期刊
CHEMICAL PHYSICS
卷 338, 期 2-3, 页码 175-185出版社
ELSEVIER
DOI: 10.1016/j.chemphys.2007.04.025
关键词
femtosecond dynamics; nonadiabatic dynamics; conical intersection; time-resolved photoelectron spectroscopy; nitrogen dioxide
Quantum wavepacket dynamics at the X(2)A(1)/A(2)B(2) conical intersection of NO2 molecule following a femtosecond pump pulse is computed, and subsequent probing of the dynamics with time-resolved fermosecond photoelectron spectroscopy is investigated theoretically. Diabatic representation of the ground and first excited state potential energy surfaces are constructed, and is used in time propagation of the vibrational wave function through pump and probe pulses in three dimensions. The Hamiltonian explicitly includes the pump interaction between the neutral states and probe interaction between the neutral and (discretized) ion continuum. Constant ionization matrix elements are used in this study. The computed photoelectron kinetic energy spectra are seen to reflect ultrafast wavepacket motion through the conical intersection region at early times. (c) 2007 Elsevier B.V. All rights reserved.
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