Facile Synthesis, Characterization, and Photocatalytic Performance of BiOF/BiFeO3 Hybrid Heterojunction for Benzylamine Coupling under Simulated Light Irradiation

Photochem Pub Date : 2023-03-21 DOI:10.3390/photochem3010012
Abdalla S. Abdelhamid, Reem H. Alzard, Lamia A. Siddig, Aya Elbahnasy, Duha Aljazmati, Zaina Kadoura, Hind Zeidane, Rufaida Elshikh, Ahmed Alzamly
{"title":"Facile Synthesis, Characterization, and Photocatalytic Performance of BiOF/BiFeO3 Hybrid Heterojunction for Benzylamine Coupling under Simulated Light Irradiation","authors":"Abdalla S. Abdelhamid, Reem H. Alzard, Lamia A. Siddig, Aya Elbahnasy, Duha Aljazmati, Zaina Kadoura, Hind Zeidane, Rufaida Elshikh, Ahmed Alzamly","doi":"10.3390/photochem3010012","DOIUrl":null,"url":null,"abstract":"Under simulated light irradiation, the aerobic oxidation of benzylamine to N,N-benzylidenebenzylamine was carried out as a model reaction to investigate the photocatalytic activity of a hydrothermally prepared composite based on BiOF and BiFeO3 materials. The prepared photocatalysts were characterized using several spectroscopic techniques, such as powder X-ray diffraction (PXRD), diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FTIR). Band gap analysis showed that the composite exhibits a band gap that lies in the UV region (3.5 eV). Nonetheless, pristine BiOF and BiFeO3 exhibited band gaps of 3.8 eV and 2.15 eV, respectively. N,N-benzylidenebenzylamine was selectively achieved with a high conversion yield of ~80% under atmospheric conditions in which the product was confirmed using 1H-NMR, 13C-NMR, and FTIR spectroscopic techniques. Various control experiments were conducted to further confirm the enhanced photocatalytic performance of the reported composite.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Photochem","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/photochem3010012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Under simulated light irradiation, the aerobic oxidation of benzylamine to N,N-benzylidenebenzylamine was carried out as a model reaction to investigate the photocatalytic activity of a hydrothermally prepared composite based on BiOF and BiFeO3 materials. The prepared photocatalysts were characterized using several spectroscopic techniques, such as powder X-ray diffraction (PXRD), diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FTIR). Band gap analysis showed that the composite exhibits a band gap that lies in the UV region (3.5 eV). Nonetheless, pristine BiOF and BiFeO3 exhibited band gaps of 3.8 eV and 2.15 eV, respectively. N,N-benzylidenebenzylamine was selectively achieved with a high conversion yield of ~80% under atmospheric conditions in which the product was confirmed using 1H-NMR, 13C-NMR, and FTIR spectroscopic techniques. Various control experiments were conducted to further confirm the enhanced photocatalytic performance of the reported composite.
模拟光照射下BiOF/BiFeO3杂化异质结苯胺偶联的合成、表征及光催化性能
在模拟光照射下,以好氧氧化法制备N,N-苄基苄基苄胺为模型反应,研究了水热法制备的BiOF和BiFeO3材料复合材料的光催化活性。采用粉末x射线衍射(PXRD)、漫反射光谱(DRS)、扫描电子显微镜(SEM)、能量色散x射线光谱(EDX)和傅里叶变换红外光谱(FTIR)等光谱技术对所制备的光催化剂进行了表征。带隙分析表明,复合材料的带隙位于紫外区(3.5 eV)。然而,原始BiOF和BiFeO3的带隙分别为3.8 eV和2.15 eV。在常压条件下选择性地合成了N,N-苄基二苄胺,转化率高达~80%,并用1H-NMR、13C-NMR和FTIR光谱技术对产物进行了证实。进行了各种对照实验,进一步证实了所报道的复合材料增强的光催化性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.60
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信