Lithographically directed materials assembly
TL;DR: In this paper, a single resistless lithography step is used to directly change the surface energy without requiring subsequent material deposition or plasma etching steps, and the resulting polystyrene features can be used as an etch mask to transfer periodic lines and spaces into a silicon substrate.
read more
Abstract: We have developed a processing method that significantly reduces the number of steps necessary to yield a surface that directs block copolymer assembly. This methodology employs a single resistless lithography step that directly changes the surface energy without requiring subsequent material deposition or plasma etching steps. The lithographically defined difference in surface energies acts as a template to direct diblock polymer self-assembly into low-defect periodic structures. Our newly developed lithographically directed self-assembly technique can produce sub-45 nm half pitch lines employing poly(styrene-b-methyl methacrylate) (PS-b-PMMA) and interference lithography. Once assembled into periodic lines of alternating materials, the PMMA block can be removed and the resulting polystyrene features can be used as an etch mask to transfer periodic lines-and-spaces into a silicon substrate.
read more
Chat with Paper
AI Agents for this Paper
Find similar papers on Google Scholar, PubMed and Arxiv
Write a critical review of this paper
Analyze citations of this paper to find unaddressed research gaps
Citations
Nanopatterning of diblock copolymer directed self-assembly lithography with wet development
Makoto Muramatsu,Mitsuaki Iwashita,Takahiro Kitano,Takayuki Toshima,Mark Somervell,Yuriko Seino,Daisuke Kawamura,Masahiro Kanno,Katsutoshi Kobayashi,Tsukasa Azuma +9 more
TL;DR: In this paper, a method for using wet development in a directed self-assembly lithography (DSAL) application is reported, which offers higher selectivity between the PMMA and PS blocks in the assembled pattern.
43
PMMA removal options by wet development in PS-b-PMMA block copolymer for nanolithographic mask fabrication
Ahmed Gharbi,Raluca Tiron,Patricia Pimenta Barros,Maxime Argoud,Isabelle Servin,Xavier Chevalier,Celia Nicolet,Christophe Navarro +7 more
TL;DR: In this article, the authors report a wet etching technique allowing an efficient removal of polymethylmethacrylate (PMMA) in PMMA cylinder-forming polystyrene-b-polymethylmethyricrylate(PS-b)-PMMA BCP in order to generate contact holes and confirm that exposure with ultraviolet (UV) light or electron beam is required for PMMA degradation before its complete removal by wet development in acetic acid.
25
Nanopatterning of diblock copolymer directed self-assembly lithography with wet development
Makoto Muramatsu,Mitsuaki Iwashita,Takahiro Kitano,Takayuki Toshima,Yuriko Seino,Daisuke Kawamura,Masahiro Kanno,Katsutoshi Kobayashi,Tsukasa Azuma +8 more
TL;DR: Wang et al. as mentioned in this paper applied wet development technique which could be higher selectivity to keep PS film thickness after pattern formation, especially, they proposed the method using low pressure mercury lamp and conventional TMAH(2.38%).
13
Patent
Methods of providing patterned chemical epitaxy templates for self-assemblable block copolymers for use in device lithography
Emiel Peeters,Wilhelmus Sebastianus Marcus Maria Ketelaars,Sander Frederik Wuister,Roelof Koole,Christianus Martinus Van Heesch,Aurélie Brizard,Henri Marie Joseph Boots,Thanh Nguyen,Oktay Yildirim +8 more
- 06 Feb 2013
TL;DR: In this paper, a patterned chemical epitaxy template for orientation of a self-assemblable block copolymer comprising first and second polymer blocks on a surface of a substrate is presented.
12
Defect recognition in line-space patterns aided by deep learning with data augmentation
Jihun Ahn,Ye Chan Kim,So Youn Kim,Su-Mi Hur,Vikram Thapar +4 more
- 24 Sep 2021
TL;DR: The outcome of this work shows that the amalgamation of an optimal network design and augmentation strategies performs satisfactorily for defectivity analysis and is generic for data not constrained to fixed settings.
References
Block Copolymer Thermodynamics: Theory and Experiment
TL;DR: Block copolymers are macromolecules composed of sequences, or blocks, of chemically distinct repeat units that make possible the sequential addition of monomers to various carbanion-ter minated ("living") linear polymer chains.
3.8K
Ultrahigh-Density Nanowire Arrays Grown in Self-Assembled Diblock Copolymer Templates
Thomas Thurn-Albrecht,Joerg Schotter,G. A. Kästle,N. Emley,Takasada Shibauchi,Takasada Shibauchi,Lia Krusin-Elbaum,Kathryn W. Guarini,Charles T. Black,Mark T. Tuominen,Thomas P. Russell +10 more
TL;DR: A simple, robust, chemical route to the fabrication of ultrahigh-density arrays of nanopores with high aspect ratios using the equilibrium self-assembled morphology of asymmetric diblock copolymers is shown.
Epitaxial self-assembly of block copolymers on lithographically defined nanopatterned substrates
Sang Ouk Kim,Harun H. Solak,Mark P. Stoykovich,Nicola J. Ferrier,Juan J. de Pablo,Paul F. Nealey +5 more
TL;DR: The integration of thin films of block copolymer with advanced lithographic techniques to induce epitaxial self-assembly of domains are demonstrated and illustrate how hybrid strategies to nanofabrication allow for molecular level control in existing manufacturing processes.
1.7K