Improved Electrochemical Cycling Behavior of ZnO-Coated Li[sub 1.05]Al[sub 0.1]Mn[sub 1.85]O[sub 3.95]F[sub 0.05] Spinel at 55°C

2006 ◽  
Vol 153 (7) ◽  
pp. A1290 ◽  
Author(s):  
Jung-Min Han ◽  
Seung-Taek Myung ◽  
Yang-Kook Sun
Keyword(s):  
Electrochemical Cycling ◽  
Cycling Behavior

Synthesis, Characterization, and Electrochemical Cycling Behavior of the Ru-Doped Spinel, Li[Mn[sub 2−x]Ru[sub x]]O[sub 4] (x=0, 0.1, and 0.25)

2009 ◽  
Vol 156 (8) ◽  
pp. A652 ◽  
Author(s):  
M. V. Reddy ◽  
S. Sundar Manoharan ◽  
Jimmy John ◽  
Brajendra Singh ◽  
G. V. Subba Rao ◽  
...  
Keyword(s):  
Electrochemical Cycling ◽  
Cycling Behavior

Electrochemical cycling behavior of LiFePO4 cathode charged with different upper voltage limits

2012 ◽  
Vol 62 ◽  
pp. 256-262 ◽  
Author(s):  
Honghe Zheng ◽  
Lili Chai ◽  
Xiangyun Song ◽  
Vince Battaglia
Keyword(s):  
Electrochemical Cycling ◽  
Lifepo4 Cathode ◽  
Cycling Behavior

scholarly journals Comparative studies on electrochemical cycling behavior of two different silica-based ionogels

2016 ◽  
Vol 301 ◽  
pp. 299-305 ◽  
Author(s):  
Shuang Wang ◽  
Ben Hsia ◽  
John P. Alper ◽  
Carlo Carraro ◽  
Zhe Wang ◽  
...  
Keyword(s):  
Comparative Studies ◽  
Electrochemical Cycling ◽  
Cycling Behavior

Dramatic Effects of Fullerene Soot Additives on the Electrochemical Cycling Behavior of Graphite Anodes

2006 ◽  
Vol 153 (10) ◽  
pp. A1880
Author(s):  
Robert E. Doe ◽  
Michael J. Erickson ◽  
Louis J. Rendek ◽  
Michael J. Wagner
Keyword(s):  
Fullerene Soot ◽  
Graphite Anodes ◽  
Electrochemical Cycling ◽  
Cycling Behavior

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>

scholarly journals 1.8 V Aqueous Symmetric Carbon-Based Supercapacitors with Agarose-Bound Activated Carbons in an Acidic Electrolyte

Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1731
Author(s):  
Chih-Chung Lai ◽  
Feng-Hao Hsu ◽  
Su-Yang Hsu ◽  
Ming-Jay Deng ◽  
Kueih-Tzu Lu ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Sulfuric Acid ◽  
Energy Density ◽  
Activated Carbons ◽  
High Energy ◽  
Aqueous Electrolytes ◽  
Alternative Material ◽  
Aqueous Cells ◽  
Acidic Electrolyte ◽  
Cycling Behavior

The specific energy of an aqueous carbon supercapacitor is generally small, resulting mainly from a narrow potential window of aqueous electrolytes. Here, we introduced agarose, an ecologically compatible polymer, as a novel binder to fabricate an activated carbon supercapacitor, enabling a wider potential window attributed to a high overpotential of the hydrogen-evolution reaction (HER) of agarose-bound activated carbons in sulfuric acid. Assembled symmetric aqueous cells can be galvanostatically cycled up to 1.8 V, attaining an enhanced energy density of 13.5 W h/kg (9.5 µW h/cm2) at 450 W/kg (315 µW/cm2). Furthermore, a great cycling behavior was obtained, with a 94.2% retention of capacitance after 10,000 cycles at 2 A/g. This work might guide the design of an alternative material for high-energy aqueous supercapacitors.

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