Defective TiO2 Nanotube Arrays for Efficient Photoelectrochemical Degradation of Organic Pollutants.

Abstract

Oxygen vacancies (OVs) are one of the most critical factors that enhance the electrical and catalytic characteristics of metal oxide-based photoelectrodes. In this work, a simple procedure was applied to prepare reduced TiO2 nanotube arrays (NTAs) (TiO2-x) via a one-step reduction method using NaBH4. A series of characterization techniques were used to study the structural, optical, and electronic properties of TiO2-x NTAs. X-ray photoelectron spectroscopy confirmed the presence of defects in TiO2-x NTAs. Photoacoustic measurements were used to estimate the electron-trap density in the NTAs. Photoelectrochemical studies show that the photocurrent density of TiO2-x NTAs was nearly 3 times higher than that of pristine TiO2. It was found that increasing OVs in TiO2 affects the surface recombination centers, enhances electrical conductivity, and improves charge transport. For the first time, a TiO2-x photoanode was used in the photoelectrochemical (PEC) degradation of a textile dye (basic blue 41, B41) and ibuprofen (IBF) pharmaceutical using in situ generated reactive chlorine species (RCS). Liquid chromatography coupled with mass spectrometry was used to study the mechanisms for the degradation of B41 and IBF. Phytotoxicity tests of B41 and IBF solutions were performed using Lepidium sativum L. to evaluate the potential acute toxicity before and after the PEC treatment. The present work provides efficient PEC degradation of the B41 dye and IBF in the presence of RCS without generating harmful products.