Discharge capacity estimation for Li-ion batteries based on particle filter under multi-operating conditions

Energy ◽  
2015 ◽  
Vol 86 ◽  
pp. 638-648 ◽  
Author(s):  
Junfu Li ◽  
Lixin Wang ◽  
Chao Lyu ◽  
Liqiang Zhang ◽  
Han Wang
2018 ◽  
Vol 6 (14) ◽  
pp. 5952-5961 ◽  
Author(s):  
M. E. Sotomayor ◽  
C. de la Torre-Gamarra ◽  
W. Bucheli ◽  
J. M. Amarilla ◽  
A. Varez ◽  
...  

Additive-free LTO ceramic anodes (thickness ∼500 μm) with high volumetric discharge capacity were prepared by powder extrusion moulding.


Batteries ◽  
2020 ◽  
Vol 6 (4) ◽  
pp. 51
Author(s):  
Davood Sabaghi ◽  
Mahmoud Madian ◽  
Ahmad Omar ◽  
Steffen Oswald ◽  
Margitta Uhlemann ◽  
...  

TiO2 represents one of the promising anode materials for lithium ion batteries due to its high thermal and chemical stability, relatively high theoretical specific capacity and low cost. However, the electrochemical performance, particularly for mesoporous TiO2, is limited and must be further developed. Elemental doping is a viable route to enhance rate capability and discharge capacity of TiO2 anodes in Li-ion batteries. Usually, elemental doping requires elevated temperatures, which represents a challenge, particularly for sulfur as a dopant. In this work, S-doped TiO2 nanotubes were successfully synthesized in situ during the electrochemical anodization of a titanium substrate at room temperature. The electrochemical anodization bath represented an ethylene glycol-based solution containing NH4F along with Na2S2O5 as the sulfur source. The S-doped TiO2 anodes demonstrated a higher areal discharge capacity of 95 µAh·cm−2 at a current rate of 100 µA·cm−2 after 100 cycles, as compared to the pure TiO2 nanotubes (60 µAh·cm−2). S-TiO2 also exhibited a significantly improved rate capability up to 2500 µA·cm−2 as compared to undoped TiO2. The improved electrochemical performance, as compared to pure TiO2 nanotubes, is attributed to a lower impedance in S-doped TiO2 nanotubes (STNTs). Thus, the direct S-doping during the anodization process is a promising and cost-effective route towards improved TiO2 anodes for Li-ion batteries.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Emre Biçer ◽  
Atilla Öktemer

In the present study, a novel organic polymer consisting of 2,2,6,6-tetramethylpiperidine-N-oxyl group as an electroactive center is employed by synthesizing it from a commercially ready polymer. An investigation on electrochemical and battery properties of this material as a cathode active material in different electrolyte salts was conducted. A coin cell shows a discharge capacity of 40 mAh g−1at 1 Cwhich is 76% of its theoretical capacity. It is observed that there is no significant decrease in capacity value even at 2 Cand 5 Cwhich indicates that it is applicable for the high-power applications. Besides, a good cycle stability is obtained with the organic radical battery.


2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Rushanah Mohamed ◽  
Shan Ji ◽  
Vladimir Linkov

Li-ion battery cathode materials were synthesised via a mechanical activation and thermal treatment process and systematically studied. LiFePO4/CNT composite cathode materials were successfully prepared from LiFePO4material. The synthesis technique involved growth of carbon nanotubes onto the LiFePO4using a novel spray pyrolysis-modified CVD technique. The technique yielded LiFePO4/CNT composite cathode material displaying good electrochemical activity. The composite cathode exhibited excellent electrochemical performances with 163 mAh/g discharge capacity with 94% cycle efficiency at a 0.1 C discharge rate in the first cycle, with a capacity fade of approximately 10% after 30 cycles. The results indicate that carbon nanotube addition can enable LiFePO4to display a higher discharge capacity at a fast rate with high efficiency. The research is of potential interest for the application of carbon nanotubes as a new conducting additive in cathode preparation and for the development of high-power Li-ion batteries for hybrid electric vehicles.


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