Quantum-Enhanced Metrology for Molecular Symmetry Violation using Decoherence-Free Subspaces
arXiv:2307.05858 · doi:10.1103/PhysRevLett.131.193602
Abstract
We propose a method to measure time-reversal symmetry violation in molecules that overcomes the standard quantum limit while leveraging decoherence-free subspaces to mitigate sensitivity to classical noise. The protocol does not require an external electric field, and the entangled states have no first-order sensitivity to static electromagnetic fields as they involve superpositions with zero average lab-frame projection of spins and dipoles. This protocol can be applied with trapped neutral or ionic species, and can be implemented using methods which have been demonstrated experimentally.
7+11 pages, 3+3 figures
References in corpus (10)
- An Al quantum-logic clock with systematic uncertainty below
- Schemes for robust quantum computation with polar molecules
- Precision Measurement of Time-Reversal Symmetry Violation with Laser-Cooled Polyatomic Molecules
- Radio Frequency Magneto-Optical Trapping of CaF with High Density
- Time-reversal symmetry violation in molecules induced by nuclear magnetic quadrupole moments
- Highly polar molecules consisting of a copper or silver atom interacting with an alkali-metal or alkaline-earth-metal atom
- Observation and laser spectroscopy of ytterbium monomethoxide, YbOCH
- Merits of Heavy-Heavy Molecules for Electron Electric Dipole Moment Searches
- Spectroscopy on the eEDM-sensitive states of ThF
- A general approach to state-dependent optical tweezer traps for polar molecules
Cited by in corpus (7)
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- Ultracold high-spin -state polar molecules for new physics searches
- Parity-Doublet Coherence Times in Optically Trapped Polyatomic Molecules
- Radioactive Molecules as Laboratories of Fundamental Physics