High-surface-area organic matrix tris(aza)pentacene supported platinum nanostructures as selective electrocatalyst for hydrogen oxidation/evolution reaction and suppressive for oxygen reduction reaction

Developing a Pt-based electrocatalytic material able to selectively catalyze hydrogen oxidation (HOR) while supressing oxygen reduction (ORR) is beneficial for durability of the fuel cells. Namely, degradation of carbon supported Pt particles is dramatically influenced by the unwanted ORR enrolling at the anode due to the air penetration during start-up/shut-down events. We present an organic matrix tris(aza)pentacene (TAP), which belongs to π-functional materials with ladder-like conjugated nitrogen-containing units, as the support for Pt to form a “smart” fuel cell anode able to selectively catalyze HOR and to suppress ORR. “Switching-on/off” of the composite material activity is provided by reversible reduction/oxidation of the TAP in the low potential region which provokes TAP - H_xTAP transition. Conductivity of the reduced H_xTAP enables supported Pt particles to effectively run HOR. In contrast, restricted conductivity of oxidized TAP analogue leads to the substantial drop in the ORR activity with respect to benchmark Pt/C catalyst.     

A topic network analysis of the system turn in the environmental sciences

Scientometrics - The concept of Earth system science denotes a shift in the scientific discourse from disciplinary accounts of isolated components of the global environment towards the holistic and...     

Interfacing perovskite strontium molybdate to molybdenum disulfide nanoplatelts for boosting HER from water

Due to low hydrogen adsorption free energy at the edges of 2D-MoS₂ layered sheets, nanostructured MoS₂ materials recently are assigned to prospective electrocatalysts for hydrogen evolution reaction (HER) from water. However, the efficiency and stability of HER onto the MoS₂ designed on the conductive substrates are poor. To significantly increase the number of active sites and achieve a long-time working stability, the design of hybrid-type electrodes is crucial. Here, we report the synthesis of a new hybrid material composed of molybdenum disulfide and molybdenum oxides heterostructured with strontium molybdate. For this, a facile one-pot hydrothermal process was developed directly onto the TiO₂ nanotube carpet substrate. The interfacing of strontium molybdate at the electrode substrate verified by X-ray photoelectron spectroscopy and Time of flight secondary ions mass spectrometry (ToF SIMS) techniques. Considerable higher catalytic activity at the surface of this hybrid film, with the onset potential of 190 mV vs RHE and a Tafel slope of 66 mV dec^?1 attaining ~80 mA cm^?2 at 0.35 V overvoltage was ascertained. Exciting HER stability in comparison with the pure synthetic MoS₂ was verified by a prolonged potential cycling from 0.05 to ?0.35 V versus RHE potential and 45 h continuous HER processing at a constant current density.     

Influence of addition of nanosize barium cerate on the microstructure and properties of top-seeded melt growth YBCO bulk superconductors

Barium cerate (BaCeO₃) is one of the possible additions to bulk YBa₂Cu₃O₇ single-grain superconductors to suppress the growth of Y₂BaCuO₅ (Y211) particles. This paper investigates the synthesis of barium cerate powder and its use in YBa₂Cu₃O₇ bulk superconductors. Crystalline barium cerate was synthesized by solid-state reaction, by co-precipitation of oxalates and by sol-gel method. Final calcination was held in air or in vacuum. It is shown that the most efficient in refining Y211 is nanocrystalline barium cerate prepared by sol-gel method calcined in vacuum. The effective refinement of Y211 particles occurred over the entire interval of nanocrystalline BaCeO₃ addition from 0.38 to 1.90 wt%. The optimal concentration of nanosize barium cerate was determined, microstructure and superconducting properties were characterized. The effect of Y211 content on trapped field in YBCO bulks with addition of nanocrystalline barium cerate is shown.     

Catalytic pyrolysis and kinetic study of real-world waste plastics: multi-layered and mixed resin types of plastics

Clean Technologies and Environmental Policy - Multi-layered and mixed resin types of plastics are a great challenge for the waste recycling industry. The majority consist of two or more types of...     

The influence of laser power on the interfaces of functionally graded materials fabricated by powder-based directed energy deposition

Journal of Materials Science - Powder-based directed energy deposition (DED) technology with separate feeders for different individual materials enables the deposition of functionally graded...     

Surface Defects on Semicoherent and Incoherent NaCl-Type Carbides Dispersed in Hot-Rolled Ferritic Steel

Metallurgical and Materials Transactions A - The interface structure of semicoherent titanium carbide (TiC) nanoparticles and incoherent micron-sized TiC precipitates in Fe–C–Ti alloy...     

A new strategy for plasticizing and stabilization of PVC mixtures

This study was undertaken to examine possible use of classic tetravalent tin‐based heat stabilizers for the preparation of a polymer plasticizer: poly(ε‐caprolactone) (PCL) and simultaneous stabilization of PVC in PVC/PCL mixtures. PCL was prepared from ε‐caprolactone (CL) by polymerization initiated by tin‐containing organic compounds and successfully used to simultaneously plasticize and stabilize PVC. Moreover, conditions under which the polymerization of CL took place directly in situ during PVC/CL mixture processing were found. The procedure yielded homogeneous plasticized PVC/PCL mixtures, which were stable and contained >90% of the original monomer content. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41066.     

Shear‐induced shish‐kebab structures in isotactic polypropylene using acicular precipitated calcium carbonate as whisker

It has been reported in the technical literature that whiskers of rodlike single crystals can be used in order to generate shish‐kebab structures or other different lamellae morphologies during isothermal or dynamic crystallization of sheared or presheared polymer melts. The expected advantage of the changed crystalline structure is a reinforcing effect of the composite. A lot of papers reported about the application of inorganic and organic whiskers such as cellulose and chitin whiskers. This study reports on an attempt to use acicular PCC as appropriate whisker for improving mechanical properties of polypropylene. In this article special attention is given to demonstrate the effect of flow induced crystallization under varying shear conditions in order to improve the mechanical properties. The effects were demonstrated using rheology, thermal analysis, tensile testing, and transmission electron microscopy. POLYM. ENG. SCI., 54:2057–2063, 2014. © 2013 Society of Plastics Engineers     

Analysis of polymer viscoelastic properties based on compressive creep tests during hot embossing for two‐dimensional polyethylene terephthalate nanochannels

Hot embossing is an emerging technology, which enables cost‐effective and high‐productivity nanofabrication. It is important to optimize the processing parameters to achieve high replication accuracy nanostructure fabrication. In this article, to reveal the interrelationship between the hot embossing conditions and replication accuracy of two‐dimensional (2D) polyethylene terephthalate (PET) nanochannels, the numerical simulations were conducted by using the generalized Maxwell model. The constants of the generalized Maxwell model were calculated by a newly established fitting formula based on experimental compressive creep curves rather than tensile stress relaxation curves. Replication accuracy of 2D PET nanochannels was evaluated by a method based on weighted averages. Orthogonal method was employed during numerical simulations to optimize the hot embossing process. Under optimized hot embossing parameters, 2D PET nanochannels, ～80 nm wide, 250 nm deep and 4 mm long, were precision‐imprinted into a PET sheet. POLYM. ENG. SCI., 54:2398–2406, 2014. © 2013 Society of Plastics Engineers