posted on 2016-03-04, 00:00authored byMichael P. Weir, David W. Johnson, Stephen C. Boothroyd, Rebecca C. Savage, Richard L. Thompson, Steven R. Parnell, Andrew
J. Parnell, Stephen M. King, Sarah E. Rogers, Karl S. Coleman, Nigel Clarke
We
study the conformation of graphene oxide as the filler in nanocomposites
of polystyrene and poly(methyl methacrylate) using inverse-space scattering
techniques and atomic force microscopy. By subtracting the polymer
scattering to estimate the scattering contribution from the graphene
oxide, we discover surface fractal scattering that spans a range of
more than two decades in reciprocal space, indicating that the graphene
oxide within these materials is rough on a very wide range of length
scales and implying extensive extrinsic wrinkling and folding. We
discover that well-exfoliated, locally flat sheets of graphene oxide
produce a crossover in the scattering at a length scale of 16 nm,
which becomes dominated by the signature of mass fractal scattering
from thin disks or sheets. We show that the local graphene oxide structure
in these polymer–graphene oxide nanocomposites is identical
to that of graphene oxide in a water solution studied on the same
length scale. Our results confirm the presence of well-exfoliated
sheets that are key to achieving high interfacial areas between polymers
and high aspect ratio filler in nanocomposites.