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Related Concept Videos

Surface Active Agents01:27

Surface Active Agents

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Surfactants, named for their behavior at interfaces, positively adsorb at the interfaces of two phases, reducing interfacial tension. Their versatility as emulsifiers, detergents, and foaming agents stems from this ability. Surfactants, often termed amphiphiles, share the property of amphipathy, with molecules having both hydrophilic and hydrophobic portions. The hydrophilic part is called the head, and the hydrophobic part, including an elongated alkyl substituent, forms the tail.Surfactants...
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Characteristics and Nomenclature of Copolymers01:24

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Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
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Anionic Chain-Growth Polymerization: Overview01:20

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The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
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Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

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Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
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Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
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Using Polystyrene-block-polyacrylic acid-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization
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Orientation Control of Block Copolymers Using Surface Active, Phase-Preferential Additives.

Ankit Vora1, Kristin Schmidt1, Gabriela Alva1

  • 1IBM Research-Almaden, 650 Harry Rd., San Jose, California 95120, United States.

ACS Applied Materials & Interfaces
|October 5, 2016
PubMed
Summary
This summary is machine-generated.

Researchers developed a new method using a surface-active polymer additive to achieve perpendicular orientation in block copolymer (BCP) nanostructures. This breakthrough enables advanced nanopatterning for semiconductor applications and beyond.

Keywords:
aliphatic polycarbonatesblock copolymersdirected self-assemblyhexafluoroalcoholhigh-χsurface active polymersthin film self-assembly

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Polymer Science

Background:

  • Controlling the orientation of thin film nanostructures from block copolymers (BCPs) is crucial for technologies like separation membranes, nanopatterning, and energy storage.
  • Achieving perpendicular orientation of BCP domains remains a significant challenge in the field.

Purpose of the Study:

  • To develop an integration-friendly approach for achieving perpendicular orientation of BCP domains.
  • To demonstrate the utility of perpendicularly oriented BCP domains in advanced semiconductor patterning and pattern transfer.

Main Methods:

  • Incorporation of a small amount of a phase-preferential, surface-active polymer (SAP) as an additive into a polycarbonate-containing BCP formulation.
  • Thermal annealing to induce self-assembly and domain orientation.
  • Pattern transfer into a hardmask layer using etch techniques and graphoepitaxy-based directed self-assembly.

Main Results:

  • Successfully obtained perpendicularly oriented BCP domains with a 19 nm natural periodicity.
  • Demonstrated the application of these vertically oriented domains for next-generation semiconductor patterning.
  • Successfully transferred patterns into a hardmask layer using established etch techniques and directed self-assembly.

Conclusions:

  • The novel formulation-based approach using SAP additives is effective for achieving perpendicular BCP domain orientation.
  • This method offers a versatile and easily extendable solution for nanopatterning applications.
  • The technique shows promise for integration into existing lithographic schemes for advanced semiconductor nodes.