Role of the TiO2 Crystalline Phase in Pt-TiO2 for Thermocatalytic Mineralization of Gaseous AcetaldehydeClick to copy article linkArticle link copied!
- Minhyung LeeMinhyung LeeDepartment of Civil & Environmental Engineering, Yonsei University, Seoul 03722, Republic of KoreaMore by Minhyung Lee
- Bupmo KimBupmo KimDepartment of Energy Engineering, Korea Institute of Energy Technology (KENTECH), Naju 58330, Republic of KoreaMore by Bupmo Kim
- Suho KimSuho KimDepartment of Civil & Environmental Engineering, Yonsei University, Seoul 03722, Republic of KoreaDepartment of Construction Test & Certification Center, Korea Institute of Civil Engineering and Building Technology, Goyang 10223, Republic of KoreaMore by Suho Kim
- Hwan KimHwan KimDepartment of Civil & Environmental Engineering, Yonsei University, Seoul 03722, Republic of KoreaEnvironmental Technology Division, Korea Testing Laboratory, Seoul 08389, Republic of KoreaMore by Hwan Kim
- Minjun ParkMinjun ParkDepartment of Civil & Environmental Engineering, Yonsei University, Seoul 03722, Republic of KoreaMore by Minjun Park
- Wonyong ChoiWonyong ChoiDepartment of Energy Engineering, Korea Institute of Energy Technology (KENTECH), Naju 58330, Republic of KoreaMore by Wonyong Choi
- Wooyul Kim*Wooyul Kim*Email: [email protected]Department of Energy Engineering, Korea Institute of Energy Technology (KENTECH), Naju 58330, Republic of KoreaMore by Wooyul Kim
- Hyoung-il Kim*Hyoung-il Kim*Email: [email protected]Department of Civil & Environmental Engineering, Yonsei University, Seoul 03722, Republic of KoreaFuture City Open Innovation Center, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of KoreaMore by Hyoung-il Kim
Abstract

Pt-TiO2 is an efficient low-temperature thermocatalyst for volatile organic compound (VOC) removal, driven by active oxygen species formation through metal–support interactions. While the role of Pt is well established, the influence of TiO2 polymorphs on active oxygen generation is less understood. This study explores the thermocatalytic removal of acetaldehyde (CH3CHO) over Pt supported on three TiO2 polymorphs: anatase, rutile, and brookite. CH3CHO mineralization at 160 °C follows the trend: Pt-anatase (99.5%) > Pt-rutile (79.3%) > Pt-brookite (56.7%). These differences correlate with the oxygen adsorption and active oxygen generation capabilities, as evidenced by electrochemical analyses and O2-temperature-programmed desorption. Density functional theory calculations further indicate that Pt supported on anatase has the highest negative charge density, which significantly enhances the formation of active oxygen species. In situ FTIR spectroscopy provides additional evidence by revealing distinct CH3CHO oxidation pathways: *HCOOH on Pt-anatase and Pt-brookite, and *CH3COOH on Pt-rutile. Despite sharing a similar pathway, Pt-anatase displayed faster kinetics due to a higher abundance of surface-active oxygen species. This study highlights the pivotal role of TiO2 polymorphs in shaping metal–support interactions and provides critical insights for designing efficient Pt-based catalysts for thermocatalytic VOC abatement.
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