The aquathermolysis of heavy oil from Riphean-Vendian complex with iron-based catalyst: FT-IR spectroscopy data

In this paper, we investigated the influence of steam treatment on structural group composition of resins and asphaltenes of heavy oil. The object of investigation was oil-saturated rocks from Riphean-Vendian complex. The extracted crude oil was determined as a high-viscous fluid. The resins and asphaltenes destructed in a small extent due to thermal treatment. The oil-soluble iron-based catalyst intensified the destructive processes. The content of sulfur compounds (-SO) in resins and asphaltenes drastically decreased due to reduction reaction of sulfoxide to sulfide and hydrogen sulfide. The results showed that catalytic aquathermolysis, even at low temperature ranges, promoted the cracking reaction of most macromolecular components and increased the content of light fractions of heavy oil. Consequently, it reduced its viscosity.     

Dihydroazulene Photoswitch Operating in Sequential Tunneling Regime: Synthesis and Single‐Molecule Junction Studies

Molecular switches play a central role for the development of molecular electronics. In this work it is demonstrated that the reproducibility and robustness of a single‐molecule dihydroazulene (DHA)/vinylheptafulvene (VHF) switch can be remarkably enhanced if the switching kernel is weakly coupled to electrodes so that the electron transport goes by sequential tunneling. To assure weak coupling, the DHA switching kernel is modified by incorporating p‐MeSC₆H₄ end‐groups. Molecules are prepared by Suzuki cross‐couplings on suitable halogenated derivatives of DHA. The synthesis presents an expansion of our previously reported bromination–elimination–cross‐coupling protocol for functionalization of the DHA core. For all new derivatives the kinetics of DHA/VHF transition has been thoroughly studied in solution. The kinetics reveals the effect of sulfur end‐groups on the thermal ring‐closure of VHF. One derivative, incorporating a p‐MeSC₆H₄ anchoring group in one end, has been placed in a silver nanogap. Conductance measurements justify that transport through both DHA (high resistivity) and VHF (low resistivity) forms goes by sequential tunneling. The switching is fairly reversible and reenterable; after more than 20 “ON‐OFF” switchings, both DHA and VHF forms are still recognizable, albeit noticeably different from the original states.     

Enhanced light trapping in solar cells using snow globe coating

A novel method, snow globe coating, is found to show significant enhancement of the short circuit current J_SC (35%) when applied as a scattering back reflector for polycrystalline silicon thin‐film solar cells. The coating is formed from high refractive index titania particles without containing binder and gives close to 100% reflectance for wavelengths above 400 nm. Snow globe coating is a physicochemical coating method executable in pH neutral media. The mild conditions of this process make this method applicable to many different types of solar cells. Copyright © 2012 John Wiley & Sons, Ltd.     

A Catalytic and Shape‐Memory Polymer Reactor

An originally designed catalytic and shape‐memory polymer reactor is reported. This reactor is made of a unique shape‐switchable polymer composed of a thermosensitive control layer and an inert substrate layer. With the inert substrate layer made of poly(acrylamide), the thermosensitive control layer consists of nickel nanoparticles and a smart polymer composite of poly(1‐vinylimidazole) (PVIm) and poly(acrylic acid) (PAAc) that exhibit switchable domains. The self‐healing and dissociation between PVIm and PAAc induce convex/concave‐switchable shapes in the resulting reactor, which cause tunable access to the encapsulated metal nanoparticles. In this way, this reactor demonstrates tunable catalytic ability. Unlike reported smart polymer reactors exhibiting tunable catalysis usually due to the thermal phase transition of poly(N‐isopropylacrylamide) (PNIPAm), this novel reactor adopts the shape‐switchable strategy for tunable catalysis. This novel design suggests a new protocol for the development of smart catalytic reactors, which opens new opportunities for controlled chemical processes.     

Environmentally Friendly Graphene Inks for Touch Screen Sensors

Graphene-based materials have attracted significant attention in many technological fields, but scaling up graphene-based technologies still faces substantial challenges. High-throughput top-down methods generally require hazardous, toxic, and high-boiling-point solvents. Here, an efficient and inexpensive strategy is proposed to produce graphene dispersions by liquid-phase exfoliation (LPE) through a combination of shear-mixing (SM) and tip sonication (TS) techniques, yielding highly concentrated graphene inks compatible with spray coating. The quality of graphene flakes (e.g., lateral size and thickness) and their concentration in the dispersions are compared using different spectroscopic and microscopy techniques. Several approaches (individual SM and TS, and their combination) are tested in three solvents (N-methyl-2-pyrrolidone, dimethylformamide, and cyrene). Interestingly, the combination of SM and TS in cyrene yields high-quality graphene dispersions, overcoming the environmental issues linked to the other two solvents. Starting from the cyrene dispersion, a graphene-based ink is prepared to spray-coat flexible electrodes and assemble a touch screen prototype. The electrodes feature a low sheet resistance (290 Ω □⁻¹) and high optical transmittance (78%), which provide the prototype with a high signal-to-noise ratio (14 dB) and multi-touch functionality (up to four simultaneous touches). These results illustrate a potential pathway toward the integration of LPE-graphene in commercial flexible electronics.     

Multifunctional Magnetic Optical Sensor Particles with Tunable Sizes for Monitoring Metabolic Parameters and as a Basis for Nanotherapeutics

Magnetic optical sensor particles with multifunctional cores and shells are synthesized via a facile nanoprecipitation method and the subsequent modification of the particle shell. The hydrophobic particle core includes optical oxygen indicators, a light harvesting system, photosensitizers, and magnetic nanoparticles. Further functionalities are introduced by modifying the shell with enzymes, antibodies, multiple layers of polyelectrolytes, stimuli‐responsive polymers, and luminescent indicator dyes. The hydrodynamic diameter is tunable by varying different precipitation parameters.     

Efficient Output Mode Converter for 30 GHz Gyroklystron at IAP

An output mode converter for Ka-band multi-MW gyroklystron in the Institute of Applied Physics (IAP) operating in the TE₅₃ mode is suggested. Two variants of the converter, aimed for different applications, are presented: the TE₅₃ to TE₀₁ mode converter with power output along the device axis and the TE₅₃ mode to Gaussian wavebeam quasi-optical converter with a visor. The suggested designs include the built-in electron beam collector. The converters were designed using a new synthesis algorithm, which implies iterative improvement of the waveguide wall shape in order to achieve high efficiency. The calculation results were proven by HFSS simulation and low-power tests of one version of the converter.     

Universal Polarization Switching Behavior of Disordered Ferroelectrics

Universal scaling features of polarization switching are established experimentally in rather different classes of disordered ferroelectrics: in well‐studied lead‐zirconate titanate (PZT) ferroelectrics, in recently synthesized Cu‐stabilized 0.94(Bi_1/2Na_1/2)TiO₃–0.06BaTiO₃ (BNT‐BT) relaxor ferroelectrics, and in classical organic ferroelectrics P(VDF‐TrFE). These scaling properties are explained by an extended concept of an inhomogeneous field mechanism (IFM) of polarization dynamics in ferroelectrics. Accordingly, disordered ferroelectrics exhibit a wide spectrum of characteristic switching times due to a statistical distribution of values of the local electric field. How this distribution can be extracted from polarization measurements is demonstrated. Generally, it is shown that the polarization response is primarily controlled by the statistical characteristics of disorder rather than by a temporal law of the local polarization switching.     

Ultra-Robust Flexible Electronics by Laser-Driven Polymer-Nanomaterials Integration

Polyethylene terephthalate (PET) is the most widely used polymer in the world. For the first time, the laser-driven integration of aluminum nanoparticles (Al NPs) into PET to realize a laser-induced graphene/Al NPs/polymer composite, which demonstrates excellent toughness and high electrical conductivity with the formation of aluminum carbide into the polymer is shown. The conductive structures show an impressive mechanical resistance against >10000 bending cycles, projectile impact, hammering, abrasion, and structural and chemical stability when in contact with different solvents (ethanol, water, and aqueous electrolytes). Devices including thermal heaters, carbon electrodes for energy storage, electrochemical and bending sensors show this technology's practical application for ultra-robust polymer electronics. This laser-based technology can be extended to integrating other nanomaterials and create hybrid graphene-based structures with excellent properties in a wide range of flexible electronics’ applications.