Porosity-dependent photoelectrochemical activity of double-layered TiO 2 thin films deposited by spin-coating method

Photoelectrochemical (PEC) cells made of low-cost, chemically stable, and abundant materials are crucial for green hydrogen production. In this regard, the fabrication of porous films with high light trapping ability and a large contact area is crucial for the production of efficient PEC cells. In t...

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Veröffentlicht in:RSC advances 2023-11, Vol.13 (49), p.34482-34488
Hauptverfasser: Rustembekkyzy, Kuralay, Zholdasbekov, Amir, Abduvalov, Alshyn, Kaikanov, Marat, Atabaev, Timur Sh
Format: Artikel
Sprache:eng
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Zusammenfassung:Photoelectrochemical (PEC) cells made of low-cost, chemically stable, and abundant materials are crucial for green hydrogen production. In this regard, the fabrication of porous films with high light trapping ability and a large contact area is crucial for the production of efficient PEC cells. In this report, anatase TiO 2 thin films with a porous double-layered structure were successfully prepared using a conventional spin-coating deposition method. Various amounts of polystyrene spheres were used as a pore-templating agent to control the porosity of the films. A range of characterization techniques, such as scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and photoluminescence were employed to assess the morphology, structural and optical properties of prepared TiO 2 films. PEC measurements revealed that prepared double-layered TiO 2 thin films exhibit porosity-dependent photocatalytic activity. For example, TiO 2 films with an optimized porous structure demonstrated an increase in photocurrent density by a factor of ∼2.23 (to 141.7 μA cm −2 ) and photoconversion efficiency improvement by a factor of ∼2.14 as compared to non-porous double-layered TiO 2 reference films. Absorbance and photoluminescence analysis confirmed that improved PEC activity can be attributed to increased light absorption by the porous structure and reduced charge carrier recombination.
ISSN:2046-2069
2046-2069
DOI:10.1039/D3RA06914A