Graphene and other two-dimensional materials display remarkable optical properties, including a simple light transparency of $T approx 1 - pi alpha$ for light in the visible region. Most theoretical rationalizations of this universal opacity employ a model coupling light to the electrons crystal momentum and put emphasis on the linear dispersion of the graphene bands. However, such a formulation of interband absorption is not allowable within band structure theory, because it conflates the crystal momentum label with the canonical momentum operator. We show that the physical origin of the optical behavior of graphene can be explained within a straightforward picture with the correct use of canonical momentum coupling. Its essence lies in the two-dimensional character of the density of states rather than in the precise dispersion relation, and therefore the discussion is applicable to other systems such as semiconductor membranes. At higher energies the calculation predicts a peak corresponding to a van Hove singularity as well as a specific asymmetry in the absorption spectrum of graphene, in agreement with previous results.
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