Mao Yuanbing, Wong Stanislaus S
Department of Chemistry, State University of New York at Stony Brook, Stony Brook, New York 11794-3400, USA.
J Am Chem Soc. 2006 Jun 28;128(25):8217-26. doi: 10.1021/ja0607483.
A size- and shape-dependent morphological transformation was demonstrated during the hydrothermal soft chemical transformation, in neutral solution, of titanate nanostructures into their anatase titania counterparts. Specifically, lepidocrocite hydrogen titanate nanotubes with diameters of approximately 10 nm were transformed into anatase nanoparticles with an average size of 12 nm. Lepidocrocite hydrogen titanate nanowires with relatively small diameters (average diameter range of < or = 200 nm) were converted into single-crystalline anatase nanowires with relatively smooth surfaces. Larger diameter (>200 nm) titanate wires were transformed into analogous anatase submicron wire motifs, resembling clusters of adjoining anatase nanocrystals with perfectly parallel, oriented fringes. Our results indicate that as-synthesized TiO2 nanostructures possessed higher photocatalytic activity than the commercial titania precursors from whence they were derived.
在水热软化学转化过程中,即在中性溶液中钛酸盐纳米结构向锐钛矿型二氧化钛对应物的转化过程中,展示了一种尺寸和形状依赖性的形态转变。具体而言,直径约为10纳米的纤铁矿型钛酸氢纳米管被转化为平均尺寸为12纳米的锐钛矿型纳米颗粒。直径相对较小(平均直径范围≤200纳米)的纤铁矿型钛酸氢纳米线被转化为表面相对光滑的单晶锐钛矿型纳米线。直径较大(>200纳米)的钛酸盐线被转化为类似的锐钛矿型亚微米线图案,类似于相邻锐钛矿型纳米晶体簇,具有完美平行的定向条纹。我们的结果表明,合成的二氧化钛纳米结构比其衍生而来的商业二氧化钛前驱体具有更高的光催化活性。