Synthesis and Characterization of Li(Li0.05Ni0.6Fe0.1Mn0.25)O2 Cathode Material for Lithim Ion Batteries

2018 ◽  
Vol 21 (1) ◽  
pp. 051-056
Author(s):  
A. Nichelson ◽  
S. Thanikaikarasan ◽  
K. Karuppasamy ◽  
S. Karthickprabhu ◽  
T. Mahalingam ◽  
...  

A new type of lithium enriched cathode material Li (Li0.05Ni0.6Fe0.1Mn0.25)O2 was synthesized by sol-gel method with citric acid as a chelating agent. The structural and morphological studies were systematically investigated through X-ray diffraction, SEM with EDS, FT-IR and Raman analyses. The crystallite size of the Li (Li0.05Ni0.6Fe0.1Mn0.25)O2 cathode material was found to be 45 nm thereby leads to the feasible movement of lithium ion all through the material. FT-IR spectroscopy was used to confirm the metal-oxygen interaction in the prepared cathode material. The electrical properties of the Li (Li0.05Ni0.6Fe0.1Mn0.25)O2 cathode material were studied by impedance and dielectric spectral analyzes. Li (Li0.05Ni0.6Fe0.1Mn0.25)O2 showed a maximum ionic conductivity of 10-6 S/cm at ambient temperature.

2014 ◽  
Vol 17 (3) ◽  
pp. 153-158
Author(s):  
A. Nichelson ◽  
S. Thanikaikarasan ◽  
Pratap Kollu ◽  
P. J. Sebastian ◽  
T. Mahalingam ◽  
...  

In the present work, layered lithium rich Li(Li0.05Ni0.4Co0.3Mn0.25)O2 cathode materials were synthesized and its structural and electrical studies were analyzed. Layered Li(Li0.05Ni0.4Co0.3Mn0.25)O2 cathode material was prepared by sol-gel technique using citric acid as chelating agent. The prepared sample was characterized by X-ray diffraction, SEM-EDS studies. The crystallite size of the Li(Li0.05Ni0.4Co0.3Mn0.25)O2 cathode material was about 57 nm in which the diffusion path of lithium ion is effectively possible. The complexation behavior of prepared cathode material was analyzed by FT-IR spectroscopy. The electrical properties of the prepared Li(Li0.05Ni0.4Co0.3Mn0.25)O2 cathode material was studied by impedance and dielectric spectral analyzes. The maximum ionic conductivity of LiLi0.05Ni0.4Co0.3Mn0.25)O2 was found to be in the order of 10-3.4 S/cm. The dielectric analysis of cathode material confirms the non-Debye type behavior.


1996 ◽  
Vol 459 ◽  
Author(s):  
E. Ching-Prado ◽  
W. Pérez ◽  
A. Reynés-Figueroa ◽  
R. S. Katiyar ◽  
D. Ravichandran ◽  
...  

ABSTRACTThin films of SrBi2Nb2O9 (SBN) with thicknesses of 0.1, 0.2, and 0.4 μ were grown by Sol-gel technique on silicon, and annealed at 650°C. The SBN films were investigated by Raman scatering for the first time. Raman spectra in some of the samples present bands around 60, 167, 196, 222, 302, 451, 560, 771, 837, and 863 cm−1, which correspond to the SBN formation. The study indicates that the films are inhomogeneous, and only in samples with thicknesses 0.4 μ the SBN material was found in some places. The prominent Raman band around 870 cm−1, which is the A1g mode of the orthorhombic symmetry, is assigned to the symmetric stretching of the NbO6 octahedrals. The frequency of this band is found to shift in different places in the same sample, as well as from sample to sample. The frequency shifts and the width of the Raman bands are discussed in term of ions in non-equilibrium positions. FT-IR spectra reveal a sharp peak at 1260 cm−1, and two broad bands around 995 and 772 cm−1. The bandwidths of the latter two bands are believed to be associated with the presence of a high degree of defects in the films. The experimental results of the SBN films are compared with those obtained in SBT (T=Ta) films. X-ray diffraction and SEM techniques are also used for the structural characterization.


2018 ◽  
Vol 15 (1) ◽  
pp. 73-80 ◽  
Author(s):  
Baghdad Science Journal

Polyaniline membranes of aniline were produced using an electrochemical method in a cell consisting of two poles. The effect of the vaccination was observed on the color of membranes of polyaniline, where analysis as of blue to olive green paints. The sanction of PANI was done by FT-IR and Raman techniques. The crystallinity of the models was studied by X-ray diffraction technique. The different electronic transitions of the PANI were determined by UV-VIS spectroscopy. The electrical conductivity of the manufactured samples was measured by using the four-probe technique at room temperature. Morphological studies have been determined by Atomic force microscopy (AFM). The structural studies have been measured by (SEM).


2013 ◽  
Vol 701 ◽  
pp. 131-135 ◽  
Author(s):  
Abdullah Abdul Samat ◽  
Mohd Azlan Mohd Ishak ◽  
Hamidi Abd Hamid ◽  
Osman Nafisah

A potential candidate for intermediate temperature solid oxide fuel cell (IT-SOFC) cathode material which is strontium-doped lanthanum cobaltite, La0.6Sr0.4CoO3-α (LSCO) has been synthesized by a complexing method. Citric acid (CA) and ethylenediaminetetraacetic acid (EDTA) were used as a combined chelating agent and ethylene glycol (EG) was employed as surfactant. The obtained powder was characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM). TGA results showed the thermal decomposition of the precursor gel was completed at 700 °C. A single perovskite phase of LSCO with cubic structure was obtained at calcination temperature of 1000 °C with heating/cooling rate of 10 °C min-1 as confirmed by XRD analysis. SEM result revealed that the morphology of the powder was spherical in shape with diameter ranging from 250 to 650 nm. Apparently, the bulk sample consists of almost homogeneous and identical particles.


Crystals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1125
Author(s):  
Dovydas Karoblis ◽  
Ramunas Diliautas ◽  
Eva Raudonyte-Svirbutaviciene ◽  
Kestutis Mazeika ◽  
Dalis Baltrunas ◽  
...  

In this study, the aqueous sol-gel method was employed for the synthesis of (1−x)SrTiO3-xBiMnO3 solid solutions. Powder X-ray diffraction analysis confirmed the formation of single-phase perovskites with a cubic structure up to x = 0.3. A further increase of the BiMnO3 content led to the formation of a negligible amount of neighboring Mn3O4 impurity, along with the major perovskite phase. Infrared (FT-IR) analysis of the synthesized specimens showed gradual spectral change associated with the superposition effect of Mn-O and Ti-O bond lengths. By introducing BiMnO3 into the SrTiO3 crystal structure, the size of the grains increased drastically, which was confirmed by means of scanning electron microscopy. Magnetization studies revealed that all solid solutions containing the BiMnO3 component can be characterized as paramagnetic materials. It was observed that magnetization values clearly correlate with the chemical composition of powders, and the gradual increase of the BiMnO3 content resulted in noticeably higher magnetization values.


2016 ◽  
Vol 34 (2) ◽  
pp. 404-411 ◽  
Author(s):  
N. Murali ◽  
K. Vijaya babu ◽  
K. Ephraim babu ◽  
V. Veeraiah

AbstractLayered oxide LiMO2 (Ni, Co, Mn) have been proposed as cathode materials for lithium-ion batteries. Mainly LiNiO2 is accepted as an attractive cathode material because of its various advantages such as low cost, high discharge capacity, good reversibility. The LiNi0.5Mn0.5O2 powders are synthesized by a sol-gel method using citric acid as a chelating agent. The structure of the synthesized material is analyzed by using XRD, FT-IR and the microstructures of the samples are observed by using FESEM. The intensities and positions of the peaks are in a good agreement with the previous results. The morphological changes are clearly observed as a result of manganese substitution. The Fourier transform infrared (FT-IR) spectra obtained with KBr pellet data reveal the structure of the oxide lattice constituted by LiO6 and NiO6 octahedra. The conductivity studies are characterized by (EIS) in the frequency range of 42 Hz to 1 MHz at room temperature to 120 °C. The dielectric properties are analyzed in the framework of complex dielectric permittivity and complex electric modulus formalisms. It indicates that the conductivity increases with increasing temperature. The fitting data of EIS plots replicate the non-Debye relaxation process with negative temperature coefficient of resistance (NTCR) behavior.


2011 ◽  
Vol 233-235 ◽  
pp. 1188-1191
Author(s):  
Hong Cai ◽  
Yan Chen ◽  
Yun Ying Wu

Nano-TiO2 particles were prepared by sol-gel method, of which the surfaces were coated by SiO2. The coating was achieved by the hydrolysis of sodium silicate (Na2SiO3) in ammonium chloride (NH4Cl). The surface bonding, phase constitution and chemical components of the samples were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction(XRD) and X-ray photoelectron spectroscopy (XPS). The mechanism of the SiO2 coating process onto TiO2 surface was analyzed. Results show that SiO2 particles were immobilized on the TiO2 surface via Ti—O—Si bondings, which formed at the interface. The SiO2 layer on TiO2 surface was amorphous, the photocatalytic performance was decreased of the TiO2 while its stability was enhanced after surface modification.


2008 ◽  
Vol 396-398 ◽  
pp. 481-484
Author(s):  
Rodrigo Jiménez-Gallegos ◽  
L. Téllez-Jurado ◽  
Luis M. Rodríguez-Lorenzo ◽  
Julio San Román

This paper focuses on the preparation of siloxane-polyurethane hybrid materials using a sol-gel method. The global aim of the project is to tailor mechanical properties, degradability rate, bioactivity and biocompatibility to design scaffolds for musculoskeletal applications. A series of seven hybrid materials were synthesized with varying the proportion of polydimethylsiloxane (PDMS), and Polyurethane (PU). The organic part ratios (by weight) employed were (% PDMS:% PU) 30:0, 35:5, 20:10, 15:15, 10:20, 5:25, and 0:30. The organic part was reacted with constant 70 % TEOS to obtain the hybrid materials. A sol-gel process was selected for the synthesis of the hybrids. The characterization of materials was carried out by the fourier-infrared spectroscopy (FT-IR), x-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electronic microscopy (SEM) and proton nuclear magnetic resonance (1H-NMR) techniques in order to analyze the structure, microstructure and chemical composition of the hybrid materials. Gelification time depends on the proportion of PU used. When no PU is employed, the gel time is 8 hours but it rises up to 18 days for 30 % of polyurethane. Materials range from opaque to translucent but with a greater fragility for greater amounts of polyurethane. No differences in the bonding of materials could be appreciated.


2011 ◽  
Vol 1326 ◽  
Author(s):  
Rene Fabian Cienfuegos ◽  
Leonardo Chávez Guerrero ◽  
Sugeheidy Carranza ◽  
Laurie Jouanin ◽  
Guillaume Marie ◽  
...  

ABSTRACTThe goal in this study was to synthesize a lanthanum - nickel phase (Ruddlesden-Popper phases) La4Ni3O10. This material was prepared using a polymeric route. An easy synthesis method is presented in order to obtain an economical cathode material, which can be used in Solid Oxide Fuel Cells (SOFC). The polymeric precursors were prepared following the Castillo method. The originality of this work was to optimize the ratio HMTA/ metallic salts from 1 to 6. The obtained powders were characterized by thermal analysis; Differential Scanning Calorimetry (DSC Q10 Instrument TA), Thermogravimetric Analysis (TGA - Q50 Instrument TA-) and X-ray diffractometer (Bruker, D8 Advance diffractometer), in order to determine the crystallized phase. Experiments 5 and 6 did not present coagulation but after few days, solution 5 was transformed into a gel. Gels 2 to 5 were heated in order to obtain a solid material. These powders are characterized by thermogravimetric and thermo-differential methods. The powders obtained at 800, 900 and 1000°C were analyzed by X-ray diffraction and it was found that the temperature to get to the La4Ni3O10 phase was 1000ºC.


2021 ◽  
Author(s):  
K. Kalaiselvi ◽  
S. Premlatha ◽  
M. Raju ◽  
Paruthimal Kalaignan Guruvaiah

Abstract LiNi1/3Mn1/3Co1/3O2 as a promising cathode material for lithium-ion batteries was synthesized by a sol-gel method using nitrate precursor calcined at 800°C for 10 hours. The crystallite nature of samples is confirmed from X-ray diffraction analysis. SEM and TEM analyses were used to investigate the surface morphology of the prepared samples. It was found that, highly crystalline polyhedral RuO2 nanoparticles are well doped on the surface of pristine LiNi1/3Mn1/3Co1/3O2 with a size of about approximately 200 nm. The chemical composition of the prepared samples was characterized by EDX and XPS analyses. The electrochemical performance of the proposed material was studied by cyclic voltammetry and charge/discharge analyses. The electrode kinetics of the samples was studied by electrochemical impedance spectroscopy. The developed RuO2 doping may provide an effective strategy to design and synthesize the advanced electrode materials for lithium ion batteries. The doping strategy has dramatically increased the capacity retention from 74 % to 90% with a high discharge capacity of 251.2 mAhg− 1. 3 % RuO2-doped LiNi1/3Mn1/3Co1/3O2 cathode materials have showed the similar characteristics of two potential plateaus obtained at 2.8 and 4.2 V compared with un doped electrode cathode material. These results revealed the enhanced performance of RuO2- doped LiNi1/3Mn1/3Co1/3O2 during insertion and extraction of lithium ions compared to pristine material.


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