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Janine C. Franz

Publications and source records attributed to Janine C. Franz.

4 recordsLinked to original sources

Dissipation across the ultrastrong-coupling regime of nanomechanical quantum Rabi systems

Mechanical resonators ultrastrongly coupled to quantum two-level systems provide a promising route towards mechanical qubits by introducing significant anharmonicity to the mechanical modes, particularly in the slow-oscillator regime. Although the resulting hybrid system is well described by the quantum Rabi model, a consistent treatment of dissipation remains challenging across the broad parameter space routinely probed in current nanotube electromechanical devices. Here, we investigate dissipation in the open quantum Rabi model using a Born-Markov framework based on the slowly varying bath spectrum approximation, yielding a Lindblad master equation applicable far beyond conventional descriptions while recovering them in their respective limits. Using this framework, we analyze experimentally accessible observables across this parameter space. As the secular approximation breaks down, phonon blockade progressively washes out. Our approach remains valid in this regime, enabling a quantitative description of the continuous evolution of phonon blockade with coupling strength and dissipation. At finite temperature, we find a suppression of the temperature-induced increase of coherence decay rate for weak anharmonicity. Under driving, our approach remains applicable to substantially stronger perturbations than conventional dressed-state master equations and shows that an apparently classical observable can coexist with Wigner negativity. We further capture the weakly anharmonic regime arising from finite detuning in the double-quantum dot. These results establish a unified description of dissipation from weakly anharmonic operating regimes to the strongly anharmonic mechanical-qubit regime and provide experimentally relevant predictions for ultrastrong electromechanical systems.

quant-ph

Tunable nonlinear electromechanics at the zero-point motion scale

Nonlinearity at the scale of zero-point motion opens new possibilities for the control and readout of nanomechanical systems, but achieving this remains a formidable challenge. Here we demonstrate that ultrastrong coupling (USC) between a nanotube mechanical oscillator and a double-quantum-dot electronic two-level system enables a mechanical Kerr (Duffing) nonlinearity at the zero-point motion scale. In the dispersive regime, this large coupling yields a mechanical anharmonicity of $α= 1.4\%$ - three orders of magnitude larger than in previous work - while preserving the predominantly mechanical nature of the lowest energy states. We further demonstrate a purely quadratic cavity-based continuous readout of the mechanical motion. This continuous nonlinear optomechanical readout is enforced by a double-quantum dot symmetry, which can be broken by gate tuning to introduce a large linear transduction. These results establish a tunable USC platform that enables strong mechanical anharmonicity and nonlinear continuous readout at the zero-point motion scale.

quant-ph

Purcell effect in chiral environments

The Purcell effect describes the modification of the spontaneous decay rate in the presence of electromagnetic media and bodies. In this work, we shed light on the dependencies and magnitude of this effect for chiral materials. Using the framework of macroscopic quantum electrodynamics and Fermi's golden rule, we study a chiral bulk medium with and without local-field corrections, an idealised chiral mirror and a chiral surface. The results imply that the chiral effect is greatest for large transition frequencies, molecules with large optical rotatory strength and media with a strong cross-susceptibility. In the case of a half space, short distances from the molecule to the interface additionally enhance the effect.

quant-ph

Photoelectron circular dichroism of a chiral molecule induced by resonant interatomic Coulombic decay from an antenna atom

We show that a nonchiral atom can act as an antenna to induce a photoelectron circular dichroism in a nearby chiral molecule in a three-step process: The donor atom (antenna) is initially resonantly excited by circularly polarized radiation. It then transfers its excess energy to the acceptor molecule by means of resonant interatomic Coulombic decay. The latter finally absorbs the energy and emits an electron which exhibits the aforementioned circular dichroism in its angular distribution. We study the process on the basis of the retarded dipole--dipole interaction and report an asymptotic analytic expression for the distance-dependent chiral asymmetry of the photoelectron as induced by resonant interatomic Coulombic decay for random line-of-sight and acceptor orientations. In the nonretarded limit, the predicted chiral asymmetry is reversed as compared to that of a direct photoelectron circular dichroism of the molecule.

physics.atm-clus