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Mariusz Mrózek

Publications and source records attributed to Mariusz Mrózek.

11 recordsLinked to original sources

Saturable absorption in NV-doped diamond studied by femtosecond Z-scan

We investigate nonlinear optical absorption in diamond crystals containing high densities of nitrogen vacancy (NV) centers using open-aperture Z-scan measurements with 230 fs laser pulses at 1032 nm, within the transparency window of diamond. While high-purity electronic-grade diamond exhibits third-order nonlinear absorption, NV-doped samples display pronounced saturable absorption that strengthens with increasing defect concentration. Linear transmission spectroscopy reveals that, in addition to NV centers, the crystals host significant populations of H2 (NVN-) defect complexes whose absorption band partially overlaps the excitation wavelength. By correlating spectroscopic data with nonlinear measurements and modeling the response using an effective two-level system, we show that the observed saturation cannot be attributed solely to NV centers but arises from the combined contribution of NV-related and H2 defects. For the highly doped sample, we determine an effective linear absorption coefficient of alpha0 = 6.52 cm-1 and a saturation intensity of Is = 40.0 GW/cm2. These findings highlight the critical role of the complex defect landscape in governing the nonlinear optical response of NV-doped diamond and underscore the necessity of accounting for ancillary defect species in the design of diamond-based nonlinear and quantum photonic devices.

physics.optics↗

Spin-lattice relaxation of NV centers in nanodiamonds adsorbed on conducting and non-conducting surfaces

The nitrogen-vacancy (NV) centers in nanodiamonds can be utilized as low-cost, highly versatile quantum sensors for studying surface properties in condensed matter physics through the application of relaxometry protocols. For such applications, a detailed knowledge of the intrinsic relaxation processes of NV centers in nanodiamonds is necessary. Here, we study the spin-lattice relaxation rates of NV ensembles in nanodiamonds with average diameters of 40 nm and 3 $μ$m between room temperature and $\sim$ 6 K. The NV relaxation curves fit to a stretched-exponential form with a stretching exponent $α\approx 0.7$, implying the large distribution of relaxation times of individual centers within nanodiamonds. We determine the Orbach-like scattering on phonons as the leading relaxation mechanism. Finally, we discuss the viability of nanodiamonds as surface sensors when deposited on a metallic substrate and emphasize the need for well-controlled surface preparation techniques.

cond-mat.mes-hall↗

Optimization and characterization of laser excitation for quantum sensing with single nitrogen-vacancy centres

In this work we present a comprehensive method of characterization and optimization of laser irradiation within a confocal microscope tailored to quantum sensing experiments using nitrogen-vacancy (NV) centres. While confocal microscopy is well-suited for such experiments, precise control and understanding of several optical parameters are essential for reliable single-emitter studies. We investigate the laser beam intensity profile, single-photon emission statistics, fluorescence response under varying polarization and saturation conditions, spectral characteristics, and the temporal profiles of readout and reinitialization pulses. The beam quality is assessed using the beam propagation factor $M^2$, determined via the razorblade technique. Optical fluorescence spectrum is recorded to confirm NV centre emission. To confirm single-emitter operation, we measure second-order autocorrelation function $g^{(2)}(τ)$. Saturation behaviour is analysed by varying laser power and recording the corresponding fluorescence, while polarization dependence is studied using a half-wave ($λ/2$) plate. Temporal laser pulse profile is examined by modulating the power of an acousto-optic modulator. After optimizing all relevant parameters, we demonstrate the microscope's capabilities in driving spin transitions of a single NV centre. This work establishes a straightforward and effective protocol for laser excitation optimization, enhancing the performance and reliability of NV-based quantum sensors.

quant-ph↗

Impact of Nitrogen-Vacancy Color Centers on the Optical Kerr Effect in Diamond: A Femtosecond Z-Scan Study

This study explores nonlinear optical effects in diamond crystals doped with nitrogen-vacancy (NV) centers, focusing on the optical Kerr effect in the infrared spectral region. By employing the Z-scan technique with 230 fs laser pulses at a wavelength of 1032~nm, we investigate the nonlinear refractive index of high-purity and NV-containing diamond crystals at NV concentrations of 0.3 ppm and 4.5 ppm. The results demonstrate a pronounced anisotropy in the nonlinear refractive index, which exhibits a four-fold rotational symmetry, with its amplitude reduced by the NV concentration. The reduction in non-linear susceptibility is linked to the negative contribution of NV centers, modeled as two-level systems upon a strong, laser field, red-detuned relative to their resonance frequency. These findings provide new insights into the interplay between NV centers and nonlinear optical properties of diamond, offering potential pathways for tunable nonlinear optics applications.

physics.optics↗

Localization of macroscopic sources of magnetic field using optical fibers doped with NV-rich sub-micron diamonds and zero-field resonance

We employ an optical fiber doped with randomly oriented fluorescent sub-micron diamonds and the novel zero-field resonance protocol to collect information on the localization and orientation of a magnetic-field source and its distribution. Many previous demonstrations of diamond-based magnetic field sensing achieved ultrahigh sensitivities down to the fT range warranted by manipulating spin states of the diamond nitrogen vacancy (NV) centers with externally applied radio or microwaves. The application of such oscillating fields is problematic in distributed magnetic-field measurements and may be incompatible with specific targets. Instead of relying on these approaches, we leveraged cross-relaxations of particular spin-state populations of the NV center under a magnetic field, thus observing zero-field resonances and making external radio frequency fields redundant. Combined with an optical fiber sensitive to the magnetic field along its entire length, remote sensing was realized that returned information on the spatial field distribution without using any moving mechanical elements in the detection system. Variation of the spatial parameters of the investigated field was achieved simply by controlling the current in a pair of induction coils easily integrable with optical fibers without limiting the fiber-specific functionality of the optical readout taking place at a fixed location at the optical fiber output. Lifting of the requirements related to the mechanical scanning of the fiber, the application of external fields, and the orientation of the NV centers against the measured field mark a very practical step forward in optically driven magnetic field sensing, not easily achievable with earlier implementations.

physics.app-ph↗

Microwave-free imaging magnetometry with nitrogen-vacancy centers in nanodiamonds at near-zero field

Magnetometry using Nitrogen-Vacancy (NV) color centers in diamond predominantly relies on microwave spectroscopy. However, microwaves may hinder certain studies involving biological systems or thin conductive samples. This work demonstrates a wide-field, microwave-free imaging magnetometer utilizing NV centers in nanodiamonds by exploiting the cross-relaxation feature near zero magnetic fields under ambient conditions without applying microwaves. For this purpose, we measure the center shift, contrast, and linewidth of the zero-field cross-relaxation in 140 nm nanodiamonds drop-cast on a current-carrying conductive pattern while scanning a background magnetic field, achieving a sensitivity of 4.5 $\mathrm{μT/\sqrt{Hz}}$. Our work allows for applying the NV zero-field feature in nanodiamonds for magnetic field sensing in the zero and low-field regimes and highlights the potential for microwave-free all-optical wide-field magnetometry based on nanodiamonds.

quant-ph↗

Multimodal Analysis of Traction Forces and Temperature Dynamics of Living Cells with Diamond-Embedded Substrate

Cells and tissues are constantly exposed to various chemical and physical signals that intricately regulate various physiological and pathological processes. This study explores the integration of two biophysical methods, Traction Force Microscopy (TFM) and Optically-Detected Magnetic Resonance (ODMR), to concurrently assess cellular traction forces and local relative temperature. We present a novel elastic substrate with embedded nitrogen-vacancy microdiamonds, that facilitate ODMR-TFM measurements. Optimization efforts have focused on minimizing the sample illumination and experiment duration to mitigate biological perturbations. Our hybrid ODMR-TFM technique yields precise TFM maps and achieves approximately 1K accuracy in relative temperature measurements. Notably, our setup, employing a simple wide-field fluorescence microscope with standard components, demonstrates the broader feasibility of these techniques in life-science laboratories. By elucidating the physical aspects of cellular behavior beyond the existing methods, this approach opens avenues for a deeper understanding and may inspire diverse biomedical applications.

physics.bio-ph↗

Near-zero-field microwave-free magnetometry with nitrogen-vacancy centers in nanodiamonds

We study the fluorescence of nanodiamond ensembles as a function of static external magnetic field and observe characteristic dip features close to the zero field with potential for magnetometry applications. We analyze the dependence of the features width and contrast of the feature on the size of the diamond (in the range 30 nm to 3 um) and on the strength of a bias magnetic field applied transversely to the field being scanned. We also perform optically detected magnetic resonance (ODMR) measurements to quantify the strain splitting of the zero-field ODMR resonance across various nanodiamond sizes and compare it with the width and contrast measurements of the zero-field fluorescence features for both nanodiamonds and bulk samples. The observed properties provide compelling evidence of cross-relaxation effects in the NV system occurring close to zero magnetic fields. Finally, the potential of this technique for use in practical magnetometry is discussed.

cond-mat.mes-hall↗

Tellurite glass rods with nanodiamonds as photonic magnetic field and temperature sensors

We present the results of work on a hybrid material composed of a tellurite glass rod doped with nanodiamonds containing nitrogen-vacancy-nitrogen and paramagnetic nitrogen-vacancy color centers. The reported results include details on tellurite glass and cane fabrication, confocal and wide-field imaging of the nanodiamond distribution in their volume, as well as on the spectroscopic characterization of their fluorescence and Optically Detected Magnetic Resonance measurements of magnetic fields and temperatures. Magnetic fields up to 50 G were examined with a sensitivity of 10$^{-5}$ T Hz$^{-1/2}$ whereas temperature measurements were simultaneously performed with a sensitivity of 74 kHz K$^{-1}$ within the 8 Kelvin range at room temperature. In that way, we demonstrate the suitability of such systems for fiber magneto- and thermometry with a reasonable performance already in the form of glass rods. At the same time, the rods constitute an interesting starting point for further processing into photonic components such as microstructured fibers or fiber tapers for the realization of specialized sensing modalities.

physics.optics↗

Volumetric incorporation of NV diamond emitters in nanostructured F2 glass magneto-optical fiber probes

Integration of optically-active nanodiamonds with glass fibers is a powerful method of scaling of diamond magnetic sensing functionality. We propose a novel approach for integration of nanodiamonds containing nitrogen-vacancy centers directly into the fiber core. The core is fabricated using nanostructurization, that is by stacking the preform from 790 soft glass canes, drawn from a single rod dip-coated with nanodiamonds suspended in isopropyl alcohol. This enables manual control over distribution of nanoscale features, here - the nanodiamonds across and along the fiber core. We verify this by mapping the nanodiamond distribution in the core using confocal microscopy. The nanodiamonds are separated longitudinally either by 15 microns or 24 microns, while in the transverse plane separation of approximately 1 micron is observed, corresponding to the individual cane diameter in the final fiber, without significant agglomeration. Filtered, red fluorescence is observed with naked eye uniformly along the fiber. Its magnetic sensitivity is confirmed by in optically detected magnetic resonance recorded with a coiled, 60-cm-long fiber sample with readout contrast limited mainly by microwave antenna coverage. NV fluorescence intensity in 0 to 35 mT magnetic field is also demonstrated, allowing magnetometry applications with a large B-field dynamic range in absence of microwaves.

cond-mat.mtrl-sci↗

Spin State Dynamics in a Bichromatic Microwave Field: Role of Bright and Dark States in coupling with Reservoir

Driving an open spin system by two strong, nearly degenerate fields enables addressing populations of individual spin states, characterisation of their interaction with thermal bath, and measurements of their relaxation/decoherence rates. With such addressing we observe nested magnetic resonances having nontrivial dependence on microwave field intensity: while the width of one of the resonances undergoes a strong power broadening, the other one exhibits a peculiar field-induced stabilization. We also observe light-induced narrowing of such composite resonances. The observations are explained by the dynamics of bright and dark superposition states and their interaction with reservoir.

quant-ph↗