Micellar dye shuttle between water and an ionic liquid

The reversible transfer of poly(2-ethyl-2-oxazoline)-block-poly(2-nonyl-2-oxazoline) nanocarriers comprising encapsulated dyes is demonstrated between water and an ionic liquid. This dye transfer concept is shown to be applicable for loading and delivery of dye molecules as well as to provide a protective environment for the encapsulated dye

Microwave-Assisted Synthesis of Core–Shell Nanoparticles—Insights into the Growth of Different Geometries

Microwave irradiation is utilized for the rapid synthesis of gold–silver core–shell bimetallic nanoparticles (NPs) in a two-step process. A strategy of establishing a bilayer organic barrier around the core using citrate and ascorbic acid as capping agents, providing a means to achieve a well-defined boundary layer between the core and the shell material, is reported. These boundary layers are essential for synthesizing different core–shell morphologies and the approach results in tunable bimetallic NPs with defined core–shell structures, both for spherical as well as for triangular seed cores. In addition, theoretical calculations of the plasmonic characteristics based on the boundary element method of different classes of NPs are conducted. These investigations enable conclusions to be drawn on the influence of the core morphology on the tunability of their localized surface plasmon resonances. © 2020 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinhei

The evolution of the footwall to the Ronda subcontinental mantle peridotites: insights from the Nieves Unit (western Betic Cordillera)

Strongly heterogeneous deformation and extreme metamorphic gradients characterize the dominantly carbonate Nieves Unit in the footwall to the Ronda mantle extrusion wedge in the western Betic Cordillera. A well-developed foliation and mineral lineation, together with isoclinal intrafolial folds, occur in silicate-bearing, calcite or dolomite marbles within a c. 1.5 km thick metamorphic aureole underlying the peridotites. For the inferred maximum pressure of 300 MPa, petrological investigations allow us to define temperature ranges for the main zones of the metamorphic aureole: >510 °C (probably c. 700 °C) for the forsterite zone; 510–430 °C for the diopside zone; 430–360 °C for the tremolite zone; 360–330 °C for the phlogopite zone. Field structural analysis integrated with petrological, microstructural and electron backscatter diffraction textural data document large finite strains consistent with general shear within the metamorphic aureole, associated with NW-directed thrusting of the peridotites. On the other hand, post-kinematic silicate growth suggests that heat diffusion from the high-temperature peridotites continued after the final emplacement of the Ronda mantle extrusion wedge, leading to final zoning of the metamorphic aureole and to local partial annealing of calcite marble textures, particularly in the highest-temperature zone of the thermally softened footwall carbonates. Following substantial cooling, renewed crustal shortening affected the whole Nieves Unit, resulting in widespread development of NE–SW-trending meso-scale folds

Emulsion polymerizations for a sustainable preparation of efficient TEMPO‐based electrodes

Organic polymer‐based batteries represent a promising alternative to present‐day metal‐based systems and a valuable step toward printable and customizable energy storage devices. However, most scientific work is focussed on the development of new redox‐active organic materials, while straightforward manufacturing and sustainable materials and production will be a necessary key for the transformation to mass market applications. Here, a new synthetic approach for 2,2,6,6‐tetramethyl‐4‐piperinidyl‐ N ‐oxyl (TEMPO)‐based polymer particles by emulsion polymerization and their electrochemical investigation are reported. The developed emulsion polymerization protocol based on an aqueous reaction medium allowed the sustainable synthesis of a redox‐active electrode material, combined with simple variation of the polymer particle size, which enabled the preparation of nanoparticles from 35 to 138 nm. Their application in cell experiments revealed a significant effect of the size of the active‐polymer particles on the performance of poly(2,2,6,6‐tetramethyl‐4‐piperinidyl‐ N ‐oxyl methacrylate) (PTMA)‐based electrodes. In particular rate capabilities were found to be reduced with larger diameters. Nevertheless, all cells based on the different particles revealed the ability to recover from temporary capacity loss due to application of very high charge/discharge rates.Sustainable and efficient organic electrode : A new synthetic approach for polymers for organic batteries includes an emulsion polymerization with adjustable particle sizes in aqueous dispersions and allows the sustainable manufacturing of active materials and composite electrodes. The electrochemical investigation shows that the influence of particle sizes and the resulting morphologies of composite films on the cell performance is as important as the active material itself

Targeted delivery of a phosphoinositide 3-kinase γ inhibitor to restore organ function in sepsis

Jaundice, the clinical hallmark of infection-associated liver dysfunction, reflects altered membrane organization of the canalicular pole of hepatocytes and portends poor outcomes. Mice lacking phosphoinositide 3-kinase-γ (PI3Kγ) are protected against membrane disintegration and hepatic excretory dysfunction. However, they exhibit a severe immune defect that hinders neutrophil recruitment to sites of infection. To exploit the therapeutic potential of PI3Kγ inhibition in sepsis, a targeted approach to deliver drugs to hepatic parenchymal cells without compromising other cells, in particular immune cells, seems warranted. Here, we demonstrate that nanocarriers functionalized through DY-635, a fluorescent polymethine dye, and a ligand of organic anion transporters can selectively deliver therapeutics to hepatic parenchymal cells. Applying this strategy to a murine model of sepsis, we observed the PI3Kγ-dependent restoration of biliary canalicular architecture, maintained excretory liver function, and improved survival without impairing host defense mechanisms. This strategy carries the potential to expand targeted nanomedicines to disease entities with systemic inflammation and concomitantly impaired barrier functionality

Nanospiral Formation by Droplet Drying: One Molecule at a Time

We have created nanospirals by self-assembly during droplet evaporation. The nanospirals, 60–70 nm in diameter, formed when solvent mixtures of methanol and m-cresol were used. In contrast, spin coating using only methanol as the solvent produced epitaxial films of stripe nanopatterns and using only m-cresol disordered structure. Due to the disparity in vapor pressure between the two solvents, droplets of m-cresol solution remaining on the substrate serve as templates for the self-assembly of carboxylic acid molecules, which in turn allows the visualization of solution droplet evaporation one molecule at a time

Strategies for Controlled Placement of Nanoscale Building Blocks

The capability of placing individual nanoscale building blocks on exact substrate locations in a controlled manner is one of the key requirements to realize future electronic, optical, and magnetic devices and sensors that are composed of such blocks. This article reviews some important advances in the strategies for controlled placement of nanoscale building blocks. In particular, we will overview template assisted placement that utilizes physical, molecular, or electrostatic templates, DNA-programmed assembly, placement using dielectrophoresis, approaches for non-close-packed assembly of spherical particles, and recent development of focused placement schemes including electrostatic funneling, focused placement via molecular gradient patterns, electrodynamic focusing of charged aerosols, and others

Nanopatterning of Octadecyltrichlorosilane (OTS) Self-Assembled Monolayers By Probe-based Lithography: Extending the Range of Substrates

Surface functionalization of oxides plays a fundamental role in nanotechnology, from microelectronics to photovoltaics [1,2]. Local oxidation by scanning probe is a powerful tool to fabricate chemical patterns at the nanometer scale, enabling the hierarchical assembly of complex structures [3,4]. Notwithstanding the paramount interest in the tailored functionalization of various kinds of oxide materials, most of the literature about probe-based electrooxidation lithography has so far focused on Si wafer substrates. The potential of titanium dioxide (TiO2) and surface-passivated aluminum (Al/AlOx) to serve as substrates for electrooxidative nanolithography is here demonstrated. The results obtained on TiO2 and Al/AlOx are compared with reference commercial substrates, such as surface-passivated silicon (Si/SiOx) and indium tin oxide (ITO). The conditions for the functionalization of the different substrate materials with n-octadecyltrichlorosilane (OTS) monolayers are reported. Next to the structural study of the formed monolayers by contact angle goniometry, Fourier Transform Infrared (FTIR) spectroscopy and Scanning Force Microscopy (SFM), the different oxidation processes on bare and OTS-functionalized substrates were studied by lateral force imaging and scanning Kelvin probe microscopy. Chemical activation was also confirmed by metallization processes