# Comparison of the Effects of Brominated Perylenediimide and Perylene Tetraester Modified G‐C₃N₄ S‐Scheme Nanocomposites on the Photocatalytic Degradation of Anionic and Cationic Dyes and Herbicide

**Authors:** Erkan Aksoy, Emre Alp

PMC · DOI: 10.1002/gch2.202500100 · 2025-04-27

## TL;DR

This study shows that modifying carbon nitride with brominated dyes improves its ability to break down certain pollutants under visible light.

## Contribution

The study introduces brominated perylenediimide and perylene tetraester as sensitizers for g-C3N4, enhancing photocatalytic degradation of dyes.

## Key findings

- g-C3N4/dBrPTE degrades rhodamine B 2.34 times faster than pure g-C3N4.
- g-C3N4/dBrPDI degrades methyl orange 2.25 times faster than pure g-C3N4.
- Photocatalytic efficiency depends on interactions between sensitizers and pollutant properties.

## Abstract

Metal‐free g‐C3N4 (graphitic carbon nitride) is a promising candidate for the next‐generation visible light‐responsive photocatalyst; however, the recombination and transfer of the photogenerated charge carriers restrict its photocatalytic performances. The exfoliated g‐C₃N₄ sensitized with brominated perylenediimide (dBrPDI) and perylene tetraester (dBrPTE) enhances the photocatalytic performance due to improved charge separation, light absorption, charge transfer and, thereby, overall efficiency in pollutant degradation. The g‐C3N4/dBrPTE hybrid composite exhibits the fastest photocatalytic degradation against rhodamine B (RhB) pollutants. The g‐C3N4/dBrPTE hybrid composite degrades RhB with a 2.34‐fold improvement over pure g‐C3N4, while the g‐C3N4/dBrPDI hybrid composite degrades with a 1.56‐fold increase over pure g‐C3N4. The g‐C3N4/dBrPDI hybrid composite shows the highest photocatalytic efficiency against methyl orange (MO) pollutants. The g‐C3N4/dBrPDI hybrid composite degrades MO with a 2.25‐fold improvement over pure g‐C3N4, while the g‐C3N4/dBrPTE hybrid composite degrades with a 1.8‐fold increase over pure g‐C3N4. Unlike MO and RhB, the perylene dye sensitization does not enhance the photocatalytic degradation of 2,4‐dichloro phenoxy acetic acid (2,4‐D) and no sustained increase in efficiency is not observed. Overall, these results suggest that photocatalytic efficiency depends not only on the sensitized photocatalyst material but also on the interaction between the sensitized photocatalyst and the chemical and ionic properties of the pollutants in the aquatic media.

Exfoliated g‐C₃N₄ sensitized with brominated perylene dyes (dBrPDI and dBrPTE) significantly enhances photocatalytic degradation of RhB and methyl orange via improved charge separation and light absorption. Performance varies by pollutant type, highlighting that photocatalytic efficiency is strongly influenced by dye–pollutant interactions in aqueous environments.

## Linked entities

- **Chemicals:** rhodamine B (PubChem CID 6694), methyl orange (PubChem CID 23673835), 2,4-dichlorophenoxyacetic acid (PubChem CID 1486)

## Full-text entities

- **Chemicals:** 2,4-D (MESH:D015084), RhB (MESH:C029773), perylene (MESH:D010569), g-C3N4 (MESH:C000629596), MO (MESH:C100258), Metal (MESH:D008670), Perylene Tetraester Modified G-C3N4 (-)

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12151797/full.md

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Source: https://tomesphere.com/paper/PMC12151797