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We present a protocol to achieve double quantum magnetometry at large static magnetic fields. This is a regime where sensitive sample parameters, such as the chemical shift, get enhanced facilitating their characterization. In particular, our method delivers two-tone stroboscopic radiation patterns with modulated Rabi frequencies to achieve larger spectral signals. Furthermore, it does not introduce inhomogeneous broadening in the sample spectrum preventing signal misinterpretation. Moreover, our protocol is designed to work under realistic conditions such as the presence of moderate microwave power and errors on the radiation fields. Albeit we particularise to nitrogen vacancy centers, our protocol is general, thus applicable to distinct quantum sensors.
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We propose a strategy to measure weak static magnetic fields with nitrogen-vacancy color center in diamond. Inspired by avian magnetoreception models, we consider the feasibility of utilizing quantum coherence phenomena to measure weak static magnetic fields. Nitrogen-vacancy (NV) color centers are regarded as the ideal platform to study quantum sciences as a result of its long coherence time up to a millisecond timescale. In high-purity diamond, hyperfine interaction with 13C nuclear spins dominates the decoherence process. In this paper, we numerically simulate the decoherence process between 0 and +1 of the individual NV color center spin in 13C nuclear baths with various of magnitudes of external magnetic fields. By applying Hahn echo into the system, we obtain the coherence of NV color center spin as a function of total evolution time and magnetic field. Furthermore we obtain the high-accuracy relationship between the three decoherence-characteristic timescales, i.e. T_W, T_R, T_2, and magnetic field B. And we draw a conclusion that T_R has the highest sensitivity about magnetic field among the three time-scales. Thus, for a certain NV color center, T_R can be the scale for the magnitude of magnetic field, or rather, the component along the NV electronic spin axis. When measuring an unknown magnetic field, we adjust the NV axis to three mutually orthogonal directions respectively. By this means, we obtain the three components of the magnetic field and thus the magnitude and direction of the actual magnetic field. The accuracy could reach 60 nT/Hz^{1/2},and could be greatly improved by using an ensemble of NV color centers or diamond crystals purified with 12C atoms.
Sensing static or slowly varying magnetic fields with high sensitivity and spatial resolution is critical to many applications in fundamental physics, bioimaging and materials science. Several versatile magnetometry platforms have emerged over the past decade, such as electronic spins associated with Nitrogen Vacancy (NV) centers in diamond. However, their high sensitivity to external fields also makes them poor sensors of DC fields. Indeed, the usual method of Ramsey magnetometry leaves them prone to environmental noise, limiting the allowable interrogation time to the short dephasing time T2*. Here we introduce a hybridized magnetometery platform, consisting of a sensor and ancilla, that allows sensing static magnetic fields with interrogation times up to the much longer T2 coherence time, allowing significant potential gains in field sensitivity. While more generally applicable, we demonstrate the method for an electronic NV sensor and a nuclear ancilla. It relies on frequency upconversion of transverse DC fields through the ancilla, allowing quantum lock-in detection with low-frequency noise rejection. In our experiments, we demonstrate sensitivities better than 6uT/vHz, comparable to the Ramsey method, and narrow-band signal noise filtering better than 64kHz. With technical optimization, we expect more than an one order of magnitude improvement in each of these parameters. Since our method measures transverse fields, in combination with the Ramsey detection of longitudinal fields, it ushers in a compelling technique for sensitive vector DC magnetometry at the nanoscale.
We theoretically study the levitation of a single magnetic domain nanosphere in an external static magnetic field. We show that apart from the stability provided by the mechanical rotation of the nanomagnet (as in the classical Levitron), the quantum spin origin of its magnetization provides two additional mechanisms to stably levitate the system. Despite of the Earnshaw theorem, such stable phases are present even in the absence of mechanical rotation. For large magnetic fields, the Larmor precession of the quantum magnetic moment stabilizes the system in full analogy with magnetic trapping of a neutral atom. For low magnetic fields, the magnetic anisotropy stabilizes the system via the Einstein-de Haas effect. These results are obtained with a linear stability analysis of a single magnetic domain rigid nanosphere with uniaxial anisotropy in a Ioffe-Pritchard magnetic field.
We introduce a double quantum (DQ) 4-Ramsey measurement protocol that enables wide-field magnetic imaging using nitrogen vacancy (NV) centers in diamond, with enhanced homogeneity of the magnetic sensitivity relative to conventional single quantum (SQ) techniques. The DQ 4-Ramsey protocol employs microwave-phase alternation across four consecutive Ramsey (4-Ramsey) measurements to isolate the desired DQ magnetic signal from any residual SQ signal induced by microwave pulse errors. In a demonstration experiment employing a 1-$mu$m-thick NV layer in a macroscopic diamond chip, the DQ 4-Ramsey protocol provides volume-normalized DC magnetic sensitivity of $eta^text{V}=34,$nTHz$^{-1/2} mu$m$^{3/2}$ across a $125,mu$m$ ,times,125,mu $m field of view, with about 5$times$ less spatial variation in sensitivity across the field of view compared to a SQ measurement. The improved robustness and magnetic sensitivity homogeneity of the DQ 4-Ramsey protocol enable imaging of dynamic, broadband magnetic sources such as integrated circuits and electrically-active cells.
We introduce an alternate route to dynamically polarize the nuclear spin host of nitrogen-vacancy (NV) centers in diamond. Our approach articulates optical, microwave and radio-frequency pulses to recursively transfer spin polarization from the NV electronic spin. Using two complementary variants of the same underlying principle, we demonstrate nitrogen nuclear spin initialization approaching 80% at room temperature both in ensemble and single NV centers. Unlike existing schemes, our approach does not rely on level anti-crossings and is thus applicable at arbitrary magnetic fields. This versatility should prove useful in applications ranging from nanoscale metrology to sensitivity-enhanced NMR.
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