Stretchable
electronic circuits are critical in a variety of next-generation
electronics applications, including soft robots, wearable technologies,
and biomedical applications. To date, printable composite conductors
comprising various types of conductive fillers have been suggested
to achieve high electrical conductance and excellent stretchability.
Among them, liquid metal particles have been considered as a viable
candidate filler that can meet the necessary prerequisites. However,
a mechanical activation process is needed to generate interconnected
liquid channels inside elastomeric polymers. In this study, we have
developed a chemical strategy of surface-functionalizing liquid metal
particles to eliminate the necessity of additional mechanical activation
processes. We found that the characteristic conformations of the polyvinylpyrrolidone
surrounding eutectic gallium indium particles are highly dependent
on the molecular weight of polyvinylpyrrolidone. By virtue of the
specific chemical roles of polyvinylpyrrolidone, the as-printed composite
layers are highly conductive and stretchable, exhibiting an electrical
conductivity approaching 8372 S/cm at 100% strain and an invariant
resistance change of 0.92 even at 75% strain after a 60,000 cycle
test. The results demonstrate that the self-activated liquid metal-based
composite conductors are applicable to traditional stretchable electronics,
healable stretchable electronics, and shape-morphable applications