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Laser irradiation in water for the novel, scalable synthesis of black TiO(x) photocatalyst for environmental remediation
Since 1970, TiO(2) photocatalysis has been considered a possible alternative for sustainable water treatment. This is due to its material stability, abundance, nontoxicity and high activity. Unfortunately, its wide band gap (≈3.2 eV) in the UV portion of the spectrum makes it inefficient under solar...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301962/ https://www.ncbi.nlm.nih.gov/pubmed/28243557 http://dx.doi.org/10.3762/bjnano.8.21 |
Sumario: | Since 1970, TiO(2) photocatalysis has been considered a possible alternative for sustainable water treatment. This is due to its material stability, abundance, nontoxicity and high activity. Unfortunately, its wide band gap (≈3.2 eV) in the UV portion of the spectrum makes it inefficient under solar illumination. Recently, so-called “black TiO(2)” has been proposed as a candidate to overcome this issue. However, typical synthesis routes require high hydrogen pressure and long annealing treatments. In this work, we present an industrially scalable synthesis of TiO(2)-based material based on laser irradiation. The resulting black TiO(x) shows a high activity and adsorbs visible radiation, overcoming the main concerns related to the use of TiO(2) under solar irradiation. We employed a commercial high repetition rate green laser in order to synthesize a black TiO(x) layer and we demonstrate the scalability of the present methodology. The photocatalyst is composed of a nanostructured titanate film (TiO(x)) synthetized on a titanium foil, directly back-contacted to a layer of Pt nanoparticles (PtNps) deposited on the rear side of the same foil. The result is a monolithic photochemical diode with a stacked, layered structure (TiO(x)/Ti/PtNps). The resulting high photo-efficiency is ascribed to both the scavenging of electrons by Pt nanoparticles and the presence of trap surface states for holes in an amorphous hydrogenated TiO(x) layer. |
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