Hydrangea‐Like Bi 4 O 5 I 2 /Na 0.5 Bi 0.5 TiO 3 Type‐II Heterojunctions For Efficient Photocatalytic Degradation of Bisphenol A
Abstract
ABSTRACT Heterojunctions hold great promise for photocatalysis due to their enhanced photo‐generated electron‐hole separation efficiency. However, the development of heterojunctions with robust interfacial contact and broad visible light response remains a critical challenge. Herein, hydrangea‐like Bi 4 O 5 I 2 /Na 0.5 Bi 0.5 TiO 3 heterojunctions with an intimate interface were rationally constructed via a facile coprecipitation method. The as‐prepared heterojunctions exhibited exceptional visible light‐driven photocatalytic performance in degrading various refractory organic pollutants, including bisphenol A (BPA), tetracycline, and Rhodamine B, outperforming the parent compounds Bi 4 O 5 I 2 and Na 0.5 Bi 0.5 TiO 3 alone. Notably, the optimized heterojunction catalyst achieved complete (100%) photocatalytic removal of BPA under visible light irradiation. The enhanced activity originates from the synergy of heterojunction formation and uniform hydrangea‐like morphology, which promotes photo‐generated electron‐hole separation/transfer and inhibits their recombination. Mechanistically, the heterojunction follows a Type‐II charge transfer pathway, where photo‐generated electrons preferentially migrate and accumulate on the conduction band of Na 0.5 Bi 0.5 TiO 3 , while photo‐generated holes transfer to and enrich on the valence band of Bi 4 O 5 I 2 . These accumulated electrons efficiently reduce adsorbed O 2 molecules to generate O 2 · − , which serves as the primary active species driving BPA degradation. This study provides a useful guideline for the design and application of bismuth‐based heterojunctions in environmental remediation.
Fields of Study & Subjects
Advanced Photocatalysis Techniques
TiO2 Photocatalysis and Solar Cells
Layered Double Hydroxides Synthesis and Applications
Publication details
- Journal / source
- ChemCatChem
- Publisher
- Wiley
- Volume
- 18
- Issue
- 1
- Publication date
- 1 January 2026
- Language
- EN