Enhancing Cycle Life of Rechargeable Zinc Hybrid Batteries in a Low-Cost, Nonfluorinated Dual-Cation Electrolyte.

Rechargeable zinc batteries (RZBs) are highly attractive as energy storage solutions due to their low cost and sustainability. Nevertheless, the use of fluorine-free zinc electrolyte systems to create affordable, ecofriendly, and safe RZBs has been largely overlooked in the battery community. Previously, we showcased the utilization of a fluorine-free, nonaqueous electrolyte comprising zinc dicyanamide (Zn(dca)2) in dimethyl sulfoxide (DMSO) to enable the electrochemical cycling of zinc. Herein we present a dual-cation-based electrolyte, [1.0 M Na(dca) +1.0 M Zn(dca)2]/DMSO, in pursuit of a rechargeable zinc hybrid battery. Fourier-transform infrared spectroscopy and molecular dynamics simulation studies indicate that the presence of Na(dca) diminishes ion-pairing in Zn(dca)2 through [dca]- anion bridging between Zn2+ and Na+ ions, thereby enhancing Zn2+ ion transport in the electrolyte. Thus, the electrolyte exhibits high ionic conductivity and transference numbers (tZn2+) of 7.9 mS cm-1 and 0.83, respectively, at 50 °C, making it particularly suitable for high-temperature battery applications. Furthermore, we demonstrate, for the first time, the cycling of a full cell with a zinc anode and triphylite sodium iron phosphate cathode (NFP) in an organic electrolyte, showcasing stable performance over 100 cycles at 0.1C rate. These encouraging findings pave the way for affordable battery technologies using, fluorine-free electrolyte.

A case study using spectroscopy and computational modelling for Co speciation in a deep eutectic solvent.

Cobalt has a vital role in the manufacturing of reliable and sustainable clean energy technologies. However, the forecasted supply deficit for cobalt is likely to reach values of 150 kT by 2030. Therefore, it is paramount to consider end-of-life devices as secondary resources for cobalt. Electrorecovery of cobalt from leached solutions has attracted attention due to the sustainability of the recovery process over solvent extraction followed by chemical precipitation. Recently, we reported Co electrorecovery from two different cobalt sources (CoCl2·6H2O and CoSO4·7H2O) using ethylene glycol : choline chloride (EG : ChCl) in a 4.5 : 1 molar ratio, leading to higher purity and easier electrodeposition when sulfate was present as an additive. Here, Co2+ speciation is reported for the two EG : ChCl systems depending on the cobalt source using several spectroscopic techniques (e.g. NMR, EPR, FTIR) in combination with molecular dynamics simulations. Monodentate coordination of SO42- to Co2+, forming the tetrahedral [CoCl3(SO4)]3- was observed as the dominant structure in the system containing CoSO4·7H2O, whereas the system comprising CoCl2·6H2O shows a homoleptic tetrahedral [CoCl4]2- as the dominant structure. This resulted in knowledge being gained regarding Co2+ speciation and the correlation with electrochemistry will contribute to the science required for designing safe electrolytes for efficient electrorecovery.

Impact of optimised quasi-block structures on the properties of polymer electrolytes.

A set of ionic quasi-block copolymers were investigated to determine the effects of their composition and structure on their performance in their application as solid-state battery electrolytes. Diffusion and electrochemical tests have shown that these new quasi-block electrolytes have comparable performance to traditional block copolymers reaching ionic conductivities of 3.8 × 10-4 S cm-1 and lithium-ion diffusion of 4.6 × 10-12 m2 s-1 at 80 °C. It was illustrated that the mechanical properties of each quasi-block electrolyte are highly dependent on the order of monomer addition in polymer synthesis while the phase morphology hints at each of the quasi-blocks' unique compositional make up.

Understanding Polymerized Ionic Liquids as Solid Polymer Electrolytes for Sodium Batteries.

Solid polymer electrolytes (SPEs) have emerged as promising candidates for sodium-based batteries due to their cost-effectiveness and excellent flexibility. However, achieving high ionic conductivity and desirable mechanical properties in SPEs remains a challenge. In this study, we investigated an AB diblock copolymer, PS-PEA(BuImTFSI), as a potential SPE for sodium batteries. We explored binary and ternary electrolyte systems by combining the polymer with salt and [C3mpyr][FSI] ionic liquid (IL) and analyzed their thermal and electrochemical properties. Differential scanning calorimetry revealed phase separation in the polymer systems. The addition of salt exhibited a plasticizing effect localized to the polyionic liquid (PIL) phase, resulting in an increased ionic conductivity in the binary electrolytes. Introducing the IL further enhanced the plasticizing effect, elevating the ionic conductivity in the ternary system. Spectroscopic analysis, for the first time, revealed that the incorporation of NaFSI and IL influences the conformation of TFSI- and weakens the interaction between TFSI- and the polymer. This establishes correlations between anions and Na+, ultimately enhancing the diffusivity of Na ions. The electrochemical properties of an optimized SPE in Na/Na symmetrical cells were investigated, showcasing stable Na plating/stripping at high current densities up to 0.7 mA cm-2, maintaining its integrity at 70 °C. Furthermore, we evaluated the performance of a Na|NaFePO4 cell cycled at different rates (C/10 and C/5) and temperatures (50 and 70 °C), revealing remarkable high-capacity retention and Coulombic efficiency. This study highlights the potential of solvent-free diblock copolymer electrolytes for high-performance sodium-based energy storage systems, contributing to advanced electrolyte materials.

Insights into the Carbon Dioxide Separation Performance of Bis(trifluoromethylsulfonyl)imide-based Plastic Crystal Composite Membranes with Fluorinated Polar Polymers.

Membrane-based gas separation technologies are one solution towards mitigating global emissions of CO2. New membrane materials with improved separation performance are still highly sought after. Composite membranes based on organic ionic plastic crystals (OIPCs) have shown preferential interaction for CO2 over N2, leading in some cases to competitive CO2/N2 selectivities. However, these ionic materials have been scarcely studied in the field of gas separation. Here, OIPCs based on the bis(trifluoromethylsulfonyl)imide ([TFSI]-) anion were investigated for use as gas separation membranes for the first time. The effect of the polymer type was also investigated, through the comparison of poly(vinylidene fluoride) (PVDF) and poly(vinylidene fluoride)-hexafluoropropylene (PVDF-HFP) OIPC membranes. A strong temperature dependence of the gas separation performance was found, particularly in the N-methyl-N-ethylpyrrolidinium-based composites where the material undergoes a solid-solid phase transition within the testing temperature range. The polymer type was noted to induce a strong effect on the structure of the composites, as well as affecting the gas and ionic transport. Thus, this research provides insights on the influence of the [TFSI]- anion on the structure and separation properties of OIPC-based composites, and new information towards the development of novel OIPC-based membranes with enhanced gas separation performance.

Atomic Layer Deposition of the Geometry Separated Lewis and Brønsted Acid Sites for Cascade Glucose Conversion.

Solid acid catalysts with bi-acidity are promising as workhouse catalysts in biorefining to produce high-quality chemicals and fuels. Herein, we report a new strategy to develop bi-acidic cascade catalysts by separating both acid sites in geometry via the atomic layer deposition (ALD) of Lewis acidic alumina on Brønsted acidic supports. Visualized by transmission electron microscopy and electron energy loss spectroscopy mapping, the ALD-deposited alumina forms a conformal alumina domain with a thickness of around 3 nm on the outermost surface of mesoporous silica-alumina. Solid state nuclear magnetic resonance investigation shows that the dominant Lewis acid sites distribute on the outermost surface, whereas intrinsic Brønsted acid sites locate inside the nanopores within the silica-rich substrate. In comparison to other bi-acidic solid catalyst counterparts, the special geometric distance of Lewis and Brønsted acid sites minimized the synergetic effect, leading to a cascade reaction environment. For cascade glucose conversion, the designed ALD catalyst showed a highly enhanced catalytic performance.

New organic ionic plastic crystals utilizing the morpholinium cation.

Organic ionic plastic crystals (OIPCs) are emerging candidates as safer, quasi solid-state ion conductors for various applications, especially for next-generation batteries. However, a fundamental understanding of these OIPC materials is required, particularly concerning how the choice of cation and anion can affect the electrolyte properties. Here, we report the synthesis and characterisation of a range of new morpholinium-based OIPCs and demonstrate the benefit of the ether functional group in the cation ring. Specifically, we investigate the 4-ethyl-4-methylmorpholinium [C2mmor]+ and 4-isopropyl-4-methylmorpholinium [C(i3)mmor]+ cations paired with bis(fluorosulfonyl)imide [FSI]- and bis(trifluoromethanesulfonyl)imide [TFSI]- anions. A fundamental study of the thermal behaviour and transport properties was performed using differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA) and electrochemical impedance spectroscopy (EIS). The free volume within the salts has been investigated by positron annihilation lifetime spectroscopy (PALS) and the ion dynamics using solid-state nuclear magnetic resonance (NMR) analysis. Finally, the electrochemical stability window was studied using cyclic voltammetry (CV). Out of the four morpholinium salts, [C2mmor][FSI] exhibits the widest phase I range from 11 to 129 °C, which is advantageous for their application. [C(i3)mmor][FSI] displayed the highest conductivity of 1 × 10-6 S cm-1 at 30 °C, whereas the largest vacancy volume of 132 Å3 was found for [C2mmor][TFSI]. These insights into the properties of new morpholinium-based OIPCs will be important for developing new electrolytes with optimised thermal and transport properties for a range of clean energy applications.

Lyotropic Liquid Crystal (LLC)-Templated Nanofiltration Membranes by Precisely Administering LLC/Substrate Interfacial Structure.

Mesoporous materials based on lyotropic liquid crystal templates with precisely defined and flexible nanostructures offer an alluring solution to the age-old challenge of water scarcity. In contrast, polyamide (PA)-based thin-film composite (TFC) membranes have long been hailed as the state of the art in desalination. They grapple with a common trade-off between permeability and selectivity. However, the tides are turning as these novel materials, with pore sizes ranging from 0.2 to 5 nm, take center stage as highly coveted active layers in TFC membranes. With the ability to regulate water transport and influence the formation of the active layer, the middle porous substrate of TFC membranes becomes an essential player in unlocking their true potential. This review delves deep into the recent advancements in fabricating active layers using lyotropic liquid crystal templates on porous substrates. It meticulously analyzes the retention of the liquid crystal phase structure, explores the membrane fabrication processes, and evaluates the water filtration performance. Additionally, it presents an exhaustive comparison between the effects of substrates on both polyamide and lyotropic liquid crystal template top layer-based TFC membranes, covering crucial aspects such as surface pore structures, hydrophilicity, and heterogeneity. To push the boundaries even further, the review explores a diverse array of promising strategies for surface modification and interlayer introduction, all aimed at achieving an ideal substrate surface design. Moreover, it delves into the realm of cutting-edge techniques for detecting and unraveling the intricate interfacial structures between the lyotropic liquid crystal and the substrate. This review is a passport to unravel the enigmatic world of lyotropic liquid crystal-templated TFC membranes and their transformative role in global water challenges.

Development of New Plastic-Crystal Based Electrolytes using Pyrrolidinium- Bis(fluorosulfonyl)imide Dicationic Salts.

Dicationic organic salts are an interesting class of solid-state electrolyte materials due to their unique structure. Here we present, for the first time, the synthesis and characterization of three dicationic-FSI salts, 1,2-bis(N-methylpyrrolidinium)ethane bi(bis(fluorosulfonyl)imide) ([C2 -Pyrr1][FSI]2 ), 1,2-bis(N-ethylpyrrolidinium)ethane bi(bis(fluorosulfonyl)imide) ([C2 -Pyrr2][FSI]2 ) and 1,2-bis(N-n-propylpyrrolidinium)ethane bi(bis(fluorosulfonyl)imide) ([C2 -Pyrr3][FSI]2 ). The structure and dynamics of the organic salts were probed using variable temperature solid-state NMR and were compared with the thermal and transport properties. The investigation revealed that [C2 -Pyrr1][FSI]2 , with shorter alkyl-side chains on the dication, displayed increased transport properties compared to [C2 -Pyrr2][FSI]2 and [C2 -Pyrr3][FSI]2 . To determine the proficiency of these dicationic-FSI salts as electrolyte materials for battery applications, 10 mol% and 50 mol% lithium bis(fluorosulfonyl)imide (LiFSI) was mixed with [C2 -Pyrr1][FSI]2 and [C2 -Pyrr2][FSI]2 . Increased transport properties were observed for [C2 -Pyrr1][FSI]2 /10 mol % LiFSI in comparison to [C2 -Pyrr2][FSI]2 /10 % LiFSI, while pulse field gradient NMR analysis revealed the highest Li+ self-diffusion ratio for [C2 -Pyrr1][FSI]2 /50 % LiFSI out of the four Li-salt-containing mixtures.

Hybrid Artificial Solid Electrolyte Interphase with Dendrite-Free Lithium Deposition and High Ion Transport Kinetics.

Interfacial issues and dendritic Li deposition in lithium metal batteries (LMBs) hamper the practical application of liquid or solid-state cells. Here, a hybrid solid electrolyte interphase (SEI), based on hydroxyl-functionalized boron nitride (BN) nanosheets and poly(vinyl alcohol), is designed to solve the unstable nature of the Li anode-electrolyte interface. Rather than acquiring a rich Li halide environment through intense electrolyte decomposition, the hybrid SEI effectively regulates electrolyte decomposition and guarantees uniform Li plating via boosting interfacial Li+ ion transport at the interface. The Li+ ion boosting kinetics were deeply analyzed using simulations and spectroscopic analysis. It is revealed that the hydroxyl-functionalized BN can decrease kinetic energy barriers for Li+ ions and strongly holds TFSI- ions, thereby ensuring faster Li+ ion migration between electrodes and electrolytes. Tailoring the interfacial Li+ ion dynamics with hybrid SEI renders the Li transference number enhancement from 0.391 to 0.562 and 0.178 to 0.327 in liquid and solid-state cells, respectively. Moreover, Li symmetric cells with hybrid SEI exhibit an ultrahigh stability over 3500 h at 2 mA cm-2 with 2 mA h cm-2, along with the improved solid-state LMB performances. Our results suggest increasing Li+ ion transport at the interface is an alternative to resolve Li anode issues.

Probing the molecular interactions and physicochemical properties of a cobalt-based redox electrolyte system for thermo-electrochemical cells.

Redox-active materials play a primary role in the high-performance electrochemical device research field. Their bulk ion dynamics and performances can be studied using different electrochemical analysis methods, but their molecular level interactions and dynamics on which these depend are often not well understood. Here, nuclear magnetic resonance (NMR) relaxation and double-stimulated echo pulsed field gradient (PFG) techniques have been used to gain insights into the molecular level interactions, exchange dynamics and self-diffusivity of the various species present in a cobalt-based redox active electrolyte system used for thermo-electrochemical applications, including how these factors depend on the oxidation state and concentration of the redox species. A series of liquid electrolyte samples consisting of a Co2+/3+(bpy)3(NTf2)2/3 redox couple (where bpy = bipyridyl and NTf2 = bis(trifluoromethanesulfonyl)imide) in 3-methoxypropionitrile (MPN) have been investigated using NMR as well as viscosity and conductivity measurements carried out over a temperature range 293 to 353 K. The results provide insights into the mobilities and interactions between the various species present, including the exchange of the NTf2- anions between the solvation shells of the Co(bpy)3 species. Such information will be useful in understanding the behaviour of these electrolytes in devices such as thermo-electrochemical cells.

Exploration of phase diagram, structural and dynamic behavior of [HMG][FSI] mixtures with NaFSI across an extended composition range.

Hexamethylguanidinium bis(fluorosulfonyl)imide ([HMG][FSI]) has recently been shown to be a promising solid state organic ionic plastic crystal with potential application in advanced alkali metal batteries. This study provides a detailed exploration of the structural and dynamic behavior of [HMG][FSI] mixtures with the sodium salt NaFSI across the whole composition range from 0 to 100 mol%. All mixtures are solids at room temperature. A combination of differential scanning calorimetry (DSC), synchrotron X-ray diffraction (SXRD) and multinuclear solid state NMR spectroscopy is employed to identify a partial phase diagram. The 25 mol% NaFSI/75 mol% [HMG][FSI] composition presents as the eutectic composition with the eutectic transition temperature at 44 °C. Both DSC and SXRD strongly support the formation of a new compound near 50 mol% NaFSI. Interestingly, the 53 mol% NaFSI [HMG][FSI] composition was consistently found to display features of a pure compound whereas the 50 mol% materials always showed a second phase. Many of the compositions examined showed unusual metastable behaviour. Moreover, the ion dynamics as determined by NMR, indicate that the Na+ and FSI- anions are signifcantly more mobile than the HMG cation in the liquid state (including the metastable state) for these materials.

Atomically-thin Schottky-like photo-electrocatalytic cross-flow membrane reactors for ultrafast remediation of persistent organic pollutants.

The remediation of persistent organic pollutants in surface and ground water represents a major environmental challenge worldwide. Conventional physico-chemical techniques do not efficiently remove such persistent organic pollutants and new remediation techniques are therefore required. Photo-electro catalytic membranes represent an emerging solution that can combine photocatalytic and electrocatalytic degradation of contaminants along with molecular sieving. Herein, macro-porous photo-electro catalytic membranes were prepared using conductive and porous stainless steel metal membranes decorated with nano coatings of semiconductor photocatalytic metal oxides (TiO2 and ZnO) via atomic layer deposition, producing highly conformal and stable coatings. The metal - semiconductor junction between the stainless steel membranes and photocatalysts provides Schottky - like characteristics to the coated membranes. The PEC membranes showed induced hydrophilicity from the nano-coatings and enhanced electro-chemical properties due to the Schottky junction. A high electron transfer rate was also induced in the coated membranes as the photocurrent efficiency increased by 4 times. The photo-electrocatalytic efficiency of the TiO2 and ZnO coated membranes were demonstrated in batch and cross flow filtration reactors for the degradation of persistent organic pollutant solution, offering increased degradation kinetic factors by 2.9 and 2.3 compared to photocatalysis and electrocatalysis, respectively. The recombination of photo-induced electron and hole pairs is mitigated during the photo-electrocatalytic process, resulting in an enhanced catalytic performance. The strategy offers outstanding perspectives to design stimuli-responsive membrane materials able to sieve and degrade simultaneously toxic contaminants towards greater process integration and self-cleaning operations.

High-Performance Cycling of Na Metal Anodes in Phosphonium and Pyrrolidinium Fluoro(sulfonyl)imide Based Ionic Liquid Electrolytes.

We have investigated the sodium electrochemistry and the evolution and chemistry of the solid-electrolyte interphase (SEI) upon cycling Na metal electrodes in two ionic liquid (IL) electrolytes. The effect of the IL cation chemistry was determined by examining the behavior of a phosphonium IL (P111i4FSI) in comparison to its pyrrolidinium-based counterpart (C3mpyrFSI) at near-saturated NaFSI salt concentrations (superconcentrated ILs) in their dry state and with water additive. The differences in their physical properties are reported, with the P111i4FSI system having a lower viscosity, higher conductivity, and higher ionicity in comparison to the C3mpyrFSI-based electrolyte, although the addition of 1000 ppm (0.1 wt %) of water had a more dramatic effect on these properties in the latter case. Despite these differences, there was little effect in the ability to sustain stable cycling at moderate current densities and capacities (being nearly identical at 1 mA cm-2 and 1 mAh cm-2). However, the IL based on the phosphonium cation is shown to support more demanding cycling with high stability (up to 4 mAh cm-2 at 1, 2, and 4 mA cm-2 current density), whereas C3mpyrFSI rapidly failed (at 1 mA cm-2 /4 mAh cm-2). The SEI was characterized ex situ using solid-state 23Na NMR, XPS, and SEM and showed that the presence of a Na complex, identified in our previous work on C3mpyrFSI to correlate with stable, dendrite-free Na metal cycling, was also more prominent and coexisted with a NaF-rich surface. The results here represent a significant breakthrough in the development of high-capacity Na metal anodes, clearly demonstrating the superior performance and stability of the P111i4FSI electrolyte, even after the addition of water (up to 1000 ppm (0.1 wt %)), and show great promise to enable future higher-temperature (50 °C) Na-metal-based batteries.

Plastic crystal-based electrolytes using novel dicationic salts.

The unique structures of dications increase the number of possible combinations of cations and anions that can be used to obtain new materials with a wide range of physicochemical properties. However, structure-property relationships related to dicationic organic salts are seldom explored. Here, we report the synthesis and characterization of two new dicationic salts, 1,2-bis(N-ethylpyrrolidinium)ethane bis(trifluoromethanesulfonyl)imide ([C2-Pyrr2][TFSI]2) and 1,2-bis(N-n-propylpyrrolidinium)ethane bis(trifluoromethanesulfonyl)imide ([C2-Pyrr3][TFSI]2). To investigate the physicochemical properties of the organic salts, local structure and dynamics were investigated by variable temperature solid-state NMR and correlated with the thermal analysis and ionic conductivity. These studies revealed that [C2-Pyrr3][TFSI]2, with the longer alkyl-side chain on the dication, showed improved transport properties compared to [C2-Pyrr2][TFSI]2. Further exploration of the organic salts as potential electrolyte materials was conducted by mixing with 10 mol% lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). This study demonstrates the effect that lithium salt addition has on thermal and ionic conductivity properties, where the largest increase in conductivity was found for [C2-Pyrr3][TFSI]2/LiTFSI (10 mol% LiTFSI). Solid-state NMR analysis revealed that Li+ and [TFSI]- ions acted as the major contributors to ionic conductivity while the dications in the bulk structure showed lower mobility.

Controlling phase and rheological behaviours of hexagonal lyotropic liquid crystalline templates for nanostructural administration and retention.

Introducing polymerizable monomers into a binary hexagonal lyotropic liquid crystalline (LLC) template is a straightforward way for retaining the nanostructure but will decrease attractive intra- and inter- aggregate interactions. It is therefore crucial to understand the interfacial interactions at nanoscale after introducing the monomers but prior to polymerization. Herein, active species, poly (ethylene glycol) diacrylate (PEGDA) and 2-hydroxyethyl methacrylate (HEMA), were introduced into hexagonal LLC of dodecyl trimethylammonium bromide and water to explore the structural variables, dimensional stability, and dynamic property. At a proper volume ratio of PEGDA/HEMA (1/4), the system presents excellent homogeneity with a higher dimensional stability and lower dynamic property from rheological assessments, thereby achieving robust, free-standing, and transparent membranes after photo-polymerization. The unique property of the system also lies in the much lower order-disorder transition temperature (45 °C) that facilitates the reorientation of mesochannels. They are in contrast inaccessible for the ternary system only with PEGDA, though the nanostructure for both systems could be retained. An insight into subtle variations in these parameters allows us to prepare a polymerizable template possessing higher dimensional stability and suitable flexibility via molecular design, thereby enabling simultaneous structural alignment and retention for the development of functional nanomaterials.

Zwitterionic materials with disorder and plasticity and their application as non-volatile solid or liquid electrolytes.

Zwitterionic materials can exhibit unique characteristics and are highly tunable by variation to the covalently bound cationic and anionic moieties. Despite the breadth of properties and potential uses reported to date, for electrolyte applications they have thus far primarily been used as additives or for making polymer gels. However, zwitterions offer intriguing promise as electrolyte matrix materials that are non-volatile and charged but non-migrating. Here we report a family of zwitterions that exhibit molecular disorder and plasticity, which allows their use as a solid-state conductive matrix. We have characterized the thermal, morphological and structural properties of these materials using techniques including differential scanning calorimetry, scanning electron microscopy, solid-state NMR and X-ray crystallography. We report the physical and transport properties of zwitterions combined with lithium salts and a lithium-functionalized polymer to form solid or high-salt-content liquid electrolytes. We demonstrate that the zwitterion-based electrolytes can allow high target ion transport and support stable lithium metal cell cycling. The ability to use disordered zwitterionic materials as electrolyte matrices for high target ion conduction, coupled with an extensive scope for varying the chemical and physical properties, has important implications for the future design of non-volatile materials that bridge the choice between traditional molecular and ionic solvent systems.

Operando magnetic resonance imaging for mapping of temperature and redox species in thermo-electrochemical cells.

Low-grade waste heat is an abundant and underutilised energy source. In this context, thermo-electrochemical cells (i.e., systems able to harvest heat to generate electricity) are being intensively studied to deliver the promises of efficient and cost-effective energy harvesting and electricity generation. However, despite the advances in performance disclosed in recent years, understanding the internal processes occurring within these devices is challenging. In order to shed light on these mechanisms, here we report an operando magnetic resonance imaging approach that can provide quantitative spatial maps of the electrolyte temperature and redox ion concentrations in functioning thermo-electrochemical cells. Time-resolved images are obtained from liquid and gel electrolytes, allowing the observation of the effects of redox reactions and competing mass transfer processes such as thermophoresis and diffusion. We also correlate the physicochemical properties of the system with the device performance via simultaneous electrochemical measurements.

Towards a High-Flux Separation Layer from Hexagonal Lyotropic Liquid Crystals for Thin-Film Composite Membranes.

Hexagonal lyotropic liquid crystals (HLLC) with uniform pore size in the range of 1~5 nm are highly sought after as promising active separation layers of thin-film composite (TFC) membranes, which have been confirmed to be efficient for water purification. The potential interaction between an amphiphile-based HLLC layer and the substrate surface, however, has not been fully explored. In this research, hydrophilic and hydrophobic microporous polyvinylidene fluoride (PVDF) substrates were chosen, respectively, to prepare TFC membranes with the active layers templated from HLLC, consisting of dodecyl trimethylammonium bromide, water, and a mixture of poly (ethylene glycol) diacrylate and 2-hydroxyethyl methacrylate. The pore size of the active layer was found to decrease by about 1.6 Å compared to that of the free-standing HLLC after polymerization, but no significant difference was observable by using either hydrophilic or hydrophobic substrates (26.9 Å vs. 27.1 Å). The water flux of the TFC membrane with the hydrophobic substrate, however, was higher than that with the hydrophilic one. A further investigation confirmed that the increase in water flux originated from a much higher porosity was due to the synergistic effect of the hydrophilic HLLC nanoporous material and the hydrophobic substrate.

New Insights into Decoupled Cation and Anion Transport and Dynamic Heterogeneity in a Diethyl(methyl)(isobutyl)phosphonium Hexafluorophosphate Organic Ionic Plastic Crystal.

Organic ionic plastic crystals (OIPCs) are an emerging family of materials with demonstrated applications in electrochemical devices such as lithium/sodium ion batteries, dye-sensitized solar cells, and hydrogen fuel cells. Herein, we present direct evidence of anion diffusion through a relatively static background of a cation lattice in an ionic plastic crystal compound, [P122i4][PF6], in an elevated temperature solid phase. We found all anions are diffusive, whereas only a small population of cations is diffusive. Two anion populations were identified with diffusion coefficients differing by 2 orders of magnitude. The slow-diffusing anion is attributed to the plastic crystal region where the cation forms a relative static background, allowing anions to diffuse possibly through a defect-assisted hopping mechanism.