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244                                Multifunctional Photocatalytic Materials for Energy

         lengths ranging from 170 to 210 nm and widths ranging from 25 to 30 nm. Fig. 11.4F
         shows the TiO 2  nanocrystallines, and the entire inner surface of the anodic aluminum
         oxide (AAO) channels was covered [88]. As a result, because of the absorption and
         reaction of the surface-related precursor molecules, the anisotropic TiO 2  nanostruc-
         tures were obtained. Maili reported an ionic liquid-assisted hydrothermal method in
         which 3-carboxymethyl-1-methylimidazoliurn bisulfate, titanium isopropoxide, HCl,
         and H 2 O were used to prepare rutile TiO 2  NRs. Fig. 11.4C shows the SEM image of
         the TiO 2  NRs [83]. By using TTIP and Ti(OC 3 H 7 ) 4  as precursors, Chen et al. produced
         well-aligned rutile TiO 2  NRs on (100) oriented sapphire substrates. The densely packed
         rutile TiO 2  NRs were grown with similar heights and all in one direction (Fig. 11.4D
         and E). A combination of chemical vapor deposition and microwave hydrothermal
         methods were also developed for the preparation TiO 2  NRs [89,90].

         11.2.2.4   TiO 2  nanofibers
         In comparison with 1D TiO 2  nanostructures, TiO 2  NFs possess additional advantages
         attributed to their special nanosize and enlarged surface area for catalytic activity
         [91–95]. The most utilized technology to fabricate TiO 2  NFs is the electrospinning
         method, which includes the following steps: (i) preparing the sol; (ii) adding sol to
         the polymer template; (iii) electrospinning the solution for NFs; and (iv) calcination
         for single-phase TiO 2  NFs [96–103]. Xia et al. obtained ultra-long TiO 2  NFs using
         Ti(OC 3 H 7 ) 4 , poly (vinyl pyrrolidone) (PVP), acetic acid, and ethanol as precursor via
         the electrospinning method [104]. In their work, the diameter of the TiO 2 /PVP NFs
         was about 78 nm, which could be varied according to the electric field, the concen-
         tration of PVP and Ti(OC 3 H 7 ) 4 , and the feeding rate. Then the samples were heated at
         500°C to remove the additional PVP in order to obtain pure TiO 2  NFs (Fig. 11.5A and
         B). Another typical structure is hollow TiO 2  NFs. Yuan and coworkers successfully
         obtained hollow TiO 2  NFs by using activated carbon fibers (ACF) as templates via
         precursor impregnation. The ACFs were immersed in a mixed solution of titanium iso-
         propoxide and anhydrous ethanol according to a designated volume ratio (1:6). Then
         the filled ACFs and solution were transferred to a stainless steel autoclave at 150°C for
         24 h. Finally, the as-prepared TiO 2  NFs were calcined at 600°C for 5 h to remove the
         template (Fig. 11.5C and D) [105].


         11.2.3   Formation of 2D TiO 2  nanostructures
         In the preparation of 1D TiO 2  nanostructures, 2D TiO 2  NSs are the intermediate part of
         the hydrothermal process, and they also play an important role in the development of
         TiO 2  materials. Therefore the key to obtaining 2D TiO 2  NSs is to precisely control the
         reaction conditions of the formation mechanism. Sun's group obtained typical TiO 2
         NSs via a traditional hydrothermal method [106,107]. By combining continuous hy-
         drothermal routes [108], room temperature synthesis [109], and ionic liquid synthesis
         approaches [110], a new organic-stabilizer-free synthesis was produced recently for
         the formation of TiO 2  NSs. Yang's group synthesized anatase TiO 2  NSs with (001)
         facets using a modified solvothermal method. A 14.5 mL mixed solution of TiF 4  and
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