected to a second high-temperature inert atmosphere anneal, within the same temperature ranges described for the first anneal, to achieve a recrystallized microstructure. However, the particular temperature or temperature range selected may be different from the first anneal. The process of the present invention includes an additional deformation step with a strain greater than or equal to 60% followed by a final inert-atmosphere anneal within the same temperature ranges described for the first anneal to recrystallize the microstructure to the desired fine grain size. Since grain size control is desired in the final anneal, the most advantageous temperature is from about 1750° F. to about 1800° F.
It may be additionally advantageous to incorporate warm deformation techniques. For example, the deformation may occur at a component temperature less than or equal to 750° F. in at least one of the stages. A temperature of from 200° F. to 750° F. may provide a greater advantage. Warm deformation in at least the last two stages, potentially three stages, of a minimum of three stages may also provide a greater advantage. Primarily, the advantage results from the yield strength of tantalum during deformation being reduced with increasing temperature. The lowered yield strength allows a greater thickness reduction, which may provide a more uniform stress distribution during deformation.
At higher temperatures, such as those used in the annealing techniques described herein, oxidation of tantalum might become a concern. Accordingly, annealing may occur in an inert atmosphere. However, deforming at 750° F. or less does not create a significant risk of tantalum oxidation and may occur in air. Deforming at 750° F. or less in air thus allows greater flexibility in thickness reduction and selection of a processing atmosphere without a significant risk of oxidation. As a practical matter, warm deformation allows the use of larger work pieces since greater thickness reductions, compared to cold deformation techniques, are possible enroute to producing a PVD component of a specified thickness. Using warm deformation, similar or improved results compared to those demonstrated in Processes 8 through 12 of Table 1 may be obtained for larger work pieces and/or may provide more uniform strain distributions.
Twelve high-purity tantalum ingots were processed according to conventional methods or according to aspects of the invention. The parameters for each experiment and the corresponding grain size and texture results are summarized in Table 1. Texture uniformity was measured by cutting samples from the target and analyzing them using an EBSD system on a scanning electron microscope (SEM). The mapped area was 7 mm×7 mm and was measured from the target surface to at least the plate mid-thickness. The lighter areas depict {111}<uvw> textures and the darker areas depict {100}<uvw> textures.
The ingots processed by conventional methods (Processes 1 through 7) exhibited a banded microstructure in both grain size and texture.
Although the experimental data show the grain size results to be less than about 50 μm it is expected that a grain size of less than 100 μm will produce similar sputtering results, so long as the texture is uniform throughout the target thickness.
Sputter trials were conducted on a conventional high-purity tantalum target and a target processed according to this invention in order to compare the sputtering characteristics.
In compliance with the statute, the invention has been described in language more or less specific as to structural and methodical features. It is to be understood, however, that the invention is not limited to the specific features shown and described, since the means herein disclosed include preferred forms of putting the invention into effect. The invention is, therefore, claimed in any of its forms or modifications within the proper scope of the appended claims appropriately interpreted in accordance with the doctrine of equivalents.
This application is a continuation-in-part of U.S. patent application Ser. No. 09/999,095, filed Oct. 30, 2001, which is a divisional application of U.S. patent application Ser. No. 09/497,079, filed Feb. 2, 2000, the entire subject matter of which is herein incorporated by reference.
Number | Date | Country | |
---|---|---|---|
Parent | 09497079 | Feb 2000 | US |
Child | 09999095 | Oct 2001 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 09999095 | Oct 2001 | US |
Child | 11331875 | Jan 2006 | US |