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Dispersion Interaction Between Thin Conducting Cylinders

Subhojit Pal, Iver Brevik, Mathias Boström

TL;DR

This work analyzes dispersion interactions between two thin conducting cylinders, addressing both ground-state van der Waals forces and excited-state resonance interactions in the non-retarded limit. Using a hydrodynamic/plasma model for conducting electrons and a scattering-matrix formalism with Matsubara sums, it derives a dispersion relation and explicit asymptotics for the inter-cylinder energy that scale as $E(R)\sim f(R)/R^2$, with $f(R)$ potentially logarithmic in $R$. The key findings reveal markedly longer-range interactions for conducting cylinders compared to non-conducting or point-like objects, including zero- and finite-temperature behaviors and a slow Förster energy transfer rate. These results have implications for energy transfer and assembly in conducting polymers, DNA-like nanostructures, and nanoscale circuit elements, highlighting strong, non-additive long-range coupling in low-dimensional metallic systems.

Abstract

The ground state and excited state resonance dipole-dipole interaction energy between two elongated conducting molecules are explored. We review the current status for ground state interactions. This interaction is found to be of a much longer range than in the case when the molecules are pointlike and nonconducting. These are well known results found earlier by Davies, Ninham, and Richmond, and later, using a different formalism, by Rubio and co-workers. We show how the theory can be extended to excited state interactions. A characteristic property following from our calculation is that the interaction energy dependence with separation ($R$) goes like $f(R)/R^2$ both for resonance and for the van der Waals case in the long range limit. In some limits $f(R)$ has a logarithmic dependency and in others it takes constant values. We predict an unusual slow decay rate for the energy transfer between conducting molecules.

Dispersion Interaction Between Thin Conducting Cylinders

TL;DR

This work analyzes dispersion interactions between two thin conducting cylinders, addressing both ground-state van der Waals forces and excited-state resonance interactions in the non-retarded limit. Using a hydrodynamic/plasma model for conducting electrons and a scattering-matrix formalism with Matsubara sums, it derives a dispersion relation and explicit asymptotics for the inter-cylinder energy that scale as , with potentially logarithmic in . The key findings reveal markedly longer-range interactions for conducting cylinders compared to non-conducting or point-like objects, including zero- and finite-temperature behaviors and a slow Förster energy transfer rate. These results have implications for energy transfer and assembly in conducting polymers, DNA-like nanostructures, and nanoscale circuit elements, highlighting strong, non-additive long-range coupling in low-dimensional metallic systems.

Abstract

The ground state and excited state resonance dipole-dipole interaction energy between two elongated conducting molecules are explored. We review the current status for ground state interactions. This interaction is found to be of a much longer range than in the case when the molecules are pointlike and nonconducting. These are well known results found earlier by Davies, Ninham, and Richmond, and later, using a different formalism, by Rubio and co-workers. We show how the theory can be extended to excited state interactions. A characteristic property following from our calculation is that the interaction energy dependence with separation () goes like both for resonance and for the van der Waals case in the long range limit. In some limits has a logarithmic dependency and in others it takes constant values. We predict an unusual slow decay rate for the energy transfer between conducting molecules.
Paper Structure (14 sections, 71 equations, 1 figure, 1 table)