
==== Front
Nat Commun
Nat Commun
Nature Communications
2041-1723
Nature Publishing Group UK London

39261483
52270
10.1038/s41467-024-52270-0
Article
Coherent spin dynamics between electron and nucleus within a single atom
http://orcid.org/0000-0002-3854-0673
Veldman Lukas M. 1
http://orcid.org/0009-0004-9582-7058
Stolte Evert W. 1
http://orcid.org/0009-0003-7929-299X
Canavan Mark P. 1
http://orcid.org/0000-0001-6684-5979
Broekhoven Rik 1
http://orcid.org/0000-0002-7215-8419
Willke Philip 2
http://orcid.org/0000-0002-5119-7013
Farinacci Laëtitia 1
http://orcid.org/0000-0003-0781-8537
Otte Sander a.f.otte@tudelft.nl

1
1 https://ror.org/02e2c7k09 grid.5292.c 0000 0001 2097 4740 Department of Quantum Nanoscience, Kavli Institute of Nanoscience, Delft University of Technology, Delft, The Netherlands
2 https://ror.org/04t3en479 grid.7892.4 0000 0001 0075 5874 Physikalisches Institut, Karlsruhe Institute of Technology, Karlsruhe, Germany
11 9 2024
11 9 2024
2024
15 795111 6 2024
30 8 2024
© The Author(s) 2024
2024
https://creativecommons.org/licenses/by-nc-nd/4.0/ Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
The nuclear spin, being much more isolated from the environment than its electronic counterpart, presents opportunities for quantum experiments with prolonged coherence times. Electron spin resonance (ESR) combined with scanning tunnelling microscopy (STM) provides a bottom-up platform to study the fundamental properties of nuclear spins of single atoms on a surface. However, access to the time evolution of nuclear spins remained a challenge. Here, we present an experiment resolving the nanosecond coherent dynamics of a hyperfine-driven flip-flop interaction between the spin of an individual nucleus and that of an orbiting electron. We use the unique local controllability of the magnetic field emanating from the STM probe tip to bring the electron and nuclear spins in tune, as evidenced by a set of avoided level crossings in ESR-STM. Subsequently, we polarize both spins through scattering of tunnelling electrons and measure the resulting free evolution of the coupled spin system using a DC pump-probe scheme. The latter reveals a complex pattern of multiple interfering coherent oscillations, providing unique insight into hyperfine physics on a single atom level.

Advancing single-atom quantum information processing necessitates a deep understanding of electron and nuclear spin dynamics. Here, using pump-probe spectroscopy, the authors detect the coherent dynamics of a nuclear and electron spin of a single hydrogenated Ti atom on MgO surface.

Subject terms

Magnetic properties and materials
Quantum information
https://doi.org/10.13039/501100003246 Nederlandse Organisatie voor Wetenschappelijk Onderzoek (Netherlands Organisation for Scientific Research) VI.C.182.016 Otte Sander https://doi.org/10.13039/100010663 EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101095574 Otte Sander https://doi.org/10.13039/501100001659 Deutsche Forschungsgemeinschaft (German Research Foundation) WI5486/1-1 Willke Philip issue-copyright-statement© Springer Nature Limited 2024
==== Body
pmcIntroduction

Nuclear spins have shown great promise as building blocks for quantum information in molecular spin qubits1,2, NV centers3,4, and donors in silicon5. They are also an excellent resource for quantum simulation6, magnetic sensing7,8 and spintronics9, and are potentially scalable via engineered molecular and atomic networks10,11. Their key advantage arises from their longer coherence times compared to their electron spin counterpart12, though the intricacies of the decoherence channels depend on the exact interaction with the environment which is hard to control in ensemble averaging techniques. Scanning tunneling microscopy (STM) constitutes an excellent means of investigation here, as it permits to address individual electron spins in electron spin resonance (ESR) experiments with sub-nanometer resolution13,14, offering atomically precise information on their environment15,16, and providing a pathway towards coherent control of the spins states17,18. In recent years, interactions involving the nuclear spin were measured indirectly by probing the hyperfine coupling in ESR-STM between the nucleus and the surrounding electrons19. In addition, the nuclear spin of individual Cu atoms could be polarized via spin pumping induced by the spin-polarized tunneling current20. However, accessing the coherent dynamics involving the nucleus remained challenging, due to its weak coupling to the tunneling electrons.

In this work, we show the free, coherent evolution between the nuclear spin and the electron spin in a single hydrogenated titanium atom. By fine-tuning the electronic Zeeman energy using the local field of the probe tip21, we identify a parameter space where electronic and nuclear spin states hybridize. In a second step, we probe the free coherent evolution of the coupled system by electric DC pump-probe experiments22. Here, we reveal an emerging beating pattern, that originates from multiple quantum oscillations with different frequencies at the points of hybridization.

We use a commercial low-temperature STM equipped with high frequency cabling to send both RF signals and nanosecond DC pulses down to the tip. The sample system consists of Ti atoms deposited on bilayer MgO islands grown on Ag(100), that become hydrogenated by residual hydrogen15,16. For all measurements, we use spin-polarized tips that are created by picking up co-deposited Fe atoms onto the tip apex. We study individual Ti adsorbed onto the oxygen sites of MgO – well-isolated from neighboring spins using atom manipulation (Fig. 1a) – which exhibit an effective electron spin S^ with magnitude S = ½15 and an anisotropic g-factor g16. Throughout this work, we focus on 47Ti isotopes, which carry a nuclear spin I^ with magnitude I = 5/2. Along the principal axes of the crystal field (x,y,z, with z out of plane), the system is described by the following Hamiltonian:﻿1 H^=∑i=x,y,zμBgiBext,i+Btip,iS^i+AiS^iI^i+QiI^i2

where μB is the Bohr magneton, and Α and Q (see Supplementary Note 3)19 are the hyperfine coupling and quadrupole contributions, respectively. The first term describes the Zeeman energy of the electron spin with contributions from both the external Bext and the tip-induced magnetic field Btip. We neglect the effect of either of these fields on the nuclear spin, since their contributions are small compared to the other terms. In Fig. 1b we show the general behavior of the interplay between the hyperfine coupling and an external magnetic field. In the low field regime, the hyperfine coupling energy dominates and the system displays avoided crossings between the different energy levels indicating superposition states. In the high field regime, we retrieve the Zeeman spin states as eigenstates.Fig. 1 Single atom nuclear polarization.

a STM topography of the single 47Ti studied in this work. A schematic drawing shows the magnetic STM tip above the electron spin (blue) and nuclear spin (red) of the single atom. b Energy diagram of the spin states of a single 47Ti. In the low field regime, avoided crossings appear between the different eigenstates. In the high field regime, the eigenstates resemble Zeeman product states. ESR transitions (purple arrows) can be driven between states with equal nuclear spin. c ESR-STM measurements at different applied DC bias (T = 1.5 K, Bext = 1.5 T, VRF = 25 mV, Iset = 2.5 pA, f0 = 11.5–12.56 GHz). The observed variation in resonance frequency f0 likely results from a combination of the tip field changing with tip height and a voltage dependence of the resonance28. Line traces at 35 mV, 80 mV, and 120 mV are shown with fits using six Fano lineshapes scaled by the Boltzmann factor in order to extract an effective temperature.

Results

State initialization via spin pumping

We start our investigation by applying a magnetic field of 1.5 T, which is large compared to the hyperfine interaction, in order to drive ESR transitions between the individual spin states of a 47Ti atom. Similar to measurements of Ti on a bridge binding site of MgO23,24, we find a large anisotropy in the hyperfine coupling A = [11, 11, 128] ± 2 ΜΗz (see Supplementary Note 4 and Supplementary Fig. 3). Since we aim for a regime in which the hyperfine interaction competes with the Zeeman splitting of the electron, the experiments are performed with an out-of-plane magnetic field.

For certain magnetic tips (see Supplementary Note 1), we observe that the hyperfine-split ESR peaks have different intensities, which indicates a strong polarization of the nuclear spin. This effect is well known in bulk NMR techniques as hyperpolarization25,26 and has been observed before on the atomic scale for single Cu atoms on MgO20. The phenomenon is explained by taking into account inelastic spin scattering events between the tunneling electrons and electron spin which are transmitted to the nucleus via the hyperfine flip-flop interaction. As shown in Fig. 1c, we find that the polarization is strongly dependent on the applied bias voltage while measuring at constant current. We believe that this may be due to the bias-dependent efficiency of the spin scattering channels involved, but a more complex mechanism involving the Ti orbital excitation16 or Pauli spin blockade27 may be at play. We find that the effective temperature of the nuclear spin population drops below 10 mK at voltages larger than 100 mV, more than two orders of magnitude lower than the actual experimental temperature of 1.5 K. While the effect of nuclear spin pumping has been observed for Cu on MgO, we here utilize it to overcome a major limitation: in previous ESR-STM experiments, the frequency ranges investigated were chosen to be compatible with sufficient spin population contrast set by the Boltzmann distribution at the experimental temperature. Finally, we point out that high bias voltages are key for efficient nuclear spin pumping, which – with few exceptions28 – has usually not been used in previous experiments involving Ti on MgO.

Tuning electron-nuclear spin entanglement

Owing to the spin pumping we can investigate a much lower frequency regime, down to ~50 MHz, in which the level of entanglement between the electron and nuclear spins can be tuned. In Fig. 2a, we show the different calculated contributions to the energy diagram of a 47Ti in a low-field regime. For the calculations we use A = [10,10,130] MHz and Q = [1.5,1.5,−3] MHz in accordance with the measurements performed in a vector field (see Supplementary Note 3). When the total electronic Zeeman energy – due to the external and tip magnetic field – is comparable to the hyperfine splitting, multiple avoided level crossings occur in the spectrum. The number of avoided crossings has increased compared to Fig. 1b which is due to a misalignment between the external field and the tip field. More precisely, an additional avoided crossing appears around Btip = 23 mT, involving a superposition of states that differ only in the electron spin projection, while the nuclear spin is the same. This electron-only hybridization will be of importance below.Fig. 2 ESR and NMR-type measurements in the low-field regime.

a Energy diagram of the atomic eigenstates as a function of hyperfine coupling, quadrupole moment, external and tip-induced magnetic field. For details on the calculations of the eigenstates, see Supplementary Note 3. b ESR-STM measurements (T = 400 mK, Bext = 20 mT, VRF = 40 mV, Iset = 2 pA, Vset = 40–200 mV) as function of tip-sample conductance. As indicated with icons, tip-sample separation decreases towards the right side of the plot, corresponding to an increasing tip-induced magnetic field. Both ESR and NMR-type transitions are observed and indicated as such. The bottom close-up is a separate dataset showing the splitting of the NMR transitions and a curve upwards of the bottom ESR transition signaling the avoided level crossing. Each trace is normalized and the average value is subtracted in order to compensate for the bias-dependent rectification current. c Separate ESR dataset (T = 400 mK, Bext = 20 mT, VRF = 40 mV, Iset = 2 pA, Vset = 100–190 mV) zoomed in to marked region of (b). d Simulations of the ESR-STM measurements (see Methods), where we consider the tip field to make an 8° angle with the out-of-plane external field. e Zoom-in to marked region of (d).

We identify these tuning points in our experiment by performing ESR measurements in the low field regime using an external field of merely 20 mT (Fig. 2b). Here, in order to fine-tune the coupled spin system, we vary the tip-induced magnetic field by changing the DC voltage while keeping the current constant. This effectively tunes the junction conductance G. At relatively large tip fields (G ≥ 20 pS) multiple ESR peaks are visible in addition to several very sharp (~3 MHz) NMR type resonances around 60 MHz. Below G ≈ 20 pS, the ESR and NMR transitions start to mix and overlap, accompanied by a redistribution of their intensities as shown in the close-up measurements in Fig. 2c. This is consistent with the presence of avoided level crossings between the energy levels, as expected from Fig. 2a and modeled in Fig. 2d, e. In Fig. 2c, we also observe that the NMR type resonances are split into multiple peaks. We attribute this to the quadrupole interaction that slightly shifts the energy of each nuclear spin state19. For the simulations we consider both ESR and NMR transitions with separately scaled intensities (see Supplementary Note 5).

Probing coherent spin dynamics

Having identified 10–20 pS as the appropriate tip-atom distances for inducing superposition states, we perform DC pump-probe experiments to explore the coupled spin dynamics. In order to increase signal amplitudes, we decrease the external field to 15 mT so that the superposition states are induced at closer tip-atom distances while using the same microtip. We use a two-pulse pumping sequence (see Supplementary Note 6 and Supplementary Fig. 4) to initialize both electron and nuclear spin states. During the pump pulses, spin-polarized electrons cause spin-flip excitations in the atom by scattering with the atom’s electron spin29. Due to the hyperfine coupling, the excitations will also affect the nuclear spin, polarizing it in the same direction20. Consequently, the combined system will be projected to a Zeeman state, ∣↓,−5/2⟩ which is not necessarily a stationary eigenstate of the Hamiltonian of Eq. (1). To probe any dynamics that might occur after the pump pulses, we then let the system evolve freely during a waiting time after which the electron spin is read out by a 5 ns probe pulse. By varying the waiting time over the course of many iterations, the dynamic evolution of the electron spin is measured8.

Using this pulse scheme we observe electron spin dynamics that, as shown in Fig. 3a, depend on the tip magnetic field. When the STM tip is close (i.e., at large conductance values) we observe fast, low-amplitude oscillations that become slower and stronger as the tip is retracted. This is the expected behavior when the system moves through an avoided crossing22. However, near G = 17 pS a beating pattern appears due to interference with a second frequency. At this point, the dynamics also appear to be longer lived compared to the single-frequency oscillation. Upon further retraction of the tip, below G = 15 pS, no spin dynamics are detected anymore. The observed dynamics occur at slightly higher conductance values compared to the detected avoided crossing measured using ESR in Fig. 2. We attribute this difference to both the slightly lower external field used for the pump-probe measurements as well as the absence of a DC bias voltage in the pump-probe experiment, which has been shown to shift the electron energy levels28.Fig. 3 Free evolution measurements and Lindblad simulations.

a Pump-probe data for different tip-atom distances set by the junction conductance (Vset = 130 mV, T = 400 mK, B = 15 mT, for details on the pulse scheme, see Supplementary Note 7). b Liouville-von Neumann simulation of the free time evolution of the electron spin when initialized to ∣↓,−5/2⟩. Simulation is convolved with a 2 mT Gaussian in the tip-field axis to simulate level broadening due to mechanical vibrations of the tip. c Corresponding simulation of the free time evolution of the nuclear spin, revealing the observed electron spin oscillations being accompanied by nuclear spin fluctuations. The calculations also show the onset of an additional oscillation in the nuclear spin at ~13 mT. However, since the period is an order of magnitude longer than the coherence time of the electron spin, it is not visible in our measurements.

Figure 3b, c show the simulated time evolution of the Sz and Iz expectation values for the electron and the nuclear spin, respectively. The calculations are performed considering the Hamiltonian shown in Eq. (1) and using the Liouville-von Neumann equation starting from the ∣↓,−5/2⟩ state30. We find excellent agreement between the data from the experiment and the electronic spin calculations, with, in particular, a beating pattern that arises when the electron and nucleus states are entangled. While the electron shows an interference pattern, the simulation shows that the dynamics of the nuclear spin are dominated by an oscillation with approximate period 40 ns.

To understand the origin of the different oscillations, we further analyze the composition of the three states forming the avoided crossings: energy eigenstates ∣4⟩, ∣5⟩ and ∣6⟩. In Fig. 4a, we show an enhanced view of the relevant region of the eigenstate energies marked by the gray box in Fig. 2a. We then take two exemplary traces from the pump-probe data presented in Fig. 3a and match the frequencies present in the spin dynamics to the energy splitting between the eigenstates. From the composition of the eigenstates at these particular tip-field amplitudes we derive the nature of the different dynamics (see Supplementary Note 3).Fig. 4 Origin of the beating pattern.

a Zoom-in on the relevant avoided level crossings of Fig. 2a. The Bloch spheres illustrate the dominating dynamics arising from the superpositions of the corresponding states. b Fit to a line trace from the pump-probe data from Fig. 3a showing a beating pattern (G = 17.7 pS). The pattern arises from two dominating frequencies and their sum frequency. c Fit to a line trace from the pump-probe data from Fig. 3a showing a single frequency oscillation (G = 21.5 pS). d Reduced density matrix of the initial state ∣↓,−5/2⟩ at 20.5 mT tip field. e Reduced density matrix of the initial state ∣↓,−5/2⟩ at 23.7 mT tip field.

At a relatively large setpoint conductance of 21.5 pS, the pump-probe data fitted in Fig. 4c show a single damped sinusoid of roughly 75 MHz. This frequency matches both the energy of the lowest ESR transition measured at the avoided crossing point in Fig. 2b as well as the calculated energy splitting between states ∣5⟩ and ∣6⟩ at the relatively large tip field of roughly 24 mT (rightmost dotted line in Fig. 4a). At this field, states ∣5⟩ and ∣6⟩ are split in energy by the in-plane component of the tip field and approximate the spin superposition states ∣↑,−5/2⟩±∣↓,−5/2⟩ (see Supplementary Fig. 2). Therefore, the reduced density matrix of the initial state ∣↓,−5/2⟩, shown in Fig. 4e, is dominated by coherences in the subspace between states ∣5⟩ and ∣6⟩. We can thus attribute the dominant frequency in the dynamics to a Larmor precession of the electron spin due to the in-plane component of the tip field as depicted in the top Bloch sphere in Fig. 4a.

In contrast, at a setpoint conductance of 17.7 pS, we need three damped sinusoids to fit the data shown in Fig. 4b: two independent frequencies, 65.9 MHz and 19.8 MHz as well as their sum. These frequencies match the energy splitting between the three states ∣4⟩, ∣5⟩ and ∣6⟩ at roughly 20 mT (leftmost dotted line in Fig. 4a). The reduced density matrix of the initial state at this field, shown in Fig. 4d, show finite coherences between all three states. This means that in addition to the Larmor contribution described above, there are two additional terms. One is a flip-flop dynamic between electron and nucleus as the subspace between states ∣4⟩ and ∣5⟩ is dominated by ∣↑,−5/2⟩±∣↓,−3/2⟩ (middle Bloch sphere in Fig. 4a). The other is an oscillation of the nuclear spin as the subspace between states ∣4⟩ and ∣6⟩ is dominated by ∣↓,−5/2⟩±∣↓,−3/2⟩ (bottom Bloch sphere in Fig. 4a).

The reduced coupling of the nuclear spin to the environment, compared to the dynamics of only the electron spin, is expected to result in an enhanced coherence time8,31,32. Indeed, fits to the data shown in Fig. 4b result in an effective coherence time of 84 ± 5 ns, whereas the oscillation in Fig. 4c has an effective coherence time of only 22 ± 1 ns. However, we point out that this is only a lower limit to the intrinsic coherence time of the combined electron-nucleus spin system. We believe that the main source of spin decoherence in our experiment is fluctuations of the magnetic field emanating from the tip caused by mechanical vibrations in the setup on the sub-picometer scale. The observed changes in coherence time may in part result from a decreased sensitivity to this magnetic tip field noise since the energy levels in Fig. 4a diverge less at 21 mT than at 23 mT, akin to a clock-transition33,34. We expect that eliminating these vibrations may result in longer coherence times in pump-probe measurements.

Discussion

Developing single-atom quantum information processing requires thorough understanding of the underlying electron and nuclear spin dynamics. This demands initialization, tuning and readout tailored on the atomic length scale. Using pump-probe spectroscopy, we revealed the collective coherent dynamics of the internal spin dynamics inside a single atom. The magnetized STM tip functioned in this work as a control knob to locally tune the nature of these dynamics. This technique has the potential to be extended to a great variety of on-surface atomic or molecular spin system. Moreover, the prospect of STM for engineering bottom-up atomic designer assemblies can provide an integral atomic-scale understanding into the fundamentals of complex coherent spin dynamics.

Methods

Extended information on used methods is provided in Supplementary Information.

Supplementary information

Supplementary Information

Peer Review File

Supplementary information

The online version contains supplementary material available at 10.1038/s41467-024-52270-0.

Acknowledgements

This work was supported by the Dutch Research Council (NWO Vici Grant VI.C.182.016) and by the European Research Council (ERC Advanced Grant No. 101095574 “HYPSTER”). P.W. acknowledges funding from the Emmy Noether Programme of the DFG (WI5486/1-1) and the Daimler and Benz Foundation.

Author contributions

L.M.V., L.F., and S.O. conceived the experiment. L.M.V., M.P.C., and E.W.S. performed the measurements. L.M.V., M.P.C., and R.B. performed the calculations. All authors analyzed and discussed the results. L.M.V., L.F., P.W., and S.O. wrote the manuscript, with input from all authors. S.O. supervised the project.

Peer review

Peer review information

Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work. A peer review file is available.

Data availability

The raw data generated in this study as well as the analysis and simulation code have been deposited in a Zenodo database under identifier 10.5281/zenodo.8316339.

Competing interests

The authors declare no competing interests.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
==== Refs
References

1. Vincent R Klyatskaya S Ruben M Wernsdorfer W Balestro F Electronic read-out of a single nuclear spin using a molecular spin transistor Nature 2012 488 357 360, 10.1038/nature11341 22895342
Vincent, R., Klyatskaya, S., Ruben, M., Wernsdorfer, W. & Balestro, F. Electronic read-out of a single nuclear spin using a molecular spin transistor. Nature 488, 357–360, (2012).22895342 10.1038/nature11341
2. Thiele S Electrically driven nuclear spin resonance in single-molecule magnets Science 2014 344 1135 1138 10.1126/science.1249802 24904159
Thiele, S. et al. Electrically driven nuclear spin resonance in single-molecule magnets. Science 344, 1135–1138 (2014).24904159 10.1126/science.1249802
3. Neumann P Single-shot readout of a single nuclear spin Science 2010 329 542 544 10.1126/science.1189075 20595582
Neumann, P. et al. Single-shot readout of a single nuclear spin. Science 329, 542–544 (2010).20595582 10.1126/science.1189075
4. Fuchs GD Burkard G Klimov PV Awschalom DD A quantum memory intrinsic to single nitrogen-vacancy centres in diamond Nat. Phys. 2011 7 789 793 10.1038/nphys2026
Fuchs, G. D., Burkard, G., Klimov, P. V. & Awschalom, D. D. A quantum memory intrinsic to single nitrogen-vacancy centres in diamond. Nat. Phys. 7, 789–793 (2011).10.1038/nphys2026
5. Pla JJ High-fidelity readout and control of a nuclear spin qubit in silicon Nature 2013 496 334 338 10.1038/nature12011 23598342
Pla, J. J. et al. High-fidelity readout and control of a nuclear spin qubit in silicon. Nature 496, 334–338 (2013).23598342 10.1038/nature12011
6. Randall J Many-body-localized discrete time crystal with a programmable spin-based quantum simulator Science 2021 374 1474 1478 10.1126/science.abk0603 34735218
Randall, J. et al. Many-body-localized discrete time crystal with a programmable spin-based quantum simulator. Science 374, 1474–1478 (2021).34735218 10.1126/science.abk0603
7. Maze JR Nanoscale magnetic sensing with an individual electronic spin in diamond Nature 2008 455 644 647 10.1038/nature07279 18833275
Maze, J. R. et al. Nanoscale magnetic sensing with an individual electronic spin in diamond. Nature 455, 644–647 (2008).18833275 10.1038/nature07279
8. Zaiser S Enhancing quantum sensing sensitivity by a quantum memory Nat. Commun. 2016 7 12279 10.1038/ncomms12279 27506596
Zaiser, S. et al. Enhancing quantum sensing sensitivity by a quantum memory. Nat. Commun. 7, 12279 (2016).27506596 10.1038/ncomms12279
9. Zutic I Fabian J Das Sarma S Spintronics: fundamentals and applications Rev. Mod. Phys. 2004 76 323 410 10.1103/RevModPhys.76.323
Zutic, I., Fabian, J. & Das Sarma, S. Spintronics: fundamentals and applications. Rev. Mod. Phys. 76, 323–410 (2004).10.1103/RevModPhys.76.323
10. Wernsdorfer W Ruben M Synthetic hilbert space engineering of molecular qudits: isotopologue chemistry Adv. Mater. 2019 31 1806687 10.1002/adma.201806687
Wernsdorfer, W. & Ruben, M. Synthetic hilbert space engineering of molecular qudits: isotopologue chemistry. Adv. Mater. 31, 1806687 (2019).10.1002/adma.201806687
11. Kane BE A silicon-based nuclear spin quantum computer Nature 1998 393 133 137 10.1038/30156
Kane, B. E. A silicon-based nuclear spin quantum computer. Nature 393, 133–137 (1998).10.1038/30156
12. Yang S High-fidelity transfer and storage of photon states in a single nuclear spin Nat. Photon. 2016 10 507 511 10.1038/nphoton.2016.103
Yang, S. et al. High-fidelity transfer and storage of photon states in a single nuclear spin. Nat. Photon. 10, 507–511 (2016).10.1038/nphoton.2016.103
13. Baumann S Electron paramagnetic resonance of individual atoms on a surface Science 2015 350 417 420 10.1126/science.aac8703 26494753
Baumann, S. et al. Electron paramagnetic resonance of individual atoms on a surface. Science 350, 417–420 (2015).26494753 10.1126/science.aac8703
14. Willke P Yang K Bae Y Heinrich AJ Lutz CP Magnetic resonance imaging of single atoms on a surface Nat. Phys. 2019 15 1005 1010 10.1038/s41567-019-0573-x
Willke, P., Yang, K., Bae, Y., Heinrich, A. J. & Lutz, C. P. Magnetic resonance imaging of single atoms on a surface. Nat. Phys. 15, 1005–1010 (2019).10.1038/s41567-019-0573-x
15. Yang K Engineering the eigenstates of coupled spin-1/2 atoms on a surface Phys. Rev. Lett. 2017 119 227206 10.1103/PhysRevLett.119.227206 29286811
Yang, K. et al. Engineering the eigenstates of coupled spin-1/2 atoms on a surface. Phys. Rev. Lett. 119, 227206 (2017).29286811 10.1103/PhysRevLett.119.227206
16. Steinbrecher M Quantifying the interplay between fine structure and geometry of an individual molecule on a surface Phys. Rev. B 2021 103 155405 10.1103/PhysRevB.103.155405
Steinbrecher, M. et al. Quantifying the interplay between fine structure and geometry of an individual molecule on a surface. Phys. Rev. B 103, 155405 (2021).10.1103/PhysRevB.103.155405
17. Yang K Coherent spin manipulation of individual atoms on a surface Science 2019 366 509 512 10.1126/science.aay6779 31649202
Yang, K. et al. Coherent spin manipulation of individual atoms on a surface. Science 366, 509–512 (2019).31649202 10.1126/science.aay6779
18. Wang Y Universal quantum control of an atomic spin qubit on a surface Npj Quant. Inf. 2023 9 48 10.1038/s41534-023-00716-6
Wang, Y. et al. Universal quantum control of an atomic spin qubit on a surface. Npj Quant. Inf. 9, 48 (2023).10.1038/s41534-023-00716-6
19. Willke P Hyperfine interaction of individual atoms on a surface Science 2018 362 336 339 10.1126/science.aat7047 30337408
Willke, P. et al. Hyperfine interaction of individual atoms on a surface. Science 362, 336–339 (2018).30337408 10.1126/science.aat7047
20. Yang K Electrically controlled nuclear polarization of individual atoms Nat. Nanotechnol. 2018 13 1120 1125 10.1038/s41565-018-0296-7 30397285
Yang, K. et al. Electrically controlled nuclear polarization of individual atoms. Nat. Nanotechnol. 13, 1120–1125 (2018).30397285 10.1038/s41565-018-0296-7
21. Yang K Tuning the exchange bias on a single atom from 1 mT to 10 T Phys. Rev. Lett. 2019 122 227203 10.1103/PhysRevLett.122.227203 31283288
Yang, K. et al. Tuning the exchange bias on a single atom from 1 mT to 10 T. Phys. Rev. Lett. 122, 227203 (2019).31283288 10.1103/PhysRevLett.122.227203
22. Veldman LM Free coherent evolution of a coupled atomic spin system initialized by electron scattering Science 2021 372 964 968 10.1126/science.abg8223 34045351
Veldman, L. M. et al. Free coherent evolution of a coupled atomic spin system initialized by electron scattering. Science 372, 964–968 (2021).34045351 10.1126/science.abg8223
23. Farinacci L Veldman LM Willke P Otte S Experimental determination of a single atom ground state orbital through hyperfine anisotropy Nano Lett. 2022 22 8470 8474 10.1021/acs.nanolett.2c02783 36305860
Farinacci, L., Veldman, L. M., Willke, P. & Otte, S. Experimental determination of a single atom ground state orbital through hyperfine anisotropy. Nano Lett. 22, 8470–8474 (2022).36305860 10.1021/acs.nanolett.2c02783
24. Kim J Anisotropic hyperfine interaction of surface-adsorbed single atoms Nano Lett. 2022 22 9766 9772 10.1021/acs.nanolett.2c02782 36317830
Kim, J. et al. Anisotropic hyperfine interaction of surface-adsorbed single atoms. Nano Lett. 22, 9766–9772 (2022).36317830 10.1021/acs.nanolett.2c02782
25. Cassidy MC Chan HR Ross BD Bhattacharya PK Marcus CM In vivo magnetic resonance imaging of hyperpolarized silicon particles Nat. Nanotechnol. 2013 8 363 368, 10.1038/nnano.2013.65 23644571
Cassidy, M. C., Chan, H. R., Ross, B. D., Bhattacharya, P. K. & Marcus, C. M. In vivo magnetic resonance imaging of hyperpolarized silicon particles. Nat. Nanotechnol. 8, 363–368, (2013).23644571 10.1038/nnano.2013.65
26. Eills J Spin hyperpolarization in modern magnetic resonance Chem. Rev. 2023 123 1417 1551 10.1021/acs.chemrev.2c00534 36701528
Eills, J. et al. Spin hyperpolarization in modern magnetic resonance. Chem. Rev. 123, 1417–1551 (2023).36701528 10.1021/acs.chemrev.2c00534
27. McMillan SR Harmon NJ Flatte ME Image of dynamic local exchange interactions in the dc magnetoresistance of spin-polarized current through a dopant Phys. Rev. Lett. 2020 125 257203 10.1103/PhysRevLett.125.257203 33416385
McMillan, S. R., Harmon, N. J. & Flatte, M. E. Image of dynamic local exchange interactions in the dc magnetoresistance of spin-polarized current through a dopant. Phys. Rev. Lett. 125, 257203 (2020).33416385 10.1103/PhysRevLett.125.257203
28. Kot P Electric control of spin transitions at the atomic scale Nat. Commun. 2023 14 6612 10.1038/s41467-023-42287-2 37857623
Kot, P. et al. Electric control of spin transitions at the atomic scale. Nat. Commun. 14, 6612 (2023).37857623 10.1038/s41467-023-42287-2
29. Loth S Etzkorn M Lutz CP Eigler DM Heinrich AJ Measurement of fast electron spin relaxation times with atomic resolution Science 2010 329 1628 1630, 10.1126/science.1191688 20929842
Loth, S., Etzkorn, M., Lutz, C. P., Eigler, D. M. & Heinrich, A. J. Measurement of fast electron spin relaxation times with atomic resolution. Science 329, 1628–1630, (2010).20929842 10.1126/science.1191688
30. Johansson JR Nation PD Nori F QuTiP: an open-source Python framework for the dynamics of open quantum systems Comput. Phys. Commun. 2012 183 1760 1772 10.1016/j.cpc.2012.02.021
Johansson, J. R., Nation, P. D. & Nori, F. QuTiP: an open-source Python framework for the dynamics of open quantum systems. Comput. Phys. Commun. 183, 1760–1772 (2012).10.1016/j.cpc.2012.02.021
31. Degen CL Reinhard F Cappellaro P Quantum sensing Rev. Mod. Phys. 2017 89 035002 10.1103/RevModPhys.89.035002
Degen, C. L., Reinhard, F. & Cappellaro, P. Quantum sensing. Rev. Mod. Phys. 89, 035002 (2017).10.1103/RevModPhys.89.035002
32. Savytskyy R An electrically driven single-atom “flip-flop” qubit Sci. Adv. 2023 9 eadd9408 10.1126/sciadv.add9408 36763660
Savytskyy, R. et al. An electrically driven single-atom “flip-flop” qubit. Sci. Adv. 9, eadd9408 (2023).36763660 10.1126/sciadv.add9408
33. Bae Y Enhanced quantum coherence in exchange coupled spins via singlet-triplet transitions Sci. Adv. 2018 4 eaau4159 10.1126/sciadv.aau4159 30430136
Bae, Y. et al. Enhanced quantum coherence in exchange coupled spins via singlet-triplet transitions. Sci. Adv. 4, eaau4159 (2018).30430136 10.1126/sciadv.aau4159
34. Shiddiq M Enhancing coherence in molecular spin qubits via atomic clock transitions Nature 2016 531 348 351 10.1038/nature16984 26983539
Shiddiq, M. et al. Enhancing coherence in molecular spin qubits via atomic clock transitions. Nature 531, 348–351 (2016).26983539 10.1038/nature16984
