2018
DOI: 10.1016/j.jallcom.2018.07.322
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The effects of Fe@C nanoparticles on the lithium storage performance of VS4 anode

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Cited by 12 publications
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“…[ 13 ] As one of the transition metal sulfides, vanadium‐based sulfides have been attracting interest due to the abundant resource and high theoretical capacity deriving in the main from their alterable valence state from V 5+ to V 0 . [ 14–16 ] The V layers of vanadium disulfide (VS 2 ) are located in the middle place between the sulfur layers and possess larger interlayer spacing of 5.76 Å, [ 17,18 ] which is much bigger than that of lithium ion (0.76 Å), [ 19 ] facilitating the dynamics process and enhancing the storage performance of lithium ions. [ 20 ] The theoretical capacity of VS 2 anode material for LIB is 466 mAh g −1 , which is superior to the 372 mAh g −1 of graphite.…”
Section: Introductionmentioning
confidence: 99%
“…[ 13 ] As one of the transition metal sulfides, vanadium‐based sulfides have been attracting interest due to the abundant resource and high theoretical capacity deriving in the main from their alterable valence state from V 5+ to V 0 . [ 14–16 ] The V layers of vanadium disulfide (VS 2 ) are located in the middle place between the sulfur layers and possess larger interlayer spacing of 5.76 Å, [ 17,18 ] which is much bigger than that of lithium ion (0.76 Å), [ 19 ] facilitating the dynamics process and enhancing the storage performance of lithium ions. [ 20 ] The theoretical capacity of VS 2 anode material for LIB is 466 mAh g −1 , which is superior to the 372 mAh g −1 of graphite.…”
Section: Introductionmentioning
confidence: 99%
“…It is composed of V 4+ ions that are coordinated with sulfur-containing dimeric S 2 2– species . Performance-wise, VS 4 , when used as an electrode material, demonstrates an exceptionally high theoretical capacity of 1196 mAh/g, a finding ascribable not only to its rich redox chemistry and high sulfur content but also to its linear-chain-like structure, which likely facilitates its favorable charge-transfer kinetics, due to weak neighboring-chain interactions . Specifically, its loose stacking structure, constructed from atomic chains held together by weak van der Waals forces and characterized by an interval of 5.83 Å, provides for a number of potential sites for ion insertion/extraction.…”
Section: Introductionmentioning
confidence: 99%
“…Among them, transition-metal chalcogenides have been extensively investigated because of their inherent advantages including high theoretical capacity, low cost, natural abundance, and intrinsic safety. In recent years, patronite (VS 4 ) has attracted growing academic interest because of its unique crystal structure and high theoretical capacity. Patronite VS 4 is monoclinic and belongs to the space group I 2/ c in which VS 8 enneahedron, composed of V 4+ ions coordinated to disulfur dianion (S 2 2– ), extends along the c axis by alternately sharing the edge and surface, forming a unique one-dimensional (1D) chain structure (Figure S1a). The theoretical capacity of the VS 4 anode for a lithium battery could be determined as 1196 mA h g –1 (VS 4 + 8Li + + 8e – ↔ 4Li 2 S + V), , and its potential advantages can be summarized as follows: (1) because the 1D chains are primarily bonded together through the van der Waals force, the large spacing between the chains can provide more potential storage sites for the lithium ion and rapid channels for charge mobility (Figure S1b), thereby improving the charge-transfer kinetics; (2) a high content of sulfur (71.6 wt %) can not only ameliorate the polarity of electrode materials but also improve the contact with the electrolyte solution; and (3) the variety of vanadium oxidation states and the transformation reaction between S 2 2– and S 2– are conducive to improving the theoretical capacity . To date, considerable efforts have been dedicated to exploring the lithium-ion storage mechanism and improving the electrochemical performance of the VS 4 anode. ,, Unfortunately, the huge volume expansion/contraction and sluggish electrode reaction kinetics during charge/discharge processes would lead to pulverization of the active materials and poor electrical contact between the current collector and the active materials, causing a rapid degradation of the capacity.…”
Section: Introductionmentioning
confidence: 99%