TY - JOUR
T1 - Potential energy surfaces and nonadiabatic transitions in the asymptotic regions of ICN photodissociation to study the interference effects in the F1 and F2 spin-rotation levels of the CN products
AU - Kashimura, Tatsuhiko
AU - Ikezaki, Tomoya
AU - Ohta, Yusuke
AU - Yabushita, Satoshi
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant No.16K05668. The computations were partly performed using the computer facilities at the Research Center for Computational Science, Okazaki National Institutes.
Publisher Copyright:
© 2018 Wiley Periodicals, Inc.
PY - 2019/1/15
Y1 - 2019/1/15
N2 - One of the most spectacular yet unsolved problems for the ICN (Formula presented.) -band photodissociation is the non-statistical spin-rotation F1 = N + 1/2 and F2 = N − 1/2 populations for each rotation level N of the CN fragment. The F1/F2 population difference function f(N) exhibits strong N and λ dependences with an oscillatory behavior. Such details were found to critically depend on the number of open-channel product states, namely, whether both I (2P3/2) and I (2P1/2) are energetically available or not as the dissociation partner. First, in the asymptotic region, the exchange and dipole-quadrupole inter-fragment interactions were studied in detail. Then, as the diabatic basis, we took the appropriate symmetry adapted products of the electronic and rotational wavefunctions for the F1 and F2 levels at the dissociation limits. We found that the adiabatic Hamiltonian exhibits Rosen–Zener–Demkov type nonadiabatic transitions reflecting the switch between the exchange interaction and the small but finite spin-rotation interaction within CN at the asymptotic region. This non-crossing type nonadiabatic transition occurs with the probability 1/2, that is, at the diabatic limit through a sudden switch of the quantization axis for CN spin S from the dissociation axis to the CN rotation axis N. We have derived semiclassical formulae for f(N) and the orientation parameters with a two-state model including the 3A′ and 4A′ electronic states, and with a four-state model including the 3A′ through 6A′ electronic states. These two kinds of interfering models explain general features of the F1 and F2 level populations observed by Zare's grousp and Hall's group, respectively.
AB - One of the most spectacular yet unsolved problems for the ICN (Formula presented.) -band photodissociation is the non-statistical spin-rotation F1 = N + 1/2 and F2 = N − 1/2 populations for each rotation level N of the CN fragment. The F1/F2 population difference function f(N) exhibits strong N and λ dependences with an oscillatory behavior. Such details were found to critically depend on the number of open-channel product states, namely, whether both I (2P3/2) and I (2P1/2) are energetically available or not as the dissociation partner. First, in the asymptotic region, the exchange and dipole-quadrupole inter-fragment interactions were studied in detail. Then, as the diabatic basis, we took the appropriate symmetry adapted products of the electronic and rotational wavefunctions for the F1 and F2 levels at the dissociation limits. We found that the adiabatic Hamiltonian exhibits Rosen–Zener–Demkov type nonadiabatic transitions reflecting the switch between the exchange interaction and the small but finite spin-rotation interaction within CN at the asymptotic region. This non-crossing type nonadiabatic transition occurs with the probability 1/2, that is, at the diabatic limit through a sudden switch of the quantization axis for CN spin S from the dissociation axis to the CN rotation axis N. We have derived semiclassical formulae for f(N) and the orientation parameters with a two-state model including the 3A′ and 4A′ electronic states, and with a four-state model including the 3A′ through 6A′ electronic states. These two kinds of interfering models explain general features of the F1 and F2 level populations observed by Zare's grousp and Hall's group, respectively.
KW - F and F spin-rotation levels
KW - Rosen-Zener-Demkov nonadiabatic transitions
KW - dipole-quadrupole interactions
KW - fine structure splitting
KW - interference effect
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U2 - 10.1002/jcc.25736
DO - 10.1002/jcc.25736
M3 - Article
C2 - 30511401
AN - SCOPUS:85057755788
SN - 0192-8651
VL - 40
SP - 482
EP - 499
JO - Journal of Computational Chemistry
JF - Journal of Computational Chemistry
IS - 2
ER -