scholarly journals Sol-Gel Synthesis of Nanocrystalline Mesoporous Li4Ti5O12 Thin-Films as Anodes for Li-Ion Microbatteries

Nanomaterials ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 1369
Author(s):  
Jadra Mosa ◽  
Mario Aparicio

The development of anodes based on Li4Ti5O12 (LTO) for lithium ion batteries has become very important in recent years on the basis that it allows a long service life (stability in charge-discharge cycling) and safety improvements. The processing of this material in the form of thin film allows for greater control of its characteristics and an improvement of its disadvantages, namely reduced electrical conductivity and low diffusion of lithium ions. In this work, we try to limit these disadvantages through the synthesis of a mesostructured carbon-doped Li4Ti5O12 thin-film with a pure spinel phase using a combination of a block-copolymer template and in situ synthesis of Li-Ti double alkoxide. Structural and electrochemical characterization has been carried out to determine the best conditions (temperature, time, atmosphere) for the thermal treatment of the material to reach a compromise between crystallinity and porosity distribution (pore size, pore volume, and interconnectivity).

Membranes ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 109 ◽  
Author(s):  
Jadra Mosa ◽  
Jonh Fredy Vélez ◽  
Mario Aparicio

Organic/inorganic hybrid membranes that are based on GTT (GPTMS-TMES-TPTE) system while using 3-Glycidoxypropyl-trimethoxysilane (GPTMS), Trimethyletoxisilane (TMES), and Trimethylolpropane triglycidyl ether (TPTE) as precursors have been obtained while using a combination of organic polymerization and sol-gel synthesis to be used as electrolytes in Li-ion batteries. Self-supported materials and thin-films solid hybrid electrolytes that were doped with Lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) were prepared. The hybrid network is based on highly cross-linked structures with high ionic conductivity. The dependency of the crosslinked hybrid structure and polymerization grade on ionic conductivity is studied. Ionic conductivity depends on triepoxy precursor (TPTE) and the accessibility of Li ions in the organic network, reaching a maximum ionic conductivity of 1.3 × 10−4 and 1.4 × 10−3 S cm−1 at room temperature and 60 °C, respectively. A wide electrochemical stability window in the range of 1.5–5 V facilitates its use as solid electrolytes in next-generation of Li-ion batteries.


2006 ◽  
Vol 301 ◽  
pp. 91-94
Author(s):  
Yasuhiro Isshiki ◽  
Kaoru Dokko ◽  
Jun Ichi Hamagami ◽  
Takashi Takei ◽  
Kiyoshi Kanamura

Thin films of lithium ion conductive ceramic Li4+xAlxSi1-xO4 were fabricated on Au substrate using sol-gel process. The sol of Li-Al-Si-O was spread on Au substrate using a spin coater, and it was gelated at room temperature. The gel was calcinated at 400 °C and heat-treated at high temperatures between 500 °C and 800 °C in air. The addition of poly(vinylpyrrolidone) (PVP) was effective in stabilizing the sol. Furthermore, the morphology of the obtained thin film was changed by the PVP additive. Li4+xAlxSi1-xO4 thin film prepared at 800 °C exhibited a Li+ ion conductivity of 10-8 S cm-1 at room temperature.


2016 ◽  
Vol 42 (10) ◽  
pp. 12371-12377 ◽  
Author(s):  
Haipeng Li ◽  
Yaqiong Wei ◽  
Yongguang Zhang ◽  
Chengwei Zhang ◽  
Gongkai Wang ◽  
...  

2004 ◽  
Vol 835 ◽  
Author(s):  
Jingsi Yang ◽  
Jun John Xu

ABSTRACTA simple organic solvent based sol-gel method for synthesis of carbon-coated LiFePO4 is developed. Phase pure LiFePO4 with uniform size of 200–300 nm and no agglomeration is obtained, with 1.8 wt % surface carbon formed in-situ. Such a material gives specific discharge capacities of 150 mAh/g and 145 mAh/g at C/5 and 2C at room temperature, respectively, with desirable cycling stability. The dependence of particle size and morphology on precursor concentrations is opposite to conventional solution based methods. Other LiMPO4 (M = Mn, Co, Ni, etc) with favorable physical characteristics can be synthesized the same way.


Rare Metals ◽  
2020 ◽  
Vol 39 (9) ◽  
pp. 1063-1071 ◽  
Author(s):  
Guang-Yin Liu ◽  
Yi-Yang Zhao ◽  
Yu-Feng Tang ◽  
Xiao-Di Liu ◽  
Miao Liu ◽  
...  

Author(s):  
G. S. Zakharova ◽  
E. Thauer ◽  
A. N. Enyashin ◽  
L. F. Deeg ◽  
Q. Zhu ◽  
...  

AbstractThe potential battery electrode material V2O3/C has been prepared using a sol–gel thermolysis technique, employing vanadyl hydroxide as precursor and different organic acids as both chelating agents and carbon sources. Composition and morphology of resultant materials were characterized by X-ray diffraction, Raman spectroscopy, scanning and transmission electron microscopies, physical sorption, and elemental analysis. Stability and electronic properties of model composites with chemically and physically integrated carbon were studied by means of quantum-chemical calculations. All fabricated composites are hierarchically structured and consist of carbon-covered microparticles assembled of polyhedral V2O3 nanograins with intrusions of amorphous carbon at the grain boundaries. Such V2O3/C phase separation is thermodynamically favored while formation of vanadium (oxy)carbides or heavily doped V2O3 is highly unlikely. When used as anode for lithium-ion batteries, the nanocomposite V2O3/C fabricated with citric acid exhibits superior electrochemical performance with an excellent cycle stability and a specific charge capacity of 335 mAh g−1 in cycle 95 at 100 mA g−1. We also find that the used carbon source has only minor effects on the materials’ electrochemical performance.


2010 ◽  
Vol 17 (01) ◽  
pp. 51-58 ◽  
Author(s):  
JEONG-HUN JU ◽  
YOUNG-MIN CHUNG ◽  
YU-RIM BAK ◽  
MOON-JIN HWANG ◽  
KWANG-SUN RYU

Carbon nano-coated LiNi 0.8 Co 0.15 Al 0.05 O 2/ C (LNCAO/C) cathode-active materials were prepared by a sol–gel method and investigated as the cathode material for lithium ion batteries. Electrochemical properties including the galvanostatic charge–discharge ability and cyclic voltammogram behavior were measured. Cyclic voltammetry (2.7–4.8 V) showed that the carbon nano-coating improved the "formation" of the LNCAO electrode, which was related to the increased electronic conductivity between the primary particles. The carbon nano-coated LNCAO/C exhibited good electrochemical performance at high C -rate. Also, the thermal stability at a highly oxidized state of the carbon nano-coated LNCAO was remarkably enhanced. The carbon nano-coating layer can serve as a physical and/or (electro-)chemical protection shell for the underlying LNCAO, which is attributed to an increase of the grain connectivity (physical part) and also to the protection of metal oxide from chemical reactions (chemical part).


2003 ◽  
Vol 02 (04n05) ◽  
pp. 299-306 ◽  
Author(s):  
CHIEN-TE HSIEH ◽  
JIN-MING CHEN ◽  
HSIU-WEN HUANG

Nanostructured SnO 2/ C composites used as anode materials were prepared by sol–gel synthesis to explore electrochemical properties in lithium-ion batteries. Surface characteristics of the SnO 2/ C nanocomposite were analyzed by X-ray diffraction (XRD) and transmission electron microscopy (TEM). It was found that nanocrystalline SnO 2/ C with a grain size of 20–50 nm was uniformly dispersed on the carbon surface. After nanocrytalline SnO 2 coated onto carbon, the discharge capacity showed an increase up to 23%, i.e., from 300 to 370 mAh/g at a current density of 0.6 mA/cm2. The nanocomposite anode can achieve a fairly stable discharge capacity and excellent Coulombic efficiency (>99.5%) over 50 cycles. Cyclic voltammograms indicated that the improvements on capacity and cycleability were due to reversible alloying of nanosized Sn and Li on carbon surface.


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