Platinum/nitrogen-co-doped TiO2 as photocatalyst and light-free catalytic adsorbent for gaseous formaldehyde
- Authors
- Lim, Daehwan; Maitlo, Hubdar Ali; Younis, Sherif A.; Boukhvalov, Danil W.; Kim, Ki Hyun; Lee, Jechan
- Issue Date
- Jan-2026
- Publisher
- Academic Press
- Keywords
- Pt/N-TiO2 catalyst; Volatile organic compounds (VOCs); Formaldehyde; Catalytic adsorption; Photocatalytic degradation; Indoor air pollution control
- Citation
- Journal of Colloid and Interface Science, v.702, pp 1 - 21
- Pages
- 21
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Colloid and Interface Science
- Volume
- 702
- Start Page
- 1
- End Page
- 21
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/208785
- DOI
- 10.1016/j.jcis.2025.138895
- ISSN
- 0021-9797
1095-7103
- Abstract
- Platinum and nitrogen co-doped titanium dioxide (Pt/N-TiO<inf>2</inf>, with 1 wt% Pt and an N/Ti molar ratio of 1) has been synthesized. This Pt/N co-doping strategy creates Schottky junctions, reduces the bandgap energy (3.25 to 2.12 eV), and introduces a new energy level (N 2p). The modified catalyst exhibits dual functionality, serving as both a photocatalyst under light irradiation (λ = 365 nm, 32 W) and a light-free catalytic adsorbent against gaseous formaldehyde (FA). The Pt/N-TiO<inf>2</inf> catalysts are immobilized on ceramic bead supports, placed in a tubular reactor system, and tested under controlled operating conditions, including FA concentrations (100–500 ppm), oxygen levels (0–21%), relative humidity (RH; 0–100%), and gas flow rates (100–500 mL min−1). The Pt/N-TiO<inf>2</inf> achieves a photocatalytic oxidation efficiency of 94.2% (reaction rate of 9.24 μmol mg−1 h−1 and apparent quantum yield of 5.58%) against 200 ppm FA (100% RH). The catalyst's efficiency stems from a synergistic dual mechanism, as evidenced by molecular simulation using density functional theory. First, N doping enhances light absorption and extends the charge carrier lifetime, while the Pt as a co-catalyst promotes charge separation by acting as an electron sink. Second, the catalyst's ability to efficiently trap H<inf>2</inf>O and O<inf>2</inf> molecules also contributes to the efficient mineralization of FA through the facile generation of reactive oxygen species. This dual functionality extends to dark conditions as a catalytic adsorbent, achieving a FA removal efficiency of 78.9% with a CO<inf>2</inf> yield of 57%. In-situ diffuse reflectance infrared Fourier transform spectroscopy analysis confirms this mechanism by identifying the generation of Pt-OH hydroxylation and •O<inf>2</inf>− radicals from H<inf>2</inf>O vapor and O<inf>2</inf>, respectively. Overall, this research provides a practical guideline for constructing an advanced VOC abatement platform.
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