Role of Ligand-to-Metal Charge Transfer in O3-Type NaFeO2-NaNiO2 Solid Solution for Enhanced Electrochemical Properties

被引:141
|
作者
Wang, Xianfen [1 ]
Liu, Guandong [1 ]
Iwao, Tatsumi [1 ]
Okubo, Masashi [1 ,2 ]
Yamada, Atsuo [1 ,3 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058568, Japan
[3] Kyoto Univ, Unit Elements Strategy Initiat Catalysts & Batter, Kyoto 6158510, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2014年 / 118卷 / 06期
关键词
SODIUM-ION BATTERIES; ENERGY-STORAGE; ELECTRODE PERFORMANCE; INTERCALATION; LITHIUM; CATHODE; DEINTERCALATION; PYROPHOSPHATE; CHALLENGES; CRYSTAL;
D O I
10.1021/jp411382r
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
Na-ion batteries have been the subjects of intensive studies for grid-scale energy storage recently. O3-type NaFeO2 is a promising candidate for the Na-ion cathode materials, though the irreversibility during Na-ion extraction/insertion seriously hinders its practical application. The present work demonstrates that partial replacement of Fe in O-3-NaFeO2 with Ni leads to the significant improvement of the electrochemical properties. The Fe-57 Mossbauer and X-ray absorption spectra show that O3-type NaFeO2 NaNiO2 solid solution forms hybridized frontier orbital of a Fe-O-Ni bond via ligand-to-metal charge transfer, which plays a dominant role in the charge discharge process. The resulting O3-NaFe0.3Ni0.7O2 delivers an initial discharge capacity of 135 mA.h.g(-1), most of which is in a high-voltage region of 2.5-3.8 V, with a high initial Coulombic efficiency of 93%, and shows enhanced cycle stability.
引用
收藏
页码:2970 / 2976
页数:7
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