Enhanced electrochemical performance of lithium rich layered cathode materials by Ca2+ substitution

被引:39
作者
Laisa, C. P. [1 ,2 ]
Ramesha, R. N. [1 ,2 ]
Ramesha, K. [1 ,2 ]
机构
[1] CSIR, Chennai Unit, Cent Electrochem Res Inst, CSIR Madras Complex, Madras 600113, Tamil Nadu, India
[2] CSIR, Acad Sci & Innovat Res AcSIR, CECRI, Karaikkudi, Tamil Nadu, India
关键词
Lithium-rich layered cathode; Electrochemical performance; Ca2+ substitution; ION BATTERIES; CYCLING STABILITY; RATE CAPABILITY; CO ELECTRODES; MANGANESE; CAPACITY; OXIDE; EFFICIENCY; FE; NI;
D O I
10.1016/j.electacta.2017.10.029
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The poor cycling stability and large voltage decay in Li-rich cathode materials is related to the layer to spinel structural transformation. It is understood that the ease of structural transformation is correlated to the amount of oxygen gas released during the first charge above 4.5 V. So one of the effective strategy to improve the electrochemical properties is by suppressing oxygen evolution through stabilizing oxygen radical intermediates by tuning metal-oxygen bond characteristics such as covalency, bond energy, iconicity, etc. through cation substitutions in Li rich phases. In this work we report that small amount of Ca substitution in Li layers of Li rich phases, Li1.2-2xCaxCo0.13Ni0.13Mn0.54O2 (x = 0.005) improves the electrochemical cycling stability as well as the rate capability. With x = 0.005 calcium substitution, the initial coulombic efficiency increased from 70% (for the pristine) to 83% and the capacity retention is improved from 71% to 87% after 100 cycles. Similarly Ca doping improves the rate capability especially at higher rates. The improved electrochemical performance of the Ca doped Li-rich cathode can be attributed to the fine-tuning of the crystal-chemical aspects manifested through enhanced structural stability and increased interlayer distance. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:10 / 18
页数:9
相关论文
共 35 条
[1]   Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[2]  
Cho J, 2001, ANGEW CHEM INT EDIT, V40, P3367, DOI 10.1002/1521-3773(20010917)40:18<3367::AID-ANIE3367>3.0.CO
[3]  
2-A
[4]  
Dean J A, 1998, LANGES HDB CHEM
[5]   Influence of Cationic Substitutions on the Oxygen Loss and Reversible Capacity of Lithium-Rich Layered Oxide Cathodes [J].
Deng, Z. Q. ;
Manthiram, A. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (14) :7097-7103
[6]   Enhanced high-rate capability and cycling stability of Na-stabilized layered Li1.2[Co0.13Ni0.13Mn0.54]O2 cathode material [J].
He, Wei ;
Yuan, Dingding ;
Qian, Jiangfeng ;
Ai, Xinping ;
Yang, Hanxi ;
Cao, Yuliang .
JOURNAL OF MATERIALS CHEMISTRY A, 2013, 1 (37) :11397-11403
[7]   A comparative study on electrochemical cycling stability of lithium rich layered cathode materials Li1.2Ni0.13M0.13Mn0.54O2 where M = Fe or Co [J].
Laisa, C. P. ;
Kumar, A. K. Nanda ;
Chandrasekaran, S. Selva ;
Murugan, P. ;
Lakshminarasimhan, N. ;
Govindaraj, R. ;
Ramesha, K. .
JOURNAL OF POWER SOURCES, 2016, 324 :462-474
[8]  
Larson A. C., 2001, J APPL CRYSTALLOGR, V34, P210, DOI DOI 10.1107/S0021889801002242
[9]   Trace level doping of lithium-rich cathode materials [J].
Lengyel, Miklos ;
Shen, Kuan-Yu ;
Lanigan, Deanna M. ;
Martin, Jonathan M. ;
Zhang, Xiaofeng ;
Axelbaum, Richard L. .
JOURNAL OF MATERIALS CHEMISTRY A, 2016, 4 (09) :3538-3545
[10]   Improve First-Cycle Efficiency and Rate Performance of Layered-Layered Li1.2Mn0.6Ni0.2O2 Using Oxygen Stabilizing Dopant [J].
Li, Jinfeng ;
Zhan, Chun ;
Lu, Jun ;
Yuan, Yifei ;
Shahbazian-Yassar, Reza ;
Qiu, Xinping ;
Amine, Khalil .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (29) :16040-16045