Dynamics and the breaking of a driven cage:: I2 in solid Ar

被引:31
作者
Bihary, Z [1 ]
Zadoyan, R [1 ]
Karavitis, M [1 ]
Apkarian, VA [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
关键词
D O I
10.1063/1.1689958
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
Pump-probe measurements of I-2 in solid Ar are reported and analyzed to extract a description of cage response to impulsive excitation, from the gentle kick, up to the breaking point. The most informative data are obtained through wavepacket motion on cage-bound, but otherwise dissociative, potentials where the chromophore acts as a transducer to drive the cage and to report on the local dynamics. This general class of dynamics is identified and analyzed as a function of energy in Ar, Kr, and Xe. The overdriven cage rebounds with a characteristic period of 1.2 ps that shows little dependence on excitation amplitude in all hosts. After rebound, the cage rings as a local resonant mode in Ar, with a period of 1 ps and dephasing time of 3 ps. This mode remains at the Debye edge in Kr and Xe, with periods of 630 and 800 fs, and dephasing times of 8 and 6 ps, respectively. In the bound B-state, the cage fluctuates toward its dilated equilibrium structure on a time scale of 3 ps, which is extracted from the down-chirp in the molecular vibrational frequency. When kicked with excess energy of 4 eV, the Ar cage breaks with 50% probability, and the molecule dissociates. The kinetics of polarization selective, multiphoton dissociation with Gaussian laser intensity profiles is delineated and the ballistics of cage breakout is described: The photodissociation proceeds by destruction of the local lattice, by creating interstitials and vacancies. During large amplitude motion on cage-bound potentials, sudden, nonadiabatic spin-flip transitions can be observed and quantified in space and time. The spin-flip occurs with unit probability in Ar when the I-*-I bond is stretched beyond 6 A. (C) 2004 American Institute of Physics.
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收藏
页码:7576 / 7589
页数:14
相关论文
共 51 条
[1]   DELAYED AND DIRECT CAGE EXIT IN PHOTODISSOCIATION OF CL2 IN SOLID AR [J].
ALIMI, R ;
GERBER, RB ;
MCCAFFREY, JG ;
KUNZ, H ;
SCHWENTNER, N .
PHYSICAL REVIEW LETTERS, 1992, 69 (05) :856-859
[2]   Molecular photodynamics in rare gas solids [J].
Apkarian, VA ;
Schwentner, N .
CHEMICAL REVIEWS, 1999, 99 (06) :1481-1514
[3]  
APKARIAN VA, 1997, J CHEM SOC FARADAY T, V108, P334
[4]   A HIGHLY ACCURATE INTERATOMIC POTENTIAL FOR ARGON [J].
AZIZ, RA .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (06) :4518-4525
[5]   Quantum control of I-2 in the gas phase and in condensed phase solid Kr matrix [J].
Bardeen, CJ ;
Che, JW ;
Wilson, KR ;
Yakovlev, VV ;
Apkarian, VA ;
Martens, CC ;
Zadoyan, R ;
Kohler, B ;
Messina, M .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (20) :8486-8503
[6]   Ultrafast solvent-induced spin-flip and nonadiabatic coupling: ClF in argon solids [J].
Bargheer, M ;
Niv, MY ;
Gerber, RB ;
Schwentner, N .
PHYSICAL REVIEW LETTERS, 2002, 89 (10)
[7]   Subpicosecond spin-flip induced by the photodissociation dynamics of ClF in an Ar matrix [J].
Bargheer, M ;
Gerber, RB ;
Korolkov, MV ;
Kühn, O ;
Manz, J ;
Schröder, M ;
Schwentner, N .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2002, 4 (22) :5554-5562
[8]   Femtosecond spectroscopy of fragment cage dynamics:: I2 in Kr [J].
Bargheer, M ;
Gühr, M ;
Dietrich, P ;
Schwentner, N .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2002, 4 (01) :75-81
[9]   Extraction of potentials and dynamics from condensed phase pump-probe spectra:: Application to I2 in Kr matrices [J].
Bargheer, M ;
Dietrich, P ;
Donovang, K ;
Schwentner, N .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (18) :8556-8564
[10]   Nonadiabatic molecular dynamics simulation of photodissociation and geminate recombination of I-2 liquid xenon [J].
Batista, VS ;
Coker, DF .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (10) :4033-4054