Journal
PHYSICAL REVIEW A
Volume 103, Issue 2, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevA.103.022802
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Funding
- National Science Centre Poland [2015/19/D/ST4/02173, 2016/23/B/ST4/03231]
- Foundation for Polish Science within the First Team program - European Union under the European Regional Development Fund
- PL-Grid Infrastructure
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The properties of highly polar diatomic molecules containing S-2-state transition-metal atoms were theoretically investigated. Various molecular properties such as potential energy curves, permanent electric dipole moments, spectroscopic constants, and leading long-range dispersion-interaction coefficients were calculated. The studied molecules exhibit strongly bound covalent or ionic bonds in the ground electronic state, resulting in very large permanent electric dipole moments.
We theoretically investigate the properties of highly polar diatomic molecules containing S-2-state transition-metal atoms. We calculate potential energy curves, permanent electric dipole moments, spectroscopic constants, and leading long-range dispersion-interaction coefficients for molecules consisting of either a Cu or Ag atom interacting with an alkali-metal (Li, Na, K, Rb, Cs, Fr) or alkaline-earth-metal (Be, Mg, Ca, Sr, Ba, Ra) atom. We use ab initio electronic structure methods, such as the coupled cluster and configuration interaction ones, with large Gaussian basis sets and small-core relativistic-energy-consistent pseudopotentials. We predict that the studied molecules in the ground electronic state are strongly bound with highly polarized covalent or ionic bonds resulting in very large permanent electric dipole moments. We find that highly excited vibrational levels have maximal electric dipole moments, e.g., exceeding 13 D for CsAg and 6 D for BaAg. Results for Cu-2, Ag-2, and CuAg are also reported. The studied molecules may find application in ultracold dipolar many-body physics, controlled chemistry, or precision measurement experiments.
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