P2-Na2/3MnO2 by Co Incorporation: As a Cathode Material of High Capacity and Long Cycle Life for Sodium-Ion Batteries

被引:50
作者
Konarov, Aishuak [1 ,2 ]
Kim, Hee Jae [1 ,2 ]
Voronina, Natalia [1 ,2 ]
Bakenov, Zhumabay [3 ]
Myung, Seung-Taek [1 ,2 ]
机构
[1] Sejong Univ, Dept Nano Technol & Adv Mat Engn, Seoul 05006, South Korea
[2] Sejong Univ, Sejong Battery Inst, Seoul 05006, South Korea
[3] Nazarbayev Univ, Natl Lab Astana, Inst Batteries LLC, 53 Kabanbay Ave, Astana 010000, Kazakhstan
基金
新加坡国家研究基金会;
关键词
layer structure; structural stability; P2-type; cathode; sodium; battery; P2-TYPE; PERFORMANCE;
D O I
10.1021/acsami.9b09317
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The P2-Na2/3MnO2 compound is one of the attractive cathodes for sodium-ion batteries due to its high initial capacity and abundance of Na and Mn elements in nature. The existence of Mn3+ Jahn-Teller ion, however, impedes electrode performance for long term. Here, we challenge to minimize the effect of the Jahn-Teller distortion caused by Mn3+ in the structure, via substitution of Mn3+ by Co3+ in P2-Na-2/3[Mn1-xCox]O-2 (x = 0-0.3). The P2-Na-2/3[Mn0.8Co0.2]O-2 compound substantializes the electrochemical performance with a capacity of about 175 mAh g(-1) (26 mA g(-1)) and retained over 90% of its initial capacity for 300 cycles at 0.1 C (26 mA g(-1)) and 10 C (2.6 A g(-1)). The operando X-ray diffraction study indicates that a single-phase reaction is associated with the insertion of sodium ions into the structure, accompanied by a small volume change of approximately 3%. Furthermore, ex situ X-ray diffraction and high-resolution transmission electron microscopy results show that the crystal structure remained after 300 continuous cycles. It is believed that such good electrode performances attribute to the structural stabilization assisted by the presence of Co3+ in the crystal structure. Our finding provides a way to take advantage of low-cost Mn-rich cathode materials for sodium-ion batteries.
引用
收藏
页码:28928 / 28933
页数:6
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