The
application of biocompostable poly(glycolic acid) (PGA) is
hindered by the conflict between its strength and ductility. In this
work, we address an effective strategy to obtain designable strength
and ductility of PGA/poly(butylene adipate-co-terephthalate)
(PBAT) films by tuning the drawing temperature. At low temperatures
(35–40 °C), the poor chain mobility leads to a predominance
of stress-induced amorphous chain orientation rather than relaxation
and crystallization, and the drawn films exhibit high tensile strength
(145 MPa) with remarkable strain hardening. Then, the chain relaxation
becomes pronounced due to the increased chain mobility at a temperature
range of 45–50 °C, resulting in a low orientation, low
crystallinity, and consequently high ductility (elongation at break
of 320%). At the high temperature region (55–60 °C), further
enhanced chain mobility facilitates the formation of oriented PGA
crystallites, which restrict chain relaxation and provide more strengthened
elements. As a result, PGA-based films with excellent strength, stiffness,
and ductility (e.g., 103 MPa, 2800 MPa, and 220%, respectively) are
achieved. Therefore, this work provides an effective route to tune
the mechanical properties of PGA materials, and in principle it should
be applicable to other semicrystalline polymeric systems as well.