Interplay of molecular and specimen length scales in the large deformation mechanical behavior of polystyrene nanofibers

- Uniaxial tension tests performed on individual PS nanofibers using MEMS.
- Brittle-to-ductile transition of PS depends on ratio of specimen to molecular size.
- Molecular confinement of PS led to dramatic increase in strength and toughness.
- A master curve for the elasto-plastic mechanical behavior of PS nanofibers.

Bulk polystyrene (PS) undergoes craze-assisted brittle failure at room temperature. In this work it is shown that the synergistic coupling of the material length scale as defined by macromolecular size, and the specimen size as defined by the nanofiber diameter, can result in extreme ductility and simultaneous strengthening and toughening for fiber diameters at the submicron scale. Combinations of PS fiber diameters between 150 nm and 5000 nm, and molecular weights between 13,000 g/mol and 9,000,000 g/mol provided a spectrum of degrees of molecular confinement, which, for particular pairs of molecular weight and fiber diameter, allowed for large fiber extensions through the process of necking followed by large homogenous deformation controlled by strain hardening. Compared to bulk PS, the combined necking and post-neck strain hardening increased the fiber strength by 350% and the fiber ductility by as much as 4000%. This mechanical response was shown to scale well with the confining parameter Dnorm, defined as the ratio of the initial fiber diameter (D0) to the root-mean-square end-to-end distance (Ree), with Dnorm ∼ 18 identified as the threshold for the transition from necking to crazing of PS nanofibers. The large deformation response of PS nanofibers with molecular weights above a threshold value is shown to obey a master true stress vs. normalized strain curve that is independent of molecular weight.