# Copper Oxide-Doped Bismuth Oxychloride Heterostructures for Heterogeneous Photocatalysis: Design, Kinetics, and Photocatalytic Degradation Mechanism for Water Decontamination

**Authors:** María F. M. Guiñez, Andrés F. Jaramillo, Norberto J. Abreu, Adriana C. Mera, Juan C. Durán-Álvarez, Amauri Serrano-Lázaro, Jonathan Usuba-Valdebenito, Rebeca Martínez-Retureta, Manuel F. Melendrez

PMC · DOI: 10.3390/molecules31050754 · 2026-02-24

## TL;DR

This study designs a copper oxide-doped bismuth oxychloride material that efficiently degrades pollutants in water under visible light.

## Contribution

The paper introduces a solvothermal method to optimize CuO loading for enhanced photocatalytic performance in water decontamination.

## Key findings

- Low CuO content (0.6 wt.%) improved surface area and photocatalytic efficiency.
- Optimal degradation (50% in 60 min) occurred at pH 4 and 0.8 g L−1 catalyst dosage.
- Hydroxyl radicals were the main oxidizing species in the degradation process.

## Abstract

Bismuth oxychloride (BiOCl)– copper oxide (CuO) heterostructures were synthesized via a solvothermal route and assessed as visible-light-driven photocatalysts for methyl orange (MO) degradation. Different CuO loadings deposited on BiOCl microspheres were investigated to identify the optimal composition. Structural and physicochemical characterization revealed that low CuO content (0.6 wt. %) promoted uniform dispersion and enhanced surface area, whereas higher loadings led to nonuniform coverage and reduced photocatalytic efficiency. Operating conditions were optimized using response surface methodology based on a central composite design, considering catalyst dosage (0.1–0.8 g L−1) and pH (4–9). The highest degradation efficiency (~50% after 60 min irradiation) was achieved at pH = 4 and a catalyst dosage of 0.8 g L−1 using the BiOCl surface modified with 0.6% CuO. Kinetic analysis followed a pseudo-first-order model. Mass spectrometry identified transient intermediates associated with demethylation and desulfonation pathways, while radical scavenger experiments confirmed hydroxyl radicals (•OH) as the dominant oxidizing species, with a secondary contribution from superoxide radicals (•O2−). These results highlight the critical role of CuO dispersion and interfacial quality in enhancing charge separation and photocatalytic performance, providing practical guidelines for the rational design of BiOX-CuO heterostructures for water remediation applications.

## Linked entities

- **Chemicals:** methyl orange (PubChem CID 23673835), Copper Oxide (PubChem CID 14829), Bismuth Oxychloride (PubChem CID 6328152)

## Full-text entities

- **Chemicals:** BiOCl (MESH:C044685), hydroxyl radicals (MESH:D017665), OH) (MESH:C031356), MO (MESH:C100258), Water (MESH:D014867), BiOX (-), CuO (MESH:C030973), O2- (MESH:D013481)

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12985650/full.md

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Source: https://tomesphere.com/paper/PMC12985650