Leveraging the Polymer Glass Transition to Access Thermally Switchable Shear Jamming Suspensions

• Published in: ACS central science 2023-04, Vol.9 (4), p.639-647
• Main Authors: Chen, Chuqiao, van der Naald, Michael, Singh, Abhinendra, Dolinski, Neil D., Jackson, Grayson L., Jaeger, Heinrich M., Rowan, Stuart J., de Pablo, Juan J.
• Format: Article
• Language: English
• Subjects: fluids; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; materials; polymer particles; polymers; suspensions
• ISSN: 2374-7943; 2374-7951
• DOI: 10.1021/acscentsci.2c01338

Suspensions of polymeric nano- and microparticles are fascinating stress-responsive material systems that, depending on their composition, can display a diverse range of flow properties under shear, such as drastic thinning, thickening, and even jamming (reversible solidification driven by shear). However, investigations to date have almost exclusively focused on nonresponsive particles, which do not allow in situ tuning of the flow properties. Polymeric materials possess rich phase transitions that can be directly tuned by their chemical structures, which has enabled researchers to engineer versatile adaptive materials that can respond to targeted external stimuli. Reported herein are suspensions of (readily prepared) micrometer-sized polymeric particles with accessible glass transition temperatures (T g) designed to thermally control their non-Newtonian rheology. The underlying mechanical stiffness and interparticle friction between particles change dramatically near T g. Capitalizing on these properties, it is shown that, in contrast to conventional systems, a dramatic and nonmonotonic change in shear thickening occurs as the suspensions transition through the particles’ T g. This straightforward strategy enables the in situ turning on (or off) of the system’s ability to shear jam by varying the temperature relative to T g and lays the groundwork for other types of stimuli-responsive jamming systems through polymer chemistry.