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Updated: Feb 4, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
Published on: April 22, 2016
Mineralización de acetaldehído por un fotocatalizador de WO3 anclado con ciclodextrina, independiente del oxígeno,
Woojung Jeon1, Seunghyun Weon2, Ye He3
1Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Abstract:
Photocatalytic degradation of volatile organic compounds (VOCs) using visible light has been widely investigated, but its practical implementation remains constrained by several limiting factors. Here, we prepared carboxymethyl-β-cyclodextrin (CMCD)-anchored WO3 that enabled visible-light-driven mineralization of acetaldehyde even under O2-free conditions. Anchoring CMCD on WO3 facilitated interfacial charge separation, enhancing the photocatalytic performance. Spectroscopic and electrochemical analyses revealed that loading CMCD on WO3 induced the formation of a charge-transfer complex via C-O-W bonding and extended the charge carrier lifetime by trapping electrons in CMCD. CMCD/WO3 sustained •OH generation under visible light (λ > 420 nm) and fully mineralized acetaldehyde even in the absence of O2. It also produced dioxygen from water oxidation in O2-free conditions, supplying O2 needed to fully mineralize VOCs to CO2, and it enabled an unconventional three-electron reduction of O2 to •OH. CMCD/WO3 exhibited a visible light degradation efficiency comparable to that of Pt-loaded WO3. In particular, CMCD/WO3 exhibited a higher carbon mass balance for acetaldehyde degradation than Pt/WO3, and this value remained nearly unchanged under both oxygen-rich and oxygen-free conditions. CMCD/WO3 also demonstrated long-term stability across repeated photocatalytic cycles with no decomposition of the CMCD structure. These findings highlight a supramolecular design strategy for developing an unconventional visible-light-active photocatalyst for indoor air purification, especially in enclosed or oxygen-depleted environments where conventional photocatalysts fail to operate.
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