O3-Type Na 2/3 Ni 1/3 Ti 2/3 O 2 Layered Oxide as a Stable and High-Rate Anode Material for Sodium Storage

Sodium-ion batteries (SIBs) are currently the most promising candidates for large-scale energy storage devices owing to their low cost and abundant resources. Titanium-based layered oxides have attracted widespread attention as promising anode materials due to delivering a safe potential of about 0....

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Veröffentlicht in:ACS applied materials & interfaces 2022-01, Vol.14 (1), p.677-683
Hauptverfasser: Zhang, Si-Yuan, Zhou, Ya-Nan, Yu, Lianzheng, Fan, Min, Chen, Wan-Ping, Xin, Sen, Yin, Ya-Xia, Xu, Sailong, Guo, Yu-Guo
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Sprache:eng
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Zusammenfassung:Sodium-ion batteries (SIBs) are currently the most promising candidates for large-scale energy storage devices owing to their low cost and abundant resources. Titanium-based layered oxides have attracted widespread attention as promising anode materials due to delivering a safe potential of about 0.7 V (vs Na /Na) and a small volume contraction during cycles; P2-type Ti-based layered oxides are typically reported, due to the challenging synthesis of the O3-type counterpart resulting from the high percentage of unstable Ti . Herein, we report an anomalous O3-Na Ni Ti O layered oxide as an ultrastable and high-rate anode material for SIBs. The anode material delivers a reversible capacity of 112 mA h g after 300 cycles at 0.1 C, a good capacity retention rate of 91% after 1400 cycles at 2 C, and, in particular, a capacity of 52 mA h g even at a high rate of 20 C (1780 mA g ). Furthermore, the X-ray diffraction monitoring reveals no phase transitions and almost zero strain both underlie the good long-cycle stability. The measured high apparent Na diffusion coefficient (2.06 × 10 cm s ) and the low migration energy barrier (0.59 eV) from density functional theory calculations are responsible for the superior rate capability. Our results promise advanced high-performance O3-type Ti-based layered oxides as promising anode materials toward application for SIBs.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.1c17554