TY - JOUR
T1 - DCl-H2O, HCl-D2O, and DCl-D2O Dimers
T2 - Inter- And Intramolecular Vibrational States and Frequency Shifts from Fully Coupled Quantum Calculations on a Full-Dimensional Neural Network Potential Energy Surface
AU - Felker, Peter M.
AU - Liu, Yang
AU - Li, Jun
AU - Bačić, Zlatko
N1 - Funding Information:
Z.B. is grateful to the National Science Foundation for its partial support of this research through the grant CHE-1566085. P.M.F. is grateful to Prof. Daniel Neuhauser for his support. Y.L. and J.L. have been financially supported by National Natural Science Foundation of China (contract no. 21973009) and Chongqing Municipal Natural Science Foundation (grant no. cstc2019jcyj-msxmX0087).
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/7/29
Y1 - 2021/7/29
N2 - We report full-dimensional and fully coupled quantum calculations of the inter- and intramolecular vibrational states of three isotopologues of the hydrogen chloride-water dimer: DCl-H2O (DH), HCl-D2O (HD), and DCl-D2O (DD). The present study extends our recent theoretical investigation of the nine-dimensional (9D) vibrational level structure of the HCl-H2O (HH) dimer [Liu, Y.; Li, J.; Felker, P. M.; Bačić, Z. Phys. Chem. Chem. Phys. 2021, 23, 7101-7114]. It employs the same accurate 9D permutation invariant polynomial-neural network potential energy surface and the highly efficient bound-state methodology. The objective of this work is to elucidate the isotopologue variations of a range of bound-state properties of the hydrogen chloride-water dimer and compare them to those of the HH dimer. In order to achieve this, for the isotopologues considered, the rigorous 9D quantum calculations performed encompass all intramolecular vibrational fundamentals, and their frequency shifts relative to the isolated monomer values, together with the low-lying intermolecular vibrational states in each of the intramolecular vibrational manifolds of interest. Moreover, for the ground state of each isotopologue, several informative vibrationally averaged intermolecular geometric properties of the dimer are computed, as well as the three rotational constants. The energies of the intermolecular inversion and rock modes, which mainly involve the motions of the water moiety, differ greatly for H2O and D2O, but are much less sensitive to whether the hydrogen chloride isotopologue is HCl or DCl. On the other hand, the excitation of the HCl/DCl stretch changes significantly the energies of the water inversion and rock modes. The DCl stretch frequency shift computed in 9D for the DD dimer, -114.91 cm-1, agrees extremely well with the corresponding experimental value of -115.20 cm-1 measured by Saykally and co-workers.
AB - We report full-dimensional and fully coupled quantum calculations of the inter- and intramolecular vibrational states of three isotopologues of the hydrogen chloride-water dimer: DCl-H2O (DH), HCl-D2O (HD), and DCl-D2O (DD). The present study extends our recent theoretical investigation of the nine-dimensional (9D) vibrational level structure of the HCl-H2O (HH) dimer [Liu, Y.; Li, J.; Felker, P. M.; Bačić, Z. Phys. Chem. Chem. Phys. 2021, 23, 7101-7114]. It employs the same accurate 9D permutation invariant polynomial-neural network potential energy surface and the highly efficient bound-state methodology. The objective of this work is to elucidate the isotopologue variations of a range of bound-state properties of the hydrogen chloride-water dimer and compare them to those of the HH dimer. In order to achieve this, for the isotopologues considered, the rigorous 9D quantum calculations performed encompass all intramolecular vibrational fundamentals, and their frequency shifts relative to the isolated monomer values, together with the low-lying intermolecular vibrational states in each of the intramolecular vibrational manifolds of interest. Moreover, for the ground state of each isotopologue, several informative vibrationally averaged intermolecular geometric properties of the dimer are computed, as well as the three rotational constants. The energies of the intermolecular inversion and rock modes, which mainly involve the motions of the water moiety, differ greatly for H2O and D2O, but are much less sensitive to whether the hydrogen chloride isotopologue is HCl or DCl. On the other hand, the excitation of the HCl/DCl stretch changes significantly the energies of the water inversion and rock modes. The DCl stretch frequency shift computed in 9D for the DD dimer, -114.91 cm-1, agrees extremely well with the corresponding experimental value of -115.20 cm-1 measured by Saykally and co-workers.
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U2 - 10.1021/acs.jpca.1c04662
DO - 10.1021/acs.jpca.1c04662
M3 - Article
C2 - 34261318
AN - SCOPUS:85111288214
SN - 1089-5639
VL - 125
SP - 6437
EP - 6449
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 29
ER -