scholarly journals Effect of Morphology and Manganese Valence on the Voltage Fade and Capacity Retention of Li[Li2/12Ni3/12Mn7/12]O2

2014 ◽  
Vol 6 (21) ◽  
pp. 18868-18877 ◽  
Author(s):  
Michael G. Verde ◽  
Haodong Liu ◽  
Kyler J. Carroll ◽  
Loïc Baggetto ◽  
Gabriel M. Veith ◽  
...  
Keyword(s):  
Capacity Retention ◽  
Voltage Fade ◽  
Manganese Valence

scholarly journals Voltage fade mitigation in the cationic dominant lithium-rich NCM cathode

2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Prem Chandan ◽  
Chung-Chieh Chang ◽  
Kuo-Wei Yeh ◽  
Chui-Chang Chiu ◽  
Dong-Ze Wu ◽  
...  
Keyword(s):  
Metal Ions ◽  
Transition Metal Ions ◽  
Lithium Content ◽  
Capacity Retention ◽  
Capacity Loss ◽  
Redox Couples ◽  
Reversible Redox ◽  
Alternative Approach ◽  
Voltage Fade ◽  
Rich Material

Abstract In the archetypal lithium-rich cathode compound Li1.2Ni0.13Co0.13Mn0.54O2, a major part of the capacity is contributed from the anionic (O2−/−) reversible redox couple and is accompanied by the transition metal ions migration with a detrimental voltage fade. A better understanding of these mutual interactions demands for a new model that helps to unfold the occurrences of voltage fade in lithium-rich system. Here we present an alternative approach, a cationic reaction dominated lithium-rich material Li1.083Ni0.333Co0.083Mn0.5O2, with reduced lithium content to modify the initial band structure, hence ~80% and ~20% of capacity are contributed by cationic and anionic redox couples, individually. A 400 cycle test with 85% capacity retention depicts the capacity loss mainly arises from the metal ions dissolution. The voltage fade usually from Mn4+/Mn3+ and/or On−/O2− reduction at around 2.5/3.0 V seen in the typical lithium-rich materials is completely eliminated in the cationic dominated cathode material.

A Self-Trapping, Bipolar Viologen Bromide Electrolyte for Aqueous Redox Flow Batteries

2020 ◽  
Author(s):  
wenda wu ◽  
Jian Luo ◽  
Fang Wang ◽  
Bing Yuan ◽  
Tianbiao Liu
Keyword(s):  
Redox Flow Battery ◽  
Capacity Retention ◽  
Redox Flow Batteries ◽  
Redox Electrolyte ◽  
Charge Process ◽  
Self Trapping ◽  
Flow Batteries ◽  
Total Capacity ◽  
Neutral Conditions ◽  
Low Solubility

Aqueous organic redox flow batteries (AORFBs) have become increasing attractive for scalable energy storage. However, it remains challenging to develop high voltage, powerful AORFBs because of the lack of catholytes with high redox potential. Herein, we report methyl viologen dibromide (<b>[MV]Br<sub>2</sub></b>) as a facile self-trapping, bipolar redox electrolyte material for pH neutral redox flow battery applications. The formation of the <b>[MV](Br<sub>3</sub>)<sub>2</sub></b> complex was computationally predicted and experimentally confirmed. The low solubility <b>[MV](Br<sub>3</sub>)<sub>2</sub></b> complex in the catholyte during the battery charge process not only mitigates the crossover of charged tribromide species (Br<sub>3</sub><sup>-</sup>) and addresses the toxicity concern of volatile bromine simultaneously. A 1.53 V bipolar MV/Br AORFB delivered outstanding battery performance at pH neutral conditions, specifically, 100% total capacity retention, 133 mW/cm<sup>2</sup> power density, and 60% energy efficiency at 40 mA/cm<sup>2</sup>.

Ultrathin Carbon Nanosheets for Highly-efficient Capacitive K-ion and Zn-ion Storage

2020 ◽  
Author(s):  
Yamin Zhang ◽  
Zhongpu Wang ◽  
Deping Li ◽  
Qing Sun ◽  
Kangrong Lai ◽  
...  
Keyword(s):  
Energy Storage ◽  
Porous Carbon ◽  
Metal Ion ◽  
Rate Capability ◽  
Energy Storage Devices ◽  
Capacity Retention ◽  
Carbon Nanosheets ◽  
Storage Devices ◽  
High Efficient ◽  
Ion Storage

<p></p><p>Porous carbon has attracted extensive attentions as the electrode material for various energy storage devices considering its advantages like high theoretical capacitance/capacity, high conductivity, low cost and earth abundant inherence. However, there still exists some disadvantages limiting its further applications, such as the tedious fabrication process, limited metal-ion transport kinetics and undesired structure deformation at harsh electrochemical conditions. Herein, we report a facile strategy, with calcium gluconate firstly reported as the carbon source, to fabricate ultrathin porous carbon nanosheets. <a>The as-prepared Ca-900 electrode delivers excellent K-ion storage performance including high reversible capacity (430.7 mAh g<sup>-1</sup>), superior rate capability (154.8 mAh g<sup>-1</sup> at an ultrahigh current density of 5.0 A g<sup>-1</sup>) and ultra-stable long-term cycling stability (a high capacity retention ratio of ~81.2% after 4000 cycles at 1.0 A g<sup>-1</sup>). </a>Similarly, when being applied in Zn-ion capacitors, the Ca-900 electrode also exhibits an ultra-stable cycling performance with ~90.9% capacity retention after 4000 cycles at 1.0 A g<sup>-1</sup>, illuminating the applicable potentials. Moreover, the origin of the fast and smooth metal-ion storage is also revealed by carefully designed consecutive CV measurements. Overall, considering the facile preparation strategy, unique structure, application flexibility and in-depth mechanism investigations, this work will deepen the fundamental understandings and boost the commercialization of high-efficient energy storage devices like potassium-ion/sodium-ion batteries, zinc-ion batteries/capacitors and aluminum-ion batteries.</p><br><p></p>

Effect of Nitric Acid Modification on LiMn2O4 Prepared by Solution Combustion Synthesis

2011 ◽  
Vol 80-81 ◽  
pp. 332-336 ◽  
Author(s):  
Yan Xia ◽  
Mei Huang ◽  
Jun Ming Guo ◽  
Ying Jie Zhang
Keyword(s):  
Nitric Acid ◽  
Combustion Synthesis ◽  
Discharge Capacity ◽  
Retention Rate ◽  
Solution Combustion Synthesis ◽  
Manganese Acetate ◽  
Solution Combustion ◽  
Acid Modification ◽  
Capacity Retention ◽  
Liquid Combustion

Effect of nitric acid and the burning time on the liquid combustion synthesis of spinel LiMn2O4 has been studied, using lithium nitrite and Manganese acetate as raw a material. The results show that the main phases are all LiMn2O4, which can be obtained at 400-600 oC. Before modified, the impurity is Mn3O4 or Mn2O3. After modified, the impurity is only Mn3O4. The aggregation obviously reduced after adding nitric acid, it is indicated that the crystalline increased. With the increasing temperatures, the modified particle size was increased and the aggregation reduced. The initial discharge capacity and cycle stability improved at some extent too. Its first discharge capacity was 104.6, 112.8 and 117.7mAh/g synthesized at 400, 500, 600 oC, respectively, and the 30th capacity retention rate were 84.89%, 80.67% and 73.24%.

scholarly journals Sample dependent performance of aqueous copper hexacyanoferrate/zinc batteries

2021 ◽  
Vol 2 (6) ◽  
pp. 2036-2044
Author(s):  
Solveig Kjeldgaard ◽  
Marnix Wagemaker ◽  
Bo Brummerstedt Iversen ◽  
Anders Bentien
Keyword(s):  
Low Ph ◽  
Capacity Retention ◽  
Copper Hexacyanoferrate ◽  
Similar Performance

The performance of aqueous CuHCF/Zn batteries are highly dependent on the CuHCF sample. With Na-based electrolyte the capacity retention improves at low pH, whereas cells with Zn-based electrolyte have similar performance at pH 2 and pH 4.

FEC-LiTFSI-Pyr1ATFSI Ionic Liquid Electrolyte to Improve Low Temperature Performance of Lithium-Ion Batteries

2014 ◽  
Vol 986-987 ◽  
pp. 80-83
Author(s):  
Xiao Xue Zhang ◽  
Zhen Feng Wang ◽  
Cui Hua Li ◽  
Jian Hong Liu ◽  
Qian Ling Zhang
Keyword(s):  
Low Temperature ◽  
Lithium Ion Batteries ◽  
Low Temperatures ◽  
Freezing Point ◽  
Lithium Ion ◽  
Liquid Electrolyte ◽  
Capacity Retention ◽  
Composite Electrolyte ◽  
Ionic Liquid Electrolyte ◽  
Fluoroethylene Carbonate

N-methyl-N-allylpyrrolidinium bis (trifluoromethanesulfonyl) imide (PYR1ATFSI) with substantial supercooling behavior is synthesized to develop low temperature electrolyte for lithium-ion batteries. Additive fluoroethylene carbonate (FEC) in LiTFSI/PYR1ATFSI/EC/PC/EMC is found that it can reduce the freezing point. LiFePO4/Li coin cells with the FEC-PYR1ATFSI electrolyte exhibit good capacity retention, reversible cycling behavior at low temperatures. The good performance can be attributed to the decrease in the freezing point and the polarization of the composite electrolyte.

A high capacity thiospinel cathode for Mg batteries

2016 ◽  
Vol 9 (7) ◽  
pp. 2273-2277 ◽  
Author(s):  
Xiaoqi Sun ◽  
Patrick Bonnick ◽  
Victor Duffort ◽  
Miao Liu ◽  
Ziqin Rong ◽  
...  
Keyword(s):  
Cathode Material ◽  
High Capacity ◽  
Capacity Retention ◽  
Full Cell

A Mg full cell with a thiospinel cathode material shows 190 mA h g−1 capacity and relatively stable capacity retention.

Overlithiation of LiNi0.8Co0.2O2 for Increased Performance in Li-Ion Batteries

2014 ◽  
Vol 938 ◽  
pp. 253-256
Author(s):  
Hashlina Rusdi ◽  
Norlida Kamarulzaman ◽  
Rusdi Roshidah ◽  
Kelimah Elong ◽  
Abd Rahman Azilah
Keyword(s):  
Cathode Materials ◽  
Structural Instability ◽  
Cation Ordering ◽  
Capacity Fading ◽  
Capacity Retention ◽  
Battery Capacity ◽  
Li Ion ◽  
Battery Application ◽  
Charge Discharge ◽  
Better Than

Layered LiNi1-xCoxO2 is one of the promising cathode materials for Li-ion battery application. However, the Ni rich cathode materials exhibit low capacity and bad capacity retention. This is due to factors such as disorder and structural instability when Li is removed during charge-discharge. Overlithiation of cathode materials is expected to improve the cation ordering and structural stability. Good cation ordering will increase the battery capacity. During charge-discharge, the irreversible Li+ loss can be replaced to a certain extent by the interstitial Li+ ions in the lattice of the LixNi0.8Co0.2O2 material. This helps reduce capacity fading of the cathode materials. In this work the overlithiation of LiNi0.8Co0.2O2 is done by interstitially doping Li+ in the LiNi0.8Co0.2O2 materials producing Li1.05Ni0.8Co0.2O2 and Li1.1Ni0.8Co0.2O2. Results showthat the performance of the overlithiated LiNi0.8Co0.2O2 materials is better than pure LiNi0.8Co0.2O2.

Sign in / Sign up

Export Citation Format

Share Document