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This study challenges established scaling laws by demonstrating anomalously long lifetimes in Rydberg states of singly charged alkaline-earth metal ions, a critical factor for improving fidelity in trapped-ion quantum computers. The research identifies distinct physical mechanisms—dipole matrix element cancellations at zero temperature and energetic level separation at room temperature—that enable these enhanced state durations. By extending the coherence time of qubits, this discovery directly addresses a primary bottleneck in scaling up quantum simulation and computing architectures.
Anomalously enhanced lifetimes of low angular momentum Rydberg states in singly charged alkaline-earth metal ions
arXiv:2609.24874v1 Announce Type: cross Abstract: Trapped ions excited to high-lying electronic states, so-called Rydberg states, open new opportunities for quantum simulation and quantum computing. Generally, the fidelity of quantum coherent operations critically depends on the longevity of Rydberg states. However, scaling laws predict that the lifetimes of Rydberg states in singly charged alkaline-earth metal ions are 16 times shorter, compared to their neutral atom counterparts. Here, we show that this is not generally the case. We report an anomalous lifetime enhancement of certain low angular momentum ionic Rydberg series by factors larger than eight. The anomaly is present at both zero and finite temperature, although it is caused by different mechanisms. At zero temperature, the anomalously enhanced lifetimes are caused by accidental cancellations of the relevant dipole transition matrix elements, while at room temperature the anomaly originates from the enlarged energetic separation of ionic Rydberg levels with respect to neutral-atom levels.
Abstract:Trapped ions excited to high-lying electronic states, so-called Rydberg states, open new opportunities for quantum simulation and quantum computing. Generally, the fidelity of quantum coherent operations critically depends on the longevity of Rydberg states. However, scaling laws predict that the lifetimes of Rydberg states in singly charged alkaline-earth metal ions are 16 times shorter, compared to their neutral atom counterparts. Here, we show that this is not generally the case. We report an anomalous lifetime enhancement of certain low angular momentum ionic Rydberg series by factors larger than eight. The anomaly is present at both zero and finite temperature, although it is caused by different mechanisms. At zero temperature, the anomalously enhanced lifetimes are caused by accidental cancellations of the relevant dipole transition matrix elements, while at room temperature the anomaly originates from the enlarged energetic separation of ionic Rydberg levels with respect to neutral-atom levels.
Atomic Physics (physics.atom-ph); Quantum Physics (quant-ph)
arXiv:2609.24874 [physics.atom-ph]
(or arXiv:2609.24874v1 [physics.atom-ph] for this version)
https://doi.org/10.48550/arXiv.2609.24874 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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Full text under the publisher's open licence · 243 words
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