scholarly journals Synthesis and Electrochemical Properties of Porous LiAl0.05Mn1.95O4 for High Power LIB by Spray Pyrolysis

2010 ◽  
Vol 445 ◽  
pp. 91-94
Author(s):  
Takayuki Kodera ◽  
Syoji Hirose ◽  
Takashi Ogihara

Spherical LiAl0.05Mn1.95O4 precursor powders were successfully prepared by spray pyrolysis. LiAl0.05Mn1.95O4 precursor powders were calcined by 800°C for 10hrs. The particles size, morphology, microstructure, crystal phases of the calcined powders were characterized by X-ray diffraction (XRD) and a scanning electron microscope (SEM). The XRD patterns showed that the crystal phases of the calcined powders were the same as spinel phase (space group: Fd3m). The particles exhibited a spherical morphology with a porous microstructure. The particle size of the primary particles was approximately 200nm. LiAl0.05Mn1.95O4 cathodes exhibited higher rechargeable capacity and cycle stability at high rates. The particle microstructure of LiAl0.05Mn1.95O4 powders was effective for the rechargeable capacity at high rates.

2011 ◽  
Vol 485 ◽  
pp. 107-110 ◽  
Author(s):  
Takayuki Kodera ◽  
Dong Ying Bi ◽  
Daisuke Ogawa ◽  
Takashi Ogihara

Spherical LiFePO4/C precursor powders were successfully prepared by spray pyrolysis. Various types of organic compounds such as glycolic acid, malic acid, citric acid, fructose and sucrose were used as carbon sources. X-ray diffraction analysis revealed that the olivine phase was obtained by calcining over 600 °C under an argon (95%)/hydrogen (5%) atmosphere. The particles exhibited a spherical morphology with approximately 1.5 μm. LiFePO4/C cathode derived from sucrose exhibited higher rechargeable capacity and cycle stability. The rechargeable capacity of LiFePO4/C cathode was approximately 154 mAh/g at 1 C. 90% of initial discharge capacity was maintained after 100 cycles.


2010 ◽  
Vol 445 ◽  
pp. 82-85
Author(s):  
Kenichi Myoujin ◽  
Araki Toriyama ◽  
Takayuki Kodera ◽  
Takashi Ogihara

Spherical La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM) precursor powders were synthesized by aerosol plasma pyrolysis using an aqueous solution of metal nitrate. As-prepared powders obtained by this method were found to have a spherical morphology with a bimodal size distribution of nanosized (primary) and submicron-sized (secondary) particles. The average size of the primary particles was less than 100 nm. X-ray diffraction (XRD) patterns showed that as-prepared powders crystallized to LSGM and other phases. XRD revealed that LSGM pellets were crystallized to a perovskite structure after sintering at 1300 °C for 10 h.


2009 ◽  
Vol 421-422 ◽  
pp. 558-561
Author(s):  
Takayuki Kodera ◽  
Kenichi Myoujin ◽  
Takashi Ogihara

Ag and Ni spherical fine powders were continuously produced by carrying out an aerosol process in a mass nanopowder production apparatus. The particles size, particle morphology, crystal phases and crystallinity of the as-prepared powders were characterized by a scanning electron microscope (SEM) and X-ray diffraction (XRD). The particles were nonaggregated and they exhibited a spherical morphology with a narrow size distribution. The average sizes of Ag and Ni particles were 500 nm and 700 nm, respectively. The crystallinity of the as-prepared powders was high. The XRD patterns showed that the crystal phases of the as-prepared powders were the same as those of their respective metals.


2013 ◽  
Vol 566 ◽  
pp. 127-130
Author(s):  
Hiroshi Kawaguchi ◽  
Takayuki Kodera ◽  
Takashi Ogihara

Spherical Li2Ti3O7precursor powders were successfully prepared by spray pyrolysis. X-ray diffraction analysis revealed that the ramsdellite phase was obtained by calcining at 1100 °C for 3 h under an argon/hydrogen (95/5 %) atmosphere. The Li2Ti3O7anode exhibited higher rechargeable capacity and excellent cycle stability. The rechargeable capacity of the Li2Ti3O7anode was approximately 168 mAh/g at 0.1 C. The discharge capacity of the Li2Ti3O7anode after 100 cycles was approximately 90% of the initial discharge capacity.


2020 ◽  
Vol 10 (03) ◽  
pp. 2050003
Author(s):  
M. R. Hassan ◽  
M. T. Islam ◽  
M. N. I. Khan

In this research, influence of adding Li2CO3 (at 0%, 2%, 4%, 6%) on electrical and magnetic properties of [Formula: see text][Formula: see text]Fe2O4 (with 60% Ni and 40% Mg) ferrite has been studied. The samples are prepared by solid state reaction method and sintered at 1300∘C for 6[Formula: see text]h. X-ray diffraction (XRD) patterns show the samples belong to single-phase cubic structure without any impurity phase. The magnetic properties (saturation magnetization and coercivity) of the samples have been investigated by VSM and found that the higher concentration of Li2CO3 reduces the hysteresis loss. DC resistivity increases with Li2CO3 contents whereas it decreases initially and then becomes constant at lower value with temperature which indicates that the studied samples are semiconductor. The dielectric dispersion occurs at a low-frequency regime and the loss peaks are formed in a higher frequency regime, which are due to the presence of resonance between applied frequency and hopping frequency of charge carriers. Notably, the loss peaks are shifted to the lower frequency with Li2CO3 additions.


2014 ◽  
Vol 937 ◽  
pp. 182-186
Author(s):  
Quan An Li ◽  
Lei Lei Chen ◽  
Wen Chuang Liu ◽  
Xing Yuan Zhang ◽  
Hui Zhen Jiang

The influence of the solution treatment (at the temperature of 500-520°C for 4-12 h) on microstructures and mechanical properties of Mg-Gd-Y-Zr alloy was investigated by means of optical microscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD) and Vickers hardness measurement. The as-cast alloy contains a microstructure consisting of α-Mg matrix, Mg5Gd phase and Mg24Y5phase. With increasing solution temperature and time, the quantity of the primary particles (Mg5Gd and Mg24Y5) in the alloy continually decreased, and the degree of recrystallization gradually increased, which result in the gradual decrease of the Vickers hardness of the solution-treated alloys.


Author(s):  
Peng Liu ◽  
Hongbin Zhang ◽  
Sinong Wang ◽  
Hui Yu ◽  
Bingjie Lu ◽  
...  

AbstractThe crystallinity indices (CrI) of Chinese handmade papers were investigated using the X-ray diffraction (XRD) method. Four Chinese handmade papers, Yingchun, Zhuma, Yuanshu and Longxucao papers were used as model substrates of mulberry bark, ramie, bamboo and Eulaliopsis binata papers, respectively. Two forms of the paper samples, paper sheets and their comminuted powders, were used in this study. The results showed that their XRD patterns belong to the cellulose-I type and Iβ dominates the cellulose microstructure of these paper samples. Moreover, it was found that the microstructures and CrIs of cellulose of these papers were changed by the grinding treatment. This work suggested that the sheet form of the handmade papers is suitable to determine CrI by XRD, despite the contribution of non-cellulosic components in the papers. The order of CrIs for these paper sheet samples was Yingchun, Zhuma, Longxucao and Yuanshu papers. Besides CrIs, differences in cross-sectional areas of the crystalline zone of cellulose can be used for comparing different types of handmade papers. It was also found that the CrIs and crystallite size of paper cellulose varied between the sheet samples and the powder samples, illustrating that the pulverisation has a negative influence on the microstructure of the handmade papers.


2014 ◽  
Vol 1061-1062 ◽  
pp. 83-86
Author(s):  
Hong Wu ◽  
De Yi Zheng

In this paper, the effects of different sintering temperature on the microstructure and piezoelectric properties of Pb(Nb2/3Zn1/3)0.03(Zr52Ti48)0.97O3(PNZZT) ceramic samples were investigated. The Pb(Nb2/3Zn1/3)0.03(Zr52Ti48)0.97O3 ceramics materials was prepared by a conventional mixed oxide method. In the period of the experiment, the relationship between crystallographic phase and microstructure were analyzed by X-ray diffraction(XRD) and scanning electron microscopy(SEM) respectively. The XRD patterns shows that all of the ceramic samples are with a tetragonal perovskite structure. Along with sintering temperature increased and the x is 0.03, the grain size gradually become big. Through this experiment, it has been found that when the x is 0.03 and sintered at 1130°C for 2 h, the grains grow well, the grain-boundary intersection of the sample combined well and the porosity of the ceramics decreased, an excellent comprehensive electrical properties of the Pb(Nb2/3Zn1/3)0.03(Zr52Ti48)0.97O3 samples can be obtained. Its best electrical properties are as follows: dielectric constant (ε) is 1105, dielectric loss(tg) is 0.017, electromechanical coupling coefficient (Kp) is 0.287, piezoelectric constant(d33) is 150PC/N


2009 ◽  
Vol 79-82 ◽  
pp. 71-74
Author(s):  
Qi Wang ◽  
Lin Qiao ◽  
Peng Song

In this paper, the resistance to H2S attack of pastes made from slag-fly ash blended cement used in oil well (SFAOW) was studied, in which fly ash (FA) was used at replacement dosages of 30% to 60% by weight of slag. Samples of SCOW and SFAOW pastes were demoulded and cured by immersion in fresh water with 2 Mp H2S insulfflation under 130oC for 15 days. After this curing period, compression strength and permeability of the samples were investigated. The reaction mechanisms of H2S with the paste were carried out through a microstructure study, which included the use of x-ray diffraction (XRD) patterns and scanning electron microscope (SEM). Based on the obtained data in this study, incorporation of FA into SCOW results in the comparable effects in the resistance to H2S attack. When the replacement dosage of slag is about 40%, the paste exhibits the best performance on resistance to H2S attack with compression strength 36.58Mp.


2013 ◽  
Vol 12 (01) ◽  
pp. 1350006
Author(s):  
AHMED E. HANNORA ◽  
FARIED F. HANNA ◽  
LOTFY K. MAREI

Mechanical alloying (MA) method has been used to produce nanocrystallite Mn -15at.% Al alloy. X-ray diffraction (XRD) patterns for the as-milled elemental α- Mn and aluminum powder samples show a mixture of α + β- MnAl phases after 20 h of milling and changes to a dominant β- MnAl phase structure after 50 h. An average crystallite size of 40 nm was determined from Hall–Williamson method analysis after 5 h of milling. Moreover, the thermal analysis results using differential thermal analysis (DTA), suggested a possible phase transformation after 20 h of milling. Isothermal treatments are carried in the temperature range of 450°C to 1000°C. Room-temperature vibrating sample magnetometer (VSM) measurements of the hysteretic response revealed that the saturation magnetization Bs and coercivity Hc for 10 h ball milled sample are ~ 2.1 emu/g and ~ 92 Oe, respectively.


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