scholarly journals Hybridization of Multiple Vibrational Modes via Strong Coupling Using Confined Light Fields

2019 ◽  
Vol 7 (18) ◽  
pp. 1900403 ◽  
Author(s):  
Kishan S. Menghrajani ◽  
Henry A. Fernandez ◽  
Geoffrey R. Nash ◽  
William L. Barnes
Keyword(s):  
Strong Coupling ◽  
Light Fields ◽  
Vibrational Modes

Strong coupling between photons of two light fields mediated by one atom

2018 ◽  
Vol 14 (9) ◽  
pp. 885-889 ◽  
Author(s):  
Christoph Hamsen ◽  
Karl Nicolas Tolazzi ◽  
Tatjana Wilk ◽  
Gerhard Rempe
Keyword(s):  
Strong Coupling ◽  
Light Fields

Quantum Strong Coupling with Protein Vibrational Modes

2016 ◽  
Vol 7 (20) ◽  
pp. 4159-4164 ◽  
Author(s):  
Robrecht M. A. Vergauwe ◽  
Jino George ◽  
Thibault Chervy ◽  
James A. Hutchison ◽  
Atef Shalabney ◽  
...  
Keyword(s):  
Strong Coupling ◽  
Vibrational Modes

scholarly journals On the SN2 reactions modified in vibrational strong coupling experiments: reaction mechanisms and vibrational mode assignments

2020 ◽  
Vol 22 (41) ◽  
pp. 23545-23552
Author(s):  
Clàudia Climent ◽  
Johannes Feist
Keyword(s):  
Strong Coupling ◽  
Reaction Mechanisms ◽  
Vibrational Mode ◽  
Vibrational Modes ◽  
Sn2 Reactions

We study the mechanism of SN2 reactions modified in vibrational strong coupling experiments and propose a new assignment of the vibrational modes.

scholarly journals Tilting a ground-state reactivity landscape by vibrational strong coupling

Science ◽  
2019 ◽  
Vol 363 (6427) ◽  
pp. 615-619 ◽  
Author(s):  
A. Thomas ◽  
L. Lethuillier-Karl ◽  
K. Nagarajan ◽  
R. M. A. Vergauwe ◽  
J. George ◽  
...  
Keyword(s):  
Strong Coupling ◽  
Activation Barrier ◽  
Bond Cleavage ◽  
Optical Cavity ◽  
Vacuum Field ◽  
Activation Entropy ◽  
Vibrational Modes ◽  
Cleavage Sites ◽  
Chemical Methods ◽  
Site Selectivity

Many chemical methods have been developed to favor a particular product in transformations of compounds that have two or more reactive sites. We explored a different approach to site selectivity using vibrational strong coupling (VSC) between a reactant and the vacuum field of a microfluidic optical cavity. Specifically, we studied the reactivity of a compound bearing two possible silyl bond cleavage sites—Si–C and Si–O, respectively—as a function of VSC of three distinct vibrational modes in the dark. The results show that VSC can indeed tilt the reactivity landscape to favor one product over the other. Thermodynamic parameters reveal the presence of a large activation barrier and substantial changes to the activation entropy, confirming the modified chemical landscape under strong coupling.

scholarly journals Nonlinear infrared polaritonic interaction between cavities mediated by molecular vibrations at ultrafast time scale

2021 ◽  
Vol 7 (19) ◽  
pp. eabf6397
Author(s):  
Bo Xiang ◽  
Jiaxi Wang ◽  
Zimo Yang ◽  
Wei Xiong
Keyword(s):  
Strong Coupling ◽  
Chemical Reactions ◽  
Time Scale ◽  
Cavity Mode ◽  
Science And Technology ◽  
Nonlinear Interactions ◽  
Vibrational Modes ◽  
Molecular Vibrations ◽  
Quantum Simulations ◽  
Molecular Vibrational Modes

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.

The vibrational spectra of ClF2SbF6, BrF2SbF6, and ClO2SbF6

1970 ◽  
Vol 48 (21) ◽  
pp. 3456-3459 ◽  
Author(s):  
H. A. Carter ◽  
F. Aubke
Keyword(s):  
Strong Coupling ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Vibrational Frequencies ◽  
Vibrational Modes ◽  
Infrared And Raman Spectra

Infrared and Raman spectra of ClF2SbF6, BrF2SbF6, and ClO2SbF6 are reported. Vibrational frequencies for the BrF2+ cation are assigned. In all compounds various degrees of anion–cation interaction are found. The symmetry of the anion is reduced but no internal similarity between the three spectra is recognizable. In addition, strong coupling of vibrational modes for BrF2SbF6 is observed.

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