# Substituent-induced oxidation-reduction molecular organic junction for interfacial hydrogen peroxide photosynthesis

**Authors:** Zhi Li, Lin An, Lijiang Guan, Jingyi Yang, Renli Yin, Shangbin Jin, Mingshan Zhu, Junhao Qin

PMC · DOI: 10.1038/s41467-026-70959-2 · 2026-03-25

## 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.

## Key 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) and photogenerated-electrons to the reduction site (triazine connected a benzene and two F-substituted benzene) via benzene bridges for a dual-pathway of water oxidation and oxygen reduction reactions to synthesize H2O2. Additionally, this heterogeneous interfacial reaction system exhibits efficient purification capability for arsenic-containing mining wastewater. This study using the separable oxidation-reduction sites for addressing the coupling reaction at manipulable active sites to improve overall catalytic efficiency via molecular junction catalyst.

Designing efficient catalysts requires precise control over where chemical reactions occur on a molecular level. This organic junction catalyst separates oxidation and reduction sites to enable high-yield hydrogen peroxide production and wastewater treatment.

## Linked entities

- **Chemicals:** hydrogen peroxide (PubChem CID 784), arsenic (PubChem CID 5359596)

## Full-text entities

- **Genes:** ESCO1 (establishment of sister chromatid cohesion N-acetyltransferase 1) [NCBI Gene 114799] {aka A930014I12Rik, CTF, ECO1, EFO1, ESO1}, CTF1 (cardiotrophin 1) [NCBI Gene 1489] {aka CT-1, CT1}, CAT (catalase) [NCBI Gene 847]
- **Chemicals:** CB (MESH:C063451), H2O2 (MESH:D006861), oxide (MESH:D010087), *O2- (MESH:D010100), cyclohexane (MESH:C506365), methanol (MESH:D000432), C (MESH:D002244), 13C (MESH:C000615229), potassium borohydride (MESH:C028371), acid (MESH:D000143), *OH (MESH:C031356), diamond (MESH:D018130), H (MESH:D006859), triazine (MESH:D014227), benzene (MESH:D001554), KI (MESH:C066186), F (MESH:D005461), H218O (-), COF (MESH:C043212), H2O (MESH:D014867), deuterium (MESH:D003903), KBr (MESH:C039004), formic acid (MESH:C030544), NaOH (MESH:D012972), N (MESH:D009584), halogen (MESH:D006219), free radicals (MESH:D005609), HCl (MESH:D006851), ammonia (MESH:D000641), p-BQ (MESH:C056194), Arsenic (MESH:D001151), metal (MESH:D008670)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13018176/full.md

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Source: https://tomesphere.com/paper/PMC13018176