Boosting the photoconversion efficiency of TiO2 nanotubes using UV radiation-assisted anodization as a prospective method: An efficient photocatalyst for eliminating resistant organic pollutants
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作者:
Aliabadi, Bahareh Ghorbani
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Univ Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, IranUniv Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, Iran
Aliabadi, Bahareh Ghorbani
[1
]
Gilani, Neda
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Univ Guilan, Dept Chem Engn, Rasht 4199613776, IranUniv Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, Iran
Gilani, Neda
[2
]
Pasikhani, Javad Vahabzade
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Univ Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, IranUniv Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, Iran
Pasikhani, Javad Vahabzade
[1
]
Pirbazari, Azadeh Ebrahimian
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Univ Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, IranUniv Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, Iran
Pirbazari, Azadeh Ebrahimian
[1
]
机构:
[1] Univ Tehran, Coll Engn, Fouman Fac Engn, POB 43515-1155, Fouman 4351666456, Iran
1D TiO2 nanotube arrays (TNTs), as versatile nanostructures, have attracted a considerable amount of scientific attention, particularly in photocatalytic applications. In the present study, UV radiation-assisted anodization method with various irradiation times (30-120 min) was employed as a preferable approach to fabricating TNTs with remarkable optical property and photocatalytic activity. The results revealed that in situ irradiation not only improved the surface area (from 30.10 to 48.5 m(2)), but also increased the roughness factor (from 77.27 to 124.73). Furthermore, UV radiation had a significant impact on optical property and by altering elemental composition, led to a red shift in absorption edge (from 3.2 to 1.4eV). Meanwhile, voltammetric experiments showed that 120 min UV radiation during anodization was able to substantially cause a surge of the photo-current density and the photoconversion efficiency of TNTs from 0.15 to 0.55 mA cm(-2) and from 13% to 40%, respectively. As a consequence of the improvement in optical property and photochemical features, anodic TNTs fabricated under 120 min UV radiation could increase the photocatalytic degradation of 2,4-DCP from 75% to 100%. Moreover, the kinetics study showed that all photocatalytic reactions followed zero-order kinetics which rate constant over the synthesized TNTs under 120 min UV radiation was about 5.1 times greater than that of conventionally fabricated TNTs. Likewise, the pathway of photocatalytic degradation and the proportion of reactive species in this process were assessed by scavenging tests. The results confirmed that holes (h(+)) play the main role that 53% of photocatalytic degradation occurred via both direct and indirect reactions with h(+) species. The rest of the degradation pathways were also allocated to e(-) and center dot O-2(-) species by accounting for 37% and 10%, respectively.
机构:
Univ Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Chong, Meng Nan
;
Jin, Bo
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Univ Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
SA Water Corp, Australian Water Qual Ctr, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Jin, Bo
;
Chow, Christopher W. K.
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SA Water Corp, Australian Water Qual Ctr, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Chow, Christopher W. K.
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Saint, Chris
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SA Water Corp, Australian Water Qual Ctr, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
机构:
Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Univ Calif Riverside, Mat Sci & Engn Program, Riverside, CA 92521 USAUniv Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Cipriano, Aaron F.
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Miller, Christopher
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Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USAUniv Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Miller, Christopher
;
Liu, Huinan
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机构:
Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Univ Calif Riverside, Mat Sci & Engn Program, Riverside, CA 92521 USA
Univ Calif Riverside, Stem Cell Ctr, Riverside, CA 92521 USAUniv Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
机构:
Univ Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Chong, Meng Nan
;
Jin, Bo
论文数: 0引用数: 0
h-index: 0
机构:
Univ Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
SA Water Corp, Australian Water Qual Ctr, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Jin, Bo
;
Chow, Christopher W. K.
论文数: 0引用数: 0
h-index: 0
机构:
SA Water Corp, Australian Water Qual Ctr, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
Chow, Christopher W. K.
;
Saint, Chris
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h-index: 0
机构:
SA Water Corp, Australian Water Qual Ctr, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Earth & Environm Sci, Adelaide, SA 5005, Australia
机构:
Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Univ Calif Riverside, Mat Sci & Engn Program, Riverside, CA 92521 USAUniv Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Cipriano, Aaron F.
;
Miller, Christopher
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h-index: 0
机构:
Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USAUniv Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Miller, Christopher
;
Liu, Huinan
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h-index: 0
机构:
Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
Univ Calif Riverside, Mat Sci & Engn Program, Riverside, CA 92521 USA
Univ Calif Riverside, Stem Cell Ctr, Riverside, CA 92521 USAUniv Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA