Abstract
Living tissue uses stress-accumulated electrical charge to close wounds,
yet to-date this piezoelectric effect has not been realised in self-repairing synthetic
materials which are typically soft amorphous materials requiring external stimuli,
prolonged physical contact and long healing times (often >24h). Here we overcome
many of these challenges using piezoelectric organic crystals, which upon mechanical
fracture, instantly recombine without any external direction, autonomously self-healing
in milliseconds with remarkable crystallographic precision. Atomic-resolution structural
studies reveal that a 3D hydrogen bonding network, with ability to store stress,
facilitates generation of stress-induced electrical charges on the fractured crystals,
creating an electrostatically-driven precise recombination of the pieces via a
diffusionless instant self-healing, as supported by spatially-resolved birefringence
experiments. Perfect, instant self-healing creates new opportunities for deployment of
molecular crystals in robust miniaturised devices, and may also spur development of
new molecular level repair mechanisms in complex biomaterials.