scholarly journals Quantum theory of collective strong coupling of molecular vibrations with a microcavity mode

2015 ◽  
Vol 17 (5) ◽  
pp. 053040 ◽  
Author(s):  
Javier del Pino ◽  
Johannes Feist ◽  
Francisco J Garcia-Vidal
ACS Photonics ◽  
2018 ◽  
Vol 5 (9) ◽  
pp. 3594-3600 ◽  
Author(s):  
Eric A. Muller ◽  
Benjamin Pollard ◽  
Hans A. Bechtel ◽  
Ronen Adato ◽  
Dordaneh Etezadi ◽  
...  

1995 ◽  
Vol 10 (11) ◽  
pp. 1611-1640 ◽  
Author(s):  
E. ABDALLA ◽  
M.C.B. ABDALLA

We consider bosonized QCD2, and prove that after one rewrites the theory in terms of gauge-invariant fields, there exists an integrability condition that is valid for the quantum theory as well. Furthermore, performing a duality type transformation we obtain an appropriate action for the description of the strong coupling limit, which is still integrable. We also prove that the model displays a complicated set of constraints, which restrict the dynamics of part of the theory, but which are necessary for maintaining the positive metric Hilbert space.


2021 ◽  
Vol 7 (19) ◽  
pp. eabf6397
Author(s):  
Bo Xiang ◽  
Jiaxi Wang ◽  
Zimo Yang ◽  
Wei Xiong

Realizing nonlinear interactions between spatially separated particles can advance molecular science and technology, including remote catalysis of chemical reactions, ultrafast processing of information in infrared (IR) photonic circuitry, and advanced platforms for quantum simulations with increased complexity. Here, we achieved nonlinear interactions at ultrafast time scale between polaritons contained in spatially adjacent cavities in the mid-IR regime, altering polaritons in one cavity by pumping polaritons in an adjacent one. This was done by strong coupling molecular vibrational modes with photon modes, a process that combines characteristics of both photon delocalization and molecular nonlinearity. The dual photon/molecule character of polaritons enables delocalized nonlinearity—a property that neither molecular nor cavity mode would have alone.


2021 ◽  
Vol 23 (1) ◽  
pp. 43-58
Author(s):  
Chantal Daniel

The correlation between electronic densities and active molecular vibrations drives the spin–vibronic mechanism of ultrafast decays in coordination chemistry.


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