SearcharxivSearch

arXiv subjects

Tim R. Eichhorn

Publications and source records attributed to Tim R. Eichhorn.

4 recordsLinked to original sources

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 ($\sim 1~μ$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

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

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

Optimizing the formation of depth-confined nitrogen vacancy center spin ensembles in diamond for quantum sensing

Spin ensembles of nitrogen vacancy (NV) centers in diamond are emerging as powerful spin-based sensors for magnetic, electric and thermal field imaging with high spatial and temporal resolution. Here we characterize the formation of depth-confined NV center ensembles, activated by electron irradiation in diamond layers grown by plasma enhanced chemical vapor deposition with nitrogen co-doping. To do so, we exploit the high magnetic sensitivity of ensembles of NV centers to probe their spin environment as a function of growth and irradiation parameters. We engineer an NV ensemble whose magnetic sensitivity is within a factor of two of the static NV-NV dipolar interaction limit, thus demonstrating a powerful platform for quantum sensing.

cond-mat.mtrl-sci