Overhauser-driven dynamic nuclear polarization for petroleum systems: literature survey and comparing with experiments

Low-field nuclear magnetic resonance (NMR) instruments are an indispensable tool in industrial research and quality control. However, the intrinsically low spin polarization at low magnetic fields severely limits their detection sensitivity and measurement throughput, preventing their widespread use in biomedical analysis. Overhauser dynamic nuclear polarization (ODNP) effectively addresses this problem by transferring the spin polarization from free electrons to protons, significantly enhancing sensitivity. In this paper, we explore the potential of using ODNP for signal enhancement in a custom-designed portable chip-based DNP-enhanced NMR platform, which is centered around a miniaturized microwave (MW) transmitter, a custom-designed NMR-on-a-chip transceiver, and two application-specific ODNP probes. The MW transmitter provides frequency synthesis, signal modulation, and power amplification, providing sufficient output power for efficient polarization transfer. The NMR-on-a-chip transceiver combines a radio frequency (RF) transmitter with a fully differential quadrature receiver, providing pulsed excitation and NMR signal down-conversion and amplification. Two custom-designed ODNP probes are used for proof-of-concept DNP-enhanced NMR relaxometry and spectroscopy measurements. The presented chip-based ODNP platform achieves a maximum MW output power of , resulting in a signal enhancement of using the relaxometry ODNP probe with of non-degassed TEMPOL solution, and an enhancement of with the spectroscopy ODNP probe using of the same solution. The proton polarization was increased from to at a low field of . Proof-of-concept measurements on radical-doped tattoo inks and acetic acid verify the potential of our chip-based ODNP platform for the analysis of biologically and medically relevant parameters such as relaxation times, chemical shifts, and hyperfine interactions.

Benchtop 13C NMR spectroscopy is highly attractive for reaction and process monitoring. However, insufficient premagnetization and low signal intensities largely prevent its application to flowing liquids. We show that hyperpolarization by Overhauser dynamic nuclear polarization (ODNP) can be used to overcome these problems, as ODNP operates on short time scales and results in strong 13C signal enhancements. Benchtop 13C NMR spectra with ODNP enhancement acquired in continuous-flow are reported here for the first time. We have investigated two ODNP approaches: direct ODNP, which transfers the polarization of unpaired electrons to 13C nuclei via direct hyperfine coupling, and indirect ODNP, in which the electron polarization is first transferred to 1H nuclei before a polarization transfer pulse sequence finally transfers the polarization to the 13C nuclei. Experiments were carried out for three pure solvents and a mixture for different flow rates. The results show significant 13C signal enhancements for both approaches. However, their performance varies for different substances, depending on the strength and type of the hyperfine interaction as well as on the relaxation properties, but by selecting a suitable approach, good single-scan 13C NMR spectra can be obtained with benchtop NMR, even at high flow rates.

TEMPOL nitroxide radicals are frequently used as a polarizing agent for liquid-state Overhauser dynamic nuclear polarization. To achieve large signal enhancements at high magnetic fields (9.4 T), fast picosecond to sub-picosecond dynamics between nitroxide and the target solvent molecule are required. Such dynamics have been predicted by molecular dynamic studies and attributed to fast inner-sphere motions of a transient radical–solvent complex. Here, we systematically study a series of nitroxide radicals with different substituents around the electron spin-bearing NO moiety and different overall sizes to quantify the contribution of the rotational dynamics of the radical to these inner-sphere dynamics. The experiments are performed at a 9.4 T magnetic field, which exhibits high sensitivity to rotational motion contributions in a low picosecond time range. We can show that the observed enhancements can be quantitatively predicted taking the rotational motion of the radical into account.

Dynamic nuclear polarization (DNP) has significantly enhanced the sensitivity of nuclear magnetic resonance (NMR) experiments. While Overhauser DNP has a well-established nuclear counterpart, the nuclear Overhauser effect (NOE), the cross-effect DNP has traditionally been considered as an exclusively electron-mediated process. Here, we present the first evidence of a nuclear counterpart to the cross effect, termed the nuclear cross effect, which mediates polarization transfer in a three-spin nuclear system. The effect was experimentally verified using single-crystal 13C-15N-labeled glycine, with results consistent with both analytical theory and numerical simulations. The experimental realization of the pulsed nuclear cross-effect in this work provides new insights into its theoretical foundations, addressing challenges posed by hardware limitations and the absence of a suitable model system for pulsed cross-effect DNP. Furthermore, the pulsed cross-effect mechanism has the potential to advance enhanced NMR applications in various fields.

We present a generally applicable approach for monitoring protein aggregation by detecting changes in surface hydration water dynamics and the changes in solvent accessibility of specific protein sites, as protein aggregation proceeds in solution state. This is made possible through the Overhauser dynamic nuclear polarization (DNP) of water interacting with stable nitroxide spin labels tethered to specific proteins sites. This effect is highly localized due to the magnetic dipolar nature of the electron-proton spin interaction, with >80% of their interaction occurring within 5 A between the unpaired electron of the spin label and the proton of water. We showcase our tool on the aggregation of tau proteins, whose fibrillization is linked to neurodegenerative disease pathologies known as taupathies. We demonstrate that the DNP approach to monitor local changes in hydration dynamics with residue specificity and local contrast can distinguish specific and neat protein-protein packing leading to fibers from non-specific protein agglomeration or precipitation. The ability to monitor tau assembly with local, residue-specific, resolution, under ambient conditions and in solution state will help unravel the mechanism and structural characteristics of the gradual process of tau aggregation into amyloid fibers, which remains unclear to this day.

While solid-liquid interfaces are ubiquitous, detecting the associated surface sites under ambient conditions remains a grand challenge. Here, we demonstrate an approach to efficiently enhance the NMR signals of solid surfaces at the solid-liquid interface at ambient temperature that is based on exchange mediated Overhauser effect dynamic nuclear polarization (OE-DNP). We use this approach to obtain DNP enhancements for the 31P signals of PPh3 ligands interacting with Rh(I) surface sites, in prototypical silica-supported materials prepared via surface organometallic chemistry. Efficient enhancement (εi) is obtained under ambient conditions simultaneously at the surface (εsurface = 20-30) and in solution (εsolution up to 50), enabling detection of species both at the surface and in solution, opening the possibility to monitor surface and interfacial chemistry.

Impact of non-polar solvents in dynamic nuclear polarization at high magnetic fields.

Dynamic nuclear polarization (DNP) at low temperature (1.2 K) and high magnetic field (3.3 T) was applied to a contrast variation study in small-angle neutron scattering (SANS) focusing on industrial rubber materials. By varying the scattering contrast by DNP, time-of-flight SANS profiles were obtained at the pulsed neutron source of the Japan Proton Accelerator Research Complex (J-PARC). The concentration of a small organic molecule, (2,2,6,6-tetramethylpiperidine-1-yl)oxy (TEMPO), was carefully controlled by a doping method using vapour sorption into the rubber specimens. With the assistance of microwave irradiation (94 GHz), almost full polarization of the paramagnetic electronic spin of TEMPO was transferred to the spin state of hydrogen (protons) in the rubber materials to obtain a high proton spin polarization (PH). The following samples were prepared: (i) a binary mixture of styrene-butadiene random copolymer (SBR) with silica particles (SBR/SP); and (ii) a ternary mixture of SBR with silica and carbon black particles (SBR/SP/CP). For the binary mixture (SBR/SP), the intensity of SANS significantly increased or decreased while keeping its q dependence for PH = -35% or PH = 40%, respectively. The q behaviour of SANS for the SBR/SP mixture can be reproduced using the form factor of a spherical particle. The intensity at low q (∼0.01 Å-1) varied as a quadratic function of PH and indicated a minimum value at PH = 30%, which can be explained by the scattering contrast between SP and SBR. The scattering intensity at high q (∼0.3 Å-1) decreased with increasing PH, which is attributed to the incoherent scattering from hydrogen. For the ternary mixture (SBR/SP/CP), the q behaviour of SANS was varied by changing PH. At PH = -35%, the scattering maxima originating from the form factor of SP prevailed, whereas at PH = 29% and PH = 38%, the scattering maxima disappeared. After decomposition of the total SANS according to inverse matrix calculations, the partial scattering functions were obtained. The partial scattering function obtained for SP was well reproduced by a spherical form factor and matched the SANS profile for the SBR/SP mixture. The partial scattering function for CP exhibited surface fractal behaviour according to q-3.6, which is consistent with the results for the SBR/CP mixture.

Overhauser dynamic nuclear polarization (O-DNP) refers to a microwave-assisted process where an unpaired electron's (e.g. a radical) spin polarization is transferred to surrounding nuclei in solution, thus increasing the nuclear magnetic resonance (NMR) signal intensity of a given substance by several orders of magnitude. The presence of the unpaired electrons, which induces relaxation of the resulting hyperpolarized state when the radiation is halted, can be avoided by electrochemically removing the radicals on demand. We report the use of Blatter-type (benzo[e][1,2,4]triazinyl) radicals as polarizing agents, potentially opening the way to highly tunable radicals for electrochemical DNP.

Structure of Membrane-Bound Huntingtin Exon 1 Reveals Membrane Interaction and Aggregation Mechanisms

Understanding the spatial distribution of the P1 centers is crucial for diamond-based sensors and quantum devices. P1 centers serve as polarization sources for dynamic nuclear polarization (DNP) quantum sensing and play a significant role in the relaxation of nitrogen vacancy (NV) centers. Additionally, the distribution of NV centers correlates with the distribution of P1 centers, as NV centers are formed through the conversion of P1 centers. We utilized DNP and pulsed electron paramagnetic resonance (EPR) techniques that revealed strong clustering of a significant population of P1 centers that exhibit exchange coupling and produce asymmetric line shapes. The 13C DNP frequency profile at a high magnetic field revealed a pattern that requires an asymmetric EPR line shape of the P1 clusters with electron-electron (e-e) coupling strengths exceeding the 13C nuclear Larmor frequency. EPR and DNP characterization at high magnetic fields was necessary to resolve energy contributions from different e-e couplings. We employed a two-frequency pump-probe pulsed electron double resonance technique to show cross-talk between the isolated and clustered P1 centers. This finding implies that the clustered P1 centers affect all of the P1 populations. Direct observation of clustered P1 centers and their asymmetric line shape offers a novel and crucial insight into understanding magnetic noise sources for quantum information applications of diamonds and for designing diamond-based polarizing agents with optimized DNP efficiency for 13C and other nuclear spins of analytes. We propose that room temperature 13C DNP at a high field, achievable through straightforward modifications to existing solution-state NMR systems, is a potent tool for evaluating and controlling diamond defects.

Water's unique thermophysical properties and how it mediates aqueous interactions between solutes have long been interpreted in terms of its collective molecular structure. The seminal work of Errington and Debenedetti [Nature 2001, 409, 318-321] revealed a striking hierarchy of relationships among the thermodynamic, dynamic, and structural properties of water, motivating many efforts to understand (1) what measures of water structure are connected to different experimentally accessible macroscopic responses and (2) how many such structural metrics are adequate to describe the collective structural behavior of water. Diffusivity constitutes a particularly interesting experimentally accessible equilibrium property to investigate such relationships because advanced NMR techniques allow the measurement of bulk and local water dynamics in nanometer proximity to molecules and interfaces, suggesting the enticing possibility of measuring local diffusivities that report on water structure. Here, we apply statistical learning methods to discover persistent structure-dynamic correlations across a variety of simulated aqueous mixtures, from alcohol-water to polypeptoid-water systems. We investigate a variety of molecular water structure metrics and find that an unsupervised statistical learning algorithm (namely, sequential feature selection) identifies only two or three independent structural metrics that are sufficient to predict water self-diffusivity accurately. Surprisingly, the translational diffusivity of water across all mixed systems studied here is strongly correlated with a measure of tetrahedral order given by water's triplet angle distribution. We also identify a separate small number of structural metrics that well predict an important thermodynamic property, the excess chemical potential of an idealized methane-sized hydrophobe in water. Ultimately, we offer a Bayesian method of inferring water structure by using only structure-dynamics linear regression models with experimental Overhauser dynamic nuclear polarization (ODNP) measurements of water self-diffusivity. This study thus quantifies the relationships among several distinct structural order parameters in water and, through statistical learning, reveals the potential to leverage molecular structure to predict fundamental thermophysical properties. In turn, these findings suggest a framework for solving the inverse problem of inferring water's molecular structure using experimental measurements such as ODNP studies that probe local water properties.

We propose a new, more efficient, and potentially cost effective, solid-state nuclear spin hyperpolarization method combining the cross-effect mechanism and electron spin optical hyperpolarization in rotating solids. We first demonstrate optical hyperpolarization in the solid state at low temperatures and low field and then investigate its field dependence to obtain the optimal condition for high-field electron spin hyperpolarization. The results are then incorporated into advanced magic-angle spinning dynamic nuclear polarization (MAS-DNP) numerical simulations that show that optically pumped MAS-DNP could yield breakthrough enhancements at very high magnetic fields. Based on these investigations, enhancements greater than the ratio of electron to nucleus magnetic moments (>658 for 1H) are possible without microwave irradiation. This could solve at once the MAS-DNP performance decrease with increasing field and the high cost of MAS-DNP instruments at very high fields.

Resonant enhancement of spin Seebeck effect (SSE) due to phonons was recently discovered in Y{}_{3}Fe{}_{5}O{}_{12} (YIG). This effect is explained by hybridization between the magnon and phonon dispersions. However, this effect was observed at low temperatures and high magnetic fields, limiting the scope for applications. Here we report observation of phonon-resonant enhancement of SSE at room temperature and low magnetic field. We observe in Lu{}_{2}BiFe{}_{4}GaO{}_{12} an enhancement 700% greater than that in a YIG film and at very low magnetic fields around 10{}^{-1} T, almost one order of magnitude lower than that of YIG. The result can be explained by the change in the magnon dispersion induced by magnetic compensation due to the presence of non-magnetic ion substitutions. Our study provides a way to tune the magnon response in a crystal by chemical doping, with potential applications for spintronic devices.

Dynamic nuclear polarization (DNP) combined with high magnetic fields and fast magic angle spinning (MAS) has opened up a new avenue for the application of exceptionally sensitive 1H NMR detection schemes to study protonated solids. Recently, it has been shown that DNP experiments at fast MAS rates lead to slower spin diffusion and hence reduced DNP enhancements for impregnated materials. However, DNP enhancements alone do not determine the overall sensitivity of a NMR experiment. Here we measure the overall sensitivity of one-dimensional 1H detected relayed DNP experiments as a function of the MAS rate in the 20–60 kHz regime using 0.7 mm diameter rotors at 21.2 T. Although faster MAS rates are detrimental for the DNP enhancement on the target material, due to slower spin diffusion, we find that with increasing spinning rates the gain in sensitivity due to 1H line-narrowing and the folding-in of sideband intensity compensates a large part of the loss of overall hyperpolarization. We find that sensitivity depends on the atomic site in the molecule, and is maximised at between 40 and 50 kHz MAS for the sample of L-histidine.HCl·H2O studied here. There is a 10–20 % difference in sensitivity between the optimum MAS rate and the fastest rate currently accessible (60 kHz).