A full-dimensional multilayer multiconfiguration time-dependent Hartree study on the ultraviolet absorption spectrum of formaldehyde oxide

• Published in: The Journal of chemical physics Vol. 141; no. 12; pp. 124309 - 20048
• Main Authors: Meng, Qingyong, Meyer, Hans-Dieter
• Format: Journal Article
• Language: English
• Published: United States American Institute of Physics 28.09.2014
• Subjects: ABSORPTION SPECTRA; APPROXIMATIONS; Chemical Sciences; COUPLING; EFFICIENCY; FORMALDEHYDE; FOURIER TRANSFORMATION; HAMILTONIANS; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; MOLECULES; Multilayers; OXIDES; Physics; SIMULATION; TIME DEPENDENCE; Ultraviolet absorption; ULTRAVIOLET RADIATION; ULTRAVIOLET SPECTRA; WAVE FUNCTIONS; MCTDH
• ISSN: 0021-9606; 1089-7690; 1089-7690
• DOI: 10.1063/1.4896201

Employing the multilayer multiconfiguration time-dependent Hartree (ML-MCTDH) method in conjunction with the multistate multimode vibronic coupling Hamiltonian (MMVCH) model, we perform a full dimensional (9D) quantum dynamical study on the simplest Criegee intermediate, formaldehyde oxide, in five lower-lying singlet electronic states. The ultraviolet (UV) spectrum is then simulated by a Fourier transform of the auto-correlation function. The MMVCH model is built based on extensive MRCI(8e,8o)/aug-cc-pVTZ calculations. To ensure a fast convergence of the final calculations, a large number of ML-MCTDH test calculations is performed to find an appropriate multilayer separations (ML-trees) of the ML-MCTDH nuclear wave functions, and the dynamical calculations are carefully checked to ensure that the calculations are well converged. To compare the computational efficiency, standard MCTDH simulations using the same Hamiltonian are also performed. A comparison of the MCTDH and ML-MCTDH calculations shows that even for the present not-too-large system (9D here) the ML-MCTDH calculations can save a considerable amount of computational resources while producing identical spectra as the MCTDH calculations. Furthermore, the present theoretical \documentclass[12pt]{minimal}\begin{document}$\tilde{B}\:{}^1A^{\prime }\leftarrow \tilde{X}\:{}^1A^{\prime }$\end{document}B̃1A′←X̃1A′ UV spectral band and the corresponding experimental measurements [J. M. Beames, F. Liu, L. Lu, and M. I. Lester, J. Am. Chem. Soc. 134, 20045–20048 (2012); L. Sheps, J. Phys. Chem. Lett. 4, 4201–4205 (2013); W.-L. Ting, Y.-H. Chen, W. Chao, M. C. Smith, and J. J.-M. Lin, Phys. Chem. Chem. Phys. 16, 10438–10443 (2014)] are discussed. To the best of our knowledge, this is the first theoretical UV spectrum simulated for this molecule including nuclear motion beyond an adiabatic harmonic approximation.