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Peter G. Kirton

Publications and source records attributed to Peter G. Kirton.

3 recordsLinked to original sources

Incoherent charge transport in an organic polariton condensate

We study how polariton condensation modifies charge transport in organic materials. In typical organic materials, charge transport proceeds via incoherent hopping. We therefore provide an approach to determine how the rate and final state of this hopping process is affected by strong matter-light coupling and polariton condensation. We show how the hopping process may create excitations when starting from a state with a finite excitation density. That is, how hopping can change the state of a lower polariton condensate by creating upper polaritons, optically inactive excitonic dark states, or by exciting vibrational sidebands. While the matrix elements for these processes can be large, for typical materials at room temperature, such excitations are suppressed by thermal factors, and ground state processes dominate. We thus study how the ground state hopping rate depends on condensate density, matter-light coupling, and cavity photon detuning. All these factors change the vibrational configuration associated with the optically active molecules, which can enhance or suppress hopping by increasing or decreasing the vibrational overlap with the state of a charged molecule. We show that hopping rates can be exponentially sensitive to detuning and condensate density, allowing an increase or decrease of hopping rate by two orders of magnitude.

cond-mat.quant-gas↗

Orientational alignment in Cavity Quantum Electrodynamics

We consider the orientational alignment of dipoles due to strong matter light coupling, for a non-vanishing density of excitations. We compare various approaches to this problem in the limit of large numbers of emitters, and show that direct Monte Carlo integration, mean-field theory, and large deviation methods match exactly in this limit. All three results show that orientational alignment develops in the presence of a macroscopically occupied polariton mode, and that the dipoles asymptotically approach perfect alignment in the limit of high density or low temperature.

cond-mat.mes-hall↗

Exact states and spectra of vibrationally dressed polaritons

Strong coupling between light and matter is possible with a variety of organic materials. In contrast to the simpler inorganic case, organic materials often have a complicated spectrum, with vibrationally dressed electronic transitions. Strong coupling to light competes with this vibrational dressing, and if strong enough, can suppress the entanglement between electronic and vibrational degrees of freedom. By exploiting symmetries, we can perform exact numerical diagonalization to find the polaritonic states for intermediate numbers of molecules, and use these to define and validate accurate expressions for the lower polariton states and strong-coupling spectrum in the thermodynamic limit. Using this approach, we find that vibrational decoupling occurs as a sharp transition above a critical matter-light coupling strength. We also demonstrate how the polariton spectrum evolves with the number of molecules, recovering classical linear optics results only at large $N$.

cond-mat.mes-hall↗