Issue 49, 2023, Issue in Progress

Porosity-dependent photoelectrochemical activity of double-layered TiO2 thin films deposited by spin-coating method

Abstract

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 TiO2 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 TiO2 films. PEC measurements revealed that prepared double-layered TiO2 thin films exhibit porosity-dependent photocatalytic activity. For example, TiO2 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 TiO2 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.

Graphical abstract: Porosity-dependent photoelectrochemical activity of double-layered TiO2 thin films deposited by spin-coating method

Supplementary files

Article information

Article type
Paper
Submitted
11 Oct 2023
Accepted
17 Nov 2023
First published
24 Nov 2023
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2023,13, 34482-34488

Porosity-dependent photoelectrochemical activity of double-layered TiO2 thin films deposited by spin-coating method

K. Rustembekkyzy, A. Zholdasbekov, A. Abduvalov, M. Kaikanov and T. Sh. Atabaev, RSC Adv., 2023, 13, 34482 DOI: 10.1039/D3RA06914A

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