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 e
lectronic 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 dressed-state, double-resonance scheme to transfer polarization from bright NV electronic spins to dark substitutional-Nitrogen (P1) electronic spins in diamond. This polarization-transfer mechanism 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.
We demonstrate preferential orientation of nitrogen-vacancy (NV) color centers along two of four possible crystallographic axes in diamonds grown by chemical vapor deposition on the {100} face. We identify the relevant growth regime and present a pos
sible explanation of this effect. We show that preferential orientation provides increased optical read-out contrast for NV multi-spin measurements, including enhanced AC magnetic field sensitivity, thus providing an important step towards high fidelity multi-spin-qubit quantum information processing, sensing and metrology.
We demonstrate a method of imaging spatially varying magnetic fields using a thin layer of nitrogen-vacancy (NV) centers at the surface of a diamond chip. Fluorescence emitted by the two-dimensional NV ensemble is detected by a CCD array, from which
a vector magnetic field pattern is reconstructed. As a demonstration, AC current is passed through wires placed on the diamond chip surface, and the resulting AC magnetic field patterns are imaged using an echo-based technique with sub-micron resolution over a 140 mu m x 140 mu m field of view, giving single-pixel sensitivity ~100 nT/sqrt{Hz}. We discuss ongoing efforts to further improve sensitivity and potential bioimaging applications such as real-time imaging of activity in functional, cultured networks of neurons.
We use multi-pulse dynamical decoupling to increase the coherence lifetime (T2) of large numbers of nitrogen-vacancy (NV) electronic spins in room temperature diamond, thus enabling scalable applications of multi-spin quantum information processing a
nd metrology. We realize an order-of-magnitude extension of the NV multi-spin T2 for diamond samples with widely differing spin environments. For samples with nitrogen impurity concentration <~1 ppm, we find T2 > 2 ms, comparable to the longest coherence time reported for single NV centers, and demonstrate a ten-fold enhancement in NV multi-spin sensing of AC magnetic fields.
For precision coherent measurements with ensembles of quantum spins the relevant Figure-of-Merit (FOM) is the product of polarized spin density and coherence lifetime, which is generally limited by the dynamics of the spin environment. Here, we apply
a coherent spectroscopic technique to characterize the dynamics of the composite solid-state spin environment of Nitrogen-Vacancy (NV) centers in room temperature diamond. For samples of very different NV densities and impurity spin concentrations, we show that NV FOM values can be almost an order of magnitude larger than previously achieved in other room-temperature solid-state spin systems, and within an order of magnitude of the state-of-the-art atomic system. We also identify a new mechanism for suppression of electronic spin bath dynamics in the presence of a nuclear spin bath of sufficient concentration. This suppression could inform efforts to further increase the FOM for solid-state spin ensemble metrology and collective quantum information processing.
