arXiv subjects

Alon Salhov

Publications and source records attributed to Alon Salhov.

10 recordsLinked to original sources

arXiv2026

PIQC: Scalable Distributed Quantum Computing via Photonic Integration of Designed Molecular Quantum Nodes

There is a growing consensus that large-scale, fault-tolerant quantum computing (FTQC) necessitates high-fidelity photonic interconnects to overcome the scaling limits of monolithic architectures. However, most current platforms were not originally designed for native photonic connectivity and require significant engineering overhead. To overcome these fundamental hardware limitations, we recently introduced a rationally designed organic molecule that serves as an ideal quantum node, featuring a robust qubit-photon interface (QPI) and a long-lived nuclear-spin register. In this work, we present PIQC (Photonic Integrated Quantum Circuits), a distributed architecture designed to scale these molecular nodes into a functional quantum computer. The PIQC framework integrates five mutually reinforcing innovations: (i) Designer molecular qubits, i.e. carbene molecules in an isosteric host that provide millisecond-coherence electron spins with high spectral stability and spin-dependent optical emission, (ii) deterministic nuclear registers made of synthetically placed $^{13}$C or $^{14}$N labels that enable fast ($\sim 1~\mu$s), high-fidelity electron-nuclear gates, (iii) hybrid photonic integration, which allows molecular films to seamlessly integrate with existing mature fabrication technologies, e.g. thin-film lithium niobate (TFLN), (iv) heralded entanglement protocols that can tolerate up to 70% photon loss, and (v) stairway Floquetification, i.e. high-rate quantum low-density parity-check (qLDPC) codes that are converted into Floquet codes, reducing syndrome extraction to weight-two Bell-pair measurements that match PIQC's networked hardware. PIQC offers a hardware-efficient, commercially viable pathway toward a utility-scale quantum computer based on distributed FTQC.

quant-ph↗

arXiv2026

A Single-Molecule Spin-Photon Interface

Optical interfaces that connect long-lived spin qubits to photons are a central requirement for quantum networking and distributed quantum information processing. Currently, solid-state atomic defects are leading candidates due to their inherent spin and optical coherence. Building on these advancements, synthetically tailored molecular systems represent a fundamental change in the field, utilizing precise atomic control and consistent bottom-up assembly. However, the lack of a robust spin-photon interface combining bright fluorescence, high spectral stability, and the persistent spin lifetimes inherent to ground-state systems has prohibited the detection of individual molecular qubits. Here we show that a triplet ground state carbene molecule, embedded within a structurally matched host crystal, functions as a robust spin-photon interface with single-molecule addressability. The system exhibits narrow zero-phonon lines, spectral stability over more than an hour, spin-selective optical transitions and single-molecule optically detected magnetic resonance. Coherent control yields millisecond-scale dynamical-decoupling coherence and tens-of-milliseconds spin relaxation at a temperature of 4.5 K. These results establish molecular qubits as a viable platform for single-emitter quantum optics while preserving the advantages of bottom-up chemical design and processable materials.

quant-ph↗

arXiv2026

Optimally Driven Dressed Qubits

The applicability and performance of qubits dressed by classical fields are limited because their control protocols give rise to an undesired counter-rotating term (CRT). This in turn forces operation in a regime where a (dressed) rotating-wave approximation (RWA) is valid, thereby restricting key aspects of their operation. Here, using only a single coupling axis in the laboratory frame, we introduce a dressed-qubit control protocol that optimally removes the CRT, eliminating the need for the RWA and delivering substantial improvements in multiple performance metrics, including single-qubit gate speed, two-qubit gate fidelity, spectroscopic range, clock stability, and coherence preservation. In addition, we provide a general parameterization together with a Floquet-based coherence-time expression, which elucidates the protocol's working principles and lowers the barrier to adoption. Collectively, these advances position our scheme as the state-of-the-art strategy for qubit control, paving the way for a wider class of quantum technologies to be realized using dressed-qubit architectures.

quant-ph↗

arXiv2025

Robust gigahertz-range ac magnetometry with an ensemble of NV centers in diamond using concatenated continuous dynamical decoupling

Sub-picotesla level magnetometry has been demonstrated using negatively-charged nitrogen-vacancy (NV) centers in diamond by increasing the number of spins simultaneously used for sensing in an NV ensemble. However, such scale-up often introduces spatial inhomogeneities in detuning and control field amplitudes, which degrade sensitivity. Although several techniques have been utilized to overcome these challenges, including pulsed dynamical decoupling or shaped pulses, these are not generally compatible with the current state-of-the-art techniques for GHz-range AC magnetometry with NV ensembles, which are typically based on Rabi oscillations. In this work we experimentally demonstrate GHz-range AC magnetometry using a large ensemble of NV centers under spatially inhomogeneous drive fields by employing concatenated continuous dynamical decoupling, which is designed for robustness against such imperfections. We compare its performance with the conventional direct Rabi method and show that the robust dressed states in our method extend significantly the measuring range to weaker signals in GHz-range AC magnetometry.

quant-ph↗

arXiv2024

Direct measurement of energy transfer in strongly driven rotating turbulence

A short, abrupt increase in energy injection rate into steady strongly-driven rotating turbulent flow is used as a probe for energy transfer in the system. The injected excessive energy is localized in time and space and its spectra differ from those of the steady turbulent flow. This allows measuring energy transfer rates, in three different domains: In real space, the injected energy propagates within the turbulent field, as a wave packet of inertial waves. In the frequency domain, energy is transferred non-locally to the low, quasi-geostrophic modes. In wavenumber space, energy locally cascades toward small wavenumbers, in a rate that is consistent with two-dimensionsal (2D) turbulence models. Surprisingly however, the inverse cascade of energy is mediated by inertial waves that propagate within the flow with small, but non-vanishing frequency. Our observations differ from measurements and theoretical predictions of weakly driven turbulence. Yet, they show that in strongly-driven rotating turbulence, inertial waves play an important role in energy transfer, even at the vicinity of the 2D manifold.

physics.flu-dyn↗

arXiv2023

Protecting Quantum Information via Destructive Interference of Correlated Noise

Decoherence and imperfect control are crucial challenges for quantum technologies. Common protection strategies rely on noise temporal autocorrelation, which is not optimal if other correlations are present. We develop and demonstrate experimentally a strategy that utilizes the cross-correlation of two noise sources. We achieve a tenfold coherence time extension by destructive interference of cross-correlated noise, improve control fidelity, and surpass the state-of-the-art sensitivity for high frequency quantum sensing, significantly expanding the applicability of noise protection strategies.

quant-ph↗

arXiv2023

Coherent manipulation of nuclear spins in the strong driving regime

Spin-based quantum information processing makes extensive use of spin-state manipulation. This ranges from dynamical decoupling of nuclear spins in quantum sensing experiments to applying logical gates on qubits in a quantum processor. Here we present an antenna for strong driving in quantum sensing experiments and theoretically address challenges of the strong driving regime. First, we designed and implemented a micron-scale planar spiral RF antenna capable of delivering intense fields to a sample. The planar antenna is tailored for quantum sensing experiments using the diamond's nitrogen-vacancy (NV) center and should be applicable to other solid-state defects. The antenna has a broad bandwidth of 22 MHz, is compatible with scanning probes, and is suitable for cryogenic and ultrahigh vacuum conditions. We measure the magnetic field induced by the antenna and estimate a field-to-current ratio of $113\pm 16$ G/A, representing a x6 increase in efficiency compared to the state-of-the-art. We demonstrate the antenna by driving Rabi oscillations in $^1$H spins of an organic sample on the diamond surface and measure $^1$H Rabi frequencies of over 500 kHz, i.e., $\mathrmπ$-pulses shorter than 1 $μs$ - faster than previously reported in NV-based nuclear magnetic resonance (NMR). Finally, we discuss the implications of driving spins with a field tilted from the transverse plane in a regime where the driving amplitude is comparable to the spin-state splitting, such that the rotating wave approximation does not describe the dynamics well. We present a recipe to optimize pulse fidelity in this regime based on a phase and offset-shifted sine drive, that may be optimized without numerical optimization procedures or precise modeling of the experiment. We consider this approach in a range of driving amplitudes and show that it is particularly efficient in the case of a tilted driving field.

quant-ph↗

arXiv2023

Towards a unified picture of polarization transfer -- pulsed DNP and chemically equivalent PHIP

Nuclear spin hyperpolarization techniques, such as dynamic nuclear polarization (DNP) and parahydrogen-induced polarization (PHIP), have revolutionized nuclear magnetic resonance and magnetic resonance imaging. In these methods, a readily available source of high spin order, either electron spins in DNP or singlet states in hydrogen for PHIP, is brought into close proximity with nuclear spin targets, enabling efficient transfer of spin order under external quantum control. Despite vast disparities in energy scales and interaction mechanisms between electron spins in DNP and nuclear singlet states in PHIP, a pseudo-spin formalism allows us to establish an intriguing equivalence. As a result, the important low-field polarization transfer regime of PHIP can be mapped onto an analogous system equivalent to pulsed-DNP. This establishes a correspondence between key polarization transfer sequences in PHIP and DNP, facilitating the transfer of sequence development concepts. This promises fresh insights and significant cross-pollination between DNP and PHIP polarization sequence developers.

quant-ph↗

arXiv2022

Radio-Frequency Sweeps at μT Fields for Parahydrogen-Induced Polarization of Biomolecules

Magnetic resonance imaging of $^{13}$C-labeled metabolites enhanced by parahydrogen-induced polarization (PHIP) can enable real-time monitoring of processes within the body. We introduce a robust, easily implementable technique for transferring parahydrogen-derived singlet order into 13C magnetization using adiabatic radio-frequency sweeps at $μ$T fields. We experimentally demonstrate the applicability of this technique to several molecules, including some molecules relevant for metabolic imaging, where we show significant improvements in the achievable polarization, in some cases reaching above 60%. Furthermore, we introduce a site-selective deuteration scheme, where deuterium is included in the coupling network of a pyruvate ester to enhance the efficiency of the polarization transfer. These improvements are enabled by the fact that the transfer protocol avoids relaxation induced by strongly coupled quadrupolar nuclei.

physics.chem-ph↗

arXiv2021

Hyperpolarized solution-state NMR spectroscopy with optically polarized crystals

Nuclear spin hyperpolarization provides a promising route to overcome the challenges imposed by the limited sensitivity of nuclear magnetic resonance. Here we demonstrate that dissolution of spin-polarized pentacene-doped naphthalene crystals enables transfer of polarization to target molecules via intermolecular cross relaxation at room temperature and moderate magnetic fields (1.45$\,$T). This makes it possible to exploit the high spin polarization of optically polarized crystals while mitigating the challenges of its transfer to external nuclei, particularly of the large distances and prohibitively weak coupling between source and target nuclei across solid-solid or solid-liquid interfaces. With this method, here we inject the highly polarized mixture into a benchtop NMR spectrometer and observe the polarization dynamics for target $^1$H nuclei. Although the spectra are radiation damped due to the high naphthalene magnetization, we describe a procedure to process the data in order to obtain more conventional NMR spectra, and extract the target nuclei polarization. With the entire process occurring on a timescale of one minute, we observe NMR signals enhanced by factors between -200 and -1730 at 1.45$\,$T for a range of small molecules.

physics.chem-ph↗