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

IF 5.062
Hadis Derikvandi , Alireza Nezamzadeh-Ejhieh
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引用次数: 74

Abstract

Mechanically prepared clinoptilolite nanoparticles (NC) and coupling were used for increasing photocatalytic 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 °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 (Z2S-NC) catalysts at pH 3. Cyclic voltammograms of the modified carbon paste electrodes with ZS-NC and Z2S-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.

Abstract Image

SnO2-ZnO/斜沸石纳米颗粒电化学和光催化活性的综合研究
采用机械制备的斜沸石纳米颗粒(NC)及其偶联剂提高ZnO和SnO2的光催化活性。采用XRD、FTIR、SEM-EDX、x射线作图、DRS、电化学阻抗谱(EIS)和BET等技术对原料和改性催化剂进行了表征。在600℃下焙烧2 h的催化剂在甲硝唑水溶液中表现出最佳的光催化活性。根据EIS结果,该催化剂在较低和较高温度下煅烧的催化剂中具有最佳的电荷转移效率。这降低了e/h复合,从而提高了光降解活性。ZnO/SnO2的摩尔比影响催化剂的降解活性,因此在pH为3时,ZnO2.4-SnO2(2.0)/NC (ZS-NC)和ZnO3.3-SnO2(2.0)/NC (Z2S-NC)催化剂的降解活性最好。ZS-NC和Z2S-NC改性碳浆电极的循环伏安图显示,磷酸盐缓冲液中的峰值电流增加,证实了ZnO和SnO2半导体在NC内的形成。此外,改性电极的峰值电流对MZ浓度的依赖性也证实了MZ的降解程度可以通过电化学方法来估计。
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审稿时长
2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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