Shi Cheng, Shin Kajita, Quan Shi, Shogo Kodate, Yuki Hayashi
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Photocatalytic ethylene decomposition using porous titania thin film formed by pulsed laser deposition
Photocatalytic oxidation using titanium dioxide (TiO2) is an effective approach for ethylene degradation due to its chemical stability and non-toxicity. In this study, we show that nanostructured TiO2 thin films can be fabricated via pulsed laser deposition (PLD) under rather high oxygen pressures, and their photocatalytic ethylene decomposition performance was evaluated. The structural and morphological characteristics of the thin films were analyzed using scanning electron microscopy (SEM), grayscale analysis, and Raman spectroscopy. The results indicate a strong dependence of photocatalytic efficiency on the oxygen pressure during the deposition process. SEM and Raman spectroscopy analyses confirm that porous TiO2 nanostructures were formed at oxygen pressures of 20 Pa and above, significantly increasing the active surface area. Subsequent calcination improved the crystallinity, resulting in a stable anatase phase and enhanced charge separation, thereby improving photocatalytic performance. These findings demonstrate that PLD is an effective method for fabricating TiO2-based photocatalysts, enabling the optimization of deposition parameters through tunable nanostructures to enhance gas-phase photocatalytic efficiency.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.