Ag4V2O6F2 (SVOF): a high silver density phase and potential new cathode material for implantable cardioverter defibrillators

The electrochemical reactivity of the cathode material Ag 4V 2O 6F 2 (SVOF) versus lithium, with a particular emphasis on the lithium insertion mechanism, was studied by means of the complementary techniques in situ X-ray diffraction, electron paramagnetic resonance, and high-resolution transmisssion electron microscopy. This study confirms the initial reports of a high capacity for SVOF of 148 mAh/g above 3 V and that the reduction of silver above 3 V (vs Li (+)/Li (0)) leads to a loss of SVOF crystallinity until it becomes completely amorphous between the third and fourth lithiums inserted. Next, vanadium is reduced between 2.5 and 1.5 V (vs Li (+)/Li (0)) for the fifth and sixth lithiums inserted. In addition, the polarization within the cathode is significantly lower for the vanadium reduction than for the silver reduction. The silver metal morphologies consisted of nanoparticles ( approximately 5 nm diameter) and dendrites and were both seen in samples of lithiated SVOF.     

Ag2V4O11: from primary to secondary battery

Journal of Solid State Electrochemistry - Ag2V4O11 (silver vanadium oxide, SVO) is the positive electrode in primary lithium/SVO batteries that had known an extraordinary success as a power source...     

V2O2F4(H2O)2·H2O: a new V4+ layer structure related to VOF3

V^IV oxyfluorides are of interest as frustrated magnets. The successful synthesis of two‐dimensionally connected vanadium(IV) oxyfluoride structures generally requires the use of ionic liquids as solvents. During solvothermal synthesis experiments aimed at producing two‐ and three‐dimensional vanadium(IV) selenites with triangular lattices, the title compound, diaquatetra‐μ‐fluorido‐dioxidodivanadium(IV) monohydrate, V₂O₂F₄(H₂O)₂·H₂O, was discovered and features a new infinite V⁴⁺‐containing two‐dimensional layer comprised of fluorine‐bridged corner‐ and edge‐sharing VOF₄(H₂O) octahedral building units. The synthesis was carried out under solvothermal conditions. The V⁴⁺ centre exhibits a typical off‐centring, with a short V=O bond and an elongated trans‐V—F bond. Hydrogen‐bonded water molecules occur between the layers. The structure is related to previously reported vanadium oxyfluoride structures, in particular, the same layer topology is seen in VOF₃.     

A new oxoanion: [IO]3- containing I(V) with a stereochemically active lone-pair in the silver uranyl iodate tetraoxoiodate(V), Ag4(UO2)4(IO3)2(IO4)2O2

The hydrothermal reaction of elemental Ag, or water-soluble silver sources, with UO3 and I2O5 at 200 degrees C for 5 days yields Ag4(UO2)4(IO3)2(IO4)2O2 in the form of orange fibrous needles. Single-crystal X-ray diffraction studies on this compound reveal a highly complex network structure consisting of three interconnected low-dimensional substructures. The first of these substructures are ribbons of UO8 hexagonal bipyramids that edge-share to form one-dimensional chains. These units further edge-share with pentagonal bipyramidal UO7 units to create ribbons. The edges of the ribbons are partially terminated by tetraoxoiodate(V), [IO4]3-, anions. The uranium oxide ribbons are joined by bridging iodate ligands to yield two-dimensional undulating sheets. These sheets help to form, and are linked together by, one-dimensional chains of edge-sharing AgO7 capped octahedral units and ribbons formed by corner-sharing capped trigonal planar AgO4 polyhedra, AgO6 capped square pyramids, and AgO6 octahedra. The [IO4]3- anions in Ag4(UO2)4(IO3)2)(IO4)2O2 are tetraoxoiodate(V), not metaperiodate, and contain I(V) with a stereochemically active lone-pair. Bond valence sum calculations are consistent with this formulation. Differential scanning calorimetry measurements show distinctly different thermal behavior of Ag4(UO2)4(IO3)2(IO4)2O2 versus other uranyl iodate compounds with endotherms at 479 and 494 degrees C. Density functional theory (DFT) calculations demonstrate that the approximate C2v geometry of the [IO4]3- anion can be attributed to a second-order Jahn-Teller distortion. DFT optimized geometry for the [IO4]3- anion is in good agreement with those measured from single-crystal X-ray diffraction studies on Ag4(UO2)4(IO3)2(IO4)2O2.     

Self-coiling of Ag2V4O11 nanobelts into perfect nanorings and microloops

Free-standing Ag2V4O11 nanorings and microloops have been synthesized by a simple hydrothermal process without any template or surfactant. The Ag2V4O11 nanorings and microloops have preferred growth direction along the [30] plane and are formed by the self-rolling of Ag2V4O11 nanobelts.     

ChemInform Abstract: V2O2F4 (H2O)2·H2O: A New V4+ Layer Structure Related to VOF3.

Single crystals of the title compound are prepared by hydrothermal reaction of VF₃ and H₂SeO₃ in ethylene glycol/HF (40%) in the presence of Et₂NH (autoclave, 393 K, 4 d).     

Synthesis and characterization of open-framework niobium silicates: Rb2(Nb2O4)(Si2O6).H2O and the dehydrated phase Rb2(Nb2O4)(Si2O6)

A new niobium(V) silicate, Rb(2)(Nb(2)O(4))(Si(2)O(6)).H(2)O, has been synthesized by a high-temperature, high-pressure hydrothermal method and characterized by single-crystal X-ray diffraction, thermogravimetric analysis, and solid-state NMR spectroscopy. It crystallizes in the tetragonal space group P4(3)22 (No. 95) with a = 7.3431(2) A, c = 38.911(3) A, and Z = 8. Its structure contains tetrameric units of the composition Nb(4)O(18), which share corners to form a layer of niobium oxide. The Nb-O layer is a slice of the pyrochlore structure. Neighboring Nb-O layers are linked by vierer single-ring silicates generating eight-ring and six-ring channels running parallel to <100> directions, in which the Rb(+) cations and water molecules reside. The tantalum analogue was prepared and characterized by powder X-ray diffraction. Upon heating to 500 degrees C, Rb(2)(Nb(2)O(4))(Si(2)O(6)).H(2)O loses lattice water molecules, while the framework structure is retained to give the anhydrous compound Rb(2)(Nb(2)O(4))(Si(2)O(6)), whose structure was also characterized by single-crystal X-ray diffraction. The dehydrated sample absorbs water reversibly, as indicated by powder X-ray diffraction. Rb(2)(Nb(2)O(4))(Si(2)O(6)) crystallizes in the tetragonal space group I4(1) (No. 80) with a = 10.2395(6) A, c = 38.832(3) A, and Z = 16.     

Determination of silver carbonate in silver oxide(Ag2O) by infrared spectroscopy

Silver carbonate in silver oxide (Ag(2)O) is determined quantitatively by infrared spectroscopy. The deviation of the results from a mean line is +/-0.2% of Ag(2)CO(3) for samples containing only normal silver carbonate, and +/-0.4% of Ag(2)CO(3) for samples containing both normal and basic silver carbonate.     

Potassium silver tin selenide,K2Ag2Sn2Se6

The title compound was synthesized by a reactive salt reaction at 773 K over a period of 5 d. It has a one-dimensional chain structure consisting of K⁺ cations and one-dimensional [Ag₂Sn₂Se₆]²⁻ anions. The chain is constructed by edge-sharing bitetrahedral [Sn₂Se₆] units connected in a 1:2 ratio via linear Ag⁺ ions.     

Subsolidus phase equilibria in the V9Mo6O40-Cr2(MoO4)3 system

The V₉Mo₆O₄₀?Cr₂(MoO₄)₃ system has been investigated using the differential thermal analysis (DTA) and X-ray phase diffraction methods. The system has been found not to be a real two-component system over the whole component system.