Using a first-principles approach we calculate the electron-phonon couplings in graphene for the transverse and longitudinal acoustic phonons. Analytic forms of the coupling matrix elements valid in the long-wavelength limit are found to give an almost quantitative description of the first-principles matrix elements even at shorter wavelengths. Using the analytic forms of the coupling matrix elements, we study the acoustic phonon-limited carrier mobility and quasiparticle lifetime observable in photoemission spectroscopy for temperatures 0--200 K and high carrier densities of 10¹²--10¹³ cm^-2. We find that the intrinsic effective acoustic deformation potential of graphene is Ξeff=6.8 eV and that the temperature dependence of the mobility μ~T^-α in the Bloch-Gr\"uneisen regime increases beyond an α=4 dependence even in the absence of screening when the true coupling matrix elements are considered. The α>4 temperature dependence of the mobility is found to originate in a similar temperature dependence of the relaxation time at the Fermi level. The large disagreement between our calculated deformation potential and those extracted from experimental measurements (18--29 eV) indicates that additional or modified acoustic phonon-scattering mechanisms are at play in experimental situations.
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Kaasbjerg et al. (2012) studied this question.
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