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Complex quantum systems and their various applications are susceptible to noise of coherent and incoherent nature. Characterization of noise and its sources is an open, key challenge in quantum technology applications, especially in terms of distinguishing between inherent incoherent noise and systematic coherent errors. In this paper, we study a scheme of repeated sequential measurements that enables the characterization of incoherent errors by reducing the effects of coherent errors. We demonstrate this approach using a coherently controlled Nitrogen Vacancy in diamond, coupled to both a natural nuclear spin bath (non-Markovian) and to experimentally controlled relaxation through an optical pumping process (nearly Markovian). Our results show mitigation of coherent errors both for Markovian and Non-Markovian incoherent noise profiles. We apply this scheme to the estimation of the dephasing time ($T_2^*$) due to incoherent noise. We observe an improved robustness against coherent errors in the estimation of dephasing time ($T_2^*$) compared to the standard (Ramsey) measurement.

Quantum sensing using local defects in solid-state systems has gained significant attention over the past several years, with impressive results demonstrated both in Academia and in Industry. Specifically, employing large volume and high density ensembles for beyond state-of-the-art sensitives is of clear interest. A major obstacle for achieving such record sensitivities is associated with the need to realize strong, homogeneous driving of the sensor defects. Here we focus on high-frequency microwave sensing using nitrogen-vacancy centers in diamond, and develop a modified split-ring resonator design to address this issue. We demonstrate enhanced drive strengths and homogeneities over large volumes compared to previous results, with prospects for enabling the desired sensitivities. We reach Rabi frequencies of up to 18 [MHz] with an efficiency ratio of 2 [$Gauss/\sqrt{Watt}$], along with an inhomogeneity of $<0.7\%$ in a volume of $0.1\:mm^3$.

Using element-specific X-ray magnetic circular dichroism (XMCD) technique we have studied different magnetic sublattices in a multiferroic Ho$_{0.5}$Nd$_{0.5}$Fe$_{3}$(BO$_{3}$)$_{4}$ single crystal. The XMCD measurements at the \emph{L}$_{2,3}$-edges of Ho and Nd, and at the Fe \emph{K}-edge have been performed at \emph{T}=2~K under a magnetic field up to 17~T applied along the trigonal \emph{c}-axis as well as in the basal \emph{ab}-plane. All three magnetic sublattices are shown to undergo a spin-reorientation transition under magnetic field applied along the \emph{c}-axis. On the contrary, when magnetic field is applied in the \emph{ab}-plane only the holmium atoms exhibit a magnetization jump. Thus, the element-specific magnetization curves revealed the Ho sublattice to be much stronger coupled to the Fe one than the Nd sublattice. The results demonstrate that the Ho$^{3+}$ subsystem plays even more dominant role in magnetic behavior of Ho$_{0.5}$Nd$_{0.5}$Fe$_{3}$(BO$_{3}$)$_{4}$ crystal than in pure HoFe$_{3}$(BO$_{3}$)$_{4}$ crystal.