Hierarchical Construction of Znbi2o4 Anchored on Flower-Like Bi2wo6 Heterojunction Photocatalyst for Removal of Alizarin Red S
Journal
Surfaces and Interfaces
ISSN
2468-0230
Date Issued
2025
Author(s)
Abstract
In this study, we investigated the fabrication and photocatalytic performance of ZnBi<inf>2</inf>O<inf>4</inf>@Bi<inf>2</inf>WO<inf>6</inf> nanocomposites for the degradation of organic pollutants. The nanocomposites were synthesized via a hydrothermal method followed by ultrasonic treatment, resulting in a unique composite structure. X-ray diffraction (XRD) confirmed successful material synthesis, and scanning electron microscopy (SEM) revealed the morphologies of Bi<inf>2</inf>WO<inf>6</inf> nanoflowers and ZnBi<inf>2</inf>O<inf>4</inf> nanocubes, with the composites exhibiting a hybrid network-like structure. UV–visible spectroscopy showed a significant redshift in the optical absorption edge, indicating that ZnBi<inf>2</inf>O<inf>4</inf> incorporation effectively reduced the band gap of the nanocomposite, enhancing its visible light absorption. Photoluminescence (PL) spectroscopy demonstrated that the nanocomposites promoted efficient charge separation and minimized recombination, critical factors for improved photocatalytic performance. Under visible light, the ZnBi<inf>2</inf>O<inf>4</inf>@Bi<inf>2</inf>WO<inf>6</inf> nanocomposites achieved a degradation efficiency of 96.8 % for alizarin red S (ARS), following pseudo-first-order kinetics. The composites also exhibited excellent stability, with only a 6.05 % loss in activity after five degradation cycles, confirming their long-term durability. Trapping experiments identified hydroxyl radicals (·OH), holes (h+), and electrons (e–) as active species in the degradation mechanism. Overall, ZnBi<inf>2</inf>O<inf>4</inf>@Bi<inf>2</inf>WO<inf>6</inf> nanocomposites show strong potential as efficient and stable photocatalysts for removing hazardous organic pollutants from wastewater, offering a sustainable solution for environmental cleanup. © 2025 Elsevier B.V.
