摘要
Hierarchical assembly of Ti(iv)/Sn(ii)-doped SnO2 nanosheets along titanate nanowires serving as both sacrificial templates and a Ti(iv) source is demonstrated, using SnCl2 as a tin precursor and Sn(ii) dopants and NaF as the morphology controlling agent. Excess fluoride inhibits the hydrolysis of SnCl2, promoting heterogeneous nucleation of Sn(ii)-doped SnO2 on the titanate nanowires due to the insufficient oxidization of Sn(ii) to Sn(iv). Simultaneously, titanate nanowires are dissolved forming Ti4+ species under the etching effect of in situ generated HF resulting in spontaneous Ti4+ ion doping of SnO 2 nanosheets formed under hydrothermal conditions. Compositional analysis indicates that Ti4+ ions are incorporated by substitution of Sn sites at a high level (16-18 at.%), with uniform distribution and no phase separation. Mössbauer spectroscopy quantified the relative content of Sn(ii) and Sn(iv) in both Sn(ii)-doped and Ti(iv)/Sn(ii) co-doped SnO 2 samples. Electrochemical properties were investigated as an anode material in lithium ion batteries, demonstrating that Ti-doped SnO2 nanosheets show improved cycle performance, which is attributed to the alleviation of inherent volume expansion of the SnO2-based anode materials by substituting part of Sn sites with Ti dopants.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 9101-9109 |
| 页数 | 9 |
| 期刊 | Nanoscale |
| 卷 | 5 |
| 期 | 19 |
| DOI | |
| 出版状态 | 已出版 - 7 10月 2013 |
| 已对外发布 | 是 |
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