LiFePO4/C Cathode Materials Prepared by One-Step Fast Carbothermal Method Using Fe2O3 as Raw Materials

2013 ◽  
Vol 773 ◽  
pp. 709-713
Author(s):  
Bao Hua Rong ◽  
Yan Wen Lu ◽  
Qing Lin Chen ◽  
Kun Tang ◽  
Xue Wen Liu ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
Raw Materials ◽  
Synthesis Temperature ◽  
Cycle Performance ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Sintering Atmosphere ◽  
X Ray ◽  
One Step ◽  
Carbothermal Method

LiFePO4/C was successfully synthesized by one-step solid-state reaction using Fe2O3, LiH2PO4 and sucrose as raw materials. The effect of synthesis temperature and sintering atmosphere on the electrochemical performance were investigated. LiFePO4/C materials were characterized by differential scanning calorimetry and thermogravimetry, X-ray diffraction, scanning electron microscopy and XPS. The results show that the synthesis temperature between 750 °C and 800 °C were appropriate and the reductive ambience can enhance the electrochemical performance effectively especially at high rates. The precursor calcined at 750°C for 5h in a N2+5%H2 atmosphere exhibited the highest discharge capacity of 155 mAh/g at 0.1C and 141 mAh/g at 1C and showed the best cycle performance.

Effects of Reductive Conditions on the Electrochemical Properties of LiFePO4/C Derived by Fe3+ Sources

2014 ◽  
Vol 1081 ◽  
pp. 313-317
Author(s):  
Yan Wen Lu ◽  
Yu Ge ◽  
Yue Feng Tang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Raw Materials ◽  
Thermal Method ◽  
X Ray Diffraction ◽  
Sintering Atmosphere ◽  
X Ray ◽  
Electrochemical Capacity ◽  
One Step ◽  
Scanning Electron

A one-step carbon thermal method was used to prepare LiFePO4/C particles by using normal Fe2O3, LiH2PO4and sucrose as raw materials. The effect of H2content in the sintering atmosphere of N2on the morphology and the electrochemical performance were investigated. LiFePO4/C materials were characterized by X-ray diffraction, scanning electron microscopy and the elemental analyzer. The results show that the precursor sintering under the atmosphere of 8%H2+N2exhibits the highest electrochemical capacity (162.3 mAh/g at 0.1C) .

Synthesis of Spherical LiFePO4/C Composites as Cathode Material of Lithium-Ion Batteries by a Novel Glucose Assisted Hydrothermal Method

2013 ◽  
Vol 787 ◽  
pp. 58-64 ◽  
Author(s):  
Xiang Feng Li ◽  
Zhao Zhang ◽  
Fang Liu ◽  
Shu Ping Zheng
Keyword(s):  
Hydrothermal Method ◽  
Raw Materials ◽  
Lithium Ion ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
High Discharge ◽  
X Ray ◽  
High Discharge Capacity ◽  
Optimal Sample ◽  
Structure Morphology

The LiFePO4/C composites with different morphology are synthesized by a novel glucose assisted hydrothermal method at various glucose concentrations (from 0 to 0.25mol/L) and the insoluble lithium source Li2CO3, (NH4)2Fe (SO4)2·6H2O and (NH4)2HPO4(n (Li):n (Fe):n (P)=1:1:1) are used as raw materials. The structure, morphology, thermal performance and electrochemical properties of the synthesized composites are characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), thermogravimetry/differential scanning calorimetry (TG-DSC), galvanostatic charge/discharge tests and cyclic voltammetry (CV). The results show that the LiFePO4/C synthesized with 0.125mol/L glucose has the relatively small particles size (0.1~0.5μm) and the well spherical morphology. The optimal sample exhibits a high discharge capacity of 160.0mAh/g at the first cycle and exhibits a good reversibility and stability in CV tests.

scholarly journals Nanocrystal, phase transformation and microstructure of Ni50Ti50 shape memory alloy

2018 ◽  
Vol 24 (02) ◽  
pp. 22-25
Author(s):  
Dovchinvanchig M ◽  
Chunwang Zhao
Keyword(s):  
Differential Scanning Calorimetry ◽  
Phase Transformation ◽  
Shape Memory Alloy ◽  
Shape Memory ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
One Step ◽  
Niti Matrix ◽  
Electronic Microscope

The nanocrystal, phase transformation and microstructure behavior of Ni50Ti50 shape memory alloy was investigated by scanning electronic microscope, X-ray diffraction and differential scanning calorimetry. The results showed that the microstructure of Ni-Ti binary alloy consists of the NiTi2 phase and the NiTi matrix phase. One-step phase transformation was observed alloy.

scholarly journals Synthesis and Crystal Structure of the Bioinorganic Complex [Sb(Hedta)]·2H2O

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Di Li ◽  
Guo-Qing Zhong
Keyword(s):  
Crystal Structure ◽  
Ethylenediaminetetraacetic Acid ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Cell Parameters ◽  
Composition And Structure ◽  
Decomposition Processes ◽  
Distorted Trigonal Bipyramid

The antimony(III) complex [Sb(Hedta)]·2H2O was synthesized with ethylenediaminetetraacetic acid (H4edta) and antimonous oxide as main raw materials in aqueous solution. The composition and structure of the complex were characterized by elemental analysis, infrared spectra, single crystal X-ray diffraction, X-ray powder diffraction, thermogravimetry, and differential scanning calorimetry. The crystal structure of the antimony(III) complex belongs to orthorhombic system, space group Pna2(1), with cell parameters ofa=18.4823(18) Å,b=10.9408(12) Å,c=7.3671(5) Å,V=1489.7(2) Å3,Z=4, andDc=1.993 g cm−3. The Sb(III) ion is five-coordinated by two amido N atoms and three carboxyl O atoms from a single Hedta3−ligand, forming a distorted trigonal bipyramid geometry. The thermal decomposition processes of the complex include dehydration, oxidation, and pyrolysis of the ligand, and the last residue is Sb2O3at the temperature of 570°C.

Electrochemical Performance Cr Doped Spinel LiMn2O4 Cathode for Lithium Ion Batteries

2014 ◽  
Vol 636 ◽  
pp. 49-53
Author(s):  
Si Qi Wen ◽  
Liang Chao Gao ◽  
Jia Li Wang ◽  
Lei Zhang ◽  
Zhi Cheng Yang ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
Lithium Ion Batteries ◽  
Electrochemical Impedance ◽  
Sol Gel ◽  
Lithium Ion ◽  
Cycling Performance ◽  
Cycle Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Discharge Test

To improve the cycle performance of spinel LiMn2O4as the cathode of 4 V class lithium ion batteries, spinel were successfully prepared using the sol-gel method. The dependence of the physicochemical properties of the spinel LiCrxMn2-xO4(x=0,0.05,0.1,0.2,0.3,0.4) powders powder has been extensively investigated by using X-ray diffraction (XRD), scanning electron microscope (SEM), charge-discharge test and electrochemical impedance spectroscopy (EIS). The results show that as Mn is replaced by Cr, the initial capacity decreases, but the cycling performance improves due to stabilization of spinel structure. Of all, the LiCr0.2Mn1.8O4has best electrochemical performance, 107.6 mAhg-1discharge capacity, 96.1% of the retention after 50 cycles.

Effects of Synthesis Temperature and Holding Time on the Electrochemical Properties of LiNi1/3Co1/3Mn1/3O2 Cathode Material Using Rheological Phase Method

2015 ◽  
Vol 814 ◽  
pp. 351-357 ◽  
Author(s):  
Hui Peng ◽  
Ze Hua Zhu ◽  
Peng Xiao Huang ◽  
Xing Li
Keyword(s):  
Electrochemical Performance ◽  
Synthesis Temperature ◽  
Holding Time ◽  
Phase Method ◽  
Phase Reaction ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
Rheological Phase Reaction ◽  
X Ray ◽  
Initial Discharge

In this paper, LiNi1/3Co1/3Mn1/3O2 was prepared via a facile rheological phase reaction method. The effect of synthesis temperature and holding time on its electrochemical performance has been investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), cyclic voltammetry (CV) tests and galvanostatic charge–discharge tests. The results suggest that the synthesis temperature and holding time greatly affect the electrochemical performance of the LiNi1/3Co1/3Mn1/3O2 and the optimized synthesis condition for the synthesis of LiNi1/3Co1/3Mn1/3O2 via rheological phase reaction method is 900 °C for 8 h. The obtained sample possesses a highly ordered layered structure and low cation mixing. It delivers an initial discharge capacity of 198 mAh g-1 at 0.2 C and 140 mAh g-1 at 1.0 C between 2.5 and 4.6 V, respectively.

Synthesis and Characterization of New Polyurethane Adhesives

2006 ◽  
Vol 514-516 ◽  
pp. 843-847 ◽  
Author(s):  
Cristina Borges Correia ◽  
João C. Bordado
Keyword(s):  
Raw Materials ◽  
Impact Resistance ◽  
Inert Atmosphere ◽  
Stray Field ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Polyurethane Adhesives ◽  
Dimer Acids

Polyurethane adhesives provide excellent flexibility, impact resistance and durability. Polyurethanes are formed through the reaction of an isocyanate component with polyether or polyester polyols or other active hydrogen compounds. This paper refers to polyurethane adhesives made from polyester polyols with long aliphatic chains (up to 36 carbon atoms) and MDI (diphenylmethane-4,4’-diisocyanate). The polyester polyols have been made from dimer acids obtained from renewable sources and short chain diols. The polyols that were used presented different degrees of unsaturation. The influence of the different raw materials in the adhesives performance is studied. The polyurethanes were produced by reaction between quasi-stoichiometric quantities of polyol and MDI, at several temperatures. The reaction was carried under inert atmosphere and at temperatures below 100°C. Performance of the adhesives was tested by carrying adhesion, hardness and water absorption tests. Characterization of both the polyester polyols and polyurethane adhesives was carried by Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), Magnetic Nuclear Resonance (NMR), X-Ray Diffraction (WAXD), Scanning RMN Imaging of 1H of Stray- Field b (MRI) and Brookfield viscometry.

scholarly journals Nano-CL-20/HMX Cocrystal Explosive for Significantly Reduced Mechanical Sensitivity

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Chongwei An ◽  
Hequn Li ◽  
Baoyun Ye ◽  
Jingyu Wang
Keyword(s):  
Spray Drying ◽  
Raw Materials ◽  
Drop Height ◽  
Drying Method ◽  
X Ray Diffraction ◽  
Mechanical Sensitivity ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Friction Sensitivity ◽  
Scanning Electron

Spray drying method was used to prepare cocrystals of hexanitrohexaazaisowurtzitane (CL-20) and cyclotetramethylene tetranitramine (HMX). Raw materials and cocrystals were characterized using scanning electron microscopy, X-ray diffraction, differential scanning calorimetry, Raman spectroscopy, and Fourier transform infrared spectroscopy. Impact and friction sensitivity of cocrystals were tested and analyzed. Results show that, after preparation by spray drying method, microparticles were spherical in shape and 0.5–5 µm in size. Particles formed aggregates of numerous tiny plate-like cocrystals, whereas CL-20/HMX cocrystals had thicknesses of below 100 nm. Cocrystals were formed by C–H⋯O bonding between –NO2 (CL-20) and –CH2– (HMX). Nanococrystal explosives exhibited drop height of 47.3 cm, and friction demonstrated explosion probability of 64%. Compared with raw HMX, cocrystals displayed significantly reduced mechanical sensitivity.

Synthesis of Al2OC Ceramic Powder by a Carbothermal Reduction Process

2014 ◽  
Vol 881-883 ◽  
pp. 1017-1020
Author(s):  
Shuang Shuang Ding ◽  
Peng Cui ◽  
Hong Xi Zhu ◽  
Cheng Ji Deng ◽  
Chao Yu
Keyword(s):  
Carbothermal Reduction ◽  
Raw Materials ◽  
Heating Temperature ◽  
Ceramic Powder ◽  
Reduction Process ◽  
Synthesis Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Argon Flow ◽  
Micro Morphology

A12OC ceramic powder was successfully synthesized via a carbothermal reduction method using Al2O3, B2O3 and activated carbon powders as raw materials. The effects of synthesis temperature on the phase transformation and micro-morphology of A12OC were investigated by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results indicated that the content of A12OC in the products was increased with the increasing heating temperature. The optimized process for preparing A12OC was heating the mixtures at 1700 °C for 2 h in argon flow. A12OC particles synthesized at 1700 °C were hexagon plate-like with thickness of 5 μm and size of about 50 μm. Keywords: A12OC, synthesis, microstructure

Glass-Ceramics Obtained from Sewage Sludge and its Characteristics Affected by Alkalinity

2014 ◽  
Vol 937 ◽  
pp. 70-73
Author(s):  
Di Wu ◽  
Jun Zhang ◽  
Xing Wang Wen ◽  
Hui Ling Liu
Keyword(s):  
Sewage Sludge ◽  
Raw Materials ◽  
Glass Ceramics ◽  
Chemical Properties ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Sludge Disposal ◽  
Physical And Chemical ◽  
And Chemical Properties

Sewage sludge was tested as component for producing glass-ceramics with the addition of analytic reagent CaO to solve the sewage sludge disposal problems. The effect of alkalinity (Ak=mCaO/mSiO2) on the characteristics of the glass-ceramics was investigated. Differential scanning calorimetry (DSC) and X-ray diffraction (XRD) were used to investigate thermal behavior and crystalline phase of the samples. It was found that the degree and characteristics of crystals in vitrified sludge significantly correlate to the alkalinity of the raw materials. The glass-ceramics with Ak = 0.36 possessed the best physical and chemical properties.

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