TWI548689B - 中性層聚合物、其製造方法,及含有該聚合物之製品 - Google Patents
中性層聚合物、其製造方法,及含有該聚合物之製品 Download PDFInfo
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- TWI548689B TWI548689B TW103121140A TW103121140A TWI548689B TW I548689 B TWI548689 B TW I548689B TW 103121140 A TW103121140 A TW 103121140A TW 103121140 A TW103121140 A TW 103121140A TW I548689 B TWI548689 B TW I548689B
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- Prior art keywords
- copolymer
- segment
- additive
- block copolymer
- free energy
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- 230000007935 neutral effect Effects 0.000 title claims description 47
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- 238000001704 evaporation Methods 0.000 claims description 6
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
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- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D153/00—Coating compositions based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D125/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Coating compositions based on derivatives of such polymers
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- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0002—Lithographic processes using patterning methods other than those involving the exposure to radiation, e.g. by stamping
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- Thermal Sciences (AREA)
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- Compositions Of Macromolecular Compounds (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
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| US14/297,095 US9382444B2 (en) | 2013-06-24 | 2014-06-05 | Neutral layer polymers, methods of manufacture thereof and articles comprising the same |
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| JP6239813B2 (ja) | 2012-07-18 | 2017-11-29 | 株式会社Screenセミコンダクターソリューションズ | 基板処理装置および基板処理方法 |
| US9802400B2 (en) | 2013-06-24 | 2017-10-31 | Dow Global Technologies Llc | Orientation control layer formed on a free top surface of a first block copolymer from a mixture of first and second block copolymers |
| US9382444B2 (en) | 2013-06-24 | 2016-07-05 | Dow Global Technologies Llc | Neutral layer polymers, methods of manufacture thereof and articles comprising the same |
| JP6702649B2 (ja) * | 2013-12-31 | 2020-06-03 | ローム アンド ハース エレクトロニック マテリアルズ エルエルシーRohm and Haas Electronic Materials LLC | ブロックコポリマーの性質を制御する方法及びブロックコポリマーから製造された物品 |
| JP2015170723A (ja) * | 2014-03-06 | 2015-09-28 | Jsr株式会社 | パターン形成方法及び自己組織化組成物 |
| US11021630B2 (en) * | 2014-12-30 | 2021-06-01 | Rohm And Haas Electronic Materials Llc | Copolymer formulation for directed self assembly, methods of manufacture thereof and articles comprising the same |
| US10294359B2 (en) | 2014-12-30 | 2019-05-21 | Rohm And Haas Electronic Materials Llc | Copolymer formulation for directed self assembly, methods of manufacture thereof and articles comprising the same |
| US10011713B2 (en) * | 2014-12-30 | 2018-07-03 | Dow Global Technologies Llc | Copolymer formulation for directed self assembly, methods of manufacture thereof and articles comprising the same |
| US9574107B2 (en) | 2015-02-16 | 2017-02-21 | International Business Machines Corporation | Fluoro-alcohol additives for orientation control of block copolymers |
| US10259907B2 (en) | 2015-02-20 | 2019-04-16 | Az Electronic Materials (Luxembourg) S.À R.L. | Block copolymers with surface-active junction groups, compositions and processes thereof |
| TWI612379B (zh) * | 2015-02-26 | 2018-01-21 | Rohm And Haas Electronic Materials Llc | 用於定向自組裝的共聚物調配物、其製造方法以及包括其的物件 |
| TWI669337B (zh) * | 2015-02-26 | 2019-08-21 | 美商羅門哈斯電子材料有限公司 | 用於定向自組裝的共聚物調配物、其製造方法以及包括其的物件 |
| TWI627219B (zh) * | 2015-02-26 | 2018-06-21 | 羅門哈斯電子材料有限公司 | 用於定向自組裝的共聚物調配物、其製造方法以及包括其的物件 |
| TWI588200B (zh) * | 2015-02-26 | 2017-06-21 | 羅門哈斯電子材料有限公司 | 用於定向自組裝的共聚物調配物、其製造方法以及包括其的物件 |
| WO2016181834A1 (ja) * | 2015-05-11 | 2016-11-17 | 国立大学法人名古屋大学 | 非共有結合性ソフトエラストマー及びその製法 |
| FR3037070B1 (fr) * | 2015-06-02 | 2019-05-31 | Arkema France | Procede de controle de l'energie de surface a l'interface entre un copolymere a blocs et un autre compose |
| FR3037071B1 (fr) * | 2015-06-02 | 2019-06-21 | Arkema France | Procede de reduction de la defectivite d'un film de copolymere a blocs |
| TWI627220B (zh) * | 2015-06-03 | 2018-06-21 | 羅門哈斯電子材料有限公司 | 用於圖案處理之組合物及方法 |
| KR101946776B1 (ko) * | 2015-06-04 | 2019-02-13 | 주식회사 엘지화학 | 중성층 조성물 |
| US9368350B1 (en) * | 2015-06-23 | 2016-06-14 | International Business Machines Corporation | Tone inverted directed self-assembly (DSA) fin patterning |
| JP6039028B1 (ja) | 2015-09-11 | 2016-12-07 | 株式会社東芝 | 自己組織化材料及びパターン形成方法 |
| KR20180112778A (ko) * | 2016-02-08 | 2018-10-12 | 제이에스알 가부시끼가이샤 | 콘택트 홀 패턴의 형성 방법 및 조성물 |
| CN109476797B (zh) * | 2016-07-21 | 2021-09-07 | 大塚化学株式会社 | 嵌段共聚物、组合物和膜 |
| US10691019B2 (en) * | 2016-10-07 | 2020-06-23 | Jsr Corporation | Pattern-forming method and composition |
| JP2018154760A (ja) * | 2017-03-17 | 2018-10-04 | 東芝メモリ株式会社 | パターン形成材料及びパターン形成方法 |
| JP6966101B2 (ja) * | 2017-07-14 | 2021-11-10 | エルジー・ケム・リミテッド | 中性層組成物 |
| US10347486B1 (en) * | 2017-12-19 | 2019-07-09 | International Business Machines Corporation | Patterning material film stack with metal-containing top coat for enhanced sensitivity in extreme ultraviolet (EUV) lithography |
| WO2019152078A1 (en) * | 2018-02-01 | 2019-08-08 | Brewer Science, Inc. | Gradient block copolymers for directed self-assembly |
| US11873243B2 (en) | 2018-06-01 | 2024-01-16 | Dow Global Technologies Llc | Inhibition of silica scale using bottle brush polymers |
| JP7135554B2 (ja) | 2018-08-03 | 2022-09-13 | Jsr株式会社 | 下層膜形成用組成物、自己組織化膜の下層膜及びその形成方法並びに自己組織化リソグラフィープロセス |
| JP7354042B2 (ja) * | 2020-03-27 | 2023-10-02 | パナソニックホールディングス株式会社 | 電気音響変換器 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4929510A (en) * | 1988-04-29 | 1990-05-29 | State University Of New York | Biocompatible polymer articles |
| TW201004862A (en) * | 2008-03-21 | 2010-02-01 | Micron Technology Inc | Methods of improving long range order in self-assembly of block copolymer films with ionic liquids |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG55445A1 (en) * | 1997-01-07 | 1998-12-21 | Denki Kagaku Kogyo Kabushili K | Block copolymer block copolymer compostion and heat shrinkable films made thereof |
| DE19829397A1 (de) * | 1998-07-01 | 2000-01-05 | Basf Ag | Verwendung mikrophasenseparierter Polymermischungen für die Herstellung von permeablen Membranen |
| US7160551B2 (en) | 2002-07-09 | 2007-01-09 | The Board Of Trustees Of The University Of Illinois | Injectable system for controlled drug delivery |
| US7407554B2 (en) | 2005-04-12 | 2008-08-05 | International Business Machines Corporation | Development or removal of block copolymer or PMMA-b-S-based resist using polar supercritical solvent |
| US20090270559A1 (en) * | 2006-05-25 | 2009-10-29 | Arkema Inc. | Acid functionalized gradient block copolymers |
| JP2008231233A (ja) | 2007-03-20 | 2008-10-02 | Kyoto Univ | 高分子薄膜、パターン基板、磁気記録用パターン媒体及びこれらの製造方法 |
| US7763319B2 (en) | 2008-01-11 | 2010-07-27 | International Business Machines Corporation | Method of controlling orientation of domains in block copolymer films |
| US9707524B2 (en) * | 2008-10-28 | 2017-07-18 | Arkema Inc. | Water flux polymer membranes |
| KR101535227B1 (ko) * | 2008-12-31 | 2015-07-08 | 삼성전자주식회사 | 블록 공중합체를 이용한 미세 패턴 형성 방법 |
| US8114306B2 (en) | 2009-05-22 | 2012-02-14 | International Business Machines Corporation | Method of forming sub-lithographic features using directed self-assembly of polymers |
| JP5300799B2 (ja) * | 2010-07-28 | 2013-09-25 | 株式会社東芝 | パターン形成方法及びポリマーアロイ下地材料 |
| US8304493B2 (en) | 2010-08-20 | 2012-11-06 | Micron Technology, Inc. | Methods of forming block copolymers |
| JP5555111B2 (ja) | 2010-09-27 | 2014-07-23 | 株式会社日立製作所 | シルセスキオキサンを有する高分子薄膜、微細構造体及びこれらの製造方法 |
| EP2643413A1 (en) * | 2010-11-24 | 2013-10-02 | Dow Corning Corporation | Controlling morphology of block copolymers |
| US9156682B2 (en) | 2011-05-25 | 2015-10-13 | The University Of Massachusetts | Method of forming oriented block copolymer line patterns, block copolymer line patterns formed thereby, and their use to form patterned articles |
| KR101999870B1 (ko) | 2011-09-15 | 2019-10-02 | 위스콘신 얼럼나이 리서어치 화운데이션 | 화학적으로 패턴화된 표면과 제2 표면 사이의 블록 공중합체 막의 유도 조립 |
| US8691925B2 (en) | 2011-09-23 | 2014-04-08 | Az Electronic Materials (Luxembourg) S.A.R.L. | Compositions of neutral layer for directed self assembly block copolymers and processes thereof |
| WO2013104499A1 (en) | 2012-01-13 | 2013-07-18 | Asml Netherlands B.V. | Self-assemblable polymer and methods for use in lithography |
| TWI478967B (zh) | 2012-02-10 | 2015-04-01 | Univ Texas | 使用化學氣相沈積膜控制嵌段共聚物薄膜中之域取向 |
| US8697810B2 (en) * | 2012-02-10 | 2014-04-15 | Rohm And Haas Electronic Materials Llc | Block copolymer and methods relating thereto |
| US9802400B2 (en) | 2013-06-24 | 2017-10-31 | Dow Global Technologies Llc | Orientation control layer formed on a free top surface of a first block copolymer from a mixture of first and second block copolymers |
| US9382444B2 (en) | 2013-06-24 | 2016-07-05 | Dow Global Technologies Llc | Neutral layer polymers, methods of manufacture thereof and articles comprising the same |
| US20140377465A1 (en) * | 2013-06-24 | 2014-12-25 | Rohm And Haas Electronic Materials Llc | Neutral layer polymers, methods of manufacture thereof and articles comprising the same |
-
2014
- 2014-06-05 US US14/297,095 patent/US9382444B2/en active Active
- 2014-06-19 TW TW103121140A patent/TWI548689B/zh active
- 2014-06-23 JP JP2014128101A patent/JP2015007233A/ja active Pending
- 2014-06-23 KR KR1020140076456A patent/KR101686059B1/ko active Active
- 2014-06-24 CN CN201710264644.5A patent/CN107459726B/zh active Active
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4929510A (en) * | 1988-04-29 | 1990-05-29 | State University Of New York | Biocompatible polymer articles |
| TW201004862A (en) * | 2008-03-21 | 2010-02-01 | Micron Technology Inc | Methods of improving long range order in self-assembly of block copolymer films with ionic liquids |
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| Publication number | Publication date |
|---|---|
| US20140378592A1 (en) | 2014-12-25 |
| CN107459726A (zh) | 2017-12-12 |
| KR20150000429A (ko) | 2015-01-02 |
| US10167411B2 (en) | 2019-01-01 |
| US20170327712A1 (en) | 2017-11-16 |
| CN104231514A (zh) | 2014-12-24 |
| CN107459726B (zh) | 2020-07-14 |
| JP2015007233A (ja) | 2015-01-15 |
| US9382444B2 (en) | 2016-07-05 |
| CN104231514B (zh) | 2017-05-17 |
| TW201518382A (zh) | 2015-05-16 |
| JP2019178339A (ja) | 2019-10-17 |
| KR101686059B1 (ko) | 2016-12-13 |
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