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Synergistic coupling {101}-{111} facet of N-doped TiO2 film enhance spatial charge separation for methylene blue photodegradation
The synthesis of N-doped TiO2 film with co-exposed {101} and {111} facets via a one-pot facile hydrothermal method had proven to enhance the photocatalytic activity of TiO2. The high-resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS) data show the incorpo...
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Published in: | Journal of alloys and compounds 2023-10, Vol.961, p.170977, Article 170977 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The synthesis of N-doped TiO2 film with co-exposed {101} and {111} facets via a one-pot facile hydrothermal method had proven to enhance the photocatalytic activity of TiO2. The high-resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS) data show the incorporation of N ions into the TiO2 accomplishes the facet modification. The shifting of the N-doped TiO2 photocatalyst adsorption bandgap toward a higher wavelength was identified as the TiO2 band gap was reduced. Up to 66 % methylene blue had successfully been degraded with the aid of N-doped TiO2 as an active photocatalyst. The enhanced photodegradation of N-doped TiO2 film is mainly attributed to the presence of {101} and {111} facets, leading to the efficient separation of carriers and lengthening the life of photogenerated carriers, consequently improving its photocatalysis potential.
•N-doped rutile-phase TiO2 film with exposed {101} and {111} facets was obtained.•A facile hydrothermal doping process was employed to fabricate the film.•The {111} facet has a higher energy facet compared to another facet.•TiO2-N 2.0 wt% based TEM results confirmed the facet changed upon doping.•The synergistic effect of {101} and {111} facets improved the spatial charge separation. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2023.170977 |