Elastocaloric effect in amorphous polymer networks undergoing mechanotropic phase transitions
arXiv:2103.02660 · doi:10.1103/PhysRevMaterials.5.L062401
Abstract
Deformations of amorphous polymer networks prepared with significant concentrations of liquid crystalline mesogens have been recently reported to undergo mechanotropic phase transitions. Here, we report that these mechanotropic phase transitions are accompanied by an elastocaloric response (). Applied uniaxial strain to the elastomeric polymer network transitions the organization of the material from a disordered, amorphous state (order parameter ) to the nematic phase (). Both the magnitude of the elastocaloric temperature change and mechanically induced order parameter are dependent on the concentration of liquid crystal mesogens in the material. While the observed temperature changes in these materials are smaller than those observed in shape memory alloys, the responsivity, defined as the temperature change divided by the input stress, is larger by an order of magnitude.
arXiv comment14 pages, 4 figures. Supplementary material: +4 pages, +2 figures
References in corpus (5)
- Elastocaloric effect associated with the martensitic transition in shape-memory alloys
- Torsional refrigeration by twisted, coiled, and supercoiled fibers
- Temperature dependence of elastocaloric effect in natural rubber
- AC Elastocaloric effect as a probe for thermodynamic signatures of continuous phase transitions
- Tunability of the elastocaloric response in main-chain liquid crystalline elastomers