A comprehensive study on electrochemical and photocatalytic activity of SnO2-ZnO/clinoptilolite nanoparticles

被引:95
作者
Derikvandi, Hadis [1 ,2 ]
Nezamzadeh-Ejhieh, Alireza [1 ,2 ,3 ]
机构
[1] Islamic Azad Univ, Shahreza Branch, Dept Chem, POB 311-86145, Shahreza, Isfahan, Iran
[2] Islamic Azad Univ, Shahreza Branch, Young Researchers & Elite Club, Shahreza, Iran
[3] Islamic Azad Univ, Shahreza Branch, RCRC, Esfahan, Iran
关键词
Clinoptilolite nanoparticles; Calcination; ZnO-SnO2; Heterogeneous photocatalysis; DOPED ZNO NANOSTRUCTURES; PHOTO-FENTON PROCESS; DIFFERENT MORPHOLOGIES; AQUEOUS-SOLUTIONS; DEGRADATION; PHOTODEGRADATION; SNO2; METRONIDAZOLE; COMPOSITE; PHARMACEUTICALS;
D O I
10.1016/j.molcata.2016.11.011
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
Mechanically prepared clinoptilolite nanoparticles (NC) and coupling were used for increasing photo catalytic activity of ZnO and SnO2. The raw and modified catalysts were characterized by XRD, FTIR, SEM-EDX, X-ray mapping, DRS, electrochemical impedance spectroscopy (EIS) and BET techniques. The calcined catalysts at 600 degrees C for 2 h showed the best photocatalytic activity in metronidazole (MZ) aqueous solution. Based on the EIS results, this catalyst has the best charge transfer efficiency with respect to other catalysts calcined at lower and higher temperatures. This caused to lower e/h recombination and hence higher photodegradation activity. The mole ratio of ZnO/SnO2 affects the degradation activity of the catalysts so the best activities were obtained for the ZnO2.4-SnO2(2.0)/NC (ZS-NC) and ZnO3.3-SnO2(2.0)/NC (Z(2)S-NC) catalysts at pH 3. Cyclic voltammograms of the modified carbon paste electrodes with ZS-NC and Z(2)S-NC showed increased peak current in phosphate buffer which confirm formation of the ZnO and SnO2 semiconductors inside NC. Also, peak current dependence of the modified electrode to MZ concentration confirmed that the degradation extent of MZ can be estimated by electrochemical methods. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:158 / 169
页数:12
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