Loading…

High-Efficacy Hierarchical Dy 2 O 3 /TiO 2 Nanoflower toward Wastewater Reclamation: A Combined Photoelectrochemical and Photocatalytic Strategy

Developing a sustainable photocatalyst is crucial to mitigate the foreseeable energy shortage and environmental pollution caused by the rapid advancement of global industry. We developed Dy O /TiO nanoflower (TNF) with a hierarchical nanoflower structure and a near-ideal anatase crystallite morpholo...

Full description

Saved in:
Bibliographic Details
Published in:ACS omega 2022-05, Vol.7 (20), p.17223-17233
Main Authors: Kaid, Mahmoud M, Khder, Abdelrahman S, Ahmed, Saleh A, Ibrahim, Amr A, Altass, Hatem M, Alsantali, Reem I, Jassas, Rabab S, Khder, Menna A, Al-Rooqi, Munirah M, Moussa, Ziad, Ahmed, Awad I
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Developing a sustainable photocatalyst is crucial to mitigate the foreseeable energy shortage and environmental pollution caused by the rapid advancement of global industry. We developed Dy O /TiO nanoflower (TNF) with a hierarchical nanoflower structure and a near-ideal anatase crystallite morphology to degrade aqueous rhodamine B solution under simulated solar light irradiation. The prepared photocatalyst was well-characterized using powder X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, energy-dispersive spectroscopy, scanning electron microscopy, Brunauer-Emmett-Teller, diffuse reflectance UV-vis spectra, and X-ray photoelectron spectroscopy. Further analysis was performed to highlight the photoelectrochemical activity of the prepared photocatalysts such as electrochemical impedance spectroscopy, linear sweep voltammetry, photocurrent response, and a Mott-Schottky study. The crystalline Dy O /TNF exhibits superb photocatalytic activity attributed to the improved charge transfer, reduced recombination rate of the electron-hole pairs, and a remarkable red-shift in light absorption.
ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.2c01090