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Showing papers on "Ionic liquid published in 2014"


Journal ArticleDOI
TL;DR: Deep Eutectic Solvents (DES) as discussed by the authors are a class of solvents that can be defined as a mixture of two or more components, which at a particular composition present a high melting point depression becoming liquids at room temperature.
Abstract: Green technology actively seeks new solvents to replace common organic solvents that present inherent toxicity and have high volatility, leading to evaporation of volatile organic compounds to the atmosphere. Over the past two decades, ionic liquids (ILs) have gained enormous attention from the scientific community, and the number of reported articles in the literature has grown exponentially. Nevertheless, IL “greenness” is often challenged, mainly due to their poor biodegradability, biocompatibility, and sustainability. An alternative to ILs are deep eutectic solvents (DES). Deep eutectic solvents are defined as a mixture of two or more components, which may be solid or liquid and that at a particular composition present a high melting point depression becoming liquids at room temperature. When the compounds that constitute the DES are primary metabolites, namely, aminoacids, organic acids, sugars, or choline derivatives, the DES are so called natural deep eutectic solvents (NADES). NADES fully represen...

1,439 citations


Journal ArticleDOI
TL;DR: Ionic liquids offer a unique suite of properties that make them important candidates for a number of energy related applications, such as fuel cell electrolytes and CO2 absorbents for post-combustion CO2 capture as mentioned in this paper.
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.

1,427 citations


Journal ArticleDOI
TL;DR: One of the advantages of RTILs as compared to their high-temperature molten salt (HTMS) “sister-systems” is that the dissolved molecules are not imbedded in a harsh high temperature environment which could be destructive for many classes of fragile (organic) molecules.
Abstract: Until recently, “room-temperature” (<100–150 °C) liquid-state electrochemistry was mostly electrochemistry of diluted electrolytes(1)–(4) where dissolved salt ions were surrounded by a considerable amount of solvent molecules. Highly concentrated liquid electrolytes were mostly considered in the narrow (albeit important) niche of high-temperature electrochemistry of molten inorganic salts(5-9) and in the even narrower niche of “first-generation” room temperature ionic liquids, RTILs (such as chloro-aluminates and alkylammonium nitrates).(10-14) The situation has changed dramatically in the 2000s after the discovery of new moisture- and temperature-stable RTILs.(15, 16) These days, the “later generation” RTILs attracted wide attention within the electrochemical community.(17-31) Indeed, RTILs, as a class of compounds, possess a unique combination of properties (high charge density, electrochemical stability, low/negligible volatility, tunable polarity, etc.) that make them very attractive substances from fundamental and application points of view.(32-38) Most importantly, they can mix with each other in “cocktails” of one’s choice to acquire the desired properties (e.g., wider temperature range of the liquid phase(39, 40)) and can serve as almost “universal” solvents.(37, 41, 42) It is worth noting here one of the advantages of RTILs as compared to their high-temperature molten salt (HTMS)(43) “sister-systems”.(44) In RTILs the dissolved molecules are not imbedded in a harsh high temperature environment which could be destructive for many classes of fragile (organic) molecules.

1,076 citations



Journal ArticleDOI
TL;DR: An overview of DESs as designer solvents to create well-defined nanomaterials including shape-controlled nanoparticles, electrodeposited films, metal-organic frameworks, colloidal assemblies, hierarchically porous carbons, and DNA/RNA architectures is provided.
Abstract: ConspectusDeep eutectic solvents (DESs) represent an alternative class of ionic fluids closely resembling room-temperature ionic liquids (RTILs), although, strictly speaking, they are distinguished by the fact that they also contain an organic molecular component (typically, a hydrogen bond donor like a urea, amide, acid, or polyol), frequently as the predominant constituent. Practically speaking, DESs are attractive alternatives to RTILs, sharing most of their remarkable qualities (e.g., tolerance to humidity, negligible vapor pressure, thermostability, wide electrochemical potential windows, tunability) while overcoming several limitations associated with their RTIL cousins. Particularly, DESs are typically, less expensive, more synthetically accessible (typically, from bulk commodity chemicals using solvent/waste-free processes), nontoxic, and biodegradable.In this Account, we provide an overview of DESs as designer solvents to create well-defined nanomaterials including shape-controlled nanoparticles,...

658 citations


Journal ArticleDOI
TL;DR: Molybdenum disulphide is identified as a promising cost-effective substitute for noble metal catalysts and shows superior carbon dioxide reduction performance compared with the noble metals with a high current density and low overpotential in an ionic liquid.
Abstract: Electrochemical reduction is one process to produce higher value chemicals from carbon dioxide, and it is typically catalysed by noble metals. Here, the authors demonstrate that molybdenum disulphide is also capable of efficiently catalysing the reaction in the presence of an ionic liquid.

616 citations


Journal ArticleDOI
TL;DR: In this paper, the authors provided accurate densities, viscosities, and refractive indices for DESs prepared using cholinium chloride as the hydrogen bond acceptor and several carboxylic acids (levulinic, glutaric, malonic, oxalic, and glycolic) as hydrogen bond donors.
Abstract: Recently, many studies concerning the environmental impact of ionic liquids (ILs) have shown that despite their unique properties and clear advantages in an ever wide range of applications and processes, ILs are not intrinsically green. In a search for biodegradable and low toxicity, a new type of ILs has been developed, the deep eutectic solvents (DESs). In this context, the aim of this work is to provide accurate densities, viscosities, and refractive indices for DESs prepared using cholinium chloride as the hydrogen bond acceptor and several carboxylic acids (levulinic, glutaric, malonic, oxalic, and glycolic) as the hydrogen bond donors. The impact of two different synthetic methodologies, heating and grinding, in the thermophysical properties of the prepared DESs was assessed. The obtained DESs were analyzed using NMR spectroscopy, FTIR, and electrospray ionization mass spectrometry in order to check their structures and purities. Thermophysical properties, densities, viscosities, and refractive indi...

532 citations


Journal ArticleDOI
TL;DR: A brief overview of the current knowledge regarding the potential risks linked to the application of ionic liquids - from preparation to their disposal, with special emphasis on their potential environmental impacts and future directions in designing inherently safer ionsic liquids are given.

507 citations


Journal ArticleDOI
TL;DR: In this paper, the roles of Ionic Liquids (ILs) and IL-based solvent systems as proposed alternative for conventional organic solvents are described and the physicochemical properties that are reviewed are thermal properties, conductivity and chemical reactivity.
Abstract: Since environmental pollution caused by chemical and energy industries has increased for several decades, there is a social expectation that scientists and engineers try to design sustainable chemical processes, to generate less hazardous materials and more environmentally friendly sources of energy production. In this review the roles of Ionic Liquids (ILs) and IL based solvent systems as proposed alternative for conventional organic solvents are described. Since there are already many reviews on benefits of ILs, after a very brief review of ILs we focus mostly on aspects that are not covered in other reviews, in particular the known limits of these solvents. In addition, different methods to measure the physicochemical properties relevant to their use in energy storage applications such as fuel cells and batteries are introduced. The physicochemical properties that are reviewed are thermal properties, conductivity and chemical reactivity. The focus of the review is on the literature after 2008, with the exception of some important historic articles on ILs.

491 citations



Journal ArticleDOI
TL;DR: It is shown that biological activity and cytotoxicity of ionic liquids dramatically depend on the nature of a biological system, and a careful selection of biological activity data is a must for the correct assessment of chemical technologies involving ionic liquid.
Abstract: Rapid progress in the field of ionic liquids in recent decades led to the development of many outstanding energy-conversion processes, catalytic systems, synthetic procedures, and important practical applications. Task-specific optimization emerged as a sharpening stone for the fine-tuning of structure of ionic liquids, which resulted in unprecedented efficiency at the molecular level. Ionic-liquid systems showed promising opportunities in the development of green and sustainable technologies; however, the chemical nature of ionic liquids is not intrinsically green. Many ionic liquids were found to be toxic or even highly toxic towards cells and living organisms. In this Review, we show that biological activity and cytotoxicity of ionic liquids dramatically depend on the nature of a biological system. An ionic liquid may be not toxic for particular cells or organisms, but may demonstrate high toxicity towards another target present in the environment. Thus, a careful selection of biological activity data is a must for the correct assessment of chemical technologies involving ionic liquids. In addition to the direct biological activity (immediate response), several indirect effects and aftereffects are of primary importance. The following principal factors were revealed to modulate toxicity of ionic liquids: i) length of an alkyl chain in the cation; ii) degree of functionalization in the side chain of the cation; iii) anion nature; iv) cation nature; and v) mutual influence of anion and cation.

Journal ArticleDOI
TL;DR: This review summarizes the recent advances in the development of new cellulose materials and technologies using ionic liquids to develop new processing technologies, cellulose functionalization methods and new cellulOSE materials including blends, composites, fibers and ion gels.
Abstract: Due to its abundance and a wide range of beneficial physical and chemical properties, cellulose has become very popular in order to produce materials for various applications. This review summarizes the recent advances in the development of new cellulose materials and technologies using ionic liquids. Dissolution of cellulose in ionic liquids has been used to develop new processing technologies, cellulose functionalization methods and new cellulose materials including blends, composites, fibers and ion gels.

Journal ArticleDOI
TL;DR: In this article, the authors proposed a dual-graphite and dual-carbon energy storage system, where the graphite was used as both anode and cathode material in a so-called dual graphite or dual carbon cell, and an ionic liquid-based electrolyte mixture was used in combination with the SEI-forming additive ethylene sulfite.
Abstract: Recently, dual-ion cells based on the anion intercalation into a graphite positive electrode have been proposed as electrochemical energy storage devices. For this technology, in particular electrolytes which display a high stability vs. oxidation are required due to the very high operation potentials of the cathode, which may exceed 5 V vs. Li/Li+. In this work, we present highly promising results for the use of graphite as both the anode and cathode material in a so-called “dual-graphite” or “dual-carbon” cell. A major goal for this system is to find suitable electrolyte mixtures which exhibit not only a high oxidative stability at the cathode but also form a stable solid electrolyte interphase (SEI) at the graphite anode. As an electrolyte system, the ionic liquid-based electrolyte mixture Pyr14TFSI-LiTFSI is used in combination with the SEI-forming additive ethylene sulfite (ES) which allows stable and highly reversible Li+ ion and TFSI− anion intercalation/de-intercalation into/from the graphite anode and cathode, respectively. By addition of ES, also the discharge capacity for the anion intercalation can be remarkably increased from 50 mA h g−1 to 97 mA h g−1. X-ray diffraction studies of the anion intercalation into graphite are conducted in order to understand the influence of the electrolyte additive on the graphite structure and on the cell performance.

Journal ArticleDOI
TL;DR: In this article, the applicability of ionic liquids and deep eutectic mixtures in a variety of extraction techniques, including but not limited to liquid-and solid-phase (micro) extraction, microwave-assisted extraction, ultrasound assisted extraction and pressurized liquid extraction, is discussed.
Abstract: In recent years, ionic liquids and deep eutectic mixtures have demonstrated great potential in extraction processes relevant to several scientific and technological activities. This review focuses on the applicability of these sustainable solvents in a variety of extraction techniques, including but not limited to liquid- and solid-phase (micro) extraction, microwave-assisted extraction, ultrasound-assisted extraction and pressurized liquid extraction. Selected applications of ionic liquids and deep eutectic mixtures on analytical method development, removal of environmental pollutants, selective isolation, and recovery of target compounds, purification of fuels, and azeotrope breaking are described and discussed.

Journal ArticleDOI
TL;DR: In this paper, the authors investigated the effect of temperature on the density and dynamic viscosities of reline, a common and popular DES composed of choline chloride and urea in 1:2 molar ratio.
Abstract: Deep eutectic solvents (DESs) have been regarded as one of the most promising environmentally benign and cost-effective alternatives to conventional ionic liquids and volatile organic solvents. Aqueous mixtures of DESs have the potential to afford modified properties for specific applications. Densities and dynamic viscosities of a common and popular DES composed of choline chloride and urea in 1:2 molar ratio, named reline, and its aqueous mixtures in the temperature range 293.15 K to 363.15 K are reported. A decrease in density with increasing temperature is found to follow a quadratic expression. Excess molar volumes of the aqueous mixtures of reline are found to be negative at all temperatures and compositions. The absolute excess molar volume is found to decrease, in general, as the temperature is increased from 293.15 K to 323.15 K. For temperatures above 323.15 K, the excess molar volume does not change much with further increase in temperature to 363.15 K. The temperature dependence of dynamic vis...

Journal ArticleDOI
Yingying Lu1, Kevin S. Korf1, Yu Kambe1, Zhengyuan Tu1, Lynden A. Archer1 
TL;DR: 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.
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.

Journal ArticleDOI
TL;DR: In the third issue of the then new journal Green Chemistry (2001, 3, 156-164), the physical properties of a few hydrophilic and hydrophobic ionic liquids (ILs) representing one of the first such studies was published.

Journal ArticleDOI
TL;DR: In this article, the authors highlight the recent use of ionic liquids (ILs) as solvents that have provided some new opportunities to efficiently convert lignin and Lignin model compounds into value-added aromatic chemicals.
Abstract: Lignin, one of the three subcomponents of lignocellulosic biomass (along with cellulose and hemicellulose), represents more than 20% of the total mass of the Earth’s biosphere. However, essentially due to its complex structure, this renewable polymer derived from biomass is mainly burned as a source of energy in the pulp and paper industry. Today, the valorization of lignin into the production of chemical feedstocks represents a real challenge in terms of both sustainability and environmental protection. This review first briefly outlines the main points of this challenge and compares the different methods investigated by chemists over the past several decades, pointing out the major difficulties met. Next, the review highlights the recent use of ionic liquids (ILs) as solvents that have provided some new opportunities to efficiently convert lignin and lignin model compounds into value-added aromatic chemicals. Particular focus is given to these new strategies in terms of selectivity, separation and the u...

Journal ArticleDOI
TL;DR: In this paper, the authors present a survey of the electrolyte composition of the lithium-sulfur battery and show that only by combining particular electrolytes with cathode materials that are designed to actively retain sulfur and its reduction products, have a relatively few studies been able to obtain the desired levels of performance.
Abstract: At first glance, the combination of the lightest, most electropositive metal (lithium) with a safe, abundant (and reasonably light) non-metal (sulfur) makes good sense as a prospective battery. However, while the lithium–sulfur battery offers a very high theoretical specific energy (∼2600 W h kg−1) the actual performance delivered is proving to be severely limited—in many cases, this is directly related to the role of the electrolyte. The fundamental issue is that the reduction of sulfur proceeds through a series of polysulfide species, which are for the most part soluble in common organic solvents, including those employed in battery electrolyte solutions. So, despite the fact that the ultimate product (Li2S) is essentially insoluble, the intermediate stages of discharge see a migration of redox-active species out of the cathode, from where they can react with the lithium anode, which sets in train a series of equilibria that cause both a loss of charging efficiency and a gradual loss of discharge capacity. In the last decade, a major stream of the research to overcome this complex situation has focused on minimizing the solubility of polysulfides. From this we now have a range of media in which the lithium–sulfur system can operate with much improved charge–discharge characteristics: ionic liquids (and blends with organic media); super-saturated salt-solvent mixtures; polymer-gelled organic media; solid polymers; solid inorganic glasses. Underlining the multi-faceted nature of interactions within the lithium–sulfur cell, though, none of these improved electrolytes has been able to bring the performance of this system up to the levels of reliability and capacity maintenance (without sacrificing high specific energy) that are benchmarks in energy storage applications. Our survey indicates that only by combining particular electrolytes with cathode materials that are designed to actively retain sulfur and its reduction products, have a relatively few studies been able to obtain the desired levels of performance. Ultimately the successful development of the lithium–sulfur battery requires careful coordination of the choice of modified electrolyte with the specific nature of the cathode material, underpinned by the assumption that the resulting electrolyte composition will meet established criteria for compatibility with the lithium anode.

Journal ArticleDOI
Xiaoyan Luo1, Yan Guo1, Fang Ding1, Hongqing Zhao1, Guokai Cui1, Haoran Li1, Congmin Wang1 
TL;DR: QC calculations, spectroscopic investigations, and calorimetric data demonstrated that multiple-site cooperative interactions between two kinds of interacting sites in the anion and CO2 resulted in superior CO2 capacities, which originated from the π-electron delocalization in the pyridine ring.
Abstract: A strategy for improving CO2 capture by new anion-functionalized ionic liquids (ILs) making use of multiple site cooperative interactions is reported An extremely high capacity of up to 160 mol CO2 per mol IL and excellent reversibility were achieved by introducing a nitrogen-based interacting site on the phenolate and imidazolate anion Quantum-chemical calculations, spectroscopic investigations, and calorimetric data demonstrated that multiple-site cooperative interactions between two kinds of interacting sites in the anion and CO2 resulted in superior CO2 capacities, which originated from the π-electron delocalization in the pyridine ring

Journal ArticleDOI
TL;DR: In this article, a review of the science and technological applications of ionic liquids confined in nano-pores is presented and a comprehensive overview is given about the experimental studies dealing with the changes in the physico-chemical properties of ionics like thermal phase transition, stability, dynamical behavior, optical properties etc.

Journal ArticleDOI
TL;DR: 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 that holds tremendous potential to advance lithium-ion battery technology by enabling the use of lithium metal anodes or to serve as membranes in high-temperature fuel cells.
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...

Journal ArticleDOI
TL;DR: In this paper, progress made in the use of ionic liquid catalysts and related systems for cycloaddition reactions of carbon dioxide with epoxides is described with the primary focus on results from the past eight years.

Journal ArticleDOI
TL;DR: A critical review of the progress in the use of Room Temperature Ionic Liquids (RTILs) as Proton Exchange Membrane (PEM) electrolytes in Fuel Cells (FCs) is provided in this article.

Journal ArticleDOI
TL;DR: In this paper, Raman data analysis supported by DFT calculations on Na+-TFSI complexes, allow to determine the sodium ion solvation and charge carrier nature as a function of salt concentration.

Journal ArticleDOI
TL;DR: In this article, the use of conducting polymers as active materials in the positive electrodes of rechargeable aluminum-based batteries operating at room temperature was demonstrated, with electrode capacities at near-theoretical levels and Coulombic efficiencies approaching 100%.
Abstract: Demonstrated here is the use of conducting polymers as active materials in the positive electrodes of rechargeable aluminum-based batteries operating at room temperature. The battery chemistry is based on chloroaluminate ionic liquid electrolytes, which allow reversible stripping and plating of aluminum metal at the negative electrode. Characterization of electrochemically synthesized polypyrrole films revealed doping of the polymers with chloroaluminate anions. Cycling of the conducting polymer electrodes occurred via the electrochemical insertion and removal of these anions. Stable galvanostatic cycling of polypyrrole and polythiophene cells was demonstrated, with electrode capacities at near-theoretical levels (30–100 mAh g–1) and Coulombic efficiencies approaching 100%. The energy density of a sealed sandwich-type cell with polythiophene at the positive electrode was estimated to be 44 Wh kg–1 relative to the total mass of active components. This energy density is competitive with state-of-the-art bat...

Journal ArticleDOI
TL;DR: The methods used for studying the protein–IL interaction are analyzed, useful in providing information about structural and conformational dynamics of protein and the affect of physico-chemical properties of ionic liquids, viz. hydrogen bond capacity and hydrophobicity on protein stability are discussed.
Abstract: Room temperatures ionic liquids are considered as miraculous solvents for biological system. Due to their inimitable properties and large variety of applications, they have been widely used in enzyme catalysis and protein stability and separation. The related information present in the current review is helpful to the researchers working in the field of biotechnology and biochemistry to design or choose an ionic liquid that can serve as a noble and selective solvent for any particular enzymatic reaction, protein preservation and other protein based applications. We have extensively analyzed the methods used for studying the protein–IL interaction which is useful in providing information about structural and conformational dynamics of protein. This can be helpful to develop and understanding about the effect of ionic liquids on stability and activity of proteins. In addition, the affect of physico-chemical properties of ionic liquids, viz. hydrogen bond capacity and hydrophobicity on protein stability are discussed.

Journal ArticleDOI
TL;DR: The experimental techniques that can be applied to study and characterise the anion speciation in these ionic liquids are reviewed and, using recent examples, how their applications base is evolving beyond traditional applications in Lewis acidic catalysis and electrochemistry is illustrated.
Abstract: Ionic liquids with chlorometallate anions may not have been the first ionic liquids, however, it was their development that lead to the recognition that ionic liquids are a distinct, and useful, class of (functional) materials. While much of the phenomenal interest and attention over the past two decades has focussed on ‘air and water stable’ ionic liquids, research and application of chlorometallate systems has continued unabated albeit largely out of the main spotlight. The defining characteristic of chlorometallates is the presence of complex anionic equilibria, which depend both on the type and on the concentration of metal present, and leads directly to their characteristic and individual properties. Here, we review the experimental techniques that can be applied to study and characterise the anion speciation in these ionic liquids and, using recent examples, illustrate how their applications base is evolving beyond traditional applications in Lewis acidic catalysis and electrochemistry through to uses as soft and component materials, in the ionothermal synthesis of semiconductors, gas storage systems and key components in the development of biomass processing.

Journal ArticleDOI
TL;DR: This perspective paper describes possible criteria for the new family of ionic liquids: "solvate" ionic liquid, originally proposed by Angell et al. in their recent review; however, their criteria remain to be debated.
Abstract: Certain concentrated mixtures of salts and solvents are not simply “solutions” anymore, but they may be described as “ionic liquids”. In this perspective paper, we describe possible criteria for the new family of ionic liquids: “solvate” ionic liquids. This subclass of ionic liquids was originally proposed by Angell et al. in their recent review; however, their criteria remain to be debated. Concentrated mixtures of lithium salts and organic solvents are useful models for these solvate ionic liquids, and the effects of the salt concentration, types of solvents, and counter anions of the lithium salts on their structure and properties have been explored to enable contrast with traditional solutions, and to help determine whether a given mixture belongs to the solvate ionic liquid or not.

Journal ArticleDOI
TL;DR: This Review provides an overview of the role of ILs in the synthesis of materials for batteries, supercapacitors, and green electrode processing.
Abstract: The advent of ionic liquids (ILs) as eco-friendly and promising reaction media has opened new frontiers in the field of electrochemical energy storage Beyond their use as electrolyte components in batteries and supercapacitors, ILs have unique properties that make them suitable as functional advanced materials, media for materials production, and components for preparing highly engineered functional products Aiming at offering an in-depth review on the newly emerging IL-based green synthesis processes of energy storage materials, this Review provides an overview of the role of ILs in the synthesis of materials for batteries, supercapacitors, and green electrode processing It is expected that this Review will assess the status quo of the research field and thereby stimulate new thoughts and ideas on the emerging challenges and opportunities of IL-based syntheses of energy materials