Characterizing Materials and Electrochemical Changes in a Range of 18650 Li-Ion Cells Cycled to 80% Initial Capacity

2021 ◽  
Vol MA2021-01 (5) ◽  
pp. 301-301
Author(s):  
Reed M Wittman ◽  
Matthieu Dubarry ◽  
Sergei Ivanov ◽  
Armando Fresquez ◽  
Jill Langendorf ◽  
...  
Keyword(s):  
Li Ion ◽  
Initial Capacity

Effect of Al(OH)3 in Enhancing PbSnF4 Anode Performances for Rechargeable Lithium-Ion Battery

2015 ◽  
Vol 245 ◽  
pp. 153-158 ◽  
Author(s):  
Denis P. Opra ◽  
Anatoly B. Podgorbunsky ◽  
Sergey V. Gnedenkov ◽  
Sergey L. Sinebryukhov ◽  
Alexander A. Sokolov ◽  
...  
Keyword(s):  
Aluminum Hydroxide ◽  
Specific Capacity ◽  
Lithium Ion ◽  
High Energy ◽  
Li Ion Batteries ◽  
Two Phase ◽  
Milling Method ◽  
Energy Ball ◽  
Li Ion ◽  
Initial Capacity

Two-phase Al(OH)3–PbSnF4 composites (concentrations of aluminum hydroxide are equal to 5 wt.%, 15 wt.% and 30 wt.%) has been prepared by high-energy ball-milling method. The materials were employed as anodes in Li-ion batteries. It was established that PbSnF4-based systems yield high initial capacity of 800–1100 mAh g–1. The reversible specific capacity of Al(OH)3–PbSnF4 (aluminum hydroxide – 15 wt.%) after 10-fold charge–discharge cycling in the range of 2.5–0.005 V attains 120 mAh g–1, while the specific capacity of pure PbSnF4 is equal only to 20 mAh g–1. It has been shown that the deviation from 15 wt.% concentration of Al (OH)3 decreases cycling stability of lead fluorostannate (II).

Growth and Electrochemical Properties of V2O5 Nanotube Arrays

2005 ◽  
Vol 879 ◽  
Author(s):  
Ying Wang ◽  
Katsunori Takahashi ◽  
Huamei Shang ◽  
Kyoungho Lee ◽  
Guozhong Cao
Keyword(s):  
Electrochemical Properties ◽  
Nanotube Arrays ◽  
Outer Diameter ◽  
Nanotube Array ◽  
Redox Cycles ◽  
Inner Diameter ◽  
Electrochemical Redox ◽  
Li Ion ◽  
Ion Intercalation ◽  
Initial Capacity

AbstractNanotube arrays of amorphous vanadium pentoxide (V2O5) were synthesized through the template-based electrodeposition and its electrochemical properties were investigated for Li-ion intercalation applications. The nanotubes have a length of 10 μm, outer-diameter of 200 nm and inner-diameter of 100 nm. Electrochemical analyses demonstrate that the V2O5 nanotube array delivers a high initial capacity of 300 mAh/g, about twice that of the electrochemically-prepared V2O5 film. Although the V2O5 nanotube array shows a more drastic degradation than the film under electrochemical redox cycles, the nanotube array reaches a stabilized capacity of 160 mAh/g which remains about 1.3 times the stabilized capacity of the film.

Microstructural Analysis of Si-Ti-Fe Alloy Anode Materials for Li-ion Secondary Batteries

2013 ◽  
Vol 51 (6) ◽  
pp. 429-436 ◽  
Author(s):  
Jeong Eun Chae ◽  
Jun-Mo Yang ◽  
Kyung Jin Park ◽  
Jung Ho Yoo ◽  
Yun Chang Park ◽  
...  
Keyword(s):  
Anode Materials ◽  
Microstructural Analysis ◽  
Alloy Anode ◽  
Li Ion

Oxidized PAN nanofibrous membrane as a separator for Li-ion battery

2014 ◽  
Author(s):  
J.H. Lee ◽  
M.H. Kim ◽  
S.H. Lee ◽  
S.Y. Jin ◽  
W.H. Park
Keyword(s):  
Nanofibrous Membrane ◽  
Li Ion Battery ◽  
Li Ion

Anionic and Cationic Redox Processes in β-Li2IrO3 and Their Structural Implications on Electrochemical Cycling in Li-Ion Cell

2019 ◽  
Author(s):  
Paul Pearce ◽  
Gaurav Assat ◽  
Antonella Iadecola ◽  
François Fauth ◽  
Rémi Dedryvère ◽  
...  
Keyword(s):  
Analytical Techniques ◽  
Charge Compensation ◽  
Coupling Mechanism ◽  
Redox Processes ◽  
Positive Electrodes ◽  
X Ray ◽  
Electrochemical Cycling ◽  
Li Ion ◽  
Electrochemical Instability ◽  
High Degree

The recent discovery of anionic redox as a means to increase the energy density of transition metal oxide positive electrodes is now a well established approach in the Li-ion battery field. However, the science behind this new phenomenon pertaining to various Li-rich materials is still debated. Thus, it is of paramount importance to develop a robust set of analytical techniques to address this issue. Herein, we use a suite of synchrotron-based X-ray spectroscopies as well as diffraction techniques to thoroughly characterize the different redox processes taking place in a model Li-rich compound, the tridimentional hyperhoneycomb β-Li2IrO3. We clearly establish that the reversible removal of Li+ from this compound is associated to a previously described reductive coupling mechanism and the formation of the M-(O-O) and M-(O-O)* states. We further show that the respective contributions to these states determine the spectroscopic response for both Ir L3-edge X-ray absorption spectroscopy (XAS) and X-ray photoemissions spectroscopy (XPS). Although the high covalency and the robust tridimentional structure of this compound enable a high degree of reversibile delithiation, we found that pushing the limits of this charge compensation mechanism has significant effects on the local as well as average structure, leading to electrochemical instability over cycling and voltage decay. Overall, this work highlights the practical limits to which anionic redox can be exploited and sheds some light on the nature of the oxidized species formed in certain lithium-rich compounds.<br>

Anionic and Cationic Redox Processes in β-Li2IrO3 and Their Structural Implications on Electrochemical Cycling in Li-Ion Cell

2019 ◽  
Author(s):  
Paul Pearce ◽  
Gaurav Assat ◽  
Antonella Iadecola ◽  
François Fauth ◽  
Rémi Dedryvère ◽  
...  
Keyword(s):  
Analytical Techniques ◽  
Charge Compensation ◽  
Coupling Mechanism ◽  
Redox Processes ◽  
Positive Electrodes ◽  
X Ray ◽  
Electrochemical Cycling ◽  
Li Ion ◽  
Electrochemical Instability ◽  
High Degree

The recent discovery of anionic redox as a means to increase the energy density of transition metal oxide positive electrodes is now a well established approach in the Li-ion battery field. However, the science behind this new phenomenon pertaining to various Li-rich materials is still debated. Thus, it is of paramount importance to develop a robust set of analytical techniques to address this issue. Herein, we use a suite of synchrotron-based X-ray spectroscopies as well as diffraction techniques to thoroughly characterize the different redox processes taking place in a model Li-rich compound, the tridimentional hyperhoneycomb β-Li2IrO3. We clearly establish that the reversible removal of Li+ from this compound is associated to a previously described reductive coupling mechanism and the formation of the M-(O-O) and M-(O-O)* states. We further show that the respective contributions to these states determine the spectroscopic response for both Ir L3-edge X-ray absorption spectroscopy (XAS) and X-ray photoemissions spectroscopy (XPS). Although the high covalency and the robust tridimentional structure of this compound enable a high degree of reversibile delithiation, we found that pushing the limits of this charge compensation mechanism has significant effects on the local as well as average structure, leading to electrochemical instability over cycling and voltage decay. Overall, this work highlights the practical limits to which anionic redox can be exploited and sheds some light on the nature of the oxidized species formed in certain lithium-rich compounds.<br>

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