Marked influence of the nature of chemical bond on CP-violating signature in molecular ions HBr+ and HI+

Abstract

Heavy polar molecules offer a great sensitivity to the electron Electric Dipole Moment(EDM). To guide emerging searches for EDMs with molecular ions, we estimate the EDM-induced energy corrections for hydrogen halide ions HBr+ and HI+ in their respective ground X 23/2 states. We find that the energy corrections due to EDM for the two ions differ by an unexpectedly large factor of fifteen. We demonstrate that a major part of this enhancement is due to a dissimilarity in the nature of the chemical bond for the two ions: the bond that is nearly of ionic character in HBr+ exhibits predominantly covalent nature in HI+. We conclude that because of this enhancement the HI+ ion may be a potentially competitive candidate for the EDM search.

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