US20050233481A1 - Novel development hastened stability of titanium nitride for APM etching rate monitor - Google Patents
Novel development hastened stability of titanium nitride for APM etching rate monitor Download PDFInfo
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- US20050233481A1 US20050233481A1 US11/157,571 US15757105A US2005233481A1 US 20050233481 A1 US20050233481 A1 US 20050233481A1 US 15757105 A US15757105 A US 15757105A US 2005233481 A1 US2005233481 A1 US 2005233481A1
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- tin
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- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 title description 40
- 238000005530 etching Methods 0.000 title description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 20
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 14
- 239000010703 silicon Substances 0.000 claims abstract description 14
- 239000000758 substrate Substances 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- 239000001301 oxygen Substances 0.000 claims abstract description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract 35
- 238000000034 method Methods 0.000 claims description 33
- 238000011282 treatment Methods 0.000 claims description 11
- 229910010421 TiNx Inorganic materials 0.000 claims description 9
- 238000005240 physical vapour deposition Methods 0.000 claims description 6
- 235000012431 wafers Nutrition 0.000 description 25
- 238000000151 deposition Methods 0.000 description 5
- 230000008021 deposition Effects 0.000 description 4
- 238000007669 thermal treatment Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- -1 for example Chemical class 0.000 description 1
- 238000004556 laser interferometry Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L22/00—Testing or measuring during manufacture or treatment; Reliability measurements, i.e. testing of parts without further processing to modify the parts as such; Structural arrangements therefor
- H01L22/20—Sequence of activities consisting of a plurality of measurements, corrections, marking or sorting steps
- H01L22/26—Acting in response to an ongoing measurement without interruption of processing, e.g. endpoint detection, in-situ thickness measurement
Definitions
- the present invention relates generally to semiconductor fabrication and more specifically to the fabrication of control wafers used to monitor etching rates.
- Control wafers may be used to monitor integrated circuit (IC) processes such as, for example, etch rates.
- IC integrated circuit
- a silicon substrate having a silicon oxide layer formed thereover.
- An initial TiN layer is formed over the silicon oxide layer.
- the silicon substrate is placed in an atmosphere having ambient oxygen for from about 22 to 26 hours to form a rested TiN layer.
- the rested TiN layer is heated at a temperature of from about 115 to 125° C. for from about 85 to 95 seconds to form a heat treated TiN layer, whereby the heat treated TiN layer is stabilized to form the stabilized TiN control wafer.
- FIGS. 1 to 3 schematically illustrate a process known to the inventors.
- FIGS. 4 to 7 schematically illustrate a preferred embodiment of the present invention.
- control wafers having an overlying titanium nitride (TiN) layer are used to monitor the APM (NH 4 +H 2 O 2 +H 2 O) etching rate of metals such as, for example, cobalt (Co).
- APM NH 4 +H 2 O 2 +H 2 O
- Co cobalt
- a layer of silicon oxide (SiO 2 ) 12 is grown over a bare silicon (Si) wafer 10 .
- the silicon oxide layer 12 has a thickness of preferably from about 1000 to 1100 ⁇ and more preferably about 1050 ⁇ .
- a layer 14 of TiN is then deposited over the silicon oxide layer 12 , preferably by a physical vapor deposition (PVD) process.
- the TiN layer 14 has a thickness of preferably from about 950 to 1050 ⁇ and more preferably about 1000 ⁇ .
- the TiN layer 14 ′ overlying wafer 10 is subjected to an APM etch rate test to ensure its stability and ability to function as a control wafer.
- the instability of TiN will induce Rs measure shift.
- the wafer 10 may then be used as a control wafer.
- the inventors attempted to subject the wafer 10 having the overlying TiN layer 14 to various thermal treatments soon after deposition of the TiN layer 14 in attempts to eliminate the at least seven day clean room storage 16 .
- the thermal treatment was a rapid thermal anneal (RTA) at the temperatures 670° C., 680° C., 690° C., 700° C. and 710° C. for about 60 seconds, and preferably about 690° C. for about 60 seconds, soon after deposition of the TiN layer 14 for five respective wafers, the uniformity of the resulting etch rates for the RTA treated TiN layers 14 was out of specification.
- the thermal treatment was a furnace anneal at about 410° C. for about 30 minutes soon after deposition of the TiN layer 14 , the inventors found that the results were unrepeatable because the thermal budget (i.e. temperature by time) was too long and not well controlled so a furnace treatment was also unacceptable.
- FIGS. 4 to 7 the inventors have discovered that by first placing a wafer 30 with an upper silicon oxide layer 32 ( FIG. 4 ) having a deposited TiN layer 34 formed over the silicon oxide layer 32 ( FIG. 5 ) in a clean room for about one (1) day (as shown at 36 in FIG. 6 ) and then treating the wafer 30 with a hot plate treatment 40 (more preferably at about 120° C. for about 90 seconds) ( FIG. 7 ) to form stabilized TiN layer 34 ′ overlying wafer 30 as described in more detail below.
- a hot plate treatment 40 more preferably at about 120° C. for about 90 seconds
- silicon substrate/wafer 30 has overlying silicon oxide layer 32 grown thereover to a thickness of preferably from about 1000 to 1100 ⁇ and more preferably about 1050 ⁇ .
- the silicon oxide layer 32 serves as a barrier layer for measuring the thickness of the TiN layer 34 as it is formed and also makes it easier to recycle to reduce damage on the bare silicon surface of silicon substrate/wafer 30 .
- a layer 34 of TiN is deposited over the silicon oxide layer 32 , preferably by a physical vapor deposition (PVD) process.
- the TiN layer 34 has a thickness of preferably from about 950 to 1050 ⁇ and more preferably about 1000 ⁇ .
- wafer 30 with topmost TiN layer 34 is stored 36 in a clean room for preferably about 22 to 26 hours and more preferably about 24 hours to partially stabilize TiN layer 34 to form partially stabilized TiN layer 34 ′ by, the inventors believe, the slow formation of a very thin TiN x O x-1 layer (not shown) over the upper surface 37 of TiN layer 34 by the reaction with ambient O 2 from the clean room (possibly from the humidity in the clean room) with the TiN of layer 34 by diffusion of oxygen into the TiN layer 34 .
- the hot plate treatment 40 is conducted at a temperature of preferably from about 115 to 125° C. for from about 85 to 95 seconds and more preferably about 120° C. for about 90 seconds.
- the use of hot plate treatment 40 permits a short thermal cycle and a low temperature to further minimize risks of TiN peeling.
- the inventors have determined that the subsequent APM etch rate of the fully stabilized TiN layer 34 ′′ formed in accordance with the method of the instant invention is within the target specification of 300 ⁇ 40 ⁇ /minute with a uniformity of less than about 20% that compares with a seven day clean room storage method without any thermal treatment. Thus a seven day process is reduced to only about 1 day using the method of the instant invention.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Chemical Vapour Deposition (AREA)
Abstract
A method of fabricating a stabilized TiN control wafer comprising the following steps. A silicon substrate is provided having a silicon oxide layer formed thereover. An initial TiN layer is formed over the silicon oxide layer. The silicon substrate is placed in an atmosphere having ambient oxygen for from about 22 to 26 hours to form a rested TiN layer. The rested TiN layer is heated at a temperature of from about 115 to 125° C. for from about 85 to 95 seconds to form a heat treated TiN layer, whereby the heat treated TiN layer is stabilized to form the stabilized TiN control wafer.
Description
- The present invention relates generally to semiconductor fabrication and more specifically to the fabrication of control wafers used to monitor etching rates.
- Control wafers may be used to monitor integrated circuit (IC) processes such as, for example, etch rates.
- U.S. Pat. No. 5,086,017 to Lu describes a laser interferometry etch rate monitor methods in a silicide process.
- U.S. Pat. No. 5,872,062 to Hsu describes a method for etching titanium nitride.
- U.S. Pat. No. 5,547,881 to Wang et al. describes an APM etch process for metal nitrides and other layers.
- U.S. Pat. No. 5,516,399 to Balconi-Lamica et al. describes etch rate monitor processes.
- Accordingly, it is an object of one or more embodiments of the present invention to provide an improved method of fabricating control wafers used to monitor an etching rate.
- Other objects will appear hereinafter.
- It has now been discovered that the above and other objects of the present invention may be accomplished in the following manner. Specifically, a silicon substrate is provided having a silicon oxide layer formed thereover. An initial TiN layer is formed over the silicon oxide layer. The silicon substrate is placed in an atmosphere having ambient oxygen for from about 22 to 26 hours to form a rested TiN layer. The rested TiN layer is heated at a temperature of from about 115 to 125° C. for from about 85 to 95 seconds to form a heat treated TiN layer, whereby the heat treated TiN layer is stabilized to form the stabilized TiN control wafer.
- The present invention will be more clearly understood from the following description taken in conjunction with the accompanying drawings in which like reference numerals designate similar or corresponding elements, regions and portions and in which:
- FIGS. 1 to 3 schematically illustrate a process known to the inventors.
- FIGS. 4 to 7 schematically illustrate a preferred embodiment of the present invention.
- Process Known to the Inventors—Not to be Considered Prior Art
- The following process is known to the inventors and is not to be considered prior art against the instant invention.
- Currently, control wafers having an overlying titanium nitride (TiN) layer are used to monitor the APM (NH4+H2O2+H2O) etching rate of metals such as, for example, cobalt (Co). The control wafers are prepared in two steps.
- In the first step and as shown in
FIG. 1 , a layer of silicon oxide (SiO2) 12 is grown over a bare silicon (Si)wafer 10. Thesilicon oxide layer 12 has a thickness of preferably from about 1000 to 1100 Å and more preferably about 1050 Å. - As shown in
FIG. 2 , alayer 14 of TiN is then deposited over thesilicon oxide layer 12, preferably by a physical vapor deposition (PVD) process. TheTiN layer 14 has a thickness of preferably from about 950 to 1050 Å and more preferably about 1000 Å. - The thickness of the
TiN layer 14 is measured by Rs-100, that is using a four-point probe method measuring the resistance (Rs) then using the formula Rs=pL/A where p=density (of TiN); L=length of measurement; and A=area of measurement. - As shown in
FIG. 3 , after depositing theTiN layer 14, the control wafer must be placed in a clean room for at least seven days (as represented by arrow 16) to form stabilizedTiN layer 14′ having an improved etch rate for the APM treatment. This is because the resistance of theTiN layer 14 is unstable after about three (3) hours from its time of deposition based upon 300 PL experimental data collected by the inventors where 300 PL=300 mm wafer pilot line—an experiment fab for 12″ wafer. - After at least seven days in a clean room, the
TiN layer 14′overlying wafer 10 is subjected to an APM etch rate test to ensure its stability and ability to function as a control wafer. The instability of TiN will induce Rs measure shift. - Once the
TiN layer 14′ passes the APM etch rate test, thewafer 10 may then be used as a control wafer. - The inventors attempted to subject the
wafer 10 having theoverlying TiN layer 14 to various thermal treatments soon after deposition of theTiN layer 14 in attempts to eliminate the at least seven dayclean room storage 16. When the thermal treatment was a rapid thermal anneal (RTA) at the temperatures 670° C., 680° C., 690° C., 700° C. and 710° C. for about 60 seconds, and preferably about 690° C. for about 60 seconds, soon after deposition of theTiN layer 14 for five respective wafers, the uniformity of the resulting etch rates for the RTA treatedTiN layers 14 was out of specification. When the thermal treatment was a furnace anneal at about 410° C. for about 30 minutes soon after deposition of theTiN layer 14, the inventors found that the results were unrepeatable because the thermal budget (i.e. temperature by time) was too long and not well controlled so a furnace treatment was also unacceptable. - Instant Invention
- As shown in FIGS. 4 to 7, the inventors have discovered that by first placing a
wafer 30 with an upper silicon oxide layer 32 (FIG. 4 ) having a depositedTiN layer 34 formed over the silicon oxide layer 32 (FIG. 5 ) in a clean room for about one (1) day (as shown at 36 inFIG. 6 ) and then treating thewafer 30 with a hot plate treatment 40 (more preferably at about 120° C. for about 90 seconds) (FIG. 7 ) to form stabilizedTiN layer 34′overlying wafer 30 as described in more detail below. - Initial Structure
- As shown in
FIG. 4 , silicon substrate/wafer 30 has overlyingsilicon oxide layer 32 grown thereover to a thickness of preferably from about 1000 to 1100 Å and more preferably about 1050 Å. Thesilicon oxide layer 32 serves as a barrier layer for measuring the thickness of theTiN layer 34 as it is formed and also makes it easier to recycle to reduce damage on the bare silicon surface of silicon substrate/wafer 30. - Formation of TiN
Layer 34 - As shown in
FIG. 5 , alayer 34 of TiN is deposited over thesilicon oxide layer 32, preferably by a physical vapor deposition (PVD) process. The TiNlayer 34 has a thickness of preferably from about 950 to 1050 Å and more preferably about 1000 Å. - Placement of Wafer 30 in
Clean Room 36 for About One Day - As shown in
FIG. 6 ,wafer 30 withtopmost TiN layer 34 is stored 36 in a clean room for preferably about 22 to 26 hours and more preferably about 24 hours to partially stabilizeTiN layer 34 to form partially stabilizedTiN layer 34′ by, the inventors believe, the slow formation of a very thin TiNxOx-1 layer (not shown) over theupper surface 37 ofTiN layer 34 by the reaction with ambient O2 from the clean room (possibly from the humidity in the clean room) with the TiN oflayer 34 by diffusion of oxygen into theTiN layer 34. -
Hot Plate Treatment 40 - Regardless of the mechanism that forms partially stabilized
TiN layer 34′, afterwafer 30 has been stored in a clean room for more preferably about 24 hours, the wafer is removed and is subjected to ahot plate treatment 40 that speeds up formation of a thicker TiNxOx-1 layer 38′ and to form fully stabilizedTiN layer 34″. Thicker TiNxOx-1 layer 38′ will be removed during a subsequent APM etch (NH4+H2O2+H2O). - The
hot plate treatment 40 is conducted at a temperature of preferably from about 115 to 125° C. for from about 85 to 95 seconds and more preferably about 120° C. for about 90 seconds. The use ofhot plate treatment 40 permits a short thermal cycle and a low temperature to further minimize risks of TiN peeling. - The inventors have determined that the subsequent APM etch rate of the fully stabilized TiN
layer 34″ formed in accordance with the method of the instant invention is within the target specification of 300±40 Å/minute with a uniformity of less than about 20% that compares with a seven day clean room storage method without any thermal treatment. Thus a seven day process is reduced to only about 1 day using the method of the instant invention. - While particular embodiments of the present invention have been illustrated and described, it is not intended to limit the invention, except as defined by the following claims.
Claims (18)
1-13. (canceled)
14. A method of fabricating a stabilized TiN control wafer, the steps comprising
providing a silicon substrate oxide layer formed thereover;
forming an initial TiN layer over the silicon oxide layer;
placing the silicon substrate in a clean room having an oxygen ambient atmosphere for from about 22 to 26 hours to form a rested TiN layer; and
subjecting the rested TiN layer to a hot plate treatment at a temperature of from about 115 to 125° C. for from about 85 to 95 seconds to form a hot plate treated TiN layer, whereby the hot plate treated TiN layer is stabilized to form the stabilized TiN control wafer.
15. The method of claim 14 , wherein the silicon oxide layer is from about 1000 to 1100 Å thick and the initial TiN layer is from about 950 to 1050 Å.
16. The method of claim 14 , wherein the silicon oxide layer is about 1050 Å thick and the initial TiN layer is about 1000 Å.
17. The method of claim 14 , wherein the silicon substrate is placed in the clean room for about 24 hours to form the rested TiN layer.
18. The method of claim 14 , wherein the hot plate treatment is conducted at a temperature of about 120° C. for about 90 seconds.
19. The method of claim 14 , wherein the initial TiN layer is formed by a physical vapor deposition method.
20. The method of claim 14 , wherein the rested TiN layer includes an overlying TiNxOx-1 layer.
21. The method of claim 14 , wherein the rested TiN layer and the stabilized TiN control wafer include an overlying TiNxOx-1.
22. The method of claim 14 , including the step of then using the control wafer to measure Rs or etch rate.
23. A method of fabricating a stabilized TiN control wafer, the steps comprising
providing a silicon substrate having a silicon oxide layer formed thereover;
forming an initial TiN layer over the silicon oxide layer;
placing the silicon substrate in a clean room having an oxygen ambient atmosphere for from about 22 to 26 hours to form a TiNxOx-1 layer over a rested TiN layer;
subjecting the TiNxOx-1 layer and the rested TiN layer to a hot plate treatment at a temperature of from about 115 to 125° C. for from about 85 to 95 seconds to form a hot plate treated TiN layer, whereby the hot plate treated TiN layer is stabilized to form the stabilized TiN control wafer; and
using the stabilized TiN control wafer to measure Rs or etch rate.
24. The method of claim 23 , wherein the silicon oxide layer is from about 1000 to 1100 Å thick and the initial TiN layer is from about 950 to 1050 Å.
25. The method of claim 23 , wherein the silicon oxide layer is about 1050 Å thick and the initial TiN layer is about 1000 Å.
26. The method of claim 23 , wherein the silicon substrate is placed in the clean room for about 24 hours to form the rested TiN layer.
27. The method of claim 23 , wherein the hot plate treatment is conducted at a temperature of about 120° C. for about 90 seconds.
28. The method of claim 23 , wherein the initial TiN layer is formed by a physical vapor deposition method.
29. The method of claim 23 , wherein the stabilized TiN control wafer has an overlying TiNxOx-1 layer.
30. The method of claim 23 , wherein the TiNxOx-1 layer partially stabilizes the rested TiN layer.
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US11/157,571 US20050233481A1 (en) | 2002-07-02 | 2005-06-21 | Novel development hastened stability of titanium nitride for APM etching rate monitor |
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US10/187,705 US6951767B1 (en) | 2002-07-02 | 2002-07-02 | Development hastened stability of titanium nitride for APM etching rate monitor |
US11/157,571 US20050233481A1 (en) | 2002-07-02 | 2005-06-21 | Novel development hastened stability of titanium nitride for APM etching rate monitor |
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US10/187,705 Division US6951767B1 (en) | 2002-07-02 | 2002-07-02 | Development hastened stability of titanium nitride for APM etching rate monitor |
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US10/187,705 Expired - Fee Related US6951767B1 (en) | 2002-07-02 | 2002-07-02 | Development hastened stability of titanium nitride for APM etching rate monitor |
US11/157,571 Abandoned US20050233481A1 (en) | 2002-07-02 | 2005-06-21 | Novel development hastened stability of titanium nitride for APM etching rate monitor |
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US6951767B1 (en) * | 2002-07-02 | 2005-10-04 | Taiwan Semiconductor Manufacturing Company, Ltd. | Development hastened stability of titanium nitride for APM etching rate monitor |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5086017A (en) * | 1991-03-21 | 1992-02-04 | Industrial Technology Research Institute | Self aligned silicide process for gate/runner without extra masking |
US5516399A (en) * | 1994-06-30 | 1996-05-14 | International Business Machines Corporation | Contactless real-time in-situ monitoring of a chemical etching |
US5547861A (en) * | 1994-04-18 | 1996-08-20 | Becton, Dickinson And Company | Detection of nucleic acid amplification |
US5872062A (en) * | 1996-05-20 | 1999-02-16 | Taiwan Semiconductor Manufacturing Company, Ltd. | Method for etching titanium nitride layers |
US6951767B1 (en) * | 2002-07-02 | 2005-10-04 | Taiwan Semiconductor Manufacturing Company, Ltd. | Development hastened stability of titanium nitride for APM etching rate monitor |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5547881A (en) | 1996-03-06 | 1996-08-20 | Taiwan Semiconductor Manufacturing Company Ltd | Method of forming a resistor for ESD protection in a self aligned silicide process |
US5710070A (en) * | 1996-11-08 | 1998-01-20 | Chartered Semiconductor Manufacturing Pte Ltd. | Application of titanium nitride and tungsten nitride thin film resistor for thermal ink jet technology |
-
2002
- 2002-07-02 US US10/187,705 patent/US6951767B1/en not_active Expired - Fee Related
-
2005
- 2005-06-21 US US11/157,571 patent/US20050233481A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5086017A (en) * | 1991-03-21 | 1992-02-04 | Industrial Technology Research Institute | Self aligned silicide process for gate/runner without extra masking |
US5547861A (en) * | 1994-04-18 | 1996-08-20 | Becton, Dickinson And Company | Detection of nucleic acid amplification |
US5516399A (en) * | 1994-06-30 | 1996-05-14 | International Business Machines Corporation | Contactless real-time in-situ monitoring of a chemical etching |
US5872062A (en) * | 1996-05-20 | 1999-02-16 | Taiwan Semiconductor Manufacturing Company, Ltd. | Method for etching titanium nitride layers |
US6951767B1 (en) * | 2002-07-02 | 2005-10-04 | Taiwan Semiconductor Manufacturing Company, Ltd. | Development hastened stability of titanium nitride for APM etching rate monitor |
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