Two-dimensional MXene@ZIF-8 hybrid-derived TiO2/TiN@N-C heterostructure as an emerging material for electrochemical sensing

IF 5.5 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Yanhong Zeng, Yong Tang, Mei Liu, Can Wu
{"title":"Two-dimensional MXene@ZIF-8 hybrid-derived TiO2/TiN@N-C heterostructure as an emerging material for electrochemical sensing","authors":"Yanhong Zeng, Yong Tang, Mei Liu, Can Wu","doi":"10.1007/s42823-024-00726-0","DOIUrl":null,"url":null,"abstract":"<p>Herein, facile room-temperature self-assembly and high-temperature pyrolysis strategy was successively conducted for in situ synthesizing novel TiO<sub>2</sub>/TiN@N-C heterostructure by using typical sandwich-like precursors (MXene/ZIF-8). Zero-dimensional (0D) TiO<sub>2</sub>, TiN and N-doped carbon nanoparticles were in situ formed and randomly anchored on the two-dimensional (2D) N-doped carbon substrate surface, making TiO<sub>2</sub>/TiN@N-C exhibit unique 0D/2D heterostructure. Relative to the extensively studied ZIF-8-derived N-doped carbon nanoparticles, TiO<sub>2</sub>/TiN@N-C heterostructure displayed greatly boosted electrochemical active specific surface. Benefiting from the enhanced electrochemical property of TiO<sub>2</sub>/TiN@N-C heterostructure, remarkable signal enhancement effect was achieved in terms of the oxidation of multiple hazardous substances, including clozapine, sunset yellow and benomyl. As a result, a novel electrochemical platform was constructed, the linear detection range were 10–1000 nM, 2.5–1250 nM, 10–1000 nM while the detection limits were evaluated to be 3.5 nM, 1.2 nM, 4.5 nM for clozapine, sunset yellow and benomyl, respectively. Besides, the practicability of the newly developed electrochemical method was verified by assessing the content of clozapine, sunset yellow and benomyl in real food samples.</p>","PeriodicalId":506,"journal":{"name":"Carbon Letters","volume":null,"pages":null},"PeriodicalIF":5.5000,"publicationDate":"2024-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1007/s42823-024-00726-0","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Herein, facile room-temperature self-assembly and high-temperature pyrolysis strategy was successively conducted for in situ synthesizing novel TiO2/TiN@N-C heterostructure by using typical sandwich-like precursors (MXene/ZIF-8). Zero-dimensional (0D) TiO2, TiN and N-doped carbon nanoparticles were in situ formed and randomly anchored on the two-dimensional (2D) N-doped carbon substrate surface, making TiO2/TiN@N-C exhibit unique 0D/2D heterostructure. Relative to the extensively studied ZIF-8-derived N-doped carbon nanoparticles, TiO2/TiN@N-C heterostructure displayed greatly boosted electrochemical active specific surface. Benefiting from the enhanced electrochemical property of TiO2/TiN@N-C heterostructure, remarkable signal enhancement effect was achieved in terms of the oxidation of multiple hazardous substances, including clozapine, sunset yellow and benomyl. As a result, a novel electrochemical platform was constructed, the linear detection range were 10–1000 nM, 2.5–1250 nM, 10–1000 nM while the detection limits were evaluated to be 3.5 nM, 1.2 nM, 4.5 nM for clozapine, sunset yellow and benomyl, respectively. Besides, the practicability of the newly developed electrochemical method was verified by assessing the content of clozapine, sunset yellow and benomyl in real food samples.

Abstract Image

作为新兴电化学传感材料的二维 MXene@ZIF-8 杂化 TiO2/TiN@N-C 异质结构
本文采用典型的三明治状前驱体(MXene/ZIF-8),先后进行了简便的室温自组装和高温热解策略,原位合成了新型TiO2/TiN@N-C异质结构。零维(0D)TiO2、TiN 和掺杂 N 的碳纳米颗粒原位形成并随机锚定在二维(2D)掺杂 N 的碳基底表面,使 TiO2/TiN@N-C 呈现出独特的 0D/2D 异质结构。与广泛研究的 ZIF-8 衍生掺杂氮的碳纳米粒子相比,TiO2/TiN@N-C 异质结构大大提高了电化学活性比表面。得益于 TiO2/TiN@N-C 异质结构电化学性能的增强,在氧化多种有害物质(包括氯氮平、日落黄和苯菌灵)方面取得了显著的信号增强效果。结果表明,构建的新型电化学平台对氯氮平、日落黄和苯菌灵的线性检测范围分别为 10-1000 nM、2.5-1250 nM 和 10-1000 nM,检测限分别为 3.5 nM、1.2 nM 和 4.5 nM。此外,通过评估实际食品样品中氯氮平、日落黄和苯菌灵的含量,验证了新开发的电化学方法的实用性。
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
Carbon Letters
Carbon Letters CHEMISTRY, MULTIDISCIPLINARY-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
7.30
自引率
20.00%
发文量
118
期刊介绍: Carbon Letters aims to be a comprehensive journal with complete coverage of carbon materials and carbon-rich molecules. These materials range from, but are not limited to, diamond and graphite through chars, semicokes, mesophase substances, carbon fibers, carbon nanotubes, graphenes, carbon blacks, activated carbons, pyrolytic carbons, glass-like carbons, etc. Papers on the secondary production of new carbon and composite materials from the above mentioned various carbons are within the scope of the journal. Papers on organic substances, including coals, will be considered only if the research has close relation to the resulting carbon materials. Carbon Letters also seeks to keep abreast of new developments in their specialist fields and to unite in finding alternative energy solutions to current issues such as the greenhouse effect and the depletion of the ozone layer. The renewable energy basics, energy storage and conversion, solar energy, wind energy, water energy, nuclear energy, biomass energy, hydrogen production technology, and other clean energy technologies are also within the scope of the journal. Carbon Letters invites original reports of fundamental research in all branches of the theory and practice of carbon science and technology.
×
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