Synthesis of two-dimensional Ti3C2TxMXene using HCl+LiF etchant: Enhanced exfoliation and delamination

Tian Zhang, Limei Pan, Huan Tang, Fei Du, Yanhua Guo, Tai Qiu, Jian Yang

科研成果: 期刊稿件文章同行评审

411 引用 (Scopus)

摘要

Herein, enhanced exfoliation and large-scale delamination of two-dimensional (2D) Ti3C2TxMXene using etchant of HCl + LiF, instead of HF, in which both etching and intercalation were achieved in exfoliation process, were thoroughly investigated with the focus on the effects of two critical factors, reaction temperature and washing solution. Increasing etching temperature promotes the exfoliation process, i.e., the transformation from Ti3AlC2to multilayer Ti3C2TxMXene, whereas simultaneously results in an aggravated surface oxidation of MXene layers formed after the extraction of Al. As a result, delamination ratio increases firstly and then decreases, and the samples etched at 35 °C show the highest delamination ratio. Compared with the distilled water, washing the exfoliation products using ethanol significantly improves the delamination ratio of Ti3C2TxMXene by co-intercalation of larger alcohol molecule and more impurity ions and a large scale delamination of Ti3C2TxMXene with a delamination ratio as high as 29.2% was obtained by simple sonication for 1 h, without additional intercalation step required, after washing using ethanol. The possible exfoliation reactions by HCl + LiF solution were proposed. Using the as-fabricated stable suspensions of delaminated Ti3C2Txflakes, flexible, free-standing Ti3C2Txpapers with tailored thickness, hydrophilic surface and excellent conductivity, typically 2 × 105S/m at 5 μm in thickness, were prepared. As anode for lithium ion batteries, the delaminated Ti3C2TxMXene obtained reversible capacities of 226.3 mAh g−1, 137.9 mAh g−1,102.0 mAh g−1and 47.9 mAh g−1respectively at the current density of 100, 300, 1000 and 3000 mA g−1, which are superior to those of the Ti3C2MXene prepared by conventional HF process.

源语言英语
页(从-至)818-826
页数9
期刊Journal of Alloys and Compounds
695
DOI
出版状态已出版 - 2017

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