Catalysis by Dark States in Vibropolaritonic Chemistry
- URL: http://arxiv.org/abs/2104.07214v3
- Date: Wed, 2 Feb 2022 08:13:34 GMT
- Title: Catalysis by Dark States in Vibropolaritonic Chemistry
- Authors: Matthew Du, Joel Yuen-Zhou
- Abstract summary: Experimental changes in thermally-activated reaction kinetics due to polariton formation appear entropically unlikely.
We show that the overlooked dark modes, while parked at the same energy as bare molecular vibrations, are robustly delocalized across $sim$2-3 molecules.
- Score: 0.0
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Collective strong coupling between a disordered ensemble of $N$ localized
molecular vibrations and a resonant optical cavity mode gives rise to 2
polariton and $N-1\gg2$ dark modes. Thus, experimental changes in
thermally-activated reaction kinetics due to polariton formation appear
entropically unlikely and remain a puzzle. Here we show that the overlooked
dark modes, while parked at the same energy as bare molecular vibrations, are
robustly delocalized across $\sim$2-3 molecules, yielding enhanced channels of
vibrational cooling, concomitantly catalyzing a chemical reaction. As an
illustration, we theoretically show a $\approx$50\% increase in an electron
transfer rate due to enhanced product stabilization. The reported effects can
arise when the homogeneous linewidths of the dark modes are smaller than their
energy spacings.
Related papers
- Can increasing the size and flexibility of a molecule reduce
decoherence? [0.0]
Extending the carbon skeleton in propynal analogs slows down decoherence and extends the duration of charge migration.
Coherent superposition of electronic states, created by ionizing a molecule, can initiate ultrafast dynamics of the electron density.
arXiv Detail & Related papers (2024-01-03T22:46:40Z) - Exploring the impact of vibrational cavity coupling strength on
ultrafast CN + $c$-C$_6$H$_{12}$ reaction dynamics [45.46706627196389]
We study the ultrafast dynamics of CN radicals interacting with a cyclohexane and chloroform.
Reaction rates remain unchanged for all extracavity, on resonance, and off-resonance cavity coupling conditions.
arXiv Detail & Related papers (2023-10-29T19:46:42Z) - Quantum field heat engine powered by phonon-photon interactions [58.720142291102135]
We present a quantum heat engine based on a cavity with two oscillating mirrors.
The engine performs an Otto cycle during which the walls and a field mode interact via a nonlinear Hamiltonian.
arXiv Detail & Related papers (2023-05-10T20:27:15Z) - Quantum Control of Atom-Ion Charge Exchange via Light-induced Conical
Intersections [66.33913750180542]
Conical intersections are crossing points or lines between two or more adiabatic electronic potential energy surfaces.
We predict significant or measurable non-adiabatic effects in an ultracold atom-ion charge-exchange reaction.
In the laser frequency window, where conical interactions are present, the difference in rate coefficients can be as large as $10-9$ cm$3$/s.
arXiv Detail & Related papers (2023-04-15T14:43:21Z) - Understanding the Energy Gap Law under Vibrational Strong Coupling [0.0]
We show that under most conditions, the collective light-matter coupling strength is not large enough to counter the entropic penalty involved with using the polariton modes.
This effect may be reversed with deep strong light-matter couplings or large detunings, both of which increase the upper polariton frequency.
arXiv Detail & Related papers (2022-10-10T19:50:08Z) - Photon generation and entanglement in a double superconducting cavity [105.54048699217668]
We study the dynamical Casimir effect in a double superconducting cavity in a quantum electrodynamics architecture.
We study the creation of photons when the walls oscillate harmonically with a small amplitude.
arXiv Detail & Related papers (2022-07-18T16:43:47Z) - Cavity-modified unimolecular dissociation reactions via intramolecular
vibrational energy redistribution [0.0]
We show that an optical cavity resonantly coupled to particular anharmonic vibrational modes can interfere with unimolecular dissociation reaction rates.
In particular, when the cavity is initially empty, the dissociation rate decreases, while when the cavity is initially hotter than the molecule, the cavity can instead accelerate the reaction rate.
arXiv Detail & Related papers (2021-09-09T14:37:39Z) - Driving chemical reactions with polariton condensates [0.0]
We study the effect of vibrational polariton condensation on the kinetics of electron transfer processes.
Compared with excitation with infrared laser sources, the condensate changes the reaction yield significantly.
Our results offer tantalizing opportunities to use condensates for driving chemical reactions.
arXiv Detail & Related papers (2021-06-23T04:57:35Z) - Algorithmic Ground-state Cooling of Weakly-Coupled Oscillators using
Quantum Logic [52.77024349608834]
We introduce a novel algorithmic cooling protocol for transferring phonons from poorly- to efficiently-cooled modes.
We demonstrate it experimentally by simultaneously bringing two motional modes of a Be$+$-Ar$13+$ mixed Coulomb crystal close to their zero-point energies.
We reach the lowest temperature reported for a highly charged ion, with a residual temperature of only $Tlesssim200mathrmmu K$ in each of the two modes.
arXiv Detail & Related papers (2021-02-24T17:46:15Z) - Collective spontaneous emission of two entangled atoms near an
oscillating mirror [50.591267188664666]
We consider the cooperative spontaneous emission of a system of two identical atoms, interacting with the electromagnetic field in the vacuum state.
Using time-dependent theory, we investigate the spectrum of the radiation emitted by the two-atom system.
We show that it is modulated in time, and that the presence of the oscillating mirror can enhance or inhibit the decay rate.
arXiv Detail & Related papers (2020-10-07T06:48:20Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.