Ionic-liquid-regulated Br-modified Bi2WO6 and Bi2WO6/BiOBr photocatalysts for simultaneous dye removal and Cr (VI) reduction: composition, crystal growth, and redox behavior

Heterojunction construction is widely used to enhance photocatalysis, yet improved charge separation does not necessarily increase the net rate of a target reduction when competing oxidative pathways are present. Here, Br-modified Bi 2 WO 6 and Bi 2 WO 6 /BiOBr heterostructures were prepared by a microwave-assisted hydrothermal method using ionic liquids (ILs) as bromine sources and morphology-directing media. Varying the IL cation chain length and dosage regulated phase evolution, facet exposure, crystallinity, nanosheet thickness, hierarchical assembly, and surface area. Low IL (1-ethyl-3-methylimidazolium bromide, [Emim]Br) loading produced Br-modified Bi 2 WO 6 without detectable crystalline BiOBr, whereas IL/Na 2 WO 4 ratios of at least 1 induced Bi 2 WO 6 /BiOBr formation. The optimized BWOE-0.1 sample combined exposure of Bi 2 WO 6 (001)-related facets, thin, densely assembled nanosheets, a high specific surface area (69.57 m 2 g −1 ), efficient interfacial charge transport, and the highest Cr(VI) reduction rate constant (0.139 min −1 ), which is 2.36 times that of pristine Bi 2 WO 6 . In contrast, Bi 2 WO 6 /BiOBr heterostructures showed lower net Cr(VI) reduction despite favorable carrier separation. EPR detection of a pronounced DMPO-X signal for (001)-dominant BiOBr indicates a strongly oxidative surface environment, supporting the interpretation that hole-driven reactions can counteract electron-mediated Cr(VI) reduction, potentially through Cr(III) re-oxidation. In a mixed Cr(VI)/methyl orange system, photogenerated electrons primarily drove Cr(VI) reduction, whereas •O 2 – dominated dye degradation. These results establish a structure–facet–redox relationship and demonstrate that photocatalyst design for mixed contaminants must optimize the balance between reduction and oxidation, rather than relying solely on charge separation.

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Journal
Journal of Alloys and Compounds
Published
2026-09-29
DOI
https://doi.org/10.1016/j.jallcom.2026.191414
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Ionic-liquid-regulated Br-modified Bi2WO6 and Bi2WO6/BiOBr photocatalysts for simultaneous dye removal and Cr (VI) reduction: composition, crystal growth, and redox behavior

Chi‐Jung Chang, Arul Pundi, Wei-Li Yuan, Tanuj Kumar et al.
Journal of Alloys and Compounds
Advanced Photocatalysis Techniques
article

Ionic-liquid-regulated Br-modified Bi2WO6 and Bi2WO6/BiOBr photocatalysts for simultaneous dye removal and Cr (VI) reduction: composition, crystal growth, and redox behavior

Chi‐Jung Chang, Arul Pundi, Wei-Li Yuan, Tanuj Kumar, Jem-Kun Chen, Zi-Yuan Su
article en

Abstract

Heterojunction construction is widely used to enhance photocatalysis, yet improved charge separation does not necessarily increase the net rate of a target reduction when competing oxidative pathways are present. Here, Br-modified Bi 2 WO 6 and Bi 2 WO 6 /BiOBr heterostructures were prepared by a microwave-assisted hydrothermal method using ionic liquids (ILs) as bromine sources and morphology-directing media. Varying the IL cation chain length and dosage regulated phase evolution, facet exposure, crystallinity, nanosheet thickness, hierarchical assembly, and surface area. Low IL (1-ethyl-3-methylimidazolium bromide, [Emim]Br) loading produced Br-modified Bi 2 WO 6 without detectable crystalline BiOBr, whereas IL/Na 2 WO 4 ratios of at least 1 induced Bi 2 WO 6 /BiOBr formation. The optimized BWOE-0.1 sample combined exposure of Bi 2 WO 6 (001)-related facets, thin, densely assembled nanosheets, a high specific surface area (69.57 m 2 g −1 ), efficient interfacial charge transport, and the highest Cr(VI) reduction rate constant (0.139 min −1 ), which is 2.36 times that of pristine Bi 2 WO 6 . In contrast, Bi 2 WO 6 /BiOBr heterostructures showed lower net Cr(VI) reduction despite favorable carrier separation. EPR detection of a pronounced DMPO-X signal for (001)-dominant BiOBr indicates a strongly oxidative surface environment, supporting the interpretation that hole-driven reactions can counteract electron-mediated Cr(VI) reduction, potentially through Cr(III) re-oxidation. In a mixed Cr(VI)/methyl orange system, photogenerated electrons primarily drove Cr(VI) reduction, whereas •O 2 – dominated dye degradation. These results establish a structure–facet–redox relationship and demonstrate that photocatalyst design for mixed contaminants must optimize the balance between reduction and oxidation, rather than relying solely on charge separation.

Journal of Alloys and CompoundsVol. 1082
National Taiwan University of Science and Technology (TW), Indian Institute of Technology Jammu (IN), Feng Chia University (TW)
National Science and Technology Council
Openalex Percentile: Top 31%
Advanced Photocatalysis Techniques
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