Shining Light on the Microscopic Resonant Mechanism Responsible for
Cavity-Mediated Chemical Reactivity
- URL: http://arxiv.org/abs/2104.12429v4
- Date: Wed, 25 May 2022 09:18:05 GMT
- Title: Shining Light on the Microscopic Resonant Mechanism Responsible for
Cavity-Mediated Chemical Reactivity
- Authors: Christian Sch\"afer, Johannes Flick, Enrico Ronca, Prineha Narang,
Angel Rubio
- Abstract summary: Strong light-matter interaction in cavity environments is emerging as a promising approach to control chemical reactions in a non-intrusive and efficient manner.
We leverage quantum-electrodynamical density-functional theory to unveil the microscopic mechanism behind the experimentally observed reduced reaction rate under cavity induced resonant vibrational strong light-matter coupling.
- Score: 0.0
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Strong light-matter interaction in cavity environments is emerging as a
promising approach to control chemical reactions in a non-intrusive and
efficient manner. The underlying mechanism that distinguishes between steering,
accelerating, or decelerating a chemical reaction has, however, remained
unclear, hampering progress in this frontier area of research. We leverage
quantum-electrodynamical density-functional theory to unveil the microscopic
mechanism behind the experimentally observed reduced reaction rate under cavity
induced resonant vibrational strong light-matter coupling. We observe multiple
resonances and obtain the thus far theoretically elusive but experimentally
critical resonant feature for a single strongly-coupled molecule undergoing the
reaction. While we do not explicitly account for collective coupling or
intermolecular interactions, the qualitative agreement with experimental
measurements suggests that our conclusions can be largely abstracted towards
the experimental realization. Specifically, we find that the cavity mode acts
as mediator between different vibrational modes. In effect, vibrational energy
localized in single bonds that are critical for the reaction is redistributed
differently which ultimately inhibits the reaction.
Related papers
- Chemical Reaction Dynamics under Vibrational Strong Coupling [0.0]
We use classical, semi-classical and quantum-mechanical methods to simulate chemical reaction dynamics inside of an optical cavity.
Recent experiments have observed significant changes in reaction rates and equilibrium constants without any external input of energy.
arXiv Detail & Related papers (2024-01-03T16:32:23Z) - 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) - Multi-level Purcell effect and the impact of vibrational modes in
molecular quantum optics [62.997667081978825]
We study a manifestation of the Purcell effect in a bio-inspired photosynthetic dimer.
We provide a theoretical picture in terms of an effective non-Hermitian Hamiltonian.
arXiv Detail & Related papers (2023-06-15T18:27:40Z) - Sensing of magnetic field effects in radical-pair reactions using a
quantum sensor [50.591267188664666]
Magnetic field effects (MFE) in certain chemical reactions have been well established in the last five decades.
We employ elaborate and realistic models of radical-pairs, considering its coupling to the local spin environment and the sensor.
For two model systems, we derive signals of MFE detectable even in the weak coupling regime between radical-pair and NV quantum sensor.
arXiv Detail & Related papers (2022-09-28T12:56:15Z) - Probing the symmetry breaking of a light--matter system by an ancillary
qubit [50.591267188664666]
Hybrid quantum systems in the ultrastrong, and even more in the deep-strong, coupling regimes can exhibit exotic physical phenomena.
We experimentally observe the parity symmetry breaking of an ancillary Xmon artificial atom induced by the field of a lumped-element superconducting resonator.
This result opens a way to experimentally explore the novel quantum-vacuum effects emerging in the deep-strong coupling regime.
arXiv Detail & Related papers (2022-09-13T06:14:08Z) - Probing dynamics of a two-dimensional dipolar spin ensemble using single
qubit sensor [62.997667081978825]
We experimentally investigate individual spin dynamics in a two-dimensional ensemble of electron spins on the surface of a diamond crystal.
We show that this anomalously slow relaxation rate is due to the presence of strong dynamical disorder.
Our work paves the way towards microscopic study and control of quantum thermalization in strongly interacting disordered spin ensembles.
arXiv Detail & Related papers (2022-07-21T18:00:17Z) - Chemical reactivity under collective vibrational strong coupling [0.0]
We study unimolecular dissociation reactions of many molecules collectively interacting with an infrared cavity mode.
We find that the reaction rate can slow down by increasing the number of aligned molecules if the cavity mode is resonant with a vibrational frequency of the molecules.
arXiv Detail & Related papers (2022-06-17T00:56:12Z) - Cavity-Altered Thermal Isomerization Rates and Dynamical Resonant
Localization in Vibro-Polaritonic Chemistry [0.0]
Reaction rates for molecules embedded in microfluidic optical cavities are altered when compared to rates observed under "ordinary" reaction conditions.
We study how strong coupling of an optical cavity mode to molecular vibrations affect the reactivity and how resonance behavior emerges.
arXiv Detail & Related papers (2021-09-28T09:06:08Z) - 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) - A roadmap toward the theory of vibrational polariton chemistry [0.0]
The field of vibrational polariton chemistry was firmly established in 2016 when a chemical reaction rate at room temperature was modified within a resonantly tuned infrared cavity without externally driving the system.
Despite intense efforts by scientists around the world to understand why the reaction rate changes, no convincing theoretical explanation exists.
arXiv Detail & Related papers (2021-07-09T18:02:47Z) - 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.