Synthesizing kinetics and characteristics of high-capacity Li1.16(Ni0.25Mn0.75)0.84O2 cathode materials for lithium-ion batteries

Ionics ◽  
2021 ◽  
Author(s):  
Min Gao ◽  
Yi He ◽  
Kun Yan ◽  
Guimei Han ◽  
Weidong Zhuang ◽  
...  
2019 ◽  
Vol 483 ◽  
pp. 1166-1173 ◽  
Author(s):  
Wei Zhao ◽  
Xunhui Xiong ◽  
Yingbang Yao ◽  
Bo Liang ◽  
Ye Fan ◽  
...  

2015 ◽  
Vol 638 ◽  
pp. 298-304 ◽  
Author(s):  
Linsen Zhang ◽  
Kai Jin ◽  
Lizhen Wang ◽  
Yong Zhang ◽  
Xiaofeng Li ◽  
...  

RSC Advances ◽  
2013 ◽  
Vol 3 (15) ◽  
pp. 5069 ◽  
Author(s):  
Bei Wang ◽  
Ying Wang ◽  
Bing Sun ◽  
Paul Munroe ◽  
Guoxiu Wang

2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Byeong Gwan Lee ◽  
Yong Joon Park

AbstractLithia-based materials are promising cathodes based on an anionic (oxygen) redox reaction for lithium ion batteries due to their high capacity and stable cyclic performance. In this study, the properties of a lithia-based cathode activated by Li2RuO3 were characterized. Ru-based oxides are expected to act as good catalysts because they can play a role in stabilizing the anion redox reaction. Their high electronic conductivity is also attractive because it can compensate for the low conductivity of lithia. The lithia/Li2RuO3 nanocomposites show stable cyclic performance until a capacity limit of 500 mAh g−1 is reached, which is below the theoretical capacity (897 mAh g−1) but superior to other lithia-based cathodes. In the XPS analysis, while the Ru 3d peaks in the spectra barely changed, peroxo-like (O2)n− species reversibly formed and dissociated during cycling. This clearly confirms that the capacity of the lithia/Li2RuO3 nanocomposites can mostly be attributed to the anionic (oxygen) redox reaction.


2019 ◽  
Vol 7 (36) ◽  
pp. 20958-20964 ◽  
Author(s):  
Yudong Zhang ◽  
Hang Li ◽  
Junxiang Liu ◽  
Jicheng Zhang ◽  
Fangyi Cheng ◽  
...  

Nickel-rich LiNi0.90Co0.07Mg0.03O2 cathode material with concentration gradient structure exhibits superior high capacity, high-rate capability and cycling stability.


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