Research articles
ScienceAsia 51 (2026): 1-8 |doi:
10.2306/scienceasia1513-1874.2026.001
Effects of calcination heating rate on the photocatalytic
activity of Al-doped TiO2 nanofibers
Watcharapon Nantaouppakan, Nattaya Comsup*
ABSTRACT: Al-dopedTiO2
nanofibersweresynthesizedusingtheone-stepelectrospinning method. Theas-synthesized
nanofiber catalyst was investigated in terms of the effect of calcination heating rate (3 to 10?C/min) at a constant
temperature of 500?C. X-ray diffraction analysis revealed that the anatase phase is the dominant phase, and a mixed
phase of rutile and anatase was formed when heating rates exceeded 3?C/min. Increasing the heating rate had almost
no effect on specific surface area, pore size, and pore volume, while the band gap energy showed a slight decrease
from 3.16 to 3.12 eV with increasing heating rate. The calcination heating rate has a distinct effect on the amount of
oxygen vacancies and chemisorbed oxygen species of Al-doped TiO2
nanofibers. The increase in heating rate decreased
the oxygen vacancies in bulk Al-doped TiO2
nanofibers, while the amount of chemisorbed oxygen increased. The
large amount of oxygen vacancies in the lattice of Al-doped TiO2
nanofibers acts as recombination centers for charge
carriers, thereby decreasing the efficiency of photocatalysis. Conversely, the large amount of chemisorbed oxygen
promotes the formation of active species, resulting in enhanced photocatalytic efficiency. Therefore, Al-doped TiO2
nanofiberscalcined with a heating rate of 10?C/minexhibitedthehighest methylenebluedegradationefficiency of 98%
within 120 min under UV light irradiation. It can be concluded that the calcination heating rate is a crucial parameter
influencing the formation of oxygen vacancies and active species, which is directly related to the photocatalytic
efficiency of Al-doped TiO2
nanofibers.
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Department of Petrochemicals and Environmental Management, Pathumwan Institute of Technology,
Bangkok 10330 Thailand |
* Corresponding author, E-mail: nattaya@pit.ac.th
Received 17 Dec 2024, Accepted 0 0000
|