Esmat Mohamed, Farghali Ahmed A, El-Dek Samaa I, Khedr Mohamed H, Yamauchi Yusuke, Bando Yoshio, Fukata Naoki, Ide Yusuke
International Center for Materials Nanoarchitechtonics (MANA) , National Institute for Materials Science (NIMS) , 1-1 Namiki , Tsukuba , Ibaraki 305-0044 , Japan.
Graduate School of Pure and Applied Sciences , University of Tsukuba , Tsukuba , Ibaraki 305-8573 , Japan.
Inorg Chem. 2019 Jun 17;58(12):7989-7996. doi: 10.1021/acs.inorgchem.9b00722. Epub 2019 May 28.
Layered titanates with one-dimensional (1D) shapes have been an important class of nanomaterials due to their combination of 1D and 2D fascinating properties. Among many layered titanates, lepidocrocite-type layered titanates have significant advantages such as superior intercalation and exfoliation properties, while the synthesis of the 1D-shape forms is still challenging. Here, we report on a facile one-pot hydrothermal conversion of a lepidocrocite-type layered titanate into the corresponding nanowire-shape form. The reaction mechanism involves the decomposition of the starting layered titanate into 1D small segments which assemble into the nanowire. This new nanowire shows properties resulting from the combination of 1D and 2D nanostructural features, excellent cation exchange ability, and high photoinduced charge separation and photocatalytic efficiency. As a demonstration, we evaluate the nanowire as a sequestrating material capable of collecting toxic cations, like Cd, from water and photoreducing them (immobilizing them tightly). We find that the nanowire shows an efficient and ultrafast photoimmobilization activity, whereas the starting layered titanate and a benchmark TiO photocatalyst (P25) show no activity under the identical conditions. The photoimmobilization rate (within 1 min) is considerably faster than the cation exchange rates reported for state-of-the-art cation exchangers (with no photoimmobilization ability). The nanowire used for photoimmobilization reactions is easily recovered from water by decantation, showing the possible practical use for safe disposal of toxic cations in the environment.
具有一维(1D)形状的层状钛酸盐因其兼具一维和二维的迷人特性而成为一类重要的纳米材料。在众多层状钛酸盐中,纤铁矿型层状钛酸盐具有显著优势,如优异的插层和剥离性能,然而一维形状形式的合成仍然具有挑战性。在此,我们报道了一种将纤铁矿型层状钛酸盐通过简易的一锅水热法转化为相应纳米线形状形式的方法。反应机理涉及起始层状钛酸盐分解为一维小片段,这些小片段组装成纳米线。这种新型纳米线展现出由一维和二维纳米结构特征相结合所产生的性能、优异的阳离子交换能力以及高光致电荷分离和光催化效率。作为一个实例,我们评估了该纳米线作为一种能够从水中收集有毒阳离子(如镉)并对其进行光还原(紧密固定)的螯合材料的性能。我们发现该纳米线表现出高效且超快的光固定活性,而起始层状钛酸盐和基准TiO光催化剂(P25)在相同条件下则无活性。光固定速率(在1分钟内)比报道的最先进阳离子交换剂(无光合固定能力)的阳离子交换速率快得多。用于光固定反应的纳米线通过倾析法很容易从水中回收,这表明其在环境中安全处置有毒阳离子方面具有实际应用的可能性。