We propose a scheme to achieve nuclear-nuclear indirect interactions mediated by a mechanically driven nitrogen-vacancy (NV) center in diamond. Here we demonstrate two-qubit entangling gates and quantum-state transfer between two carbon nuclei in diamond. In such a system, the NV center interacts with a nearby nuclear spin via a dipole-dipole interaction. Under the quantum Zeno condition, the scheme is robust against decoherence caused by coupling between the NV center (nuclear spins) and the environment. Conveniently, precise control of dipole coupling is not required so this scheme is insensitive to fluctuating positions of the nuclear spins and the NV center. Our scheme provides a general blueprint for multi-nuclear-spin gates and for multi-party communication in a polygon geometry with each vertex occupied by a nuclear spin.
We theoretically investigate spin decoherence of a single nitrogen-vacancy (NV) center in diamond. Using the spin coherent-state
P-representation method, we simulate coherence evolution of the NV center coupled to surrounding nitrogen electron (N) spins. In the system, the strength of N-N coupling is the same order as that of NV-N coupling (the strong intrabath coupling regime). We find that spin decoherence time as well as free-induction decay of the NV center depend on the spatial configuration of N spins. Both the spin decoherence rate (
1/T2) and dephasing rate (
1/T2∗) of the NV center increase linearly with the concentration of the N spins. Using the
P-representation method, we also demonstrate extracting the noise spectrum of the N spin bath. The capability to calculate the noise spectrum will provide promising pathways to suppress decoherence of spin systems in the strong intrabath coupling regime.
The coupled negatively charged nitrogen-vacancy (NV − ) center system is a promising candidate for scalable quantum information techniques. In this work, ionized nitrogen molecules are implanted into bulk diamond to generate coupled NV − center pairs. The two-photon autocorrelation measurement and optically detected magnetic resonance measurement are carried out to confirm the production of the NV − center pair. Also, both 1.3 μs decoherence time and 4.9 kHz magnetic coupling strength of the NV − center pair are measured by controlling and detecting the spin states. Along with nanoscale manipulation and detection methods, such coupled NV − centers through short distance dipole-dipole interaction would show high potential in scalable quantum information processes.
We present a custom-designed ultrahigh vacuum (UHV) cluster tool developed for studying shallow nitrogen-vacancy (NV) centers in diamond, enabling in situ diamond surface preparation, characterization, and single NV center dynamics measurements within a single connected platform. The system combines a surface science chamber for controlled surface modification and analysis with a cryogenic confocal microscope chamber dedicated to NV spin and optical measurements. This integrated approach enables a direct correlation between diamond surface chemistry and the resulting NV spin and charge properties. The instrument provides a versatile platform for systematic studies of surface-induced decoherence mechanisms and charge dynamics for shallow NV centers, and establishes a pathway toward reproducible surface engineering for quantum sensing applications.