Electrical conductivity measured in atomic carbon chains

The first electrical conductivity measurements of monoatomic carbon chains are reported in this study. The chains were obtained by unraveling carbon atoms from graphene ribbons while an electrical current flowed through the ribbon and, successively, through the chain. The formation of the chains was accompanied by a characteristic drop in the electrical conductivity. The conductivity of carbon chains was much lower than previously predicted for ideal chains. First-principles calculations using both density functional and many-body perturbation theory show that strain in the chains determines the conductivity in a decisive way. Indeed, carbon chains are always under varying non-zero strain that transforms its atomic structure from cumulene to polyyne configuration, thus inducing a tunable band gap. The modified electronic structure and the characteristics of the contact to the graphitic periphery explain the low conductivity of the locally constrained carbon chain.Comment: 21 pages, 9 figure

How to teach an old dog new (electrochemical) tricks: Aziridine-functionalized CNTs as efficient electrocatalysts for the selective CO<inf>2</inf> reduction to CO

© 2018 The Royal Society of Chemistry. The electrocatalytic conversion of CO2 to energy-rich chemicals or energy vectors is a highly challenging approach to cope with an ever increasing demand for energy storage and valorization of renewable resources. Herein we report on the electrocatalytic reduction of CO2 to CO using covalently N-decorated carbon nanotubes as highly efficient and chemoselective metal-free electrocatalysts. At odds with more conventional synthetic methods for the production of N-doped nanocarbons, chemical functionalization warrants a unique control of "surface N-defects" available for the process, ruling out any synergistic contribution to electrocatalysis coming from other surface or bulk N-containing groups. With a CO faradaic efficiency (FECO) close to 90% and productivity as high as 48 NLCO gN-1 h-1, NH-aziridine functionalized MWCNTs have shown CO2RR performance that is among the highest reported so far for related metal-free systems. At the same time, it has offered a unique view-point for the comprehension of the underlying structure-reactivity relationship

Helminth eggs die-off and nutrients : human excreta storage experiment

Are the current practices of handling human excreta for agricultural purposes by farmers in Vietnam good enough?This study set up an excreta storage experiment to research how to inactivate Ascaris lumbricoides eggs and stillmaintain the nutrient value of human excreta

Flexural-strengthening efficiency of cfrp sheets for unbonded post-tensioned concrete T-beams

There has been a limited number of studies about the flexural behavior of unbonded post-tensioned concrete (UPC) beams strengthened with carbon fibre reinforced polymer (CFRP) and these studies have not systematically examined the effect of CFRP sheets on the tendon strain as well as the strengthening efficiency. Moreover, current design guides for the FRP strengthening techniques have not provided any design procedure for UPC structures. This study, thus, investigates the influence of CFRP sheet ratio on the flexural behavior of CFRP-strengthened UPC T-beams and quantifies its effect upon tendon behavior in this kind of UPC beams. The testing program consisted of nine large-scale UPC T-beams strengthened by different layers of CFRP sheets with or without CFRP U-wrapped anchors. The experimental results have shown that the use of CFRP sheets and CFRP U-wrapped anchors significantly affected the tendon strain. The FRP reinforcement ratio governed the flexural capacity, the crack width, the mid-span displacement, and the ductility of the beams in which the strengthening efficiency reduces with the increased number of CFRP layers. The configuration of the CFRP U-wrapped anchors affected the strain of the CFRP sheets, the failure mode and thus the beam behavior. In addition, semi-empirical equations were proposed to estimate the actual strain of unbonded tendons in which the effect of the CFRP sheets and CFRP U-wrapped anchors have been taken into consideration. The proposed equations, which are simple to use, yield reliable predictions with a small variation

A 3D insight on the catalytic nanostructuration of few-layer graphene

The catalytic cutting of few-layer graphene is nowadays a hot topic in materials research due to its potential applications in the catalysis field and the graphene nanoribbons fabrication. We show here a 3D analysis of the nanostructuration of few-layer graphene by iron-based nanoparticles under hydrogen flow. The nanoparticles located at the edges or attached to the steps on the FLG sheets create trenches and tunnels with orientations, lengths and morphologies defined by the crystallography and the topography of the carbon substrate. The cross-sectional analysis of the 3D volumes highlights the role of the active nanoparticle identity on the trench size and shape, with emphasis on the topographical stability of the basal planes within the resulting trenches and channels, no matter the obstacle encountered. The actual study gives a deep insight on the impact of nanoparticles morphology and support topography on the 3D character of nanostructures built up by catalytic cutting

Pyridine-decorated carbon nanotubes as a metal-free heterogeneous catalyst for mild CO<inf>2</inf>reduction to methanol with hydroboranes

© 2017 The Royal Society of Chemistry. Pyridine decorated multi-walled carbon nanotubes (N Py -MW) have been successfully employed as a catalyst for the reduction of carbon dioxide to methyl borinate (R 2 BO-CH 3 ) in the presence of 9-borabicyclo[3.3.1]nonane. N Py -MW represents the first example of a heterogeneous, metal-free and durable catalyst for CO 2 hydroboration to methanol. A mechanistic cycle has been proposed on the basis of targeted blank experiments and a quantum chemical study, highlighting the non-innocent role played by the nanotube carrier in the final N Py -MW catalytic performance

Tridimensional few-layer graphene-like structures from sugar-salt mixtures as high-performance supercapacitor electrodes

© 2018 Elsevier Ltd This work describes a straightforward approach to the production of highly-performing and cost-effective C-based materials for energy storage application while proposing an original and effective method to the control of the final material morphology. Indeed, robust few-layer graphene-like and highly open-cell structures have been prepared by a modified chemical activation procedure starting from costless sugar/salt mixtures. The as-prepared C-samples ensure high ion-accessible surface area and low ion transport resistance, two key features for the fabrication of effective electrochemical double layer supercapacitors. A selected sample from this series exhibits high specific capacitance (Cg) (312 and 234 F g−1 at 0.5 and 50 A g−1, respectively, in 0.5 M H2SO4), particularly at high current density values, along with excellent cycling stability and Cg retention for increasing charge–discharge rates

Efficient hierarchically structured composites containing cobalt catalyst for clean synthetic fuel production from Fischer-Tropsch synthesis

We report a straightforward preparation method to synthesize hierarchical composite consisting of TiO2-coated multi-walled carbon nanotubes (CNTs) decorating a macroscopic host structure of alpha-Al2O3. The obtained composite possesses moderate specific surface area and very open porous structure, as well as moderate interaction with active sites, which significantly improve the cobalt nanoparticles dispersion and the mass diffusion during the reaction. The Co/TiO2/CNT-alpha-Al2O3 (CoTiCNTA) catalyst is then used in the Fischer-Tropsch synthesis (FTS) process. This hierarchical catalyst achieves a FTS rate to C5+ of 0.80 g(C5+) g(cat)(-1) h(-1) along with a long-chain hydrocarbons (C5+) selectivity of 85%, which can be pointed out as the most outstanding noble promoter-free catalyst for the FTS process. The as-synthesized catalyst also exhibits an extremely high stability as a function of time on stream which is also one of the prerequisites for the development of future FTS catalysts, especially for the Biomass-to-Liquids process where trace amount of impurities and/or moisture could have an impact on the catalyst stability. The present work also introduces a new investigation methodology based on the use of zero field Co-59 NMR, which allows one to map in a precise manner the cobalt active phase distribution and to correlate it with the FTS performance. It is expected that such technique would be extremely helpful for the understanding of the catalyst structure-performance relationship and for future optimization in the FTS process as well as in other fields of investigation where cobalt particles are involved. (C) 2014 Elsevier Inc. All rights reserved

Chemical functionalization of N-doped carbon nanotubes: A powerful approach to cast light on the electrochemical role of specific N-functionalities in the oxygen reduction reaction

© 2016 The Royal Society of Chemistry.In this paper, we describe the combination of two different synthetic approaches to carbon nanotube N-decoration/doping: the chemical functionalization with tailored N-pyridinic groups and the classical Chemical Vapor Deposition (CVD) technique. Accordingly, CVD-prepared N-doped CNMs (NMWs) and their N-decorated (chemically functionalized) counterparts (NMW@N1,2) have been prepared and used as metal-free electrocatalysts for the oxygen reduction reaction (ORR). It has been demonstrated that chemical functionalization occurs on the NMW surface sites responsible for their inherent electrochemical properties and "switches them off". As a result, the ORR promoted by NMW@N1,2 is fully controlled by the appended N-heterocycles. A comparative analysis of N-functionalized samples and N-doped (CVD prepared) materials is used to foster the hypothesis of a unique N-configuration (N-pyridinic) responsible for the overall electrochemical performance in NMWs. In addition to that, original electrochemical insights unveiled during the study are discussed and the truly metal-free action of NMW in ORR catalysis is demonstrated