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Nicolas Staudenmaier

Publications and source records attributed to Nicolas Staudenmaier.

6 recordsLinked to original sources

Quantum Memory Enhanced Multipoint Correlation Spectroscopy for Statistically Polarized NMR

Nuclear magnetic resonance spectroscopy with solid-state spin sensors is a promising pathway for the detection of nuclear spins at the micro- and nanoscale. Although many nanoscale experiments rely on a single sensor spin for the detection of the signal, leveraging spin ensembles can enhance sensitivity, particularly in cases in which the signal merely originates from statistically polarized nuclear spins. In this work, we introduce multipoint correlation spectroscopy, that combines the advantages of two well-established methods -- correlation spectroscopy and quantum heterodyne detection -- to enable temporally efficient measurements of statistically polarized samples at the nanoscale with spin ensembles. We present a theoretical framework for this approach and demonstrate an experimental proof of concept with a nitrogen vacancy center in diamond. We achieve single hertz uncertainty in the estimated signal frequency, highlighting the potential applications of the technique for nanoscale nuclear magnetic resonance.

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Robust Noise Suppression and Quantum Sensing by Continuous Phased Dynamical Decoupling

We propose and demonstrate experimentally continuous phased dynamical decoupling (CPDD), where we apply a continuous field with discrete phase changes for quantum sensing and robust compensation of environmental and amplitude noise. CPDD does not use short pulses, making it particularly suitable for experiments with limited driving power or nuclear magnetic resonance at high magnetic fields. It requires control of the timing of the phase changes, offering much greater precision than the Rabi frequency control needed in standard continuous sensing schemes. We successfully apply our method to nanoscale nuclear magnetic resonance and combine it with quantum heterodyne detection, achieving microhertz uncertainty in the estimated signal frequency for a 120 s measurement. Our Letter expands significantly the applicability of dynamical decoupling and opens the door for a wide range of experiments, e.g., in nitrogen-vacancy centers, trapped ions, or trapped atoms.

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Optimal Sensing Protocol for Statistically Polarized Nano-NMR with NV Centers

Diffusion noise represents a major constraint to successful liquid state nano-NMR spectroscopy. Using the Fisher information as a faithful measure, we theoretically calculate and experimentally show that phase sensitive protocols are superior in most experimental scenarios, as they maximize information extraction from correlations in the sample. We derive the optimal experimental parameters for quantum heterodyne detection (Qdyne) and present the most accurate statistically polarized nano-NMR Qdyne detection experiments to date, leading the way to resolve chemical shifts and $J$ couplings at the nanoscale.

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Power-law scaling of correlations in statistically polarised nano-NMR

Diffusion noise is a major source of spectral line broadening in liquid state nano-scale nuclear magnetic resonance with shallow nitrogen-vacancy centres, whose main consequence is a limited spectral resolution. This limitation arises by virtue of the widely accepted assumption that nuclear spin signal correlations decay exponentially in nano-NMR. However, a more accurate analysis of diffusion shows that correlations survive for a longer time due to a power-law scaling, yielding the possibility for improved resolution and altering our understanding of diffusion at the nano-scale. Nevertheless, such behaviour remains to be demonstrated in experiments. Using three different experimental setups and disparate measurement techniques, we present overwhelming evidence of power-law decay of correlations. These result in sharp-peaked spectral lines, for which diffusion broadening need not be a limitation to resolution.

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Phase sensitive quantum spectroscopy with high frequency resolution

Classical sensors for spectrum analysis are widely used but lack micro- or nanoscale spatial resolution. On the other hand, quantum sensors, capable of working with nanoscale precision, do not provide precise frequency resolution over a wide range of frequencies. Using a single spin in diamond, we present a measurement protocol for quantum probes which enables full signal reconstruction on a nanoscale spatial resolution up to potentially 100\,GHz. We achieve $58\,\mathrm{nT/\sqrt{Hz}}$ amplitude and $0.095\,\mathrm{rad/\sqrt{Hz}}$ phase sensitivity and a relative frequency uncertainty of $10^{-12}$ for a $1.51\,\mathrm{GHz}$ signal within $10\,\mathrm{s}$ of integration. This technique opens the way to quantum spectrum analysis methods with potential applications in electron spin detection and nanocircuitry in quantum technologies.

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Experimental test of fluctuation relations for driven open quantum systems with an NV center

The experimental verification of quantum fluctuation relations for driven open quantum system is currently a challenge, due to the conceptual and operative difficulty of distinguishing work and heat. The Nitrogen-Vacancy center in diamond has been recently proposed as a controlled test bed to study fluctuation relations in the presence of an engineered dissipative channel, in absence of work [Hernández-Gómez et al., Phys. Rev. Research 2, 023327 (2020)]. Here, we extend those studies to exploring the validity of quantum fluctuation relations in a driven-dissipative scenario, where the spin exchanges energy both with its surroundings because of a thermal gradient, and with an external work source. We experimentally prove the validity of the quantum fluctuation relations in the presence of cyclic driving in two cases, when the spin exchanges energy with an effective infinite-temperature reservoir, and when the total work vanishes at stroboscopic times -- although the power delivered to the NV center is non-null. Our results represent the first experimental study of quantum fluctuation relation in driven open quantum systems.

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