Showing papers on "Ionic conductivity published in 2014"

Energy applications of ionic liquids

Abstract: Ionic liquids offer a unique suite of properties that make them important candidates for a number of energy related applications. Cation–anion combinations that exhibit low volatility coupled with high electrochemical and thermal stability, as well as ionic conductivity, create the possibility of designing ideal electrolytes for batteries, super-capacitors, actuators, dye sensitised solar cells and thermo-electrochemical cells. In the field of water splitting to produce hydrogen they have been used to synthesize some of the best performing water oxidation catalysts and some members of the protic ionic liquid family co-catalyse an unusual, very high energy efficiency water oxidation process. As fuel cell electrolytes, the high proton conductivity of some of the protic ionic liquid family offers the potential of fuel cells operating in the optimum temperature region above 100 °C. Beyond electrochemical applications, the low vapour pressure of these liquids, along with their ability to offer tuneable functionality, also makes them ideal as CO2 absorbents for post-combustion CO2 capture. Similarly, the tuneable phase properties of the many members of this large family of salts are also allowing the creation of phase-change thermal energy storage materials having melting points tuned to the application. This perspective article provides an overview of these developing energy related applications of ionic liquids and offers some thoughts on the emerging challenges and opportunities.

A sulphide lithium super ion conductor is superior to liquid ion conductors for use in rechargeable batteries

Abstract: We report that a heat-treated Li2S–P2S5 glass-ceramic conductor has an extremely high ionic conductivity of 1.7 × 10−2 S cm−1 and the lowest conduction activation energy of 17 kJ mol−1 at room temperature among lithium-ion conductors reported to date. The optimum conditions of the heat treatment reduce the grain boundary resistance, and the influence of voids, to increase the Li+ ionic conductivity of the solid electrolyte so that it is greater than the conductivities of liquid electrolytes, when the transport number of lithium ions in the inorganic electrolyte is unity.

A family of oxide ion conductors based on the ferroelectric perovskite Na0.5Bi0.5TiO3

Abstract: Oxide ion conductors find important technical applications in electrochemical devices such as solid-oxide fuel cells (SOFCs), oxygen separation membranes and sensors. Na0.5Bi0.5TiO3 (NBT) is a well-known lead-free piezoelectric material; however, it is often reported to possess high leakage conductivity that is problematic for its piezo- and ferroelectric applications. Here we report this high leakage to be oxide ion conduction due to Bi-deficiency and oxygen vacancies induced during materials processing. Mg-doping on the Ti-site increases the ionic conductivity to ~0.01 S cm(-1) at 600 °C, improves the electrolyte stability in reducing atmospheres and lowers the sintering temperature. This study not only demonstrates how to adjust the nominal NBT composition for dielectric-based applications, but also, more importantly, gives NBT-based materials an unexpected role as a completely new family of oxide ion conductors with potential applications in intermediate-temperature SOFCs and opens up a new direction to design oxide ion conductors in perovskite oxides.

Block copolymer electrolytes for rechargeable lithium batteries

Abstract: Ion-conducting block copolymers (BCPs) have attracted significant interest as conducting materials in solid-state lithium batteries. BCP self-assembly offers promise for designing ordered materials with nanoscale domains. Such nanostructures provide a facile method for introducing sufficient mechanical stability into polymer electrolyte membranes, while maintaining the ionic conductivity at levels similar to corresponding solvent-free homopolymer electrolytes. This ability to simultaneously control conductivity and mechanical integrity provides opportunities for the fabrication of sturdy, yet easily processable, solid-state lithium batteries. In this review, we first introduce several fundamental studies of ion conduction in homopolymers for the understanding of ion transport in the conducting domain of BCP systems. Then, we summarize recent experimental studies of BCP electrolytes with respect to the effects of salt-doping and morphology on ionic conductivity. Finally, we present some remaining challenges for BCP electrolytes and highlight several important areas for future research. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014, 52, 1–16

Concentrated electrolytes: decrypting electrolyte properties and reassessing Al corrosion mechanisms

Abstract: Highly concentrated electrolytes containing carbonate solvents with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) have been investigated to determine the influence of eliminating bulk solvent (i.e., uncoordinated to a Li+ cation) on electrolyte properties. The phase behavior of ethylene carbonate (EC)–LiTFSI mixtures indicates that two crystalline solvates form—(EC)3:LiTFSI and (EC)1:LiTFSI. Crystal structures for these were determined to obtain insight into the ion and solvent coordination. Between these compositions, however, a crystallinity gap exists. A Raman spectroscopic analysis of the EC solvent bands for the 3–1 and 2–1 EC–LiTFSI liquid electrolytes indicates that ∼86 and 95%, respectively, of the solvent is coordinated to the Li+ cations. This extensive coordination results in significantly improved anodic oxidation and thermal stabilities as compared with more dilute (i.e., 1 M) electrolytes. Further, while dilute EC–LiTFSI electrolytes extensively corrode the Al current collector at high potential, the concentrated electrolytes do not. A new mechanism for electrolyte corrosion of Al in Li-ion batteries is proposed to explain this. Although the ionic conductivity of concentrated EC–LiTFSI electrolytes is somewhat low relative to the current state-of-the-art electrolyte formulations used in commercial Li-ion batteries, using an EC–diethyl carbonate (DEC) mixed solvent instead of pure EC markedly improves the conductivity.

Ionic-Liquid–Nanoparticle Hybrid Electrolytes: Applications in Lithium Metal Batteries†

Abstract: Development of rechargeable lithium metal battery (LMB) remains a challenge because of uneven lithium deposition during repeated cycles of charge and discharge. Ionic liquids have received intensive scientific interest as electrolytes because of their exceptional thermal and electrochemical stabilities. Ionic liquid and ionic-liquid–nanoparticle hybrid electrolytes based on 1-methy-3-propylimidazolium (IM) and 1-methy-3-propylpiperidinium (PP) have been synthesized and their ionic conductivity, electrochemical stability, mechanical properties, and ability to promote stable Li electrodeposition investigated. PP-based electrolytes were found to be more conductive and substantially more efficient in suppressing dendrite formation on cycled lithium anodes; as little as 11 wt % PP-IL in a PC-LiTFSI host produces more than a ten-fold increase in cell lifetime. Both PP- and IM-based nanoparticle hybrid electrolytes provide up to 10 000-fold improvements in cell lifetime than anticipated based on their mechanical modulus alone. Galvanostatic cycling measurements in Li/Li4Ti5O12 half cells using IL–nanoparticle hybrid electrolytes reveal more than 500 cycles of trouble-free operation and enhanced rate capability.

Air-stable, high-conduction solid electrolytes of arsenic-substituted Li4SnS4

Abstract: Lithium-ion-conducting solid electrolytes show promise for enabling high-energy secondary battery chemistries and solving safety issues associated with conventional lithium batteries. Achieving the combination of high ionic conductivity and outstanding chemical stability in solid electrolytes is a grand challenge for the synthesis of solid electrolytes. Herein we report the design of aliovalent substitution of Li4SnS4 to achieve high conduction and excellent air stability based on the hard and soft acids and bases theory. The solid electrolyte of composition Li3.833Sn0.833As0.166S4 has a high ionic conductivity of 1.39 mS cm−1 at 25 °C. Considering the high Li+ transference number, this phase conducts Li+ as well as carbonate-based liquid electrolytes. This research also addresses the compatibility of the sulfide-based solid electrolytes through chemical passivation.

High-Modulus, High-Conductivity Nanostructured Polymer Electrolyte Membranes via Polymerization-Induced Phase Separation

Abstract: The primary challenge in solid-state polymer electrolyte membranes (PEMs) is to enhance properties, such as modulus, toughness, and high temperature stability, without sacrificing ionic conductivity. We report a remarkably facile one-pot synthetic strategy based on polymerization-induced phase separation (PIPS) to generate nanostructured PEMs that exhibit an unprecedented combination of high modulus and ionic conductivity. Simple heating of a poly(ethylene oxide) macromolecular chain transfer agent dissolved in a mixture of ionic liquid, styrene and divinylbenzene, leads to a bicontinuous PEM comprising interpenetrating nanodomains of highly cross-linked polystyrene and poly(ethylene oxide)/ionic liquid. Ionic conductivities higher than the 1 mS/cm benchmark were achieved in samples with an elastic modulus approaching 1 GPa at room temperature. Crucially, these samples are robust solids above 100 °C, where the conductivity is significantly higher. This strategy holds tremendous potential to advance lithiu...

A Composite Gel Polymer Electrolyte with High Performance Based on Poly(Vinylidene Fluoride) and Polyborate for Lithium Ion Batteries

Abstract: A composite membrane based on electrospun poly(vinylidene fluoride) (PVDF) and lithium polyvinyl alcohol oxalate borate (LiPVAOB) exhibiting high safety (self-extinguishing) and good mechanical property is prepared. The ionic conductivity of the as-prepared gel polymer electrolyte from this composite membrane saturated with 1 mol L−1 LiPF6 electrolyte at ambient temperature can be up to 0.26 mS cm−1, higher than that of the corresponding well-used commercial separator (Celgard 2730), 0.21 mS cm−1. Moreover, the lithium ion transference in the gel polymer electrolyte at room temperature is 0.58, twice as that in the commercial separator (0.27). Furthermore, the absorbed electrolyte solvent is difficult to evaporate at elevated temperature. Its electrochemical performance is evaluated by using LiFePO4 cathode. The obtained results suggest that this gel-type composite membrane shows great possibilities for use in large-capacity lithium ion batteries that require high safety.

A metal-organic framework-based material for electrochemical sensing of carbon dioxide.

Abstract: The free primary hydroxyl groups in the metal–organic framework of CDMOF-2, an extended cubic structure containing units of six γ-cyclodextrin tori linked together in cube-like fashion by rubidium ions, has been shown to react with gaseous CO2 to form alkyl carbonate functions. The dynamic covalent carbon–oxygen bond, associated with this chemisorption process, releases CO2 at low activation energies. As a result of this dynamic covalent chemistry going on inside a metal–organic framework, CO2 can be detected selectively in the atmosphere by electrochemical impedance spectroscopy. The “as-synthesized” CDMOF-2 which exhibits high proton conductivity in pore-filling methanolic media, displays a ∼550-fold decrease in its ionic conductivity on binding CO2. This fundamental property has been exploited to create a sensor capable of measuring CO2 concentrations quantitatively even in the presence of ambient oxygen.

Electrochemical stability of non-aqueous electrolytes for sodium-ion batteries and their compatibility with Na0.7CoO2

Abstract: The present study compares the physico-chemical properties of non-aqueous liquid electrolytes based on NaPF6, NaClO4 and NaCF3SO3 salts in the binary mixture of ethylene carbonate (EC) and dimethyl carbonate (DMC). The ionic conductivity of the electrolytes is determined as a function of salt concentration and temperature. It is found that the electrolytes containing NaClO4 and NaPF6 exhibit ionic conductivities ranging from 5 mS cm−1 to 7 mS cm−1 at ambient temperature. The electrochemical stability window of the different electrolytes is studied by linear sweep voltammetry (LSV) and cyclic voltammetry (CV) measurements with respect to a variety of working electrodes (WE) such as glassy carbon (GC), graphite and a carbon gas diffusion layer (GDL). Electrolytes containing NaPF6 and NaClO4 are found to be electrochemically stable with respect to GC and GDL electrodes up to 4.5 V vs. Na/Na+, with some side reactions starting from around 3.0 V for the latter salt. The results further show that aluminium is preferred over different steels as a cathode current collector. Copper is stable up to a potential of 3.5 V vs. Na/Na+. In view of practical Na-ion battery systems, the electrolytes are electrochemically tested with Na0.7CoO2 as a positive electrode. It is inferred that the electrolyte NaPF6–EC : DMC is favorable for the formation of a stable surface film and the reversibility of the above cathode material.

Atomic-scale origin of the large grain-boundary resistance in perovskite Li-ion-conducting solid electrolytes

Abstract: Li-ion-conducting solid electrolytes are the potential solution to the severe safety issues that occur with conventional batteries based on solvent-based electrolytes. The ionic conductivity of solid electrolytes is in general too low, however, due to a high grain-boundary (GB) resistance. A thorough understanding of the ionic transport mechanism at GBs in these materials is critical for a revolutionary development of next-generation Li batteries. Herein we present the first atomic-scale study to reveal the origin of the large GB resistance; (Li3xLa2/3−x)TiO3 was chosen as a prototype material to demonstrate the concept. A strikingly severe structural and chemical deviation of about 2–3 unit cells thick was revealed at the grain boundaries. Instead of preserving the ABO3 perovskite framework, such GBs were shown to consist of a binary Ti–O compound, which prohibits the abundance and transport of the charge carrier Li+. This observation has led to a potential strategy for tailoring the grain boundary structures. This study points out, for the first time, the importance of the atomic-scale grain-boundary modification to the macroscopic Li+ conductivity. Such a discovery paves the way for the search and design of solid electrolytes with superior performance.

Thin, Deformable, and Safety‐Reinforced Plastic Crystal Polymer Electrolytes for High‐Performance Flexible Lithium‐Ion Batteries

Abstract: A new class of highly thin, deformable, and safety-reinforced plastic crystal polymer electrolytes (N-PCPEs) is demonstrated as an innovative solid electrolyte for potential use in high-performance flexible lithium-ion batteries with aesthetic versatility and robust safety. The unusual N-PCPEs are fabricated by combining a plastic crystal polymer electrolyte with a porous polyethylene terephthalate (PET) nonwoven. Herein, the three-dimensional reticulated plastic crystal polymer electrolyte matrix is formed directly inside the PET nonwoven skeleton via in-situ UV-crosslinking of ethoxylated trimethylolpropane triacrylate (ETPTA) monomer, under co-presence of plastic crystal electrolyte. The PET nonwoven is incorporated as a compliant skeleton to enhance mechanical/dimensional strength of N-PCPE. Owing to this structural uniqueness, the N-PCPE shows significant improvements in the film thickness and deformability with maintaining advantageous features (such as high ionic conductivity and thermal stability) of the PCE. Based on structural/physicochemical characterization of N-PCPE, its potential application as a solid electrolyte for flexible lithium-ion batteries is explored by scrutinizing the electrochemical performance of cells. The high ionic conductance of N-PCPE, along with its excellent deformability, plays a viable role in improving cell performance (particularly at high current densities and also mechanically deformed states). Notably, the cell assembled with N-PCPE exhibits stable electrochemical performance even under a severely wrinkled state, without suffering from internal short-circuit failures between electrodes.

Dielectric and Viscoelastic Responses of Imidazolium-Based Ionomers with Different Counterions and Side Chain Lengths

Abstract: A molecular-level understanding of dynamics in imidazolium-based ionomers with different counterions and side chain lengths was investigated using X-ray scattering, oscillatory shear, and dielectric relaxation spectroscopy (DRS). Variations of the counterion size and side chain length lead to changes in glass transition temperature (Tg), extent of ionic aggregation, and dielectric constant, with consequences for ion transport. A physical model of electrode polarization is used to determine the number density of simultaneously conducting ions and their mobility. Imidazolium-based ionomers with larger counterion and longer side chain have lower Tg, resulting in higher ionic conductivity and mobility. The ionic mobility is coupled to ion motions that are directly measured as a second segmental process in DRS, as these are observed to share the same Vogel temperature. Time–temperature superposition (tTS) was applied to create linear viscoelasticity master curves and to investigate the delay in chain motion re...

Morphology–Conductivity Relationship of Single-Ion-Conducting Block Copolymer Electrolytes for Lithium Batteries

Abstract: A significant limitation of rechargeable lithium-ion batteries arises because most of the ionic current is carried by the anion, the ion that does not participate in energy-producing reactions. Single-ion-conducting block copolymer electrolytes, wherein all of the current is carried by the lithium cations, have the potential to dramatically improve battery performance. The relationship between ionic conductivity and morphology of single-ion-conducting poly(ethylene oxide)-b-polystyrenesulfonyllithium(trifluoromethylsulfonyl)imide (PEO–PSLiTFSI) diblock copolymers was studied by small-angle X-ray scattering and ac impedance spectroscopy. At low temperatures, an ordered lamellar phase is obtained, and the “mobile” lithium ions are trapped in the form of ionic clusters in the glassy polystyrene-rich microphase. An increase in temperature results in a thermodynamic transition to a disordered phase. Above this transition temperature, the lithium ions are released from the clusters, and ionic conductivity incre...

Ionic Liquid of a Gold Nanocluster: A Versatile Matrix for Electrochemical Biosensors

Abstract: Ionic liquids are room-temperature molten salts that are increasingly used in electrochemical devices, such as batteries, fuel cells, and sensors, where their intrinsic ionic conductivity is exploited. Here we demonstrate that combining anionic, redox-active Au25 clusters with imidazolium cations leads to a stable ionic liquid possessing both ionic and electronic conductivity. The Au25 ionic liquid was found to act as a versatile matrix for amperometric enzyme biosensors toward the detection of glucose. Enzyme electrodes prepared by incorporating glucose oxidase in the Au25 ionic liquid show high electrocatalytic activity and substrate affinity. Au25 clusters in the electrode were found to act as effective redox mediators as well as electronic conductors determining the detection sensitivity. With the unique electrochemical properties and almost unlimited structural tunability, the ionic liquids of quantum-sized gold clusters may serve as versatile matrices for a variety of electrochemical biosensors.

Computational and Experimental Investigation of Li-Doped Ionic Liquid Electrolytes: [pyr14][TFSI], [pyr13][FSI], and [EMIM][BF4]

Abstract: We employ molecular dynamics (MD) simulation and experiment to investigate the structure, thermodynamics, and transport of N-methyl-N-butylpyrrolidinium bis(trifluoromethylsufonyl)imide ([pyr14][TFSI]), N-methyl-N-propylpyrrolidinium bis(fluorosufonyl)imide ([pyr13][FSI]), and 1-ethyl-3-methylimidazolium boron tetrafluoride ([EMIM][BF4]), as a function of Li-salt mole fraction (0.05 ≤ xLi(+) ≤ 0.33) and temperature (298 K ≤ T ≤ 393 K). Structurally, Li(+) is shown to be solvated by three anion neighbors in [pyr14][TFSI] and four anion neighbors in both [pyr13][FSI] and [EMIM][BF4], and at all levels of xLi(+) we find the presence of lithium aggregates. Pulsed field gradient spin-echo NMR measurements of diffusion and electrochemical impedance spectroscopy measurements of ionic conductivity are made for the neat ionic liquids as well as 0.5 molal solutions of Li-salt in the ionic liquids. Bulk ionic liquid properties (density, diffusion, viscosity, and ionic conductivity) are obtained with MD simulations and show excellent agreement with experiment. While the diffusion exhibits a systematic decrease with increasing xLi(+), the contribution of Li(+) to ionic conductivity increases until reaching a saturation doping level of xLi(+) = 0.10. Comparatively, the Li(+) conductivity of [pyr14][TFSI] is an order of magnitude lower than that of the other liquids, which range between 0.1 and 0.3 mS/cm. Our transport results also demonstrate the necessity of long MD simulation runs (∼200 ns) to converge transport properties at room temperature. The differences in Li(+) transport are reflected in the residence times of Li(+) with the anions (τ(Li/-)), which are revealed to be much larger for [pyr14][TFSI] (up to 100 ns at the highest doping levels) than in either [EMIM][BF4] or [pyr13][FSI]. Finally, to comment on the relative kinetics of Li(+) transport in each liquid, we find that while the net motion of Li(+) with its solvation shell (vehicular) significantly contributes to net diffusion in all liquids, the importance of transport through anion exchange increases at high xLi(+) and in liquids with large anions.