The present invention relates to a method for manufacturing semiconductor devices, and more particularly, to a method for depositing titanium layers on a substrate.
Device density in integrated circuits (ICs) is constantly being increased. To enable the increase in density, device dimensions are being reduced. As the dimensions of device contacts get smaller, device contact resistance increases, and device performance is adversely affected. Methods for decreasing device contact resistance in ICs are needed to obtain enhanced device and IC performance.
Device contacts with reduced resistance may be created by forming certain metals on a silicon semiconductor base layer. These metals react with the underlying silicon, for example, to form silicides. Silicide device contacts are desirable because they reduce the native oxide on silicon. The native oxide is undesirable because it increases the contact resistance.
In one embodiment, titanium is used to form silicide device contacts for two reasons. First, titanium silicide has superior gettering qualities. Also, titanium silicide forms low resistance contacts on both polysilicon and single-crystal silicon.
Titanium silicide device contacts are normally formed with the following process. First, a thin layer of titanium is formed on top of the silicon base layer, such as a substrate. The titanium adjoins active regions exposed by contact holes in an isolating layer, such as an oxide, above the silicon base layer. Then, the silicon base layer is annealed. As a result, the titanium reacts with the active regions of silicon to form titanium silicide.
However, because titanium cannot be readily deposited in a pure form, additional processing steps are required to form titanium silicide device contacts. Titanium precursors, such as titanium tetrachloride, are commonly available and can be used to form titanium. Titanium tetrachloride, though, can only be reduced at temperatures exceeding 1000 degrees Celsius with certain reducing agents. At these temperatures, the silicon base layer will be damaged. Therefore, there is a need for a method of forming titanium from titanium precursors at lower temperatures.
Furthermore, the resistance of device contacts can be adversely increased by conductive layers coupled between the device contacts and other components. The conductive layers may be formed by the same metal layer used to form the device contacts. As device dimensions shrink, the contact holes become relatively deeper and narrower. Also, the walls of the contact holes become steeper, and closer to vertical. As a result, most metal deposition techniques form conductive layers having relatively small step coverage, and hence relatively high resistance. Step coverage is the ratio of the minimum thickness of a film as it crosses a step, to the nominal thickness of the film on flat regions, where thickness is generally measured perpendicular to the surfaces of the step and flat regions, and where the resultant value is usually expressed as a percentage. Thus, the effective contact resistance is increased at lower values of step coverage. Therefore, there is also a need for a method of forming conductive layers having increased step coverage to reduce effective device contact resistance.
Conformal layers of titanium having good step coverage have been previously formed at lower temperatures with chemical vapor deposition. Such techniques are disclosed in U.S. Pat. Nos. 5,173,327, 5,273,783 and 5,278,100, which are hereby incorporated by reference. However, alternative, effective and efficient techniques for forming titanium films are desired.
The present invention provides a method, and a corresponding resulting structure, for forming conformal titanium films supported on a substrate of an integrated circuit (IC) by forming a seed layer supported by the substrate, and then reducing a titanium precursor with the seed layer. In one embodiment, the seed layer comprises a main group element selected from the group consisting of zinc, cadmium, mercury, aluminum, gallium, indium, tin, silicon, germanium, lead, arsenic and antimony. The seed layer is formed by combining a first precursor and a reducing agent by chemical vapor deposition (CVD). Then, titanium is formed by combining a second precursor with the seed layer by CVD.
In another embodiment, the present invention may further comprise the step of annealing the titanium to form titanium silicide.
In another embodiment, forming the seed layer further comprises forming a seed layer according to the following chemical process (I):
MRx+H2→M+alkanes,
wherein:
In one embodiment, chemical process (I) is performed at a temperature between approximately 100 and 600 degrees Celsius.
In yet another embodiment, the step of forming titanium further comprises the step of combining the seed layer with the second precursor that is titanium tetrachloride according to the following chemical process (II):
TiCl4+M→Ti+MClx
In one embodiment, chemical process (II) is performed at a temperature between approximately 100 and 600 degrees Celsius.
In yet another embodiment, titanium may be formed in a single step according to the following chemical process (III):
TiCl4+M(source)→Ti+MClx
In one embodiment, chemical process (III) is performed at a temperature between approximately 100 and 700 degrees Celsius.
In yet a further embodiment, the present invention may be an IC comprising a layer of a titanium alloy, coupled to a titanium silicide contact. In yet another embodiment, the present invention may be a memory comprising a memory array operatively coupled to a control circuit and an I/O circuit. The memory array, control circuit and I/O circuit comprise a layer of a titanium alloy coupled to titanium silicide contacts. In yet another embodiment, the titanium alloy may comprise titanium and an element selected from the group consisting of zinc, cadmium, mercury, aluminum, gallium, indium, tin, silicon, germanium, lead, arsenic and antimony. In still another embodiment, the titanium alloy may comprise titanium and zinc.
It is a benefit of the present invention that high step coverage metal layers can be formed. Further features and advantages of the present invention, as well as the structure and operations of various embodiments of the present invention, are described in detail below with reference to the accompanying drawings.
In the following detailed description of the preferred embodiments, reference is made to the accompanying drawings which form a part hereof, and in which is shown by way of illustration specific preferred embodiments in which the inventions may be practiced. These embodiments are described in sufficient detail to enable persons skilled in the art to practice the invention, and it is to be understood that other embodiments may be utilized and that logical, mechanical and electrical changes may be made without departing from the spirit and scope of the present invention. The terms wafer and substrate used in the following description include any semiconductor-based structure having an exposed surface with which to form the integrated circuit structure of the invention. Wafer and substrate are used interchangeably to refer to semiconductor structures during processing, and may include other layers that have been fabricated thereupon. Both wafer and substrate include doped and undoped semiconductors, epitaxial semiconductor layers supported by a base semiconductor or insulator, as well as other semiconductor structures well known to one skilled in the art. The following detailed description is, therefore, not to be taken in a limiting sense, and the scope of the present invention is defined only by the appended claims.
The subsequently described methods will be in the context of using zinc as a metal seed layer. However, other seed layers are suitable for use with the various embodiments of the invention, as will be described.
In order to manufacture a device contact in an integrated circuit 19, a contact hole 10, as shown in
Chemical vapor deposition (CVD) is used to form a conformal layer of titanium or titanium alloy on the integrated circuit 19 by a subsequently described method. CVD is further described in U.S. Pat. No. 5,278,100. In one embodiment, the conformal layer has a step coverage of at least one hundred percent in the contact hole 10, even for a high aspect ratio contact hole (i.e., a contact hole that is much deeper than it is wide). As a result, a low resistance layer of titanium or titanium alloy 16 is formed on the insulating layer 12, as shown in
In another embodiment, a cold wall-hot substrate reactor is used to form the conformal layer of titanium or titanium alloy. In one embodiment, a cold wall-hot substrate reactor is used for blanket depositions as this design is efficient in regard to precursor consumption. In one embodiment, first, a conformal film of a seed layer 22 comprising zinc is deposited on the insulator 12 and substrate 14, as shown in
When performing this step, the integrated circuit 19 is mounted on a substrate holder in the CVD reactor 29. The substrate 14 is heated to a temperature within a range of approximately 100 to 600 degrees Celsius and at a pressure approximately between 1 millitorr and 1 atmosphere. Alternatively, the temperature may range from approximately 300 to 550 degrees Celsius, or approximately 350 to 450 degrees Celsius. In one embodiment, the temperature is approximately 400 degrees Celsius. Also, alternatively, the pressure may range from approximately 10 millitorr to 100 torr. In one embodiment, the pressure is approximately 1 torr. A carrier gas of helium, argon or nitrogen may be used at a flow rate of between approximately 1 and 200 sccm. Alternatively, the flow rate may range between approximately 20 sccm and 1 liter. In one embodiment, the pressure is approximately 200 sccm. The first precursor 26 and the reducing agent 24 contact the heated silicon base layer and insulating layer 12, and form the seed layer 22 on the integrated circuit 19. This chemical process (I) is exemplified below:
ZnR2(gas)+H2(gas)→Zn(solid)+alkanes(gas), (I)
where R is an alkyl group.
First reaction products 28, such as gaseous alkanes, resulting from the formation of the seed layer 22 exit from the CVD reactor 29 through an exhaust manifold. The thickness of the seed layer 22 formed on the integrated circuit 19 is between approximately 5 and 50 angstroms. However, the present invention envisions forming a seed layer 22 that is thicker.
Next, the seed layer 22 is converted to a layer 16 of titanium or a titanium alloy. As illustrated in
When performing this step, the integrated circuit 19 is mounted and heated in the CVD reactor 29 to a temperature within a range of approximately 100 to 600 degrees Celsius and at a pressure approximately between 1 millitorr and 1 atmosphere. Alternatively, the temperature may range from approximately 100 to 700 degrees Celsius, approximately 300 to 550 degrees Celsius, or approximately 350 to 450 degrees Celsius. In one embodiment, the temperature is approximately 400 degrees Celsius. Also, alternatively, the pressure may range from approximately 10 millitorr to 100 torr. In one embodiment, the pressure is approximately 1 torr. A carrier gas of helium, argon or nitrogen may be used at a flow of between approximately 1 and 200 sccm. Alternatively, the flow rate may range between approximately 20 sccm and 1 liter. In one embodiment, the pressure is approximately 200 sccm. When the titanium precursor 32 contacts the seed layer 22 on the integrated circuit 19, the compounds form a conformal layer 16 of titanium or a titanium alloy. The chemical process (II) is exemplified below:
TiCl4(gas)+Zn(solid)→Ti(solid)+ZnCl2(gas) (II)
Second reaction products 34 resulting from the formation of the titanium or titanium alloy exit from the CVD reactor 29 through the exhaust manifold. Part or all of the seed layer 22 is converted to a layer 16 of titanium or titanium alloy. If this process step is conducted for a sufficient period of time, all of the seed layer 22 will be converted to a layer 16 of titanium. However, if not all of the seed layer 22 is converted to a layer 16 of titanium, a layer 16 of titanium alloy, including the seed layer 22, will be formed on the integrated circuit 19. These steps may be repeated to form thicker layers.
In another embodiment, the layer 16 of titanium or titanium alloy can be formed during a single CVD step, as exemplified by chemical process (III) below:
TiCl4+Zn(source)→Ti+ZnCl2 (III)
The zinc can be provided from one of many types of sources, including gaseous and solid sources. In one embodiment of such a single CVD step, the seed and titanium layers 22, 16 can be formed substantially simultaneously. The titanium or titanium alloy layer 16 can be formed by combining a first precursor 26, such as a dialkyl or trimethyl zinc compound, with a reducing agent 24, such as hydrogen, and a titanium precursor 32, such as titanium tetrachloride. When performing the CVD step, the integrated circuit 19 is mounted and heated in the CVD reactor 29 to a temperature within a range of approximately 100 to 600 degrees Celsius at a pressure of approximately between 1 millitorr and 1 atmosphere. Alternatively, the temperature may range from approximately 100 to 700 degrees Celsius, approximately 300 to 550 degrees Celsius, or approximately 350 to 450 degrees Celsius. In one embodiment, the temperature is approximately 400 degrees Celsius. Also, alternatively, the pressure may range from approximately 10 millitorr to 100 torr. In one embodiment, the pressure is approximately 1 torr. A carrier gas of helium, argon or nitrogen may be used at a flow rate of between approximately 1 and 200 sccm. Alternatively, the flow rate may range between approximately 20 sccm and 1 liter. In one embodiment, the pressure is approximately 200 sccm. When the first precursor 26 and the reducing agent 24 contact the heated silicon base layer and insulating layer 12, they form the seed layer 22 on the integrated circuit 19. Then, when the titanium precursor 32 contacts the seed layer 22, a conformal layer 16 of titanium or titanium alloy is formed on the integrated circuit. The resulting layer 16 of titanium or titanium alloy has a thickness between approximately 5 and 50 angstroms. However, the present invention envisions forming a thicker layer 16 titanium or titanium alloy. The chemical process (IV) is exemplified below:
ZnR2(gas)+H2(gas)+TiCl4(gas)→Ti(solid)+ZnCl2(gas)+alkanes(gas), (IV)
where R is an alkyl group.
The reaction products 28, 34 exit from the CVD reactor 29 through the exhaust manifold.
Subsequently, the integrated circuit 19 is annealed at a temperature of between approximately 250 to 750 degrees Celsius. Alternatively, the temperature may range from approximately 250 to 800 degrees Celsius. In one embodiment, the temperature is approximately 700 degrees Celsius. As a result, the titanium in the layer 16 of titanium or titanium alloy proximate to the silicon is converted to titanium silicide (TiSi, TiSi2, Ti3Si5 or combinations thereof) to form the low resistance device contact 18. For via level applications, the anneal is not required. The via comprises a tungsten or aluminum fill 42 on top of the layer 16 which is formed on top of a conductor (also represented by reference number 17) with an optional TiN layer 40 between layer 16 and the fill material 42.
In yet another embodiment, the low resistance device contact 18 of titanium silicide may be formed over the active region 17 when the layer 16 of titanium or titanium alloy is formed by CVD on the integrated circuit 19 at a temperature of between approximately 250 to 750 degrees Celsius. Alternatively, the temperature may range from approximately 250 to 800 degrees Celsius. In one embodiment, the temperature is approximately 700 degrees Celsius. Upon device contact 18 formation, additional metal layers, such as titanium nitride and tungsten, may be subsequently formed over the device contact 18 and layer 16 of titanium or titanium alloy.
In another embodiment, the integrated circuit 19 is a memory 300 in
As noted above, other seed layers are suitable for use with the various embodiments of the invention. In one embodiment, the first precursor 26 is an alkane of the form MRx, where M is an element selected from the group consisting of zinc, cadmium, mercury, aluminum, gallium, indium, tin, silicon, germanium, lead, arsenic and antimony; R is an alkyl group; and x is some integer value determined by the valence of M. The value of x is generally equal to a valence of M, e.g., when M has a valence of 3 as does aluminum, x equals 3. M may be capable of having more than one valence. Such alkane precursors may be used to form the seed layer 22. Chemical process (I) for the formation of seed layer 22 may then be written in its more general form:
MRx(gas)+H2(gas)→M(solid)+alkanes(gas), (I)
wherein:
In similar fashion, chemical process (II) for the formation of the layer 16 of titanium or titanium alloy may be written more generally as:
TiCl4(gas)+M(solid)→Ti(solid)+MClx(gas) (II)
wherein:
In another embodiment, where the formation of the layer 16 of titanium or titanium alloy is performed in a single step, chemical process (III) may be written more generally as:
TiCl4+M(source)→Ti+MClx (III)
wherein:
In a further embodiment, where the formation of the layer 16 of titanium or titanium alloy is performed in a single CVD step, chemical process (IV) may be written more generally as:
MRx(gas)+H2(gas)+TiCl4(gas)→Ti(solid)+MClx(gas)+alkanes(gas), (IV)
wherein:
The various embodiments of the present invention provide high step coverage, low resistivity titanium silicide device contacts to silicon, or titanium contacts to metal at the via level, formed at a relatively low temperature. Use of the various alkane precursors permits formation of a titanium layer without depletion of an underlying silicon or other base layer.
It is to be understood that the above description is intended to be illustrative, and not restrictive. Many other embodiments will be apparent to those of skill in the art upon reviewing the above description. For example, other titanium precursors, such as tetradimethyl amino titanium (TDMAT) can be used to form layers 16 and device contacts 18. Additionally, the present invention may be implemented with any CVD apparatus 29, including hot wall reactors, cold wall reactors, radiation beam assisted reactors, plasma-assisted reactors, and the like. Furthermore, the seed layer 22 may be formed in any manner which provides a desired thickness film. Hence, the scope of the invention should, therefore, be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.
This application is a divisional of U.S. application Ser. No. 11/146,609, filed Jun. 7, 2005 now U.S. Pat. No. 7,443,032, which is a continuation of U.S. application Ser. No. 09/941,125, filed Aug. 28, 2001, now issued as U.S. Pat. No. 6,830,838, which is a divisional of U.S. application Ser. No. 09/489,187, filed Jan. 20, 2000, now issued as U.S. Pat. No. 6,284,316, which is a continuation-in-part of U.S. application Ser. No. 09/030,705, filed Feb. 25, 1998, now issued as U.S. Pat. No. 6,143,362. These applications are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3900312 | Terry et al. | Aug 1975 | A |
4340617 | Deutsch et al. | Jul 1982 | A |
4343870 | Heller et al. | Aug 1982 | A |
4359490 | Lehrer | Nov 1982 | A |
4527184 | Fischer | Jul 1985 | A |
4713258 | Umemura | Dec 1987 | A |
4721631 | Endo et al. | Jan 1988 | A |
4751101 | Joshi | Jun 1988 | A |
4782380 | Shankar et al. | Nov 1988 | A |
4829024 | Klein et al. | May 1989 | A |
4868005 | Ehrlich et al. | Sep 1989 | A |
4876112 | Kaito et al. | Oct 1989 | A |
4884123 | Dixit et al. | Nov 1989 | A |
4923717 | Gladfelter et al. | May 1990 | A |
4957777 | Ilderem et al. | Sep 1990 | A |
4971655 | Stefano et al. | Nov 1990 | A |
4994410 | Sun et al. | Feb 1991 | A |
5005519 | Egermeier et al. | Apr 1991 | A |
5015330 | Okumura et al. | May 1991 | A |
5022905 | Grundy et al. | Jun 1991 | A |
5032233 | Yu et al. | Jul 1991 | A |
5049975 | Ajika et al. | Sep 1991 | A |
5124780 | Sandhu et al. | Jun 1992 | A |
5136362 | Grief et al. | Aug 1992 | A |
5147819 | Yu et al. | Sep 1992 | A |
5173327 | Sandhu et al. | Dec 1992 | A |
5192589 | Sandhu | Mar 1993 | A |
5196360 | Doan et al. | Mar 1993 | A |
5202579 | Fujii et al. | Apr 1993 | A |
5227331 | Westmoreland | Jul 1993 | A |
5227334 | Sandhu | Jul 1993 | A |
5229643 | Ohta et al. | Jul 1993 | A |
5232873 | Geva et al. | Aug 1993 | A |
5239196 | Ikeda et al. | Aug 1993 | A |
5240739 | Doan et al. | Aug 1993 | A |
5246881 | Sandhu et al. | Sep 1993 | A |
5252518 | Sandhu et al. | Oct 1993 | A |
5254499 | Sandhu et al. | Oct 1993 | A |
5258096 | Sandhu et al. | Nov 1993 | A |
5273783 | Wanner | Dec 1993 | A |
5275715 | Tuttle | Jan 1994 | A |
5278100 | Doan et al. | Jan 1994 | A |
5306951 | Lee et al. | Apr 1994 | A |
5320880 | Sandhu et al. | Jun 1994 | A |
5341016 | Prall et al. | Aug 1994 | A |
5344792 | Sandhu et al. | Sep 1994 | A |
5355020 | Lee et al. | Oct 1994 | A |
5374591 | Hasegawa et al. | Dec 1994 | A |
5376405 | Doan et al. | Dec 1994 | A |
5381302 | Sandhu et al. | Jan 1995 | A |
5384284 | Doan et al. | Jan 1995 | A |
5384289 | Westmoreland | Jan 1995 | A |
5391410 | Nii et al. | Feb 1995 | A |
5393564 | Westmoreland et al. | Feb 1995 | A |
5399379 | Sandhu | Mar 1995 | A |
5401674 | Anjum et al. | Mar 1995 | A |
5416045 | Kauffman et al. | May 1995 | A |
5425392 | Thakur et al. | Jun 1995 | A |
5444018 | Yost et al. | Aug 1995 | A |
5453640 | Kinoshita | Sep 1995 | A |
5459353 | Kanazawa | Oct 1995 | A |
5488245 | Shimizu et al. | Jan 1996 | A |
5496762 | Sandhu et al. | Mar 1996 | A |
5506166 | Sandhu et al. | Apr 1996 | A |
5508066 | Akahori | Apr 1996 | A |
5534716 | Takemura | Jul 1996 | A |
5567243 | Foster et al. | Oct 1996 | A |
5571572 | Sandhu | Nov 1996 | A |
5575708 | Chau et al. | Nov 1996 | A |
5595784 | Kaim et al. | Jan 1997 | A |
5600591 | Takagi | Feb 1997 | A |
5607722 | Vaartstra et al. | Mar 1997 | A |
5633200 | Hu | May 1997 | A |
5641545 | Sandhu | Jun 1997 | A |
5644166 | Honeycutt et al. | Jul 1997 | A |
5654577 | Nakamura et al. | Aug 1997 | A |
5693557 | Hirao et al. | Dec 1997 | A |
5703403 | Sobue et al. | Dec 1997 | A |
5725739 | Hu | Mar 1998 | A |
5747116 | Sharan et al. | May 1998 | A |
5773890 | Uchiyama et al. | Jun 1998 | A |
5828131 | Cabral, Jr. et al. | Oct 1998 | A |
5834371 | Ameen et al. | Nov 1998 | A |
5838052 | McTeer | Nov 1998 | A |
5846881 | Sandhu et al. | Dec 1998 | A |
5924012 | Vaartstra | Jul 1999 | A |
5956595 | Zenke | Sep 1999 | A |
5970309 | Ha et al. | Oct 1999 | A |
5973402 | Shinriki et al. | Oct 1999 | A |
5976976 | Doan et al. | Nov 1999 | A |
6016012 | Chatila et al. | Jan 2000 | A |
6031288 | Todorobaru et al. | Feb 2000 | A |
6051880 | Kikuta | Apr 2000 | A |
6066891 | Yamaoka et al. | May 2000 | A |
6120844 | Chen et al. | Sep 2000 | A |
6140230 | Li | Oct 2000 | A |
6143362 | Sandhu et al. | Nov 2000 | A |
6143649 | Tang | Nov 2000 | A |
6153490 | Xing et al. | Nov 2000 | A |
6197686 | Taguchi et al. | Mar 2001 | B1 |
6208033 | Doan et al. | Mar 2001 | B1 |
6217721 | Xu et al. | Apr 2001 | B1 |
6255216 | Doan et al. | Jul 2001 | B1 |
6284316 | Sandhu et al. | Sep 2001 | B1 |
6294420 | Tsu et al. | Sep 2001 | B1 |
6294469 | Kulkarni et al. | Sep 2001 | B1 |
6320213 | Kirlin et al. | Nov 2001 | B1 |
6326690 | Wang et al. | Dec 2001 | B2 |
6420262 | Farrar | Jul 2002 | B1 |
6433430 | Sharan et al. | Aug 2002 | B2 |
6433434 | Sandhu et al. | Aug 2002 | B1 |
6472756 | Doan et al. | Oct 2002 | B2 |
6503803 | Todorobaru et al. | Jan 2003 | B2 |
6509278 | Chen | Jan 2003 | B1 |
6531736 | Koike | Mar 2003 | B1 |
6605533 | Trivedi | Aug 2003 | B2 |
6803318 | Qiao et al. | Oct 2004 | B1 |
6830820 | Sandhu et al. | Dec 2004 | B2 |
6830838 | Sandhu et al. | Dec 2004 | B2 |
6903462 | Sandhu et al. | Jun 2005 | B2 |
6940172 | Sandhu et al. | Sep 2005 | B2 |
6969671 | Shimazu et al. | Nov 2005 | B2 |
7223689 | Park et al. | May 2007 | B2 |
7443032 | Sandhu et al. | Oct 2008 | B2 |
20010042505 | Vaartstra | Nov 2001 | A1 |
20010045661 | Yang et al. | Nov 2001 | A1 |
20020000263 | Sandhu et al. | Jan 2002 | A1 |
20020000662 | Sandhu et al. | Jan 2002 | A1 |
20020006525 | Sandhu et al. | Jan 2002 | A1 |
20020011615 | Nagata et al. | Jan 2002 | A1 |
20020017724 | Sandhu et al. | Feb 2002 | A1 |
20050009325 | Chung et al. | Jan 2005 | A1 |
20050255698 | Sandhu et al. | Nov 2005 | A1 |
20070235709 | Kostylev et al. | Oct 2007 | A1 |
20090142474 | Gandikota et al. | Jun 2009 | A1 |
Number | Date | Country |
---|---|---|
0798777 | Oct 1997 | EP |
04-196419 | Jul 1992 | JP |
404196419 | Jul 1992 | JP |
56995 | Jan 1993 | JP |
40-7097679 | Apr 1995 | JP |
8-176823 | Jul 1996 | JP |
WO-9834445 | Aug 1998 | WO |
Entry |
---|
Bachmann, P., et al., “Plasma-Assisted Chemical Vapor Deposition Processes”, MRS Bulletin, (Dec. 1988), 52-59. |
Bouteville, A., et al., “TiSi2 Selective Growth in a rapid thermal low pressure chemical vapor depositoin system”, Journal of the Electrochemical Society, 139, (Aug. 1992), 2260-2263. |
Cowher, M., et al., “Low Temperature CVD Garnet Growth”, Journal of Crystal Growth, 46, (1979), 399-402. |
Engqvist, Jan, et al., “Selective deposition of TiSi2 from H2-TiCl4 Gas mixtures and si: Aspects of Thermodynamics including Critical evaluation of thermochemical data in the Ti-Si System”, Journal of the Electrochemical Society, 139, (Nov. 1992), 3197-3205. |
Esquivel, A., et al., “Electrical and Physical Characteristics of Dry Oxygen, High Pressure Oxidation for SUB-0.5 um CMOS Isolation”, Abst. Int'l Electron Devices Meeting, (1994). |
Herman, I., “Laser-Assisted Deposition of Thin Films from Gas-Phase and Surface-Adsorbed Molecules”, Chem. Rev., 89, (1989), 1323, 1346-1349. |
Ilderem, V., et al., “Optimized Deposition Parameters for Low Pressure Chemical Vapor Deposited Titanium Silicide”, J. Electrochemical Soc. : Solid State Science and Technology , (Oct. 1988), 2590-2596. |
Lee, Jaegab, et al., “Plasma enhanced chemical vapor deposition of blanket TiSi2 on oxide patterned wafers”, Journal of the Electrochemical Society, 139, (Apr. 1992), 1159-1165. |
Lie, L., et al., “High Pressure Oxidation of Silicon in Dry Oxygen”, J. Electrochemical Soc. : Solid State Sceince and Technology, 129, (Dec. 1982), 2828-2834. |
Moeller, T., et al., “Semiconducting Elements, Ch. 30”, In: Chemistry with Inorganic Qualitative Analysis, 2nd Edition, Academic Press, (1984), 995-996. |
Morosanu, C., Thin Films by Chemical Vapor Deposition, Elsevier, N.Y., (1990), 42-54 & 460-475. |
Panson, A., et al., “Chemical Vapor Deposition of YBa(2)Cu(3)O(7) Using Metalorganic Chelate Precursors”, Appl. Phys. Lett., 53, (Oct. 1988), 1756-1758. |
Rosler, R., et al., “Plasma-Enhanced CVD of Titanium Silicide”, J. Vacuum Science Tech., B2(4), (Oct./Dec. 198), 733-737. |
Wolf, S., Silicon Processing for the VLSI Era, vol. 2: Process Integration, Lattice Press, Sunset Beach, California, (1990), 202-203. |
Yu, M., et al., “Surface Chemistry of the WF(6)-Based Chemical Vapor Deposition of Tungsten”, IBM J. Research Development, 34, (Nov. 1990), 875-883. |
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20090039517 A1 | Feb 2009 | US |
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