Nancy Sottos

She is the Swanlund Endowed Chair and the head of the Department of Materials Science and Engineering at the University of Illinois at Urbana–Champaign.

[2] She is also a co-chair of the Molecular and Electronic Nanostructures Research Theme at the Beckman Institute for Advanced Science and Technology.

[5] She is a pioneer in the area of adaptive materials, creating the first self-healing polymers with Jeffrey S. Moore, Scott R. White, and others as of 2000.

[10] She was appointed co-chair of the Molecular and Electronic Nanostructures Research Theme at the Beckman Institute for Advanced Science and Technology in 2004, succeeding Jeffrey Moore.

[14][15] She was elected a member of the National Academy of Engineering in 2020 for contributions to the design and applications of self-healing and multifunctional materials.

[16] Sottos helped develop the first polymeric self-healing material with colleagues including Jeffrey Moore and Scott White.

Using dicyclopentadiene (DCPD) and Grubbs' catalyst in an epoxy matrix, polycyclopendiene was formed to seal cracks, recovering up to 75% of the original fracture toughness.

[18][19] Sottos has also focused on the design of microvascular networks for the distribution of active fluids in autonomous materials systems.

Such designs offer possibilities for "self-healing, regeneration, self-sensing, self-protection and self-cooling" properties, similar to those of biological systems.

This approach has potential applications in the design and use of fiberglass and other composite materials for structures including airplanes and wind turbines.

[23] A team led by Sottos and Wenle Li[24] has developed polymeric structural materials that can indicate the presence of damage by changing color.

This autonomous visual indicator can enable engineers to detect mechanical damage and intervene before a structure is compromised.

The orientation of the MC subspecies relative to the tensile force could be characterized based on the anisotropy of the fluorescence polarization.

[30][31] The researchers have also demonstrated that mechanical force can power a chemical response in the polymer, changing the covalent bonding.