Non-adiabatic transitions from I2(E0g+ and D0u+) states induced by collisions with M = I2(X0g+) and H2O

被引:17
作者
Akopyan, M. E. [1 ]
Baturo, V. V. [1 ]
Lukashov, S. S. [1 ]
Poretsky, S. A. [1 ]
Pravilov, A. M. [1 ]
机构
[1] St Petersburg State Univ, Fac Phys, VA Fock Inst Phys, St Petersburg 198504, Russia
关键词
ION-PAIR STATES; AMPLIFIED SPONTANEOUS EMISSION; LASER-INDUCED-FLUORESCENCE; MI2 VDW COMPLEXES; MOLECULAR-IODINE; OPTICAL POPULATION; DIPOLE-MOMENT; DISSOCIATION LIMIT; ENERGY-TRANSFER; I-2;
D O I
10.1063/1.4725541
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 stepwise two-step two-color and three-step three-color laser excitation schemes are used for selective population of rovibronic levels of the first-tier ion-pair E0(g)(+) and D0(u)(+) states of molecular iodine and studies of non-adiabatic transitions to the D and E states induced by collisions with M = I-2(X) and H2O. Collection and analysis of the luminescence after excitation of the upsilon(E) = 8, 13 and upsilon(D) = 13, 18 vibronic levels of the E and D states in the pure iodine vapor and the gas-phase mixtures with H2O provide rate constants for the non-adiabatic transitions to the D and E state induced by collisions with these molecules. Vibrational distributions for the I-2(E, upsilon(E) (M)<-> D, upsilon(D)) collision-induced non-adiabatic transitions (CINATs) are obtained. Rather strong lambda(max)(lum) approximate to 3400 angstrom luminescence band is observed in the I-2 + H2O mixtures, whereas its intensity is similar to 100 times less in pure iodine vapor. Radiative lifetimes and quenching rate constants of the I-2(E,nu(E) = 8, 13 and D,nu(D) = 13, 18) vibronic state are also determined. Rate constants of the I-2(E, upsilon(E) (I2(X))-> D, upsilon(D)), upsilon(E) = 8-54, CINATs are measured again and compared with those obtained earlier. New data confirm resonance characters of the CINATs found in our laboratory about 10 years ago. Possible reasons of differences between rate constant values obtained in this and earlier works are discussed. It is shown, in particular, that differences in rate constants of non-resonant CINATs are due to admixture of water vapor in iodine. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4725541]
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页数:11
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共 51 条
[1]   Non-adiabatic transitions from the I2(E) induced by the transition dipole moment of I2(E-D) and the electric dipole moment of collision partners [J].
Akopyan, M. E. ;
Lukashov, S. ;
Maslennikova, Yu. D. ;
Poretsky, S. A. ;
Pravilov, A. M. ;
Torgashkova, A. S. .
CHEMICAL PHYSICS LETTERS, 2008, 458 (1-3) :29-34
[2]   Non-adiabatic E(M)over-right-arrow D,D′,β,γ,δ transitions in the first ion-pair tier of molecular iodine induced by collisions with I2, N2 and CO2 [J].
Akopyan, M. E. ;
Lukashov, S. S. ;
Khadikova, E. I. ;
Nikandrova, E. A. ;
Poretsky, S. A. ;
Pravilov, A. M. ;
Torgashkova, A. S. .
CHEMICAL PHYSICS, 2007, 342 (1-3) :173-183
[3]   Non-adiabatic E → D, D′, β, γ, δ transitions in the first ion-pair tier of molecular iodine induced by collisions with I2, He, Ar, Kr, Xe [J].
Akopyan, M. E. ;
Buchachenko, A. A. ;
Lukashov, S. S. ;
Poretsky, S. A. ;
Pravilov, A. M. ;
Suleimanov, Yu. V. ;
Torgashkova, A. S. ;
Tscherbul, T. V. .
CHEMICAL PHYSICS LETTERS, 2007, 436 (1-3) :1-6
[4]   Resonant optical excitation of the I2 ion-pair states through the RgI2 complexes in the valence states correlating to the 2P1/2+2P1/2 limit [J].
Akopyan, M. E. ;
Buchachenko, A. A. ;
Lukashov, S. S. ;
Novikova, I. Yu. ;
Poretsky, S. A. ;
Pravilov, A. M. .
CHEMICAL PHYSICS LETTERS, 2006, 427 (4-6) :259-264
[5]   Dipole moment functions of the iodine D′2g -A′2u, D0u+-a′ 0g+, D0u+-X0g+ and E0g+-B0u+ transitions [J].
Akopyan, M. E. ;
Baturo, V. V. ;
Lukashov, S. S. ;
Poretsky, S. A. ;
Pravilov, A. M. .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2011, 44 (20)
[6]   Dynamics and mechanism of the non-adiabatic transitions from the ungerade I2(D0u+) state induced by collisions with rare gas atoms [J].
Akopyan, M. E. ;
Khadikova, E. I. ;
Lukashov, S. S. ;
Poretsky, S. A. ;
Pravilov, A. M. ;
Buchachenko, A. A. ;
Suleimanov, Yu V. .
JOURNAL OF CHEMICAL PHYSICS, 2010, 133 (24)
[7]   Time resolved studies of decay of the XeI2(IP) complexes [J].
Akopyan, M. E. ;
Lukashov, S. S. ;
Maslennikova, Yu. D. ;
Poretsky, S. A. ;
Pravilov, A. M. .
CHEMICAL PHYSICS, 2009, 362 (1-2) :27-33
[8]   On mechanism of population of the I2(β) state under photolysis of the I2 + SF6 mixture [J].
Akopyan, M. E. ;
Lukashov, S. S. ;
Poretsky, S. A. ;
Pravilov, A. M. ;
Torgashkova, A. S. .
CHEMICAL PHYSICS LETTERS, 2009, 470 (4-6) :191-195
[9]   Collision-induced nonadiabatic transitions in the second-tier ion-pair states of iodine molecule:: Experimental and theoretical study of the I2(f0g+) collisions with rare gas atoms -: art. no. 214318 [J].
Akopyan, ME ;
Novikova, IY ;
Poretsky, SA ;
Pravilov, AM ;
Smolin, AG ;
Tscherbul, TV ;
Buchachenko, AA .
JOURNAL OF CHEMICAL PHYSICS, 2005, 122 (20)
[10]   The iodine E0g+-B0u+ and D0u+-X0g+ transition dipole moment functions [J].
Akopyan, ME ;
Bibinov, NK ;
Kokh, DB ;
Pravilov, AM ;
Stepanov, MB .
CHEMICAL PHYSICS, 1999, 242 (02) :253-261