Porosity-dependent photoelectrochemical activity of double-layered TiO 2 thin films deposited by spin-coating method.
Kuralay RustembekkyzyAmir ZholdasbekovAlshyn AbduvalovMarat I KaikanovTimur Sh AtabaevPublished in: RSC advances (2023)
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.
Keyphrases
- visible light
- quantum dots
- electron microscopy
- room temperature
- highly efficient
- low cost
- high resolution
- induced apoptosis
- metal organic framework
- sensitive detection
- reduced graphene oxide
- tissue engineering
- transition metal
- ionic liquid
- single molecule
- carbon nanotubes
- dna damage
- endoplasmic reticulum stress
- density functional theory
- energy transfer
- single cell
- magnetic resonance
- oxidative stress
- signaling pathway
- ion batteries
- cell death
- crystal structure