“…Remarkably, the V B – coherence in electron-irradiated sample is close to the 18 μs upper limit, theoretically predicted for spin defects in hBN using a cluster expansion method and assuming that decoherence is mainly caused by the entanglement between the electron spin and the nuclear spin bath of the host atoms . It is thus within the common range of the coherence for high-density spin defects in diamond , and SiC, , though well below the millisecond range established for single defects in these materials. , (ii) The observed stretched exponential decay indicates that the total coherence time, in addition to spin–spin relaxation, is determined by spectral diffusion, which is commonly characterized by a typical value of n between 1 and 4 depending on the regime of spectral diffusion . The latter indicates coherent interaction of the V B – defect spin with the random and temporally fluctuating local (effective) magnetic field associated with the dipolar-interaction induced flip-flops of nuclear spin pairs of 10 B, 11 B, and 14 N.…”