构建 ZnCo2O4/Ag3PO4 复合光催化剂以提高光催化性能

IF 1.5 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Micro & Nano Letters Pub Date : 2024-09-23 DOI:10.1049/mna2.12202
Jiayi Liu, Jiafeng Hu, Hao Hu, Xiaotao Zhou, Qiwei Wang, Weizhi Wei, Wenhui Liu
{"title":"构建 ZnCo2O4/Ag3PO4 复合光催化剂以提高光催化性能","authors":"Jiayi Liu,&nbsp;Jiafeng Hu,&nbsp;Hao Hu,&nbsp;Xiaotao Zhou,&nbsp;Qiwei Wang,&nbsp;Weizhi Wei,&nbsp;Wenhui Liu","doi":"10.1049/mna2.12202","DOIUrl":null,"url":null,"abstract":"<p>In this study, ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> composite catalyst was prepared by the precipitation method, and their performance in the photocatalytic degradation of methyl orange (MO) was studied. The catalysts were characterized by scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, selected area electron diffraction, X-ray photoelectron spectroscopy, and UV-Vis diffuse reflectance spectroscopy. The results indicate that the 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> composite system has good photocatalytic activity in the degradation of methyl orange. Under simulated sunlight conditions, the degradation rate can reach 94% after 30 min. The maximum reaction rate constant of 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> was 0.05301 min<sup>−1</sup>, which is 3 times and 52 times the rate constant of pure Ag<sub>3</sub>PO<sub>4</sub> and pure ZnCo<sub>2</sub>O<sub>4</sub>, respectively. In catalyst recycling experiments, 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> still degraded methyl orange at a rate of 84.4% after three cycles. Trapping experiments showed that holes and superoxide radicals mostly contributed to the photocatalytic degradation of methyl orange by the catalyst, while hydroxyl radicals played a partial role. The energy level structure of ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> is conducive to the effective separation of photogenerated electrons and holes, improving the lifespan of photogenerated charges. In the investigated catalyst series, 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> demonstrated the best photocatalytic performance.</p>","PeriodicalId":18398,"journal":{"name":"Micro & Nano Letters","volume":"19 5","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1049/mna2.12202","citationCount":"0","resultStr":"{\"title\":\"Construction of ZnCo2O4/Ag3PO4 composite photocatalyst for enhanced photocatalytic performance\",\"authors\":\"Jiayi Liu,&nbsp;Jiafeng Hu,&nbsp;Hao Hu,&nbsp;Xiaotao Zhou,&nbsp;Qiwei Wang,&nbsp;Weizhi Wei,&nbsp;Wenhui Liu\",\"doi\":\"10.1049/mna2.12202\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In this study, ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> composite catalyst was prepared by the precipitation method, and their performance in the photocatalytic degradation of methyl orange (MO) was studied. The catalysts were characterized by scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, selected area electron diffraction, X-ray photoelectron spectroscopy, and UV-Vis diffuse reflectance spectroscopy. The results indicate that the 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> composite system has good photocatalytic activity in the degradation of methyl orange. Under simulated sunlight conditions, the degradation rate can reach 94% after 30 min. The maximum reaction rate constant of 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> was 0.05301 min<sup>−1</sup>, which is 3 times and 52 times the rate constant of pure Ag<sub>3</sub>PO<sub>4</sub> and pure ZnCo<sub>2</sub>O<sub>4</sub>, respectively. In catalyst recycling experiments, 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> still degraded methyl orange at a rate of 84.4% after three cycles. Trapping experiments showed that holes and superoxide radicals mostly contributed to the photocatalytic degradation of methyl orange by the catalyst, while hydroxyl radicals played a partial role. The energy level structure of ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> is conducive to the effective separation of photogenerated electrons and holes, improving the lifespan of photogenerated charges. In the investigated catalyst series, 0.1 ZnCo<sub>2</sub>O<sub>4</sub>/Ag<sub>3</sub>PO<sub>4</sub> demonstrated the best photocatalytic performance.</p>\",\"PeriodicalId\":18398,\"journal\":{\"name\":\"Micro & Nano Letters\",\"volume\":\"19 5\",\"pages\":\"\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1049/mna2.12202\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Micro & Nano Letters\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1049/mna2.12202\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Micro & Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1049/mna2.12202","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

本研究采用沉淀法制备了 ZnCo2O4/Ag3PO4 复合催化剂,并研究了其在光催化降解甲基橙 (MO) 中的性能。采用扫描电子显微镜、高分辨透射电子显微镜、X 射线衍射、能量色散 X 射线光谱、选区电子衍射、X 射线光电子能谱和紫外可见光漫反射光谱对催化剂进行了表征。结果表明,0.1 ZnCo2O4/Ag3PO4 复合体系在降解甲基橙方面具有良好的光催化活性。在模拟日光条件下,30 分钟后降解率可达 94%。0.1 ZnCo2O4/Ag3PO4 的最大反应速率常数为 0.05301 min-1,分别是纯 Ag3PO4 和纯 ZnCo2O4 的 3 倍和 52 倍。在催化剂循环实验中,0.1 ZnCo2O4/Ag3PO4 经过三个循环后,甲基橙的降解率仍高达 84.4%。捕集实验表明,空穴和超氧自由基是催化剂光催化降解甲基橙的主要成分,而羟自由基则起了部分作用。ZnCo2O4/Ag3PO4 的能级结构有利于光生电子和空穴的有效分离,提高了光生电荷的寿命。在所研究的催化剂系列中,0.1 ZnCo2O4/Ag3PO4 的光催化性能最好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Construction of ZnCo2O4/Ag3PO4 composite photocatalyst for enhanced photocatalytic performance

In this study, ZnCo2O4/Ag3PO4 composite catalyst was prepared by the precipitation method, and their performance in the photocatalytic degradation of methyl orange (MO) was studied. The catalysts were characterized by scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, selected area electron diffraction, X-ray photoelectron spectroscopy, and UV-Vis diffuse reflectance spectroscopy. The results indicate that the 0.1 ZnCo2O4/Ag3PO4 composite system has good photocatalytic activity in the degradation of methyl orange. Under simulated sunlight conditions, the degradation rate can reach 94% after 30 min. The maximum reaction rate constant of 0.1 ZnCo2O4/Ag3PO4 was 0.05301 min−1, which is 3 times and 52 times the rate constant of pure Ag3PO4 and pure ZnCo2O4, respectively. In catalyst recycling experiments, 0.1 ZnCo2O4/Ag3PO4 still degraded methyl orange at a rate of 84.4% after three cycles. Trapping experiments showed that holes and superoxide radicals mostly contributed to the photocatalytic degradation of methyl orange by the catalyst, while hydroxyl radicals played a partial role. The energy level structure of ZnCo2O4/Ag3PO4 is conducive to the effective separation of photogenerated electrons and holes, improving the lifespan of photogenerated charges. In the investigated catalyst series, 0.1 ZnCo2O4/Ag3PO4 demonstrated the best photocatalytic performance.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Micro & Nano Letters
Micro & Nano Letters 工程技术-材料科学:综合
CiteScore
3.30
自引率
0.00%
发文量
58
审稿时长
2.8 months
期刊介绍: Micro & Nano Letters offers express online publication of short research papers containing the latest advances in miniature and ultraminiature structures and systems. With an average of six weeks to decision, and publication online in advance of each issue, Micro & Nano Letters offers a rapid route for the international dissemination of high quality research findings from both the micro and nano communities. Scope Micro & Nano Letters offers express online publication of short research papers containing the latest advances in micro and nano-scale science, engineering and technology, with at least one dimension ranging from micrometers to nanometers. Micro & Nano Letters offers readers high-quality original research from both the micro and nano communities, and the materials and devices communities. Bridging this gap between materials science and micro and nano-scale devices, Micro & Nano Letters addresses issues in the disciplines of engineering, physical, chemical, and biological science. It places particular emphasis on cross-disciplinary activities and applications. Typical topics include: Micro and nanostructures for the device communities MEMS and NEMS Modelling, simulation and realisation of micro and nanoscale structures, devices and systems, with comparisons to experimental data Synthesis and processing Micro and nano-photonics Molecular machines, circuits and self-assembly Organic and inorganic micro and nanostructures Micro and nano-fluidics
期刊最新文献
Catalytic oxidation of CO over CuO@TiO2 catalyst: The relationship between activity and adsorption performance Anticancer effect of surface functionalized nano titanium dioxide with 5-fluorouracil on oral cancer cell line—An in vitro study Green synthesis of cerium oxide nanoparticles via Linum usitatissimum seeds extract and assessment of its biological effects Graphene nanoribbon FET technology-based OTA for optimizing fast and energy-efficient electronics for IoT application: Next-generation circuit design Construction of ZnCo2O4/Ag3PO4 composite photocatalyst for enhanced photocatalytic performance
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1