Chong Zu

Quantum-enhanced multiparameter sensing is often associated with distributed architectures or 2-anticoherent states, whereas squeezing in a single collective ensemble is typically limited to single-parameter metrology. Here, we show that a single ensemble can support simultaneous multiparameter squeezing when each sensor is promoted from a qubit to a qudit (i.e., spin with $d$ energy levels). We develop a general framework in which the optimal product probe state, the corresponding global readout observables, and the associated squeezing parameters are all determined from the single-site quantum Fisher information matrix. We then present a minimal qudit construction for two-parameter vector magnetic field sensing with local dimension $d=3$. We further identify a collective twisting-like interacting Hamiltonian that generates such multiparameter-squeezed states and numerically demonstrate scalable metrological gain. In particular, for a trapped-ion qutrit chain with power-law interactions, we obtain up to 12 dB enhancement in two-parameter sensing for $N=256$ sensors. Our results establish qudit-enabled multiparameter squeezing in a single ensemble as a distinct route to multiparameter quantum metrology with global readout, and highlight its potential advantage over distributed multi-ensemble strategies in the fixed-sensor-budget regime.

While spin squeezing has been traditionally considered in all-to-all interacting models, recent works have shown that it can also occur in systems with power-law interactions, enabling direct tests in Rydberg atoms, trapped ions, ultracold atoms, and nitrogen-vacancy (NV) centers in diamond. For the latter, Wu et al. Nature 646 (2025) demonstrated that spin squeezing is heavily affected by positional disorder, reducing any capacity for a practical squeezing advantage, which requires scalability with the system size. In this Letter we explore the robustness of spin squeezing in two-dimensional lattices with a fraction of unoccupied lattice sites. Using semiclassical modeling, we demonstrate the existence of scalable squeezing in power-law interacting XXZ models up to a disorder threshold, above which squeezing is not scalable. We produce a phase diagram for scalable squeezing, and explain its absence in the aforementioned NV experiment. Our work illustrates the maximum disorder allowed for realizing scalable spin squeezing in a host of quantum simulators, highlights a regime with substantial tolerance to disorder, and identifies controlled defect creation as a promising route for scalable squeezing in solid-state systems.

Probing electrical and magnetic properties in aqueous environments remains a frontier challenge in nanoscale sensing. Our inability to do so with quantitative accuracy imposes severe limitations, for example, on our understanding of the ionic environments in a diverse array of systems, ranging from novel materials to the living cell. The Nitrogen-Vacancy (NV) center in fluorescent nanodiamonds (FNDs) has emerged as a good candidate to sense temperature, pH, and the concentration of paramagnetic species at the nanoscale, but comes with several hurdles such as particle-to-particle variation which render calibrated measurements difficult, and the challenge to tightly confine and precisely position sensors in aqueous environment. To address this, we demonstrate relaxometry with NV centers within optically-trapped FNDs. In a proof of principle experiment, we show that optically-trapped FNDs enable highly reproducible nanomolar sensitivity to the paramagnetic ion, (\mathrm{Gd}^{3+}). We capture the three distinct phases of our experimental data by devising a model analogous to nanoscale Langmuir adsorption combined with spin coherence dynamics. Our work provides a basis for routes to sense free paramagnetic ions and molecules in biologically relevant conditions.

Levitated diamond particles in high vacuum with internal spin qubits have been proposed for exploring macroscopic quantum mechanics, quantum gravity, and precision measurements. The coupling between spins and particle rotation can be utilized to study quantum geometric phase, create gyroscopes and rotational matter-wave interferometers. However, previous efforts in levitated diamonds struggled with vacuum level or spin state readouts. To address these gaps, we fabricate an integrated surface ion trap with multiple stabilization electrodes. This facilitates on-chip levitation and, for the first time, optically detected magnetic resonance measurements of a nanodiamond levitated in high vacuum. The internal temperature of our levitated nanodiamond remains moderate below $10^{-5}$ Torr. Impressively, we have driven a nanodiamond to rotate up to 20 MHz ($1.2 \times 10^{9}$ rpm), surpassing typical nitrogen-vacancy (NV) center electron spin dephasing rates. Using these NV spins, we observe the effect of the Berry phase arising from particle rotation. In addition, we demonstrate quantum control of spins in a rotating nanodiamond. These results mark an important development in interfacing mechanical rotation with spin qubits, expanding our capacity to study quantum phenomena.