Ag2CrO4/ZnO复合光催化剂的制备及光催化性能研究

黄凤萍1, 李春花1*, 辛萌1, 刘博学1, 周鑫敏1, 丁力2

化工新型材料 ›› 2020, Vol. 48 ›› Issue (9) : 105 -110.

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化工新型材料 ›› 2020, Vol. 48 ›› Issue (9) : 105-110. DOI: 10.19817/j.cnki.issn 1006-3536.2020.09.023
新材料与新技术

Ag2CrO4/ZnO复合光催化剂的制备及光催化性能研究

    黄凤萍1, 李春花1*, 辛萌1, 刘博学1, 周鑫敏1, 丁力2
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Preparation and photocatalytic performance of Ag2CrO4/ZnO composite photocatalyst

  • Huang Fengping1, Li Chunhua1, Xin Meng1, Liu Boxue1, Zhou Xinmin1, Ding Li2
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摘要

采用沉淀法制备具有高催化性能的Ag2CrO4/ZnO复合光催化剂。通过X射线衍射仪、扫描电子显微镜、透射电子显微镜、X射线光电子能谱仪、紫外-可见分光光度计等测试手段对催化剂的结构和形貌进行了表征。利用可见光催化降解有机染料罗丹明B(RhB),考察复合光催化剂的光催化性能及稳定性。结果表明:Ag2CrO4均匀地附着在ZnO纳米棒上,当Ag2CrO4与ZnO摩尔比为1:2时催化剂表现出最优的光催化性能,90min内对RhB的降解率可达86%。经过5次循环实验,复合光催化剂对RhB的降解率仍可达82%,而纯Ag2CrO4降解率仅为24%。Ag2CrO4/ZnO复合光催化剂表现出的优异光催化活性及稳定性,主要由于Ag2CrO4和ZnO之间稳定地负载,能有效分离光生电子和空穴,降低了活性位点,提高了催化剂的光催化活性和稳定性。

Abstract

Ag2CrO4/ZnO composite photocatalyst with high catalytic performance was prepared by precipitation method.The structure and morphology of the catalyst were characterized by XRD,SEM,TEM,XPS and UV-Vis.The photocatalytic performance and stability of the photocatalyst were investigated by visible light photocatalytic degradation of organic dyes (RhB).The results shown that Ag2CrO4 was uniformly attached to ZnO nanorods.When the composite molar ratio of Ag2CrO4 to ZnO is 1:2,the catalyst exhibits the best photocatalytic performance,and the degradation rate of RhB can reach 86% within 90min.After 5 cycles of experiments,the degradation rate of RhB was still up to 82%,while pure Ag2CrO4 was only 24%.The research shown that the excellent photocatalytic activity and stability of Ag2CrO4/ZnO were mainly due to the stable loading between Ag2CrO4 and ZnO,which can effectively separate photogenerated electrons and holes,reduced the active sites and improved the photocatalytic activity and stability of the catalyst.

关键词

沉淀法 / 光催化性能 / 氧化锌 / 铬酸银 / 复合光催化剂

Key words

precipitation method / photocatalytic performance / ZnO / Ag2CrO4 / composite photocatalyst

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Ag2CrO4/ZnO复合光催化剂的制备及光催化性能研究[J]. 化工新型材料, 2020, 48(9): 105-110 DOI:10.19817/j.cnki.issn 1006-3536.2020.09.023

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基金资助

“十三五”国家重点研发计划(2016YFC0700904)

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