Creating Useful Nanostructured Soft Materials by Directed Self-Assembly

Originally delivered Nov 18, 2020
  • Type:
    Archived Webinar
  • Level:
    Intermediate
  • Duration:
    1.25 hours
  • PDHs:
    1.00

Share This Post:

Controlling structure and thereby manipulating the use properties of condensed matter is a central concern in materials science. A striking disparity exists in our ability to enact such structural control in self-assembled soft materials, relative to hard condensed matter systems. This talk examines strategies for directing self-assembly in nanostructured soft matter to create useful materials, including single crystals and materials with bespoke textures. Our focus is on self-assembly of block copolymers and small molecule mesogens.

The ability to precisely control their chemical functionality combined with the readily tunable characteristic length scales (~1-100 nm) of their self-assembled mesophases position these systems as a versatile and attractive class of materials for compelling applications ranging from membranes for size and chemo-selective transport, to optics, and lithography. As a result there is intense interest in elucidating the physical processes relevant for directing their self-assembly to create application relevant structures, with a goal of exploiting such fundamental understanding to create useful materials or devices.

This presentation discusses such directed self-assembly of soft nanostructured materials and emerging methods for generating highly ordered and heterostructured systems. In particular, we focus on recent advances in the creation of highly ordered nanostructured membranes for water purification, and small length scale structures for lithography in microelectronics. While much of the progress to date has involved the use of a single ‘field’ to direct self-assembly (e.g. shear, magnetic, electric fields; surface forces/confinement), the use of more than one stimulus to control structural order has the potential to produce materials with true single crystal texture.

We show that such single-crystal textures can be produced over unprecedented length scales in a small molecule columnar mesophase. Texture control is accomplished by judicious application of magnetic fields and physical confinement, or by sequential applications of dynamic and static magnetic fields across pertinent phase transitions. We discuss the physical origin of the unique biaxial texture control as revealed by in situ X-ray scattering experiments.

Presenter(s): 

Chinedum Osuji

Prof. Osuji received his Ph.D. in Materials Science and Engineering from MIT in 2003, for studies of structure-property relationships and self-assembly of liquid crystalline block copolymers. From 2003-2005 he was a Senior Scientist at Surface Logix Inc. where he worked on soft lithography, and from 2005-2007 was a Postdoctoral Associate in Applied Physics at Harvard University where he studied shear-induced structure and dynamics of colloidal gels. From 2007-2018 he was on the faculty at Yale University in the Department...Read more

This Live Event was conducted on Wednesday, November 18, 2020, 10:45am EST. Registration for this event is now closed.
Once the content has been viewed and you have attested to it, you will be able to download and print a certificate for PDH credits. If you have already viewed this content, please click here to login.

Checkout

Checkout

Do you already own this?

Pricing


Individuals

AIChE Members Free
AIChE Graduate Student Members Free
AIChE Undergraduate Student Members Free
Non-Members $109.00
Webinar content is available with the kind permission of the author(s) solely for the purpose of furthering AIChE’s mission to educate, inform and improve the practice of professional chemical engineering. All other uses are forbidden without the express consent of the author(s).