Andrew J. Ilott

Correlating Microstructural Lithium Metal Growth with Electrolyte Salt Depletion in Lithium Batteries Using 7Li MRI

Lithium dendrite growth in lithium ion and lithium rechargeable batteries is associated with severe safety concerns. To overcome these problems, a fundamental understanding of the growth mechanism of dendrites under working conditions is needed. In this work, in situ (7)Li magnetic resonance (MRI) is performed on both the electrolyte and lithium metal electrodes in symmetric lithium cells, allowing the behavior of the electrolyte concentration gradient to be studied and correlated with the type and rate of microstructure growth on the Li metal electrode. For this purpose, chemical shift (CS) imaging of the metal electrodes is a particularly sensitive diagnostic method, enabling a clear distinction to be made between different types of microstructural growth occurring at the electrode surface and the eventual dendrite growth between the electrodes. The CS imaging shows that mossy types of microstructure grow close to the surface of the anode from the beginning of charge in every cell studied, while dendritic growth is triggered much later. Simple metrics have been developed to interpret the MRI data sets and to compare results from a series of cells charged at different current densities. The results show that at high charge rates, there is a strong correlation between the onset time of dendrite growth and the local depletion of the electrolyte at the surface of the electrode observed both experimentally and predicted theoretical (via the Sands time model). A separate mechanism of dendrite growth is observed at low currents, which is not governed by salt depletion in the bulk liquid electrolyte. The MRI approach presented here allows the rate and nature of a process that occurs in the solid electrode to be correlated with the concentrations of components in the electrolyte.

Multinuclear in situ magnetic resonance imaging of electrochemical double-layer capacitors

The last decade has seen an intensified interest in the development and use of electrochemical double-layer capacitors, fuelled by the availability of new electrode materials. The use of nanoporous carbons, in particular, with extremely high surface areas for ion adsorption has enabled the development of working devices with significantly increased capacitances that have become viable alternatives to lithium-ion batteries in certain applications. An understanding of the charge storage mechanism and the ion dynamics inside the nanopores is only just emerging, with the most compelling evidence coming from simulation. Here we present the first in situ magnetic resonance imaging experiments of electrochemical double-layer capacitors. These experiments overcome the limitations of other techniques and give spatially resolved chemical information about the electrolyte ions in real time for a working capacitor of standard geometry. The results provide insight into the predominant capacitive processes occurring at different states of charge and discharge.

Paramagnetic electrodes and bulk magnetic susceptibility effects in the in situ NMR studies of batteries: application to Li1.08Mn1.92O4 spinels.

To date, in situ nuclear magnetic resonance (NMR) studies of working batteries have been performed in static mode, i.e., in the absence of magic angle spinning (MAS). Thus, it is extremely challenging to apply the method to paramagnetic systems such as the cathodes spinels Li(1+x)Mn(2-x)O4 primarily due to three factors: (1) the resonance lines are broadened severely; (2) spectral analysis is made more complicated by bulk magnetic susceptibility (BMS) effects, which depend on the orientation and shape of the object under investigation; (3) the difficulty in untangling the BMS effects induced by the paramagnetic and metallic components on other (often diamagnetic) components in the system, which result in additional shifts and line broadening. Here we evaluate the orientation-dependence of the BMS effect of Li1.08Mn1.92O4, analyzing the experimental results by using a simple long-distance Li-electron dipolar coupling model. In addition, we discuss the shape and packing density dependence of the BMS effect and its influence on the observed frequencies of other components, such as the Li metal and the electrolyte in the battery. Finally, we show that by taking these effects into account we are able to minimize the BMS induced shift by orienting the cell at a rotation angle, αi=54.7° which facilitates the interpretation of the in situ NMR spectra of a working battery with the paramagnetic Li1.08Mn1.92O4 cathode.

Visualizing skin effects in conductors with MRI: 7Li MRI experiments and calculations

While experiments on metals have been performed since the early days of NMR (and DNP), the use of bulk metal is normally avoided. Instead, often powders have been used in combination with low fields, so that skin depth effects could be neglected. Another complicating factor of acquiring NMR spectra or MRI images of bulk metal is the strong signal dependence on the orientation between the sample and the radio frequency (rf) coil, leading to non-intuitive image distortions and inaccurate quantification. Such factors are particularly important for NMR and MRI of batteries and other electrochemical devices. Here, we show results from a systematic study combining rf field calculations with experimental MRI of (7)Li metal to visualize skin depth effects directly and to analyze the rf field orientation effect on MRI of bulk metal. It is shown that a certain degree of selectivity can be achieved for particular faces of the metal, simply based on the orientation of the sample. By combining rf field calculations with bulk magnetic susceptibility calculations accurate NMR spectra can be obtained from first principles. Such analyses will become valuable in many applications involving battery systems, but also metals, in general.

Real-time 3D imaging of microstructure growth in battery cells using indirect MRI

Significance Lithium metal is an ideal anode material for rechargeable Li-ion batteries, but its use is prevented by the growth of lithium deposits, or “dendrites,” during charging that can cause performance loss and serious safety concerns. Understanding the growth of dendrites in situ is crucial for the progress of this technology. MRI has been limited to directly studying the lithium signal until now, resulting in low sensitivity, limited resolution, and long experiment times. We present here an approach that detects the “shadows” of dendrites growing through the electrolyte, allowing the dendrites’ growth to be imaged very quickly in 3D with high resolution. This technique can also be applied to other electrodes, such as those based on sodium, zinc, and magnesium. Lithium metal is a promising anode material for Li-ion batteries due to its high theoretical specific capacity and low potential. The growth of dendrites is a major barrier to the development of high capacity, rechargeable Li batteries with lithium metal anodes, and hence, significant efforts have been undertaken to develop new electrolytes and separator materials that can prevent this process or promote smooth deposits at the anode. Central to these goals, and to the task of understanding the conditions that initiate and propagate dendrite growth, is the development of analytical and nondestructive techniques that can be applied in situ to functioning batteries. MRI has recently been demonstrated to provide noninvasive imaging methodology that can detect and localize microstructure buildup. However, until now, monitoring dendrite growth by MRI has been limited to observing the relatively insensitive metal nucleus directly, thus restricting the temporal and spatial resolution and requiring special hardware and acquisition modes. Here, we present an alternative approach to detect a broad class of metallic dendrite growth via the dendrites’ indirect effects on the surrounding electrolyte, allowing for the application of fast 3D 1H MRI experiments with high resolution. We use these experiments to reconstruct 3D images of growing Li dendrites from MRI, revealing details about the growth rate and fractal behavior. Radiofrequency and static magnetic field calculations are used alongside the images to quantify the amount of the growing structures.

MRI and Unilateral NMR Study of Reindeer Skin Tanning Processes

The study of arctic or subarctic indigenous skin clothing material, known for its design and ability to keep the body warm, provides information about the tanning materials and techniques. The study also provides clues about the culture that created it, since tanning processes are often specific to certain indigenous groups. Untreated skin samples and samples treated with willow (Salix sp) bark extract and cod liver oil are compared in this study using both MRI and unilateral NMR techniques. The two types of samples show different proton spatial distributions and different relaxation times, which may also provide information about the tanning technique and aging behavior.

Rechargeable lithium-ion cell state of charge and defect detection by in-situ inside-out magnetic resonance imaging

When and why does a rechargeable battery lose capacity or go bad? This is a question that is surprisingly difficult to answer; yet, it lies at the heart of progress in the fields of consumer electronics, electric vehicles, and electrical storage. The difficulty is related to the limited amount of information one can obtain from a cell without taking it apart and analyzing it destructively. Here, we demonstrate that the measurement of tiny induced magnetic field changes within a cell can be used to assess the level of lithium incorporation into the electrode materials, and diagnose certain cell flaws that could arise from assembly. The measurements are fast, can be performed on finished and unfinished cells, and most importantly, can be done nondestructively with cells that are compatible with commercial design requirements with conductive enclosures.The development of noninvasive methodology plays an important role in advancing lithium ion battery technology. Here the authors utilize the measurement of tiny magnetic field changes within a cell to assess the lithiation state of the active material, and detect defects.

Correlation of Phosphorus Cross-Linking to Hydration Rates in Sodium Starch Glycolate Tablet Disintegrants Using MRI

Understanding the behavior of tablet disintegrants is valuable in the development of pharmaceutical solid dosage formulations. In this study, high-resolution magnetic resonance imaging has been used to understand the hydration behavior of a series of commercial sodium starch glycolate (SSG) samples, providing robust estimates of tablet disintegration rate that could be correlated with physicochemical properties of the SSGs, such as the extent of phosphorus (P) cross-linking as obtained from infra-red spectroscopy. Furthermore, elemental analysis together with powder X-ray diffraction has been used to quantify the presence of carboxymethyl groups and salt impurities, which also contribute to the disintegration behavior. The utility of Fast Low Angle SHot magnetic resonance imaging has been demonstrated as an approach to rapidly acquire approximations of the volume of a disintegrating tablet and, together with a robust voxel analysis routine, extract tablet disintegration rates. In this manner, a complete characterization of a series of SSG grades from different sources has been performed, showing the variability in their physicochemical properties and demonstrating a correlation between their disintegration rates and intrinsic characteristics. The insights obtained will be a valuable aid in the choice of disintegrant source as well as in managing SSG variability to ensure robustness of drug products containing SSG.

Super-resolution Surface Microscopy of Conductors using Magnetic Resonance

The spatial resolution of traditional Magnetic Resonance Imaging (MRI) techniques is typically dictated by the strength of the applied magnetic field gradients, resulting in hard resolution limits of the order of 20–50 μm in favorable circumstances. We demonstrate here a technique which is suitable for the interrogation of regions at specified distances below the surface of conducting objects with a resolution well below these limiting values. This approach does not rely on magnetic field gradients, but rather on the spatial variation of the radiofrequency field within a conductor. Samples of aluminium and lithium metal with different sizes and morphologies are examined with this technique using 27Al and 7Li NMR. In this implementation, the slice selectivity depends on the conductivity of the material, as well as on the frequency of operation, although in the most general case, the technique could also be used to provide spatial selectivity with arbitrary B1 field distributions in non-conductors.

1H NMR study and multivariate data analysis of reindeer skin tanning methods

Reindeer skin clothing has been an essential component in the lives of indigenous people of the arctic and sub‐arctic regions, keeping them warm during harsh winters. However, the skin processing technology, which often conveys the history and tradition of the indigenous group, has not been well documented. In this study, NMR spectra and relaxation behaviors of reindeer skin samples treated with a variety of vegetable tannin extracts, oils and fatty substances are studied and compared. With the assistance of principal component analysis (PCA), one can recognize patterns and identify groupings of differently treated samples. These methods could be important aids in efforts to conserve museum leather artifacts with unknown treatment methods and in the analysis of reindeer skin tanning processes. Copyright