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Three-Dimensional Printable, Extremely Soft, Stretchable, and Reversible Elastomers from Molecular Architecture-Directed Assembly

Shifeng Nian, Jinchang Zhu, Haozhe Zhang, Zihao Gong, Guillaume Freychet, Mikhail Zhernenkov, Baoxing Xu, Li‐Heng Cai

2021Chemistry of Materials37 citationsDOIOpen Access PDF

Abstract

3D printing elastomers enables the fabrication of many technologically important structures and devices such as tissue scaffolds, sensors, actuators, and soft robots. However, conventional 3D printable elastomers are intrinsically stiff; moreover, the process of printing often requires external mechanical support and/or post-treatment. Here, we exploit the self-assembly of a responsive linear-bottlebrush-linear triblock copolymer to create stimuli-reversible, extremely soft, and stretchable elastomers and demonstrate their applicability as inks for in situ direct-write printing 3D structures without the aid of external mechanical support or post-treatment. By developing a procedure for controlled synthesis of such architecturally designed block copolymers, we create elastomers with extensibility up to 600% and Young’s moduli down to ∼102 Pa, 106 times softer than plastics and more than 102 times softer than all existing 3D printable elastomers. Moreover, the elastomers are thermostable and remain to be solid up to 180 °C, yet they are 100% solvent-reprocessable. Their extreme softness, stretchability, thermostability, and solvent-reprocessability bode well for future applications.

Topics & Concepts

ElastomerMaterials scienceSoft roboticsThermoplastic elastomerCopolymer3D printingActuatorNanotechnologyAmphiphileStretchable electronicsExtensibilityPolymer scienceFabricationComposite materialPolymerComputer scienceElectronicsChemistryAlternative medicineOperating systemPhysical chemistryMedicinePathologyArtificial intelligenceAdvanced Sensor and Energy Harvesting MaterialsAdvanced Materials and MechanicsPolymer composites and self-healing
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