Programmable Shape Change in Semicrystalline Liquid Crystal Elastomers
Source abstract
Abstract
Liquid crystal elastomers (LCEs) are stimuli-responsive materials capable of reversible and programmable shape change in response to an environmental stimulus. Despite the highly responsive nature of these materials, the modest elastic modulus and blocking stress exhibited by these actuating materials can be limiting in some engineering applications. Here, we engineer a semicrystalline LCE, where the incorporation of semicrystallinity in a lightly cross-linked liquid crystalline network yields tough and highly responsive materials. Directed self-assembly can be employed to program director profiles through the thickness of the semicrystalline LCE. In short, we use the alignment of a liquid crystal monomer phase to pattern the anisotropy of a semicrystalline polymer network. Both the semicrystalline-liquid crystalline and liquid crystalline-isotropic phase transition temperatures provide controllable shape transformations. A planarly aligned sample's normalized dimension parallel to the nematic director decreases from 1 at room temperature to 0.42 at 250 °C. The introduction of the semicrystalline nature also enhances the mechanical properties exhibited by the semicrystalline LCE. Semicrystalline LCEs have a storage modulus of 390 MPa at room temperature, and monodomain samples are capable of generating a contractile stress of 2.7 MPa on heating from 25 to 50 °C, far below the nematic to isotropic transition temperature. The robust mechanical properties of this material combined with the high actuation strain can be leveraged for applications such as soft robotics and actuators capable of doing significant work.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Materials and Mechanics · Polymer composites and self-healing · Advanced Sensor and Energy Harvesting Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States
Department of Materials Science and Engineering, Texas A&M University, College Station, Texas 77843, United States
University of Cambridge, Cambridge CB2 1TN, UK
Air Force Research Laboratory, Dayton, Ohio 45433, United States
University of Science and Technology Beijing, Beijing 100083, China
North Dakota State University, Fargo, North Dakota 58108, United States
Funding
National Science Foundation
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