# Double Z-scheme biochar-based g-C3N4/Bi2WO6/Ag3PO4 nanocomposite for efficient removal of antibiotics and synergistic mechanisms

**Authors:** Tongtong Wang, Di Zhang, Hui Shi, Jiyong Zheng, Huixia Wang, Eric Lichtfouse

PMC · DOI: 10.1038/s42004-026-01923-w · Communications Chemistry · 2026-02-03

## TL;DR

A new nanocomposite material efficiently removes antibiotics from water using a unique photocatalytic mechanism.

## Contribution

The study introduces a biochar-based nanocomposite with a double Z-scheme heterojunction for enhanced photocatalytic antibiotic removal.

## Key findings

- The nanocomposite achieved nearly complete tetracycline removal in 120 minutes with a high removal rate.
- It showed over 85% antibiotic removal in real wastewater and 99% bacterial sterilization within 48 hours.
- The composite's structure and heteroatoms significantly enhance photocatalytic activity through radical generation.

## Abstract

Photocatalysis research has evolved towards increasingly sophisticated structural regulation and material design. The synergistic enhancement of photocatalysis by multi-component semiconductors and biochar warrants detailed investigation. This study introduces an innovative biochar-based g-C3N4/Bi2WO6/Ag3PO4 nanocomposite (CN/Bi/Ag@ACB), which was applied to the efficient removal of antibiotic pollutants represented by tetracycline (TC). Findings reveal that CN/Bi/Ag@ACB forms a double Z-scheme heterojunction, significantly reducing photogenerated carrier recombination. It absorbs light in the 200-800 nm range, with a band gap of 1.91 eV. Under 120 min of illumination, the composite nearly completely removed 50 mg·L-1 of TC, achieving a removal rate of 0.0351 min-1, which is 8.56-13.50 times higher than that of the individual semiconductors. In real wastewater, TC removal exceeded 85.95%, with concurrent removal of other antibiotics, and achieved 99% sterilization of E. coli and S. aureus within 48 hours. The catalytic system was predominantly driven by ·O2-, h+, and ·OH radicals. The unique structure and surface characteristics of the composite, along with the incorporation of heteroatoms, substantially enhance photocatalytic activity. The TC degradation process is associated with the conversion of fulvic and humic acids, with three potential degradation pathways proposed. This study elucidates the synergistic mechanisms of photocatalysis enhancement by multi-component semiconductors and biochar.

Although photocatalysis research has evolved towards increasingly sophisticated structural regulation and material design, the synergistic enhancement of photocatalysis by multi-component semiconductors and biochar remains underexplored. Here, the authors present a biochar-based g-C3N4/Bi2WO6/Ag3PO4 nanocomposite and apply it to the efficient removal of tetracycline, showing that it forms a double Z-scheme heterojunction that significantly reduces photogenerated carrier recombination.

## Linked entities

- **Chemicals:** tetracycline (PubChem CID 54675776)

## Full-text entities

- **Chemicals:** Ag3PO4 (MESH:C039072), Bi2WO6 (MESH:C000626718), biochar (MESH:C540010), g-C3N4 (MESH:C000629596), TC (MESH:D013752), Ag@ACB (-), Bi (MESH:D001729)
- **Species:** Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954125/full.md

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Source: https://tomesphere.com/paper/PMC12954125