Electron and nuclear spin dynamics in the thermal mixing model of dynamic nuclear polarization

A novel mathematical treatment is proposed for computing the time evolution of dynamic nuclear polarization processes in the low temperature thermal mixing regime. Without assuming any a priori analytical form for the electron polarization, our approach provides a quantitative picture of the steady state that recovers the well known Borghini prediction based on thermodynamics arguments, as long as the electrons-nuclei transition rates are fast compared to the other relevant time scales. Substantially different final polarization levels are achieved instead when the latter assumption is relaxed in the presence of a nuclear leakage term, even though very weak, suggesting a possible explanation for the deviation between the measured steady state polarizations and the Borghini prediction. The proposed methodology also allows to calculate nuclear polarization and relaxation times, once specified the electrons/nuclei concentration ratio and the typical rates of the microscopic processes involving the two spin species. Numerical results are shown to account for the manifold dynamical behaviours of typical DNP samples.Comment: 11 pages, 11 figure

Design and performance of a DNP prepolarizer coupled to a rodent MRI scanner

For most of the last forty years, the techniques of Dynamic Nuclear Polarization (DNP) have been confined to particle-physics laboratories building polarized targets, but recently it has been shown that samples similar to a solid target can be transformed into room temperature liquid solutions while retaining a high nuclear polarization. This method of "hyperpolarization" is of interest in NMR/MRI/MRS. We describe a 3.35 T DNP/9.4 T MRI installation based on a continuous-flow cryostat, using a standard wide-bore low-field NMR magnet as prepolarizer magnet and a widely available radical as polarizing agent. The interfacing to a rodent scanner requires that the infusion of the polarized solution in the animal be remotely controlled, because of limited access inside the magnet bore. Physiological constraints on the infusion rate can be a serious source of polarization loss, and the discussion of efficiency is therefore limited to that of the prepolarizer itself, i.e., the spin temperatures obtained in the solid state. To put our results in context, we summarize data obtained in targets with different types of radicals, and provide a short review of the DNP mechanisms needed in their discussion. (C) 2007 Wiley Periodicals, Inc

CdTe solar cells in a novel configuration

Polycrystalline thin-film CdTe/CdS solar cells have been developed in a configuration in which a transparent conducting layer of indium tin oxide (ITO) has been used for the first time as a back electrical contact on p-CdTe. Solar cells of 7.9% efficiency were developed on SnOx:F-coated glass substrates with a low-temperature (<450\ub0C) high-vacuum evaporation method. After the CdCl2 annealing treatment of the CdTe/CdS stack, a bromine methanol solution was used for etching the CdTe surface prior to the ITO deposition. The unique features of this solar cell with both front and back contacts being transparent and conducting are that the cell can be illuminated from either or both sides simultaneously like a 'bi-facial' cell, and it can be used in tandem solar cells. The solar cells with transparent conducting oxide back contact show long-term stable performance under accelerated test conditions

Hyperpolarized lithium-6 as a sensor of nanomolar contrast agents.

Lithium is widely used in psychotherapy. The (6)Li isotope has a long intrinsic longitudinal relaxation time T(1) on the order of minutes, making it an ideal candidate for hyperpolarization experiments. In the present study we demonstrated that lithium-6 can be readily hyperpolarized within 30 min, while retaining a long polarization decay time on the order of a minute. We used the intrinsically long relaxation time for the detection of 500 nM contrast agent in vitro. Hyperpolarized lithium-6 was administered to the rat and its signal retained a decay time on the order of 70 sec in vivo. Localization experiments imply that the lithium signal originated from within the brain and that it was detectable up to 5 min after administration. We conclude that the detection of submicromolar contrast agents using hyperpolarized NMR nuclei such as (6)Li may provide a novel avenue for molecular imaging

Dynamic nuclear polarization of small labelled molecules in frozen water-alcohol solutions

In recent years methods of creating 'hyperpolarized' substances have gained considerable attention in biomedical magnetic resonance and dynamic nuclear polarization (DNP) is one of the most promising, especially for imaging applications. Here we present results of DNP studies on protons and C-13 nuclei in frozen solutions of sodium acetate and glycine, dissolved in water-ethanol and water-glycerol, doped with TEMPO free radicals and EHBA-Cr-V complexes. Up to 14% C-13 polarization and close to 50% proton polarization were achieved at similar to 1.2K in a magnetic field of similar to 3.5 T under irradiation with similar to 97 GHz microwaves, which corresponds to an enhancement of more than 15 000 with respect to thermal equilibrium polarization in a 9.4 T magnet at room temperature. For all investigated samples the main DNP mechanism was found to be thermal mixing. The absolute polarization values achieved are mainly depending on the type of solvent, the water-alcohol ratio, its degree of deuteration and the concentration of paramagnetic centres. This allows application of the so-established sample preparation and DNP procedure to other molecules in future experiments. Two further examples of DNP of molecules in solution underline the general applicability of the method to a wide variety of organic compounds

A 140 GHz prepolarizer for dissolution dynamic nuclear polarization

Apart from their very classical use to build polarized targets for particle physics, the methods of dynamic nuclear polarization (DNP) have more recently found application for sensitivity enhancement in high-resolution NMR, both in the solid and in the liquid state. It is often thought that the possible signal enhancement in such applications deteriorates when the DNP is performed at higher fields. We show that for a dissolution-DNP method that uses conventional (2,2,6,6-tetramethylpiperidine 1-oxyl) radicals as the paramagnetic agent, this is not the case for fields up to 5 T. (C) 2008 American Institute of Physics

Feasibility of in vivo N-15 MRS detection of hyperpolarized N-15 labeled choline in rats

The increase of total choline in tumors has become an important biomarker in cancer diagnosis. Choline and choline metabolites can be measured in vivo and in vitro using multinuclear MRS. Recent in vivo C-13 MRS studies using labeled substrates enhanced via dynamic nuclear polarization demonstrated the tremendous potential of hyperpolarization for real-time metabolic studies. The present study demonstrates the feasibility of detecting hyperpolarized N-15 labeled choline in vivo in a rat head at 9.4 T. We furthermore report the in vitro (172 +/- 16 s) and in vivo (126 +/- 15 s) longitudinal relaxation times. We conclude that with appropriate infusion protocols it is feasible to detect hyperpolarized N-15 labeled choline in live animals