Interfacially Assembled Fluorescent Nanofilm for Ultra-Sensitive Formic Acid Detection via Hydrogen Bonding Affinity and Recognition

IF 4.3 3区 化学 Q2 POLYMER SCIENCE Macromolecular Rapid Communications Pub Date : 2025-02-17 DOI:10.1002/marc.202401048
Linxuan Huang, Xinxiang Gao, Xinyao Mao, Ishfaq Ullah, Zhijie Zhou, Ejaz Hussain, Yinghui Xiao, Haonan Peng, Yu Fang
{"title":"Interfacially Assembled Fluorescent Nanofilm for Ultra-Sensitive Formic Acid Detection via Hydrogen Bonding Affinity and Recognition","authors":"Linxuan Huang,&nbsp;Xinxiang Gao,&nbsp;Xinyao Mao,&nbsp;Ishfaq Ullah,&nbsp;Zhijie Zhou,&nbsp;Ejaz Hussain,&nbsp;Yinghui Xiao,&nbsp;Haonan Peng,&nbsp;Yu Fang","doi":"10.1002/marc.202401048","DOIUrl":null,"url":null,"abstract":"<p>High-performance film-based sensors are key innovations driving advancements in sensing technologies. An ultra-sensitive formic acid sensor based on a polymer fluorescent nanofilm synthesized via interfacial assembly using a tetraphenylethylene derivative functionalized with aldehyde and hydroxyl groups is reported. These groups promote imine bond formation and enhance selectivity. The nanofilm, prepared through dynamic condensation with 4,4′-diaminodiphenyl ether at the air-DMSO interface, exhibits excellent luminescence, flexibility, and tunable surface topography. Its bright fluorescence is primarily due to the aggregation-induced emission (AIE) property and hydrogen bonding interactions within the film structure. Imines serve as recognition sites for formic acid, where weak hydrogen bonding alters the electronic environment of the imine groups, blocking proton donors (─OH) and promoting non-radiative decay, leading to selective fluorescence quenching. The sensor achieves an ultra-low detection limit of 550 ppt, a rapid response time of 0.3 s, and excellent reversibility. It also demonstrates high selectivity for formic acid over other VOCs, making it suitable for real-time monitoring. Additionally, the nanofilm's multimodal sensing capabilities, including responses to HCl and NH<sub>3</sub>, highlight its potential for diverse environmental and industrial applications.</p>","PeriodicalId":205,"journal":{"name":"Macromolecular Rapid Communications","volume":"46 9","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecular Rapid Communications","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/marc.202401048","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

High-performance film-based sensors are key innovations driving advancements in sensing technologies. An ultra-sensitive formic acid sensor based on a polymer fluorescent nanofilm synthesized via interfacial assembly using a tetraphenylethylene derivative functionalized with aldehyde and hydroxyl groups is reported. These groups promote imine bond formation and enhance selectivity. The nanofilm, prepared through dynamic condensation with 4,4′-diaminodiphenyl ether at the air-DMSO interface, exhibits excellent luminescence, flexibility, and tunable surface topography. Its bright fluorescence is primarily due to the aggregation-induced emission (AIE) property and hydrogen bonding interactions within the film structure. Imines serve as recognition sites for formic acid, where weak hydrogen bonding alters the electronic environment of the imine groups, blocking proton donors (─OH) and promoting non-radiative decay, leading to selective fluorescence quenching. The sensor achieves an ultra-low detection limit of 550 ppt, a rapid response time of 0.3 s, and excellent reversibility. It also demonstrates high selectivity for formic acid over other VOCs, making it suitable for real-time monitoring. Additionally, the nanofilm's multimodal sensing capabilities, including responses to HCl and NH3, highlight its potential for diverse environmental and industrial applications.

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
基于氢键亲和和识别的超灵敏甲酸检测界面组装荧光纳米膜。
高性能薄膜传感器是推动传感技术进步的关键创新。本文报道了一种基于四苯基乙烯衍生物与醛和羟基功能化界面组装合成的聚合物荧光纳米膜的超灵敏甲酸传感器。这些基团促进亚胺键形成,提高选择性。通过与4,4′-二氨基二苯醚在空气- dmso界面上的动态缩合制备的纳米膜具有优异的发光性、柔韧性和可调的表面形貌。其明亮的荧光主要是由于聚集诱导发射(AIE)性质和薄膜结构内的氢键相互作用。亚胺是甲酸的识别位点,其中弱氢键改变了亚胺基的电子环境,阻断质子供体(OH)并促进非辐射衰变,导致选择性荧光猝灭。该传感器实现了550 ppt的超低检测限,0.3 s的快速响应时间,以及出色的可逆性。它对甲酸的选择性也高于其他VOCs,适合于实时监测。此外,纳米膜的多模态传感能力,包括对HCl和NH3的响应,突出了其在各种环境和工业应用中的潜力。
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 去求助
来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
期刊最新文献
Phase Transition Mechanism and Research Progress of LCST-Type Thermosensitive Hydrogels. Special Issue on Polymer Chemistry Research in Kyoto Institute of Polymer Science. Dynamic Polymers for Transient Electronics. Polysialic Acid Hydrogel for Reducing Foreign Body Reactions in Implanted Polyurethane Materials. Chemical Upcycling of Commodity Thermoset Polyurethane toward Multi-functional Materials based on Oxime-urethane Moiety.
×
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:604180095
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