Prospects for All-Optical Alignment and Quantum State Control of Nonpolar Molecules

2002 ◽  
pp. 304-319
Author(s):  
A. M. Lyyra ◽  
F. C. Spano ◽  
J. Qi ◽  
T. Kirova
Keyword(s):  
Quantum State ◽  
State Control ◽  
All Optical ◽  
Optical Alignment ◽  
Nonpolar Molecules

Erratum: Autler-Townes Splitting in Molecular Lithium: Prospects for All-Optical Alignment of Nonpolar Molecules [Phys. Rev. Lett. 83, 288 (1999)]

2002 ◽  
Vol 88 (22) ◽  
Author(s):  
Jianbing Qi ◽  
Guenadiy Lazarov ◽  
Xuejun Wang ◽  
Li Li ◽  
Lorenzo M. Narducci ◽  
...  
Keyword(s):  
All Optical ◽  
Optical Alignment ◽  
Nonpolar Molecules

Autler-Townes Splitting in Molecular Lithium: Prospects for All-Optical Alignment of Nonpolar Molecules

1999 ◽  
Vol 83 (2) ◽  
pp. 288-291 ◽  
Author(s):  
Jianbing Qi ◽  
Guenadiy Lazarov ◽  
Xuejun Wang ◽  
Li Li ◽  
Lorenzo M. Narducci ◽  
...  
Keyword(s):  
All Optical ◽  
Optical Alignment ◽  
Nonpolar Molecules

Autler–Townes splitting and the AC Stark effect in nonpolar molecules: Prospects for all-optical alignment

2001 ◽  
Vol 79 (2-3) ◽  
pp. 547-559
Author(s):  
A M Lyyra ◽  
J Qi ◽  
F C Spano
Keyword(s):  
Stark Effect ◽  
Continuous Wave ◽  
Molecular System ◽  
Triple Resonance ◽  
Atomic Systems ◽  
Molecular Systems ◽  
All Optical ◽  
Optical Alignment ◽  
Ac Stark Effect ◽  
Nonpolar Molecules

This paper describes an extension of the familiar coherence effects from atomic systems to the molecular regime. Such effects are inherent in the interaction of multiple laser fields with molecular systems. We have observed Autler–Townes splitting and the AC Stark shift in diatomic Lithium using the continuous wave all-optical triple resonance (AOTR) techniques. By using the Autler–Townes effect, we have partially resolved the magnetic sublevels of a molecular rovibrational level in a Doppler broadened sample, allowing all-optical alignment of the angular momentum in excited states of nonpolar molecules. The Autler–Townes effect in a molecular system extends the rovibrational state selectivity of the AOTR excitation technique to magnetic sublevels. PACS Nos.: 33.40tf, 42.50Hz

Quantum state control on the chemical reactivity of a transition metal vanadium cation in carbon dioxide activation

2019 ◽  
Vol 21 (13) ◽  
pp. 6868-6877 ◽  
Author(s):  
Yih Chung Chang ◽  
Yuntao Xu ◽  
Cheuk-Yiu Ng
Keyword(s):  
Carbon Dioxide ◽  
Transition Metal ◽  
Electronic State ◽  
Quantum State ◽  
Electron Spin ◽  
Chemical Reactivity ◽  
Ion Source ◽  
Atomic Transition ◽  
Spin Orbit ◽  
State Control

By utilizing a newly developed spin-orbit electronic state selected ion source for atomic transition metal vanadium cation (V+), the chemical reactivity of V+ with CO2 has been examined in detail, indicating that the titled reaction is dominantly governed by electron spin conservation, and thus the chemical reactivity can be controlled by quantum electronic state selections.

scholarly journals All optical quantum control of a spin-quantum state and ultrafast transduction into an electric current

2013 ◽  
Vol 3 (1) ◽  
Author(s):  
K. Müller ◽  
T. Kaldewey ◽  
R. Ripszam ◽  
J. S. Wildmann ◽  
A. Bechtold ◽  
...  
Keyword(s):  
Electric Current ◽  
Quantum State ◽  
Quantum Control ◽  
Spin Quantum ◽  
All Optical

Quantum State Control with Atoms and Cavities

CLEO: 2015 ◽  
2015 ◽  
Author(s):  
Jean-Michel Raimond ◽  
Theo Rybarczyk ◽  
Bruno Peaudecerf ◽  
Mariane Penasa ◽  
Stefan Gerlich ◽  
...  
Keyword(s):  
Quantum State ◽  
State Control
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