The last two hydrogen molecular ion isotopologues, DT+ and T2+, receive high-precision variational ro-vibrational energies, dipole transition amplitudes, relativistic corrections, and hyperfine coefficients.
Quantum control of a single $\mathrm{H}_2^+$ molecular ion
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abstract
Science is founded on the benchmarking of theoretical models against experimental measurements, with the challenge that for all but the simplest systems, the calculations required for high precision become extremely challenging. $\mathrm{H}_2^+$ is the simplest stable molecule, and its structure is calculable to high precision. However, studying $\mathrm{H}_2^+$ experimentally presents significant challenges: Standard control methods such as laser cooling are not applicable due to the long lifetimes of its rotational and vibrational states. Here we solve this issue by combining buffer gas cooling to quench the $\mathrm{H}_2^+$ rovibrational excitation with quantum logic operations between $\mathrm{H}_2^+$ and a co-trapped 'helper' ion to control the molecule's hyperfine structure. This enables us to perform pure quantum state preparation, coherent control, and non-destructive readout, which we use to demonstrate high-resolution microwave spectroscopy in the hyperfine structure of $\mathrm{H}_2^+$ with a precision of 2 Hz. Our results pave the way for high precision spectroscopy of $\mathrm{H}_2^+$ in both the microwave and optical domains. Due to the wide applicability of buffer gas cooling, our method provides a general tool for molecular ion species that are hard to control with quantum logic tools alone.
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Variational studies of ro-vibrational spectra of DT$^+$ and T$_2^+$ ions
The last two hydrogen molecular ion isotopologues, DT+ and T2+, receive high-precision variational ro-vibrational energies, dipole transition amplitudes, relativistic corrections, and hyperfine coefficients.