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Konstantin Tamarov

Publications and source records attributed to Konstantin Tamarov.

4 recordsLinked to original sources

Score-based diffusion models for severely ill-posed problems in diffuse optical tomography

Score-based diffusion models are a recently developed framework for posterior sampling in Bayesian inverse problems, enabling high-quality reconstructions in inverse problems by leveraging expressive prior distributions learned from empirical data. Despite their strong empirical performance and growing interest within the machine learning community, their behaviour in realistic, severely ill-posed inverse problems with experimental measurement data remains under-explored. Diffuse optical tomography (DOT) is an inverse boundary value problem that uses boundary measurements of near-infrared light to recover spatially varying absorption and scattering parameters in biological tissue. The problem is highly ill-posed and particularly sensitive to both measurement noise and modelling errors. We introduce a regularization strategy by constructing a mixed score consisting of a learned component and a model-based component. We show that the resulting mixed score approximates the score of a corresponding mixture distribution locally and in the small diffusion-time regime, providing a theoretical justification for the approach. We compare four approaches for difference imaging in DOT: a classical model-based method, an approximate score-based diffusion method (DPS), an exact posterior sampling method (UCoS) and a novel, regularized version of UCoS. We show that both the model-based approach and approximate diffusion-based sampling degrade significantly in the presence of limited-view geometry and real experimental data, whereas UCoS yields more accurate reconstructions.

stat.ML

Temperature-dependent dynamic nuclear polarization of diamond

Dynamic nuclear polarization (DNP) can increase nuclear magnetic resonance (NMR) signals by orders of magnitude. DNP in diamond proceeds through different DNP mechanisms with a possible temperature-dependence. We report on 13C dynamic nuclear polarization (DNP) experiments in diamonds at 3.4 T and 7 T between 300 K and 1.7 K. Nuclear polarization enhancements between 100 and 600 were measured for all temperatures, corresponding to polarizations at 7 T between 0.1% (300 K) and 38% (1.7 K). A strong temperature dependence of the DNP profiles was observed. Longitudinal-detected (LOD) electron paramagnetic resonance (EPR) experiments revealed an additional broad temperature-dependent electron line centered around the mI = 0 line of the P1 triplet transitions. Our results suggest that nuclei are preferentially polarized via a direct hyperfine mediated polarization transfer while spin diffusion in the sample plays a minor role.

cond-mat.mtrl-sci

The role of nuclear spin diffusion in dynamic nuclear polarization of crystalline nanoscale silicon particles

Hyperpolarized nanoparticles (NPs) offer high polarization levels with room temperature relaxation times exceeding half an hour. In this work, we demonstrate that the achievable hyperpolarization enhancement and relaxation (decay) time at room temperature are largely independent of the particle size contrary to previous assumptions. This is explained through first-principles spin-diffusion coefficient calculations and finite-element polarization simulations. The simulated zero-quantum (flip-flop) line width governing the spin diffusion is found to agree with the experimentally accessible single-quantum (single spin flip, e.g. radio-frequency pulse) line width. The transport of hyperpolarization from strongly hyperfine-coupled spins towards the bulk is most likelybelieved to be responsible for the slow polarization dynamics including long room temperature decay time. The line width and spin-diffusion simulations are extended to other cubic crystal structures and analytical expressions, which only require insertion of the gyromagnetic ratio, lattice constant, isotope abundance and measured spectral density distribution (nuclear line width), are fitted. The presented simulations can be adjusted to study spin diffusion in other materials.

quant-ph

Controlled synthesis and characterization of porous silicon nanoparticles for dynamic nuclear polarization

Si nanoparticles (NPs) have been actively developed as a hyperpolarized magnetic resonance imaging (MRI) contrast agent with an imaging window close to one hour. However, the progress in the development of NPs has been hampered by the incomplete understanding of their structural properties that correspond to efficient hyperpolarization buildup and long polarization decays. In this work we study dynamic nuclear polarization (DNP) of single crystal porous Si (PSi) NPs with defined doping densities ranging from nominally undoped to highly doped with boron or phosphorus. To develop such PSi NPs we perform low-load metal-assisted catalytic etching for electronic grade Si powder followed by thermal oxidation to form the dangling bonds in the Si/SiO$_2$ interface, the $P_b$ centers. $P_b$ centers are the endogenous source of the unpaired electron spins necessary for DNP. The controlled fabrication and oxidation procedures allow us to thoroughly investigate the impact of the magnetic field, temperature and doping on the DNP process. We argue that the buildup and decay rate constants are independent of size of Si crystals between approximately 10 and 60 nm. Instead, the rates are limited by the polarization transfer across the nuclear spin diffusion barrier determined by the large hyperfine shift of the central $^{29}$Si nuclei of the $P_b$ centers. The size-independent rates are then weakly affected by the doping degree for low and moderately doped Si although slight doping is required to achieve the highest polarization. Thus, we find the room temperature relaxation of low boron doped PSi NPs reaching $75 \pm 3$ minutes and nuclear polarization levels exceeding $\sim 6$ % when polarized at 6.7 T and 1.4 K. Our study thus establishes solid grounds for further development of Si NPs as hyperpolarized contrast agents.

cond-mat.mtrl-sci