Functional Polymer Zwitterions as Reactive Surfactants for Nanoparticle Capture
Not provided.
Materials Science↗
Engineering topics
Emrick, Todd
Publications and source records attributed to Emrick, Todd.
Polymer Zwitterions for Stabilization of CsPbBr 3 Perovskite Nanoparticles and Nanocomposite Films
Abstract Functional polymers with sulfobetaine or phosphorylcholine zwitterions as pendent groups are demonstrated as both ligands and host matrices for CsPbBr 3 perovskite nanoparticles (PNPs). These polymers produce nanocomposite films with excellent NP dispersion, optical transparency, and impressive resistance to NP degradation upon exposure to water. Multidentate interactions of the zwitterion‐containing copolymers with the PNPs induce dispersed or weakly aggregated nanocomposite morphologies, depending on the extent of zwitterionic functionality in the polymer. Incorporating additional functionality into the polymers, such as benzophenone pendent groups, yields lithographically patternable films, while time‐resolved photoluminescence measurements provide insight into the electronic impact of PNPs in zwitterionic polymer matrices.
Kim, Hyunki↗
Polymer Zwitterions for Stabilization of CsPbBr 3 Perovskite Nanoparticles and Nanocomposite Films
Functional polymers with sulfobetaine or phosphorylcholine zwitterions as pendent groups are demonstrated as both ligands and host matrices for CsPbBr 3 perovskite nanoparticles (PNPs). These polymers produce nanocomposite films with excellent NP dispersion, optical transparency, and impressive resistance to NP degradation upon exposure to water. Multidentate interactions of the zwitterion-containing copolymers with the PNPs induce dispersed or weakly aggregated nanocomposite morphologies, depending on the extent of zwitterionic functionality in the polymer. Incorporating additional functionality into the polymers, such as benzophenone pendent groups, yields lithographically patternable films, while time-resolved photoluminescence measurements provide insight into the electronic impact of PNPs in zwitterionic polymer matrices.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Tailoring Biomimetic Phosphorylcholine-Containing Block Copolymers as Membrane-Targeting Cellular Rescue Agents
Some synthetic polymers can block cell death when applied following an injury that would otherwise kill the cell. This cellular rescue occurs through interactions of the polymers with cell membranes. However, general principles for designing synthetic polymers to ensure strong, but nondisruptive, cell membrane targeting are not fully elucidated. Here, we tailored biomimetic phosphorylcholine-containing block copolymers to interact with cell membranes and determined their efficacy in blocking neuronal death following oxygen-glucose deprivation. By adjusting the hydrophilicity and membrane affinity of poly(2-methacryloyloxyethyl phosphorylcholine) (polyMPC)-based triblock copolymers, the surface active regime in which the copolymers function effectively as membrane-targeting cellular rescue agents was determined. We identified nonintrusive interactions between the polymer and the cell membrane that alter the collective dynamics of the membrane by inducing rigidification without disrupting lipid packing or membrane thickness. Furthermore, our results open new avenues for biological applications of polyMPC-based polymers and provide an approach to designing membrane-targeting agents to block cell death after injury.
59 BASIC BIOLOGICAL SCIENCES↗
Functional polymers for growth and stabilization of CsPbBr 3 perovskite nanoparticles
We introduce an approach to synthesize polymer-stabilized CsPbBr 3 perovskite nanoparticles (NPs) using ammonium bromide-functionalized polymers as both bromide precursors and stabilizing ligands. The polymer-passivated NPs exhibit significant advantages over conventional perovskite NPs owing to their facile dispersion in polymer matrices and enhanced optoelectronic stability.
36 MATERIALS SCIENCE↗
Simultaneous “Clean-and-Repair” of Surfaces Using Smart Droplets
An autonomous self-healing system, inspired by transportation processes inherent to biology, is described for materials transportation and repair. The selected model system combines inorganic nanoparticles (NPs) on damaged substrates with functional emulsion droplets that pick up the particles from pristine portions of the substrate and deposit them into damaged regions. The droplets are stabilized by polymer surfactants containing phosphorylcholine groups, a polymer composition selected to impart surfactant properties for droplet stabilization as well as fouling resistance to prevent irreversible droplet adsorption on the substrates. Both the NP pickup (cleaning) and drop off (repair) steps are conducted in a system driven by an imposed flow and characterized by fluorescence microscopy. To evaluate and optimize the efficiency of this NP transportation process, the effect of both the chemical composition of the polymer surfactant and the NP surface chemistry is investigated in this work. Interfacial interactions proved enabling for these NP transportation processes, specifically those involving NP/droplet, NP/substrate, and droplet/substrate interactions. Ultimately, droplets capable of both picking up and dropping off NPs are realized by adjusting fluid/fluid and fluid/substrate interactions, with electrostatic interactions between NPs and droplets proving most effective.
36 MATERIALS SCIENCE↗
Hydrophilic conjugated polymers, and methods of preparation and use thereof
The invention provides novel hydrophilic conjugated polymers, e.g., hydrophilic poly(arylene vinylenes) or PAVs, and preparation thereof, and methods and devices for their application in photovoltaics, and the resulting improved solar cells.
36 MATERIALS SCIENCE↗
Functional interlayers of fullerene derivatives and applications in organic solar cells
The invention provides novel materials, methods and designs to enable improved power conversion efficiencies of organic photovoltaics (OPVs). In particular, the invention provides novel materials and interlayers for polymer-based solar cells. Novel functional fullerene-based interlayers are disclosed that enable high efficiency devices in conjunction with numerous active layer and electrode materials.
14 SOLAR ENERGY↗
Conjugated polymer zwitterions and solar cells comprising conjugated polymer zwitterions
A conjugated polymer zwitterion includes repeating units having structure (I), (II), or a combination thereof ##STR00001## wherein Ar is independently at each occurrence a divalent substituted or unsubstituted C 3-30 arylene or heteroarylene group; L is independently at each occurrence a divalent C 1-16 alkylene group, C 6-30 arylene or heteroarylene group, or alkylene oxide group; and R 1 is independently at each occurrence a zwitterion. A polymer solar cell including the conjugated polymer zwitterion is also disclosed.
14 SOLAR ENERGY↗
Scientists Print All-Liquid 3-D Structures
Berkeley Lab scientists have developed a way to print 3-D structures composed entirely of liquids. Using a modified 3-D printer, they injected threads of water into silicone oil — sculpting tubes made of one liquid within another liquid. They envision their all-liquid material could be used to construct liquid electronics that power flexible, stretchable devices. The scientists also foresee chemically tuning the tubes and flowing molecules through them, leading to new ways to separate molecules or precisely deliver nanoscale building blocks to under-construction compounds.
3-D LIQUID STRUCTURES↗
Reconfigurable Printed Liquids
Abstract Liquids lack the spatial order required for advanced functionality. Interfacial assemblies of colloids, however, can be used to shape liquids into complex, 3D objects, simultaneously forming 2D layers with novel magnetic, plasmonic, or structural properties. Fully exploiting all‐liquid systems that are structured by their interfaces would create a new class of biomimetic, reconfigurable, and responsive materials. Here, printed constructs of water in oil are presented. Both form and function are given to the system by the assembly and jamming of nanoparticle surfactants, formed from the interfacial interaction of nanoparticles and amphiphilic polymers that bear complementary functional groups. These yield dissipative constructs that exhibit a compartmentalized response to chemical cues. Potential applications include biphasic reaction vessels, liquid electronics, novel media for the encapsulation of cells and active matter, and dynamic constructs that both alter, and are altered by, their external environment.
Forth, Joe↗
Chemical and Morphological Control of Interfacial Self-Doping for Efficient Organic Electronics
Solution-based processing of materials for electrical doping of organic semiconductor interfaces is attractive for boosting the efficiency of organic electronic devices with multilayer structures. In order to simplify this process, self-doping perylene diimide (PDI)-based ionene polymers are synthesized, in which the semiconductor PDI components are embedded together with electrolyte dopants in the polymer backbone. Functionality contained within the PDI monomers suppresses their aggregation, affording self-doping interlayers with controllable thickness when processed from solution into organic photovoltaic devices (OPVs). Optimal results for interfacial self-doping lead to increased power conversion efficiencies (PCEs) of the fullerene-based OPVs, from 2.62% to 10.64%, and of the nonfullerene-based OPVs, from 3.34% to 10.59%. These PDI–ionene interlayers enable chemical and morphological control of interfacial doping and conductivity, demonstrating that the conductive channels are crucial for charge transport in doped organic semiconductor films. Using these novel interlayers with efficient doping and high conductivity, both fullerene- and nonfullerene-based OPVs are achieved with PCEs exceeding 9% over interlayer thicknesses ranging from ≈3 to 40 nm.
36 MATERIALS SCIENCE↗
Stabilizing liquid drops of arbitrary shape by the interfacial jamming of nanoparticles
A stabilized assembly including a first liquid phase of non-spherical droplets in a second liquid phase, wherein the second liquid phase is immiscible with the first phase, and nanoparticle surfactants assembled at an interface of the non-spherical droplets and the second phase is disclosed. The nanoparticle surfactants include nanoparticles and end-functionalized polymers that can interact through ligand type interactions, and the first phase is stabilized by a disordered, jammed layer of nanoparticle surfactants. A method of preparing a stabilized assembly is also disclosed.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Amino-fulleropyrrolidines as electrotropic additives to enhance organic photovoltaics
The synthesis, device fabrication, and electric poling of novel amino-functionalized fulleropyrrolidines in polymer solar cells is reported. Systematically varying the tether lengths between the fullerene cage and tertiary amines provides insight into enhanced device efficiency and stability after poling. DFT calculations in an external electric field result in alignment of molecular dipole moments, which corroborates our hypothesis that electrotropic polarization causes an increased built-in electrostatic potential difference across the device, and results in enhance performance.
solar (photovoltaic), charge transport, materials ↗
Assembly of P3HT/CdSe nanowire networks in an insulating polymer host
Hybrid nanowire networks of electron donors and acceptors were achieved by the combination of phase separation, interfacial segregation, and crystallization in multicomponent blends.
Chemistry↗
Transition in Dynamics as Nanoparticles Jam at the Liquid/Liquid Interface
Nanoparticles (NPs) segregated to the liquid/liquid interface form disordered or liquid-like assemblies that show diffusive motions in the plane of the interface. As the areal density of NPs at the interface increases, the available interfacial area decreases, and the interfacial dynamics of the NP assemblies change when the NPs jam. In this work, dynamics associated with jamming was investigated by X-ray photon correlation spectroscopy. Water-in-toluene emulsions, formed by a self-emulsification at the liquid/liquid interface and stabilized by ligand-capped CdSe–ZnS NPs, provided a simple, yet powerful platform, to investigate NP dynamics. In contrast to a single planar interface, these emulsions increased the number of NPs in the incident beam and decreased the absorption of X-rays in comparison to the same path length in pure water. A transition from diffusive to confined dynamics was manifested by intermittent dynamics, indicating a transition from a liquid-like to a jammed state.
36 MATERIALS SCIENCE↗