Issue 37, 2015

Enhanced visible-light-driven photoactivities of single-walled carbon nanotubes coated with N doped TiO2 nanoparticles

Abstract

A two-step hydrothermal method is used to prepare N doped single-walled carbon nanotube–TiO2 (SWCNT–N/TiO2) hybrids with different contents of SWCNTs from 1.25 wt% to 10 wt%. The photocatalysts were characterized by X-ray diffraction analysis, UV-vis diffuse reflectance spectroscopy, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The UV-vis diffuse reflectance spectra show an apparent enhancement of absorption throughout the visible light region. Raman spectroscopy further confirms the chemical interaction between N/TiO2 and SWCNTs in the hybrid. SWCNT–N/TiO2 hybrid presents a superior photocatalytic activity to DWCNT–N/TiO2 (N doped double-walled carbon nanotube–TiO2) and MWCNT–N/TiO2 (N doped multi-walled carbon nanotube–TiO2) based on the results of the photocatalytic degradation of sulfathiazole under visible light irradiation, which is attributed to the synergetic effects of SWCNT modification and N doping. N doping induces visible light absorption by either introducing localized electronic states within the band gap or contributing electrons to the valence band and metal-like SWCNT can act as an electron conductor to facilitate the fast injection of the photogenerated electrons into the conduction band of N/TiO2, leading to significantly enhanced visible-light-driven photocatalytic activity.

Graphical abstract: Enhanced visible-light-driven photoactivities of single-walled carbon nanotubes coated with N doped TiO2 nanoparticles

Article information

Article type
Paper
Submitted
18 Dec 2014
Accepted
18 Mar 2015
First published
18 Mar 2015

RSC Adv., 2015,5, 28973-28979

Author version available

Enhanced visible-light-driven photoactivities of single-walled carbon nanotubes coated with N doped TiO2 nanoparticles

T. Gao, G. Sun, F. Cheng, K. Dai, H. Chen, K. Deng and Q. Huang, RSC Adv., 2015, 5, 28973 DOI: 10.1039/C4RA16597G

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