4.6 Article

Generalized first-principles method to study near-field heat transfer mediated by Coulomb interaction

Journal

PHYSICAL REVIEW B
Volume 104, Issue 12, Pages -

Publisher

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.104.L121409

Keywords

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Funding

  1. FRC Grant [R-144-000-427-114]
  2. MOE tier 2 Grant [R-144-000-411-112]

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A general microscopic first-principles method was presented to study Coulomb-interaction-mediated heat transfer in the near field, focusing on screened Coulomb potential and spectrum function of polarizability. Using single-layer graphene as an example, it was found that heat flux saturates at the extreme near field and differs from the 1/d dependence of local response functions.
We present a general microscopic first-principles method to study the Coulomb-interaction-mediated heat transfer in the near field. Using the nonequilibrium Green's function formalism, we derive Caroli formulas for heat transfers between materials with translational invariance. The central physical quantities are the screened Coulomb potential and the spectrum function of polarizability. Within the random phase approximation, we calculate the polarizability using the linear response density functional theory and obtain the screened Coulomb potential from a retarded Dyson equation. We show that the heat transfer mediated by the Coulomb interaction is consistent with that of the p-polarized evanescent waves which dominate the heat transfer in the near field. We adopt single-layer graphene as an example to calculate heat transfers between two parallel sheets separated by a vacuum gap d. Our results show a saturation of heat flux at the extreme near field which is different from the reported 1/d dependence for local response functions. The calculated heat flux is up to 5 x 10(4) times more than the blackbody limit, and a 1/d(2) dependence is shown at large separations. From the spectrum of energy current density, we infer that the near-field enhancement of heat transfer stems from electron transitions around the Fermi energy. With a uniform strain, the heat flux increases for most of the distances, while a negative correlation is shown at the moderate field. Our method is valid for inhomogeneous materials in which the macroscopic response function used in conventional theory of fluctuational electrodynamics would fail at the subnanometer scale.

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