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Transition metal oxides with various valence states have high specific capacitance and have attracted much attention. However, the poor cycle stability caused by material agglomeration seriously limits the play of its high activity. Herein, we create a stress dispersion structure (CuxO composite porous carbon net) by in situ lyophilization and one-step carbonization, effectively anchoring highly reactive copper oxides and highly conductive carbon networks combined with high nitrogen doping of 10.7%, to investigate their electrochemical performance in supercapacitors. Specifically, the specific capacitance of CuxO@NPC can be as high as 392 F/g (0.5 A/g) in the three-electrode system with 6 mol/L KOH as electrolyte. When applied to the two-electrode system, the cycle stability of the whole device can reach 97% after 10,000 cycles.

A facile carbothermal route was adopted to obtain niobium carbide nanoparticles (NPs) embedded in carbon network from Nb2O5 to study photocatalytic behavior. Optimization of synthesis parameters to obtain single phase NbC NPs has been successfully done. The phase identification, morphology and nature of carbon were determined with the help of X-ray diffraction, transmission electron microscopy (TEM) and Raman spectroscopy. X-ray photoelectron spectroscopy (XPS) suggested the presence of multiple oxidation states of Nb associated to NbC and NbCxOy centers on the surface of NPs. Due to the presence of NbCxOy on the surface of NPs, absorption under visible region of EM spectrum has been observed by UV-visible spectroscopy. Different organic dyes (RhB, MB and MO) were used to study the effect of holding time on the photocatalytic performance of as-synthesized samples. RhB dye was found to be the most sensitive organic molecule among all the considered dyes and degraded 78% in 120 min.

A three-dimensional MnO/C nanocomposite is fabricated through a simple route of immersion and subsequent calcination. The carbon content and morphology of the sample are adjusted by adjusting the calcination temperature. This material combines the excellent lithium storage performance of MnO and the good stability of carbon. Because MnO is embedded in the three-dimensional carbon networks, it can provide proper space to alleviate the volume effect during discharging and charging. The unique architecture and large surface area enable the composites to exhibit remarkable lithium storage properties with outstanding rate performance, high reversible capacity, and cycle life. The optimized sample (MnO/C-750) has excellent performance of 1067.95 mAh g−1 at 0.2 A g−1 over 200 cycles and 722.32 mAh g−1 at 1 A g−1 over 600 cycles.

Through this work, a carbon network/aluminum matrix porous composite material was analyzed for its susceptibility to material degradation in sulfuric acid and seawater corrosive media. Simple potentiodynamic electrochemical testing was implemented, and from polarization curves, the Tafel coefficients and exchange current densities were obtained for a comparative analysis. The pseudo exchange current densities for corrosion of the composite material were compared to those found for Al 1235 and 6061-T6. By relating the pseudo icorr of these materials in each environment, an understanding regarding the relative propensity to corrosion was determined. According to the recovered data, the composite had the lowest pseudo icorr in all corrosion systems and was consequently inferred the least likely to corrode. The factor that primarily contests this conclusion is the material&rsquo, s relatively large exposed surface area. The existence of carbon along the grain boundaries in the C/Al composite improved its corrosion behavior. Further discussion concerning the implication of &beta, c is offered. Electrochemical impedance spectroscopic (EIS) tests were performed in the frequency range from 0.001 Hz to 100 kHz. An immersion corrosion test was conducted to calculate the corrosion rate in different environments. Morphological observation on the corrosion surface was also carried out to evaluate the corrosion product deposition on each material.

trans-Diethynylethene [(E)-hex-3-ene-1,5-diyne (1 a)], geminal-diethynylethene [3-ethynyl-but-3-ene-1-yne (1 b)], and tetraethynylethene [3,4-diethynyl-hex-3-ene-1,5-diyne (2)] are flexible molecular building blocks for pi-conjugated polymers with interesting electronic and photonic properties. The type of functionalization, the length of the polymer chain, and the choice of pi-conjugation pattern, play a crucial role in determining the properties of these compounds. To rationalize the impact of the different delocalization pathways in the various types of isomers (trans or geminal) on the molecular and electronic structure, a detailed theoretical investigation is presented. We develop a method based on the natural bond orbital (NBO) analysis of Weinhold, which allows one to correlate electron delocalization with molecular and electronic structure observables. The method reveals that the difference between trans (or through) and geminal (or cross) conjugation is not only due to the vertical pi conjugation, but also to the in-plane sigma hyperconjugation. The method is used to correlate the changes in molecular and electronic observables, such as the bond lengths or the absorption frequencies, with the electronic structure of the compounds under investigation. Moreover, this method allows us to predict how a certain substituent will affect the molecular structure and the electronic properties of a given backbone.

The fragmentation of molecular hydrogen on N-doped carbon networks was investigated by using molecular (polyaromatic macrocycles) as well as truncated and periodic (carbon nanotubes) models. The computational study was focused on the ergonicity analysis of the reaction and on the properties of the transition states involved when constellations of three or four pyridinic nitrogen atom defects are present in the carbon network. Calculations show that whenever N-defects are embedded in species characterized by large conjugated π-systems, either in polyaromatic macrocycles or carbon nanotubes, the corresponding H2 bond cleavage is largely exergonic. The fragmentation Gibbs free energy is affected by the final arrangement of the hydrogen atoms on the defect and by the extension of the π-electron cloud, but it is not influenced by the curvature of the system.

All rights reserved. The production of high-quality graphene-oxide interfaces is normally achieved by graphene growth via chemical vapour deposition on a metallic surface, followed by transfer of the C layer onto the oxide, by atomic layer and physical vapour deposition of the oxide on graphene or by carbon deposition on top of oxide surfaces. These methods, however, come with a series of issues: they are complex, costly and can easily result in damage to the carbon network, with detrimental effects on the carrier mobility. Here we show that the growth of a graphene layer on a bimetallic Ni3Al alloy and its subsequent exposure to oxygen at 520 K result in the formation of a 1.5 nm thick alumina nanosheet underneath graphene. This new, simple and low-cost strategy based on the use of alloys opens a promising route to the direct synthesis of a wide range of interfaces formed by graphene and high-κ dielectrics., The research activities of L.O., E.M., F.O. and A.B. have received funding from the MIUR within the programme PRIN 2010-2011 for the project entitled ‘GRAF. Frontiers in Graphene Research: understanding and controlling Advanced Functionalities’ (No.20105ZZTSE_001). E.R.H. acknowledges support of the Spanish Research and Innovation Office through project FIS2012-31713. E.R.H. and D.A. acknowledge support from the Leverhulme Trust. M.B., S.U. and P.H. acknowledge support from the VILLUM foundation, The Danish Council for Independent Research/Technology and Production Sciences.