Abstract:
Our society has made significant advancements in technology as it continues to
grow in size which in turn has led to an accumulating amount of toxic threats. Some types
of harmful pollution our society is currently facing includes industrial waste such as non
biodegradable organic compounds, heavy metals and pathogens. Therefore, it is imperative
to develop green and efficient technologies to control and reduce the growth of
environmental hazards. In recent years, photocatalysis using titanium dioxide (TiO2) has
become a promising route to degrading organic pollutants. However, Anatase phase of TiO2
has a band gap of 3.2 eV. This limits its practical application under sunlight because the
light with energy greater than 3.2 eV constitutes only 3 ~ 4 % of the total solar energy
reaching the earth. Therefore, modifications of TiO2 are needed to allow TiO2 to efficiently
utilize the solar spectrum. Electrospun TiO2 nanofibers present a unique class of active
materials with optimized photoactivity and cost efficiency due to ease of synthesis and
fabrication in bulk. The high aspect ratios of these nanostructured materials shorten the
transportation length of electrons and holes from the crystal interface to the surface, thus
accelerating their migration to the active surface sites. The primary goal of this dissertation
is to develop TiO2 nanofibers as an efficient and cost-effective catalyst for practical and
multi-purpose application in water remediation. To achieve this, various strategies were
employed including doping, photosensitization with a low bandgap material, modification
of the surface chemical states, and incorporating second-phase materials in TiO2
nanofibers. The detailed characterization of the prepared nanofibers was carried out by
SEM, TEM, XRD, XPS, UV-vis DRS, FTIR and PL.
TiO2 nanofibers were prepared through sol-gel solution followed by electrospinning
and calcination treatment. The electrospun nanofibers were successfully doped by phosphorus and the surface of nanofibers were decorated by silver nanoparticles. The
synergistic effect of P-doping and Ag NPs resulted in a decrease in the bandgap and
enhanced charge separation. Consequently, the rate constant of Cr(VI) photoreduction by
Ag-PTNFs was 96 % higher than unmodified nanofibers and the rate constant of MB
photoreduction was 83 % higher than that of the unmodified nanofibers. Another strategy
was to make composite TiO2 nanofibers by incorporation of g-C3N4 in TiO2 nanofibers and
the effect of making heterojunctions with Ag NPs was studied. The prepared composite
nanofiber exhibited remarkable photocatalytic activity for degradation of MB, reduction of
Cr(VI) and antibacterial activity against E. coli and S. aureus under simulated solar
irradiation. TiO2 nanofibers were also successfully photosensitized with low bandgap Ag2S
nanoparticles of 11, 17, 23 and 40 nm mean sizes. 17 nm Ag2S@TiO2 nanofibers exhibited
optimal activity in the photodegradation of methylene blue and photoreduction of Cr(VI)
under simulated sunlight. Whereas, 11 nm Ag2S@TiO2 nanofibers displayed excellent
bactericidal activity under dark and simulated solar irradiation. Furthermore, a UV-O3
surface treatment induced excess Ti3+ surface states and oxygen vacancies which
synergistically enhanced the photocatalytic activity. This was attributed to the efficient
charge separation and transfer driven by increased visible-light absorption, bandgap
narrowing and reduced electron-hole recombination rates. This dissertation demonstrates
the potential utilization of modified TiO2 nanofibers in multifunctional filtration
membranes for remediation of pollutants from wastewater under solar irradiation.