Glassy gels toughened by solvent.

Glassy polymers are generally stiff and strong yet have limited extensibility1. By swelling with solvent, glassy polymers can become gels that are soft and weak yet have enhanced extensibility1-3. The marked changes in properties arise from the solvent increasing free volume between chains while weakening polymer-polymer interactions. Here we show that solvating polar polymers with ionic liquids (that is, ionogels4,5) at appropriate concentrations can produce a unique class of materials called glassy gels with desirable properties of both glasses and gels. The ionic liquid increases free volume and therefore extensibility despite the absence of conventional solvent (for example, water). Yet, the ionic liquid forms strong and abundant non-covalent crosslinks between polymer chains to render a stiff, tough, glassy, and homogeneous network (that is, no phase separation)6, at room temperature. Despite being more than 54 wt% liquid, the glassy gels exhibit enormous fracture strength (42 MPa), toughness (110 MJ m-3), yield strength (73 MPa) and Young's modulus (1 GPa). These values are similar to those of thermoplastics such as polyethylene, yet unlike thermoplastics, the glassy gels can be deformed up to 670% strain with full and rapid recovery on heating. These transparent materials form by a one-step polymerization and have impressive adhesive, self-healing and shape-memory properties.

Electrothermally Actuated Semitransparent Shape Memory Polymer Composite with Application as a Wearable Touch Sensor.

A semitransparent shape memory polymer (SMP):silver nanowire (AgNW) composite is demonstrated to be capable of low-temperature actuation, thus making it attractive for wearable electronics applications that require intimate contact with the human body. We demonstrate that the SMP:AgNW composite has tunable electrical and optical transparency through variation of the AgNW loading and that the AgNW loading did not significantly change the mechanical behavior of the SMP. The SMP composite is also capable of electrical actuation through Joule heating, where applying a 4 V bias across the AgNWs resulted in full shape recovery. The SMP was found to have high strain sensitivity at both small (<1%) and large (over 10%) applied strain. The SMP could sense strains as low as 0.6% with a gauge factor of 8.2. The SMP composite was then utilized as a touch sensor, able to sense and differentiate tapping and pressing. Finally, the composite was applied as a wearable ring that was thermally actuated to conformably fit onto a finger as a touch sensor. The ring sensor was able to sense finger tapping, pressing, and bending with high signal-to-noise ratios. These results demonstrate that SMP:AgNW composites are a promising design approach for application in wearable electronics.

Dynamic Mechanical Analysis of Polymer Thin Films Using a Kirigami-Inspired Support.

A method of determining the mechanical relaxation behavior of polymer thin films is presented that employs a kirigami-inspired sample support. The film of interest is placed on the kirigami support and loaded into a dynamic mechanical analyzer. When the composite is placed in tension, the substrate effectively transfers the load to the film of interest. We demonstrate the approach using a number of polymers and conjugated polymer: small molecule blends relevant for organic photovoltaics. The kirigami-inspired method is found to provide an accurate view of thermal relaxation behavior in polymer thin films, including a quantitative assessment of the film storage modulus. The method is particularly valuable in thin films where film morphology is highly dependent on processing conditions. We show that differences in casting conditions have a clear impact on the thermal relaxation of both the neat and blend conjugated polymer films.