Affiliation:
1. Departamento PAMS, Instituto de Física Fundamental (IFF-CSIC), CSIC, Serrano 123, 28006 Madrid, Spain
2. Departamento de Física, Universidad Nacional de Colombia, Calle 26, Cra 39, Edificio 404, Bogotá, Colombia
Abstract
The protonated hydrogen dimer, H
5
+
, is the smallest system including proton transfer, and has been of long-standing interest since its first laboratory observation in 1962. H
5
+
and its isotopologues are the intermediate complexes in deuterium fractionation reactions, and are of central importance in molecular astrophysics. The recently recorded infrared spectra of both H
5
+
and D
5
+
reveal a rich vibrational dynamics of the cations, which presents a challenge for standard theoretical approaches. Although H
5
+
is a four-electron ion, which makes highly accurate electronic structure calculations tractable, the construction of
ab initio
-based potential energy and dipole moment surfaces has proved a hard task. In the same vein, the difficulties in treating the nuclear motion could also become cumbersome due to their high dimensionality, floppiness and/or symmetry. These systems are prototypical examples for studying large-amplitude motions, as they are highly delocalized, interconverting between equivalent minima through internal rotation and proton transfer motions requiring state-of-the-art treatments. Recent advances in the computational vibrational spectroscopy of the H
5
+
cation and its isotopologues are reported from full quantum spectral simulations, providing important information in a rigorous manner, and open perspectives for further future investigations.
This article is part of a discussion meeting issue ‘Advances in hydrogen molecular ions: H
3
+
, H
5
+
and beyond’.
Subject
General Physics and Astronomy,General Engineering,General Mathematics
Cited by
1 articles.
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1. Hydrogen molecular ions: H
3
+
, H
5
+
and beyond;Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences;2019-08-05