scholarly journals Sodium-Vanadium Bronze Na9V14O35: An Electrode Material for Na-Ion Batteries

Molecules ◽  
2021 ◽  
Vol 27 (1) ◽  
pp. 86
Author(s):  
Maria A. Kirsanova ◽  
Alexey S. Akmaev ◽  
Mikhail V. Gorbunov ◽  
Daria Mikhailova ◽  
Artem M. Abakumov
Keyword(s):  
Negative Electrode ◽  
X Ray Diffraction ◽  
Conversion Reaction ◽  
X Ray ◽  
Electroactive Material ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Electrochemical Capacity ◽  
Silica Ampoule ◽  
Electron Energy Loss

Na9V14O35 (η-NaxV2O5) has been synthesized via solid-state reaction in an evacuated sealed silica ampoule and tested as electroactive material for Na-ion batteries. According to powder X-ray diffraction, electron diffraction and atomic resolution scanning transmission electron microscopy, Na9V14O35 adopts a monoclinic structure consisting of layers of corner- and edge-sharing VO5 tetragonal pyramids and VO4 tetrahedra with Na cations positioned between the layers, and can be considered as sodium vanadium(IV,V) oxovanadate Na9V104.1+O19(V5+O4)4. Behavior of Na9V14O35 as a positive and negative electrode in Na half-cells was investigated by galvanostatic cycling against metallic Na, synchrotron powder X-ray diffraction and electron energy loss spectroscopy. Being charged to 4.6 V vs. Na+/Na, almost 3 Na can be extracted per Na9V14O35 formula, resulting in electrochemical capacity of ~60 mAh g−1. Upon discharge below 1 V, Na9V14O35 uptakes sodium up to Na:V = 1:1 ratio that is accompanied by drastic elongation of the separation between the layers of the VO4 tetrahedra and VO5 tetragonal pyramids and volume increase of about 31%. Below 0.25 V, the ordered layered Na9V14O35 structure transforms into a rock-salt type disordered structure and ultimately into amorphous products of a conversion reaction at 0.1 V. The discharge capacity of 490 mAh g−1 delivered at first cycle due to the conversion reaction fades with the number of charge-discharge cycles.

High Spatial Resolution Compositional Analysis at Interfaces

1980 ◽  
Vol 38 ◽  
pp. 356-359
Author(s):  
John B. Vander Sande ◽  
Thomas F. Kelly ◽  
Douglas Imeson
Keyword(s):  
Electron Microscope ◽  
High Spatial Resolution ◽  
Compositional Analysis ◽  
Scanning Transmission Electron Microscope ◽  
Thin Specimen ◽  
X Ray ◽  
Volume Of Interest ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Electron Energy Loss

In the scanning transmission electron microscope (STEM) a fine probe of electrons is scanned across the thin specimen, or the probe is stationarily placed on a volume of interest, and various products of the electron-specimen interaction are then collected and used for image formation or microanalysis. The microanalysis modes usually employed in STEM include, but are not restricted to, energy dispersive X-ray analysis, electron energy loss spectroscopy, and microdiffraction.

Phase Transformation of Powdered Material by Using Metal Jet

2012 ◽  
Vol 706-709 ◽  
pp. 741-744 ◽  
Author(s):  
Akio Kira ◽  
Ryuichi Tomoshige ◽  
Kazuyuki Hokamoto ◽  
Masahiro Fujita
Keyword(s):  
Phase Transformation ◽  
Powdered Material ◽  
Scanning Transmission Electron Microscope ◽  
Ultrahigh Pressure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Metal Jet ◽  
Very High

The various techniques of phase transformation of the material have been proposed by many researchers. We have developed several devices to generate the ultrahigh pressure by using high explosive. One of them uses metal jets. It is expected that the ultrahigh pressure occurs by the head-on collision between metal jets, because the velocity of the metal jet is very high. By mixing a powdered material with metal jets, the pressure of the material becomes high. The purpose of this study is to transform the phase of the powdered material by using this high pressure. The powders of the graphite and hBN were applied. The synthesis to the diamond and cBN was confirmed by X-ray diffraction (XRD). In this paper, the mechanism of the generation of the ultrahigh pressure is explained and the results of the observation of the powder by using scanning transmission electron microscope (STEM) are reported.

Core–shell structures with metallic silver as nucleation agent of low expansion phases in BaO/SrO/ZnO/SiO2 glasses

CrystEngComm ◽  
2019 ◽  
Vol 21 (29) ◽  
pp. 4373-4386 ◽  
Author(s):  
Christian Thieme ◽  
Michael Kracker ◽  
Katrin Thieme ◽  
Christian Patzig ◽  
Thomas Höche ◽  
...  
Keyword(s):  
Scanning Transmission Electron Microscopy ◽  
Nucleating Agent ◽  
Shell Structures ◽  
Metallic Silver ◽  
X Ray Diffraction ◽  
Nucleation Agent ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Transmission

The role of silver as a nucleating agent in BaO/SrO/ZnO/SiO2 glasses is studied with a range of microstructure-characterization techniques, such as scanning transmission electron microscopy, ultraviolet-visible spectroscopy, and X-ray diffraction.

High-Pressure, High-Temperature Synthesis of Superhard Boron Suboxide

1995 ◽  
Vol 410 ◽  
Author(s):  
H. Hubert ◽  
L. A. J. Garvie ◽  
K. Leinenweber ◽  
P. R. Buseck ◽  
W. T. Petuskeyt ◽  
...  
Keyword(s):  
Pressure Range ◽  
X Ray Diffraction ◽  
Temperature Synthesis ◽  
X Ray ◽  
High Temperature Synthesis ◽  
Transmission Electron ◽  
High Pressure High Temperature ◽  
Boron Suboxide ◽  
Electron Energy Loss ◽  
Rhombohedral Boron

ABSTRACTA multianvil device was used to investigate the formation of BxO phases produced in the 2 to 10 GPa pressure range with temperatures between 1000 and 1800 °C.Amorphous and crystalline B and BP were oxidized using B2O3 and CrO3. Using powder X-ray diffraction and parallel electron energy-loss spectroscopy (PEELS), we were unable to detect graphitic or diamondstructured B2O, reported in previous studies. The refractory boride B6O, which has the α-rhombohedral boron structure, is the dominant suboxide in the P and T range of our investigation. PEELS with a transmission electron microscope was used to characterize the boron oxides.

Obtaining the structure factors for an epitaxial film using Cu X-ray radiation

2013 ◽  
Vol 46 (6) ◽  
pp. 1749-1754 ◽  
Author(s):  
P. Wadley ◽  
A. Crespi ◽  
J. Gázquez ◽  
M.A. Roldán ◽  
P. García ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Thin Films ◽  
Structure Factor ◽  
Tetragonal Symmetry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Structure Factors ◽  
Scanning Transmission

Determining atomic positions in thin films by X-ray diffraction is, at present, a task reserved for synchrotron facilities. Here an experimental method is presented which enables the determination of the structure factor amplitudes of thin films using laboratory-based equipment (Cu Kα radiation). This method was tested using an epitaxial 130 nm film of CuMnAs grown on top of a GaAs substrate, which unlike the orthorhombic bulk phase forms a crystal structure with tetragonal symmetry. From the set of structure factor moduli obtained by applying this method, the solution and refinement of the crystal structure of the film has been possible. The results are supported by consistent high-resolution scanning transmission electron microscopy and stoichiometry analyses.

Fabrication of boron carbonitride (BCN) nanotubes and giant fullerene cages

2010 ◽  
Vol 88 (12) ◽  
pp. 1256-1261 ◽  
Author(s):  
Guifang Sun ◽  
Faming Gao ◽  
Li Hou
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
The Novel ◽  
X Ray Diffraction ◽  
Boron Carbonitride ◽  
X Ray ◽  
Transmission Electron ◽  
New Form ◽  
First Time ◽  
Electron Energy Loss

Boron carbonitride (BCN) nanotubes have been successfully prepared using NH4Cl, KBH4, and ZnBr2 as the reactants at 480 °C for 12 h by a new benzene-thermal approach in a N2 atmosphere. As its by-product, a new form of carbon regular hexagonal nanocages are observed. The samples are characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), transmission electron diffraction (TED), electron energy loss spectroscopy (EELS), and high-resolution transmission electron microscopy (HRTEM). The prepared nanotubes have uniform outer diameters in the range of 150 to 500 nm and a length of up to several micrometerss. The novel carbon hexagonal nanocages have a typical size ranging from 100 nm to 1.5 µm, which could be the giant fullerene cages of [Formula: see text] (N = 17∼148). So, high fullerenes are observed for the first time. The influences of reaction temperature and ZnBr2 on products and the formation mechanism of BCN nanotubes are discussed.

scholarly journals Synthesis and Structure of novel Luminescent lanthanide organic frameworks.

2014 ◽  
Vol 70 (a1) ◽  
pp. C1259-C1259
Author(s):  
Mohammed S. M. Abdelbaky ◽  
Zakariae Amghouz ◽  
Santiago Granda
Keyword(s):  
Thermal Analyses ◽  
Luminescence Properties ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Carboxylate Groups ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Conventional Electrode ◽  
Li Ion

Lanthanide-Organic frameworks (LnOFs) are currently attracting increasing attention due to their excellent luminescence properties, in which both Ln3+ and organic linkers can be used to give rise to luminescence materials with increased brightness and emission quantum yield [1,2]. Lithium doped MOFs are of particular interest due to the recent studies showing enhanced H2 uptake, as well as promising candidates for replacing the conventional electrode in Li-ion batteries [3,4]. Herein, novel Lithium-lanthanide frameworks based on a rigid dicarboxylic acid, formulated as [LiLn(BDC)2(H2O)·2(H2O)] (Ln = Y, Dy, Ho, Er, Yb, Y1-xEux, Y1-xTbx and H2BDC = Terephthalic acid), have been obtained as single phases under hydrothermal conditions. The crystal structures were solved by single-crystal X-ray diffraction and the bulk characterized by powder X-ray diffraction (PXRD), thermal analyses (TG-MS and DSC), vibrational spectroscopy (FTIR), scanning/transmission electron microscopy (SEM-EDX, TEM, SAED, STEM-EDX), and powder X-ray thermodiffractometry (HT-XRD). All compounds are isostructural (monoclinic P21/c, a = 11.6365(7) Å, b =16.0920(2) Å, c = 13.2243(8) Å and β = 132.23(1)° for Ln = Y [5]) and possess a 3D framework with 1D trigonal channels running along the [101] direction contain water molecules. The structure is built up of unusual four-membered rings formed by edge- and vertex-shared {LnO8} and {LiO4} polyhedra. The four-membered rings are isolated and connected to each other via carboxylate groups. Topologically, the 3D frameworks belongs to a new 2-nodal 3,10-c net with point symbol of {4.5^2}2{4^14.5^10.6^18.7.8^2}. HT-XRD reveals that the compounds undergo phase transformation upon dehydration process which is a reversible process involving a spontaneous rehydration characterized by fast kinetic. The luminescence properties of selected compounds are also studied.

Above Room-Temperature Ferromagnetism in GaN Powders by Calcinations with CuO

2006 ◽  
Vol 941 ◽  
Author(s):  
Lori Noice ◽  
Bjoern Seipel ◽  
Rolf Erni ◽  
Amita Gupta ◽  
Chunfei Li ◽  
...  
Keyword(s):  
Copper Oxide ◽  
Room Temperature Ferromagnetism ◽  
Scanning Probe ◽  
Electronic Effects ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Oxide Phases ◽  
Probe Transmission ◽  
Electron Energy Loss

ABSTRACTGallium nitride powders were calcined with copper oxide in either air or N2 and analyzed by means of powder X-ray diffraction (XRD), high-resolution parallel illumination (HRTEM) and scanning probe transmission electron microscopy (STEM), energy dispersive X-ray spectroscopy (EDXS), and electron energy loss spectroscopy (EELS) in order to address the structural and electronic effects of Cu-incorporation into GaN. Gallium oxide and multiple copper oxide phases corresponding to the calcination environment were detected. Significant changes in the lattice parameters and electronic structure of the N2-processed GaN indicate incorporation of both copper and oxygen into the GaN lattice as well as changes in the chemical bonding due to the calcinations process. SQUID magnetometer measurements at 300 K demonstrated ferromagnetism in selected samples.

scholarly journals MINERALOGICAL AND SPECTROSCOPIC STUDY OF NESQUEHONITE SYNTHESIZED BY REACTION OF GASEOUS CO2 WITH MG CHLORIDE SOLUTION

2017 ◽  
Vol 50 (4) ◽  
pp. 2009
Author(s):  
V. Skliros ◽  
A. Anagnostopoulou ◽  
P. Tsakiridis ◽  
M. Perraki
Keyword(s):  
Scanning Transmission Electron Microscopy ◽  
Chloride Solution ◽  
Raw Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Raman Spectroscopic ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Permanent Storage ◽  
Ir And Raman

Nesquehonite, a hydrous carbonate with promising uses such as building raw material and treatment of wastewaters, was synthesized under low pressure conditions by reaction of gaseous CO2 with Mg chloride solution and it was studied by means of X-Ray Diffraction, optical and scanning/transmission electron microscopy, and FTIR and Raman spectroscopic methods. Synthesized nesquehonite forms elongated fibers, exhibiting transparent to translucent diaphaneity and vitreous luster. It is characterized by high crystallinity. IR and Raman spectroscopy indicated the presence of OHand HCO3 - in the crystal structure of nesquehonite. The nesquehonite synthesis described herein constitutes a potential permanent storage of CO2 emissions.

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