The fundamental vibrational interval of H2+ has been determined to be
ΔG1/2=2191.126614(17) cm−1 by continuous-wave laser
spectroscopy of Stark manifolds of Rydberg states of H2 with the H2+
ion core in the ground and first vibrationally excited states. Extrapolation of
the Stark shifts to zero field yields the zero-quantum-defect positions
−RH2/n2, from which ionization energies can be determined.
Our new result represents a four-order-of-magnitude improvement compared to
earlier measurements. It agrees, within the experimental uncertainty, with the
value of 2191.126\,626\,344(17)(100) cm−1 determined in non-relativistic
quantum electrodynamic calculations V. Korobov, L. Hilico and J.-Ph. Karr,
Phys. Rev. Lett. 118, 233001 (2017)
http://doi.org/10.1103/PhysRevLett.118.233001