scholarly journals LiMnPO4 Olivine as a Cathode for Lithium Batteries

2011 ◽  
Vol 5 (1) ◽  
pp. 222-227 ◽  
Author(s):  
Zhumabay Bakenov ◽  
Izumi Taniguchi

The olivine structured mixed lithium-transition metal phosphates LiMPO4 (M = Fe, Mn, Co) have attracted tremendous attention of many research teams worldwide as a promising cathode materials for lithium batteries. Among them, lithium manganese phosphate LiMnPO4 is the most promising considering its high theoretical capacity and operating voltage, low cost and environmental safety. Various techniques were applied to prepare this perspective cathode for lithium batteries. The solution based synthetic routes such as spray pyrolysis, precipitation, sol-gel, hydrothermal and polyol synthesis allow preparing nanostructured powders of LiMnPO4 with enhanced electrochemical properties, which is mostly attributed to the higher chemical homogeneity and narrow particle size distribution of the material. Up-to-date, the LiMnPO4/C composites prepared by the spray pyrolysis route have the best electrochemical performance among the reported in the literature.

Author(s):  
Elena V. Tomina ◽  
Dmitry A. Lastochkin ◽  
Sergey A. Maltsev

Due to rare earth doping, phosphates and vanadates are the leading materials for the synthesis of phosphors due to their thermal stability, low sintering temperature, and chemical stability. Phosphors in the nanoscale state are of particular interest. The simple, fast, and scalable synthesis of nanophosphors with high chemical homogeneity is a priority task. The purpose of this work was to synthesize powders of mixed yttrium vanadate-phosphate crystals of various compositions by coprecipitation under the action of microwave radiation and spray pyrolysis, as well as to compare the characteristics ofthe obtained samples. Samples of YVхP1–хO4 of different compositions were synthesized by coprecipitation under the action of microwave radiation and spray pyrolysis in different modes. In the case of the synthesis of yttrium vanadate-phosphate YVхP1–хO4 by spray pyrolysis followed by annealing, according to the X-ray phase analysis data, single-phase nanopowders were formed. The morphological characteristics of the samples were revealed by the methods of transmission electron microscopy and scanning electron microscopy. Depending on the annealing conditions, the samples were either faceted or spherical particlesless than 100 nm in size. The composition of the YVхP1–хO4 , samples synthesized by the coprecipitation method under the action of microwave radiation strongly depended on the pH of the precursor solution. The minimum content of impurity phases was reached at pH 9.Spray pyrolysis allows the synthesis of yttrium vanadate phosphate YVхP1–хO4 nanopowders of high chemical homogeneity with a particle size of less than 100 nm. The maximum chemical homogeneity of yttrium vanadate-phosphate powders was achieved at pH = 9 during the synthesis of YVхP1–хO4 by coprecipitation under the action of microwave radiation. However, the particle size dispersion was large, within the range of 2–60 μm.       References 1. Wu C., Wang Y., Jie W. Hydrothermal synthesisand luminescent properties of LnPO4:Tb (Ln = La, Gd)phosphors under VUV excitation. Journal of Alloys andCompounds. 2007;436: 383–386. DOI: https://doi.org/10.1016/j.jallcom.2006.07.0562. Huang J., Tang L., Chen N., Du G. Broadeningthe photoluminescence excitation spectral bandwidthof YVO4:Eu3+ nanoparticles via a novel core-shell andhybridization approach. Materials. 2019;12: 3830. DOI:https://doi.org/10.3390/ma122338303. Wu Y., Zhang Z., Suo H., Zhao X., Guo C. 808 nmlight triggered up-conversion optical nano-thermometerYPO4:Nd3+/Yb3+/Er3+ based on FIR technology.Journal of Luminescence. 2019;214: 116478. DOI:https://doi.org/10.1016/j.jlumin.2019.1165784. Xiu Z., Wu Y., Hao X., Li X., Zhang L. Uniformand well-dispersed Y2O3:Eu/YVO4:Eu composite microsphereswith high photoluminescence prepared bychemical corrosion approach. Colloids Surf. A.2012;401(5): 68–73. DOI: https://doi.org/10.1016/j.colsurfa.2012.03.0215. Vats B. G., Gupta S. K., Keskar M., Phatak R.,Mukherjee S., Kannan S. The effect of vanadium substitutionon photoluminescent properties of KSrLa(-PO4)x(VO4)2x:Eu3+ phosphors, a new variant of phosphovanadates.New Journal of Chemistry. 2016;40(2):1799–1806. DOI: https://doi.org/10.1039/c5nj02951a6. Riwotzki K., Haase M. Colloidal YVO4:Eu andYP0.95V0.05O4:Eu nanoparticles: luminescence and energytransfer processes. The Journal of Physical ChemistryB. 2001;105(51): 12709–12713. DOI: https://doi.org/10.1021/jp01137357. Wu C.-C., Chen K.-B., Lee C.-S., Chen T.-M.,Cheng B.-M. Synthesis and VUV photoluminescencecharacterization of (Y,Gd)(V,P)O4:Eu3+ as a potentialred-emitting PDP phosphor. Chem. Mater. 2007;19(13):3278–3285. DOI: https://doi.org/10.1021/cm061042a8. Shimomura Y., Kurushima T., Olivia R., Kijima N.Synthesis of Y(P,V)O4:Eu3+ red phosphor by spray pyrolysiswithout postheating. The Japan Society of Applied.2005;44(3): 1356–1360. DOI: https://doi.org/10.1143/JJAP.44.13569. Lai H, Chen B., Xu W., Xie Y., Wang X., Di W. Fineparticles (Y,Gd)PxV1−xO4:Eu3+ phosphor for PDP preparedby coprecipitation reaction. Materials Letters.2006; 60 (11): 1341-1343. DOI: https://doi.org/10.1016/j.matlet.2005.11.05110. Singh V., Takami S., Aoki N., Hojo D., Arita T.,Adschiri T. Hydrothermal synthesis of luminescentGdVO4:Eu nanoparticles with dispersibility in organicsolvents. Journal of Nanoparticle Research. 2014;16(5):2378. DOI: https://doi.org/10.1007/s11051-014-2378-211. Song W.-S., Kim Y.-S., Yang H. Hydrothermalsynthesis of self-emitting Y(V,P)O4 nanophosphors forfabrication of transparent blue-emitting display device.Journal of Luminescence. 2012;132(5): 1278–1284.DOI: https://doi.org/10.1016/j.jlumin.2012.01.01512. Yu M., Lin J., Fu J., Han Y. Sol–gel fabrication,patterning and photoluminescent properties ofLaPO4:Ce3+, Tb3+ nanocrystalline thin films. ChemicalPhysics Letters. 2003;5(1-2): 178–183. DOI: https://doi.org/10.1016/S0009-2614(03)00239-213. Raoufi D., Raoufi T. The effect of heat treatmenton the physical properties of sol–gel derived ZnO thinfilms. Applied Surface Science. 2009;255(11): 5812–5817. DOI: https://doi.org/10.1016/j.ap-susc.2009.01.01014. Shao J., Yan J., Li X., Li S., Hu T. Novel fluorescentlabel based on YVO4:Bi3+, Eu3+ for latent fingerprintdetection. Dyes and Pigments. 2019;160: 555–562.DOI: https://doi.org/10.1016/j.dyepig.2018.08.03315. Dolinskaya Yu. A., Kolesnikov I. E., KurochkinA. V., Man’shina A. A., Mikhailov M. D., SemenchaA. V. Sol-Gel synthesis and luminescent propertiesof YVO4: Eu nanoparticles. Glass Physics and Chemistry.2013;39(3): 308–310. DOI: https://doi.org/10.1134/s108765961303006116. Tomina E. V., Sladkopevtsev B. V., Knurova M. V.,Latyshev A.N., Mittova I. Y., Mittova V. O. Microwavesynthesis and luminescence properties of YVO4:Eu3+.Inorganic Materials. 2016;52(5): 495–498. DOI: https://doi.org/10.7868/S0002337X1605017117. Tomina E. V., Mittova I. J., Burtseva N. A.,Sladkopevtsev B. V. Method for synthesis of yttrium orthovanadate-based phosphor: patent for invention No2548089. The patent holder FGBOU VPO “Voronezhstate University” No 2013133382/05; declared12.11.2013; published. 20.05.2015.18. Tomina E. V., Kurkin N. A., & Mal’tsev S. A.Microwave synthesis of yttrium orthoferrite dopedwith nickel. Kondensirovannye sredy i mezhfaznyegranitsy = Condensed Matter and Interphases.2019;21(2): 306–312. DOI:https://doi.org/10.17308/kcmf.2019.21/768 (In Russ., abstract in Eng.)19. Huang J., Gao R., Lu Z., Qian D., Li W., Huang B.,He X. Sol–gel preparation and photoluminescenceenhancement of Li+ and Eu3+ co-doped YPO4 nanophosphors.Optical Materials. 2010;32(9): 857–861.DOI: https://doi.org/10.1016/j.optmat.2009.12.01120. Brandon D., Kaplan W. D. MicrostructuralCharacterization of Materials. John Wiley & Sons Ltd;1999. 409 p. DOI: https://doi.org/10.1002/9780470727133


2020 ◽  
Author(s):  
Martin E. Oviedo ◽  
Fernando Alvira ◽  
Agustin Apaolaza ◽  
Juan F. Martiarena ◽  
Matías R. Tejerina

This work presents a design of a low-cost spray pyrolysis automatized system which allows to manufacture high quality thin films. In particular, the thermal component of this instrument is modelled in different operation conditions, analyzed, and controlled. Also, different configurations for the whole instrument are analyzed.


2020 ◽  
Author(s):  
Martin E. Oviedo ◽  
Fernando Alvira ◽  
Agustin Apaolaza ◽  
Juan F. Martiarena ◽  
Matías R. Tejerina

This work presents a design of a low-cost spray pyrolysis automatized system which allows to manufacture high quality thin films. In particular, the thermal component of this instrument is modelled in different operation conditions, analyzed, and controlled. Also, different configurations for the whole instrument are analyzed.


2012 ◽  
Vol 584 ◽  
pp. 345-349 ◽  
Author(s):  
P. Prahasini ◽  
Marimuthu Sivakumar ◽  
Rengapillai Subadevi ◽  
Fu Ming Wang

LiCoO2 is the most studied cathode material for lithium batteries. The doping effect gives a better cycle life in such materials. Apart from the doping effect, the preparation technique also plays an important role. Presently, the layer structured Cu doped LiCoO2 cathode material has been prepared via microwave assisted sol gel route; better cycle life and capacity retention have been attained. It was found that this method could reduce the synthesis time to 30 minutes. The espousal of the microwave method in synthesis could develop a highly efficient, low cost process for synthesis. The surface morphology of the material has been observed using SEM and it is inhomogeneous in nature. The capacity retention is higher than that of pure LiCoO2 material. Compositional analysis was made through EDX. The Cu doped material has a voltage plateau about 4.0V which is obtained from the cyclic voltammetry.


2010 ◽  
Vol 12 (3,4) ◽  
pp. 201
Author(s):  
I. Belharouak ◽  
Q. Yan ◽  
Y-K. Sun ◽  
K. Amine

<p>Nano-sized and micron-sized LiFePO<sub>4</sub> electrode materials were prepared by a sol gel and coprecipitation reactions. An improvement of the cycling and rate performances in lithium cells was observed for the carbon coated LiFePO<sub>4</sub> materials. The coating process uses a solid/gas-phase reaction which consists of decomposing propylene gas, as carbon source, inside a reactor containing olivine LiFePO<sub>4</sub> materials. Optimized LiFePO<sub>4</sub> electrode cells, cycled at RT between 3.0 and 4.3 V at a C/10 rate, do not show any sign of capacity fade during the first 50 cycles. Combination of the high volumetric energy density and low cost preparation method makes the micron-sized LiFePO<sub>4</sub> olivine an attractive safe cathode for lithium-ion batteries.</p>


RSC Advances ◽  
2021 ◽  
Vol 11 (13) ◽  
pp. 7732-7737
Author(s):  
Fenying Wang ◽  
Dan Wang ◽  
Tingting Wang ◽  
Yu Jin ◽  
Baoping Ling ◽  
...  

Fluorescent molecularly imprinted polymer (FMIP) gains great attention in many fields due to their low cost, good biocompatibility and low toxicity. Here, a high-performance FMIP was prepared based on the autocatalytic silica sol–gel reaction.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Md Atiqur Rahman ◽  
Mohammad Tariqul Islam ◽  
Mandeep Singh Jit Singh ◽  
Md Samsuzzaman ◽  
Muhammad E. H. Chowdhury

AbstractIn this article, we propose SNG (single negative) metamaterial fabricated on Mg–Zn ferrite-based flexible microwave composites. Firstly, the flexible composites are synthesized by the sol-gel method having four different molecular compositions of MgxZn(1−x)Fe2O4, which are denoted as Mg20, Mg40, Mg60, and Mg80. The structural, morphological, and microwave properties of the synthesized flexible composites are analyzed using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and conventional dielectric assessment kit (DAK) to justify their possible application as dielectric substrate at microwave frequency regime. Thus the average grain size is found from 20 to 24 nm, and the dielectric constants are 6.01, 5.10, 4.19, and 3.28, as well as loss tangents, are 0.002, 0.004, 0.006, and 0.008 for the prepared Mg–Zn ferrites, i.e., Mg20, Mg40, Mg60, and Mg80 respectively. Besides, the prepared low-cost Mg–Zn ferrite composites exhibit high flexibility and lightweight, which makes them a potential candidate as a metamaterial substrate. Furthermore, a single negative (SNG) metamaterial unit cell is fabricated on the prepared, flexible microwave composites, and their essential electromagnetic behaviors are observed. Very good effective medium ratios (EMR) vales are obtained from 14.65 to 18.47, which ensure the compactness of the fabricated prototypes with a physical dimension of 8 × 6.5 mm2. Also, the proposed materials have shown better performances comparing with conventional FR4 and RO4533 materials, and they have covered S-, C-, X-, Ku-, and K-band of microwave frequency region. Thus, the prepared, flexible SNG metamaterials on MgxZn(1−x)Fe2O4 composites are suitable for microwave and flexible technologies.


Electronics ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1099
Author(s):  
Ye-Ji Han ◽  
Se Hyeong Lee ◽  
So-Young Bak ◽  
Tae-Hee Han ◽  
Sangwoo Kim ◽  
...  

Conventional sol-gel solutions have received significant attention in thin-film transistor (TFT) manufacturing because of their advantages such as simple processing, large-scale applicability, and low cost. However, conventional sol-gel processed zinc tin oxide (ZTO) TFTs have a thermal limitation in that they require high annealing temperatures of more than 500 °C, which are incompatible with most flexible plastic substrates. In this study, to overcome the thermal limitation of conventional sol-gel processed ZTO TFTs, we demonstrated a ZTO TFT that was fabricated at low annealing temperatures of 350 °C using self-combustion. The optimized device exhibited satisfactory performance, with μsat of 4.72 cm2/V∙s, Vth of −1.28 V, SS of 0.86 V/decade, and ION/OFF of 1.70 × 106 at a low annealing temperature of 350 °C for one hour. To compare a conventional sol-gel processed ZTO TFT with the optimized device, thermogravimetric and differential thermal analyses (TG-DTA) and X-ray photoelectron spectroscopy (XPS) were implemented.


Metals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 463
Author(s):  
Srecko Stopic ◽  
Felix Wenz ◽  
Tatjana-Volkov Husovic ◽  
Bernd Friedrich

Silica has sparked strong interest in hydrometallurgy, catalysis, the cement industry, and paper coating. The synthesis of silica particles was performed at 900 °C using the ultrasonic spray pyrolysis (USP) method. Ideally, spherical particles are obtained in one horizontal reactor from an aerosol. The controlled synthesis of submicron particles of silica was reached by changing the concentration of precursor solution. The experimentally obtained particles were compared with theoretically calculated values of silica particles. The characterization was performed using a scanning electron microscope (SEM) and energy-dispersive X-ray spectroscopy (EDS). X-ray diffraction, frequently abbreviated as XRD, was used to analyze the structure of obtained materials. The obtained silica by ultrasonic spray pyrolysis had an amorphous structure. In comparison to other methods such as sol–gel, acidic treatment, thermal decomposition, stirred bead milling, and high-pressure carbonation, the advantage of the ultrasonic spray method for preparation of nanosized silica controlled morphology is the simplicity of setting up individual process segments and changing their configuration, one-step continuous synthesis, and the possibility of synthesizing nanoparticles from various precursors.


2014 ◽  
Vol 989-994 ◽  
pp. 316-319 ◽  
Author(s):  
Jing Zhu ◽  
Yong Guang Liu ◽  
Qing Qing Tian ◽  
Ling Wang ◽  
Ji Lin Cao

Li0.95Na0.05Ti2(PO4)3/C nanocomposite was prepared by sol-gel method.The structure and morphology of the samples were characterized by XRD, SEM which showed the particles had typical NASICON structure and diameter range from 400~500nm. The electrochemical performance were tested by cyclic voltammetry and galvanostatic charge–discharge. Results show Li0.95Na0.05Ti2(PO4)3/C nanocomposite exhibitsmuch better electrochemical performance than bare Li0.95Na0.05Ti2(PO4)3.


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