Relevant bibliographies by topics / Self-Assembly of block copolymers

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Self-Assembly of block copolymers'

Author: Grafiati
Published: 7 July 2024
Last updated: 31 July 2025

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Journal articles on the topic "Self-Assembly of block copolymers"

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Abetz, Volker. "Self-Assembly of Block Copolymers." Polymers 12, no. 4 (2020): 794. http://dx.doi.org/10.3390/polym12040794.

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Kuperkar, Ketan, Dhruvi Patel, Leonard Ionut Atanase, and Pratap Bahadur. "Amphiphilic Block Copolymers: Their Structures, and Self-Assembly to Polymeric Micelles and Polymersomes as Drug Delivery Vehicles." Polymers 14, no. 21 (2022): 4702. http://dx.doi.org/10.3390/polym14214702.

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Self-assembly of amphiphilic block copolymers display a multiplicity of nanoscale periodic patterns proposed as a dominant tool for the ‘bottom-up’ fabrication of nanomaterials with different levels of ordering. The present review article focuses on the recent updates to the self-association of amphiphilic block copolymers in aqueous media into varied core-shell morphologies. We briefly describe the block copolymers, their types, microdomain formation in bulk and micellization in selective solvents. We also discuss the characteristic features of block copolymers nanoaggregates viz., polymer mi
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Yoon, Jongseung, Wonmok Lee, and Edwin L. Thomas. "Self-Assembly of Block Copolymers for Photonic-Bandgap Materials." MRS Bulletin 30, no. 10 (2005): 721–26. http://dx.doi.org/10.1557/mrs2005.270.

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AbstractSelf-assembled block copolymer systems with an appropriate molecular weight to produce a length scale that will interact with visible light are an alternative platform material for the fabrication of large-area, well-ordered photonic-bandgap structures at visible and near-IR frequencies.Over the past years, one-, two-, and three-dimensional photonic crystals have been demonstrated with various microdomain structures created through microphase separation of block copolymers. The size and shape of periodic microstructures of block copolymers can be readily tuned by molecular weight, rela
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Ma, Shuhui, Yushuang Hou, Jinlin Hao, Cuncai Lin, Jiawei Zhao, and Xin Sui. "Well-Defined Nanostructures by Block Copolymers and Mass Transport Applications in Energy Conversion." Polymers 14, no. 21 (2022): 4568. http://dx.doi.org/10.3390/polym14214568.

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With the speedy progress in the research of nanomaterials, self-assembly technology has captured the high-profile interest of researchers because of its simplicity and ease of spontaneous formation of a stable ordered aggregation system. The self-assembly of block copolymers can be precisely regulated at the nanoscale to overcome the physical limits of conventional processing techniques. This bottom-up assembly strategy is simple, easy to control, and associated with high density and high order, which is of great significance for mass transportation through membrane materials. In this review,
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Benmouna, A., R. Benmouna, M. R. Bockstaller, and I. F. Hakem. "Self-Organization Schemes towards Thermodynamic Stable Bulk Heterojunction Morphologies: A Perspective on Future Fabrication Strategies of Polymer Photovoltaic Architectures." Advances in Physical Chemistry 2013 (April 16, 2013): 1–8. http://dx.doi.org/10.1155/2013/948189.

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Research efforts to improve our understanding of electronic polymers are developing fast because of their promising advantages over silicon in photovoltaic solar cells. A major challenge in the development of polymer photovoltaic devices is the viable fabrication strategies of stable bulk heterojunction architecture that will retain functionality during the expected lifetime of the device. Block copolymer self-assembly strategies have attracted particular attention as a scalable means toward thermodynamically stable microstructures that combine the ideal geometrical characteristics of a bulk h
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Xie, Yihui, Nicolas Moreno, Victor M. Calo, et al. "Synthesis of highly porous poly(tert-butyl acrylate)-b-polysulfone-b-poly(tert-butyl acrylate) asymmetric membranes." Polymer Chemistry 7, no. 18 (2016): 3076–89. http://dx.doi.org/10.1039/c6py00215c.

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For the first time, self-assembly and non-solvent induced phase separation was applied to polysulfone-based linear block copolymers, reaching mechanical stability much higher than other block copolymer membranes used in this method, which were mainly based on polystyrene blocks.
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Wang, Zihao, Susu Tao, Yanyan Chu, Xiaoyan Xu, and Qinggang Tan. "Diameter of Carbon Nanotube-Directed Self-Assembly of Amphiphilic Block Copolymers." Materials 12, no. 10 (2019): 1606. http://dx.doi.org/10.3390/ma12101606.

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The cooperative self-assembly of nanoparticles and amphiphilic block copolymers has attracted increasing interests as it offers effective routes to achieve nanocomposite supramolecular structures with desired structure and properties. The incorporation of nanoparticles usually tunes the self-assembly structure of block copolymers, as the copolymer–nanoparticle interactions may change the relative volume ratio of hydrophobic block/hydrophilic block copolymers. It should be noted that the micro-size length and the strong nonpolar feature of carbon nanotubes (CNTs) may cause the block copolymer–C
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Choi, Young Joo, Hyeong Min Jin, Bong Hoon Kim, Ju Young Kim, and Sang Ouk Kim. "Self-Assembly Nanofabrication via Mussel-Inspired Interfacial Engineering." Applied Mechanics and Materials 229-231 (November 2012): 2749–52. http://dx.doi.org/10.4028/www.scientific.net/amm.229-231.2749.

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We present that polydopamineassistedinterfacial engineering can be synergistically integratedwith block copolymer lithography for surface nanopatterningof low-surface-energy substrate materials, includingTeflon, graphene, and gold. Block copolymer lithography is aself-assembly based nanofabrication that holds greatpromise for sub-10-nm scale patterning. The directed self-assemblyof block copolymers into device-oriented nanopatternsgenerally requires organic modification of a substrate surface.In this work, the versatility of the polydopamine treatment was demonstrated by the surface modificati
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Bailly, Nathalie, Gwenaelle Pound-Lana, and Bert Klumperman. "Synthesis, Characterization, and Self-Assembly of Poly(N-vinylpyrrolidone)-block-poly(vinyl acetate)." Australian Journal of Chemistry 65, no. 8 (2012): 1124. http://dx.doi.org/10.1071/ch12185.

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Poly(N-vinylpyrrolidone)-block-poly(vinyl acetate) (PVP-b-PVAc) block copolymers of varying molar mass and hydrophobic block lengths were synthesized by xanthate-mediated radical polymerization. In order to control the molar mass of the hydrophilic PVP block, a xanthate chain transfer agent, S-(2-cyano-2-propyl) O-ethyl xanthate, was used. The PVP-b-PVAc block copolymer is composed of a hydrophilic and hydrophobic segment, and has the ability to self-assemble in aqueous solution. The PVP-b-PVAc block copolymers were characterized by 1H NMR spectroscopy to confirm their self-assembly in water.
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Tirrell, Matthew V., and Alexander Katz. "Self-Assembly in Materials Synthesis." MRS Bulletin 30, no. 10 (2005): 700–704. http://dx.doi.org/10.1557/mrs2005.205.

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AbstractThe synthesis of materials via self-assembly typically involves the spontaneous and reversible organization of small building blocks for the purpose of creating conglomerate structures over larger length scales. This introductory article describes self-assembly processes on several length scales, from subnanometer up to millimeter scales, and briefly summarizes some of the incredible diversity of materials that exhibit selfassembly. Articles in this issue cover self-assembly using zeolitic structures, organic molecular crystals, block copolymers, surfactants, mesoscale templates, and s
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Dissertations / Theses on the topic "Self-Assembly of block copolymers"

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Valverde, Serrano Clara. "Self-assembly behavior in hydrophilic block copolymers." Phd thesis, Universität Potsdam, 2011. http://opus.kobv.de/ubp/volltexte/2011/5416/.

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Block copolymers are receiving increasing attention in the literature. Reports on amphiphilic block copolymers have now established the basis of their self-assembly behavior: aggregate sizes, morphologies and stability can be explained from the absolute and relative block lengths, the nature of the blocks, the architecture and also solvent selectiveness. In water, self-assembly of amphiphilic block copolymers is assumed to be driven by the hydrophobic. The motivation of this thesis is to study the influence on the self-assembly in water of A b B type block copolymers (with A hydrophilic) of th
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Cheng, Li-Chen Ph D. Massachusetts Institute of Technology. "Templated self-assembly of novel block copolymers." Thesis, Massachusetts Institute of Technology, 2019. https://hdl.handle.net/1721.1/122156.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2019<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references.<br>Self-assembly of block copolymers (BCPs) is emerging as a promising route for numerous technological applications to fabricate a variety of nanoscopic structures. The resulting feature sizes range from a few to several hundred nanometers, and are readily tunable by varying the molecular weights of block copolymers. Directed self-assembly of block copolymer is an effective way to pattern periodic arrays o
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Mohd, Yusoff Siti Fairus. "Crystallization-driven self-assembly of polyferrocenylsilane-based block copolymers." Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546192.

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Jung, Yeon Sik. "Templated self-assembly of siloxane block copolymers for nanofabrication." Thesis, Massachusetts Institute of Technology, 2009. http://hdl.handle.net/1721.1/52791.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2009.<br>This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.<br>Cataloged from student submitted PDF version of thesis.<br>Includes bibliographical references.<br>Monolayer patterns of block copolymer (BCP) microdomains have been pursued for applications in below sub-30 nm nanolithography. BCP selfassembly processing is scalable and low cost, and is well-suited for integration with existing semiconduct
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Cowie, Lauren. "The synthesis and self-assembly of MPC block copolymers." Thesis, Durham University, 2013. http://etheses.dur.ac.uk/7341/.

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Biocompatible and biodegradable poly(lactide)-2-methacryloyloxyethyl phosphorylcholine (PLA-PMPC) amphiphilic block copolymers were synthesized by a combination of Ring Opening Polymerization (ROP) and Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization techniques. The PLA-macroRAFT agent was synthesized by the derivatization of PLA-OH with RAFT agent 4-cyano-4-(phenylcarbonothioylthio)pentanoic acid (CPADB) achieving high levels of functionalization and narrow weight distributions (PDI range of 1.02-1.17). PLA-PMPC with varied MPC block lengths were synthesized yielding pol
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BERTANI, DANIELA. "Synthesis and self-assembly of biocompatible amphiphilic block copolymers." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2018. http://hdl.handle.net/10281/199109.

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Il drug delivery attira molto interesse a causa della necessità di migliorare efficienza e selettività delle terapie farmacologiche. Capsule polimeriche per i farmaci sono una strategia promettente per prolungarne i tempi di circolazione, migliorarne il trasporto nel sangue, e modularne nel tempo il rilascio. In questo ambito, l’organizzazione spontanea dei copolimeri a blocchi (CB) in nanoparticelle (NP) compartimentalizzate in ambiente acquoso è uno strumento potente per la fabbricazione di sistemi per il drug delivery. In questa tesi vengono investigati la sintesi e l’autoassemblaggio (AS)
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Gomes, Correia Cindy. "Directed self-assembly strategies for orientation-controlled block copolymers for advanced lithography." Thesis, Bordeaux, 2019. http://www.theses.fr/2019BORD0393.

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L’objectif de ce travail était de mettre en évidence le potentiel du PDMSBb-PS pour des applications en nanolithographie avancée. Pour cela, nous avons fourni une compréhension du comportement d’auto-assemblage du PDMSB-b-PS en masse et en film mince. Nous avons réalisé l’auto-assemblage de ce copolymère semicristallin en cylindre et gyroïde bien définis avec des périodicités inférieures à 20 nm grâce à un paramètre d’interaction de Flory-Huggins élevé (Chapitre 2). Nous avons par la suite proposé une approche pour obtenir des lamelles perpendiculaires du PDMSB-b-PS en film mince grâce à l’uti
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Evangelio, Araujo Laura. "Directed self-assembly of block copolymers on chemically nanopatterned surfaces." Doctoral thesis, Universitat Autònoma de Barcelona, 2017. http://hdl.handle.net/10803/406119.

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La tesi doctoral titulada “Auto-assemblatge de copolímers de bloc per modificació química de la superfície”, presenta com a objectiu principal el desenvolupament, implementació i caracterització d’un mètode de guiatge de copolímers de bloc basat en la modificació química de la superfície. El desenvolupament d’aquest mètode de nanofabricació contribueix a la futura generació de dispositius i circuits nanoelectrònics. Primer de tot, es presenten els aspectes generals sobre l’auto-assemblatge dirigit de copolímers de bloc, així com el seu rol dins del futur de la nanoelectrònica comparat amb alt
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Weiß, Jan. "Synthesis and self-assembly of multiple thermoresponsive amphiphilic block copolymers." Phd thesis, Universität Potsdam, 2011. http://opus.kobv.de/ubp/volltexte/2011/5336/.

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In the present thesis, the self-assembly of multi thermoresponsive block copolymers in dilute aqueous solution was investigated by a combination of turbidimetry, dynamic light scattering, TEM measurements, NMR as well as fluorescence spectroscopy. The successive conversion of such block copolymers from a hydrophilic into a hydrophobic state includes intermediate amphiphilic states with a variable hydrophilic-to-lipophilic balance. As a result, the self-organization is not following an all-or-none principle but a multistep aggregation in dilute solution was observed. The synthesis of double the
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Parras, Petros. "Self-assembly and dynamics in block copolymers with hierarchical order." Thesis, University of Reading, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493799.

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Incorporation of peptide or mesogenic units into block copolymers enables hierarchical order, whereby an interplay between microphase separation and peptide secondary structure formation or liquid crystal ordering occurs. This thesis concerns the self-assembly process and dynamics in block copolymers with hierarchical order. The second and third chapters discuss peptide-based poly(γ-benzyl-Lglutamate)-poly(ethylene glycol)-poly(γ-benzyl-L-glutamate) triblock copolymers and side-group liquid crystal polystyrene-poly [2-(((3-cholesteryl)-oxy)carbonyl)decyl methacrylate)] diblock copolymers. In t
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Books on the topic "Self-Assembly of block copolymers"

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1942-, Lindman Björn, and Alexandridis Paschalis, eds. Amphiphilic block copolymers: Self-assembly and applications. Elsevier, 2000.

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Salvatore, Stefano. Optical Metamaterials by Block Copolymer Self-Assembly. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-05332-5.

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Borisov, Oleg, and Axel H. E. Müller. Self organized nanostructures of amphiphilic block copolymers. Springer, 2011.

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Müller, Axel H. E., and Oleg Borisov, eds. Self Organized Nanostructures of Amphiphilic Block Copolymers II. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-22297-9.

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Müller, Axel H. E., and Oleg Borisov, eds. Self Organized Nanostructures of Amphiphilic Block Copolymers I. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-22486-7.

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Lindman, B., and P. Alexandridis. Amphiphilic Block Copolymers: Self-Assembly and Applications. Elsevier Science & Technology Books, 2000.

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Massey, Jason. Self-assembly of block copolymers containing poly(ferrocene). Dept of Chemistry, U of Toronto, 2000.

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Block Copolymers with Crystallizable Blocks: Synthesis, Self-Assembly and Applications. MDPI, 2022. http://dx.doi.org/10.3390/books978-3-0365-3325-4.

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Schmalz, Holger. Block Copolymers with Crystallizable Blocks: Synthesis, Self-Assembly and Applications. Mdpi AG, 2022.

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Gronheid, Roel, and Paul Nealey. Directed Self-Assembly of Block Co-polymers for Nano-manufacturing. Elsevier Science & Technology, 2015.

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Book chapters on the topic "Self-Assembly of block copolymers"

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Hrub&xFD, Martin, Sergey K. Filippov, and Petr &xt&xBp&xEnek. "Biomedical Application of Block Copolymers." In Macromolecular Self&;#x02010;assembly. John Wiley &;#38; Sons, Inc., 2016. http://dx.doi.org/10.1002/9781118887813.ch8.

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Liu, Chi-chun, Kenji Yoshimoto, Juan de Pablo, and Paul Nealey. "Directed Self-Assembly of Block Copolymers." In Microlithography. CRC Press, 2020. http://dx.doi.org/10.1201/9781315117171-13.

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Chenkual, Laltanpuii, Dimple S. Lalchandani, Amruta Prabhakar Padakanti, Naveen Chella, and Pawan Kumar Porwal. "Synthesis and Self-Assembly of Block Copolymers." In Block Co-polymeric Nanocarriers: Design, Concept, and Therapeutic Applications. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-6917-3_4.

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DeWit, Matthew A., Ali Nazemi, Solmaz Karamdoust, Annelise Beaton, and Elizabeth R. Gillies. "Design, Synthesis and Assembly of Self-Immolative Linear Block Copolymers." In Non-Conventional Functional Block Copolymers. American Chemical Society, 2011. http://dx.doi.org/10.1021/bk-2011-1066.ch002.

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Xie, Ru, Carlos R. López-Barrón, and Norman J. Wagner. "Self-Assembly of Block Copolymers in Ionic Liquids." In ACS Symposium Series. American Chemical Society, 2017. http://dx.doi.org/10.1021/bk-2017-1250.ch005.

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Gowd, E. Bhoje, Mallikarjuna Shroff Rama, and Manfred Stamm. "Nanostructures Based on Self-Assembly of Block Copolymers." In Nanofabrication. Springer Vienna, 2011. http://dx.doi.org/10.1007/978-3-7091-0424-8_8.

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Whittell, George R., Jessica Gwyther, David A. Rider, and Ian Manners. "Self-Assembly and Applications of Polyferrocenylsilane Block Copolymers." In Complex Macromolecular Architectures. John Wiley & Sons (Asia) Pte Ltd, 2011. http://dx.doi.org/10.1002/9780470825150.ch16.

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Quémener, D., A. Deratani, and S. Lecommandoux. "Dynamic Assembly of Block-Copolymers." In Constitutional Dynamic Chemistry. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/128_2011_258.

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Karayianni, Maria, and Stergios Pispas. "Self-Assembly of Amphiphilic Block Copolymers in Selective Solvents." In Fluorescence Studies of Polymer Containing Systems. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26788-3_2.

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Wang, Xiaosong, Mitchell A. Winnik, and Ian Manners. "Synthesis, Self-Assembly, and Applications of Polyferrocenylsilane Block Copolymers." In ACS Symposium Series. American Chemical Society, 2006. http://dx.doi.org/10.1021/bk-2006-0928.ch020.

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Conference papers on the topic "Self-Assembly of block copolymers"

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Uranga-Granados, Iker, Berke Erbas, Pol Torres-Vila, et al. "Combination of thermal scanning probe lithography and directed self-assembly of block copolymers." In Novel Patterning Technologies 2025, edited by Richard A. Farrell and Ricardo Ruiz. SPIE, 2025. https://doi.org/10.1117/12.3050036.

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Monreal, Victor, Sachin Bobade, Deepak Dharmangadan, et al. "Roughness improvements with new high-chi block copolymers for EUV rectification directed self-assembly." In Novel Patterning Technologies 2025, edited by Richard A. Farrell and Ricardo Ruiz. SPIE, 2025. https://doi.org/10.1117/12.3051517.

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Janes, Dustin W., and Jon-l. Innocent-dolor. "Improving 28nm pitch line and space EUV patterns by the directed self-assembly of block copolymers." In Novel Patterning Technologies 2025, edited by Richard A. Farrell and Ricardo Ruiz. SPIE, 2025. https://doi.org/10.1117/12.3052802.

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Rahman, Md S., Tomohiro Iwaki, Xianfeng Gao, et al. "Directed self-assembly of medium-chi and high-chi block copolymers for DRAM C/H patterning." In Novel Patterning Technologies 2025, edited by Richard A. Farrell and Ricardo Ruiz. SPIE, 2025. https://doi.org/10.1117/12.3051487.

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Wu, Zhiyong, Jiacheng Luo, Qingshu Dong, et al. "Quadruple-hole multiplication by directed self-assembly of block copolymer." In 8th International Workshop on Advanced Patterning Solutions (IWAPS 2024), edited by Yayi Wei and Tianchun Ye. SPIE, 2024. https://doi.org/10.1117/12.3055274.

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Nealey, Paul F. "Design of block copolymers for directed self-assembly." In Novel Patterning Technologies 2021, edited by Eric M. Panning and J. Alexander Liddle. SPIE, 2021. http://dx.doi.org/10.1117/12.2584926.

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Angelini, Angelo, Irdi Murataj, Marwan Channab, et al. "Self-assembly of di-block copolymers for hyperbolic metasurfaces." In CLEO: Applications and Technology. OSA, 2020. http://dx.doi.org/10.1364/cleo_at.2020.jtu2b.25.

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Okabe, Kye, He Yi, Maryann C. Tung, et al. "Cross-sectional imaging of directed self-assembly block copolymers." In SPIE Advanced Lithography, edited by Douglas J. Resnick and Christopher Bencher. SPIE, 2015. http://dx.doi.org/10.1117/12.2087569.

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Doerk, Gregory S., Joy Y. Cheng, Charles T. Rettner, Srinivasan Balakrishnan, Noel Arellano, and Daniel P. Sanders. "Deterministically isolated gratings through the directed self-assembly of block copolymers." In SPIE Advanced Lithography, edited by William M. Tong and Douglas J. Resnick. SPIE, 2013. http://dx.doi.org/10.1117/12.2011629.

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Ito, Natsuko, Gregory Blachut, Yusuke Asano, et al. "Block copolymers for sub-10nm directed self-assembly lithography (Conference Presentation)." In Novel Patterning Technologies 2018, edited by Eric M. Panning and Martha I. Sanchez. SPIE, 2018. http://dx.doi.org/10.1117/12.2297030.

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Reports on the topic "Self-Assembly of block copolymers"

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Jenekhe, S. A., and X. L. Chen. Self-Assembly of Rod-Coil Block Copolymers. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada366979.

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Determan, Michael Duane. Synthesis and Characterization of Stimuli Responsive Block Copolymers, Self-Assembly Behavior and Applications. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/861607.

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Thomas, Edwin L. Tunable PhoXonic Band Gap Materials from Self-Assembly of Block Copolymers and Colloidal Nanocrystals (NBIT Phase II). Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada591353.

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Hiszpanski, Anna M. Directed-Assembly of Block Copolymers for Large-Scale, Three-Dimensional, Optical Metamaterials at Visible Wavelengths. Final LDRD Report. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1410019.

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Wu, Sangwook. Theory for dynamical self arrest and gelation in microemulsions and the block copolymer systems. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/850055.

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Su, Wei-Fangg, L.-Y. Wang, C.-A. Dai, and C.-W. Chen. High Efficiency Photovoltaic Devices Fabricated from Self-Assemble Block Insulating-Conducting Copolymer Containing Semiconducting Nanoparticles. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada473098.

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Luckett, DeBorah C., Andrew L. Bowman, Andrew M. Lessel, et al. High-Rate Characterization and Modeling of a Hyperelastic Block Copolymer Subjected to Ballistic Impact. U.S. Army Engineer Research and Development Center, 2024. http://dx.doi.org/10.21079/11681/49416.

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Abstract:
polystyrene-polyisobutylene-polystyrene star-block copolymer (PS-PIB-PS) is a thermoplastic elastomer with visco hyperelastic characteristics that displays a high level of toughness and performs well in shock attenuating applications. The research goal is to investigate experimentally and numerically the capacity of PS-PIB-PS to dissipate kinetic energy and examine its deformation and failure modes under impact by spherical steel projectiles at speed ranges of 200–1,700 m/s. First, PS-PIB-PS is characterized using a Split-Hopkinson Pressure Bar to measure high strain rate response and calibrat
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8

Thomas, Edwin. Tunable PhoXonic Band Gap Materials from Self-Assembly of Block Copoliymers and Colloidal Nanocrystals (NBIT Phase II). Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada542359.

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