Morphology controlled hydrothermal synthesis and photocatalytic properties of ZnFe2O4 nanostructures

被引:104
|
作者
Dhiman, Manisha [1 ]
Sharma, Rimi [1 ]
Kumar, Vinod [2 ]
Singhal, Sonal [1 ]
机构
[1] Panjab Univ, Dept Chem, Chandigarh 160014, India
[2] Icon Analyt Equipment Pvt Ltd, Bombay, Maharashtra, India
关键词
Morphology based synthesis; Hydrothermal route; Photo-Fenton catalysis; Surface area; Band gap; MAGNETIC-PROPERTIES; ASSISTED SYNTHESIS; CATALYTIC-ACTIVITY; FERRITE; NI; MN; MICROSPHERES; DEGRADATION; NANOSPHERES; NANOCRYSTAL;
D O I
10.1016/j.ceramint.2016.04.115
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The present work is focused on studying morphology dependent catalysis of spinel ZnFe2O4 nanostructures. Different morphologies i.e. porous nanorods, nanoparticles, nanoflowers and hollow micro spheres were designed hydrothermally. The as prepared nanomaterials were characterized using Fourier Transform Infra-Red (FTIR), field emission scanning electron microscopy (FE-SEM), high resolution transmission electron microscopy (HR-TEM), powder X-ray diffraction (XRD), vibrating sample magnetometer (VSM), Brunauer-Emmett-Teller (BET) technique and UV-visible spectrophotometer. The results confirmed formation of desired morphologies of cubic spinel ZnFe2O4 with high surface areas (92-138 m(2)/g) and narrow band gaps (1.76-1.97 eV). It suggested the use of ZnFe2O4 nanostructures as potential visible light photocatalysts. Therefore, the application of synthesized ZnFe2O4 nanostructures was studied in photo-Fenton degradation of dyes. The results indicated shape dependent relationship with photocatalytic activity as the degradation of dyes followed the order porous nanorods > nanoparticles > nanoflowers > hollow microspheres. The role of main active species in the reaction i.e. (OH)-O-center dot was also confirmed. All the materials exhibited stability and magnetic separability hence could act as potential photo-Fenton catalysts for wastewater treatment. (C) 2016 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:12594 / 12605
页数:12
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