Abstract:In this study, an ionic liquid (IL), 1-butyl-3-methylimidazolium acetate, was used to prepare ionogels with microcrystalline cellulose (MCC) and halloysite (Hal). SEM, XRD, TG, DSC, FTIR spectroscopy, conductometry and mechanical tests were used to study the morphology, structure, thermal behaviour and electrophysical and mechanical characteristics of synthesised ionogels. XRD analysis showed a slight decrease in the interlayer space of halloysite in ionogels containing MCC, which may have been associated with… Show more
“…For example, the T g value became almost 12 • C higher compared to the ionic liquid. A similar conclusion concerning the influence of the clay mineral was made by us earlier for the BMImAc/Halloysite ionogels [26] as well as for the BMImNTf 2 /Bent and BMImNTf 2 /Na-MMT ionogels [36]. The presented data indicate the confinement in the IL/clay systems.…”
Section: Phase Transitions In the Bmimac/na-bent/mcc Ionogelssupporting
confidence: 90%
“…The presented data indicate that the interaction with bentonite nanoparticles hinders the decomposition of the IL molecules. It should be noted that earlier [26], when studying the thermal behavior of the BMI-mAc/Halloysite composites, we made the opposite conclusion. Namely, we reported that BMImAc confined in the halloysite nanotubes decomposed easier than bulk IL.…”
Section: Thermal Decomposition Of Starting Materials and Ionogels Bmi...contrasting
confidence: 53%
“…The electrical conductivity of both triple IL/Na-Bent/MCC and binary IL/MCC ionogels was non-monotonous. The present paper is a continuation of our studies of triple ionogels with halloysite as a clay filler [26]. Therefore, the information on the properties of triple ionogels (but with bentonite as a clay filler) obtained in the current study is new and can be used in describing the effect of the clay filler nature in such systems.…”
Section: Preparation Of the Bmimac/na-bent/mcc Composite Materialsmentioning
For the synthesis of ionogels containing microcrystalline cellulose (MCC) and Na-bentonite (Na-Bent), ionic liquid (IL) 1-butyl-3-methylimidazolium acetate was used as an MCC solvent. Characterization and research of the physicochemical properties of the synthesized materials were carried out using methods such as SEM, WAXS, thermal analysis, FTIR, conductometry, and viscometry. WAXS analysis showed an increase in the interlayer distance of Na-bentonite in composites due to the intercalation of IL molecules. Based on the data on the characteristic temperatures of thermal degradation, enhanced thermal stability of triple IL/Na-Bent/MCC ionogels was revealed compared to that for cellulose-free systems. It was found that the electrical conductivity of both triple IL/Na-Bent/MCC and binary IL/MCC ionogels was non-monotonous. The data obtained can be used in the formation of multifunctional coatings with enhanced thermal stability.
“…For example, the T g value became almost 12 • C higher compared to the ionic liquid. A similar conclusion concerning the influence of the clay mineral was made by us earlier for the BMImAc/Halloysite ionogels [26] as well as for the BMImNTf 2 /Bent and BMImNTf 2 /Na-MMT ionogels [36]. The presented data indicate the confinement in the IL/clay systems.…”
Section: Phase Transitions In the Bmimac/na-bent/mcc Ionogelssupporting
confidence: 90%
“…The presented data indicate that the interaction with bentonite nanoparticles hinders the decomposition of the IL molecules. It should be noted that earlier [26], when studying the thermal behavior of the BMI-mAc/Halloysite composites, we made the opposite conclusion. Namely, we reported that BMImAc confined in the halloysite nanotubes decomposed easier than bulk IL.…”
Section: Thermal Decomposition Of Starting Materials and Ionogels Bmi...contrasting
confidence: 53%
“…The electrical conductivity of both triple IL/Na-Bent/MCC and binary IL/MCC ionogels was non-monotonous. The present paper is a continuation of our studies of triple ionogels with halloysite as a clay filler [26]. Therefore, the information on the properties of triple ionogels (but with bentonite as a clay filler) obtained in the current study is new and can be used in describing the effect of the clay filler nature in such systems.…”
Section: Preparation Of the Bmimac/na-bent/mcc Composite Materialsmentioning
For the synthesis of ionogels containing microcrystalline cellulose (MCC) and Na-bentonite (Na-Bent), ionic liquid (IL) 1-butyl-3-methylimidazolium acetate was used as an MCC solvent. Characterization and research of the physicochemical properties of the synthesized materials were carried out using methods such as SEM, WAXS, thermal analysis, FTIR, conductometry, and viscometry. WAXS analysis showed an increase in the interlayer distance of Na-bentonite in composites due to the intercalation of IL molecules. Based on the data on the characteristic temperatures of thermal degradation, enhanced thermal stability of triple IL/Na-Bent/MCC ionogels was revealed compared to that for cellulose-free systems. It was found that the electrical conductivity of both triple IL/Na-Bent/MCC and binary IL/MCC ionogels was non-monotonous. The data obtained can be used in the formation of multifunctional coatings with enhanced thermal stability.
“…Furthermore, when exfoliated, their structured aluminosilicate layers provide high gravimetric surface area that results in robust nanocomposite mechanical properties . The most common clays utilized are montmorillonite, vermiculite, and halloysite for nanofillers or matrices in polymer, − polymer gel, − and ionogel − electrolytes. In these cases, the nanoclay provides mechanical support, increasing the electrolyte mechanical modulus and decreasing polymer crystallinity that enhances ionic conductivity. , Despite the breadth of demonstrated clay nanocomposite electrolytes, the most naturally abundant clay variety, kaolinite, has rarely been utilized. , The 1:1 structure of silica and alumina layers within bulk kaolinite results in strong hydrogen bonding between the layers making exfoliation difficult relative to other clay varieties. , Although kaolinite nanocomposites produced through chemical intercalation have been demonstrated, this process is time-intensive and limited to a small subset of molecules, restricting potential applications. , Only one reported system to date has shown direct liquid-phase exfoliation of kaolinite, albeit with the assistance of a large fraction of graphene oxide (GO) dispersing agent (i.e., 5:1 GO/kaolinite) and no reported yield for the process. , Therefore, a need remains for a highly scalable kaolinite exfoliation process that will enable broader use of kaolinite in SSEs and related clay nanocomposite applications.…”
Lithium-ion batteries are the leading energy storage technology for portable electronics and vehicle electrification. However, demands for enhanced energy density, safety, and scalability necessitate solid-state alternatives to traditional liquid electrolytes. Moreover, the rapidly increasing utilization of lithium-ion batteries further requires that next-generation electrolytes are derived from earth-abundant raw materials in order to minimize supply chain and environmental concerns. Toward these ends, clay-based nanocomposite electrolytes hold significant promise since they utilize earth-abundant materials that possess superlative mechanical, thermal, and electrochemical stability, which suggests their compatibility with energy-dense lithium metal anodes. Despite these advantages, nanocomposite electrolytes rarely employ kaolinite, the most abundant variety of clay, due to strong interlayer interactions that have historically precluded efficient exfoliation of kaolinite. Overcoming this limitation, here we demonstrate a scalable liquid-phase exfoliation process that produces kaolinite nanoplatelets (KNPs) with high gravimetric surface area, thus enabling the formation of mechanically robust nanocomposites. In particular, KNPs are combined with a succinonitrile (SN) liquid electrolyte to form a nanocomposite gel electrolyte with high room-temperature ionic conductivity (1 mS cm −1 ), stiff storage modulus (>10 MPa), wide electrochemical stability window (4.5 V vs Li/Li + ), and excellent thermal stability (>100 °C). The resulting KNP-SN nanocomposite gel electrolyte is shown to be suitable for high-rate rechargeable lithium metal batteries that employ high-voltage LiNi 0.8 Co 0.15 Al 0.05 O 2 (NCA) cathodes. While the primary focus here is on solid-state batteries, our strategy for kaolinite liquid-phase exfoliation can serve as a scalable manufacturing platform for a wide variety of other kaolinite-based nanocomposite applications.
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