263 research outputs found
Magnetodielectric effect of Graphene-PVA Nanocomposites
Graphene-Polyvinyl alcohol (PVA) nanocomposite films with thickness were synthesized by solidification of PVA in a solution with dispersed
graphene nanosheets. Electrical conductivity data were explained as arising due
to hopping of carriers between localized states formed at the graphene-PVA
interface. Dielectric permittivity data as a function of frequency indicated
the occurrence of Debye-type relaxation mechanism. The nanocomposites showed a
magnetodielectric effect with the dielectric constant changing by 1.8% as the
magnetic field was increased to 1 Tesla. The effect was explained as arising
due to Maxwell-Wagner polarization as applied to an inhomogeneous
two-dimensional,two-component composite model. This type of nanocomposite may
be suitable for applications involving nanogenerators.Comment: 13 pages, 11 figure
Multiple Redox Modes in the Reversible Lithiation of High-Capacity, Peierls-Distorted Vanadium Sulfide.
This is the author accepted manuscript. The final version is available from ACS via http://dx.doi.org/10.1021/jacs.5b03395Vanadium sulfide VS4 in the patronite mineral structure is a linear chain compound comprising vanadium atoms coordinated by disulfide anions [S2](2-). (51)V NMR shows that the material, despite having V formally in the d(1) configuration, is diamagnetic, suggesting potential dimerization through metal-metal bonding associated with a Peierls distortion of the linear chains. This is supported by density functional calculations, and is also consistent with the observed alternation in V-V distances of 2.8 and 3.2 Å along the chains. Partial lithiation results in reduction of the disulfide ions to sulfide S(2-), via an internal redox process whereby an electron from V(4+) is transferred to [S2](2-) resulting in oxidation of V(4+) to V(5+) and reduction of the [S2](2-) to S(2-) to form Li3VS4 containing tetrahedral [VS4](3-) anions. On further lithiation this is followed by reduction of the V(5+) in Li3VS4 to form Li3+xVS4 (x = 0.5-1), a mixed valent V(4+)/V(5+) compound. Eventually reduction to Li2S plus elemental V occurs. Despite the complex redox processes involving both the cation and the anion occurring in this material, the system is found to be partially reversible between 0 and 3 V. The unusual redox processes in this system are elucidated using a suite of short-range characterization tools including (51)V nuclear magnetic resonance spectroscopy (NMR), S K-edge X-ray absorption near edge spectroscopy (XANES), and pair distribution function (PDF) analysis of X-ray data.SB acknowledges Schlumberger Stichting Fund and European Research Council (EU ERC) for funding. JC thanks BK21 plus project of Korea. We thank Phoebe Allan and Andrew J. Morris, University of Cambridge, for useful discussions. We also thank Trudy Bolin and Tianpin Wu of Beamline 9-BM, Argonne National Laboratory for help with XANES measurements. The DFT calculations were performed at the UCSB Center for Scientific Computing at UC Santa Barbara, supported by the California Nanosystems Institute (NSF CNS-0960316), Hewlett-Packard, and the Materials Research Laboratory (DMR-1121053). This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357
Effect of feeding ratios on the structure and electrochemical performance of graphite oxide/polypyrrole nanocomposites
High-conductivity graphene nanocomposite via facile, covalent linkage of gold nanoparticles to graphene oxide
Electrocatalytic Hydrogen Evolution and Oxygen Reduction on Polyoxotungstates/Graphene Nanocomposite Multilayers
Advantaging Synergy Photocatalysis with Graphene‐Related Carbon as a Counterpart Player of Titania
Synthesis of a stable sol of Mn2+-doped ZnS nanoparticles by low-temperature heating of sulfide precipitate in ethylene glycol
Epoxidization of allyl chloride by combined oxidation with ethylbenzene on layered compounds of graphite with transition-metal chlorides
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