Self-organized sodium titanate/titania nanoforest for the negative electrode of sodium-ion microbatteries

被引:13
作者
Cabello, Marta [1 ]
Ortiz, Gregorio F. [1 ]
Lopez, Maria C. [1 ]
Alcantara, Ricardo [1 ]
Gonzalez, Jose R. [1 ]
Tirado, Jose L. [1 ]
Stoyanova, Radostina [2 ]
Zhecheva, Ekaterina [2 ]
机构
[1] Univ Cordoba, Lab Quim Inorgan, E-14071 Cordoba, Spain
[2] Bulgarian Acad Sci, Inst Gen & Inorgan Chem, BU-1113 Sofia, Bulgaria
关键词
Nanostructured materials; Thin films; Energy storage materials; Nanofabrications; Electron paramagnetic resonance; Self-organized nanotrees; ELECTROCHEMICAL NA; HIGH-VOLTAGE; NANOTUBES; LITHIUM; NA2TI6O13; INSERTION; STORAGE; ANODE; STABILITY; BATTERIES;
D O I
10.1016/j.jallcom.2015.06.183
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
A nanocomposite of sodium titanate/titania nanotrees self-organized in a parallel fashion to form nanoforests is successfully prepared and used as high-performance anode for Na-ion microbatteries. The first step of the synthesis is the anodic oxidation of Ti foils to form self-organized amorphous TiO2 nanotubes followed by insertion of sodium in aqueous media at room temperature. Then the composite is thermally dehydrated and crystallized as monoclinic Na2Ti6O13/rutile nanotrees. EPR spectra evidence a significant increase in Ti3+ content during sodium/proton insertion and a decrease on heating. SEM images reveal that while the height of the nanotubes is similar to the nanoforest (c.a. 8.0 mm) the morphology changes from aligned nanotubes to nanotrees of complex texture. The electrochemical results of sodium test cells in non-aqueous electrolyte using the Na2Ti6O13/TiO2 nanocomposite electrodes show flat profiles of sodium insertion and de-insertion at 0.7 and 0.9 V, respectively. The observed reversible capacity of 130 mu A h cm(-2) over 150 cycles is almost threefold the value of titania nanotubes annealed at a same temperature. Both characteristics are of great interest to achieve safe and efficient Na-ion microbatteries. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:816 / 826
页数:11
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