Identification of beryllium fluoride complexes in mechanically distorted gels using quadrupolar split 9Be NMR spectra resolved with solution-state selective cross-polarization.

The uniformly anisotropic media afforded by hydrogels are being increasingly exploited in analytical (structure elucidation) nuclear magnetic resonance (NMR) spectroscopy, and in studies of mechanosensitive biophysical and biochemical properties of living cells. The 9Be NMR parameters of beryllium fluoride complexes formed in aqueous solutions are sensitive markers of the anisotropic molecular environments produced by gelatin gels. The electric quadrupole moment of the 9Be nucleus (spin I = 3/2) interacts with the electric field gradient tensor in a stretched (or compressed) gel, giving rise to the splitting of peaks in 9Be NMR spectra. These are in addition to those produced by scalar coupling to the 19F nuclei. Thus, an equilibrium mixture of beryllofluoride complexes (BeF2, BeF3-, and BeF42-) in mechanically distorted gels generates an envelope of overlapping 9Be NMR multiplets. In the present work, the multiplets were dissected apart by using selective excitation of 9Be-19F cross-polarization; and the spectral components were quantified with multi-parameter line-shape decomposition, coupled with SpinDynamica simulations. The effects of gel density and Bloom number (a measure of gelatin-gel rigidity under standard conditions of sample preparation) on residual quadrupolar splittings were examined. Cross-polarization experiments revealed a bimodal distribution of  residual quadrupolar coupling constants (RQC) of the BeF3- complexes. The average RQC of the dominant BeF3- population was ∼3 times larger than that of BeF42-. The secondary BeF3- population existed in a tetrahedral configuration. It was attributed to BeF3- complexes associated with negatively charged -COO- groups of the denatured collagen matrix.

Enhanced Ca2+ influx in mechanically distorted erythrocytes measured with 19F nuclear magnetic resonance spectroscopy.

We present the first direct nuclear magnetic resonance (NMR) evidence of enhanced entry of Ca2+ ions into human erythrocytes (red blood cells; RBCs), when these cells are mechanically distorted. For this we loaded the RBCs with the fluorinated Ca2+ chelator, 1,2-bis(2-amino-5-fluorophenoxy)ethane-N,N,N',N'-tetraacetic acid (5FBAPTA), and recorded 19F NMR spectra. The RBCs were suspended in gelatin gel in a special stretching/compression apparatus. The 5FBAPTA was loaded into the cells as the tetraacetoxymethyl ester; and 13C NMR spectroscopy with [1,6-13C]D-glucose as substrate showed active glycolysis albeit at a reduced rate in cell suspensions and gels. The enhancement of Ca2+ influx is concluded to be via the mechanosensitive cation channel Piezo1. The increased rate of influx brought about by the activator of Piezo1, 2-[5-[[(2,6-dichlorophenyl)methyl]thio]-1,3,4-thiadiazol-2-yl]-pyrazine (Yoda1) supported this conclusion; while the specificity of the cation-sensing by 5FBAPTA was confirmed by using the Ca2+ ionophore, A23187.

Distortion-free inside-out imaging for rapid diagnostics of rechargeable Li-ion cells.

Safety risks associated with modern high energy-dense rechargeable cells highlight the need for advanced battery screening technologies. A common rechargeable cell exposed to a uniform magnetic field creates a characteristic field perturbation due to the inherent magnetism of electrochemical materials. The perturbation pattern depends on the design, state of charge, accumulated mechanical defects, and manufacturing flaws of the device. The quantification of the induced magnetic field with MRI provides a basis for noninvasive battery diagnostics. MRI distortions and rapid signal decay are the main challenges associated with strongly magnetic components present in most commercial cells. These can be avoided by using Single-Point Ramped Imaging with T1 enhancement (SPRITE). The method is immune to image artifacts arising from strong background gradients and eddy currents. Due to its superior image quality, SPRITE is highly sensitive to defects and the state of charge distribution in commercial Li-ion cells.

New insights into the thermal behaviour of organic ionic plastic crystals: magnetic resonance imaging of polycrystalline morphology alterations induced by solid-solid phase transitions.

Organic ionic plastic crystals (OIPCs) show strong potential as solid-state electrolytes for lithium battery applications, demonstrating promising electrochemical performance and eliminating the need for a volatile and flammable liquid electrolyte. The ionic conductivity (σ) in these systems has recently been shown to depend strongly on polycrystalline morphology, which is largely determined by the sample's thermal history. [K. Romanenko et al., J. Am. Chem. Soc., 2014, 136, 15638]. Tailoring this morphology could lead to conductivities sufficiently high for battery applications, so a more complete understanding of how phenomena such as solid-solid phase transitions can affect the sample morphology is of significant interest. Anisotropic relaxation of nuclear spin magnetisation provides a new MRI based approach for studies of polycrystalline materials at both a macroscopic and molecular level. In this contribution, morphology alterations induced by solid-solid phase transitions in triisobutyl(methyl)phosphonium bis(fluorosulfonyl)imide (P1444FSI) and diethyl(methyl)(isobutyl)phosphonium hexafluorophosphate (P1224PF6) are examined using magnetic resonance imaging (MRI), alongside nuclear magnetic resonance (NMR) spectroscopy, diffusion measurements and conductivity data. These observations are linked to molecular dynamics and structural behaviour crucial for the conductive properties of OIPCs. A distinct correlation is established between the conductivity at a given temperature, σ(T), and the intensity of the narrow NMR signal that is attributed to a mobile fraction, fm(T), of ions in the OIPC. To explain these findings we propose an analogy with the well-studied relationship between permeability (k) and void fraction (θ) in porous media, with k(θ) commonly quantified by a power-law dependence that can also be employed to describe σ(fm).

New opportunities for quantitative and time efficient 3D MRI of liquid and solid electrochemical cell components: Sectoral Fast Spin Echo and SPRITE.

The ability to image electrochemical processes in situ using nuclear magnetic resonance imaging (MRI) offers exciting possibilities for understanding and optimizing materials in batteries, fuel cells and supercapacitors. In these applications, however, the quality of the MRI measurement is inherently limited by the presence of conductive elements in the cell or device. To overcome related difficulties, optimal methodologies have to be employed. We show that time-efficient three dimensional (3D) imaging of liquid and solid lithium battery components can be performed by Sectoral Fast Spin Echo and Single Point Imaging with T1 Enhancement (SPRITE), respectively. The former method is based on the generalized phase encoding concept employed in clinical MRI, which we have adapted and optimized for materials science and electrochemistry applications. Hard radio frequency pulses, short echo spacing and centrically ordered sectoral phase encoding ensure accurate and time-efficient full volume imaging. Mapping of density, diffusivity and relaxation time constants in metal-containing liquid electrolytes is demonstrated. 1, 2 and 3D SPRITE approaches show strong potential for rapid high resolution (7)Li MRI of lithium electrode components.

Anisotropic MRI contrast reveals enhanced ionic transport in plastic crystals.

Organic ionic plastic crystals (OIPCs) are attractive as solid-state electrolytes for electrochemical devices such as lithium-ion batteries and solar and fuel cells. OIPCs offer high ionic conductivity, nonflammability, and versatility of molecular design. Nevertheless, intrinsic ion transport behavior of OIPCs is not fully understood, and their measured properties depend heavily on thermal history. Solid-state magnetic resonance imaging experiments reveal a striking image contrast anisotropy sensitive to the orientation of grain boundaries in polycrystalline OIPCs. Probing triethyl(methyl)phosphonium bis(fluorosulfonyl)imide (P1222FSI) samples with different thermal history demonstrates vast variations in microcrystallite alignment. Upon slow cooling from the melt, microcrystallites exhibit a preferred orientation throughout the entire sample, leading to an order of magnitude increase in conductivity as probed using impedance spectroscopy. This investigation describes both a new conceptual window and a new characterization method for understanding polycrystalline domain structure and transport in plastic crystals and other solid-state conductors.

Spatially resolved measurements of mean spin-spin relaxation time constants.

Magnetic Resonance measurements of the T2 distribution have become very common and they are a powerful way to probe microporous fluid bearing solids. While the structure of the T2 distribution, and changes in the structure, are often very informative, it is common to reduce the T2 distribution to a mean numeric quantity in order to provide a quantitative interpretation of the distribution. Magnetic Resonance Imaging measurements of the T2 distribution have recently been introduced, but they are time consuming, especially for 2 and 3 spatial dimensions. In this paper we explore a direct MRI measurement of the arithmetic mean of 1/T2, characterizing the distribution by using the initial slope of the spatially resolved T2 decay in a CPMG prepared Centric Scan SPRITE experiment. The methodology is explored with a test phantom sample and realistic petroleum reservoir core plug samples. The arithmetic mean of 1/T2 is related to the harmonic mean of T2. The mean obtained from the early decay is explored through measurements of uniform saturated core plug samples and by comparison to other means determined from the complete T2 distribution. Complementary data were obtained using SE-SPI T2 distribution MRI measurements. The utility of the arithmetic mean 1/T2 is explored through measurements of centrifuged core plug samples where the T2 distribution varies spatially. The harmonic mean T2 obtained from the early decay was employed to estimate the irreducible water saturation for core plug samples.

Velocity field measurements in sedimentary rock cores by magnetization prepared 3D SPRITE.

A time-efficient MRI method suitable for quantitative mapping of 3-D velocity fields in sedimentary rock cores, and granular samples is discussed. The method combines the 13-interval Alternating-Pulsed-Gradient Stimulated-Echo (APGSTE) scheme and three-dimensional Single Point Ramped Imaging with T(1) Enhancement (SPRITE). Collecting a few samples near the q-space origin and employing restricted k-space sampling dramatically improves the performance of the imaging method. The APGSTE-SPRITE method is illustrated through mapping of 3-D velocity field in a macroscopic bead pack and heterogeneous sandstone and limestone core plugs. The observed flow patterns are consistent with a general trend for permeability to increase with the porosity. Domains of low permeability obstruct the flow within the core volume. Water tends to flow along macroscopic zones of higher porosity and across zones of lower porosity.

(35)Cl profiling using centric scan SPRITE with variable flip angle excitation.

An efficient MRI technique for quantitative density profiling of samples with fast spin-lattice relaxation (T(1)<5ms) is introduced. The pulse scheme is based on the 1D centric scan SPRITE technique. Strong excitation of the sample at the k-space origin improves the sensitivity with respect to the original centric scan SPRITE technique. Radio frequency pulse durations are defined so as to provide uniform excitation of the sample at every k-space point. For a particular k-space point the pulse duration is required to be less than the inverse sample bandwidth. Simulations permit one to examine distortions from ideal profile geometry due to flip angle and spin-lattice relaxation effects. The proposed technique is especially suitable for the observation of low sensitivity samples, in particular, low-gamma nuclei like (35)Cl. In some cases, this strategy permits one to reduce the number of scans, i.e. the experiment time, by a factor of 100, depending on hardware, sample length and tolerable resolution loss. The designed pulse scheme is tested on cylindrical agar gel and type 1 Portland cement paste phantoms prepared to provide (1)H and (35)Cl signals, respectively.

Solid state NMR characterization of individual compounds and solid solutions formed in Sc(2)O(3)--V(2)O(5)--Nb(2)O(5)--Ta(2)O(5) system.

In this study, (51)V, (45)Sc and (93)Nb MAS NMR combined with satellite transition spectroscopy analysis were used to characterize the complex solid mixtures: VNb(9(1-x))Ta(9x)O(25), ScNb((1-x))Ta(x)O(4) and ScNb(2(1-x))Ta(2x)VO(9) (x = 0, 0.3, 0.5, 0.7, 1.0). This led us to describe the structures of Sc and V sites. The conclusions were based on accurate values for (51)V quadrupole coupling and chemical shift tensors obtained with (51)V MAS NMR/SATRAS for VNb(9)O(25), VTa(9)O(25) and ScVO(4). The (45)Sc NMR parameters have been obtained for Sc(2)O(3), ScVO(4), ScNbO(4) and ScTaO(4). On the basis of (45)Sc NMR and data available from literature, the ranges of the (45)Sc chemical shift have been established for ScO(6) and ScO(8). The gradual change of the (45)Sc and (51)V NMR parameters with x confirms the formation of solid solutions in the process of synthesis of VNb(9(1-x))Ta(9x)O(25) and ScNb((1-x))Ta(x)O(4), in contrast to ScNb(2(1-x))Ta(2x)VO(9). The cation sublattice of ScNb((1-x))Ta(x)O(4) is found to be in octahedral coordination. The V sites in VNb(9(1-x))Ta(9x)O(25) are present in the form of slightly distorted tetrahedra. The (93)Nb NMR parameters have been obtained for VNb(9)O(25).

129Xe nuclear magnetic resonance study of pitch-based activated carbon modified by air oxidation/pyrolysis cycles: a new approach to probe the micropore size.

(129)Xe NMR has been used to study a series of homologous activated carbons obtained from a KOH-activated pitch-based carbon molecular sieve modified by air oxidation/pyrolysis cycles. A clear correlation between the pore size of microporous carbons and the (129)Xe NMR of adsorbed xenon is proposed for the first time. The virial coefficient delta(Xe)(-)(Xe) arising from binary xenon collisions varied linearly with the micropore size and appeared to be a better probe of the microporosity than the chemical shift extrapolated to zero pressure. This correlation was explained by the fact that the xenon collision frequency increases with increasing micropore size. The chemical shift has been shown to vary very little with temperature (less than 9 ppm) for xenon trapped inside narrow and wide micropores. This is indicative of a smooth xenon-surface interaction potential.

93Nb NMR chemical shift scale for niobia systems.

93Nb solid-state NMR spectra of a series of inorganic niobates with Nb in different oxygen coordination environments were measured. For all studied compounds the chemical shielding and quadrupole tensor parameters were determined using conventional and ultrahigh field NMR facilities, ultrahigh speed MAS, DQ STMAS, solid-echo and computer modeling. It has been demonstrated that the 93Nb isotropic chemical shift is sensitive to the coordination number of Nb sites. For the first time the 93Nb NMR chemical shift scale for NbOx polyhedra in solid materials has been proposed: for four-coordinated Nb sites, the isotropic shifts occur from -650 to -950 ppm; five-coordinated Nb sites have the isotropic shifts in the range of -900 to -980 ppm; for six-coordinated Nb sites the isotropic shifts vary from -900 to -1360 ppm; the shifts from -1200 to -1600 ppm are typical for seven-coordinated Nb sites; for eight-coordinated Nb sites the shifts are higher than -1400 ppm. The possible correlation between the value of the isotropic chemical shift and the ionic character of the NbOx-MOy polyhedra association has been suggested. The magnitude of the 93Nb quadrupole coupling constant depends on the local symmetry of Nb sites and may vary from hundreds of kHz to hundreds of MHz.

95Mo magic angle spinning NMR at high field: improved measurements and structural analysis of the quadrupole interaction in monomolybdates and isopolymolybdates.

In this study, 95Mo quadrupole couplings in various molydbates were measured easily and accurately with magic angle spinning (MAS) NMR under a directing field of 19.6 T. The resonance frequency of 54 MHz was sufficiently high to remove acoustic ringing artifacts, and the spectra could be analyzed in the usual terms of chemical shift and quadrupolar line shapes. For monomolybdates and molybdite, the quadrupole coupling dominated the NMR response, and the quadrupole parameters could be measured with better accuracy than in previous lower field studies. Moreover, despite the low symmetry of the molybdenum coordination, the usefulness of such measurements to probe molybdenum environments was established by ab initio density functional theory (DFT) calculations of the electric field gradient from known structures. The experimental NMR data correlated perfectly with the refined structures. In isopolymolybdates, the resonances were shapeless and DFT calculations were impossible because of the large and low symmetry unit cells. Nevertheless, empirical but clear NMR signatures were obtained from the spinning sidebands analysis or the MQMAS spectra. This was possible for the first time thanks to the improved baseline and sensitivity at high fields. With the generalization of NMR spectrometers operating above 17 T, it was predicted that 95Mo MAS NMR could evolve as a routine characterization tool for ill-defined structures such as supported molybdates in catalysis.