Iterative Diagonalization in the Multiconfigurational Time-Dependent Hartree Approach: Ro-vibrational Eigenstates
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- 作者：Robert Wodraszka ; Uwe Manthe
- 刊名：The Journal of Physical Chemistry A
- 出版年：2013
- 出版时间：August 15, 2013
- 年：2013
- 卷：117
- 期：32
- 页码：7246-7255
- 全文大小：363K
- 年卷期：v.117,no.32(August 15, 2013)
- ISSN：1520-5215
文摘
A scheme to efficiently calculate ro-vibrational (J > 0) eigenstates within the framework of the multiconfigurational time-dependent Hartree (MCTDH) approach is introduced. It employs a basis of MCTDH wave packets which is generated in the calculation of vibrational (J = 0) eigenstates via existing MCTDH-based iterative diagonalization approaches. The subsequent ro-vibrational calculations for total angular momenta J > 0 use direct products of these wave packets and the Wigner rotation matrices. In this ro-vibrational basis, the Hamiltonian matrix can be computed and diagonalized with minor numerical effort for any value of J. Accurate ro-vibrational states are obtained if the number of iterations in the J = 0 calculations and the basis set sizes in the MCTDH wave function representation are converged. Test calculations studying CH2D show that ro-vibrational eigenstates for moderately large J can be converged within wavenumber accuracy with the same MCTDH basis sets and only slightly increased iteration counts compared to purely vibrational (J = 0) calculations. If large J鈥檚 are considered or very high accuracies are required, the number of iterations required to obtain convergence increases significantly. Comparing the theoretical results with experimental data for the out-of-plane bend, symmetric stretch, and antisymmetric stretch fundamentals, the accuracy of the ab initio potential energy surface employed is investigated.