Inelastic collisions of cold polar molecules in nonparallel electric and magnetic fields

被引:48
作者
Abrahamsson, E. [1 ]
Tscherbul, T. V. [1 ]
Krems, R. V. [1 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1063/1.2748770
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The authors present a detailed study of low-temperature collisions between CaD molecules and He atoms in superimposed electric and magnetic fields with arbitrary orientations. Electric fields do not interact with the electron spin of the molecules directly but modify their rotational structure and, consequently, the spin-rotation interactions. The authors examine molecular Stark and Zeeman energy levels as functions of the angle between the fields and show that rotating fields may induce and shift avoided crossings between the Zeeman levels of the rotationally ground and rotationally excited states of the molecule. The dynamics of molecular collisions are extremely sensitive to external fields near these avoided crossings and it is shown that molecular collisions may be controlled by varying both the strength and the relative orientation of the fields. The effects observed in this study are due to interactions of the isolated molecules with external fields so the conclusions should be relevant for collisions of molecules with other atoms or collisions of molecules with each other. This study demonstrates that electric fields may be used to enhance or suppress spin-rotation interactions in molecules. The spin-rotation interactions induce nonadiabatic couplings between states of different total spins in systems of two open-shell species and it is suggested that electric fields might be used for controlling nonadiabatic spin transitions and spin-forbidden chemical reactions of cold molecules in a magnetic trap. (C) 2007 American Institute of Physics.
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页数:10
相关论文
共 57 条
[1]   VELOCITY DEPENDENCE OF COLLISIONAL ALIGNMENT OF OXYGEN MOLECULES IN GASEOUS EXPANSIONS [J].
AQUILANTI, V ;
ASCENZI, D ;
CAPPELLETTI, D ;
PIRANI, F .
NATURE, 1994, 371 (6496) :399-402
[2]   SCATTERING OF ROTATIONALLY ALIGNED OXYGEN MOLECULES AND THE MEASUREMENT OF ANISOTROPIES OF VAN-DER-WAALS FORCES [J].
AQUILANTI, V ;
ASCENZI, D ;
CAPPELLETTI, D ;
FRANCESCHINI, S ;
PIRANI, F .
PHYSICAL REVIEW LETTERS, 1995, 74 (15) :2929-2932
[3]   Suppression of inelastic collisions of polar 1Σ state molecules in an electrostatic field [J].
Avdeenkov, AV ;
Kajita, M ;
Bohn, JL .
PHYSICAL REVIEW A, 2006, 73 (02)
[4]  
Avdeenkov AV, 2004, PHYS REV A, V69, DOI 10.1103/PhysRevA.69.012710
[5]   Collisional dynamics of ultracold OH molecules in an electrostatic field [J].
Avdeenkov, AV ;
Bohn, JL .
PHYSICAL REVIEW A, 2002, 66 (05) :10
[6]   Magnetic trapping of buffer-gas-cooled chromium atoms and prospects for the extension to paramagnetic molecules [J].
Bakker, Joost M. ;
Stoll, Michael ;
Weise, Dennis R. ;
Vogelsang, Oliver ;
Meijer, Gerard ;
Peters, Achim .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2006, 39 (19) :S1111-S1123
[7]   The He-CaH(2Σ+) interaction.: II.: Collisions at cold and ultracold temperatures [J].
Balakrishnan, N ;
Groenenboom, GC ;
Krems, RV ;
Dalgarno, A .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (16) :7386-7393
[8]   Photoassociation of 85Rb atoms into 0+u states near the 5S+5P atomic limits [J].
Bergeman, T. ;
Qi, J. ;
Wang, D. ;
Huang, Y. ;
Pechkis, H. K. ;
Eyler, E. E. ;
Gould, P. L. ;
Stwalley, W. C. ;
Cline, R. A. ;
Miller, J. D. ;
Heinzen, D. J. .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2006, 39 (19) :S813-S823
[9]   Fine structure, alignment, and orientation of 32S16O and 16O18O molecules in congruent electric and magnetic fields [J].
Boca, A ;
Friedrich, B .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (08) :3609-3619
[10]   Imaging the alignment angular distribution: State symmetries, coherence effects, and nonadiabatic interactions in photodissociation [J].
Bracker, AS ;
Wouters, ER ;
Suits, AG ;
Vasyutinskii, OS .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (14) :6749-6765