Wu Chunjin, Hua Weibo, Zhang Zheng, Zhong Benhe, Yang Zuguang, Feng Guilin, Xiang Wei, Wu Zhenguo, Guo Xiaodong
School of Chemical Engineering Sichuan University Chengdu 610065 P. R. China.
Adv Sci (Weinh). 2018 Jul 1;5(9):1800519. doi: 10.1002/advs.201800519. eCollection 2018 Sep.
A novel complementary approach for promising anode materials is proposed. Sodium titanates with layered NaTiO and tunnel NaTiO hybrid structure are presented, fabricated, and characterized. The hybrid sample exhibits excellent cycling stability and superior rate performance by the inhibition of layered phase transformation and synergetic effect. The structural evolution, reaction mechanism, and reaction dynamics of hybrid electrodes during the sodium insertion/desertion process are carefully investigated. In situ synchrotron X-ray powder diffraction (SXRD) characterization is performed and the result indicates that Na inserts into tunnel structure with occurring solid solution reaction and intercalates into NaTiO structure with appearing a phase transition in a low voltage. The reaction dynamics reveals that sodium ion diffusion of tunnel NaTiO is faster than that of layered NaTiO. The synergetic complementary properties are significantly conductive to enhance electrochemical behavior of hybrid structure. This study provides a promising candidate anode for advanced sodium ion batteries (SIBs).
提出了一种用于有前景的阳极材料的新型互补方法。展示、制备并表征了具有层状NaTiO和隧道状NaTiO混合结构的钛酸钠。通过抑制层状相变和协同效应,混合样品表现出优异的循环稳定性和卓越的倍率性能。仔细研究了混合电极在钠嵌入/脱嵌过程中的结构演变、反应机理和反应动力学。进行了原位同步辐射X射线粉末衍射(SXRD)表征,结果表明Na在发生固溶体反应时插入隧道结构,并在低电压下出现相变时插入NaTiO结构。反应动力学表明,隧道状NaTiO的钠离子扩散速度比层状NaTiO快。协同互补特性对增强混合结构的电化学行为具有显著的促进作用。本研究为先进钠离子电池(SIBs)提供了一种有前景的候选阳极。