Interface-rich mixed P2+T phase NaxCo0.1Mn0.9O2 (0.44 ≤ x ≤ 0.7) toward fast and high capacity sodium storage

被引:77
作者
Gao, Guofeng [1 ]
Tie, Da [1 ]
Ma, Hao [2 ]
Yu, Haijun
Shi, Shanshan [1 ]
Wang, Bo [1 ]
Xu, Shengming [3 ]
Wang, Linlin [4 ]
Zhao, Yufeng [1 ]
机构
[1] Yanshan Univ, Key Lab Appl Chem, Qinhuangdao 066004, Peoples R China
[2] Beijing Univ Technol, Coll Mat Sci & Engn, Beijing 100124, Peoples R China
[3] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing 100084, Peoples R China
[4] Shanghai Univ Engn Sci, Coll Chem & Chem Engn, 333 Longteng Rd, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金;
关键词
CATHODE MATERIALS; ION BATTERIES; NA0.44MNO2; P2-TYPE; INTERCALATION; MODULATION; TRANSITION; DIFFUSION; VOLTAGE; OXIDES;
D O I
10.1039/c8ta00206a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, we report a novel design of mixed P2 + T phase NaxCo0.1Mn0.9O2 (0.44 <= x <= 0.7) with interface rich characteristics for high performance sodium storage, whereby the tunneled T phase offers fast Na ion diffusivity and excellent structural stability, the layered P2 phase contributes to high specific capacity, and the P2 + T phase interface offers additional channels and active sites for charge transfer and excess charge storage. Consequently, the as-prepared NaxCo0.1Mn0.9O2 (0.44 <= x <= 0.7) demonstrates an excellent discharge capacity of 219 mA h g(-1) at a current rate of 0.1C (1C = 176 mA g(-1)), and retains 117 mA h g(-1) even at a high rate of 5C. This outstanding performance is significantly superior to that of pure T-type Na0.44Co0.1Mn0.9O2 and P2-type Na0.7Co0.1Mn0.9O2, and also outperforms state-of-the-art manganese-based cathodes. The kinetic analysis indicates the drastically improved Na+ diffusion coefficient of the P2 + T phase, which is 6 and 200 times that of the pure T and P phases, respectively. The good reversibility and structural stability is evidenced through an ex situ XRD study.
引用
收藏
页码:6675 / 6684
页数:10
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