Synthesis and Characterization of LiVOPO4 Cathode Material by Solid-State Method

2012 ◽  
Vol 554-556 ◽  
pp. 436-439 ◽  
Author(s):  
An Ping Tang ◽  
Ze Qiang He ◽  
Jie Shen ◽  
Guo Rong Xu

Lithium vanadyl phosphate (β-LiVOPO4) cathode material for lithium ion batteries was prepared via a novel solid state method. The microstructure and electrochemical properties of the sample were characterized by X-ray diffraction, scanning electron microscopy, galvanostatically discharge/discharge and cyclic voltammetry techniques, respectively. X-ray diffraction patterns showed that β-LiVOPO4 has an orthorhombic structure with space group of Pnma. The discharge capacity of LiVOPO4 sample is 89.9 mAh•g-1 in the first cycle, and in the 50th cycle it is 76.2 mAh•g-1 at the current density of 10 mA•g-1 between 3.0-4.5 V. The chemical diffusion coefficient ( ) value determined from CV is about 10-11 cm2 s-1. Experimental results indicate that further efforts are needed to improve electrochemical performances of LiVOPO4 material synthesized by solid state method; however, it has a higher discharge plateau around 3.9 V.

2011 ◽  
Vol 391-392 ◽  
pp. 1363-1367
Author(s):  
Yong Mei Liu ◽  
Hui Juan Li ◽  
Jie Ni

A series of yttrium-doped lithium trivanadates LiV3-yYyO8 (y=0, 0.01, 0.03, 0.05, 0.1 and 0.2) were synthesized by a solid-state reaction. X-ray diffraction (XRD) tests show that a proper amount of yttrium doping in LiV3O8 can modify its structure. Charge-discharge tests show that doped samples with a proper amount of yttrium display good cycling stability compared with undoped sample. The cyclic voltammetry (CV) tests indicate that the proper amount of yttrium doping in LiV3O8 can stabilize its original structure. Yttrium doping is a convenient and effective method for improving the electrochemical performances of LiV3O8.


2016 ◽  
Vol 703 ◽  
pp. 316-320
Author(s):  
Hai Feng Chen ◽  
Jing Ling Hu ◽  
Bing Xu

Using NH4VO3, Bi (NO3)3•5H2O and Co (NO3)2•6H2O as raw materials, Co doped BiVO4 (Co/BiVO4) photocatalysts were successfully prepared by solid state method. And the photo catalytic properties were test in this work. Crystal structures of these samples were characterized by X-ray diffraction (XRD). The Methyl Orange (MO) was simulated as the sewage under the visible light to explorer the influence of the illumination time and the mass of photocatalyst. The visible-light absorption spectrum of BiVO4 was broadening with doping Co. It was found that the Co/BiVO4 had higher photocatalytic activity than pure BiVO4 .The reason of enhanced catalytic effect also had been analyzed and discussed in the article.


Author(s):  
Adelyna Oktavia ◽  
Kurnia Sembiring ◽  
Slamet Priyono

Hospho-material of olivine, LiMnPO4 identified as promising for cathode material generation next Lithium-ion battery and has been successfully synthesized by solid-state method with Li2Co3, 2MnO2, 2NH4H2PO4 as raw material. The influence of initial concentration of precursors at kalsinasi temperatures (400-800 ° C) flows with nitrogen. The purity and composition phase verified by x-ray diffraction analysis (XRD), scanning electron microscopy (SEM), spectroscopy, energy Dispersive x-ray Analysis (EDS), Raman spectra. General investigation shows that there is a correlation between the concentration of precursors, the temperature and the temperature of sintering kalsinasi that can be exploited to design lithium-ion next generation.


2011 ◽  
Vol 412 ◽  
pp. 61-64
Author(s):  
Xiao Bo Wu ◽  
Da Zhi Sun ◽  
Dan Yu Jiang ◽  
Hai Fang Xu ◽  
De Xin Huang ◽  
...  

3Y-TZP powder has been successfully synthesized by gel solid-state method. The structural phases of powder particles were analyzed by X-ray diffraction and the morphology was analyzed by scanning electron microscopy. The average size of grains was 230 nm. The sintering behavior, mechanical properties and microstructure of 3Y-TZP ceramics sintered by this powder were investigated. The experiment results showed that the mechanical properties of ceramics were excellent.


2014 ◽  
Vol 2014 ◽  
pp. 1-9
Author(s):  
Hamadi Hamza ◽  
Mohamed Faouzi Zid ◽  
Ahmed Driss

LiNa5K3Mo11As3O45 is a new inorganic compound. It was synthesized by a solid state method. The crystal structure has been studied by single crystal X-ray analysis. The R-values reached 2.8%. The title compound crystallizes in the triclinic system, space group P-1, with a = 10.550 (2) Å, b = 11.723 (2) Å, c = 17.469 (3) Å, α = 102.35 (3)°, β = 87.61 (2)°, and γ = 111.03 (3)°. The anionic unit [Mo11As3O45]9− is formed by nine MoO6 octahedra, two MoO5 trigonal bipyramids, and three AsO4 tetrahedra. The association of [Mo11As3O45]9− units, running along [010], leads to a one-dimensional framework. Li, K, and Na are located in the space surrounding the anionic ribbons. This material was characterized by SEM microscopy, IR spectroscopy, and powder X-ray diffraction. The electrical conductivity was investigated from 528 K to 673 K by impedance complex followed by DSC spectroscopy.


2018 ◽  
Vol 14 (5) ◽  
pp. 440-447 ◽  
Author(s):  
Gang Sun ◽  
Chenxiao Jia ◽  
Shuanlong Di ◽  
Jianning Zhang ◽  
Qinghua Du ◽  
...  

Background: LiNi1/3Mn1/3Co1/3O2 derived from the solid-state method suffers from the problem of significant irreversible charge-discharge behavior. To improve the electrochemical performance of LiNi1/3Mn1/3Co1/3O2, there are several important factors, such as starting raw materials, precursor, preparation method and conditions. In this work, the layered LiNi1/3Mn1/3 Co1/3O2 material was prepared by solid-state reaction. By varying the temperature and duration of synthesis thermal treatment, the greater crystallinity and well-ordered layered LiNi1/3Mn1/3Co1/3O2 cathode material has been successfully synthesized. The structural properties, morphology and electrochemical properties of LiNi1/3Mn1/3Co1/3O2 powders have been investigated in detail. Methods: LiNi1/3Co1/3Mn1/3O2 cathode material was synthesized via a high-temperature solid-state method. Stoichiometric amounts of Ni(CH3COO)2•4H2O, Co(CH3COO)2•4H2O, Mn(CH3COO)2• 4H2O, and Li2CO3 as raw materials were homogenized mixed in a ball mill for 8 h at 240 rpm. By varying the temperature and duration of synthesis thermal treatment, LiNi1/3Co1/3Mn1/3O2 cathode materials with different electrochemistry performance were achieved. (a) The effect of the temperature of synthesis thermal treatment on electrochemistry performance of LiNi1/3Co1/3Mn1/3O2 was explored by calcining the above mixed powder at 800°C, 850°C, 900°C, 950°C, and 1000°C for 12 h in air at a rate of 5°C min-1. Then the target product was prepared at last. The obtained compound was named as N-800, N-850, N-900, N-950 and N-1000, respectively. (b) In order to explore the effect of the duration of synthesis thermal treatment on electrochemistry performance of LiNi1/3 Co1/3Mn1/3O2 cathode material, the above mixed raw materials were calcined at 900°C for 4 h, 8 h, 12 h, 16 h and 20 h in air at a rate of 5°C min-1. The obtained compound was named as N-4, N-8, N- 12, N-16 and N-20, respectively. The N-900 and N-12 are the same sample. Results: The cathode material sintered at 900°C for 12 h revealed the best electrochemical performance, with high-capacity and recyclability compared with other materials. Its initial discharge capacity attains 182.4 mAh g-1 at 0.2 C in the voltage range of 2.5-4.6 V, which can be attributed to its greater crystallinity and well-ordered layered structure. Compared with other studies on lithium-ion batteries given in literature, this work provides a sample, optimal and mild synthetic conditions to synthesize the cathode materials with great electrochemistry performance. Conclusion: A greater crystallinity and well-ordered layered LiNi1/3Mn1/3Co1/3O2 powders had been successfully synthesized by mixing raw materials under various temperatures and duration of synthesis thermal treatment. The XRD results indicated the I(003)/I(104) values of N-900 (N-12) is 1.591 larger than 1.2, which illustrates no undesirable cation mixing to be occurred. In this work, from the results of electrochemical property experiments, it can be indicated that the optimal synthesized conditions are 900°C for 12 h. When the calcination temperature is too low and the calcined time is too short, the material is poorly crystalline and has a poor layer structure. When the calcination temperature is too high and the calcined time is too long, lithium salt is evaporated completely during the calcination process resulting in a poor electrochemistry performance.


2017 ◽  
Vol 715 ◽  
pp. 304-310 ◽  
Author(s):  
Yunlong He ◽  
Jie Zhang ◽  
Qiu Li ◽  
Yong Hao ◽  
Jianwen Yang ◽  
...  

2014 ◽  
Vol 633-634 ◽  
pp. 495-498
Author(s):  
Xiao Bing Huang ◽  
Hong Hui Chen ◽  
Shi Biao Zhou ◽  
Yuan Dao Chen ◽  
Bei Ping Liu ◽  
...  

Spinel Li4-xKxTi5O12(x=0, 0.03) were successfully synthesized by a traditional solid-state method and systematically investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and the charge-discharge test, respectively. The results demonstrated that Li3.97K0.03Ti5O12exhibited much better rate performance in comparsion with Li4Ti5O12. At 0.2 C and 10 C, it delivered a discharge capacity of 173 mAh g-1and 124 mAh g-1respectively, and after 100 cycles at 10 C, 96.1% of its initial capacity was retained.


Sign in / Sign up

Export Citation Format

Share Document