Nitrate Ionic Liquid Research Articles

Multiphase Coexistence in an Ionic Liquid: 1-Decyl-3-methylimidazolium Nitrate.

Complicated phase transitions were observed in a single-component 1-decyl-3-methylimidazolium nitrate ([C10mim][NO3]) ionic liquid (IL) using Raman spectroscopy and synchrotron small- and wide-angle X-ray scattering (SWAXS). Time-resolved synchrotron SWAXS could distinguish the phase transitions depending upon the cooling rate. Low-Q peaks representing a few kinds of layered structures were decomposed. Multiphase coexistence was observed in [C10mim][NO3] at specific cooling rates (8-9 K/min). Ionic liquid crystals (ILCs), hybrid-layered crystals, and hexagonal close-packed structures coexisted simultaneously. At the cooling rate region, the reentrant phase transition of the ILC phase upon heating was observed.

The Degradation of the 2-Hydroxyethylhydrazinium Nitrate Ionic Liquid System.

The mechanism by which the 2-hydroxyethylhydrazinium nitrate (HEHN) ionic liquid (IL) dissociates via the formation and loss of nitric acid is investigated utilizing the effective fragment potential (EFP) method and various ab initio methods. Additionally, the interactions that dictate the stability of the HEHN IL and contribute to the formation of nitric acid are further assessed using the quasi-atomic orbital (QUAO) bonding analysis. From this work, it is suggested that the formation of nitric acid is dictated by the presence of hydrogen-bonding interactions which appear to become increasingly ionic in nature as the system approaches the bulk, limiting the formation of nitric acid.

Cyphos Nitrate Selectively Separates Y(III) from Sr(II) Present in Acidic Feed Solution: An Efficient Ionic Liquid based Extraction Process

AbstractMutual separation of Y(III) and Sr(II) from their waste solution has been an emerging research domain due to their various industrial applications. In this investigation, we emphasize the feasibility of selective separation of Y(III) from Sr(II) present in nitric acid medium using undiluted cyphos nitrate ionic liquid (IL): trihexyl(tetradecyl)phosphonium nitrate ([P66614][NO3]) as the ligating phase. The set experimental parameters were the feed phase acidity, initial nitrate ion concentration, initial feed metal ion concentration, equilibration time and temperature to unveil the efficacy of the proposed system. Efficient extraction of Y(III) selectively in presence of Sr(II) using only a salting agent in aqueous phase without additional extractant in IL phase was highlighted. A remarkable separation factor (SF) obtained for Y(III) over Sr(II) explored the efficacy of the proposed IL system. Y(III) loading in IL phase both in unirradiated and irradiated conditions was compared to evaluate the coordination behavior of irradiated moieties. In addition, a most important advantage of the proposed system is that it employs Milli‐Q water for the back extraction (stripping) of the loaded Y(III) from IL phase and does not demand any complexing agent (water soluble). This undoubtedly corroborates the economic and environmental benefits of the proposed IL system.

Evaluation of the synergistic effect of nanocomposite hydrogel based on imidazolium nitrate ionic liquids for enhanced oil recovery

A comprehensive research study was conducted to examine the synergistic properties of ionic liquids, and hydrogels. Two nanocomposite hydrogel samples were created: one with ionic liquid and the other without. The samples were made using hydrogel with acrylamide (AM) backbone, Al2O3 nanoparticles, and ionic liquid [C8mim][NO3]. The effectiveness of a nanocomposite hydrogel containing an ionic liquid was tested to improve the wettability alteration and sweeping efficiency of reservoirs. Various tests were performed including IFT, electroconductivity, micromodel, SEM, and equilibrium swelling tests. The tests showed that the presence of the ionic liquid increased the swelling up to 102 %. IL increased conductivity by 124.24 % and 44.86 % at ambient temperature and 90 °C respectively. In the strain sweep test, the maximum elastic modulus for NCH-IL was recorded as 40,350 Pa, while for the sample without ionic liquid, it was 27,100 Pa. The frequency sweep test confirmed the three-dimensional structure of the gel. IL increased the maximum elastic modulus from 13,200 Pa to 27,400 Pa. The critical frequency value also increased by 87.5 %. Moreover, the suspension, which contains 1 wt% of Nanocomposite Hydrogel based on Imidazolium Nitrate Ionic Liquids, has shear-thinning properties, making it easy to inject into reservoirs. The reduction of the contact angle from 109° to 14.2° demonstrated the ability of IL to alter the wettability of NCHs. This result stemmed from the release of part of the ionic liquid within the hydrogel structure, as confirmed by the UV test. During the emulsion stability test, it was observed that the NCH-IL sample created a stable emulsion and a more complete two-phase separation than the sample without the ionic liquid. The sample that contained IL recorded 85 % and 78.4 % oil recovery in homogeneous and heterogeneous micromodels, respectively. Whereas, the sample without IL recorded 71.27 % and 60.73 % in the same micromodels.

Nano silicated-FeAl2O4 functionalized by DL-alaninium nitrate ionic liquid (FeAl2O4-SiO2@[DL-Ala][NO3]) as versatile promotor for aqua-mediated synthesis of spiro[chromenopyrazole-indene-triones and spiro[chromenopyrazole-indoline-diones

In this work, the spinel FeAl2O4 was prepared and functionalized step-by-step with silica and alaninium nitrate ionic liquid ([DL-Ala][NO3]) to produce a bio-based multi-layered nanostructure (nano FeAl2O4-SiO2@[DL-Ala][NO3]). The obtained magnetized inorganic-bioorganic nanohybrid characterized by Fourier transform infrared spectroscopy (FT-IR), vibrating-sample magnetometry (VSM), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDAX), transmission electron microscopy (TEM), thermogravimetric analysis/differential scanning calorimetry (TGA/DSC), X-ray fluorescence (XRF), and X-Ray diffraction (XRD) analysis. A facile synthesis of some tricyclic dihydro-spiro[chromeno[2,3-c]pyrazole-4,2′-indene]triones and dihydro-spiro[chromeno[2,3-c]pyrazole-4,3′-indoline]diones via domino four-component one-pot reaction of various hydrazine derivatives, ethyl acetoacetate, heterocyclic 1,2-ketones (ninhydrin, isatin, 5-bromoisatin) and cyclic 1,3-diketones (dimedone and 1,3-cyclohexanedine), examined in the presence of nano FeAl2O4-SiO2@[DL-Ala][NO3] nanohybrid in refluxing aqueous media, successfully. The multi-aspect characteristics of the nanohybrid which consist of magnetized inorganic and bioorganic parts, could be the reason of its special catalytic efficacy. The recovery and reusability of the FeAl2O4-SiO2@[DL-Ala][NO3] magnetized nanoparticles (MNPs) were performed in two runs without significant activity loss.

Effect of alkyl chain length on the thermal properties and toxicity of n-alkyl-ammonium nitrate ionic liquids (n = 2, 3, 4, 5, 6, 8) for energy applications

AbstractThe most currently used ionic liquids (ILs) are protic ionic liquids (PILs), subject to extensive investigation regarding their physical properties. These compounds along with their mixtures with other substances such as salts and solvents, serve as electrolytes in next generation electrochemical smart devices, and emerge as viable candidates to replace conventional Heat Transfer Fluids (HTFs) in various energy applications. Despite the extensive number of studies, important information about this kind of compounds is still unknown, such as the effect of alkyl chain length on thermal and thermophysical properties, as well as toxicity. This work, extending previous studies of our group, summarizes the liquid range, heat capacity and acute toxicity level of six ammonium ILs: specifically, n-alkyl-ammonium nitrate ILs with increasing alkyl chain length (n = 2, 3, 4, 5, 6, 8). For this study, the synthesis of the three ILs with the longest alkyl chain was performed, along with DSC, TGA and toxicity measurements. It was observed that an increase in alkyl chain length resulted in a decrease in short-term thermal stability and an increase in melting temperature, indicating a reduction in the liquid range. A compensation effect between enthalpy and entropy of melting was observed for the studied chain lengths. The isobaric specific and molar heat capacities increase with temperature for all the compounds studied here, and good correlations were obtained between molar heat capacity and the number of carbon atoms in the alkyl chain for every temperature. Finally, most of the ILs are non-toxic, although toxicity increases with alkyl chain length.

NMR study of nitrate ionic liquids confined between micrometer-spaced plates

This review paper presents the results of a study conducted using nuclear magnetic resonance (NMR) methods to investigate the dynamic behaviour of ionic liquid-based compositions in micrometre-spaced confinement. Ethylammonium nitrate (EAN) and other ionic liquid (IL) systems with nitrate anion in glass or quartz spaced confinement demonstrate anomalous cation dynamics that differ from those observed in bulk and in nano-confinement. It was demonstrated that the principal axis of the nitrate anion exhibits preferential orientation to the surface, akin to that in liquid crystals. It was shown that the cation translational mobility reversibly changes during exposure to a static magnetic field. This phenomenon was interpreted as a result of intermolecular structure transformations occurring in the confined ILs. The mechanisms of these transformations were discussed.

Evaluation of the thermal hazard and pyrolysis mechanism of 1-allyl-3-methylimidazole nitrate and 1-propyl-3-methylimidazole nitrate via thermal analysis and DFT calculation: Effect of structural characteristics

Imidazole ionic liquid, as a green solvent, is one of the most widely used ionic liquids. Understanding its thermal safety characteristics and mechanism is the essential basis for its safe application. In this paper, the thermal hazard characteristics of two ionic liquids with typical structural characteristics are systematically studied, which were 1-allyl-3-methylimidazole nitrate and 1-propyl-3-methylimidazole nitrate ionic liquids. The thermal decomposition peculiarities of two ionic liquids were systematically analyzed by thermogravimetric analyzer, differential scanning calorimetry and accelerating rate calorimeter techniques, and the risk of thermal runaway is also evaluated. In addition, the pyrolysis products and microscopic pyrolysis mechanism of ionic liquids were studied via thermogravimetry-Fourier transform infrared spectroscopy, thermogravimetric mass spectrometry and density functional theory calculation, and the essential mechanism of thermal hazard were determined. The influence of substituent structure on the thermal hazard characteristics of imidazole nitrate ionic liquid was preliminarily analyzed from macroscopic experiment and microscopic mechanism two aspects. This study provides a theoretical basis for the safe application, design and development of imidazole nitrate ionic liquids.

Thermal hazard evaluation and risk assessment of 1-allyl-3-methylimidazole nitrate ionic liquid

Imidazole ionic liquids (ILs) have broad application prospects in batteries and other fields. Researching the thermal decomposition features of ILs holds paramount importance for the application in battery electrolyte. 1-allyl-3-methylimidazole nitrate ionic liquid (IL) as a new functional IL, and its related thermal decomposition properties are unknown. In this paper, the thermal decomposition peculiarities of 1-allyl-3-methylimidazole nitrate IL were systematically analyzed by thermogravimetric analyzer, differential scanning calorimetry, and accelerating rate calorimeter techniques, and the relevant thermodynamic parameters and thermal decomposition models were derived. In addition, 1-allyl-3-methylimidazole nitrate IL possesses strong thermal runaway characteristics and the risk of thermal runaway is also evaluated. The main gaseous products formed by the pyrolysis of 1-allyl-3-methylimidazole nitrate IL was detected and analyzed by thermogravimetry-Fourier transform infrared spectroscopy and thermogravimetric-photoionization mass spectrometry techniques. The results showed that flammable gas, toxic gas, and asphyxiating gas are formed during the pyrolysis of 1-allyl-3-methylimidazole nitrate IL. This study lays a theoretical foundation for the safe application and the formulation of corresponding safety protection measures of 1-allyl-3-methylimidazole nitrate IL.

(Invited) On the Inhibition Mechanism of an Alkylammonium Nitrate Ionic Liquid Family on Al Alloys: Electrochemical and XPS/in Situ PM-IRRAS Studies

AA2024 are high strength Al alloys widely used in the aerospace industry due to their excellent strength to weight ratio. However, their high susceptibility to localised corrosion, caused by the presence of intermetallic particles embedded in the Al matrix, requires the use of chromate-based surface treatment formulations1. Several alternatives have been explored in the last decades, such as vanadates, chromium (III) based conversion coatings, rare-earth inhibitors or more recently, lithium containing conversion coatings2. However, these alternatives are often not versatile (cannot be transposed to all alloy systems) or are not as cost effective as chromates. Ionic liquids (ILs), usually defined as salts with a melting point below 100°C, can be considered as promising corrosion inhibitors due to their low vapour pressure, chemical and thermal stability3. In addition, they can exhibit versatile inhibition properties associated with the quasi-infinite possible anion-cation combinations3–5. In previous work, the effect of an alkylammonium nitrate IL family, namely ethylammonium nitrate (EAN), propylammonium nitrate (PAN), and butylammonium nitrate (BAN) as potential corrosion inhibitors for an AA2024-T6 Al alloy was investigated6. Electrochemical tests such as potentiodynamic polarisation and electrochemical impedance spectroscopy were performed to identify the effect of the anion and cation on the anodic and cathodic kinetics. Herein, surface analysis was performed to rationalise the electrochemical results, particularly on the reactivity of NO3 - and R-NH3 + on the Cu-rich intermetallic particles. To this end, electrospray ionisation of EAN, BAN and NaNO3 was realised on Cu. The effect of the IL concentration and cation chain length, using PM-IRRAS (polarisation modulation -infrared reflection adsorption spectroscopy) was used to investigate molecule orientation and surface-molecule bonding as a function of surface coverage; The results provided new insights on the inhibition mechanism of this IL family. O. Gharbi, S. Thomas, C. Smith, and N. Birbilis, Npj Mater Degrad, 2, 12 (2018) http://www.nature.com/articles/s41529-018-0034-5.A. Kosari et al., Corros Sci, 190, 109651 (2021) https://doi.org/10.1016/j.corsci.2021.109651.C. Verma, E. E. Ebenso, and M. A. Quraishi, J Mol Liq, 233, 403–414 (2017) http://dx.doi.org/10.1016/j.molliq.2017.02.111.J. Sun, P. C. Howlett, D. R. MacFarlane, J. Lin, and M. Forsyth, Electrochim Acta, 54, 254–260 (2008).N. V. Likhanova et al., Corros Sci, 52, 2088–2097 (2010) http://dx.doi.org/10.1016/j.corsci.2010.02.030.A. Z. Benbouzid et al., Corrosion Communications, 9, 57–64 (2023).

A comprehensive investigation of 1,3-dibutylimidazolium nitrate ionic liquid as a green energetic oxidizer: From design to thermal stability assessment

The present work introduces a novel energetic ionic liquid (EIL), the 1,3-dibutyl-imidazolium nitrate [BBIm][NO3], that demonstrates interesting features such as symmetrical cation’s structure [BBIm] and the presence of nitrate anion [NO3], which confers the explosophoric oxidizing character. This EIL was synthesized by a simple green method and its chemical structure was fully characterized by 1-D 1H, 13C, 15N NMR, 2-D NMR, and FTIR spectroscopy. Besides, DSC and non-isothermal TGA analyses demonstrated that the [BBIm][NO3] displayed two stages of exothermicity and good thermal stability at temperatures ≤230 °C, which reduced its thermal hazard and enhanced its safe handling. Furthermore, the non-isothermal TGA data combined with isoconversional kinetic methods, i.e., TAS, it-KAS, and Vyazovkin/CE were used to determine the kinetics of its thermal decomposition. The obtained results revealed that the prepared [BBIm][NO3] EIL presents promising reactivity features, which may promote its further use in practical applications.

Evolution of the La(III) ion coordination sphere in ethylammonium nitrate solution upon water addition

A thorough structural study of La(NO3)3 salt solutions in mixtures of the ethylammonium nitrate (EAN) ionic liquid (IL) and water with EAN molar fraction (χEAN) ranging from 0 to 1 has been carried out by means of X-ray absorption spectroscopy (XAS) measurements at the La K-edge and molecular dynamics (MD) simulations. Both the XAS and MD outcomes agree in finding that the composition of the La3+ ion first solvation shell undergoes steadily changes when moving from pure water to pure EAN. Upon increasing of the IL concentration, the La3+ solvation complexes progressively lose water molecules to accommodate more and more nitrate anions, and the ratio between the two ligands continuously changes across the explored composition range. The nitrate ligands coordinate the metal ion only in a monodentate fashion for the lower EAN contents, while the percentage of bidentate nitrates becomes more and more predominant as the EAN concentration increases. When moving from pure water to pure EAN, the La3+ ion coordination passes from a 9-fold tricapped trigonal prismatic geometry to a 12-fold icosahedral one, while a 10-fold coordination with bicapped square antiprism geometry is the dominant species for the mixed compositions. The remarkable flexibility of this solvation complex in accommodating a variable amount of water molecules and nitrate ligands at dependence of the system composition is key for its predominance in all the EAN/water mixtures.

Low-temperature and high-pressure phase transitions in 1-decyl-3-methylimidazolium nitrate ionic liquid

The phase behavior of 1-decyl-3-methylimidazolium nitrate ([C10mim][NO3]) was investigated at a low temperature (LT) under ambient pressure and a high pressure (HP) under ambient temperature. [C10mim][NO3] is an ionic liquid (IL) possessing a long alkyl chain length. Detailed crystal structures of the IL at LT and HP were determined by synchrotron radiation experiments. The weak Bragg reflections in the low wavevector (Q) region were clearly observed. At LT, the Bragg reflection at the lowest Q was positioned differently than the prepeak in the liquid state. The 00ℓ Bragg reflections at Q00ℓ indicate a hybrid-layered structure with a lattice constant of 4.3 nm. In addition to the 00ℓ Bragg reflections, the double peak occurred in the region of Q002 at HP; thus new HP crystal structures were observed in [C10mim][NO3].

Thermophysical properties of n-alkyl-ammonium nitrate ionic liquids (n = 2,3,4) pure and water saturated for energy applications

Phase transition temperatures of three ionic liquids (ILs) with ammonium cations of different alkyl chain length and nitrate common anion were determined in this paper by differential scanning calorimetry. Thermal stability of these ILs in air and nitrogen atmosphere and the maximum operation temperatures of the compounds were also studied using a thermogravimetric analyser. Furthermore, thermophysical properties as density, viscosity, thermal conductivity, and heat capacity against temperature of these pure ionic liquids were determined and compared with the corresponding values for water saturated samples. For this purpose, different techniques were employed: for density and viscosity a rotational automated viscodensimeter; for thermal conductivity measurements a thermal conductimeter that follows the transient hot-wire method; and for heat capacity measurements a microdifferential scanning calorimeter. Different behaviours were observed depending on the analysed thermophysical properties. In case of dried samples, density and thermal conductivity decrease with alkyl chain; for saturated samples, same tendency is observed for density but is the opposite in case of thermal conductivity. Isobaric specific heat and viscosity increase with alkyl chain length in case of dried samples; for saturated samples same tendency is observed for the viscosity, whereas the tendency is the contrary in case of isobaric specific heat.

Molecular dynamics simulation studies of 1,3-dimethyl imidazolium nitrate ionic liquid with water.

The fundamental understanding of intermolecular interactions of ionic liquids (ILs) with water is essential in predicting IL-water thermodynamic properties. In this study, intermolecular or noncovalent interactions were studied for 1,3-dimethyl imidazolium [DMIM]+ cation and nitrate [NO3]- anion with water, employing quantum mechanics and molecular dynamics simulations. Molecular dynamics simulations were performed using a revised multipolar polarizable force field. The effect of water on ionic liquids was evaluated in terms of thermodynamic and dynamic properties. Thermodynamic properties included liquid densities ρ, excess molar volumes ΔVE, and liquid structures gr. Dynamic properties included self-diffusion coefficients D of mixture constituents as a function of water concentration. The density of ionic liquid-water mixtures monotonically decrease with increasing concentration of water. A negative excess volume was obtained for low and high water concentrations, demonstrating strong intermolecular interactions of water with ionic liquid components. Liquid structures of ionic liquid-water mixtures revealed a tendency for anions to interact with cations at shorter intermolecular distances when the water concentration is increased. Diffusion rates were found to increase for all mixture components with increase in the fraction of water. A significant change in the diffusion rate was found at ∼0.3 weight fraction of water. However, the water self-diffusion coefficient was dominant at all concentrations. The ratio of water/anion and anion/cation self-diffusion coefficients was found to decrease linearly with increasing concentration of water molecules.

Ionic liquid route for the corrosion inhibition of Al alloys: the effect of butylammonium nitrate on the corrosion of AA2024-T6

In this work, the effect of an ammonium nitrate ionic liquid on the corrosion susceptibility of an Al-Cu-Mg alloy was investigated. The effect of the nitrate anion and the ammonium cation on the anodic and cathodic kinetics were studied separately using potentiodynamic polarisation testing, electrochemical impedance spectroscopy and scanning electron microscopy. The results revealed a significant anodic inhibition, associated with a cation/anion synergy. The cathodic kinetics however increase with the presence of nitrates, associated with nitrate reduction reaction. Conversely, longer alkyl chain seemed to reduce the effect of nitrates. Such findings are promising in the context of developing ecofriendly chromate alternatives.

Formation and fragmentation of 2-hydroxyethylhydrazinium nitrate (HEHN) cluster ions: a combined electrospray ionization mass spectrometry, molecular dynamics and reaction potential surface study.

The 2-hydroxyethylhydrazinium nitrate ([HOCH2CH2NH2NH2]+NO3-, HEHN) ionic liquid has the potential to power both electric and chemical thrusters and provide a wider range of specific impulse needs. To characterize its capabilities as an electrospray propellant, we report the formation of HEHN cluster ions in positive electrospray ionization (ESI) and their collision-induced dissociation. The experiment was carried out using ESI guided-ion beam mass spectrometry which mimics an electrospray thruster in terms of ion emission, injection into a vacuum and fragmentation in space. Measurements include compositions of primary ions in the electrospray plume and their individual dissociation product ion cross sections and threshold energies. The results were interpreted in light of theoretical modeling. To determine cluster structures that are comprised of [HE + H]+ and NO3- constituents, classical mechanics simulations were used to create initial guesses; and for clusters that are formed by reactions between ionic constituents, quasi-classical direct dynamics trajectory simulations were used to mimic covalent bond formation and structures. All candidate structures were subject to density functional theory optimization, from which global minimum structures were identified and used for construction of reaction potential energy surface. The comparison between experimental values and calculated dissociation thermodynamics was used to verify the structures for the emitted species [(HEHN)nHE + H]+, [(HEHN)n(HE)2 + H]+, [(HE)n+1 + H]+ and [(HE)nC2H4OH]+ (n = 0-2), of which [(HE)1-2 + H]+ dominates. Due to the protic nature of HEHN, cluster fragmentation can be rationalized by proton transfer-mediated elimination of HNO3, HE and HE·HNO3, and the latter two become dominant in larger clusters. [(HE)2 + H]+ and [(HE)nC2H4OH]+ contain H-bonded water and consequently are featured by water elimination in fragmentation. These findings help to evaluate ion formation and fragmentation efficiencies and their impacts on electrospray propulsion.

Enabling uniform Li deposition behavior by introducing a NO3−-based ionic liquid additive into carbonate electrolyte for high-voltage Li metal batteries

The nonuniform lithium deposition behavior and low deposition/dissolution reversibility are the most significant obstacles for practical high-energy-density lithium metal batteries (LMBs). Herein, a novel 1-ethyl-3-methylimidazolium nitrate ionic liquid ([EMIm][NO3] IL) is proposed to incorporate into the conventional carbonate electrolyte with a small amount of 1,2-dimethoxyethane (DME) as the cosolvent. A high solubility of 0.5 M [EMIm][NO3] in the carbonate electrolyte is achieved for high-voltage LMBs by replacing traditional lithium nitrate with [EMIm][NO3] IL, where the DME cosolvent with high donicity enables the solvation of NO3− in the electrolyte system. Benefitting from the electrochemical reduction of NO3− anions, the designed electrolyte promotes the formation of highly conductive and stable solid electrolyte interface abundant with N-containing species and achieves stable Li stripping/plating behavior. As a result, the IL-modified electrolyte enables excellent electrochemical performances with improved Coulombic efficiency (>98.5%) in Li|Cu cell and stable cyclability (900 h) in Li|Li symmetric cell, respectively. More importantly, a Li|LiNi0.8Co0.1Mn0.1O2 pouch-type battery composed of high mass loading cathode (20 mg cm−2) and thin Li foil (50 μm) maintains an impressive cycling lifespan of 100 cycles. The exploration of NO3− containing IL as a novel electrolyte additive offers a promising opportunity for achieving high-performance Li metal batteries.

Tuning a Solvation Structure of Lithium Ions Coordinated with Nitrate Anions through Ionic Liquid‐Based Solvent for Highly Stable Lithium Metal Batteries

AbstractRational design of promising electrolyte is considered as an effective strategy to improve the cycling stability of lithium metal batteries (LMBs). Here, an elaborately designed ionic liquid‐based electrolyte is proposed that is composed of lithium bis(trifluoromethanesulfonyl)imide as the lithium salt, 1‐ethyl‐3‐methylimidazolium nitrate ionic liquid ([EMIm][NO3] IL) and fluoroethylene carbonate (FEC) as the functional solvents, and 1,2‐dimethoxyethane (DME) as the diluent solvent. Using [EMIm][NO3] IL as the solvent component facilitates a special Li+‐coordinated NO3− solvation structure, which enables the continues electrochemical reduction of solvated NO3− and the formation of remarkably stable and conductive solid electrolyte interface. With FEC as another functional solvent and DME as the diluent solvent, the formulated electrolyte delivers high oxidative stability and ionic conductivity, and endows improved electrochemical reaction kinetics. Therefore, the formulated electrolyte demonstrates exceedingly reversible and stable Li stripping/plating behavior with high average Coulombic efficiency (98.8%) and ultralong cycling stability (3500 h). Notably, the high‐voltage Li|LiNi0.8Co0.1Mn0.1O2 full cell with IL‐based electrolyte exhibits enhanced cyclability with a capacity retention of 65% after 200 cycles under harsh conditions of low negative/positive ratio (3.1) and lean electrolyte (2.5 µL mg−1). This study creates the first NO3−‐based ionic liquid electrolyte and evokes the avenue for practical high‐voltage LMBs.

Nanopockets with a Thermoresponsive Nitrate Ionic Liquid for Highly Efficient Uranium Extraction at High Acidity

Nanopockets with a Thermoresponsive Nitrate Ionic Liquid for Highly Efficient Uranium Extraction at High Acidity