Flat interface for a metal-silicon contract barrier film

Abstract

A conductive contact having an atomically flat interface. The contact includes, in order, a silicon substrate, a highly disordered silicide layer, and a titanium oxynitride layer. The silicide layer is formed of titanium, silicon, and one of the elements tungsten, tantalum, and molybdenum. The interface between the silicon substrate and the silicide layer is atomically flat. The flat interface prevents diffusion of conductive materials into the underlying silicon substrate. The contact is useful especially for very small devices and shallow junctions, such as are required for ULSI shallow junctions.

Description

TECHNICAL FIELD

The present invention relates to the formation of conductive contacts during the fabrication of semiconductor integrated circuits. More particularly, this invention relates to a method for forming an atomically flat interface that prevents diffusion of the conductive material into the underlying semiconductor layer.

BACKGROUND OF THE INTENTION

The continuing increase in semiconductor device circuit speed and density has been accompanied both by a decrease in the vertical dimensions of devices and by a need for reliable dense wiring. The decrease in vertical dimension has produced shallower device junctions.

In the processing of integrated circuits, individual devices that are comprised of silicon are connected into circuits by subsequent metal layers. Great care must be given to the metal-to-silicon interface because the metal-silicon junction is prone to certain problems that require process attention. Two such problems are high-ohmic connections, which may electrically look like open circuits, and poisoning of the device by the contacting metal.

During formation of an interconnect, a contact hole is created in an insulating layer, typically silicon dioxide, to expose the underlying semiconductor substrate, typically a N+ region set in a P− well, or a P+ region set in a N− well. To form the interconnect, the appropriate metal is deposited in the contact hole by standard techniques. If the metal is placed in direct contact with the semiconductor substrate, the metal can diffuse into the semiconductor during subsequent processing of the device, especially at temperatures above 400° C., which are encountered during device packaging.

Diffusion produces spiking of the metal into the semiconductor. Spiking typically extends for less than about 0.5 micron into the semiconductor, and thus is not a particular problem when the device is greater than 0.5 micron thick. For high-density circuits in which the device is less than 0.5 micron thick, however, spiking can short the metal to the underlying P-well or N-well, rendering the device inoperative.

Metal silicides are typically used to provide good ohmic contact to device junctions. Titanium silicide (TiSi 2 ) has become the most widely used silicide for self-aligned silicide applications in the Ultra Large Scale Integration (ULSI) industry because of its low resistivity, its ability to be self-aligned, and its relatively good thermal stability. Titanium is deposited into the contact hole by standard deposition techniques. Silicidation is conducted by subsequently heating the substrate and metal to about 500° C. to 700° C.

To minimize junction leakage, the device junction must be kept below the silicide. This distance is determined by the amount of metal deposited in the contact hole, the amount of silicon consumed during heating, and the planarity of the reaction front during heating. The amount of silicon consumed is determined by the stoichiometry and crystal structure of the silicide formed as well as by the anneal time and anneal temperature. For titanium silicide, the molar ratio of metal to silicon is two to one. The planarity of the silicide reaction front is controlled by many variables, such as the cleanliness of the silicon surface before metal deposition and the reaction temperature. Typical semiconductor fabrication sequences produce non-planar, cusped reaction fronts. Junction depths could be made shallower by using a silicidation process that consumed less silicon, produced a more nearly planar reaction front, or both.

To prevent diffusion, many semiconductor fabrication sequences use a diffusion barrier between the metal and the silicon substrate. In a common process sequence, titanium nitride (TiN) is used as a barrier against attack by tungsten hexafluoride and by fluorine during the deposition of tungsten, a commonly used conductive material, by chemical vapor deposition from tungsten hexafluoride. A preferred method for forming the titanium nitride barrier conducts the silicidation reaction in a nitrogen-containing atmosphere, such as nitrogen gas, ammonia vapor, or forming gas. Titanium nitride is formed at the same time as titanium silicide.

The topography of the resulting interface limits the usefulness of this method in the development of smaller shallow junction devices. The method involves competing reactions in a very narrow region: formation of TiO y N z from above and formation of TiSi 2 from below. Thus, it is difficult to control the layer thickness of the bilayer, and the layer is typically nitrogen deficient. Formation of the titanium silicide layer consumes silicon from the substrate and the layer can be cusped.

The rough interface between titanium silicides and silicon is not good for shallow junctions or small devices. The layer is an unreliable barrier against attack during the chemical vapor deposition of tungsten, which can lead to tungsten encroachment and ruin the device. Although the barrier properties of the layer can be improved by incorporating oxygen during deposition of the titanium and the subsequent anneal, the non-uniformity in thickness of the TiO y N z layer, which degrades its effectiveness as a barrier, remains a problem.

U.S. Pat. No. 5,567,652 issued to Nishio discloses a method in which (1) a silicon dioxide layer is formed on the surface of the silicon substrate; (2) a layer of titanium is deposited on the oxide layer; (3) a layer of cobalt is deposited on the titanium layer; and (4) the substrate is heat treated in a nitrogen-containing atmosphere. On heat treatment, the titanium reacts with the silicon dioxide to form silicon at the interface. Then, some of the cobalt migrates through the titanium to form a layer of CoSi 2 at the interface. The layer of CoSi 2 formed at the interface reflects the crystal orientation of the silicon substrate. Consequently, a very flat layer of CoSi 2 is formed at the interface.

Several additional steps are introduced into the processing sequence, however, by this method. Initially, it is necessary to form the silicon dioxide layer. Two layers of metal, a layer of titanium and a layer of cobalt, must be individually deposited instead of a single layer of metal. Following heat treatment, it is necessary to remove both the oxygen-containing titanium nitride layer formed during heat treatment and the unreacted cobalt layer before a metal can be deposited on the CoSi 2 layer. Removal of each of these layers requires a separate step.

U.S. Pat. No. 5,047,367 issued to Wei discloses a process for the formation of a titanium nitride/cobalt silicide bilayer. The bilayer is formed by (1) depositing a layer of titanium on the silicon layer; (2) depositing a layer of cobalt on the titanium layer; and (3) annealing in a nitrogen-containing atmosphere. An additional step is required, deposition of the cobalt layer, and the final temperature of the anneal is high, about 850-950° C.

Thus, a need exists for a method for forming a barrier layer and a silicide layer in which (1) formation of the silicide layer consumes less silicon than a disilicide; (2) the interface formed between the silicide layer and the silicon substrate is a flat interface, preferably an atomically flat interface; and (3) the barrier layer is uniform in thickness. In addition, the method should be readily integratable into the procedures currently used to form semiconductor devices and, preferably, does not introduce additional processing steps.

SUMMARY OF THE INVENTION

The invention is a method for forming a semiconductor device with electrical interconnections that have low contact resistance and for forming a barrier layer that prevents undesired diffusion into the silicon substrate. The method comprises:

a) depositing a layer consisting essentially of titanium and an element selected from the group consisting of cobalt, tungsten, tantalum, and molybdenum on a silicon substrate, in which the amount of the element selected from the group consisting of cobalt, tungsten, tantalum, and molybdenum present in the layer does not exceed 20 atomic percent of the total amount of the element and titanium present in the layer;

b) annealing the substrate and the layer in a nitrogen-containing atmosphere at about 500° C. to about 700° C.; and

c) depositing a conductive material on the layer.

The method produces an atomically flat interface between the silicides formed during processing and the silicon substrate. The flat interface is critical for contacts for very small devices and shallow junctions, such as are required for ULSI shallow junctions. The uniform TiO y N z (titanium oxynitride, tioxynitride) layer formed by this method is a good barrier against attack by tungsten hexafluoride and fluorine during the chemical vapor deposition of tungsten.

Although not intending to be bound by any theory or explanation, it is believed that the cobalt in the titanium-cobalt alloy layer plays two roles during the annealing. First, the cobalt migrates to the silicon surface and slows formation of the silicide. Second, because of differences in both atomic radius and electronic structure between the cobalt and titanium atoms, each of these atoms bonds differently to silicon. This difference in bonding to silicon destroys the long-range spatial and electronic peniodicity of the silicide crystal and allows formation of highly disordered nano-crystalline or amorphous silicide. The highly disordered silicide forms, in turn, an atomically flat interface between silicon and the silicide. Highly disordered silicide also causes formation of a uniformly thick TiO y N z layer. Thus, a much more reliable barrier against attack of the silicon by metal or fluorine is created. In addition, a better-controlled silicide interface, which is more suitable for contact in shallow junction applications, is formed.

Unlike cobalt, the elements tungsten, tantalum, and molybdenum have atomic diameters that are similar to that of titanium. However, they have different electronic structures. Because of these differences in electronic structure, each of these atoms bonds differently to silicon, destroying the long-range spatial and electronic periodicity of the silicide crystal. As in the case of cobalt, this forms a highly disordered nano-crystalline or amorphous silicide.

In another embodiment, the invention is a contact in which the interface between the silicon substrate and its adjacent layer is atomically flat. In still another embodiment, the invention is a contact formed by the method of the invention. It is to be understood that both the foregoing general description and the following detailed description are exemplary, but are not restrictive, of the invention.

BRIEF DESCRIPTION OF THE DRAWING

The invention is best understood from the following detailed description when read in connection with the accompanying drawing. It is emphasized that, according to common practice, the various features of the drawing are not to scale. On the contrary, the dimensions of the various features are arbitrarily expanded or reduced for clarity. Included in the drawing are the following figures:

FIG. 1 is a cross-section of a silicon substrate with a titanium-cobalt alloy layer formed on the substrate;

FIG. 2 a is a cross-section of the multi-layer structure formed on anneal;

FIG. 2 b is a cross-section of a contact formed by the method of the present invention;

FIG. 3 shows a transmission electron microscopy (TEM) micrograph of a cross-section of a cobalt-containing, multi-layer structure formed on anneal;

FIG. 4 shows at higher magnification the TEM micrograph of the cross-section of the multi-layer structure formed on anneal;

FIG. 5 shows a cross-section of a tungsten-containing, multi-layer structure formed on anneal;

FIG. 6 shows a cross-section of a tantalum-containing, multi-layer structure formed on anneal; and

FIG. 7 shows a cross-section of a molybdenum-containing, multi-layer structure formed on anneal.

DETAILED DESCRIPTION OF THE INVENTION

The present invention includes a process for forming an atomically flat interface between a silicon substrate and a (Ti,M)Si x /TiO y N z layer, in which M is selected from the group consisting of cobalt (Co), tungsten (W), tantalum (Ta), and molybdenum (Mo), for use in self-aligned silicide technology and as a contact via fill. The layer serves as a barrier against attack on the silicon substrate during subsequent processing steps, such as attack by tungsten hexa-fluoride and fluorine during subsequent chemical vapor deposition of tungsten from tungsten hexafluoride.

The invention will now be described by reference to the accompanying figures. Throughout the specification, similar reference characters refer to similar elements in all of the figures. Although certain aspects of the invention will be described with respect to the use of cobalt, except where indicted the description also applies to the use of tungsten, to the use of tantalum, and to the use of molybdenum in place of cobalt.

Referring to FIG. 1 , silicon substrate 10 may be either mono-crystalline or poly-crystalline silicon. Using methods well known to those skilled in the art, such as are described, for example, by S. A. Campbell in The Science and Engineering of Microelectronic Fabrication, Oxford University Press, New York, 1996, the silicon substrate can be provided, for example, by formation of a contact hole, or via, in the dielectric layer over the region of a silicon substrate at which a connection is desired. Typically, the contact hole is formed over an N+ region set in a P-well or a P+ region set in an N-well.

A titanium-cobali alloy layer 12 is deposited on the surface of silicon substrate 10 by any one of several techniques known in the art. Deposition techniques include, for example, physical vapor deposition, chemical vapor deposition, plasma-enhanced chemical vapor deposition, flash evaporation, sputtering, electron beam evaporation, and ion-assisted deposition. The apparatus and techniques for vacuum deposition are well known to those skilled in the art.

The titanium and the cobalt may be deposited from different sources or from a source of titanium that also contains cobalt. For example, if the layer is deposited by sputtering, a sputtering target of titanium and cobalt is prepared such that a titanium layer containing the desired atomic percentage of cobalt is deposited on the silicon substrate. Alternatively, the layer can be deposited by co-sputtering titanium and cobalt such that a titanium film containing the desired atomic percentage of cobalt is deposited on the silicon substrate. When the physical vapor deposition process of evaporation is used, the titanium and cobalt are deposited from two different sources at appropriate rates to achieve the desired atomic percentage of cobalt. Other processes known in the art may also be used to deposit titanium-cobalt alloy layer 12 .

The amount of cobalt present in titanium-cobalt alloy layer 12 should not exceed about 20 atomic percent of the total amount of cobalt and titanium present in the layer, typically about 0.1 to about 20 atomic percent cobalt. Titanium-cobalt alloy layer 12 preferably contains about 1 to about 10 atomic percent cobalt, more preferably about 3 to about 7 atomic percent cobalt, and most preferably about 5 atomic percent cobalt.

Titanium-cobalt alloy layer 12 typically has a thickness of about 5 nm to about 100 nm, preferably about 5 nm to about 30 nm, more preferably about 5 nm to about 20 nm. Most preferably, titanium-cobalt alloy layer 12 is about 6 nm to about 10 nm thick.

Following deposition of titanium-cobalt alloy layer 12 , substrate 10 and layer 12 are annealed in a nitrogen-containing atmosphere, such as ammonia vapor, forming gas (a mixture of nitrogen and hydrogen), or nitrogen gas. The time and temperature are selected to ensure formation of the (Ti,Co)Si x and TiO y N z layers. The annealing step may be conducted at about 500° C. to about 700° C. for about 0.5 hour to about 2 hours. Above about 700° C., agglomeration of the (Ti,Co)Si x is observed. Preferably, the annealing step is conducted at about 550° C. for about 0.5 hour. The anneal may be done by methods well known to those skilled in the art, such as in a conventional annealing furnace or by rapid thermal anneal.

FIG. 2 a shows the multi-layer structure formed on anneal. The multi-layer structure consists of silicon substrate 10 , a cobalt silicide (CoSi w) layer 14 , a highly disordered silicide ((Ti,Co)Si x ) layer 16 , and a titanium oxynitride or tioxynitride (TiO y N z ) layer 18 .

During the initial stages of anneal, the titanium present in titanium-cobalt alloy layer 12 removes any silicon dioxide present on the surface of silicon substrate 10 . Generally, this oxide layer is only about 0.1 to 0.5 nm (1 to 5 Å) thick. Silicon dioxide dissolves into the titanium. Subsequently, the oxygen is rejected into the TiO y N z layer 18 by the growing silicide layer.

During anneal, cobalt in the (titanium-cobalt) alloy migrates to the silicon(titanium-cobalt) alloy boundary while silicon and the (titanium-cobalt) alloy form alloyed silicide. Within (Ti,Co)Si x layer 16 , cobalt segregates toward the interface between silicon and the alloyed silicide layer and forms CoSi w layer 14 at the boundary between the silicon and the alloyed silicide layer. CoSi w layer 14 is believed to be about a monolayer thick. CoSi w layer 14 has been detected by TEM analysis, nano-probe electron energy loss spectroscopy, and energy dispersive X-ray analysis.

TEM analysis has detected formation of an analogous tungsten silicide layer when tungsten is used in place of cobalt. The tungsten silicide layer is about a monolayer thick and is atomically flat. Although analogous silicide layers may be formed when tantalum or molybdenum is used in place of cobalt, formation of these layers has not been detected by TEM analysis.

The cobalt remaining in the silicide layer destroys the long-range spatial and electronic periodicity of the silicide crystal, producing a highly disordered layer of silicide. “Highly disordered” means that (Ti,Co)Si x layer 16 is either nano-crystalline or amorphous. As is well known to those skilled in the art, “nano-crystalline” means that there is some localized, short range order in the layer, typically about a few nanometers, while “amorphous” means that there is no order in the layer greater than a few Å. Highly disordered (Ti,Co)Si x layer 16 causes formation of an atomically flat interface between silicon substrate 10 and highly disordered (Ti,Co)Si x layer 16 .

Due to segregation of the cobalt during anneal, the amount of cobalt in highly disordered (Ti,Co)Si x layer 16 is greater that the amount present in titanium-cobalt alloy layer 12 . The amount of cobalt in highly disordered (Ti,Co)Si x layer 16 is typically about 0.2 to about 35 atomic percent, preferably about 2 to about 15 atomic percent, more preferably about 5 to about 10 atomic percent, and most preferably about 8 atomic percent, based on the total amount of cobalt and titanium present in (Ti,Co)Si x layer 16 . If the amount of cobalt in titanium-cobalt alloy layer 12 is about 5 atomic percent of the total amount of cobalt and titanium present in titanium-cobalt layer 12 , the amount of cobalt in (Ti,Co)Si x layer 16 is typically about 8 atomic percent of the total amount of cobalt and titanium present in (Ti,Co)Si x layer 16 .

Highly disordered (Ti,Co)Si x layer 16 is typically slightly more than half as thick as titanium-cobalt alloy layer 12 . (Ti,Co)Si x layer 16 typically has a thickness of about 3 nm to about 60 nm, preferably about 3 nm to about 20 nm, more preferably about 3 nm to about 12 nm. Most preferably, (Ti,Co)Si x layer 16 is about 4 nm to about 7 nm thick. When titanium-cobalt alloy layer 12 is about 9 nm thick, highly disordered (Ti,Co)Si x layer 16 is typically about 5 nm thick. Although the exact value of x depends on the conditions under which (Ti,Co)Si x layer 16 is formed (i.e., the amount of cobalt in titanium-cobalt alloy layer 12 , the thickness of titanium-cobalt alloy layer 12 , the anneal temperature, and the like), x has a value between one and two.

The titanium in titanium-cobalt alloy layer 12 reacts with nitrogen in the nitrogen-containing atmosphere and the oxygen that was present on the surface of titanium-cobalt alloy layer 12 to form TiO y N z layer 18 . No detectable cobalt remains in TiO y N z layer 18 . Due to the atomically flat interface between silicon substrate 10 and (Ti,Co)Si x layer 16 , TiO y N z layer 18 is very uniform in thickness, which makes it a more reliable barrier against attack by metals and by fluorine during subsequent processing steps.

TiO y N z layer 18 is typically slightly less than half as thick as titanium-cobalt alloy layer 12 . TiO y N z layer 18 typically has a thickness of about 2 nm to about 40 nm, preferably about 2 nm to about 15 nm, more preferably about 2 nm to about 8 nm. Most preferably, TiO y N z layer 18 is about 3 nm to about 6 nm thick. When titanium-cobalt alloy layer 12 is about 9 nm thick, TiO y N z layer 18 is typically about 4 nm thick.

The values of y and z depend on the reaction conditions and typically vary across the cross-section of TiO y N z layer 18 . Typically, the amount of oxygen near the interface with highly disordered (Ti,Co)Si x layer 16 is greater than the amount of oxygen at the surface, and the amount of nitrogen is greater at the surface than the amount of nitrogen near the interface with (Ti,Co)Si z layer 16 .

After anneal, it is unnecessary to remove any of the layers formed on anneal. A conductive material can be deposited directly on top of the interface by methods well known to those skilled in the art. Typical conductive materials include, for example, tungsten, aluminum, copper, gold, tantalum, aluminum-copper alloy, and aluminum-silicon-copper alloy. A preferred conductive material is tungsten. Tungsten may be deposited by chemical vapor deposition of tungsten hexa-fluoride (WF 6 ). FIG. 2 b shows conductive material 20 over TiO y N z layer 18 .

Following the procedures described above, a contact comprising, in order: a) a silicon substrate; b) a silicide layer, in which the silicide layer consists essentially of silicon and an element selected from the group consisting of tungsten, tantalum, and molybdenum; c) a highly disordered silicide layer comprising titanium, silicon, and the same element present in the highly disordered silicide layer; and d) a titanium oxynitride layer can be prepared. The interface between the silicon substrate and the highly disordered silicide layer is atomically flat. The preferred element for combination with the silicon to form the silicide layer is tungsten.

INDUSTRIAL APPLICABILITY

The invention can be used in the manufacture of semiconductor devices, which are used in, for example, digital computers. The method produces an atomically flat interface for a tungsten barrier plug film, which provides an improved plug for ULSI shallow junctions. The junction can be used to form the source and drain elements for semiconductor devices. The method may be readily integrated into present semiconductor fabrication techniques that currently use titanium silicide layers formed from undoped titanium.

The advantageous properties of this invention can be observed by reference to the following examples, which illustrate but do not limit the invention.

EXAMPLES

Example 1

This example describes preparation of an interface by the method of the invention. Silicon substrate 10 was undoped monocrystalline silicon about 0.7 mm thick. Doped silicon and polycrystalline silicon, typically a N+ region set in a P-well or a P+ region set in an N-well, can also be used. A cobalt-containing titanium layer was deposited on the silicon substrate by co-evaporation. The layer contained 5 atomic percent cobalt and was 10 nm thick. The substrate was annealed at 550° C. for 0.5 hour in nitrogen gas. An anneal was conducted in a conventional annealing furnace.

The resulting structure contains TiO y N z layer 18 , highly disordered (Ti,Co)Si x layer 16 , CoSi w layer 14 , and silicon substrate 10 . The structure was analyzed by TEM imaging, nano-probe analytical TEM with energy dispersive X-ray and electron energy loss spectroscopy, Auger, and X-ray diffraction.

TEM analysis of a cross-section of the multi-layer structure formed on anneal is shown in FIG. 3 and FIG. 4 . Visible are silicon substrate 10 , CoSi w layer 14 , highly disordered (Ti,Co)Si x layer 16 , and TiO y N z layer 18 . As shown in the figures, CoSi w layer 14 is about a monolayer thick, having a thickness of about 0.63 nm (6.3 Å) and is atomically flat. The flat interface between silicon substrate 10 and CoSi w layer 14 and the flat interface between CoSi w layer 14 and highly disordered (Ti,Co)Si x layer 16 are also visible.

CoSi w layer 14 can also be detected by nano-probe electron energy loss spectroscopy and energy dispersive x-ray analysis.

Example 2

The procedure of Example 1 was repeated using tungsten in place of cobalt. The resulting structure contains a TiO y N z layer 118 , a highly disordered (Ti,W)Si x layer 116 , a WSi w layer 114 , and a silicon substrate 110 .

TEM analysis of a cross-section of the multi-layer structure formed on anneal is shown in FIG. 5 . Visible are silicon substrate 110 , WSi w layer 114 , highly disordered (Ti,W)Si x layer 116 , and TiO y N z layer 118 . As shown in FIG. 5 , WSi w layer 114 is about a monolayer thick, having a thickness of about 0.7-1.0 nm (7-10 Å) and is atomically flat. The flat interface between silicon substrate 110 and WSi w layer 114 and the flat interface between WSi w layer 114 and highly disordered (Ti,W)Si x layer 116 are also visible.

Example 3

The procedure of Example 1 was repeated using tantalum in place of cobalt. The resulting structure contains a TiO y N z layer 218 , a highly disordered (Ti,Ta)Si x layer 216 , and a silicon substrate 210 .

TEM analysis of a cross-section of the multi-layer structure formed on anneal is shown in FIG. 6 . Visible are silicon substrate 210 , highly disordered (Ti,Ta)Si x layer 216 , and TiO y N z layer 218 . The flat interface between silicon substrate 210 and highly disordered (Ti,Ta)Si x layer 216 is also visible.

Example 4

The procedure of Example 1 was repeated using molybdenum in place of cobalt. The resulting structure contains a TiO y N z layer 318 , a highly disordered (Ti,Mo)Si x layer 316 , and a silicon substrate 310 .

TEM analysis of a cross-section of the multi-layer structure formed on anneal is shown in FIG. 7 . Visible are silicon substrate 310 , highly disordered (Ti,Mo)Si x layer 316 , and TiO y N z layer 318 . The flat interface between silicon substrate 310 and highly disordered (Ti,Mo)Si x layer 316 is also visible.

Although illustrated and described above with reference to certain specific embodiments, the present invention is nevertheless not intended to be limited to the details shown. Rather, various modifications may be made in the details within the scope and range of equivalents of the claims and without departing from the spirit of the invention.

Claims

1. A contact comprising, in order:a) a silicon substrate; b) a highly disordered silicide layer comprising titanium, silicon, and the element selected from the group consisting of tungsten, tantalum, and molybdenum; and c) a titanium oxynitride layer; in which the interface between the silicon substrate and the highly disordered silicide layer is atomically flat.

2. The contact of claim 1 in which the titanium oxynitride layer is uniformly thick.

3. The contact of claim 1 in which the highly disordered silicide layer is nano-crystalline and consists essentially of titanium, silicon, and the element selected from the group consisting of tungsten, tantalum, and molybdenum.

4. The contact of claim 1 in which the highly disordered silicide layer is amorphous and consists essentially of titanium, silicon, and the element selected from the group consisting of tungsten, tantalum, and molybdenum.

5. The contact of claim 1 in which the highly disordered silicide layer comprises about 2 to about 15 atomic percent of the element selected from the group consisting of tungsten, tantalum, and molybdenum, based on the total amount of the element and titanium present in the silicide layer.

6. The contact of claim 1 in which:the highly disordered silicide layer consists essentially of titanium, silicon, and the element selected from the group consisting of tungsten, tantalum, and molybdenum; the highly disordered silicide layer is about 3 nm to 20 nm thick; and the titanium oxynitride layer is about 2 nm to about 15 nm thick.

7. The contact of claim 6 in which the highly disordered silicide layer contains about 5 to about 10 atomic percent of the element selected from the group consisting of tungsten, tantalum, and molybdenum, based on the total amount of the element and titanium present in the silicide layer.

8. The contact of claim 7 in which the element is tantalum.

9. The contact of claim 7 in which the element is molybdenum.

10. The contact of claim 1 additionally comprising (d) a layer of conductive material disposed adjacent to the titanium oxynitride layer and opposite the highly disordered silicide layer.

11. The contact of claim 10 in which the conductive material is selected from the group consisting of tungsten, aluminum, copper, gold, tantalum, aluminum-copper alloy, and aluminum-silicon-copper alloy.

12. The contact of claim 11 in which the conductive material is tungsten.

13. The contact of claim 12 in which the titanium oxynitride layer is uniformly thick.

14. The contact of claim 13 in which the highly disordered silicide layer is nano-crystalline and consists essentially of titanium, silicon, and the element selected from the group consisting of tungsten, tantalum, and molybdenum.

15. The contact of claim 13 in which the highly disordered silicide layer is amorphous and consists essentially of titanium, silicon, and the element selected from the group consisting of tungsten, tantalum, and molybdenum.

16. The contact of claim 13 in which:the silicide layer consists essentially of titanium, silicon, and the element selected from the group consisting of tungsten, tantalum, and molybdenum; the highly disordered silicide layer contains about 2 to about 15 atomic percent of the element selected from the group consisting of tungsten, tantalum, and molybdenum, based on the total amount of the element and titanium present in the silicide layer; the highly disordered silicide layer is about 3 nm to 20 nm thick; and the titanium oxynitride layer is about 2 nm to about 15 nm thick.

17. The contact of claim 16 in which the element is tungsten.

18. The contact of claim 17 additionally comprising a tungsten silicide layer forming the interface between the silicon substrate and the highly disordered silicide layer, in which the tungsten silicide layer is about a monolayer thick and is atomically flat.

19. The contact of claim 16 in which the element is tantalum.

20. The contact of claim 16 in which the element is molybdenum.