scholarly journals Spherical Li4Ti5O12/NiO Composite With Enhanced Capacity and Rate Performance as Anode Material for Lithium-Ion Batteries

2020 ◽  
Vol 8 ◽  
Author(s):  
Jiequn Liu ◽  
Shengkui Zhong ◽  
Qingrong Chen ◽  
Luchao Meng ◽  
Qianyi Wang ◽  
...  

Compositing with metal oxides is proved to be an efficient strategy to improve electrochemical performance of anode material Li4Ti5O12 for lithium-ion batteries. Herein, spherical Li4Ti5O12/NiO composite powders have been successfully prepared via a spray drying method. X-ray diffraction and high-resolution transmission electron microscopy results demonstrate that crystal structure of the powders is spinel. Scanning electron microscopy results show that NiO uniformly distributes throughout Li4Ti5O12 matrix. It is found that compositing with NiO increases both discharge platform capacity and rate stability of Li4Ti5O12. The as-prepared Li4Ti5O12/NiO (5%) exhibits a high initial discharge capacity of 381.3 mAh g−1 at 0.1 C, and a discharge capacity of 194.7 mAh g−1 at an ultrahigh rate of 20 C.

2015 ◽  
Vol 2015 ◽  
pp. 1-8
Author(s):  
Liwei Su ◽  
Yali Sha ◽  
Jingkang Jiang ◽  
Lianbang Wang ◽  
Yuanhao Wang

Ultrathin carbon-coated LiMnPO4(ULMP/C) nanoplates were prepared through an ethylene glycol- (EG-) assisted pyrolysis method. Different from most of LiMnPO4/C works, the obtained ULMP/C possessed relatively small particle size (less than 50 nm in thickness) and preferable carbon coating (~1 nm in thickness, 2 wt.%). As a reference, LiMnPO4/C (LMP/C) composites were also fabricated via the traditional hydrothermal method. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), thermogravimetric analysis (TG), galvanostatic charge-discharge, and cyclic voltammetry (CV) were performed to characterize the crystalline phase, morphology, structure, carbon content, and electrochemical behaviors of samples. The electrochemical performance of bare and carbon-coated LiMnPO4was evaluated as cathodes in lithium ion batteries. As a result, the obtained ULMP/C nanoplates demonstrated much higher reversible capacities (110.9 mAh g−1after 50 cycles at 0.1 C) and rate performances than pure LMP and LMP/C composites. This facile and efficient EG-assisted pyrolysis method can enlighten us on exploiting advanced routes to modify active materials with ultrathin and homogeneous carbon layers.


2013 ◽  
Vol 4 ◽  
pp. 699-704 ◽  
Author(s):  
Raju Prakash ◽  
Katharina Fanselau ◽  
Shuhua Ren ◽  
Tapan Kumar Mandal ◽  
Christian Kübel ◽  
...  

A carbon-encapsulated Fe3O4 nanocomposite was prepared by a simple one-step pyrolysis of iron pentacarbonyl without using any templates, solvents or surfactants. The structure and morphology of the nanocomposite was investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Brunauer–Emmett–Teller analysis and Raman spectroscopy. Fe3O4 nanoparticles are dispersed intimately in a carbon framework. The nanocomposite exhibits well constructed core–shell and nanotube structures, with Fe3O4 cores and graphitic shells/tubes. The as-synthesized material could be used directly as anode in a lithium-ion cell and demonstrated a stable capacity, and good cyclic and rate performances.


2020 ◽  
Vol 20 (3) ◽  
pp. 1962-1967
Author(s):  
Zhen Liu ◽  
Wei Zhou ◽  
Guilin Zeng ◽  
Yuling Zhang ◽  
Zebin Wu ◽  
...  

Oroxylum as a traditional Chinese medicine, was used as a green and novel bio-template to synthesize tremella-like Li3V2(PO4)3/C composite (LVPC) cathode materials by adopting a facile immersion method. The microstructures were analyzed by X-ray diffraction analysis, scanning electron microscopy, and transmission electron microscopy. The electrochemical properties were investigated by galvanostatic charge–discharge experiments. The LVPC revealed specific capacity of 95 mAh·g-1 at 1 C rate within potential range of 3.0–4.3 V. After 100 cycles at 0.2 C, the retention of discharge capacity was 96%. The modified electrochemical performance is mainly resulted from the distinct tremella-like structure.


2020 ◽  
Vol 20 (5) ◽  
pp. 2911-2916
Author(s):  
Zhen Zhang ◽  
Xiao Chen ◽  
Guangxue Zhang ◽  
Chuanqi Feng

The MoO3/V2O5/C, MoO3/C and V2O5/C are synthesized by electrospinning combined with heat treatment. These samples are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy and thermogravimetric analysis (TG) techniques. The results show that sample MoO3/V2O5/C is a composite composed from MoO3, V2O5 and carbon. It takes on morphology of the nanofibers with the diameter of 200~500 nm. The TG analysis result showed that the carbon content in the composite is about 40.63%. Electrochemical properties for these samples are studied. When current density is 0.2 A g−1, the MoO3/V2O5/C could retain the specific capacity of 737.6 mAh g−1 after 200 cycles and its coulomb efficiency is 92.99%, which proves that MoO3/V2O5/C has better electrochemical performance than that of MoO3/C and V2O5/C. The EIS and linear Warburg coefficient analysis results show that the MoO3/V2O5/C has larger Li+ diffusion coefficient and superior conductivity than those of MoO3/C or V2O5/C. So MoO3/V2O5/C is a promising anode material for lithium ion battery application.


2015 ◽  
Vol 60 (2) ◽  
pp. 1145-1149 ◽  
Author(s):  
S.M. Shin ◽  
G.J. Jung ◽  
Woo-Jin Lee ◽  
C.Y. Kang ◽  
J.P. Wang

Abstract This study was focused on recycling process newly proposed to recover electrodic powder enriched in cobalt (Co) and lithium (Li) from spent lithium ion battery. In addition, this new process was designed to prevent explosion of batteries during thermal treatment under inert atmosphere. Spent lithium ion batteries (LIBs) were heated over the range of 300°C to 600°C for 2 hours and each component was completely separated inside reactor after experiment. Electrodic powder was successfully recovered from bulk components containing several pieces of metals through sieving operation. The electrodic powder obtained was examined by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), and atomic absorption spectroscopy (AA) and furthermore image of the powder was taken by scanning electron microscopy (SEM). It was finally found that cobalt and lithium were mainly recovered to about 49 wt.% and 4 wt.% in electrodic powder, respectively.


2008 ◽  
Vol 8 (6) ◽  
pp. 3203-3207 ◽  
Author(s):  
Changjie Mao ◽  
Xingcai Wu ◽  
Jun-Jie Zhu

A large number of β-AgVO3 nanowires with diameter of 30–60 nm, and length of 1.5–3 μm have been successfully synthesized by a simple and facile low-temperature sonochemical route. The morphologies and structures of the nanowires were characterized by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning transmission electron microscopy (SEM), and thermal gravimetric analysis (TGA). Cyclic voltammetry and charge–discharge experiments were applied to characterize the electrochemical properties of the nanowires as cathode materials for lithium-ion batteries. In the initial discharge and charge process, the as-prepared β-AgVO3 nanowires showed the initial charge and discharge capacities of 69 and 102 (mAh)/g, respectively. It is anticipated that the β-AgVO3 nanostructures are promising cathode candidates in the application of primary lithium-ion batteries.


2018 ◽  
Vol 271 ◽  
pp. 9-17 ◽  
Author(s):  
Lkhagvajav Sarantuya ◽  
Galsan Sevjidsuren ◽  
Pagvajav Altantsog ◽  
Namsrai Tsogbadrakh

Nanosized spinel Li4Ti5O12 was successfully synthesized by a solid state reaction method at 800°C according to the Li4Ti5O12cubic spinel phase structure. In this synthesizing process, anatase TiO2and Li2CO3were used as reactants. The average grain size of the synthesized powders was around 200 nm. The synthesized Li4Ti5O12powder was characterized X-ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray spectrometry (EDS), and Specific Surface Area Analyzer (BET, Brunner-Emmett-Teller) respectively. X-ray diffraction results show that calcination temperature and time have the important effects on the crystal structure of Li4Ti5O12powder. In this study, we used a first principle method, based on the density functional theory to explore electronic and structural properties of Li4Ti5O12, as anode material for lithium ion batteries. Differences on these properties between delithiation state Li4Ti5O12and lithiation state Li7Ti5O12are compared. All the predicted structural and electrochemical properties agree closely with the experimental findings in literature. The average intercalation voltage of 1.4V during charging/discharging were obtained. We have shown that the Li4Ti5O12material exhibits insulating behavior with the band gap of 3.16 and 3.90 eV using the GGA and GGA+U+J0calculations respectively. Li7Ti5O12becomes metallic as Li atoms inserted in Li4Ti5O12material. Spinel Li4Ti5O12has been regarded as an attractive anode material for the development of high-power lithium-ion batteries because of its unique attributes of high safety and rate capability.


2014 ◽  
Vol 905 ◽  
pp. 56-60
Author(s):  
Dan Feng Qiu ◽  
Yong Jun Xia ◽  
He Qing Ma ◽  
Gang Bu

Graphene-NiO nanocomposites were prepared via a solvothermal method. The nanostructure and morphology of the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). SEM and TEM results indicated that NiO nanoplates distributed homogeneously on graphene sheets. The electrochemical properties of the samples as active anode materials for lithium-ion batteries were examined by constant current charge-discharge cycling. With graphene as conductive matrix, homogeneous distribution of NiO nanoplates can be ensured and volume changes of thenanocomposite during the charge and discharge processes can be accomodated effectively, which results in good electrochemical performance of the composites.


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