Environmental Engineering Reference
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Fig. 9 SEM images of a 20-lm-long TiO
2
nanotube array from anodization of the Ti film
sputter-deposited on FTO-coated glass: a cross-sectional view and b top view. The current-
voltage characteristics (c) and the incident photon-to-current conversion efficiency (IPCE) spectra
of DSSCs fabricated using transparent nanotube array films of various lengths. (Reprinted with
permission from Ref. [
188
]. Copyright American Chemical Society)
incoming light using back illumination mode is partially reflected by the counter
electrode and partially absorbed by the counter electrode and iodine in the elec-
trolyte before striking TiO
2
nanotubes, leading to a loss of *25 % of the incident
solar energy [
180
]. Furthermore, sintering of the TiO
2
for transformation from
amorphous phase to crystalline phase (i.e. anatase or rutile) can introduce the
formation of a barrier layer between the nanotubes and the underlying Ti substrate.
This enables recombination of electrons and holes when the nanotube layers are
used for photoelectrochemical water splitting [
181
]. Fortunately, several strategies
have been explored to solve this deadlock. One straightforward alternative solution
is to deposit titanium as a thin film on a transparent substrate (e.g., FTO glass)
before anodizing. The deposition process is usually performed by physical
methods, for example, radio-frequency (RF) or direct-current (DC) magnetron
sputtering [
182
-
187
]. Through anodization of sputtered titanium into nanotube
layers on transparent substrate (Fig.
9
a, b), a power conversion efficiency of 6.9 %
for the resulting DSSCs was obtained (Fig.
9
c, d) [
188
]. The length of the
nanotubes is limited by the difficulty of growing a high quality, thick Ti film on the
conductive glass via sputter deposition [
189
]. Therefore, a large-area free-standing
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