Microwave-assisted synthesis of biomass-derived N-doped carbon dots for metal ion sensing.

Carbon research.. Pub Date : 2025-01-01 Epub Date: 2025-06-22 DOI:10.1007/s44246-025-00215-7
Mehedi Hasan, Balachandran Baheerathan, Shrikanta Sutradhar, Ronak Shahbandinejad, Sudip Rakshit, Janusz Kozinski, Dongbing Li, Yulin Hu, Kang Kang
{"title":"Microwave-assisted synthesis of biomass-derived N-doped carbon dots for metal ion sensing.","authors":"Mehedi Hasan, Balachandran Baheerathan, Shrikanta Sutradhar, Ronak Shahbandinejad, Sudip Rakshit, Janusz Kozinski, Dongbing Li, Yulin Hu, Kang Kang","doi":"10.1007/s44246-025-00215-7","DOIUrl":null,"url":null,"abstract":"<p><p>Biomass-derived carbon dots (CDs) have gained significant research interest for environmental monitoring applications thanks to their cost-effectiveness and sustainability. Using eco-friendly biowastes as precursors for CDs production offers an alternative to expensive and unsustainable inorganic and chemically synthesized CDs. This study presents the findings regarding the successful synthesis of biomass-based nitrogen-doped carbon dots (N-CDs) via a rapid, cost-effective, and environmentally friendly microwave-assisted method. Carboxymethyl cellulose (CMC) and glycine were used as carbon precursors and nitrogen dopants for the first time. The N-CDs exhibited a moderately high quantum yield of 31.6 ± 1.5% with an optimal fluorescence excitation wavelength of 400 nm. FTIR, CHNS, and SEM-EDX analyses characterized the N-CDs' surface functional groups and elemental composition. The optical stability of the N-CDs was validated across varying pH levels and NaCl concentrations. The N-CDs displayed notable selectivity and sensitivity for Fe<sup>3</sup>⁺, Cu<sup>2</sup>⁺, and Hg<sup>2</sup>⁺ ions. The primary quenching mechanisms involve electrostatic interactions, π-π interactions, inner filter effects, and energy transfer. <i>Stern-Volmer</i> analysis revealed strong linear quenching for Fe<sup>3</sup>⁺, Cu<sup>2</sup>⁺, and Hg<sup>2</sup>⁺ ions within the 0-10 µM range concentrations, with detection limits (LOD) of 6.0 µM, 1.41 µM and 1.36 µM for Fe<sup>3</sup>⁺, Cu<sup>2</sup>⁺, and Hg<sup>2</sup>⁺, respectively. The fluorescence quenching for Fe<sup>3</sup>⁺ ions enhanced sensitivity at higher concentrations, while selectivity decreased at lower concentrations. These findings highlight the potential of these N-CDs as a cost-effective and sustainable tool for environmental monitoring, offering a promising approach to addressing critical water contamination issues.</p><p><strong>Graphical abstract: </strong></p>","PeriodicalId":520918,"journal":{"name":"Carbon research..","volume":"4 1","pages":"49"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12212424/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon research..","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s44246-025-00215-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/22 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Biomass-derived carbon dots (CDs) have gained significant research interest for environmental monitoring applications thanks to their cost-effectiveness and sustainability. Using eco-friendly biowastes as precursors for CDs production offers an alternative to expensive and unsustainable inorganic and chemically synthesized CDs. This study presents the findings regarding the successful synthesis of biomass-based nitrogen-doped carbon dots (N-CDs) via a rapid, cost-effective, and environmentally friendly microwave-assisted method. Carboxymethyl cellulose (CMC) and glycine were used as carbon precursors and nitrogen dopants for the first time. The N-CDs exhibited a moderately high quantum yield of 31.6 ± 1.5% with an optimal fluorescence excitation wavelength of 400 nm. FTIR, CHNS, and SEM-EDX analyses characterized the N-CDs' surface functional groups and elemental composition. The optical stability of the N-CDs was validated across varying pH levels and NaCl concentrations. The N-CDs displayed notable selectivity and sensitivity for Fe3⁺, Cu2⁺, and Hg2⁺ ions. The primary quenching mechanisms involve electrostatic interactions, π-π interactions, inner filter effects, and energy transfer. Stern-Volmer analysis revealed strong linear quenching for Fe3⁺, Cu2⁺, and Hg2⁺ ions within the 0-10 µM range concentrations, with detection limits (LOD) of 6.0 µM, 1.41 µM and 1.36 µM for Fe3⁺, Cu2⁺, and Hg2⁺, respectively. The fluorescence quenching for Fe3⁺ ions enhanced sensitivity at higher concentrations, while selectivity decreased at lower concentrations. These findings highlight the potential of these N-CDs as a cost-effective and sustainable tool for environmental monitoring, offering a promising approach to addressing critical water contamination issues.

Graphical abstract:

微波辅助合成生物质来源的金属离子传感n掺杂碳点。
由于其成本效益和可持续性,生物质衍生碳点(CDs)在环境监测应用中获得了重要的研究兴趣。使用生态友好的生物废物作为cd生产的前体,为昂贵且不可持续的无机和化学合成cd提供了另一种选择。本研究介绍了通过快速、经济、环保的微波辅助方法成功合成生物质基氮掺杂碳点(N-CDs)的研究结果。首次将羧甲基纤维素(CMC)和甘氨酸作为碳前驱体和氮掺杂剂。在最佳荧光激发波长为400 nm时,N-CDs的量子产率为31.6±1.5%。FTIR、CHNS和SEM-EDX分析表征了N-CDs的表面官能团和元素组成。在不同的pH和NaCl浓度下验证了N-CDs的光学稳定性。N-CDs对Fe3 +、Cu2 +和Hg2 +表现出显著的选择性和敏感性。主要的猝灭机制包括静电相互作用、π-π相互作用、内部过滤效应和能量转移。Stern-Volmer分析显示,Fe3 +、Cu2 +和Hg2 +在0-10µM浓度范围内呈强线性猝灭,Fe3 +、Cu2 +和Hg2 +的检出限(LOD)分别为6.0µM、1.41µM和1.36µM。Fe3 +的荧光猝灭在较高浓度下增强了灵敏度,而在较低浓度下选择性降低。这些发现突出了这些N-CDs作为一种具有成本效益和可持续的环境监测工具的潜力,为解决关键的水污染问题提供了一种有希望的方法。图形化的简介:
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
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:604180095
Book学术官方微信