Substituent-induced oxidation-reduction molecular organic junction for interfacial hydrogen peroxide photosynthesis
Zhi Li, Lin An, Lijiang Guan, Jingyi Yang, Renli Yin, Shangbin Jin, Mingshan Zhu, Junhao Qin

TL;DR
This paper introduces a new organic catalyst that separates oxidation and reduction sites to efficiently produce hydrogen peroxide and treat wastewater.
Contribution
A fluorine-substituted molecular organic junction catalyst with spatially separated redox sites is developed for enhanced photocatalytic performance.
Findings
The catalyst achieves a hydrogen peroxide production rate of 4664 µmol g−1 h−1 under simulated sunlight and ultrasonic forces.
The design enables dual-pathway water oxidation and oxygen reduction reactions via benzene bridges.
The system effectively purifies arsenic-containing mining wastewater.
Abstract
The distribution of catalytic active sites critically dictates photocatalytic efficiency, but existing catalyst design operate at the same or adjacent sites still remain limitations toward photocatalytic reaction. To address this, a kind of spatially separable oxidation-reduction assignment in fluorine substituted molecular organic junction catalyst (covalent triazine framework, CTF-TF-0.5) is constructed. By modulating the coordination of F-substituted benzene linkers, we controlled the redox nature of triazine ring in CTFs to obtain the separable oxidation-reduction assignment. It achieves a interfacial hydrogen peroxide (H2O2) photosynthesis rate of 4664 µmol g−1 h−1 at triphasic interface with simulated sunlight and ultrasonic forces. With external forces, the photogenerated-holes allow to transfer to the oxidation site (triazine connected two benzene and a F-substituted benzene)…
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Taxonomy
TopicsAdvanced Photocatalysis Techniques · Covalent Organic Framework Applications · Advanced oxidation water treatment
