Ionic Liquid-Containing Pickering Emulsions Stabilized by Graphene Oxide-Based Surfactants.

Emulsions stabilized by particles (i.e., Pickering emulsions) are complementary to those stabilized by small molecules or polymers and most commonly consist of oil droplets dispersed in a continuous water phase, with particles assembled at the fluid-fluid interface. New particle surfactants and different fluid-fluid interfaces are critical for developing next-generation systems for a number of advanced applications. Herein we report the preparation of IL-containing emulsions stabilized by graphene oxide (GO)-based nanoparticles using the IL [Bmim][PF6]: GO nanosheets stabilize IL-in-water emulsions, and alkylated GO nanosheets (C18-GO) stabilize IL-in-oil emulsions. The impact of particle concentration, fluid-fluid ratio, and addition of acid or base on emulsion formation and stability is studied, with distinct effects for the water and oil systems observed. We then illustrate the broad applicability of GO-based particle surfactants by preparing emulsions with different ILs and preparing inverted emulsions (water-in-IL and oil-in-IL emulsions). The latter systems were accessed by tuning the polarity of GO nanosheets by functionalization with a perfluorinated alkyl chain such that they were dispersible in IL. This work provides insight into the preparation of different IL-containing emulsions and lays a foundation for the architecture of dissimilar materials into composite systems.

Disparate Regions of the Human Chemokine CXCL10 Exhibit Broad-Spectrum Antimicrobial Activity against Biodefense and Antibiotic-Resistant Bacterial Pathogens.

CXCL10 is a pro-inflammatory chemokine produced by the host in response to microbial infection. In addition to canonical, receptor-dependent actions affecting immune-cell migration and activation, CXCL10 has also been found to directly kill a broad range of pathogenic bacteria. Prior investigations suggest that the bactericidal effects of CXCL10 occur through two distinct pathways that compromise the cell envelope. These observations raise the intriguing notion that CXCL10 features a separable pair of antimicrobial domains. Herein, we affirm this possibility through peptide-based mapping and structure/function analyses, which demonstrate that discrete peptides derived from the N- and C-terminal regions of CXCL10 mediate bacterial killing. The N-terminal derivative, peptide P1, exhibited marked antimicrobial activity against Bacillus anthracis vegetative bacilli and spores, as well as antibiotic-resistant clinical isolates of Klebsiella pneumoniae, Acinetobacter baumannii, Enterococcus faecium, and Staphylococcus aureus, among others. At bactericidal concentrations, peptide P1 had a minimal degree of chemotactic activity, but did not cause red blood cell hemolysis or cytotoxic effects against primary human cells. The C-terminal derivative, peptide P9, exhibited antimicrobial effects, but only against Gram-negative bacteria in low-salt medium─conditions under which the peptide can adopt an α-helical conformation. The introduction of a hydrocarbon staple induced and stabilized α-helicity; accordingly, stapled peptide P9 displayed significantly improved bactericidal effects against both Gram-positive and Gram-negative bacteria in media containing physiologic levels of salt. Together, our findings identify and characterize the antimicrobial regions of CXCL10 and functionalize these novel determinants as discrete peptides with potential therapeutic utility against difficult-to-treat pathogens.

Molecular engineering of antimicrobial peptide (AMP)-polymer conjugates.

As antimicrobial resistance becomes an increasing threat, bringing significant economic and health burdens, innovative antimicrobial treatments are urgently needed. While antimicrobial peptides (AMPs) are promising therapeutics, exhibiting high activity against resistant bacterial strains, limited stability and toxicity to mammalian cells has hindered clinical development. Attaching AMPs to polymers provides opportunities to present AMPs in a way that maximizes bacterial killing while enhancing compatibility with mammalian cells, stability, and solubility. Conjugation of an AMP to a linear hydrophilic polymer yields the desired improvements in stability, mammalian cell compatibility, and solubility, yet often markedly reduces bactericidal effects. Non-linear polymer architectures and supramolecular assemblies that accommodate multiple AMPs per polymer chain afford AMP-polymer conjugates that strike a superior balance of antimicrobial activity, mammalian cell compatibility, stability, and solubility. Therefore, we review the design criteria, building blocks, and synthetic strategies for engineering AMP-polymer conjugates, emphasizing the connection between molecular architecture and antimicrobial performance to inspire and enable further innovation to advance this emerging class of biomaterials.

Encapsulation of Ionic Liquids for Tailored Applications.

This spotlight article highlights the favorable impact encapsulation of ionic liquids (ILs) has on multiple advanced applications. ILs are molten salts with many attractive properties such as negligible vapor pressure, good thermal stability, and high ionic conductivity; however, their widespread implementation in advanced applications is hampered by their relatively high viscosity, which makes them difficult to handle and results in slow mass transfer rates. The ability to encapsulate IL in a shell holds potential to impact many applications, including separations, gas sequestration, and energy storage and management, given that the capsule structure provides high surface area compared to that of bulk IL and also allows handling of the IL as a solid. Herein, we discuss encapsulation of ILs using different approaches and highlight the contributions from our lab in both capsule preparation and application. Specifically, we have developed the ability to use 2D carbon nanoparticle surfactants and interfacial polymerization to prepare capsules of IL using both IL-in-water and IL-in-oil Pickering emulsions as templates. This facile, one-step method to encapsulate ILs gives structures with beneficial performance in supercapacitors, separations, and CO2 sequestration, as discussed herein. We conclude this spotlight with an outlook on how to improve upon these systems for next-generation applications.

Hybrid Ionic Liquid Capsules for Rapid CO2 Capture.

The CO2 absorption by ionic liquids (ILs) were enhanced by the use of hybrid capsules composed of a core of IL and shell of polyurea and alkylated graphene oxide (GO). These composite structures were synthesized using a Pickering emulsion as a template and capsules of two different ILs were prepared. The contribution of the encapsulated IL on the CO2 absorption of the capsules is consistent with agitated neat IL, but with improved kinetics of absorption across different pressures. This novel materials design allows for CO2 to be absorbed significantly faster compared to bulk IL and provides insight into improved carbon capture technologies.

Pickering Emulsion-Templated Encapsulation of Ionic Liquids for Contaminant Removal.

Ionic liquids (ILs) have received attention for a diverse range of applications, but their liquid nature can make them difficult to handle and process and their high viscosities can lead to suboptimal performance. As such, encapsulated ILs are attractive for their ease of handling and high surface area and have potential for improved performance in energy storage, gas uptake, extractions, and so forth. Herein, we report a facile method to encapsulate a variety of ILs using Pickering emulsions as templates, graphene oxide (GO)-based nanosheets as particle surfactants, and interfacial polymerization for stabilization. The capsules contain up to 80% IL in the core, and the capsule shells are composed of polyurea and GO. We illustrate that capsules can be prepared from IL-in-water or IL-in-oil emulsions and explore the impact of monomer and IL identity, thereby accessing different compositions. The spherical, discrete capsules are characterized by optical microscopy, scanning electron microscopy, infrared spectroscopy, Raman spectroscopy, thermogravimetric analysis, and 1H NMR spectroscopy. We illustrate the application of these IL capsules as a column material to remove phenol from oil, demonstrating ≥98% phenol removal after passage of >170 column volumes. This simple method to prepare capsules of IL will find widespread use across diverse applications.

Carbon Capsules of Ionic Liquid for Enhanced Performance of Electrochemical Double-Layer Capacitors.

Ion accessibility, large surface area, and complete wetting of a carbonaceous electrode by the electrolyte are crucial for high-performance electrochemical double-layer capacitors. Herein, we report a facile and scalable method to prepare electrode-electrolyte hybrid materials, where an ionic liquid (IL) electrolyte is encapsulated within a shell of reduced graphene oxide (rGO) nanosheets as the active electrode material (called rGO-IL capsules). These structures were templated using a Pickering emulsion consisting of a dispersed phase of 1-methyl-3-butylimidazolium hexafluorophosphate ([bmim][PF6]) and a continuous water phase; graphene oxide nanosheets were used as the surfactant, and interfacial polymerization yielded polyurea that bound the nanosheets together to form the capsule shell. This method prevents the aggregation and restacking of GO nanosheets and allows wetting of the materials by IL. The chemical composition, thermal properties, morphology, and electrochemical behavior of these new hybrid architectures are fully characterized. Specific capacitances of 80 F g-1 at 18 °C and 127 F g-1 at 60 °C were achieved at a scan rate of 10 mV s-1 for symmetric coin cells of rGO-IL capsules. These architected materials have higher capacitance at low temperature (18 °C) across many scan rates (10-500 mV s-1) compared with analogous cells with the porous carbon YP-50. These results demonstrate a distinct and important methodology to enhance the performance of electrochemical double-layer capacitors by incorporating electrolyte and carbon material together during synthesis.

2D Particles at Fluid-Fluid Interfaces: Assembly and Templating of Hybrid Structures for Advanced Applications.

Fluid-fluid interfaces have widespread applications in personal care products, the food industry, oil recovery, mineral processes, etc. and are also important and versatile platforms for generating advanced materials. In Pickering emulsions, particles stabilize the fluid-fluid interface, and their presence reduces the interfacial energy between the two fluids. To date, most Pickering emulsions stabilized by 2D particles make use of clay platelets or GO nanosheets. These systems have been used to template higher order hybrid, functional materials, most commonly, armored polymer particles, capsules, and Janus nanosheets. This review discusses the experimental and computational study of the assembly of sheet-like 2D particles at fluid-fluid interfaces, with an emphasis on the impact of chemical composition, and the use of these assemblies to prepare composite structures of dissimilar materials. The review culminates in a perspective on the future of Pickering emulsions using 2D particle surfactants, including new chemical modification and types of particles as well as the realization of properties and applications not possible with currently accessible systems, such as lubricants, porous structures, delivery, coatings, etc.

Distinct Chemical and Physical Properties of Janus Nanosheets.

Janus particles have recently garnered significant attention for their distinct properties compared to particles that are homogeneously functionalized. Moreover, high aspect ratio Janus particles that are rod-like or planar (i.e., nanosheets) are especially intriguing considering their interfacial properties as well as their ability to assemble into higher order and hybrid structures. To date, major challenges facing the exploration and utilization of 2D Janus particles are scalability of synthesis, characterization of tailored chemical functionalization, and ability to introduce a diverse set of functionalities. Herein, a facile method to access Janus 2D graphene oxide (GO) nanosheets by combining a Pickering-type emulsion and grafting-from polymerization via ATRP is reported. Janus GO nanosheets bearing PMMA on one face as well as the symmetrically functionalized analogue are prepared, and the chemical, thermal, structural, surface, and interfacial properties of these materials are characterized. Time-of-flight secondary ion mass spectrometry coupled with Langmuir-Blodgett films is shown to be an ideal route to conclusively establish asymmetric functionalization of 2D materials. This work not only provides a facile route for the preparation of Janus nanosheets but also demonstrates the direct visualization of polymer grown from the surface of GO.