Efficiently Visible-Light Driven Photoelectrocatalytic Oxidation of As(III) at Low Positive Biasing Using Pt/TiO2 Nanotube Electrode

• Published in: Nanoscale research letters Vol. 11; no. 1; p. 32
• Main Authors: Qin, Yanyan, Li, Yilian, Tian, Zhen, Wu, Yangling, Cui, Yanping
• Format: Journal Article
• Language: English
• Published: New York Springer US 19.01.2016; Springer Nature B.V
• Subjects: Chemistry and Materials Science; Materials Science; Molecular Medicine; Nano Express; Nanochemistry; Nanoscale Science and Technology; Nanotechnology; Nanotechnology and Microengineering; nanotubes; Pt/TiO; Anode electrolytic tanks; As(III); Photoelectrocatalytic oxidation; Pt/TiO2 nanotubes
• ISSN: 1931-7573; 1556-276X
• DOI: 10.1186/s11671-016-1248-5

A constant current deposition method was selected to load highly dispersed Pt nanoparticles on TiO 2 nanotubes in this paper, to extend the excited spectrum range of TiO 2 -based photocatalysts to visible light. The morphology, elemental composition, and light absorption capability of as-obtained Pt/TiO 2 nanotubes electrodes were characterized by FE-SEM, energy dispersive spectrometer (EDS), X-ray photoelectron spectrometer (XPS), and UV-vis spectrometer. The photocatalytic and photoelectrocatalytic oxidation of As(III) using a Pt/TiO 2 nanotube arrays electrode under visible light ( λ  > 420 nm) irradiation were investigated in a divided anode/cathode electrolytic tank. Compared with pure TiO 2 which had no As(III) oxidation capacity under visible light, Pt/TiO 2 nanotubes exhibited excellent visible-light photocatalytic performance toward As(III), even at dark condition. In anodic cell, As(III) could be oxidized with high efficiency by photoelectrochemical process with only 1.2 V positive biasing. Experimental results showed that photoelectrocatalytic oxidation process of As(III) could be well described by pseudo-first-order kinetic model. Rate constants depended on initial concentration of As(III), applied bias potential and solution pH. At the same time, it was interesting to find that in cathode cell, As(III) was also continuously oxidized to As(V). Furthermore, high-arsenic groundwater sample (25 m underground) with 0.32 mg/L As(III) and 0.35 mg/L As(V), which was collected from Daying Village, Datong basin, Northern China, could totally transform to As(V) after 200 min under visible light in this system.