Long-Lived Mechanically-Detected Molecular Spins for Quantum Sensing

Abstract:Quantum sensors based on individual spins provide unprecedented access to local magnetic fields in condensed matter, chemistry, and biology, with solid-state defect spins emerging as the leading platform. However, their molecular-sensing capabilities are limited by confinement to a host lattice, which prevents placement in close proximity to a target molecule. Molecular spins offer an alternative, enabling chemical tunability and flexible positioning relative to the target system. Here we present a nanoscale sensing platform that combines molecular electron spins, ultrasensitive mechanical readout, and Hamiltonian engineering. Using a modified XYXY dipolar decoupling sequence, we suppress electron-electron dipolar interactions across a broad distribution of control fields, extending coherence times to $\sim 400~\mu$s in an attoliter-scale droplet containing $\sim$100 trityl-OX063 radicals. Leveraging this sequence, we demonstrate frequency-selective detection of nanotesla-scale AC fields and perform sensing and spectroscopy of small, local nuclear-spin ensembles. Collectively, these results establish SQUINT (Spin-based QUantum Integrated Nanomechanical Transduction) as a framework for quantum sensing that affords molecular-level control over sensor properties and enables direct integration into complex molecular targets.

Quantum Physics (quant-ph); Mesoscale and Nanoscale Physics (cond-mat.mes-hall)

arXiv:2603.04708 [quant-ph]

(or arXiv:2603.04708v2 [quant-ph] for this version)

https://doi.org/10.48550/arXiv.2603.04708 Focus to learn more arXiv-issued DOI via DataCite

https://doi.org/10.1103/c994-bzx7 Focus to learn more DOI(s) linking to related resources

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