Radial alignment of c-channel nanorods in 3D porous TiO2 for eliciting enhanced Li storage performance

2015 ◽  
Vol 51 (81) ◽  
pp. 15019-15022 ◽  
Author(s):  
Jayeon Baek ◽  
Soomin Park ◽  
Chyan Kyung Song ◽  
Tae Yong Kim ◽  
Inho Nam ◽  
...  

Motivated by anisotropic Li mobility inside a rutile crystal, the c-channel specialized nanorods are radially assembled to form a 3D dendritic TiO2 sphere, which facilitate Li movement during the charge/discharge process.


Author(s):  
Xu Han ◽  
Zeyun Zhang ◽  
Xuefei Xu

To suppress the shuttle effect of lithium polysulfides and promote fast kinetics of charge−discharge process in Li−S batteries, it is essential to search promising catalysts with sufficient stability and high...



Author(s):  
Mahboobeh Nazarian-Samani ◽  
Masoud Nazarian-Samani ◽  
Safa Haghighat-Shishavan ◽  
Kwang-Bum Kim






2021 ◽  
pp. 162261
Author(s):  
Dong Wang ◽  
Gaohui Du ◽  
Di Han ◽  
Qingmei Su ◽  
Shukai Ding ◽  
...  


Nanoscale ◽  
2012 ◽  
Vol 4 (5) ◽  
pp. 1541 ◽  
Author(s):  
Xiangpeng Fang ◽  
Bingkun Guo ◽  
Yifeng Shi ◽  
Bin Li ◽  
Chunxiu Hua ◽  
...  


2011 ◽  
Vol 1333 ◽  
Author(s):  
R. Prasada Rao ◽  
L. Kangle ◽  
S. Adams ◽  
M.V. Reddy ◽  
B.V.R. Chowdari

ABSTRACTThe electrochemical storage performance of anatase TiO2 nanotubes (NT) is compared to the performance of TiO2 nanotubes covered by sulfur. Charge/discharge curves and cycling performance of TiO2 NT with and without sulfur deposition with respect to lithium anodes are demonstrated in electrochemical test cells. At 0.5C cycle rate the TiO2 NT exhibited a first cycle specific charge/discharge capacity of 180/155 mAh/g, whereas the TiO2 NT deposited with sulfur showed a remarkably higher performance at 0.5C cycle rate with first cycle charge/ discharge specific capacities of 258/260 mAh/g and a coulombic efficiency of 98%.



2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Tomoyuki Matsuda ◽  
Yutaka Moritomo

We investigated the charge/discharge properties, valence states, and structural properties of a nanoporous cathode materialLixMn[Fe(CN)6]0.83·3.5H2O. The film-type electrode ofLixMn[Fe(CN)6]0.83·3.5H2Oexhibited a high charge capacity(=128 mAh g-1)and a good cyclability (87% of the initial value after 100 cycles) and is one of the promising candidates for Li-ion battery cathode. X-ray absorption spectra near the Fe and Mn K-edges revealed that the charge/discharge process is a two-electron reaction; that is,MnII–NC–FeII,MnII–NC–FeIII, andMnIII–NC–FeIII. We further found that the crystal structure remains cubic throughout the charge/discharge process. The lattice constant slightly increased during the[FeII(CN)6]4-/[FeIII(CN)6]3-oxidization reaction while decreased during theMnII/MnIIIoxidization reaction. The two-electron reaction without structural phase transition is responsible for the high charge capacity and the good cyclability.



Energies ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 3487
Author(s):  
Ashraf Abdel-Ghany ◽  
Ahmed M. Hashem ◽  
Alain Mauger ◽  
Christian M. Julien

Lithium-rich layered oxides are recognized as promising materials for Li-ion batteries, owing to higher capacity than the currently available commercialized cathode, for their lower cost. However, their voltage decay and cycling instability during the charge/discharge process are problems that need to be solved before their practical application can be envisioned. These problems are mainly associated with a phase transition of the surface layer from the layered structure to the spinel structure. In this paper, we report the AlF3-coating of the Li-rich Co-free layered Li1.2Ni0.2Mn0.6O2 (LLNMO) oxide as an effective strategy to solve these problems. The samples were synthesized via the hydrothermal route that insures a very good crystallization in the layered structure, probed by XRD, energy-dispersive X-ray (EDX) spectroscopy, and Raman spectroscopy. The hydrothermally synthesized samples before and after AlF3 coating are well crystallized in the layered structure with particle sizes of about 180 nm (crystallites of ~65 nm), with high porosity (pore size 5 nm) determined by Brunauer–Emmett–Teller (BET) specific surface area method. Subsequent improvements in discharge capacity are obtained with a ~5-nm thick coating layer. AlF3-coated Li1.2Ni0.2Mn0.6O2 delivers a capacity of 248 mAh g−1 stable over the 100 cycles, and it exhibits a voltage fading rate of 1.40 mV per cycle. According to the analysis from galvanostatic charge-discharge and electrochemical impedance spectroscopy, the electrochemical performance enhancement is discussed and compared with literature data. Post-mortem analysis confirms that the AlF3 coating is a very efficient surface modification to improve the stability of the layered phase of the Li-rich material, at the origin of the significant improvement of the electrochemical properties.



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