Laser probing of rotational-state-dependent velocity distributions of N2+ (ν″=0,J) drifted in He

2000 ◽  
Vol 112 (23) ◽  
pp. 10269-10281 ◽  
Author(s):  
Eric B. Anthony ◽  
Michael J. Bastian ◽  
Veronica M. Bierbaum ◽  
Stephen R. Leone
Keyword(s):  
Rotational State ◽  
Laser Probing ◽  
State Dependent

Rotational state-dependent mixings between resonance states of vibrationally highly excited DCO (X̃ 2A′)

2004 ◽  
Vol 120 (22) ◽  
pp. 10530-10542 ◽  
Author(s):  
J. Wei ◽  
A. Tröllsch ◽  
C. Tesch ◽  
F. Temps
Keyword(s):  
Rotational State ◽  
Resonance States ◽  
State Dependent

Rotational state-dependent attachment of He atoms to cold molecular ions: An action spectroscopic scheme for rotational spectroscopy

2017 ◽  
Vol 332 ◽  
pp. 67-78 ◽  
Author(s):  
Sandra Brünken ◽  
Lars Kluge ◽  
Alexander Stoffels ◽  
Jesús Pérez-Ríos ◽  
Stephan Schlemmer
Keyword(s):  
Molecular Ions ◽  
Rotational State ◽  
Rotational Spectroscopy ◽  
State Dependent

Rotational-State-Dependent Dispersion of Molecules by Pulsed Optical Standing Waves

2015 ◽  
Vol 115 (22) ◽  
Author(s):  
Xing Nan Sun ◽  
Lee Yeong Kim ◽  
Bum Suk Zhao ◽  
Doo Soo Chung
Keyword(s):  
Standing Waves ◽  
Rotational State ◽  
State Dependent

scholarly journals Scattering of adiabatically aligned molecules by nonresonant optical standing waves

2020 ◽  
Vol 6 (14) ◽  
pp. eaaz0682
Author(s):  
Lee Yeong Kim ◽  
Byung Gwun Jin ◽  
Tae Woo Kim ◽  
Ju Hyeon Lee ◽  
Bum Suk Zhao
Keyword(s):  
Standing Wave ◽  
Transverse Velocity ◽  
Translational Motion ◽  
Central Peak ◽  
Peak Position ◽  
Rotational State ◽  
Molecular Scattering ◽  
Optical Fields ◽  
Rotational States ◽  
State Dependent

We study the effect of rotational state–dependent alignment in the scattering of molecules by optical fields. CS2 molecules in their lowest few rotational states are adiabatically aligned and transversely accelerated by a nonresonant optical standing wave. The width of the measured transverse velocity distribution increases to 160 m/s with the field intensity, while its central peak position moves from 10 to −10 m/s. These changes are well reproduced by numerical simulations based on the rotational state–dependent alignment but cannot be modeled when ignoring these effects. Moreover, the molecular scattering by an off-resonant optical field amounts to manipulating the translational motion of molecules in a rotational state–specific way. Conversely, our results demonstrate that scattering from a nonresonant optical standing wave is a viable method for rotational state selection of nonpolar molecules.

On the problem of rotational-state-dependent molecule–surface interaction: Relaxation, accommodation and trapping at low J

2000 ◽  
Vol 112 (19) ◽  
pp. 8680-8686 ◽  
Author(s):  
A. Yu. Pankov ◽  
S. Yu. Krylov ◽  
E. J. van Duijn ◽  
L. J. F. Hermans
Keyword(s):  
Surface Interaction ◽  
Rotational State ◽  
State Dependent ◽  
Molecule Surface

Laser-induced fluorescence of hydrogen via the transition: Rotational-state-dependent collisional quenching

2011 ◽  
Vol 504 (4-6) ◽  
pp. 136-141 ◽  
Author(s):  
K. Niki ◽  
M. Fujiwara ◽  
Y. Motoshima ◽  
T. Kawauchi ◽  
K. Fukutani
Keyword(s):  
Laser Induced Fluorescence ◽  
Rotational State ◽  
Collisional Quenching ◽  
State Dependent

scholarly journals Effect of rotational-state-dependent molecular alignment on the optical dipole force

2016 ◽  
Vol 94 (1) ◽  
Author(s):  
Lee Yeong Kim ◽  
Ju Hyeon Lee ◽  
Hye Ah Kim ◽  
Sang Kyu Kwak ◽  
Bretislav Friedrich ◽  
...  
Keyword(s):  
Molecular Alignment ◽  
Rotational State ◽  
State Dependent ◽  
Dipole Force

Rotational-state dependent selectivity in the bond fission of C2HD (5ν1)

1997 ◽  
Vol 268 (1-2) ◽  
pp. 163-168 ◽  
Author(s):  
T. Arusi-Parpar ◽  
R.P. Schmid ◽  
R.-J. Li ◽  
I. Bar ◽  
S. Rosenwaks
Keyword(s):  
Rotational State ◽  
State Dependent
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