Although
experimental evidence for shear-banding flows in concentrated
polymer solutions has accumulated over the last 20 years, the origin
of such shear-banding flows is still under heated debate. Experiments
that probe the microscopic dynamics of shear-banding polymer solutions
are still scarce. Here, using a custom-built high-resolution rheo-confocal
shear cell, we experimentally study the dynamics of DNA-bridged colloidal
dumbbells in the shear-banding flow of concentrated double-stranded
DNA (dsDNA) solutions under large amplitude oscillatory shear. We
synthesize dumbbells consisting of two spherical colloids linked by
λ-DNA and track their 2D-projected configurations in sheared
dsDNA solutions. We first confirm that the velocity profile of the
concentrated dsDNA solutions is inhomogeneous at high Weissenberg
numbers and exhibits strong shear banding with two distinct shear
bands. We then measure the orientational distribution of the DNA-bridged
dumbbells and investigate their translational and rotational dynamics
within the two shear bands. The preferred alignment of the dumbbells
along the flow direction in the high-shear-rate band suggests the
dominant role of elastic stresses in that band. In contrast, a bimodal
distribution of dumbbell orientations is observed in the low-shear-rate
band, indicating more balanced contributions from both normal and
elastic stresses. Furthermore, exclusively in the high-shear-rate
band, we also find spatially localized correlated enhanced translational
and rotational motions and a strong coupling between enhanced translation
and chain extension. These unique conformational and dynamic features
suggest shear-induced breakage of the local entanglement network in
the high-shear band, which we postulate leads to puddles of low viscosity
within an otherwise high-viscosity fluid. Together, our quantitative
analyses of the spatially distinct dynamics of dsDNA-bridged dumbbells
in coexisting shear bands provide important insights into the microscopic
origin of shear-banding flows in concentrated polymer solutions.