Transversal structure of a sum-frequency beam generated from the surface of a chiral medium

2009 ◽  
Vol 11 (7) ◽  
pp. 074008 ◽  
Author(s):  
V A Makarov ◽  
I A Perezhogin
2022 ◽  
Author(s):  
Kirill Grigoriev ◽  
Vladimir Makarov

Abstract Aiming to study the nonlinear response of the surface of isotropic chiral medium, we obtained analytical expression relating the transverse amplitudes of the spatial Fourier-spectra of two incident arbitrary polarized fundamental beams and one signal reflected beam at the sum-frequency within the first-order approximation by their divergence angles. The calculations, carried out in paraxial approximation, simultaneously take into account the spatial dispersion of the bulk of the medium, its near-surface heterogeneity and the transverse finiteness of the three interacting light beams with arbitrary amplitude profiles and orientation in space. A special compact form for the final formulas was found, which makes use of effective nonlinear transformation tensors, the components of which are solely determined by the geometry of incidence of the beams and the material constants of the medium. A possibility of ``switching off'' the certain mechanisms of nonlinear response by choosing the specific polarization states of the incident beams is discussed.


1995 ◽  
Vol 5 (7) ◽  
pp. 913-918 ◽  
Author(s):  
Frédéric Guérin ◽  
Akhlesh Lakhtakia

2018 ◽  
Author(s):  
Daniel R. Moberg ◽  
Shelby C. Straight ◽  
Francesco Paesani

<div> <div> <div> <p>The temperature dependence of the vibrational sum-frequency generation (vSFG) spectra of the the air/water interface is investigated using many-body molecular dynamics (MB-MD) simulations performed with the MB-pol potential energy function. The total vSFG spectra calculated for different polarization combinations are then analyzed in terms of molecular auto-correlation and cross-correlation contributions. To provide molecular-level insights into interfacial hydrogen-bonding topologies, which give rise to specific spectroscopic features, the vSFG spectra are further investigated by separating contributions associated with water molecules donating 0, 1, or 2 hydrogen bonds to neighboring water molecules. This analysis suggests that the low frequency shoulder of the free OH peak which appears at ∼3600 cm−1 is primarily due to intermolecular couplings between both singly and doubly hydrogen-bonded molecules. </p> </div> </div> </div>


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