Efficient Charge Carrier Separation in l-Alanine Acids Derived N-TiO2 Nanospheres: The Role of Oxygen Vacancies in Tetrahedral Ti4+ Sites

N-doped TiO2 with oxygen vacancies exhibits many advantages for photocatalysis, such as enhanced visible light absorbency, inhibition of the photogenerated charge carrier recombination, etc. However, preparation of N-doped TiO2 with oxygen vacancies under mild conditions is still a challenge. Herein, N-doped TiO2 nanospheres with tetrahedral Ti4+ sites were synthesized by using dodecylamine as template and assisted by l-alanine acids. The obtained samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV–Vis diffuse reflectance spectra (UV–Vis DRS). It was found that the dodecylamine as a neutral surfactant controlled the structure of TiO2 spherical, while l-alanine acids provided a nitrogen source. The existence of tetrahedral Ti4+ sites in N-doped TiO2 was also confirmed. The N-doped TiO2 sample with tetrahedral Ti4+ sites exhibited significantly improved photocatalytic performance for degradation of methylene blue solution under UV light or visible light irradiation. A combined time-resolved infrared (IR) spectroscopy study reveals that the enhanced photocatalytic performance could be attributed to a large amount of photogenerated charge carriers and efficient charge separation. It is demonstrated that the shallow donor state produced by oxygen vacancies of tetrahedral Ti4+ sites can effectively promote separation of charge carriers besides capturing electrons.

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The Photocatalytic and Antibacterial Performance of Nitrogen-Doped TiO2: Surface-Structure Dependence and Silver-Deposition Effect

Nanomaterials ◽

10.3390/nano10112261 ◽

2020 ◽

Vol 10 (11) ◽

pp. 2261 ◽

Cited By ~ 2

Author(s):

Abdul Wafi ◽

Erzsébet Szabó-Bárdos ◽

Ottó Horváth ◽

Mihály Pósfai ◽

Éva Makó ◽

...

Keyword(s):

Electron Microscopy ◽

Visible Light ◽

Surface Area ◽

Photocatalytic Performance ◽

Visible Region ◽

Bet Surface Area ◽

Doped Tio2 ◽

X Ray ◽

Nitrogen Doped ◽

Visible Light Driven

Catalysts for visible-light-driven oxidative cleaning processes and antibacterial applications (also in the dark) were developed. In order to extend the photoactivity of titanium dioxide into the visible region, nitrogen-doped TiO2 catalysts with hollow and non-hollow structures were synthesized by co-precipitation (NT-A) and sol–gel (NT-U) methods, respectively. To increase their photocatalytic and antibacterial efficiencies, various amounts of silver were successfully loaded on the surfaces of these catalysts by using a facile photo-deposition technique. Their physical and chemical properties were evaluated by using scanning electron microscopy (SEM), transmission electron microscopy–energy dispersive X-ray spectroscopy (TEM–EDS), Brunauer–Emmett–Teller (BET) surface area, X-ray diffraction (XRD), and diffuse reflectance spectra (DRS). The photocatalytic performances of the synthesized catalysts were examined in coumarin and 1,4-hydroquinone solutions. The results showed that the hollow structure of NT-A played an important role in obtaining high specific surface area and appreciable photoactivity. In addition, Ag-loading on the surface of non-hollow structured NT-U could double the photocatalytic performance with an optimum Ag concentration of 10−6 mol g−1, while a slight but monotonous decrease was caused in this respect for the hollow surface of NTA upon increasing Ag concentration. Comparing the catalysts with different structures regarding the photocatalytic performance, silverized non-hollow NT-U proved competitive with the hollow NT-A catalyst without Ag-loading for efficient visible-light-driven photocatalytic oxidative degradations. The former one, due to the silver nanoparticles on the catalyst surface, displayed an appreciable antibacterial activity, which was comparable to that of a reference material practically applied for disinfection in polymer coatings.

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Enhanced Photodecomposition of Methylene Blue in Water with Sr1−xKxTiO3−δ@PC-polyHIPEs under UV and Visible Light

Journal of Chemistry ◽

10.1155/2018/9365147 ◽

2018 ◽

Vol 2018 ◽

pp. 1-10 ◽

Cited By ~ 1

Author(s):

Yonghua Gao ◽

Tao Zhang ◽

Qipeng Guo ◽

Lizhen Gao

Keyword(s):

Methylene Blue ◽

Visible Light ◽

Room Temperature ◽

Oxygen Vacancies ◽

Photocatalytic Performance ◽

Uv Light ◽

Water Solution ◽

Internal Phase ◽

Water Pollutant ◽

First Time

Photocatalytic method was investigated to remove water pollutant methylene blue (MB) produced in textile, plastic, and dye industries. PC-polyHIPEs were prepared by light-induced polymerization of dopamine in transparent polyHIPEs which were synthesized by polymerization within high internal phase emulsions. Sr1-xKxTiO3-δ (x = 0–0.5) nanoparticles were incorporated and adhered to PC-polyHIPEs to form Sr1-xKxTiO3-δ@PC-polyHIPEs for the first time. The catalysts were characterized by XRD, FTIR, TGA, UV-Vis DRS, and SEM and their photocatalytic properties for MB decomposition were measured over UV-Vis spectrometer. The PC-polyHIPEs were of interconnected porous structure with around 100 μm pores and 30 μm windows. Sr1−xKxTiO3−δ@PC-polyHIPEs showed excellent MB decomposition activity under either UV or visible light although Sr1−xKxTiO3−δ alone worked only under UV light. When x = 0.3, Sr1−xKxTiO3−δ@PC-polyHIPEs showed the highest photocatalytic performance due to the existence of more oxygen vacancies. When the water solution with 50 mg L−1 MB and 1.6 gcat. L−1 Sr0.7K0.3TiO3−δ@PC-polyHIPEs was exposed to visible light for 160 min at room temperature, 88.3% of MB was decomposed. After being used for eight cycles, 87.6% activity of fresh Sr0.7K0.3TiO3−δ@PC-polyHIPEs still remained. The influences of salinity, temperature, and catalyst concentration on the catalytic activity were studied. For MB decomposition under visible light, the activation energy of Sr0.7K0.3TiO3−δ@PC-polyHIPEs was calculated to be 12.3 kJ mol−1 and the kinetics analysis revealed that the photocatalysis followed the second-order reaction. These findings demonstrated that Sr1−xKxTiO3−δ@PC-polyHIPEs were an effective candidate for real application in decomposition of MB in water.

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