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Published on: June 20, 2019
Photoinduced ordering of block copolymers
Vikram K Daga1, Evan L Schwartz, Curran M Chandler
1Department of Chemical Engineering, University of Massachusetts , Amherst, Massachusetts 01003, United States.
Photoinduced ordering of disordered block copolymers (BCPs) is achieved by blending with an additive. This method creates well-ordered nanostructures on demand in specific material regions.
Area of Science:
- Materials Science
- Polymer Chemistry
- Nanotechnology
Background:
- Block copolymers (BCPs) self-assemble into ordered nanostructures.
- Achieving controlled, on-demand ordering in specific regions remains challenging.
- Existing methods for nanostructure formation can be intrusive or lack spatial control.
Purpose of the Study:
- To develop a nonintrusive, on-demand method for photoinduced ordering of disordered block copolymers.
- To create well-defined nanostructures in arbitrarily chosen regions of BCP materials.
- To establish a generalizable strategy applicable to various block copolymers.
Main Methods:
- Blending disordered block copolymers with a photo-convertible additive.
- Utilizing photoconversion of the additive to induce specific interactions with one BCP block.
- Applying light to initiate ordering in targeted areas of the BCP blend.
- Leveraging hydrogen bonding capabilities for enhanced interactions.
Main Results:
- Successfully induced photoordering in disordered BCPs using a simple blending approach.
- Demonstrated the ability to form well-ordered nanostructures in specific, arbitrarily defined regions.
- Established that the strategy is effective for BCPs with chain segments capable of hydrogen bonding with the additive.
- The process is rapid and nonintrusive.
Conclusions:
- Photoinduced ordering of disordered BCPs is achievable through additive blending and photoconversion.
- This method offers a versatile and controllable route for fabricating nanostructured materials.
- The strategy holds promise for applications requiring precise control over nanostructure formation in block copolymers.
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