Abstract
Water contaminated with dyes severely impacts human health and the aquatic ecosystem, thus becoming a global problem. Photocatalysis is considered the most promising method for dye remediation and degradation. In this context, titanium dioxide (TiO2) is considered an ideal photocatalyst due to its nontoxicity, biodegradability, abundance, recyclability, and improved properties. However, the application of TiO2 for the removal of organic pollutants faces numerous challenges, including its wide band-gap, low affinity, mass transfer limits, particle aggregation, and regeneration issues. Due to its superior physical and chemical properties compared to pure TiO2, considerable efforts have been made to modify TiO2 with various materials. Structural modifications can be achieved in various ways, particularly through the introduction of dopants and the use of support materials. These factors are important for increasing the number of active sites and slowing the recombination rate of photogenerated electron-hole pairs. This review presents photo-assisted dye degradation and recent advances in supported and doped TiO2 photocatalysts. Furthermore, the role of dopants and support materials and their contribution to improving the photocatalytic potential of TiO2 were reported. The structural properties of TiO2 and possible mechanisms of TiO2-mediated dye degradation, as well as its future potential, are also discussed.
| Original language | English |
|---|---|
| Article number | 113852 |
| Journal | Materials Research Bulletin |
| Volume | 195 |
| DOIs | |
| State | Published - Mar 2026 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2025 Elsevier Ltd
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Degradation
- Doping
- Photocatalysis
- Structural modification
- Titanium dioxide
ASJC Scopus subject areas
- General Materials Science
- Condensed Matter Physics
- Mechanics of Materials
- Mechanical Engineering
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