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Nitrogen-vacancy (NV) center in diamond is an ideal candidate for quantum sensors because of its excellent optical and coherence property. However, previous studies are usually conducted at low or room temperature. The lack of full knowledge of coherence properties of the NV center at high temperature limits NVs further applications. Here, we systematically explore the coherence properties of the NV center ensemble at temperatures from 300 K to 600 K. Coherence time $T_2$ decreases rapidly from $184 mu s$ at 300 K to $30 mu s$ at 600 K, which is attributed to the interaction with paramagnetic impurities. Single-quantum and double-quantum relaxation rates show an obvious temperature-dependent behavior as well, and both of them are dominated by the two phonon Raman process. While the inhomogeneous dephasing time $T_2^*$ and thermal echo decoherence time $T_{TE}$ remain almost unchanged as temperature rises. Since $T_{TE}$ changed slightly as temperature rises, a thermal-echo-based thermometer is demonstrated to have a sensitivity of $41 mK/sqrt{Hz}$ at 450 K. These findings will help to pave the way toward NV-based high-temperature sensing, as well as to have a more comprehensive understanding of the origin of decoherence in the solid-state qubit.
We investigated the depth dependence of coherence times of nitrogen-vacancy (NV) centers through precisely depth controlling by a moderately oxidative at 580{deg}C in air. By successive nanoscale etching, NV centers could be brought close to the diam
Stimulated emission is the process fundamental to laser operation, thereby producing coherent photon output. Despite negatively-charged nitrogen-vacancy (NV$^-$) centres being discussed as a potential laser medium since the 1980s, there have been no
Solid-state spin systems including nitrogen-vacancy (NV) centers in diamond constitute an increasingly favored quantum sensing platform. However, present NV ensemble devices exhibit sensitivities orders of magnitude away from theoretical limits. The
Significant attention has been recently focused on the realization of high precision nano-thermometry using the spin-resonance temperature shift of the negatively charged nitrogen-vacancy (NV-) center in diamond. However, the precise physical origins
The negatively-charged nitrogen-vacancy (NV) center in diamond is at the frontier of quantum nano-metrology and bio-sensing. Recent attention has focused on the application of high-sensitivity thermometry using the spin resonances of NV centers in na