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OO13.01 - Rotational Disorder in Twisted Bilayer Graphene 
Date/Time:
April 24, 2014   8:00am - 8:15am
 
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Conventional means of stacking two-dimensional (2D) crystals inevitably leads to imperfections. To examine the ramifications of these imperfections, rotational disorder and strain are quantified in twisted bilayer graphene (TBG) using a combination of Raman spectroscopic and low-energy electron diffraction imaging. The twist angle between TBG layers varies on the order of 2° within large (50-100 μm) single-crystalline grains resulting in changes of the emergent Raman response by over an order of magnitude. Rotational disorder does not evolve continuously across the large grains but rather comes about by variations in the local twist angles between differing contiguous sub-grains , ~1 μm in size, that themselves exhibit virtually no twist angle variation (ΔΘ~0.1°). Owing to weak out of plane van der Waals bonding between azimuthally rotated graphene layers, these sub-grains evolve in conjunction with the 0.3% strain variation observed both within and between the atomic layers. Importantly, the emergent Raman response is altered, but not removed, by these extrinsic perturbations. Interlayer interactions are therefore resilient to strain and rotational disorder, a fact that gives promise to the prospect of designer 2D-solid heterostructures created via transfer processes.
 


 
 
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