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arXiv:1205.6938 · Europhysics Letters (EPL)

Robust dynamical decoupling for arbitrary quantum states of a single NV center in diamond

J. H. Shim, I. Niemeyer, J. Zhang, Dieter Suter

Published Aug 1, 2012• 36 citations
arXivHTMLPDF

Abstract

Dynamical decoupling is a powerful technique for extending the coherence time ( T 2 ) of qubits. We apply this technique to the electron spin qubit of a single nitrogen-vacancy center in type-IIa diamond. In a crystal with natural abundance of 13 C nuclear spins, we extend the decoherence time up to 2.2 ms. This is close to the T 1 value of this NV center (4 ms). Since dynamical decoupling must perform well for arbitrary initial conditions, we measured the dependence on the initial state and compared the performance of different sequences with respect to initial state dependence and robustness to experimental imperfections.

DOI
10.1209/0295-5075/99/40004

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Dynamical decoupling is a powerful technique for extending the coherence time ( T 2 ) of qubits. We apply this technique to the electron spin qubit of a single nitrogen-vacancy center in type-IIa diamond. In a crystal with natural abundance of 13 C nuclear spins, we extend the decoherence time up to 2.2 ms. This is close to the T 1 value of this NV center (4 ms). Since dynamical decoupling must perform well for arbitrary initial conditions, we measured the dependence on the initial state and compared the performance of different sequences with respect to initial state dependence and robustness to experimental imperfections.
We experimentally demonstrate over 2 orders of magnitude increase in the room-temperature coherence time of nitrogen-vacancy centers in diamond by implementing decoupling techniques. We show that equal pulse spacing decoupling performs just as well as nonperiodic Uhrig decoupling and also allows us to take advantage of revivals in the echo to explore the longest coherence times. At short times, we can extend the coherence of particular quantum states out from T2*=2.7 μs out to an effective T2>340 μs. For preserving arbitrary states we show the experimental importance of using pulse sequences that compensate the imperfections of individual pulses for all input states through judicious choice of the phase of the pulses. We use these compensated sequences to enhance the echo revivals and show a coherence time of over 1.6 ms in ultrapure natural abundance 13C diamond.
In this work, we optimize a dynamical decoupling (DD) protocol to improve the spin coherence properties of a dense ensemble of nitrogen-vacancy (NV) centers in diamond. Using liquid nitrogen-based cooling and DD microwave pulses, we increase the transverse coherence time T2 from ∼ 0.7 ms up to ∼ 30 ms. We extend previous work of single-axis (Carr-Purcell-Meiboom-Gill) DD towards the preservation of arbitrary spin states. After performing a detailed analysis of pulse and detuning errors, we compare the performance of various DD protocols. We identify that the concatenated XY8 pulse sequences serves as the optimal control scheme for preserving an arbitrary spin state. Finally, we use the concatenated sequences to demonstrate an immediate improvement of the AC magnetic sensitivity up to a factor of two at 250 kHz. For future work, similar protocols may be used to increase coherence times up to NV-NV interaction time scales, a major step toward the creation of quantum collective NV spin states.
We use multipulse dynamical decoupling to increase the coherence lifetime (T2{T}_{2}T2​) of large numbers of nitrogen-vacancy (NV) electronic spins in room temperature diamond, thus enabling scalable applications of multispin quantum information processing and metrology. We realize an order-of-magnitude extension of the NV multispin T2{T}_{2}T2​ in three diamond samples with widely differing spin impurity environments. In particular, for samples with nitrogen impurity concentration $\ensuremath{\lesssim}$1 ppm, we extend T2{T}_{2}T2​ to $>$2 ms, comparable to the longest coherence time reported for single NV centers, and demonstrate a tenfold enhancement in NV multispin sensing of ac magnetic fields.
We perform a detailed theoretical-experimental study of the dynamical decoupling (DD) of the nitrogen-vacancy (NV) center in diamond. We investigate the DD sequences applied to suppress the dephasing of the electron spin of the NV center induced by the coupling to a spin bath composed of the substitutional nitrogen atoms. The decoupling efficiency of various DD schemes is studied, including both periodic and aperiodic pulse sequences. For ideal control pulses, we find that the DD protocols with the Carr-Purcell-Meiboom-Gill (CPMG) timing of the pulses provides best performance. We show that, as the number of control pulses increases, the decoupling fidelity scaling differs qualitatively from the predictions of the Magnus expansion, and explain the origin of this difference. In particular, more advanced symmetrized or concatenated protocols do not improve the DD performance. Next, we investigate the impact of the systematic instrumental pulse errors in different periodic and aperiodic pulse sequences. The DD protocols with the single-axis control do not preserve all spin components in the presence of the pulse errors, and the two-axis control is needed. We demonstrate that the two-axis control sequence with the CPMG timing is very robust with respect to the pulse errors. The impact of the pulse errors can be diminished further by symmetrizing this protocol. For all protocols studied here, we present a detailed account of the pulse error parameters which make the strongest impact on the DD performance. In conclusion, we give specific recommendations about choosing the decoupling protocol for the system under investigation.
Abstract A nitrogen-vacancy (NV) center in a diamond enables the access to an electron spin, which is expected to present highly sensitive quantum sensors. Although exploiting a nitrogen nuclear spin improves the sensitivity, manipulating it using a resonant pulse requires a long gate time owing to its small gyromagnetic ratio. Another technique to control nuclear spins is a conditional rotation gate based on dynamical decoupling, which is faster but unavailable for nitrogen spins owing to the lack of transverse hyperfine coupling with the electron spin. In this study, we generated effective transverse coupling by applying a weak off-axis magnetic field. An effective coupling depends on the off-axis field; the conditional rotation gate on the nitrogen-14 spins of an NV center was demonstrated within 4.2 μs under an 1.8% off-axis field and a longitudinal field of approximately 280 mT. We estimated that a population transfer from the electron to nitrogen spins can be implemented with 8.7 μs. Our method is applicable to an ensemble of NV centers, in addition to a single NV center.
We demonstrate significant improvements of the spin coherence time of a dense ensemble of nitrogen-vacancy (NV) centers in diamond through optimized dynamical decoupling (DD). Cooling the sample down to 77 K suppresses longitudinal spin relaxation T1{T}_{1}T1​ effects and DD microwave pulses are used to increase the transverse coherence time T2{T}_{2}T2​ from $\ensuremath{\sim}0.7\phantom{\rule{0.28em}{0ex}}\mathrm{ms}$ up to $\ensuremath{\sim}30\phantom{\rule{0.28em}{0ex}}\mathrm{ms}$. We extend previous work of single-axis (Carr-Purcell-Meiboom-Gill) DD towards the preservation of arbitrary spin states. Following a theoretical and experimental characterization of pulse and detuning errors, we compare the performance of various DD protocols. We identify that the optimal control scheme for preserving an arbitrary spin state is a recursive protocol, the concatenated version of the XY8 pulse sequence. The improved spin coherence might have an immediate impact on improvements of the sensitivities of ac magnetometry. Moreover, the protocol can be used on denser diamond samples to increase coherence times up to NV-NV interaction time scales, a major step towards the creation of quantum collective NV spin states.