High Capacity Positive Electrode Material for Room Temperature Na Ion Battery: NaxMn2/3Co1/6Ni1/6O2

被引:32
作者
Kataoka, Riki [1 ]
Mukai, Takashi [1 ]
Yoshizawa, Akihiro [1 ]
Inoue, Kenshi [1 ]
Kiyobayashi, Tetsu [1 ]
Sakai, Tetsuo [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Res Inst Ubiquitous Energy Devices, Ikeda, Osaka 5638577, Japan
关键词
X-RAY-DIFFRACTION; CATHODE MATERIAL; ELECTROCHEMICAL INTERCALATION; LAYERED OXIDE; SODIUM; DEINTERCALATION; PERFORMANCE; BEHAVIOR; NI; CO;
D O I
10.1149/2.0181504jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A layered compound, NaxMn2/3Co1/6Ni1/6O2 (NMCN), prepared by a solid-state reaction, served as a high capacity positive electrode material with the reversible capacity of ca. 200 mA.h.g(-1) using a Na foil as the counter electrode. A high-resolution synchrotron X-ray diffraction (XRD) analysis revealed that, whereas the NMCN sample had the P3 structure (R3m) when the precursor was heated below 700 degrees C, the P-2 structure (P6(3)/mmc) was obtained when heated above 800 degrees C. The latter excels over the former in both capacity and cycle stability; i.e., the initial discharge capacities and potentials of the P2 and P3-NMCN were 216 mA.h.g(-1), 2.87 V vs. Na+/Na and 206 mA.h.g(-1), 2.78 V vs. Na+/Na, respectively. The P2-MNCN retained 80% of its initial discharge capacity while the P3-NMCN dropped to 69% after 30 cycles in the potential range of 1.0-4.5 V vs. Na+/Na. An in-situ XRD analysis revealed that the lattice volume of the P2-NMCN contracts and expands by 20% during the charge and discharge (i.e., Na extraction and insertion) without drastically changing its crystallographic structure. (C) 2015 The Electrochemical Society. All rights reserved.
引用
收藏
页码:A553 / A558
页数:6
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