2D montmorillonite-supported Ga-doped In-MOF composite for high-efficiency photocatalytic degradation of tetracycline

IF 2.8 4区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR
Xueying Ma, Guomin Yu, Yinghua Li, Hui Li, Hongfang Wang, Xu Jia, Tiebing Cui
{"title":"2D montmorillonite-supported Ga-doped In-MOF composite for high-efficiency photocatalytic degradation of tetracycline","authors":"Xueying Ma,&nbsp;Guomin Yu,&nbsp;Yinghua Li,&nbsp;Hui Li,&nbsp;Hongfang Wang,&nbsp;Xu Jia,&nbsp;Tiebing Cui","doi":"10.1007/s11243-025-00695-x","DOIUrl":null,"url":null,"abstract":"<div><p>To address the challenge of antibiotic residue remediation, this study employed a hydrothermal method to in-situ construct a bimetallic indium/gallium-based MIL-68 heterostructure on the surface of two-dimensional montmorillonite (MMT). By integrating metal node electronic structure regulation with interface engineering strategies, it provides a feasible approach to improve the low charge carrier separation efficiency in metal-organic framework (MOFs) materials. Experimental results demonstrate that when the MMT loading is 20%, the composite material exhibits obvious enhanced photocatalytic performance for the degradation of 40 mg/L tetracycline solution, with a degradation rate of up to 97% within 60 min using 10 mg of catalyst. This improvement is attributed to the synergistic effect of In/Ga bimetals and the interface charge transfer channels of the MMT 2D matrix, which together induce a Z-type charge carrier migration mechanism, enhancing the separation efficiency of photo-induced electron-hole pairs. After four cycles, the MIL-68(In/Ga)/MMT composite showed good cycling stability and demonstrated broad-spectrum degradation capability, achieving degradation rates of 99% and 79% for rhodamine B and methyl orange, respectively. This composite material shows good photocatalytic performance in dye degradation, providing new research insights for the field of photocatalytic degradation of pollutants.</p></div>","PeriodicalId":803,"journal":{"name":"Transition Metal Chemistry","volume":"51 1","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transition Metal Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11243-025-00695-x","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

To address the challenge of antibiotic residue remediation, this study employed a hydrothermal method to in-situ construct a bimetallic indium/gallium-based MIL-68 heterostructure on the surface of two-dimensional montmorillonite (MMT). By integrating metal node electronic structure regulation with interface engineering strategies, it provides a feasible approach to improve the low charge carrier separation efficiency in metal-organic framework (MOFs) materials. Experimental results demonstrate that when the MMT loading is 20%, the composite material exhibits obvious enhanced photocatalytic performance for the degradation of 40 mg/L tetracycline solution, with a degradation rate of up to 97% within 60 min using 10 mg of catalyst. This improvement is attributed to the synergistic effect of In/Ga bimetals and the interface charge transfer channels of the MMT 2D matrix, which together induce a Z-type charge carrier migration mechanism, enhancing the separation efficiency of photo-induced electron-hole pairs. After four cycles, the MIL-68(In/Ga)/MMT composite showed good cycling stability and demonstrated broad-spectrum degradation capability, achieving degradation rates of 99% and 79% for rhodamine B and methyl orange, respectively. This composite material shows good photocatalytic performance in dye degradation, providing new research insights for the field of photocatalytic degradation of pollutants.

二维蒙脱石负载的掺ga In-MOF复合材料用于四环素的高效光催化降解
为了解决抗生素残留修复的难题,本研究采用水热法在二维蒙脱土(MMT)表面原位构建了双金属铟/镓基MIL-68异质结构。将金属节点电子结构调控与界面工程策略相结合,为提高金属有机骨架(MOFs)材料的低载流子分离效率提供了一条可行的途径。实验结果表明,当MMT负载为20%时,复合材料对40 mg/L四环素溶液的光催化性能明显增强,在10 mg催化剂的作用下,60 min的降解率可达97%。这种改善是由于In/Ga双金属和MMT二维矩阵的界面电荷转移通道的协同作用,共同诱导了z型载流子迁移机制,提高了光致电子-空穴对的分离效率。经过4次循环,MIL-68(In/Ga)/MMT复合材料表现出良好的循环稳定性和广谱降解能力,对罗丹明B和甲基橙的降解率分别达到99%和79%。该复合材料在染料降解中表现出良好的光催化性能,为光催化降解污染物领域提供了新的研究思路。
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
Transition Metal Chemistry
Transition Metal Chemistry 化学-无机化学与核化学
CiteScore
3.60
自引率
0.00%
发文量
32
审稿时长
1.3 months
期刊介绍: Transition Metal Chemistry is an international journal designed to deal with all aspects of the subject embodied in the title: the preparation of transition metal-based molecular compounds of all kinds (including complexes of the Group 12 elements), their structural, physical, kinetic, catalytic and biological properties, their use in chemical synthesis as well as their application in the widest context, their role in naturally occurring systems etc. Manuscripts submitted to the journal should be of broad appeal to the readership and for this reason, papers which are confined to more specialised studies such as the measurement of solution phase equilibria or thermal decomposition studies, or papers which include extensive material on f-block elements, or papers dealing with non-molecular materials, will not normally be considered for publication. Work describing new ligands or coordination geometries must provide sufficient evidence for the confident assignment of structural formulae; this will usually take the form of one or more X-ray crystal structures.
×
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:604180095
Book学术官方微信
小红书