Novel high potential visible-light-active photocatalyst of CNT/Mo, S-codoped TiO2 hetero-nanostructure

被引:28
|
作者
Hamadanian, M. [1 ,2 ]
Shamshiri, M. [2 ]
Jabbari, V. [1 ]
机构
[1] Univ Kashan, Inst Nanosci & Nanotechnol, Kashan, Iran
[2] Univ Kashan, Fac Chem, Dept Phys Chem, Kashan, Iran
关键词
TiO2; CNT; CNT/Mo; S-codoped TiO2; Nanocomposite; Nano catalyst; WALL CARBON NANOTUBES; DOPED TITANIA; SOLAR-CELLS; COMPOSITE; DEGRADATION; NANOPARTICLES; ENHANCEMENT; NANOCOMPOSITES; DECOMPOSITION; CATALYSTS;
D O I
10.1016/j.apsusc.2014.08.123
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The current study deals with synthesize of novel nanophotocatalysts of CNT/Mo,S-codoped TiO2 by reacting between titanium isopropoxide (Ti(C3H7)(4)) and CNT in aqueous ammonia and subsequent calcining of hydrolysis of the products. The prepared catalysts were characterized by N-2 adsorption-desorption measurements, XRD, SEM, TEM, EDX, FT-IR, and UV-vis DRS spectroscopy. SEM and TEM images exhibited uniform coverage of CNT with anatase TiO2 nanoclusters. It was also demonstrated that the presence of S and Mo within the TiO2 acts as electrons traps and prevents the charge recombination and also enables the TiO2 photocatalyst to be active in visible-light region. Moreover, the CNT/Mo,S-doped TiO2 nanohybrids has been proven to has a excellent photocatalytic performance in photodecomposition of Congored (CR), at which the rate of decomposition reaches 100% in only 20 and 30 min under UV and visible-light irradiation, respectively. The enhanced photocatalytic activity was ascribed to the synergetic effects of excellent electrical property of CNT and metal-non-metal codoping. Finally, which to best of our knowledge is done for the first time, we have demonstrated that Mo- and S-doped TiO2 decorated over CNT, or CNT/Mo,S-codoped TiO2, may have high potential applications in photocatalysis and environmental protection with superior catalytic activity under visible-light illumination. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:302 / 311
页数:10
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