Photocatalytic degradation of organic contaminants under solar light using carbon dot/titanium dioxide nanohybrid, obtained through a facile approach

被引:70
作者
Hazarika, Deepshikha [1 ]
Karak, Niranjan [1 ]
机构
[1] Tezpur Univ, Dept Chem Sci, Ctr Polymer Sci & Technol, Adv Polymer & Nanomat Lab, Tezpur 784028, Assam, India
关键词
Carbon dot; Nanohybrid; Carbon dot/titanium dioxide; Photocatalyst; Degradation; VISIBLE-LIGHT; QUANTUM DOTS; GREEN SYNTHESIS; NANOCOMPOSITES; EFFICIENT; NANODOTS; TIO2; NANOPARTICLES; IRRADIATION; COMPOSITES;
D O I
10.1016/j.apsusc.2016.03.165
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
In the present study, a novel, simple and green method was developed to synthesize highly luminescent nitrogen containing carbon dot (CD) using carbon resources like bio-based citric acid and glycerol in the presence of cost free cow urine. The as-synthesized CD showed exciting wavelength dependent down and up-conversion flourescence properties. To utilize the advantage of up-conversion flourescence, a nanohybrid (CD@TiO2) was synthesized from the above carbon resources and titanium butoxide through a facile one pot single step hydrothermal protocol. Nanomaterials like bare TiO2 and nanohybrid of TiO2 in presence of CD (CD/TiO2) were also synthesized for comparison purpose. The optical properties and structural characteristics of the prepared CD, bare TiO2, CD@TiO2 and CD/TiO2 were examined by Fourier transform infrared (FTIR), UV-vis and fluorescence spectroscopic, scanning electron microscopic (SEM), transmission electron microscopic (TEM) and X-ray diffraction (XRD) studies. The elemental compositions of bare CD and CD@TiO2 nanohybrid were obtained from EDX analyses. The poor crystalline nature and narrow distribution of spherical CD and anatase form of TiO2 were confirmed from XRD and TEM studies. Amongst the studied nanomaterials, CD@TiO2 exhibited the most promising photocatalytic degradation of organic pollutants like benzene and phenol as well as an anthrogenic pesticide under sunlight. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:276 / 285
页数:10
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