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A comprehensive variable temperature, pressure and frequency multinuclear (1H, 2H, and 19F) magnetic resonance study was undertaken on selectively deuterated 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide (BMIM TFSA) ionic liquid isotopologues. This study builds on our earlier investigation of the effects of increasing alkyl chain length on diffusion and dynamics in imidazolium-based TFSA ionic liquids. Fast field cycling 1H T1 data revealed multiple modes of motion. Through calculation of diffusion coefficient (D) values and activation energies, the low- and high-field regimes were assigned to the translational and reorientation dynamics respectively. Variable-pressure 2H T1 measurements reveal site-dependent interactions in the cation with strengths in the order MD3 > CD3 > CD2, indicating dissimilarities in the electric field gradients along the alkyl chain, with the CD2 sites having the largest gradient. Additionally, the α saturation effect in T1 vs. P was observed for all three sites, suggesting significant reduction of the short-range rapid reorientational dynamics. This reduction was also deduced from the variable pressure 1H T1 data, which showed an approach to saturation for both the methyl and butyl group terminal methyl sites. Pressure-dependent D measurements show independent motions for both cations and anions, with the cations having greater D values over the entire pressure range.

Redox flow batteries (RFBs) are a burgeoning electrochemical platform for long-duration energy storage, but present embodiments are too expensive for broad adoption. Nonaqueous redox flow batteries (NAqRFBs) seek to reduce system costs by leveraging the large electrochemical stability window of organic solvents (> 3 V) to operate at high cell voltages and to facilitate the use of redox couples that are incompatible with aqueous electrolytes. However, a key challenge for emerging nonaqueous chemistries is the lack of membranes/separators with suitable combinations of selectivity, conductivity, and stability. Single-ion conducting ceramics, integrated with polymeric fillers to make flexible composites, may offer a pathway to the performance attributes needed for competitive nonaqueous systems. Here, we explore composite polymer-inorganic binder-filler membranes for lithium-based NAqRFBs, investigating two different ceramic compounds with NASICON-type (NASICON: sodium (Na) Super Ionic CONductor) crystal structure, Li1.3Al0.3Ti1.7(PO4)3 (LATP) and Li1.4Al0.4Ge0.2Ti1.4(PO4)3 (LAGTP), blended with a polyvinylidene fluoride (PVDF) polymeric matrix. We characterize the physicochemical and electrochemical properties of the synthesized membranes as a function of processing conditions and formulation using a range of microscopic, spectroscopic, and electrochemical techniques. We then integrate select composite membranes into a single electrolyte flow cell configuration and perform polarization measurements with different redox electrolyte compositions. We find that mechanically robust, chemically stable LATP/PVDF composites can support > 40 mA cm −2 at 400 mV cell overpotential, but further improvements are needed in selectivity. The insights gained through this work begin to establish the foundational knowledge needed to advance composite polymer-inorganic membranes/separators for NAqRFBs.

Sodium alanate has proven to be a feasible candidate for electrochemical applications. Within a lithium cell, NaAlH 4 closely approaches its theoretical capacity of 1985 mAhg −1 upon the first discharge. Despite its high specific capacity, NaAlH 4 suffers from poor cycle efficiency, mostly due to the severe volume expansion following the conversion reaction and resulting in damage to electrode mechanical integrity with loss of electrical contact. Synthesis of an appropriate composite alanate/carbon by high energy ball milling demonstrates an ability to mitigate these deleterious effects, whereby large improvements in terms of electrochemical reversibility can be achieved. In order to highlight the effects of mechanochemical treatment on the electrochemical properties of NaAlH 4 , new insights on such NaAlH 4 /C composites are reported. Solid state NMR has been used to study the impact of ball milling on the NaAlH 4 crystal structure, while, the hydrogen content and associated desorption properties have been evaluated by thermal programmed desorption measurements. Also, electrochemical features have been analyzed via the combined application of potentiodynamic cycling with galvanostatic acceleration and electrochemical impedance spectroscopy measurements. Finally, new evidence concerning the reversibility of the conversion processes has been obtained by ex-situ NMR measurements on cycled electrodes.