WO2002069395B1 - INTEGRATION OF LOW ⊂ THIN FILMS AND Ta INTO Cu DAMASCENE - Google Patents

INTEGRATION OF LOW ⊂ THIN FILMS AND Ta INTO Cu DAMASCENE

Info

Publication number
WO2002069395B1
WO2002069395B1 PCT/US2002/005470 US0205470W WO02069395B1 WO 2002069395 B1 WO2002069395 B1 WO 2002069395B1 US 0205470 W US0205470 W US 0205470W WO 02069395 B1 WO02069395 B1 WO 02069395B1
Authority
WO
WIPO (PCT)
Prior art keywords
polymer
film
polymer film
precursor
moiety
Prior art date
Application number
PCT/US2002/005470
Other languages
French (fr)
Other versions
WO2002069395A3 (en
WO2002069395A2 (en
Inventor
Chung J Lee
Original Assignee
Dielectric Systems Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dielectric Systems Inc filed Critical Dielectric Systems Inc
Priority to AU2002306571A priority Critical patent/AU2002306571A1/en
Publication of WO2002069395A2 publication Critical patent/WO2002069395A2/en
Publication of WO2002069395A3 publication Critical patent/WO2002069395A3/en
Publication of WO2002069395B1 publication Critical patent/WO2002069395B1/en

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/70Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
    • H01L21/71Manufacture of specific parts of devices defined in group H01L21/70
    • H01L21/768Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
    • H01L21/76838Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
    • H01L21/76841Barrier, adhesion or liner layers
    • H01L21/76843Barrier, adhesion or liner layers formed in openings in a dielectric
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
    • C08G61/025Polyxylylenes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L65/00Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L65/00Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
    • C08L65/04Polyxylenes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02107Forming insulating materials on a substrate
    • H01L21/02109Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
    • H01L21/02112Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
    • H01L21/02118Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer carbon based polymeric organic or inorganic material, e.g. polyimides, poly cyclobutene or PVC
    • H01L21/0212Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer carbon based polymeric organic or inorganic material, e.g. polyimides, poly cyclobutene or PVC the material being fluoro carbon compounds, e.g.(CFx) n, (CHxFy) n or polytetrafluoroethylene
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02107Forming insulating materials on a substrate
    • H01L21/02225Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
    • H01L21/0226Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
    • H01L21/02263Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
    • H01L21/02271Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/70Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
    • H01L21/71Manufacture of specific parts of devices defined in group H01L21/70
    • H01L21/768Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
    • H01L21/76801Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
    • H01L21/76802Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing by forming openings in dielectrics
    • H01L21/76814Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing by forming openings in dielectrics post-treatment or after-treatment, e.g. cleaning or removal of oxides on underlying conductors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/70Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
    • H01L21/71Manufacture of specific parts of devices defined in group H01L21/70
    • H01L21/768Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
    • H01L21/76801Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
    • H01L21/76822Modification of the material of dielectric layers, e.g. grading, after-treatment to improve the stability of the layers, to increase their density etc.
    • H01L21/76828Modification of the material of dielectric layers, e.g. grading, after-treatment to improve the stability of the layers, to increase their density etc. thermal treatment
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/70Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
    • H01L21/71Manufacture of specific parts of devices defined in group H01L21/70
    • H01L21/768Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
    • H01L21/76801Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
    • H01L21/76829Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing characterised by the formation of thin functional dielectric layers, e.g. dielectric etch-stop, barrier, capping or liner layers
    • H01L21/76831Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing characterised by the formation of thin functional dielectric layers, e.g. dielectric etch-stop, barrier, capping or liner layers in via holes or trenches, e.g. non-conductive sidewall liners
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/34Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
    • C08G2261/342Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing only carbon atoms
    • C08G2261/3424Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing only carbon atoms non-conjugated, e.g. paracyclophanes or xylenes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2365/00Characterised by the use of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Derivatives of such polymers
    • C08J2365/04Polyxylylenes

Abstract

New precursors and processes to generate fluorinated poly(para-xylylenes) ('PPX') and their chemically modified films suitable for fabrications of integrated circuit ('Ics') of <0.15 µm are disclosed. The films so prepared have low dielectric constants ('⊂') and are able to keep the integrity of the dielectric, Cu, and the barrier metal, such as Ta. Hence, the reliability of Ics can be assured.

Claims

AMENDED CLAIMS
[received by the International Bureau on 09 May 2003 (09.05.03) original claims 1, 12, 14-18, 22, 24, 28, 30-34, 38-47, 52-56 amended, claims 35, 48 cancelled, claims 57-59 added]
WHAT IS CLAIMED IS:
1. A polymer film prepared from a method comprising: co-polymerizing an intermediate (A) and an intermediate (B); wherein, co-polymerizing precursor intermediates having a feed rate onto a substrate having a substrate temperature is conducted under vacuum or inert atmosphere with a slow system leakage rate, the substrate temperature being below a melting temperature of the intermediate (A); the intermediate (A) is an aromatic group consisting of n' reactive sites with n' unpaired electrons and n' is an integer of at least 2 but is smaller than, or equal to, the maximum number of sites for the sp C substitution in the intermediate (A); the intermediate (B) is a bridging compound consisting of n" reactive sites with n" unpaired electrons; and n" is an integer of at least 2 but is smaller than, or equal to, the maximum number of sites for the sp3C substitution in the intermediate (B); and the polymer film having a thermal stable crystalline form suitable for use as a dielectric thin film in fabrication of an integrated circuit.
2. The polymer film of claim 1 , wherein the vacuum is lower than about 30 mTorrs and the system leakage rate is less than about 2 mTorrs per minute.
3. The polymer film of claim 1 , wherein the inert atmosphere is an atmosphere that is substantially devoid from either a free radical scavenger or a compound containing an active hydrogen.
4. The polymer film of claim 3, wherein the free radical scavenger comprises water and oxygen.
5. The polymer film of claim 3, wherein the active hydrogen comprises a compound containing an -OH, an -SH, or an -KNH group.
26
6. The polymer film of claim 1 , wherein the intermediate (A) is a benzyne.
7. The polymer of claim 1 , wherein the intermediate (A) is a fully-fluorinated benzyne or a partially-fluorinated benzyne.
8. The polymer film of claim 1, wherein the intermediate (B) has a general chemical structure of • C • (Z' Z"), in which each of Z' and Z" is independently H, F, or -CόF5.
9. The polymer film of claim 1, wherein the intermediate (B) is a divalent carbon.
10. The polymer film of claim 1, wherein the intermediate (B) is a carbene.
11. The polymer film of claim 1 , wherein the intermediate (B) is a fully- fluorinated carbene or a partially-fluorinated carbene.
12. An intermediate (A) made by a chemical process of manufacture from a precursor having a general chemical structure of:
(X')m-Ar-(X")n , wherein,
X' and X" are each leaving groups;
Ar is an aromatic group; and n and m are independently 0 or an integer, and (n+m) is at least 2 but can equal to the total sp2C substitutions in the aromatic group Ar; wherein, the chemical process of manufacture is conducted under vacuum or inert atmosphere with a slow system lealcage rate, the system leakage rate is less than about 2 mTorrs per minute; and the intermediate (A) is useful for producing a polymer film having a thermal stable crystalline form suitable for use as a dielectric thin film in fabrication of an integrated circuit.
27
13. The intermediate (A) of claim 12, wherein the leaving group X' or X" is independently a ketene, -COOH, ~Br, -I, -NR2, -~N , -SR, -SO2R, -OR, =N+=N\ -C(O)- N2, or CF3-CF(-O-)-, wherein R is an alkyl or an aromatic group.
14. The intermediate (A) of claim 12, wherein both of the leaving groups X' and X" are -COOH, Br, or I, and n = m = 1.
15. The intermediate (A) of claim 12, wherein the Ar is a phenyl moiety, a naphthenyl moiety, a di-phenyl moiety, an anthracenyl moiety, a phenanthrenyl moiety, or a pyrenyl moiety.
27-A
1 . The intermediate (A) of claim 12, wherein the chemical process of manufacture comprises irradiation, using photons or electron; or cracking, using heat or plasma; or combination thereof.
1 . The intermediate (A) of claim 16, wherein the chemical process of manufacture comprises cracking using a heated reactor.
18. An intermediate (A) made by a chemical process of manufacture from a precursor having a general chemical structure of: (X)m-Ar-(CZ Z Y)n, wherein,
X' and Y are each leaving groups;
Ar is an aromatic group;
Z' and Z" similar or different and individually H, F or -C6Fs;
n and m are similar or different and independently 0 or an integer; and (n+m) is at least 2 but can equal to the total sp2C substitutions in the aromatic group Ar;
wherein,
the chemical process of manufacture is conducted under vacuum or inert atmosphere with a slow system leakage rate, the system leakage rate is less than about 2 mTorrs per minute; and the intermediate (A) is useful for producing a polymer film having a thermal stable crystalline foπn suitable for use as a dielectric thin film in fabrication of an integrated circuit.
19. The intermediate (A) of claim 18, wherein the leaving group X' or Y is independently a ketene, -COOH, -Br, -I, -MR2, -N Rs, -SR, -SO2R, -OR, ^N^N", -C(O)- N2, or CF3-CF(-O-)-, wherein R is an alkyl or an aromatic group.
28
20. The intermediate (A) of claim 18, wherein the Ar is a phenyl moiety, a naphthenyl moiety, a di-phenyl moiety, an anthracenyl moiety, a phenanthrenyl moiety, or a pyrenyl moiety.
21. The intermediate (A) of claim 18, wherein the chemical process of manufacture comprises irradiation, using photons or electron, or cracking, using heat or plasma, or any combination of the above.
22. The intermediate (A) of claim 18, wherein the chemical process of manufacture comprises of an IR - assisted thermal cracking.
23. The intermediate (A) of claim 18, wherein X' is -COOH, -Br, or -I, and n = m = l.
28-A
24. An intermediate (B) made by a chemical process of manufacture from a precursor having a general chemical structure of:
X-C(Z' Z")
wherein,
X is a leaving group; and
Z" and Z" are similar or different and independently H, F, or -CδFs. wherein, the chemical process of manufacture is conducted under vacuum or inert atmosphere with a system leakage rate less than about 2 mTorrs per minute; and the intermediate (B) is useful for producing a polymer film having a thermal stable crystalline form suitable for use as a dielectric thin film in fabrication of an integrated circuit.
25. The intermediate (B) of claim 24, wherein X is a ketene, -C(O)-N2, or CF3- CF(-0-)-.
26. The intermediate (B) of claim 24, wherein the chemical process of manufacture comprises irradiation, using photons or electron, or cracking, using heat or plasma, or any combination of the above.
27. The intermediate (B) of claim 26, wherein the chemical process comprises of thermal cracking using a heated reactor.
29
28. A polymer film suitable for use as a dielectric thin film in fabrication of an integrated circuit, wherein,
the polymer film is prepared from polymerization or co-polymerization of at least two reactive precursor intermediates,
co-polymerizing of precursor intermediates having a feed rate onto a substrate having a substrate temperature is conducted under vacuum or inert atmosphere with a system leakage rate less than about 2 mTorrs per minute; and
the polymer film comprises fully- or partially- fluorinated polymers; and
the polymer film comprises a thermal stable crystalline form.
29. The polymer film of claim 28, wherein the fluorinated polymers is a polymer or copolymer of -CF2C6H CF2-,-CF2C6F4CF2-, -C6H4CF2-, or -C6F4CF2-.
30. The polymer film of claim 28, wherein the film is heterogeneous film comprising of semicrystalline polymers.
1. The polymer film of claim 30, further comprising a layer of amorphous polymer.
32. The polymer film of claim 28, wherein the film is homogeneous film.
33. The polymer film of claim 28, wherein the film is suitable for fabrication of optical devices.
29-A
34. A semicrystalline polymer made by a chemical process of manufacture comprising: polymerizing precursor intermediates having a feed rate onto a substrate having a substrate temperature in a deposition chamber; wherein, the precursor has a general chemical structure comprising;
(X')m-Ar-(CZ'Z"Y)n, wherein,
Ar is an aromatic group;
X' and Y are leaving groups and are a ketene, -COOH, -Br, -I, -NR.>, -l^R;), - SR, -SO2R, -OR, =KΗN-, -C(O)-N2, (CF3-CF(0))-, wherein R is an alkyl or aromatic group;
Z' and Z" are similar or different and are H, F or -CQFS; n and m are similar or different and independently 0 or an integer, and (n + m) is at least 2 and can equal the total sp2C substitutions in the aromatic group, Ar; the semicrystalline polymer is prepared under a vacuum with a low system- leakage-rate, an inert atmosphere, or both; and the semicrystalline polymer comprises a thermal stable crystalline form suitable for use as a dielectric thin film in fabrication of an integrated circuit.
35. Cancel.
36. A semicrystalline polymer of claim 34, wherein both the leaving groups X' and Y is -COOH, Br, or I, and n = m = 1.
30
37. A semicrystalline polymer of claim 34, wherein the Ar is a phenyl moiety, a naphthenyl moiety, a di-phenyl moiety, an anthracenyl moiety, a phenanthrenyl moiety, or a pyrenyl moiety.
38. The semicrystalline polymer of claim 34, wherein the chemical process of manufacture further comprises: generating precursor intermediates by irradiation with photons or electron; cracking with heat or plasma; or any combination thereof.
39. The semicrystalline polymer of claim 34, wherein the chemical process of manufacture further comprises: generating precursor intermediates by thermal cracking with a heated reactor.
40. The semicrystalline polymer of claim 34, wherein the semicrystalline polymer is at least 30% crystalline.
41. The semicrystalline polymer of claim 34, wherein the semicrystalline polymer is defined by polymer chains oriented at no more than 45 degrees to the xy-plane of the dielectric thin film.
30-A
42. The semicrystalline polymer of claim 34, wherein the thermal stable crystalline form is not altered more than 15% after being heated at temperatures greater than 400 °C.
43. The semicrystalline polymer of claim 34, wherein the chemical process of manufacture further comprises post-annealing the semicrystalline polymer at a high temperature ranging from 350 to 400 °C, the post-annealing step forming a film having more than 30% to 50% crystalline polymers in the thermal stable crystalline.
44. The semicrystalline polymer of claim 43, wherein the film is PPX-F or PF- PPX.
45. The semicrystalline polymer of claim 43, wherein the crystalline polymers have their polymer chains orientated at less than 45 degrees to the xy-plane of the film.
46. The semicrystalline polymer of claim 34, wherein the feed rate for precursor intermediates is less than 10 mmoles/min per meter2 of the substrate.
47. The semicrystalline polymer of claim 34, wherein the substrate temperature is less than -20°C, but no less than -65°C.
48. Cancel.
49. A method of making polymer thin films comprising:
providing a precursor vapor under a vacuum or inert atmosphere;
generating reactive precursor intermediates from the precursor vapor; and
transporting the reactive precursor intermediates to a substrate for film growth;
wherein,
31 there are at least two different reactive precursor intermediates;
the reactive precursor intermediates have a feed rate onto the substrate;
the substrate has a substrate temperature;
the polymer film comprises a thermal stable crystalline form that is suitable for use as a dielectric thin film in fabrication of an integrated circuit.
50. The method of claim 49, wherein the vacuum is lower than about 30 mTorrs and the system leakage rate is less than about 2 mTorrs per minute.
31-A
51. The method of claim 49, wherein the inert atmosphere is an atmosphere that is substantially devoid from either a free radical scavenger or a compound containing an active hydrogen.
52. The method of claim 51 , wherein the free radical scavenger comprises water and oxygen.
53. The method of claim 51 , wherein the active hydrogen comprises a compound containing an -OH, an -SH, or an -R H group.
54. A system for deposition of thin films comprising:
a precursor reservoir;
a reactor thereto for producing reactive precursor intermediates;
a diffusor;
a cold trap; and
a pump;
wherein,
the system is useful for providing a precursor vapor under a vacuum or inert atmosphere, then generating reactive precursor intermediates from the precursor vapor, and transporting the reactive precursor intermediates to a substrate for film growth;
wherein,
there are at least two different reactive precursor inteπnediates;
the reactive precursor intermediates have a feed rate onto the substrate;
32 the substrate has a substrate temperature;
the polymer film comprises a thermal stable crystalline form that is suitable for use as a dielectric thin film in fabrication of an integrated circuit
55. A. thin film transistor ("TFT") in active matrix liquid crystal display ("AMLCD") comprising the polymer film of claim 1.
56, A color filter in an active matrix liquid crystal display ("AMLCD") comprising the polymer film of claim 1.
32-A
57. The semicrystalline polymer of claim 45, wherein the crystalline polymers have their polymer chains orientated at less than 20 degrees to the xy-plane of the film.
58. The semicrystalline polymer of claim 34, wherein the feed rate for precursor intermediates is less than 10 mmoles/ in per meter2 of the substrate.
59. The semicrystalline polymer of claim 34, wherein the substrate temperature is -30°C.
32-B
PCT/US2002/005470 2001-02-26 2002-02-22 INTEGRATION OF LOW ⊂ THIN FILMS AND Ta INTO Cu DAMASCENE WO2002069395A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2002306571A AU2002306571A1 (en) 2001-02-26 2002-02-22 Integration of low thin films and ta into cu damascene

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/795,217 2001-02-26
US09/795,217 US6825303B2 (en) 2001-02-26 2001-02-26 Integration of low ε thin films and Ta into Cu dual damascene

Publications (3)

Publication Number Publication Date
WO2002069395A2 WO2002069395A2 (en) 2002-09-06
WO2002069395A3 WO2002069395A3 (en) 2003-08-21
WO2002069395B1 true WO2002069395B1 (en) 2004-07-08

Family

ID=25165034

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2002/005470 WO2002069395A2 (en) 2001-02-26 2002-02-22 INTEGRATION OF LOW ⊂ THIN FILMS AND Ta INTO Cu DAMASCENE

Country Status (3)

Country Link
US (1) US6825303B2 (en)
AU (1) AU2002306571A1 (en)
WO (1) WO2002069395A2 (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6824879B2 (en) 1999-06-10 2004-11-30 Honeywell International Inc. Spin-on-glass anti-reflective coatings for photolithography
CA2374944A1 (en) 1999-06-10 2000-12-21 Nigel Hacker Spin-on-glass anti-reflective coatings for photolithography
US20040255862A1 (en) * 2001-02-26 2004-12-23 Lee Chung J. Reactor for producing reactive intermediates for low dielectric constant polymer thin films
US20050274322A1 (en) * 2001-02-26 2005-12-15 Lee Chung J Reactor for producing reactive intermediates for low dielectric constant polymer thin films
AU2002227106A1 (en) 2001-11-15 2003-06-10 Honeywell International Inc. Spin-on anti-reflective coatings for photolithography
US8053159B2 (en) 2003-11-18 2011-11-08 Honeywell International Inc. Antireflective coatings for via fill and photolithography applications and methods of preparation thereof
US6962871B2 (en) * 2004-03-31 2005-11-08 Dielectric Systems, Inc. Composite polymer dielectric film
US7094661B2 (en) * 2004-03-31 2006-08-22 Dielectric Systems, Inc. Single and dual damascene techniques utilizing composite polymer dielectric film
US7309395B2 (en) 2004-03-31 2007-12-18 Dielectric Systems, Inc. System for forming composite polymer dielectric film
US20060201426A1 (en) * 2004-05-25 2006-09-14 Lee Chung J Reactor for Producing Reactive Intermediates for Transport Polymerization
US20060046044A1 (en) * 2004-08-24 2006-03-02 Lee Chung J Porous composite polymer dielectric film
US20060274474A1 (en) * 2005-06-01 2006-12-07 Lee Chung J Substrate Holder
US20060275547A1 (en) * 2005-06-01 2006-12-07 Lee Chung J Vapor Phase Deposition System and Method
US7993972B2 (en) * 2008-03-04 2011-08-09 Stats Chippac, Ltd. Wafer level die integration and method therefor
US8642246B2 (en) 2007-02-26 2014-02-04 Honeywell International Inc. Compositions, coatings and films for tri-layer patterning applications and methods of preparation thereof
US8557877B2 (en) 2009-06-10 2013-10-15 Honeywell International Inc. Anti-reflective coatings for optically transparent substrates
US8864898B2 (en) 2011-05-31 2014-10-21 Honeywell International Inc. Coating formulations for optical elements
EP3194502A4 (en) 2015-04-13 2018-05-16 Honeywell International Inc. Polysiloxane formulations and coatings for optoelectronic applications
US11390718B2 (en) 2019-04-10 2022-07-19 Specialty Coating Systems, Inc. Elastic parylene

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB650947A (en) 1947-09-19 1951-03-07 Michael Mojzesz Szwarc The production of new polymers
GB673651A (en) 1949-02-07 1952-06-11 Michael Mojzesz Szwarc New polymers
US3274267A (en) 1963-09-23 1966-09-20 Union Carbide Corp Cyclic alpha-perfluoro-di-p-xylylenes
US3332891A (en) 1963-09-23 1967-07-25 Union Carbide Corp Process for the preparation of alpha-per-fluoro-p-xylylene polymers
US3379803A (en) 1964-05-04 1968-04-23 Union Carbide Corp Coating method and apparatus for deposition of polymer-forming vapor under vacuum
US3349045A (en) 1964-07-09 1967-10-24 Union Carbide Corp Poly (alpha, alpha, alpha', alpha'-tetrachloro-p-xylylene) films
US3280202A (en) 1964-07-09 1966-10-18 Union Carbide Corp Process for producing p-xylylene-containing compositions
US3342754A (en) * 1966-02-18 1967-09-19 Union Carbide Corp Para-xylylene polymers
US3288728A (en) 1966-02-18 1966-11-29 Union Carbide Corp Para-xylylene copolymers
US3509075A (en) 1966-05-04 1970-04-28 Union Carbide Corp Polymerization process and product thereof
US3626032A (en) 1968-04-24 1971-12-07 Us Navy Preparation of poly-{60 ,{60 ,2,3,5,6,-hexafluoro-p-xylylene
US3503903A (en) 1969-01-13 1970-03-31 Union Carbide Corp Polymers of improved performance capabilities and processes therefor
US3694495A (en) 1970-12-02 1972-09-26 Us Navy Preparation of poly alpha, alpha 2,3,5,6-hexafluoro-p-xylylene
US3940530A (en) 1972-05-24 1976-02-24 Union Carbide Corporation Support media with supported object
NL8801524A (en) 1988-06-15 1990-01-02 Union Carbide Corp PROCESS FOR MANUFACTURING HIGH TENSILE POLYMERIC PRODUCTS
US5531857A (en) 1988-07-08 1996-07-02 Cauldron Limited Partnership Removal of surface contaminants by irradiation from a high energy source
US5153986A (en) 1991-07-17 1992-10-13 International Business Machines Method for fabricating metal core layers for a multi-layer circuit board
US5268202A (en) 1992-10-09 1993-12-07 Rensselaer Polytechnic Institute Vapor deposition of parylene-F using 1,4-bis (trifluoromethyl) benzene
AU7682594A (en) 1993-09-08 1995-03-27 Uvtech Systems, Inc. Surface processing
JP3773065B2 (en) 1995-08-25 2006-05-10 第三化成株式会社 Dichloro-tetrafluoro- [2,2] -paracyclophane and process for producing the same
US5538758A (en) 1995-10-27 1996-07-23 Specialty Coating Systems, Inc. Method and apparatus for the deposition of parylene AF4 onto semiconductor wafers
TW297147B (en) 1995-10-27 1997-02-01 Specialty Coating Systems Inc Multi-level circuit structure including fluorinated parylene polymer dielectric interlayers
US5879808A (en) 1995-10-27 1999-03-09 Alpha Metals, Inc. Parylene polymer layers
JP3808102B2 (en) 1995-10-27 2006-08-09 スペシャルティ、コーティング、システムズ、インコーポレイテッド Deposition method of Parylene AF4 on a semiconductor wafer
US5958510A (en) 1996-01-08 1999-09-28 Applied Materials, Inc. Method and apparatus for forming a thin polymer layer on an integrated circuit structure
US5888591A (en) 1996-05-06 1999-03-30 Massachusetts Institute Of Technology Chemical vapor deposition of fluorocarbon polymer thin films
US5965679A (en) 1996-09-10 1999-10-12 The Dow Chemical Company Polyphenylene oligomers and polymers
KR20010005944A (en) 1997-04-03 2001-01-15 캠벨 존 에스 Low dielectric constant material with improved dielectric strength
US6140456A (en) * 1997-10-24 2000-10-31 Quester Techology, Inc. Chemicals and processes for making fluorinated poly(para-xylylenes)
US6020458A (en) 1997-10-24 2000-02-01 Quester Technology, Inc. Precursors for making low dielectric constant materials with improved thermal stability
US6051321A (en) 1997-10-24 2000-04-18 Quester Technology, Inc. Low dielectric constant materials and method
JP3199006B2 (en) 1997-11-18 2001-08-13 日本電気株式会社 Method of forming interlayer insulating film and insulating film forming apparatus
US6033939A (en) 1998-04-21 2000-03-07 International Business Machines Corporation Method for providing electrically fusible links in copper interconnection
US6015918A (en) 1998-11-10 2000-01-18 Sharp Laboratories Of America, Inc. Allyl-derived precursor and synthesis method
US6265320B1 (en) 1999-12-21 2001-07-24 Novellus Systems, Inc. Method of minimizing reactive ion etch damage of organic insulating layers in semiconductor fabrication

Also Published As

Publication number Publication date
WO2002069395A3 (en) 2003-08-21
AU2002306571A1 (en) 2002-09-12
US6825303B2 (en) 2004-11-30
US20020120083A1 (en) 2002-08-29
WO2002069395A2 (en) 2002-09-06

Similar Documents

Publication Publication Date Title
WO2002069395B1 (en) INTEGRATION OF LOW ⊂ THIN FILMS AND Ta INTO Cu DAMASCENE
US6514801B1 (en) Method for manufacturing thin-film transistor
EP0608633B1 (en) Method for multilayer CVD processing in a single chamber
US6881447B2 (en) Chemically and electrically stabilized polymer films
EP1085579B1 (en) Method of manufacturing solar cell
KR100412744B1 (en) Method of manufacturing thin-film transistor
US6703462B2 (en) Stabilized polymer film and its manufacture
KR100436319B1 (en) Method for forming silicon film
US20100140756A1 (en) Apparatus for manufacturing silicon oxide thin film and method for forming the silicon oxide thin film
US7192645B2 (en) Porous low E (&lt;2.0) thin films by transport co-polymerization
Li et al. Constructing Additives Synergy Strategy to Doctor‐Blade Efficient CH3NH3PbI3 Perovskite Solar Cells under a Wide Range of Humidity from 45% to 82%
JPH10289902A (en) Film formation device
US20060046044A1 (en) Porous composite polymer dielectric film
JP3384487B2 (en) Method of forming insulating film and multilayer wiring
JP4076245B2 (en) Low dielectric constant insulating film, method for forming the same, and interlayer insulating film
KR100382370B1 (en) Preventive treatment method of susceptor of CVD device
JP3494572B2 (en) Method for forming low dielectric polymer film
JPH09326388A (en) Forming method of low specific dielectric constant polymer film, forming method of interlayer insulating film and low specific dielectric constant polymer film forming apparatus
JP3957811B2 (en) Method for forming low dielectric constant polymer film
KR100454758B1 (en) Method of depositing tantalum oxide layer
KR20160041036A (en) Method for manufacturing pedot film having ultra-high conductivity prepared by using weak base (dudo) and electronic device including the same
CN108668450A (en) A kind of adhesion without adhesiver dosage form flexible copper-clad plate and preparation method thereof
JPS58218177A (en) Manufacture of semiconductor device
KR20000055083A (en) a method of manufacturing thin films used for semiconductor devices
JPH0424432B2 (en)

Legal Events

Date Code Title Description
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase
B Later publication of amended claims

Effective date: 20030509

NENP Non-entry into the national phase

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP