Single-mode laser fluorescence of NO2 excited at 488 nm

1981 ◽  
Vol 59 (4) ◽  
pp. 559-566 ◽  
Author(s):  
M. J. Armstrong ◽  
J. C. D. Brand ◽  
C. di Lauro

The 488 nm line of the Ar+ laser operated in a single cavity mode excites absorption–fluorescence cycles in which an unusually high proportion exhibit anomalies in the selection rules, including transitions to a1 vibrational levels with values of ΔK = Kinitial – Kfinal of 4,2,0, and −2. Many transitions in the fluorescence, especially the weaker bands, show an intensity distribution different from that expected for type A bands of a 2B2–2A1 transition; this is attributed to interference between the dominant μa moment and a secondary, perpendicular transition moment considered to result from a perturbation of the intermediate state of the cycle by the 2B1 state.Data from about 20 fluorescence bands are used to determine the coefficient of a sextic anharmonic resonance, ν1ν2ν3, ν1, − 3, ν2 + 1, ν3 + 2 in the ground state of NO2.

2020 ◽  
Author(s):  
Johan Triana ◽  
Felipe Herrera

<p>We study the infrared photodissociation dynamics of a single hydrogen fluoride (HF) molecule in a single-mode cavity vacuum, and compare it with the case of strong cw laser driving. We show that in the absence of additional IR sources, a single cavity mode can efficiently dissociate a polar diatomic molecule prepared in the ground vibrational level. We predict dissociation probabilities of up to 20%, for a vacuum field that is resonant with the fundamental vibration frequency at the onset of the ultrastrong coupling regime. In contrast, similar dissociation rates can only be achieved in free space using resonant laser fields with intensities not smaller than 10<sup>14</sup> W/cm<sup>2</sup>. Our work highlights the fundamental differences that can be expected for reactive dynamical processes inside infrared cavities.</p>


2021 ◽  
Author(s):  
D. Koenen ◽  
B. Willenberg ◽  
J. Pupeikis ◽  
S. Camenzind ◽  
C. R. Phillips ◽  
...  

2020 ◽  
Author(s):  
Johan Triana ◽  
Felipe Herrera

<p>We study the infrared photodissociation dynamics of a single hydrogen fluoride (HF) molecule in a single-mode cavity vacuum, and compare it with the case of strong cw laser driving. We show that in the absence of additional IR sources, a single cavity mode can efficiently dissociate a polar diatomic molecule prepared in the ground vibrational level. We predict dissociation probabilities of up to 20%, for a vacuum field that is resonant with the fundamental vibration frequency at the onset of the ultrastrong coupling regime. In contrast, similar dissociation rates can only be achieved in free space using resonant laser fields with intensities not smaller than 10<sup>14</sup> W/cm<sup>2</sup>. Our work highlights the fundamental differences that can be expected for reactive dynamical processes inside infrared cavities.</p>


1997 ◽  
Vol 44 (11-12) ◽  
pp. 2427-2439 ◽  
Author(s):  
K. Jacobs ◽  
P. L. Knight ◽  
V. Vedral

2012 ◽  
Vol 42 (6) ◽  
pp. 561-564 ◽  
Author(s):  
S I Derzhavin ◽  
O A Dyukel' ◽  
N M Lyndin

1990 ◽  
Vol 145 (4) ◽  
pp. 159-165 ◽  
Author(s):  
Li Cao ◽  
Da-jin Wu

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