Structural and Electrochemical Investigation of Na+ Insertion Into λ-Mn1-xNixO2

2015 ◽  
Vol 1810 ◽  
Author(s):  
J. R. Kim ◽  
G. G. Amatucci
Keyword(s):  
High Voltage ◽  
Low Cost ◽  
Electrochemical Techniques ◽  
Positive Electrode ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
Positive Electrodes ◽  
Insertion Mechanism ◽  
First Time

AbstractIncreased demand for low cost energy storage options has expanded the scope of Na+ batteries considerably; and with the growing interest in Na-based chemistries, the importance of high voltage positive electrodes is quickly realized as the Na/Na+ redox introduces lower operating voltages as compared to Li/Li+ based electrochemical cells. The 4.7V LiMn1.5Ni0.5O4 spinel has exhibited considerable properties as a high voltage Li+ positive electrode, with a host structure (λ-Mn0.75Ni0.25O2) that may provide an analogous high voltage Na+ positive electrode. Structural and electrochemical properties of NaxMn1.56Ni0.44O4 and NaxMn2O4 are investigated for the first time[1] utilizing ex-situ, in-situ X-ray diffraction, and high-resolution electrochemical techniques to provide an insightful study of the Na+ insertion mechanism.

scholarly journals Study of ZnAl2O4 spinel nanoparticles synthesized using gelatin as organic precursor

Cerâmica ◽  
2019 ◽  
Vol 65 (374) ◽  
pp. 180-184
Author(s):  
H. P. Macedo ◽  
R. L. B. A. Medeiros ◽  
R. A. B. Nascimento ◽  
A. A. S. Oliveira ◽  
G. P. Figueredo ◽  
...  
Keyword(s):  
Spinel Structure ◽  
Pechini Method ◽  
Low Cost ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
Organic Precursor ◽  
In Situ Xrd ◽  
Znal2o4 Spinel ◽  
Adsorption Desorption

Abstract In this work, zinc aluminate spinel powders were prepared by a fast, simple, eco-friendly and low-cost modified Pechini method using commercial gelatin as the organic precursor. The materials were calcinated at 600, 700 and 800 °C and characterized by thermogravimetric analysis, in situ and ex situ X-ray diffraction (XRD), N2-adsorption/desorption isotherms and scanning electron microscopy. The results showed that single phase ZnAl2O4 particles with spinel structure were successfully obtained resulting in a high purity, nanometric, homogeneous and mesoporous materials. The in situ XRD results showed that the crystalline spinel structure of ZnAl2O4 started forming at a temperature lower than 600 °C, revealing powders with crystallite size smaller than 40 nm, which increased with increasing the temperature (91% of increase between 600 and 800 °C). The effect of calcination time showed that the materials calcinated at 600 °C for 3 h presented the higher percentage of crystallite growth due to the increase of crystallinity. The ZnAl2O4 samples retained their pore size up to 700 °C.

In Situ X-Ray Diffraction Investigations during Diffusion Anneals of Ni-Cu Thin Film Diffusion Couples

2010 ◽  
Vol 89-91 ◽  
pp. 503-508 ◽  
Author(s):  
J. Sheng ◽  
U. Welzel ◽  
Eric J. Mittemeijer
Keyword(s):  
Thermal Stresses ◽  
Stress Generation ◽  
Ex Situ ◽  
Diffusion Annealing ◽  
X Ray Diffraction ◽  
Individual Layer ◽  
X Ray ◽  
Bilayer System ◽  
Stress Changes

The stress evolution during diffusion annealing of Ni-Cu bilayers (individual layer thicknesses of 50 nm) was investigated employing ex-situ and in-situ X-ray diffraction measurements. Annealing at relatively low homologous temperatures (about 0.3 - 0.4 Tm) for durations up to about 100 hours results in considerable diffusional intermixing, as demonstrated by Auger-electron spectroscopy investigations (in combination with sputter-depth profiling). In addition to thermal stresses due to differences of the coefficients of thermal expansion of layers and substrate, tensile stress con-tributions in the sublayers arise during the diffusion anneals. The obtained stress data have been discussed in terms of possible mechanisms of stress generation. The influence of diffusion on stress development in the sublayers of the diffusion couple during heating and isothermal annealing was investigated by comparing stress changes in the bilayer system with corresponding results obtained under identical conditions for single layers of the components in the bilayer system. The specific residual stresses that emerge due to diffusion between the (sub)layers in the bilayer could thereby be identified.

scholarly journals Monoclinic and Orthorhombic NaMnO2 for Secondary Batteries: A Comparative Study

Energies ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1230
Author(s):  
Jessica Manzi ◽  
Annalisa Paolone ◽  
Oriele Palumbo ◽  
Domenico Corona ◽  
Arianna Massaro ◽  
...  
Keyword(s):  
Structural Parameters ◽  
Reversible Capacity ◽  
Beta Phase ◽  
X Ray Diffraction ◽  
Positive Electrodes ◽  
Detailed Structural Analysis ◽  
Physico Chemical ◽  
Sodium Batteries ◽  
The Impact ◽  
First Time

In this manuscript, we report a detailed physico-chemical comparison between the α- and β-polymorphs of the NaMnO2 compound, a promising material for application in positive electrodes for secondary aprotic sodium batteries. In particular, the structure and vibrational properties, as well as electrochemical performance in sodium batteries, are compared to highlight differences and similarities. We exploit both laboratory techniques (Raman spectroscopy, electrochemical methods) and synchrotron radiation experiments (Fast-Fourier Transform Infrared spectroscopy, and X-ray diffraction). Notably the vibrational spectra of these phases are here reported for the first time in the literature as well as the detailed structural analysis from diffraction data. DFT+U calculations predict both phases to have similar electronic features, with structural parameters consistent with the experimental counterparts. The experimental evidence of antisite defects in the beta-phase between sodium and manganese ions is noticeable. Both polymorphs have been also tested in aprotic batteries by comparing the impact of different liquid electrolytes on the ability to de-intercalated/intercalate sodium ions. Overall, the monoclinic α-NaMnO2 shows larger reversible capacity exceeding 175 mAhg−1 at 10 mAg−1.

Size dependent behavior of Fe3O4crystals during electrochemical (de)lithiation: an in situ X-ray diffraction, ex situ X-ray absorption spectroscopy, transmission electron microscopy and theoretical investigation

2017 ◽  
Vol 19 (31) ◽  
pp. 20867-20880 ◽  
Author(s):  
David C. Bock ◽  
Christopher J. Pelliccione ◽  
Wei Zhang ◽  
Janis Timoshenko ◽  
K. W. Knehr ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Structural Changes ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
X Ray ◽  
Size Dependent ◽  
Transmission Electron ◽  
Dependent Behavior ◽  
X Ray Absorption

Crystal and atomic structural changes of Fe3O4upon electrochemical (de)lithiation were determined.

scholarly journals A study on preparation and characterization of carbon doped TiO2 nanotubes

2014 ◽  
Vol 6 (1) ◽  
Author(s):  
Srimala Sreekantan ◽  
Roshasnorlyza Hazan ◽  
Zainovia Lockman ◽  
Ishak Mat
Keyword(s):  
Methyl Orange ◽  
Tio2 Nanotubes ◽  
Pure Tio2 ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
Methyl Orange Degradation ◽  
Doped Tio2 ◽  
X Ray ◽  
Carbon Doped

The present study is directed to clarify the influence of carbon doping on the degradation of methyl orange. TiO2 nanotubes were prepared by anodizing titanium foils in a two electrode configuration bath with titanium foil as the anode and platinum as the counter electrode. The electrochemical bathconsists of 1 M Na2SO4 with 0.7 g ammonium fluoride, NH4F. The nanotubes obtained were further doped with carbon via in-situ and ex-situ method. Incorporation of carbon on TiO2 via in-situ method is accomplished during the anodization process by introducing oxalic acid into electrolyte while theex-situ doping involves carbon incorporation into pre-fabricated TiO2 nanotube via flame annealing using carbon blackN330. Characterization such as Scanning Electron Microscope (SEM), Energy Dispersive X-ray Analysis (EDX), and X-Ray Diffraction (XRD) are used to determine the surfacemorphology, composition of dopants, and phases exists. Well ordered nanotube with good adherence and smooth surface was obtained for both methods. When the oxide was annealed, X-ray diffraction analysis revealed the presence of anatase and rutile phase. The photocatalytic properties of thepure TiO2 and carbon doped TiO2 were tested for methyl orange degradation and the result indicated that the in-situ doped TiO2 has much better degradation than the ex-situ and pure TiO2. The percentage of methyl orange degradation for in-situ was 20% and 41% higher than ex-situ doped TiO2 and pure TiO2, respectively.

scholarly journals The Viscosity and Atomic Structure of Volatile-Bearing Melilititic Melts at High Pressure and Temperature and the Transport of Deep Carbon

Minerals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 267 ◽  
Author(s):  
Vincenzo Stagno ◽  
Veronica Stopponi ◽  
Yoshio Kono ◽  
Annalisa D’Arco ◽  
Stefano Lupi ◽  
...  
Keyword(s):  
Experimental Data ◽  
High Pressure ◽  
Atomic Structure ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
High Pressure And Temperature ◽  
X Ray ◽  
Falling Sphere ◽  
Basaltic Melts

Understanding the viscosity of mantle-derived magmas is needed to model their migration mechanisms and ascent rate from the source rock to the surface. High pressure–temperature experimental data are now available on the viscosity of synthetic melts, pure carbonatitic to carbonate–silicate compositions, anhydrous basalts, dacites and rhyolites. However, the viscosity of volatile-bearing melilititic melts, among the most plausible carriers of deep carbon, has not been investigated. In this study, we experimentally determined the viscosity of synthetic liquids with ~31 and ~39 wt% SiO2, 1.60 and 1.42 wt% CO2 and 5.7 and 1 wt% H2O, respectively, at pressures from 1 to 4.7 GPa and temperatures between 1265 and 1755 °C, using the falling-sphere technique combined with in situ X-ray radiography. Our results show viscosities between 0.1044 and 2.1221 Pa·s, with a clear dependence on temperature and SiO2 content. The atomic structure of both melt compositions was also determined at high pressure and temperature, using in situ multi-angle energy-dispersive X-ray diffraction supported by ex situ microFTIR and microRaman spectroscopic measurements. Our results yield evidence that the T–T and T–O (T = Si,Al) interatomic distances of ultrabasic melts are higher than those for basaltic melts known from similar recent studies. Based on our experimental data, melilititic melts are expected to migrate at a rate ~from 2 to 57 km·yr−1 in the present-day or the Archaean mantle, respectively.

Nanocomposite cellulose fabrics with in situ generated silver nanoparticles by bioreduction method

2020 ◽  
pp. 152808372092473 ◽  
Author(s):  
Suchart Siengchin ◽  
Pawinee Boonyasopon ◽  
Vajja Sadanand ◽  
Anumakonda Varada Rajulu
Keyword(s):  
Silver Nanoparticles ◽  
Size Range ◽  
Low Cost ◽  
Aqueous Dispersion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gram Positive Bacteria ◽  
Bed Materials ◽  
Cellulose Fabrics

In the present work, nanocomposite cellulose fabrics with in situ generated silver nanoparticles were prepared by bioreduction method employing aqueous dispersion of low-cost natural turmeric powder as a reducing agent and different concentrated aqueous AgNO3 as source solutions. The prepared nanocomposite cellulose fabrics were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, and antibacterial tests. The nanocomposite cellulose fabrics had roughly spherical silver nanoparticles in the size range of 41–130 nm with an overall average of 78 nm. The X-ray analysis indicated the generation of both silver nanoparticles and Ag2O nanoparticles in the nanocomposite cellulose fabrics. The nanocomposite cellulose fabrics retained the generated AgNPs even after repeated detergent washings. The prepared nanocomposite cellulose fabrics exhibited excellent antibacterial activity against both the Gram-negative and Gram-positive bacteria and hence can be considered as antibacterial hospital-bed materials, apparels, etc.

PHASE FORMATION AND TEXTURE DEVELOPMENT IN AG-SHEATHED Bi, Pb(2223) TAPES STUDIED BY DIFFERENT IN-SITU AND EX-SITU DIFFRACTION TECHNIQUES

2000 ◽  
Vol 14 (25n27) ◽  
pp. 2688-2693 ◽  
Author(s):  
E. GIANNINI ◽  
E. BELLINGERI ◽  
F. MARTI ◽  
M. DHALLÉ ◽  
V. HONKIMÄKI ◽  
...  
Keyword(s):  
High Energy ◽  
Texture Development ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scattering Geometry ◽  
Reflection Geometry ◽  
Comparison Of The Results ◽  
In Situ Neutron Diffraction

In-situ and ex-situ high energy (80÷88 keV) X-Ray diffraction from a synchrotron radiation source were performed on multifilamentary Bi, Pb(2223)/Ag tapes using a transmission scattering geometry. Several thermo-mechanical procedures were compared, focusing mainly on the texture development of both Bi, Pb(2212) and Bi, Pb(2223) phases. The effect of the periodic pressing on the texture and on the critical current is elucidated. The texture development of the Bi, Pb(2212) phase prior to its transformation into Bi, Pb(2223) was directly observed in-situ at high temperature by using a dedicated high-energy X-ray compatible furnace and a high resolution Image Plate detector. A sharp increase of the Bi, Pb(2212) grain orientation along the [00l] direction was found to occur only above 750°C. Normal state transport measurements are in full agreement with the formation mechanism and with the texture development observed. A comparison of the results with the ones provided by in-situ neutron diffraction and standard low-energy XRD in a reflection geometry is presented.

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