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Piotr Put

Publications and source records attributed to Piotr Put.

8 recordsLinked to original sources

Nanoscale magnetometry via collective many-body dynamics in diamond

Many-body dynamics constitutes a promising approach for creating correlations between quantum particles which can be used for applications in sensing and metrology. However, utilizing this potential for substantial gains in practical settings is a challenging task with only a very few applications realized to date. Here, we demonstrate an approach to nanoscale magnetic sensing enabled by strongly interacting electronic spins in a room temperature solid. By coherently controlling collective many-body dynamics of a dipolar ensemble of $\sim 10^4$ nitrogen-vacancy (NV) centres in diamond with pulsed magnetic field gradients, we demonstrate practical metrological gain up to $7.9(2)\,\mathrm{dB}$ for magnetic signal detection and $8.8(3)\,\mathrm{dB}$ for magnetic noise sensing, fully accounting for experimental overheads. Finally, we combine these methods to demonstrate a momentum-space-resolved sensing modality that enables detection of spatially correlated magnetic noise at continuously tunable length scales down to 50 nanometers. These observations open the door toward practical applications of interaction-enhanced quantum sensors for nanoscale biological imaging and material characterization.

quant-ph

Quantum Sensors for Chemistry and Materials Science

The advancement of chemistry and materials science relies on transformative analytical tools which can overcome the sensitivity, spatial resolution, and throughput limitations of conventional techniques. This review explores the application of quantum sensors - specifically optically pumped magnetometers (OPMs) and nitrogen-vacancy (NV) centers in diamond - as robust platforms for molecular and materials analysis. We contrast the extreme magnetic sensitivity of macroscopic OPM ensembles with the atomic-scale resolution and multimodal capabilities of solid-state NV centers. We highlight their deployment in zero- to ultralow-field and nanoscale NMR spectroscopy, real-time reaction monitoring, and transient radical and pH detection. Furthermore, we discuss their integration into high-throughput chemical assays and non-destructive materials diagnostics, such as operando battery monitoring. With the ongoing commercialization of these technologies and advances in quantum-enhanced sensitivities, quantum sensors are poised to routinely address complex real-world analytical challenges.

quant-ph

Dressed-state Hamiltonian engineering in a strongly interacting solid-state spin ensemble

In quantum science applications, ranging from many-body physics to quantum metrology, dipolar interactions in spin ensembles are controlled via Floquet engineering. However, this technique typically reduces the interaction strength between spins, and effectively weakens the coupling to a target sensing field, limiting the metrological sensitivity. In this work, we develop and demonstrate a method for direct tuning of the native interaction in an ensemble of nitrogen-vacancy (NV) centers in diamond. Our approach utilizes dressed-state qubit encoding under a magnetic field perpendicular to the crystal lattice orientation. This method leads to a $3.2\times$ enhancement of the dimensionless coherence parameter $JT_2$ compared to state-of-the-art Floquet engineering, and a $2.6\times$ ($8.3~$dB) enhanced sensitivity in AC magnetometry. Utilizing the extended coherence we experimentally probe spin transport at intermediate to late times. Our results provide a powerful Hamiltonian engineering tool for future studies with NV ensembles and other interacting higher-spin ($S>\frac{1}{2}$) systems.

quant-ph

Collective many-body dynamics in a solid-state quantum sensor controlled through nanoscale magnetic gradients

Coherent collective dynamics of strongly interacting qubits are a central resource in quantum information science, with applications from quantum computing and simulation to metrology. While electronic spins interact strongly via dipolar couplings in dense solid-state ensembles, imperfections and positional disorder pose major obstacles to coherent correlated behavior, limiting their usefulness. Here, we realize collective many-body dynamics by combining time-dependent magnetic field gradients with global coherent control of dense electron spin ensembles in diamond. We control and probe the dynamics of nanometer-scale spin spirals, and, by exploiting Hamiltonian engineering that enhances the microscopic symmetry of the interactions, we observe a disorder-resilient collective spin evolution. Our results establish a pathway to interaction-enhanced quantum metrology and nanoscale imaging of materials and biological systems under ambient conditions.

quant-ph

Wideband covariance magnetometry below the diffraction limit

We experimentally demonstrate a method for measuring correlations of wideband magnetic signals with spatial resolution below the optical diffraction limit. Our technique employs two nitrogen-vacancy (NV) centers in diamond as nanoscale magnetometers, spectrally resolved by inhomogeneous optical transitions. Using high-fidelity optical readout and long spin coherence time, we probe correlated MHz-range noise with sensitivity of 15 nT Hz$^{-1/4}$. In addition, we use this system for correlated $T_1$ relaxometry, enabling correlation measurements of GHz-range noise. Under such externally applied noise, while individual NV centers exhibit featureless relaxation, their correlation displays rich coherent and incoherent dynamics reminiscent of superradiance physics. This capability to probe high-frequency correlations provides a powerful tool for investigating a variety of condensed-matter phenomena characterized by nonlocal correlations.

quant-ph

Signal amplification in a solid-state quantum sensor via asymmetric time-reversal of many-body dynamics

Electronic spins of nitrogen vacancy (NV) centers in diamond constitute a promising system for micro- and nano-scale magnetic sensing, due to their operation under ambient conditions, ease of placement in close proximity to sensing targets, and biological compatibility. At high densities, the electronic spins interact through dipolar coupling, which typically limits but can also potentially enhance sensing performance. Here we report the experimental demonstration of many-body signal amplification in a solid-state, room temperature quantum sensor. Our approach utilizes time-reversed two-axis-twisting interactions, engineered through dynamical control of the quantization axis and Floquet engineering in a two-dimensional ensemble of NV centers. Strikingly, we observe that the optimal amplification occurs when the backward evolution time equals twice the forward evolution time, in sharp contrast to the conventional Loschmidt echo. These observations can be understood as resulting from an underlying time-reversed mirror symmetry of the microscopic dynamics, providing key insights into signal amplification and opening the door towards entanglement-enhanced practical quantum sensing.

quant-ph

Nonlinear magneto-optical rotation with parametric resonance

We report on investigations of nonlinear magneto-optical rotation (NMOR) in rubidium vapor subjected to a modulated magnetic field and continuous-wave (CW) laser-light illumination. By superimposing modulation and a static (DC) magnetic field, we demonstrate the appearance of resonances at both small and large (compared to the ground-state relaxation rate) values of the static field. Since in conventional NMOR, there is no rotation at high fields, this suggests an existence of a novel mechanism generating anisotropy in the considered case, which we identify as parametric resonance. The experiments are performed using light of small ellipticity and rotation signals are significantly enhanced by combining atom-induced polarization rotation with a passive rotation induced with a wave plate. All the observations are supported with theoretical simulations. The density-matrix formalism and angular-momentum probability surfaces are used to provide intuitive explanation of the observed signals.

physics.atom-ph

Different sensitivities of two optical magnetometers realized in the same experimental arrangement

In this article, operation of optical magnetometers detecting static (DC) and oscillating (AC) magnetic fields is studied and comparison of the devices is performed. To facilitate the comparison, the analysis is carried out in the same experimental setup, exploiting nonlinear magneto-optical rotation. In such a system, a control over static-field magnitude or oscillating-field frequency provides detection of strength of the DC or AC fields. Polarization rotation is investigated for various light intensities and AC-field amplitudes, which allows to determine optimum sensitivity to both fields. With the results, we demonstrate that under optimal conditions the AC magnetometer is about ten times more sensitive than its DC counterpart, which originates from different response of the atoms to the fields. Bandwidth of the magnetometers is also analyzed, revealing its different dependence on the light power. Particularly, we demonstrate that bandwidth of the AC magnetometer can be significantly increased without strong deterioration of the magnetometer sensitivity. This behavior, combined with the ability to tune the resonance frequency of the AC magnetometer, provide means for ultra-sensitive measurements of the AC field in a broad but spectrally-limited range, where detrimental role of static-field instability is significantly reduced.

physics.atom-ph