Optical magnetic imaging of living cells.

Magnetic imaging is a powerful tool for probing biological and physical systems. However, existing techniques either have poor spatial resolution compared to optical microscopy and are hence not generally applicable to imaging of sub-cellular structure (for example, magnetic resonance imaging), or entail operating conditions that preclude application to living biological samples while providing submicrometre resolution (for example, scanning superconducting quantum interference device microscopy, electron holography and magnetic resonance force microscopy). Here we demonstrate magnetic imaging of living cells (magnetotactic bacteria) under ambient laboratory conditions and with sub-cellular spatial resolution (400 nanometres), using an optically detected magnetic field imaging array consisting of a nanometre-scale layer of nitrogen-vacancy colour centres implanted at the surface of a diamond chip. With the bacteria placed on the diamond surface, we optically probe the nitrogen-vacancy quantum spin states and rapidly reconstruct images of the vector components of the magnetic field created by chains of magnetic nanoparticles (magnetosomes) produced in the bacteria. We also spatially correlate these magnetic field maps with optical images acquired in the same apparatus. Wide-field microscopy allows parallel optical and magnetic imaging of multiple cells in a population with submicrometre resolution and a field of view in excess of 100 micrometres. Scanning electron microscope images of the bacteria confirm that the correlated optical and magnetic images can be used to locate and characterize the magnetosomes in each bacterium. Our results provide a new capability for imaging bio-magnetic structures in living cells under ambient conditions with high spatial resolution, and will enable the mapping of a wide range of magnetic signals within cells and cellular networks.

Sensing Coherent Dynamics of Electronic Spin Clusters in Solids.

We observe coherent spin exchange between identical electronic spins in the solid state, a key step towards full quantum control of electronic spin registers in room temperature solids. In a diamond substrate, a single nitrogen vacancy (NV) center coherently couples to two adjacent S=1/2 dark electron spins via the magnetic dipolar interaction. We quantify NV-electron and electron-electron couplings via detailed spectroscopy, with good agreement to a model of strongly interacting spins. The electron-electron coupling enables an observation of coherent flip-flop dynamics between electronic spins in the solid state, which occur conditionally on the state of the NV. Finally, as a demonstration of coherent control, we selectively couple and transfer polarization between the NV and the pair of electron spins. Our observations enable the realization of fast quantum gate operations and quantum state transfer in a scalable, room temperature, quantum processor.

Dressed-state resonant coupling between bright and dark spins in diamond.

Under ambient conditions, spin impurities in solid-state systems are found in thermally mixed states and are optically "dark"; i.e., the spin states cannot be optically controlled. Nitrogen-vacancy (NV) centers in diamond are an exception in that the electronic spin states are "bright"; i.e., they can be polarized by optical pumping, coherently manipulated with spin-resonance techniques, and read out optically, all at room temperature. Here we demonstrate a scheme to resonantly couple bright NV electronic spins to dark substitutional-nitrogen (P1) electronic spins by dressing their spin states with oscillating magnetic fields. This resonant coupling mechanism can be used to transfer spin polarization from NV spins to nearby dark spins and could be used to cool a mesoscopic bath of dark spins to near-zero temperature, thus providing a resource for quantum information and sensing, and aiding studies of quantum effects in many-body spin systems.

Broadband loop gap resonator for nitrogen vacancy centers in diamond.

We present an S-band tunable loop gap resonator (LGR), which provides strong, homogeneous, and directionally uniform broadband microwave (MW) drive for nitrogen-vacancy (NV) ensembles. With 42 dBm of input power, the composite device provides drive field amplitudes approaching 5 G over a circular area ≳50 mm2 or cylindrical volume ≳250 mm3. The wide 80 MHz device bandwidth allows driving all NV Zeeman resonances for bias magnetic fields below 20 G. The device realizes percent-scale MW drive inhomogeneity; we measure a fractional root-mean-square inhomogeneity σ rms = 1.6% and a peak-to-peak variation σ pp = 3% over a circular area of 11 mm2 and σ rms = 3.2% and σ pp = 10.5% over a larger 32 mm2 circular area. We demonstrate incident MW power coupling to the LGR using two methodologies: a printed circuit board-fabricated exciter antenna for deployed compact bulk sensors and an inductive coupling coil suitable for microscope-style imaging. The inductive coupling coil allows for approximately 2π steradian combined optical access above and below the device, ideal for envisioned and existing NV imaging and bulk sensing applications.

Solid-state electronic spin coherence time approaching one second.

Solid-state spin systems such as nitrogen-vacancy colour centres in diamond are promising for applications of quantum information, sensing and metrology. However, a key challenge for such solid-state systems is to realize a spin coherence time that is much longer than the time for quantum spin manipulation protocols. Here we demonstrate an improvement of more than two orders of magnitude in the spin coherence time (T2) of nitrogen-vacancy centres compared with previous measurements: T2≈0.6 s at 77 K. We employed dynamical decoupling pulse sequences to suppress nitrogen-vacancy spin decoherence, and found that T2 is limited to approximately half of the longitudinal spin relaxation time over a wide range of temperatures, which we attribute to phonon-induced decoherence. Our results apply to ensembles of nitrogen-vacancy spins, and thus could advance quantum sensing, enable squeezing and many-body entanglement, and open a path to simulating driven, interaction-dominated quantum many-body Hamiltonians.

Suppression of spin-bath dynamics for improved coherence of multi-spin-qubit systems.

Multi-qubit systems are crucial for the advancement and application of quantum science. Such systems require maintaining long coherence times while increasing the number of qubits available for coherent manipulation. For solid-state spin systems, qubit coherence is closely related to fundamental questions of many-body spin dynamics. Here we apply a coherent spectroscopic technique to characterize the dynamics of the composite solid-state spin environment of nitrogen-vacancy colour centres in room temperature diamond. We identify a possible new mechanism in diamond for suppression of electronic spin-bath dynamics in the presence of a nuclear spin bath of sufficient concentration. This suppression enhances the efficacy of dynamical decoupling techniques, resulting in increased coherence times for multi-spin-qubit systems, thus paving the way for applications in quantum information, sensing and metrology.