Related Experiment Video
Updated: Dec 31, 2025

11:42
Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
8.2K
Strain-Dependent Nanowrinkle Confinement of Block Copolymers
Nano Letters
|January 14, 2020
Summary
This study demonstrates soft templated assembly of block copolymers (BCPs) using nanowrinkles. Researchers controlled BCP alignment for advanced nanolithography in soft electronics.
Area of Science:
- Materials Science
- Polymer Science
- Nanotechnology
Background:
- Block copolymers (BCPs) are crucial for nanolithography.
- Controlling BCP alignment is challenging, especially on flexible substrates.
Purpose of the Study:
- To develop a soft, templated assembly method for BCPs.
- To achieve programmable alignment of BCPs using polymeric nanowrinkles.
- To explore BCP structural formation mechanisms and control strategies.
Main Methods:
- Utilized polymeric nanowrinkles as a confining scaffold for BCP assembly.
- Manipulated substrate strain to control BCP alignment relative to wrinkle orientation.
- Employed self-consistent field theory (SCFT) modeling to understand BCP formation.
- Investigated various copolymer molecular weights and functional wrinkle surfaces.
Main Results:
- Achieved programmable parallel or perpendicular alignment of poly(styrene)-block-poly(dimethylsiloxane) (PS-b-PDMS) BCPs.
- Demonstrated that wrinkle curvature and surface affinity dictate BCP structural formation.
- Showcased control over BCP alignment on complex wrinkle geometries and functionalized surfaces.
Conclusions:
- Developed an all-soft, templated assembly technique for BCPs.
- Established a method for programmable BCP alignment on flexible 3D architectures.
- This approach offers a promising nanolithography route for next-generation soft electronics.
More Related Videos
Related Concept Videos
Characteristics and Nomenclature of Copolymers
3.1K
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...
3.1K
Polymers: Molecular Weight Distribution
4.5K
For any given polymer, the weight average molecular weight (Mw) is higher than, if not equal to, the number average molecular weight (Mn). The only situation in which the weight average molecular weight and the number average molecular weight are equal is when a polymer consists only of chains with equal molecular weight. However, this never happens in a synthetic polymer, since it is difficult to control the polymerization process up to a molecular level with accuracy to a hundred percent.
4.5K
Cationic Chain-Growth Polymerization: Mechanism
2.7K
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...
2.7K
Ziegler–Natta Chain-Growth Polymerization: Overview
3.8K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.8K
Radical Chain-Growth Polymerization: Chain Branching
2.4K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
2.4K
Anionic Chain-Growth Polymerization: Mechanism
2.4K
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...
2.4K

