Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:2509.23170

Room-temperature quantum entanglement in a van der Waals material

Xingyu Gao, Ge, Zhun, Saakshi Dikshit, Sumukh Vaidya, Peng Ju, Tongcang Li

Published Sep 27, 2025• 0 citations
arXivHTMLPDF

Abstract

Entanglement is central to quantum science and technology. Atomic defects in two-dimensional (2D) van der Waals (vdW) materials offer exciting prospects for quantum sensing, with spatial resolution reaching 1 nm demonstrated using scanning probe techniques. However, entangling qubits in vdW materials remains elusive. Here we report room-temperature quantum entanglement between an optically addressable electron spin and a strongly coupled $^{13}$C nuclear spin in hexagonal boron nitride (hBN). We extend the electron spin coherence to 38 $μ$s with dynamical decoupling, and create maximally entangled Bell states with a fidelity up to 0.89. We further use the nuclear spin as a long-lived quantum memory to enhance AC magnetic field sensing via correlation spectroscopy. These results establish entangled spin qubits in hBN as a robust platform for advanced quantum technologies based on 2D materials.

DOI
10.48550/arxiv.2509.23170

Related papers

Room-Temperature Electrical Readout of Spin Defects in van der Waals Materials

Shihao Ru, Liheng An, Haidong Liang +14 more

Negatively charged boron vacancy ($\mathrm{V_B^-}$) in hexagonal boron nitride (hBN) is the most extensively studied room-temperature quantum spin system in two-dimensional (2D) materials. Nevertheless, the current effective readout of $\mathrm{V_B^-}$ spin states is carried out by systematically optical methods. This limits their exploitation in compact and miniaturized quantum devices, which would otherwise hold substantial promise to address quantum sensing and quantum information tasks. In this study, we demonstrated a photoelectric spin readout technique for $\mathrm{V_B^-}$ spins in hBN. The observed photocurrent signals stem from the spin-dependent ionization dynamics of boron vacancies, mediated by spin-dependent non-radiative transitions to a metastable state. We further extend this electrical detection technique to enable the readout of dynamical decoupling sequences, including the Carr-Purcell-Meiboom-Gill (CPMG) protocols, and of nuclear spins via electron-nuclear double resonance. These results provide a pathway toward on-chip integration and real-field exploitation of quantum functionalities based on 2D material platforms.

quant-pharXiv:2511.08874•Nov 13, 2025

Room-Temperature Storage of Entanglement in a Silicon Carbide Quantum Node

Shuo Ren, Rui-Jian Liang, Qi-Cheng Hu +8 more

Robust entanglement at room temperature is a central challenge for solid-state quantum information processing and quantum-enhanced sensing. Here we demonstrate room-temperature storage of entanglement in a silicon carbide (SiC) quantum node by coherently transferring an electron-nuclear entangled state onto long-lived nuclear-spin memory qubits. Using a shallow single color center in 4H-SiC, conventionally denoted PL6, we realize a fully addressable three-qubit register composed of one electron-spin processor and two strongly coupled $^{29}$Si nuclear-spin memory qubits. This platform enables the deterministic generation of high-fidelity entangled states, including a nuclear-spin Bell state with a fidelity of $94 \pm 2\%$ and a three-qubit Greenberger-Horne-Zeilinger (GHZ)-type state with a fidelity of $89 \pm 4\%$. By implementing a SWAP-gate protocol in the strong hyperfine-coupling regime, the electron-nuclear entanglement is transferred to the nuclear-spin memory with a fidelity of $92.5 \pm 2.5\%$, extending the entanglement lifetime by a factor of 240. We further confirm the generality of this approach in an additional heterogeneous $^{29}$Si-$^{13}$C nuclear-spin register and, through a statistical survey of 200 single PL6 centers, show that multi-nuclear-spin registers occur naturally with probabilities above 10%. These results position shallow SiC color centers as a powerful platform for entanglement-assisted quantum sensing and scalable room-temperature quantum technologies.

quant-pharXiv:2609.13744•Physical Review Letters•Sep 15, 2026•0 citations

Tuning Boron-Vacancy Qubit Coherence through Layer Number in hBN

Juan M. Florez, Eric Suárez Morell

The negatively charged boron vacancy ($\VB$) in hexagonal boron nitride (\hBN{}) was the first optically addressable spin qubit identified inside a van der Waals crystal, allowing atomically defined placement relative to a target. Its coherence in bulk \hBN{} is limited by the boron nuclei of the layers flanking the defect plane, which a thin flake removes. Here, we use a generalized cluster-correlation expansion with an extended central-spin block to calculate the Hahn-echo coherence time of $\VB$ in h$^{11}$B$^{15}$N as a function of layer number. Our results show that $T_2$ rises from $199\ns$ in the bulk limit to $653\ns$ in a monolayer, a factor of $3.3$ that is already saturated at three layers and that a sublattice decomposition attributes entirely to boron. The enhancement is confined to low field, is insensitive to stacking registry and twist angle, and requires alignment to within about two degrees, an onset we reproduce with no free parameters. Under dynamical decoupling, a $1/e$ threshold returns $206\ns$ for every thickness, but this is a zero of the first-shell modulation rather than a decay: measured without a threshold, the layer contrast survives and reaches a factor of $170$. Layer number thus emerges as a design parameter for $\VB$-based sensing.

cond-mat.mes-hallCross-listedarXiv:2609.01812•Sep 3, 2026

Optically Addressable Molecular Spins at 2D Surfaces

Xuankai Zhou, Yan-Tung Kong, Cheuk Kit Cheung +18 more

Optically addressable spins at material surfaces have represented a long-standing ambition in quantum sensing, providing atomic resolution and quantum-limited sensitivity. However, they are constrained by a finite depth at which the quantum spins can be stabilized. Here, we demonstrate a hybrid molecular-2D architecture that realizes quantum spin sensors directly on top of the surface. By anchoring spin-active molecules onto hexagonal boron nitride (hBN), we eliminate the depth of the quantum sensor while also exhibiting robust spin properties from 4~K to room temperature (RT). The Hahn-echo spin coherence time exceeds \(T_2 = 3.4~\upmu\text{s}\) at 4~K, outperforming values in bulk organic crystals and overturning the prevailing expectation that spin inevitably deteriorates upon approaching the surface. By chemically tuning the molecule through deuteration, \(T_2\) improves by more than 10-fold, and under dynamic decoupling, coherence is prolonged to the intrinsic lifetime limit, exceeding 300~\(\upmu\text{s}\). Proximal proton spins and the magnetic response of two-dimensional magnets beneath the hBN layer have been detected at RT. These molecular spins form surface quantum sensors with long coherence, optical addressability, and interfacial versatility, enabling a scalable, adaptable architecture beyond what conventional solid-state platforms offer.

quant-pharXiv:2601.19988•Jan 29, 2026

A Surface-Scaffolded Molecular Qubit

Tian-Xing Zheng, M. Iqbal Bakti Utama, Xingyu Gao +24 more

Fluorescent spin qubits are central building blocks of quantum technologies. Placing these qubits at surfaces maximizes coupling to nearby spins and fields, enabling nanoscale sensing and facilitating integration with photonic and superconducting devices. However, reducing the dimensions or size of established qubit systems without sacrificing the qubit performance or degrading the coherence lifetime remains challenging. Here, we introduce a surface molecular qubit formed by pentacene molecules scaffolded on a two-dimensional (2D) material, hexagonal boron nitride (hBN). The qubit exhibits stable fluorescence and optically detected magnetic resonance (ODMR) from cryogenic to ambient conditions. With fully deuterated pentacene, the Hahn-echo coherence reaches 22 $μ$s and further extends to 214 $μ$s under dynamical decoupling, outperforming state-of-the-art shallow NV centers in diamond, despite being positioned directly on the surface. We map the local spin environment, resolving couplings to nearby nuclear and electron spins that can serve as auxiliary quantum resources. This platform combines true surface integration, long qubit coherence, and scalable fabrication, opening routes to quantum sensing, quantum simulation, and hybrid quantum devices. It also paves the way for a broader family of 2D material-supported molecular qubits.

quant-pharXiv:2601.19976•Jan 29, 2026

Room-temperature hybrid 2D-3D quantum spin system for enhanced magnetic sensing and many-body dynamics

Haoyu Sun, Pei Yu, Xu Zhou +10 more

Abstract Advances in hybrid quantum systems and their precise control are pivotal for developing advanced quantum technologies. Two-dimensional (2D) materials with optically accessible spin defects have emerged as a promising platform for building integrated quantum spin systems due to their exceptional flexibility and scalability. However, experimentally realizing such systems and demonstrating their superiority remains challenging. Here, we present a hybrid spin system operating under ambient conditions, integrating boron vacancy ( $${{\rm{V}}}_{{\rm{B}}}^{-}$$ V B − ) spins in 2D hexagonal boron nitride flakes with a single nitrogen vacancy (NV) center in 3D single-crystal diamonds. This combined system achieves full controllability and exhibits enhanced performance for nanoscale magnetic sensing, including an improved dynamic range. Moreover, we investigate the rich many-body spin dynamics within the hybrid system, which enables us to estimate the concentration of $${{\rm{V}}}_{{\rm{B}}}^{-}$$ V B − spins. This work provides a critical foundation for advancing the development of 2D-3D integrated quantum spin systems.

arXiv:2504.10815•npj Quantum Information•Dec 6, 2025•2 citations
Entanglement is central to quantum science and technology. Atomic defects in two-dimensional (2D) van der Waals (vdW) materials offer exciting prospects for quantum sensing, with spatial resolution reaching 1 nm demonstrated using scanning probe techniques. However, entangling qubits in vdW materials remains elusive. Here we report room-temperature quantum entanglement between an optically addressable electron spin and a strongly coupled 13^{13}13C nuclear spin in hexagonal boron nitride (hBN). We extend the electron spin coherence to 38 μμμs with dynamical decoupling, and create maximally entangled Bell states with a fidelity up to 0.89. We further use the nuclear spin as a long-lived quantum memory to enhance AC magnetic field sensing via correlation spectroscopy. These results establish entangled spin qubits in hBN as a robust platform for advanced quantum technologies based on 2D materials.
Negatively charged boron vacancy (VB−\mathrm{V_B^-}VB−​) in hexagonal boron nitride (hBN) is the most extensively studied room-temperature quantum spin system in two-dimensional (2D) materials. Nevertheless, the current effective readout of VB−\mathrm{V_B^-}VB−​ spin states is carried out by systematically optical methods. This limits their exploitation in compact and miniaturized quantum devices, which would otherwise hold substantial promise to address quantum sensing and quantum information tasks. In this study, we demonstrated a photoelectric spin readout technique for VB−\mathrm{V_B^-}VB−​ spins in hBN. The observed photocurrent signals stem from the spin-dependent ionization dynamics of boron vacancies, mediated by spin-dependent non-radiative transitions to a metastable state. We further extend this electrical detection technique to enable the readout of dynamical decoupling sequences, including the Carr-Purcell-Meiboom-Gill (CPMG) protocols, and of nuclear spins via electron-nuclear double resonance. These results provide a pathway toward on-chip integration and real-field exploitation of quantum functionalities based on 2D material platforms.
Robust entanglement at room temperature is a central challenge for solid-state quantum information processing and quantum-enhanced sensing. Here we demonstrate room-temperature storage of entanglement in a silicon carbide (SiC) quantum node by coherently transferring an electron-nuclear entangled state onto long-lived nuclear-spin memory qubits. Using a shallow single color center in 4H-SiC, conventionally denoted PL6, we realize a fully addressable three-qubit register composed of one electron-spin processor and two strongly coupled 29^{29}29Si nuclear-spin memory qubits. This platform enables the deterministic generation of high-fidelity entangled states, including a nuclear-spin Bell state with a fidelity of 94±2%94 \pm 2\%94±2% and a three-qubit Greenberger-Horne-Zeilinger (GHZ)-type state with a fidelity of 89±4%89 \pm 4\%89±4%. By implementing a SWAP-gate protocol in the strong hyperfine-coupling regime, the electron-nuclear entanglement is transferred to the nuclear-spin memory with a fidelity of 92.5±2.5%92.5 \pm 2.5\%92.5±2.5%, extending the entanglement lifetime by a factor of 240. We further confirm the generality of this approach in an additional heterogeneous 29^{29}29Si-13^{13}13C nuclear-spin register and, through a statistical survey of 200 single PL6 centers, show that multi-nuclear-spin registers occur naturally with probabilities above 10%. These results position shallow SiC color centers as a powerful platform for entanglement-assisted quantum sensing and scalable room-temperature quantum technologies.
The negatively charged boron vacancy ($\VB$) in hexagonal boron nitride (\hBN{}) was the first optically addressable spin qubit identified inside a van der Waals crystal, allowing atomically defined placement relative to a target. Its coherence in bulk \hBN{} is limited by the boron nuclei of the layers flanking the defect plane, which a thin flake removes. Here, we use a generalized cluster-correlation expansion with an extended central-spin block to calculate the Hahn-echo coherence time of $\VB$ in h11^{11}11B15^{15}15N as a function of layer number. Our results show that T2T_2T2​ rises from $199\ns$ in the bulk limit to $653\ns$ in a monolayer, a factor of 3.33.33.3 that is already saturated at three layers and that a sublattice decomposition attributes entirely to boron. The enhancement is confined to low field, is insensitive to stacking registry and twist angle, and requires alignment to within about two degrees, an onset we reproduce with no free parameters. Under dynamical decoupling, a 1/e1/e1/e threshold returns $206\ns$ for every thickness, but this is a zero of the first-shell modulation rather than a decay: measured without a threshold, the layer contrast survives and reaches a factor of 170170170. Layer number thus emerges as a design parameter for $\VB$-based sensing.
Optically addressable spins at material surfaces have represented a long-standing ambition in quantum sensing, providing atomic resolution and quantum-limited sensitivity. However, they are constrained by a finite depth at which the quantum spins can be stabilized. Here, we demonstrate a hybrid molecular-2D architecture that realizes quantum spin sensors directly on top of the surface. By anchoring spin-active molecules onto hexagonal boron nitride (hBN), we eliminate the depth of the quantum sensor while also exhibiting robust spin properties from 4~K to room temperature (RT). The Hahn-echo spin coherence time exceeds \(T_2 = 3.4~\upmu\text{s}\) at 4~K, outperforming values in bulk organic crystals and overturning the prevailing expectation that spin inevitably deteriorates upon approaching the surface. By chemically tuning the molecule through deuteration, T2T_2T2​ improves by more than 10-fold, and under dynamic decoupling, coherence is prolonged to the intrinsic lifetime limit, exceeding 300~\(\upmu\text{s}\). Proximal proton spins and the magnetic response of two-dimensional magnets beneath the hBN layer have been detected at RT. These molecular spins form surface quantum sensors with long coherence, optical addressability, and interfacial versatility, enabling a scalable, adaptable architecture beyond what conventional solid-state platforms offer.
Fluorescent spin qubits are central building blocks of quantum technologies. Placing these qubits at surfaces maximizes coupling to nearby spins and fields, enabling nanoscale sensing and facilitating integration with photonic and superconducting devices. However, reducing the dimensions or size of established qubit systems without sacrificing the qubit performance or degrading the coherence lifetime remains challenging. Here, we introduce a surface molecular qubit formed by pentacene molecules scaffolded on a two-dimensional (2D) material, hexagonal boron nitride (hBN). The qubit exhibits stable fluorescence and optically detected magnetic resonance (ODMR) from cryogenic to ambient conditions. With fully deuterated pentacene, the Hahn-echo coherence reaches 22 μμμs and further extends to 214 μμμs under dynamical decoupling, outperforming state-of-the-art shallow NV centers in diamond, despite being positioned directly on the surface. We map the local spin environment, resolving couplings to nearby nuclear and electron spins that can serve as auxiliary quantum resources. This platform combines true surface integration, long qubit coherence, and scalable fabrication, opening routes to quantum sensing, quantum simulation, and hybrid quantum devices. It also paves the way for a broader family of 2D material-supported molecular qubits.
Abstract Advances in hybrid quantum systems and their precise control are pivotal for developing advanced quantum technologies. Two-dimensional (2D) materials with optically accessible spin defects have emerged as a promising platform for building integrated quantum spin systems due to their exceptional flexibility and scalability. However, experimentally realizing such systems and demonstrating their superiority remains challenging. Here, we present a hybrid spin system operating under ambient conditions, integrating boron vacancy ( VB−{{\rm{V}}}_{{\rm{B}}}^{-}VB−​ V B − ) spins in 2D hexagonal boron nitride flakes with a single nitrogen vacancy (NV) center in 3D single-crystal diamonds. This combined system achieves full controllability and exhibits enhanced performance for nanoscale magnetic sensing, including an improved dynamic range. Moreover, we investigate the rich many-body spin dynamics within the hybrid system, which enables us to estimate the concentration of VB−{{\rm{V}}}_{{\rm{B}}}^{-}VB−​ V B − spins. This work provides a critical foundation for advancing the development of 2D-3D integrated quantum spin systems.