Department of Chemistry and Biology, Beihua University, Jilin, China.
Nanoscale. 2014 May 21;6(10):5329-37. doi: 10.1039/c4nr00236a.
In this work, we report a novel approach to fabricate hierarchical TiO2 microspheres (HTMS) assembled by ultrathin nanoribbons where an anatase/TiO2(B) heterojunction and high energy facet coexist. The as-adopted approach involves (1) nonaqueous solvothermal treatment of a mixture of tetrabutyl titanate and acetic acid and (2) topotactical transformation into HTMS via thermal annealing. By this approach, the TiO2(B) phase usually synthesized from an alkaline treatment route could be initially formed. Subsequently, phase transition from TiO2(B) to anatase TiO2 occurs upon thermal treatment. It is demonstrated that such phase transition is accompanied by crystallographic orientation along the c-axis of anatase and TiO2(B) crystals, resulting in not only a coherent interface between two phases but also oriented attachment of anatase mesocrystals along the [001] direction, and finally high-energy (001) facet exposure. Interestingly, this work provides an alternative fluorine-free route for the synthesis of TiO2 crystals with high-energy (001) facet exposure. The structural analysis reveals that lattice-match induced topotactic transformation from TiO2(B) to anatase is the sole reason for the (001) facet exposure of anatase TiO2. The photocatalytic test for acetaldehyde decomposition shows that HTMS with anatase/TiO2(B) heterojunction and high-energy (001) facet exhibits superior photocatalytic efficiency compared with the relevant commercial product P25, which can be ascribed to the synergistic effect of large surface area, anatase/TiO2(B) heterojunction as well as high-energy facet exposure.
在这项工作中,我们报告了一种制造由超薄纳米带组装的分级 TiO2 微球(HTMS)的新方法,其中存在锐钛矿/TiO2(B)异质结和高能面。所采用的方法包括 (1) 钛酸四丁酯和乙酸的非水溶剂热处理,以及 (2) 通过热退火转化为 HTMS 的拓扑转化。通过这种方法,可以最初形成通常通过碱性处理路线合成的 TiO2(B)相。随后,在热处理过程中,TiO2(B)相发生向锐钛矿 TiO2 的相变。证明这种相变伴随着锐钛矿和 TiO2(B)晶体沿 c 轴的晶面取向,不仅在两相之间形成了相干界面,而且沿[001]方向定向连接了锐钛矿介晶,最终暴露了高能(001)面。有趣的是,这项工作为具有高能(001)面暴露的 TiO2 晶体的合成提供了一种替代无氟的方法。结构分析表明,晶格匹配诱导的从 TiO2(B)到锐钛矿的拓扑转化是锐钛矿 TiO2 暴露(001)面的唯一原因。对于乙醛分解的光催化测试表明,具有锐钛矿/TiO2(B)异质结和高能(001)面的 HTMS 表现出比相关商业产品 P25 更高的光催化效率,这归因于大比表面积、锐钛矿/TiO2(B)异质结以及高能面暴露的协同效应。