scholarly journals Influence of particle size and fluorination ratio of CF x precursor compounds on the electrochemical performance of C–FeF2 nanocomposites for reversible lithium storage

2013 ◽  
Vol 4 ◽  
pp. 705-713 ◽  
Author(s):  
Ben Breitung ◽  
M Anji Reddy ◽  
Venkata Sai Kiran Chakravadhanula ◽  
Michael Engel ◽  
Christian Kübel ◽  
...  
Keyword(s):  
Particle Size ◽  
Electrochemical Performance ◽  
Cathode Materials ◽  
Electrochemical Performances ◽  
X Ray Diffraction ◽  
Lithium Storage ◽  
One Pot ◽  
Electrically Conductive ◽  
X Ray ◽  
Electron Energy Loss

Systematical studies of the electrochemical performance of CF x -derived carbon–FeF2 nanocomposites for reversible lithium storage are presented. The conversion cathode materials were synthesized by a simple one-pot synthesis, which enables a reactive intercalation of nanoscale Fe particles in a CF x matrix, and the reaction of these components to an electrically conductive C–FeF2 compound. The pretreatment and the structure of the utilized CF x precursors play a crucial role in the synthesis and influence the electrochemical behavior of the conversion cathode material. The particle size of the CF x precursor particles was varied by ball milling as well as by choosing different C/F ratios. The investigations led to optimized C–FeF2 conversion cathode materials that showed specific capacities of 436 mAh/g at 40 °C after 25 cycles. The composites were characterized by Raman spectroscopy, X-Ray diffraction measurements, electron energy loss spectroscopy and TEM measurements. The electrochemical performances of the materials were tested by galvanostatic measurements.

scholarly journals Formation of ZnO/Zn0.5Cd0.5Se Alloy Quantum Dots in the Presence of High Oleylamine Contents

Nanomaterials ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 999
Author(s):  
Yi-An Chen ◽  
Kuo-Hsien Chou ◽  
Yi-Yang Kuo ◽  
Cheng-Ye Wu ◽  
Po-Wen Hsiao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Particle Size ◽  
X Ray Diffraction ◽  
One Pot ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Alloy Quantum Dots ◽  
First Time

To the best of our knowledge, this report presents, for the first time, the schematic of the possible chemical reaction for a one-pot synthesis of Zn0.5Cd0.5Se alloy quantum dots (QDs) in the presence of low/high oleylamine (OLA) contents. For high OLA contents, high-resolution transmission electron microscopy (HRTEM) results showed that the average size of Zn0.5Cd0.5Se increases significantly from 4 to 9 nm with an increasing OLA content from 4 to 10 mL. First, [Zn(OAc)2]–OLA complex can be formed by a reaction between Zn(OAc)2 and OLA. Then, Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) data confirmed that ZnO is formed by thermal decomposition of the [Zn(OAc)2]–OLA complex. The results indicated that ZnO grew on the Zn0.5Cd0.5Se surface, thus increasing the particle size. For low OLA contents, HRTEM images were used to estimate the average sizes of the Zn0.5Cd0.5Se alloy QDs, which were approximately 8, 6, and 4 nm with OLA loadings of 0, 2, and 4 mL, respectively. We found that Zn(OAc)2 and OLA could form a [Zn(OAc)2]–OLA complex, which inhibited the growth of the Zn0.5Cd0.5Se alloy QDs, due to the decreasing reaction between Zn(oleic acid)2 and Se2−, which led to a decrease in particle size.

scholarly journals Continuous Composition Spread and Electrochemical Studies of Low Cobalt Content Li(Ni,Mn,Co)O2 Cathode Materials

Coatings ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 366 ◽  
Author(s):  
JongSeok Jung ◽  
Haena Yim ◽  
Narendra Singh Parmar ◽  
Jae-Seung Lee ◽  
Ji-Won Choi
Keyword(s):  
Thin Film ◽  
Electrochemical Performance ◽  
Cathode Materials ◽  
Electrochemical Impedance ◽  
Cobalt Content ◽  
Electrochemical Studies ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wide Range ◽  
X Ray Absorption

Many scientific efforts have been undertaken toward reducing the Co content in LiMn1/3Ni1/3Co1/3O2 cathode materials for thin-film batteries. In this study, we present cathodes with a wide range of Li(Ni, Mn, Co)O2 compositions to determine the material with the best electrochemical performance by changing the ratio of Ni to Mn at a fixed 0.1 at.% of Co by the continuous composition spread sputtering method. The cathode composition measurements by Rutherford backscattering spectroscopy show that the best electrochemical performance is obtained for a composition of Ni:Mn:Co = 19:71:10. The reasons for this improved electrochemical performance are further investigated by X-ray diffraction, electrochemical impedance spectroscopy, Fourier-transform infrared spectroscopy, and X-ray absorption near edge spectroscopy.

Electrochemical Performance of Spherical Li3V2(PO4)3/C Synthesized by Spray Drying Method

2017 ◽  
Vol 727 ◽  
pp. 738-743 ◽  
Author(s):  
Zong Lin Zuo ◽  
Jin Wang ◽  
Jian Qiu Deng ◽  
Qing Rong Yao ◽  
Zhong Min Wang ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
Spray Drying ◽  
Cathode Materials ◽  
Lithium Ion ◽  
Drying Method ◽  
X Ray Diffraction ◽  
Capacity Retention ◽  
Voltage Range ◽  
X Ray ◽  
Discharge Capacities

Spherical Li3V2(PO4)3/C cathode materials have been successfully synthesized by a spray drying method. The structure and morphology of the cathode materials are characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM) and thermogravimetric (TG) analysis. The results show that synthesized monoclinic Li3V2(PO4)3 with high purities exhibits spherical morphology, in favor of enhancing the capacities and cycling stability of Li3V2(PO4)3/C cathode materials for lithium-ion battery. The Li3V2(PO4)3/C cathode materials sintered at 750 °C present best electrochemical performance among all the samples. It exhibits high initial discharge capacities of 99.2 mAhg-1 and capacity retention of 93.6% after 200 cycles at a rate of 1C within a voltage range of 3.0–4.3 V.

Fe Content Effects on Electrochemical Properties of 0.3Li2MnO3•0.7LiMnxNixFe(1-2x)/2 O2 Cathode Materials

2011 ◽  
Vol 347-353 ◽  
pp. 3518-3521
Author(s):  
Dong Li ◽  
Fang Lian ◽  
Wei Hua Qiu ◽  
Fu Shen Li ◽  
Kuo Chih Chou
Keyword(s):  
Electrochemical Properties ◽  
Cathode Materials ◽  
Reversible Capacity ◽  
Solid State Reaction Method ◽  
Electrochemical Performances ◽  
Fe Doping ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Fe Content

The cathode materials 0.3Li2MnO3•0.7LiMnxNixFe(1-2x)/2O2(0.35≤x≤0.5) were synthesized via low-heating solid-state reaction method. The prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), thermogravimetric analysis (TG) and differential thermal analysis (DTA), and their electrochemical performances were also investigated here. The FESEM images of samples revealed that the particle of Fe-substituted samples became smaller and size distribution got narrower compared with the materials without Fe-doping. The results showed that electrochemical properties of the material depended on the content of Fe. 0.3Li2MnO3• 0.7LiMn0.4 Ni0.4Fe2O2 maintained 99.5% of the reversible capacity after 60 cycles

scholarly journals Mining Wastes of an Albite Deposit as Raw Materials for Vitrified Mullite Ceramics

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada
Keyword(s):  
Particle Size ◽  
Raw Materials ◽  
Phase Evolution ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Mining Wastes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Value

In this work, an examination of mining wastes of an albite deposit in south Spain was carried out using X-ray Fluorescence (XRF), X-ray diffraction (XRD), particle size analysis, thermo-dilatometry and Differential Thermal Analysis (DTA) and Thermogravimetric (TG) analysis, followed by the determination of the main ceramic properties. The albite content in two selected samples was high (65–40 wt. %), accompanied by quartz (25–40 wt. %) and other minor minerals identified by XRD, mainly kaolinite, in agreement with the high content of silica and alumina determined by XRF. The content of Na2O was in the range 5.44–3.09 wt. %, being associated with albite. The iron content was very low (<0.75 wt. %). The kaolinite content in the waste was estimated from ~8 to 32 wt. %. The particle size analysis indicated values of 11–31 wt. % of particles <63 µm. The ceramic properties of fired samples (1000–1350 °C) showed progressive shrinkage by the thermal effect, with water absorption and open porosity almost at zero at 1200–1250 °C. At 1200 °C, the bulk density reached a maximum value of 2.38 g/cm3. An abrupt change in the phase evolution by XRD was found from 1150 to 1200 °C, with the disappearance of albite by melting in accordance with the predictions of the phase diagram SiO2-Al2O3-Na2O and the system albite-quartz. These fired materials contained as main crystalline phases quartz and mullite. Quartz was present in the raw samples and mullite was formed by decomposition of kaolinite. The observation of mullite forming needle-shape crystals was revealed by Scanning Electron Microscopy (SEM). The formation of fully densified and vitrified mullite materials by firing treatments was demonstrated.

scholarly journals Synthesis of magnesium carbonate hydrate from natural talc

2020 ◽  
Vol 18 (1) ◽  
pp. 951-961
Author(s):  
Qiuju Chen ◽  
Tao Hui ◽  
Hongjuan Sun ◽  
Tongjiang Peng ◽  
Wenjin Ding
Keyword(s):  
Crystal Structure ◽  
Particle Size ◽  
Crystal Growth ◽  
Crystal Morphology ◽  
Magnesium Carbonate ◽  
Organic Additives ◽  
X Ray Diffraction ◽  
Morphological Transformation ◽  
X Ray ◽  
Carbonation Process

AbstractVarious morphologies of magnesium carbonate hydrate had been synthesized without using any organic additives by carefully adjusting the reaction temperature and time during the talc carbonation process. At lower temperatures, magnesium carbonate hydrate was prone to display needle-like morphology. With the further increase of the carbonation temperature, the sheet-like crystallites became the preferred morphology, and at higher aging temperatures, these crystallites tended to assemble into layer-like structures with diverse morphologies, such as rose-like particles and nest-like structure. The reaction time had no effect on the crystal morphology, but it affected the particle size and situation of the crystal growth. X-Ray diffraction results showed that these various morphologies were closely related to their crystal structure and compositions. The needle-like magnesium carbonate hydrate had a formula of MgCO3·3H2O, whereas with the morphological transformation from needle-like to sheet-like, rose-like, and nest-like structure, their corresponding compositions also changed from MgCO3·3H2O to 4MgCO3·Mg(OH)2·8H2O, 4MgCO3·Mg(OH)2·5H2O, and 4MgCO3·Mg(OH)2·4H2O.

scholarly journals Thermal, Structural, and Physical Properties of Freeze Dried Tropical Fruit Powder

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
K. A. Athmaselvi ◽  
C. Kumar ◽  
M. Balasubramanian ◽  
Ishita Roy
Keyword(s):  
Particle Size ◽  
Physical Properties ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Tropical Fruit ◽  
X Ray ◽  
Freeze Dried ◽  
Fruit Powder ◽  
Lcr Meter

This study evaluates the physical properties of freeze dried tropical (guava, sapota, and papaya) fruit powders. Thermal stability and weight loss were evaluated using TGA-DSC and IR, which showed pectin as the main solid constituent. LCR meter measured electrical conductivity, dielectric constant, and dielectric loss factor. Functional groups assessed by FTIR showed presence of chlorides, and O–H and N–H bonds in guava, chloride and C–H bond in papaya, and chlorides, and C=O and C–H bonds in sapota. Particle size and type of starch were evaluated by X-ray diffraction and microstructure through scanning electronic microscopy. A semicrystalline profile and average particle size of the fruit powders were evidenced by X-ray diffraction and lamellar/spherical morphologies by SEM. Presence of A-type starch was observed in all three fruits. Dependence of electric and dielectric properties on frequency and temperature was observed.

Effect of Synthesis Temperature on Particles Size and Morphology of Zirconium Oxide Nanoparticle

2017 ◽  
Vol 50 ◽  
pp. 18-31 ◽  
Author(s):  
Rudzani Sigwadi ◽  
Simon Dhlamini ◽  
Touhami Mokrani ◽  
Patrick Nonjola
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Zirconium Oxide ◽  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Crystallite Sizes ◽  
Ft Ir

The paper presents the synthesis and investigation of zirconium oxide (ZrO2) nanoparticles that were synthesised by precipitation method with the effects of the temperatures of reaction on the particles size, morphology, crystallite sizes and stability at high temperature. The reaction temperature effect on the particle size, morphology, crystallite sizes and stabilized a higher temperature (tetragonal and cubic) phases was studied. Thermal decomposition, band structure and functional groups were analyzed by Brunauer-Emmett-Teller (BET), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Thermo-gravimetric analysis (TGA) and Fourier transform infrared (FT-IR). The crystal structure was determined using X-ray diffraction. The morphology and the particle size were studied using (SEM) and (TEM). The shaped particles were confirmed through the SEM analysis. The transmission electron microscopic analysis confirmed the formation of the nanoparticles with the particle size. The FT-IR spectra showed the strong presence of ZrO2 nanoparticles.

Replacing sulfonate by carboxylate: application of pyridyliminocarboxylato copper(II) complexes in rac-lactide polymerization and Chan–Evans–Lam coupling

2019 ◽  
Vol 97 (3) ◽  
pp. 178-190 ◽  
Author(s):  
Valérie Hardouin Duparc ◽  
Clémentine Dimeck ◽  
Frank Schaper
Keyword(s):  
Molecular Sieves ◽  
Weight Control ◽  
Phenylboronic Acid ◽  
Side Reactions ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
One Pot ◽  
X Ray ◽  
Induction Periods ◽  
Lactide Polymerization

Copper(II) complexes carrying pyridylmethyleneaminobenzoate or –propanoate ligands, LCuX, were prepared in one-pot reactions from pyridinecarboxaldehyde, aminobenzoic acid or β-alanine, and CuX2 (X = Cl, NO3, OAc, or OTf). All complexes were characterized by single-crystal X-ray diffraction studies and formed either dimers, tetramers, or coordination polymers. Attempted preparation of the respective alkoxide complexes, LCu(OR), was unsuccessful, but use of LCuX/NaOMe mixtures in rac-lactide polymerization indicated under some conditions coordination–insertion polymerization via a copper alkoxide as the mechanism. The complexes performed poorly in rac-lactide polymerization, showing low activities (12 h to completion at 140 °C), low to moderate heterotacticity (Pr = 0.6–0.8), and poor polymer molecular weight control (intramolecular transesterification). They were competent catalysts for Chan–Evans–Lam couplings with phenylboronic acid, without any indication of side reactions such as deboration or aryl homocoupling. The complexes were active in undried methanol, without addition of base, ligand, or molecular sieves. Aniline, n-octylamine, and cyclohexylamine were coupled quantitatively under identical reaction conditions. There is only little influence of the anion on activities (less than a factor of 2) but a strong influence on induction periods. The complexes were not active in CEL coupling with alcohols, phenols, or alkylboronic acids.

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