Crystal Composition Research Articles

Supramolecular gels: a versatile crystallization toolbox.

Supramolecular gels are unique materials formed through the self-assembly of molecular building blocks, typically low molecular weight gelators (LMWGs), driven by non-covalent interactions. The process of crystallization within supramolecular gels has broadened the scope of the traditional gel-phase crystallization technique offering the possibility of obtaining crystals of higher quality and size. The broad structural diversity of LMWGs allows crystallization in multiple organic and aqueous solvents, favouring screening and optimization processes and the possibility to search for novel polymorphic forms. These supramolecular gels have been used for the crystallization of inorganic, small organic compounds of pharmaceutical interest, and proteins. Results have shown that these gels are not only able to produce crystals of high quality but also to influence polymorphism and physicochemical properties of the crystals, giving rise to crystals with potential new bio- and technological applications. Thus, understanding the principles of crystallization in supramolecular gels is essential for tailoring their properties and applications, ranging from drug delivery systems to composite crystals with tunable stability properties. In this review, we summarize the use of LMWG-based supramolecular gels as media to grow single crystals of a broad range of compounds.

Seriation of Enzyme-Functionalized Multilayers for the Design of Scalable Biomimetic Mineralized Structures.

Biomimetic hydroxyapatites are widely explored for their potential applications in the repair of mineralized tissues, particularly dental enamel, which is acellular and, thus, not naturally reformed after damage. Enamel is formed with a highly-controlled hierarchical structure, which is difficult to replicate up to the macroscale. A biomimetic approach is thus warranted, based on the same principles that drive biomineralization in vivo. Herein, a strategy for the design of enamel-like architectures is described, utilizing enzymes embedded in polyelectrolyte multilayers to generate inorganic phosphate locally, and provide a favorable chemical environment for the nucleation and growth of minerals. Moreover, a method is proposed to build up seriated mineral layers with scalable thicknesses, continuous mineral growth, and tunable morphology. Results show the outstanding growth of cohesive mineral layers, yielding macroscopic standalone fluoride and/or carbonate-substituted hydroxyapatite materials with comparable crystal structure and composition to native human mineralized tissues. This strategy presents a promising path forward for the biomimetic design of biomineral materials, particularly relevant for restorative applications, with an exquisite level of synthetic control over multiple orders of magnitude.

Exploring the molarity of Lithium Fluoride in minimally intensive layer delamination (MILD) method for efficient room temperature synthesis of high quality Ti3C2Tx free-standing film

In recent years, MXene has become the most demanding material in the 2D family, leading to their increased use in research for a diverse range of applications, such as energy storage, water purification, optoelectronics, electromagnetic interference (EMI) shielding and medicine. However, recent research has made it increasingly important to synthesize high-quality MXene in a safe, reliable, fast, reproducible, and good-yielding single-step method. To achieve high-quality MXene by etching the MAX phase precursors, it is very important to critically optimize synthesis parameters, such as etching method, etchant concentrations, temperature, time, etc. Minimally intensive layer delamination (MILD) method for MXene synthesis using Lithium Fluoride (LiF) salt and hydrochloric (HCl) acid seems to be a better choice in the context of improved performance in different applications as well as its scalability and reproducibility. Here, the molar ratio of HCL/LIF is critical for Aluminium etching at room temperature to produce a high-quality MXene with = O, -OH, -F termination groups in the MILD method. However, in case of MILD method the effect of LiF/HCL concentrations on quality of MXene need to be addressed. In this study, we focus on room temperature etching of Ti3AlC2 using MILD method to synthesize quasi two-dimensional carbide (Ti3C2) MXene. The influence of molarity concentration of etchants (LiF and HCl) on quality of MXene has been thoroughly investigated. Different molar concentrations of Lithium Fluoride (LiF) with fixed HCL concentration were tested at room temperature for 24 h in the etching process. The crystal structure, microstructure and composition of the MXene were characterized using X-ray diffraction, Raman spectroscopy, and electron microscopy. Flexible free-standing MXene film with largest shift in the characteristic (002) peak, indicating large interplanar spacing, has been successfully achieved repeatedly for an optimum molar concentration of etchants at room temperature.

Sensitivity of Mild Hydrothermal Synthesis to the Reaction Conditions: Targeting Mixed-Metal Hexagonal Tungsten Bronze Fluorides AxM2+xM3+(1-x)F3 to Investigate Their Magnetic Behavior.

The synthesis of five quaternary hexagonal tungsten bronze (HTB) fluorides, AxM2+xM3+(1-x)F3, (A = Cs and Rb; M2+ = Co2+, Ni2+, and Zn2+; and M3+ = V3+) via a mild hydrothermal route is reported. The crystal structures and compositions were determined using a combination of single-crystal X-ray diffraction, Rietveld refinement of powder X-ray diffraction data, and inductively coupled plasma optical emission spectroscopy analysis. This study highlights the sensitivity of the mild hydrothermal method on the reaction temperature, solvent system, and quantity of starting reagents that directly influence the selective synthesis of kinetically stabilized fluoride materials, including hydrated fluorides, β-pyrochlores, and HTB. The magnetic susceptibility and isothermal magnetization data for all five compounds were collected, which revealed the existence of a strong antiferromagnetic component in these phases. The presence of the Kagome layer in the structure results in geometrical frustration and leads to frustration indexes ranging from 7 to 13 for these compounds.

Rationalizing the Influence of Small-Molecule Dopants on Guanine Crystal Morphology.

Many spectacular optical phenomena in animals are produced by reflective assemblies of guanine crystals. The crystals comprise planar H-bonded layers of π-stacked molecules with a high in-plane refractive index. By preferentially expressing the highly reflective π-stacked (100) crystal face and controlling its cross-sectional shape, organisms generate a diverse array of photonic superstructures. How is this precise control over crystal morphology achieved? Recently, it was found that biogenic guanine crystals are composites, containing high quantities of hypoxanthine and xanthine in a molecular alloy. Here, we crystallized guanine in the presence of these dopants and used computations to rationalize their influence on the crystal morphology and energy. Exceptional quantities of hypoxanthine are incorporated into kinetically favored solid solutions, indicating that fast crystallization kinetics underlies the heterogeneous compositions of biogenic guanine crystals. We find that weakening of H-bonding interactions by additive incorporation elongates guanine crystals along the stacking direction-the opposite morphology of biogenic crystals. However, by modulation of the strength of competing in-plane H-bonding interactions, additive incorporation strongly influences the cross-sectional shape of the crystals. Our results suggest that small-molecule H-bond disrupting additives may be simultaneously employed with π-stack blocking additives to generate reflective platelet crystal morphologies exhibited by organisms.

The Solid‐State Battery Applicational Technology: Material Characteristics and Charge–Discharge Mechanisms of Iron Chloride Electrodes

ABSTRACTThis study delves into the unique characteristics of an iron chloride cathode with a solid‐state electrolyte (SSE) and the construction of a button cell battery (BT cell) for its evaluation. The iron ions in this system can provide either divalent or trivalent ions, which possess a higher electrical capacity (~200 mAh/g) and competitive advantages. The solid‐state electrolyte materials, iron compounds (chloride, oxide), exhibit high activation in electrochemistry. After the cycle test, the ferric chloride electrolyte transforms into another iron hydroxide compound due to its high activation. The study examines iron, ferric oxide (Fe2O3), and ferrous chloride (FeCl2) as cathode materials and evaluates their impact on the battery. Cyclic voltammetry compares the potential and current values of the redox reactions among the three. Finally, transmission electron microscopy (TEM) explores the ferric chloride layer and iron hydroxide in ferrous chloride. The study focuses on the high electrochemical activity of the iron chloride layer and explores the crystal structure and composition for electrochemical analysis. The findings of this study are crucial for understanding the potential of iron‐ion batteries and the role of iron compounds in improving battery performance.

Microscopic mechanism of the L12–D019 phase transformation in a Co-base single crystal superalloy

In γ′-strengthened superalloys based on the Co-Al-W system, the stability of the γ′ phase is often limited, as it is found to transform into other phases such as B2 and D019 after long-term annealing. To explore the details behind the annealing-induced transformation from the metastable L12-γ′ phase to the thermodynamically stable D019-χ phase in the single-crystalline Co-base superalloy ERBOCo-VF60 (Co79.8Al8.9W9.0Ta2.3 in at.%), scanning transmission electron microscopy and atom probe tomography are employed. Due to the structural similarity between the L12 and D019 structures, coherent plate-shaped χ precipitates are formed in the γ/γ′ microstructure parallel to {111} planes through a shear-based transformation mechanism. While the χ phase precipitates slowly during isothermal aging, its formation can be significantly accelerated locally by coating the superalloy with a Cr-rich layer, which indirectly stabilizes the χ phase as revealed by thermodynamic calculations. This procedure allowed us to obtain an intermediate (incomplete) state of χ-phase formation in terms of both crystal structure and composition. By characterizing the partial dislocations at the tip of growing χ precipitates, the microscopic details of the shear-based cubic-to-hexagonal transformation from L12 to D019 are uncovered. The compositional aspect of the transformation involves a significant diffusion-mediated enrichment of W in the χ phase, accompanied by a simultaneous W depletion in the γ′ phase, leading to its transformation to the γ phase.

An UHF band planar resonator temperature sensor constructed from high-performance titanium dioxide system microwave dielectric ceramics: Toward integrated ceramic-based sensor devices

With the rapid fusion of temperature sensing technology and microwave technology, microwave temperature sensors have become the protagonist of competing research. We propose a planar resonator temperature sensor that combines substrate material modifications with sensor structure design. To realize this concept, high-performance TiO2-xwt. % ZnO (0 ≤ x ≤ 3) microwave dielectric ceramics are prepared. The various factors influencing dielectric properties, including crystal structure, phase composition, Raman vibration, microstructure, element valence, and oxygen vacancy, are completely investigated. The TiO2-0.7 wt. % ZnO ceramic exhibiting exceptional properties (εr = 106.6, Qf = 46 000 GHz, τf = 426.0 ppm/°C) is selected for substrate fabrication. The frequency and temperature dependence of εr and tan δ are analyzed at 2–4.5 GHz from −50 to 100 °C, revealing a good linearity between εr and temperature. A CSRR temperature sensor employing this substrate material is designed, simulated, fabricated, and validated from −50 to 90 °C. This sensor generates two resonance frequencies (around 0.5 and 1.4 GHz) in the UHF band, demonstrating sensitivities of 2.2 MHz/10 °C and 6.3 MHz/10 °C at the first and second resonance frequencies, along with an outstanding normalized sensitivity of approximately 0.045. Through a comprehensive analysis of the physical mechanisms affecting the sensor's sensitivity and quality factor, the design of the sensor is strengthened from the perspective of optimizing the performance of microwave dielectric ceramics. The regulation mechanism of dielectric characteristics is enriched and clarified, thereby achieving a synergistic improvement in sensor performance. This work expands the application scope of microwave dielectric ceramics and provides an innovative approach to environmental monitoring.

Combine Improvement for Dye-Sensitized Solar Cells

Dye Sensitized-Solar Cells (DSSC) represent a third-generation solar cell technology based on photoelectrochemical principles. This study explores the use of Clitoria ternatea (butterfly pea) extract as an organic dye for DSSCs, focusing on its ability to absorb sunlight effectively. Excitation of electrons triggered by light in photocatalysis is strongly influenced by the position of the band gap. To be effective as a photocatalyst, the material must have a conduction band with a high positive potential compared to the electron accepting potential. Doping metal oxides such as CuO, MgO, Fe2O3, and ZnO into TiO2 can change the band edge properties or surface states which can increase light absorption. This research presents the synthesis of TiO2 nanoparticles as photoanodes doped using metal oxides to evaluate characteristic that can influence DSSC performance. TiO2 nanoparticles doped with metal oxide were synthesized using the solvothermal method and characterized by XRD, SEM-EDX, FTIR, and UV-Vis. Comprehensive analysis of samples doped with metal oxides significantly affects the crystal structure, morphology, elemental composition, and optical properties of the material. The results showed that Cu-doped TiO2 samples allowed for the most significant performance improvement in DSSC, followed by Fe-doped TiO2, Mg-doped TiO2, and Zn-doped TiO2, with pure TiO2 having the lowest performance potential. These results provide important insights into material optimization to improve DSSC efficiency.

Solid-State Oxide Fuel Cells

Solid-State Oxide Fuel Cell (SOFC) is an efficient energy conversion device that directly covers fuel's chemical energy into electricity. With a high energy conversion efficiency, it is not limited by the Carnot cycle. Fuel adaptability is wide, clean and pollution-free, all solid structure, do not use precious metal catalyst and other advantages. It is of great significance to achieve the goal of carbon peak and carbon neutrality target in China. However, there are some problems, mainly including: conductivity, relatively low conductivity of medium-temperature solid oxide fuel cells, which limits the performance of batteries, sintering, cost, and stability. To improve the conductivity, researchers are exploring different material combinations and doping strategies to optimize the crystal structure and chemical composition of the electrolyte. Finally, the importance of the electrolyte, the role of the oxygen vacancy, the influence of the doping elements, and the balance of the performance and the cost are drawn.

Fabrication of novel N-rich g-C3N5 decorated cubic spinel Co2SnO4 hybrids: Studies on morphology, degradation efficacy, pathway and mechanism

Managing interfacial charge transfer is a crucial and challenging problem in promoting the migration/separation of photogenerated carriers for heterojunction photocatalysts. The innovative dual Z-scheme heterojunction is crucial in effectively removing organic pollutants by enhancing the separation of charge carriers. A novel Co2SnO4/g-C3N5 (CoSn/CN) nanocomposite heterojunction is synthesized using a simple hydrothermal approach. The resulting nanocomposite is then studied in terms of its crystal phases, optical characteristics, surface morphologies, and compositions. The charge separation efficiency is significantly enhanced, resulting in a high-efficiency photocatalytic degradation performance. The CoSn/CN photocatalyst exhibits a degradation efficiency of 99.11 % and 98.08 % for Congo red (CR) and Rose Bengal (RB) respectively, within 75 minutes and 50 minutes under visible light conditions. In addition, scavenging tests demonstrated the generation of active radical species, specifically •OH, h+, and •O2−. The hypothesized CR and RB degradation process and potential pathways were derived from the proper experimental study. The primary objective of this project is to create a novel photocatalytic material that can effectively degrade dyes. Additionally, the study aims to construct a larger-scale photocatalytic system, determine the cost of the wastewater treatment unit, and analyze the life cycle of the entire process. In addition, the Co2SnO4/g-C3N5 heterojunction also demonstrates the expected stability as no substantial drop was observed after 5 cycles. The exceptional degrading performance and stability of the system can be attributed to the enhanced separation of photo-induced charge carriers and the strong contact at the interface, achieved through the formation of a Z-Scheme charge transfer.

Studies of the phase composition and ultrafine structure of the initial domestic raw materials of proppants

The results of the study of intracrystalline electric and magnetic fields in samples on 57Fe nuclei by the ultrafine method of the Mossbauer effect are considered. The source of gamma radiation was 57Co in the chromium matrix. The spectra of the samples were measured on 57Fe nuclei using the MS1104Em spectrometer in the mode of constant accelerations at room temperature for absorption. The crystal structure, phase composition, and electronic states of individual components of the proppants are given. The measurements were carried out on the d8 Advance universal complex (Bruker, Germany). The data of parameters recorded on detectors of secondary energy characteristics of X-rays corresponding to K, L, M, N and O levels of electronic transitions using computer processing of elemental compositions and their ratios in samples are analyzed. The data of X-ray studies of the composition of fly ash are presented, determining its potential application in various industries, including the production of proppants. The results of the analysis of the chemical composition of bauxite samples obtained by X-ray diffraction analysis are presented. The silicon modulus (µSi) has been determined, which is the ratio of Al2O3 to SiO2 to characterize the quality of bauxite. The main components of bauxite were Al2O3 (aluminum oxide) and SiO2 (silicon dioxide). A significant content of Fe2O3 (iron oxide) was also noted, which is 24-33 wt. % for bauxite.

Crystal field optimization, luminescence enhancement and thermal stability of novel K2NaAl0.4Ga0.6F6:Mn4+ solid solution red phosphor for high-performance warm WLED

Mn4+-doped fluoride phosphors have important application value in the background light and WLED lighting fields. Therefore, the synthesis of efficient and stable Mn4+-doped red phosphor is of great application value. In this study, a series of red-emitting K2NaAl1-yGayF6:xMn4+ (y = 0, 0.2, 0.4, 0.6, 0.8 and 1) (x = 0.01, 0.03, 0.05, 0.07 and 0.09) solid solution phosphors are successfully synthesized by simple coprecipitation method. The synthesis strategy of simple crystal structure optimization is proposed to realize simultaneously the crystal field optimization, luminescence enhancement and thermal stability of red phosphor. The calculation and theoretical analysis of crystal field strength are used to prove that solid solution matrix K2NaAl0.4Ga0.6F6 is the most ideal matrix material. X-ray powder diffraction, energy-dispersive X-ray spectrometer and scanning electron microscope are employed to determine the crystal structure, composition and morphology of all samples. Optical properties are characterized using excitation spectra, emission spectra and fluorescence lifetime curves. Moreover, the CIE coordinates of red-light show that the phosphor has low correlated color temperature and excellent color purity. Intriguingly, the as-prepared K2NaAl0.4Ga0.6F6:Mn4+ phosphor possesses admirable thermal quenching behavior and color stability at high temperature. At a temperature of 423 K, the photoluminescence intensity can be maintained at 52 % of the original intensity (298 K). The activation energy, the chromaticity shift and chromaticity coordinate variation are also systematically calculated. More importantly, A high-performance warm WLED with low correlated color temperature (CCT = 3982 K) and high color rendering index (Ra = 93.7) is achieved by using K2NaAl0.4Ga0.6F6:Mn4+ as a red-emitting material. These results demonstrate that K2NaAl0.4Ga0.6F6:Mn4+ red phosphor provides a novel choice for the warm WLED required for indoor lighting.

Regularities of Martensitic Transformations in New Medium-Entropy Single Crystals of CoNiAlFe Alloys

This paper deals with the martensitic transformation and functional properties in the quenched single crystals of the Co35Ni35Al28Fe2 medium-entropy alloy, oriented along the [001]B2-direction. The microstructure and chemical composition of the single crystals have been studied in detail using transmission and scanning electron microscopy. The {111}L10 martensite twins up to 10-20 nm width and γ/γ′-phase precipitations larger than 100 μm are detected. The thermoelastic B2-L10 martensitic transformation upon stress-free cooling/heating in single crystals of Co35Ni35Al28Fe2 alloy is characterized by the accumulation of elastic energy, which is the driving force of the reverse martensitic transformation, and the low dissipation energy. The reverse transformation starts at lower temperatures than the forward transformation Ms>As. The regularities of the stress-induced B2-L10 martensitic transformation change due to an increase in the contribution of the dissipated energy and Msσ<Asσ. There is shape memory effect with the reversible strain (3.2±0.3)% and high temperature superelasticity with the reversible strain (3.3±0.3)% in the temperature range from 323 K to ≥548 K in the [001]B2-oriented single crystals. These crystals withstand stress up to 1200 MPa in compression without destruction.

Topotaxial mutual-exchange growth of magnetic Zintl Eu3In2As4 nanowires with axion insulator classification.

Due to quasi-one-dimensional confinement, nanowires possess unique electronic properties, which can promote specific device architectures. However, nanowire growth presents paramount challenges, limiting the accessible crystal structures and elemental compositions. Here we demonstrate solid-state topotactic exchange that converts wurtzite InAs nanowires into Zintl Eu3In2As4. Molecular-beam-epitaxy-based in situ evaporation of Eu and As onto InAs nanowires results in the mutual exchange of Eu from the shell and In from the core. Therefore, a single-phase Eu3In2As4 shell grows, which gradually consumes the InAs core. The mutual exchange is supported by the substructure of the As matrix, which is similar across the wurtzite InAs and Zintl Eu3In2As4 and therefore is topotactic. The Eu3In2As4 nanowires undergo an antiferromagnetic transition at a Néel temperature of ~6.5 K. Ab initio calculations confirm the antiferromagnetic ground state and classify Eu3In2As4 as a C2T axion insulator, hosting both chiral hinge modes and unpinned Dirac surface states. The topotactic mutual-exchange nanowire growth will, thus, enable the exploration of intricate magneto-topological states in Eu3In2As4 and potentially in other exotic compounds.

ZIF-67 MOF derived in-doped Co3O4 nanoflowers for H2S gas-sensing performances

Hydrogen sulfide (H2S) is a colorless toxic acidic gas, so the development of gas sensors that can effectively detect H2S in the environment is critical to protecting human health. Metal-organic frameworks (MOFs) are emerging as promising template for semiconductor materials in gas sensor technology, offering unique structural advantages for various sensing applications. This study aimed to understand the properties of Indium-doped ZIF-67 nanoflowers by analyzing their crystal structure, surface morphology, and chemical composition. It also investigated the hydrogen sulfide (H2S) gas-sensitive properties of these materials to fully comprehend their capabilities and limitations. It is demonstrated that the Co3O4 sensor doped with 5 % In displays excellent stability, gas selectivity, and responsiveness. Specifically, the Co3O4 sensor doped with 5 % In showed a response of 19–50 ppm H2S at an operating temperature of 180 °C, which was significantly higher than that of the pure Co3O4 sensor. This is mainly due to the high content of oxygen vacancy (11.26 %). In the 5 % In doped sample, and the relatively large specific surface area (60.58 m2g-1).

The interactions of protein-calcium oxalate in crystallization process

Understanding the pathogenic crystallization of calcium oxalate (CaOx), a major constituent of kidney stones, is crucial in developing effective treatment strategies. In this work, the interactions between lysozyme and CaOx during crystallization have been investigated. Further investigations into the crystal morphology, size, quantity, and nucleation time of the lysozyme have been designed. The results reveal that CaCl2 could act as an effective precipitant for lysozyme crystallization. The formation process and structure of the distinctive composite CaOx-lysozyme crystal has been investigated. The addition of lysozyme promoted the formation of individual CaOx crystals by preventing the crystal aggregation in the solution. The presence of lysozyme induced a transformation in the CaOx crystals from calcium oxalate monohydrate to calcium oxalate dihydrate. These findings contribute to a better understanding of protein-CaOx interactions and their implications in kidney stone pathogenesis.

Microscopic instabilities in single crystal matrix composites

A finite strain micromechanical analysis is presented for the prediction of the loss of microscopic stability of a class of metal matrix composites that are subjected to axial compressive loading and undergoing large deformations. The metallic constituent behavior is modeled by the single crystal anisotropic plasticity theory in which, due to the resolved shear stresses, plastic deformations occur along certain pre-defined slip planes. Thus, this incremental plasticity theory is capable of providing the effect of the applied axial loading on the induced shear stresses which dominate the microbuckling. The composites are assumed to possess slight imperfections at the interfaces, and in order to satisfy the interfacial conditions, a perturbation expansion is employed which yields zero and first order micromechanical analysis problems. The zero order problem corresponds to the micromechanical modeling of the composite with no imperfections, whereas the solution of the first order problem is utilized to obtain the critical stresses and deformations at which bifurcation buckling occurs. Both problems are solved by employing the finite strain high-fidelity generalized method of cells (HFGMC) micromechanics. Applications are given for various types of single crystal matrix composites including layered, particulate, continuous and short fiber composites. Finally, a comparison between the compressive strengths of a standard metal matrix boron/aluminum and SiC/single crystal composites is presented and discussed.

Constructing Multifunctional Composite Single Crystals via Polymer Gel Incorporation.

The non-uniformity of a single crystal can sometimes be found in biominerals, where surrounding biomacromolecules are incorporated into the growing crystals. This unique composite structure, combining heterogeneity and long-range ordering, enables the functionalization of single crystals. Polymer gel media are often used to prepare composite single crystals, in which the growing crystals incorporate gel networks and form a bi-continuous interpenetrating structure without any disruption to single crystallinity. Moreover, dyes and many kinds of nanoparticles can be occluded into single crystals under the guidance of gel incorporation. On this basis, the bio-inspired method has been applied in crystal morphology control, crystal dyeing, mechanical reinforcement, and organic bulk heterojunction-based optoelectronics. In this paper, the composite structure, the incorporation mechanisms, and the multiple functions of gel-incorporated single crystals are reviewed.

Composite organic ionic plastic crystal membranes: The effect of ether-functionalized cations on light-gas separation performance

In light of increasing concerns about climate change, there is a growing need for innovative solutions to address CO2 emissions. Addressing this urgency, this work presents a unique approach to CO2 separation utilizing composite membranes of organic ionic plastic crystals (OIPCs) with ether-functionalized cations and poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP). Here we report the gas separation performance of OIPC-based membranes of 3,3-dimethyloxazolidinium [C1moxa]+, 4-ethyl-4-methylmorpholinium [C2mmor]+ and 4-isopropyl-4-methylmorpholinium [Ci3mmor]+ cations paired with the bis(fluorosulfonyl)imide [FSI]- anion. These composites demonstrated very good gas separation properties, especially [C1moxa][FSI] which produced a permeability of 63 barrer for CO2 and an overall selectivity (CO2/N2) of 205, which is the highest amongst all the OIPCs reported so far. Additionally, a large change in separation performance was observed for the [Ci3mmor][FSI] membrane upon heating above the solid-solid phase transition (II - I) at 48 °C; the CO2 permeability increased from 7 to 163 barrer and an approximately 3-fold increase in selectivity was observed. These findings advance the design of composite membranes based on OIPCs towards increased selectivity and sustained effectiveness in the separation of light gases.