Using
environmentally controlled, high-speed atomic force microscopy
(AFM), we examine dynamic fluctuations of topographically confined
poly(styrene-block-methyl methacrylate) (PS-b-PMMA) cylinders. During thermal annealing, fluctuations
drive perturbations of the block copolymer (BCP) interface between
polymer domains, leading to pattern roughness. Whereas previous investigations
have examined roughness in room-temperature and kinetically quenched
samples, we directly visualize the dynamics of PS/PMMA interfaces
in real space and time at in situ temperatures above
the glass transition temperature, T
g.
Imaging under these experimentally challenging thermal annealing conditions
is critical to understanding the inherent connection between thermal
fluctuations and BCP pattern assembly. Through the use of slow-scan-disabled
AFM, we dramatically improve the imaging time resolution for tracking
polymer dynamics. Fluctuations increase in intensity with temperature
and, at high temperatures, become spatially coherent across their
confining potential. Additionally, we observe that topographic confinement
suppresses fluctuations and correlations in the proximity of the guiding
field. In situ imaging at annealing temperatures
represents a significant step in capturing the dynamics of chain mobility
at BCP interfaces.