arXiv subjects

Michal Gulka

Publications and source records attributed to Michal Gulka.

6 recordsLinked to original sources

arXiv2026

Exploiting ionization dynamics in the nitrogen vacancy center for rapid, high-contrast spin and charge state initialization

We propose and experimentally demonstrate a method to strongly increase the sensitivity of spin measurements on nitrogen-vacancy (NV) centers in diamond, which can be readily implemented in existing quantum sensing experiments. While charge state transitions of this defect are generally considered a parasitic effect to be avoided, we show here that these can be used to significantly increase the NV center's spin contrast, a key quantity for high sensitivity magnetometry and high fidelity state readout. The protocol consists of a two-step procedure, in which the charge state of the defect is first purified by a strong laser pulse, followed by weak illumination to obtain high spin polarization. We observe a relative improvement of the readout contrast by 17 %, and infer a reduction of the initialization error of more than 50 %. The contrast enhancement is accompanied by a beneficial increase of the readout signal. For long sequence durations, typically encountered in high-resolution magnetometry, a measurement speedup by a factor of >1.5 is extracted, and we find that the technique is beneficial for sequences of any duration. Additionally, our findings give detailed insight into the charge and spin polarization dynamics of the NV center, and provide actionable insights for direct optical, spin-to-charge, and electrical readout of solid-state spin centres.

quant-ph↗

arXiv2026

Long Spin Relaxation Times in CVD-Grown Nanodiamonds

Currently, the primary applications of fluorescent nanodiamonds (FNDs) are in the area of biosensing, by using photoluminescence or spin properties of colour centres, mainly represented by the Nitrogen Vacancy (NV) point defect. The sensitivity of NV-FNDs to external fields is, however, limited by crystallographic defects, which influence their key quantum state characteristics - the spin longitudinal (\textit{T$_1$}) and spin transversal (\textit{T$_2$}) relaxation and coherence times, respectively. We report on utilising an advanced FND growth technique consisting of heterogeneous nucleation on pre-engineered sites to create FNDs averaging around 60 nm in size, with mean longitudinal coherence times of 800 $\mu$s and a maximum over 1.8 ms, close to bulk theoretical values. This is a major, nearly ten-fold improvement over commercially available nanodiamonds for the same size range of 50 to 150 nm. Heavy-N doped nanodiamond shells, important for sensing events in nm proximity to the diamond surface, are fabricated and discussed in terms of re-nucleation and twinning on \{111\} crystal facets. We also discuss scalability issues in order to enable the production of FND volumes matching the needs of sensing applications.

cond-mat.mes-hall↗

arXiv2025

Modelling and experimental verification of photoelectrical response of NV diamond spin centres

We report on a mathematical model of the photoelectric response of NV colour centres in diamond, that can be employed for sensing and quantum science information applications. Although the model applies to NV centre in diamond, it can be applied with small modifications to other semiconducting solid state qubits. In our model, we include the drift and collection of charge carriers as well as the presence of other defects via generation and recombination dynamics. Though the photoluminescence readout and the associated dynamics of the NV defect has been extensively studied experimentally and theoretically, so far, there has been no precise model for photocurrent readout, including these effects. In our description, we use a multilevel-level system including mS=0, mS=+-1 ground and excited states, singlet state and the NV0 neutral state. Also, the presence of substitutional nitrogen (NS), which for example determines the spin coherence via the paramagnetic spin bath, is discussed together with presence of acceptor defects. We model the time-dependent occupation of all electronic sublevels and also consider the electronic charge transport from the Boltzmann transport equation, leading to information about the charge state transitions and recombination dynamics. ODMR and PDMR response as well as their quantum efficiencies, are calculated. On this basis, we determine an optimal parameter space for qubit operations, including the highest spin contrast and especially relate those to NS presence. The model is confirmed experimentally and can become a useful tool for optimisation of the performance of NV qubit photoelectric readout.

quant-ph↗

arXiv2021

Room-temperature control and electrical readout of individual nitrogen-vacancy nuclear spins

Nuclear spins in semiconductors are leading candidates for quantum technologies, including quantum computation, communication, and sensing. Nuclear spins in diamond are particularly attractive due to their extremely long coherence lifetime. With the nitrogen-vacancy (NV) centre, such nuclear qubits benefit from an auxiliary electronic qubit, which has enabled entanglement mediated by photonic links. The transport of quantum information by the electron itself, via controlled transfer to an adjacent centre or via the dipolar interaction, would enable even faster and smaller processors, but optical readout of arrays of such nodes presents daunting challenges due to the required sub-diffraction inter-site distances. Here, we demonstrate the electrical readout of a basic unit of such systems - a single 14N nuclear spin coupled to the NV electron. Our results provide the key ingredients for quantum gate operations and electrical readout of nuclear qubit registers, in a manner compatible with nanoscale electrode structures. This demonstration is therefore a milestone towards large-scale diamond quantum devices with semiconductor scalability.

cond-mat.mes-hall↗

arXiv2020

Nanoscale Dynamic Readout of a Chemical Redox Process Using Radicals Coupled with Nitrogen-Vacancy Centers in Nanodiamonds

Biocompatible nanoscale probes for sensitive detection of paramagnetic species and molecules associated with their (bio)chemical transformations would provide a desirable tool for a better understanding of cellular redox processes. Here, we describe an analytical tool based on quantum sensing techniques. We magnetically coupled negatively charged nitrogen-vacancy (NV) centers in nanodiamonds (NDs) with nitroxide radicals present in a bioinert polymer coating of the NDs. We demonstrated that the T1 spin relaxation time of NV centers is very sensitive to the number of nitroxide radicals, with a resolution down to ~10 spins per ND (detection of approximately $ 10^-23 $ mol in a localized volume). The detection is based on T1 shortening upon the radical attachment and we propose a theoretical model describing this phenomenon. We further show this colloidally stable, water-soluble system can be used dynamically for spatiotemporal readout of a redox chemical process (oxidation of ascorbic acid) occurring near the ND surface in an aqueous environment under ambient conditions.

physics.app-ph↗

arXiv2016

Pulsed photoelectric coherent manipulation and detection of NV centre spins in diamond

Hybrid photoelectric detection of NV magnetic resonances (PDMR) is anticipated to lead to scalable quantum chip technology. To achieve this goal, it is crucial to prove that PDMR readout is compatible with the coherent spin control. Here we present PDMR MW pulse protocols that filter background currents related to ionization of NS0 defects and achieve a high contrast and S/N ratio. We demonstrate Rabi and Ramsey protocols on shallow nitrogen-implanted electronic grade diamond and the coherent readout of ~ 5 NV spins, as a first step towards the fabrication of scalable photoelectric quantum devices.

cond-mat.mes-hall↗