Synthesis of urchin-like rutile titania carbon nanocomposites by iron-facilitated phase transformation of MXene for environmental remediation

被引:175
作者
Zou, Guodong [1 ]
Guo, Jianxin [1 ,2 ]
Peng, Qiuming [1 ]
Zhou, Aiguo [3 ]
Zhang, Qingrui [4 ]
Liu, Baozhong [3 ]
机构
[1] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Peoples R China
[2] Hebei Univ, Coll Phys Sci & Technol, Hebei Prov Key Lab Optoelect Informat Mat, Baoding 071002, Peoples R China
[3] Henan Polytech Univ, Sch Mat Sci & Engn, Jiaozuo 454000, Peoples R China
[4] Yanshan Univ, Sch Environm & Chem Engn, Hebei Key Lab Appl Chem, Qinhuangdao 066004, Peoples R China
关键词
001; FACETS; TIO2; ANATASE; SURFACE; CHEMISTRY; OXIDATION; REMOVAL; CR(VI); GROWTH; INTERCALATION;
D O I
10.1039/c5ta07343j
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
Self-assembling has been confirmed as an effective pathway to achieve some unique properties. The recently developed two-dimensional transition metal carbides (termed MXene) provide more potential opportunities to modify the surfaces of layered materials relative to simple graphene. Here we describe a one-step method for preparing an urchin-like rutile TiO2-C (u-RTC) nano-composite with a high amount of (110) facets by in situ phase transformation of MXene (Ti3C2(OH)(0.8)F-1.2) under FeCl3 conditions. A layered anatase TiO2-C (l-ATC) nano-composite with a high percentage of (001) facets first forms, and then it changes into u-RTC due to the Fe(III) ion induction. The u-RTC displays a high Cr(VI) adsorption capacity of similar to 225 mg g(-1), which is higher than that of the primitive MXene (similar to 62 mg g(-1)) and the l-ATC precursor (similar to 11 mg g(-1)), owing to the inhibition of H2O molecule adsorption by bridging oxo groups in terms of the first principles calculations. Apart from the fact that the finding leads to a desirable aligned oxide-carbon material, this approach may set up a new trajectory to self-assemble functional surfaces of other MXene derivatives.
引用
收藏
页码:489 / 499
页数:11
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