scholarly journals Strong light-matter coupling in quantum chemistry and quantum photonics

Nanophotonics ◽  
2018 ◽  
Vol 7 (9) ◽  
pp. 1479-1501 ◽  
Author(s):  
Johannes Flick ◽  
Nicholas Rivera ◽  
Prineha Narang

AbstractIn this article, we review strong light-matter coupling at the interface of materials science, quantum chemistry, and quantum photonics. The control of light and heat at thermodynamic limits enables exciting new opportunities for the rapidly converging fields of polaritonic chemistry and quantum optics at the atomic scale from a theoretical and computational perspective. Our review follows remarkable experimental demonstrations that now routinely achieve the strong coupling limit of light and matter. In polaritonic chemistry, many molecules couple collectively to a single-photon mode, whereas, in the field of nanoplasmonics, strong coupling can be achieved at the single-molecule limit. Theoretical approaches to address these experiments, however, are more recent and come from a spectrum of fields merging new developments in quantum chemistry and quantum electrodynamics alike. We review these latest developments and highlight the common features between these two different limits, maintaining a focus on the theoretical tools used to analyze these two classes of systems. Finally, we present a new perspective on the need for and steps toward merging, formally and computationally, two of the most prominent and Nobel Prize-winning theories in physics and chemistry: quantum electrodynamics and electronic structure (density functional) theory. We present a case for how a fully quantum description of light and matter that treats electrons, photons, and phonons on the same quantized footing will unravel new quantum effects in cavity-controlled chemical dynamics, optomechanics, nanophotonics, and the many other fields that use electrons, photons, and phonons.

2021 ◽  
Vol 118 (41) ◽  
pp. e2110464118
Author(s):  
Christian Schäfer ◽  
Florian Buchholz ◽  
Markus Penz ◽  
Michael Ruggenthaler ◽  
Angel Rubio

Strong light–matter coupling provides a promising path for the control of quantum matter where the latter is routinely described from first principles. However, combining the quantized nature of light with this ab initio tool set is challenging and merely developing as the coupled light–matter Hilbert space is conceptually different and computational cost quickly becomes overwhelming. In this work, we provide a nonperturbative photon-free formulation of quantum electrodynamics (QED) in the long-wavelength limit, which is formulated solely on the matter Hilbert space and can serve as an accurate starting point for such ab initio methods. The present formulation is an extension of quantum mechanics that recovers the exact results of QED for the zero- and infinite-coupling limit and the infinite-frequency as well as the homogeneous limit, and we can constructively increase its accuracy. We show how this formulation can be used to devise approximations for quantum-electrodynamical density-functional theory (QEDFT), which in turn also allows us to extend the ansatz to the full minimal-coupling problem and to nonadiabatic situations. Finally, we provide a simple local density–type functional that takes the strong coupling to the transverse photon degrees of freedom into account and includes the correct frequency and polarization dependence. This QEDFT functional accounts for the quantized nature of light while remaining computationally simple enough to allow its application to a large range of systems. All approximations allow the seamless application to periodic systems.


2005 ◽  
Vol 892 ◽  
Author(s):  
Ian Sellers ◽  
Fabrice Semond ◽  
Mathieu Leroux ◽  
Jean Massies ◽  
Pierre Disseix ◽  
...  

AbstractWe present experimental results demonstrating strong-light matter coupling at low and room temperature in bulk GaN microcavities. Angle dependent reflectivity measurements demonstrate strong-coupling with a Rabi-energy of 50meV at room temperature which is well reproduced with transfer matrix simulations. The absence of strong coupling in the photoluminescence is attributed to the low finesse of the microcavity (Q=60) and is confirmed by simulations which indicate a quality factor of 90 is required to observe strong-coupling in the emission.


Nature ◽  
2004 ◽  
Vol 431 (7005) ◽  
pp. 162-167 ◽  
Author(s):  
A. Wallraff ◽  
D. I. Schuster ◽  
A. Blais ◽  
L. Frunzio ◽  
R.- S. Huang ◽  
...  

2018 ◽  
Vol 190 ◽  
pp. 04001
Author(s):  
Andrey Anisimov ◽  
Victor Soltamov ◽  
Pavel Baranov ◽  
Georgy Astakhov ◽  
Vladimir Dyakonov

Atomic-scale colour centres in bulk and nanocrystalline SiC are promising systems for quantum photonics compatible with fiber optics, quantum information processing and sensing at ambient conditions. Colour centres which acts as stable single photon sources in SiC can be key elements for quantum photonics and communications. It has been shown that there are at least two families of colour centres in SiC with S = 1 and S = 3/2, which have the property of optical alignment of the spin levels even at room temperature and above. The spin state can be initialized, manipulated and readout by means of optically detected magnetic resonance (ODMR), level anticrossing and cross-relaxation. Recently, we observed the effects of “hole burning” in the ODMR spectra, which made it possible to narrow the ODMR line by approximately an order of magnitude, which substantially increases the possibilities of technological applications of spin centres.


Author(s):  
Wassie Mersha Takele ◽  
Lukasz Piatkowski ◽  
Frank Wackenhut ◽  
Sylwester Gawinkowski ◽  
Alfred J. Meixner ◽  
...  

Changes in the Raman spectra under vibrational strong coupling do not necessarily result from the coupling effect but rather they can be caused by the surface enhancement effect.


Author(s):  
Tao E. Li ◽  
Bingyu Cui ◽  
Joseph E. Subotnik ◽  
Abraham Nitzan

Chemical manifestations of strong light–matter coupling have recently been a subject of intense experimental and theoretical studies. Here we review the present status of this field. Section 1 is an introduction to molecular polaritonics and to collective response aspects of light–matter interactions. Section 2 provides an overview of the key experimental observations of these effects, while Section 3 describes our current theoretical understanding of the effect of strong light–matter coupling on chemical dynamics. A brief outline of applications to energy conversion processes is given in Section 4. Pending technical issues in the construction of theoretical approaches are briefly described in Section 5. Finally, the summary in Section 6 outlines the paths ahead in this exciting endeavor. Expected final online publication date for the Annual Review of Physical Chemistry, Volume 73 is April 2022. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.


2021 ◽  
Vol 2058 (1) ◽  
pp. 012001
Author(s):  
I Nabiev

Abstract Resonant interaction between excitonic transitions of molecules and localized electromagnetic field forms the hybrid polaritonic states. Tuneable microresonators may change the light-matter coupling strength and modulate them from weak to strong and ultra-strong coupling regimes. In this work we have realised strong coupling between the tuneable open-access cavity mode and the excitonic transitions in oligonucleotide-based molecular beacons with their terminus labelled with a pair of organic dye molecules demonstrating an efficient donor-to-acceptor Förster resonance energy transfer (FRET). We show that the predominant strong coupling of the cavity photon to the exciton transition in the donor dye molecule can lead to such a large an energy shift that the energy transfer from the acceptor exciton reservoir to the mainly donor lower polaritonic state can be achieved, thus yielding the chromophores’ donor–acceptor role reversal or “carnival effect”. The data show the possibility for confined electromagnetic fields to control and mediate polariton-assisted remote energy transfer. Obtained results open the avenues to quantum optical switching and other applications.


2019 ◽  
Author(s):  
S. Giarrusso ◽  
Paola Gori-Giorgi

We analyze in depth two widely used definitions (from the theory of conditional probablity amplitudes and from the adiabatic connection formalism) of the exchange-correlation energy density and of the response potential of Kohn-Sham density functional theory. We introduce a local form of the coupling-constant-dependent Hohenberg-Kohn functional, showing that the difference between the two definitions is due to a corresponding local first-order term in the coupling constant, which disappears globally (when integrated over all space), but not locally. We also design an analytic representation for the response potential in the strong-coupling limit of density functional theory for a model single stretched bond.<br>


Sign in / Sign up

Export Citation Format

Share Document