Carson T. Riche

Two-phase microfluidic droplet flows of ionic liquids for the synthesis of gold and silver nanoparticles.

Droplet-based microfluidic platforms have the potential to provide superior control over mixing as compared to traditional batch reactions. Ionic liquids have advantageous properties for metal nanoparticle synthesis as a result of their low interfacial tension and complexing ability; however, droplet formation of ionic liquids within microfluidic channels in a two-phase system has not yet been attained because of their complex interfacial properties and high viscosities. Here, breakup of an imidazolium-based ionic liquid into droplets in a simple two-phase system has for the first time been achieved and characterized by using a microchannel modified with a thin film fluoropolymer. This microfluidic/ionic liquid droplet system was used to produce small, spherical gold (4.28 ± 0.84 nm) and silver (3.73 ± 0.77 nm) nanoparticles.

Flow invariant droplet formation for stable parallel microreactors.

The translation of batch chemistries onto continuous flow platforms requires addressing the issues of consistent fluidic behaviour, channel fouling and high-throughput processing. Droplet microfluidic technologies reduce channel fouling and provide an improved level of control over heat and mass transfer to control reaction kinetics. However, in conventional geometries, the droplet size is sensitive to changes in flow rates. Here we report a three-dimensional droplet generating device that exhibits flow invariant behaviour and is robust to fluctuations in flow rate. In addition, the droplet generator is capable of producing droplet volumes spanning four orders of magnitude. We apply this device in a parallel network to synthesize platinum nanoparticles using an ionic liquid solvent, demonstrate reproducible synthesis after recycling the ionic liquid, and double the reaction yield compared with an analogous batch synthesis.

Effect of Ionic Liquid Impurities on the Synthesis of Silver Nanoparticles

Imidazolium-based ionic liquids have been widely utilized as versatile solvents for metal nanoparticle synthesis; however, reactions to synthesize silver nanoparticles that are performed identically in different commercially obtained lots of 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM-BF(4)) give divergent results. This suggests that impurities in these nominally identical solvents play an important role in the resulting silver nanoparticle quality. To test the effect that impurities have on the quality of silver nanoparticles synthesized in BMIM-BF(4), silver nanoparticles were synthesized in carefully prepared and purified BMIM-BF(4) and compared against silver nanoparticles that were synthesized in the purified BMIM-BF(4) that had been spiked with trace amounts of water, chloride, and 1-methylimidazole. It was clearly demonstrated that trace amounts of these common ionic liquid impurities cause significant deviation in size and shape (creating polydisperse and irregularly shaped ensembles of both large and small particles), and also negatively impact the stabilization of the resulting silver nanoparticles.

The dynamics of giant unilamellar vesicle oxidation probed by morphological transitions.

We have studied the dynamics of Lissamine Rhodamine B dye sensitization-induced oxidation of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) giant unilamellar vesicles (GUVs), where the progression of the underlying chemical processes was followed via vesicle membrane area changes. The surface-area-to-volume ratio of our spherical GUVs increased after as little as ten seconds of irradiation. The membrane area expansion was coupled with high amplitude fluctuations not typical of GUVs in isoosmotic conditions. To accurately measure the area of deformed and fluctuating membranes, we utilized a dual-beam optical trap (DBOT) to stretch GUV membranes into a geometrically regular shape. Further oxidation led to vesicle contraction, and the GUVs became tense, with micron-scale pores forming in the bilayer. We analyzed the GUV morphological behaviors as two consecutive rate-limiting steps. We also considered the effects of altering DOPC and 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(lissamine rhodamine B sulfonyl) (RhDPPE) concentrations. The resulting kinetic model allows us to measure how lipid molecular area changes during oxidation, as well as to determine the rate constants controlling how quickly oxidation products are formed. Controlled membrane oxidation leading to permeabilization is also a potential tool for drug delivery based on engineered photosensitizer-containing lipid vesicles.

Chalcogenol Ligand Toolbox for CdSe Nanocrystals and Their Influence on Exciton Relaxation Pathways

We have employed a simple modular approach to install small chalcogenol ligands on the surface of CdSe nanocrystals. This versatile modification strategy provides access to thiol, selenol, and tellurol ligand sets via the in situ reduction of R2E2 (R=tBu, Bn, Ph; E=S, Se, Te) by diphenylphosphine (Ph2PH). The ligand exchange chemistry was analyzed by solution NMR spectroscopy, which reveals that reduction of the R2E2 precursors by Ph2PH directly yields active chalcogenol ligands that subsequently bind to the surface of the CdSe nanocrystals. Thermogravimetric analysis, FT-IR spectroscopy, and energy dispersive X-ray spectroscopy provide further evidence for chalcogenol addition to the CdSe surface with a concomitant reduction in overall organic content from the displacement of native ligands. Time-resolved and low temperature photoluminescence measurements showed that all of the phenylchalcogenol ligands rapidly quench the photoluminescence by hole localization onto the ligand. Selenol and tellurol ligands exhibit a larger driving force for hole transfer than thiol ligands and therefore quench the photoluminescence more efficiently. The hole transfer process could lead to engineering long-lived, partially separated excited states.

Responsive polymer welds via solution casting for stabilized self-assembly.

We present a simple solution casting technique to apply polymer welds to stabilize capillary-force directed self-assembled systems including arrays of pillars and microbeads. The strength of the polymer welds can be enhanced by increasing either the polymer concentration or molecular weight. The use of responsive polymers to form the welds allow for the fabrication of hierarchical structures that actuate in response to external stimuli. For example, temperature-responsive and pH-responsive microstructures can be formed by solution casting poly(vinyl methyl ether) and poly(methacrylic acid), respectively. We demonstrate that polymer welds formed using biocompatible alginate allows for controllable release of microbeads in microfluidic channels, which has potential applications in drug delivery.

G Protein-Coupled Receptors Incorporated into Rehydrated Diblock Copolymer Vesicles Retain Functionality

G protein-coupled receptor (GPCR) is incorporated into polymeric vesicles made up of diblock copolymer bilayers. Successfully incorporated GPCRs exhibit correct biased physiological orientation and respond to various ligands. After extended dehydrated storage via lyophilization and subsequent rehydration, diblock copolymer polymersomes retain their shape and incorporated GPCR retains its function.

Scale-up modeling for manufacturing nanoparticles using microfluidic T-junction

ABSTRACT Nanoparticles have great potential to revolutionize industry and improve our lives in various fields such as energy, security, medicine, food, and environmental science. Droplet-based microfluidic reactors serve as an important tool to facilitate monodisperse nanoparticles with a high yield. Depending on process settings, droplet formation in a typical microfluidic T-junction is explained by different mechanisms, squeezing, dripping, or squeezing-to-dripping. Therefore, the manufacturing process can potentially operate under multiple physical domains due to uncertainties. Although mechanistic models have been developed for individual domains, a modeling approach for the scale-up manufacturing of droplet formation across multiple domains does not exist. Establishing an integrated and scalable droplet formation model, which is vital for scaling up microfluidic reactors for large-scale production, faces two critical challenges: the high dimensionality of the modeling space; and ambiguity among the boundaries of physical domains. This work establishes a novel and generic formulation for the scale-up of multiple-domain manufacturing processes and provides a scalable modeling approach for the quality control of products, which enables and supports the scale-up of manufacturing processes that can potentially operate under multiple physical domains due to uncertainties.