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High Order Split Operators for the Time-Dependent Wavepacket method of Triatomic Reactive Scattering in Hyperspherical Coordinates
Since the introduction of a series of methods for solving the time-dependent Schrödinger equation (TDSE) in the 80s of the last centry, such as the Fourier transform, the split operator (SO), the Chebyshev polynomial propagator, and complex absorbing potential, investigation of the molecular dynamic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7514310/ http://dx.doi.org/10.3390/e21100979 |
Sumario: | Since the introduction of a series of methods for solving the time-dependent Schrödinger equation (TDSE) in the 80s of the last centry, such as the Fourier transform, the split operator (SO), the Chebyshev polynomial propagator, and complex absorbing potential, investigation of the molecular dynamics within quantum mechanics principle have become popular. In this paper, the application of the time-dependent wave packet (TDWP) method using high-order SO propagators in hyperspherical coordinates for solving triatomic reactive scattering was investigated. The fast sine transform was applied to calculate the derivatives of the wave function of the radial degree of freedom. These high-order SO propagators are examined in different forms, i.e., TVT (Kinetic–Potential–Kinetic) and VTV (Potential–Kinetic–Potential) forms with three typical triatomic reactions, H + H [Formula: see text] , O + O [Formula: see text] and F + HD. A little difference has been observed among the performances of high-order SO propagators in the TVT and VTV representations in the hyperspherical coordinate. For obtaining total reaction probabilities with 1% error, some of the S class high-order SO propagators, which have symmetric forms, are more efficient than second order SO for reactions involving long lived intermediate states. High order SO propagators are very efficient for obtaining total reaction probabilities. |
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