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Composites of (C4F)n and (CF)n Synthesized by Uncatalyzed Fluorination of Graphite

A new solid-state 19F magic-angle spinning NMR signal at an isotropic 19F chemical shift of −53 ppm is measured from graphite fluoride synthesized by reaction of graphite with F2 at temperatures above 750 K with no catalyst. Two-dimensional NMR suggests the −53 ppm 19F NMR signal originates from covalent fluoromethanetriyl groups belonging to ordered (CyF)n bulk domains composited with the major (CF)n domains. Quantitative 19F and 13C NMR find y=4.32±0.64. DFT calculations of NMR chemical shifts for unsaturated fluorographene models show that a (C4F)n phase with fluorine bound covalently to a single side of the carbon layer best explains the observed NMR chemical shifts. We assign the new phase to this (C4F)n structure, which constitutes up to 15% of the carbon in our graphite fluoride composites. The (C4F)n content of the composite affects bulk electrochemical properties in a manner similar to graphite fluorides produced by conventional, catalyzed fluorination processes.

Walder, Brennan J. (ORCID:0000000274539143)↗

Density impact on performance of composite Si/graphite electrodes

The ability of alkali-substituted binders for composite Si and graphite negative electrodes to minimize capacity fade for lithium ion batteries is investigated. Polymer films and electrodes are described and characterized by FTIR following immersion in electrolyte (1:2 EC:DMC) for 24 h. FTIR analysis following electrode formation displayed similar alkali-ion dependent shifts in peak location suggesting that changes in the vibrational structure of the binder are maintained after electrode formation. The Si and graphite composite electrodes prepared using the alkali-substituted polyacrylates were also exposed to electrochemical cycling and it has been found that the performance of the Na-substituted binder is superior to a comparable density K-substituted system. However, in comparing performance across many different electrode densities attention needs to be placed on making comparisons at similar densities, as low density electrodes tend to exhibit lower capacity fade over cycling. This is highlighted by a 6% difference between a low density K-substituted electrode and a high density Na-substituted sample. As a result, this low variance between the two systems makes it difficult to quickly make a direct evaluation of binder performance unless electrode density is tightly controlled.

25 ENERGY STORAGE↗

Damage-Tolerance Characteristics of Composite Fuselage Sandwich Structures with Thick Facesheets

Damage tolerance characteristics and results from experimental and analytical studies of a composite fuselage keel sandwich structure subjected to low-speed impact damage and discrete-source damage are presented. The test specimens are constructed from graphite-epoxy skins borided to a honeycomb core, and they are representative of a highly loaded fuselage keel structure. Results of compression-after-impact (CAI) and notch-length sensitivity studies of 5-in.-wide by 10-in.long specimens are presented. A correlation between low-speed-impact dent depth, the associated damage area, and residual strength for different impact-energy levels is described; and a comparison of the strength for undamaged and damaged specimens with different notch-length-to-specimen-width ratios is presented. Surface strains in the facesheets of the undamaged specimens as well as surface strains that illustrate the load redistribution around the notch sites in the notched specimens are presented and compared with results from finite element analyses. Reductions in strength of as much as 53.1 percent for the impacted specimens and 64.7 percent for the notched specimens are observed.

McGowan, David M.↗

Metastability of diamond ramp-compressed to 2 terapascals

Carbon is the fourth-most prevalent element in the Universe and essential for all known life. In the elemental form it is found in multiple allotropes, including graphite, diamond and fullerenes, and it has long been predicted that even more structures can exist at pressures greater than those at Earth’s core. Several phases have been predicted to exist in the multi-terapascal regime, which is important for accurate modelling of the interiors of carbon-rich exoplanets. By compressing solid carbon to 2 terapascals (20 million atmospheres; more than five times the pressure at Earth’s core) using ramp-shaped laser pulses and simultaneously measuring nanosecond-duration time-resolved X-ray diffraction, we found that solid carbon retains the diamond structure far beyond its regime of predicted stability. The results confirm predictions that the strength of the tetrahedral molecular orbital bonds in diamond persists under enormous pressure, resulting in large energy barriers that hinder conversion to more-stable high-pressure allotropes, just as graphite formation from metastable diamond is kinetically hindered at atmospheric pressure. In conclusion, this work nearly doubles the highest pressure at which X-ray diffraction has been recorded on any material.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

X-ray Absorption Spectroscopy Studies of a Molecular CO 2 -Reduction Catalyst Deposited on Graphitic Carbon Nitride

Metal-ligand complexes have been extensively explored as well-defined molecular catalysts in small molecule activation reactions such as carbon dioxide (CO 2 ) reduction. Many hybrid photocatalysts have been prepared by coupling such complexes with photoactive surfaces for use in solar CO 2 reduction. In this work, we employ X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopies, density functional theory (DFT) and computational XANES modeling to interrogate the structure of a hybrid photocatalyst consisting of a macrocyclic cobalt complex deposited on graphitic carbon nitride (C 3 N 4 ). Results show that the cobalt complex binds on C 3 N 4 through surface OH or NH 2 groups. By refining the local geometry and binding sites of this well-defined molecular cobalt complex on C 3 N 4 , here we established an important benchmark for modeling a large class of molecular catalysts that can be adapted to in situ/operando studies and further enhanced by applying chemometrics-based approaches and machine learning methods of XANES data analysis.

36 MATERIALS SCIENCE↗

Modification of surface functionality and interlayer spacing of multi-walled carbon nanotubes using {gamma}-rays

The surface functionality and interlayer spacing changes induced by {gamma}-ray irradiation were investigated in multi-walled carbon nanotubes (MWCNTs). The modification effect of MWCNTs irradiated in air and epoxy chloropropane (ECP) was characterized by x-ray photoelectron spectroscopy, Raman spectroscopy, and x-ray diffraction. The results indicated that {gamma}-ray irradiation in two different media improved the amount of oxygen-containing functional groups on nanotube surface, and the irradiation in ECP was more efficient. Compared with the pristine MWCNTs, the MWCNTs irradiated in air exhibited a decrease in width of G band and intensity ratio of D to G band in the Raman spectra and an increase in intensity and diffraction angle of (002) characteristic x-ray peak. However, the MWCNTs tended to show the opposite behaviors in Raman spectra and x-ray diffraction patterns after they were irradiated in ECP. This preliminary study suggests that {gamma}-ray irradiation in air can meaningfully decrease the interlayer distance of MWCNTs and improve the graphitization of MWCNTs, while irradiation in ECP disorders and breaks the structure of MWCNTs. It is worth expecting that MWCNTs can be functionalized by {gamma}-rays in reactive liquid and also be employed for preventing {gamma}-ray radiation from reaching sensitive materials at least for short term experiments in air.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

The electric current effect on electrochemical deconsolidation of spherical fuel elements - 18447

For High-Temperature Gas-cooled Reactor in China, fuel particles are bonded into spherical fuel elements by a carbonaceous matrix. In conjunction with the development of a system to determine fuel failure fractions through {gamma}-analysis of individual and undamaged fuel particles, an automated electrochemical deconsolidation apparatus was developed in this study to separate the particles from the carbonaceous matrix by disintegrating the matrix into fine graphite powder, based on the anodic oxidation of graphite in an electrolyte containing nitric acid. A series of tests were conducted under a range of deconsolidation conditions to develop procedures and refine the equipment. The easy-handle un-irradiated spherical fuel elements were used as samples for initial tests. It is found that the morphology, size, and element content of deconsolidated graphite matrix and free particles were notably affected by electric current intensity. During the electrolysis, the nitric acid electrolyte gradually infiltrated into the micropores of graphite matrix, and the electrochemical reaction would take place around micropore structure as well as matrix surface. With much higher surface reaction capability due to the large specific area of micropore structure, the expansion stress originated from inner surface of micropores widened the c-spacing of the layer lattice of carbonaceous matrix, which was thought to be one of the main driving force of deconsolidation. (authors)

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Thermoelectric Properties of Sb 2 Te 3 -Based Nanocomposites with Graphite

Antimony-telluride-based nanocomposite samples containing different weight fractions of graphite (Sb 2 Te 3 + x% graphite, where x = 0.0, 0.5, 1.0, and 2.5%) are synthesized and studied. The samples are produced by a solid-state reaction with the use of a ball mill. X-ray diffraction measurements show that the Sb 2 Te 3 phase is present in the nanocomposites. All of the diffraction peaks are identified as corresponding to the rhombohedral structure of symmetry R 3-bar m. No additional peaks related to graphite are observed because of its low content. Moreover, the X-ray data show the insolubility of graphite in Sb 2 Te 3 : the peaks related to Sb 2 Te 3 remain unchanged upon the addition of graphite. The thermal conductivity, thermoelectric power, and resistivity of the samples are studied in the temperature range 80 K ≤ T ≤ 320 K. The thermal conductivity k of the nanocomposite decreases several times compared to the thermal conductivity of single-crystal Sb 2 Te 3 and reaches k ≈ 0.95 W m -1 K -1 at x = 0.5%. The parameter k unsteadily depends on the content of graphite. The thermoelectric power of the nanocomposites with graphite at x = 1.0% is higher compared to that of nanostructured Sb 2 Te 3 .

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

The Influence of Fabrication Methods on Structure and Microwave Absorption Property of Fe{sub 3}O{sub 4}/rGO Composites

In this study, flake graphite is used as raw material and oxidized to produce graphene oxide (GO), and then two kinds of ferroferric oxide/reduced graphene oxide (Fe{sub 3}O{sub 4}/rGO) composites are fabricated with one-step and two-step methods, respectively. The influence of composite methods on structure and performance is investigated by FT-IR, XRD, SEM, TEM, and testing of electromagnetic parameters. The results show that there are many advantages in the one-step method for fabrication of Fe{sub 3}O{sub 4}/rGO composite, such as the composite process is simplified, the time is shortened, and the Fe{sub 3}O{sub 4}/rGO composite fabricated with the one-step method has the best microwave impedance matching property in the frequency range of 2.5–6 GHz. At the same time, it can be found that there is the Fe–O–C bond in Fe{sub 3}O{sub 4}/rGO composites fabricated with the one-step method, which results in two ways of physical recombination and chemical bonding between Fe{sub 3}O{sub 4} and rGO sheet particulates. In addition, when the mass ratio of GO and FeCl{sub 3} is 1:10, the R{sub L} value of the Fe{sub 3}O{sub 4}/rGO composite fabricated with the one-step method is minimum, and the increase of sample thickness is beneficial to improve the impedance matching property of Fe{sub 3}O{sub 4}/rGO composite in the frequency range of 2.5–6 GHz.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

“Wiring” Fe-N x -Embedded Porous Carbon Framework onto 1D Nanotubes for Efficient Oxygen Reduction Reaction in Alkaline and Acidic Media

This study presents a novel metal-organic-framework-engaged synthesis route based on porous tellurium nanotubes as a sacrificial template for hierarchically porous 1D carbon nanotubes. Furthermore, an ultrathin Fe-ion-containing polydopamine layer has been introduced to generate highly effective FeN x C active sites into the carbon framework and to induce a high degree of graphitization. The synergistic effects between the hierarchically porous 1D carbon structure and the embedded FeN x C active sites in the carbon framework manifest in superior catalytic activity toward oxygen reduction reaction (ORR) compared to Pt/C catalyst in both alkaline and acidic media. A rechargeable zinc-air battery assembled in a decoupled configuration with the nonprecious pCNT@Fe@GL/CNF ORR electrode and Ni-Fe LDH/NiF oxygen evolution reaction (OER) electrode exhibits charge–discharge overpotentials similar to the counterparts of Pt/C ORR electrode and IrO 2 OER electrode.

1D nanotubes↗

3D polymer hydrogel for high-performance atomic iron-rich catalysts for oxygen reduction in acidic media

Current platinum group metal (PGM)-free carbon nanocomposite catalysts for the oxygen reduction reaction (ORR) in acidic electrolyte often suffer from rapid degradation associated with carbon corrosion due to the use of large amount of amorphoous carbon black supports. Here, we developed a new concept of using freestanding 3D hydrogel to design support-free Fe-N-C catalysts. A 3D polyaniline (PANI)-based hydrogel was used for preparing a new type of single atomic iron site-rich catalyst, which has exhibited exceptionally enhanced activity and stability compared to conventional Fe-N-C catalysts supported on amorphous carbon blacks. The achieved performance metric on the hydrogel PANI-Fe catalysts is one of the best ever reported PGM-free catalysts, reaching a half-wave potential up to 0.83 V vs. RHE and only leaving 30 mV gap with Pt/C catalysts (60 μgPt/cm2) in challenging acidic media. Remarkable ORR stability was accomplished as well on the same catalyst evidenced by using harsh potential cycling tests. The well dispersion of atomic iron into partially graphitized carbon, featured with dominance of micropores and porous network structures, is capable of accommodating increased number of active sites, strengthening local bonding among iron, nitrogen and carbon, and facilitating mass transfer. The 3D polymer hydrogel approach would be a new pathway to advance PGM-free catalysts.

32 ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATI↗

Magmatic, hydrothermal and ore element transfer processes of the southeastern Archean Superior Province implied from electrical resistivity structure

Although magmatic- and metamorphic- derived fluids are widely recognized mineralizing agents, the role of crustal architecture in defining source and sink zones within the middle to lower crust and upper mantle of ancient orogens remains enigmatic. The globally largest and best-preserved Archean greenstone belts lie in the Superior Province, Canada. They provide an ideal location to investigate the influence of igneous construction and subsequent syn-deformational plutonism and metamorphism on the localization of metal-rich melts and fluids throughout the crustal column. Integration of three-dimensional magnetotelluric modelling and seismic reflection sections across the Abitibi subprovince reveals details of a 'whole-of-crust' magmatic and hydrothermal system. East-west low resistivity structures broadly underlie the surface traces of the major deformation zones that are host to significant gold endowment (>200 Moz), while mid-crustal cross trends suggest mineralized fluids flowed along 'pipes' within fault planes. Most low resistivity structures are inferred to represent domains containing interconnected zones of graphite and/or sulfide. Furthermore, these delineate relict mantle source/transit domains and crustal pathways enriched by the flow of magmas or metamorphic fluids genetically related to a late-stage pulse of ore-bearing magmatism, possibly as a result of slab break-off or delamination. Using the combined MT and seismic data, we develop a 3-D crustal-scale model which highlights how evolving orogenic architecture-controlled mass transfer and metallogenic processes developed.

58 GEOSCIENCES↗

Effect of growth temperature on the CVD grown Fe filled multi-walled carbon nanotubes using a modified photoresist

Fe filled carbon nanotubes were synthesized by atmospheric pressure chemical vapor deposition using a simple mixture of iron(III) acetylacetonate (Fe(acac){sub 3}) with a conventional photoresist and the effect of growth temperature (550-950 {sup o}C) on Fe filled nanotubes has been studied. Scanning electron microscopy results show that, as the growth temperature increases from 550 to 950 {sup o}C, the average diameter of the nanotubes increases while their number density decreases. High resolution transmission electron microscopy along with energy dispersive X-ray investigation shows that the nanotubes have a multi-walled structure with partial Fe filling for all growth temperatures. The graphitic nature of the nanotubes was observed via X-ray diffraction pattern. Raman analysis demonstrates that the degree of graphitization of the carbon nanotubes depends upon the growth temperature.

36 MATERIALS SCIENCE↗

Tin asymmetric membranes for high capacity sodium ion battery anodes

Sodium-ion batteries have attracted tremendous research attention as promising candidates for next generation energy storage systems due to low-cost and high abundancy. Furthermore, comparing to current Li-ion battery technology, limitations on the anode side seriously hinder the cell performance since sodium does not easily intercalate into graphite materials. Here, tin nanoparticles embedded in various asymmetric membrane structures were developed to leverage the high capacity of tin (847 mA h g -1 based on Na 15 Sn 4 ) and accommodate the significant volume expansion for long cycle life. It was demonstrated 762 mA h g -1 reversible capacity at 50 mA g -1 and stable cycling performance over 100 cycles with 92.1% capacity retention at 100 mA g -1 can be achieved for the tin asymmetric membrane electrode synthesized using polysulfone and tin tert-butoxide precursor.

25 ENERGY STORAGE↗

Structural Characteristics and Graphitizability of Tars from Thermal versus Microwave Plasma Pyrolysis of Coals

This work investigates the structural characteristics and graphitizability of tars obtained from thermal pyrolysis versus the reactive microwave (MW) plasma pyrolysis of coals. Powder River Basin (PRB) coal tars obtained by thermal pyrolysis have been compared with tars obtained from MW plasma pyrolysis containing H 2 . To study the effect of coal rank and MW plasma environment, the PRB tars have been compared with Middle Kittanning (MK) coal tars obtained from an argon–hydrogen MW plasma (hp) and an argon-CO 2 MW plasma (cdp) environment. Fourier transform infrared spectroscopy has been used for investigating the structural differences among the tar samples. The tars have been graphitized (GR-) at 2500 °C and the graphitic quality assessment has been performed using X-ray diffraction and transmission electron microscopy. MW plasma-derived tars have higher aromaticity, lower condensation, and lower oxygenated molecules compared to thermally derived tars. These advantageous features of MW plasma-derived tars lead to the formation of crystallites several times larger than thermally derived tars after graphitization. When considering coal of the same rank (bituminous), the choice of the MW plasma environment has a substantial impact on the graphitic quality of the tars. The utilization of MW plasma containing H 2 leads to a significant increase in both the crystallite diameter (by 60%) and stacking height (by 40%) compared to MW plasma containing CO 2 . Furthermore, within the same MW plasma environment, the coal rank plays a significant role in determining the crystallite diameter and stacking height of the GR-tars. In particular, GR-MK tar obtained from hp exhibits a 135% larger crystallite diameter and 85% larger stacking height compared with GR-PRB tar obtained from hp. These findings demonstrate the potential to tailor the composition of coal-derived tars and consequently influence their graphitizability by adjusting the reactive environment during MW plasma treatment.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Superconductivity at 28 K in CaB{sub 3}C{sub 3} predicted from first-principles

The structural parameters, electronic properties, and superconducting state in the graphite-like B{sub x}C{sub 1−x} intercalation compound, CaB{sub 3}C{sub 3}, have been studied using pseudopotential density functional theory within the generalized gradient approximation. Electronic and electron–phonon coupling calculations reveal that CaB{sub 3}C{sub 3} is hole conducting and superconducting with critical temperature 28.2 K, which is much higher than that of CaC{sub 6} (11.5 K). The excellent superconducting state in CaB{sub 3}C{sub 3} stems from the simultaneous presence of highly mobile and extremely confined conduction electrons, which enhances electron pairing and superconductivity. The current calculations might stimulate further theoretical and experimental investigation in search of new superconducting states in graphite-like B{sub x}C{sub 1−x} intercalated compounds.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Role of ripples in altering the electronic and chemical properties of graphene

Ripples of graphene are known to manipulate electronic and hydrogenation properties of graphitic materials. More detailed work is needed to elucidate the structure–property relationship of these systems. In this work, the density functional theory is used to compute the energy and electronic structure of the graphene models with respect to variable curvatures and hydrogen adsorption sites. The magnitude of finite bandgap opening depends on the orientation of ripples, and the hydrogen adsorption energy depends on the local curvature of graphene. An adsorbed hydrogen alters the local curvature, resulting in relatively weakened adsorption on the neighboring three sites, which gives a rationale to experimentally observed dynamic equilibrium stoichiometry (H:C = 1:4) of hydrogenated graphene. The surface diffusion transition state energy of adsorbed hydrogen is computed, which indicates that the Eley–Rideal surface recombination mechanism may be important to establish the dynamic equilibrium, instead of the commonly assumed Langmuir–Hinshelwood mechanism.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗