Multiscale Structure of Poly(ionic liquid)s in Bulk and Solutions by Small-Angle Neutron Scattering

Poly(ionic liquid)s (PILs), similar to their ionic liquid (IL) analogues, present a nanostructure arising from local interactions. The influence of this nanostructure on the macromolecular conformation of polymer chains is investigated for the first time by means of an extensive use of small-angle neutron scattering on a series of poly(1-vinyl-3-alkylimidazolium)s with varying alkyl side-chain length and counter-anion, both in bulk and in dilute solutions. Radii of gyration are found to increase with the side-chain length in solution as a consequence of crowding interactions between neighboring monomers. In bulk, however, a nonmonotonic evolution of the radius of gyration reflects a change in chain flexibility and a potential screening of electrostatic interactions. Additionally, at a smaller scale, SANS provides an experimental estimation of both the chain diameter and the correlation length between neighboring chains, comparison of which unveils clear evidence of interdigitation of the alkyl side chains. These structural features bring precious insights into the understanding of the dynamic properties of PILs.

Automated summary

This study investigates the influence of nanostructure of poly(ionic liquid)s on the macromolecular conformation of polymer chains using small-angle neutron scattering. The results show that the nanostructure of poly(ionic liquid)s leads to an increase in the radius of gyration of polymer chains in solution and a nonmonotonic evolution in bulk. Furthermore, evidence of interdigitation of alkyl side chains is observed.