Comparison of the structural evolution of the O3 and P2 phases of Na2/3Fe2/3Mn1/3O2 during electrochemical cycling

被引:14
|
作者
Sharma, Neeraj [1 ]
Al Bahri, Othman Khalfan [1 ]
Han, Man Huon [2 ]
Gonzalo, Elena [2 ]
Pramudita, James Christian [1 ]
Rojo, Teofilo [2 ,3 ]
机构
[1] UNSW Australia, Sch Chem, Sydney, NSW 2052, Australia
[2] CIC Energigune, Parque Tecnol Alava,Albert Einstein 48,ED CIC, Minano 01510, Spain
[3] Univ Pais Vasco UPV EHU, Dept Quim Inorgan, POB 644, Bilbao 48080, Spain
关键词
in-situ synchrotron XRD; variable current rate; mid-long term structural evolution in coin; cells; NA-ION BATTERIES; CATHODE MATERIALS; V3+/V4+;
D O I
10.1016/j.electacta.2016.04.008
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The recent development and the in-depth analysis of O-3 -phase Na2/3Fe2/3Mn1/3O2 has enriched the understanding of the overall electrochemical performance relating to the phase transitions during cycling of layered oxide cathodes. In order to understand the correlation between the initial polymorphs, their phase transitions during cycling without bias from starting Na concentration, we directly compare the structural evolution of O-3(-) and P2-phase Na2/3Fe2/3Mn1/3O2 utilizing time -resolved in situ synchrotron X-ray diffraction data. The complex phase transitions along with multiple regions of solid solution and biphasic evolution are identified based on time (or voltage) of cycling progress. The focus of this work is at relatively high C -rates of 1C and C/2.5, where a direct comparison of the evolution of the O-3 and P2 type Na2/3Fe2/3Mn1/3O2 phases are made, showing striking differences which do have ramifications on the short and long-term electrochemical performance of these electrodes. An example of the mid-term structural evolution of the O-3 electrode shows that it can transform to the P2 electrode with electrochemical cycling. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:189 / 197
页数:9
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