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# Magnetic ordering of nitrogen-vacancy centers in diamond via resonator-mediated coupling

*EPJ Quantum Technology*
**volume 2**, Article number: 18 (2015)

## Abstract

Nitrogen-vacancy centers in diamond, being a promising candidate for quantum information processing, may also be an ideal platform for simulating many-body physics. However, it is difficult to realize interactions between nitrogen-vacancy centers strong enough to form a macroscopically ordered phase under realistic temperatures. Here we propose a scheme to realize long-range ferromagnetic Ising interactions between distant nitrogen-vacancy centers by using a mechanical resonator as a medium. Since the critical temperature in the long-range Ising model is proportional to the number of spins, a ferromagnetic order can be formed at a temperature of tens of millikelvin for a sample with ∼10^{4} nitrogen-vacancy centers. This method may provide a new platform for studying many-body physics using qubit systems.

## Introduction

The negatively charged nitrogen-vacancy (NV) centers in high-purity diamond have been considered as a promising candidate for solid state quantum information processing due to their long coherence time [1–3] and high feasibility in initialization, control, and readout of their spin states [4]. Simulation of many-body physics using NV centers, in analogue to cold atom physics [5, 6], has been proposed [7–10]. To realize phase transitions in NV center qubit systems under realistic temperatures, however, sufficiently strong interactions between NV centers located sufficiently close (<30 nm) is till highly challenging [7, 8, 11]. A new opportunity is to use resonators as mediators [7, 12–15], which has potential of coupling NV centers at distance.

In this paper, we propose to realize long-range coupling between many separated NV centers via a mechanical resonator. A remarkable feature of the long-range interacting system is: the critical temperature for ferromagnetic phase transitions is proportional to the number of spins, so a ferromagnetic order could be formed at a temperature of tens of millikelvin (mK) for a sample with ∼10^{4} NV centers, even though the mediated coupling between two NV centers is less than 200 kHz (∼10 μK).

## Microscopic model

The essential idea can be understood by considering a prototype system shown in Figure 1(a). A mechanical resonator with frequency \(\omega_{r}\) is attached with a magnet. The NV sample is placed right under the magnet with a distance *d*. The oscillation of the mechanical resonator generates a time dependent magnetic field that causes Zeeman shift of the spins in the sample. In contrast to the schemes of direct dipolar coupling between NV centers, our scheme does not require short distance between NV centers. We use a diamond sample where the orientation axes of the NV color centers can lie along one of the four possible crystallographic axes in diamonds, \([111]\) (Figure 1(b)) which can be grown by chemical vapor deposition method [16, 17]. The NV centers have a spin triplet ground state (\(S=1\)) with a large zero field splitting \(\Delta=2.87\mbox{ GHz}\). We apply a static magnetic field \(B_{\mathrm{NV}}\) along the \([111]\) direction of the sample so that two Zeeman states of the electron spin qubits with magnetic quantum number \(|1\rangle\) and \(|0\rangle\) are nearly degenerate, \(\delta\equiv(\Delta -\gamma_{e}B_{\mathrm{NV}})\sim0\) (Figure 1(c)).

We make use of the two Zeeman states of the electron spin \(|1\rangle\) and \(|0\rangle\) and define a pseudo-spin by \(\sigma_{z}=|1\rangle\langle 1|-|0\rangle\langle0|\) and the corresponding spin flip operators \(\sigma^{+} =|1\rangle\langle0|\) and \(\sigma^{-}=|0\rangle\langle1|\). In each NV center there is a ^{14}N nuclear spin which interacts with the on-site NV center spin. The Hamiltonian of the NV center near the degenerate point (\(\delta\approx0\)) is \(H_{\mathrm{NV}}=\sum_{j}[\Delta _{N}(I_{j}^{z})^{2}-\gamma_{N}I_{j}^{z} B_{\mathrm{NV}}+A I_{j}\cdot\sigma_{j}+\delta\sigma _{j}^{z}]\), where \(\Delta_{N}=5.1\mbox{ MHz}\) is the ^{14}N nuclear spin quadrupole splitting [18], \(\gamma_{N}\) is the gyromagnetic ratio of the nitrogen nuclear spin and \(A\approx2\mbox{ MHz}\) is the hyperfine coupling between the electronic spin and the ^{14}N nuclear spin [18].

The motion of the mechanical resonator is described by the Hamiltonian \(H_{r}=\omega_{r}b^{\dagger}b\), with \(\omega_{r}\) as the frequency of the fundamental vibration mode of the resonator and *b* as the corresponding annihilation operator. For example a silicon nitride string resonator has dimensions \((325\times0.35\times0.1 )\mbox{ $\upmu$m}\) with \(\omega_{r}=2\pi\times1.0\mbox{ MHz}\) and \(Q =1.3\times10^{6}\) at room temperature [19].

The magnetic field felt by the electronic spin of the NV centers can be approximated by a magnetic dipole [20], \(\vec {B}(d_{j}-x(t))=\vec{B}(d_{j})-G_{m}\vec{x}(t)+o(x^{2})\), where \(d_{j}\) is the distance between the equilibrium position of the resonator and *j*th NV center, \(G_{m}\) is the magnetic field gradient at the position of the NV centers and *x* is the amplitude of mechanical resonator oscillation (\(x\sim10^{-12}\mbox{ m}\) at temperature of mK). This magnetic field will induce a Zeeman shift to the NV spins with Hamiltonian \(H_{z}=\sum_{j}\eta_{j}\sigma_{j}^{x}(b+b^{\dagger})\) and \(\eta_{j}=\gamma _{e}|G_{m}|a_{0}\), where \(\gamma_{e}\) is the gyromagnetic ratio for electron and \(a_{0}=\sqrt{\hbar/2m\omega_{r}}\) is the amplitude of zero point fluctuations for a resonator of mass *m*.

Due to the distance distribution of the NV centers to the magnet, the coupling of the NV centers to the mechanical resonator have a distribution. A magnetic tip with size of 100 nm produces a magnetic gradient \(G_{m}\sim7.8\times10^{6}\mbox{ T/m}\) at a distance 25 nm away from the tip [21]. In such case \(\eta/2\pi\) could reach 200 kHz. For a sample with typical distance of NV centers ∼20 nm, the neighbor NV centers have a direct dipolar interaction with strength ∼5 kHz (∼0.25 μK), much less than the critical temperature to be discussed later. For the sake of simplicity, in the following we assume the coupling between the mechanical resonator and NV centers to be uniform and neglect the direct dipolar coupling between NV centers. Without these assumptions, however, the results in this paper would only be quantitatively affected. The coupling constant \(\eta/2\pi\sim200\mbox{ kHz}\) considerably exceeds both the electronic spin decoherence rate (∼kHz) of the NV centers and the intrinsic damping rate of the mechanical resonator, \(\gamma=\omega_{r}/Q\) [19]. We neglect the interaction between the mechanical resonator and the ^{14}N nuclear spins since it is three orders of magnitude smaller than that between the NV center and the mechanical resonator.

Summarizing the three terms described above, the total microscopic Hamiltonian including the spin qubits in the NV centers, nitrogen nuclear spins, the mechanical resonator and the interaction among them is,

## Effective long-range Ising model

To obtain the effective interactions between NV centers, we calculate the partition function of the hybrid system \(Z=\operatorname{Tr}[e^{-\beta H}]\). We shall neglect the Zeeman energy of the ^{14}N nuclear spin since its strength (∼0.3 MHz) is much smaller than the zero field splitting ∼5 MHz and the hyperfine interaction ∼3 MHz. The hyperfine interaction between the electronic spin and the ^{14}N nuclear spin term \(AI\cdot\sigma\) can be separated into the diagonal term \(AI^{x}\sigma^{x}\) and the flip-flop term \(A(I^{y}\sigma ^{y}+I^{z}\sigma^{z})\). Let us first neglect the flip-flop term and the qubit splitting (\(\delta=0\)). By partial trace of the phonon bath and the nuclear spins, the partition function can be factorised as

where \(Z_{\mathrm{phonon}}\) is the partition function of an independent phonon bath, \(Z_{^{14}\mathrm{N}}\) is the partition function of the nuclear spins. A unitary transformation of the form, \(U=\exp(\sum_{j}\eta_{j}\sigma _{j}^{x}(b-b^{\dagger})/\omega_{r})\), can be applied to the Hamiltonian in equation (1), with the Zeeman splitting *δ* and flip-flop term neglected, to obtain an effective Hamiltonian for the NV electron spins up to the second order in \(\eta/\omega_{r}\),

with \(h(\beta)=\beta^{-1}\ln[(1+2\cosh(\beta A_{x}))/3]\) being an effective magnetic field resulting from the on-site interaction between the NV center and the ^{14}N nuclear spin. Note that in equation (3) all the NV center spins interact with each other, making an effectively *N*-dimensional model. The physics for the effective long-range interactions between the NV centers is that an NV center spin flips by virtually emitting a phonon, and then the phonon is virtually absorbed by another NV center spin far away with a spin flip. Therefore two NV spins at distance can flip-flop via virtual exchange of phonons, which leads to long-range \(\sigma_{i}^{x}\sigma_{j}^{x}\) coupling. In the temperature range we are interested in (∼10 mK), the effective field, \(h(\beta )\sim0.3\mbox{ $\upmu$K}\), is negligible. Therefore the distant NV centers interact through an effective long-range ferromagnetic Ising interaction with the Hamiltonian

where the ferromagnetic coupling strength \(J=2\eta^{2}/\omega_{r}\). If the flip-flop term of the hyperfine interaction is taken into account, it would contribute an effective transverse field to the electronic spins, which, however, is ∼0.3 μK and hence negligible.

## Ferromagnetic ordering

The long-range Ising model can be solved by mapping the ensemble onto to a single large spin. With the notation \(S_{x}=\sum_{j=1}^{N}\sigma_{j}^{x}/2\), the Hamiltonian of the long-range Ising model can be written as

The spin quantum number *S* takes values \(0,1,2,\ldots, N/2\) for even *N* and \(1/2,3/2,\ldots,N/2\) for odd *N*. Moreover, the spin degeneracy in each large spin subspace is \(D[S]=C_{N}^{N/2-S}-C_{N}^{N/2-S-1}\) where \(C_{N}^{j}\) is the binomial coefficient. Then the electron spin partition function

In the large *N* limit [22]

where \(\varphi=(1/2+X)\ln(1/2+X)+(1/2-X)\ln(1/2-X)-2\tilde{\beta}X^{2}\) and \(\tilde{\beta}=\beta NJ\). The integration in the partition function can be evaluated by the saddle point approximation method. For \(\tilde {\beta}<1\), the saddle point appears at \(X=0\), and for \(\tilde{\beta }>1\), there are two symmetric saddle point located respectively within \((-1/2,0)\) and \((0,1/2)\). Therefore \(\tilde{\beta}=1\) is the critical point for the ferromagnetic phase transition in the long-range Ising model. So the critical temperature for the long-range ferromagnetic Ising model, \(k_{B}T_{c}=NJ\), is proportional to the number of spins and the coupling strength [23]. The mean-field theory gives a good estimation of the phase transition temperature in the long-range Ising model, which becomes exact in the thermodynamic limit.

We present the scaled free energy of the long-range Ising model as a function of the spin magnetization \(M_{x}\equiv\langle S_{x}\rangle/N\) for different temperatures in Figure 2. One can see that at high temperature (Figure 2(a)) the free energy minimum is situated at \(M_{x}=0\) and a paramagnetic state is stable, while at low temperature (Figure 2(b)) the free energy minimum is doubly degenerated with \(M_{x}\approx1\) or \(M_{x}\approx-1\), and a ferromagnetic state is preferred.

For the hybrid system, the phase transition temperature can be controlled through the detuning from the degeneracy point between the NV spin states \(|1\rangle\) and \(|0\rangle\). If the NV qubits have a small splitting \(\delta=\Delta-\gamma B_{\mathrm{NV}}\), the resonator mediated interaction between the NV centers becomes

The critical temperature becomes

Here the magnetic field is tuned so that the NV spin states \(|1\rangle\) and \(|0\rangle\) are nearly degenerate. Hence the splitting *δ* is much smaller than the frequency of the resonator. In Figure 3 we plot the phase diagrams of the NV centers as a function of splitting for \(N=10\mbox{,}000\). In a diamond sample with NV concentration ∼50 ppb, coupling between a resonator and such many NV centers is possible. A ferromagnetic order can be formed at the temperature of 50 mK. The magnetization of the large number of spins would cause a displacement of the resonator \({\sim} 2 a_{0} \eta N \langle M_{x}\rangle / (\hbar\omega_{r}) \approx2\mbox{ nm}\) for \(N=10^{4}\mbox{ NV}\) centers, which can be detected by optical reflection as done in atomic force microscopy.

In Figure 4(a), we present the numerical and the mean field results of the order parameter as a function of reduced temperature, \(k_{B}T/NJ\). One can see that the order parameter vanishes at and above the critical temperature \(k_{B}T/NJ=1\) and also the finite size numerical results approach to that of the mean field predictions reasonably well as the number of spins increases. The specific heat shown in Figure 4(b) has a finite jump which signals a second order phase transitions occurs.

## Conclusion

In summary, we propose a scheme to realize ferromagnetic ordering of distant nitrogen-vacancy centers by using a mechanical resonator to mediate long-range Ising-type interaction. The critical temperature for the ferromagnetic phase transition in the long-range Ising model is proportional to the number of spins, so the ferromagnetic order could be formed at the temperature of tens of millikelvin for a sample with ten thousand nitrogen-vacancy centers. In addition, it may also be possible to use a superconducting resonator [24, 25] as a medium to realize the long-range ferromagnetic coupling between the NV centers. Since the interactions between the NV centers mediated by a superconducting resonator is usually small compared to that by a mechanical resonator, high density NV samples are required to observe the magnetic ordering in the NV centers.

## References

- 1.
Kennedy T-A, Colton J-S, Butler J-E, Linares R-C, Doering P-J. Long coherence times at 300 K for nitrogen-vacancy center spins in diamond grown by chemical vapor deposition. Appl Phys Lett. 2004;83:4190.

- 2.
Gaebel T, Domhan M, Popa I, Wittmann C, Neumann P, Jelezko F, Rabeau J-R, Stavrias N, Greentree A-D, Prawer S, Meijer J, Twamley J, Hemmer P-R, Wrachtrup J. Room-temperature coherent coupling of single spins in diamond. Nat Phys. 2006;2:408.

- 3.
Balasubramanian G, Neumann P, Twitchen D, Markham M, Kolesov R, Mizuochi M, Isoya J, Achard J, Beck J, Tissler J, Jacques V, Hemmer P-R, Jelezko F, Wrachtrup J. Ultralong spin coherence time in isotopically engineered diamond. Nat Mater. 2009;8:383.

- 4.
Gruber A, Dräbenstedt A, Tietz C, Fleury L, Wrachtrup J, von Borczyskowski C. Scanning confocal optical microscopy and magnetic resonance on single defect centers. Science. 1997;276:2012.

- 5.
Lewenstein M, Sanpera A, Ahufinger V, Damski B, Sen(De) A, Sen U. Ultracold atomic gases in optical lattices: mimicking condensed matter physics and beyond. Adv Phys. 2007;56:243.

- 6.
Bloch I, Dalibard J, Zwerger W. Many-body physics with ultracold gases. Rev Mod Phys. 2008;80:885.

- 7.
Rabl P, Kolkowitz S-J, Koppens F-H-L, Harris J-G-E, Zoller P, Lukin M-D. A quantum spin transducer based on nanoelectromechanical resonator arrays. Nat Phys. 2010;6:602.

- 8.
Yao N-Y, Jiang L, Gorshkov A-V, Maurer P-C, Giedke G, Cirac J-I, Lukin M-D. Scalable architecture for a room temperature solid-state quantum information processor. Nat Commun. 2012;3:800.

- 9.
Cai J-M, Retzker A, Jelezko F, Plenio M-B. A large-scale quantum simulator on a diamond surface at room temperature. Nat Phys. 2013;9:168.

- 10.
Chen S-W, Jiang Z-F, Liu R-B. Quantum criticality at high temperature revealed by spin echo. New J Phys. 2013;15:043032.

- 11.
Dolde F, Jakobi I, Naydenov B, Zhao N, Pezzagna S, Trautmann C, Meijer J, Neumann P, Jelezko F, Wrachtrup J. Room-temperature entanglement between single defect spins in diamond. Nat Phys. 2013;9:139.

- 12.
Rabl P, Cappellaro P, Gurudev Dutt M-V, Jiang L, Maze J-R, Lukin M-D. Strong magnetic coupling between an electronic spin qubit and a mechanical resonator. Phys Rev B. 2009;79:041302.

- 13.
Xu Z-Y, Hu Y-M, Yang W-L, Feng M, Du J-F. Deterministically entangling distant nitrogen-vacancy centers by a nanomechanical cantilever. Phys Rev A. 2009;80:022335.

- 14.
Arcizet O, Jacques V, Siria A, Poncharal P, Vincent P, Seidelin S. A single nitrogen-vacancy defect coupled to a nanomechanical oscillator. Nat Phys. 2011;7:879.

- 15.
Li P-B, Liu Y-C, Gao S-Y, Xiang Z-L, Rabl P, Li F-L, Xiao Y-F. arXiv:1503.02437 (2015).

- 16.
Lesik M, Tetienne J-P, Tallaire A, Achard J, Mille V, Gicquel A, Roch J-F, Jacques V. arXiv:1401.2795 (2014).

- 17.
Michl J, Teraji T, Zaiser S, Jakobi I, Waldherr G, Dolde F, Neumann P, Doherty M-W, Manson N-B, Isoya J, Wrachtrup J. arXiv:1401.4106 (2014).

- 18.
He X-F, Manson N-B, Fisk P-T-H. Paramagnetic resonance of photoexcited N-V defects in diamond. II. Hyperfine interaction with the

^{14}N nucleus. Phys Rev B. 1993;47:8816. - 19.
Verbridge S-S, Craighead H-G, Parpia J-M. A megahertz nanomechanical resonator with room temperature quality factor over a million. Appl Phys Lett. 2008;92:013112.

- 20.
Hunger D, Camerer S, Korppi M, Jöckel A, Hänsch T-W, Treutlein P. Coupling ultracold atoms to mechanical oscillators. C R Phys. 2011;12:871.

- 21.
Mamin H-J, Poggio M, Degen C-L, Rugar D. Nuclear magnetic resonance imaging with 90-nm resolution. Nat Nanotechnol. 2007;2:301.

- 22.
Wilms J, Vidal J, Verstraete F, Dusuel S. Finite-temperature mutual information in a simple phase transition. J Stat Mech. 2012;2012:P01023.

- 23.
Huang K. Statistical mechanics. New York: Wiley; 1987.

- 24.
Zhu X-B, Saito S, Kemp A, Kakuyanagi K, Karimoto S-I, Nakano H, Munro W-J, Tokura Y, Everitt M-S, Nemoto K, Kasu M, Mizuochi N, Semba K. Coherent coupling of a superconducting flux qubit to an electron spin ensemble in diamond. Nature. 2011;478:221.

- 25.
Kubo Y, Grezes C, Dewes A, Umeda T, Isoya J, Sumiya H, Morishita N, Abe H, Onoda S, Ohshima T, Jacques V, Dréau A, Roch J-F, Diniz I, Auffeves A, Vion D, Esteve D, Bertet P. Hybrid quantum circuit with a superconducting qubit coupled to a spin ensemble. Phys Rev Lett. 2011;107:220501.

## Acknowledgements

We are grateful to P Bertet for useful discussions. This work was supported by National Basic Research Program of China Grant 2014CB921402, Hong Kong RGC/GRF 401413, Hong Kong RGC/CRF CUHK4/CRF/12G, and CUHK VC’s One-Off Discretionary Fund.

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### Competing interests

The authors declare that they have no competing interests.

### Authors’ contributions

RBL conceived the idea, RBL & BBW formulated the theory, RBL, BBW, CB & JW designed the physical system, BBW carried out the calculation, BBW & RBL wrote the paper, and all authors commented on the manuscript.

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Wei, B., Burk, C., Wrachtrup, J. *et al.* Magnetic ordering of nitrogen-vacancy centers in diamond via resonator-mediated coupling.
*EPJ Quantum Technol.* **2, **18 (2015) doi:10.1140/epjqt/s40507-015-0032-2

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### Keywords

- nitrogen-vacancy centers
- ferromagnetism
- resonators