scholarly journals Doped Nanoscale NMC333 as Cathode Materials for Li-Ion Batteries

Materials ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 2899 ◽  
Author(s):  
Hashem ◽  
Abdel-Ghany ◽  
Scheuermann ◽  
Indris ◽  
Ehrenberg ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Chelating Agent ◽  
Li Ion Batteries ◽  
X Ray Diffraction ◽  
Al Doping ◽  
X Ray ◽  
Transmission Electron ◽  
Li Ion ◽  
Diffraction Patterns

A series of Li(Ni1/3Mn1/3Co1/3)1−xMxO2 (M = Al, Mg, Zn, and Fe, x = 0.06) was prepared via sol-gel method assisted by ethylene diamine tetra acetic acid as a chelating agent. A typical hexagonal α-NaFeO2 structure (R-3m space group) was observed for parent and doped samples as revealed by X-ray diffraction patterns. For all samples, hexagonally shaped nanoparticles were observed by scanning electron microscopy and transmission electron microscopy. The local structure was characterized by infrared, Raman, and Mössbauer spectroscopy and 7Li nuclear magnetic resonance (Li-NMR). Cyclic voltammetry and galvanostatic charge-discharge tests showed that Mg and Al doping improved the electrochemical performance of LiNi1/3Mn1/3Co1/3O2 in terms of specific capacities and cyclability. In addition, while Al doping increases the initial capacity, Mg doping is the best choice as it improves cyclability for reasons discussed in this work.

Sol-gel processing of nanocrystalline haematite thin films

1997 ◽  
Vol 12 (6) ◽  
pp. 1441-1444 ◽  
Author(s):  
L. Armelao ◽  
A. Armigliato ◽  
R. Bozio ◽  
P. Colombo
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Transmission Electron Microscopy ◽  
Raman Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Single Particles ◽  
X Ray ◽  
Transmission Electron ◽  
Gel Processing

The microstructure of Fe2O3 sol-gel thin films, obtained from Fe(OCH2CH3)3, was investigated by x-ray diffraction (XRD), transmission electron microscopy (TEM), and Raman spectroscopy. Samples were nanocrystalline from 400 °C to 1000 °C, and the crystallized phase was haematite. In the coatings, the α–Fe2O3 clusters were dispersed as single particles in a network of amorphous ferric oxide.

Homogeneity in the Polyether Alkoxide Sol‐Gel Synthesis of YBa2Cu3O7-δ

1994 ◽  
Vol 346 ◽  
Author(s):  
Carol S. Houk ◽  
Gary A. Burgoine ◽  
Catherine J. Page
Keyword(s):  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Diffraction Patterns ◽  
Mapping Techniques ◽  
Starting Solutions ◽  
Average Size ◽  
Sol Gel Synthesis ◽  
Elemental Maps

ABSTRACTWe have investigated the homogeneity of sol‐gel derived YBa2Cu307‐s from the solution phase to the final product using transmission electron microscopy (TEM), x‐ray diffraction (XRD), and Energy Dispersive X‐ray (EDX) lateral mapping techniques. The starting solutions contain stoichiometric amounts of the metal 2‐(2‐methoxyethoxy)ethoxide components in 2‐(2‐methoxyethoxy)ethanol and appear to be homogeneous by TEM with a uniform distribution of particles having an average size of less than 40 â. Through elemental mapping we see elemental segregation in the high temperature (950 °C) products, which are orthorhombic by XRD. In elemental maps of gel samples fired to 700 °C, which are tetragonal by XRD, we also see elemental inhomogeneity within particles and phase zoning in maps of products from finely ground gels. A comparison of elemental maps and x‐ray diffraction patterns of the products from gel processing and conventional solid state processing is made.

scholarly journals Surface Modification of LiMn2O4for Lithium Batteries by Nanostructured LiFePO4Phosphate

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
B. Sadeghi ◽  
R. Sarraf-Mamoory ◽  
H. R. Shahverdi
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Dip Coating ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electrochemical Tests ◽  
Transmission Electron ◽  
Coating Method ◽  
Dip Coating Method ◽  
Spinel Cathode

LiMn2O4spinel cathode materials have been successfully synthesized by solid-state reaction. Surface of these particles was modified by nanostructured LiFePO4via sol gel dip coating method. Synthesized products were characterized by thermally analyzed thermogravimetric and differential thermal analysis (TG/DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX). The results of electrochemical tests showed that the charge/discharge capacities improved and charge retention of battery enhanced. This improved electrochemical performance is caused by LiFePO4phosphate layer on surfaces of LiMn2O4cathode particles.

Lithium chromium pyrophosphate as an insertion material for Li-ion batteries

2015 ◽  
Vol 71 (6) ◽  
pp. 661-667 ◽  
Author(s):  
Martin Reichardt ◽  
Sébastien Sallard ◽  
Petr Novák ◽  
Claire Villevieille
Keyword(s):  
Sol Gel ◽  
Insertion Reaction ◽  
Li Ion Batteries ◽  
Conductivity Measurements ◽  
X Ray Diffraction ◽  
Theoretical Limit ◽  
X Ray ◽  
Electrochemically Active ◽  
Carbon Coated ◽  
Li Ion

Lithium chromium pyrophosphate (LiCrP2O7) and carbon-coated LiCrP2O7 (LiCrP2O7/C) were synthesized by solid-state and sol–gel routes, respectively. The materials were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and conductivity measurements. LiCrP2O7 powder has a conductivity of ∼ 10−8 S cm−1, ∼ 104 times smaller than LiCrP2O7/C (∼ 10−4 S cm−1). LiCrP2O7/C is electrochemically active, mainly between 1.8 and 2.2 V versus Li+/Li (Cr3+/Cr2+ redox couple), whereas LiCrP2O7 has limited electrochemical activity. LiCrP2O7/C delivers a reversible specific charge up to ∼ 105 mAh g−1 after 100 cycles, close to the theoretical limit of 115 mAh g−1. Operando XRD experiments show slight peak shifts between 2.2 and 4.8 V versus Li+/Li, and a reversible amorphization between 1.8 and 2.2 V versus Li+/Li, suggesting an insertion reaction mechanism.

Synthesis of MoO3/V2O5/C Composite as Novel Anode for Li-Ion Battery Application

2020 ◽  
Vol 20 (5) ◽  
pp. 2911-2916
Author(s):  
Zhen Zhang ◽  
Xiao Chen ◽  
Guangxue Zhang ◽  
Chuanqi Feng
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Specific Capacity ◽  
Lithium Ion ◽  
Li Ion Battery ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Li Ion ◽  
Battery Application

The MoO3/V2O5/C, MoO3/C and V2O5/C are synthesized by electrospinning combined with heat treatment. These samples are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy and thermogravimetric analysis (TG) techniques. The results show that sample MoO3/V2O5/C is a composite composed from MoO3, V2O5 and carbon. It takes on morphology of the nanofibers with the diameter of 200~500 nm. The TG analysis result showed that the carbon content in the composite is about 40.63%. Electrochemical properties for these samples are studied. When current density is 0.2 A g−1, the MoO3/V2O5/C could retain the specific capacity of 737.6 mAh g−1 after 200 cycles and its coulomb efficiency is 92.99%, which proves that MoO3/V2O5/C has better electrochemical performance than that of MoO3/C and V2O5/C. The EIS and linear Warburg coefficient analysis results show that the MoO3/V2O5/C has larger Li+ diffusion coefficient and superior conductivity than those of MoO3/C or V2O5/C. So MoO3/V2O5/C is a promising anode material for lithium ion battery application.

Preparation and Application of Carboxyl-Functioned Magnetic Nanoparticles for Arylsulfatase Immobilization

2016 ◽  
Vol 13 (10) ◽  
pp. 7408-7415
Author(s):  
Yongxing Li ◽  
Qiong Xiao ◽  
Qin Yin ◽  
Hui Ni ◽  
Yanbing Zhu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Magnetic Nanoparticles ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
Sulfate Ester ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Mean Diameter ◽  
Diffraction Patterns

Arylsulfatase, one of a few enzymes that can enhance the gelling strength of agar by cleaving the sulfate ester bonds in agar, was covalently immobilized with carboxyl functioned magnetic nanoparticles (CMNPs). The resultant CMNPs and immobilized arylsulfatase were characterized by transmission electron microscopy (TEM), Dynamic Light scattering (DLS), X-ray diffraction (XRD), vibrating sample magnetometry (VSM) and thermogravimetric analysis (TGA). The TEM result indicated that the CMNPs and immobilized arylsulfatase had a similar mean particle size of 10 nm. The arylsulfatase-CMNPs had a mean diameter of 1200 nm in aqueous solution determined by the DLS, which was much bigger than the CMNPs (433.6 nm). The different sizes demonstrated that the arylsulfatase was coated on CMNPs successfully. XRD showed that diffraction patterns of the CMNPs and arylsulfatase-CMNPs were close to the standard XRD pattern of Fe3O4. Saturation magnetizations were 52.1 emu/g for carriers and 47.9 emu/g for immobilized arylsulfatase, which indicated that the particles had superparamagnetic characteristics. The TGA revealed that the amount of arylsulfatase bound to the surface of CMNPs was 5.65%. The arylsulfatase exhibited better thermal stability and reusability after immobilization, the immobilized arylsulfatase can retain more than 50% enzyme activity up to the 9th cycle.

Synthesis of Ni-Mo-W Sulfide Nanorods as Catalyst for Hydrodesulfurization of Dibenzothiophene

2008 ◽  
Vol 8 (12) ◽  
pp. 6406-6413 ◽  
Author(s):  
F. Paraguay-Delgado ◽  
R. García-Alamilla ◽  
J. A. Lumbreras ◽  
E. Cizniega ◽  
G. Alonso-Núñez
Keyword(s):  
Electron Microscopy ◽  
Physical Adsorption ◽  
Atomic Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxide Precursor ◽  
Transmission Electron ◽  
Adsorption Of Nitrogen ◽  
Diffraction Patterns ◽  
Scanning Electron

Two trimetallic sulfurs, MoWNiS and MoWSNi, were synthesized to be used as a catalyst in hydrodesulfurization reactions. The mixed oxide mesoporous nanostructured MoO3-WO3 with an Mo:W atomic ratio of 1:1 was used as the precursor. The first catalyst was prepared by impregnating nickel in the oxide precursor and then subsequent sulfiding with an H2S/H2 mix at 400 °C for 2 hours. The second catalyst was prepared by sulfiding the precursor and then impregnating the nickel, and finally reducing the material with a H2/N2 at 350 °C. In both catalysts the Mo:W:Ni atomic ratio was maintained at 1:1:0.5. The materials obtained were characterized by physical adsorption of nitrogen, X-ray diffraction, scanning electron microscopy, transmission electron microscopy. Furthermore, the materials obtained were evaluated by a dibenzothiophene hydrodesulfuration reaction. The diffraction patterns show that both materials are polycrystalline and mainly of MoS2 and WS2 phases.

Paper 24: Dry Wear of Steel as Revealed by Electron Microscopy and X-Ray Diffraction

1967 ◽  
Vol 182 (14) ◽  
pp. 201-213
Author(s):  
T. F. J. Quinn
Keyword(s):  
Electron Microscopy ◽  
Medium Carbon Steel ◽  
X Ray Diffraction ◽  
Medium Carbon ◽  
X Ray ◽  
Ambient Temperatures ◽  
Transmission Electron ◽  
Steel Aisi ◽  
Diffraction Patterns ◽  
Fatigue Failures

Low-alloy, medium-carbon steel (AISI 4340) pins have been worn against discs of the same material at various loads under unlubricated (‘dry’) sliding conditions. Shadowed carbon replicas have been obtained from the surfaces of selected pins and discs. Transmission electron microscopy of these replicas revealed several interesting features, the most interesting being the presence of reproducible crack systems occurring in those parts of the surface at which the wear is taking place. These cracks are very similar to those obtained in fatigue failures. X-ray diffraction patterns were also obtained from these specimens, and from the corresponding wear debris. These indicated that oxidation had occurred at temperatures considerably in excess of the measured ambient temperatures. The various topographic and crystallographic features revealed by the electron microscopy and X-ray diffraction techniques are discussed in relation to a possible mechanism of ‘dry’ wear

scholarly journals Sol-Gel Derived Eu3+-Doped Gd2Ti2O7Pyrochlore Nanopowders

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Sanja Ćulubrk ◽  
Željka Antić ◽  
Vesna Lojpur ◽  
Milena Marinović-Cincović ◽  
Miroslav D. Dramićanin
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Structural Changes ◽  
Sol Gel ◽  
Pyrochlore Phase ◽  
Structural Defects ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Synthesis

Herein we presented hydrolytic sol-gel synthesis and photoluminescent properties of Eu3+-doped Gd2Ti2O7pyrochlore nanopowders. According to Gd2Ti2O7precursor gel thermal analysis a temperature of 840°C is identified for the formation of the crystalline pyrochlore phase. Obtained samples were systematically characterized by powder X-ray diffraction, scanning and transmission electron microscopy, and photoluminescence spectroscopy. The powders consist of well-crystalline cubic nanocrystallites of approximately 20 nm in size as evidenced from X-ray diffraction. The scanning and transmission electron microscopy shows that investigated Eu3+-doped Gd2Ti2O7nanopowders consist of compact, dense aggregates composed entirely of nanoparticles with variable both shape and dimension. The influence of Eu3+ions concentration on the optical properties, namely, photoluminescence emission and decay time, is measured and discussed. Emission intensity as a function of Eu3+ions concentration shows that Gd2Ti2O7host can accept Eu3+ions in concentrations up to 10 at.%. On the other hand, lifetime values are similar up to 3 at.% (~2.7 ms) and experience decrease at higher concentrations (2.4 ms for 10 at.% Eu3+). Moreover, photoluminescent spectra and lifetime values clearly revealed presence of structural defects in sol-gel derived materials proposing photoluminescent spectroscopy as a sensitive tool for monitoring structural changes in both steady state and lifetime domains.

Sign in / Sign up

Export Citation Format

Share Document