30 research outputs found

    Solid state lithiation-delithiation of sulphur in sub-nano confinement: a new concept for designing lithium-sulphur batteries.

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    We investigate the detailed effects and mechanisms of sub-nano confinement on lithium-sulfur (Li-S) electrochemical reactions in both ether-based and carbonate-based electrolytes. Our results demonstrate a clear correlation between the size of sulfur confinement and the resulting Li-S electrochemical mechanisms. In particular, when sulfur is confined within sub-nano pores, we observe identical lithium-sulfur electrochemical behavior, which is distinctly different from conventional Li-S reactions, in both ether and carbonate electrolytes. Taken together, our results highlight the critical importance of sub-nano confinement effects on controlling solid-state reactions in Li-S electrochemical systems

    Templated fabrication of InSb nanowires for nanoelectronics

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    Among various ways to produce nanowires, anodic alumina membrane-(AAM-) based synthesis has constantly received much attention, because AAM has a uniform and parallel porous nanostructure which makes it an ideal template material for fabricating highly ordered nanostructures. In this paper, we report fabrication of InSb nanowire arrays with diameter of 200 nm and 30 nm by direct current electrodeposition inside the nanochannels of anodic alumina membranes without subsequent annealing. The nanowires have four major growth directions, (220) being the most dominant with structure defects such as twins. The transmission electron microscopy (TEM) and scanning electron microscopy (SEM) results demonstrate that these InSb nanowires are uniform with diameters about 200 nm and 30 nm, corresponding to the pore diameter of the AAMs. The I-V measurement of a single nanowire is also reported with encouraging preliminary results

    Time-resolved dissolution elucidates the mechanism of zeolite MFI crystallization

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    Zeolite crystal growth mechanisms are not fully elucidated owing to their complexity wherein the formation of a particular zeolite can occur by more than one crystallization pathway. Here, we have conducted time-resolved dissolution experiments of MFI-type zeolite crystals in ammonium fluoride medium where detailed structural analysis allowed us to extrapolate and elucidate the possible mechanism of nucleation and crystal growth. A combination of electron and scanning probe microscopy shows that dissolution initiates preferentially at lattice defects and progressively removes defect zones to reveal a mosaic structure of crystalline domains within each zeolite crystal. This mosaic architecture evolves during the growth process, reflecting the changing conditions of zeolite formation that can be retroactively assessed during zeolite crystal dissolution. Moreover, a more general implication of this study is the establishment that dissolution can be used successfully as an ex situ technique to uncover details about crystal growth features inaccessible by other methods

    Electrochemical Lithiation of Covalently Bonded Sulfur in Vulcanized Polyisoprene

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    We report the synthesis of vulcanized polyisoprene (SPIP) nanowires and an investigation of the electrochemical lithiation mechanism of the covalently bonded sulfur bridges in SPIP. Electrochemical analysis demonstrates that the sulfur chains in SPIP have distinct electrochemical signatures from those that are characteristic of bulk elemental sulfur. The cyclic voltammetry and galvanostatic cycling data show a distinct multistep charge-transfer process and solid-state lithium–sulfur reaction behavior, and it is clear that this new material provides a promising basis for the development of cathodes for rechargeable batteries. Chemical changes due to the lithiation process are studied using Raman and X-ray photoelectron spectroscopy, on the basis of which new lithiation mechanisms of covalently bonded sulfur are proposed
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