Coherence of nitrogen-vacancy electronic spin ensembles in diamond

We present an experimental and theoretical study of electronic spin decoherence in ensembles of nitrogen-vacancy (NV) color centers in bulk high-purity diamond at room temperature. Under appropriate conditions, we find ensemble NV spin coherence times (T(2)) comparable to that of single NV with T(2) > 600 mu s for a sample with natural abundance of (13)C and paramagnetic impurity density similar to 10(15) cm(-3). We also observe a sharp decrease in the coherence time with misalignment of the static magnetic field relative to the NV electronic spin axis, consistent with theoretical modeling of NV coupling to a (13)C nuclear-spin bath. The long coherence times and increased signal-to-noise provided by room-temperature NV ensembles will aid many applications of NV centers in precision magnetometry and quantum information.