Identification of molecular quantum states using phase-sensitive forces
arXiv:2004.05306 · doi:10.1038/s41467-020-18170-9
Abstract
Quantum-logic techniques used to manipulate quantum systems are now increasingly being applied to molecules. Previous experiments on single trapped diatomic species have enabled state detection with excellent fidelities and highly precise spectroscopic measurements. However, for complex molecules with a dense energy-level structure improved methods are necessary. Here, we demonstrate an enhanced quantum protocol for molecular state detection using state-dependent forces. Our approach is based on interfering a reference and a signal force applied to a single atomic and molecular ion, respectively, in order to extract their relative phase. We use this phase information to identify states embedded in a dense molecular energy-level structure and to monitor state-to-state inelastic scattering processes. This method can also be used to exclude a large number of states in a single measurement when the initial state preparation is imperfect and information on the molecular properties is incomplete. While the present experiments focus on N, the method is general and is expected to be of particular benefit for polyatomic systems.
References in corpus (10)
- Supplementary information for "Quantum supremacy using a programmable superconducting processor"
- The Quantum Internet
- An Al quantum-logic clock with systematic uncertainty below
- Quantum information transfer using photons
- Enhanced sensitivity to variation of the fine structure constant and m_p/m_e in diatomic molecules
- Quantum entanglement between an atom and a molecule
- Quantum non-demolition state detection and spectroscopy of single trapped molecules
- Precision frequency-comb terahertz spectroscopy on pure quantum states of a single molecular ion
- From megahertz to terahertz qubits encoded in molecular ions: theoretical analysis of dipole-forbidden spectroscopic transitions in N
- State-selective coherent motional excitation as a new approach for the manipulation, spectroscopy and state-to-state chemistry of single molecular ions