Soft, Super-Elastic, All-Polymer Piezoelectric Elastomer for Artificial Electronic Skin.

Piezoelectric sensors are widely used in wearable devices to mimic the functions of human skin. However, it is considerably challenging to develop soft piezoelectric materials that can exhibit high sensitivity, stretchability, super elasticity, and suitable modulus. In this study, a soft skin-like piezoelectric polymer elastomer composed of poly(vinylidene fluoride) (PVDF) and a novel elastic substrate polyacrylonitrile is prepared by combining the radical polymerization and freeze-drying processes. Dipole-dipole interaction results in the phase transition of PVDF (α phase to ß phase), which enhances the electrical and mechanical performances. Thus, we achieve a high piezoelectric coefficient (d33max = 63 pC/N), good stretchability (211.3-259.3%), super compressibility (subjected to 99% compression strain without cracking), and super elasticity (100% recovery after extreme compression) simultaneously for the elastomer. The soft composite elastomer produces excellent electrical signal output (Vocmax = 253 mV) and responds rapidly (15 ms) to stress-induced polarization effects. In addition, the elastomer-based sensor accurately detects various physiological signals such as gestures, throat vibrations, and pulse waves. The developed elastomers exhibit excellent mechanical properties and high sensitivity, which helps facilitate their application as artificial electronic skin to sense subtle external pressure in real time.

Elastomeric conductive hybrid hydrogels with continuous conductive networks.

Elastomeric conductive hybrid hydrogels (ECHs) combining conducting polymers with elastomeric hydrogels have recently attracted interest due to their wide range of applications in bioelectronics such as wearable or implantable sensing devices. However, the conductivity of ECHs is typically compromised when conductive polymers are used as fillers in hydrogel networks because the inherent limitations of ECHs severely restrict their applicability. Here, we significantly improved the electrical conductivity of ECHs by using a bioinspired catechol derivative, dopamine (DA), as the dopant and mediator for the in situ polymerization of conducting polypyrrole (PPy) within the elastomeric hydrogel dual-networks. In general, ECHs prepared by conventional methods tend to form separate island structures of conductive polymers dispersed within porous hydrogel matrices. We found that a continuous conductive PPy network prepared using the DA mediator facilitated fast electron transfer within the ECHs, which showed good elastomeric mechanical properties, excellent biocompatibility and high force- or strain-responsiveness suitable for implantable strain-sensing applications.