Anodization Of Titania Nanotube Arrays In Electrolyte Ontaining Hydrogen Peroxide
It is well-accepted that anodization conducted in H2O2 as oxidant could facilitate rapid growth of nanotube for photocatalyst application. However, the corrosion behaviour, formation mechanism of compact oxide layer and nanotube associated with anodization in electrolyte containing H2O2 remains u...
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| 格式: | Thesis |
| 语言: | English |
| 出版: |
2018
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| 主题: | |
| 在线阅读: | http://eprints.usm.my/47427/1/Anodization%20Of%20Titania%20Nanotube%20Arrays%20In%20Electrolyte%20Ontaining%20Hydrogen%20Peroxide.pdf |
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| 总结: | It is well-accepted that anodization conducted in H2O2 as oxidant could
facilitate rapid growth of nanotube for photocatalyst application. However, the
corrosion behaviour, formation mechanism of compact oxide layer and nanotube
associated with anodization in electrolyte containing H2O2 remains unanswered.
Therefore, anodization of titania nanotube (TNT) in H2O2-based electrolyte are
studied relative to H2O for better understanding on the formation of TNT nanotube as
well as the formation of its surface oxide layer. Besides, the study aimed to explore
the by product in anodic waste electrolyte for chemical recycling of Ti4+ species.
Two-electrode anodization is conducted at 60 V for 1 hour by connecting the Ti and
Pt foils to positive and negative terminal respectively using ethylene glycol,
ammonium fluoride and different oxidants (H2O and H2O2) as electrolyte. Based on
the current-time transient profiles, it is well-verified that the presence of •OOH and
OOH- species facilitate stronger electrochemical reactions on substrate surface. It is
found that presence of Ti4+(H2O2) species in the electrolyte raises the electrolyte
temperature up to 55 °C, promoting the fluoride activity and leading to corrosion of
substrate. Under similar temperature profile, sample anodized in H2O experiences a
more severe corrosion. The observation fulfils the expectance where H2O2 species
demonstrates a stronger passivation tendency. The investigation on the origin of
compact oxide was made based on the nanotube-splitting model and initiation model.
The formation of compact oxide layer can be more accurately described by initiation
layer model. On this premise, it is suggested that nanotube is grown at the metalmetal
oxide interface. Experimental works on single-sided (SA) vs double sided anodization (DA) configuration showed that SA produces a thick wall nanotube array
which exhibits a much higher and stable photocurrent of 1.6 mA cm-2 at 0 V. Based
on the morphology changes observed, formation mechanism of nanotube is greatly
influenced by the compact oxide layer present above. Therefore, the compact oxide
formation must be taken into consideration when devising nanotube growth model.
Besides, the post-anodized electrolyte is filtered, dried and characterized. The byproduct
extracted from waste anodic electrolyte was identified as (NH4)3TiOF5, with
highly symmetrical F(m3m) octahedral structure. Annealing at 200 °C decomposes
the yellowish powder, (NH4)3TiOF5 into (NH4)TiOF3 and (NH4)2TiF6. |
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